A36G (p.Ala36Gly) variant of SLC12A1 (Q13621)
A36G (p.Ala36Gly) in SLC12A1 (Q13621) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
A36G (p.Ala36Gly) variant details
- p.Ala36Gly
- NCI-TCGA Cosmic COSV1003
- cosmic curated COSV10037
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available