E69K (p.Glu69Lys) variant of SRSF2 (Q01130)
E69K (p.Glu69Lys) in SRSF2 (Q01130) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
E69K (p.Glu69Lys) variant details
- p.Glu69Lys
- NCI-TCGA Cosmic COSV5797
- cosmic curated COSV57971
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.