P89H (p.Pro89His) variant of SLC22A6 (Q4U2R8)
P89H (p.Pro89His) 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.
P89H (p.Pro89His) variant details
- p.Pro89His
- NCI-TCGA Cosmic COSV6456
- cosmic curated COSV64560
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available