S13R (p.Ser13Arg) variant of HCN1 (O60741)
S13R (p.Ser13Arg) in HCN1 (O60741) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data and structural context.
S13R (p.Ser13Arg) variant details
- p.Ser13Arg
- TOPMed rs1194673599
- gnomAD rs1194673599
- Missense
- Variant Prioritization Score for Impact Estimate 0.34
- REVEL 0.32
- CADD 20.70
- PolyPhen-2 0.09
- SIFT 0.10
- Population evidence available
- Structural context available