Annotation Detail
Information
- Associated Genes
- TGM1
- Associated Variants
-
TGM1 p.Gly218Ser (p.G218S)
(
ENST00000544573.5,
ENST00000206765.11 )
TGM1 p.Gly218Ser (p.G218S) ( ENST00000206765.11, ENST00000544573.5 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000359.3(TGM1):c.652G>A (p.Gly218Ser) AND not provided
- ClinVar Allele ID
- 27539
- ClinVar RefSeq Alternation Syntax
- NM_000359.3:c.652G>A
- Clinical Significance Description
- Pathogenic/Likely pathogenic
- Clinical Significance Last Update
- 2024-01-13
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001219929
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs