F116L (p.Phe116Leu) variant of SLC22A6 (Q4U2R8)
F116L (p.Phe116Leu) 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.
F116L (p.Phe116Leu) variant details
- p.Phe116Leu
- NCI-TCGA Cosmic COSV1008
- cosmic curated COSV10084
- NCI-TCGA Cosmic COSV6456
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available