Name: rs116261102
Published: September 21, 2022
License: Open Access

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.

rs116261102

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:17613168 (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: T>C
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.000019 (5/264690, TOPMED)
C=0.000004 (1/250892, GnomAD_exome)
C=0.000029 (4/140152, GnomAD) (+ 7 more)
C=0.000017 (2/120218, ExAC)
C=0.00007 (2/28258, 14KJPN)
C=0.00006 (1/16760, 8.3KJPN)
C=0.00000 (0/14050, ALFA)
C=0.00015 (2/13006, GO-ESP)
C=0.0002 (1/6404, 1000G_30x)
C=0.0002 (1/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ARHGEF10L : Synonymous 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	14050	T=1.00000	C=0.00000
European	Sub	9690	T=1.0000	C=0.0000
African	Sub	2898	T=1.0000	C=0.0000
African Others	Sub	114	T=1.000	C=0.000
African American	Sub	2784	T=1.0000	C=0.0000
Asian	Sub	112	T=1.000	C=0.000
East Asian	Sub	86	T=1.00	C=0.00
Other Asian	Sub	26	T=1.00	C=0.00
Latin American 1	Sub	146	T=1.000	C=0.000
Latin American 2	Sub	610	T=1.000	C=0.000
South Asian	Sub	98	T=1.00	C=0.00
Other	Sub	496	T=1.000	C=0.000

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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	T=0.999981	C=0.000019
gnomAD - Exomes	Global	Study-wide	250892	T=0.999996	C=0.000004
gnomAD - Exomes	European	Sub	135252	T=0.999993	C=0.000007
gnomAD - Exomes	Asian	Sub	48842	T=1.00000	C=0.00000
gnomAD - Exomes	American	Sub	34392	T=1.00000	C=0.00000
gnomAD - Exomes	African	Sub	16252	T=1.00000	C=0.00000
gnomAD - Exomes	Ashkenazi Jewish	Sub	10044	T=1.00000	C=0.00000
gnomAD - Exomes	Other	Sub	6110	T=1.0000	C=0.0000
gnomAD - Genomes	Global	Study-wide	140152	T=0.999971	C=0.000029
gnomAD - Genomes	European	Sub	75908	T=0.99999	C=0.00001
gnomAD - Genomes	African	Sub	42000	T=0.99995	C=0.00005
gnomAD - Genomes	American	Sub	13650	T=1.00000	C=0.00000
gnomAD - Genomes	Ashkenazi Jewish	Sub	3320	T=1.0000	C=0.0000
gnomAD - Genomes	East Asian	Sub	3126	T=0.9997	C=0.0003
gnomAD - Genomes	Other	Sub	2148	T=1.0000	C=0.0000
ExAC	Global	Study-wide	120218	T=0.999983	C=0.000017
ExAC	Europe	Sub	73020	T=0.99999	C=0.00001
ExAC	Asian	Sub	24330	T=1.00000	C=0.00000
ExAC	American	Sub	11574	T=1.00000	C=0.00000
ExAC	African	Sub	10392	T=0.99990	C=0.00010
ExAC	Other	Sub	902	T=1.000	C=0.000
14KJPN	JAPANESE	Study-wide	28258	T=0.99993	C=0.00007
8.3KJPN	JAPANESE	Study-wide	16760	T=0.99994	C=0.00006
Allele Frequency Aggregator	Total	Global	14050	T=1.00000	C=0.00000
Allele Frequency Aggregator	European	Sub	9690	T=1.0000	C=0.0000
Allele Frequency Aggregator	African	Sub	2898	T=1.0000	C=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	610	T=1.000	C=0.000
Allele Frequency Aggregator	Other	Sub	496	T=1.000	C=0.000
Allele Frequency Aggregator	Latin American 1	Sub	146	T=1.000	C=0.000
Allele Frequency Aggregator	Asian	Sub	112	T=1.000	C=0.000
Allele Frequency Aggregator	South Asian	Sub	98	T=1.00	C=0.00
GO Exome Sequencing Project	Global	Study-wide	13006	T=0.99985	C=0.00015
GO Exome Sequencing Project	European American	Sub	8600	T=1.0000	C=0.0000
GO Exome Sequencing Project	African American	Sub	4406	T=0.9995	C=0.0005
1000Genomes_30x	Global	Study-wide	6404	T=0.9998	C=0.0002
1000Genomes_30x	African	Sub	1786	T=0.9994	C=0.0006
1000Genomes_30x	Europe	Sub	1266	T=1.0000	C=0.0000
1000Genomes_30x	South Asian	Sub	1202	T=1.0000	C=0.0000
1000Genomes_30x	East Asian	Sub	1170	T=1.0000	C=0.0000
1000Genomes_30x	American	Sub	980	T=1.000	C=0.000
1000Genomes	Global	Study-wide	5008	T=0.9998	C=0.0002
1000Genomes	African	Sub	1322	T=0.9992	C=0.0008
1000Genomes	East Asian	Sub	1008	T=1.0000	C=0.0000
1000Genomes	Europe	Sub	1006	T=1.0000	C=0.0000
1000Genomes	South Asian	Sub	978	T=1.000	C=0.000
1000Genomes	American	Sub	694	T=1.000	C=0.000

