Annotation Detail
Information
- Associated Genes
- SMPD1
- Associated Variants
-
SMPD1 p.Arg476Trp (p.R476W)
(
ENST00000527275.5,
ENST00000342245.9 )
SMPD1 p.Arg476Trp (p.R476W) ( 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.1426C>T (p.Arg476Trp) AND multiple conditions
- ClinVar Allele ID
- 99222
- ClinVar RefSeq Alternation Syntax
- NM_001007593.3:c.1423C>T
- ClinVar RefSeq Alternation Syntax
- NR_027400.3:n.1379C>T
- ClinVar RefSeq Alternation Syntax
- NM_001318087.2:c.1426C>T
- ClinVar RefSeq Alternation Syntax
- NM_001318088.2:c.505C>T
- ClinVar RefSeq Alternation Syntax
- NM_000543.5:c.1426C>T
- ClinVar RefSeq Alternation Syntax
- NM_001365135.2:c.1294C>T
- ClinVar RefSeq Alternation Syntax
- NR_134502.2:n.898C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2023-11-04
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000688387
- ClinVar Disease
- Niemann-Pick disease, type A
- ClinVar Disease
- Niemann-Pick disease, type B
- Observed Origin Sample
- germline
Drugs