G78D (p.Gly78Asp) variant of VSIR (Q9H7M9)
G78D (p.Gly78Asp) 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.
G78D (p.Gly78Asp) variant details
- p.Gly78Asp
- 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