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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.

rs776861168

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr16:57656528 (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
C>T
Variation Type
SNV Single Nucleotide Variation
Frequency
T=0.000004 (1/264690, TOPMED)
T=0.000004 (1/251486, GnomAD_exome)
T=0.000008 (1/121370, ExAC) (+ 1 more)
T=0.00000 (0/10680, ALFA)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
ADGRG1 : 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 10680 C=1.00000 T=0.00000
European Sub 6962 C=1.0000 T=0.0000
African Sub 2294 C=1.0000 T=0.0000
African Others Sub 84 C=1.00 T=0.00
African American Sub 2210 C=1.0000 T=0.0000
Asian Sub 108 C=1.000 T=0.000
East Asian Sub 84 C=1.00 T=0.00
Other Asian Sub 24 C=1.00 T=0.00
Latin American 1 Sub 146 C=1.000 T=0.000
Latin American 2 Sub 610 C=1.000 T=0.000
South Asian Sub 94 C=1.00 T=0.00
Other Sub 466 C=1.000 T=0.000


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 C=0.999996 T=0.000004
gnomAD - Exomes Global Study-wide 251486 C=0.999996 T=0.000004
gnomAD - Exomes European Sub 135408 C=1.000000 T=0.000000
gnomAD - Exomes Asian Sub 49010 C=0.99998 T=0.00002
gnomAD - Exomes American Sub 34592 C=1.00000 T=0.00000
gnomAD - Exomes African Sub 16256 C=1.00000 T=0.00000
gnomAD - Exomes Ashkenazi Jewish Sub 10080 C=1.00000 T=0.00000
gnomAD - Exomes Other Sub 6140 C=1.0000 T=0.0000
ExAC Global Study-wide 121370 C=0.999992 T=0.000008
ExAC Europe Sub 73330 C=1.00000 T=0.00000
ExAC Asian Sub 25160 C=0.99996 T=0.00004
ExAC American Sub 11574 C=1.00000 T=0.00000
ExAC African Sub 10398 C=1.00000 T=0.00000
ExAC Other Sub 908 C=1.000 T=0.000
Allele Frequency Aggregator Total Global 10680 C=1.00000 T=0.00000
Allele Frequency Aggregator European Sub 6962 C=1.0000 T=0.0000
Allele Frequency Aggregator African Sub 2294 C=1.0000 T=0.0000
Allele Frequency Aggregator Latin American 2 Sub 610 C=1.000 T=0.000
Allele Frequency Aggregator Other Sub 466 C=1.000 T=0.000
Allele Frequency Aggregator Latin American 1 Sub 146 C=1.000 T=0.000
Allele Frequency Aggregator Asian Sub 108 C=1.000 T=0.000
Allele Frequency Aggregator South Asian Sub 94 C=1.00 T=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 16 NC_000016.10:g.57656528C>T
GRCh37.p13 chr 16 NC_000016.9:g.57690440C>T
ADGRG1 RefSeqGene NG_011643.1:g.41531C>T
Gene: ADGRG1, adhesion G protein-coupled receptor G1 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
ADGRG1 transcript variant 3 NM_201525.4:c.1078C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform b precursor NP_958933.1:p.His360Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant 1 NM_005682.7:c.1078C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform a precursor NP_005673.3:p.His360Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant 29 NM_001370454.1:c.553C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform f NP_001357383.1:p.His185Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant 18 NM_001370434.1:c.1075C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform i precursor NP_001357363.1:p.His359Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant 17 NM_001370433.1:c.1093C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform c precursor NP_001357362.1:p.His365Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant 22 NM_001370438.1:c.1078C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform b precursor NP_001357367.1:p.His360Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant 12 NM_001370428.1:c.1078C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform a precursor NP_001357357.1:p.His360Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant 24 NM_001370440.1:c.1078C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform b precursor NP_001357369.1:p.His360Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant 