D118V (p.Asp118Val) variant of ATP1A3 (P13637)
D118V (p.Asp118Val) in ATP1A3 (P13637) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.63 / 1. The record also includes population frequency data and structural context.
D118V (p.Asp118Val) variant details
- p.Asp118Val
- TOPMed rs2075301704
- gnomAD rs2075301704
- Missense
- Variant Prioritization Score for Impact Estimate 0.631
- CADD 25.90
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available