P47H (p.Pro47His) variant of IL12RB1 (P42701)
P47H (p.Pro47His) in IL12RB1 (P42701) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
P47H (p.Pro47His) variant details
- p.Pro47His
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact. (in dbSNP:rs17887176)