L49F (p.Leu49Phe) variant of ABCC2 (Q92887)
L49F (p.Leu49Phe) in ABCC2 (Q92887) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
L49F (p.Leu49Phe) variant details
- p.Leu49Phe
- NCI-TCGA Cosmic COSV6497
- cosmic curated COSV64970
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available