L29F (p.Leu29Phe) variant of TNNC1 (P63316)
L29F (p.Leu29Phe) 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.
L29F (p.Leu29Phe) variant details
- p.Leu29Phe
- gnomAD 19-55156349-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.0933
- CADD 1.79
- Most common in the Non-Finnish European population (allele frequency 2.7e-06)
- Structural context available
- Literature evidence available