Annotation Detail
Information
- Associated Genes
- CDH1
- Associated Variants
-
CDH1 p.Leu667SerfsTer12 (p.L667Sfs*12)
(
ENST00000422392.6,
ENST00000261769.10 )
CDH1 p.Leu667SerfsTer12 (p.L667Sfs*12) ( ENST00000261769.10, ENST00000422392.6 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_004360.5(CDH1):c.1999del (p.Leu667fs) AND not provided
- ClinVar Allele ID
- 184440
- ClinVar RefSeq Alternation Syntax
- NM_001317184.2:c.1816del
- ClinVar RefSeq Alternation Syntax
- NM_001317186.2:c.34del
- ClinVar RefSeq Alternation Syntax
- NM_001317185.2:c.451del
- ClinVar RefSeq Alternation Syntax
- NM_004360.5:c.1999del
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2022-03-11
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000376724
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
- Observed Origin Sample
- unknown
Drugs