Run ID: ERR4831744
Sample name:
Date: 01-04-2023 21:05:46
Number of reads: 1550998
Percentage reads mapped: 98.78
Strain: lineage2.2.1
Drug-resistance: MDR-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 | 1.0 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.97 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Trp | missense_variant | 1.0 | rifampicin |
rpsL | 781822 | p.Lys88Arg | missense_variant | 1.0 | streptomycin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.12 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
embB | 4247429 | p.Met306Val | missense_variant | 0.88 | ethambutol |
ethA | 4327345 | c.128delG | frameshift_variant | 0.1 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7789 | p.Pro163Arg | missense_variant | 0.1 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490923 | p.Gln47His | missense_variant | 0.17 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575235 | c.-113G>T | upstream_gene_variant | 0.12 |
mshA | 575480 | p.Arg45Ser | missense_variant | 0.13 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 575921 | p.Asp192Tyr | missense_variant | 0.15 |
mshA | 575933 | p.Pro196Thr | missense_variant | 0.13 |
mshA | 576024 | p.Ser226Trp | missense_variant | 0.13 |
mshA | 576730 | c.1383G>T | synonymous_variant | 0.33 |
mshA | 576754 | c.1407C>A | synonymous_variant | 0.11 |
ccsA | 619795 | c.-96C>T | upstream_gene_variant | 0.25 |
ccsA | 619838 | c.-53G>T | upstream_gene_variant | 0.2 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
ccsA | 620741 | p.Thr284Lys | missense_variant | 0.13 |
rpoB | 760903 | p.His366Pro | missense_variant | 0.12 |
rpoB | 760995 | p.Arg397Gly | missense_variant | 0.12 |
rpoB | 761196 | c.1390C>T | synonymous_variant | 0.13 |
rpoB | 761388 | p.Asp528His | missense_variant | 0.2 |
rpoB | 761399 | c.1593C>T | synonymous_variant | 0.14 |
rpoB | 761571 | p.Pro589Ala | missense_variant | 0.1 |
rpoB | 761701 | p.Ala632Asp | missense_variant | 0.14 |
rpoB | 762333 | p.Gly843Arg | missense_variant | 0.11 |
rpoB | 762522 | p.Pro906Ala | missense_variant | 0.11 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764010 | p.Arg214His | missense_variant | 0.17 |
rpoC | 764521 | p.Asn384Lys | missense_variant | 0.13 |
rpoC | 764545 | c.1176C>G | synonymous_variant | 0.12 |
rpoC | 765342 | p.Pro658Leu | missense_variant | 0.14 |
rpoC | 765347 | p.Asp660His | missense_variant | 0.14 |
rpoC | 765407 | p.Gly680Ser | missense_variant | 0.13 |
rpoC | 765625 | c.2256C>A | synonymous_variant | 0.13 |
rpoC | 765678 | p.Arg770His | missense_variant | 0.15 |
rpoC | 765731 | p.Ala788Ser | missense_variant | 0.13 |
rpoC | 766051 | c.2682G>A | synonymous_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775644 | p.Arg946Leu | missense_variant | 0.12 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 776298 | p.Ser728Ile | missense_variant | 0.11 |
mmpL5 | 777044 | c.1437C>G | synonymous_variant | 0.1 |
mmpL5 | 777318 | p.Arg388His | missense_variant | 0.25 |
mmpL5 | 777743 | c.738C>G | synonymous_variant | 0.12 |
mmpL5 | 777907 | p.Leu192Val | missense_variant | 0.14 |
mmpL5 | 778419 | p.Arg21Gln | missense_variant | 0.22 |
mmpL5 | 779172 | c.-692C>T | upstream_gene_variant | 0.22 |
mmpR5 | 779347 | p.Val120Leu | missense_variant | 0.12 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801282 | c.474G>C | synonymous_variant | 0.18 |
fbiC | 1304038 | p.Pro370Thr | missense_variant | 0.13 |
fbiC | 1304117 | p.Pro396His | missense_variant | 0.12 |
fbiC | 1304231 | p.Pro434Gln | missense_variant | 0.15 |
fbiC | 1305060 | c.2130C>T | synonymous_variant | 0.14 |
Rv1258c | 1406750 | c.591C>A | synonymous_variant | 0.18 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1407148 | p.Ala65Ser | missense_variant | 0.2 |
