Annotation Detail
Information
- Associated Genes
- ARSA
- Associated Variants
-
ARSA p.Thr276Met (p.T276M)
(
ENST00000216124.10,
ENST00000356098.9,
ENST00000395619.3,
ENST00000395621.7,
ENST00000453344.6 )
ARSA p.Thr276Met (p.T276M) ( ENST00000216124.10, ENST00000356098.9, ENST00000395619.3, ENST00000395621.7, ENST00000453344.6 ) - Associated Disease
- ARSA-related disorder
- Source Database
- ClinVar
- Description
- NM_000487.6(ARSA):c.827C>T (p.Thr276Met) AND ARSA-related disorder
- ClinVar Allele ID
- 18114
- ClinVar RefSeq Alternation Syntax
- NM_001085428.3:c.569C>T
- ClinVar RefSeq Alternation Syntax
- NM_001085425.3:c.827C>T
- ClinVar RefSeq Alternation Syntax
- NM_001085426.3:c.827C>T
- ClinVar RefSeq Alternation Syntax
- NM_001085427.3:c.827C>T
- ClinVar RefSeq Alternation Syntax
- NM_000487.6:c.827C>T
- ClinVar RefSeq Alternation Syntax
- NM_001362782.2:c.569C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2023-11-07
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003904799
- ClinVar Disease
- ARSA-related disorder
- Observed Origin Sample
- germline
Drugs