V13G (p.Val13Gly) variant of SLC22A6 (Q4U2R8)
V13G (p.Val13Gly) in SLC22A6 (Q4U2R8) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
V13G (p.Val13Gly) variant details
- p.Val13Gly
- NCI-TCGA Cosmic COSV6456
- cosmic curated COSV64560
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available