25 NM_001370441.1:c.1075C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform g precursor NP_001357370.1:p.His359Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant 2 NM_201524.4:c.1078C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform b precursor NP_958932.1:p.His360Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant 27 NM_001370451.1:c.553C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform f NP_001357380.1:p.His185Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant 16 NM_001370432.1:c.1078C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform a precursor NP_001357361.1:p.His360Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant 23 NM_001370439.1:c.1078C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform b precursor NP_001357368.1:p.His360Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant 9 NM_001290142.2:c.568C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform d precursor NP_001277071.1:p.His190Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant 11 NM_001290144.2:c.553C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform f NP_001277073.1:p.His185Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant 26 NM_001370442.1:c.922C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform h precursor NP_001357371.1:p.His308Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant 20 NM_001370436.1:c.1078C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform b precursor NP_001357365.1:p.His360Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant 28 NM_001370453.1:c.553C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform f NP_001357382.1:p.His185Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant 19 NM_001370435.1:c.1078C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform b precursor NP_001357364.1:p.His360Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant 10 NM_001290143.2:c.553C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform e NP_001277072.1:p.His185Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant 6 NM_001145772.3:c.1078C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform b precursor NP_001139244.1:p.His360Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant 5 NM_001145770.3:c.1078C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform b precursor NP_001139242.1:p.His360Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant 4 NM_001145771.3:c.1078C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform a precursor NP_001139243.1:p.His360Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant 15 NM_001370431.1:c.1078C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform a precursor NP_001357360.1:p.His360Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant 7 NM_001145774.3:c.1078C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform b precursor NP_001139246.1:p.His360Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant 21 NM_001370437.1:c.1078C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform b precursor NP_001357366.1:p.His360Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant 8 NM_001145773.3:c.1093C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform c precursor NP_001139245.1:p.His365Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant 14 NM_001370430.1:c.1078C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform a precursor NP_001357359.1:p.His360Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant 13 NM_001370429.1:c.1078C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform a precursor NP_001357358.1:p.His360Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant X1 XM_005256238.3:c.1093C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform X1 XP_005256295.1:p.His365Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant X2 