L29P (p.Leu29Pro) variant of TNNC1 (P63316)
L29P (p.Leu29Pro) in TNNC1 (P63316) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data, published literature, and structural context.
L29P (p.Leu29Pro) variant details
- p.Leu29Pro
- rs2085729878
- gnomAD 19-55156348-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.101
- CADD 2.92
- Most common in the African/African-American population (allele frequency 3e-05)
- Structural context available
- Literature evidence available