N118S (p.Asn118Ser) variant of SPTBN2 (O15020)
N118S (p.Asn118Ser) in SPTBN2 (O15020) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
N118S (p.Asn118Ser) variant details
- p.Asn118Ser
- NCI-TCGA Cosmic COSV5945
- cosmic curated COSV59458
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.