Run ID: SRR4035834
Sample name:
Date: 04-04-2023 07:19:40
Number of reads: 1051269
Percentage reads mapped: 99.44
Strain: lineage4.1.2
Drug-resistance: Other
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 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
pncA | 2289026 | p.Cys72Trp | missense_variant | 0.13 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7319 | c.18G>A | synonymous_variant | 0.13 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7448 | p.Lys49Asn | missense_variant | 0.11 |
gyrA | 7463 | c.162G>C | synonymous_variant | 0.11 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7805 | c.504C>T | synonymous_variant | 0.29 |
gyrA | 7820 | c.519G>A | synonymous_variant | 0.13 |
gyrA | 7828 | p.Asn176Ile | missense_variant | 0.13 |
gyrA | 8061 | p.Arg254Cys | missense_variant | 1.0 |
gyrA | 8634 | p.Ala445Ser | missense_variant | 0.12 |
gyrA | 8862 | p.Thr521Ala | missense_variant | 0.14 |
gyrA | 9033 | p.Arg578Trp | missense_variant | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9388 | p.Ala696Gly | missense_variant | 0.1 |
gyrA | 9453 | p.Arg718Ser | missense_variant | 0.12 |
fgd1 | 490592 | c.-191C>A | upstream_gene_variant | 0.17 |
fgd1 | 491518 | p.Thr246Ala | missense_variant | 0.22 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575504 | p.His53Tyr | missense_variant | 0.22 |
ccsA | 620017 | p.Gly43Arg | missense_variant | 0.13 |
ccsA | 620359 | p.Tyr157His | missense_variant | 0.11 |
ccsA | 620630 | p.Gly247Asp | missense_variant | 0.15 |
rpoB | 760017 | c.211C>A | synonymous_variant | 0.12 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 760747 | p.Leu314His | missense_variant | 0.2 |
rpoB | 760758 | p.Val318Ile | missense_variant | 0.15 |
rpoB | 760770 | p.Ile322Val | missense_variant | 0.13 |
rpoB | 760783 | p.Thr326Lys | missense_variant | 0.15 |
rpoC | 763103 | c.-267G>T | upstream_gene_variant | 0.13 |
rpoC | 763899 | p.Leu177Pro | missense_variant | 0.22 |
rpoC | 763974 | p.Glu202Gly | missense_variant | 0.12 |
rpoC | 764263 | c.894G>A | synonymous_variant | 1.0 |
rpoC | 764811 | p.Pro481Arg | missense_variant | 0.11 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765228 | p.Met620Lys | missense_variant | 0.14 |
rpoC | 765275 | p.Arg636Trp | missense_variant | 0.2 |
rpoC | 765866 | p.Pro833Thr | missense_variant | 0.14 |
rpoC | 766488 | p.Pro1040Leu | missense_variant | 0.15 |
rpoC | 766779 | p.Glu1137Gly | missense_variant | 0.11 |
rpoC | 766899 | p.Pro1177Leu | missense_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776205 | p.Gly759Val | missense_variant | 0.22 |
mmpL5 | 776339 | p.His714Gln | missense_variant | 0.12 |
mmpL5 | 777083 | c.1398C>T | synonymous_variant | 0.15 |
mmpL5 | 777320 | c.1161C>G | synonymous_variant | 1.0 |
mmpL5 | 777922 | p.Thr187Ala | missense_variant | 0.11 |
mmpS5 | 778554 | p.Val118Ile | missense_variant | 0.15 |
mmpS5 | 778704 | p.Asn68Asp | missense_variant | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304320 | p.Ser464Cys | missense_variant | 0.25 |
fbiC | 1304338 | p.Phe470Leu | missense_variant | 0.18 |
fbiC | 1304404 | p.Asp492His | missense_variant | 0.2 |
Rv1258c | 1406810 | c.531C>A | synonymous_variant | 0.25 |
Rv1258c | 1407028 | p.Val105Leu | missense_variant | 0.15 |
Rv1258c | 1407430 | c.-90A>G | upstream_gene_variant | 0.14 |
embR | 1416434 | p.Ala305Val | missense_variant | 0.13 |
embR | 1416438 | p.Gln304* | stop_gained | 0.12 |
atpE | 1460858 | c.-187C>A | upstream_gene_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473802 | n.145C>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474492 | n.839_840delCG | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475200 | n.1543T>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.12 |
fabG1 | 1673714 | p.Ser92Phe | missense_variant | 0.14 |
fabG1 | 1674181 | c.742T>C | stop_lost&splice_region_variant | 0.12 |
inhA | 1674711 | c.510G>C | synonymous_variant | 0.12 |
inhA | 1674720 | p.Arg173Ser | missense_variant | 0.11 |
inhA | 1674756 | c.555T>C | synonymous_variant | 0.12 |
rpsA | 1833380 | c.-162G>A | upstream_gene_variant | 0.18 |
rpsA | 1833463 | c.-79C>A | upstream_gene_variant | 0.22 |
rpsA | 1834829 | p.Ala430Pro | missense_variant | 0.12 |
rpsA | 1834853 | p.Ala438Thr | missense_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918177 | p.Ala80Thr | missense_variant | 0.19 |
