G78R (p.Gly78Arg) variant of ADH1B (P00325)
G78R (p.Gly78Arg) in ADH1B (P00325) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G78R (p.Gly78Arg) variant details
- p.Gly78Arg
- NCI-TCGA Cosmic COSV5929
- cosmic curated COSV59299
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available