S9N (p.Ser9Asn) variant of MYPN (Myopalladin)
S9N (p.Ser9Asn) in MYPN (Myopalladin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data, published literature, and structural context.
S9N (p.Ser9Asn) variant details
- p.Ser9Asn
- gnomAD 10-68109678-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.305
- CADD 16.00
- SIFT 1.00
- Most common in the Non-Finnish European population (allele frequency 6.3e-06)
- Structural context available
- Literature evidence available