Annotation Detail
Information
- Associated Genes
- GNPTAB
- Associated Variants
-
GNPTAB p.Cys442Tyr (p.C442Y)
(
ENST00000299314.12,
ENST00000549940.5 )
GNPTAB p.Cys442Tyr (p.C442Y) ( ENST00000299314.12, ENST00000549940.5 ) - Associated Disease
- Pseudo-Hurler polydystrophy Mucolipidosis type II
- Source Database
- ClinVar
- Description
- NM_024312.5(GNPTAB):c.1325G>A (p.Cys442Tyr) AND multiple conditions
- ClinVar Allele ID
- 47632
- ClinVar RefSeq Alternation Syntax
- NM_024312.5:c.1325G>A
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2023-07-03
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001037653
- ClinVar Disease
- Pseudo-Hurler polydystrophy
- ClinVar Disease
- Mucolipidosis type II
- Observed Origin Sample
- germline
Drugs