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. 2012 Apr;86(8):4631–4643. doi: 10.1128/JVI.06265-11

Table 1.

Potential compensatory mutations within the 5′ UTR and Nsp1 coding region of progeny from the B142-173/M chimera

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a

Plaque purified clones were selected at virus passage 0 (VP0) and identified as small (S) or large (L).

b

Number of base pairs within the base-pairing window (identified as positions 145 to 169 in the 5′ UTR and 347 to 363 in the Nsp1 cistron).

c

See Fig. 3 for descriptions of the folding patterns.

d

Causes K52E.

e

Causes P47T.

f

Causes K48N.

g

Causes M128V.

h

Causes K50T.

i

Causes F11L.