Run ID: ERR4816127
Sample name:
Date: 01-04-2023 14:15:11
Number of reads: 358784
Percentage reads mapped: 94.7
Strain: lineage1.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1.1 | Indo-Oceanic | EAI3;EAI4;EAI5;EAI6 | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrB | 6929 | p.Ala564Pro | missense_variant | 0.25 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
ccsA | 620512 | p.Gly208Ser | missense_variant | 0.15 |
ccsA | 620744 | p.Ala285Glu | missense_variant | 0.13 |
ccsA | 620755 | p.Asp289Tyr | missense_variant | 0.14 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.29 |
rpoB | 760611 | c.805T>C | synonymous_variant | 0.25 |
rpoB | 760629 | c.823C>T | synonymous_variant | 0.43 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.38 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.43 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.5 |
rpoB | 760670 | c.864G>C | synonymous_variant | 0.75 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.6 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.5 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.5 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.5 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.5 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.5 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.75 |
rpoB | 761645 | c.1839C>G | synonymous_variant | 0.5 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.5 |
rpoB | 761657 | c.1851C>G | synonymous_variant | 0.43 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.18 |
rpoB | 761954 | c.2148C>G | synonymous_variant | 0.18 |
rpoB | 761972 | c.2166C>G | synonymous_variant | 0.29 |
rpoB | 762008 | c.2202C>T | synonymous_variant | 0.4 |
rpoB | 762014 | c.2208C>T | synonymous_variant | 0.67 |
rpoB | 762017 | c.2211A>G | synonymous_variant | 0.67 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763158 | c.-212C>T | upstream_gene_variant | 0.22 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.22 |
rpoC | 763190 | c.-180C>T | upstream_gene_variant | 0.25 |
rpoC | 763202 | c.-168A>G | upstream_gene_variant | 0.25 |
rpoC | 763402 | c.33C>G | synonymous_variant | 0.2 |
rpoC | 763411 | c.42T>G | synonymous_variant | 0.2 |
rpoC | 763414 | c.45T>C | synonymous_variant | 0.2 |
rpoC | 763438 | p.Trp23* | stop_gained | 0.25 |
rpoC | 763441 | c.72C>T | synonymous_variant | 0.25 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.25 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.4 |
rpoC | 763853 | p.Val162Ile | missense_variant | 0.67 |
rpoC | 763858 | c.489A>G | synonymous_variant | 0.67 |
rpoC | 763872 | p.Gly168Ala | missense_variant | 0.67 |
rpoC | 763876 | p.Glu169Asp | missense_variant | 0.67 |
rpoC | 763879 | c.510A>G | synonymous_variant | 0.67 |
rpoC | 763888 | c.519G>C | synonymous_variant | 0.67 |
rpoC | 763891 | c.522G>C | synonymous_variant | 0.67 |
rpoC | 763894 | c.525A>G | synonymous_variant | 0.67 |
rpoC | 763900 | c.531G>C | synonymous_variant | 0.5 |
rpoC | 764317 | c.948C>T | synonymous_variant | 0.29 |
rpoC | 764353 | c.984G>T | synonymous_variant | 0.2 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.25 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.22 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 0.22 |
rpoC | 764713 | c.1344G>C | synonymous_variant | 0.33 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.33 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.29 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.25 |
rpoC | 764797 | c.1428G>C | synonymous_variant | 0.5 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.5 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.5 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.4 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.33 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.43 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.38 |
rpoC | 764932 | c.1563C>A | synonymous_variant | 0.5 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.33 |
rpoC | 765171 | p.Pro601Leu | missense_variant | 1.0 |
rpoC | 766861 | c.3492G>T | synonymous_variant | 0.33 |
rpoC | 766864 | c.3495G>C | synonymous_variant | 0.33 |
rpoC | 766945 | c.3576A>G | synonymous_variant | 0.4 |
rpoC | 766972 | c.3603G>C | synonymous_variant | 0.4 |
rpoC | 766978 | c.3609C>A | synonymous_variant | 0.4 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.6 |
rpoC | 767012 | c.3643C>T | synonymous_variant | 0.6 |
rpoC | 767032 | c.3663G>T | synonymous_variant | 0.75 |
rpoC | 767035 | c.3666G>T | synonymous_variant | 0.67 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.5 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.6 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781622 | c.63C>G | synonymous_variant | 0.29 |
rplC | 801066 | c.258G>A | synonymous_variant | 0.29 |
fbiC | 1303388 | p.Ala153Val | missense_variant | 0.17 |
Rv1258c | 1406888 | c.453C>T | synonymous_variant | 0.29 |
Rv1258c | 1407201 | c.139delG | frameshift_variant | 0.33 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474803 | n.1146G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 1.0 |
inhA | 1674509 | c.311delG | frameshift_variant | 0.4 |
inhA | 1674601 | p.Leu134Ala | missense_variant | 0.22 |
inhA | 1674624 | c.423A>C | synonymous_variant | 0.29 |
inhA | 1674636 | c.435C>G | synonymous_variant | 0.25 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.67 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.5 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.5 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.5 |
rpsA | 1833748 | c.207C>G | synonymous_variant | 0.5 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.67 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.67 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 0.67 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.5 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.33 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.33 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.33 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.33 |
rpsA | 1834297 | c.756C>T | synonymous_variant | 0.67 |
rpsA | 1834303 | c.762T>G | synonymous_variant | 0.5 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.4 |
rpsA | 1834319 | p.Val260Ile | missense_variant | 0.6 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.5 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.6 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.75 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.75 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.75 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.75 |
rpsA | 1834438 | c.897C>G | synonymous_variant | 0.75 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.6 |
rpsA | 1834465 | c.924T>C | synonymous_variant | 0.6 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.5 |
rpsA | 1834474 | c.933C>G | synonymous_variant | 0.5 |
rpsA | 1834547 | p.Gln336Lys | missense_variant | 0.25 |
rpsA | 1834753 | c.1212T>C | synonymous_variant | 0.5 |
rpsA | 1834759 | c.1218A>C | synonymous_variant | 0.5 |
rpsA | 1834765 | p.Glu408Asp | missense_variant | 0.6 |
rpsA | 1834775 | p.Ala412Thr | missense_variant | 0.5 |
rpsA | 1834780 | c.1239A>G | synonymous_variant | 0.4 |
rpsA | 1834786 | c.1245A>G | synonymous_variant | 0.4 |
rpsA | 1834789 | c.1248T>C | synonymous_variant | 0.4 |
rpsA | 1834792 | c.1251G>C | synonymous_variant | 0.4 |
rpsA | 1834798 | c.1257C>G | synonymous_variant | 0.33 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102218 | c.825C>A | synonymous_variant | 0.4 |
ndh | 2102227 | c.816C>T | synonymous_variant | 0.5 |
ndh | 2102230 | c.813G>C | synonymous_variant | 0.5 |
ndh | 2102233 | c.810G>A | synonymous_variant | 0.5 |
ndh | 2102245 | c.798C>G | synonymous_variant | 0.4 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2156532 | c.-421C>A | upstream_gene_variant | 0.5 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167983 | p.Gly877Asp | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289149 | c.93C>A | synonymous_variant | 0.29 |
pncA | 2290105 | c.-864G>C | upstream_gene_variant | 0.4 |
kasA | 2517950 | c.-165C>G | upstream_gene_variant | 0.15 |
kasA | 2517974 | c.-141T>C | upstream_gene_variant | 0.17 |
kasA | 2517989 | c.-126T>C | upstream_gene_variant | 0.25 |
kasA | 2517993 | c.-122G>T | upstream_gene_variant | 0.25 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2519248 | c.1135delG | frameshift_variant | 0.25 |
eis | 2714571 | c.762G>A | synonymous_variant | 0.5 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
folC | 2746308 | p.Arg431Ser | missense_variant | 0.22 |
