R16G (p.Arg16Gly) variant of SF3B1 (Splicing factor 3B subunit 1)
R16G (p.Arg16Gly) in SF3B1 (Splicing factor 3B subunit 1) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
R16G (p.Arg16Gly) variant details
- p.Arg16Gly
- NCI-TCGA Cosmic COSV5921
- cosmic curated COSV59217
- NCI-TCGA Cosmic COSV5922
- Ensembl rs2106015585
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available