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Gene | CHEK2 |
Variant | V198Ffs*7 |
Impact List | frameshift |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | CHEK2 V198Ffs*7 indicates a shift in the reading frame starting at amino acid 198 and terminating seven residues downstream causing a premature truncation of the 543 amino acid Chek2 protein (UniProt.org). V198Ffs*7 has not been characterized, however, due to the effects of other truncation mutations downstream of V198 resulting in disruption of the protein kinase domain (PMID: 11053450, PMID: 16982735, PMID: 31050813), is predicted to lead to a loss of Chek2 protein function. |
Associated Drug Resistance | |
Category Variants Paths |
CHEK2 mutant CHEK2 inact mut CHEK2 V198Ffs*7 |
Transcript | NM_007194.4 |
gDNA | chr22:g.28724977delC |
cDNA | c.592+1delG |
Protein | p.V198Ffs*7 |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_007194.3 | chr22:g.28724977delC | c.592+1delG | p.V198Ffs*7 | RefSeq | GRCh38/hg38 |
NM_007194.4 | chr22:g.28724977delC | c.592+1delG | p.V198Ffs*7 | RefSeq | GRCh38/hg38 |
NM_145862.2 | chr22:g.28724977delC | c.592+1delG | p.V198Ffs*7 | RefSeq | GRCh38/hg38 |
NM_145862.2 | chr22:g.28724977delC | c.592+1delG | p.V198Ffs*7 | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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