Annotation Detail
Information
- Associated Genes
- ARSA
- Associated Variants
-
ARSA p.Pro427Thr (p.P427T)
(
ENST00000216124.10,
ENST00000356098.9,
ENST00000395619.3,
ENST00000395621.7,
ENST00000453344.6 )
ARSA p.Pro427Thr (p.P427T) ( ENST00000216124.10, ENST00000356098.9, ENST00000395619.3, ENST00000395621.7, ENST00000453344.6 ) - Associated Disease
- Metachromatic leukodystrophy, juvenile type
- Source Database
- ClinVar
- Description
- NM_000487.6(ARSA):c.1279C>A (p.Pro427Thr) AND Metachromatic leukodystrophy, juvenile type
- ClinVar Allele ID
- 18133
- ClinVar RefSeq Alternation Syntax
- NM_001085428.3:c.1021C>A
- ClinVar RefSeq Alternation Syntax
- NM_000487.6:c.1279C>A
- ClinVar RefSeq Alternation Syntax
- NM_001085427.3:c.1279C>A
- ClinVar RefSeq Alternation Syntax
- NM_001362782.2:c.1021C>A
- ClinVar RefSeq Alternation Syntax
- NM_001085426.3:c.1279C>A
- ClinVar RefSeq Alternation Syntax
- NM_001085425.3:c.1279C>A
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2003-06-20
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000003240
- ClinVar Disease
- Metachromatic leukodystrophy, juvenile type
- Observed Origin Sample
- germline
- Pubmed
- 10220151
- Pubmed
- 12788103
- Pubmed
- 12503099
Drugs