P41P (p.Pro41Pro) variant of MYPN (Myopalladin)
P41P (p.Pro41Pro) in MYPN (Myopalladin) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.46 / 1. The record also includes population frequency data, published literature, and structural context.
P41P (p.Pro41Pro) variant details
- p.Pro41Pro
- rs2042242365
- gnomAD 10-68121561-T-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.455
- CADD 12.10
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available