ACAP3
ArfGAP with coiled-coil, ankyrin repeat and PH domains 3
Summary
Predicted to enable GTPase activator activity and zinc ion binding activity. Predicted to act upstream of or within neuron migration and regulation of neuron projection development. Predicted to be located in endosome membrane and growth cone. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants57 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1363653048 | 1:1,228,992 | G/C | — | uncertain significance |
| rs1193444415 | 1:1,229,038 | G/A | — | uncertain significance |
| rs1341647247 | 1:1,229,234 | C/G | — | uncertain significance |
| rs1011452948 | 1:1,229,256 | C/G | — | uncertain significance |
| rs758335799 | 1:1,229,515 | C/T | — | uncertain significance |
| rs769370839 | 1:1,229,537 | C/T | — | uncertain significance |
| rs771214380 | 1:1,229,867 | G/A | — | uncertain significance |
| rs1467968072 | 1:1,229,902 | G/C | — | uncertain significance |
| rs771507543 | 1:1,229,951 | G/A | — | uncertain significance |
| rs564887554 | 1:1,230,134 | C/T | — | uncertain significance |
| rs1641043848 | 1:1,230,185 | C/T | — | uncertain significance |
| rs144585204 | 1:1,230,833 | G/T | — | uncertain significance |
| rs774062574 | 1:1,230,851 | C/T | — | uncertain significance |
| rs746691582 | 1:1,231,146 | C/T | — | uncertain significance |
| rs775873154 | 1:1,231,166 | C/T | — | uncertain significance |
| rs2522635734 | 1:1,231,190 | G/A | — | uncertain significance |
| rs749761079 | 1:1,231,205 | A/G | — | likely benign |
| rs2522636196 | 1:1,231,212 | T/G | — | uncertain significance |
| rs141926737 | 1:1,231,245 | C/T | — | uncertain significance |
| rs750075234 | 1:1,231,266 | G/A | — | uncertain significance |
| rs748796567 | 1:1,231,317 | G/T | — | uncertain significance |
| rs1287688403 | 1:1,231,431 | C/G | — | uncertain significance |
| rs762644301 | 1:1,231,631 | C/T | — | uncertain significance |
| rs768250680 | 1:1,231,632 | G/A | — | uncertain significance |
| rs563840123 | 1:1,231,862 | C/T | — | uncertain significance |
| rs1040631059 | 1:1,231,863 | G/A | — | uncertain significance |
| rs570241461 | 1:1,231,871 | G/C | — | uncertain significance |
| rs371372231 | 1:1,231,885 | G/T | — | likely benign |
| rs759899820 | 1:1,231,944 | C/T | — | uncertain significance |
| rs1401130731 | 1:1,231,949 | C/T | — | uncertain significance |
| rs1295329148 | 1:1,231,959 | T/A | — | likely benign |
| rs1250518263 | 1:1,231,975 | G/C | — | uncertain significance |
| rs753749956 | 1:1,231,985 | G/A | — | uncertain significance |
| rs970592193 | 1:1,232,003 | C/G | — | uncertain significance |
| rs149746396 | 1:1,232,004 | G/A | — | uncertain significance |
| rs749605784 | 1:1,233,215 | C/T | — | uncertain significance |
| rs558870678 | 1:1,233,223 | G/T | — | uncertain significance |
| rs749874984 | 1:1,233,246 | T/C | — | uncertain significance |
| rs374801017 | 1:1,233,304 | C/G | — | uncertain significance |
| rs1641271120 | 1:1,233,412 | C/T | — | uncertain significance |
| rs141328101 | 1:1,233,490 | C/T | — | uncertain significance |
| rs575628799 | 1:1,233,763 | T/C | — | uncertain significance |
| rs2522676933 | 1:1,233,790 | G/A | — | uncertain significance |
| rs368349562 | 1:1,233,966 | C/T | — | uncertain significance |
| rs1160420340 | 1:1,234,052 | G/C | — | uncertain significance |
| rs367626962 | 1:1,235,212 | C/T | — | uncertain significance |
| rs2522695600 | 1:1,235,275 | A/C | — | uncertain significance |
| rs2522698843 | 1:1,235,543 | C/T | — | uncertain significance |
| rs761584739 | 1:1,235,554 | A/T | — | uncertain significance |
| rs753494129 | 1:1,235,578 | T/C | — | uncertain significance |
| rs746294144 | 1:1,235,948 | C/T | — | uncertain significance |
| rs1279897299 | 1:1,237,369 | C/T | — | uncertain significance |
| rs137985693 | 1:1,238,554 | G/T | — | uncertain significance |
| rs766387958 | 1:1,238,640 | T/C | — | uncertain significance |
| rs762794456 | 1:1,238,648 | C/T | — | uncertain significance |
| rs991594822 | 1:1,243,191 | G/A | — | uncertain significance |
| rs144003672 | 1:1,245,104 | C/A | missense variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.