S33G (p.Ser33Gly) variant of MYPN (Myopalladin)
S33G (p.Ser33Gly) in MYPN (Myopalladin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.43 / 1. The record also includes population frequency data and structural context.
S33G (p.Ser33Gly) variant details
- p.Ser33Gly
- gnomAD rs923169496
- Missense
- Variant Prioritization Score for Impact Estimate 0.431
- REVEL 0.39
- CADD 26.10
- PolyPhen-2 0.73
- SIFT 0.02
- Most common in the South Asian population (allele frequency 0.00021)
- Structural context available