Run ID: SRR6896296
Sample name:
Date: 04-04-2023 18:01:31
Number of reads: 229132
Percentage reads mapped: 97.5
Strain: lineage2
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761076 | p.Phe424Leu | missense_variant | 0.4 | rifampicin |
ethA | 4327166 | c.306_307delCA | frameshift_variant | 0.13 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5370 | p.His44Pro | missense_variant | 0.15 |
gyrB | 5689 | c.450T>C | synonymous_variant | 0.18 |
gyrB | 5830 | p.Met197Ile | missense_variant | 0.14 |
gyrB | 6158 | p.Thr307Ala | missense_variant | 0.25 |
gyrA | 6346 | c.-956C>T | upstream_gene_variant | 0.15 |
gyrB | 6524 | p.Arg429Ser | missense_variant | 0.11 |
gyrB | 7025 | p.Lys596Glu | missense_variant | 0.17 |
gyrA | 7317 | c.16T>C | synonymous_variant | 0.13 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8353 | p.Gly351Val | missense_variant | 0.33 |
gyrA | 8649 | p.Arg450Cys | missense_variant | 0.14 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9762 | p.Glu821* | stop_gained | 0.5 |
fgd1 | 491006 | p.Leu75Arg | missense_variant | 0.22 |
fgd1 | 491043 | c.261T>C | synonymous_variant | 0.18 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620267 | p.Ala126Glu | missense_variant | 0.22 |
ccsA | 620388 | c.498A>G | synonymous_variant | 0.14 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
ccsA | 620647 | c.759delA | frameshift_variant | 0.5 |
ccsA | 620703 | c.813G>A | synonymous_variant | 0.4 |
rpoB | 759788 | c.-19A>G | upstream_gene_variant | 0.14 |
rpoB | 759999 | p.Arg65Gly | missense_variant | 0.14 |
rpoB | 760405 | p.Pro200Gln | missense_variant | 0.22 |
rpoB | 760868 | c.1062C>A | synonymous_variant | 0.5 |
rpoB | 761229 | p.Gly475Cys | missense_variant | 0.2 |
rpoB | 761723 | c.1917A>G | synonymous_variant | 0.2 |
rpoB | 762835 | p.Gly1010Asp | missense_variant | 0.25 |
rpoC | 762971 | c.-399G>A | upstream_gene_variant | 0.14 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763646 | p.Gly93Ser | missense_variant | 0.2 |
rpoC | 763809 | p.Glu147Ala | missense_variant | 0.25 |
rpoC | 765846 | p.Asn826Ser | missense_variant | 0.2 |
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 | 776797 | p.Val562Ile | missense_variant | 0.11 |
mmpR5 | 778070 | c.-920G>A | upstream_gene_variant | 0.33 |
mmpL5 | 778959 | c.-479T>C | upstream_gene_variant | 0.13 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
mmpS5 | 779656 | c.-751G>T | upstream_gene_variant | 0.22 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781428 | c.-132C>A | upstream_gene_variant | 0.29 |
rplC | 800660 | c.-148delA | upstream_gene_variant | 0.22 |
fbiC | 1303309 | p.Glu127* | stop_gained | 0.13 |
fbiC | 1303404 | c.474A>G | synonymous_variant | 0.18 |
fbiC | 1304263 | p.Gly445Cys | missense_variant | 0.29 |
fbiC | 1304669 | p.Ser580Leu | missense_variant | 0.18 |
fbiC | 1305207 | c.2277C>A | synonymous_variant | 0.38 |
fbiC | 1305243 | c.2313T>C | synonymous_variant | 0.33 |
fbiC | 1305268 | p.Arg780Ser | missense_variant | 0.33 |
fbiC | 1305272 | p.Ile781Thr | missense_variant | 0.33 |
fbiC | 1305481 | p.Tyr851Asn | missense_variant | 0.25 |
Rv1258c | 1406107 | p.Asp412Asn | missense_variant | 0.22 |
Rv1258c | 1406291 | c.1050G>T | synonymous_variant | 0.33 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1406827 | p.Thr172Ala | missense_variant | 0.25 |
Rv1258c | 1407313 | p.Phe10Val | missense_variant | 0.13 |
embR | 1416291 | c.1055_1056dupTG | frameshift_variant | 0.15 |
embR | 1416383 | c.964delA | frameshift_variant | 0.25 |
embR | 1416632 | c.715delC | frameshift_variant | 0.25 |
embR | 1417460 | c.-113G>C | upstream_gene_variant | 0.67 |
atpE | 1461193 | p.Phe50Ser | missense_variant | 0.17 |
atpE | 1461220 | p.Leu59Ser | missense_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471790 | n.-56T>C | upstream_gene_variant | 0.12 |
rrs | 1472072 | n.227A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472499 | n.654A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472530 | n.685G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472677 | n.834delT | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474005 | n.348T>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474115 | n.458C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474195 | n.538A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474265 | n.608G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474305 | n.649delA | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474810 | n.1153G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474921 | n.1268delG | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475001 | n.1344A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475387 | n.1733delA | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475593 | n.1941delG | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475627 | n.1970G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475635 | n.1978G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476065 | n.2408A>G | non_coding_transcript_exon_variant | 0.11 |
fabG1 | 1673315 | c.-125_-124insGG | upstream_gene_variant | 0.67 |
fabG1 | 1674183 | c.744A>G | stop_lost&splice_region_variant | 0.29 |
rpsA | 1833646 | c.105T>C | synonymous_variant | 1.0 |
rpsA | 1834170 | c.631_633delATC | conservative_inframe_deletion | 0.2 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1918739 | p.Gly267Val | missense_variant | 0.25 |
ndh | 2102620 | c.423C>A | synonymous_variant | 0.25 |
ndh | 2102821 | c.222C>A | synonymous_variant | 0.18 |
ndh | 2102838 | p.Ala69Ser | missense_variant | 0.22 |
katG | 2154163 | p.Ser650Tyr | missense_variant | 0.18 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168697 | p.Ile639Thr | missense_variant | 0.13 |
PPE35 | 2168801 | c.1812A>G | synonymous_variant | 0.13 |
PPE35 | 2169092 | c.1521G>T | synonymous_variant | 0.29 |
PPE35 | 2169675 | p.Asn313Ser | missense_variant | 0.11 |
Rv1979c | 2221724 | p.Arg481Gly | missense_variant | 0.22 |
Rv1979c | 2221822 | p.Ser448* | stop_gained | 0.15 |
Rv1979c | 2221863 | p.Tyr434* | stop_gained | 0.17 |
Rv1979c | 2222129 | p.Tyr346His | missense_variant | 0.2 |
Rv1979c | 2222570 | p.Ala199Ser | missense_variant | 0.14 |
Rv1979c | 2223002 | p.Gly55Arg | missense_variant | 0.29 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288865 | p.Asp126Val | missense_variant | 0.25 |
pncA | 2289831 | c.-590A>G | upstream_gene_variant | 0.5 |
kasA | 2517943 | c.-172A>G | upstream_gene_variant | 0.18 |
kasA | 2518259 | p.Glu49* | stop_gained | 0.33 |
eis | 2714195 | p.Ser380Pro | missense_variant | 0.18 |
eis | 2714659 | p.Leu225Pro | missense_variant | 0.4 |
eis | 2714690 | p.Phe215Leu | missense_variant | 0.33 |
eis | 2714829 | c.504C>A | synonymous_variant | 0.2 |
eis | 2714839 | p.Leu165Ser | missense_variant | 0.2 |
ahpC | 2726167 | c.-26T>G | upstream_gene_variant | 0.2 |
ahpC | 2726388 | p.Ala66Pro | missense_variant | 0.13 |
ahpC | 2726436 | p.Ile82Val | missense_variant | 0.13 |
folC | 2746491 | p.Phe370Leu | missense_variant | 0.18 |
folC | 2747775 | c.-177C>T | upstream_gene_variant | 0.2 |
pepQ | 2859738 | c.681C>T | synonymous_variant | 0.22 |
pepQ | 2859797 | p.Thr208Ser | missense_variant | 0.18 |
pepQ | 2860485 | c.-67C>T | upstream_gene_variant | 0.33 |
ribD | 2986936 | c.100_104dupTATCC | frameshift_variant | 0.33 |
ribD | 2987574 | p.Asp246Tyr | missense_variant | 0.2 |
Rv2752c | 3064602 | c.1590T>C | synonymous_variant | 0.29 |
Rv2752c | 3065036 | p.Asn386His | missense_variant | 0.5 |
thyX | 3067801 | p.Lys49Glu | missense_variant | 0.4 |
