G5D (p.Gly5Asp) variant of HCN1 (O60741)
G5D (p.Gly5Asp) in HCN1 (O60741) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.45 / 1. The record also includes population frequency data and structural context.
G5D (p.Gly5Asp) variant details
- p.Gly5Asp
- Ensembl rs1740007331
- Missense
- Variant Prioritization Score for Impact Estimate 0.445
- REVEL 0.33
- CADD 20.20
- PolyPhen-2 0.01
- SIFT 0.14
- Most common in the Non-Finnish European population (allele frequency 1e-06)
- Structural context available