Run ID: ERR2245360
Sample name:
Date: 31-03-2023 17:39:32
Number of reads: 1690755
Percentage reads mapped: 98.87
Strain: lineage3.1.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
lineage3.1.1 | East-African-Indian | CAS1-Kili | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5443 | c.204G>T | synonymous_variant | 0.18 |
gyrB | 5699 | p.Glu154* | stop_gained | 0.27 |
gyrB | 5747 | p.Thr170Ala | missense_variant | 0.22 |
gyrB | 6350 | p.Thr371Ala | missense_variant | 0.18 |
gyrB | 6393 | p.Gln385Leu | missense_variant | 0.18 |
gyrB | 6437 | p.Pro400Thr | missense_variant | 0.3 |
gyrA | 6739 | c.-563C>A | upstream_gene_variant | 0.22 |
gyrB | 6993 | p.Arg585His | missense_variant | 0.17 |
gyrA | 7147 | c.-155G>T | upstream_gene_variant | 0.4 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7503 | p.Arg68Cys | missense_variant | 0.33 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8917 | p.Arg539Leu | missense_variant | 0.18 |
gyrA | 8925 | p.Lys542Glu | missense_variant | 0.17 |
gyrA | 8978 | c.1677C>T | synonymous_variant | 0.17 |
gyrA | 9003 | p.Leu568Val | missense_variant | 0.2 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9780 | p.Ala827Thr | missense_variant | 0.22 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
fgd1 | 491757 | p.Gln325His | missense_variant | 0.25 |
mshA | 575920 | c.573C>A | synonymous_variant | 0.5 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.38 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 760078 | p.Glu91Gly | missense_variant | 0.29 |
rpoB | 760290 | p.Ile162Phe | missense_variant | 0.33 |
rpoB | 760481 | c.675G>A | synonymous_variant | 0.29 |
rpoB | 760638 | p.Gly278Cys | missense_variant | 0.22 |
rpoB | 760658 | p.Glu284Asp | missense_variant | 0.22 |
rpoB | 760749 | p.Gly315Trp | missense_variant | 0.2 |
rpoB | 761267 | p.Asn487Lys | missense_variant | 0.33 |
rpoB | 761961 | p.Pro719Thr | missense_variant | 0.22 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763117 | p.Glu1104Ala | missense_variant | 0.4 |
rpoB | 763263 | p.Ala1153Thr | missense_variant | 0.14 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.2 |
rpoC | 763865 | p.Arg166Cys | missense_variant | 0.29 |
rpoC | 764234 | p.Lys289Gln | missense_variant | 0.22 |
rpoC | 764912 | p.Met515Val | missense_variant | 0.17 |
rpoC | 765237 | p.Asp623Ala | missense_variant | 0.5 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776073 | p.Val803Gly | missense_variant | 0.2 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpR5 | 778106 | c.-884G>T | upstream_gene_variant | 0.29 |
mmpS5 | 778799 | p.Gly36Val | missense_variant | 0.14 |
mmpR5 | 779082 | p.Ser31Arg | missense_variant | 0.17 |
mmpR5 | 779322 | p.Met111Ile | missense_variant | 0.17 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781688 | p.Lys43Asn | missense_variant | 0.13 |
fbiC | 1304645 | p.Gly572Val | missense_variant | 0.33 |
fbiC | 1304914 | p.Asp662Tyr | missense_variant | 0.22 |
fbiC | 1305183 | p.Leu751Phe | missense_variant | 0.18 |
fbiC | 1305286 | p.Thr786Ser | missense_variant | 0.4 |
Rv1258c | 1406504 | c.837C>T | synonymous_variant | 0.4 |
Rv1258c | 1406873 | c.468C>T | synonymous_variant | 0.29 |
Rv1258c | 1407068 | c.273G>T | synonymous_variant | 0.25 |
embR | 1416459 | p.Ser297Thr | missense_variant | 0.5 |
