dbSNP Short Genetic Variations
Welcome to the Reference SNP (rs) Report
All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.
Reference SNP (rs) Report
This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.
rs6695710
Current Build 156
Released September 21, 2022
- Organism
- Homo sapiens
- Position
-
chr1:17664557 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
- Alleles
- C>A / C>G / C>T
- Variation Type
- SNV Single Nucleotide Variation
- Frequency
-
T=0.000144 (38/264690, TOPMED)T=0.000057 (11/192918, ALFA)T=0.000107 (15/140228, GnomAD) (+ 6 more)
- Clinical Significance
- Not Reported in ClinVar
- Gene : Consequence
- ARHGEF10L : Missense Variant
- Publications
- 0 citations
- Genomic View
- See rs on genome
ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.
Release Version: 20230706150541
| Population | Group | Sample Size | Ref Allele | Alt Allele |
|---|---|---|---|---|
| Total | Global | 208962 | C=0.999933 | T=0.000067 |
| European | Sub | 176358 | C=0.999955 | T=0.000045 |
| African | Sub | 10032 | C=0.99960 | T=0.00040 |
| African Others | Sub | 358 | C=1.000 | T=0.000 |
| African American | Sub | 9674 | C=0.9996 | T=0.0004 |
| Asian | Sub | 3414 | C=1.0000 | T=0.0000 |
| East Asian | Sub | 2728 | C=1.0000 | T=0.0000 |
| Other Asian | Sub | 686 | C=1.000 | T=0.000 |
| Latin American 1 | Sub | 798 | C=1.000 | T=0.000 |
| Latin American 2 | Sub | 1002 | C=1.0000 | T=0.0000 |
| South Asian | Sub | 296 | C=1.000 | T=0.000 |
| Other | Sub | 17062 | C=0.99988 | T=0.00012 |
Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").
Download| Study | Population | Group | Sample Size | Ref Allele | Alt Allele |
|---|---|---|---|---|---|
| TopMed | Global | Study-wide | 264690 | C=0.999856 | T=0.000144 |
| Allele Frequency Aggregator | Total | Global | 192918 | C=0.999943 | T=0.000057 |
| Allele Frequency Aggregator | European | Sub | 166540 | C=0.999958 | T=0.000042 |
| Allele Frequency Aggregator | Other | Sub | 15650 | C=0.99987 | T=0.00013 |
| Allele Frequency Aggregator | African | Sub | 5218 | C=0.9996 | T=0.0004 |
| Allele Frequency Aggregator | Asian | Sub | 3414 | C=1.0000 | T=0.0000 |
| Allele Frequency Aggregator | Latin American 2 | Sub | 1002 | C=1.0000 | T=0.0000 |
| Allele Frequency Aggregator | Latin American 1 | Sub | 798 | C=1.000 | T=0.000 |
| Allele Frequency Aggregator | South Asian | Sub | 296 | C=1.000 | T=0.000 |
| gnomAD - Genomes | Global | Study-wide | 140228 | C=0.999893 | T=0.000107 |
| gnomAD - Genomes | European | Sub | 75950 | C=1.00000 | T=0.00000 |
| gnomAD - Genomes | African | Sub | 42016 | C=0.99967 | T=0.00033 |
| gnomAD - Genomes | American | Sub | 13660 | C=0.99993 | T=0.00007 |
| gnomAD - Genomes | Ashkenazi Jewish | Sub | 3320 | C=1.0000 | T=0.0000 |
| gnomAD - Genomes | East Asian | Sub | 3128 | C=1.0000 | T=0.0000 |
| gnomAD - Genomes | Other | Sub | 2154 | C=1.0000 | T=0.0000 |
| The PAGE Study | Global | Study-wide | 78646 | C=0.99978 | T=0.00022 |
| The PAGE Study | AfricanAmerican | Sub | 32496 | C=0.99966 | T=0.00034 |
| The PAGE Study | Mexican | Sub | 10804 | C=0.99972 | T=0.00028 |
| The PAGE Study | Asian | Sub | 8310 | C=1.0000 | T=0.0000 |
| The PAGE Study | PuertoRican | Sub | 7916 | C=0.9999 | T=0.0001 |
| The PAGE Study | NativeHawaiian | Sub | 4524 | C=1.0000 | T=0.0000 |
| The PAGE Study | Cuban | Sub | 4228 | C=0.9995 | T=0.0005 |
| The PAGE Study | Dominican | Sub | 3824 | C=1.0000 | T=0.0000 |
| The PAGE Study | CentralAmerican | Sub | 2450 | C=1.0000 | T=0.0000 |
| The PAGE Study | SouthAmerican | Sub | 1982 | C=1.0000 | T=0.0000 |
| The PAGE Study | NativeAmerican | Sub | 1260 | C=1.0000 | T=0.0000 |
| The PAGE Study | SouthAsian | Sub | 852 | C=1.000 | T=0.000 |
| 14KJPN | JAPANESE | Study-wide | 28258 | C=0.99996 | T=0.00004 |
| 1000Genomes_30x | Global | Study-wide | 6404 | C=0.9998 | T=0.0002 |
| 1000Genomes_30x | African | Sub | 1786 | C=0.9994 | T=0.0006 |
| 1000Genomes_30x | Europe | Sub | 1266 | C=1.0000 | T=0.0000 |
| 1000Genomes_30x | South Asian | Sub | 1202 | C=1.0000 | T=0.0000 |
| 1000Genomes_30x | East Asian | Sub | 1170 | C=1.0000 | T=0.0000 |
| 1000Genomes_30x | American | Sub | 980 | C=1.000 | T=0.000 |
| KOREAN population from KRGDB | KOREAN | Study-wide | 2930 | C=0.0000 | A=0.0000, G=0.0000 |
Help
Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.
