Annotation Detail

Information
Associated Genes
CDH1
Associated Variants
CDH1 p.Trp20Ter (p.W20*) ( ENST00000261769.10, ENST00000422392.6 )
CDH1 p.Trp20Ter (p.W20*) ( ENST00000261769.10, ENST00000422392.6 )
Associated Disease
Hereditary diffuse gastric adenocarcinoma
Source Database
ClinVar
Description
NM_004360.5(CDH1):c.59G>A (p.Trp20Ter) AND Hereditary diffuse gastric adenocarcinoma
ClinVar Allele ID
27278
ClinVar RefSeq Alternation Syntax
NM_001317184.2:c.59G>A
ClinVar RefSeq Alternation Syntax
NM_001317185.2:c.-1557G>A
ClinVar RefSeq Alternation Syntax
NM_004360.5:c.59G>A
ClinVar RefSeq Alternation Syntax
NM_001317186.2:c.-1761G>A
Clinical Significance Description
Pathogenic
Clinical Significance Last Update
2023-06-08
Clinical Significance Review Status
criteria provided, multiple submitters, no conflicts
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV000013026
ClinVar Disease
Hereditary diffuse gastric adenocarcinoma
Observed Origin Sample
germline
Observed Origin Sample
unknown
Pubmed
10072428
Drugs