P36T (p.Pro36Thr) variant of CALCB (P10092)
P36T (p.Pro36Thr) in CALCB (P10092) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data and structural context.
P36T (p.Pro36Thr) variant details
- p.Pro36Thr
- cosmic curated COSV60834
- TOPMed rs1267624517
- gnomAD rs1267624517
- Missense
- Variant Prioritization Score for Impact Estimate 0.251
- REVEL 0.08
- CADD 3.18
- PolyPhen-2 0.01
- SIFT 0.82
- Most common in the Non-Finnish European population (allele frequency 2.9e-05)
- Structural context available