D77Y (p.Asp77Tyr) variant of CHM (P24386)
D77Y (p.Asp77Tyr) in CHM (P24386) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
D77Y (p.Asp77Tyr) variant details
- p.Asp77Tyr
- NCI-TCGA Cosmic COSV6256
- cosmic curated COSV62566
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available