ARL15
ARF like GTPase 15
Summary
Predicted to enable GTP binding activity and GTPase activity. Located in extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants47 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs774701068 | 5:53,182,507 | C/T | — | uncertain significance |
| rs761221301 | 5:53,182,522 | C/G | — | uncertain significance |
| rs2253601 | 5:53,222,781 | A/T | intron variant | — |
| rs788517 | 5:53,247,386 | C/T | coding sequence variant | — |
| rs1694089 | 5:53,247,394 | A/C | coding sequence variant | — |
| rs702634 | 5:53,271,420 | G/A | intron variant | — |
| rs4865796 | 5:53,272,664 | G/C | — | — |
| rs28499105 | 5:53,274,467 | G/A | intron variant | — |
| rs1664791 | 5:53,283,827 | C/G | intron variant | — |
| rs7719168 | 5:53,292,390 | A/C | intron variant | — |
| rs143859456 | 5:53,294,978 | C/T | intron variant | — |
| rs59061738 | 5:53,296,557 | A/G | intron variant | — |
| rs6450176 | 5:53,298,025 | G/C | — | — |
| rs3776717 | 5:53,298,762 | G/A | intron variant | — |
| rs4311394 | 5:53,300,662 | A/C | — | — |
| rs4334836 | 5:53,300,835 | T/G | — | — |
| rs16881971 | 5:53,301,207 | T/G | — | — |
| rs11738093 | 5:53,301,425 | A/G | — | — |
| rs2448 | 5:53,302,354 | T/C | intron variant | — |
| rs3776712 | 5:53,304,179 | T/C | regulatory region variant | — |
| rs80138475 | 5:53,304,991 | C/T | intron variant | — |
| rs112838464 | 5:53,308,819 | G/A | intron variant | — |
| rs7735249 | 5:53,310,139 | C/G | intron variant | — |
| rs255758 | 5:53,311,502 | C/A | intron variant | — |
| rs255749 | 5:53,318,596 | G/A | intron variant | — |
| rs40480 | 5:53,325,481 | C/G | intron variant | — |
| rs144915300 | 5:53,358,490 | T/C | intron variant | — |
| rs10069589 | 5:53,366,153 | T/C | intron variant | — |
| rs156380 | 5:53,378,450 | T/G | — | — |
| rs273218 | 5:53,380,555 | T/C | intron variant | — |
| rs1054253877 | 5:53,409,069 | T/C | — | uncertain significance |
| rs1202641397 | 5:53,409,147 | A/G | — | uncertain significance |
| rs700910 | 5:53,439,777 | C/T | intron variant | — |
| rs2531328445 | 5:53,450,407 | T/A | — | uncertain significance |
| rs151804 | 5:53,452,060 | A/G | intron variant | — |
| rs278064 | 5:53,458,923 | T/C | intron variant | — |
| rs39671 | 5:53,465,786 | T/C | intron variant | — |
| rs2530648918 | 5:53,467,683 | C/T | — | uncertain significance |
| rs2530649234 | 5:53,467,712 | T/A | — | uncertain significance |
| rs1754729751 | 5:53,467,718 | C/T | — | uncertain significance |
| rs139330292 | 5:53,503,097 | A/T | intron variant | — |
| rs35926 | 5:53,578,554 | G/A | intron variant | — |
| rs35929 | 5:53,580,425 | G/A | intron variant | — |
| rs35931 | 5:53,581,743 | C/G | regulatory region variant | — |
| rs35951 | 5:53,592,361 | G/A | — | — |
| rs35942 | 5:53,603,593 | G/A | — | — |
| rs35941 | 5:53,606,295 | T/C | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.