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Gene | BRIP1 |
Variant | L358P |
Impact List | missense |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | BRIP1 L358P lies within the helicase ATP-binding domain of the Brip1 protein (UniProt.org). L358P does not confer resistance to interstrand crosslinking agents in a BRIP1-deficient cell line in culture (PMID: 33619228), and therefore, is predicted to lead to a loss of Brip1 protein function. |
Associated Drug Resistance | |
Category Variants Paths |
BRIP1 mutant BRIP1 inact mut BRIP1 L358P |
Transcript | NM_032043.3 |
gDNA | chr17:g.61801320A>G |
cDNA | c.1073T>C |
Protein | p.L358P |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_032043 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_011525333.4 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_011525336.2 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_011525340.3 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_011525335 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_011525341.4 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
NM_032043.2 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_047436896.1 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_011525336 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_047436899.1 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_011525340 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_011525337.2 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_011525333 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_047436900.1 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_011525339.3 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_047436891.1 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_011525340.4 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_047436897.1 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_011525339.4 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_011525332 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_011525333.3 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_011525337 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_011525335.4 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_011525334.3 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_047436892.1 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_011525332.4 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_011525339 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_011525334 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_011525341.3 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_047436904.1 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_047436901.1 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
NM_032043.3 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_047436894.1 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_047436902.1 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_011525341 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_047436893.1 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_011525334.2 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_011525335.3 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_047436895.1 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_011525332.3 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_011525336.3 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
XM_047436903.1 | chr17:g.61801320A>G | c.1073T>C | p.L358P | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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