Run ID: ERR4816192
Sample name:
Date: 01-04-2023 14:17:29
Number of reads: 581950
Percentage reads mapped: 98.52
Strain: lineage3
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5852 | p.Thr205Ala | missense_variant | 0.25 |
gyrB | 6007 | c.768C>A | synonymous_variant | 0.14 |
gyrB | 6645 | p.Ser469Asn | missense_variant | 0.22 |
gyrA | 7269 | c.-32_-30delCAA | upstream_gene_variant | 0.22 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7379 | c.78C>T | synonymous_variant | 0.29 |
gyrA | 7763 | c.462T>C | synonymous_variant | 0.14 |
gyrA | 7799 | c.498A>G | synonymous_variant | 0.15 |
gyrA | 8370 | c.1069C>A | synonymous_variant | 0.12 |
gyrA | 8993 | p.His564Gln | missense_variant | 0.18 |
gyrA | 9024 | c.1723C>A | synonymous_variant | 0.18 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9596 | c.2295G>T | synonymous_variant | 1.0 |
gyrA | 9777 | p.Asn826Asp | missense_variant | 1.0 |
fgd1 | 490847 | p.Glu22Val | missense_variant | 0.18 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575520 | p.Ala58Val | missense_variant | 0.67 |
mshA | 576751 | p.Lys468Asn | missense_variant | 0.25 |
ccsA | 620100 | c.210G>T | synonymous_variant | 0.12 |
ccsA | 620148 | c.258G>T | synonymous_variant | 0.29 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 760687 | p.Phe294Tyr | missense_variant | 0.2 |
rpoB | 760888 | p.Thr361Asn | missense_variant | 0.11 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoB | 762636 | p.Lys944Glu | missense_variant | 1.0 |
rpoB | 762834 | p.Gly1010Cys | missense_variant | 0.5 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.33 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.18 |
rpoB | 763075 | p.Thr1090Ile | missense_variant | 0.18 |
rpoB | 763077 | p.Val1091His | missense_variant | 0.18 |
rpoC | 763088 | c.-282C>G | upstream_gene_variant | 0.13 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.15 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.22 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.22 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.18 |
rpoB | 763137 | p.Ile1111Val | missense_variant | 0.18 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.13 |
rpoC | 763445 | c.78_79delCG | frameshift_variant | 0.33 |
rpoC | 764181 | p.Asp271Gly | missense_variant | 1.0 |
rpoC | 764404 | c.1035C>T | synonymous_variant | 0.14 |
rpoC | 764751 | p.Val461Ala | missense_variant | 0.4 |
rpoC | 764773 | p.Asn468Lys | missense_variant | 0.4 |
rpoC | 765023 | p.Gln552* | stop_gained | 0.14 |
rpoC | 765258 | p.Arg630Leu | missense_variant | 0.21 |
mmpL5 | 775616 | c.2865G>A | synonymous_variant | 0.15 |
mmpL5 | 775629 | p.Pro951Leu | missense_variant | 0.18 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpR5 | 777995 | c.-995G>T | upstream_gene_variant | 0.14 |
mmpL5 | 778185 | p.Arg99Gln | missense_variant | 0.29 |
mmpR5 | 778283 | c.-707G>T | upstream_gene_variant | 0.2 |
mmpL5 | 778564 | c.-84C>T | upstream_gene_variant | 0.17 |
mmpS5 | 778739 | p.Val56Ala | missense_variant | 0.14 |
mmpR5 | 779308 | p.Arg107Cys | missense_variant | 0.4 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303413 | p.Trp161* | stop_gained | 0.17 |
fbiC | 1304094 | p.Met388Ile | missense_variant | 0.2 |
fbiC | 1305267 | c.2337C>A | synonymous_variant | 0.18 |
embR | 1416887 | p.Arg154His | missense_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474482 | n.825G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474487 | n.830G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474496 | n.839C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474517 | n.860C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474552 | n.895C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475391 | n.1734T>C | non_coding_transcript_exon_variant | 0.5 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.17 |
fabG1 | 1673987 | c.551delG | frameshift_variant | 0.14 |
rpsA | 1834136 | p.Arg199Ser | missense_variant | 0.17 |
rpsA | 1834705 | c.1164C>A | synonymous_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102772 | p.His91Tyr | missense_variant | 0.2 |
katG | 2154069 | c.2043G>A | synonymous_variant | 0.11 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155697 | p.Ala139Thr | missense_variant | 0.17 |
PPE35 | 2167696 | p.Ile973Val | missense_variant | 0.2 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169642 | p.Ala324Glu | missense_variant | 0.25 |
PPE35 | 2169885 | p.Gly243Val | missense_variant | 0.29 |
PPE35 | 2170147 | p.Ser156Ala | missense_variant | 0.5 |
PPE35 | 2170371 | p.Thr81Val | missense_variant | 0.33 |
PPE35 | 2170769 | c.-157C>T | upstream_gene_variant | 1.0 |
Rv1979c | 2221965 | p.Gln400His | missense_variant | 0.14 |
