GPRC6A
G protein-coupled receptor class C group 6 member A
Summary
Members of family C of the G protein-coupled receptor (GPCR) superfamily, such as GPRC6A, are characterized by an evolutionarily conserved amino acid-sensing motif linked to an intramembranous 7-transmembrane loop region. Several members of GPCR family C, including GPRC6A, also have a long N-terminal domain (summary by Pi et al., 2005 [PubMed 16199532]).[supplied by OMIM, Nov 2010]
Known Variants54 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs370144882 | 6:117,113,429 | C/T | — | uncertain significance |
| rs142518238 | 6:117,113,432 | G/T | — | benign |
| rs765958789 | 6:117,113,507 | C/G | — | uncertain significance |
| rs201038107 | 6:117,113,533 | C/G | — | uncertain significance |
| rs142053954 | 6:117,113,558 | A/G | — | likely benign |
| rs777182062 | 6:117,113,566 | C/G | — | uncertain significance |
| rs367740558 | 6:117,113,585 | C/A | — | uncertain significance |
| rs751214810 | 6:117,113,588 | T/C | — | uncertain significance |
| rs147708254 | 6:117,113,724 | T/G | — | uncertain significance |
| rs778404819 | 6:117,113,741 | T/C | — | uncertain significance |
| rs767813992 | 6:117,113,810 | A/G | — | uncertain significance |
| rs369623666 | 6:117,113,858 | T/C | — | uncertain significance |
| rs200330140 | 6:117,113,901 | T/C | — | likely benign |
| rs746438567 | 6:117,113,924 | A/G | — | uncertain significance |
| rs142578038 | 6:117,113,951 | G/A | — | uncertain significance |
| rs139961413 | 6:117,113,975 | G/A | — | uncertain significance |
| rs6901250 | 6:117,114,025 | G/A | synonymous variant | — |
| rs751876928 | 6:117,114,032 | A/C | — | uncertain significance |
| rs118009892 | 6:117,114,050 | G/A | — | likely benign |
| rs2482250118 | 6:117,114,095 | G/A | — | uncertain significance |
| rs1772364435 | 6:117,114,170 | C/T | — | uncertain significance |
| rs2482250550 | 6:117,114,192 | C/G | — | uncertain significance |
| rs374630779 | 6:117,114,204 | C/T | — | uncertain significance |
| rs771905528 | 6:117,114,251 | C/A | — | uncertain significance |
| rs1772372980 | 6:117,114,341 | T/A | — | uncertain significance |
| rs1222703481 | 6:117,114,386 | T/C | — | uncertain significance |
| rs1772376995 | 6:117,114,394 | T/G | — | uncertain significance |
| rs2482257253 | 6:117,116,954 | C/G | — | uncertain significance |
| rs372316877 | 6:117,116,961 | C/T | — | uncertain significance |
| rs770428595 | 6:117,121,751 | A/G | — | uncertain significance |
| rs2482269781 | 6:117,121,788 | T/C | — | uncertain significance |
| rs774093168 | 6:117,121,790 | A/G | — | uncertain significance |
| rs144356533 | 6:117,127,570 | C/T | — | uncertain significance |
| rs199602706 | 6:117,127,591 | A/G | — | uncertain significance |
| rs766660334 | 6:117,127,705 | G/A | — | uncertain significance |
| rs1772851193 | 6:117,127,838 | G/A | — | uncertain significance |
| rs145960158 | 6:117,127,923 | A/G | — | likely benign |
| rs2482285982 | 6:117,127,934 | T/C | — | uncertain significance |
| rs1042017666 | 6:117,128,071 | A/G | — | uncertain significance |
| rs530814514 | 6:117,128,105 | C/T | — | uncertain significance |
| rs1308612511 | 6:117,128,192 | T/C | — | uncertain significance |
| rs149304182 | 6:117,128,198 | C/A | — | uncertain significance |
| rs550250199 | 6:117,128,221 | G/C | — | uncertain significance |
| rs985198078 | 6:117,128,238 | C/A | — | uncertain significance |
| rs772965129 | 6:117,128,241 | G/C | — | uncertain significance |
| rs374928227 | 6:117,128,284 | T/A | — | uncertain significance |
| rs200835880 | 6:117,128,326 | C/T | — | uncertain significance |
| rs767566797 | 6:117,130,541 | C/T | — | uncertain significance |
| rs2114599532 | 6:117,130,550 | G/A | — | uncertain significance |
| rs375116535 | 6:117,130,625 | A/G | — | uncertain significance |
| rs185709000 | 6:117,130,673 | T/C | — | uncertain significance |
| rs375283736 | 6:117,150,007 | C/G | — | uncertain significance |
| rs759939366 | 6:117,150,106 | G/A | — | uncertain significance |
| rs753372835 | 6:117,150,131 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.