Annotation Detail
Information
- Associated Genes
- TGFB1
- Associated Variants
-
TGFB1 p.Arg25Pro (p.R25P)
(
ENST00000221930.6,
ENST00000600196.2,
ENST00000677934.1,
ENST00000539627.5 )
TGFB1 p.Arg25Pro (p.R25P) ( ENST00000221930.6, ENST00000600196.2, ENST00000677934.1, ENST00000539627.5 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000660.7(TGFB1):c.74G>C (p.Arg25Pro) AND not provided
- ClinVar Allele ID
- 47505
- ClinVar RefSeq Alternation Syntax
- NM_000660.7:c.74G>C
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2024-01-31
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001514681
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs