Annotation Detail
Information
- Associated Genes
- CDH1
- Associated Variants
-
CDH1 p.Gln641Ter (p.Q641*)
(
ENST00000261769.10,
ENST00000422392.6 )
CDH1 p.Gln641Ter (p.Q641*) ( ENST00000261769.10, ENST00000422392.6 ) - Associated Disease
- Hereditary cancer-predisposing syndrome
- Source Database
- ClinVar
- Description
- NM_004360.5(CDH1):c.1921C>T (p.Gln641Ter) AND Hereditary cancer-predisposing syndrome
- ClinVar Allele ID
- 152540
- ClinVar RefSeq Alternation Syntax
- NM_001317185.2:c.373C>T
- ClinVar RefSeq Alternation Syntax
- NM_001317186.2:c.-45C>T
- ClinVar RefSeq Alternation Syntax
- NM_004360.5:c.1921C>T
- ClinVar RefSeq Alternation Syntax
- NM_001317184.2:c.1738C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2023-06-22
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000132257
- ClinVar Disease
- Hereditary cancer-predisposing syndrome
- Observed Origin Sample
- germline
Drugs