S19N (p.Ser19Asn) variant of GABRA1 (P14867)
S19N (p.Ser19Asn) in GABRA1 (P14867) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S19N (p.Ser19Asn) variant details
- p.Ser19Asn
- NCI-TCGA Cosmic COSV9919
- cosmic curated COSV99196
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available