XM_006721339.5:c.1093C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform X1 XP_006721402.1:p.His365Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant X3 XM_006721340.4:c.1093C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform X1 XP_006721403.1:p.His365Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant X4 XM_006721338.3:c.1093C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform X1 XP_006721401.1:p.His365Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant X5 XM_047434906.1:c.1093C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform X1 XP_047290862.1:p.His365Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant X6 XM_005256240.5:c.1093C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform X1 XP_005256297.1:p.His365Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant X7 XM_005256237.3:c.1093C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform X1 XP_005256294.1:p.His365Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant X8 XM_011523462.3:c.1093C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform X1 XP_011521764.1:p.His365Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant X9 XM_005256242.5:c.1093C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform X1 XP_005256299.1:p.His365Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant X10 XM_005256239.3:c.1093C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform X1 XP_005256296.1:p.His365Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant X11 XM_005256244.4:c.1093C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform X1 XP_005256301.1:p.His365Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant X12 XM_005256241.5:c.1093C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform X1 XP_005256298.1:p.His365Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant X13 XM_005256245.3:c.1093C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform X1 XP_005256302.1:p.His365Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant X14 XM_006721342.3:c.1078C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform X2 XP_006721405.1:p.His360Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant X15 XM_005256246.3:c.1078C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform X2 XP_005256303.1:p.His360Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant X16 XM_011523466.3:c.1078C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform X2 XP_011521768.1:p.His360Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant X17 XM_005256254.3:c.1078C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform X2 XP_005256311.1:p.His360Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant X18 XM_005256248.3:c.1078C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform X2 XP_005256305.1:p.His360Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant X19 XM_005256252.3:c.1078C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform X2 XP_005256309.1:p.His360Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant X20 XM_011523468.3:c.1078C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform X2 XP_011521770.1:p.His360Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant X21 XM_006721347.3:c.1093C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform X3 XP_006721410.1:p.His365Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant X22 XM_047434907.1:c.1093C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform X3 XP_047290863.1:p.His365Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant X23 XM_047434908.1:c.1093C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform X3 XP_047290864.1:p.His365Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant X24 XM_047434909.1:c.1093C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform X3 XP_047290865.1:p.His365Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant X25 