Annotation Detail

Information
Associated Genes
IDUA
Associated Variants
IDUA p.Leu490Pro (p.L490P) ( ENST00000247933.9, ENST00000514224.2 )
IDUA p.Leu490Pro (p.L490P) ( ENST00000247933.9, ENST00000514224.2 )
Associated Disease
not provided
Source Database
ClinVar
Description
NM_000203.5(IDUA):c.1469T>C (p.Leu490Pro) AND not provided
ClinVar Allele ID
26958
ClinVar RefSeq Alternation Syntax
NM_000203.5:c.1469T>C
ClinVar RefSeq Alternation Syntax
NM_001363576.1:c.1073T>C
ClinVar RefSeq Alternation Syntax
NR_110313.1:n.1557T>C
Clinical Significance Description
Pathogenic
Clinical Significance Last Update
2023-06-08
Clinical Significance Review Status
criteria provided, multiple submitters, no conflicts
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV000790664
ClinVar Disease
not provided
Observed Origin Sample
germline
Drugs