Annotation Detail
Information
- Associated Genes
- GNPTAB
- Associated Variants
-
GNPTAB p.Tyr56Ter (p.Y56*)
(
ENST00000549165.1,
ENST00000392919.4,
ENST00000299314.12,
ENST00000549940.5 )
GNPTAB p.Tyr56Ter (p.Y56*) ( ENST00000299314.12, ENST00000392919.4, ENST00000549165.1, ENST00000549940.5 ) - Associated Disease
- Pseudo-Hurler polydystrophy
- Source Database
- ClinVar
- Description
- NM_024312.5(GNPTAB):c.168T>A (p.Tyr56Ter) AND Pseudo-Hurler polydystrophy
- ClinVar Allele ID
- 47641
- ClinVar RefSeq Alternation Syntax
- NM_024312.5:c.168T>A
- Clinical Significance Description
- not provided
- Clinical Significance Review Status
- no assertion provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000032303
- ClinVar Disease
- Pseudo-Hurler polydystrophy
- Observed Origin Sample
- unknown
Drugs