Run ID: SRR5535687
Sample name:
Date: 04-04-2023 10:37:48
Number of reads: 1705670
Percentage reads mapped: 99.33
Strain: lineage4.1.3
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.3 | Euro-American | T;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761110 | p.Asp435Val | missense_variant | 1.0 | rifampicin |
fabG1 | 1673432 | c.-8T>A | upstream_gene_variant | 1.0 | isoniazid |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289073 | p.His57Tyr | missense_variant | 1.0 | pyrazinamide |
pncA | 2289235 | p.Ala3Pro | missense_variant | 0.12 | pyrazinamide |
embB | 4247431 | p.Met306Ile | missense_variant | 1.0 | ethambutol |
gid | 4407967 | p.Leu79Ser | missense_variant | 1.0 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5187 | c.-53C>A | upstream_gene_variant | 0.13 |
gyrA | 6304 | c.-998C>A | upstream_gene_variant | 0.18 |
gyrB | 7097 | p.Glu620* | stop_gained | 0.17 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9557 | c.2256G>C | synonymous_variant | 1.0 |
fgd1 | 490860 | c.79delG | frameshift_variant | 0.11 |
fgd1 | 491110 | p.Ala110Ser | missense_variant | 0.11 |
fgd1 | 491754 | p.Phe324Leu | missense_variant | 0.13 |
rpoB | 763207 | p.Ser1134Ile | missense_variant | 0.13 |
rpoC | 763447 | c.78C>A | synonymous_variant | 0.17 |
rpoC | 764196 | p.Ser276* | stop_gained | 0.13 |
rpoC | 764438 | p.Leu357Met | missense_variant | 0.12 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 767125 | c.3756G>T | synonymous_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776079 | p.Ala801Asp | missense_variant | 0.21 |
mmpL5 | 776131 | p.Leu784Ile | missense_variant | 0.14 |
mmpL5 | 776150 | p.Met777Ile | missense_variant | 0.12 |
mmpL5 | 776767 | p.Ala572Pro | missense_variant | 0.5 |
mmpR5 | 779144 | p.Ser52Tyr | missense_variant | 0.12 |
mmpR5 | 779471 | p.Thr161Ile | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781421 | c.-139C>A | upstream_gene_variant | 0.91 |
fbiC | 1304610 | c.1680C>T | synonymous_variant | 1.0 |
atpE | 1461242 | c.198C>A | synonymous_variant | 0.25 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472007 | n.162G>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472290 | n.445C>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472391 | n.546C>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473154 | n.1309C>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473394 | n.-264C>A | upstream_gene_variant | 0.3 |
rrl | 1473718 | n.61G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474497 | n.840G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476714 | n.3057G>C | non_coding_transcript_exon_variant | 0.25 |
fabG1 | 1673924 | p.Gly162Val | missense_variant | 0.22 |
fabG1 | 1674058 | p.Pro207Thr | missense_variant | 0.13 |
inhA | 1674102 | c.-100C>A | upstream_gene_variant | 0.2 |
inhA | 1674450 | c.249G>T | synonymous_variant | 0.2 |
inhA | 1674719 | p.Arg173Met | missense_variant | 0.13 |
rpsA | 1833570 | p.Gln10Arg | missense_variant | 0.11 |
rpsA | 1833813 | p.Leu91Arg | missense_variant | 0.14 |
rpsA | 1833880 | p.Trp113Cys | missense_variant | 0.12 |
rpsA | 1834486 | p.Glu315Asp | missense_variant | 0.22 |
rpsA | 1834816 | c.1275C>T | synonymous_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102632 | c.411C>A | synonymous_variant | 0.18 |
ndh | 2103162 | c.-120G>T | upstream_gene_variant | 0.13 |
PPE35 | 2168227 | p.Thr796Ala | missense_variant | 0.22 |
Rv1979c | 2221869 | p.Tyr432* | stop_gained | 0.2 |
Rv1979c | 2221885 | p.Gly427Val | missense_variant | 0.2 |
Rv1979c | 2222785 | p.Trp127Leu | missense_variant | 0.22 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289369 | c.-128C>A | upstream_gene_variant | 0.17 |
pncA | 2289657 | c.-416G>T | upstream_gene_variant | 0.14 |
eis | 2714263 | p.Gly357Asp | missense_variant | 0.15 |
ahpC | 2726233 | p.Gln14Arg | missense_variant | 0.13 |
folC | 2747566 | c.33G>T | synonymous_variant | 0.13 |
Rv2752c | 3064629 | c.1563C>A | synonymous_variant | 0.14 |
Rv2752c | 3065512 | p.Arg227Gln | missense_variant | 1.0 |
Rv2752c | 3065892 | p.Ile100Met | missense_variant | 0.14 |
thyA | 3074215 | p.Asp86Val | missense_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448956 | c.453G>A | synonymous_variant | 0.15 |
Rv3083 | 3449465 | p.Ile321Thr | missense_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474135 | c.129G>A | synonymous_variant | 0.18 |
Rv3236c | 3612936 | p.Gly61Ser | missense_variant | 0.15 |
fbiB | 3642863 | c.1329T>C | synonymous_variant | 0.11 |
clpC1 | 4039071 | p.Pro545Leu | missense_variant | 0.17 |
clpC1 | 4039540 | p.Tyr389Asp | missense_variant | 0.11 |
clpC1 | 4039882 | p.Glu275* | stop_gained | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embB | 4249211 | p.Leu900Phe | missense_variant | 0.12 |
aftB | 4266969 | p.Pro623Gln | missense_variant | 0.18 |
aftB | 4266971 | c.1866C>T | synonymous_variant | 0.18 |
aftB | 4268005 | c.832T>C | synonymous_variant | 0.13 |
aftB | 4268641 | p.Leu66Met | missense_variant | 0.18 |
ubiA | 4269382 | p.Cys151Phe | missense_variant | 0.18 |
ethA | 4327067 | p.Leu136Arg | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407596 | p.Val203Met | missense_variant | 0.11 |