D41G (p.Asp41Gly) variant of SLC12A1 (Q13621)
D41G (p.Asp41Gly) 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.
D41G (p.Asp41Gly) variant details
- p.Asp41Gly
- NCI-TCGA Cosmic COSV5770
- cosmic curated COSV57709
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available