Annotation Detail
Information
- Associated Genes
- ARSA
- Associated Variants
-
ARSA p.Gly88Asp (p.G88D)
(
ENST00000216124.10,
ENST00000356098.9,
ENST00000395619.3,
ENST00000395621.7,
ENST00000453344.6 )
ARSA p.Gly88Asp (p.G88D) ( ENST00000216124.10, ENST00000356098.9, ENST00000395619.3, ENST00000395621.7, ENST00000453344.6 ) - Associated Disease
- Metachromatic leukodystrophy, severe
- Source Database
- ClinVar
- Description
- NM_000487.6(ARSA):c.263G>A (p.Gly88Asp) AND Metachromatic leukodystrophy, severe
- ClinVar Allele ID
- 18100
- ClinVar RefSeq Alternation Syntax
- NM_001085427.3:c.263G>A
- ClinVar RefSeq Alternation Syntax
- NM_001362782.2:c.5G>A
- ClinVar RefSeq Alternation Syntax
- NM_000487.6:c.263G>A
- ClinVar RefSeq Alternation Syntax
- NM_001085426.3:c.263G>A
- ClinVar RefSeq Alternation Syntax
- NM_001085428.3:c.5G>A
- ClinVar RefSeq Alternation Syntax
- NM_001085425.3:c.263G>A
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2018-11-07
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000003207
- ClinVar Disease
- Metachromatic leukodystrophy, severe
- Observed Origin Sample
- germline
- Pubmed
- 1671769
Drugs