Run ID: ERR6336712
Sample name:
Date: 02-04-2023 02:00:16
Number of reads: 667680
Percentage reads mapped: 98.81
Strain: lineage1.2.1.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 1.0 |
lineage1.2.1 | Indo-Oceanic | EAI2 | RD239 | 1.0 |
lineage1.2.1.2 | Indo-Oceanic | NA | RD239 | 1.0 |
lineage1.2.1.2.1 | Indo-Oceanic | NA | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5327 | p.Pro30Ser | missense_variant | 0.12 |
gyrB | 6057 | p.Ser273Thr | missense_variant | 0.12 |
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrB | 6930 | p.Ala564Val | missense_variant | 0.15 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7473 | p.Ala58Thr | missense_variant | 0.18 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8287 | c.987delT | frameshift_variant | 0.14 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9239 | c.1938C>T | synonymous_variant | 1.0 |
gyrA | 9249 | p.Ala650Thr | missense_variant | 0.12 |
gyrA | 9255 | p.Asn652Asp | missense_variant | 0.12 |
gyrA | 9260 | c.1959G>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9591 | p.Gly764Arg | missense_variant | 0.14 |
fgd1 | 490724 | c.-59G>A | upstream_gene_variant | 0.22 |
fgd1 | 491081 | p.Arg100Leu | missense_variant | 0.12 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
fgd1 | 491761 | p.Asp327Asn | missense_variant | 0.12 |
mshA | 575307 | c.-41G>A | upstream_gene_variant | 0.2 |
mshA | 575368 | c.21T>C | synonymous_variant | 1.0 |
mshA | 575809 | c.462C>T | synonymous_variant | 0.12 |
mshA | 576164 | p.Arg273Cys | missense_variant | 0.33 |
mshA | 576217 | c.873delC | frameshift_variant | 0.25 |
mshA | 576456 | p.Val370Gly | missense_variant | 0.2 |
rpoB | 760867 | p.Gly354Asp | missense_variant | 0.22 |
rpoB | 760999 | p.Met398Thr | missense_variant | 0.4 |
rpoB | 761844 | p.Gln680* | stop_gained | 0.14 |
rpoB | 762198 | p.Gly798Ser | missense_variant | 0.12 |
rpoB | 762409 | p.Ala868Asp | missense_variant | 0.13 |
rpoC | 762524 | c.-846G>A | upstream_gene_variant | 0.18 |
rpoC | 762875 | c.-495C>T | upstream_gene_variant | 0.12 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763198 | p.Val1131Ala | missense_variant | 0.12 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.14 |
rpoC | 763470 | p.Ile34Thr | missense_variant | 0.13 |
rpoC | 763531 | c.162G>C | synonymous_variant | 1.0 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
rpoC | 764117 | p.Glu250* | stop_gained | 0.29 |
rpoC | 765111 | c.1744delG | frameshift_variant | 0.15 |
rpoC | 766110 | p.Pro914Leu | missense_variant | 0.25 |
rpoC | 766147 | c.2778C>G | synonymous_variant | 0.29 |
rpoC | 766463 | p.Gln1032Glu | missense_variant | 0.4 |
rpoC | 766701 | p.Leu1111Pro | missense_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775732 | p.Asp917His | missense_variant | 0.13 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776225 | p.Glu752Asp | missense_variant | 0.12 |
mmpL5 | 776243 | c.2238C>T | synonymous_variant | 0.14 |
mmpL5 | 776430 | p.Arg684His | missense_variant | 0.2 |
mmpL5 | 776503 | p.Glu660Lys | missense_variant | 0.17 |
mmpL5 | 777071 | c.1410G>A | synonymous_variant | 0.25 |
mmpL5 | 778311 | p.Gly57Ala | missense_variant | 0.12 |
mmpL5 | 778483 | c.-3C>T | upstream_gene_variant | 0.17 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781660 | p.Cys34Tyr | missense_variant | 0.15 |
rplC | 800772 | c.-37G>C | upstream_gene_variant | 0.14 |
rplC | 800986 | p.Arg60Cys | missense_variant | 0.17 |
fbiC | 1304503 | p.Leu525Met | missense_variant | 0.17 |
fbiC | 1304596 | p.Asn556Asp | missense_variant | 0.17 |
fbiC | 1304689 | p.Arg587Trp | missense_variant | 0.18 |
Rv1258c | 1406141 | c.1200G>A | synonymous_variant | 0.12 |
Rv1258c | 1406312 | c.1029T>C | synonymous_variant | 1.0 |
Rv1258c | 1406697 | p.Gly215Glu | missense_variant | 0.18 |
embR | 1416259 | c.1089G>C | synonymous_variant | 0.17 |
embR | 1416262 | c.1086G>C | synonymous_variant | 0.14 |
embR | 1416388 | c.959delT | frameshift_variant | 0.17 |
embR | 1416480 | p.Ala290Pro | missense_variant | 0.25 |
embR | 1416639 | p.Asp237Asn | missense_variant | 0.17 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
embR | 1417134 | p.Ile72Val | missense_variant | 0.33 |
embR | 1417280 | p.Ile23Thr | missense_variant | 0.12 |
embR | 1417371 | c.-24A>T | upstream_gene_variant | 0.2 |
atpE | 1460907 | c.-138T>C | upstream_gene_variant | 1.0 |
atpE | 1461219 | c.175T>C | synonymous_variant | 0.1 |
atpE | 1461251 | c.207G>C | synonymous_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473024 | n.1179G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473694 | n.37C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474170 | n.513G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476244 | n.2587G>A | non_coding_transcript_exon_variant | 0.22 |
inhA | 1674057 | c.-145C>T | upstream_gene_variant | 0.22 |
inhA | 1674162 | c.-40C>T | upstream_gene_variant | 1.0 |
rpsA | 1833920 | p.Lys127Glu | missense_variant | 0.12 |
rpsA | 1834015 | c.474G>A | synonymous_variant | 0.13 |
rpsA | 1834260 | p.Leu240Pro | missense_variant | 0.11 |
rpsA | 1834267 | p.Lys243Arg | missense_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918664 | p.Trp242Leu | missense_variant | 0.4 |
ndh | 2102165 | p.Ser293Leu | missense_variant | 0.25 |
ndh | 2102237 | p.Ile269Asn | missense_variant | 0.18 |
ndh | 2102685 | p.Gly120Cys | missense_variant | 0.15 |
ndh | 2102957 | p.Ala29Val | missense_variant | 0.15 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169690 | p.Gly308Val | missense_variant | 0.15 |
PPE35 | 2169695 | p.Gln306His | missense_variant | 0.15 |
Rv1979c | 2222082 | c.1083C>T | synonymous_variant | 0.12 |
Rv1979c | 2222085 | c.1080G>T | synonymous_variant | 0.12 |
Rv1979c | 2222302 | p.Thr288Ile | missense_variant | 0.22 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2222492 | p.Thr225Ala | missense_variant | 0.25 |
Rv1979c | 2222503 | p.Met221Lys | missense_variant | 0.22 |
Rv1979c | 2222654 | p.Ala171Thr | missense_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288681 | c.561A>G | stop_lost&splice_region_variant | 0.29 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2519048 | p.Gly312Ser | missense_variant | 1.0 |
kasA | 2519162 | p.Val350Ile | missense_variant | 0.2 |
eis | 2714819 | p.Arg172Cys | missense_variant | 0.15 |
eis | 2714988 | c.345C>T | synonymous_variant | 0.14 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
