Annotation Detail
Information
- Associated Genes
- PRX
- Associated Variants
-
PRX p.Arg1048Ter (p.R1048*)
(
ENST00000291825.11,
ENST00000324001.8,
ENST00000673881.1,
ENST00000674005.2,
ENST00000674773.1 )
PRX p.Arg1048Ter (p.R1048*) ( ENST00000291825.11, ENST00000324001.8, ENST00000673881.1, ENST00000674005.2, ENST00000674773.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_181882.3(PRX):c.2857C>T (p.Arg953Ter) AND not provided
- ClinVar Allele ID
- 19826
- ClinVar RefSeq Alternation Syntax
- NM_020956.2:c.*3062C>T
- ClinVar RefSeq Alternation Syntax
- NM_181882.3:c.2857C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2019-03-11
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000236836
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs