RGS12
regulator of G protein signaling 12
Summary
This gene encodes a member of the 'regulator of G protein signaling' (RGS) gene family. The encoded protein may function as a guanosine triphosphatase (GTPase)-activating protein as well as a transcriptional repressor. This protein may play a role in tumorigenesis. Multiple transcript variants encoding distinct isoforms have been identified for this gene. Other alternative splice variants have been described but their biological nature has not been determined. [provided by RefSeq, Jul 2008]
Known Variants115 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs191970356 | 4:3,297,280 | G/A | intron variant | — |
| rs192941415 | 4:3,313,998 | T/C | upstream gene variant | — |
| rs370267778 | 4:3,317,962 | G/A | — | uncertain significance |
| rs144806041 | 4:3,317,977 | G/A | — | uncertain significance |
| rs144976826 | 4:3,318,195 | G/A | — | uncertain significance |
| rs751007677 | 4:3,318,201 | T/C | — | likely benign |
| rs747380453 | 4:3,318,216 | A/T | — | uncertain significance |
| rs748359816 | 4:3,318,224 | A/C | — | uncertain significance |
| rs770854466 | 4:3,318,238 | A/G | — | uncertain significance |
| rs2474255665 | 4:3,318,501 | G/A | — | uncertain significance |
| rs1724793919 | 4:3,318,502 | T/C | — | uncertain significance |
| rs554044371 | 4:3,318,508 | A/T | — | uncertain significance |
| rs779962906 | 4:3,318,583 | C/T | — | uncertain significance |
| rs1724805632 | 4:3,318,631 | C/G | — | likely benign |
| rs773699575 | 4:3,318,771 | G/A | — | uncertain significance |
| rs150593377 | 4:3,318,807 | G/A | — | uncertain significance |
| rs779601274 | 4:3,318,814 | C/T | — | uncertain significance |
| rs201477940 | 4:3,318,846 | A/G | — | uncertain significance |
| rs75068773 | 4:3,318,860 | C/G | — | likely benign |
| rs780725638 | 4:3,318,864 | G/A | — | uncertain significance |
| rs145505565 | 4:3,318,891 | G/A | — | uncertain significance |
| rs1437366588 | 4:3,318,932 | C/G | — | uncertain significance |
| rs375410795 | 4:3,318,967 | G/T | — | uncertain significance |
| rs2474259398 | 4:3,319,012 | G/C | — | uncertain significance |
| rs148633904 | 4:3,319,027 | C/T | — | uncertain significance |
| rs1341540921 | 4:3,319,035 | C/T | — | uncertain significance |
| rs566876780 | 4:3,319,069 | G/A | — | uncertain significance |
| rs374990339 | 4:3,319,105 | G/A | — | uncertain significance |
| rs2474260590 | 4:3,319,153 | G/T | — | uncertain significance |
| rs757227717 | 4:3,319,170 | G/A | — | uncertain significance |
| rs753058839 | 4:3,319,237 | C/T | — | uncertain significance |
| rs370026603 | 4:3,319,248 | G/A | — | uncertain significance |
| rs1220399165 | 4:3,319,254 | G/A | — | uncertain significance |
| rs772585191 | 4:3,319,290 | G/A | — | likely benign |
| rs148700456 | 4:3,319,300 | G/C | — | uncertain significance |
| rs764405169 | 4:3,319,302 | G/A | — | uncertain significance |
| rs200806401 | 4:3,319,306 | C/G | — | uncertain significance |
| rs139665491 | 4:3,319,378 | G/C | — | uncertain significance |
| rs1182487493 | 4:3,319,425 | G/A | — | uncertain significance |
| rs561441862 | 4:3,319,458 | C/A | — | uncertain significance |
| rs370188931 | 4:3,319,527 | C/T | — | uncertain significance |
| rs2474264583 | 4:3,319,572 | G/T | — | uncertain significance |
| rs545077720 | 4:3,319,674 | C/T | — | uncertain significance |
| rs146835102 | 4:3,319,687 | C/T | — | uncertain significance |
| rs754357222 | 4:3,319,690 | C/G | — | uncertain significance |
