Run ID: SRR7645929
Sample name:
Date: 04-04-2023 19:59:07
Number of reads: 683720
Percentage reads mapped: 95.43
Strain: lineage2.2.1
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
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 |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.12 | kanamycin, capreomycin, aminoglycosides, amikacin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289202 | p.Cys14Arg | missense_variant | 1.0 | pyrazinamide |
thyX | 3067961 | c.-16C>T | upstream_gene_variant | 1.0 | para-aminosalicylic_acid |
thyA | 3073808 | p.Arg222Gly | missense_variant | 1.0 | para-aminosalicylic_acid |
embB | 4247730 | p.Gly406Asp | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6525 | p.Arg429His | missense_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8952 | p.Gln551* | stop_gained | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 576357 | p.Ala337Val | missense_variant | 0.14 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
ccsA | 620681 | p.Lys264Thr | missense_variant | 0.11 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763041 | p.Leu1079Met | missense_variant | 0.12 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.12 |
rpoC | 763551 | p.Tyr61Ser | missense_variant | 0.13 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.18 |
rpoC | 763578 | p.Phe70Tyr | missense_variant | 0.2 |
rpoC | 766333 | c.2964G>T | synonymous_variant | 0.15 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 1.0 |
rpoC | 766779 | p.Glu1137Gly | 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 |
mmpR5 | 779291 | p.Ala101Val | missense_variant | 0.2 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781478 | c.-82C>T | upstream_gene_variant | 0.12 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
atpE | 1461059 | c.15C>T | synonymous_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473164 | n.1319C>T | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474830 | n.1173A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476091 | n.2434T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.13 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834612 | c.1071G>T | synonymous_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101839 | p.Ala402Thr | missense_variant | 0.13 |
katG | 2154259 | p.Thr618Met | missense_variant | 0.12 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518642 | c.528A>G | synonymous_variant | 0.17 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087494 | c.675C>A | synonymous_variant | 0.12 |
Rv3083 | 3448583 | c.84delC | frameshift_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiB | 3641810 | c.276G>C | synonymous_variant | 1.0 |
alr | 3840576 | p.Ala282Val | missense_variant | 0.16 |
rpoA | 3877773 | c.735G>A | synonymous_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
ubiA | 4269529 | p.Ala102Gly | missense_variant | 0.17 |
ethA | 4326339 | p.Asn379Asp | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |