S18F (p.Ser18Phe) variant of GNA11 (P29992)
S18F (p.Ser18Phe) in GNA11 (P29992) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S18F (p.Ser18Phe) variant details
- p.Ser18Phe
- NCI-TCGA Cosmic COSV5001
- NCI-TCGA Cosmic COSV9931
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available