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| Gene | BRIP1 |
| Variant | A349P |
| Impact List | missense |
| Protein Effect | loss of function |
| Gene Variant Descriptions | BRIP1 A349P lies within the Fe-S domain of the Brip1 protein (PMID: 20639400). A349P demonstrates ATPase activity and single stranded DNA translocation similar to wild-type Brip1, however, fails to destabilize DNA-bound protein, and results in reduced iron binding and loss of DNA helicase activity (PMID: 20639400, PMID: 16973432), and leads to reduced protein stability, chromosomal aberrations, alterations in the cell cycle, and failure to rescue mitomycin-induced DNA cross-linking damage in cell culture (PMID: 31822495). |
| Associated Drug Resistance | |
| Category Variants Paths |
BRIP1 mutant BRIP1 inact mut BRIP1 A349P |
| Transcript | NM_032043.3 |
| gDNA | chr17:g.61801348C>G |
| cDNA | c.1045G>C |
| Protein | p.A349P |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| XM_047436899.1 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_011525335 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_011525332 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_011525341.4 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_011525337 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_011525336 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_047436892.1 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_011525334.3 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_047436900.1 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_011525332.3 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_047436891.1 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_011525340.4 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_011525339 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_047436901.1 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_011525333 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_011525341.3 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_047436895.1 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_011525336.3 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| NM_032043.2 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_011525339.3 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_047436897.1 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_011525333.4 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| NM_032043.3 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_011525332.4 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_047436904.1 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_011525339.4 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| NM_032043 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_011525340 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_047436903.1 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_011525334 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_011525336.2 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_047436896.1 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_011525341 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_011525337.2 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_011525335.3 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_047436893.1 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_047436902.1 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_011525333.3 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_011525340.3 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_011525334.2 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_011525335.4 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| XM_047436894.1 | chr17:g.61801348C>G | c.1045G>C | p.A349P | RefSeq | GRCh38/hg38 |
| Molecular Profile | Protein Effect | Treatment Approaches |
|---|---|---|
| BRIP1 A349P | loss of function | Olaparib |