Annotation Detail
Information
- Associated Genes
- CDH1
- Associated Variants
-
CDH1 c.1137+2T>C
(
ENST00000422392.6,
ENST00000261769.10 )
CDH1 c.1137+2T>C ( ENST00000261769.10, ENST00000422392.6 ) - Associated Disease
- Hereditary diffuse gastric adenocarcinoma
- Source Database
- ClinVar
- Description
- NM_004360.5(CDH1):c.1137+2T>C AND Hereditary diffuse gastric adenocarcinoma
- ClinVar Allele ID
- 184374
- ClinVar RefSeq Alternation Syntax
- NM_001317185.2:c.-479+2T>C
- ClinVar RefSeq Alternation Syntax
- NM_001317186.2:c.-683+2T>C
- ClinVar RefSeq Alternation Syntax
- NM_004360.5:c.1137+2T>C
- ClinVar RefSeq Alternation Syntax
- NM_001317184.2:c.1137+2T>C
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2020-01-31
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001195172
- ClinVar Disease
- Hereditary diffuse gastric adenocarcinoma
- Observed Origin Sample
- germline
Drugs