Abstract: Three polymorphic regions in the human genome were found to be associated with EBV variation: one at the amino acid level (BRLF1:p.Lys316Glu); and two at the gene level (burden testing of rare variants in BALF5 and BBRF1).
Result: 2B) and the EBV amino acid BRLF1:p.Lys316Glu.
Result: BRLF1:p.Lys316Glu and BRLF1:p.Glu377Ala are in moderate LD (r2 = 0.55) in our dataset.
Result: BRLF1:p.Lys316Glu has not been described previously, but variation at the nearby residue 377 (BRLF1:
EBV mutation literature information.
PMID: 
2021
Scientific reports