Rv1979c | 2222882 | p.Gly95Cys | missense_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
pncA | 2290039 | c.-798C>T | upstream_gene_variant | 0.22 |
kasA | 2517932 | c.-182delT | upstream_gene_variant | 0.2 |
kasA | 2518089 | c.-26C>A | upstream_gene_variant | 0.13 |
eis | 2715432 | c.-100C>T | upstream_gene_variant | 1.0 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726266 | p.Lys25Arg | missense_variant | 0.2 |
ahpC | 2726752 | p.Ala187Val | missense_variant | 0.18 |
folC | 2746206 | p.Gly465Arg | missense_variant | 0.17 |
folC | 2746318 | c.1281C>T | synonymous_variant | 0.4 |
folC | 2746379 | p.Gly407Glu | missense_variant | 0.4 |
folC | 2747125 | p.Met158Ile | missense_variant | 0.2 |
folC | 2747167 | p.Lys144Asn | missense_variant | 0.12 |
pepQ | 2859359 | p.Thr354Ala | missense_variant | 1.0 |
ribD | 2987136 | p.Val100Phe | missense_variant | 0.12 |
ribD | 2987161 | p.Ala108Asp | missense_variant | 0.12 |
ribD | 2987601 | p.Tyr255His | missense_variant | 0.13 |
Rv2752c | 3065092 | p.Gln367Pro | missense_variant | 0.12 |
Rv2752c | 3065627 | p.Ser189Thr | missense_variant | 0.13 |
Rv2752c | 3067086 | c.-896delG | upstream_gene_variant | 0.25 |
thyA | 3074089 | p.Ile128Asn | missense_variant | 0.12 |
thyA | 3074287 | p.Phe62Ser | missense_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087432 | p.Arg205Trp | missense_variant | 0.14 |
ald | 3087456 | p.Gly213Ser | missense_variant | 0.17 |
ald | 3087742 | p.Thr308Lys | missense_variant | 0.33 |
fbiD | 3339742 | c.625C>A | synonymous_variant | 0.5 |
Rv3083 | 3448328 | c.-176G>A | upstream_gene_variant | 0.2 |
Rv3083 | 3448635 | c.132C>T | synonymous_variant | 0.18 |
Rv3083 | 3449134 | p.Gln211* | stop_gained | 0.67 |
Rv3083 | 3449776 | p.Asp425Asn | missense_variant | 0.14 |
Rv3083 | 3449871 | c.1368C>A | synonymous_variant | 0.17 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474601 | p.Arg199Cys | missense_variant | 0.15 |
fprA | 3475350 | c.1344C>A | synonymous_variant | 0.14 |
fbiA | 3640891 | p.Gln117Lys | missense_variant | 0.12 |
fbiB | 3642018 | p.Asp162Asn | missense_variant | 0.5 |
alr | 3841442 | c.-22G>A | upstream_gene_variant | 0.12 |
alr | 3841539 | c.-119C>T | upstream_gene_variant | 0.12 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.13 |
rpoA | 3877664 | p.Asp282Asn | missense_variant | 0.14 |
ddn | 3987248 | p.Asp135Glu | missense_variant | 0.15 |
clpC1 | 4038348 | p.Ser786* | stop_gained | 0.12 |
clpC1 | 4039645 | p.His354Asp | missense_variant | 0.1 |
clpC1 | 4040180 | c.525C>A | synonymous_variant | 0.25 |
embC | 4239780 | c.-83G>T | upstream_gene_variant | 0.12 |
embC | 4240475 | p.Ala205Ser | missense_variant | 0.18 |
embC | 4240480 | c.618G>A | synonymous_variant | 0.18 |
embC | 4240489 | c.627A>G | synonymous_variant | 0.18 |
embC | 4240495 | c.633T>C | synonymous_variant | 0.17 |
embC | 4240512 | p.Ser217Thr | missense_variant | 0.17 |
embC | 4240514 | p.Val218Ile | missense_variant | 0.17 |
embC | 4240519 | c.657T>C | synonymous_variant | 0.17 |
embC | 4240543 | c.681G>C | synonymous_variant | 0.11 |
embC | 4240769 | p.Val303Met | missense_variant | 0.25 |
embC | 4241245 | c.1383C>T | synonymous_variant | 0.11 |
embC | 4241928 | p.Arg689Pro | missense_variant | 0.14 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embC | 4242255 | p.Pro798Leu | missense_variant | 0.22 |
embC | 4242264 | p.Glu801Val | missense_variant | 0.13 |
embC | 4242449 | p.Met863Val | missense_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242950 | p.Gly1030Arg | missense_variant | 0.13 |
embA | 4243710 | p.Gly160Trp | missense_variant | 0.18 |
embA | 4244065 | p.Leu278Gln | missense_variant | 0.25 |
embA | 4244214 | p.Ala328Thr | missense_variant | 0.2 |
embA | 4245340 | p.Gly703Asp | missense_variant | 0.18 |
embA | 4245387 | c.2157delC | frameshift_variant | 0.15 |
embB | 4246587 | p.Gly25Glu | missense_variant | 0.25 |
embB | 4247097 | p.Pro195His | missense_variant | 0.17 |
embB | 4247772 | p.Glu420Gly | missense_variant | 0.33 |
aftB | 4267003 | c.1834C>A | synonymous_variant | 0.22 |
aftB | 4267130 | c.1707C>T | synonymous_variant | 0.14 |
aftB | 4267338 | p.Leu500His | missense_variant | 0.2 |
aftB | 4268741 | c.96G>A | synonymous_variant | 0.17 |
ubiA | 4269837 | c.-4T>G | upstream_gene_variant | 0.33 |
ethA | 4326078 | p.Arg466Trp | missense_variant | 0.17 |
ethA | 4326155 | p.Leu440Pro | missense_variant | 0.14 |
ethA | 4327424 | p.Val17Asp | missense_variant | 0.4 |
ethR | 4327928 | p.Ala127Asp | missense_variant | 0.22 |
ethA | 4328270 | c.-797C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4408470 | c.-268G>A | upstream_gene_variant | 0.18 |