D77H (p.Asp77His) variant of IFT172 (Q9UG01)
D77H (p.Asp77His) in IFT172 (Q9UG01) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
D77H (p.Asp77His) variant details
- p.Asp77His
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available