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.17613168T>C
GRCh37.p13 chr 1	NC_000001.10:g.17939663T>C
ARHGEF10L RefSeqGene	NG_050860.1:g.97972T>C

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.610-2926… NM_001011722.2:c.610-2926T>C	N/A	Intron Variant
ARHGEF10L transcript variant 3	NM_001319837.1:c.610-2926… NM_001319837.1:c.610-2926T>C	N/A	Intron Variant
ARHGEF10L transcript variant 4	NM_001319838.1:c.	N/A	Genic Upstream Transcript Variant
ARHGEF10L transcript variant 5	NM_001328124.1:c.	N/A	Genic Upstream Transcript Variant
ARHGEF10L transcript variant 1	NM_018125.4:c.720T>C	D [GAT] > D [GAC]	Coding Sequence Variant
rho guanine nucleotide exchange factor 10-like protein isoform 1	NP_060595.3:p.Asp240=	D (Asp) > D (Asp)	Synonymous Variant
ARHGEF10L transcript variant 6	NR_137287.2:n.1019T>C	N/A	Non Coding Transcript Variant
ARHGEF10L transcript variant 7	NR_137288.2:n.	N/A	Intron Variant
ARHGEF10L transcript variant X2	XM_005245923.3:c.613-2926… XM_005245923.3:c.613-2926T>C	N/A	Intron Variant
ARHGEF10L transcript variant X13	XM_005245925.3:c.610-2926… XM_005245925.3:c.610-2926T>C	N/A	Intron Variant
ARHGEF10L transcript variant X3	XM_006710728.1:c.613-2926… XM_006710728.1:c.613-2926T>C	N/A	Intron Variant
ARHGEF10L transcript variant X11	XM_006710729.2:c.610-2926… XM_006710729.2:c.610-2926T>C	N/A	Intron Variant
ARHGEF10L transcript variant X10	XM_006710731.1:c.610-2926… XM_006710731.1:c.610-2926T>C	N/A	Intron Variant
ARHGEF10L transcript variant X12	XM_011541691.3:c.613-2926… XM_011541691.3:c.613-2926T>C	N/A	Intron Variant
ARHGEF10L transcript variant X14	XM_011541692.3:c.613-2926… XM_011541692.3:c.613-2926T>C	N/A	Intron Variant
ARHGEF10L transcript variant X24	XM_017001617.2:c.610-2926… XM_017001617.2:c.610-2926T>C	N/A	Intron Variant
ARHGEF10L transcript variant X27	XM_017001619.2:c.613-2926… XM_017001619.2:c.613-2926T>C	N/A	Intron Variant
ARHGEF10L transcript variant X28	XM_017001620.2:c.613-2926… XM_017001620.2:c.613-2926T>C	N/A	Intron Variant
ARHGEF10L transcript variant X4	XM_024448059.2:c.613-2926… XM_024448059.2:c.613-2926T>C	N/A	Intron Variant
ARHGEF10L transcript variant X6	XM_024448061.2:c.613-2926… XM_024448061.2:c.613-2926T>C	N/A	Intron Variant
ARHGEF10L transcript variant X5	XM_024448062.1:c.613-2926… XM_024448062.1:c.613-2926T>C	N/A	Intron Variant
