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| Gene | BRIP1 |
| Variant | S919P |
| Impact List | missense |
| Protein Effect | unknown |
| Gene Variant Descriptions | BRIP1 S919P lies within the BRCA1-interacting region of the Brip1 protein (UniProt.org). S919P has been identified in the scientific literature (PMID: 29221171, PMID: 38962713, PMID: 28415781), but has not been biochemically characterized and therefore, its effect on Brip1 protein function is unknown (PubMed, Dec 2025). |
| Associated Drug Resistance | |
| Category Variants Paths |
BRIP1 mutant BRIP1 S919P |
| Transcript | NM_032043.3 |
| gDNA | chr17:g.61685986A>G |
| cDNA | c.2755T>C |
| Protein | p.S919P |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| NM_032043.3 | chr17:g.61685986A>G | c.2755T>C | p.S919P | RefSeq | GRCh38/hg38 |
| XM_047436891.1 | chr17:g.61685986A>G | c.2755T>C | p.S919P | RefSeq | GRCh38/hg38 |
| XM_047436892.1 | chr17:g.61685986A>G | c.2755T>C | p.S919P | RefSeq | GRCh38/hg38 |
| XM_011525335.4 | chr17:g.61685986A>G | c.2755T>C | p.S919P | RefSeq | GRCh38/hg38 |
| XM_011525335 | chr17:g.61685986A>G | c.2755T>C | p.S919P | RefSeq | GRCh38/hg38 |
| NM_032043 | chr17:g.61685986A>G | c.2755T>C | p.S919P | RefSeq | GRCh38/hg38 |
| NM_032043.2 | chr17:g.61685986A>G | c.2755T>C | p.S919P | RefSeq | GRCh38/hg38 |
| XM_011525335.3 | chr17:g.61685986A>G | c.2755T>C | p.S919P | RefSeq | GRCh38/hg38 |
| Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
|---|---|---|---|---|---|---|---|
| BRIP1 mutant | ovarian cancer | not applicable | N/A | Guideline | Risk Factor | Germline BRIP1 mutations are associated with increased risk of developing ovarian cancer (NCCN.org). | detail... |