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Gene | CHEK2 |
Variant | R95* |
Impact List | nonsense |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | CHEK2 R95* results in a premature truncation of the Chek2 protein at amino acid 95 of 543 (UniProt.org). R95* has not been characterized, however, due to the effects of other truncation mutations downstream of R95 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 R95* |
Transcript | NM_007194.4 |
gDNA | chr22:g.28734439G>A |
cDNA | c.283C>T |
Protein | p.R95* |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_047441104.1 | chr22:g.28734439G>A | c.283C>T | p.R95* | RefSeq | GRCh38/hg38 |
XM_047441105.1 | chr22:g.28734439G>A | c.283C>T | p.R95* | RefSeq | GRCh38/hg38 |
XM_011529843 | chr22:g.28734439G>A | c.283C>T | p.R95* | RefSeq | GRCh38/hg38 |
NM_007194 | chr22:g.28734439G>A | c.283C>T | p.R95* | RefSeq | GRCh38/hg38 |
NM_001349956.1 | chr22:g.28734439G>A | c.283C>T | p.R95* | RefSeq | GRCh38/hg38 |
XM_047441106.1 | chr22:g.28734439G>A | c.283C>T | p.R95* | RefSeq | GRCh38/hg38 |
NM_007194.4 | chr22:g.28734439G>A | c.283C>T | p.R95* | RefSeq | GRCh38/hg38 |
NM_145862.2 | chr22:g.28734439G>A | c.283C>T | p.R95* | RefSeq | GRCh38/hg38 |
NM_001349956.2 | chr22:g.28734439G>A | c.283C>T | p.R95* | RefSeq | GRCh38/hg38 |
NM_145862.2 | chr22:g.28734439G>A | c.283C>T | p.R95* | RefSeq | GRCh38/hg38 |
NM_001005735.1 | chr22:g.28734439G>A | c.283C>T | p.R95* | RefSeq | GRCh38/hg38 |
XM_011529841.1 | chr22:g.28734439G>A | c.283C>T | p.R95* | RefSeq | GRCh38/hg38 |
NM_145862 | chr22:g.28734439G>A | c.283C>T | p.R95* | RefSeq | GRCh38/hg38 |
NM_007194.3 | chr22:g.28734439G>A | c.283C>T | p.R95* | RefSeq | GRCh38/hg38 |
XM_011529841 | chr22:g.28734439G>A | c.283C>T | p.R95* | RefSeq | GRCh38/hg38 |
NM_001005735 | chr22:g.28734439G>A | c.283C>T | p.R95* | RefSeq | GRCh38/hg38 |
NM_001005735.2 | chr22:g.28734439G>A | c.283C>T | p.R95* | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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