Annotation Detail
Information
- Associated Genes
- TGM1
- Associated Variants
-
TGM1 p.Val379Leu (p.V379L)
(
ENST00000544573.5,
ENST00000206765.11 )
TGM1 p.Val379Leu (p.V379L) ( ENST00000206765.11, ENST00000544573.5 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000359.3(TGM1):c.1135G>C (p.Val379Leu) AND not provided
- ClinVar Allele ID
- 27525
- ClinVar RefSeq Alternation Syntax
- NM_000359.3:c.1135G>C
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2023-12-30
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000413167
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs