Run ID: ERR4832067
Sample name:
Date: 01-04-2023 21:18:03
Number of reads: 572955
Percentage reads mapped: 78.78
Strain: lineage2.2.1.1
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 |
lineage2.2.1.1 | East-Asian (Beijing) | Beijing-RD150 | RD105;RD207;RD181;RD150 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 0.96 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
katG | 2155999 | p.Trp38* | stop_gained | 0.18 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5710 | c.471C>G | synonymous_variant | 0.15 |
gyrA | 6460 | c.-842G>T | upstream_gene_variant | 0.33 |
gyrA | 6916 | c.-386G>C | upstream_gene_variant | 0.12 |
gyrB | 6922 | c.1688delT | frameshift_variant | 0.13 |
gyrB | 6979 | p.Phe580Leu | missense_variant | 0.13 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8645 | c.1344C>G | synonymous_variant | 0.11 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491284 | p.Gly168Arg | missense_variant | 0.2 |
fgd1 | 491289 | c.507C>A | synonymous_variant | 0.33 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
fgd1 | 491746 | p.Glu322* | stop_gained | 0.17 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 762487 | p.Pro894Gln | missense_variant | 0.12 |
rpoB | 762522 | p.Pro906Thr | missense_variant | 0.12 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 765725 | p.Gly786Ser | missense_variant | 0.14 |
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 | 776418 | p.Ser688* | stop_gained | 0.29 |
mmpL5 | 776695 | p.Val596Phe | missense_variant | 0.14 |
mmpL5 | 778918 | c.-438G>T | upstream_gene_variant | 0.33 |
mmpR5 | 779192 | p.Ser68Ile | missense_variant | 0.15 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781444 | c.-116C>A | upstream_gene_variant | 0.13 |
rpsL | 781453 | c.-107C>G | upstream_gene_variant | 0.13 |
rpsL | 781465 | c.-95G>T | upstream_gene_variant | 0.13 |
rplC | 800921 | p.Arg38His | missense_variant | 0.18 |
rplC | 800967 | c.159C>A | synonymous_variant | 0.12 |
fbiC | 1304672 | p.Val581Ala | missense_variant | 0.1 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
embR | 1416232 | c.1116T>C | synonymous_variant | 0.1 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471870 | n.25G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472861 | n.1016G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472885 | n.1040T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473082 | n.1237G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474097 | n.440C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474904 | n.1247G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475721 | n.2064C>A | non_coding_transcript_exon_variant | 0.5 |
fabG1 | 1673944 | p.Arg169Cys | missense_variant | 0.12 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834352 | c.811C>A | synonymous_variant | 0.12 |
rpsA | 1834535 | p.Glu332* | stop_gained | 0.29 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102449 | p.Lys198Asn | missense_variant | 0.17 |
ndh | 2102772 | p.His91Asn | missense_variant | 0.18 |
katG | 2154389 | p.Ser575Pro | missense_variant | 0.12 |
katG | 2154426 | p.Asn562Lys | missense_variant | 0.13 |
katG | 2154703 | p.Ser470Leu | missense_variant | 0.17 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2154780 | c.1332G>A | synonymous_variant | 0.14 |
PPE35 | 2167743 | p.Gly957Val | missense_variant | 0.12 |
PPE35 | 2167886 | p.Phe909Leu | missense_variant | 0.13 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168579 | c.2034C>A | synonymous_variant | 0.12 |
PPE35 | 2168604 | p.Pro670His | missense_variant | 0.13 |
PPE35 | 2169032 | p.Phe527Leu | missense_variant | 0.22 |
PPE35 | 2169560 | c.1053G>T | synonymous_variant | 0.4 |
PPE35 | 2170581 | p.Asn11Ser | missense_variant | 0.1 |
Rv1979c | 2222680 | p.Ala162Asp | missense_variant | 0.25 |
Rv1979c | 2222927 | p.Ala80Ser | missense_variant | 0.12 |
Rv1979c | 2222947 | p.Arg73Lys | missense_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv1979c | 2223330 | c.-166C>T | upstream_gene_variant | 0.33 |
pncA | 2289294 | c.-53G>C | upstream_gene_variant | 0.12 |
pncA | 2290204 | c.-963G>A | upstream_gene_variant | 0.22 |
pncA | 2290210 | c.-969G>A | upstream_gene_variant | 0.2 |
kasA | 2518195 | c.81G>A | synonymous_variant | 0.5 |
eis | 2714846 | p.Val163Ile | missense_variant | 1.0 |
ahpC | 2726670 | p.Glu160* | stop_gained | 0.13 |
ahpC | 2726735 | c.543C>A | synonymous_variant | 0.12 |
ahpC | 2726773 | p.Ser194Leu | missense_variant | 0.13 |
Rv2752c | 3064596 | c.1596G>T | synonymous_variant | 0.12 |
Rv2752c | 3064908 | p.Ser428Arg | missense_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087053 | p.Ile78Met | missense_variant | 0.2 |
Rv3083 | 3448312 | c.-192T>A | upstream_gene_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568408 | p.Val91Ala | missense_variant | 0.11 |
whiB7 | 3568648 | p.Pro11Arg | missense_variant | 0.2 |
whiB7 | 3568772 | c.-93C>A | upstream_gene_variant | 0.67 |
Rv3236c | 3612391 | c.726G>T | synonymous_variant | 0.15 |
Rv3236c | 3612425 | p.Ala231Glu | missense_variant | 0.14 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
rpoA | 3878268 | c.240C>A | synonymous_variant | 0.33 |
ddn | 3987125 | c.282C>A | synonymous_variant | 0.18 |
clpC1 | 4038643 | p.Asn688Asp | missense_variant | 0.33 |
clpC1 | 4039752 | p.Gln318Arg | missense_variant | 0.11 |
panD | 4043995 | p.Ala96Asp | missense_variant | 0.4 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4245175 | p.Ser648* | stop_gained | 0.12 |
embB | 4248115 | c.1602C>T | synonymous_variant | 1.0 |
embB | 4249550 | p.Arg1013Ser | missense_variant | 0.13 |
embB | 4249739 | p.Ala1076Ser | missense_variant | 0.17 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
ethA | 4326290 | p.Ala395Asp | missense_variant | 0.12 |
ethR | 4327369 | c.-180C>T | upstream_gene_variant | 0.12 |
ethA | 4327638 | c.-165G>T | upstream_gene_variant | 0.14 |
whiB6 | 4338286 | p.Val79Asp | missense_variant | 0.12 |
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 |