G19V (p.Gly19Val) variant of SLC2A10 (O95528)
G19V (p.Gly19Val) in SLC2A10 (O95528) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G19V (p.Gly19Val) variant details
- p.Gly19Val
- NCI-TCGA Cosmic COSV6371
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available