D111G (p.Asp111Gly) variant of SLC22A2 (O15244)
D111G (p.Asp111Gly) in SLC22A2 (O15244) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
D111G (p.Asp111Gly) variant details
- p.Asp111Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available