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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.

rs752973367

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr20:46725988 (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
A>G
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.000004 (1/264690, TOPMED)
G=0.000004 (1/251060, GnomAD_exome)
G=0.000008 (1/121180, ExAC) (+ 1 more)
G=0.00000 (0/10680, ALFA)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
SLC2A10 : 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 27034 A=0.99996 G=0.00004
European Sub 17046 A=1.00000 G=0.00000
African Sub 7130 A=0.9999 G=0.0001
African Others Sub 268 A=1.000 G=0.000
African American Sub 6862 A=0.9999 G=0.0001
Asian Sub 108 A=1.000 G=0.000
East Asian Sub 84 A=1.00 G=0.00
Other Asian Sub 24 A=1.00 G=0.00
Latin American 1 Sub 146 A=1.000 G=0.000
Latin American 2 Sub 610 A=1.000 G=0.000
South Asian Sub 94 A=1.00 G=0.00
Other Sub 1900 A=1.0000 G=0.0000


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").

Download
Study Population Group Sample Size Ref Allele Alt Allele
TopMed Global Study-wide 264690 A=0.999996 G=0.000004
gnomAD - Exomes Global Study-wide 251060 A=0.999996 G=0.000004
gnomAD - Exomes European Sub 135018 A=1.000000 G=0.000000
gnomAD - Exomes Asian Sub 49004 A=0.99998 G=0.00002
gnomAD - Exomes American Sub 34588 A=1.00000 G=0.00000
gnomAD - Exomes African Sub 16242 A=1.00000 G=0.00000
gnomAD - Exomes Ashkenazi Jewish Sub 10076 A=1.00000 G=0.00000
gnomAD - Exomes Other Sub 6132 A=1.0000 G=0.0000
ExAC Global Study-wide 121180 A=0.999992 G=0.000008
ExAC Europe Sub 73184 A=1.00000 G=0.00000
ExAC Asian Sub 25156 A=0.99996 G=0.00004
ExAC American Sub 11572 A=1.00000 G=0.00000
ExAC African Sub 10366 A=1.00000 G=0.00000
ExAC Other Sub 902 A=1.000 G=0.000
Allele Frequency Aggregator Total Global 10680 A=1.00000 G=0.00000
Allele Frequency Aggregator European Sub 6962 A=1.0000 G=0.0000
Allele Frequency Aggregator African Sub 2294 A=1.0000 G=0.0000
Allele Frequency Aggregator Latin American 2 Sub 610 A=1.000 G=0.000
Allele Frequency Aggregator Other Sub 466 A=1.000 G=0.000
Allele Frequency Aggregator Latin American 1 Sub 146 A=1.000 G=0.000
Allele Frequency Aggregator Asian Sub 108 A=1.000 G=0.000
Allele Frequency Aggregator South Asian Sub 94 A=1.00 G=0.00
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 20 NC_000020.11:g.46725988A>G
GRCh37.p13 chr 20 NC_000020.10:g.45354627A>G
SLC2A10 RefSeqGene NG_016284.1:g.21349A>G
Gene: SLC2A10, solute carrier family 2 member 10 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
SLC2A10 transcript NM_030777.4:c.952A>G S [AGC] > G [GGC] Coding Sequence Variant
solute carrier family 2, facilitated glucose transporter member 10 NP_110404.1:p.Ser318Gly S (Ser) > G (Gly) Missense Variant
SLC2A10 transcript variant X1 XM_011529060.3:c.1015A>G S [AGC] > G [GGC] Coding Sequence Variant
solute carrier family 2, facilitated glucose transporter member 10 isoform X1 XP_011527362.1:p.Ser339Gly S (Ser) > G (Gly) Missense Variant
SLC2A10 transcript variant X2 XM_011529061.3:c.961A>G S [AGC] > G [GGC] Coding Sequence Variant
solute carrier family 2, facilitated glucose transporter member 10 isoform X2 XP_011527363.1:p.Ser321Gly S (Ser) > G (Gly) Missense Variant
SLC2A10 transcript variant X3 XM_047440528.1:c.1015A>G S [AGC] > G [GGC] Coding Sequence Variant
solute carrier family 2, facilitated glucose transporter member 10 isoform X3 XP_047296484.1:p.Ser339Gly S (Ser) > G (Gly) Missense Variant
SLC2A10 transcript variant X4 XM_011529062.3:c.1015A>G S [AGC] > G [GGC] Coding Sequence Variant
solute carrier family 2, facilitated glucose transporter member 10 isoform X4 XP_011527364.1:p.Ser339Gly S (Ser) > G (Gly) Missense Variant
SLC2A10 transcript variant X5 XM_011529063.3:c.1015A>G S [AGC] > G [GGC] Coding Sequence Variant
solute carrier family 2, facilitated glucose transporter member 10 isoform X5 XP_011527365.1:p.Ser339Gly S (Ser) > G (Gly) Missense Variant
SLC2A10 transcript variant X6 XM_047440529.1:c.952A>G S [AGC] > G [GGC] Coding Sequence Variant
solute carrier family 2, facilitated glucose transporter member 10 isoform X6 XP_047296485.1:p.Ser318Gly S (Ser) > G (Gly) Missense Variant
SLC2A10 transcript variant X7 XM_011529064.3:c.1015A>G S [AGC] > G [GGC] Coding Sequence Variant
solute carrier family 2, facilitated glucose transporter member 10 isoform X7 XP_011527366.1:p.Ser339Gly S (Ser) > G (Gly) Missense Variant
SLC2A10 transcript variant X8 XM_011529065.3:c.1015A>G S [AGC] > G [GGC] Coding Sequence Variant
solute carrier family 2, facilitated glucose transporter member 10 isoform X8 XP_011527367.1:p.Ser339Gly S (Ser) > G (Gly) Missense Variant
SLC2A10 transcript variant X9 XM_017028087.3:c.952A>G S [AGC] > G [GGC] Coding Sequence Variant
solute carrier family 2, facilitated glucose transporter member 10 isoform X9 XP_016883576.1:p.Ser318Gly S (Ser) > G (Gly) 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 A= G
GRCh38.p14 chr 20 NC_000020.11:g.46725988= NC_000020.11:g.46725988A>G
GRCh37.p13 chr 20 NC_000020.10:g.45354627= NC_000020.10:g.45354627A>G
SLC2A10 RefSeqGene NG_016284.1:g.21349= NG_016284.1:g.21349A>G
SLC2A10 transcript NM_030777.4:c.952= NM_030777.4:c.952A>G
SLC2A10 transcript NM_030777.3:c.952= NM_030777.3:c.952A>G
SLC2A10 transcript variant X2 XM_011529061.3:c.961= XM_011529061.3:c.961A>G
SLC2A10 transcript variant X2 XM_011529061.2:c.961= XM_011529061.2:c.961A>G
SLC2A10 transcript variant X2 XM_011529061.1:c.961= XM_011529061.1:c.961A>G
SLC2A10 transcript variant X1 XM_011529060.3:c.1015= XM_011529060.3:c.1015A>G
SLC2A10 transcript variant X1 XM_011529060.2:c.1015= XM_011529060.2:c.1015A>G
SLC2A10 transcript variant X1 XM_011529060.1:c.1015= XM_011529060.1:c.1015A>G
SLC2A10 transcript variant X4 XM_011529062.3:c.1015= XM_011529062.3:c.1015A>G
SLC2A10 transcript variant X4 XM_011529062.2:c.1015= XM_011529062.2:c.1015A>G
SLC2A10 transcript variant X4 XM_011529062.1:c.1015= XM_011529062.1:c.1015A>G
SLC2A10 transcript variant X8 XM_011529065.3:c.1015= XM_011529065.3:c.1015A>G
SLC2A10 transcript variant X7 XM_011529065.2:c.1015= XM_011529065.2:c.1015A>G
SLC2A10 transcript variant X7 XM_011529065.1:c.1015= XM_011529065.1:c.1015A>G
