P47S (p.Pro47Ser) variant of MYPN (Myopalladin)
P47S (p.Pro47Ser) in MYPN (Myopalladin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes population frequency data and structural context.
P47S (p.Pro47Ser) variant details
- p.Pro47Ser
- TOPMed rs1043762674
- gnomAD rs1043762674
- Missense
- Variant Prioritization Score for Impact Estimate 0.272
- REVEL 0.15
- CADD 9.68
- SIFT 0.79
- Most common in the Latino/Admixed American population (allele frequency 6.5e-05)
- Structural context available