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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.

rs761146881

Current Build 152

Released October 2, 2018

Organism
Homo sapiens
Position
chr6:30160799 (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
C>G
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.00000 (1/246010, GnomAD)
G=0.00001 (1/120734, ExAC)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
TRIM10 : Missense Variant
Publications
0 citations
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 6 NC_000006.12:g.30160799C>G
GRCh37.p13 chr 6 NC_000006.11:g.30128576C>G
GRCh38.p12 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.3:g.1640605C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.2:g.1640711C>G
GRCh38.p12 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.2:g.1415927C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.1:g.1421523C>G
GRCh38.p12 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.2:g.1416715C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.1:g.1422300C>G
GRCh38.p12 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.2:g.1459726C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.1:g.1459024C>G
GRCh38.p12 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.2:g.1471520C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.1:g.1477140C>G
GRCh38.p12 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.2:g.1504876C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.1:g.1510461C>G
GRCh38.p12 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.2:g.1418894C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.1:g.1368810C>G
Gene: TRIM10, tripartite motif containing 10 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
TRIM10 transcript variant 2 NM_052828.2:c.60G>C Q [CAG] > H [CAC] Coding Sequence Variant
tripartite motif-containing protein 10 isoform 2 NP_439893.2:p.Gln20His Q (Gln) > H (His) Missense Variant
TRIM10 transcript variant 1 NM_006778.3:c.60G>C Q [CAG] > H [CAC] Coding Sequence Variant
tripartite motif-containing protein 10 isoform 1 NP_006769.2:p.Gln20His Q (Gln) > H (His) Missense Variant
TRIM10 transcript variant X1 XM_011514221.1:c. N/A Splice Acceptor Variant
TRIM10 transcript variant X2 XM_011514222.2:c. N/A Splice Acceptor Variant
TRIM10 transcript variant X3 XM_011514223.2:c. N/A Splice Acceptor Variant
TRIM10 transcript variant X4 XM_011514225.1:c. N/A Splice Acceptor 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").

Download
Study Population Group Sample Size Ref Allele Alt Allele
gnomAD - Exomes Global Study-wide 246010 C=1.00000 G=0.00000
gnomAD - Exomes European Sub 133786 C=0.99999 G=0.00001
gnomAD - Exomes Asian Sub 48018 C=1.0000 G=0.0000
gnomAD - Exomes American Sub 33578 C=1.0000 G=0.0000
gnomAD - Exomes African Sub 15304 C=1.0000 G=0.0000
gnomAD - Exomes Ashkenazi Jewish Sub 9844 C=1.000 G=0.000
gnomAD - Exomes Other Sub 5480 C=1.000 G=0.000
ExAC Global Study-wide 120734 C=0.99999 G=0.00001
ExAC Europe Sub 72872 C=1.0000 G=0.0000
ExAC Asian Sub 25076 C=1.0000 G=0.0000
ExAC American Sub 11552 C=1.0000 G=0.0000
ExAC African Sub 10338 C=1.0000 G=0.0000
ExAC Other Sub 896 C=1.00 G=0.00
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= G Note
GRCh38.p12 chr 6 NC_000006.12:g.30160799C= NC_000006.12:g.30160799C>G
GRCh37.p13 chr 6 NC_000006.11:g.30128576C= NC_000006.11:g.30128576C>G
GRCh38.p12 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.3:g.1640605C= NT_113891.3:g.1640605C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.2:g.1640711C= NT_113891.2:g.1640711C>G
GRCh38.p12 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.2:g.1415927C= NT_167248.2:g.1415927C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.1:g.1421523C= NT_167248.1:g.1421523C>G
GRCh38.p12 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.2:g.1416715C= NT_167245.2:g.1416715C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.1:g.1422300C= NT_167245.1:g.1422300C>G
GRCh38.p12 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.2:g.1459726C= NT_167249.2:g.1459726C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.1:g.1459024C= NT_167249.1:g.1459024C>G
GRCh38.p12 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.2:g.1471520C= NT_167246.2:g.1471520C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.1:g.1477140C= NT_167246.1:g.1477140C>G
GRCh38.p12 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.2:g.1504876C= NT_167247.2:g.1504876C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.1:g.1510461C= NT_167247.1:g.1510461C>G
GRCh38.p12 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.2:g.1418894C= NT_167244.2:g.1418894C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.1:g.1368810C= NT_167244.1:g.1368810C>G
TRIM10 transcript variant 1 NM_006778.3:c.60G= NM_006778.3:c.60G>C
TRIM10 transcript variant 2 NM_052828.2:c.60G= NM_052828.2:c.60G>C
tripartite motif-containing protein 10 isoform 1 NP_006769.2:p.Gln20= NP_006769.2:p.Gln20His
tripartite motif-containing protein 10 isoform 2 NP_439893.2:p.Gln20= NP_439893.2:p.Gln20His
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, 2 Frequency submissions
No Submitter Submission ID Date (Build)
1 EVA_EXAC ss1688214217 Apr 01, 2015 (144)
2 GNOMAD ss2735622514 Nov 08, 2017 (151)
3 ExAC NC_000006.11 - 30128576 Oct 12, 2018 (152)
4 gnomAD - Exomes NC_000006.11 - 30128576 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).

Added to this RefSNP Cluster:
Submission ids Observation SPDI Canonical SPDI Source RSIDs
8237919, 3794750, ss1688214217, ss2735622514 NC_000006.11:30128575:C= NC_000006.12:30160798:C= (self)
8237919, 3794750, ss1688214217, ss2735622514 NC_000006.11:30128575:C>G NC_000006.12:30160798:C>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 rs761146881

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.post58+e54ea20