K66N (p.Lys66Asn) variant of C3 (Complement C3)
K66N (p.Lys66Asn) in C3 (Complement C3) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
K66N (p.Lys66Asn) variant details
- p.Lys66Asn
- NCI-TCGA TCGA novel
- TOPMed rs1968116239
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available