Annotation Detail
Information
- Associated Genes
- SMPD1
- Associated Variants
-
SMPD1 p.Arg498Cys (p.R498C)
(
ENST00000527275.5,
ENST00000342245.9 )
SMPD1 p.Arg498Cys (p.R498C) ( ENST00000342245.9, ENST00000527275.5 ) - Associated Disease
- Niemann-Pick disease, type A
- Source Database
- ClinVar
- Description
- NM_000543.5(SMPD1):c.1492C>T (p.Arg498Cys) AND Niemann-Pick disease, type A
- ClinVar Allele ID
- 195256
- ClinVar RefSeq Alternation Syntax
- NM_001365135.2:c.1360C>T
- ClinVar RefSeq Alternation Syntax
- NM_000543.5:c.1492C>T
- ClinVar RefSeq Alternation Syntax
- NR_134502.2:n.984C>T
- ClinVar RefSeq Alternation Syntax
- NM_001318088.2:c.571C>T
- ClinVar RefSeq Alternation Syntax
- NR_027400.3:n.1445C>T
- ClinVar RefSeq Alternation Syntax
- NM_001007593.3:c.1489C>T
- ClinVar RefSeq Alternation Syntax
- NM_001318087.2:c.1512C>T
- Clinical Significance Description
- Pathogenic/Likely pathogenic
- Clinical Significance Last Update
- 2023-09-05
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000674497
- ClinVar Disease
- Niemann-Pick disease, type A
- Observed Origin Sample
- germline
- Observed Origin Sample
- unknown
Drugs