Annotation Detail
Information
- Associated Genes
- PRX
- Associated Variants
-
PRX p.Asp860ThrfsTer10 (p.D860Tfs*10)
(
ENST00000291825.11,
ENST00000324001.8,
ENST00000673881.1,
ENST00000674005.2,
ENST00000674773.1 )
PRX p.Asp860ThrfsTer10 (p.D860Tfs*10) ( ENST00000291825.11, ENST00000324001.8, ENST00000673881.1, ENST00000674005.2, ENST00000674773.1 ) - Associated Disease
- Autosomal recessive Dejerine-Sottas syndrome
- Source Database
- ClinVar
- Description
- NM_181882.3(PRX):c.2289del (p.Asp765fs) AND Autosomal recessive Dejerine-Sottas syndrome
- ClinVar Allele ID
- 205189
- ClinVar RefSeq Alternation Syntax
- NM_181882.3:c.2289del
- ClinVar RefSeq Alternation Syntax
- NM_020956.2:c.*2494del
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2001-02-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000005056
- ClinVar Disease
- Autosomal recessive Dejerine-Sottas syndrome
- Observed Origin Sample
- germline
- Pubmed
- 11133365
Drugs