S99N (p.Ser99Asn) variant of SLC22A2 (O15244)
S99N (p.Ser99Asn) in SLC22A2 (O15244) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S99N (p.Ser99Asn) variant details
- p.Ser99Asn
- NCI-TCGA Cosmic COSV6526
- cosmic curated COSV65266
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available