P42S (p.Pro42Ser) variant of SLC12A1 (Q13621)
P42S (p.Pro42Ser) in SLC12A1 (Q13621) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
P42S (p.Pro42Ser) variant details
- p.Pro42Ser
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available