P37P (p.Pro37Pro) variant of MYPN (Myopalladin)
P37P (p.Pro37Pro) in MYPN (Myopalladin) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data, published literature, and structural context.
P37P (p.Pro37Pro) variant details
- p.Pro37Pro
- rs776759477
- gnomAD 10-68121549-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.124
- CADD 6.09
- Most common in the South Asian population (allele frequency 7e-05)
- Structural context available
- Literature evidence available