embR | 1416837 | p.Val171Ile | missense_variant | 0.4 |
embR | 1417194 | p.Val52Ile | missense_variant | 0.25 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472717 | n.872C>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473314 | n.1469A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475513 | n.1856T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476336 | n.2679C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476558 | n.2901G>T | non_coding_transcript_exon_variant | 0.33 |
inhA | 1673925 | c.-277C>A | upstream_gene_variant | 1.0 |
rpsA | 1833969 | p.Gly143Val | missense_variant | 0.25 |
rpsA | 1834335 | c.795delC | frameshift_variant | 0.22 |
rpsA | 1834962 | p.Arg474Gln | missense_variant | 0.4 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1917982 | p.Gly15Cys | missense_variant | 0.29 |
tlyA | 1918176 | c.237C>A | synonymous_variant | 0.4 |
katG | 2154177 | c.1935G>A | synonymous_variant | 0.25 |
katG | 2154548 | p.Glu522* | stop_gained | 0.25 |
katG | 2154974 | p.Thr380Ser | missense_variant | 0.33 |
katG | 2155302 | c.810C>T | synonymous_variant | 0.4 |
katG | 2156306 | c.-195C>A | upstream_gene_variant | 0.18 |
katG | 2156335 | c.-224C>A | upstream_gene_variant | 0.25 |
katG | 2156454 | c.-343G>T | upstream_gene_variant | 0.17 |
katG | 2156551 | c.-440C>A | upstream_gene_variant | 0.33 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168018 | c.2595C>A | synonymous_variant | 0.29 |
PPE35 | 2168876 | p.Phe579Leu | missense_variant | 0.29 |
PPE35 | 2168882 | c.1731T>A | synonymous_variant | 0.25 |
PPE35 | 2169498 | p.Phe372Ser | missense_variant | 0.12 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.17 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.17 |
PPE35 | 2170059 | p.Val185Gly | missense_variant | 0.18 |
PPE35 | 2170141 | p.Ala158Ser | missense_variant | 0.5 |
PPE35 | 2170439 | p.Gln58His | missense_variant | 0.4 |
PPE35 | 2170461 | p.Gly51Glu | missense_variant | 1.0 |
Rv1979c | 2222032 | p.Ala378Val | missense_variant | 0.25 |
Rv1979c | 2222226 | p.Phe313Leu | missense_variant | 0.33 |
Rv1979c | 2222423 | p.Pro248Ala | missense_variant | 0.29 |
Rv1979c | 2222918 | p.Thr83Pro | missense_variant | 0.18 |
Rv1979c | 2223195 | c.-31A>T | upstream_gene_variant | 0.22 |
Rv1979c | 2223291 | c.-127G>T | upstream_gene_variant | 0.33 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289059 | c.183A>C | synonymous_variant | 0.25 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
pncA | 2289933 | c.-692G>T | upstream_gene_variant | 0.25 |
kasA | 2518288 | c.174C>A | synonymous_variant | 0.17 |
eis | 2714568 | c.765C>A | synonymous_variant | 0.17 |
eis | 2715570 | c.-238C>T | upstream_gene_variant | 0.33 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
folC | 2746302 | p.Ala433Ser | missense_variant | 0.33 |
folC | 2746439 | p.Val387Ala | missense_variant | 0.4 |
folC | 2747081 | p.Val173Gly | missense_variant | 0.29 |
folC | 2747132 | p.Thr156Ile | missense_variant | 0.22 |
pepQ | 2859912 | p.Glu169Asp | missense_variant | 0.25 |
pepQ | 2860159 | p.Ala87Val | missense_variant | 0.33 |
pepQ | 2860586 | c.-168C>A | upstream_gene_variant | 0.5 |
ribD | 2987412 | p.Thr192Ala | missense_variant | 0.4 |
Rv2752c | 3064566 | c.1626G>C | synonymous_variant | 0.33 |
