Annotation Detail
Information
- Associated Genes
- DES
- Associated Variants
-
DES p.Pro419Ser (p.P419S)
(
ENST00000373960.4 )
DES p.Pro419Ser (p.P419S) ( ENST00000373960.4 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_001927.4(DES):c.1255C>T (p.Pro419Ser) AND not provided
- ClinVar Allele ID
- 48317
- ClinVar RefSeq Alternation Syntax
- NM_001927.4:c.1255C>T
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2016-03-07
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000056783
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
- Observed Origin Sample
- not provided
Drugs