D29G (p.Asp29Gly) variant of LRP2 (P98164)
D29G (p.Asp29Gly) 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.
D29G (p.Asp29Gly) variant details
- p.Asp29Gly
- NCI-TCGA Cosmic COSV9979
- cosmic curated COSV99790
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available