A99P (p.Ala99Pro) variant of MYH11 (Myosin-11)
A99P (p.Ala99Pro) in MYH11 (Myosin-11) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.68 / 1. The record also includes population frequency data and structural context.
A99P (p.Ala99Pro) variant details
- p.Ala99Pro
- gnomAD rs1245092974
- Missense
- Variant Prioritization Score for Impact Estimate 0.684
- REVEL 0.64
- CADD 24.30
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available