GIMAP8
GTPase, IMAP family member 8
Summary
This gene encodes a protein belonging to the GTP-binding superfamily and to the immuno-associated nucleotide (IAN) subfamily of nucleotide-binding proteins. In humans, the IAN subfamily genes are located in a cluster at 7q36.1. [provided by RefSeq, Jul 2008]
Known Variants51 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs746636931 | 7:150,163,811 | T/C | — | uncertain significance |
| rs150937690 | 7:150,163,850 | G/C | — | uncertain significance |
| rs2486753122 | 7:150,163,932 | G/T | — | uncertain significance |
| rs758956378 | 7:150,163,938 | G/C | — | uncertain significance |
| rs375220398 | 7:150,164,004 | T/C | — | uncertain significance |
| rs140677657 | 7:150,164,052 | T/G | — | uncertain significance |
| rs903724377 | 7:150,164,060 | C/G | — | uncertain significance |
| rs149849472 | 7:150,164,111 | G/A | missense variant | — |
| rs2486753827 | 7:150,164,129 | A/G | — | likely benign |
| rs866044980 | 7:150,164,153 | G/A | — | uncertain significance |
| rs774306095 | 7:150,164,160 | C/T | — | uncertain significance |
| rs143212982 | 7:150,164,189 | C/A | — | likely benign |
| rs767618404 | 7:150,164,225 | T/C | — | uncertain significance |
| rs776872577 | 7:150,164,293 | C/A | — | uncertain significance |
| rs200592029 | 7:150,164,346 | G/T | — | uncertain significance |
| rs746261806 | 7:150,164,372 | A/G | — | uncertain significance |
| rs147231393 | 7:150,164,375 | G/A | — | uncertain significance |
| rs1307163542 | 7:150,164,400 | A/G | — | likely benign |
| rs765889995 | 7:150,167,927 | A/G | — | uncertain significance |
| rs753707877 | 7:150,167,930 | A/G | — | uncertain significance |
| rs552649813 | 7:150,168,798 | G/C | — | — |
| rs2486766565 | 7:150,171,118 | T/C | — | uncertain significance |
| rs759454503 | 7:150,171,135 | G/A | — | uncertain significance |
| rs750543849 | 7:150,171,154 | C/T | — | uncertain significance |
| rs1023463864 | 7:150,171,184 | G/A | — | uncertain significance |
| rs147409428 | 7:150,171,186 | G/A | — | uncertain significance |
| rs964326185 | 7:150,171,272 | C/G | — | uncertain significance |
| rs1172539544 | 7:150,171,349 | A/C | — | uncertain significance |
| rs774971235 | 7:150,171,363 | G/A | — | uncertain significance |
| rs375143235 | 7:150,171,482 | C/A | — | uncertain significance |
| rs140725618 | 7:150,171,544 | C/T | — | uncertain significance |
| rs368806122 | 7:150,174,242 | A/G | — | uncertain significance |
| rs200837107 | 7:150,174,251 | A/C | — | likely benign |
| rs201505121 | 7:150,174,269 | C/T | — | uncertain significance |
| rs180888093 | 7:150,174,380 | G/A | — | uncertain significance |
| rs1338376937 | 7:150,174,477 | G/A | — | uncertain significance |
| rs146125013 | 7:150,174,507 | C/G | — | uncertain significance |
| rs770094053 | 7:150,174,632 | C/T | — | uncertain significance |
| rs200505163 | 7:150,174,633 | G/A | — | uncertain significance |
| rs139453539 | 7:150,174,635 | C/T | — | uncertain significance |
| rs758668369 | 7:150,174,642 | T/C | — | uncertain significance |
| rs2486775588 | 7:150,174,644 | A/G | — | uncertain significance |
| rs2486775760 | 7:150,174,668 | G/A | — | uncertain significance |
| rs2486775787 | 7:150,174,672 | T/C | — | uncertain significance |
| rs1443843856 | 7:150,174,696 | C/T | — | uncertain significance |
| rs2486775924 | 7:150,174,708 | A/G | — | uncertain significance |
| rs1297123568 | 7:150,174,735 | A/G | — | uncertain significance |
| rs889114847 | 7:150,174,756 | G/C | — | uncertain significance |
| rs749134661 | 7:150,174,762 | C/T | — | uncertain significance |
| rs765752735 | 7:150,174,834 | A/T | — | uncertain significance |
| rs778809911 | 7:150,174,850 | A/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.