W49C (p.Trp49Cys) variant of ABCC9 (O60706)
W49C (p.Trp49Cys) in ABCC9 (O60706) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
W49C (p.Trp49Cys) variant details
- p.Trp49Cys
- cosmic curated COSV10879
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available