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Gene | CHEK2 |
Variant | R117G |
Impact List | missense |
Protein Effect | loss of function |
Gene Variant Descriptions | CHEK2 R117G lies within the FHA domain of the Chek2 protein (UniProt.org). R117G confers a loss of function to the Chek2 protein as demonstrated by reduced kinase activity (PMID: 16835864), and results in decreased Kap1 phosphorylation upon ionizing radiation in cell culture (PMID: 34903604). |
Associated Drug Resistance | |
Category Variants Paths |
CHEK2 mutant CHEK2 inact mut CHEK2 R117G |
Transcript | NM_007194.4 |
gDNA | chr22:g.28725338T>C |
cDNA | c.349A>G |
Protein | p.R117G |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_145862.2 | chr22:g.28725338T>C | c.349A>G | p.R117G | RefSeq | GRCh38/hg38 |
NM_007194.3 | chr22:g.28725338T>C | c.349A>G | p.R117G | RefSeq | GRCh38/hg38 |
NM_145862 | chr22:g.28725338T>C | c.349A>G | p.R117G | RefSeq | GRCh38/hg38 |
NM_007194 | chr22:g.28725338T>C | c.349A>G | p.R117G | RefSeq | GRCh38/hg38 |
NM_145862.2 | chr22:g.28725338T>C | c.349A>G | p.R117G | RefSeq | GRCh38/hg38 |
NM_001349956.1 | chr22:g.28725338T>C | c.349A>G | p.R117G | RefSeq | GRCh38/hg38 |
XM_011529843 | chr22:g.28725338T>C | c.349A>G | p.R117G | RefSeq | GRCh38/hg38 |
NM_001349956.2 | chr22:g.28725338T>C | c.349A>G | p.R117G | RefSeq | GRCh38/hg38 |
NM_007194.4 | chr22:g.28725338T>C | c.349A>G | p.R117G | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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