Run ID: ERR8665510
Sample name:
Date: 02-04-2023 07:30:12
Number of reads: 211257
Percentage reads mapped: 99.57
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 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7582 | p.Asp94Gly | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
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 |
rrs | 1473246 | n.1401A>G | non_coding_transcript_exon_variant | 1.0 | kanamycin, capreomycin, aminoglycosides, amikacin |
fabG1 | 1673432 | c.-8T>C | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
embB | 4247431 | p.Met306Ile | missense_variant | 1.0 | ethambutol |
ethA | 4326087 | c.1386delA | frameshift_variant | 1.0 | ethionamide, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6665 | p.Gln476Lys | missense_variant | 0.5 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9326 | c.2025G>T | synonymous_variant | 0.33 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 766190 | p.Gly941Cys | missense_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 776357 | p.Phe708Leu | missense_variant | 0.29 |
mmpL5 | 777902 | c.579C>A | synonymous_variant | 0.4 |
mmpL5 | 778400 | p.Met27Ile | missense_variant | 0.67 |
mmpL5 | 778431 | p.Arg17Met | missense_variant | 0.4 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
mmpS5 | 779651 | c.-746G>T | upstream_gene_variant | 0.67 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800906 | p.Pro33His | missense_variant | 0.4 |
Rv1258c | 1406263 | p.Gly360Cys | missense_variant | 0.29 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1406789 | c.552C>A | synonymous_variant | 0.4 |
embR | 1417186 | c.162C>A | synonymous_variant | 0.5 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472755 | n.910G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472950 | n.1105C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474108 | n.451C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474573 | n.916C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474874 | n.1217A>G | non_coding_transcript_exon_variant | 0.18 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834585 | c.1044C>A | synonymous_variant | 0.33 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103036 | p.Pro3Thr | missense_variant | 0.29 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2154848 | p.Pro422Thr | missense_variant | 0.6 |
katG | 2156006 | p.Gln36Lys | missense_variant | 0.2 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169527 | c.1086G>T | synonymous_variant | 0.5 |
PPE35 | 2170427 | c.186G>A | synonymous_variant | 0.29 |
Rv1979c | 2221893 | c.1272C>A | synonymous_variant | 0.33 |
Rv1979c | 2223162 | c.3G>T | synonymous_variant | 0.33 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289240 | c.2T>C | start_lost | 1.0 |
eis | 2714568 | c.765C>A | synonymous_variant | 0.29 |
eis | 2714599 | p.Thr245Asn | missense_variant | 0.25 |
ribD | 2987295 | p.Arg153Ser | missense_variant | 0.29 |
Rv2752c | 3065738 | p.Asp152Tyr | missense_variant | 0.25 |
ald | 3086731 | c.-89A>G | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086846 | c.32delA | frameshift_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiB | 3640980 | c.-555C>A | upstream_gene_variant | 0.29 |
fbiB | 3642282 | p.Glu250* | stop_gained | 0.33 |
rpoA | 3878297 | p.Glu71* | stop_gained | 0.25 |
ddn | 3987026 | c.183C>A | synonymous_variant | 0.18 |
ddn | 3987070 | p.Ala76Glu | missense_variant | 0.15 |
clpC1 | 4038707 | c.1998C>A | synonymous_variant | 0.29 |
clpC1 | 4038760 | p.Asp649Tyr | missense_variant | 0.5 |
clpC1 | 4039674 | p.Pro344Gln | missense_variant | 0.4 |
panD | 4044036 | c.246G>T | synonymous_variant | 0.4 |
embC | 4240436 | p.Asp192Tyr | missense_variant | 0.33 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243346 | c.114A>G | synonymous_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4245152 | c.1920C>A | synonymous_variant | 0.38 |
embA | 4245155 | c.1923C>A | synonymous_variant | 0.25 |
embB | 4245779 | c.-735C>A | upstream_gene_variant | 0.5 |
embB | 4247323 | c.810G>T | synonymous_variant | 0.5 |
embB | 4249271 | p.Asp920Tyr | missense_variant | 0.33 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268344 | p.Arg165Ser | missense_variant | 0.22 |
ethA | 4327479 | c.-6G>T | upstream_gene_variant | 0.17 |
whiB6 | 4338371 | p.Thr51Pro | missense_variant | 1.0 |
whiB6 | 4338404 | p.Arg40Ser | missense_variant | 0.25 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338676 | c.-156delG | upstream_gene_variant | 0.2 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |