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Gene | CHEK2 |
Variant | W93Gfs*17 |
Impact List | frameshift |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | CHEK2 W93Gfs*17 indicates a shift in the reading frame starting at amino acid 93 and terminating 17 residues downstream causing a premature truncation of the 543 amino acid Chek2 protein (UniProt.org). W93Gfs*17 is predicted to lead to a loss of Chek2 protein function as indicated by decreased Kap1 phosphorylation in culture (PMID: 34903604). |
Associated Drug Resistance | |
Category Variants Paths |
CHEK2 mutant CHEK2 inact mut CHEK2 W93Gfs*17 |
Transcript | NM_007194.4 |
gDNA | chr22:g.28734445delA |
cDNA | c.277delT |
Protein | p.W93Gfs*17 |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_007194 | chr22:g.28734445delA | c.277delT | p.W93Gfs*17 | RefSeq | GRCh38/hg38 |
NM_001349956.2 | chr22:g.28734445delA | c.277delT | p.W93Gfs*17 | RefSeq | GRCh38/hg38 |
NM_001005735.2 | chr22:g.28734445_28734446insTTGGGCC | c.276_277insGGCCCAA | p.W93Gfs*17 | RefSeq | GRCh38/hg38 |
NM_145862.2 | chr22:g.28734445delA | c.277delT | p.W93Gfs*17 | RefSeq | GRCh38/hg38 |
NM_007194.3 | chr22:g.28734445delA | c.277delT | p.W93Gfs*17 | RefSeq | GRCh38/hg38 |
NM_001005735.1 | chr22:g.28734445_28734446insTTGGGCC | c.276_277insGGCCCAA | p.W93Gfs*17 | RefSeq | GRCh38/hg38 |
NM_001005735 | chr22:g.28734446_28734447insCGGGCCG | c.276_277insGGCCCGC | p.W93Gfs*17 | RefSeq | GRCh38/hg38 |
NM_007194.4 | chr22:g.28734445delA | c.277delT | p.W93Gfs*17 | RefSeq | GRCh38/hg38 |
NM_145862.2 | chr22:g.28734445delA | c.277delT | p.W93Gfs*17 | RefSeq | GRCh38/hg38 |
XM_047441105.1 | chr22:g.28734445_28734446insTTGGGCC | c.276_277insGGCCCAA | p.W93Gfs*17 | RefSeq | GRCh38/hg38 |
XM_011529841.1 | chr22:g.28734445_28734446insTTGGGCC | c.276_277insGGCCCAA | p.W93Gfs*17 | RefSeq | GRCh38/hg38 |
XM_047441106.1 | chr22:g.28734445_28734446insTTGGGCC | c.276_277insGGCCCAA | p.W93Gfs*17 | RefSeq | GRCh38/hg38 |
XM_047441104.1 | chr22:g.28734445_28734446insTTGGGCC | c.276_277insGGCCCAA | p.W93Gfs*17 | RefSeq | GRCh38/hg38 |
XM_011529841 | chr22:g.28734446_28734447insCGGGCCG | c.276_277insGGCCCGC | p.W93Gfs*17 | RefSeq | GRCh38/hg38 |
NM_145862 | chr22:g.28734445delA | c.277delT | p.W93Gfs*17 | RefSeq | GRCh38/hg38 |
XM_011529843 | chr22:g.28734445delA | c.277delT | p.W93Gfs*17 | RefSeq | GRCh38/hg38 |
NM_001349956.1 | chr22:g.28734445delA | c.277delT | p.W93Gfs*17 | RefSeq | GRCh38/hg38 |
Molecular Profile | Protein Effect | Treatment Approaches |
---|---|---|
CHEK2 W93Gfs*17 | loss of function - predicted | Olaparib |