Annotation Detail
Information
- Associated Genes
- TGM1
- Associated Variants
-
TGM1 p.Arg143His (p.R143H)
(
ENST00000544573.5,
ENST00000206765.11 )
TGM1 p.Arg143His (p.R143H) ( ENST00000206765.11, ENST00000544573.5 ) - Source Database
- ClinVar
- Description
- NM_000359.3(TGM1):c.428G>A (p.Arg143His) AND Abnormality of the skin
- ClinVar Allele ID
- 27520
- ClinVar RefSeq Alternation Syntax
- NM_000359.3:c.428G>A
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2021-07-10
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001836706
- Observed Origin Sample
- germline
Drugs