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dbSNP Short Genetic Variations

Examples: rs268, BRCA1 and more Advanced search

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.

rs866269762

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr4:152329754 (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
G>A / G>C / G>T
Variation Type
SNV Single Nucleotide Variation
Frequency
None
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
FBXW7 : Missense Variant
Publications
0 citations
Genomic View
See rs on genome
Help

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").

None
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 4 NC_000004.12:g.152329754G>A
GRCh38.p14 chr 4 NC_000004.12:g.152329754G>C
GRCh38.p14 chr 4 NC_000004.12:g.152329754G>T
GRCh37.p13 chr 4 NC_000004.11:g.153250906G>A
GRCh37.p13 chr 4 NC_000004.11:g.153250906G>C
GRCh37.p13 chr 4 NC_000004.11:g.153250906G>T
FBXW7 RefSeqGene (LRG_1141) NG_029466.2:g.212120C>T
FBXW7 RefSeqGene (LRG_1141) NG_029466.2:g.212120C>G
FBXW7 RefSeqGene (LRG_1141) NG_029466.2:g.212120C>A
Gene: FBXW7, F-box and WD repeat domain containing 7 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
FBXW7 transcript variant 4 NM_001257069.1:c. N/A Genic Downstream Transcript Variant
FBXW7 transcript variant 1 NM_033632.3:c.1154C>T T [ACA] > I [ATA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform 1 NP_361014.1:p.Thr385Ile T (Thr) > I (Ile) Missense Variant
FBXW7 transcript variant 1 NM_033632.3:c.1154C>G T [ACA] > R [AGA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform 1 NP_361014.1:p.Thr385Arg T (Thr) > R (Arg) Missense Variant
FBXW7 transcript variant 1 NM_033632.3:c.1154C>A T [ACA] > K [AAA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform 1 NP_361014.1:p.Thr385Lys T (Thr) > K (Lys) Missense Variant
FBXW7 transcript variant 2 NM_018315.5:c.914C>T T [ACA] > I [ATA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform 2 NP_060785.2:p.Thr305Ile T (Thr) > I (Ile) Missense Variant
FBXW7 transcript variant 2 NM_018315.5:c.914C>G T [ACA] > R [AGA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform 2 NP_060785.2:p.Thr305Arg T (Thr) > R (Arg) Missense Variant
FBXW7 transcript variant 2 NM_018315.5:c.914C>A T [ACA] > K [AAA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform 2 NP_060785.2:p.Thr305Lys T (Thr) > K (Lys) Missense Variant
FBXW7 transcript variant 3 NM_001013415.2:c.800C>T T [ACA] > I [ATA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform 3 NP_001013433.1:p.Thr267Ile T (Thr) > I (Ile) Missense Variant
FBXW7 transcript variant 3 NM_001013415.2:c.800C>G T [ACA] > R [AGA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform 3 NP_001013433.1:p.Thr267Arg T (Thr) > R (Arg) Missense Variant
FBXW7 transcript variant 3 NM_001013415.2:c.800C>A T [ACA] > K [AAA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform 3 NP_001013433.1:p.Thr267Lys T (Thr) > K (Lys) Missense Variant
FBXW7 transcript variant 5 NM_001349798.2:c.1154C>T T [ACA] > I [ATA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform 1 NP_001336727.1:p.Thr385Ile T (Thr) > I (Ile) Missense Variant
FBXW7 transcript variant 5 NM_001349798.2:c.1154C>G T [ACA] > R [AGA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform 1 NP_001336727.1:p.Thr385Arg T (Thr) > R (Arg) Missense Variant
FBXW7 transcript variant 5 NM_001349798.2:c.1154C>A T [ACA] > K [AAA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform 1 NP_001336727.1:p.Thr385Lys T (Thr) > K (Lys) Missense Variant
FBXW7 transcript variant X1 XM_047415897.1:c.1154C>T T [ACA] > I [ATA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X1 XP_047271853.1:p.Thr385Ile T (Thr) > I (Ile) Missense Variant
FBXW7 transcript variant X1 XM_047415897.1:c.1154C>G T [ACA] > R [AGA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X1 XP_047271853.1:p.Thr385Arg T (Thr) > R (Arg) Missense Variant
FBXW7 transcript variant X1 XM_047415897.1:c.1154C>A T [ACA] > K [AAA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X1 XP_047271853.1:p.Thr385Lys T (Thr) > K (Lys) Missense Variant
FBXW7 transcript variant X2 XM_047415898.1:c.1154C>T T [ACA] > I [ATA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X1 XP_047271854.1:p.Thr385Ile T (Thr) > I (Ile) Missense Variant
FBXW7 transcript variant X2 XM_047415898.1:c.1154C>G T [ACA] > R [AGA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X1 XP_047271854.1:p.Thr385Arg T (Thr) > R (Arg) Missense Variant
FBXW7 transcript variant X2 XM_047415898.1:c.1154C>A T [ACA] > K [AAA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X1 XP_047271854.1:p.Thr385Lys T (Thr) > K (Lys) Missense Variant
FBXW7 transcript variant X3 XM_047415899.1:c.1154C>T T [ACA] > I [ATA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X1 XP_047271855.1:p.Thr385Ile T (Thr) > I (Ile) Missense Variant
FBXW7 transcript variant X3 XM_047415899.1:c.1154C>G T [ACA] > R [AGA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X1 XP_047271855.1:p.Thr385Arg T (Thr) > R (Arg) Missense Variant
FBXW7 transcript variant X3 XM_047415899.1:c.1154C>A T [ACA] > K [AAA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X1 XP_047271855.1:p.Thr385Lys T (Thr) > K (Lys) Missense Variant
FBXW7 transcript variant X4 XM_047415900.1:c.1154C>T T [ACA] > I [ATA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X1 XP_047271856.1:p.Thr385Ile T (Thr) > I (Ile) Missense Variant
FBXW7 transcript variant X4 XM_047415900.1:c.1154C>G T [ACA] > R [AGA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X1 XP_047271856.1:p.Thr385Arg T (Thr) > R (Arg) Missense Variant
FBXW7 transcript variant X4 XM_047415900.1:c.1154C>A T [ACA] > K [AAA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X1 XP_047271856.1:p.Thr385Lys T (Thr) > K (Lys) Missense Variant
FBXW7 transcript variant X5 XM_011532084.3:c.1154C>T T [ACA] > I [ATA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X1 XP_011530386.1:p.Thr385Ile T (Thr) > I (Ile) Missense Variant
FBXW7 transcript variant X5 XM_011532084.3:c.1154C>G T [ACA] > R [AGA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X1 XP_011530386.1:p.Thr385Arg T (Thr) > R (Arg) Missense Variant
FBXW7 transcript variant X5 XM_011532084.3:c.1154C>A T [ACA] > K [AAA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X1 XP_011530386.1:p.Thr385Lys T (Thr) > K (Lys) Missense Variant
FBXW7 transcript variant X6 XM_011532085.3:c.1154C>T T [ACA] > I [ATA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X1 XP_011530387.1:p.Thr385Ile T (Thr) > I (Ile) Missense Variant
FBXW7 transcript variant X6 XM_011532085.3:c.1154C>G T [ACA] > R [AGA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X1 XP_011530387.1:p.Thr385Arg T (Thr) > R (Arg) Missense Variant
FBXW7 transcript variant X6 XM_011532085.3:c.1154C>A T [ACA] > K [AAA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X1 XP_011530387.1:p.Thr385Lys T (Thr) > K (Lys) Missense Variant
FBXW7 transcript variant X7 XM_024454123.2:c.1154C>T T [ACA] > I [ATA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X1 XP_024309891.1:p.Thr385Ile T (Thr) > I (Ile) Missense Variant
FBXW7 transcript variant X7 XM_024454123.2:c.1154C>G T [ACA] > R [AGA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X1 XP_024309891.1:p.Thr385Arg T (Thr) > R (Arg) Missense Variant
FBXW7 transcript variant X7 XM_024454123.2:c.1154C>A T [ACA] > K [AAA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X1 XP_024309891.1:p.Thr385Lys T (Thr) > K (Lys) Missense Variant
FBXW7 transcript variant X8 XM_047415901.1:c.1154C>T T [ACA] > I [ATA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X1 XP_047271857.1:p.Thr385Ile T (Thr) > I (Ile) Missense Variant
FBXW7 transcript variant X8 XM_047415901.1:c.1154C>G T [ACA] > R [AGA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X1 XP_047271857.1:p.Thr385Arg T (Thr) > R (Arg) Missense Variant
FBXW7 transcript variant X8 XM_047415901.1:c.1154C>A T [ACA] > K [AAA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X1 XP_047271857.1:p.Thr385Lys T (Thr) > K (Lys) Missense Variant
FBXW7 transcript variant X9 XM_011532087.3:c.1070C>T T [ACA] > I [ATA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X2 XP_011530389.1:p.Thr357Ile T (Thr) > I (Ile) Missense Variant
FBXW7 transcript variant X9 XM_011532087.3:c.1070C>G T [ACA] > R [AGA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X2 XP_011530389.1:p.Thr357Arg T (Thr) > R (Arg) Missense Variant
FBXW7 transcript variant X9 XM_011532087.3:c.1070C>A T [ACA] > K [AAA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X2 XP_011530389.1:p.Thr357Lys T (Thr) > K (Lys) Missense Variant
FBXW7 transcript variant X10 XM_011532086.3:c.1070C>T T [ACA] > I [ATA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X2 XP_011530388.1:p.Thr357Ile T (Thr) > I (Ile) Missense Variant
FBXW7 transcript variant X10 XM_011532086.3:c.1070C>G T [ACA] > R [AGA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X2 XP_011530388.1:p.Thr357Arg T (Thr) > R (Arg) Missense Variant
FBXW7 transcript variant X10 XM_011532086.3:c.1070C>A T [ACA] > K [AAA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X2 XP_011530388.1:p.Thr357Lys T (Thr) > K (Lys) Missense Variant
FBXW7 transcript variant X11 XM_047415902.1:c.1070C>T T [ACA] > I [ATA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X2 XP_047271858.1:p.Thr357Ile T (Thr) > I (Ile) Missense Variant
FBXW7 transcript variant X11 XM_047415902.1:c.1070C>G T [ACA] > R [AGA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X2 XP_047271858.1:p.Thr357Arg T (Thr) > R (Arg) Missense Variant
FBXW7 transcript variant X11 XM_047415902.1:c.1070C>A T [ACA] > K [AAA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X2 XP_047271858.1:p.Thr357Lys T (Thr) > K (Lys) Missense Variant
FBXW7 transcript variant X12 XM_024454126.2:c.653C>T T [ACA] > I [ATA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X3 XP_024309894.1:p.Thr218Ile T (Thr) > I (Ile) Missense Variant
FBXW7 transcript variant X12 XM_024454126.2:c.653C>G T [ACA] > R [AGA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X3 XP_024309894.1:p.Thr218Arg T (Thr) > R (Arg) Missense Variant
FBXW7 transcript variant X12 XM_024454126.2:c.653C>A T [ACA] > K [AAA] Coding Sequence Variant
F-box/WD repeat-containing protein 7 isoform X3 XP_024309894.1:p.Thr218Lys T (Thr) > K (Lys) Missense 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 G= A C T
GRCh38.p14 chr 4 NC_000004.12:g.152329754= NC_000004.12:g.152329754G>A NC_000004.12:g.152329754G>C NC_000004.12:g.152329754G>T
GRCh37.p13 chr 4 NC_000004.11:g.153250906= NC_000004.11:g.153250906G>A NC_000004.11:g.153250906G>C NC_000004.11:g.153250906G>T
