Annotation Detail
Information
- Associated Genes
- CDH1
- Associated Variants
-
CDH1 c.387+1G>A
(
ENST00000261769.10,
ENST00000422392.6 )
CDH1 c.387+1G>A ( ENST00000261769.10, ENST00000422392.6 ) - Associated Disease
- Hereditary cancer-predisposing syndrome
- Source Database
- ClinVar
- Description
- NM_004360.5(CDH1):c.387+1G>A AND Hereditary cancer-predisposing syndrome
- ClinVar Allele ID
- 151375
- ClinVar RefSeq Alternation Syntax
- NM_001317185.2:c.-1229+1G>A
- ClinVar RefSeq Alternation Syntax
- NM_001317184.2:c.387+1G>A
- ClinVar RefSeq Alternation Syntax
- NM_001317186.2:c.-1433+1G>A
- ClinVar RefSeq Alternation Syntax
- NM_004360.5:c.387+1G>A
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2023-03-30
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000130267
- ClinVar Disease
- Hereditary cancer-predisposing syndrome
- Observed Origin Sample
- germline
Drugs