folC | 2746321 | c.1278A>G | synonymous_variant | 0.2 |
folC | 2746328 | p.Arg424Ala | missense_variant | 0.29 |
folC | 2746335 | p.Gly422Arg | missense_variant | 0.29 |
folC | 2746336 | c.1263C>G | synonymous_variant | 0.29 |
folC | 2746345 | c.1254G>C | synonymous_variant | 0.25 |
folC | 2746393 | c.1206C>G | synonymous_variant | 0.22 |
folC | 2746451 | p.Gly383Ala | missense_variant | 0.2 |
folC | 2746477 | p.Phe374Tyr | missense_variant | 0.18 |
folC | 2746480 | c.1119A>C | synonymous_variant | 0.18 |
folC | 2746494 | c.1103_1104delAT | frameshift_variant | 0.25 |
folC | 2746498 | c.1100_1101insCG | frameshift_variant | 0.29 |
folC | 2746507 | c.1092A>G | synonymous_variant | 0.29 |
folC | 2746510 | c.1089A>G | synonymous_variant | 0.29 |
folC | 2746516 | c.1083T>G | synonymous_variant | 0.29 |
folC | 2746519 | p.Ser360Ala | missense_variant | 0.29 |
folC | 2746525 | c.1074G>C | synonymous_variant | 0.29 |
pepQ | 2859969 | c.450C>T | synonymous_variant | 0.18 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 1.0 |
Rv2752c | 3065689 | p.Thr168Ile | missense_variant | 0.29 |
thyX | 3067316 | c.630A>G | synonymous_variant | 0.11 |
thyX | 3067850 | c.96A>C | synonymous_variant | 0.17 |
thyX | 3067853 | c.93C>T | synonymous_variant | 0.18 |
thyX | 3067869 | p.Thr26Ser | missense_variant | 0.25 |
thyX | 3067874 | c.72C>G | synonymous_variant | 0.27 |
thyX | 3067883 | c.63C>G | synonymous_variant | 0.31 |
thyX | 3067886 | c.60A>C | synonymous_variant | 0.31 |
thyX | 3067889 | c.57C>G | synonymous_variant | 0.29 |
thyX | 3067898 | p.Asp16Glu | missense_variant | 0.31 |
thyX | 3067935 | p.Thr4Ile | missense_variant | 0.17 |
thyX | 3068151 | c.-206T>C | upstream_gene_variant | 0.2 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
Rv3083 | 3449508 | c.1005G>T | synonymous_variant | 0.25 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
fprA | 3475315 | p.His437Asn | missense_variant | 0.17 |
whiB7 | 3568872 | c.-193C>T | upstream_gene_variant | 0.29 |
Rv3236c | 3613053 | p.Gly22Arg | missense_variant | 0.29 |
fbiA | 3641408 | c.868delG | frameshift_variant | 0.2 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.2 |
rpoA | 3877679 | p.Ala277Ser | missense_variant | 0.22 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.22 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.22 |
rpoA | 3877704 | c.804G>T | synonymous_variant | 0.22 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.18 |
rpoA | 3877887 | c.621G>C | synonymous_variant | 0.25 |
rpoA | 3877896 | c.612G>C | synonymous_variant | 0.25 |
rpoA | 3877900 | p.Ser203Asn | missense_variant | 0.22 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.2 |
rpoA | 3877908 | p.Asn200Ser | missense_variant | 0.2 |
rpoA | 3877920 | c.588G>C | synonymous_variant | 0.3 |
rpoA | 3877926 | c.582G>C | synonymous_variant | 0.3 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.43 |
rpoA | 3877986 | c.522G>C | synonymous_variant | 0.5 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.4 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.4 |
clpC1 | 4039973 | p.Asp244Glu | missense_variant | 0.4 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
clpC1 | 4040675 | c.30C>G | synonymous_variant | 0.11 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242886 | c.-347G>A | upstream_gene_variant | 0.13 |
embA | 4242892 | c.-341G>C | upstream_gene_variant | 0.13 |
embA | 4242901 | c.-332G>C | upstream_gene_variant | 0.12 |
embA | 4243848 | p.Val206Met | missense_variant | 1.0 |
embA | 4244096 | c.864C>T | synonymous_variant | 1.0 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embA | 4246347 | p.Thr1039Ala | missense_variant | 0.12 |
embB | 4246727 | c.217_218dupTC | frameshift_variant | 0.17 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
aftB | 4266972 | p.Gly622Asp | missense_variant | 0.33 |
aftB | 4268904 | c.-68C>T | upstream_gene_variant | 0.2 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
ubiA | 4269532 | p.Leu101Pro | missense_variant | 0.2 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ethA | 4328340 | c.-867A>G | upstream_gene_variant | 0.18 |
ethA | 4328363 | c.-890A>G | upstream_gene_variant | 0.22 |
whiB6 | 4338242 | p.Gln94Glu | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407832 | p.Val124Gly | missense_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |