G20W (p.Gly20Trp) variant of HCN4 (Q9Y3Q4)
G20W (p.Gly20Trp) in HCN4 (Q9Y3Q4) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.75 / 1. The record also includes population frequency data and structural context.
G20W (p.Gly20Trp) variant details
- p.Gly20Trp
- gnomAD rs868149827
- Missense
- Variant Prioritization Score for Impact Estimate 0.754
- REVEL 0.69
- MetaLR 0.97
- MetaSVM 1.10
- CADD 27.10
- PolyPhen-2 0.99
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 1.8e-05)
- Structural context available