Y91F (p.Tyr91Phe) variant of HCN1 (O60741)
Y91F (p.Tyr91Phe) 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.
Y91F (p.Tyr91Phe) variant details
- p.Tyr91Phe
- NCI-TCGA TCGA novel
- Ensembl rs1739997647
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available