Run ID: SRR8791320
Sample name:
Date: 04-04-2023 21:56:25
Number of reads: 235022
Percentage reads mapped: 98.83
Strain:
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7582 | p.Asp94Gly | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
rrs | 1473246 | n.1401A>G | non_coding_transcript_exon_variant | 1.0 | kanamycin, capreomycin, aminoglycosides, amikacin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289054 | p.Asp63Ala | missense_variant | 1.0 | pyrazinamide |
ddn | 3987106 | p.Trp88* | stop_gained | 1.0 | delamanid |
embB | 4247574 | p.Asp354Ala | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5206 | c.-34C>A | upstream_gene_variant | 0.33 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8266 | p.Ala322Val | missense_variant | 0.33 |
gyrA | 8380 | p.Gln360Arg | missense_variant | 0.29 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9431 | c.2130G>T | synonymous_variant | 0.33 |
gyrA | 9476 | c.2175G>T | synonymous_variant | 0.33 |
gyrA | 9484 | p.Ser728* | stop_gained | 0.33 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575339 | c.-9C>T | upstream_gene_variant | 0.33 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620447 | p.Phe186Ser | missense_variant | 0.17 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
ccsA | 620725 | p.Leu279Met | missense_variant | 0.2 |
rpoB | 760177 | p.Ala124Glu | missense_variant | 0.25 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 765179 | p.Gly604Trp | missense_variant | 0.25 |
rpoC | 765546 | p.Arg726His | missense_variant | 1.0 |
rpoC | 765680 | p.Asn771Asp | missense_variant | 0.5 |
rpoC | 765698 | p.Ile777Val | missense_variant | 0.5 |
rpoC | 766802 | p.Gln1145* | stop_gained | 0.25 |
rpoC | 767102 | p.Leu1245Ile | missense_variant | 0.5 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 777484 | p.Gln333Lys | missense_variant | 0.25 |
mmpL5 | 778231 | p.Glu84* | stop_gained | 0.29 |
mmpR5 | 778238 | c.-752C>A | upstream_gene_variant | 0.22 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1302889 | c.-42G>T | upstream_gene_variant | 1.0 |
fbiC | 1303547 | p.Pro206Gln | missense_variant | 0.5 |
fbiC | 1304164 | p.Gly412* | stop_gained | 0.2 |
fbiC | 1304585 | p.Ile552Asn | missense_variant | 0.25 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1406894 | c.447C>T | synonymous_variant | 0.4 |
rrs | 1471656 | n.-190G>T | upstream_gene_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472115 | n.270C>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472148 | n.303T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472313 | n.468G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474164 | n.507C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474590 | n.933A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474798 | n.1141C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474933 | n.1276A>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475637 | n.1980T>C | non_coding_transcript_exon_variant | 0.22 |
fabG1 | 1673165 | c.-275A>G | upstream_gene_variant | 1.0 |
inhA | 1674629 | p.Ser143Tyr | missense_variant | 0.25 |
inhA | 1674673 | p.Tyr158His | missense_variant | 0.25 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834934 | p.Ala465Ser | missense_variant | 0.33 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102071 | c.972C>A | synonymous_variant | 0.25 |
ndh | 2102114 | p.Ser310Tyr | missense_variant | 0.25 |
ndh | 2102591 | p.Ile151Thr | missense_variant | 0.25 |
ndh | 2102850 | p.Glu65Lys | missense_variant | 1.0 |
katG | 2154045 | p.Trp689Cys | missense_variant | 0.29 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155529 | p.Glu195* | stop_gained | 0.5 |
katG | 2155834 | p.Ala93Gly | missense_variant | 0.67 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168288 | c.2325C>A | synonymous_variant | 0.29 |
PPE35 | 2168326 | p.Asp763Asn | missense_variant | 0.29 |
PPE35 | 2168435 | c.2178C>A | synonymous_variant | 0.33 |
PPE35 | 2168494 | p.Gly707Cys | missense_variant | 0.4 |
PPE35 | 2169057 | p.Pro519Arg | missense_variant | 0.4 |
PPE35 | 2169926 | c.687C>T | synonymous_variant | 0.29 |
Rv1979c | 2221809 | c.1356C>A | synonymous_variant | 0.15 |
Rv1979c | 2222520 | p.Lys215Asn | missense_variant | 0.33 |
Rv1979c | 2222845 | p.Gly107Val | missense_variant | 0.18 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288937 | p.Ala102Val | missense_variant | 0.33 |
pncA | 2289906 | c.-665T>C | upstream_gene_variant | 0.33 |
kasA | 2518887 | p.Gly258Asp | missense_variant | 0.25 |
eis | 2714155 | p.Asp393Gly | missense_variant | 0.33 |
ribD | 2987035 | p.Gly66Asp | missense_variant | 0.22 |
ribD | 2987230 | p.Ala131Val | missense_variant | 0.2 |
Rv2752c | 3065966 | p.Ala76Ser | missense_variant | 0.5 |
Rv2752c | 3066275 | c.-84G>A | upstream_gene_variant | 0.33 |
thyX | 3067634 | c.312C>A | synonymous_variant | 0.33 |
thyX | 3067662 | p.Arg95Leu | missense_variant | 0.25 |
thyA | 3073928 | p.Ala182Ser | missense_variant | 0.25 |
thyA | 3074264 | p.Gly70Ser | missense_variant | 0.2 |
ald | 3086731 | c.-89A>G | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087018 | p.Asp67Asn | missense_variant | 0.33 |
fbiD | 3339614 | p.Ser166* | stop_gained | 0.5 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474342 | c.336G>A | synonymous_variant | 0.4 |
fprA | 3474412 | p.Pro136Thr | missense_variant | 0.17 |
Rv3236c | 3613149 | c.-33G>T | upstream_gene_variant | 0.25 |
alr | 3841078 | p.Pro115Thr | missense_variant | 0.17 |
alr | 3841115 | c.306T>G | synonymous_variant | 0.17 |
rpoA | 3877956 | p.Glu184Asp | missense_variant | 1.0 |
ddn | 3987084 | p.Gly81Cys | missense_variant | 0.33 |
clpC1 | 4038646 | p.Glu687* | stop_gained | 0.14 |
clpC1 | 4039591 | p.Val372Leu | missense_variant | 0.18 |
clpC1 | 4040479 | p.Gly76Arg | missense_variant | 0.4 |
clpC1 | 4040724 | c.-20G>T | upstream_gene_variant | 0.25 |
embC | 4240478 | p.Gly206Trp | missense_variant | 0.25 |
embC | 4240542 | p.Thr227Lys | missense_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243346 | c.114A>G | synonymous_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4244401 | p.Leu390Pro | missense_variant | 1.0 |
embB | 4245956 | c.-558G>T | upstream_gene_variant | 0.5 |
embA | 4246425 | p.Pro1065Ser | missense_variant | 0.5 |
embB | 4248903 | p.Thr797Lys | missense_variant | 0.25 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268623 | p.Trp72Arg | missense_variant | 0.5 |
ubiA | 4269707 | p.Gly43Ser | missense_variant | 0.2 |
ubiA | 4269756 | p.Trp26Cys | missense_variant | 0.2 |
ubiA | 4269882 | c.-49G>T | upstream_gene_variant | 0.18 |
whiB6 | 4338185 | p.Ala113Pro | missense_variant | 0.5 |
whiB6 | 4338371 | p.Thr51Pro | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |