P7L (p.Pro7Leu) variant of SRSF2 (Q01130)
P7L (p.Pro7Leu) in SRSF2 (Q01130) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact.
P7L (p.Pro7Leu) variant details
- p.Pro7Leu
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.