S9P (p.Ser9Pro) variant of MYPN (Myopalladin)
S9P (p.Ser9Pro) in MYPN (Myopalladin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data and structural context.
S9P (p.Ser9Pro) variant details
- p.Ser9Pro
- gnomAD rs2042239798
- Missense
- Variant Prioritization Score for Impact Estimate 0.334
- REVEL 0.14
- CADD 22.40
- SIFT 0.69
- Most common in the South Asian population (allele frequency 0.00021)
- Structural context available