Annotation Detail
Information
- Associated Genes
- PRX
- Associated Variants
-
PRX p.Arg1165Ter (p.R1165*)
(
ENST00000291825.11,
ENST00000324001.8,
ENST00000673881.1,
ENST00000674005.2,
ENST00000674773.1 )
PRX p.Arg1165Ter (p.R1165*) ( ENST00000291825.11, ENST00000324001.8, ENST00000673881.1, ENST00000674005.2, ENST00000674773.1 ) - Associated Disease
- Dejerine-Sottas disease
- Source Database
- ClinVar
- Description
- NM_181882.3(PRX):c.3208C>T (p.Arg1070Ter) AND Dejerine-Sottas disease
- ClinVar Allele ID
- 19833
- ClinVar RefSeq Alternation Syntax
- NM_181882.3:c.3208C>T
- ClinVar RefSeq Alternation Syntax
- NM_020956.2:c.*3413C>T
- Clinical Significance Description
- Pathogenic/Likely pathogenic
- Clinical Significance Last Update
- 2022-01-03
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000005061
- ClinVar Disease
- Dejerine-Sottas disease
- Observed Origin Sample
- germline
- Observed Origin Sample
- inherited
Drugs