Run ID: ERR4818355
Sample name:
Date: 01-04-2023 15:30:46
Number of reads: 805954
Percentage reads mapped: 90.36
Strain: lineage3
Drug-resistance: Other
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 |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.66 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8904 | p.Arg535Cys | missense_variant | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490772 | c.-11A>G | upstream_gene_variant | 0.12 |
fgd1 | 491173 | p.Arg131Trp | missense_variant | 0.12 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576257 | p.Ser304Gly | missense_variant | 0.13 |
mshA | 576641 | p.Asn432Tyr | missense_variant | 0.2 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 761542 | p.Gln579Leu | missense_variant | 0.12 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.17 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.17 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.2 |
rpoB | 762177 | p.Arg791Thr | missense_variant | 0.2 |
rpoB | 762181 | p.Asp792Ala | missense_variant | 0.22 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.22 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 0.17 |
rpoB | 762200 | c.2394C>T | synonymous_variant | 0.17 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.17 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763700 | p.Pro111Thr | missense_variant | 0.1 |
rpoC | 765590 | p.Arg741Cys | missense_variant | 0.22 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776973 | p.Met503Thr | missense_variant | 0.17 |
mmpL5 | 777032 | c.1449C>G | synonymous_variant | 0.17 |
mmpL5 | 777035 | c.1446G>A | synonymous_variant | 0.18 |
mmpL5 | 777191 | c.1290C>A | synonymous_variant | 0.18 |
mmpL5 | 777196 | p.Glu429Gln | missense_variant | 0.2 |
mmpL5 | 777735 | p.Phe249Ser | missense_variant | 0.25 |
mmpL5 | 777820 | c.661C>T | synonymous_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.13 |
rpsL | 781766 | c.207C>T | synonymous_variant | 0.13 |
rpsL | 781772 | c.213C>T | synonymous_variant | 0.19 |
rpsL | 781796 | p.Met79Ile | missense_variant | 0.22 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.2 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.2 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.2 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.19 |
fbiC | 1304676 | c.1746A>C | synonymous_variant | 1.0 |
Rv1258c | 1406937 | p.Ala135Val | missense_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474634 | n.977T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474866 | n.1209C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474869 | n.1212G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475974 | n.2317A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476141 | n.2484A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.4 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.18 |
rpsA | 1833732 | p.Pro64Leu | missense_variant | 0.2 |
rpsA | 1833736 | c.195C>T | synonymous_variant | 0.18 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.18 |
rpsA | 1834100 | p.Arg187Cys | missense_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918724 | p.Arg262Leu | missense_variant | 0.12 |
ndh | 2102167 | p.Gln292His | missense_variant | 0.2 |
ndh | 2103005 | p.Arg13His | missense_variant | 0.22 |
katG | 2153992 | p.Leu707Arg | missense_variant | 1.0 |
katG | 2154249 | c.1863C>T | synonymous_variant | 0.2 |
katG | 2154402 | c.1710C>T | synonymous_variant | 0.11 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167667 | c.2945delT | frameshift_variant | 0.22 |
PPE35 | 2167729 | p.Ala962Thr | missense_variant | 0.13 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168651 | p.Leu654Phe | missense_variant | 1.0 |
PPE35 | 2169182 | c.1431G>A | synonymous_variant | 0.18 |
PPE35 | 2169683 | c.930C>T | synonymous_variant | 0.15 |
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 | 2290125 | c.-884C>T | upstream_gene_variant | 1.0 |
kasA | 2518090 | c.-25A>G | upstream_gene_variant | 0.14 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
pepQ | 2860399 | p.Arg7Gln | missense_variant | 1.0 |
Rv2752c | 3066118 | p.Asn25Ser | missense_variant | 0.12 |
ald | 3086756 | c.-64A>G | upstream_gene_variant | 0.2 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087169 | p.Tyr117Cys | missense_variant | 0.12 |
fbiD | 3339218 | p.Thr34Ile | missense_variant | 0.12 |
fbiD | 3339366 | c.249G>A | synonymous_variant | 0.2 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474142 | c.141dupG | frameshift_variant | 0.11 |
fprA | 3475228 | p.Asp408Asn | missense_variant | 0.13 |
Rv3236c | 3612372 | p.Leu249Phe | missense_variant | 0.15 |
fbiB | 3642809 | c.1275G>A | synonymous_variant | 0.13 |
alr | 3841473 | c.-53G>A | upstream_gene_variant | 1.0 |
clpC1 | 4040569 | p.Ala46Thr | missense_variant | 0.11 |
clpC1 | 4040815 | c.-111C>G | upstream_gene_variant | 0.11 |
embC | 4240189 | c.327G>C | synonymous_variant | 0.17 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embC | 4242184 | c.2322C>A | synonymous_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243216 | c.-17G>T | upstream_gene_variant | 0.11 |
embA | 4243834 | p.Ala201Val | missense_variant | 0.13 |
embB | 4248067 | p.Trp518Cys | missense_variant | 0.11 |
ubiA | 4269124 | p.Ala237Asp | missense_variant | 0.17 |
ethA | 4327529 | c.-56T>C | upstream_gene_variant | 0.1 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407704 | p.Ala167Thr | missense_variant | 0.18 |
gid | 4408252 | c.-50A>G | upstream_gene_variant | 0.12 |