Run ID: SRR14782658
Sample name:
Date: 03-04-2023 11:34:28
Number of reads: 4690716
Percentage reads mapped: 99.46
Strain: lineage4.2.1;lineage2.2.1
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.28 |
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.73 |
lineage4.2 | Euro-American | H;T;LAM | None | 0.73 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 0.28 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.26 |
lineage4.2.1 | Euro-American (TUR) | H3;H4 | None | 0.77 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 0.25 | streptomycin |
rpsL | 781822 | p.Lys88Arg | missense_variant | 0.78 | streptomycin |
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 0.73 | isoniazid, ethionamide |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288887 | p.Trp119Arg | missense_variant | 0.23 | pyrazinamide |
pncA | 2289040 | p.Trp68Arg | missense_variant | 0.71 | pyrazinamide |
eis | 2715344 | c.-12C>T | upstream_gene_variant | 0.72 | kanamycin |
embB | 4247402 | p.Ser297Ala | missense_variant | 0.69 | ethambutol |
embB | 4247469 | p.Tyr319Ser | missense_variant | 0.26 | ethambutol |
ethA | 4327033 | p.Tyr147* | stop_gained | 0.3 | 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 | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491247 | c.465C>T | synonymous_variant | 0.83 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.28 |
mshA | 575907 | p.Ala187Val | missense_variant | 0.29 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.17 |
mshA | 576613 | c.1266A>C | synonymous_variant | 0.22 |
mshA | 576616 | c.1269G>C | synonymous_variant | 0.31 |
ccsA | 619969 | p.Val27Ile | missense_variant | 0.76 |
ccsA | 620625 | p.Ile245Met | missense_variant | 0.2 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.25 |
rpoC | 764367 | p.Gly333Ala | missense_variant | 0.15 |
rpoC | 764817 | p.Val483Gly | missense_variant | 0.7 |
rpoC | 764840 | p.Ile491Val | missense_variant | 0.26 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 0.24 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 0.99 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.28 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 0.3 |
mmpL5 | 777883 | p.Gly200Arg | missense_variant | 0.18 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 0.23 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 0.27 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673553 | p.Asp38Glu | missense_variant | 0.23 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.4 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102817 | p.Leu76Val | missense_variant | 0.18 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.25 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 0.24 |
PPE35 | 2169879 | p.Phe245Cys | missense_variant | 0.78 |
PPE35 | 2170065 | p.Ala183Gly | missense_variant | 0.19 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519071 | p.Asp319Glu | missense_variant | 0.23 |
pepQ | 2860159 | p.Ala87Gly | missense_variant | 0.19 |
Rv2752c | 3064823 | p.Val457Leu | missense_variant | 0.16 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 0.71 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.99 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.73 |
fbiD | 3339746 | p.Ala210Gly | missense_variant | 0.38 |
fbiD | 3339749 | p.Val211Gly | missense_variant | 0.38 |
fbiD | 3339751 | p.Ala212Pro | missense_variant | 0.21 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568425 | c.255T>G | synonymous_variant | 0.2 |
whiB7 | 3568428 | c.252A>G | synonymous_variant | 0.35 |
whiB7 | 3568431 | c.249C>G | synonymous_variant | 0.25 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 0.14 |
fbiB | 3640830 | c.-705C>A | upstream_gene_variant | 0.79 |
rpoA | 3878590 | c.-83G>C | upstream_gene_variant | 0.3 |
rpoA | 3878597 | c.-90G>C | upstream_gene_variant | 0.2 |
rpoA | 3878609 | c.-102T>G | upstream_gene_variant | 0.22 |
rpoA | 3878613 | c.-106A>C | upstream_gene_variant | 0.38 |
rpoA | 3878628 | c.-121G>T | upstream_gene_variant | 0.4 |
rpoA | 3878637 | c.-130G>C | upstream_gene_variant | 0.67 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.77 |
embC | 4240409 | p.Pro183Ala | missense_variant | 0.34 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243225 | c.-8C>A | upstream_gene_variant | 0.26 |
embA | 4243460 | c.228C>T | synonymous_variant | 0.3 |
embB | 4246527 | p.Ala5Gly | missense_variant | 0.28 |
embB | 4247020 | c.507C>G | synonymous_variant | 0.21 |
embB | 4248324 | p.Ala604Gly | missense_variant | 0.18 |
embB | 4248328 | c.1815G>C | synonymous_variant | 0.26 |
embB | 4249594 | c.3081G>A | synonymous_variant | 0.72 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 0.16 |
ethA | 4326632 | p.His281Pro | missense_variant | 0.77 |
ethA | 4328376 | c.-903G>C | upstream_gene_variant | 0.82 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.26 |
gid | 4407927 | p.Glu92Asp | missense_variant | 0.29 |