| rs778847850 | 4:3,344,709 | C/T | — | uncertain significance |
| rs979908968 | 4:3,344,722 | G/A | — | uncertain significance |
| rs60208975 | 4:3,364,530 | A/G | regulatory region variant | — |
| rs881817 | 4:3,365,381 | A/G | intron variant | — |
| rs10155132 | 4:3,369,500 | A/G | intron variant | — |
| rs560524789 | 4:3,391,893 | A/G | — | — |
| rs9291160 | 4:3,392,947 | G/C | — | — |
| rs772460923 | 4:3,415,870 | G/C | — | uncertain significance |
| rs2474732987 | 4:3,415,966 | T/G | — | uncertain significance |
| rs2474738139 | 4:3,416,534 | A/T | — | uncertain significance |
| rs541977869 | 4:3,417,721 | G/A | — | uncertain significance |
| rs200267242 | 4:3,417,807 | C/T | — | uncertain significance |
| rs147243770 | 4:3,417,811 | C/T | — | likely benign |
| rs146573735 | 4:3,417,821 | A/G | — | likely benign |
| rs60154162 | 4:3,418,714 | G/A | — | benign |
| rs140454822 | 4:3,418,737 | C/T | — | uncertain significance |
| rs369954430 | 4:3,418,784 | G/A | — | likely benign |
| rs868458630 | 4:3,419,203 | C/T | — | uncertain significance |
| rs370795017 | 4:3,419,212 | G/T | — | uncertain significance |
| rs559823702 | 4:3,419,224 | C/T | — | uncertain significance |
| rs762461946 | 4:3,419,238 | A/C | — | uncertain significance |
| rs61748737 | 4:3,419,252 | C/T | — | likely benign |
| rs764810699 | 4:3,419,254 | G/A | — | uncertain significance |
| rs1258097404 | 4:3,422,375 | T/C | — | uncertain significance |
| rs367586320 | 4:3,424,104 | C/T | — | uncertain significance |
| rs2474797996 | 4:3,424,170 | C/T | — | uncertain significance |
| rs754410879 | 4:3,424,185 | G/A | — | uncertain significance |
| rs762050159 | 4:3,424,241 | G/C | — | uncertain significance |
| rs768504028 | 4:3,424,280 | C/G | — | uncertain significance |
| rs2474799400 | 4:3,424,290 | G/A | — | uncertain significance |
| rs775956737 | 4:3,424,681 | G/A | — | uncertain significance |
| rs2474810479 | 4:3,425,285 | A/G | — | uncertain significance |
| rs73193395 | 4:3,425,300 | G/A | — | uncertain significance |
| rs368849204 | 4:3,425,304 | C/T | — | uncertain significance |
| rs148923822 | 4:3,427,247 | G/C | — | uncertain significance |
| rs750160314 | 4:3,429,864 | G/A | — | uncertain significance |
| rs2474848067 | 4:3,429,882 | A/C | — | uncertain significance |
| rs777956928 | 4:3,429,895 | C/T | — | uncertain significance |
| rs2474866366 | 4:3,432,205 | G/T | — | uncertain significance |
| rs200477499 | 4:3,432,263 | C/G | — | uncertain significance |
| rs752445196 | 4:3,432,302 | G/C | — | uncertain significance |
| rs142339779 | 4:3,432,319 | C/G | — | uncertain significance |
| rs774712714 | 4:3,432,320 | G/A | — | uncertain significance |
| rs762240572 | 4:3,432,326 | G/C | — | uncertain significance |
| rs768201061 | 4:3,432,329 | C/T | — | uncertain significance |
| rs773830368 | 4:3,432,331 | T/C | — | likely benign |
| rs2474868021 | 4:3,432,383 | C/A | — | uncertain significance |
| rs202050160 | 4:3,432,393 | G/A | — | likely benign |
| rs761279798 | 4:3,432,400 | G/C | — | uncertain significance |
| rs762315278 | 4:3,432,428 | C/T | — | uncertain significance |
| rs535694501 | 4:3,432,436 | C/T | — | uncertain significance |
| rs201575073 | 4:3,432,437 | C/A | — | uncertain significance |
| rs778998135 | 4:3,432,482 | C/T | — | uncertain significance |
| rs747391665 | 4:3,432,485 | T/G | — | uncertain significance |
| rs771255511 | 4:3,432,487 | T/A | — | uncertain significance |
Showing 100 of 115 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.