S39N (p.Ser39Asn) variant of SLC12A3 (P55017)
S39N (p.Ser39Asn) in SLC12A3 (P55017) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S39N (p.Ser39Asn) variant details
- p.Ser39Asn
- NCI-TCGA Cosmic COSV9934
- cosmic curated COSV99344
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available