Run ID: ERR8665507
Sample name:
Date: 02-04-2023 07:30:07
Number of reads: 214499
Percentage reads mapped: 99.56
Strain: lineage2.2.1
Drug-resistance: Pre-XDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
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 | 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 | 5234 | c.-6C>A | upstream_gene_variant | 0.18 |
gyrB | 5511 | p.Ser91Tyr | missense_variant | 0.43 |
gyrB | 5888 | p.Glu217* | stop_gained | 0.29 |
gyrB | 6824 | p.Leu529Met | missense_variant | 0.22 |
gyrA | 7573 | p.Ser91* | stop_gained | 0.25 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8011 | p.Ser237Tyr | missense_variant | 0.2 |
gyrA | 8013 | p.Gln238Lys | missense_variant | 0.18 |
gyrA | 8200 | p.Ser300Tyr | missense_variant | 0.25 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9618 | p.Glu773Gln | missense_variant | 0.29 |
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 |
rpoB | 760490 | c.684C>A | synonymous_variant | 0.17 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763654 | c.285C>A | synonymous_variant | 0.4 |
rpoC | 766723 | c.3354G>A | synonymous_variant | 0.18 |
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 | 776704 | p.Asp593Tyr | missense_variant | 0.33 |
mmpL5 | 777211 | p.Asp424Tyr | missense_variant | 0.2 |
mmpS5 | 779489 | c.-584C>A | upstream_gene_variant | 0.33 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800747 | c.-62C>A | upstream_gene_variant | 0.17 |
fbiC | 1305070 | p.Asp714Tyr | missense_variant | 0.25 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471866 | n.21C>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473173 | n.1328C>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473514 | n.-144C>A | upstream_gene_variant | 0.25 |
rrl | 1475214 | n.1557G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475450 | n.1793C>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476297 | n.2640C>A | non_coding_transcript_exon_variant | 0.25 |
rpsA | 1833409 | c.-133C>A | upstream_gene_variant | 0.4 |
rpsA | 1834093 | c.552G>T | synonymous_variant | 0.5 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918402 | p.Leu155Met | missense_variant | 0.5 |
ndh | 2103065 | c.-23G>T | upstream_gene_variant | 0.25 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2156006 | p.Gln36Lys | missense_variant | 0.29 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2221731 | c.1434G>T | synonymous_variant | 0.25 |
Rv1979c | 2222328 | c.837G>T | synonymous_variant | 0.29 |
Rv1979c | 2222420 | p.Asp249Tyr | missense_variant | 0.5 |
Rv1979c | 2223045 | c.120C>A | synonymous_variant | 0.33 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288898 | p.Pro115Gln | missense_variant | 0.29 |
pncA | 2289240 | c.2T>C | start_lost | 1.0 |
kasA | 2518610 | p.Thr166Ala | missense_variant | 1.0 |
eis | 2715087 | c.246C>A | synonymous_variant | 0.67 |
ahpC | 2726171 | c.-22C>A | upstream_gene_variant | 0.2 |
ahpC | 2726256 | p.Asp22Tyr | missense_variant | 0.22 |
folC | 2747420 | p.Pro60His | missense_variant | 0.4 |
Rv2752c | 3066308 | c.-117G>T | upstream_gene_variant | 0.29 |
thyA | 3074356 | p.Ser39* | stop_gained | 0.33 |
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 |
ald | 3087076 | p.Arg86Leu | missense_variant | 0.4 |
ald | 3087348 | p.Gly177Ser | missense_variant | 0.29 |
ald | 3087723 | p.Pro302Thr | missense_variant | 0.17 |
fbiD | 3338940 | c.-178C>A | upstream_gene_variant | 0.22 |
Rv3083 | 3449865 | p.Gln454His | missense_variant | 0.33 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474720 | c.714G>T | synonymous_variant | 0.33 |
Rv3236c | 3612471 | p.Glu216* | stop_gained | 0.5 |
Rv3236c | 3612477 | p.Asp214Tyr | missense_variant | 0.5 |
Rv3236c | 3612793 | c.324C>A | synonymous_variant | 0.29 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiB | 3641960 | c.426C>A | synonymous_variant | 0.67 |
alr | 3840626 | c.795C>A | synonymous_variant | 0.25 |
clpC1 | 4038555 | p.Ile717Asn | missense_variant | 0.29 |
clpC1 | 4038832 | p.Asp625Tyr | missense_variant | 0.29 |
clpC1 | 4039883 | p.Lys274Asn | missense_variant | 0.4 |
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 |
embB | 4245794 | c.-720G>T | upstream_gene_variant | 0.25 |
embB | 4248109 | c.1596C>A | synonymous_variant | 0.33 |
embB | 4249201 | p.Gln896His | missense_variant | 0.33 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
ethA | 4327359 | p.Glu39* | stop_gained | 0.33 |
ethA | 4328245 | c.-772C>A | upstream_gene_variant | 0.4 |
whiB6 | 4338371 | p.Thr51Pro | missense_variant | 1.0 |
whiB6 | 4338558 | c.-37G>T | upstream_gene_variant | 0.22 |
whiB6 | 4338592 | c.-71G>T | upstream_gene_variant | 0.25 |
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 |