D67N (p.Asp67Asn) variant of SRSF2 (Q01130)
D67N (p.Asp67Asn) in SRSF2 (Q01130) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
D67N (p.Asp67Asn) variant details
- p.Asp67Asn
- NCI-TCGA Cosmic COSV5797
- cosmic curated COSV57972
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.