G29D (p.Gly29Asp) variant of BCR (P11274)
G29D (p.Gly29Asp) in BCR (P11274) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data and structural context.
G29D (p.Gly29Asp) variant details
- p.Gly29Asp
- cosmic curated COSV59934
- ESP rs367800501
- ExAC rs367800501
- TOPMed rs367800501
- Missense
- Variant Prioritization Score for Impact Estimate 0.4
- REVEL 0.18
- CADD 24.90
- PolyPhen-2 0.68
- SIFT 0.05
- Most common in the HGDP:YAKUT population (allele frequency 0.04)
- Structural context available