S33R (p.Ser33Arg) variant of MYPN (Myopalladin)
S33R (p.Ser33Arg) 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.
S33R (p.Ser33Arg) variant details
- p.Ser33Arg
- gnomAD rs1311518691
- Missense
- Variant Prioritization Score for Impact Estimate 0.333
- REVEL 0.40
- CADD 22.90
- PolyPhen-2 0.95
- SIFT 0.03
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available