RALGPS2
Ral GEF with PH domain and SH3 binding motif 2
Summary
Predicted to enable guanyl-nucleotide exchange factor activity. Predicted to be involved in Ras protein signal transduction. Predicted to be located in cytoplasm. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2773080 | 1:178,696,750 | T/C | regulatory region variant | — |
| rs138964290 | 1:178,711,335 | C/A | downstream gene variant | — |
| rs745958556 | 1:178,745,934 | A/T | — | uncertain significance |
| rs1460102100 | 1:178,745,939 | G/T | — | uncertain significance |
| rs1558114586 | 1:178,745,940 | C/G | — | uncertain significance |
| rs560285002 | 1:178,745,946 | C/T | — | uncertain significance |
| rs748539541 | 1:178,753,625 | G/A | — | uncertain significance |
| rs2527821123 | 1:178,753,650 | A/G | — | uncertain significance |
| rs2527824644 | 1:178,754,693 | G/A | — | uncertain significance |
| rs774239123 | 1:178,754,741 | A/T | — | uncertain significance |
| rs564676440 | 1:178,761,531 | C/T | — | — |
| rs12064534 | 1:178,763,469 | G/T | intron variant | — |
| rs547607293 | 1:178,769,338 | A/G | — | — |
| rs60070265 | 1:178,770,673 | A/T | intron variant | — |
| rs575671452 | 1:178,773,730 | G/A | — | — |
| rs1330720337 | 1:178,780,474 | A/C | — | uncertain significance |
| rs12131426 | 1:178,780,650 | A/T | — | — |
| rs373250030 | 1:178,790,769 | T/C | — | uncertain significance |
| rs1655511948 | 1:178,790,781 | T/C | — | uncertain significance |
| rs546210783 | 1:178,797,607 | C/G | — | — |
| rs181385249 | 1:178,800,479 | C/G | intron variant | — |
| rs779308103 | 1:178,802,578 | A/G | — | uncertain significance |
| rs1656124619 | 1:178,802,628 | A/G | — | uncertain significance |
| rs138528833 | 1:178,802,629 | A/G | — | uncertain significance |
| rs140883827 | 1:178,802,647 | T/C | — | uncertain significance |
| rs1294330725 | 1:178,852,642 | C/T | — | uncertain significance |
| rs61758797 | 1:178,854,226 | C/T | — | uncertain significance |
| rs2528222869 | 1:178,854,265 | G/A | — | uncertain significance |
| rs1042167507 | 1:178,854,313 | A/G | — | uncertain significance |
| rs767721965 | 1:178,855,169 | A/T | — | uncertain significance |
| rs780683289 | 1:178,855,201 | G/A | — | uncertain significance |
| rs747971729 | 1:178,855,210 | C/G | — | uncertain significance |
| rs368999235 | 1:178,858,787 | T/A | — | uncertain significance |
| rs770309544 | 1:178,861,387 | G/A | — | uncertain significance |
| rs373862016 | 1:178,861,418 | A/G | — | uncertain significance |
| rs764684407 | 1:178,861,429 | A/G | — | uncertain significance |
| rs1245456491 | 1:178,866,824 | C/T | — | uncertain significance |
| rs888632393 | 1:178,866,826 | G/A | — | uncertain significance |
| rs773270931 | 1:178,871,257 | A/G | — | uncertain significance |
| rs758545019 | 1:178,871,319 | C/G | — | uncertain significance |
| rs762927733 | 1:178,875,917 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.