Q33H (p.Gln33His) variant of CALCRL (Q16602)
Q33H (p.Gln33His) in CALCRL (Q16602) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data and structural context.
Q33H (p.Gln33His) variant details
- p.Gln33His
- cosmic curated COSV66473
- TOPMed rs1053976961
- gnomAD rs1053976961
- Missense
- Variant Prioritization Score for Impact Estimate 0.0757
- REVEL 0.05
- CADD 0.06
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available