P52T (p.Pro52Thr) variant of TNNC1 (P63316)
P52T (p.Pro52Thr) in TNNC1 (P63316) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.66 / 1. The record also includes population frequency data, published literature, and structural context.
P52T (p.Pro52Thr) variant details
- p.Pro52Thr
- rs1345623490
- gnomAD 19-55156343-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.664
- CADD 10.50
- Most common in the Latino/Admixed American population (allele frequency 2.3e-05)
- Structural context available
- Literature evidence available