M1V (p.Met1Val) variant of MYPN (Myopalladin)
M1V (p.Met1Val) in MYPN (Myopalladin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data, published literature, and structural context.
M1V (p.Met1Val) variant details
- p.Met1Val
- gnomAD 10-68106800-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.306
- MetaLR 0.05
- MetaSVM -1.02
- CADD 15.20
- SIFT 0.54
- Most common in the Non-Finnish European population (allele frequency 3.2e-06)
- Structural context available
- Literature evidence available