G12W (p.Gly12Trp) variant of RARA (Retinoic acid receptor alpha)
G12W (p.Gly12Trp) in RARA (Retinoic acid receptor alpha) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G12W (p.Gly12Trp) variant details
- p.Gly12Trp
- NCI-TCGA Cosmic COSV9956
- cosmic curated COSV99564
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available