E26Q (p.Glu26Gln) variant of CALCRL (Q16602)
E26Q (p.Glu26Gln) in CALCRL (Q16602) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.19 / 1. The record also includes population frequency data and structural context.
E26Q (p.Glu26Gln) variant details
- p.Glu26Gln
- gnomAD rs1326868810
- Missense
- Variant Prioritization Score for Impact Estimate 0.188
- REVEL 0.05
- CADD 16.10
- PolyPhen-2 0.01
- SIFT 0.42
- Most common in the Finnish in Finland (FIN) population (allele frequency 3.8e-05)
- Structural context available