G39S (p.Gly39Ser) variant of TIGIT (Q495A1)
G39S (p.Gly39Ser) in TIGIT (Q495A1) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G39S (p.Gly39Ser) variant details
- p.Gly39Ser
- NCI-TCGA Cosmic COSV6732
- cosmic curated COSV67329
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available