SLC2A10 transcript variant X9 XM_017028087.3:c.952= XM_017028087.3:c.952A>G
SLC2A10 transcript variant X8 XM_017028087.2:c.952= XM_017028087.2:c.952A>G
SLC2A10 transcript variant X8 XM_017028087.1:c.952= XM_017028087.1:c.952A>G
SLC2A10 transcript variant X5 XM_011529063.3:c.1015= XM_011529063.3:c.1015A>G
SLC2A10 transcript variant X5 XM_011529063.2:c.1015= XM_011529063.2:c.1015A>G
SLC2A10 transcript variant X5 XM_011529063.1:c.1015= XM_011529063.1:c.1015A>G
SLC2A10 transcript variant X7 XM_011529064.3:c.1015= XM_011529064.3:c.1015A>G
SLC2A10 transcript variant X6 XM_011529064.2:c.1015= XM_011529064.2:c.1015A>G
SLC2A10 transcript variant X6 XM_011529064.1:c.1015= XM_011529064.1:c.1015A>G
SLC2A10 transcript variant X6 XM_047440529.1:c.952= XM_047440529.1:c.952A>G
SLC2A10 transcript variant X3 XM_047440528.1:c.1015= XM_047440528.1:c.1015A>G
solute carrier family 2, facilitated glucose transporter member 10 NP_110404.1:p.Ser318= NP_110404.1:p.Ser318Gly
solute carrier family 2, facilitated glucose transporter member 10 isoform X2 XP_011527363.1:p.Ser321= XP_011527363.1:p.Ser321Gly
solute carrier family 2, facilitated glucose transporter member 10 isoform X1 XP_011527362.1:p.Ser339= XP_011527362.1:p.Ser339Gly
solute carrier family 2, facilitated glucose transporter member 10 isoform X4 XP_011527364.1:p.Ser339= XP_011527364.1:p.Ser339Gly
solute carrier family 2, facilitated glucose transporter member 10 isoform X8 XP_011527367.1:p.Ser339= XP_011527367.1:p.Ser339Gly
solute carrier family 2, facilitated glucose transporter member 10 isoform X9 XP_016883576.1:p.Ser318= XP_016883576.1:p.Ser318Gly
solute carrier family 2, facilitated glucose transporter member 10 isoform X5 XP_011527365.1:p.Ser339= XP_011527365.1:p.Ser339Gly
solute carrier family 2, facilitated glucose transporter member 10 isoform X7 XP_011527366.1:p.Ser339= XP_011527366.1:p.Ser339Gly
solute carrier family 2, facilitated glucose transporter member 10 isoform X6 XP_047296485.1:p.Ser318= XP_047296485.1:p.Ser318Gly
solute carrier family 2, facilitated glucose transporter member 10 isoform X3 XP_047296484.1:p.Ser339= XP_047296484.1:p.Ser339Gly
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#.

3 SubSNP, 4 Frequency submissions
No Submitter Submission ID Date (Build)
1 EVA_EXAC ss1694025945 Apr 01, 2015 (144)
2 GNOMAD ss2744652870 Nov 08, 2017 (151)
3 TOPMED ss5090358413 Apr 26, 2021 (155)
4 ExAC NC_000020.10 - 45354627 Oct 12, 2018 (152)
5 gnomAD - Exomes NC_000020.10 - 45354627 Jul 13, 2019 (153)
6 TopMed NC_000020.11 - 46725988 Apr 26, 2021 (155)
7 ALFA NC_000020.11 - 46725988 Apr 26, 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).

Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
5582772, 13975329, ss1694025945, ss2744652870 NC_000020.10:45354626:A:G NC_000020.11:46725987:A:G (self)
365467358, 4592506335, ss5090358413 NC_000020.11:46725987:A:G NC_000020.11:46725987:A:G (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 rs752973367

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
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.

Software version is: 2.0.1.post761+d5e8e07