Annotation Detail
Information
- Associated Genes
- TGM1
- Associated Variants
-
TGM1 p.Gln582Ter (p.Q582*)
(
ENST00000206765.11,
ENST00000544573.5 )
TGM1 p.Gln582Ter (p.Q582*) ( ENST00000206765.11, ENST00000544573.5 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000359.3(TGM1):c.1744C>T (p.Gln582Ter) AND not provided
- ClinVar Allele ID
- 48122
- ClinVar RefSeq Alternation Syntax
- NM_000359.3:c.1744C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2024-01-19
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001235335
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs