Run ID: SRR7517752
Sample name:
Date: 04-04-2023 19:35:54
Number of reads: 1186677
Percentage reads mapped: 94.63
Strain: lineage2.2
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rpoC | 764724 | p.Phe452Ser | missense_variant | 0.88 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
eis | 2715342 | c.-10G>A | upstream_gene_variant | 1.0 | kanamycin |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6980 | p.Ala581Thr | missense_variant | 0.5 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8249 | c.948C>A | synonymous_variant | 0.2 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
fgd1 | 491783 | p.Arg334Leu | missense_variant | 0.5 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 762679 | p.Leu958Pro | missense_variant | 0.33 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763753 | c.384C>A | synonymous_variant | 0.29 |
rpoC | 763841 | p.Glu158* | stop_gained | 0.18 |
rpoC | 764192 | p.Glu275* | stop_gained | 0.22 |
rpoC | 766424 | p.Gly1019Cys | missense_variant | 0.17 |
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 | 776872 | p.Glu537* | stop_gained | 0.4 |
mmpL5 | 777398 | c.1083G>T | synonymous_variant | 0.21 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1305094 | p.His722Asn | missense_variant | 0.22 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474844 | n.1187G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474866 | n.1209C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475877 | n.2220C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476204 | n.2547C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 1.0 |
inhA | 1674936 | c.735G>T | synonymous_variant | 0.4 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834420 | c.879C>A | synonymous_variant | 0.4 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2156246 | c.-135C>T | upstream_gene_variant | 0.29 |
katG | 2156268 | c.-157G>T | upstream_gene_variant | 0.2 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168474 | c.2139C>A | synonymous_variant | 0.4 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv1979c | 2223340 | c.-176T>C | upstream_gene_variant | 0.67 |
Rv1979c | 2223360 | c.-196G>T | upstream_gene_variant | 0.67 |
pncA | 2289313 | c.-72G>T | upstream_gene_variant | 0.18 |
pncA | 2289735 | c.-494C>A | upstream_gene_variant | 0.5 |
ahpC | 2725994 | c.-199G>T | upstream_gene_variant | 0.17 |
ahpC | 2726192 | c.-1C>A | upstream_gene_variant | 0.33 |
pepQ | 2859600 | c.819G>T | synonymous_variant | 0.5 |
pepQ | 2859663 | c.756G>A | synonymous_variant | 0.29 |
thyA | 3074382 | p.Phe30Leu | missense_variant | 0.29 |
ald | 3086731 | c.-89A>G | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086890 | p.Ala24Val | missense_variant | 0.25 |
ald | 3087144 | p.Asp109Tyr | missense_variant | 0.33 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474717 | c.711C>T | synonymous_variant | 0.17 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
alr | 3841606 | c.-186G>T | upstream_gene_variant | 0.29 |
rpoA | 3877847 | p.Leu221Met | missense_variant | 0.5 |
rpoA | 3877917 | p.Glu197Asp | missense_variant | 0.2 |
ddn | 3986963 | c.120C>A | synonymous_variant | 0.29 |
clpC1 | 4040476 | p.His77Tyr | missense_variant | 0.5 |
embC | 4241752 | p.Leu630Phe | missense_variant | 0.18 |
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 | 4249734 | p.Pro1074His | missense_variant | 0.29 |
aftB | 4267594 | p.Ala415Thr | missense_variant | 0.2 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4269156 | c.-320C>A | upstream_gene_variant | 0.4 |
ubiA | 4269208 | p.Ser209* | stop_gained | 0.4 |
aftB | 4269456 | c.-620G>T | upstream_gene_variant | 0.17 |
ethA | 4326606 | p.Asp290Tyr | missense_variant | 0.5 |
ethR | 4326625 | c.-924G>A | upstream_gene_variant | 0.75 |
whiB6 | 4338371 | p.Thr51Pro | missense_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 |