G86V (p.Gly86Val) variant of HCN1 (O60741)
G86V (p.Gly86Val) in HCN1 (O60741) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G86V (p.Gly86Val) variant details
- p.Gly86Val
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available