Annotation Detail
Information
- Associated Genes
- DES
- Associated Variants
-
DES p.Gln389Pro (p.Q389P)
(
ENST00000373960.4 )
DES p.Gln389Pro (p.Q389P) ( ENST00000373960.4 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_001927.4(DES):c.1166A>C (p.Gln389Pro) AND not provided
- ClinVar Allele ID
- 31869
- ClinVar RefSeq Alternation Syntax
- NM_001927.4:c.1166A>C
- Clinical Significance Description
- not provided
- Clinical Significance Review Status
- no assertion provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000056776
- ClinVar Disease
- not provided
- Observed Origin Sample
- not provided
Drugs