A77G (p.Ala77Gly) variant of ABCA1 (O95477)
A77G (p.Ala77Gly) in ABCA1 (O95477) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
A77G (p.Ala77Gly) variant details
- p.Ala77Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available