ARHGEF10L transcript variant X1	XM_047424065.1:c.613-2926… XM_047424065.1:c.613-2926T>C	N/A	Intron Variant
ARHGEF10L transcript variant X7	XM_047424070.1:c.613-2926… XM_047424070.1:c.613-2926T>C	N/A	Intron Variant
ARHGEF10L transcript variant X8	XM_047424071.1:c.613-2926… XM_047424071.1:c.613-2926T>C	N/A	Intron Variant
ARHGEF10L transcript variant X9	XM_047424075.1:c.613-2926… XM_047424075.1:c.613-2926T>C	N/A	Intron Variant
ARHGEF10L transcript variant X15	XM_047424089.1:c.613-2926… XM_047424089.1:c.613-2926T>C	N/A	Intron Variant
ARHGEF10L transcript variant X16	XM_047424093.1:c.613-2926… XM_047424093.1:c.613-2926T>C	N/A	Intron Variant
ARHGEF10L transcript variant X17	XM_047424096.1:c.613-2926… XM_047424096.1:c.613-2926T>C	N/A	Intron Variant
ARHGEF10L transcript variant X18	XM_047424097.1:c.613-2926… XM_047424097.1:c.613-2926T>C	N/A	Intron Variant
ARHGEF10L transcript variant X19	XM_047424098.1:c.610-2926… XM_047424098.1:c.610-2926T>C	N/A	Intron Variant
ARHGEF10L transcript variant X20	XM_047424100.1:c.610-2926… XM_047424100.1:c.610-2926T>C	N/A	Intron Variant
ARHGEF10L transcript variant X21	XM_047424105.1:c.610-2926… XM_047424105.1:c.610-2926T>C	N/A	Intron Variant
ARHGEF10L transcript variant X22	XM_047424111.1:c.610-2926… XM_047424111.1:c.610-2926T>C	N/A	Intron Variant
ARHGEF10L transcript variant X23	XM_047424112.1:c.610-2926… XM_047424112.1:c.610-2926T>C	N/A	Intron Variant
ARHGEF10L transcript variant X29	XM_047424158.1:c.613-2926… XM_047424158.1:c.613-2926T>C	N/A	Intron Variant
ARHGEF10L transcript variant X30	XM_047424159.1:c.613-2926… XM_047424159.1:c.613-2926T>C	N/A	Intron Variant
ARHGEF10L transcript variant X31	XM_047424165.1:c.613-2926… XM_047424165.1:c.613-2926T>C	N/A	Intron Variant
ARHGEF10L transcript variant X32	XM_047424167.1:c.610-2926… XM_047424167.1:c.610-2926T>C	N/A	Intron Variant
ARHGEF10L transcript variant X33	XM_047424175.1:c.613-2926… XM_047424175.1:c.613-2926T>C	N/A	Intron Variant
ARHGEF10L transcript variant X35	XM_047424190.1:c.613-2926… XM_047424190.1:c.613-2926T>C	N/A	Intron Variant
ARHGEF10L transcript variant X36	XM_047424201.1:c.610-2926… XM_047424201.1:c.610-2926T>C	N/A	Intron Variant
ARHGEF10L transcript variant X26	XM_005245929.4:c.	N/A	Genic Upstream Transcript Variant
ARHGEF10L transcript variant X25	XR_946686.4:n.	N/A	Intron Variant
ARHGEF10L transcript variant X34	XR_946691.3:n.	N/A	Intron Variant

