W18R (p.Trp18Arg) variant of ABCC1 (P33527)
W18R (p.Trp18Arg) in ABCC1 (P33527) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
W18R (p.Trp18Arg) variant details
- p.Trp18Arg
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available