RGL1
ral guanine nucleotide dissociation stimulator like 1
Summary
Predicted to enable guanyl-nucleotide exchange factor activity. Predicted to be involved in Ras protein signal transduction. Predicted to be located in cytosol. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs149988897 | 1:183,610,696 | C/G | downstream gene variant | — |
| rs10911390 | 1:183,616,884 | C/T | missense variant | — |
| rs4507976 | 1:183,666,920 | G/A | intron variant | — |
| rs1356612840 | 1:183,711,326 | G/A | — | uncertain significance |
| rs1208953162 | 1:183,711,328 | G/C | — | uncertain significance |
| rs1369212636 | 1:183,711,354 | A/G | — | uncertain significance |
| rs4132276 | 1:183,728,476 | C/G | upstream gene variant | — |
| rs567136875 | 1:183,766,630 | C/T | — | — |
| rs1661344482 | 1:183,775,591 | C/T | — | uncertain significance |
| rs2491441 | 1:183,802,259 | T/C | intron variant | — |
| rs3002647 | 1:183,819,123 | A/G | intron variant | — |
| rs9425320 | 1:183,824,421 | C/T | intron variant | — |
| rs752067488 | 1:183,835,152 | A/T | — | uncertain significance |
| rs4651156 | 1:183,837,032 | A/C | — | — |
| rs768803586 | 1:183,849,853 | C/T | — | uncertain significance |
| rs10797919 | 1:183,852,914 | G/C | splice region variant | — |
| rs775475058 | 1:183,852,934 | A/G | — | uncertain significance |
| rs143787133 | 1:183,853,003 | T/C | — | uncertain significance |
| rs754144884 | 1:183,853,036 | A/G | — | uncertain significance |
| rs1480866006 | 1:183,866,992 | G/C | — | uncertain significance |
| rs7527758 | 1:183,870,073 | T/A | — | — |
| rs1431579697 | 1:183,871,724 | A/G | — | uncertain significance |
| rs10911463 | 1:183,873,585 | T/G | — | — |
| rs370100542 | 1:183,874,024 | C/T | — | uncertain significance |
| rs749217257 | 1:183,874,102 | A/C | — | uncertain significance |
| rs770515511 | 1:183,876,167 | T/G | — | uncertain significance |
| rs200500728 | 1:183,876,208 | G/A | — | uncertain significance |
| rs1140534 | 1:183,881,362 | C/T | — | uncertain significance |
| rs73049207 | 1:183,881,409 | A/G | — | benign |
| rs1206378405 | 1:183,885,623 | G/T | — | uncertain significance |
| rs1368460377 | 1:183,885,701 | C/G | — | uncertain significance |
| rs780012312 | 1:183,885,746 | C/T | — | uncertain significance |
| rs749146764 | 1:183,885,773 | G/T | — | uncertain significance |
| rs762555890 | 1:183,885,789 | G/A | — | uncertain significance |
| rs773977972 | 1:183,891,411 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.