Annotation Detail
Information
- Associated Genes
- TGM1
- Associated Variants
-
TGM1 p.Asp490Gly (p.D490G)
(
ENST00000544573.5,
ENST00000206765.11 )
TGM1 p.Asp490Gly (p.D490G) ( ENST00000206765.11, ENST00000544573.5 ) - Associated Disease
- autosomal recessive congenital ichthyosis 1
- Source Database
- ClinVar
- Description
- NM_000359.3(TGM1):c.1469A>G (p.Asp490Gly) AND Autosomal recessive congenital ichthyosis 1
- ClinVar Allele ID
- 27530
- ClinVar RefSeq Alternation Syntax
- NM_000359.3:c.1469A>G
- Clinical Significance Description
- Conflicting interpretations of pathogenicity
- Clinical Significance Last Update
- 2023-06-12
- Clinical Significance Review Status
- criteria provided, conflicting interpretations
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000013313
- ClinVar Disease
- Autosomal recessive congenital ichthyosis 1
- Observed Origin Sample
- germline
- Observed Origin Sample
- unknown
- Pubmed
- 12542526
Drugs