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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), decreased Kap1 phosphorylation upon ionizing radiation in cell culture (PMID: 34903604), and decreased Kap1 phosphorylation and Chek2 autophosphorylation in culture (PMID: 37449874). |
| 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_001349956.1 | 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 |
| 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_007194.3 | 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 |
| NM_145862.2 | 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 |
| Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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