Annotation Detail
Information
- Associated Genes
- SMPD1
- Associated Variants
-
SMPD1 p.Trp32Ter (p.W32*)
(
ENST00000342245.9,
ENST00000527275.5 )
SMPD1 p.Trp32Ter (p.W32*) ( ENST00000342245.9, ENST00000527275.5 ) - Associated Disease
- Niemann-Pick disease, type A Niemann-Pick disease, type B
- Source Database
- ClinVar
- Description
- NM_000543.5(SMPD1):c.96G>A (p.Trp32Ter) AND multiple conditions
- ClinVar Allele ID
- 186823
- ClinVar RefSeq Alternation Syntax
- NM_000543.5:c.96G>A
- ClinVar RefSeq Alternation Syntax
- NM_001318088.2:c.-866G>A
- ClinVar RefSeq Alternation Syntax
- NM_001365135.2:c.96G>A
- ClinVar RefSeq Alternation Syntax
- NR_027400.3:n.221G>A
- ClinVar RefSeq Alternation Syntax
- NM_001007593.3:c.96G>A
- ClinVar RefSeq Alternation Syntax
- NM_001318087.2:c.96G>A
- ClinVar RefSeq Alternation Syntax
- NR_134502.2:n.221G>A
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2023-07-28
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001219345
- ClinVar Disease
- Niemann-Pick disease, type A
- ClinVar Disease
- Niemann-Pick disease, type B
- Observed Origin Sample
- germline
- Observed Origin Sample
- unknown
Drugs