F53V (p.Phe53Val) variant of MYL2 (P10916)
F53V (p.Phe53Val) in MYL2 (P10916) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.19 / 1. The record also includes population frequency data and structural context.
F53V (p.Phe53Val) variant details
- p.Phe53Val
- NCI-TCGA Cosmic COSV9996
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.188
- CADD 5.28
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the South Asian population (allele frequency 7.3e-05)
- Structural context available