E107R (p.Glu107Arg) variant of CNGA1 (P29973)
E107R (p.Glu107Arg) in CNGA1 (P29973) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
E107R (p.Glu107Arg) variant details
- p.Glu107Arg
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available