Run ID: SRR1172987
Sample name:
Date: 03-04-2023 03:14:21
Number of reads: 169824
Percentage reads mapped: 13.65
Strain: lineage4.9
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 0.8 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.8 | streptomycin |
rrs | 1473246 | n.1401A>G | non_coding_transcript_exon_variant | 0.3 | kanamycin, capreomycin, aminoglycosides, amikacin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
embA | 4243217 | c.-16C>G | upstream_gene_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8672 | c.1371A>G | synonymous_variant | 0.4 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9489 | p.Gly730Cys | missense_variant | 1.0 |
gyrA | 9764 | p.Glu821Asp | missense_variant | 0.29 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 0.8 |
rpoB | 760060 | p.Tyr85Leu | missense_variant | 0.67 |
rpoB | 760067 | c.261G>C | synonymous_variant | 0.4 |
rpoB | 760070 | c.264T>G | synonymous_variant | 0.4 |
rpoB | 760091 | c.285G>C | synonymous_variant | 0.33 |
rpoB | 760101 | c.295T>C | synonymous_variant | 0.33 |
rpoB | 760112 | c.306T>C | synonymous_variant | 0.33 |
rpoB | 760118 | c.312T>G | synonymous_variant | 0.5 |
rpoB | 760121 | c.315T>C | synonymous_variant | 0.5 |
rpoB | 760130 | p.Asp108Glu | missense_variant | 0.5 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.25 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 0.75 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.4 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.67 |
rpoC | 762932 | c.-438G>T | upstream_gene_variant | 0.6 |
rpoC | 762938 | c.-432G>C | upstream_gene_variant | 0.33 |
rpoC | 762944 | c.-426C>T | upstream_gene_variant | 0.33 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.4 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 0.4 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.67 |
rpoC | 763067 | c.-303C>G | upstream_gene_variant | 0.4 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.4 |
rpoB | 763074 | p.Thr1090Val | missense_variant | 0.4 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.33 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.5 |
rpoC | 765404 | p.Leu679Val | missense_variant | 0.5 |
rpoC | 765409 | c.2040T>C | synonymous_variant | 0.33 |
rpoC | 765451 | c.2082C>A | synonymous_variant | 0.25 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.33 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.6 |
rpoC | 765529 | c.2160C>T | synonymous_variant | 0.75 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 1.0 |
rpoC | 766378 | c.3009C>T | synonymous_variant | 0.5 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.4 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.4 |
rpoC | 766387 | c.3018C>G | synonymous_variant | 0.4 |
rpoC | 766408 | c.3039C>T | synonymous_variant | 0.5 |
rpoC | 766411 | c.3042C>G | synonymous_variant | 0.5 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777094 | p.Leu463Val | missense_variant | 1.0 |
mmpL5 | 777751 | p.Arg244Cys | missense_variant | 0.4 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800814 | c.6A>G | synonymous_variant | 0.29 |
rplC | 800817 | c.9A>T | synonymous_variant | 0.29 |
fbiC | 1304937 | c.2007G>C | synonymous_variant | 0.5 |
fbiC | 1304958 | c.2028T>G | synonymous_variant | 0.5 |
rrs | 1472069 | n.224G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472123 | n.278A>G | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472150 | n.305T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472504 | n.659A>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472505 | n.660G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472574 | n.729T>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472836 | n.991G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472874 | n.1029C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472875 | n.1030T>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472974 | n.1129A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472977 | n.1133dupT | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473089 | n.1244A>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473346 | n.1501G>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1473697 | n.40C>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473698 | n.41G>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473699 | n.42A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473718 | n.61G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473840 | n.183A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473884 | n.227C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473888 | n.231T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473889 | n.232G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473896 | n.239C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473899 | n.242A>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1473911 | n.254G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474093 | n.436G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474099 | n.442G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474130 | n.473C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474199 | n.542G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474202 | n.545T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474253 | n.596A>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474351 | n.694G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474527 | n.870T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474542 | n.885A>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474784 | n.1127C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474798 | n.1141C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474803 | n.1146G>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474825 | n.1168G>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474837 | n.1180A>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474901 | n.1244A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474921 | n.1264C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475562 | n.1905C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475659 | n.2002G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475713 | n.2056C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475757 | n.2101_2104delACCC | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475902 | n.2245T>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475993 | n.2336C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476080 | n.2423T>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476085 | n.2428G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476251 | n.2594T>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476298 | n.2641C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476300 | n.2643G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476307 | n.2650A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476309 | n.2652G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476535 | n.2878G>A | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.5 |
rpsA | 1834096 | c.555G>C | synonymous_variant | 0.2 |
rpsA | 1834099 | c.558C>G | synonymous_variant | 0.2 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.3 |
rpsA | 1834105 | c.564C>G | synonymous_variant | 0.25 |
rpsA | 1834108 | c.567C>G | synonymous_variant | 0.25 |
rpsA | 1834123 | c.582C>G | synonymous_variant | 0.33 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.67 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.67 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.67 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.67 |
rpsA | 1834510 | c.969C>T | synonymous_variant | 0.67 |
rpsA | 1834513 | c.972C>G | synonymous_variant | 0.67 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1917987 | c.48G>A | synonymous_variant | 0.4 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2168715 | p.Gln633Pro | missense_variant | 0.33 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
kasA | 2518093 | c.-22C>A | upstream_gene_variant | 0.4 |
kasA | 2518162 | c.48G>A | synonymous_variant | 0.29 |
kasA | 2518174 | c.60A>G | synonymous_variant | 0.33 |
kasA | 2518754 | p.Arg214Trp | missense_variant | 0.25 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
folC | 2747355 | p.Val82Ile | missense_variant | 0.67 |
folC | 2747359 | c.240C>G | synonymous_variant | 0.67 |
folC | 2747362 | c.237G>C | synonymous_variant | 0.67 |
folC | 2747394 | p.Ile69Val | missense_variant | 0.5 |
folC | 2747395 | c.204T>C | synonymous_variant | 0.5 |
Rv2752c | 3066118 | p.Asn25Ser | missense_variant | 0.29 |
thyX | 3067349 | c.597G>C | synonymous_variant | 0.67 |
thyX | 3067355 | c.591A>C | synonymous_variant | 0.67 |
thyA | 3074439 | c.33G>T | synonymous_variant | 0.67 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087817 | p.Cys333Phe | missense_variant | 0.29 |
Rv3083 | 3449029 | p.Ser176Ala | missense_variant | 0.33 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568670 | c.10C>T | synonymous_variant | 1.0 |
rpoA | 3878698 | c.-191A>G | upstream_gene_variant | 1.0 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.6 |
clpC1 | 4038623 | c.2082A>G | synonymous_variant | 0.67 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.67 |
clpC1 | 4038845 | c.1860G>C | synonymous_variant | 1.0 |
clpC1 | 4038951 | p.Phe585Cys | missense_variant | 0.29 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.29 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 0.4 |
embC | 4241140 | c.1278A>G | synonymous_variant | 0.4 |
embC | 4241146 | c.1284C>G | synonymous_variant | 0.4 |
embC | 4241170 | c.1308G>C | synonymous_variant | 0.4 |
embC | 4241173 | c.1311C>T | synonymous_variant | 0.4 |
embC | 4241179 | c.1317G>A | synonymous_variant | 0.4 |
embC | 4241203 | c.1341T>C | synonymous_variant | 0.33 |
embC | 4241206 | c.1344G>C | synonymous_variant | 0.4 |
embC | 4241218 | c.1356G>C | synonymous_variant | 0.4 |
embC | 4241479 | c.1617C>G | synonymous_variant | 0.4 |
embC | 4241480 | c.1618T>C | synonymous_variant | 0.4 |
embC | 4241488 | c.1626G>C | synonymous_variant | 0.4 |
embC | 4242075 | p.Arg738Gln | missense_variant | 0.67 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245101 | c.1869G>C | synonymous_variant | 0.5 |
embA | 4245137 | c.1905T>C | synonymous_variant | 0.5 |
embB | 4246055 | c.-459T>C | upstream_gene_variant | 0.22 |
embB | 4246064 | c.-450T>C | upstream_gene_variant | 0.22 |
embA | 4246080 | p.Pro950Ser | missense_variant | 0.22 |
embB | 4246088 | c.-426A>G | upstream_gene_variant | 0.22 |
embB | 4247655 | p.Lys381Thr | missense_variant | 0.4 |
aftB | 4269390 | c.-554G>T | upstream_gene_variant | 0.67 |
whiB6 | 4338262 | p.Ala87Glu | missense_variant | 0.5 |
whiB6 | 4338371 | p.Thr51Pro | missense_variant | 0.4 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407758 | p.Ser149Arg | missense_variant | 1.0 |