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. 2016 Nov 1;32(10-11):1031–1045. doi: 10.1089/aid.2015.0330

Table 5.

Residues in Vpr That Differed in Frequency of the Dominant Amino Acid

Codon Infection stage Residue frequency Signature residue p q
19 Chronic A0.27, I0.01, T0.72 A .180 0.70
  t/f T0.88, A0.12      
22 Chronic L0.49, I0.45, V0.05, M0.01 L .007 0.14
  t/f L0.82, I0.18      
41 Chronic S0.5, G0.24, N0.2 D0.04, A0.01, H0.01, I0.01 S .332 0.80
  t/f S0.65, G0.35      
55 Chronic T0.79, A0.13, M0.04, L0.01, P0.01, R0.01, S0.01, I0.01 T .143 0.70
  t/f T0.65, A0.12, V0.12, E0.06, I0.06      
60 Chronic I0.58, L0.39, M0.02, V0.01 I .147 0.70
  t/f I0.76, L0.18, M0.06      
61 Chronic I0.83, L0.08, M0.03, T0.05, V0.01 I .193 0.70
  t/f I0.71, L0.18, T0.06, V0.06      
70 Chronic I0.82, V0.11, T0.06, M0.01 I .023 0.28
  t/f I0.59, V0.29, T0.12      
84 Chronic L0.63, I0.11, M0.11, V0.07, W0.04, T0.02, G0.01, S0.01 L .209 0.70
  t/f L0.47, I0.12, M0.12, V0.12, A0.06, S0.06, T0.06      
93 Chronic A0.9, S0.06, T0.03, D0.01, P0.01 A .005 0.14
  t/f A0.65, S0.18, P0.12, N0.06      

The bold values highlight residues that can more likely be explored as possible transmission signatures that have a p-value < 0.05 and a q-value threshold < 0.3 to correct for multiple hypothesis testing, for which we used the Benjamini-Hochberg procedure to compute false discovery rate-adjusted p-values (q-values).