D48G (p.Asp48Gly) variant of SRSF2 (Q01130)
D48G (p.Asp48Gly) in SRSF2 (Q01130) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
D48G (p.Asp48Gly) variant details
- p.Asp48Gly
- NCI-TCGA Cosmic COSV1003
- cosmic curated COSV10033
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.