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. 2013 Nov 7;19(41):6995–7023. doi: 10.3748/wjg.v19.i41.6995

Table 1.

Main amino acid variants described in the hepatitis B virus genome and its effect

ORF Amino acid variant Effect
P A181T and M204 I/V (compensatory: L80I/V, T128N , R153Q, V173L L180M, A200V1, V207I1) LMV resistance
N236T (compensatory: A181 T/V/S. Low sensitivity: V84M, S85A, L217R, I233V) ADV resistance
I169T, T184S, S202C/I/G, M250I ETV resistance2
A194T1 TDF resistance
S G145R W156Stop, W163Stop, W172Stop, W196Stop Immune therapy failure
D144A, P142S, K141E, Q129H, I/T126N, T131I, M133L HBsAg structural alterations
X I130M, V131I, F132Y Contribution to HCC development
C
preCore A1762T and G1764A HBeAg negative forms
Core G1896A and G1899A Disease progression
P5H/L/T, D32N/H, C/E43K, cP50A/H/Y, E83D, I97F/L, L100I, A131G/N/P, S181H/P and C/Q182K/stop HCC development
Regions 50-69 and 74-84 Immune scape variants
1

Antiviral treatment resistances not completely defined[58];

2

Linked to lamivudine (LMV) signature (L180M + M204V). ORF: Open reading frames; ADV: Adefovir; ETV: Entecavir; TDF: Tenofovir; HBsAg: Hepatitis B virus (HBV) surface antigen; HBeAg: HBV e antigen; HCC: Hepatocellular carcinoma.