Run ID: SRR6046659
Sample name:
Date: 04-04-2023 12:21:15
Number of reads: 578235
Percentage reads mapped: 98.46
Strain: lineage2.2.1
Drug-resistance: Pre-XDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 0.98 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7570 | p.Ala90Val | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 760314 | p.Val170Phe | missense_variant | 1.0 | rifampicin |
katG | 2155129 | p.Trp328Leu | missense_variant | 1.0 | isoniazid |
pncA | 2289202 | p.Cys14Arg | missense_variant | 1.0 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5135 | c.-105G>T | upstream_gene_variant | 0.14 |
gyrB | 5423 | p.Ala62Thr | missense_variant | 0.14 |
gyrB | 5875 | p.Arg212Ser | missense_variant | 0.22 |
gyrB | 6329 | p.Glu364Lys | missense_variant | 0.2 |
gyrA | 6625 | c.-677G>T | upstream_gene_variant | 0.25 |
gyrB | 6785 | p.Glu516* | stop_gained | 0.18 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8008 | p.Gly236Val | missense_variant | 0.17 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490897 | p.Asp39Tyr | missense_variant | 0.22 |
fgd1 | 490927 | p.Gly49Cys | missense_variant | 0.2 |
fgd1 | 491521 | c.739C>A | synonymous_variant | 0.12 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575476 | p.Asp43Glu | missense_variant | 1.0 |
mshA | 575751 | p.Gly135Val | missense_variant | 0.15 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 576112 | c.765C>A | synonymous_variant | 0.14 |
mshA | 576467 | p.Val374Leu | missense_variant | 0.29 |
mshA | 576585 | p.Arg413Leu | missense_variant | 0.13 |
mshA | 576755 | p.Arg470Ser | missense_variant | 0.5 |
ccsA | 620492 | p.Ser201Trp | missense_variant | 0.18 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 759620 | c.-187A>C | upstream_gene_variant | 0.2 |
rpoB | 759629 | c.-178T>C | upstream_gene_variant | 0.17 |
rpoB | 759855 | p.Arg17Ser | missense_variant | 0.33 |
rpoB | 760309 | p.Val168Ala | missense_variant | 1.0 |
rpoB | 761386 | p.Ala527Val | missense_variant | 0.22 |
rpoB | 762117 | p.Ser771Ala | missense_variant | 0.13 |
rpoB | 762326 | p.Lys840Asn | missense_variant | 0.22 |
rpoC | 762380 | c.-990T>C | upstream_gene_variant | 0.4 |
rpoB | 762825 | p.Gly1007Trp | missense_variant | 0.33 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763317 | p.Leu1171Ile | missense_variant | 0.15 |
rpoC | 764245 | c.876C>A | synonymous_variant | 0.22 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.12 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.12 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.12 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.12 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.12 |
rpoC | 764500 | c.1131C>G | synonymous_variant | 0.14 |
rpoC | 764525 | p.Arg386Ser | missense_variant | 0.18 |
rpoC | 764842 | p.Ile491Met | missense_variant | 0.13 |
rpoC | 765232 | c.1863G>C | synonymous_variant | 0.14 |
rpoC | 765271 | p.Lys634Asn | missense_variant | 0.17 |
rpoC | 765284 | p.Gln639Lys | missense_variant | 0.15 |
rpoC | 766011 | p.Ser881Tyr | missense_variant | 0.12 |
rpoC | 766361 | p.Val998Leu | missense_variant | 0.17 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 1.0 |
rpoC | 766798 | c.3429C>G | synonymous_variant | 0.11 |
rpoC | 766857 | p.Arg1163His | missense_variant | 0.33 |
rpoC | 767148 | p.Ala1260Gly | missense_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775800 | p.Ser894* | stop_gained | 0.33 |
mmpL5 | 775940 | c.2541C>T | synonymous_variant | 0.18 |
