Annotation Detail
Information
- Associated Genes
- GNPTAB
- Associated Variants
-
GNPTAB p.Arg375Ter (p.R375*)
(
ENST00000549940.5,
ENST00000299314.12 )
GNPTAB p.Arg375Ter (p.R375*) ( ENST00000299314.12, ENST00000549940.5 ) - Associated Disease
- GNPTAB-related disorder
- Source Database
- ClinVar
- Description
- NM_024312.5(GNPTAB):c.1123C>T (p.Arg375Ter) AND GNPTAB-related disorder
- ClinVar Allele ID
- 47625
- ClinVar RefSeq Alternation Syntax
- NM_024312.5:c.1123C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2022-04-21
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV004528150
- ClinVar Disease
- GNPTAB-related disorder
- Observed Origin Sample
- unknown
Drugs