F18S (p.Phe18Ser) variant of SLC22A2 (O15244)
F18S (p.Phe18Ser) in SLC22A2 (O15244) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes variant effect predictions and structural context.
F18S (p.Phe18Ser) variant details
- p.Phe18Ser
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- SIFT 0.24
- UniProt: Variant assessed as somatic; high impact.
- Structural context available