H26Y (p.His26Tyr) variant of MYPN (Myopalladin)
H26Y (p.His26Tyr) 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.
H26Y (p.His26Tyr) variant details
- p.His26Tyr
- gnomAD rs1465652949
- Missense
- Variant Prioritization Score for Impact Estimate 0.428
- REVEL 0.17
- CADD 24.80
- PolyPhen-2 0.78
- SIFT 0.03
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available