D62N (p.Asp62Asn) variant of HCN1 (O60741)
D62N (p.Asp62Asn) in HCN1 (O60741) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.42 / 1. The record also includes population frequency data and structural context.
D62N (p.Asp62Asn) variant details
- p.Asp62Asn
- gnomAD rs1275868182
- Missense
- Variant Prioritization Score for Impact Estimate 0.417
- REVEL 0.30
- CADD 21.90
- PolyPhen-2 0.01
- SIFT 0.08
- Most common in the South Asian population (allele frequency 2.6e-05)
- Structural context available