G29C (p.Gly29Cys) variant of BCR (P11274)
G29C (p.Gly29Cys) in BCR (P11274) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data and structural context.
G29C (p.Gly29Cys) variant details
- p.Gly29Cys
- gnomAD rs1441899010
- Missense
- Variant Prioritization Score for Impact Estimate 0.331
- REVEL 0.21
- CADD 25.00
- PolyPhen-2 0.92
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available