K49N (p.Lys49Asn) variant of SPTBN2 (O15020)
K49N (p.Lys49Asn) in SPTBN2 (O15020) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
K49N (p.Lys49Asn) variant details
- p.Lys49Asn
- NCI-TCGA Cosmic COSV5944
- cosmic curated COSV59449
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.