ACTR8
actin related protein 8
Summary
Predicted to enable ATP binding activity. Involved in several processes, including chromatin remodeling; regulation of chromosome organization; and regulation of nucleobase-containing compound metabolic process. Located in centrosome and nucleoplasm. Part of Ino80 complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants34 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs758113135 | 3:53,902,754 | C/T | — | uncertain significance |
| rs761315684 | 3:53,902,792 | C/T | — | uncertain significance |
| rs1385458995 | 3:53,902,841 | A/C | — | uncertain significance |
| rs770170566 | 3:53,904,071 | T/G | — | uncertain significance |
| rs2474680344 | 3:53,904,127 | A/C | — | uncertain significance |
| rs373055423 | 3:53,905,343 | T/C | — | uncertain significance |
| rs199775265 | 3:53,905,393 | C/G | — | uncertain significance |
| rs769409988 | 3:53,905,397 | G/C | — | uncertain significance |
| rs1030608705 | 3:53,905,447 | G/A | — | uncertain significance |
| rs2474684621 | 3:53,906,460 | T/A | — | uncertain significance |
| rs371924812 | 3:53,906,548 | G/A | — | uncertain significance |
| rs201796393 | 3:53,906,551 | C/A | — | uncertain significance |
| rs2474686117 | 3:53,907,132 | T/C | — | uncertain significance |
| rs184519138 | 3:53,907,798 | C/G | intron variant | — |
| rs376401536 | 3:53,908,263 | T/G | — | uncertain significance |
| rs2474689044 | 3:53,908,300 | T/C | — | uncertain significance |
| rs752599288 | 3:53,910,036 | C/T | — | uncertain significance |
| rs749555757 | 3:53,910,078 | C/T | — | uncertain significance |
| rs2474693599 | 3:53,910,710 | T/A | — | uncertain significance |
| rs758841076 | 3:53,910,712 | T/C | — | uncertain significance |
| rs1273252274 | 3:53,911,404 | A/C | — | uncertain significance |
| rs150103066 | 3:53,911,715 | T/C | — | uncertain significance |
| rs780432704 | 3:53,911,729 | G/A | — | uncertain significance |
| rs768886722 | 3:53,911,738 | T/C | — | uncertain significance |
| rs1416966322 | 3:53,911,753 | C/T | — | uncertain significance |
| rs899734209 | 3:53,911,768 | T/G | — | uncertain significance |
| rs1208579176 | 3:53,911,771 | G/C | — | uncertain significance |
| rs149202945 | 3:53,911,774 | C/T | — | uncertain significance |
| rs201378833 | 3:53,911,785 | A/C | — | benign |
| rs1218703426 | 3:53,912,392 | G/C | — | uncertain significance |
| rs2474697939 | 3:53,912,419 | T/C | — | uncertain significance |
| rs928554394 | 3:53,913,974 | C/T | — | uncertain significance |
| rs752053283 | 3:53,914,030 | C/T | — | uncertain significance |
| rs772847580 | 3:53,914,058 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.