FBXW7 RefSeqGene (LRG_1141) NG_029466.2:g.212120= NG_029466.2:g.212120C>T NG_029466.2:g.212120C>G NG_029466.2:g.212120C>A
FBXW7 transcript variant 2 NM_018315.5:c.914= NM_018315.5:c.914C>T NM_018315.5:c.914C>G NM_018315.5:c.914C>A
FBXW7 transcript variant 2 NM_018315.4:c.914= NM_018315.4:c.914C>T NM_018315.4:c.914C>G NM_018315.4:c.914C>A
FBXW7 transcript variant 1 NM_033632.3:c.1154= NM_033632.3:c.1154C>T NM_033632.3:c.1154C>G NM_033632.3:c.1154C>A
FBXW7 transcript variant 5 NM_001349798.2:c.1154= NM_001349798.2:c.1154C>T NM_001349798.2:c.1154C>G NM_001349798.2:c.1154C>A
FBXW7 transcript variant 5 NM_001349798.1:c.1154= NM_001349798.1:c.1154C>T NM_001349798.1:c.1154C>G NM_001349798.1:c.1154C>A
FBXW7 transcript variant 3 NM_001013415.2:c.800= NM_001013415.2:c.800C>T NM_001013415.2:c.800C>G NM_001013415.2:c.800C>A
FBXW7 transcript variant 3 NM_001013415.1:c.800= NM_001013415.1:c.800C>T NM_001013415.1:c.800C>G NM_001013415.1:c.800C>A
FBXW7 transcript variant X10 XM_011532086.3:c.1070= XM_011532086.3:c.1070C>T XM_011532086.3:c.1070C>G XM_011532086.3:c.1070C>A
FBXW7 transcript variant X7 XM_011532086.2:c.1070= XM_011532086.2:c.1070C>T XM_011532086.2:c.1070C>G XM_011532086.2:c.1070C>A
FBXW7 transcript variant X5 XM_011532086.1:c.1070= XM_011532086.1:c.1070C>T XM_011532086.1:c.1070C>G XM_011532086.1:c.1070C>A
FBXW7 transcript variant X9 XM_011532087.3:c.1070= XM_011532087.3:c.1070C>T XM_011532087.3:c.1070C>G XM_011532087.3:c.1070C>A
FBXW7 transcript variant X9 XM_011532087.2:c.1070= XM_011532087.2:c.1070C>T XM_011532087.2:c.1070C>G XM_011532087.2:c.1070C>A
FBXW7 transcript variant X6 XM_011532087.1:c.1070= XM_011532087.1:c.1070C>T XM_011532087.1:c.1070C>G XM_011532087.1:c.1070C>A
FBXW7 transcript variant X5 XM_011532084.3:c.1154= XM_011532084.3:c.1154C>T XM_011532084.3:c.1154C>G XM_011532084.3:c.1154C>A
FBXW7 transcript variant X5 XM_011532084.2:c.1154= XM_011532084.2:c.1154C>T XM_011532084.2:c.1154C>G XM_011532084.2:c.1154C>A
FBXW7 transcript variant X3 XM_011532084.1:c.1154= XM_011532084.1:c.1154C>T XM_011532084.1:c.1154C>G XM_011532084.1:c.1154C>A
FBXW7 transcript variant X6 XM_011532085.3:c.1154= XM_011532085.3:c.1154C>T XM_011532085.3:c.1154C>G XM_011532085.3:c.1154C>A
FBXW7 transcript variant X6 XM_011532085.2:c.1154= XM_011532085.2:c.1154C>T XM_011532085.2:c.1154C>G XM_011532085.2:c.1154C>A
FBXW7 transcript variant X4 XM_011532085.1:c.1154= XM_011532085.1:c.1154C>T XM_011532085.1:c.1154C>G XM_011532085.1:c.1154C>A
FBXW7 transcript variant X7 XM_024454123.2:c.1154= XM_024454123.2:c.1154C>T XM_024454123.2:c.1154C>G XM_024454123.2:c.1154C>A
FBXW7 transcript variant X3 XM_024454123.1:c.1154= XM_024454123.1:c.1154C>T XM_024454123.1:c.1154C>G XM_024454123.1:c.1154C>A
FBXW7 transcript variant X12 XM_024454126.2:c.653= XM_024454126.2:c.653C>T XM_024454126.2:c.653C>G XM_024454126.2:c.653C>A
FBXW7 transcript variant X11 XM_024454126.1:c.653= XM_024454126.1:c.653C>T XM_024454126.1:c.653C>G XM_024454126.1:c.653C>A
FBXW7 transcript variant X1 XM_047415897.1:c.1154= XM_047415897.1:c.1154C>T XM_047415897.1:c.1154C>G XM_047415897.1:c.1154C>A
FBXW7 transcript variant X3 XM_047415899.1:c.1154= XM_047415899.1:c.1154C>T XM_047415899.1:c.1154C>G XM_047415899.1:c.1154C>A
FBXW7 transcript variant X8 XM_047415901.1:c.1154= XM_047415901.1:c.1154C>T XM_047415901.1:c.1154C>G XM_047415901.1:c.1154C>A
FBXW7 transcript variant X11 XM_047415902.1:c.1070= XM_047415902.1:c.1070C>T XM_047415902.1:c.1070C>G XM_047415902.1:c.1070C>A
