A18T (p.Ala18Thr) variant of KCNJ11 (Q14654)
A18T (p.Ala18Thr) in KCNJ11 (Q14654) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
A18T (p.Ala18Thr) variant details
- p.Ala18Thr
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact. (in dbSNP:rs41309072)
- Structural context available