Missing content? – Request curation!
Request curation for specific Genes, Variants, or PubMed publications.
Have questions, comments, or suggestions? - Let us know!
Email us at : ckbsupport@genomenon.com
Gene | CHEK2 |
Variant | R474L |
Impact List | missense |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | CHEK2 R474L lies within the protein kinase domain of the Chek2 protein (UniProt.org). R474L results in reduced Kap1 phosphorylation upon ionizing radiation in culture (PMID: 34903604), and therefore, is predicted to lead to a loss of Chek2 protein function. |
Associated Drug Resistance | |
Category Variants Paths |
CHEK2 mutant CHEK2 inact mut CHEK2 R474L |
Transcript | NM_007194.4 |
gDNA | chr22:g.28694072C>A |
cDNA | c.1421G>T |
Protein | p.R474L |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_007194.3 | chr22:g.28694072C>A | c.1421G>T | p.R474L | RefSeq | GRCh38/hg38 |
NM_001005735.2 | chr22:g.28695210_28695211delAGinsCT | c.1420_1421delAGinsCT | p.R474L | RefSeq | GRCh38/hg38 |
NM_007194.4 | chr22:g.28694072C>A | c.1421G>T | p.R474L | RefSeq | GRCh38/hg38 |
XM_024452149.2 | chr22:g.28689199_28689200delAGinsCT | c.1420_1421delAGinsCT | p.R474L | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
---|