P33S (p.Pro33Ser) variant of SRC (P12931)
P33S (p.Pro33Ser) 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.
P33S (p.Pro33Ser) variant details
- p.Pro33Ser
- NCI-TCGA Cosmic COSV1006
- cosmic curated COSV10065
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available
- SRC SH3 domain domainome 1.0: score 0.115