S30N (p.Ser30Asn) variant of NSD1 (Q96L73)
S30N (p.Ser30Asn) in NSD1 (Q96L73) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S30N (p.Ser30Asn) variant details
- p.Ser30Asn
- NCI-TCGA TCGA novel
- Ensembl rs2149755309
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available