Run ID: ERR4832054
Sample name:
Date: 01-04-2023 21:17:38
Number of reads: 693534
Percentage reads mapped: 98.43
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 | 0.99 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.99 |
lineage2.2.1.1 | East-Asian (Beijing) | Beijing-RD150 | RD105;RD207;RD181;RD150 | 0.96 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761109 | p.Asp435Tyr | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 0.89 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
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 | 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 |
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 | 776464 | p.Ser673Thr | missense_variant | 0.18 |
mmpL5 | 776473 | p.Gln670Lys | missense_variant | 0.17 |
mmpL5 | 777163 | p.Gln440Lys | missense_variant | 0.11 |
mmpL5 | 778101 | p.Gln127Pro | missense_variant | 0.11 |
mmpL5 | 779010 | c.-530G>T | upstream_gene_variant | 0.14 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 0.9 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800764 | c.-45C>A | upstream_gene_variant | 0.14 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472099 | n.254G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472404 | n.559G>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473280 | n.1435G>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474134 | n.477G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474408 | n.751G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474507 | n.850G>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475062 | n.1405A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475953 | n.2296A>G | non_coding_transcript_exon_variant | 0.17 |
fabG1 | 1673507 | p.Gly23Glu | missense_variant | 0.15 |
inhA | 1673660 | c.-542C>A | upstream_gene_variant | 0.12 |
rpsA | 1833558 | p.Val6Ala | missense_variant | 0.18 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.12 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.13 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154456 | c.1656A>T | synonymous_variant | 0.15 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155523 | p.Tyr197Asn | missense_variant | 0.14 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168804 | p.Gly603Arg | missense_variant | 0.13 |
PPE35 | 2169432 | p.Pro394Gln | missense_variant | 0.13 |
Rv1979c | 2222090 | c.1075T>C | synonymous_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288857 | p.Asp129Tyr | missense_variant | 1.0 |
eis | 2714846 | p.Val163Ile | missense_variant | 1.0 |
thyA | 3073952 | p.Val174Leu | missense_variant | 0.25 |
ald | 3086782 | c.-38T>C | upstream_gene_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448902 | c.399C>T | synonymous_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568427 | p.Arg85Ser | missense_variant | 0.12 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
rpoA | 3878154 | c.354G>T | synonymous_variant | 0.15 |
ddn | 3986939 | c.96C>T | synonymous_variant | 0.12 |
clpC1 | 4039068 | p.Ser546* | stop_gained | 0.14 |
clpC1 | 4040550 | p.Leu52Ser | missense_variant | 0.11 |
embC | 4241432 | p.Met524Val | missense_variant | 0.1 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 0.98 |
embA | 4245169 | p.Val646Gly | missense_variant | 0.11 |
embB | 4248115 | c.1602C>T | synonymous_variant | 1.0 |
embB | 4248339 | p.Leu609Pro | missense_variant | 0.12 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4267922 | c.915G>T | synonymous_variant | 0.11 |
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 |