H26L (p.His26Leu) variant of MYPN (Myopalladin)
H26L (p.His26Leu) in MYPN (Myopalladin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.41 / 1. The record also includes population frequency data, published literature, and structural context.
H26L (p.His26Leu) variant details
- p.His26Leu
- gnomAD 10-68109699-A-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.406
- CADD 18.50
- SIFT 0.05
- Most common in the Non-Finnish European population (allele frequency 6.3e-06)
- Structural context available
- Literature evidence available