G28A (p.Gly28Ala) variant of MYPN (Myopalladin)
G28A (p.Gly28Ala) in MYPN (Myopalladin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.42 / 1. The record also includes population frequency data, published literature, and structural context.
G28A (p.Gly28Ala) variant details
- p.Gly28Ala
- gnomAD 10-68121521-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.423
- REVEL 0.24
- CADD 25.20
- PolyPhen-2 0.70
- SIFT 0.17
- Most common in the Non-Finnish European population (allele frequency 9e-06)
- Structural context available
- Literature evidence available