Genomic Placements
| Sequence name | Change |
|---|---|
| GRCh38.p14 chr 1 | NC_000001.11:g.17664557C>A |
| GRCh38.p14 chr 1 | NC_000001.11:g.17664557C>G |
| GRCh38.p14 chr 1 | NC_000001.11:g.17664557C>T |
| GRCh37.p13 chr 1 | NC_000001.10:g.17991052T>C |
| GRCh37.p13 chr 1 | NC_000001.10:g.17991052T>A |
| GRCh37.p13 chr 1 | NC_000001.10:g.17991052T>G |
| ARHGEF10L RefSeqGene | NG_050860.1:g.149361C>A |
| ARHGEF10L RefSeqGene | NG_050860.1:g.149361C>G |
| ARHGEF10L RefSeqGene | NG_050860.1:g.149361C>T |
Gene: ARHGEF10L, Rho guanine nucleotide exchange factor 10 like
(plus strand)
| Molecule type | Change | Amino acid[Codon] | SO Term |
|---|---|---|---|
| ARHGEF10L transcript variant 2 | NM_001011722.2:c.2854C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform 2 | NP_001011722.2:p.Arg952= | R (Arg) > R (Arg) | Synonymous Variant |
| ARHGEF10L transcript variant 2 | NM_001011722.2:c.2854C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform 2 | NP_001011722.2:p.Arg952Gly | R (Arg) > G (Gly) | Missense Variant |
| ARHGEF10L transcript variant 2 | NM_001011722.2:c.2854C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform 2 | NP_001011722.2:p.Arg952Trp | R (Arg) > W (Trp) | Missense Variant |
| ARHGEF10L transcript variant 3 | NM_001319837.1:c.2839C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform 3 | NP_001306766.1:p.Arg947= | R (Arg) > R (Arg) | Synonymous Variant |
| ARHGEF10L transcript variant 3 | NM_001319837.1:c.2839C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform 3 | NP_001306766.1:p.Arg947Gly | R (Arg) > G (Gly) | Missense Variant |
| ARHGEF10L transcript variant 3 | NM_001319837.1:c.2839C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform 3 | NP_001306766.1:p.Arg947Trp | R (Arg) > W (Trp) | Missense Variant |
| ARHGEF10L transcript variant 4 | NM_001319838.1:c.2080C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform 4 | NP_001306767.1:p.Arg694= | R (Arg) > R (Arg) | Synonymous Variant |
| ARHGEF10L transcript variant 4 | NM_001319838.1:c.2080C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform 4 | NP_001306767.1:p.Arg694Gly | R (Arg) > G (Gly) | Missense Variant |
| ARHGEF10L transcript variant 4 | NM_001319838.1:c.2080C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform 4 | NP_001306767.1:p.Arg694Trp | R (Arg) > W (Trp) | Missense Variant |
| ARHGEF10L transcript variant 5 | NM_001328124.1:c.2305C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform 5 | NP_001315053.1:p.Arg769= | R (Arg) > R (Arg) | Synonymous Variant |
| ARHGEF10L transcript variant 5 | NM_001328124.1:c.2305C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform 5 | NP_001315053.1:p.Arg769Gly | R (Arg) > G (Gly) | Missense Variant |
| ARHGEF10L transcript variant 5 | NM_001328124.1:c.2305C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform 5 | NP_001315053.1:p.Arg769Trp | R (Arg) > W (Trp) | Missense Variant |
| ARHGEF10L transcript variant 1 | NM_018125.4:c.2971C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform 1 | NP_060595.3:p.Arg991= | R (Arg) > R (Arg) | Synonymous Variant |
| ARHGEF10L transcript variant 1 | NM_018125.4:c.2971C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform 1 | NP_060595.3:p.Arg991Gly | R (Arg) > G (Gly) | Missense Variant |
| ARHGEF10L transcript variant 1 | NM_018125.4:c.2971C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform 1 | NP_060595.3:p.Arg991Trp | R (Arg) > W (Trp) | Missense Variant |
| ARHGEF10L transcript variant 6 | NR_137287.2:n.4014C>A | N/A | Non Coding Transcript Variant |
| ARHGEF10L transcript variant 6 | NR_137287.2:n.4014C>G | N/A | Non Coding Transcript Variant |
| ARHGEF10L transcript variant 6 | NR_137287.2:n.4014C>T | N/A | Non Coding Transcript Variant |
| ARHGEF10L transcript variant 7 | NR_137288.2:n.3894C>A | N/A | Non Coding Transcript Variant |
| ARHGEF10L transcript variant 7 | NR_137288.2:n.3894C>G | N/A | Non Coding Transcript Variant |
| ARHGEF10L transcript variant 7 | NR_137288.2:n.3894C>T | N/A | Non Coding Transcript Variant |
| ARHGEF10L transcript variant X29 | XM_047424158.1:c. | N/A | Genic Downstream Transcript Variant |
| ARHGEF10L transcript variant X30 | XM_047424159.1:c. | N/A | Genic Downstream Transcript Variant |
| ARHGEF10L transcript variant X31 | XM_047424165.1:c. | N/A | Genic Downstream Transcript Variant |
| ARHGEF10L transcript variant X32 | XM_047424167.1:c. | N/A | Genic Downstream Transcript Variant |
| ARHGEF10L transcript variant X33 | XM_047424175.1:c. | N/A | Genic Downstream Transcript Variant |
| ARHGEF10L transcript variant X35 | XM_047424190.1:c. | N/A | Genic Downstream Transcript Variant |
| ARHGEF10L transcript variant X36 | XM_047424201.1:c. | N/A | Genic Downstream Transcript Variant |
| ARHGEF10L transcript variant X3 | XM_006710728.1:c.2866C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_006710791.1:p.Arg956= | R (Arg) > R (Arg) | Synonymous Variant |
| ARHGEF10L transcript variant X3 | XM_006710728.1:c.2866C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_006710791.1:p.Arg956Gly | R (Arg) > G (Gly) | Missense Variant |
| ARHGEF10L transcript variant X3 | XM_006710728.1:c.2866C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_006710791.1:p.Arg956Trp | R (Arg) > W (Trp) | Missense Variant |
| ARHGEF10L transcript variant X10 | XM_006710731.1:c.2863C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X2 | XP_006710794.1:p.Arg955= | R (Arg) > R (Arg) | Synonymous Variant |
| ARHGEF10L transcript variant X10 | XM_006710731.1:c.2863C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X2 | XP_006710794.1:p.Arg955Gly | R (Arg) > G (Gly) | Missense Variant |
| ARHGEF10L transcript variant X10 | XM_006710731.1:c.2863C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X2 | XP_006710794.1:p.Arg955Trp | R (Arg) > W (Trp) | Missense Variant |
| ARHGEF10L transcript variant X5 | XM_024448062.1:c.2866C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_024303830.1:p.Arg956= | R (Arg) > R (Arg) | Synonymous Variant |
| ARHGEF10L transcript variant X5 | XM_024448062.1:c.2866C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_024303830.1:p.Arg956Gly | R (Arg) > G (Gly) | Missense Variant |
| ARHGEF10L transcript variant X5 | XM_024448062.1:c.2866C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_024303830.1:p.Arg956Trp | R (Arg) > W (Trp) | Missense Variant |
| ARHGEF10L transcript variant X1 | XM_047424065.1:c.2866C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_047280021.1:p.Arg956= | R (Arg) > R (Arg) | Synonymous Variant |
| ARHGEF10L transcript variant X1 | XM_047424065.1:c.2866C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_047280021.1:p.Arg956Gly | R (Arg) > G (Gly) | Missense Variant |
| ARHGEF10L transcript variant X1 | XM_047424065.1:c.2866C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_047280021.1:p.Arg956Trp | R (Arg) > W (Trp) | Missense Variant |
| ARHGEF10L transcript variant X2 | XM_005245923.3:c.2866C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_005245980.2:p.Arg956= | R (Arg) > R (Arg) | Synonymous Variant |