mmpL5 | 775945 | p.Val846Leu | missense_variant | 0.13 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 776973 | p.Met503Thr | missense_variant | 0.29 |
mmpL5 | 777501 | p.Thr327Asn | missense_variant | 0.15 |
mmpL5 | 777526 | p.Gly319Cys | missense_variant | 0.18 |
mmpS5 | 778588 | p.Gln106His | missense_variant | 1.0 |
mmpS5 | 778614 | p.Ser98Pro | missense_variant | 0.12 |
mmpR5 | 779335 | p.Asp116Tyr | missense_variant | 0.18 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 0.83 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303597 | p.Phe223Ile | missense_variant | 0.25 |
fbiC | 1303813 | p.Phe295Leu | missense_variant | 0.29 |
fbiC | 1304262 | p.Trp444Cys | missense_variant | 0.4 |
fbiC | 1304265 | c.1335C>T | synonymous_variant | 0.4 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1407154 | c.186delC | frameshift_variant | 0.25 |
embR | 1416841 | c.507C>T | synonymous_variant | 0.29 |
embR | 1417444 | c.-97T>C | upstream_gene_variant | 0.25 |
atpE | 1461079 | p.Gly12Asp | missense_variant | 0.25 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472863 | n.1018T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473329 | n.1484G>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1473832 | n.175C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1473836 | n.179A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473839 | n.182G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473862 | n.205C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476780 | n.3123C>A | non_coding_transcript_exon_variant | 0.5 |
fabG1 | 1673723 | p.Ala95Val | missense_variant | 0.17 |
inhA | 1673982 | c.-220G>T | upstream_gene_variant | 0.2 |
inhA | 1674153 | c.-49G>T | upstream_gene_variant | 0.17 |
rpsA | 1833365 | c.-177G>A | upstream_gene_variant | 0.25 |
rpsA | 1833597 | p.Ser19Asn | missense_variant | 0.13 |
rpsA | 1833643 | c.102C>T | synonymous_variant | 0.2 |
rpsA | 1833779 | p.Val80Phe | missense_variant | 0.15 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918711 | p.Asp258Tyr | missense_variant | 0.12 |
ndh | 2102875 | c.168C>T | synonymous_variant | 0.14 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2154893 | p.Glu407* | stop_gained | 0.18 |
katG | 2155407 | c.705G>T | synonymous_variant | 0.18 |
katG | 2155446 | c.666G>A | synonymous_variant | 0.13 |
katG | 2156012 | p.Gly34* | stop_gained | 0.15 |
PPE35 | 2167884 | p.Gly910Asp | missense_variant | 0.67 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168041 | p.Ala858Thr | missense_variant | 0.22 |
PPE35 | 2168898 | p.Ala572Gly | missense_variant | 0.29 |
PPE35 | 2169351 | p.Ala421Gly | missense_variant | 0.11 |
PPE35 | 2169724 | p.Ile297Val | missense_variant | 0.12 |
PPE35 | 2169736 | p.Gly293Ser | missense_variant | 0.12 |
PPE35 | 2170368 | p.Gln82Arg | missense_variant | 0.22 |
PPE35 | 2170370 | p.Thr81Ala | missense_variant | 0.22 |
PPE35 | 2170379 | c.234G>T | synonymous_variant | 0.22 |
PPE35 | 2170382 | c.231C>T | synonymous_variant | 0.22 |
PPE35 | 2170387 | c.226C>T | synonymous_variant | 0.22 |
PPE35 | 2170403 | c.210C>G | synonymous_variant | 0.22 |
PPE35 | 2170406 | p.Ala69Glu | missense_variant | 0.22 |
PPE35 | 2170566 | p.Phe16Tyr | missense_variant | 0.67 |
PPE35 | 2170792 | c.-180T>C | upstream_gene_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288968 | p.Ala92Ser | missense_variant | 0.12 |
pncA | 2289221 | c.21C>A | synonymous_variant | 0.15 |
kasA | 2517920 | c.-195G>T | upstream_gene_variant | 0.5 |
kasA | 2518048 | c.-67C>G | upstream_gene_variant | 0.2 |
kasA | 2518515 | p.Pro134His | missense_variant | 0.4 |
kasA | 2518639 | c.525G>T | synonymous_variant | 1.0 |
eis | 2714627 | p.Ala236Ser | missense_variant | 0.13 |
eis | 2714709 | c.624C>A | synonymous_variant | 0.2 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.33 |
folC | 2746170 | p.Ala477Ser | missense_variant | 0.14 |
folC | 2746483 | p.Phe372Leu | missense_variant | 0.13 |
folC | 2746614 | p.Gly329Arg | missense_variant | 0.33 |
folC | 2746643 | p.Arg319His | missense_variant | 0.33 |
folC | 2746983 | p.Gly206Ser | missense_variant | 0.17 |
folC | 2747130 | p.Ala157Ser | missense_variant | 0.33 |
pepQ | 2859361 | p.Glu353Ala | missense_variant | 0.12 |
pepQ | 2859524 | p.Gly299Cys | missense_variant | 0.18 |
pepQ | 2859919 | p.Arg167Leu | missense_variant | 0.17 |
ribD | 2986976 | c.138C>A | synonymous_variant | 0.12 |
ribD | 2987231 | c.393G>T | synonymous_variant | 0.15 |
ribD | 2987362 | p.Glu175Gly | missense_variant | 0.18 |
Rv2752c | 3064578 | c.1614C>A | synonymous_variant | 0.13 |
Rv2752c | 3064721 | p.His491Tyr | missense_variant | 0.14 |
Rv2752c | 3064742 | p.Gly484Cys | missense_variant | 0.14 |
Rv2752c | 3064781 | p.Gly471Ser | missense_variant | 0.17 |
Rv2752c | 3065139 | c.1053C>A | synonymous_variant | 0.12 |
Rv2752c | 3065475 | c.717C>A | synonymous_variant | 0.18 |
Rv2752c | 3065539 | p.Val218Glu | missense_variant | 0.2 |
Rv2752c | 3065744 | p.Thr150Ser | missense_variant | 0.14 |
Rv2752c | 3065750 | p.His148Asn | missense_variant | 0.17 |
Rv2752c | 3067155 | c.-964C>A | upstream_gene_variant | 0.33 |
thyX | 3067393 | p.Val185Leu | missense_variant | 0.33 |
thyX | 3067621 | p.Val109Leu | missense_variant | 0.15 |
thyX | 3068047 | c.-102C>A | upstream_gene_variant | 0.25 |
thyA | 3074169 | p.Trp101Cys | missense_variant | 0.14 |
thyA | 3074280 | c.192C>T | synonymous_variant | 0.17 |
thyA | 3074645 | c.-174T>G | upstream_gene_variant | 0.33 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087247 | p.Gln143Arg | missense_variant | 0.22 |
ald | 3087732 | p.Val305Met | missense_variant | 0.12 |
ald | 3087910 | p.Thr364Ile | missense_variant | 0.25 |
Rv3083 | 3448634 | p.Thr44Asn | missense_variant | 0.22 |
Rv3083 | 3449016 | c.513A>G | synonymous_variant | 0.18 |
Rv3083 | 3449207 | p.Pro235Leu | missense_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474142 | p.Trp46Arg | missense_variant | 0.18 |
fprA | 3474160 | p.Gly52Trp | missense_variant | 0.15 |
fprA | 3474665 | p.Gly220Val | missense_variant | 0.12 |
fprA | 3474672 | c.666C>T | synonymous_variant | 0.12 |
Rv3236c | 3612433 | c.684C>A | synonymous_variant | 0.5 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
Rv3236c | 3612867 | p.Ser84Gly | missense_variant | 0.25 |
fbiB | 3640572 | c.-963C>T | upstream_gene_variant | 0.14 |
fbiA | 3641276 | p.Pro245Leu | missense_variant | 0.2 |
fbiB | 3642789 | p.Glu419Lys | missense_variant | 0.15 |
alr | 3840270 | p.Gly384Asp | missense_variant | 0.13 |
alr | 3840706 | p.Ala239Ser | missense_variant | 0.14 |
alr | 3840716 | c.705G>T | synonymous_variant | 0.14 |
alr | 3840753 | p.Arg223Leu | missense_variant | 0.18 |
alr | 3840846 | p.Gly192Glu | missense_variant | 0.4 |
alr | 3841467 | c.-48_-47insAGGC | upstream_gene_variant | 0.25 |
alr | 3841475 | c.-55C>A | upstream_gene_variant | 0.25 |
rpoA | 3877675 | p.Arg278Leu | missense_variant | 0.14 |
rpoA | 3878190 | c.318C>T | synonymous_variant | 0.33 |
rpoA | 3878344 | p.Arg55Leu | missense_variant | 0.12 |