thyX | 3068043 | c.-98A>G | upstream_gene_variant | 0.25 |
thyA | 3073756 | p.Phe239Ser | missense_variant | 0.2 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087015 | c.198delC | frameshift_variant | 0.5 |
ald | 3087728 | c.909C>A | synonymous_variant | 0.12 |
Rv3083 | 3448422 | c.-82T>C | upstream_gene_variant | 0.22 |
Rv3083 | 3448471 | c.-33T>C | upstream_gene_variant | 0.2 |
Rv3083 | 3448840 | p.Gln113Glu | missense_variant | 0.33 |
fprA | 3473928 | c.-79T>G | upstream_gene_variant | 0.22 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474048 | c.42G>A | synonymous_variant | 0.5 |
fprA | 3474961 | p.Val319Leu | missense_variant | 1.0 |
whiB7 | 3568704 | c.-28_-26delCCA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
Rv3236c | 3612816 | p.Ala101Thr | missense_variant | 0.29 |
fbiA | 3640810 | c.269delA | frameshift_variant | 0.25 |
fbiA | 3641470 | p.Met310Val | missense_variant | 1.0 |
fbiB | 3641718 | p.Pro62Ser | missense_variant | 0.25 |
fbiB | 3641977 | p.Ile148Thr | missense_variant | 0.22 |
alr | 3840357 | p.Leu355Pro | missense_variant | 0.29 |
alr | 3841116 | p.Ala102Val | missense_variant | 0.4 |
rpoA | 3877804 | p.Gly235Val | missense_variant | 0.33 |
rpoA | 3878278 | p.Ile77Thr | missense_variant | 0.22 |
rpoA | 3878411 | p.Thr33Ala | missense_variant | 0.2 |
clpC1 | 4038512 | c.2193C>A | synonymous_variant | 0.22 |
clpC1 | 4038954 | p.Glu584Gly | missense_variant | 0.25 |
clpC1 | 4039625 | p.Lys360Asn | missense_variant | 0.25 |
clpC1 | 4040396 | c.309C>T | synonymous_variant | 0.15 |
panD | 4043998 | p.Asp95Gly | missense_variant | 0.5 |
embC | 4239774 | c.-89C>A | upstream_gene_variant | 0.33 |
embC | 4239880 | c.18C>T | synonymous_variant | 0.33 |
embC | 4240470 | p.Asp203Gly | missense_variant | 0.67 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242868 | c.-365C>A | upstream_gene_variant | 0.33 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4244414 | c.1182G>C | synonymous_variant | 1.0 |
embA | 4244689 | p.Lys486Arg | missense_variant | 0.18 |
embA | 4244746 | p.Leu505Pro | missense_variant | 0.4 |
embA | 4246392 | c.3164delG | frameshift_variant | 0.25 |
embB | 4247817 | p.Val435Ala | missense_variant | 0.25 |
embB | 4248395 | p.Phe628Leu | missense_variant | 0.22 |
embB | 4248434 | p.Ala641Ser | missense_variant | 0.18 |
embB | 4249548 | p.Phe1012Ser | missense_variant | 0.29 |
aftB | 4267500 | p.Pro446Leu | missense_variant | 0.2 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268143 | p.Tyr232His | missense_variant | 0.25 |
aftB | 4268291 | p.Ser182Arg | missense_variant | 0.2 |
ethA | 4326216 | p.Glu420* | stop_gained | 0.17 |
ethA | 4326345 | p.Ile377Val | missense_variant | 0.15 |
ethA | 4326404 | p.Asp357Gly | missense_variant | 0.14 |
ethA | 4326441 | p.Asn345His | missense_variant | 0.12 |
ethA | 4326498 | c.976C>A | synonymous_variant | 0.12 |
ethA | 4326552 | p.Gly308Trp | missense_variant | 0.18 |
ethA | 4326720 | p.Ala252Pro | missense_variant | 0.33 |
ethR | 4326778 | c.-771G>A | upstream_gene_variant | 0.2 |
ethA | 4326840 | p.Ile212Val | missense_variant | 0.14 |
ethA | 4327062 | p.Ser138Arg | missense_variant | 0.22 |
ethA | 4327158 | p.Ser106Gly | missense_variant | 0.13 |
ethA | 4328206 | c.-734delA | upstream_gene_variant | 0.22 |
whiB6 | 4338473 | c.49A>C | synonymous_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338668 | c.-148delC | upstream_gene_variant | 0.14 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407603 | c.600G>A | synonymous_variant | 0.33 |
gid | 4407620 | p.Tyr195His | missense_variant | 1.0 |
gid | 4407762 | p.Lys147Asn | missense_variant | 0.33 |
gid | 4407870 | c.333C>T | synonymous_variant | 0.22 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |
gid | 4408440 | c.-238C>G | upstream_gene_variant | 0.5 |