R47L (p.Arg47Leu) variant of SRSF2 (Q01130)
R47L (p.Arg47Leu) in SRSF2 (Q01130) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
R47L (p.Arg47Leu) variant details
- p.Arg47Leu
- NCI-TCGA Cosmic COSV1003
- cosmic curated COSV10033
- NCI-TCGA Cosmic COSV5797
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.