E36G (p.Glu36Gly) variant of MYPN (Myopalladin)
E36G (p.Glu36Gly) 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.
E36G (p.Glu36Gly) variant details
- p.Glu36Gly
- TOPMed rs2042241903
- Missense
- Variant Prioritization Score for Impact Estimate 0.332
- REVEL 0.21
- CADD 24.00
- PolyPhen-2 0.00
- SIFT 0.03
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available