M1? variant of SRSF2 (Q01130)
M1? in SRSF2 (Q01130) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact.
M1? variant details
- NCI-TCGA Cosmic COSV1003
- cosmic curated COSV10033
- NCI-TCGA Cosmic COSV5797
- cosmic curated COSV57975
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.