ahpC | 2726311 | p.Ser40Asn | missense_variant | 0.18 |
ahpC | 2726428 | p.Asp79Ala | missense_variant | 0.15 |
folC | 2746322 | p.Gly426Ala | missense_variant | 0.2 |
folC | 2746325 | p.Phe425Cys | missense_variant | 0.18 |
folC | 2746641 | p.Gln320* | stop_gained | 0.18 |
folC | 2746890 | c.707_708delGT | frameshift_variant | 0.2 |
folC | 2747524 | c.75G>A | synonymous_variant | 0.22 |
Rv2752c | 3064548 | c.1644G>A | synonymous_variant | 0.12 |
Rv2752c | 3064553 | p.Arg547Cys | missense_variant | 0.12 |
Rv2752c | 3064866 | c.1326G>A | synonymous_variant | 0.25 |
Rv2752c | 3065301 | c.891C>T | synonymous_variant | 0.2 |
Rv2752c | 3066152 | p.Gly14Ser | missense_variant | 0.22 |
thyX | 3067222 | p.Ala242Pro | missense_variant | 0.29 |
thyX | 3067726 | p.Glu74Lys | missense_variant | 0.13 |
thyX | 3067882 | p.Asp22Asn | missense_variant | 0.15 |
thyX | 3068039 | c.-94C>G | upstream_gene_variant | 0.15 |
thyA | 3074357 | p.Ser39Ala | missense_variant | 0.25 |
thyA | 3074385 | c.87G>C | synonymous_variant | 0.4 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087618 | p.Ile267Val | missense_variant | 0.1 |
ald | 3087740 | c.921G>A | synonymous_variant | 0.15 |
fbiD | 3339417 | c.300A>G | synonymous_variant | 1.0 |
fbiD | 3339488 | p.Glu124Ala | missense_variant | 0.11 |
Rv3083 | 3448522 | p.Val7Leu | missense_variant | 0.11 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
Rv3083 | 3448720 | p.Lys73Glu | missense_variant | 0.17 |
Rv3083 | 3449183 | p.Ser227Phe | missense_variant | 0.5 |
Rv3083 | 3449280 | c.777G>A | synonymous_variant | 0.14 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474002 | c.-5C>A | upstream_gene_variant | 0.14 |
fprA | 3474426 | c.420G>A | synonymous_variant | 0.25 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
whiB7 | 3568488 | c.191delG | frameshift_variant | 1.0 |
whiB7 | 3568572 | c.108C>T | synonymous_variant | 0.15 |
whiB7 | 3568646 | c.33dupC | frameshift_variant | 0.18 |
Rv3236c | 3612094 | c.1023C>T | synonymous_variant | 0.17 |
fbiB | 3640557 | c.-978T>C | upstream_gene_variant | 1.0 |
fbiA | 3640652 | p.Ala37Val | missense_variant | 0.29 |
fbiA | 3640679 | p.Asn46Ile | missense_variant | 0.33 |
fbiA | 3640841 | p.Asp100Val | missense_variant | 0.15 |
fbiB | 3641529 | c.-6G>A | upstream_gene_variant | 0.2 |
fbiB | 3642868 | p.Leu445Pro | missense_variant | 0.13 |
alr | 3840212 | c.1209C>T | synonymous_variant | 0.14 |
alr | 3840270 | p.Gly384Ala | missense_variant | 0.22 |
alr | 3840834 | p.His196Leu | missense_variant | 0.17 |
rpoA | 3877492 | c.1015delC | frameshift_variant | 0.17 |
rpoA | 3877591 | p.Leu306Ala | missense_variant | 0.13 |
rpoA | 3877639 | p.Gly290Val | missense_variant | 0.15 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.13 |
ddn | 3986794 | c.-50G>C | upstream_gene_variant | 0.17 |
clpC1 | 4038398 | c.2307G>A | synonymous_variant | 0.15 |
clpC1 | 4038740 | c.1965G>C | synonymous_variant | 0.12 |
clpC1 | 4038752 | p.Gln651His | missense_variant | 0.13 |
clpC1 | 4039924 | p.Tyr261His | missense_variant | 0.12 |
clpC1 | 4039929 | p.Ser259Thr | missense_variant | 0.12 |
clpC1 | 4039932 | p.Gly258Ala | missense_variant | 0.12 |
