G19S (p.Gly19Ser) variant of CD7 (T-cell antigen CD7)
G19S (p.Gly19Ser) in CD7 (T-cell antigen CD7) is a missense change. Clinical records from ClinVar 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 0.18 / 1. The record also includes population frequency data.
G19S (p.Gly19Ser) variant details
- p.Gly19Ser
- 1000Genomes rs372973906
- ESP rs372973906
- ExAC rs372973906
- TOPMed rs372973906
- Uncertain significance
- not specified
- Missense
- Variant Prioritization Score for Impact Estimate 0.177
- REVEL 0.02
- CADD 0.04
- PolyPhen-2 0.06
- SIFT 0.90
- ClinVar: Uncertain significance (not specified)
- UniProt: Uncertain significance
- Most common in the 1KG:MSL population (allele frequency 0.0063)