E886Q (p.Glu886Gln) variant of CACNA2D2 (Q9NY47)
E886Q (p.Glu886Gln) in CACNA2D2 (Q9NY47) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
E886Q (p.Glu886Gln) variant details
- p.Glu886Gln
- NCI-TCGA Cosmic COSV5657
- cosmic curated COSV56570
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available