G4R (p.Gly4Arg) variant of MYD88 (Q99836)
G4R (p.Gly4Arg) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.49 / 1. The record also includes population frequency data and structural context.
G4R (p.Gly4Arg) variant details
- p.Gly4Arg
- cosmic curated COSV10589
- Ensembl rs752325925
- Missense
- Variant Prioritization Score for Impact Estimate 0.489
- CADD 16.80
- PolyPhen-2 0.09
- SIFT 0.04
- Most common in the HGDP:MBUTI population (allele frequency 0.083)
- Structural context available