BRAP
BRCA1 associated protein
Summary
The protein encoded by this gene was identified by its ability to bind to the nuclear localization signal of BRCA1 and other proteins. It is a cytoplasmic protein which may regulate nuclear targeting by retaining proteins with a nuclear localization signal in the cytoplasm. [provided by RefSeq, Jul 2008]
Known Variants37 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs777109467 | 12:112,082,016 | T/C | — | uncertain significance |
| rs150778696 | 12:112,082,022 | C/T | — | uncertain significance |
| rs778523849 | 12:112,082,025 | C/A | — | uncertain significance |
| rs1332115393 | 12:112,082,052 | C/T | — | uncertain significance |
| rs781582359 | 12:112,082,056 | C/G | — | uncertain significance |
| rs764106592 | 12:112,082,085 | A/G | — | uncertain significance |
| rs779071140 | 12:112,082,242 | C/T | — | uncertain significance |
| rs374914110 | 12:112,082,248 | C/T | — | uncertain significance |
| rs780046712 | 12:112,082,340 | G/C | — | uncertain significance |
| rs11065991 | 12:112,083,162 | C/T | intron variant | — |
| rs61739319 | 12:112,087,805 | C/T | — | benign |
| rs749237684 | 12:112,088,447 | T/A | — | — |
| rs184354242 | 12:112,092,462 | G/A | — | — |
| rs746619992 | 12:112,093,422 | C/T | — | uncertain significance |
| rs1178512876 | 12:112,096,584 | C/T | — | uncertain significance |
| rs151101195 | 12:112,097,057 | C/T | — | benign |
| rs3742002 | 12:112,097,099 | G/A | — | benign |
| rs780327818 | 12:112,098,429 | T/G | — | uncertain significance |
| rs2542166018 | 12:112,098,441 | A/G | — | uncertain significance |
| rs747386868 | 12:112,098,448 | C/T | — | uncertain significance |
| rs752397283 | 12:112,103,488 | T/G | — | uncertain significance |
| rs61999323 | 12:112,103,589 | G/A | — | benign |
| rs3782886 | 12:112,110,489 | T/C | synonymous variant | — |
| rs1225814022 | 12:112,110,490 | C/T | — | uncertain significance |
| rs61308437 | 12:112,117,009 | A/G | — | benign |
| rs200004698 | 12:112,117,022 | T/C | — | uncertain significance |
| rs2542196015 | 12:112,117,095 | T/C | — | uncertain significance |
| rs11066001 | 12:112,119,171 | T/C | upstream gene variant | — |
| rs1356325887 | 12:112,119,557 | T/G | — | uncertain significance |
| rs2542199784 | 12:112,119,568 | G/T | — | uncertain significance |
| rs751880237 | 12:112,120,965 | T/C | — | uncertain significance |
| rs753294379 | 12:112,120,983 | C/G | — | uncertain significance |
| rs2542202577 | 12:112,121,049 | C/T | — | uncertain significance |
| rs80229432 | 12:112,121,068 | G/A | — | benign |
| rs1234250530 | 12:112,121,078 | G/C | — | uncertain significance |
| rs601663 | 12:112,123,284 | A/T | — | — |
| rs1208447449 | 12:112,123,578 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.