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Gene | CHEK2 |
Variant | N185fs |
Impact List | frameshift |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | CHEK2 N185fs results in a change in the amino acid sequence of the Chek2 protein beginning at aa 185 of 543, likely resulting in premature truncation of the functional protein (UniProt.org). N185fs has not been characterized, however, due to the effects of other truncation mutations downstream of N185 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 N185fs |
Transcript | NM_007194.4 |
gDNA | chr22:g.(28725016_28725017) |
cDNA | c.(553_552) |
Protein | p.N185fs |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_145862.2 | chr22:g.(28725016_28725017) | c.(553_552) | p.N185fs | RefSeq | GRCh38/hg38 |
NM_145862.2 | chr22:g.(28725016_28725017) | c.(553_552) | p.N185fs | RefSeq | GRCh38/hg38 |
NM_007194.4 | chr22:g.(28725016_28725017) | c.(553_552) | p.N185fs | RefSeq | GRCh38/hg38 |
XM_047441104.1 | chr22:g.(28725109_28725110) | c.(553_552) | p.N185fs | RefSeq | GRCh38/hg38 |
NM_007194.3 | chr22:g.(28725016_28725017) | c.(553_552) | p.N185fs | RefSeq | GRCh38/hg38 |
XM_047441106.1 | chr22:g.(28725109_28725110) | c.(553_552) | p.N185fs | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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