Run ID: ERR4821712
Sample name:
Date: 01-04-2023 17:24:33
Number of reads: 400549
Percentage reads mapped: 74.23
Strain:
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1.2.2 | Indo-Oceanic | EAI1 | RD239 | 1.0 |
lineage1.2.2.2 | Indo-Oceanic | NA | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5075 | c.-165C>T | upstream_gene_variant | 1.0 |
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrB | 6971 | p.Pro578Ser | missense_variant | 0.25 |
gyrA | 7268 | c.-34C>T | upstream_gene_variant | 1.0 |
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 |
mshA | 576565 | c.1218G>A | synonymous_variant | 0.22 |
ccsA | 620368 | p.Ala160Ser | missense_variant | 0.25 |
rpoB | 760094 | c.288G>T | synonymous_variant | 0.15 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.25 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.25 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.25 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.25 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.25 |
rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 0.27 |
rpoB | 761150 | c.1344A>T | synonymous_variant | 0.29 |
rpoB | 761159 | c.1353G>C | synonymous_variant | 0.29 |
rpoB | 762625 | c.2820_2821delCG | frameshift_variant | 0.18 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763798 | c.431_433delGCC | disruptive_inframe_deletion | 0.4 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.25 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.25 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.43 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.43 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.5 |
rpoC | 764503 | c.1134G>T | synonymous_variant | 0.67 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.67 |
rpoC | 764512 | c.1143G>C | synonymous_variant | 0.67 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.8 |
rpoC | 764524 | c.1155C>T | synonymous_variant | 0.4 |
rpoC | 764530 | c.1161C>T | synonymous_variant | 0.5 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.5 |
rpoC | 764543 | p.Thr392Ala | missense_variant | 0.57 |
rpoC | 764548 | c.1179G>C | synonymous_variant | 0.5 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.43 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.22 |
rpoC | 764647 | c.1278C>T | synonymous_variant | 0.2 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777321 | p.Val387Ala | missense_variant | 0.14 |
mmpL5 | 779269 | c.-789G>T | upstream_gene_variant | 0.22 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303828 | p.His300Tyr | missense_variant | 0.29 |
Rv1258c | 1406104 | c.1237C>A | synonymous_variant | 0.14 |
embR | 1416220 | p.Phe376Leu | missense_variant | 0.14 |
embR | 1416461 | p.Ala296Ile | missense_variant | 0.29 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473122 | n.1281delA | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473288 | n.1443C>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473300 | n.1455C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474551 | n.894G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474555 | n.898T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474558 | n.901G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474581 | n.924C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474601 | n.944C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474794 | n.1137C>T | 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 |
rrl | 1474831 | n.1174A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474832 | n.1175A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476164 | n.2507A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476179 | n.2522C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476194 | n.2537A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476204 | n.2547C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476207 | n.2550T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.25 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.21 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.2 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.14 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.15 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102240 | p.Arg268His | missense_variant | 1.0 |
katG | 2153937 | c.2175C>T | synonymous_variant | 0.12 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2156160 | c.-49T>C | upstream_gene_variant | 0.29 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167928 | c.2685G>A | synonymous_variant | 1.0 |
PPE35 | 2168742 | p.Gly624Asp | missense_variant | 1.0 |
PPE35 | 2169805 | p.Ala270Thr | missense_variant | 0.22 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
eis | 2714901 | c.432A>G | synonymous_variant | 0.17 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
ahpC | 2726240 | c.48C>A | synonymous_variant | 0.18 |
pepQ | 2860490 | c.-72G>A | upstream_gene_variant | 0.13 |
thyX | 3068063 | c.-119_-118insG | upstream_gene_variant | 0.29 |
ald | 3086672 | c.-148C>T | upstream_gene_variant | 0.4 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087601 | p.Gly261Val | missense_variant | 1.0 |
ald | 3087675 | p.Pro286Ala | missense_variant | 0.2 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
Rv3083 | 3449601 | p.Gln366His | missense_variant | 0.12 |
Rv3083 | 3449781 | c.1278G>A | synonymous_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3474602 | p.Arg199Leu | missense_variant | 0.25 |
fprA | 3474793 | p.Gly263Arg | missense_variant | 1.0 |
fprA | 3475090 | p.Arg362Ser | missense_variant | 0.15 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
Rv3236c | 3613249 | c.-133A>T | upstream_gene_variant | 0.25 |
rpoA | 3878464 | p.Thr15Ile | missense_variant | 0.25 |
clpC1 | 4039645 | p.His354Asp | missense_variant | 0.29 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
clpC1 | 4040523 | p.Ser61Ile | missense_variant | 0.25 |
clpC1 | 4040719 | c.-15A>G | upstream_gene_variant | 1.0 |
panD | 4044455 | c.-174G>T | upstream_gene_variant | 0.13 |
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 | 4244926 | p.Phe565Tyr | missense_variant | 0.25 |
embA | 4245072 | p.Leu614Val | missense_variant | 0.17 |
embB | 4245704 | c.-810G>A | upstream_gene_variant | 0.25 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
aftB | 4269252 | c.-416C>T | upstream_gene_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ethA | 4326148 | c.1326G>T | synonymous_variant | 1.0 |
ethA | 4326439 | p.Asn345Lys | missense_variant | 1.0 |
whiB6 | 4338203 | p.Arg107Cys | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
gid | 4407566 | c.637C>A | synonymous_variant | 0.2 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407848 | p.Ala119Thr | missense_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |
gid | 4407926 | p.Pro93Ser | missense_variant | 1.0 |