Q14R (p.Gln14Arg) variant of BCR (P11274)
Q14R (p.Gln14Arg) in BCR (P11274) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.42 / 1. The record also includes population frequency data and structural context.
Q14R (p.Gln14Arg) variant details
- p.Gln14Arg
- 1000Genomes rs2146187452
- Missense
- Variant Prioritization Score for Impact Estimate 0.422
- REVEL 0.30
- CADD 25.50
- PolyPhen-2 0.97
- SIFT 0.00
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00019)
- Structural context available