Annotation Detail
Information
- Associated Genes
- SMPD1
- Associated Variants
-
SMPD1 p.Pro477Leu (p.P477L)
(
ENST00000527275.5,
ENST00000342245.9 )
SMPD1 p.Pro477Leu (p.P477L) ( 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.1430C>T (p.Pro477Leu) AND multiple conditions
- ClinVar Allele ID
- 186827
- ClinVar RefSeq Alternation Syntax
- NM_001318087.2:c.1430C>T
- ClinVar RefSeq Alternation Syntax
- NM_000543.5:c.1430C>T
- ClinVar RefSeq Alternation Syntax
- NM_001318088.2:c.509C>T
- ClinVar RefSeq Alternation Syntax
- NR_027400.3:n.1383C>T
- ClinVar RefSeq Alternation Syntax
- NM_001007593.3:c.1427C>T
- ClinVar RefSeq Alternation Syntax
- NM_001365135.2:c.1298C>T
- ClinVar RefSeq Alternation Syntax
- NR_134502.2:n.902C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2023-11-24
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000802459
- ClinVar Disease
- Niemann-Pick disease, type A
- ClinVar Disease
- Niemann-Pick disease, type B
- Observed Origin Sample
- germline
Drugs