G72S (p.Gly72Ser) variant of CD79B (P40259)
G72S (p.Gly72Ser) in CD79B (P40259) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as likely benign in the context of not specified. The available variant effect predictions contribute to a CATVariant prioritization score of 0.11 / 1. The record also includes population frequency data and structural context.
G72S (p.Gly72Ser) variant details
- p.Gly72Ser
- rs373078798
- ClinGen CA8708606
- ClinVar RCV004435542
- 1000Genomes rs373078798
- Likely benign
- not specified
- Missense
- Variant Prioritization Score for Impact Estimate 0.106
- REVEL 0.14
- CADD 0.68
- PolyPhen-2 0.01
- SIFT 0.41
- ClinVar: Likely benign (not specified)
- EBI: Likely benign
- UniProt: Likely benign
- Most common in the 1KG:PEL population (allele frequency 0.0059)
- Structural context available