P47Q (p.Pro47Gln) variant of SCN9A (Nav1.7)
P47Q (p.Pro47Gln) in SCN9A (Nav1.7) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
P47Q (p.Pro47Gln) variant details
- p.Pro47Gln
- rs1281216048
- NCI-TCGA Cosmic COSV1003
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available