E14D (p.Glu14Asp) variant of SLC22A2 (O15244)
E14D (p.Glu14Asp) 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.
E14D (p.Glu14Asp) variant details
- p.Glu14Asp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- SIFT 0.07
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available