H26R (p.His26Arg) variant of MYPN (Myopalladin)
H26R (p.His26Arg) 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.
H26R (p.His26Arg) variant details
- p.His26Arg
- rs1376779535
- gnomAD 10-68109693-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.313
- CADD 19.30
- SIFT 0.31
- Most common in the East Asian population (allele frequency 0.00022)
- Structural context available
- Literature evidence available