T40T (p.Thr40Thr) variant of CALCB (P10092)
T40T (p.Thr40Thr) in CALCB (P10092) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data, published literature, and structural context.
T40T (p.Thr40Thr) variant details
- p.Thr40Thr
- rs1438673634
- gnomAD 11-15075094-A-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.0976
- CADD 2.39
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available
- Literature evidence available