embR | 1416222 | p.Phe376Leu | missense_variant | 0.11 |
embR | 1416232 | p.Cys372Gly | missense_variant | 0.11 |
embR | 1416280 | c.1068A>C | synonymous_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1473812 | n.155G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1473814 | n.157A>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1473815 | n.158T>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1473839 | n.182G>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474477 | n.820C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474519 | n.862G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474561 | n.904G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475247 | n.1590G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475325 | n.1668C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476131 | n.2474C>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476338 | n.2685delG | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476576 | n.2919C>G | non_coding_transcript_exon_variant | 0.17 |
inhA | 1674062 | c.-140C>A | upstream_gene_variant | 0.14 |
inhA | 1674210 | c.9A>C | synonymous_variant | 1.0 |
inhA | 1674331 | p.Leu44Met | missense_variant | 0.11 |
inhA | 1674765 | c.564C>T | synonymous_variant | 0.14 |
rpsA | 1833959 | p.Leu140Val | missense_variant | 0.11 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918218 | c.279C>T | synonymous_variant | 0.14 |
ndh | 2102242 | c.801G>T | synonymous_variant | 0.13 |
ndh | 2102535 | p.Leu170Ile | missense_variant | 0.12 |
katG | 2153991 | c.2121T>G | synonymous_variant | 0.12 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155351 | p.Arg254His | missense_variant | 0.14 |
katG | 2155364 | p.Glu250Lys | missense_variant | 0.17 |
katG | 2155397 | p.Pro239Thr | missense_variant | 0.13 |
katG | 2156328 | c.-217C>G | upstream_gene_variant | 0.17 |
katG | 2156431 | c.-320A>G | upstream_gene_variant | 0.12 |
katG | 2156515 | c.-404G>A | upstream_gene_variant | 0.22 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170264 | p.Leu117Val | missense_variant | 0.12 |
PPE35 | 2170402 | p.Pro71Thr | missense_variant | 0.12 |
PPE35 | 2170516 | p.Gly33Trp | missense_variant | 0.13 |
Rv1979c | 2222062 | p.Arg368Leu | missense_variant | 0.12 |
Rv1979c | 2222417 | p.Arg250Gly | missense_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289423 | c.-182A>G | upstream_gene_variant | 0.12 |
kasA | 2518758 | p.Ala215Asp | missense_variant | 0.2 |
kasA | 2518976 | p.Gly288Arg | missense_variant | 0.18 |
kasA | 2519033 | p.His307Asp | missense_variant | 0.22 |
kasA | 2519197 | c.1083G>T | synonymous_variant | 0.22 |
kasA | 2519206 | c.1092C>T | synonymous_variant | 0.22 |
eis | 2715041 | p.Arg98Gly | missense_variant | 0.25 |
eis | 2715164 | p.Glu57* | stop_gained | 0.12 |
eis | 2715481 | c.-149G>A | upstream_gene_variant | 0.13 |
eis | 2715583 | c.-251G>T | upstream_gene_variant | 0.29 |
ahpC | 2726265 | p.Lys25Gln | missense_variant | 0.19 |
ahpC | 2726351 | p.Trp53Cys | missense_variant | 0.14 |
folC | 2746635 | p.Asp322Asn | missense_variant | 1.0 |
folC | 2747138 | p.Val154Gly | missense_variant | 0.15 |
folC | 2747466 | p.Pro45Thr | missense_variant | 0.12 |
pepQ | 2859721 | p.Met233Thr | missense_variant | 0.12 |
pepQ | 2859944 | p.Ala159Ser | missense_variant | 0.12 |
Rv2752c | 3064536 | c.1656G>T | synonymous_variant | 0.11 |
Rv2752c | 3064582 | p.Val537Ala | missense_variant | 0.11 |
Rv2752c | 3065060 | p.Ala378Thr | missense_variant | 0.12 |
Rv2752c | 3065304 | c.888G>C | synonymous_variant | 0.12 |
Rv2752c | 3065520 | c.672G>T | synonymous_variant | 0.12 |
Rv2752c | 3066107 | p.Arg29Gly | missense_variant | 0.14 |
