V186G (p.Val186Gly) variant of TH (Tyrosine 3-monooxygenase)
V186G (p.Val186Gly) in TH (Tyrosine 3-monooxygenase) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
V186G (p.Val186Gly) variant details
- p.Val186Gly
- NCI-TCGA Cosmic COSV1001
- cosmic curated COSV10014
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available