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 | S140N |
| Impact List | missense |
| Protein Effect | loss of function - predicted |
| Gene Variant Descriptions | CHEK2 S140N lies within the FHA domain of the Chek2 protein (UniProt.org). S140N results in reduced phosphorylation of Chek2 and Kap1 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 S140N |
| Transcript | NM_007194.4 |
| gDNA | chr22:g.28725268C>T |
| cDNA | c.419G>A |
| Protein | p.S140N |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| NM_145862.2 | chr22:g.28725268C>T | c.419G>A | p.S140N | RefSeq | GRCh38/hg38 |
| NM_007194.4 | chr22:g.28725268C>T | c.419G>A | p.S140N | RefSeq | GRCh38/hg38 |
| NM_001349956.1 | chr22:g.28725268C>T | c.419G>A | p.S140N | RefSeq | GRCh38/hg38 |
| NM_145862.2 | chr22:g.28725268C>T | c.419G>A | p.S140N | RefSeq | GRCh38/hg38 |
| NM_007194.3 | chr22:g.28725268C>T | c.419G>A | p.S140N | RefSeq | GRCh38/hg38 |
| NM_001349956.2 | chr22:g.28725268C>T | c.419G>A | p.S140N | RefSeq | GRCh38/hg38 |
| Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
|---|