T38N (p.Thr38Asn) variant of GABRG2 (P18507)
T38N (p.Thr38Asn) in GABRG2 (P18507) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
T38N (p.Thr38Asn) variant details
- p.Thr38Asn
- NCI-TCGA Cosmic COSV1007
- cosmic curated COSV10072
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available