SGSM1
small G protein signaling modulator 1
Summary
Enables GTPase activator activity and small GTPase binding activity. Predicted to act upstream of or within positive regulation of transcription by RNA polymerase II. Located in cytoplasmic vesicle membrane and cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants76 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs570924820 | 22:25,201,408 | G/A | — | — |
| rs67760767 | 22:25,212,905 | C/T | intron variant | — |
| rs7291042 | 22:25,220,606 | C/T | intron variant | — |
| rs576385352 | 22:25,233,533 | G/A | — | — |
| rs1240922218 | 22:25,240,936 | T/G | — | uncertain significance |
| rs200042106 | 22:25,243,618 | G/A | — | uncertain significance |
| rs776946803 | 22:25,243,627 | G/A | — | uncertain significance |
| rs2517417344 | 22:25,243,639 | C/T | — | uncertain significance |
| rs779612530 | 22:25,243,664 | A/G | — | uncertain significance |
| rs2517417494 | 22:25,243,718 | A/G | — | uncertain significance |
| rs2517420571 | 22:25,246,250 | A/C | — | uncertain significance |
| rs753571655 | 22:25,246,263 | G/T | — | uncertain significance |
| rs1947300080 | 22:25,251,281 | A/G | — | uncertain significance |
| rs1930704106 | 22:25,251,282 | T/A | — | uncertain significance |
| rs749576223 | 22:25,251,342 | G/A | — | uncertain significance |
| rs200297927 | 22:25,251,378 | C/A | — | uncertain significance |
| rs138255291 | 22:25,251,516 | A/G | — | uncertain significance |
| rs371782129 | 22:25,251,552 | C/T | — | uncertain significance |
| rs375907759 | 22:25,251,570 | C/T | — | uncertain significance |
| rs771120349 | 22:25,251,604 | G/A | — | uncertain significance |
| rs201253300 | 22:25,255,683 | A/G | — | uncertain significance |
| rs573738280 | 22:25,255,689 | G/A | — | uncertain significance |
| rs375323027 | 22:25,263,061 | G/A | — | uncertain significance |
| rs764252074 | 22:25,263,071 | A/G | — | uncertain significance |
| rs367830127 | 22:25,263,088 | C/T | — | uncertain significance |
| rs149525948 | 22:25,263,217 | G/A | intron variant | — |
| rs61744681 | 22:25,264,353 | C/T | — | benign |
| rs953221485 | 22:25,264,417 | G/A | — | uncertain significance |
| rs760691824 | 22:25,264,493 | C/T | — | uncertain significance |
| rs375693724 | 22:25,264,712 | G/C | — | uncertain significance |
| rs529211960 | 22:25,264,729 | G/C | — | uncertain significance |
| rs1035628397 | 22:25,264,799 | A/G | — | uncertain significance |
| rs377645874 | 22:25,270,471 | G/A | — | uncertain significance |
| rs543827291 | 22:25,270,498 | A/G | — | uncertain significance |
| rs563632035 | 22:25,270,499 | G/T | — | uncertain significance |
| rs762938788 | 22:25,270,503 | G/C | — | uncertain significance |
| rs763875141 | 22:25,270,507 | A/G | — | likely benign |
| rs1188787901 | 22:25,272,559 | T/C | — | uncertain significance |
| rs771885403 | 22:25,272,564 | G/A | — | uncertain significance |
| rs200354936 | 22:25,272,606 | C/T | — | uncertain significance |
| rs191833638 | 22:25,272,645 | G/A | — | uncertain significance |
| rs776637794 | 22:25,275,435 | C/T | — | likely benign |
| rs1932473129 | 22:25,280,039 | C/A | — | uncertain significance |
| rs2517459441 | 22:25,280,121 | G/A | — | uncertain significance |
| rs372740239 | 22:25,280,131 | C/T | — | uncertain significance |
| rs757539280 | 22:25,282,669 | G/A | — | uncertain significance |
| rs199841996 | 22:25,282,688 | G/C | — | uncertain significance |
| rs61741166 | 22:25,289,448 | G/A | — | benign |
| rs201092835 | 22:25,289,468 | G/A | — | uncertain significance |
| rs1601963996 | 22:25,289,573 | G/A | — | uncertain significance |
| rs755807901 | 22:25,291,209 | C/T | — | uncertain significance |
| rs533760799 | 22:25,291,212 | G/T | — | uncertain significance |
| rs373305837 | 22:25,291,214 | C/T | — | uncertain significance |
| rs915344083 | 22:25,291,253 | A/G | — | uncertain significance |
| rs762208193 | 22:25,293,939 | G/A | — | uncertain significance |
| rs144859640 | 22:25,293,954 | G/A | — | uncertain significance |
| rs980603823 | 22:25,294,026 | G/A | — | uncertain significance |
| rs1932969500 | 22:25,294,036 | C/T | — | uncertain significance |
| rs777891959 | 22:25,294,137 | G/A | — | uncertain significance |
| rs535041194 | 22:25,294,143 | C/T | — | uncertain significance |
| rs776810655 | 22:25,294,144 | G/A | — | uncertain significance |
| rs774658152 | 22:25,294,156 | C/A | — | uncertain significance |
| rs375076898 | 22:25,294,182 | G/A | — | uncertain significance |
| rs2073202 | 22:25,294,376 | C/T | synonymous variant | — |
| rs745861489 | 22:25,294,404 | A/G | — | uncertain significance |
| rs775314441 | 22:25,294,413 | A/G | — | uncertain significance |
| rs772283914 | 22:25,294,515 | G/A | — | uncertain significance |
| rs751977222 | 22:25,297,836 | C/T | — | uncertain significance |
| rs771321195 | 22:25,308,655 | A/T | — | uncertain significance |
| rs147428507 | 22:25,308,671 | C/T | — | benign |
| rs1377060503 | 22:25,308,690 | C/T | — | uncertain significance |
| rs199780735 | 22:25,308,697 | C/A | — | likely benign |
| rs201954600 | 22:25,315,810 | G/A | — | uncertain significance |
| rs200983507 | 22:25,315,903 | C/T | — | uncertain significance |
| rs2517509802 | 22:25,320,158 | G/T | — | uncertain significance |
| rs1371116809 | 22:25,320,174 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.