S34G (p.Ser34Gly) variant of CALCB (P10092)
S34G (p.Ser34Gly) 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.
S34G (p.Ser34Gly) variant details
- p.Ser34Gly
- NCI-TCGA Cosmic COSV6083
- cosmic curated COSV60834
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available