D9N (p.Asp9Asn) variant of ATP1A3 (P13637)
D9N (p.Asp9Asn) in ATP1A3 (P13637) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data and structural context.
D9N (p.Asp9Asn) variant details
- p.Asp9Asn
- TOPMed rs2075307477
- Missense
- Variant Prioritization Score for Impact Estimate 0.182
- CADD 15.80
- PolyPhen-2 0.00
- SIFT 0.36
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available