N60D (p.Asn60Asp) variant of MYL2 (P10916)
N60D (p.Asn60Asp) in MYL2 (P10916) 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.
N60D (p.Asn60Asp) variant details
- p.Asn60Asp
- gnomAD rs2071674753
- Missense
- Variant Prioritization Score for Impact Estimate 0.676
- REVEL 0.71
- CADD 24.60
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available