Run ID: SRR7645936
Sample name:
Date: 04-04-2023 19:59:21
Number of reads: 1271178
Percentage reads mapped: 23.37
Strain: lineage2.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.99 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 1.0 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5932 | c.694delT | frameshift_variant | 0.13 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7569 | p.Ala90Ser | missense_variant | 0.31 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7592 | c.291G>C | synonymous_variant | 0.22 |
gyrA | 7605 | p.Pro102Asp | missense_variant | 0.24 |
gyrA | 7609 | p.Trp103Phe | missense_variant | 0.25 |
gyrA | 7623 | p.Pro108Thr | missense_variant | 0.17 |
gyrA | 7631 | c.330G>C | synonymous_variant | 0.22 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491631 | c.849C>T | synonymous_variant | 0.11 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575815 | p.Trp156* | stop_gained | 0.12 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620439 | c.553delG | frameshift_variant | 0.11 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
ccsA | 620644 | p.Glu252Lys | missense_variant | 0.2 |
rpoB | 760191 | p.Val129Ile | missense_variant | 0.17 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.35 |
rpoB | 762911 | p.Ile1035Met | missense_variant | 0.43 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.42 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.42 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.44 |
rpoB | 762939 | p.Met1045Leu | missense_variant | 0.42 |
rpoB | 762942 | p.Ile1046Val | missense_variant | 0.44 |
rpoC | 762947 | c.-423C>G | upstream_gene_variant | 0.41 |
rpoC | 762968 | c.-402G>A | upstream_gene_variant | 0.55 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 0.48 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.44 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.4 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.17 |
rpoC | 764618 | c.1249C>T | synonymous_variant | 0.3 |
rpoC | 764623 | c.1254C>G | synonymous_variant | 0.3 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.29 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.33 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.42 |
rpoC | 764665 | c.1296C>G | synonymous_variant | 0.48 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 0.5 |
rpoC | 764671 | c.1302G>A | synonymous_variant | 0.5 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.5 |
rpoC | 764680 | c.1311G>A | synonymous_variant | 0.5 |
rpoC | 764701 | c.1332C>G | synonymous_variant | 0.62 |
rpoC | 764713 | c.1344G>T | synonymous_variant | 0.36 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.22 |
rpoC | 764722 | c.1353G>T | synonymous_variant | 0.18 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 1.0 |
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 | 776864 | p.Met539Ile | missense_variant | 0.13 |
mmpS5 | 778750 | c.155delA | frameshift_variant | 0.11 |
mmpR5 | 779181 | p.Ser64Arg | missense_variant | 0.12 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781588 | p.Lys10Arg | missense_variant | 0.11 |
fbiC | 1303672 | p.Ala248Thr | missense_variant | 0.12 |
Rv1258c | 1406723 | c.618A>G | synonymous_variant | 0.11 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
embR | 1416314 | p.Arg345Gln | missense_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472153 | n.308G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472210 | n.365A>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472235 | n.390G>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472242 | n.397C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472256 | n.411T>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472277 | n.432C>G | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472328 | n.483G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472333 | n.488G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472389 | n.544G>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472390 | n.545T>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472391 | n.546C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472707 | n.862A>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472709 | n.864T>G | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472715 | n.870C>G | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472716 | n.871C>A | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472785 | n.940G>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472786 | n.941C>G | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472814 | n.969G>A | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472887 | n.1042G>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473038 | n.1193A>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473044 | n.1199C>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473075 | n.1230A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473139 | n.1294T>C | non_coding_transcript_exon_variant | 0.34 |
rrs | 1473147 | n.1302G>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473164 | n.1319C>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.63 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.72 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.76 |
rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473288 | n.1443C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1473602 | n.-56G>A | upstream_gene_variant | 0.12 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474221 | n.564T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474228 | n.571T>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474253 | n.596A>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474488 | n.831G>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474494 | n.837C>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474495 | n.838G>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1474503 | n.846G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474507 | n.850G>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474509 | n.852G>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474516 | n.859C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474528 | n.871T>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474530 | n.873G>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474539 | n.882C>A | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474541 | n.884G>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474573 | n.916C>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1474576 | n.919T>A | non_coding_transcript_exon_variant | 0.68 |
rrl | 1474583 | n.926C>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1474584 | n.927C>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1474586 | n.929T>A | non_coding_transcript_exon_variant | 0.63 |
rrl | 1474587 | n.930G>A | non_coding_transcript_exon_variant | 0.63 |
rrl | 1474601 | n.944C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474608 | n.951T>A | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474609 | n.952G>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474610 | n.953C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1475783 | n.2126T>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475787 | n.2130C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.37 |
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 | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476384 | n.2727G>A | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476470 | n.2813C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476483 | n.2826G>A | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476501 | n.2844C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.54 |
fabG1 | 1673648 | p.Arg70His | missense_variant | 0.14 |
rpsA | 1833683 | c.145delG | frameshift_variant | 0.11 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917866 | c.-74C>T | upstream_gene_variant | 0.2 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918081 | p.Asp48Asn | missense_variant | 0.14 |
tlyA | 1918353 | c.414C>T | synonymous_variant | 0.11 |
ndh | 2102397 | p.Ala216Thr | missense_variant | 0.11 |
katG | 2154696 | c.1416A>T | synonymous_variant | 0.14 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155563 | c.549C>T | synonymous_variant | 0.15 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289776 | c.-535C>T | upstream_gene_variant | 0.14 |
pepQ | 2859957 | c.462G>T | synonymous_variant | 0.11 |
Rv2752c | 3064731 | p.Leu487Phe | missense_variant | 1.0 |
thyX | 3067512 | c.433delG | frameshift_variant | 0.25 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiA | 3641324 | p.Ser261Leu | missense_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242701 | p.Ala947Thr | missense_variant | 0.14 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4244812 | p.Cys527Tyr | missense_variant | 0.22 |
embA | 4246452 | p.Val1074Ile | missense_variant | 0.17 |
embB | 4247163 | p.Leu217Pro | missense_variant | 0.11 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
ethA | 4326699 | p.Arg259Cys | missense_variant | 0.12 |
ethR | 4327093 | c.-456G>A | upstream_gene_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 0.95 |