M1? variant of SCN10A (Q9Y5Y9)
M1? in SCN10A (Q9Y5Y9) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
M1? variant details
- NCI-TCGA Cosmic COSV1014
- cosmic curated COSV10147
- NCI-TCGA Cosmic COSV7186
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available