D79G (p.Asp79Gly) variant of SLC6A3 (Q01959)
D79G (p.Asp79Gly) in SLC6A3 (Q01959) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
D79G (p.Asp79Gly) variant details
- p.Asp79Gly
- NCI-TCGA TCGA novel
- Ensembl rs1755441811
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available