Run ID: SRR3675272
Sample name:
Date: 04-04-2023 05:25:03
Number of reads: 288736
Percentage reads mapped: 98.88
Strain: lineage3
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2155573 | p.Thr180Lys | missense_variant | 0.14 | isoniazid |
ahpC | 2726145 | c.-48G>T | upstream_gene_variant | 0.17 | isoniazid |
ethA | 4327132 | c.341dupA | frameshift_variant | 0.29 | ethionamide, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8667 | p.Ala456Ser | missense_variant | 0.2 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491027 | p.Asn82Thr | missense_variant | 0.25 |
fgd1 | 491057 | p.Thr92Ile | missense_variant | 0.25 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576751 | p.Lys468Asn | missense_variant | 0.33 |
ccsA | 620537 | p.Val216Gly | missense_variant | 1.0 |
rpoB | 759620 | c.-187A>C | upstream_gene_variant | 0.25 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 761592 | c.1788delC | frameshift_variant | 0.25 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764566 | c.1197C>A | synonymous_variant | 0.22 |
rpoC | 765538 | p.Trp723Cys | missense_variant | 0.33 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777158 | c.1323C>A | synonymous_variant | 0.18 |
mmpR5 | 778016 | c.-974G>T | upstream_gene_variant | 0.22 |
mmpL5 | 778537 | c.-57G>A | upstream_gene_variant | 1.0 |
mmpL5 | 778570 | c.-90C>A | upstream_gene_variant | 0.2 |
mmpS5 | 778872 | p.Leu12Met | missense_variant | 0.18 |
mmpS5 | 779680 | c.-775G>T | upstream_gene_variant | 0.25 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473666 | n.9G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473774 | n.117G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474319 | n.662C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475008 | n.1351C>A | non_coding_transcript_exon_variant | 0.95 |
ndh | 2103221 | c.-179C>T | upstream_gene_variant | 1.0 |
katG | 2154051 | c.2061G>T | synonymous_variant | 0.15 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155007 | p.Gly369Ser | missense_variant | 0.22 |
katG | 2156289 | c.-178G>A | upstream_gene_variant | 0.2 |
PPE35 | 2167865 | c.2748G>C | synonymous_variant | 0.2 |
PPE35 | 2167868 | c.2745A>C | synonymous_variant | 0.2 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.15 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.13 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.39 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.47 |
Rv1979c | 2221884 | c.1281G>T | synonymous_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
pncA | 2289783 | c.-542G>T | upstream_gene_variant | 0.29 |
eis | 2715172 | p.Pro54Gln | missense_variant | 0.22 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
Rv2752c | 3064917 | p.Asn425Lys | missense_variant | 0.18 |
Rv2752c | 3065791 | p.Thr134Ile | missense_variant | 0.25 |
thyA | 3074531 | c.-60G>T | upstream_gene_variant | 0.4 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448397 | c.-107G>A | upstream_gene_variant | 0.29 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
alr | 3840975 | p.Gly149Asp | missense_variant | 0.22 |
ddn | 3986840 | c.-4C>A | upstream_gene_variant | 0.4 |
panD | 4044109 | p.Tyr58Phe | missense_variant | 0.29 |
embC | 4240648 | c.786C>T | synonymous_variant | 0.29 |
embC | 4241424 | p.Arg521Leu | missense_variant | 0.33 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245320 | c.2088C>A | synonymous_variant | 0.25 |
embA | 4245372 | p.Pro714Ser | missense_variant | 1.0 |
embB | 4247652 | p.Ser380Ile | missense_variant | 0.15 |
embB | 4249456 | c.2943G>A | synonymous_variant | 1.0 |
aftB | 4268390 | c.447G>T | synonymous_variant | 0.22 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |