A34T (p.Ala34Thr) variant of HCN1 (O60741)
A34T (p.Ala34Thr) in HCN1 (O60741) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data and structural context.
A34T (p.Ala34Thr) variant details
- p.Ala34Thr
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.316
- REVEL 0.16
- AlphaMissense 0.10
- MetaLR 0.63
- MetaSVM -0.22
- CADD 14.30
- PolyPhen-2 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available