XM_047434910.1:c.1093C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform X3 XP_047290866.1:p.His365Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant X26 XM_047434911.1:c.1093C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform X3 XP_047290867.1:p.His365Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant X27 XM_047434912.1:c.1093C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform X3 XP_047290868.1:p.His365Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant X28 XM_005256255.3:c.1078C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform X4 XP_005256312.1:p.His360Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant X29 XM_047434913.1:c.1078C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform X4 XP_047290869.1:p.His360Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant X30 XM_017023892.2:c.1078C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform X4 XP_016879381.1:p.His360Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant X31 XM_047434914.1:c.1078C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform X4 XP_047290870.1:p.His360Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant X32 XM_047434915.1:c.1078C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform X4 XP_047290871.1:p.His360Tyr H (His) > Y (Tyr) Missense Variant
ADGRG1 transcript variant X33 XM_047434916.1:c.1078C>T H [CAT] > Y [TAT] Coding Sequence Variant
adhesion G-protein coupled receptor G1 isoform X4 XP_047290872.1:p.His360Tyr H (His) > Y (Tyr) 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 C= T
GRCh38.p14 chr 16 NC_000016.10:g.57656528= NC_000016.10:g.57656528C>T
GRCh37.p13 chr 16 NC_000016.9:g.57690440= NC_000016.9:g.57690440C>T
ADGRG1 RefSeqGene NG_011643.1:g.41531= NG_011643.1:g.41531C>T
ADGRG1 transcript variant 1 NM_005682.7:c.1078= NM_005682.7:c.1078C>T
ADGRG1 transcript variant 1 NM_005682.6:c.1078= NM_005682.6:c.1078C>T
GPR56 transcript variant 1 NM_005682.5:c.1078= NM_005682.5:c.1078C>T
ADGRG1 transcript variant 2 NM_201524.4:c.1078= NM_201524.4:c.1078C>T
ADGRG1 transcript variant 2 NM_201524.3:c.1078= NM_201524.3:c.1078C>T
GPR56 transcript variant 2 NM_201524.2:c.1078= NM_201524.2:c.1078C>T
ADGRG1 transcript variant 3 NM_201525.4:c.1078= NM_201525.4:c.1078C>T
ADGRG1 transcript variant 3 NM_201525.3:c.1078= NM_201525.3:c.1078C>T
GPR56 transcript variant 3 NM_201525.2:c.1078= NM_201525.2:c.1078C>T
ADGRG1 transcript variant 6 NM_001145772.3:c.1078= NM_001145772.3:c.1078C>T
ADGRG1 transcript variant 6 NM_001145772.2:c.1078= NM_001145772.2:c.1078C>T
GPR56 transcript variant 6 NM_001145772.1:c.1078= NM_001145772.1:c.1078C>T
ADGRG1 transcript variant 4 NM_001145771.3:c.1078= NM_001145771.3:c.1078C>T
ADGRG1 transcript variant 4 NM_001145771.2:c.1078= NM_001145771.2:c.1078C>T
GPR56 transcript variant 4 NM_001145771.1:c.1078= NM_001145771.1:c.1078C>T
ADGRG1 transcript variant 7 NM_001145774.3:c.1078= NM_001145774.3:c.1078C>T
ADGRG1 transcript variant 7 NM_001145774.2:c.1078= NM_001145774.2:c.1078C>T
GPR56 transcript variant 7 NM_001145774.1:c.1078= NM_001145774.1:c.1078C>T
ADGRG1 transcript variant 5 NM_001145770.3:c.1078= NM_001145770.3:c.1078C>T
ADGRG1 transcript variant 5 NM_001145770.2:c.1078= NM_001145770.2:c.1078C>T
GPR56 transcript variant 5 NM_001145770.1:c.1078= NM_001145770.1:c.1078C>T
ADGRG1 transcript variant 8 NM_001145773.3:c.1093= NM_001145773.3:c.1093C>T
ADGRG1 transcript variant 8 NM_001145773.2:c.1093= NM_001145773.2:c.1093C>T
GPR56 transcript variant 8 NM_001145773.1:c.1093= NM_001145773.1:c.1093C>T
ADGRG1 transcript variant 11 NM_001290144.2:c.553= NM_001290144.2:c.553C>T
ADGRG1 transcript variant 11 NM_001290144.1:c.553= NM_001290144.1:c.553C>T
ADGRG1 transcript variant 10 NM_001290143.2:c.553= NM_001290143.2:c.553C>T
ADGRG1 transcript variant 10 NM_001290143.1:c.553= NM_001290143.1:c.553C>T
ADGRG1 transcript variant 9 NM_001290142.2:c.568= NM_001290142.2:c.568C>T
