T53N (p.Thr53Asn) variant of TNNC1 (P63316)
T53N (p.Thr53Asn) in TNNC1 (P63316) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Cardiovascular phenotype. The record also includes structural context.
T53N (p.Thr53Asn) variant details
- p.Thr53Asn
- rs2471444614
- ClinGen CA353168510
- ClinVar RCV002398394
- Uncertain significance
- Cardiovascular phenotype
- Missense
- ClinVar: Uncertain significance (Cardiovascular phenotype)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available