A27P (p.Ala27Pro) variant of ARID1B (Q8NFD5)
A27P (p.Ala27Pro) in ARID1B (Q8NFD5) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
A27P (p.Ala27Pro) variant details
- p.Ala27Pro
- NCI-TCGA TCGA novel
- Ensembl rs2114958637
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available