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

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	T=	C
GRCh38.p14 chr 1	NC_000001.11:g.17613168=	NC_000001.11:g.17613168T>C
GRCh37.p13 chr 1	NC_000001.10:g.17939663=	NC_000001.10:g.17939663T>C
ARHGEF10L RefSeqGene	NG_050860.1:g.97972=	NG_050860.1:g.97972T>C
ARHGEF10L transcript variant 1	NM_018125.4:c.720=	NM_018125.4:c.720T>C
ARHGEF10L transcript variant 1	NM_018125.3:c.720=	NM_018125.3:c.720T>C
ARHGEF10L transcript variant 6	NR_137287.2:n.1019=	NR_137287.2:n.1019T>C
ARHGEF10L transcript variant 6	NR_137287.1:n.882=	NR_137287.1:n.882T>C
rho guanine nucleotide exchange factor 10-like protein isoform 1	NP_060595.3:p.Asp240=	NP_060595.3:p.Asp240=
ARHGEF10L transcript variant 2	NM_001011722.2:c.610-2926=	NM_001011722.2:c.610-2926T>C
ARHGEF10L transcript variant 3	NM_001319837.1:c.610-2926=	NM_001319837.1:c.610-2926T>C
ARHGEF10L transcript variant X3	XM_005245923.1:c.613-2926=	XM_005245923.1:c.613-2926T>C
ARHGEF10L transcript variant X2	XM_005245923.3:c.613-2926=	XM_005245923.3:c.613-2926T>C
ARHGEF10L transcript variant X4	XM_005245924.1:c.613-2926=	XM_005245924.1:c.613-2926T>C
ARHGEF10L transcript variant X5	XM_005245925.1:c.610-2926=	XM_005245925.1:c.610-2926T>C
ARHGEF10L transcript variant X13	XM_005245925.3:c.610-2926=	XM_005245925.3:c.610-2926T>C
ARHGEF10L transcript variant X6	XM_005245926.1:c.610-2926=	XM_005245926.1:c.610-2926T>C
ARHGEF10L transcript variant X8	XM_005245928.1:c.43-2926=	XM_005245928.1:c.43-2926T>C
ARHGEF10L transcript variant X3	XM_006710728.1:c.613-2926=	XM_006710728.1:c.613-2926T>C
ARHGEF10L transcript variant X11	XM_006710729.2:c.610-2926=	XM_006710729.2:c.610-2926T>C
ARHGEF10L transcript variant X10	XM_006710731.1:c.610-2926=	XM_006710731.1:c.610-2926T>C
ARHGEF10L transcript variant X12	XM_011541691.3:c.613-2926=	XM_011541691.3:c.613-2926T>C
ARHGEF10L transcript variant X14	XM_011541692.3:c.613-2926=	XM_011541692.3:c.613-2926T>C
ARHGEF10L transcript variant X24	XM_017001617.2:c.610-2926=	XM_017001617.2:c.610-2926T>C
ARHGEF10L transcript variant X27	XM_017001619.2:c.613-2926=	XM_017001619.2:c.613-2926T>C
ARHGEF10L transcript variant X28	XM_017001620.2:c.613-2926=	XM_017001620.2:c.613-2926T>C
ARHGEF10L transcript variant X4	XM_024448059.2:c.613-2926=	XM_024448059.2:c.613-2926T>C
ARHGEF10L transcript variant X6	XM_024448061.2:c.613-2926=	XM_024448061.2:c.613-2926T>C
ARHGEF10L transcript variant X5	XM_024448062.1:c.613-2926=	XM_024448062.1:c.613-2926T>C
ARHGEF10L transcript variant X1	XM_047424065.1:c.613-2926=	XM_047424065.1:c.613-2926T>C
ARHGEF10L transcript variant X7	XM_047424070.1:c.613-2926=	XM_047424070.1:c.613-2926T>C
ARHGEF10L transcript variant X8	XM_047424071.1:c.613-2926=	XM_047424071.1:c.613-2926T>C
ARHGEF10L transcript variant X9	XM_047424075.1:c.613-2926=	XM_047424075.1:c.613-2926T>C
ARHGEF10L transcript variant X15	XM_047424089.1:c.613-2926=	XM_047424089.1:c.613-2926T>C
ARHGEF10L transcript variant X16	XM_047424093.1:c.613-2926=	XM_047424093.1:c.613-2926T>C
ARHGEF10L transcript variant X17	XM_047424096.1:c.613-2926=	XM_047424096.1:c.613-2926T>C
ARHGEF10L transcript variant X18	XM_047424097.1:c.613-2926=	XM_047424097.1:c.613-2926T>C
ARHGEF10L transcript variant X19	XM_047424098.1:c.610-2926=	XM_047424098.1:c.610-2926T>C
ARHGEF10L transcript variant X20	XM_047424100.1:c.610-2926=	XM_047424100.1:c.610-2926T>C
ARHGEF10L transcript variant X21	XM_047424105.1:c.610-2926=	XM_047424105.1:c.610-2926T>C
ARHGEF10L transcript variant X22	XM_047424111.1:c.610-2926=	XM_047424111.1:c.610-2926T>C
ARHGEF10L transcript variant X23	XM_047424112.1:c.610-2926=	XM_047424112.1:c.610-2926T>C
ARHGEF10L transcript variant X29	XM_047424158.1:c.613-2926=	XM_047424158.1:c.613-2926T>C
ARHGEF10L transcript variant X30	XM_047424159.1:c.613-2926=	XM_047424159.1:c.613-2926T>C
ARHGEF10L transcript variant X31	XM_047424165.1:c.613-2926=	XM_047424165.1:c.613-2926T>C
ARHGEF10L transcript variant X32	XM_047424167.1:c.610-2926=	XM_047424167.1:c.610-2926T>C
ARHGEF10L transcript variant X33	XM_047424175.1:c.613-2926=	XM_047424175.1:c.613-2926T>C
ARHGEF10L transcript variant X35	XM_047424190.1:c.613-2926=	XM_047424190.1:c.613-2926T>C
ARHGEF10L transcript variant X36	XM_047424201.1:c.610-2926=	XM_047424201.1:c.610-2926T>C

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#.

17 SubSNP, 10 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	1000GENOMES	ss217411014	Jul 14, 2010 (132)
2	1000GENOMES	ss488654920	May 04, 2012 (137)
3	NHLBI-ESP	ss712280413	Apr 25, 2013 (138)
4	1000GENOMES	ss1289865737	Aug 21, 2014 (142)
5	EVA_EXAC	ss1685350622	Apr 01, 2015 (144)
6	HUMAN_LONGEVITY	ss2160378745	Dec 20, 2016 (150)
7	GNOMAD	ss2731191738	Nov 08, 2017 (151)
8	GNOMAD	ss2746239722	Nov 08, 2017 (151)
9	GNOMAD	ss2752192106	Nov 08, 2017 (151)
10	EVA	ss3745885634	Jul 12, 2019 (153)
11	EVA	ss3823569010	Apr 25, 2020 (154)
12	TOPMED	ss4440704549	Apr 27, 2021 (155)
13	TOMMO_GENOMICS	ss5142731587	Apr 27, 2021 (155)
14	EVA	ss5317061376	Oct 12, 2022 (156)
15	1000G_HIGH_COVERAGE	ss5513196273	Oct 12, 2022 (156)
16	TOMMO_GENOMICS	ss5667108974	Oct 12, 2022 (156)
17	EVA	ss5907223090	Oct 12, 2022 (156)
18	1000Genomes	NC_000001.10 - 17939663	Oct 11, 2018 (152)
19	1000Genomes_30x	NC_000001.11 - 17613168	Oct 12, 2022 (156)
20	ExAC	NC_000001.10 - 17939663	Oct 11, 2018 (152)
21	gnomAD - Genomes	NC_000001.11 - 17613168	Apr 27, 2021 (155)
22	gnomAD - Exomes	NC_000001.10 - 17939663	Jul 12, 2019 (153)
23	GO Exome Sequencing Project	NC_000001.10 - 17939663	Oct 11, 2018 (152)
24	8.3KJPN	NC_000001.10 - 17939663	Apr 27, 2021 (155)
25	14KJPN	NC_000001.11 - 17613168	Oct 12, 2022 (156)
26	TopMed	NC_000001.11 - 17613168	Apr 27, 2021 (155)
27	ALFA	NC_000001.11 - 17613168	Apr 27, 2021 (155)

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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss217411014	NC_000001.9:17812249:T:C	NC_000001.11:17613167:T:C	(self)
548199, 4533187, 204302, 27728, 700894, ss488654920, ss712280413, ss1289865737, ss1685350622, ss2731191738, ss2746239722, ss2752192106, ss3745885634, ss3823569010, ss5142731587, ss5317061376	NC_000001.10:17939662:T:C	NC_000001.11:17613167:T:C	(self)
722208, 3840453, 946078, 4310884, 1547578278, ss2160378745, ss4440704549, ss5513196273, ss5667108974, ss5907223090	NC_000001.11:17613167:T:C	NC_000001.11:17613167:T:C	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs116261102

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
Top▲ Help
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.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs116261102