R32M (p.Arg32Met) variant of MYPN (Myopalladin)
R32M (p.Arg32Met) in MYPN (Myopalladin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.47 / 1. The record also includes population frequency data, published literature, and structural context.
R32M (p.Arg32Met) variant details
- p.Arg32Met
- gnomAD 10-68121533-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.472
- REVEL 0.28
- CADD 22.70
- PolyPhen-2 0.29
- SIFT 0.60
- Most common in the Ashkenazi Jewish population (allele frequency 3.8e-05)
- Structural context available
- Literature evidence available