ADGRG1 transcript variant 9 NM_001290142.1:c.568= NM_001290142.1:c.568C>T
ADGRG1 transcript variant 12 NM_001370428.1:c.1078= NM_001370428.1:c.1078C>T
ADGRG1 transcript variant 24 NM_001370440.1:c.1078= NM_001370440.1:c.1078C>T
ADGRG1 transcript variant 20 NM_001370436.1:c.1078= NM_001370436.1:c.1078C>T
ADGRG1 transcript variant 28 NM_001370453.1:c.553= NM_001370453.1:c.553C>T
ADGRG1 transcript variant 15 NM_001370431.1:c.1078= NM_001370431.1:c.1078C>T
ADGRG1 transcript variant 18 NM_001370434.1:c.1075= NM_001370434.1:c.1075C>T
ADGRG1 transcript variant 27 NM_001370451.1:c.553= NM_001370451.1:c.553C>T
ADGRG1 transcript variant 21 NM_001370437.1:c.1078= NM_001370437.1:c.1078C>T
ADGRG1 transcript variant 13 NM_001370429.1:c.1078= NM_001370429.1:c.1078C>T
ADGRG1 transcript variant 14 NM_001370430.1:c.1078= NM_001370430.1:c.1078C>T
ADGRG1 transcript variant 22 NM_001370438.1:c.1078= NM_001370438.1:c.1078C>T
ADGRG1 transcript variant 29 NM_001370454.1:c.553= NM_001370454.1:c.553C>T
ADGRG1 transcript variant 19 NM_001370435.1:c.1078= NM_001370435.1:c.1078C>T
ADGRG1 transcript variant 16 NM_001370432.1:c.1078= NM_001370432.1:c.1078C>T
ADGRG1 transcript variant 17 NM_001370433.1:c.1093= NM_001370433.1:c.1093C>T
ADGRG1 transcript variant 23 NM_001370439.1:c.1078= NM_001370439.1:c.1078C>T
ADGRG1 transcript variant 25 NM_001370441.1:c.1075= NM_001370441.1:c.1075C>T
ADGRG1 transcript variant 26 NM_001370442.1:c.922= NM_001370442.1:c.922C>T
ADGRG1 transcript variant X2 XM_006721339.5:c.1093= XM_006721339.5:c.1093C>T
ADGRG1 transcript variant X3 XM_006721339.4:c.1093= XM_006721339.4:c.1093C>T
ADGRG1 transcript variant X3 XM_006721339.3:c.1093= XM_006721339.3:c.1093C>T
ADGRG1 transcript variant X3 XM_006721339.2:c.1093= XM_006721339.2:c.1093C>T
GPR56 transcript variant X21 XM_006721339.1:c.1093= XM_006721339.1:c.1093C>T
ADGRG1 transcript variant X9 XM_005256242.5:c.1093= XM_005256242.5:c.1093C>T
ADGRG1 transcript variant X12 XM_005256242.4:c.1093= XM_005256242.4:c.1093C>T
ADGRG1 transcript variant X11 XM_005256242.3:c.1093= XM_005256242.3:c.1093C>T
GPR56 transcript variant X6 XM_005256242.2:c.1093= XM_005256242.2:c.1093C>T
GPR56 transcript variant X6 XM_005256242.1:c.1093= XM_005256242.1:c.1093C>T
ADGRG1 transcript variant X12 XM_005256241.5:c.1093= XM_005256241.5:c.1093C>T
ADGRG1 transcript variant X10 XM_005256241.4:c.1093= XM_005256241.4:c.1093C>T
ADGRG1 transcript variant X12 XM_005256241.3:c.1093= XM_005256241.3:c.1093C>T
GPR56 transcript variant X5 XM_005256241.2:c.1093= XM_005256241.2:c.1093C>T
GPR56 transcript variant X5 XM_005256241.1:c.1093= XM_005256241.1:c.1093C>T
ADGRG1 transcript variant X6 XM_005256240.5:c.1093= XM_005256240.5:c.1093C>T
ADGRG1 transcript variant X8 XM_005256240.4:c.1093= XM_005256240.4:c.1093C>T
ADGRG1 transcript variant X8 XM_005256240.3:c.1093= XM_005256240.3:c.1093C>T
GPR56 transcript variant X4 XM_005256240.2:c.1093= XM_005256240.2:c.1093C>T
GPR56 transcript variant X4 XM_005256240.1:c.1093= XM_005256240.1:c.1093C>T
ADGRG1 transcript variant X3 XM_006721340.4:c.1093= XM_006721340.4:c.1093C>T
ADGRG1 transcript variant X5 XM_006721340.3:c.1093= XM_006721340.3:c.1093C>T
ADGRG1 transcript variant X5 XM_006721340.2:c.1093= XM_006721340.2:c.1093C>T
GPR56 transcript variant X22 XM_006721340.1:c.1093= XM_006721340.1:c.1093C>T
ADGRG1 transcript variant X11 XM_005256244.4:c.1093= XM_005256244.4:c.1093C>T
ADGRG1 transcript variant X14 XM_005256244.3:c.1093= XM_005256244.3:c.1093C>T
ADGRG1 transcript variant X14 XM_005256244.2:c.1093= XM_005256244.2:c.1093C>T
GPR56 transcript variant X8 XM_005256244.1:c.1093= XM_005256244.1:c.1093C>T
ADGRG1 transcript variant X10 XM_005256239.3:c.1093= XM_005256239.3:c.1093C>T
ADGRG1 transcript variant X6 XM_005256239.2:c.1093= XM_005256239.2:c.1093C>T
ADGRG1 transcript variant X6 XM_005256239.1:c.1093= XM_005256239.1:c.1093C>T
