Annotation Detail
Information
- Associated Genes
- SMPD1
- Associated Variants
-
SMPD1 p.His423Tyr (p.H423Y)
(
ENST00000527275.5,
ENST00000342245.9 )
SMPD1 p.His423Tyr (p.H423Y) ( ENST00000342245.9, ENST00000527275.5 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000543.5(SMPD1):c.1267C>T (p.His423Tyr) AND not provided
- ClinVar Allele ID
- 18031
- ClinVar RefSeq Alternation Syntax
- NM_001318088.2:c.346C>T
- ClinVar RefSeq Alternation Syntax
- NM_001365135.2:c.1135C>T
- ClinVar RefSeq Alternation Syntax
- NR_027400.3:n.1220C>T
- ClinVar RefSeq Alternation Syntax
- NM_001318087.2:c.1267C>T
- ClinVar RefSeq Alternation Syntax
- NM_000543.5:c.1267C>T
- ClinVar RefSeq Alternation Syntax
- NM_001007593.3:c.1264C>T
- ClinVar RefSeq Alternation Syntax
- NR_134502.2:n.739C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2021-03-02
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000723415
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs