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Gene | BRIP1 |
Variant | A89V |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | BRIP1 A89V lies within the helicase ATP-binding domain of the Brip1 protein (UniProt.org). A89V confers a partial resistance to interstrand crosslinking agents compared to wild-type protein in BRIP1-deficient cells in culture (PMID: 33619228), but has not been fully biochemically characterized and therefore, its effect on Brip1 protein function is unknown. |
Associated Drug Resistance | |
Category Variants Paths |
BRIP1 mutant BRIP1 A89V |
Transcript | NM_032043.3 |
gDNA | chr17:g.61857171G>A |
cDNA | c.266C>T |
Protein | p.A89V |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_047436901.1 | chr17:g.61857171G>A | c.266C>T | p.A89V | RefSeq | GRCh38/hg38 |
XM_011525335.4 | chr17:g.61857171G>A | c.266C>T | p.A89V | RefSeq | GRCh38/hg38 |
XM_047436895.1 | chr17:g.61857171G>A | c.266C>T | p.A89V | RefSeq | GRCh38/hg38 |
XM_011525341.3 | chr17:g.61857171G>A | c.266C>T | p.A89V | RefSeq | GRCh38/hg38 |
XM_047436893.1 | chr17:g.61857171G>A | c.266C>T | p.A89V | RefSeq | GRCh38/hg38 |
XM_011525333.3 | chr17:g.61857171G>A | c.266C>T | p.A89V | RefSeq | GRCh38/hg38 |
XM_047436904.1 | chr17:g.61857171G>A | c.266C>T | p.A89V | RefSeq | GRCh38/hg38 |
XM_011525336.3 | chr17:g.61857171G>A | c.266C>T | p.A89V | RefSeq | GRCh38/hg38 |
XM_047436897.1 | chr17:g.61857171G>A | c.266C>T | p.A89V | RefSeq | GRCh38/hg38 |
XM_047436894.1 | chr17:g.61857171G>A | c.266C>T | p.A89V | RefSeq | GRCh38/hg38 |
XM_011525334.3 | chr17:g.61857171G>A | c.266C>T | p.A89V | RefSeq | GRCh38/hg38 |
XM_011525336.2 | chr17:g.61857171G>A | c.266C>T | p.A89V | RefSeq | GRCh38/hg38 |
XM_011525339.3 | chr17:g.61857171G>A | c.266C>T | p.A89V | RefSeq | GRCh38/hg38 |
XM_011525332.3 | chr17:g.61857171G>A | c.266C>T | p.A89V | RefSeq | GRCh38/hg38 |
XM_047436891.1 | chr17:g.61857171G>A | c.266C>T | p.A89V | RefSeq | GRCh38/hg38 |
XM_047436902.1 | chr17:g.61857171G>A | c.266C>T | p.A89V | RefSeq | GRCh38/hg38 |
XM_047436896.1 | chr17:g.61857171G>A | c.266C>T | p.A89V | RefSeq | GRCh38/hg38 |
XM_011525337.2 | chr17:g.61857171G>A | c.266C>T | p.A89V | RefSeq | GRCh38/hg38 |
NM_032043.2 | chr17:g.61857171G>A | c.266C>T | p.A89V | RefSeq | GRCh38/hg38 |
XM_011525340.4 | chr17:g.61857171G>A | c.266C>T | p.A89V | RefSeq | GRCh38/hg38 |
XM_011525333.4 | chr17:g.61857171G>A | c.266C>T | p.A89V | RefSeq | GRCh38/hg38 |
XM_047436903.1 | chr17:g.61857171G>A | c.266C>T | p.A89V | RefSeq | GRCh38/hg38 |
XM_047436899.1 | chr17:g.61857171G>A | c.266C>T | p.A89V | RefSeq | GRCh38/hg38 |
XM_011525341.4 | chr17:g.61857171G>A | c.266C>T | p.A89V | RefSeq | GRCh38/hg38 |
XM_011525339.4 | chr17:g.61857171G>A | c.266C>T | p.A89V | RefSeq | GRCh38/hg38 |
XM_011525335.3 | chr17:g.61857171G>A | c.266C>T | p.A89V | RefSeq | GRCh38/hg38 |
XM_047436892.1 | chr17:g.61857171G>A | c.266C>T | p.A89V | RefSeq | GRCh38/hg38 |
XM_011525334.2 | chr17:g.61857171G>A | c.266C>T | p.A89V | RefSeq | GRCh38/hg38 |
XM_047436900.1 | chr17:g.61857171G>A | c.266C>T | p.A89V | RefSeq | GRCh38/hg38 |
XM_011525340.3 | chr17:g.61857171G>A | c.266C>T | p.A89V | RefSeq | GRCh38/hg38 |
NM_032043.3 | chr17:g.61857171G>A | c.266C>T | p.A89V | RefSeq | GRCh38/hg38 |
XM_011525332.4 | chr17:g.61857171G>A | c.266C>T | p.A89V | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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