EVI5
ecotropic viral integration site 5
Summary
Enables GTPase activator activity and small GTPase binding activity. Involved in positive regulation of GTPase activity and retrograde transport, endosome to Golgi. Located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants82 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs6690764 | 1:92,976,590 | G/T | — | — |
| rs144597007 | 1:92,979,279 | C/T | — | likely benign |
| rs1659409038 | 1:92,979,298 | C/T | — | uncertain significance |
| rs2524822408 | 1:92,979,316 | T/A | — | uncertain significance |
| rs6603979 | 1:92,979,354 | A/G | — | benign |
| rs142905346 | 1:92,979,365 | C/T | — | likely benign |
| rs201450382 | 1:92,979,403 | T/C | — | uncertain significance |
| rs747893888 | 1:92,979,467 | T/C | — | uncertain significance |
| rs1283685554 | 1:92,979,520 | C/T | — | uncertain significance |
| rs184721335 | 1:92,981,236 | T/G | intron variant | — |
| rs3903212 | 1:92,984,055 | A/T | — | — |
| rs6603980 | 1:92,985,335 | C/A | — | — |
| rs2027061 | 1:93,001,430 | C/T | intron variant | — |
| rs11164771 | 1:93,005,084 | A/G | intron variant | — |
| rs10874708 | 1:93,005,124 | T/C | — | — |
| rs11804321 | 1:93,009,313 | T/C | intron variant | — |
| rs7515577 | 1:93,009,438 | C/G | — | — |
| rs6603984 | 1:93,011,572 | A/G | intron variant | — |
| rs28764836 | 1:93,012,762 | T/C | intron variant | — |
| rs145341911 | 1:93,014,343 | C/G | — | — |
| rs12753280 | 1:93,016,228 | T/A | — | — |
| rs771112779 | 1:93,029,215 | G/A | — | uncertain significance |
| rs138806513 | 1:93,029,275 | T/G | — | uncertain significance |
| rs6422513 | 1:93,032,467 | G/C | — | — |
| rs6603991 | 1:93,032,583 | T/G | — | — |
| rs11586076 | 1:93,072,481 | C/A | — | — |
| rs770316787 | 1:93,073,163 | C/T | — | uncertain significance |
| rs201906216 | 1:93,073,184 | G/C | — | uncertain significance |
| rs11808092 | 1:93,073,228 | C/A | missense variant | benign |
| rs141343784 | 1:93,073,240 | C/T | — | benign |
| rs1650748304 | 1:93,073,253 | G/A | — | uncertain significance |
| rs781351466 | 1:93,073,259 | C/T | — | uncertain significance |
| rs2524913608 | 1:93,073,284 | T/C | — | uncertain significance |
| rs11589122 | 1:93,083,903 | C/T | intron variant | — |
| rs200068198 | 1:93,089,776 | T/C | — | uncertain significance |
| rs201719783 | 1:93,089,803 | C/T | — | uncertain significance |
| rs7514716 | 1:93,089,823 | T/C | — | benign |
| rs553860119 | 1:93,089,824 | T/C | — | uncertain significance |
| rs1461426278 | 1:93,089,840 | C/T | — | uncertain significance |
| rs377644327 | 1:93,089,862 | C/G | — | uncertain significance |
| rs773362486 | 1:93,089,865 | T/G | — | uncertain significance |
| rs201423013 | 1:93,089,878 | C/G | — | uncertain significance |
| rs201103592 | 1:93,089,879 | G/A | — | uncertain significance |
| rs142784307 | 1:93,089,891 | G/A | — | uncertain significance |
| rs1557931063 | 1:93,091,409 | G/A | — | uncertain significance |
| rs1655569406 | 1:93,091,468 | C/A | — | uncertain significance |
| rs10735781 | 1:93,121,107 | G/C | intron variant | — |
| rs200507358 | 1:93,131,516 | G/A | — | uncertain significance |
| rs146140626 | 1:93,142,746 | G/A | — | uncertain significance |
| rs114036942 | 1:93,143,278 | C/A | — | — |
| rs11810217 | 1:93,148,377 | C/T | intron variant | — |
| rs6690641 | 1:93,149,678 | T/G | — | — |
| rs146386533 | 1:93,152,374 | G/A | intron variant | — |
| rs147990139 | 1:93,152,380 | A/C | intron variant | — |
| rs11809700 | 1:93,152,635 | C/T | intron variant | — |
| rs1669880247 | 1:93,159,410 | T/C | — | uncertain significance |
| rs569327954 | 1:93,159,450 | G/C | — | uncertain significance |
| rs773804312 | 1:93,159,926 | C/A | — | uncertain significance |
| rs117711462 | 1:93,159,927 | G/A | missense variant | — |
| rs143611208 | 1:93,160,880 | A/G | — | likely benign |
| rs2391199 | 1:93,160,902 | T/C | — | benign |
| rs2526791500 | 1:93,160,913 | A/G | — | uncertain significance |
| rs200758588 | 1:93,160,916 | G/A | — | uncertain significance |
| rs367754544 | 1:93,160,954 | C/A | — | uncertain significance |
| rs781444194 | 1:93,163,436 | T/C | — | uncertain significance |
| rs756234245 | 1:93,163,445 | C/A | — | uncertain significance |
| rs200747400 | 1:93,163,529 | T/G | — | uncertain significance |
| rs2526928073 | 1:93,167,699 | T/C | — | uncertain significance |
| rs200157317 | 1:93,167,754 | G/A | — | uncertain significance |
| rs886149591 | 1:93,167,765 | G/C | — | uncertain significance |
| rs114138180 | 1:93,168,083 | C/T | upstream gene variant | — |
| rs141479784 | 1:93,169,052 | T/C | — | uncertain significance |
| rs773081130 | 1:93,169,091 | T/C | — | uncertain significance |
| rs751785118 | 1:93,169,113 | C/T | — | uncertain significance |
| rs1489130472 | 1:93,170,284 | C/T | — | uncertain significance |
| rs6680578 | 1:93,176,878 | T/G | — | — |
| rs748294903 | 1:93,201,973 | T/C | — | uncertain significance |
| rs756848081 | 1:93,202,060 | G/A | — | uncertain significance |
| rs780400268 | 1:93,202,173 | G/C | — | uncertain significance |
| rs6604014 | 1:93,215,718 | T/A | — | — |
| rs370949072 | 1:93,257,940 | G/T | — | uncertain significance |
| rs2524370294 | 1:93,257,941 | T/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.