Q94R (p.Gln94Arg) variant of CD7 (T-cell antigen CD7)
Q94R (p.Gln94Arg) in CD7 (T-cell antigen CD7) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not specified. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data and structural context.
Q94R (p.Gln94Arg) variant details
- p.Gln94Arg
- rs2052020578
- ClinGen CA401572894
- ClinVar RCV004344713
- gnomAD rs2052020578
- Uncertain significance
- not specified
- Missense
- Variant Prioritization Score for Impact Estimate 0.228
- REVEL 0.07
- CADD 8.86
- PolyPhen-2 0.13
- SIFT 0.02
- ClinVar: Uncertain significance (not specified)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available