Annotation Detail
Information
- Associated Genes
- PRX
- Associated Variants
-
PRX p.Cys810Ter (p.C810*)
(
ENST00000291825.11,
ENST00000324001.8,
ENST00000673881.1,
ENST00000674005.2,
ENST00000674773.1 )
PRX p.Cys810Ter (p.C810*) ( ENST00000291825.11, ENST00000324001.8, ENST00000673881.1, ENST00000674005.2, ENST00000674773.1 ) - Associated Disease
- Inborn genetic diseases
- Source Database
- ClinVar
- Description
- NM_181882.3(PRX):c.2145T>A (p.Cys715Ter) AND Inborn genetic diseases
- ClinVar Allele ID
- 19831
- ClinVar RefSeq Alternation Syntax
- NM_181882.3:c.2145T>A
- ClinVar RefSeq Alternation Syntax
- NM_020956.2:c.*2350T>A
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2019-09-23
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002426489
- ClinVar Disease
- Inborn genetic diseases
- Observed Origin Sample
- germline
Drugs