| ARHGEF10L transcript variant X2 | XM_005245923.3:c.2866C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_005245980.2:p.Arg956Gly | R (Arg) > G (Gly) | Missense Variant |
| ARHGEF10L transcript variant X2 | XM_005245923.3:c.2866C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_005245980.2:p.Arg956Trp | R (Arg) > W (Trp) | Missense Variant |
| ARHGEF10L transcript variant X4 | XM_024448059.2:c.2866C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_024303827.1:p.Arg956= | R (Arg) > R (Arg) | Synonymous Variant |
| ARHGEF10L transcript variant X4 | XM_024448059.2:c.2866C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_024303827.1:p.Arg956Gly | R (Arg) > G (Gly) | Missense Variant |
| ARHGEF10L transcript variant X4 | XM_024448059.2:c.2866C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_024303827.1:p.Arg956Trp | R (Arg) > W (Trp) | Missense Variant |
| ARHGEF10L transcript variant X6 | XM_024448061.2:c.2866C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_024303829.1:p.Arg956= | R (Arg) > R (Arg) | Synonymous Variant |
| ARHGEF10L transcript variant X6 | XM_024448061.2:c.2866C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_024303829.1:p.Arg956Gly | R (Arg) > G (Gly) | Missense Variant |
| ARHGEF10L transcript variant X6 | XM_024448061.2:c.2866C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_024303829.1:p.Arg956Trp | R (Arg) > W (Trp) | Missense Variant |
| ARHGEF10L transcript variant X7 | XM_047424070.1:c.2866C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_047280026.1:p.Arg956= | R (Arg) > R (Arg) | Synonymous Variant |
| ARHGEF10L transcript variant X7 | XM_047424070.1:c.2866C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_047280026.1:p.Arg956Gly | R (Arg) > G (Gly) | Missense Variant |
| ARHGEF10L transcript variant X7 | XM_047424070.1:c.2866C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_047280026.1:p.Arg956Trp | R (Arg) > W (Trp) | Missense Variant |
| ARHGEF10L transcript variant X8 | XM_047424071.1:c.2866C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_047280027.1:p.Arg956= | R (Arg) > R (Arg) | Synonymous Variant |
| ARHGEF10L transcript variant X8 | XM_047424071.1:c.2866C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_047280027.1:p.Arg956Gly | R (Arg) > G (Gly) | Missense Variant |
| ARHGEF10L transcript variant X8 | XM_047424071.1:c.2866C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_047280027.1:p.Arg956Trp | R (Arg) > W (Trp) | Missense Variant |
| ARHGEF10L transcript variant X9 | XM_047424075.1:c.2866C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_047280031.1:p.Arg956= | R (Arg) > R (Arg) | Synonymous Variant |
| ARHGEF10L transcript variant X9 | XM_047424075.1:c.2866C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_047280031.1:p.Arg956Gly | R (Arg) > G (Gly) | Missense Variant |
| ARHGEF10L transcript variant X9 | XM_047424075.1:c.2866C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_047280031.1:p.Arg956Trp | R (Arg) > W (Trp) | Missense Variant |
| ARHGEF10L transcript variant X11 | XM_006710729.2:c.2863C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X2 | XP_006710792.1:p.Arg955= | R (Arg) > R (Arg) | Synonymous Variant |
| ARHGEF10L transcript variant X11 | XM_006710729.2:c.2863C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X2 | XP_006710792.1:p.Arg955Gly | R (Arg) > G (Gly) | Missense Variant |
| ARHGEF10L transcript variant X11 | XM_006710729.2:c.2863C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X2 | XP_006710792.1:p.Arg955Trp | R (Arg) > W (Trp) | Missense Variant |
| ARHGEF10L transcript variant X12 | XM_011541691.3:c.2857C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X3 | XP_011539993.1:p.Arg953= | R (Arg) > R (Arg) | Synonymous Variant |
| ARHGEF10L transcript variant X12 | XM_011541691.3:c.2857C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X3 | XP_011539993.1:p.Arg953Gly | R (Arg) > G (Gly) | Missense Variant |
| ARHGEF10L transcript variant X12 | XM_011541691.3:c.2857C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X3 | XP_011539993.1:p.Arg953Trp | R (Arg) > W (Trp) | Missense Variant |
| ARHGEF10L transcript variant X13 | XM_005245925.3:c.2854C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X4 | XP_005245982.2:p.Arg952= | R (Arg) > R (Arg) | Synonymous Variant |
| ARHGEF10L transcript variant X13 | XM_005245925.3:c.2854C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X4 | XP_005245982.2:p.Arg952Gly | R (Arg) > G (Gly) | Missense Variant |
| ARHGEF10L transcript variant X13 | XM_005245925.3:c.2854C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X4 | XP_005245982.2:p.Arg952Trp | R (Arg) > W (Trp) | Missense Variant |
| ARHGEF10L transcript variant X14 | XM_011541692.3:c.2851C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X5 | XP_011539994.1:p.Arg951= | R (Arg) > R (Arg) | Synonymous Variant |
| ARHGEF10L transcript variant X14 | XM_011541692.3:c.2851C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X5 | XP_011539994.1:p.Arg951Gly | R (Arg) > G (Gly) | Missense Variant |
| ARHGEF10L transcript variant X14 | XM_011541692.3:c.2851C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X5 | XP_011539994.1:p.Arg951Trp | R (Arg) > W (Trp) | Missense Variant |
| ARHGEF10L transcript variant X15 | XM_047424089.1:c.2842C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X6 | XP_047280045.1:p.Arg948= | R (Arg) > R (Arg) | Synonymous Variant |
| ARHGEF10L transcript variant X15 | XM_047424089.1:c.2842C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X6 | XP_047280045.1:p.Arg948Gly | R (Arg) > G (Gly) | Missense Variant |
| ARHGEF10L transcript variant X15 | XM_047424089.1:c.2842C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X6 | XP_047280045.1:p.Arg948Trp | R (Arg) > W (Trp) | Missense Variant |
| ARHGEF10L transcript variant X16 | XM_047424093.1:c.2842C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X6 | XP_047280049.1:p.Arg948= | R (Arg) > R (Arg) | Synonymous Variant |
| ARHGEF10L transcript variant X16 | XM_047424093.1:c.2842C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X6 | XP_047280049.1:p.Arg948Gly | R (Arg) > G (Gly) | Missense Variant |
| ARHGEF10L transcript variant X16 | XM_047424093.1:c.2842C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X6 | XP_047280049.1:p.Arg948Trp | R (Arg) > W (Trp) | Missense Variant |
| ARHGEF10L transcript variant X17 | XM_047424096.1:c.2842C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X6 | XP_047280052.1:p.Arg948= | R (Arg) > R (Arg) | Synonymous Variant |
| ARHGEF10L transcript variant X17 | XM_047424096.1:c.2842C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X6 | XP_047280052.1:p.Arg948Gly | R (Arg) > G (Gly) | Missense Variant |
| ARHGEF10L transcript variant X17 | XM_047424096.1:c.2842C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X6 | XP_047280052.1:p.Arg948Trp | R (Arg) > W (Trp) | Missense Variant |
