S129F (p.Ser129Phe) variant of SLC22A6 (Q4U2R8)
S129F (p.Ser129Phe) 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.
S129F (p.Ser129Phe) variant details
- p.Ser129Phe
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available