G77D (p.Gly77Asp) variant of SLC22A2 (O15244)
G77D (p.Gly77Asp) in SLC22A2 (O15244) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes variant effect predictions and structural context.
G77D (p.Gly77Asp) variant details
- p.Gly77Asp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.44
- MetaSVM -0.24
- SIFT 0.56
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available