A346G (p.Ala346Gly) variant of SMC1A (Q14683)
A346G (p.Ala346Gly) 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.
A346G (p.Ala346Gly) variant details
- p.Ala346Gly
- NCI-TCGA Cosmic COSV1004
- cosmic curated COSV10044
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available