clpC1 | 4040032 | p.Val225Ile | missense_variant | 0.14 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.14 |
clpC1 | 4040087 | c.618G>A | synonymous_variant | 0.18 |
clpC1 | 4040219 | c.486C>T | synonymous_variant | 0.15 |
clpC1 | 4040356 | p.Glu117Lys | missense_variant | 0.15 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
panD | 4044319 | c.-38G>A | upstream_gene_variant | 0.15 |
embC | 4239677 | c.-186C>T | upstream_gene_variant | 0.14 |
embC | 4239735 | c.-128C>A | upstream_gene_variant | 0.2 |
embC | 4240661 | c.801delG | frameshift_variant | 0.18 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embC | 4242368 | p.Arg836Gly | missense_variant | 0.17 |
embC | 4242416 | p.Gly852Ser | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242904 | p.Asp1014Glu | missense_variant | 0.22 |
embA | 4242964 | c.-269C>T | upstream_gene_variant | 0.25 |
embA | 4243272 | p.Arg14Cys | missense_variant | 0.13 |
embA | 4243291 | p.Ser20Leu | missense_variant | 0.13 |
embA | 4243580 | c.348G>A | synonymous_variant | 1.0 |
embA | 4243703 | c.471C>T | synonymous_variant | 0.15 |
embA | 4244343 | p.Ala371Thr | missense_variant | 0.13 |
embA | 4244420 | c.1188G>C | synonymous_variant | 1.0 |
embA | 4245194 | c.1962G>A | synonymous_variant | 0.12 |
embA | 4245651 | p.Thr807Ala | missense_variant | 0.17 |
embA | 4245660 | p.Ala810Thr | missense_variant | 0.14 |
embA | 4245772 | p.Asn847Ile | missense_variant | 0.14 |
embA | 4245782 | c.2551delA | frameshift_variant | 0.18 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4246567 | c.54_55insT | frameshift_variant | 0.4 |
embB | 4247041 | c.528C>T | synonymous_variant | 1.0 |
embB | 4247105 | p.Pro198Ser | missense_variant | 0.2 |
embB | 4247109 | p.Gly199Glu | missense_variant | 0.2 |
embB | 4247578 | c.1065G>A | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4247875 | c.1362G>T | synonymous_variant | 0.14 |
embB | 4248683 | p.Ala724Ser | missense_variant | 0.13 |
embB | 4248694 | c.2181G>A | synonymous_variant | 0.13 |
embB | 4248699 | p.Gln729Pro | missense_variant | 0.13 |
embB | 4248773 | p.Leu754Phe | missense_variant | 0.13 |
aftB | 4267085 | c.1752G>A | synonymous_variant | 0.15 |
aftB | 4267695 | p.Gly381Glu | missense_variant | 0.24 |
aftB | 4268108 | c.729G>A | synonymous_variant | 0.25 |
aftB | 4268444 | c.393C>T | synonymous_variant | 0.4 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
ubiA | 4269468 | c.365delC | frameshift_variant | 0.15 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ubiA | 4269864 | c.-32delG | upstream_gene_variant | 1.0 |
ethA | 4326228 | p.Thr416Ala | missense_variant | 0.15 |
ethA | 4326350 | p.Ser375Tyr | missense_variant | 0.12 |
ethA | 4327389 | p.Thr29Ala | missense_variant | 0.18 |
ethA | 4327419 | p.Ala19Pro | missense_variant | 0.15 |
ethA | 4328291 | c.-818C>T | upstream_gene_variant | 0.13 |
whiB6 | 4338289 | p.Gly78Glu | missense_variant | 0.15 |
whiB6 | 4338361 | p.Arg54Gln | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
gid | 4407535 | p.Thr223Met | missense_variant | 0.12 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |
gid | 4408107 | p.Glu32Asp | missense_variant | 0.25 |