G15E (p.Gly15Glu) variant of CHM (P24386)
G15E (p.Gly15Glu) in CHM (P24386) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G15E (p.Gly15Glu) variant details
- p.Gly15Glu
- NCI-TCGA Cosmic COSV6256
- cosmic curated COSV62565
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available