| ARHGEF10L transcript variant X18 | XM_047424097.1:c.2842C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X6 | XP_047280053.1:p.Arg948= | R (Arg) > R (Arg) | Synonymous Variant |
| ARHGEF10L transcript variant X18 | XM_047424097.1:c.2842C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X6 | XP_047280053.1:p.Arg948Gly | R (Arg) > G (Gly) | Missense Variant |
| ARHGEF10L transcript variant X18 | XM_047424097.1:c.2842C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X6 | XP_047280053.1:p.Arg948Trp | R (Arg) > W (Trp) | Missense Variant |
| ARHGEF10L transcript variant X19 | XM_047424098.1:c.2839C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X7 | XP_047280054.1:p.Arg947= | R (Arg) > R (Arg) | Synonymous Variant |
| ARHGEF10L transcript variant X19 | XM_047424098.1:c.2839C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X7 | XP_047280054.1:p.Arg947Gly | R (Arg) > G (Gly) | Missense Variant |
| ARHGEF10L transcript variant X19 | XM_047424098.1:c.2839C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X7 | XP_047280054.1:p.Arg947Trp | R (Arg) > W (Trp) | Missense Variant |
| ARHGEF10L transcript variant X20 | XM_047424100.1:c.2839C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X7 | XP_047280056.1:p.Arg947= | R (Arg) > R (Arg) | Synonymous Variant |
| ARHGEF10L transcript variant X20 | XM_047424100.1:c.2839C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X7 | XP_047280056.1:p.Arg947Gly | R (Arg) > G (Gly) | Missense Variant |
| ARHGEF10L transcript variant X20 | XM_047424100.1:c.2839C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X7 | XP_047280056.1:p.Arg947Trp | R (Arg) > W (Trp) | Missense Variant |
| ARHGEF10L transcript variant X21 | XM_047424105.1:c.2839C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X7 | XP_047280061.1:p.Arg947= | R (Arg) > R (Arg) | Synonymous Variant |
| ARHGEF10L transcript variant X21 | XM_047424105.1:c.2839C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X7 | XP_047280061.1:p.Arg947Gly | R (Arg) > G (Gly) | Missense Variant |
| ARHGEF10L transcript variant X21 | XM_047424105.1:c.2839C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X7 | XP_047280061.1:p.Arg947Trp | R (Arg) > W (Trp) | Missense Variant |
| ARHGEF10L transcript variant X22 | XM_047424111.1:c.2839C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X7 | XP_047280067.1:p.Arg947= | R (Arg) > R (Arg) | Synonymous Variant |
| ARHGEF10L transcript variant X22 | XM_047424111.1:c.2839C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X7 | XP_047280067.1:p.Arg947Gly | R (Arg) > G (Gly) | Missense Variant |
| ARHGEF10L transcript variant X22 | XM_047424111.1:c.2839C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X7 | XP_047280067.1:p.Arg947Trp | R (Arg) > W (Trp) | Missense Variant |
| ARHGEF10L transcript variant X23 | XM_047424112.1:c.2839C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X7 | XP_047280068.1:p.Arg947= | R (Arg) > R (Arg) | Synonymous Variant |
| ARHGEF10L transcript variant X23 | XM_047424112.1:c.2839C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X7 | XP_047280068.1:p.Arg947Gly | R (Arg) > G (Gly) | Missense Variant |
| ARHGEF10L transcript variant X23 | XM_047424112.1:c.2839C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X7 | XP_047280068.1:p.Arg947Trp | R (Arg) > W (Trp) | Missense Variant |
| ARHGEF10L transcript variant X24 | XM_017001617.2:c.2839C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X7 | XP_016857106.1:p.Arg947= | R (Arg) > R (Arg) | Synonymous Variant |
| ARHGEF10L transcript variant X24 | XM_017001617.2:c.2839C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X7 | XP_016857106.1:p.Arg947Gly | R (Arg) > G (Gly) | Missense Variant |
| ARHGEF10L transcript variant X24 | XM_017001617.2:c.2839C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X7 | XP_016857106.1:p.Arg947Trp | R (Arg) > W (Trp) | Missense Variant |
| ARHGEF10L transcript variant X26 | XM_005245929.4:c.2290C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X8 | XP_005245986.2:p.Arg764= | R (Arg) > R (Arg) | Synonymous Variant |
| ARHGEF10L transcript variant X26 | XM_005245929.4:c.2290C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X8 | XP_005245986.2:p.Arg764Gly | R (Arg) > G (Gly) | Missense Variant |
| ARHGEF10L transcript variant X26 | XM_005245929.4:c.2290C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X8 | XP_005245986.2:p.Arg764Trp | R (Arg) > W (Trp) | Missense Variant |
| ARHGEF10L transcript variant X27 | XM_017001619.2:c.2866C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X9 | XP_016857108.1:p.Arg956= | R (Arg) > R (Arg) | Synonymous Variant |
| ARHGEF10L transcript variant X27 | XM_017001619.2:c.2866C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X9 | XP_016857108.1:p.Arg956Gly | R (Arg) > G (Gly) | Missense Variant |
| ARHGEF10L transcript variant X27 | XM_017001619.2:c.2866C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X9 | XP_016857108.1:p.Arg956Trp | R (Arg) > W (Trp) | Missense Variant |
| ARHGEF10L transcript variant X28 | XM_017001620.2:c.2851C>A | R [CGG] > R [AGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X10 | XP_016857109.1:p.Arg951= | R (Arg) > R (Arg) | Synonymous Variant |
| ARHGEF10L transcript variant X28 | XM_017001620.2:c.2851C>G | R [CGG] > G [GGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X10 | XP_016857109.1:p.Arg951Gly | R (Arg) > G (Gly) | Missense Variant |
| ARHGEF10L transcript variant X28 | XM_017001620.2:c.2851C>T | R [CGG] > W [TGG] | Coding Sequence Variant |
| rho guanine nucleotide exchange factor 10-like protein isoform X10 | XP_016857109.1:p.Arg951Trp | R (Arg) > W (Trp) | Missense Variant |
| ARHGEF10L transcript variant X25 | XR_946686.4:n.2909C>A | N/A | Non Coding Transcript Variant |
| ARHGEF10L transcript variant X25 | XR_946686.4:n.2909C>G | N/A | Non Coding Transcript Variant |
| ARHGEF10L transcript variant X25 | XR_946686.4:n.2909C>T | N/A | Non Coding Transcript Variant |
| ARHGEF10L transcript variant X34 | XR_946691.3:n. | N/A | Genic Downstream Transcript Variant |
Help
Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.
Not Reported in ClinVar
Help
Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".
| Placement | C= | A | G | T |
|---|---|---|---|---|
| GRCh38.p14 chr 1 | NC_000001.11:g.17664557= | NC_000001.11:g.17664557C>A | NC_000001.11:g.17664557C>G | NC_000001.11:g.17664557C>T |
| GRCh37.p13 chr 1 | NC_000001.10:g.17991052T>C | NC_000001.10:g.17991052T>A | NC_000001.10:g.17991052T>G | NC_000001.10:g.17991052= |
| ARHGEF10L RefSeqGene | NG_050860.1:g.149361= | NG_050860.1:g.149361C>A | NG_050860.1:g.149361C>G | NG_050860.1:g.149361C>T |
| ARHGEF10L transcript variant 1 | NM_018125.4:c.2971= | NM_018125.4:c.2971C>A | NM_018125.4:c.2971C>G | NM_018125.4:c.2971C>T |
| ARHGEF10L transcript variant 1 | NM_018125.3:c.2971= | NM_018125.3:c.2971C>A | NM_018125.3:c.2971C>G | NM_018125.3:c.2971C>T |
| ARHGEF10L transcript variant 6 | NR_137287.2:n.4014= | NR_137287.2:n.4014C>A | NR_137287.2:n.4014C>G | NR_137287.2:n.4014C>T |
