Run ID: ERR773806
Sample name:
Date: 02-04-2023 05:36:49
Number of reads: 850247
Percentage reads mapped: 21.52
Strain: lineage2.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 1.0 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490972 | p.Arg64Cys | missense_variant | 0.12 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 619837 | c.-54G>T | upstream_gene_variant | 0.17 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoC | 762863 | c.-507T>C | upstream_gene_variant | 0.38 |
rpoB | 762872 | p.Met1022Ile | missense_variant | 0.44 |
rpoB | 762878 | p.Ile1024Met | missense_variant | 0.46 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.46 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.59 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.68 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.68 |
rpoB | 762925 | p.Thr1040Ile | missense_variant | 0.71 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.71 |
rpoB | 762939 | p.Met1045Leu | missense_variant | 0.69 |
rpoB | 762942 | p.Ile1046Val | missense_variant | 0.69 |
rpoC | 762980 | c.-390T>C | upstream_gene_variant | 0.51 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.51 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.52 |
rpoC | 762998 | c.-372G>A | upstream_gene_variant | 0.42 |
rpoB | 763005 | p.Cys1067Val | missense_variant | 0.24 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764070 | p.Leu234Pro | missense_variant | 0.13 |
rpoC | 764338 | c.969G>A | synonymous_variant | 0.25 |
rpoC | 764344 | c.975C>T | synonymous_variant | 0.25 |
rpoC | 764348 | p.Met327Leu | missense_variant | 0.24 |
rpoC | 764355 | p.Gln329Pro | missense_variant | 0.29 |
rpoC | 764359 | c.990C>G | synonymous_variant | 0.29 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 0.2 |
rpoC | 764377 | c.1008C>G | synonymous_variant | 0.23 |
rpoC | 764383 | c.1014C>G | synonymous_variant | 0.14 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 0.13 |
rpoC | 764401 | c.1032C>T | synonymous_variant | 0.13 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.22 |
rpoC | 764410 | c.1041G>C | synonymous_variant | 0.38 |
rpoC | 764419 | c.1050C>G | synonymous_variant | 0.47 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.47 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.49 |
rpoC | 764435 | c.1066_1068delAGGinsCGC | synonymous_variant | 0.49 |
rpoC | 764446 | p.Asp359Glu | missense_variant | 0.51 |
rpoC | 764450 | p.Gly361Arg | missense_variant | 0.51 |
rpoC | 764461 | p.Glu364Asp | missense_variant | 0.53 |
rpoC | 764468 | p.Val367Ile | missense_variant | 0.53 |
rpoC | 764471 | p.Asn368Arg | missense_variant | 0.55 |
rpoC | 764479 | c.1110G>A | synonymous_variant | 0.53 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.54 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.5 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.39 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.32 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.11 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.31 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.39 |
rpoC | 764660 | p.Val431Thr | missense_variant | 0.39 |
rpoC | 764665 | c.1296C>G | synonymous_variant | 0.38 |
rpoC | 764671 | c.1302G>C | synonymous_variant | 0.38 |
rpoC | 764672 | p.Gln435Glu | missense_variant | 0.39 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.38 |
rpoC | 764687 | p.Gln440Glu | missense_variant | 0.38 |
rpoC | 764695 | c.1326T>C | synonymous_variant | 0.41 |
rpoC | 764705 | p.Leu446Lys | missense_variant | 0.39 |
rpoC | 764874 | p.Pro502His | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 776459 | c.2022G>T | synonymous_variant | 0.12 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 0.96 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303016 | p.Val29Gly | missense_variant | 0.18 |
fbiC | 1304445 | c.1515G>C | synonymous_variant | 0.17 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471876 | n.31G>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1471877 | n.32A>G | non_coding_transcript_exon_variant | 0.35 |
rrs | 1471892 | n.47G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1471893 | n.48T>G | non_coding_transcript_exon_variant | 0.39 |
rrs | 1471896 | n.51T>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1471917 | n.72G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1471918 | n.74_78delAAGGT | non_coding_transcript_exon_variant | 0.36 |
rrs | 1471934 | n.89A>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1471935 | n.92_96delCTCGA | non_coding_transcript_exon_variant | 0.36 |
rrs | 1471948 | n.103A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472128 | n.283G>C | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472129 | n.284G>A | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472135 | n.290C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472138 | n.293C>T | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472147 | n.302G>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472153 | n.308G>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472240 | n.395G>C | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472242 | n.397C>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472338 | n.493A>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472349 | n.504A>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472374 | n.529T>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472379 | n.534T>G | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472382 | n.537G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472390 | n.545T>C | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472391 | n.546C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472412 | n.567A>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472415 | n.570T>G | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472694 | n.849C>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472715 | n.870C>A | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472812 | n.967A>C | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472887 | n.1042G>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473147 | n.1302G>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473148 | n.1303G>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473149 | n.1304G>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473162 | n.1317C>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473163 | n.1318C>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473164 | n.1319C>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473352 | n.1507C>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473353 | n.1508C>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473358 | n.1513G>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473359 | n.1514G>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474838 | n.1181C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474869 | n.1212G>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474875 | n.1218G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474876 | n.1219T>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474883 | n.1226T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474893 | n.1236G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474899 | n.1242T>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474910 | n.1253C>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474913 | n.1256T>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474920 | n.1263G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474928 | n.1271C>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475499 | n.1842C>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1475526 | n.1869C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1475538 | n.1881T>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475540 | n.1883C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 0.34 |
rrl | 1475550 | n.1893A>G | non_coding_transcript_exon_variant | 0.34 |
rrl | 1475553 | n.1896G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475555 | n.1898T>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475571 | n.1914A>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1475575 | n.1918C>A | non_coding_transcript_exon_variant | 0.46 |
rrl | 1475577 | n.1920C>G | non_coding_transcript_exon_variant | 0.46 |
rrl | 1475589 | n.1932G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475591 | n.1934G>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475791 | n.2134A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.37 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.39 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476238 | n.2581T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476266 | n.2609G>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476279 | n.2622G>C | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476281 | n.2624T>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476339 | n.2682G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476356 | n.2699C>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476384 | n.2727G>A | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476443 | n.2786G>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476455 | n.2798C>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476470 | n.2813C>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476501 | n.2844C>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476512 | n.2855C>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.19 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.89 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102540 | p.Ala168Gly | missense_variant | 0.17 |
katG | 2154046 | p.Trp689Leu | missense_variant | 0.11 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 0.9 |
PPE35 | 2170026 | p.Pro196Leu | missense_variant | 0.2 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2715117 | c.216T>G | synonymous_variant | 0.11 |
thyA | 3073806 | c.666C>G | synonymous_variant | 0.2 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339273 | c.156T>G | synonymous_variant | 0.38 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiA | 3641332 | p.Gly264Arg | missense_variant | 1.0 |
fbiB | 3642772 | p.Asp413Ala | missense_variant | 0.29 |
rpoA | 3878412 | p.Tyr32* | stop_gained | 0.12 |
ddn | 3986740 | c.-104G>T | upstream_gene_variant | 0.12 |
clpC1 | 4039484 | c.1221T>G | synonymous_variant | 0.38 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embB | 4246737 | p.Thr75Met | missense_variant | 0.12 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |