G53T (p.Gly53Thr) variant of SLC6A19 (Q695T7)
G53T (p.Gly53Thr) in SLC6A19 (Q695T7) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G53T (p.Gly53Thr) variant details
- p.Gly53Thr
- NCI-TCGA Cosmic COSV1004
- NCI-TCGA Cosmic COSV5866
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available