V28G (p.Val28Gly) variant of TNNC1 (P63316)
V28G (p.Val28Gly) in TNNC1 (P63316) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data, published literature, and structural context.
V28G (p.Val28Gly) variant details
- p.Val28Gly
- rs1428949969
- gnomAD 19-55156363-A-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.121
- CADD 5.68
- Population evidence available
- Structural context available
- Literature evidence available