Annotation Detail
Information
- Associated Genes
- TFR2
- Associated Variants
-
TFR2 p.Arg455Gln (p.R455Q)
(
ENST00000223051.8,
ENST00000431692.5,
ENST00000462107.1 )
TFR2 p.Arg455Gln (p.R455Q) ( ENST00000223051.8, ENST00000431692.5, ENST00000462107.1 ) - Associated Disease
- TFR2-related disorder
- Source Database
- ClinVar
- Description
- NM_003227.4(TFR2):c.1364G>A (p.Arg455Gln) AND TFR2-related disorder
- ClinVar Allele ID
- 20422
- ClinVar RefSeq Alternation Syntax
- NM_003227.4:c.1364G>A
- ClinVar RefSeq Alternation Syntax
- NM_001206855.3:c.851G>A
- Clinical Significance Description
- Likely benign
- Clinical Significance Last Update
- 2020-10-09
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003914812
- ClinVar Disease
- TFR2-related disorder
- Observed Origin Sample
- germline
Drugs