M1? variant of SRC (P12931)
M1? in SRC (P12931) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes experimental measurements and structural context.
M1? variant details
- NCI-TCGA Cosmic COSV1006
- cosmic curated COSV10065
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available
- SRC SH3 domain domainome 1.0: score 0.0124