G111R (p.Gly111Arg) variant of C9ORF72 (Q96LT7)
G111R (p.Gly111Arg) in C9ORF72 (Q96LT7) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G111R (p.Gly111Arg) variant details
- p.Gly111Arg
- NCI-TCGA Cosmic COSV6615
- cosmic curated COSV66154
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available