G362A (p.Gly362Ala) variant of SMC1A (Q14683)
G362A (p.Gly362Ala) in SMC1A (Q14683) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G362A (p.Gly362Ala) variant details
- p.Gly362Ala
- NCI-TCGA Cosmic COSV5912
- cosmic curated COSV59127
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available