R49E (p.Arg49Glu) variant of KRIT1 (O00522)
R49E (p.Arg49Glu) in KRIT1 (O00522) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
R49E (p.Arg49Glu) variant details
- p.Arg49Glu
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available