R32G (p.Arg32Gly) variant of MYPN (Myopalladin)
R32G (p.Arg32Gly) in MYPN (Myopalladin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data and structural context.
R32G (p.Arg32Gly) variant details
- p.Arg32Gly
- gnomAD rs1220705857
- Missense
- Variant Prioritization Score for Impact Estimate 0.298
- REVEL 0.27
- CADD 23.30
- PolyPhen-2 0.47
- SIFT 0.07
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available