P37T (p.Pro37Thr) variant of MYPN (Myopalladin)
P37T (p.Pro37Thr) in MYPN (Myopalladin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data, published literature, and structural context.
P37T (p.Pro37Thr) variant details
- p.Pro37Thr
- gnomAD 10-68109695-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.339
- CADD 16.70
- SIFT 0.05
- Population evidence available
- Structural context available
- Literature evidence available