A49G (p.Ala49Gly) variant of ITGA6 (Integrin alpha-6)
A49G (p.Ala49Gly) in ITGA6 (Integrin alpha-6) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
A49G (p.Ala49Gly) variant details
- p.Ala49Gly
- NCI-TCGA Cosmic COSV9990
- cosmic curated COSV99906
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available