RASEF
RAS and EF-hand domain containing
Summary
This gene is a member of the Rab family of GTPases that are involved in regulation of membrane traffic. The encoded protein contains an N-terminal EF-hand domain, a coiled-coil motif and a C-terminal Rab domain. A potential role as tumor suppressor has been indicated for this gene. [provided by RefSeq, Nov 2012]
Known Variants58 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs759426460 | 9:85,597,615 | T/C | — | uncertain significance |
| rs774307482 | 9:85,597,621 | G/A | — | uncertain significance |
| rs202043132 | 9:85,597,686 | T/C | — | uncertain significance |
| rs745464677 | 9:85,607,906 | A/G | — | uncertain significance |
| rs760993989 | 9:85,607,918 | G/A | — | uncertain significance |
| rs140679572 | 9:85,607,922 | C/T | — | likely benign |
| rs10867921 | 9:85,609,781 | G/C | — | — |
| rs1828959695 | 9:85,613,290 | C/A | — | uncertain significance |
| rs1228485117 | 9:85,613,329 | C/A | — | uncertain significance |
| rs771496936 | 9:85,613,333 | A/C | — | uncertain significance |
| rs748326357 | 9:85,615,206 | T/C | — | uncertain significance |
| rs770704145 | 9:85,615,210 | C/T | — | uncertain significance |
| rs2537796773 | 9:85,615,222 | C/T | — | uncertain significance |
| rs775469651 | 9:85,615,355 | G/A | — | uncertain significance |
| rs760608840 | 9:85,615,356 | A/G | — | uncertain significance |
| rs147216417 | 9:85,615,377 | T/C | — | uncertain significance |
| rs767597750 | 9:85,615,397 | C/G | — | uncertain significance |
| rs541159158 | 9:85,615,398 | C/T | — | uncertain significance |
| rs1829012479 | 9:85,615,417 | G/T | — | likely benign |
| rs777910876 | 9:85,615,418 | G/C | — | uncertain significance |
| rs747670115 | 9:85,615,470 | C/T | — | uncertain significance |
| rs2118445605 | 9:85,615,849 | C/T | — | uncertain significance |
| rs373103397 | 9:85,615,853 | G/C | — | uncertain significance |
| rs1829025576 | 9:85,615,882 | T/C | — | uncertain significance |
| rs781056649 | 9:85,615,975 | T/C | — | uncertain significance |
| rs756110127 | 9:85,616,007 | G/T | — | uncertain significance |
| rs745517292 | 9:85,616,031 | G/C | — | uncertain significance |
| rs375599945 | 9:85,616,038 | G/A | — | uncertain significance |
| rs1177790284 | 9:85,616,043 | G/A | — | uncertain significance |
| rs145846912 | 9:85,619,426 | G/C | — | uncertain significance |
| rs781201987 | 9:85,620,347 | T/C | — | uncertain significance |
| rs369002992 | 9:85,620,356 | C/T | — | uncertain significance |
| rs778406601 | 9:85,620,386 | T/C | — | uncertain significance |
| rs1167611090 | 9:85,622,397 | T/A | — | uncertain significance |
| rs770820253 | 9:85,622,400 | G/A | — | uncertain significance |
| rs372693188 | 9:85,622,403 | C/T | — | uncertain significance |
| rs767015983 | 9:85,622,410 | T/C | — | uncertain significance |
| rs2537821104 | 9:85,627,359 | T/C | — | uncertain significance |
| rs748960349 | 9:85,627,423 | C/T | — | uncertain significance |
| rs747530514 | 9:85,630,775 | C/T | — | uncertain significance |
| rs148666621 | 9:85,630,776 | G/A | — | uncertain significance |
| rs765553596 | 9:85,630,799 | T/A | — | uncertain significance |
| rs774009940 | 9:85,630,800 | C/G | — | uncertain significance |
| rs142200322 | 9:85,630,809 | G/A | — | uncertain significance |
| rs139684719 | 9:85,640,744 | C/T | — | uncertain significance |
| rs373085493 | 9:85,640,745 | G/A | — | uncertain significance |
| rs182283403 | 9:85,674,962 | T/C | intron variant | — |
| rs916350899 | 9:85,677,355 | G/C | — | uncertain significance |
| rs766500257 | 9:85,677,369 | T/G | — | uncertain significance |
| rs2537907414 | 9:85,677,430 | G/C | — | uncertain significance |
| rs1249449344 | 9:85,677,530 | G/A | — | uncertain significance |
| rs2537907910 | 9:85,677,565 | C/A | — | uncertain significance |
| rs770726589 | 9:85,677,707 | C/T | — | uncertain significance |
| rs767625674 | 9:85,677,712 | C/T | — | uncertain significance |
| rs753491627 | 9:85,677,722 | C/A | — | uncertain significance |
| rs554402618 | 9:85,677,732 | G/T | — | uncertain significance |
| rs17400257 | 9:85,812,953 | C/A | downstream gene variant | — |
| rs182522830 | 9:85,835,260 | G/A | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.