Annotation Detail
Information
- Associated Genes
- ARSA
- Associated Variants
-
ARSA p.Gly101Asp (p.G101D)
(
ENST00000216124.10,
ENST00000395621.7,
ENST00000356098.9,
ENST00000453344.6,
ENST00000395619.3 )
ARSA p.Gly101Asp (p.G101D) ( ENST00000356098.9, ENST00000395619.3, ENST00000216124.10, ENST00000395621.7, ENST00000453344.6 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000487.6(ARSA):c.302G>A (p.Gly101Asp) AND not provided
- ClinVar Allele ID
- 18092
- ClinVar RefSeq Alternation Syntax
- NM_001085425.3:c.302G>A
- ClinVar RefSeq Alternation Syntax
- NM_001085426.3:c.302G>A
- ClinVar RefSeq Alternation Syntax
- NM_001085427.3:c.302G>A
- ClinVar RefSeq Alternation Syntax
- NM_001085428.3:c.44G>A
- ClinVar RefSeq Alternation Syntax
- NM_000487.6:c.302G>A
- ClinVar RefSeq Alternation Syntax
- NM_001362782.2:c.44G>A
- Clinical Significance Description
- Pathogenic/Likely pathogenic
- Clinical Significance Last Update
- 2024-02-01
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000724149
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs