R69Q (p.Arg69Gln) variant of HLA-DRA (P01903)
R69Q (p.Arg69Gln) in HLA-DRA (P01903) 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.
R69Q (p.Arg69Gln) variant details
- p.Arg69Gln
- TOPMed rs1348828850
- gnomAD rs1348828850
- cosmic curated COSV10531
- Missense
- Variant Prioritization Score for Impact Estimate 0.396
- REVEL 0.19
- CADD 26.40
- PolyPhen-2 1.00
- SIFT 0.06
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available