G26S (p.Gly26Ser) variant of SRC (P12931)
G26S (p.Gly26Ser) in SRC (P12931) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes experimental measurements and structural context.
G26S (p.Gly26Ser) variant details
- p.Gly26Ser
- NCI-TCGA Cosmic COSV6244
- cosmic curated COSV62441
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available
- SRC SH3 domain domainome 1.0: score -0.0804