P36Q (p.Pro36Gln) variant of CALCB (P10092)
P36Q (p.Pro36Gln) in CALCB (P10092) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data and structural context.
P36Q (p.Pro36Gln) variant details
- p.Pro36Gln
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.237
- REVEL 0.11
- CADD 19.10
- PolyPhen-2 0.52
- SIFT 0.35
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available