S97L (p.Ser97Leu) variant of LRP2 (P98164)
S97L (p.Ser97Leu) in LRP2 (P98164) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S97L (p.Ser97Leu) variant details
- p.Ser97Leu
- NCI-TCGA Cosmic COSV9978
- cosmic curated COSV99787
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available