Run ID: SRR6257061
Sample name:
Date: 04-04-2023 13:24:53
Number of reads: 443699
Percentage reads mapped: 97.96
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 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rpoC | 764841 | p.Ile491Thr | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288878 | p.Gln122* | stop_gained | 1.0 | pyrazinamide |
embA | 4243221 | c.-12C>T | upstream_gene_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6729 | p.Leu497Pro | missense_variant | 0.12 |
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 | 491331 | p.Lys183Asn | missense_variant | 0.22 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575602 | c.255G>A | synonymous_variant | 0.17 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 760250 | p.Met148Ile | missense_variant | 0.15 |
rpoB | 762154 | p.Ile783Thr | missense_variant | 0.15 |
rpoB | 762156 | c.2350_2351insA | frameshift_variant | 0.14 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 1.0 |
mmpL5 | 775595 | c.2886C>A | synonymous_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775736 | c.2745C>G | synonymous_variant | 0.13 |
mmpL5 | 775741 | c.2740C>T | synonymous_variant | 0.15 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 777119 | p.His454Gln | missense_variant | 0.29 |
mmpL5 | 777122 | c.1359C>T | synonymous_variant | 0.29 |
mmpL5 | 777128 | c.1353A>G | synonymous_variant | 0.4 |
mmpS5 | 778770 | p.Asp46Tyr | missense_variant | 0.2 |
mmpR5 | 779318 | p.Ala110Glu | missense_variant | 0.15 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304871 | c.1941G>A | synonymous_variant | 0.2 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
embR | 1416222 | p.Phe376Leu | missense_variant | 0.17 |
embR | 1416232 | p.Cys372Gly | missense_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475084 | n.1427G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475102 | n.1445C>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475188 | n.1531C>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475714 | n.2057G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476186 | n.2529T>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476681 | n.3024T>C | non_coding_transcript_exon_variant | 0.15 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.28 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.28 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.24 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.24 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.24 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.5 |
rpsA | 1833476 | c.-66T>C | upstream_gene_variant | 0.29 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103216 | c.-174G>A | upstream_gene_variant | 0.13 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2156315 | c.-204T>C | upstream_gene_variant | 0.12 |
PPE35 | 2167814 | c.2799C>T | synonymous_variant | 0.16 |
PPE35 | 2167865 | c.2748G>C | synonymous_variant | 0.23 |
PPE35 | 2167868 | c.2745A>C | synonymous_variant | 0.23 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167939 | c.2673_2674insAC | frameshift_variant | 0.11 |
PPE35 | 2168231 | c.2382T>C | synonymous_variant | 0.22 |
PPE35 | 2168234 | c.2379G>T | synonymous_variant | 0.22 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.11 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.11 |
PPE35 | 2169302 | p.Met437Phe | missense_variant | 0.14 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.44 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.44 |
Rv1979c | 2222112 | c.1052dupT | frameshift_variant | 1.0 |
Rv1979c | 2222848 | p.Trp106Leu | missense_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518577 | p.Gly155Ser | missense_variant | 0.2 |
kasA | 2519140 | c.1026G>C | synonymous_variant | 0.5 |
kasA | 2519143 | c.1029G>C | synonymous_variant | 0.5 |
eis | 2714964 | c.369C>T | synonymous_variant | 0.15 |
eis | 2715248 | p.Gly29Ser | missense_variant | 0.14 |
eis | 2715276 | c.57G>T | synonymous_variant | 0.15 |
eis | 2715450 | c.-118T>C | upstream_gene_variant | 0.2 |
eis | 2715585 | c.-253C>A | upstream_gene_variant | 1.0 |
ahpC | 2726341 | p.Val50Gly | missense_variant | 0.29 |
Rv2752c | 3065200 | p.Gly331Val | missense_variant | 0.13 |
Rv2752c | 3066137 | p.Thr19Ala | missense_variant | 0.25 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339452 | p.Val112Glu | missense_variant | 0.14 |
fbiD | 3339694 | p.Ala193Thr | missense_variant | 0.25 |
Rv3083 | 3449775 | c.1272C>A | synonymous_variant | 0.13 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474109 | p.Ala35Thr | missense_variant | 0.2 |
fprA | 3475360 | p.Arg452Trp | missense_variant | 0.22 |
Rv3236c | 3612687 | p.Gly144Ser | missense_variant | 0.22 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
Rv3236c | 3613168 | c.-52A>G | upstream_gene_variant | 0.13 |
fbiA | 3640367 | c.-176A>G | upstream_gene_variant | 1.0 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.27 |
rpoA | 3878483 | p.Leu9Met | missense_variant | 0.2 |
ddn | 3986931 | p.Arg30Ser | missense_variant | 1.0 |
clpC1 | 4039642 | p.Thr355Ser | missense_variant | 0.14 |
clpC1 | 4039829 | p.Leu292Phe | missense_variant | 0.12 |
panD | 4044320 | c.-39C>T | upstream_gene_variant | 0.2 |
embC | 4239863 | c.1A>T | initiator_codon_variant | 0.25 |
embC | 4240757 | p.Thr299Gly | missense_variant | 0.2 |
embC | 4241275 | c.1413A>G | synonymous_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4243063 | p.Tyr1067* | stop_gained | 0.4 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4244457 | p.Ala409Thr | missense_variant | 0.25 |
embA | 4244832 | p.Val534Met | missense_variant | 0.25 |
embA | 4245950 | p.Gln906His | missense_variant | 0.22 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.25 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.25 |
embB | 4247395 | c.882C>T | synonymous_variant | 0.12 |
embB | 4247512 | c.999T>C | synonymous_variant | 0.18 |
embB | 4247516 | p.Asn335Asp | missense_variant | 0.18 |
embB | 4247695 | c.1182G>C | synonymous_variant | 0.22 |
embB | 4247699 | p.Met396Leu | missense_variant | 0.22 |
embB | 4247986 | c.1473C>T | synonymous_variant | 0.17 |
embB | 4248019 | c.1506G>T | synonymous_variant | 0.14 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4267831 | p.Gly336Cys | missense_variant | 0.4 |
ethA | 4326437 | p.Leu346Pro | missense_variant | 0.15 |
ethA | 4328302 | c.-829C>A | upstream_gene_variant | 0.22 |
whiB6 | 4338214 | c.306_307dupCG | frameshift_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |