R7G (p.Arg7Gly) variant of HLA-B (P01889)
R7G (p.Arg7Gly) in HLA-B (P01889) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes population frequency data and structural context.
R7G (p.Arg7Gly) variant details
- p.Arg7Gly
- NCI-TCGA Cosmic COSV6952
- cosmic curated COSV69521
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.205
- REVEL 0.23
- CADD 14.30
- PolyPhen-2 0.26
- SIFT 0.13
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 3.1e-06)
- Structural context available