Annotation Detail
Information
- Associated Genes
- TNNC1
- Associated Variants
-
TNNC1 p.Asp145= (p.D145=)
(
ENST00000232975.8 )
TNNC1 p.Asp145= (p.D145=) ( ENST00000232975.8 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_003280.3(TNNC1):c.435C>T (p.Asp145=) AND not provided
- ClinVar Allele ID
- 229105
- ClinVar RefSeq Alternation Syntax
- NM_003280.3:c.435C>T
- Clinical Significance Description
- Likely benign
- Clinical Significance Last Update
- 2023-01-01
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001711996
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs