S9S (p.Ser9Ser) variant of MYPN (Myopalladin)
S9S (p.Ser9Ser) in MYPN (Myopalladin) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.14 / 1. The record also includes population frequency data, published literature, and structural context.
S9S (p.Ser9Ser) variant details
- p.Ser9Ser
- rs1212177605
- gnomAD 10-68121465-T-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.139
- CADD 8.27
- Most common in the Latino/Admixed American population (allele frequency 0.00046)
- Structural context available
- Literature evidence available