Run ID: SRR1173725
Sample name:
Date: 03-04-2023 03:30:33
Number of reads: 1926526
Percentage reads mapped: 93.57
Strain: lineage8
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage8 | Lineage 8 | None | None | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761109 | p.Asp435Tyr | missense_variant | 1.0 | rifampicin |
rpoB | 761127 | p.Ser441Ala | missense_variant | 0.5 | rifampicin |
inhA | 1674481 | p.Ser94Ala | missense_variant | 1.0 | isoniazid, ethionamide |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288988 | p.Leu85Arg | missense_variant | 0.19 | pyrazinamide |
pncA | 2289081 | p.Pro54Gln | missense_variant | 0.78 | pyrazinamide |
embA | 4243222 | c.-11C>A | upstream_gene_variant | 0.71 | ethambutol |
embB | 4247495 | p.Asp328Tyr | missense_variant | 0.46 | 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 | 8553 | p.Arg418Trp | missense_variant | 1.0 |
gyrA | 9088 | p.Val596Ala | missense_variant | 0.15 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
mmpL5 | 775611 | p.Ser957* | stop_gained | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpR5 | 779192 | p.Ser68Ile | missense_variant | 0.46 |
mmpS5 | 779536 | c.-631G>A | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406466 | p.Ser292Leu | missense_variant | 1.0 |
embR | 1417464 | c.-117C>T | upstream_gene_variant | 1.0 |
atpE | 1461057 | p.Ile5Leu | missense_variant | 0.25 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472770 | n.925C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472905 | n.1060C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475841 | n.2184T>G | non_coding_transcript_exon_variant | 0.22 |
fabG1 | 1673219 | c.-221C>T | upstream_gene_variant | 0.12 |
tlyA | 1917786 | c.-154G>A | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155155 | c.957C>T | synonymous_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168701 | p.Val638Ile | missense_variant | 1.0 |
PPE35 | 2168924 | c.1689G>T | synonymous_variant | 0.99 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 0.92 |
eis | 2714418 | c.915C>T | synonymous_variant | 1.0 |
ahpC | 2726247 | p.Ile19Val | missense_variant | 0.29 |
pepQ | 2859482 | p.Ala313Thr | missense_variant | 1.0 |
thyA | 3074400 | c.72C>G | synonymous_variant | 1.0 |
thyA | 3074591 | c.-120T>G | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449865 | c.1362G>A | synonymous_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
Rv3236c | 3612035 | p.Val361Gly | missense_variant | 0.15 |
Rv3236c | 3612540 | p.Leu193Phe | missense_variant | 1.0 |
alr | 3840800 | c.621C>A | synonymous_variant | 1.0 |
rpoA | 3878403 | c.105C>A | synonymous_variant | 0.14 |
clpC1 | 4039645 | p.His354Asp | missense_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243225 | c.-8C>A | upstream_gene_variant | 0.29 |
embA | 4245411 | p.Ser727Cys | missense_variant | 0.2 |
embB | 4247252 | p.Ser247Ala | missense_variant | 1.0 |
embB | 4247483 | p.Gly324Arg | missense_variant | 0.58 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4248022 | p.Leu503Phe | missense_variant | 1.0 |
embB | 4248206 | p.Ser565Gly | missense_variant | 1.0 |
aftB | 4267683 | p.Trp385Ser | missense_variant | 0.18 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ethA | 4326264 | p.Arg404Cys | missense_variant | 1.0 |
ethA | 4327442 | p.Gly11Asp | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407760 | c.442_443insC | frameshift_variant | 1.0 |