Annotation Detail
Information
- Associated Genes
- SMPD1
- Associated Variants
-
SMPD1 p.Cys159Arg (p.C159R)
(
ENST00000527275.5,
ENST00000342245.9 )
SMPD1 p.Cys159Arg (p.C159R) ( ENST00000342245.9, ENST00000527275.5 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000543.5(SMPD1):c.475T>C (p.Cys159Arg) AND not provided
- ClinVar Allele ID
- 177267
- ClinVar RefSeq Alternation Syntax
- NM_000543.5:c.475T>C
- ClinVar RefSeq Alternation Syntax
- NR_027400.3:n.600T>C
- ClinVar RefSeq Alternation Syntax
- NM_001365135.2:c.475T>C
- ClinVar RefSeq Alternation Syntax
- NM_001318088.2:c.-487T>C
- ClinVar RefSeq Alternation Syntax
- NM_001007593.3:c.472T>C
- ClinVar RefSeq Alternation Syntax
- NM_001318087.2:c.475T>C
- Clinical Significance Description
- Pathogenic/Likely pathogenic
- Clinical Significance Last Update
- 2023-07-10
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000723416
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs