S13N (p.Ser13Asn) variant of CALCB (P10092)
S13N (p.Ser13Asn) in CALCB (P10092) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S13N (p.Ser13Asn) variant details
- p.Ser13Asn
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available