AGFG2
ArfGAP with FG repeats 2
Summary
This gene is a member of the HIV-1 Rev binding protein (HRB) family and encodes a protein with one Arf-GAP zinc finger domain, several phe-gly (FG) motifs, and four asn-pro-phe (NPF) motifs. This protein interacts with Eps15 homology (EH) domains and plays a role in the Rev export pathway, which mediates the nucleocytoplasmic transfer of proteins and RNAs. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Feb 2013]
Known Variants27 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs536503624 | 7:100,137,121 | C/T | — | uncertain significance |
| rs1800566629 | 7:100,146,492 | C/T | — | uncertain significance |
| rs1027374743 | 7:100,146,525 | C/A | — | uncertain significance |
| rs781652659 | 7:100,148,085 | C/G | — | uncertain significance |
| rs1018491385 | 7:100,150,977 | C/T | — | uncertain significance |
| rs377262869 | 7:100,150,981 | C/T | — | uncertain significance |
| rs748209980 | 7:100,151,741 | C/T | — | uncertain significance |
| rs200779668 | 7:100,151,791 | G/C | — | uncertain significance |
| rs749263005 | 7:100,151,851 | C/A | — | uncertain significance |
| rs375233200 | 7:100,153,239 | C/T | — | uncertain significance |
| rs748296459 | 7:100,153,309 | C/G | — | uncertain significance |
| rs2485862592 | 7:100,159,891 | A/T | — | uncertain significance |
| rs139318752 | 7:100,159,897 | C/T | — | uncertain significance |
| rs1350732442 | 7:100,159,953 | G/A | — | likely benign |
| rs1800894170 | 7:100,159,977 | G/A | — | uncertain significance |
| rs1426936536 | 7:100,160,255 | C/G | — | uncertain significance |
| rs149626460 | 7:100,160,261 | C/T | — | uncertain significance |
| rs142258495 | 7:100,160,269 | G/A | — | likely benign |
| rs570722771 | 7:100,160,275 | G/A | — | uncertain significance |
| rs1349193397 | 7:100,160,287 | A/G | — | uncertain significance |
| rs1800904420 | 7:100,160,302 | G/C | — | uncertain significance |
| rs780962444 | 7:100,160,564 | C/T | — | uncertain significance |
| rs202000689 | 7:100,161,513 | A/C | — | uncertain significance |
| rs766106894 | 7:100,161,525 | G/A | — | uncertain significance |
| rs766941813 | 7:100,161,544 | C/T | — | uncertain significance |
| rs776048198 | 7:100,161,855 | G/A | — | uncertain significance |
| rs767900026 | 7:100,161,872 | G/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.