S19P (p.Ser19Pro) variant of STK11 (Q15831)
S19P (p.Ser19Pro) in STK11 (Q15831) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S19P (p.Ser19Pro) variant details
- p.Ser19Pro
- NCI-TCGA TCGA novel
- Ensembl rs2145404634
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available