A35G (p.Ala35Gly) variant of MYPN (Myopalladin)
A35G (p.Ala35Gly) in MYPN (Myopalladin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.44 / 1. The record also includes population frequency data, published literature, and structural context.
A35G (p.Ala35Gly) variant details
- p.Ala35Gly
- gnomAD 10-68121542-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.44
- REVEL 0.22
- CADD 23.40
- PolyPhen-2 0.31
- SIFT 0.05
- Most common in the East Asian population (allele frequency 7.6e-05)
- Structural context available
- Literature evidence available