ADGRG1 transcript variant X4 XM_006721338.3:c.1093= XM_006721338.3:c.1093C>T
ADGRG1 transcript variant X2 XM_006721338.2:c.1093= XM_006721338.2:c.1093C>T
ADGRG1 transcript variant X2 XM_006721338.1:c.1093= XM_006721338.1:c.1093C>T
ADGRG1 transcript variant X1 XM_005256238.3:c.1093= XM_005256238.3:c.1093C>T
ADGRG1 transcript variant X1 XM_005256238.2:c.1093= XM_005256238.2:c.1093C>T
ADGRG1 transcript variant X1 XM_005256238.1:c.1093= XM_005256238.1:c.1093C>T
ADGRG1 transcript variant X15 XM_005256246.3:c.1078= XM_005256246.3:c.1078C>T
ADGRG1 transcript variant X16 XM_005256246.2:c.1078= XM_005256246.2:c.1078C>T
ADGRG1 transcript variant X15 XM_005256246.1:c.1078= XM_005256246.1:c.1078C>T
ADGRG1 transcript variant X14 XM_006721342.3:c.1078= XM_006721342.3:c.1078C>T
ADGRG1 transcript variant X15 XM_006721342.2:c.1078= XM_006721342.2:c.1078C>T
ADGRG1 transcript variant X16 XM_006721342.1:c.1078= XM_006721342.1:c.1078C>T
ADGRG1 transcript variant X21 XM_006721347.3:c.1093= XM_006721347.3:c.1093C>T
ADGRG1 transcript variant X33 XM_006721347.2:c.1093= XM_006721347.2:c.1093C>T
ADGRG1 transcript variant X33 XM_006721347.1:c.1093= XM_006721347.1:c.1093C>T
ADGRG1 transcript variant X28 XM_005256255.3:c.1078= XM_005256255.3:c.1078C>T
ADGRG1 transcript variant X34 XM_005256255.2:c.1078= XM_005256255.2:c.1078C>T
ADGRG1 transcript variant X34 XM_005256255.1:c.1078= XM_005256255.1:c.1078C>T
ADGRG1 transcript variant X8 XM_011523462.3:c.1093= XM_011523462.3:c.1093C>T
ADGRG1 transcript variant X11 XM_011523462.2:c.1093= XM_011523462.2:c.1093C>T
ADGRG1 transcript variant X10 XM_011523462.1:c.1093= XM_011523462.1:c.1093C>T
ADGRG1 transcript variant X16 XM_011523466.3:c.1078= XM_011523466.3:c.1078C>T
ADGRG1 transcript variant X25 XM_011523466.2:c.1078= XM_011523466.2:c.1078C>T
ADGRG1 transcript variant X24 XM_011523466.1:c.1078= XM_011523466.1:c.1078C>T
ADGRG1 transcript variant X13 XM_005256245.3:c.1093= XM_005256245.3:c.1093C>T
ADGRG1 transcript variant X13 XM_005256245.2:c.1093= XM_005256245.2:c.1093C>T
ADGRG1 transcript variant X13 XM_005256245.1:c.1093= XM_005256245.1:c.1093C>T
ADGRG1 transcript variant X17 XM_005256254.3:c.1078= XM_005256254.3:c.1078C>T
ADGRG1 transcript variant X28 XM_005256254.2:c.1078= XM_005256254.2:c.1078C>T
ADGRG1 transcript variant X28 XM_005256254.1:c.1078= XM_005256254.1:c.1078C>T
ADGRG1 transcript variant X7 XM_005256237.3:c.1093= XM_005256237.3:c.1093C>T
ADGRG1 transcript variant X9 XM_005256237.2:c.1093= XM_005256237.2:c.1093C>T
ADGRG1 transcript variant X9 XM_005256237.1:c.1093= XM_005256237.1:c.1093C>T
ADGRG1 transcript variant X18 XM_005256248.3:c.1078= XM_005256248.3:c.1078C>T
ADGRG1 transcript variant X27 XM_005256248.2:c.1078= XM_005256248.2:c.1078C>T
ADGRG1 transcript variant X26 XM_005256248.1:c.1078= XM_005256248.1:c.1078C>T
ADGRG1 transcript variant X19 XM_005256252.3:c.1078= XM_005256252.3:c.1078C>T
ADGRG1 transcript variant X24 XM_005256252.2:c.1078= XM_005256252.2:c.1078C>T
ADGRG1 transcript variant X27 XM_005256252.1:c.1078= XM_005256252.1:c.1078C>T
ADGRG1 transcript variant X20 XM_011523468.3:c.1078= XM_011523468.3:c.1078C>T
ADGRG1 transcript variant X31 XM_011523468.2:c.1078= XM_011523468.2:c.1078C>T
ADGRG1 transcript variant X31 XM_011523468.1:c.1078= XM_011523468.1:c.1078C>T
ADGRG1 transcript variant X30 XM_017023892.2:c.1078= XM_017023892.2:c.1078C>T
ADGRG1 transcript variant X35 XM_017023892.1:c.1078= XM_017023892.1:c.1078C>T
ADGRG1 transcript variant X24 XM_047434909.1:c.1093= XM_047434909.1:c.1093C>T
ADGRG1 transcript variant X26 XM_047434911.1:c.1093= XM_047434911.1:c.1093C>T
ADGRG1 transcript variant X22 XM_047434907.1:c.1093= XM_047434907.1:c.1093C>T
ADGRG1 transcript variant X5 XM_047434906.1:c.1093= XM_047434906.1:c.1093C>T
ADGRG1 transcript variant X29 XM_047434913.1:c.1078= XM_047434913.1:c.1078C>T
