G78V (p.Gly78Val) variant of VSIR (Q9H7M9)
G78V (p.Gly78Val) in VSIR (Q9H7M9) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G78V (p.Gly78Val) variant details
- p.Gly78Val
- NCI-TCGA Cosmic COSV5648
- NCI-TCGA Cosmic COSV9982
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available