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Gene | BRIP1 |
Variant | F108S |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | BRIP1 F108S lies within the helicase ATP-binding domain of the Brip1 protein (UniProt.org). F108S has not been characterized in the scientific literature and therefore, its effect on Brip1 protein function is unknown (PubMed, Feb 2024). |
Associated Drug Resistance | |
Category Variants Paths |
BRIP1 mutant BRIP1 F108S |
Transcript | NM_032043.3 |
gDNA | chr17:g.61857114A>G |
cDNA | c.323T>C |
Protein | p.F108S |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_011525337.2 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_047436901.1 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_011525334.2 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_047436894.1 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_011525339.4 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_047436903.1 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_011525337 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_047436895.1 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_011525339 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_011525336.3 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_047436904.1 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_047436900.1 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_047436892.1 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_011525334 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_011525335.3 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
NM_032043.2 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_047436902.1 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_047436896.1 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_011525340.4 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_011525333 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_011525336 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_011525333.3 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_011525334.3 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_047436899.1 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_011525332.3 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_011525333.4 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_047436893.1 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_011525339.3 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_011525332 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_011525340 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_047436891.1 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_011525341.4 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
NM_032043.3 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_047436897.1 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_011525340.3 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_011525341.3 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
NM_032043 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_011525335 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_011525336.2 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_011525335.4 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_011525341 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
XM_011525332.4 | chr17:g.61857114A>G | c.323T>C | p.F108S | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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