N137T (p.Asn137Thr) variant of GNAQ (P50148)
N137T (p.Asn137Thr) in GNAQ (P50148) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
N137T (p.Asn137Thr) variant details
- p.Asn137Thr
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available