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. 2017 Jan 3;114(3):E386–E395. doi: 10.1073/pnas.1619242114

Table 1.

Mutations detected in individual lineages of Min L at the end of P6 (second passage at 39 °C) of the temperature stress test present at ≥45% frequency

Gene Nucleotide mutation Amino acid mutation Percentage of reads with mutation in indicated lineage no.*
1 2 3 4 5 6 7 8 9 10
Intergenic NS2-N g1123a / 85
P a2687u E114V 96
M u3798a N179K 61
SH c4369a H22Q 81
SH c4387g I28M 71
G a5384g E232 (silent) 47
M2-1 g7823u A73S 99 93 61 48 83 63 87 57
M2-1 c7870a N88K 94 96
M2-1 a8013g E136G 48
L u10548c Y684H 97
L u10797c S767P 82
L g12933a A1479T 63 85
L a13783c Y1762S 83
5′ Extragenic (trailer) u15100c / 75

“/” indicates that the amino acid mutation is not applicable for this particular mutation as the given mutation is localized in a nontranslated region.

*

Percentage of reads with the indicated mutation; only mutations present in ≥45% of the reads are shown. Nucleotide numbering is based on RSV sequence M74568 (biological WT RSV strain A2). Mutations present in ≥5% of reads from this same experiment are shown in Table S1.

Mutation involving a codon that had been changed as part of CPD of the L ORF.

Mutation involving a nucleotide position that had been changed as part of CPD of the L ORF.

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