ddn | 3987166 | p.Asp108Val | missense_variant | 0.15 |
clpC1 | 4039344 | p.Glu454Gly | missense_variant | 0.15 |
clpC1 | 4040009 | c.696C>A | synonymous_variant | 0.18 |
clpC1 | 4040150 | c.555C>A | synonymous_variant | 0.12 |
clpC1 | 4040396 | p.Ile103Met | missense_variant | 0.12 |
panD | 4043993 | p.Arg97Trp | missense_variant | 0.18 |
embC | 4240586 | p.Gly242Ser | missense_variant | 0.2 |
embC | 4240862 | p.Trp334Arg | missense_variant | 0.13 |
embC | 4241619 | p.Trp586Leu | missense_variant | 0.5 |
embC | 4241786 | c.1925delA | frameshift_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242740 | p.Leu960Ile | missense_variant | 0.18 |
embC | 4243115 | p.Leu1085Met | missense_variant | 0.17 |
embC | 4243139 | p.Arg1093Ser | missense_variant | 0.33 |
embA | 4243410 | p.Ala60Thr | missense_variant | 0.33 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4243798 | p.Val189Glu | missense_variant | 0.25 |
embA | 4243953 | p.Arg241Ser | missense_variant | 0.25 |
embA | 4244184 | p.Ser318Leu | missense_variant | 0.13 |
embA | 4244240 | p.Trp336* | stop_gained | 0.17 |
embA | 4244429 | c.1197G>T | synonymous_variant | 0.18 |
embA | 4244445 | c.1213C>T | synonymous_variant | 0.17 |
embA | 4244750 | c.1518C>A | synonymous_variant | 0.12 |
embA | 4244771 | c.1539G>T | synonymous_variant | 0.14 |
embA | 4245377 | c.2145T>C | synonymous_variant | 0.17 |
embB | 4245677 | c.-837G>T | upstream_gene_variant | 0.25 |
embA | 4245987 | p.Gln919Arg | missense_variant | 0.17 |
embA | 4246477 | p.Pro1082His | missense_variant | 0.15 |
embA | 4246510 | p.Leu1093Arg | missense_variant | 0.17 |
embB | 4246532 | c.19A>C | synonymous_variant | 0.22 |
embB | 4247094 | p.Gly194Glu | missense_variant | 0.25 |
embB | 4247821 | c.1308T>C | synonymous_variant | 0.12 |
embB | 4247976 | p.Val488Gly | missense_variant | 0.12 |
embB | 4248173 | p.Val554Leu | missense_variant | 0.22 |
embB | 4248646 | c.2133C>T | synonymous_variant | 0.14 |
embB | 4248826 | c.2313G>T | synonymous_variant | 0.25 |
embB | 4248986 | p.Gly825Cys | missense_variant | 0.14 |
embB | 4249534 | c.3021C>A | synonymous_variant | 0.29 |
aftB | 4267002 | p.Arg612Pro | missense_variant | 0.18 |
aftB | 4267207 | p.Val544Leu | missense_variant | 0.17 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268131 | p.Val236Phe | missense_variant | 0.14 |
aftB | 4268155 | p.Arg228Trp | missense_variant | 0.22 |
aftB | 4268728 | p.Thr37Ser | missense_variant | 0.25 |
ethA | 4326046 | p.Glu476Asp | missense_variant | 0.12 |
ethA | 4326120 | p.Arg452Cys | missense_variant | 0.11 |
ethA | 4326156 | p.Leu440Met | missense_variant | 0.14 |
ethA | 4326423 | p.Gly351Trp | missense_variant | 0.18 |
ethR | 4326679 | c.-870C>A | upstream_gene_variant | 0.14 |
ethA | 4326698 | p.Arg259Leu | missense_variant | 0.17 |
ethA | 4327361 | p.Arg38Leu | missense_variant | 0.15 |
ethR | 4327417 | c.-132C>A | upstream_gene_variant | 0.14 |
ethA | 4327905 | c.-432C>A | upstream_gene_variant | 0.14 |
ethR | 4327916 | p.Ala123Val | missense_variant | 0.13 |
ethA | 4328376 | c.-903G>T | upstream_gene_variant | 0.13 |
ethA | 4328464 | c.-991C>G | upstream_gene_variant | 0.22 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338654 | c.-133A>G | upstream_gene_variant | 0.17 |
whiB6 | 4338719 | c.-198T>A | upstream_gene_variant | 0.29 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407809 | p.Asp132Tyr | missense_variant | 0.17 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |
gid | 4408256 | c.-54G>T | upstream_gene_variant | 0.17 |