| ARHGEF10L transcript variant 6 | NR_137287.1:n.3877= | NR_137287.1:n.3877C>A | NR_137287.1:n.3877C>G | NR_137287.1:n.3877C>T |
| ARHGEF10L transcript variant 7 | NR_137288.2:n.3894= | NR_137288.2:n.3894C>A | NR_137288.2:n.3894C>G | NR_137288.2:n.3894C>T |
| ARHGEF10L transcript variant 7 | NR_137288.1:n.3757= | NR_137288.1:n.3757C>A | NR_137288.1:n.3757C>G | NR_137288.1:n.3757C>T |
| ARHGEF10L transcript variant 2 | NM_001011722.2:c.2854= | NM_001011722.2:c.2854C>A | NM_001011722.2:c.2854C>G | NM_001011722.2:c.2854C>T |
| ARHGEF10L transcript variant 3 | NM_001319837.1:c.2839= | NM_001319837.1:c.2839C>A | NM_001319837.1:c.2839C>G | NM_001319837.1:c.2839C>T |
| ARHGEF10L transcript variant 5 | NM_001328124.1:c.2305= | NM_001328124.1:c.2305C>A | NM_001328124.1:c.2305C>G | NM_001328124.1:c.2305C>T |
| ARHGEF10L transcript variant 4 | NM_001319838.1:c.2080= | NM_001319838.1:c.2080C>A | NM_001319838.1:c.2080C>G | NM_001319838.1:c.2080C>T |
| ARHGEF10L transcript variant X26 | XM_005245929.4:c.2290= | XM_005245929.4:c.2290C>A | XM_005245929.4:c.2290C>G | XM_005245929.4:c.2290C>T |
| ARHGEF10L transcript variant X15 | XM_005245929.3:c.2290= | XM_005245929.3:c.2290C>A | XM_005245929.3:c.2290C>G | XM_005245929.3:c.2290C>T |
| ARHGEF10L transcript variant X13 | XM_005245929.2:c.2290= | XM_005245929.2:c.2290C>A | XM_005245929.2:c.2290C>G | XM_005245929.2:c.2290C>T |
| ARHGEF10L transcript variant X9 | XM_005245929.1:c.2290T>C | XM_005245929.1:c.2290T>A | XM_005245929.1:c.2290T>G | XM_005245929.1:c.2290= |
| ARHGEF10L transcript variant X25 | XR_946686.4:n.2909= | XR_946686.4:n.2909C>A | XR_946686.4:n.2909C>G | XR_946686.4:n.2909C>T |
| ARHGEF10L transcript variant X13 | XR_946686.3:n.2995= | XR_946686.3:n.2995C>A | XR_946686.3:n.2995C>G | XR_946686.3:n.2995C>T |
| ARHGEF10L transcript variant X10 | XR_946686.2:n.2995= | XR_946686.2:n.2995C>A | XR_946686.2:n.2995C>G | XR_946686.2:n.2995C>T |
| ARHGEF10L transcript variant X10 | XR_946686.1:n.2909= | XR_946686.1:n.2909C>A | XR_946686.1:n.2909C>G | XR_946686.1:n.2909C>T |
| ARHGEF10L transcript variant X2 | XM_005245923.3:c.2866= | XM_005245923.3:c.2866C>A | XM_005245923.3:c.2866C>G | XM_005245923.3:c.2866C>T |
| ARHGEF10L transcript variant X2 | XM_005245923.2:c.2866= | XM_005245923.2:c.2866C>A | XM_005245923.2:c.2866C>G | XM_005245923.2:c.2866C>T |
| ARHGEF10L transcript variant X3 | XM_005245923.1:c.2866T>C | XM_005245923.1:c.2866T>A | XM_005245923.1:c.2866T>G | XM_005245923.1:c.2866= |
| ARHGEF10L transcript variant X13 | XM_005245925.3:c.2854= | XM_005245925.3:c.2854C>A | XM_005245925.3:c.2854C>G | XM_005245925.3:c.2854C>T |
| ARHGEF10L transcript variant X9 | XM_005245925.2:c.2854= | XM_005245925.2:c.2854C>A | XM_005245925.2:c.2854C>G | XM_005245925.2:c.2854C>T |
| ARHGEF10L transcript variant X5 | XM_005245925.1:c.2854T>C | XM_005245925.1:c.2854T>A | XM_005245925.1:c.2854T>G | XM_005245925.1:c.2854= |
| ARHGEF10L transcript variant X12 | XM_011541691.3:c.2857= | XM_011541691.3:c.2857C>A | XM_011541691.3:c.2857C>G | XM_011541691.3:c.2857C>T |
| ARHGEF10L transcript variant X8 | XM_011541691.2:c.2857= | XM_011541691.2:c.2857C>A | XM_011541691.2:c.2857C>G | XM_011541691.2:c.2857C>T |
| ARHGEF10L transcript variant X5 | XM_011541691.1:c.2857= | XM_011541691.1:c.2857C>A | XM_011541691.1:c.2857C>G | XM_011541691.1:c.2857C>T |
| ARHGEF10L transcript variant X14 | XM_011541692.3:c.2851= | XM_011541692.3:c.2851C>A | XM_011541692.3:c.2851C>G | XM_011541692.3:c.2851C>T |
| ARHGEF10L transcript variant X10 | XM_011541692.2:c.2851= | XM_011541692.2:c.2851C>A | XM_011541692.2:c.2851C>G | XM_011541692.2:c.2851C>T |
| ARHGEF10L transcript variant X7 | XM_011541692.1:c.2851= | XM_011541692.1:c.2851C>A | XM_011541692.1:c.2851C>G | XM_011541692.1:c.2851C>T |
| ARHGEF10L transcript variant X27 | XM_017001619.2:c.2866= | XM_017001619.2:c.2866C>A | XM_017001619.2:c.2866C>G | XM_017001619.2:c.2866C>T |
| ARHGEF10L transcript variant X17 | XM_017001619.1:c.2866= | XM_017001619.1:c.2866C>A | XM_017001619.1:c.2866C>G | XM_017001619.1:c.2866C>T |
| ARHGEF10L transcript variant X28 | XM_017001620.2:c.2851= | XM_017001620.2:c.2851C>A | XM_017001620.2:c.2851C>G | XM_017001620.2:c.2851C>T |
| ARHGEF10L transcript variant X18 | XM_017001620.1:c.2851= | XM_017001620.1:c.2851C>A | XM_017001620.1:c.2851C>G | XM_017001620.1:c.2851C>T |
| ARHGEF10L transcript variant X11 | XM_006710729.2:c.2863= | XM_006710729.2:c.2863C>A | XM_006710729.2:c.2863C>G | XM_006710729.2:c.2863C>T |
| ARHGEF10L transcript variant X7 | XM_006710729.1:c.2863= | XM_006710729.1:c.2863C>A | XM_006710729.1:c.2863C>G | XM_006710729.1:c.2863C>T |
| ARHGEF10L transcript variant X24 | XM_017001617.2:c.2839= | XM_017001617.2:c.2839C>A | XM_017001617.2:c.2839C>G | XM_017001617.2:c.2839C>T |
| ARHGEF10L transcript variant X12 | XM_017001617.1:c.2839= | XM_017001617.1:c.2839C>A | XM_017001617.1:c.2839C>G | XM_017001617.1:c.2839C>T |
| ARHGEF10L transcript variant X4 | XM_024448059.2:c.2866= | XM_024448059.2:c.2866C>A | XM_024448059.2:c.2866C>G | XM_024448059.2:c.2866C>T |
| ARHGEF10L transcript variant X3 | XM_024448059.1:c.2866= | XM_024448059.1:c.2866C>A | XM_024448059.1:c.2866C>G | XM_024448059.1:c.2866C>T |
| ARHGEF10L transcript variant X6 | XM_024448061.2:c.2866= | XM_024448061.2:c.2866C>A | XM_024448061.2:c.2866C>G | XM_024448061.2:c.2866C>T |
| ARHGEF10L transcript variant X4 | XM_024448061.1:c.2866= | XM_024448061.1:c.2866C>A | XM_024448061.1:c.2866C>G | XM_024448061.1:c.2866C>T |
| ARHGEF10L transcript variant X3 | XM_006710728.1:c.2866= | XM_006710728.1:c.2866C>A | XM_006710728.1:c.2866C>G | XM_006710728.1:c.2866C>T |
| ARHGEF10L transcript variant X10 | XM_006710731.1:c.2863= | XM_006710731.1:c.2863C>A | XM_006710731.1:c.2863C>G | XM_006710731.1:c.2863C>T |
| ARHGEF10L transcript variant X15 | XM_047424089.1:c.2842= | XM_047424089.1:c.2842C>A | XM_047424089.1:c.2842C>G | XM_047424089.1:c.2842C>T |
| ARHGEF10L transcript variant X22 | XM_047424111.1:c.2839= | XM_047424111.1:c.2839C>A | XM_047424111.1:c.2839C>G | XM_047424111.1:c.2839C>T |
| ARHGEF10L transcript variant X16 | XM_047424093.1:c.2842= | XM_047424093.1:c.2842C>A | XM_047424093.1:c.2842C>G | XM_047424093.1:c.2842C>T |
| ARHGEF10L transcript variant X19 | XM_047424098.1:c.2839= | XM_047424098.1:c.2839C>A | XM_047424098.1:c.2839C>G | XM_047424098.1:c.2839C>T |
| ARHGEF10L transcript variant X1 | XM_047424065.1:c.2866= | XM_047424065.1:c.2866C>A | XM_047424065.1:c.2866C>G | XM_047424065.1:c.2866C>T |
| ARHGEF10L transcript variant X20 | XM_047424100.1:c.2839= | XM_047424100.1:c.2839C>A | XM_047424100.1:c.2839C>G | XM_047424100.1:c.2839C>T |
| ARHGEF10L transcript variant X18 | XM_047424097.1:c.2842= | XM_047424097.1:c.2842C>A | XM_047424097.1:c.2842C>G | XM_047424097.1:c.2842C>T |
| ARHGEF10L transcript variant X23 | XM_047424112.1:c.2839= | XM_047424112.1:c.2839C>A | XM_047424112.1:c.2839C>G | XM_047424112.1:c.2839C>T |
| ARHGEF10L transcript variant X9 | XM_047424075.1:c.2866= | XM_047424075.1:c.2866C>A | XM_047424075.1:c.2866C>G | XM_047424075.1:c.2866C>T |
| ARHGEF10L transcript variant X8 | XM_047424071.1:c.2866= | XM_047424071.1:c.2866C>A | XM_047424071.1:c.2866C>G | XM_047424071.1:c.2866C>T |
| ARHGEF10L transcript variant X7 | XM_047424070.1:c.2866= | XM_047424070.1:c.2866C>A | XM_047424070.1:c.2866C>G | XM_047424070.1:c.2866C>T |
| ARHGEF10L transcript variant X5 | XM_024448062.1:c.2866= | XM_024448062.1:c.2866C>A | XM_024448062.1:c.2866C>G | XM_024448062.1:c.2866C>T |
| ARHGEF10L transcript variant X17 | XM_047424096.1:c.2842= | XM_047424096.1:c.2842C>A | XM_047424096.1:c.2842C>G | XM_047424096.1:c.2842C>T |
| ARHGEF10L transcript variant X21 | XM_047424105.1:c.2839= | XM_047424105.1:c.2839C>A | XM_047424105.1:c.2839C>G | XM_047424105.1:c.2839C>T |
| rho guanine nucleotide exchange factor 10-like protein isoform 1 | NP_060595.3:p.Arg991= | NP_060595.3:p.Arg991= | NP_060595.3:p.Arg991Gly | NP_060595.3:p.Arg991Trp |
| rho guanine nucleotide exchange factor 10-like protein isoform 2 | NP_001011722.2:p.Arg952= | NP_001011722.2:p.Arg952= | NP_001011722.2:p.Arg952Gly | NP_001011722.2:p.Arg952Trp |
| rho guanine nucleotide exchange factor 10-like protein isoform 3 | NP_001306766.1:p.Arg947= | NP_001306766.1:p.Arg947= | NP_001306766.1:p.Arg947Gly | NP_001306766.1:p.Arg947Trp |
| rho guanine nucleotide exchange factor 10-like protein isoform 5 | NP_001315053.1:p.Arg769= | NP_001315053.1:p.Arg769= | NP_001315053.1:p.Arg769Gly | NP_001315053.1:p.Arg769Trp |
| rho guanine nucleotide exchange factor 10-like protein isoform 4 | NP_001306767.1:p.Arg694= | NP_001306767.1:p.Arg694= | NP_001306767.1:p.Arg694Gly | NP_001306767.1:p.Arg694Trp |
| rho guanine nucleotide exchange factor 10-like protein isoform X8 | XP_005245986.2:p.Arg764= | XP_005245986.2:p.Arg764= | XP_005245986.2:p.Arg764Gly | XP_005245986.2:p.Arg764Trp |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_005245980.2:p.Arg956= | XP_005245980.2:p.Arg956= | XP_005245980.2:p.Arg956Gly | XP_005245980.2:p.Arg956Trp |
| rho guanine nucleotide exchange factor 10-like protein isoform X4 | XP_005245982.2:p.Arg952= | XP_005245982.2:p.Arg952= | XP_005245982.2:p.Arg952Gly | XP_005245982.2:p.Arg952Trp |
| rho guanine nucleotide exchange factor 10-like protein isoform X3 | XP_011539993.1:p.Arg953= | XP_011539993.1:p.Arg953= | XP_011539993.1:p.Arg953Gly | XP_011539993.1:p.Arg953Trp |
| rho guanine nucleotide exchange factor 10-like protein isoform X5 | XP_011539994.1:p.Arg951= | XP_011539994.1:p.Arg951= | XP_011539994.1:p.Arg951Gly | XP_011539994.1:p.Arg951Trp |
| rho guanine nucleotide exchange factor 10-like protein isoform X9 | XP_016857108.1:p.Arg956= | XP_016857108.1:p.Arg956= | XP_016857108.1:p.Arg956Gly | XP_016857108.1:p.Arg956Trp |
| rho guanine nucleotide exchange factor 10-like protein isoform X10 | XP_016857109.1:p.Arg951= | XP_016857109.1:p.Arg951= | XP_016857109.1:p.Arg951Gly | XP_016857109.1:p.Arg951Trp |
| rho guanine nucleotide exchange factor 10-like protein isoform X2 | XP_006710792.1:p.Arg955= | XP_006710792.1:p.Arg955= | XP_006710792.1:p.Arg955Gly | XP_006710792.1:p.Arg955Trp |
| rho guanine nucleotide exchange factor 10-like protein isoform X7 | XP_016857106.1:p.Arg947= | XP_016857106.1:p.Arg947= | XP_016857106.1:p.Arg947Gly | XP_016857106.1:p.Arg947Trp |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_024303827.1:p.Arg956= | XP_024303827.1:p.Arg956= | XP_024303827.1:p.Arg956Gly | XP_024303827.1:p.Arg956Trp |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_024303829.1:p.Arg956= | XP_024303829.1:p.Arg956= | XP_024303829.1:p.Arg956Gly | XP_024303829.1:p.Arg956Trp |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_006710791.1:p.Arg956= | XP_006710791.1:p.Arg956= | XP_006710791.1:p.Arg956Gly | XP_006710791.1:p.Arg956Trp |
| rho guanine nucleotide exchange factor 10-like protein isoform X2 | XP_006710794.1:p.Arg955= | XP_006710794.1:p.Arg955= | XP_006710794.1:p.Arg955Gly | XP_006710794.1:p.Arg955Trp |
| rho guanine nucleotide exchange factor 10-like protein isoform X6 | XP_047280045.1:p.Arg948= | XP_047280045.1:p.Arg948= | XP_047280045.1:p.Arg948Gly | XP_047280045.1:p.Arg948Trp |
| rho guanine nucleotide exchange factor 10-like protein isoform X7 | XP_047280067.1:p.Arg947= | XP_047280067.1:p.Arg947= | XP_047280067.1:p.Arg947Gly | XP_047280067.1:p.Arg947Trp |
| rho guanine nucleotide exchange factor 10-like protein isoform X6 | XP_047280049.1:p.Arg948= | XP_047280049.1:p.Arg948= | XP_047280049.1:p.Arg948Gly | XP_047280049.1:p.Arg948Trp |
| rho guanine nucleotide exchange factor 10-like protein isoform X7 | XP_047280054.1:p.Arg947= | XP_047280054.1:p.Arg947= | XP_047280054.1:p.Arg947Gly | XP_047280054.1:p.Arg947Trp |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_047280021.1:p.Arg956= | XP_047280021.1:p.Arg956= | XP_047280021.1:p.Arg956Gly | XP_047280021.1:p.Arg956Trp |
| rho guanine nucleotide exchange factor 10-like protein isoform X7 | XP_047280056.1:p.Arg947= | XP_047280056.1:p.Arg947= | XP_047280056.1:p.Arg947Gly | XP_047280056.1:p.Arg947Trp |
| rho guanine nucleotide exchange factor 10-like protein isoform X6 | XP_047280053.1:p.Arg948= | XP_047280053.1:p.Arg948= | XP_047280053.1:p.Arg948Gly | XP_047280053.1:p.Arg948Trp |
| rho guanine nucleotide exchange factor 10-like protein isoform X7 | XP_047280068.1:p.Arg947= | XP_047280068.1:p.Arg947= | XP_047280068.1:p.Arg947Gly | XP_047280068.1:p.Arg947Trp |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_047280031.1:p.Arg956= | XP_047280031.1:p.Arg956= | XP_047280031.1:p.Arg956Gly | XP_047280031.1:p.Arg956Trp |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_047280027.1:p.Arg956= | XP_047280027.1:p.Arg956= | XP_047280027.1:p.Arg956Gly | XP_047280027.1:p.Arg956Trp |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_047280026.1:p.Arg956= | XP_047280026.1:p.Arg956= | XP_047280026.1:p.Arg956Gly | XP_047280026.1:p.Arg956Trp |
| rho guanine nucleotide exchange factor 10-like protein isoform X1 | XP_024303830.1:p.Arg956= | XP_024303830.1:p.Arg956= | XP_024303830.1:p.Arg956Gly | XP_024303830.1:p.Arg956Trp |
| rho guanine nucleotide exchange factor 10-like protein isoform X6 | XP_047280052.1:p.Arg948= | XP_047280052.1:p.Arg948= | XP_047280052.1:p.Arg948Gly | XP_047280052.1:p.Arg948Trp |
| rho guanine nucleotide exchange factor 10-like protein isoform X7 | XP_047280061.1:p.Arg947= | XP_047280061.1:p.Arg947= | XP_047280061.1:p.Arg947Gly | XP_047280061.1:p.Arg947Trp |
| Rho guanine nucleotide exchange factor (GEF) 10-like isoform X3 | XP_005245980.1:p.Trp956Arg | XP_005245980.1:p.Trp956Arg | XP_005245980.1:p.Trp956Gly | XP_005245980.1:p.Trp956= |
| Rho guanine nucleotide exchange factor (GEF) 10-like isoform X5 | XP_005245982.1:p.Trp952Arg | XP_005245982.1:p.Trp952Arg | XP_005245982.1:p.Trp952Gly | XP_005245982.1:p.Trp952= |
| Rho guanine nucleotide exchange factor (GEF) 10-like isoform X9 | XP_005245986.1:p.Trp764Arg | XP_005245986.1:p.Trp764Arg | XP_005245986.1:p.Trp764Gly | XP_005245986.1:p.Trp764= |
Help
Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.
