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. 2017 Nov 14;91(23):e00942-17. doi: 10.1128/JVI.00942-17

TABLE 5.

SNVs unique to the primary or recurrent infection in subject A or B

Gene Nucleotide/amino acid position Nucleotide variant
Amino acid variant
Function
Primary infection (sample 8) ≫ recurrent infection (sample 14) Primary (sample 16) ≫ recurrent (sample 19) Primary infection Recurrent infection
Subject A
    UL13a,b 569/190 C (86)c, T (14)C (98), T (1), A (1) A (86), V (14) A (98) Protein kinase
    UL13b 685/229 G (100) ≫ G (90), T (10) D (100) D (90), Y (10) Protein kinase
    UL14 321/107 T (10), C (90)T (74), C (26) Tegument protein
    UL14 334/112 C (70), T (30) ≫ C (99), A (1) R (70), C(30) R (100) Tegument protein
    UL27 206/69 C (100) ≫ T (52), C (48) P (100) L (52), P (48) Glycoprotein B
    UL30 3398/1133 C (98), T (1), A (1) ≫ T (60), C (40) P (98) L (60), P (40) DNA polymerase
    UL36 7942/2648 G (100) ≫ G (65), A (35) A (100) A (65), T (35) Tegument protein
    UL37b 1478/493 A (7), C (93) ≫ A (99), G (1) P (93) H (99) Tegument protein
    UL44 321/107 G (82), C (15), A (1), T (2) ≫ G (91), C (8), T (1) Tegument protein
    Intergenic space 145807d G (89), A (11) ≫ G (99), A (1)
Subject B
    UL12 1305/435 C (100) ≫ T (24), C (76) DNase
    UL13b 862/288 C (86), T (14) ≫ C (98), T (2) R (86), STOP (14) R (98) Protein kinase
    UL13b 1133/378 G (100) ≫ G (86), T (14) G (100) G (86), V (14) Protein kinase
    UL14 241/81 G (99), T (1) ≫ G (79), A (21) V (99) V (79), M (21) Tegument protein
    UL14 321/107 T (81), C (19)T (45), C (55) Tegument protein
    UL14 396/132 C (100) ≫ C (90), T (10) Tegument protein
    UL21b 1039/347 G (67), A (33) ≫ G (100) A (67), T (33) A (100) Tegument protein
    UL24 165/55 G (89), A (11) ≫ G (100) Nuclear protein
    UL30b 2852/951 G (80), A (20) ≫ G (100) C (80), Y (20) C (100) DNA polymerase
a

Boldface indicates nonsynonymous substitutions.

b

The secondary and tertiary structures of the protein that contained the polymorphisms were analyzed using the Phyre2 Web portal (Table 6).

c

The numbers in parentheses are the percentages of Novoalign mapped reads supporting each polymorphism. The reported polymorphisms appeared in ≥10% of mapped reads. Underlining indicates the polymorphic variant allele.

d

Polymorphism position observed in an intergenic space derived from the Novoalign alignments (BAM files).