A59S (p.Ala59Ser) variant of SCN10A (Q9Y5Y9)
A59S (p.Ala59Ser) in SCN10A (Q9Y5Y9) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes variant effect predictions and structural context.
A59S (p.Ala59Ser) variant details
- p.Ala59Ser
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.95
- MetaSVM 1.09
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available