ADGRG1 transcript variant X25 XM_047434910.1:c.1093= XM_047434910.1:c.1093C>T
ADGRG1 transcript variant X23 XM_047434908.1:c.1093= XM_047434908.1:c.1093C>T
ADGRG1 transcript variant X31 XM_047434914.1:c.1078= XM_047434914.1:c.1078C>T
ADGRG1 transcript variant X27 XM_047434912.1:c.1093= XM_047434912.1:c.1093C>T
ADGRG1 transcript variant X32 XM_047434915.1:c.1078= XM_047434915.1:c.1078C>T
ADGRG1 transcript variant X33 XM_047434916.1:c.1078= XM_047434916.1:c.1078C>T
adhesion G-protein coupled receptor G1 isoform a precursor NP_005673.3:p.His360= NP_005673.3:p.His360Tyr
adhesion G-protein coupled receptor G1 isoform b precursor NP_958932.1:p.His360= NP_958932.1:p.His360Tyr
adhesion G-protein coupled receptor G1 isoform b precursor NP_958933.1:p.His360= NP_958933.1:p.His360Tyr
adhesion G-protein coupled receptor G1 isoform b precursor NP_001139244.1:p.His360= NP_001139244.1:p.His360Tyr
adhesion G-protein coupled receptor G1 isoform a precursor NP_001139243.1:p.His360= NP_001139243.1:p.His360Tyr
adhesion G-protein coupled receptor G1 isoform b precursor NP_001139246.1:p.His360= NP_001139246.1:p.His360Tyr
adhesion G-protein coupled receptor G1 isoform b precursor NP_001139242.1:p.His360= NP_001139242.1:p.His360Tyr
adhesion G-protein coupled receptor G1 isoform c precursor NP_001139245.1:p.His365= NP_001139245.1:p.His365Tyr
adhesion G-protein coupled receptor G1 isoform f NP_001277073.1:p.His185= NP_001277073.1:p.His185Tyr
adhesion G-protein coupled receptor G1 isoform e NP_001277072.1:p.His185= NP_001277072.1:p.His185Tyr
adhesion G-protein coupled receptor G1 isoform d precursor NP_001277071.1:p.His190= NP_001277071.1:p.His190Tyr
adhesion G-protein coupled receptor G1 isoform a precursor NP_001357357.1:p.His360= NP_001357357.1:p.His360Tyr
adhesion G-protein coupled receptor G1 isoform b precursor NP_001357369.1:p.His360= NP_001357369.1:p.His360Tyr
adhesion G-protein coupled receptor G1 isoform b precursor NP_001357365.1:p.His360= NP_001357365.1:p.His360Tyr
adhesion G-protein coupled receptor G1 isoform f NP_001357382.1:p.His185= NP_001357382.1:p.His185Tyr
adhesion G-protein coupled receptor G1 isoform a precursor NP_001357360.1:p.His360= NP_001357360.1:p.His360Tyr
adhesion G-protein coupled receptor G1 isoform i precursor NP_001357363.1:p.His359= NP_001357363.1:p.His359Tyr
adhesion G-protein coupled receptor G1 isoform f NP_001357380.1:p.His185= NP_001357380.1:p.His185Tyr
adhesion G-protein coupled receptor G1 isoform b precursor NP_001357366.1:p.His360= NP_001357366.1:p.His360Tyr
adhesion G-protein coupled receptor G1 isoform a precursor NP_001357358.1:p.His360= NP_001357358.1:p.His360Tyr
adhesion G-protein coupled receptor G1 isoform a precursor NP_001357359.1:p.His360= NP_001357359.1:p.His360Tyr
adhesion G-protein coupled receptor G1 isoform b precursor NP_001357367.1:p.His360= NP_001357367.1:p.His360Tyr
adhesion G-protein coupled receptor G1 isoform f NP_001357383.1:p.His185= NP_001357383.1:p.His185Tyr
adhesion G-protein coupled receptor G1 isoform b precursor NP_001357364.1:p.His360= NP_001357364.1:p.His360Tyr
adhesion G-protein coupled receptor G1 isoform a precursor NP_001357361.1:p.His360= NP_001357361.1:p.His360Tyr
adhesion G-protein coupled receptor G1 isoform c precursor NP_001357362.1:p.His365= NP_001357362.1:p.His365Tyr
adhesion G-protein coupled receptor G1 isoform b precursor NP_001357368.1:p.His360= NP_001357368.1:p.His360Tyr
adhesion G-protein coupled receptor G1 isoform g precursor NP_001357370.1:p.His359= NP_001357370.1:p.His359Tyr
adhesion G-protein coupled receptor G1 isoform h precursor NP_001357371.1:p.His308= NP_001357371.1:p.His308Tyr
adhesion G-protein coupled receptor G1 isoform X1 XP_006721402.1:p.His365= XP_006721402.1:p.His365Tyr
adhesion G-protein coupled receptor G1 isoform X1 XP_005256299.1:p.His365= XP_005256299.1:p.His365Tyr
