RAD51AP1
RAD51 associated protein 1
Summary
Enables DNA binding activity and RNA binding activity. Involved in DNA repair; cellular response to ionizing radiation; and positive regulation of DNA recombination. Located in chromatin and nucleus. Part of protein-containing complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants26 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs11063218 | 12:4,651,060 | C/G | — | benign |
| rs11063219 | 12:4,651,098 | T/C | — | benign |
| rs34810644 | 12:4,653,063 | A/C | — | benign |
| rs2907493 | 12:4,654,939 | T/C | — | benign |
| rs2497736804 | 12:4,655,489 | A/T | — | uncertain significance |
| rs137998180 | 12:4,655,540 | A/G | — | uncertain significance |
| rs1247301681 | 12:4,657,301 | G/C | — | uncertain significance |
| rs147167939 | 12:4,657,876 | G/A | — | uncertain significance |
| rs114193736 | 12:4,657,882 | G/A | missense variant | — |
| rs780901436 | 12:4,657,886 | G/A | — | uncertain significance |
| rs775499438 | 12:4,657,935 | G/C | — | uncertain significance |
| rs768706534 | 12:4,657,949 | T/C | — | uncertain significance |
| rs200919420 | 12:4,657,996 | G/A | — | uncertain significance |
| rs765982514 | 12:4,657,999 | C/T | — | uncertain significance |
| rs750733051 | 12:4,662,211 | A/G | — | likely benign |
| rs61752091 | 12:4,662,220 | A/T | — | likely benign |
| rs2497768926 | 12:4,662,221 | G/C | — | uncertain significance |
| rs201318970 | 12:4,662,299 | A/G | — | uncertain significance |
| rs61400910 | 12:4,665,519 | T/C | — | uncertain significance |
| rs761332048 | 12:4,665,659 | G/A | — | uncertain significance |
| rs140432356 | 12:4,668,029 | C/T | — | uncertain significance |
| rs73255448 | 12:4,668,031 | G/A | — | benign |
| rs532205268 | 12:4,668,068 | T/C | — | uncertain significance |
| rs766590782 | 12:4,668,091 | A/G | — | uncertain significance |
| rs142518068 | 12:4,668,130 | C/A | — | uncertain significance |
| rs1944602520 | 12:4,668,154 | A/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.