D41Y (p.Asp41Tyr) variant of SCN9A (Q15858)
D41Y (p.Asp41Tyr) in SCN9A (Q15858) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
D41Y (p.Asp41Tyr) variant details
- p.Asp41Tyr
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available