A71G (p.Ala71Gly) variant of SRSF2 (Q01130)
A71G (p.Ala71Gly) in SRSF2 (Q01130) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
A71G (p.Ala71Gly) variant details
- p.Ala71Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.