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dbSNP Short Genetic Variations

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.

rs8314

Current Build 153

Released July 9, 2019

Organism
Homo sapiens
Position
chr10:5001610 (GRCh38.p12) 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>A
Variation Type
SNV Single Nucleotide Variation
Frequency
None
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
AKR1C2 : Synonymous Variant
Publications
1 citation
Genomic View
See rs on genome
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.p12 chr 10 NC_000010.11:g.5001610T>A
GRCh37.p13 chr 10 fix patch HG871_PATCH NW_003871071.1:g.31276T>A
AKR1C2 RefSeqGene NG_031852.1:g.21406A>T
GRCh37.p13 chr 10 NC_000010.10:g.5043802T>A
Gene: AKR1C2, aldo-keto reductase family 1 member C2 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
AKR1C2 transcript variant 1 NM_001354.5:c.156A>T A [GCA] > A [GCT] Coding Sequence Variant
aldo-keto reductase family 1 member C2 isoform 1 NP_001345.1:p.Ala52= A (Ala) > A (Ala) Synonymous Variant
AKR1C2 transcript variant 2 NM_205845.2:c.156A>T A [GCA] > A [GCT] Coding Sequence Variant
aldo-keto reductase family 1 member C2 isoform 1 NP_995317.1:p.Ala52= A (Ala) > A (Ala) Synonymous Variant
AKR1C2 transcript variant 3 NM_001135241.2:c.156A>T A [GCA] > A [GCT] Coding Sequence Variant
aldo-keto reductase family 1 member C2 isoform 2 NP_001128713.1:p.Ala52= A (Ala) > A (Ala) Synonymous Variant
AKR1C2 transcript variant 4 NM_001321027.1:c.156A>T A [GCA] > A [GCT] Coding Sequence Variant
aldo-keto reductase family 1 member C2 isoform 3 NP_001307956.1:p.Ala52= A (Ala) > A (Ala) Synonymous 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

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

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= A Note
GRCh38.p12 chr 10 NC_000010.11:g.5001610= NC_000010.11:g.5001610T>A
GRCh37.p13 chr 10 fix patch HG871_PATCH NW_003871071.1:g.31276= NW_003871071.1:g.31276T>A
AKR1C2 RefSeqGene NG_031852.1:g.21406= NG_031852.1:g.21406A>T
AKR1C2 transcript variant 1 NM_001354.5:c.156= NM_001354.5:c.156A>T
AKR1C2 transcript variant 2 NM_205845.2:c.156= NM_205845.2:c.156A>T
AKR1C2 transcript variant 3 NM_001135241.2:c.156= NM_001135241.2:c.156A>T
AKR1C2 transcript variant 4 NM_001321027.1:c.156= NM_001321027.1:c.156A>T
GRCh37.p13 chr 10 NC_000010.10:g.5043802= NC_000010.10:g.5043802T>A
aldo-keto reductase family 1 member C2 isoform 1 NP_001345.1:p.Ala52= NP_001345.1:p.Ala52=
aldo-keto reductase family 1 member C2 isoform 1 NP_995317.1:p.Ala52= NP_995317.1:p.Ala52=
aldo-keto reductase family 1 member C2 isoform 2 NP_001128713.1:p.Ala52= NP_001128713.1:p.Ala52=
aldo-keto reductase family 1 member C2 isoform 3 NP_001307956.1:p.Ala52= NP_001307956.1:p.Ala52=
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#.

2 SubSNP submissions
No Submitter Submission ID Date (Build)
1 LEE ss4438230 May 29, 2002 (106)
2 GNOMAD ss2738086957 Oct 12, 2018 (152)
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)
rs3207906 Jul 03, 2002 (106)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss2738086957 NC_000010.10:5043801:T:A NC_000010.11:5001609:T:A (self)
ss4438230 NT_008705.16:4983801:T:A NC_000010.11:5001609:T:A (self)
Help

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

1 citation for rs8314
PMID Title Author Year Journal
19877174 Single nucleotide differences (SNDs) in the dbSNP database may lead to errors in genotyping and haplotyping studies. Musumeci L et al. 2010 Human mutation

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.post270+ab078da