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. 2017 Jun 21;23(23):4222–4232. doi: 10.3748/wjg.v23.i23.4222

Table 5.

Frequency and patterns of 3 types of NAr Mutations related to hepatocellular carcinoma

Mutations No. of patients
Nucleotide sequences Codons in RT genes (patients) Codons in HBsAg genes (patients) P value
CH HCC
rtL80I 0 5 GGCTAT→GGATAT CTA(L)→ATA(I) (5) TAT(Y)→TAT(Y) (5) 0.036
rtN139K/T/H (sT131N/P) 0 8 GGAACC→GGAAAC AAC(N)→AAA(K) (4) ACC(T)→AAC(N) (4)
→GGCACC →CAC(H) (3) →ACC(T) (3) 0.008
→GGACCC →ACC(T) (1) →CCC(P) (1)
rtM204I/V (sW196L/S/W) 0 9 ATATGG→ATATTG ATG(M)→ATT(I) (7) TGG(W)→TTG(L) (7)
→ATATCG →ATC(I) (1) →TCG(S) (1) 0.004
→ATGTGG →GTG(V) (1) →TGG(W) (1)

The point mutation bases of the three truncations are shown in bold and italic. H: Histidine; I: Isoleucine; K: Lysine; L: Leucine; M: Methionine; N: Asparagine; P: Proline; S: Serine; T: Threonine; V: Valine; W: Tryptophan; Y: Tyrosine; CH: Chronic hepatitis; HCC: Hepatocellular carcinoma.