RALGPS1
Ral GEF with PH domain and SH3 binding motif 1
Summary
Enables guanyl-nucleotide exchange factor activity. Involved in regulation of Ral 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 Variants30 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs371196451 | 9:129,728,166 | A/G | — | uncertain significance |
| rs374751575 | 9:129,728,189 | G/A | — | uncertain significance |
| rs62580791 | 9:129,757,851 | A/T | — | — |
| rs7861804 | 9:129,780,929 | A/G | — | — |
| rs146032431 | 9:129,796,764 | G/A | — | uncertain significance |
| rs4292797 | 9:129,810,248 | G/C | intron variant | — |
| rs778033944 | 9:129,812,372 | A/G | — | uncertain significance |
| rs2789512 | 9:129,855,105 | T/G | intron variant | — |
| rs538049645 | 9:129,855,714 | G/T | — | — |
| rs138423884 | 9:129,855,937 | A/G | regulatory region variant | — |
| rs868852 | 9:129,899,510 | T/G | — | — |
| rs955934 | 9:129,913,597 | C/A | intron variant | — |
| rs10465114 | 9:129,917,824 | G/A | intron variant | — |
| rs2496376152 | 9:129,928,414 | A/G | — | uncertain significance |
| rs2496820037 | 9:129,937,013 | C/T | — | uncertain significance |
| rs2059758718 | 9:129,937,026 | C/T | — | uncertain significance |
| rs146196583 | 9:129,944,671 | C/T | intron variant | — |
| rs183996093 | 9:129,957,387 | G/A | — | likely benign |
| rs2497981364 | 9:129,957,390 | T/G | — | uncertain significance |
| rs937258252 | 9:129,957,406 | G/A | — | uncertain significance |
| rs199975640 | 9:129,957,448 | C/T | — | uncertain significance |
| rs2061288528 | 9:129,957,459 | G/A | — | uncertain significance |
| rs1158666861 | 9:129,958,869 | C/T | — | uncertain significance |
| rs998492186 | 9:129,958,897 | T/G | — | uncertain significance |
| rs201112223 | 9:129,974,943 | G/A | — | uncertain significance |
| rs2498930316 | 9:129,974,973 | C/T | — | uncertain significance |
| rs776124423 | 9:129,974,978 | C/T | — | uncertain significance |
| rs199937278 | 9:129,975,289 | G/A | — | uncertain significance |
| rs368997146 | 9:129,977,116 | C/T | — | uncertain significance |
| rs3780318 | 9:129,979,758 | G/A | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.