G67A (p.Gly67Ala) variant of HCN1 (O60741)
G67A (p.Gly67Ala) in HCN1 (O60741) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data and structural context.
G67A (p.Gly67Ala) variant details
- p.Gly67Ala
- TOPMed rs941855168
- Missense
- Variant Prioritization Score for Impact Estimate 0.239
- REVEL 0.27
- CADD 15.60
- Most common in the Non-Finnish European population (allele frequency 1.6e-05)
- Structural context available