GIMAP7
GTPase, IMAP family member 7
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 Variants33 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7784108 | 7:150,210,148 | T/A | coding sequence variant | — |
| rs7784050 | 7:150,213,314 | C/A | regulatory region variant | — |
| rs7808446 | 7:150,214,465 | T/C | — | — |
| rs145339506 | 7:150,217,082 | G/C | — | likely benign |
| rs748612836 | 7:150,217,096 | G/A | — | uncertain significance |
| rs142322540 | 7:150,217,112 | C/G | — | uncertain significance |
| rs372010180 | 7:150,217,127 | G/A | — | uncertain significance |
| rs114459899 | 7:150,217,137 | G/A | synonymous variant | — |
| rs781166918 | 7:150,217,145 | T/A | — | uncertain significance |
| rs114367962 | 7:150,217,150 | G/C | — | uncertain significance |
| rs2486843823 | 7:150,217,178 | C/T | — | uncertain significance |
| rs778322751 | 7:150,217,211 | C/T | — | uncertain significance |
| rs769439572 | 7:150,217,229 | G/C | — | uncertain significance |
| rs761682617 | 7:150,217,255 | C/T | — | uncertain significance |
| rs545570989 | 7:150,217,302 | A/T | — | uncertain significance |
| rs3735080 | 7:150,217,309 | C/T | — | benign |
| rs267601406 | 7:150,217,322 | C/T | — | uncertain significance |
| rs942866533 | 7:150,217,343 | C/T | — | uncertain significance |
| rs760524047 | 7:150,217,348 | G/T | — | uncertain significance |
| rs369222429 | 7:150,217,419 | T/A | — | uncertain significance |
| rs115164158 | 7:150,217,441 | A/G | — | uncertain significance |
| rs2486844941 | 7:150,217,527 | C/G | — | uncertain significance |
| rs2486845038 | 7:150,217,550 | G/A | — | uncertain significance |
| rs767533437 | 7:150,217,585 | A/G | — | likely benign |
| rs144503420 | 7:150,217,591 | G/C | — | uncertain significance |
| rs2486845335 | 7:150,217,660 | T/G | — | uncertain significance |
| rs761959705 | 7:150,217,708 | C/T | — | uncertain significance |
| rs780035145 | 7:150,217,800 | G/T | — | uncertain significance |
| rs372605250 | 7:150,217,871 | G/C | — | uncertain significance |
| rs1795182237 | 7:150,217,888 | G/A | — | uncertain significance |
| rs2486846040 | 7:150,217,923 | A/G | — | uncertain significance |
| rs975579781 | 7:150,217,940 | C/T | — | uncertain significance |
| rs58391005 | 7:150,218,137 | G/A | 3 prime UTR variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.