G30A (p.Gly30Ala) variant of TNNC1 (P63316)
G30A (p.Gly30Ala) in TNNC1 (P63316) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data, published literature, and structural context.
G30A (p.Gly30Ala) variant details
- p.Gly30Ala
- gnomAD 19-55156360-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.0879
- CADD 1.02
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available