P37R (p.Pro37Arg) variant of MYPN (Myopalladin)
P37R (p.Pro37Arg) in MYPN (Myopalladin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data, published literature, and structural context.
P37R (p.Pro37Arg) variant details
- p.Pro37Arg
- gnomAD 10-68121548-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.404
- REVEL 0.14
- CADD 24.40
- PolyPhen-2 0.47
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available