D9N (p.Asp9Asn) variant of MYH11 (Myosin-11)
D9N (p.Asp9Asn) in MYH11 (Myosin-11) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.59 / 1. The record also includes population frequency data and structural context.
D9N (p.Asp9Asn) variant details
- p.Asp9Asn
- gnomAD rs1301566011
- Missense
- Variant Prioritization Score for Impact Estimate 0.586
- REVEL 0.47
- CADD 23.70
- PolyPhen-2 0.33
- SIFT 0.03
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)
- Structural context available