120 SubSNP,
7 Frequency
submissions
| No | Submitter | Submission ID | Date (Build) |
|---|---|---|---|
| 1 | BCM_SSAHASNP | ss9888636 | Jul 11, 2003 (116) |
| 2 | CSHL-HAPMAP | ss16421131 | Feb 27, 2004 (120) |
| 3 | CSHL-HAPMAP | ss19123276 | Feb 27, 2004 (120) |
| 4 | SSAHASNP | ss20591923 | Apr 05, 2004 (121) |
| 5 | ABI | ss41263970 | Mar 15, 2006 (126) |
| 6 | BCMHGSC_JDW | ss87264591 | Mar 23, 2008 (129) |
| 7 | HUMANGENOME_JCVI | ss97922335 | Feb 04, 2009 (130) |
| 8 | BGI | ss105126443 | Dec 01, 2009 (131) |
| 9 | 1000GENOMES | ss108025958 | Jan 22, 2009 (130) |
| 10 | 1000GENOMES | ss110122892 | Jan 24, 2009 (130) |
| 11 | ILLUMINA-UK | ss118530933 | Feb 14, 2009 (130) |
| 12 | ENSEMBL | ss137822210 | Dec 01, 2009 (131) |
| 13 | ENSEMBL | ss139152085 | Dec 01, 2009 (131) |
| 14 | GMI | ss154706502 | Dec 01, 2009 (131) |
| 15 | SEATTLESEQ | ss159696411 | Dec 01, 2009 (131) |
| 16 | ILLUMINA | ss161043416 | Dec 01, 2009 (131) |
| 17 | COMPLETE_GENOMICS | ss163130991 | Jul 04, 2010 (132) |
| 18 | COMPLETE_GENOMICS | ss163900989 | Jul 04, 2010 (132) |
| 19 | ILLUMINA | ss169005457 | Jul 04, 2010 (132) |
| 20 | BUSHMAN | ss198097455 | Jul 04, 2010 (132) |
| 21 | BCM-HGSC-SUB | ss205429700 | Jul 04, 2010 (132) |
| 22 | 1000GENOMES | ss217314438 | Jul 14, 2010 (132) |
| 23 | 1000GENOMES | ss217390892 | Jul 14, 2010 (132) |
| 24 | 1000GENOMES | ss217392133 | Jul 14, 2010 (132) |
| 25 | 1000GENOMES | ss217400011 | Jul 14, 2010 (132) |
| 26 | 1000GENOMES | ss217410558 | Jul 14, 2010 (132) |
| 27 | 1000GENOMES | ss217411067 | Jul 14, 2010 (132) |
| 28 | 1000GENOMES | ss218260191 | Jul 14, 2010 (132) |
| 29 | 1000GENOMES | ss230444736 | Jul 14, 2010 (132) |
| 30 | 1000GENOMES | ss238156083 | Jul 15, 2010 (132) |
| 31 | BL | ss252952390 | May 09, 2011 (134) |
| 32 | GMI | ss275736187 | May 04, 2012 (137) |
| 33 | GMI | ss284010220 | Apr 25, 2013 (138) |
| 34 | PJP | ss290703119 | May 09, 2011 (134) |
| 35 | NHLBI-ESP | ss341939288 | May 09, 2011 (134) |
| 36 | ILLUMINA | ss479406936 | Sep 08, 2015 (146) |
| 37 | 1000GENOMES | ss489724847 | May 04, 2012 (137) |
| 38 | EXOME_CHIP | ss491287928 | May 04, 2012 (137) |
| 39 | CLINSEQ_SNP | ss491587189 | May 04, 2012 (137) |
| 40 | ILLUMINA | ss532739607 | Sep 08, 2015 (146) |
| 41 | TISHKOFF | ss553844168 | Apr 25, 2013 (138) |
| 42 | SSMP | ss647610663 | Apr 25, 2013 (138) |
| 43 | ILLUMINA | ss780806683 | Sep 08, 2015 (146) |
| 44 | ILLUMINA | ss783488359 | Sep 08, 2015 (146) |
| 45 | JMKIDD_LAB | ss974433576 | Aug 21, 2014 (142) |
| 46 | JMKIDD_LAB | ss1067417155 | Aug 21, 2014 (142) |
| 47 | JMKIDD_LAB | ss1067702819 | Aug 21, 2014 (142) |
| 48 | 1000GENOMES | ss1289867486 | Aug 21, 2014 (142) |
| 49 | DDI | ss1425730861 | Apr 01, 2015 (144) |
| 50 | EVA_GENOME_DK | ss1573914517 | Apr 01, 2015 (144) |
| 51 | EVA_FINRISK | ss1584005286 | Apr 01, 2015 (144) |
| 52 | EVA_UK10K_ALSPAC | ss1599636743 | Apr 01, 2015 (144) |
| 53 | EVA_UK10K_TWINSUK | ss1642630776 | Apr 01, 2015 (144) |
| 54 | EVA_EXAC | ss1685351440 | Apr 01, 2015 (144) |
| 55 | EVA_MGP | ss1710892586 | Apr 01, 2015 (144) |
| 56 | ILLUMINA | ss1751884321 | Sep 08, 2015 (146) |
| 57 | HAMMER_LAB | ss1793989397 | Sep 08, 2015 (146) |
| 58 | ILLUMINA | ss1917723748 | Feb 12, 2016 (147) |
| 59 | WEILL_CORNELL_DGM | ss1918112746 | Feb 12, 2016 (147) |
| 60 | ILLUMINA | ss1945986417 | Feb 12, 2016 (147) |
| 61 | ILLUMINA | ss1958247735 | Feb 12, 2016 (147) |
| 62 | GENOMED | ss1966695086 | Jul 19, 2016 (147) |
| 63 | JJLAB | ss2019567664 | Sep 14, 2016 (149) |
| 64 | USC_VALOUEV | ss2147570014 | Dec 20, 2016 (150) |
| 65 | HUMAN_LONGEVITY | ss2160382239 | Dec 20, 2016 (150) |
| 66 | SYSTEMSBIOZJU | ss2624300125 | Nov 08, 2017 (151) |
| 67 | GRF | ss2697473821 | Nov 08, 2017 (151) |
| 68 | GNOMAD | ss2731192976 | Nov 08, 2017 (151) |
| 69 | GNOMAD | ss2746240092 | Nov 08, 2017 (151) |
| 70 | GNOMAD | ss2752196310 | Nov 08, 2017 (151) |
| 71 | SWEGEN | ss2986397178 | Nov 08, 2017 (151) |
| 72 | ILLUMINA | ss3021061017 | Nov 08, 2017 (151) |
| 73 | CSHL | ss3343346061 | Nov 08, 2017 (151) |
| 74 | ILLUMINA | ss3626037349 | Oct 11, 2018 (152) |
| 75 | ILLUMINA | ss3634309716 | Oct 11, 2018 (152) |
| 76 | ILLUMINA | ss3635985981 | Oct 11, 2018 (152) |
| 77 | ILLUMINA | ss3637740155 | Oct 11, 2018 (152) |
| 78 | ILLUMINA | ss3640017080 | Oct 11, 2018 (152) |
| 79 | ILLUMINA | ss3644482267 | Oct 11, 2018 (152) |
| 80 | OMUKHERJEE_ADBS | ss3646225702 | Oct 11, 2018 (152) |
| 81 | ILLUMINA | ss3651385523 | Oct 11, 2018 (152) |
| 82 | ILLUMINA | ss3725001227 | Jul 12, 2019 (153) |
| 83 | ACPOP | ss3726831929 | Jul 12, 2019 (153) |
| 84 | ILLUMINA | ss3744340430 | Jul 12, 2019 (153) |
| 85 | ILLUMINA | ss3744610679 | Jul 12, 2019 (153) |
| 86 | EVA | ss3745886176 | Jul 12, 2019 (153) |
| 87 | PAGE_CC | ss3770789337 | Jul 12, 2019 (153) |
| 88 | ILLUMINA | ss3772112260 | Jul 12, 2019 (153) |
| 89 | PACBIO | ss3783341086 | Jul 12, 2019 (153) |
| 90 | PACBIO | ss3789012458 | Jul 12, 2019 (153) |
