G7D (p.Gly7Asp) variant of ABCC9 (O60706)
G7D (p.Gly7Asp) in ABCC9 (O60706) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.86 / 1. The record also includes population frequency data and structural context.
G7D (p.Gly7Asp) variant details
- p.Gly7Asp
- gnomAD rs1475114116
- Missense
- Variant Prioritization Score for Impact Estimate 0.857
- REVEL 0.92
- CADD 25.90
- Most common in the HGDP:BANTUSOUTHAFRICA population (allele frequency 0.062)
- Structural context available