P37Q (p.Pro37Gln) variant of MYPN (Myopalladin)
P37Q (p.Pro37Gln) in MYPN (Myopalladin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.51 / 1. The record also includes population frequency data, published literature, and structural context.
P37Q (p.Pro37Gln) variant details
- p.Pro37Gln
- gnomAD 10-68106768-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.511
- MetaLR 0.08
- MetaSVM -1.08
- CADD 14.10
- SIFT 0.02
- Population evidence available
- Structural context available
- Literature evidence available