Rv2752c | 3066287 | c.-96G>C | upstream_gene_variant | 0.14 |
Rv2752c | 3066329 | c.-138C>A | upstream_gene_variant | 0.13 |
thyX | 3067495 | p.Glu151* | stop_gained | 0.2 |
thyX | 3067538 | c.408C>A | synonymous_variant | 0.18 |
thyX | 3067907 | c.39C>T | synonymous_variant | 0.17 |
thyX | 3068018 | c.-73G>A | upstream_gene_variant | 0.14 |
thyX | 3068115 | c.-170C>T | upstream_gene_variant | 0.12 |
thyX | 3068135 | c.-190G>C | upstream_gene_variant | 0.12 |
thyA | 3073701 | p.Ile257Met | missense_variant | 0.13 |
thyA | 3074614 | c.-143G>T | upstream_gene_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087887 | c.1068C>T | synonymous_variant | 0.14 |
fbiD | 3339563 | p.Ala149Val | missense_variant | 0.18 |
Rv3083 | 3449031 | c.528C>G | synonymous_variant | 0.11 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475256 | p.Leu417Pro | missense_variant | 0.12 |
fprA | 3475266 | c.1260G>C | synonymous_variant | 0.14 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiA | 3640478 | c.-65G>C | upstream_gene_variant | 0.2 |
fbiB | 3641127 | c.-408T>G | upstream_gene_variant | 0.14 |
fbiB | 3641199 | c.-336C>T | upstream_gene_variant | 0.22 |
fbiA | 3641372 | p.Gly277Val | missense_variant | 0.18 |
fbiB | 3641625 | p.Ala31Thr | missense_variant | 1.0 |
fbiB | 3641678 | c.144T>C | synonymous_variant | 0.11 |
fbiB | 3641913 | p.Ala127Ser | missense_variant | 0.25 |
fbiB | 3642798 | p.Gly422Ser | missense_variant | 0.13 |
alr | 3840905 | p.Phe172Leu | missense_variant | 0.12 |
alr | 3841105 | p.Thr106Pro | missense_variant | 0.11 |
alr | 3841195 | p.Arg76Cys | missense_variant | 0.12 |
ddn | 3987055 | p.Gly71Val | missense_variant | 0.12 |
ddn | 3987058 | p.Arg72Gln | missense_variant | 0.12 |
clpC1 | 4038449 | c.2256C>G | synonymous_variant | 0.11 |
clpC1 | 4039105 | p.Arg534Ser | missense_variant | 0.12 |
clpC1 | 4040244 | p.Gly154Ala | missense_variant | 0.12 |
embA | 4242286 | c.-947C>T | upstream_gene_variant | 0.12 |
embC | 4242372 | p.Ala837Asp | missense_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242802 | c.-431G>T | upstream_gene_variant | 0.12 |
embA | 4243388 | c.156C>T | synonymous_variant | 0.2 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4243488 | p.Gly86Ser | missense_variant | 0.14 |
embA | 4243796 | c.564C>A | synonymous_variant | 0.14 |
embA | 4244347 | p.Trp372* | stop_gained | 0.13 |
embA | 4245603 | p.Gly791Trp | missense_variant | 0.2 |
embA | 4245733 | p.Pro834Leu | missense_variant | 0.15 |
embA | 4246462 | p.Gly1077Asp | missense_variant | 0.17 |
embB | 4246874 | p.Gln121Lys | missense_variant | 0.12 |
embB | 4247079 | p.Phe189Ser | missense_variant | 0.14 |
embB | 4247427 | p.Gly305Ala | missense_variant | 0.11 |
embB | 4247443 | c.930C>A | synonymous_variant | 0.14 |
embB | 4247885 | p.Gly458Cys | missense_variant | 0.14 |
embB | 4248594 | p.Gly694Asp | missense_variant | 0.12 |
embB | 4248868 | c.2355G>A | synonymous_variant | 0.14 |
embB | 4249132 | c.2619G>A | synonymous_variant | 0.13 |
embB | 4249140 | p.Val876Gly | missense_variant | 0.14 |
embB | 4249147 | c.2634C>T | synonymous_variant | 0.15 |
embB | 4249522 | c.3009C>T | synonymous_variant | 0.15 |
embB | 4249635 | p.Asp1041Ala | missense_variant | 0.12 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268201 | c.636G>T | synonymous_variant | 0.14 |
whiB6 | 4338251 | p.Ala91Pro | missense_variant | 0.17 |
whiB6 | 4338256 | p.Ala89Glu | missense_variant | 0.2 |
whiB6 | 4338308 | p.Ala72Thr | missense_variant | 0.17 |
whiB6 | 4338342 | p.Trp60* | stop_gained | 0.17 |
whiB6 | 4338369 | c.153C>G | synonymous_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407532 | p.Ala224Glu | missense_variant | 0.13 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |