W52C (p.Trp52Cys) variant of ITGA6 (Integrin alpha-6)
W52C (p.Trp52Cys) in ITGA6 (Integrin alpha-6) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
W52C (p.Trp52Cys) variant details
- p.Trp52Cys
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available