adhesion G-protein coupled receptor G1 isoform X1 XP_005256298.1:p.His365= XP_005256298.1:p.His365Tyr
adhesion G-protein coupled receptor G1 isoform X1 XP_005256297.1:p.His365= XP_005256297.1:p.His365Tyr
adhesion G-protein coupled receptor G1 isoform X1 XP_006721403.1:p.His365= XP_006721403.1:p.His365Tyr
adhesion G-protein coupled receptor G1 isoform X1 XP_005256301.1:p.His365= XP_005256301.1:p.His365Tyr
adhesion G-protein coupled receptor G1 isoform X1 XP_005256296.1:p.His365= XP_005256296.1:p.His365Tyr
adhesion G-protein coupled receptor G1 isoform X1 XP_006721401.1:p.His365= XP_006721401.1:p.His365Tyr
adhesion G-protein coupled receptor G1 isoform X1 XP_005256295.1:p.His365= XP_005256295.1:p.His365Tyr
adhesion G-protein coupled receptor G1 isoform X2 XP_005256303.1:p.His360= XP_005256303.1:p.His360Tyr
adhesion G-protein coupled receptor G1 isoform X2 XP_006721405.1:p.His360= XP_006721405.1:p.His360Tyr
adhesion G-protein coupled receptor G1 isoform X3 XP_006721410.1:p.His365= XP_006721410.1:p.His365Tyr
adhesion G-protein coupled receptor G1 isoform X4 XP_005256312.1:p.His360= XP_005256312.1:p.His360Tyr
adhesion G-protein coupled receptor G1 isoform X1 XP_011521764.1:p.His365= XP_011521764.1:p.His365Tyr
adhesion G-protein coupled receptor G1 isoform X2 XP_011521768.1:p.His360= XP_011521768.1:p.His360Tyr
adhesion G-protein coupled receptor G1 isoform X1 XP_005256302.1:p.His365= XP_005256302.1:p.His365Tyr
adhesion G-protein coupled receptor G1 isoform X2 XP_005256311.1:p.His360= XP_005256311.1:p.His360Tyr
adhesion G-protein coupled receptor G1 isoform X1 XP_005256294.1:p.His365= XP_005256294.1:p.His365Tyr
adhesion G-protein coupled receptor G1 isoform X2 XP_005256305.1:p.His360= XP_005256305.1:p.His360Tyr
adhesion G-protein coupled receptor G1 isoform X2 XP_005256309.1:p.His360= XP_005256309.1:p.His360Tyr
adhesion G-protein coupled receptor G1 isoform X2 XP_011521770.1:p.His360= XP_011521770.1:p.His360Tyr
adhesion G-protein coupled receptor G1 isoform X4 XP_016879381.1:p.His360= XP_016879381.1:p.His360Tyr
adhesion G-protein coupled receptor G1 isoform X3 XP_047290865.1:p.His365= XP_047290865.1:p.His365Tyr
adhesion G-protein coupled receptor G1 isoform X3 XP_047290867.1:p.His365= XP_047290867.1:p.His365Tyr
adhesion G-protein coupled receptor G1 isoform X3 XP_047290863.1:p.His365= XP_047290863.1:p.His365Tyr
adhesion G-protein coupled receptor G1 isoform X1 XP_047290862.1:p.His365= XP_047290862.1:p.His365Tyr
adhesion G-protein coupled receptor G1 isoform X4 XP_047290869.1:p.His360= XP_047290869.1:p.His360Tyr
adhesion G-protein coupled receptor G1 isoform X3 XP_047290866.1:p.His365= XP_047290866.1:p.His365Tyr
adhesion G-protein coupled receptor G1 isoform X3 XP_047290864.1:p.His365= XP_047290864.1:p.His365Tyr
adhesion G-protein coupled receptor G1 isoform X4 XP_047290870.1:p.His360= XP_047290870.1:p.His360Tyr
adhesion G-protein coupled receptor G1 isoform X3 XP_047290868.1:p.His365= XP_047290868.1:p.His365Tyr
adhesion G-protein coupled receptor G1 isoform X4 XP_047290871.1:p.His360= XP_047290871.1:p.His360Tyr
adhesion G-protein coupled receptor G1 isoform X4 XP_047290872.1:p.His360= XP_047290872.1:p.His360Tyr
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 ss1692321337 Apr 01, 2015 (144)
2 GNOMAD ss2742014065 Nov 08, 2017 (151)
3 TOPMED ss5016791213 Apr 26, 2021 (155)
4 ExAC NC_000016.9 - 57690440 Oct 12, 2018 (152)
5 gnomAD - Exomes NC_000016.9 - 57690440 Jul 13, 2019 (153)
6 TopMed NC_000016.10 - 57656528 Apr 26, 2021 (155)
7 ALFA NC_000016.10 - 57656528 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
2730438, 11294432, ss1692321337, ss2742014065 NC_000016.9:57690439:C:T NC_000016.10:57656527:C:T (self)
232336874, 6875806916, ss5016791213 NC_000016.10:57656527:C:T NC_000016.10:57656527:C:T (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 rs776861168

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