L29V (p.Leu29Val) variant of TNNC1 (P63316)
L29V (p.Leu29Val) 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.
L29V (p.Leu29Val) variant details
- p.Leu29Val
- rs1013144337
- gnomAD 19-55156349-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.089
- CADD 1.50
- Most common in the African/African-American population (allele frequency 4.8e-05)
- Structural context available
- Literature evidence available