Table 1:
Summary of minor variant mutations analysis of PB2 D701 Cluster sequences
| Chromosome / Segment | Genome position | Referen ce allele | Alternative allele | Alternative allele frequency / Position (Annotate allele) | Allele effect | Allele impact | CDS variation | CDS length | Protein variation | Comments | ||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 240524-2/2023 | 240265/2023 | 240270-1/2023 | ||||||||||
| OQ352545.1. / Seg 1 (PB2) | 1590 | T | A | 78,32 / 535 (A) | 76,92 / 65 (A) | 75,61 / 123 (A) | synonymous variant | LOW | 1563T>A | 2280 | T521T | |
| 2128 | G | A | 52,94 / 527 (A) | 70,88 / 1092 (A) | 65,19 / 135 (A) | missense variant | MODERATE | 2101G>A | 2280 | D701N | ||
| 2160 | T | C | 65,08 / 524 (C) | 87,35 / 1289 (C) | 90,37 / 135 (C) | synonymous variant | LOW | 2133T>C | 2280 | N711N | ||
| OQ352546.1 / Seg 2 (PB1) | 96 | A | G | 100 / 3 (G) | 73,53 / 170 (G) | 86,15 / 65 (G) | synonymous variant | LOW | 69A>G | 2274 | P23P | |
| 705 | A | G | 100 / 3 (G) | 78,46 / 65 (G) | 85,94 / 65 /G) | synonymous variant | LOW | 678A>G | 2274 | T226T | ||
| 723 | G | A | 33,33 / 3 (A) | 78,12 / 64 (A) | 84,38 / 64 (A) | synonymous variant | LOW | 696G>A | 2274 | E232E | ||
| 1570 | T | G | 75 / 4 (G) | 76,27 / 118 (G) | 81,82 /154 (G) | missense variant | MODERATE | 1543T>G | 2274 | S515A | ||
| OQ352547.1 / Seg 3 (PA) | 150 | A | G | 77,39 / 115 (G) | 77,39 / 115 (G) | 79,37 / 63 (G) | synonymous variant | LOW | 126A>G | 2151 | L42L | |
| 1692 | A | G | 73,39 / 124 (G) | 70,63 / 126 (G) | 73,13 / 67 (G) | synonymous variant | LOW | 1668A>G | 2151 | Q556Q | ||
| 150 | A | G | 77,39 / 115 (G) | 77,39 / 115 (G) | 79,37 / 63 (G) | synonymous variant | LOW | 126A>G | 759 | L42L | ||
| OQ352548.1 / Seg 4 (HA) | 610 | T | C | 89,97 / 3130 (C) | 88,94 / 461 (C) | 88,19 / 415 (C) | synonymous variant | LOW | 582T>C | 1704 | I194I | |
| OQ352549.1 / Seg 5 (NP) | 401 | T | C | 79,47 / 5255 (C) | 76,75 / 1045 (C) | 77,12 / 813 (C) | missense variant | MODERATE | 356T>C | 1497 | I119T | |
| 714 | C | T | 63,24 / 5283 (T) | 60,36 / 1047 (T) | 62,41 / 814 /T) | synonymous variant | LOW | 669C>T | 1497 | C223C | ||
| OQ352551.1 / Seg 7 (M) | 691 | T | C | 47,79 / 15659 (C) | 59,61 / 3442 (C) | 59,31 /3728 (C) | synonymous variant | LOW | 666T>C | 759 | H222H | |
| 691 | T | C | 47,79 / 15659 (C) | 59,61 / 3422 (C) | 59,31 /3728 (C) | intron variant | MODIFIER | 27–49T>C | 294 | |||
| OQ352552.1 / Seg 8 (NS) | 102 | G | A | 52,86 / 32303 (A) | 64,3 / 372 (A) | 62,81 / 5230 (A) | intron variant | MODIFIER | 30+46G>A | 366 | ||
| 703 | T | C | 70,9 / 33304 (C) | 83 / 3700 (C) | 82,62 / 5312 (C) | synonymous variant | LOW | 205T>C | 366 | L69L | ||
| 102 | G | A | 52,86 / 32302 (A) | 64,3 / 3712 (A) | 62,81 / 5230 (A) | missense variant | MODERATE | 76G>A | 693 | E26K | ||
| 703 | T | C | 70,9 / 33304 (C) | 83 / 3700 (C) | 82,62 / 5312 (C) | missense variant | MODERATE | 677T>C | 693 | I226T | ||