| 91 | PACBIO | ss3793884919 | Jul 12, 2019 (153) |
| 92 | EVA | ss3823569196 | Apr 25, 2020 (154) |
| 93 | EVA | ss3825555490 | Apr 25, 2020 (154) |
| 94 | EVA | ss3826047777 | Apr 25, 2020 (154) |
| 95 | EVA | ss3836412035 | Apr 25, 2020 (154) |
| 96 | SGDP_PRJ | ss3848317189 | Apr 25, 2020 (154) |
| 97 | KRGDB | ss3893221167 | Apr 25, 2020 (154) |
| 98 | FSA-LAB | ss3983920000 | Apr 27, 2021 (155) |
| 99 | FSA-LAB | ss3983920001 | Apr 27, 2021 (155) |
| 100 | EVA | ss3984452965 | Apr 27, 2021 (155) |
| 101 | EVA | ss3986009365 | Apr 27, 2021 (155) |
| 102 | EVA | ss3986103713 | Apr 27, 2021 (155) |
| 103 | TOPMED | ss4440717944 | Apr 27, 2021 (155) |
| 104 | TOMMO_GENOMICS | ss5142733178 | Apr 27, 2021 (155) |
| 105 | EVA | ss5314596635 | Oct 12, 2022 (156) |
| 106 | EVA | ss5317064229 | Oct 12, 2022 (156) |
| 107 | 1000G_HIGH_COVERAGE | ss5513198397 | Oct 12, 2022 (156) |
| 108 | EVA | ss5623913217 | Oct 12, 2022 (156) |
| 109 | EVA | ss5623988963 | Oct 12, 2022 (156) |
| 110 | SANFORD_IMAGENETICS | ss5625029216 | Oct 12, 2022 (156) |
| 111 | TOMMO_GENOMICS | ss5667111023 | Oct 12, 2022 (156) |
| 112 | EVA | ss5800078877 | Oct 12, 2022 (156) |
| 113 | EVA | ss5831609251 | Oct 12, 2022 (156) |
| 114 | EVA | ss5847527766 | Oct 12, 2022 (156) |
| 115 | EVA | ss5848250767 | Oct 12, 2022 (156) |
| 116 | EVA | ss5907224834 | Oct 12, 2022 (156) |
| 117 | EVA | ss5936508892 | Oct 12, 2022 (156) |
| 118 | EVA | ss5936841964 | Oct 12, 2022 (156) |
| 119 | EVA | ss5979939267 | Oct 12, 2022 (156) |
| 120 | EVA | ss5981191092 | Oct 12, 2022 (156) |
| 121 | 1000Genomes_30x | NC_000001.11 - 17664557 | Oct 12, 2022 (156) |
| 122 | gnomAD - Genomes | NC_000001.11 - 17664557 | Apr 27, 2021 (155) |
| 123 | KOREAN population from KRGDB | NC_000001.10 - 17991052 | Apr 25, 2020 (154) |
| 124 | The PAGE Study | NC_000001.11 - 17664557 | Jul 12, 2019 (153) |
| 125 | 14KJPN | NC_000001.11 - 17664557 | Oct 12, 2022 (156) |
| 126 | TopMed | NC_000001.11 - 17664557 | Apr 27, 2021 (155) |
| 127 | ALFA | NC_000001.11 - 17664557 | Apr 27, 2021 (155) |
Help
History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).
| Associated ID | History Updated (Build) |
|---|---|
| rs117515171 | Aug 16, 2010 (132) |
Added to this RefSNP Cluster:
| Submission IDs | Observation SPDI | Canonical SPDI | Source RSIDs |
|---|---|---|---|
| 398561, ss3893221167 | NC_000001.10:17991051:T:A | NC_000001.11:17664556:C:A | (self) |
| ss198097455 | NC_000001.9:17863638:T:G | NC_000001.11:17664556:C:G | (self) |
| 398561, ss3893221167 | NC_000001.10:17991051:T:G | NC_000001.11:17664556:C:G | (self) |
| ss87264591, ss108025958, ss110122892, ss118530933, ss163130991, ss163900989, ss198097455, ss205429700, ss217314438, ss217390892, ss217392133, ss217400011, ss217410558, ss217411067, ss252952390, ss275736187, ss284010220, ss290703119, ss491587189 | NC_000001.9:17863638:T:T | NC_000001.11:17664556:C:T | (self) |
| 398561, ss218260191, ss230444736, ss238156083, ss341939288, ss479406936, ss489724847, ss491287928, ss532739607, ss553844168, ss647610663, ss780806683, ss783488359, ss974433576, ss1067417155, ss1067702819, ss1289867486, ss1425730861, ss1573914517, ss1584005286, ss1599636743, ss1642630776, ss1685351440, ss1710892586, ss1751884321, ss1793989397, ss1917723748, ss1918112746, ss1945986417, ss1958247735, ss1966695086, ss2019567664, ss2147570014, ss2624300125, ss2697473821, ss2731192976, ss2746240092, ss2752196310, ss2986397178, ss3021061017, ss3343346061, ss3626037349, ss3634309716, ss3635985981, ss3637740155, ss3640017080, ss3644482267, ss3646225702, ss3651385523, ss3726831929, ss3744340430, ss3744610679, ss3745886176, ss3772112260, ss3783341086, ss3789012458, ss3793884919, ss3823569196, ss3825555490, ss3826047777, ss3836412035, ss3848317189, ss3893221167, ss3983920000, ss3983920001, ss3984452965, ss3986009365, ss3986103713, ss5142733178, ss5314596635, ss5317064229, ss5623913217, ss5623988963, ss5625029216, ss5800078877, ss5831609251, ss5847527766, ss5848250767, ss5936508892, ss5936841964, ss5979939267, ss5981191092 | NC_000001.10:17991051:T:T | NC_000001.11:17664556:C:T | (self) |
| 724332, 3851006, 10806, 948127, 4324279, 8414040972, ss2160382239, ss3725001227, ss3770789337, ss4440717944, ss5513198397, ss5667111023, ss5907224834 | NC_000001.11:17664556:C:T | NC_000001.11:17664556:C:T | (self) |
| ss41263970, ss97922335, ss105126443, ss137822210, ss139152085, ss154706502, ss159696411, ss161043416, ss169005457 | NT_004610.19:4671139:T:T | NC_000001.11:17664556:C:T | (self) |
| ss9888636 | NT_030584.9:815393:T:T | NC_000001.11:17664556:C:T | (self) |
| ss16421131, ss19123276, ss20591923 | NT_030584.10:815393:T:T | NC_000001.11:17664556:C:T | (self) |
Help
Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.
No publications for rs6695710
Help
The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.
Genome context:
Select flank length:
Genomic regions, transcripts, and products
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NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.