FBXW7 transcript variant X4 XM_047415900.1:c.1154= XM_047415900.1:c.1154C>T XM_047415900.1:c.1154C>G XM_047415900.1:c.1154C>A
FBXW7 transcript variant X2 XM_047415898.1:c.1154= XM_047415898.1:c.1154C>T XM_047415898.1:c.1154C>G XM_047415898.1:c.1154C>A
F-box/WD repeat-containing protein 7 isoform 2 NP_060785.2:p.Thr305= NP_060785.2:p.Thr305Ile NP_060785.2:p.Thr305Arg NP_060785.2:p.Thr305Lys
F-box/WD repeat-containing protein 7 isoform 1 NP_361014.1:p.Thr385= NP_361014.1:p.Thr385Ile NP_361014.1:p.Thr385Arg NP_361014.1:p.Thr385Lys
F-box/WD repeat-containing protein 7 isoform 1 NP_001336727.1:p.Thr385= NP_001336727.1:p.Thr385Ile NP_001336727.1:p.Thr385Arg NP_001336727.1:p.Thr385Lys
F-box/WD repeat-containing protein 7 isoform 3 NP_001013433.1:p.Thr267= NP_001013433.1:p.Thr267Ile NP_001013433.1:p.Thr267Arg NP_001013433.1:p.Thr267Lys
F-box/WD repeat-containing protein 7 isoform X2 XP_011530388.1:p.Thr357= XP_011530388.1:p.Thr357Ile XP_011530388.1:p.Thr357Arg XP_011530388.1:p.Thr357Lys
F-box/WD repeat-containing protein 7 isoform X2 XP_011530389.1:p.Thr357= XP_011530389.1:p.Thr357Ile XP_011530389.1:p.Thr357Arg XP_011530389.1:p.Thr357Lys
F-box/WD repeat-containing protein 7 isoform X1 XP_011530386.1:p.Thr385= XP_011530386.1:p.Thr385Ile XP_011530386.1:p.Thr385Arg XP_011530386.1:p.Thr385Lys
F-box/WD repeat-containing protein 7 isoform X1 XP_011530387.1:p.Thr385= XP_011530387.1:p.Thr385Ile XP_011530387.1:p.Thr385Arg XP_011530387.1:p.Thr385Lys
F-box/WD repeat-containing protein 7 isoform X1 XP_024309891.1:p.Thr385= XP_024309891.1:p.Thr385Ile XP_024309891.1:p.Thr385Arg XP_024309891.1:p.Thr385Lys
F-box/WD repeat-containing protein 7 isoform X3 XP_024309894.1:p.Thr218= XP_024309894.1:p.Thr218Ile XP_024309894.1:p.Thr218Arg XP_024309894.1:p.Thr218Lys
F-box/WD repeat-containing protein 7 isoform X1 XP_047271853.1:p.Thr385= XP_047271853.1:p.Thr385Ile XP_047271853.1:p.Thr385Arg XP_047271853.1:p.Thr385Lys
F-box/WD repeat-containing protein 7 isoform X1 XP_047271855.1:p.Thr385= XP_047271855.1:p.Thr385Ile XP_047271855.1:p.Thr385Arg XP_047271855.1:p.Thr385Lys
F-box/WD repeat-containing protein 7 isoform X1 XP_047271857.1:p.Thr385= XP_047271857.1:p.Thr385Ile XP_047271857.1:p.Thr385Arg XP_047271857.1:p.Thr385Lys
F-box/WD repeat-containing protein 7 isoform X2 XP_047271858.1:p.Thr357= XP_047271858.1:p.Thr357Ile XP_047271858.1:p.Thr357Arg XP_047271858.1:p.Thr357Lys
F-box/WD repeat-containing protein 7 isoform X1 XP_047271856.1:p.Thr385= XP_047271856.1:p.Thr385Ile XP_047271856.1:p.Thr385Arg XP_047271856.1:p.Thr385Lys
F-box/WD repeat-containing protein 7 isoform X1 XP_047271854.1:p.Thr385= XP_047271854.1:p.Thr385Ile XP_047271854.1:p.Thr385Arg XP_047271854.1:p.Thr385Lys
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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#.

2 SubSNP submissions
No Submitter Submission ID Date (Build)
1 GENOMED ss1966658503 Feb 12, 2016 (147)
2 EVA ss5935726156 Oct 13, 2022 (156)
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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
ss5935726156 NC_000004.11:153250905:G:A NC_000004.12:152329753:G:A
ss5935726156 NC_000004.11:153250905:G:C NC_000004.12:152329753:G:C
ss1966658503, ss5935726156 NC_000004.11:153250905:G:T NC_000004.12:152329753:G:T (self)
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Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs866269762

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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.

Software version is: 2.0.1.post761+d5e8e07