D42Y (p.Asp42Tyr) variant of SCN9A (Q15858)
D42Y (p.Asp42Tyr) 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.
D42Y (p.Asp42Tyr) variant details
- p.Asp42Tyr
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available