S19T (p.Ser19Thr) variant of MYPN (Myopalladin)
S19T (p.Ser19Thr) 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.
S19T (p.Ser19Thr) variant details
- p.Ser19Thr
- gnomAD 10-68106773-T-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.313
- MetaLR 0.11
- MetaSVM -1.02
- CADD 18.20
- SIFT 0.47
- Most common in the Non-Finnish European population (allele frequency 3.2e-06)
- Structural context available
- Literature evidence available