Annotation Detail
Information
- Associated Genes
- CHEK2
- Associated Variants
-
CHEK2 p.Arg566His (p.R566H)
(
ENST00000402731.6,
ENST00000405598.5,
ENST00000403642.5,
ENST00000382580.6,
ENST00000404276.6,
ENST00000348295.7,
ENST00000425190.7,
ENST00000464581.6,
ENST00000650281.1,
ENST00000649563.1 )
CHEK2 p.Arg566His (p.R566H) ( ENST00000348295.7, ENST00000382580.6, ENST00000402731.6, ENST00000403642.5, ENST00000404276.6, ENST00000405598.5, ENST00000425190.7, ENST00000464581.6, ENST00000649563.1, ENST00000650281.1 ) - Associated Disease
- Hereditary cancer-predisposing syndrome
- Source Database
- ClinVar
- Description
- NM_007194.4(CHEK2):c.1568G>A (p.Arg523His) AND Hereditary cancer-predisposing syndrome
- ClinVar Allele ID
- 471821
- ClinVar RefSeq Alternation Syntax
- NM_001257387.2:c.905G>A
- ClinVar RefSeq Alternation Syntax
- NM_001005735.2:c.1697G>A
- ClinVar RefSeq Alternation Syntax
- NM_001349956.2:c.1367G>A
- ClinVar RefSeq Alternation Syntax
- NM_007194.4:c.1568G>A
- ClinVar RefSeq Alternation Syntax
- NM_145862.2:c.1481G>A
- Clinical Significance Description
- Conflicting interpretations of pathogenicity
- Clinical Significance Last Update
- 2021-11-22
- Clinical Significance Review Status
- criteria provided, conflicting interpretations
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000572698
- ClinVar Disease
- Hereditary cancer-predisposing syndrome
- Observed Origin Sample
- germline
Drugs