tlyA | 1918183 | p.Ala82Ser | missense_variant | 0.12 |
tlyA | 1918248 | c.309T>G | synonymous_variant | 0.12 |
ndh | 2102729 | p.Gly105Ala | missense_variant | 0.17 |
katG | 2153966 | p.Ala716Ser | missense_variant | 0.18 |
katG | 2154141 | c.1971C>T | synonymous_variant | 0.14 |
katG | 2155922 | p.Tyr64His | missense_variant | 0.13 |
PPE35 | 2169918 | c.694dupC | frameshift_variant | 0.15 |
PPE35 | 2170467 | p.Thr49Lys | missense_variant | 0.14 |
Rv1979c | 2221986 | c.1179C>T | synonymous_variant | 0.13 |
Rv1979c | 2222814 | c.351G>C | synonymous_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289389 | c.-148A>T | upstream_gene_variant | 0.15 |
pncA | 2289532 | c.-291T>A | upstream_gene_variant | 0.14 |
pncA | 2289551 | c.-310C>T | upstream_gene_variant | 0.14 |
pncA | 2289824 | c.-583T>C | upstream_gene_variant | 0.15 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
eis | 2714707 | p.Gly209Asp | missense_variant | 0.12 |
folC | 2747146 | p.Lys151Asn | missense_variant | 0.13 |
folC | 2747692 | c.-94A>G | upstream_gene_variant | 0.18 |
pepQ | 2859332 | p.Thr363Ala | missense_variant | 0.14 |
pepQ | 2859767 | p.Val218Met | missense_variant | 0.15 |
pepQ | 2859980 | p.Cys147Arg | missense_variant | 0.14 |
pepQ | 2859989 | p.Arg144* | stop_gained | 0.15 |
pepQ | 2860403 | p.Arg6Cys | missense_variant | 0.14 |
ribD | 2987253 | p.Ala139Thr | missense_variant | 0.25 |
ribD | 2987604 | p.Val256Ile | missense_variant | 0.18 |
Rv2752c | 3065310 | c.882G>A | synonymous_variant | 0.12 |
Rv2752c | 3065817 | c.375C>T | synonymous_variant | 0.2 |
Rv2752c | 3066269 | c.-78A>G | upstream_gene_variant | 0.12 |
thyA | 3074652 | c.-181T>A | upstream_gene_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339255 | c.138G>A | synonymous_variant | 0.13 |
fbiD | 3339368 | p.Thr84Ile | missense_variant | 0.13 |
Rv3083 | 3448640 | p.Asp46Gly | missense_variant | 0.12 |
Rv3083 | 3448957 | p.Asp152Asn | missense_variant | 0.14 |
Rv3083 | 3448984 | p.Gly161Ser | missense_variant | 0.17 |
fprA | 3473947 | c.-60G>T | upstream_gene_variant | 0.13 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474831 | c.825G>T | synonymous_variant | 0.15 |
fprA | 3475267 | p.Ala421Thr | missense_variant | 0.12 |
Rv3236c | 3611974 | c.1143A>C | synonymous_variant | 1.0 |
Rv3236c | 3612147 | p.Leu324Val | missense_variant | 0.2 |
Rv3236c | 3612576 | p.Ala181Ser | missense_variant | 0.13 |
fbiB | 3641664 | p.Asp44Asn | missense_variant | 0.14 |
fbiB | 3642668 | c.1134A>G | synonymous_variant | 0.12 |
alr | 3840857 | c.564C>G | synonymous_variant | 0.11 |
ddn | 3986782 | c.-62G>A | upstream_gene_variant | 0.15 |
ddn | 3986795 | c.-49C>T | upstream_gene_variant | 0.14 |
ddn | 3986826 | c.-18G>T | upstream_gene_variant | 0.13 |
ddn | 3986850 | p.Lys3Glu | missense_variant | 0.12 |
clpC1 | 4039927 | p.Arg260Ser | missense_variant | 0.13 |
clpC1 | 4040416 | p.Gln97* | stop_gained | 0.13 |
embC | 4240396 | c.534G>A | synonymous_variant | 0.15 |
embC | 4240411 | c.549G>A | synonymous_variant | 0.13 |
embC | 4241157 | p.Gly432Val | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4244051 | p.Asp273Glu | missense_variant | 0.14 |
embA | 4244056 | p.Gly275Ala | missense_variant | 0.15 |
embA | 4244679 | p.Ala483Pro | missense_variant | 0.13 |
embA | 4244904 | p.Val558Leu | missense_variant | 0.18 |
embA | 4244947 | p.Val572Ala | missense_variant | 0.13 |
embA | 4246101 | p.Thr957Pro | missense_variant | 0.25 |
embB | 4247220 | p.Leu236Ser | missense_variant | 0.17 |
embB | 4247353 | c.840C>T | synonymous_variant | 0.17 |
embB | 4248209 | p.Val566Met | missense_variant | 0.12 |
embB | 4249047 | p.Ala845Val | missense_variant | 0.13 |
aftB | 4268277 | p.Pro187Arg | missense_variant | 0.11 |
aftB | 4268550 | p.Val96Glu | missense_variant | 0.17 |
ubiA | 4268986 | c.847dupG | frameshift_variant | 0.18 |
ubiA | 4269140 | p.Cys232Arg | missense_variant | 0.11 |
ubiA | 4269334 | p.Ala167Asp | missense_variant | 0.15 |
ubiA | 4269875 | c.-42G>A | upstream_gene_variant | 0.18 |
ubiA | 4269991 | c.-158C>T | upstream_gene_variant | 0.2 |
ethA | 4326852 | p.Ser208Pro | missense_variant | 0.11 |
ethA | 4327071 | p.Phe135Leu | missense_variant | 0.12 |
ethA | 4327422 | p.Ser18Gly | missense_variant | 0.18 |
ethR | 4327429 | c.-120G>T | upstream_gene_variant | 0.17 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338635 | c.-114A>G | upstream_gene_variant | 0.12 |