T37A (p.Thr37Ala) variant of CALCRL (Q16602)
T37A (p.Thr37Ala) in CALCRL (Q16602) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes population frequency data and structural context.
T37A (p.Thr37Ala) variant details
- p.Thr37Ala
- TOPMed rs1688053741
- gnomAD rs1688053741
- Missense
- Variant Prioritization Score for Impact Estimate 0.269
- REVEL 0.10
- CADD 19.40
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available