Rv2752c | 3065800 | p.Gly131Ala | missense_variant | 0.18 |
thyX | 3067479 | p.Asp156Ala | missense_variant | 0.4 |
thyA | 3074506 | c.-35C>A | upstream_gene_variant | 0.2 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087456 | p.Gly213Cys | missense_variant | 0.29 |
fbiD | 3339605 | p.Gly163Val | missense_variant | 0.29 |
fbiD | 3339727 | p.Gly204Trp | missense_variant | 0.4 |
Rv3083 | 3448668 | c.165G>T | synonymous_variant | 0.5 |
Rv3083 | 3448948 | p.Tyr149Asn | missense_variant | 0.4 |
Rv3083 | 3449171 | p.Val223Gly | missense_variant | 0.33 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474445 | p.Gly147Cys | missense_variant | 0.18 |
fprA | 3475275 | p.Trp423Cys | missense_variant | 0.4 |
fbiA | 3641015 | p.Asp158Ala | missense_variant | 0.25 |
fbiB | 3641866 | p.Ser111Tyr | missense_variant | 0.4 |
rpoA | 3877495 | p.Glu338Ala | missense_variant | 0.33 |
rpoA | 3878144 | p.Gly122Cys | missense_variant | 0.29 |
rpoA | 3878164 | p.Gly115Val | missense_variant | 0.2 |
rpoA | 3878490 | c.18C>G | synonymous_variant | 0.5 |
clpC1 | 4038538 | p.Thr723Pro | missense_variant | 0.4 |
clpC1 | 4038893 | c.1812C>T | synonymous_variant | 0.29 |
clpC1 | 4039031 | c.1674T>C | synonymous_variant | 0.17 |
clpC1 | 4039045 | p.Pro554Thr | missense_variant | 0.18 |
clpC1 | 4039109 | c.1596C>A | synonymous_variant | 0.2 |
clpC1 | 4039730 | c.975C>G | synonymous_variant | 0.29 |
clpC1 | 4039892 | p.Lys271Asn | missense_variant | 0.29 |
clpC1 | 4040344 | p.Ala121Thr | missense_variant | 0.4 |
clpC1 | 4040500 | p.Gln69Lys | missense_variant | 0.18 |
embC | 4240084 | c.222G>T | synonymous_variant | 0.25 |
embC | 4240172 | p.Val104Met | missense_variant | 1.0 |
embC | 4240290 | p.Pro143Gln | missense_variant | 0.25 |
embC | 4241491 | c.1629G>T | synonymous_variant | 0.29 |
embC | 4241562 | p.Arg567His | missense_variant | 1.0 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243899 | p.Ala223Ser | missense_variant | 0.33 |
embA | 4244821 | p.Gly530Val | missense_variant | 0.33 |
embA | 4245245 | c.2013C>T | synonymous_variant | 0.2 |
embB | 4245716 | c.-798G>T | upstream_gene_variant | 0.5 |
embA | 4245723 | p.Gly831Arg | missense_variant | 0.5 |
embB | 4247164 | c.651G>T | synonymous_variant | 0.4 |
embB | 4247300 | p.Gly263Cys | missense_variant | 0.18 |
embB | 4247636 | p.Pro375Ser | missense_variant | 0.2 |
embB | 4248441 | p.Thr643Asn | missense_variant | 0.25 |
embB | 4248499 | p.Lys662Asn | missense_variant | 0.14 |
embB | 4249052 | p.Thr847Pro | missense_variant | 0.4 |
aftB | 4267318 | p.Gln507Lys | missense_variant | 0.33 |
aftB | 4267422 | p.Thr472Ile | missense_variant | 0.33 |
aftB | 4268619 | p.Val73Gly | missense_variant | 0.4 |
aftB | 4269222 | c.-386T>G | upstream_gene_variant | 0.22 |
ethA | 4326141 | p.Glu445* | stop_gained | 0.2 |
ethA | 4326204 | p.Ser424Ala | missense_variant | 0.18 |
ethA | 4326223 | c.1251G>T | synonymous_variant | 0.22 |
ethA | 4326979 | p.Gln165His | missense_variant | 0.29 |
ethA | 4327006 | p.Asp156Glu | missense_variant | 0.22 |
ethR | 4327045 | c.-504G>A | upstream_gene_variant | 0.29 |
ethA | 4327863 | c.-390G>A | upstream_gene_variant | 0.33 |
ethR | 4328055 | p.His169Gln | missense_variant | 0.29 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |