Run ID: SRR3732710
Sample name:
Date: 04-04-2023 05:38:24
Number of reads: 1489483
Percentage reads mapped: 99.73
Strain: lineage4.3.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 0.99 |
lineage4.3.2 | Euro-American (LAM) | LAM3 | None | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6175 | p.Glu312Asp | missense_variant | 0.29 |
gyrB | 6488 | p.Arg417Ser | missense_variant | 0.33 |
gyrA | 6496 | c.-806G>A | upstream_gene_variant | 0.4 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7950 | p.Ala217Ser | missense_variant | 0.4 |
gyrA | 8323 | p.Phe341Tyr | missense_variant | 0.2 |
gyrA | 8700 | p.Asp467Tyr | missense_variant | 0.17 |
gyrA | 8769 | p.His490Asn | missense_variant | 0.22 |
gyrA | 8987 | c.1686C>A | synonymous_variant | 0.13 |
gyrA | 9226 | p.Ser642Tyr | missense_variant | 0.14 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490949 | p.Ser56Phe | missense_variant | 0.22 |
fgd1 | 491027 | p.Asn82Thr | missense_variant | 0.5 |
fgd1 | 491186 | p.Ser135* | stop_gained | 0.15 |
mshA | 575339 | c.-9C>A | upstream_gene_variant | 0.17 |
ccsA | 620107 | p.Asp73Tyr | missense_variant | 0.17 |
rpoB | 759710 | c.-97C>A | upstream_gene_variant | 0.4 |
rpoB | 759984 | p.Gly60Ser | missense_variant | 0.22 |
rpoB | 760397 | p.Lys197Asn | missense_variant | 0.14 |
rpoB | 760455 | p.Gly217Ser | missense_variant | 0.17 |
rpoB | 760783 | p.Thr326Lys | missense_variant | 0.18 |
rpoB | 760838 | p.Glu344Asp | missense_variant | 0.22 |
rpoB | 761647 | p.Arg614His | missense_variant | 0.15 |
rpoB | 762007 | p.Arg734His | missense_variant | 0.17 |
rpoB | 762285 | p.Arg827Ser | missense_variant | 0.25 |
rpoB | 762972 | p.Gln1056Lys | missense_variant | 0.25 |
rpoB | 763096 | p.Tyr1097Cys | missense_variant | 0.18 |
rpoC | 763950 | p.Arg194Leu | missense_variant | 0.14 |
rpoC | 764535 | p.Arg389Leu | missense_variant | 0.18 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 765302 | p.Glu645* | stop_gained | 0.13 |
rpoC | 766622 | p.Arg1085Trp | missense_variant | 0.29 |
rpoC | 767234 | p.Glu1289* | stop_gained | 0.21 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775828 | p.Gly885Trp | missense_variant | 0.2 |
mmpL5 | 775934 | p.Asp849Glu | missense_variant | 0.18 |
mmpL5 | 776039 | c.2442C>A | synonymous_variant | 0.5 |
mmpL5 | 776165 | p.Asn772Lys | missense_variant | 0.17 |
mmpL5 | 777655 | p.Asp276Tyr | missense_variant | 0.15 |
mmpL5 | 777983 | c.498G>T | synonymous_variant | 0.18 |
mmpL5 | 778059 | p.Ser141Ile | missense_variant | 0.15 |
mmpR5 | 778190 | c.-800G>T | upstream_gene_variant | 0.15 |
mmpL5 | 778416 | p.Pro22Gln | missense_variant | 0.25 |
mmpL5 | 778422 | p.Ala20Glu | missense_variant | 0.25 |
mmpS5 | 779595 | c.-690G>T | upstream_gene_variant | 0.33 |
mmpS5 | 779625 | c.-720G>T | upstream_gene_variant | 0.29 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781830 | p.Pro91Thr | missense_variant | 0.17 |
rplC | 801044 | p.Arg79Leu | missense_variant | 0.33 |
fbiC | 1302915 | c.-16G>T | upstream_gene_variant | 0.33 |
fbiC | 1303270 | p.Leu114Ile | missense_variant | 0.25 |
fbiC | 1303508 | p.Pro193Gln | missense_variant | 0.57 |
fbiC | 1303611 | c.681G>T | synonymous_variant | 0.18 |
fbiC | 1303743 | c.813C>A | synonymous_variant | 0.22 |
fbiC | 1303762 | p.Arg278Ser | missense_variant | 0.4 |
fbiC | 1304091 | c.1161C>T | synonymous_variant | 1.0 |
fbiC | 1304138 | p.Ala403Val | missense_variant | 0.13 |
fbiC | 1304626 | p.Ala566Ser | missense_variant | 0.17 |
fbiC | 1304653 | p.Asp575Tyr | missense_variant | 0.14 |
fbiC | 1304866 | p.Gly646Trp | missense_variant | 0.22 |
Rv1258c | 1406366 | c.975C>T | synonymous_variant | 0.15 |
Rv1258c | 1406372 | c.969G>A | synonymous_variant | 0.17 |
embR | 1416735 | p.Glu205* | stop_gained | 0.18 |
atpE | 1461078 | p.Gly12Ser | missense_variant | 0.67 |
atpE | 1461229 | p.Ala62Glu | missense_variant | 0.33 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473022 | n.1177G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475045 | n.1388C>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475394 | n.1737G>A | non_coding_transcript_exon_variant | 0.33 |
inhA | 1673460 | c.-742A>G | upstream_gene_variant | 0.33 |
inhA | 1673839 | c.-363C>A | upstream_gene_variant | 0.4 |
fabG1 | 1674118 | p.Glu227* | stop_gained | 0.15 |
inhA | 1674432 | c.231G>T | synonymous_variant | 0.25 |
inhA | 1674820 | p.Leu207Ile | missense_variant | 0.14 |
rpsA | 1833854 | p.Lys105Glu | missense_variant | 0.22 |
rpsA | 1833908 | p.Asp123Tyr | missense_variant | 0.2 |
rpsA | 1833970 | c.429G>T | synonymous_variant | 0.29 |
rpsA | 1834000 | c.459G>T | synonymous_variant | 0.22 |
rpsA | 1834100 | p.Arg187Ser | missense_variant | 0.2 |
rpsA | 1834513 | c.972C>A | synonymous_variant | 0.4 |
rpsA | 1834733 | p.Ala398Thr | missense_variant | 0.2 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918395 | c.456G>A | synonymous_variant | 0.2 |
ndh | 2101933 | p.Met370Ile | missense_variant | 0.18 |
ndh | 2102956 | c.87G>T | synonymous_variant | 0.4 |
ndh | 2103074 | c.-32C>A | upstream_gene_variant | 0.33 |
katG | 2153997 | c.2115G>T | synonymous_variant | 0.18 |
katG | 2154863 | p.His417Asn | missense_variant | 0.15 |
katG | 2154926 | p.Arg396Cys | missense_variant | 0.18 |
katG | 2154975 | c.1137C>A | synonymous_variant | 0.18 |
PPE35 | 2167682 | c.2931G>T | synonymous_variant | 0.25 |
PPE35 | 2167808 | c.2805C>T | synonymous_variant | 0.25 |
PPE35 | 2168096 | c.2517C>A | synonymous_variant | 0.22 |
PPE35 | 2169516 | p.Ser366Tyr | missense_variant | 0.67 |
Rv1979c | 2221842 | c.1323G>T | synonymous_variant | 0.18 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288835 | p.Asp136Val | missense_variant | 0.14 |
pncA | 2288963 | c.279G>A | synonymous_variant | 0.14 |
pncA | 2289480 | c.-239G>T | upstream_gene_variant | 0.25 |
pncA | 2290041 | c.-800C>A | upstream_gene_variant | 0.15 |
kasA | 2518058 | c.-57G>T | upstream_gene_variant | 0.25 |
kasA | 2518252 | c.138C>A | synonymous_variant | 0.22 |
ahpC | 2725933 | c.-260G>T | upstream_gene_variant | 0.14 |
folC | 2746959 | p.Gly214Trp | missense_variant | 0.22 |
folC | 2747158 | c.441G>T | synonymous_variant | 0.22 |
pepQ | 2859639 | c.780T>A | synonymous_variant | 0.12 |
ribD | 2986693 | c.-146C>A | upstream_gene_variant | 0.25 |
ribD | 2986850 | c.12T>C | synonymous_variant | 0.17 |
ribD | 2987041 | p.Arg68Leu | missense_variant | 0.17 |
Rv2752c | 3065756 | p.Val146Ile | missense_variant | 0.15 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3087645 | p.Glu276Lys | missense_variant | 0.18 |
ald | 3087726 | p.Ala303Thr | missense_variant | 0.18 |
Rv3083 | 3448588 | p.Asp29Tyr | missense_variant | 0.4 |
Rv3083 | 3448624 | p.Leu41Met | missense_variant | 0.25 |
Rv3083 | 3448701 | p.Phe66Leu | missense_variant | 0.18 |
Rv3083 | 3449013 | c.510C>A | synonymous_variant | 0.2 |
Rv3083 | 3449315 | p.Trp271Leu | missense_variant | 0.18 |
Rv3083 | 3449366 | p.Pro288Gln | missense_variant | 0.17 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474062 | p.Ala19Glu | missense_variant | 0.2 |
fprA | 3475005 | c.999G>A | synonymous_variant | 0.33 |
fprA | 3475215 | c.1209C>A | synonymous_variant | 0.14 |
whiB7 | 3568471 | c.207_208dupGA | frameshift_variant | 0.15 |
whiB7 | 3568761 | c.-82G>T | upstream_gene_variant | 0.25 |
Rv3236c | 3612180 | p.Ala313Ser | missense_variant | 0.17 |
Rv3236c | 3613030 | c.87G>T | synonymous_variant | 0.29 |
Rv3236c | 3613060 | c.57G>T | synonymous_variant | 0.22 |
Rv3236c | 3613274 | c.-158C>T | upstream_gene_variant | 0.4 |
fbiA | 3641332 | p.Gly264Trp | missense_variant | 0.14 |
alr | 3840289 | p.Asp378Tyr | missense_variant | 0.15 |
alr | 3840309 | p.Arg371Leu | missense_variant | 0.25 |
alr | 3841556 | c.-136C>A | upstream_gene_variant | 0.15 |
alr | 3841612 | c.-193_-192insC | upstream_gene_variant | 1.0 |
ddn | 3986745 | c.-99A>C | upstream_gene_variant | 0.18 |
ddn | 3986962 | p.Thr40Asn | missense_variant | 0.22 |
ddn | 3987161 | c.318G>T | synonymous_variant | 0.18 |
clpC1 | 4038225 | p.Pro827Gln | missense_variant | 0.18 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4038656 | p.Lys683Asn | missense_variant | 0.2 |
clpC1 | 4039071 | p.Pro545Gln | missense_variant | 0.15 |
clpC1 | 4039145 | p.Gly520Cys | missense_variant | 0.22 |
clpC1 | 4039277 | c.1428C>T | synonymous_variant | 0.18 |
clpC1 | 4039359 | p.Ser449Ile | missense_variant | 0.18 |
clpC1 | 4039362 | p.Ala448Asp | missense_variant | 0.18 |
clpC1 | 4039365 | p.Ala447Asp | missense_variant | 0.18 |
clpC1 | 4039372 | p.Glu445* | stop_gained | 0.2 |
panD | 4044211 | p.Gly24Val | missense_variant | 0.22 |
embC | 4239783 | c.-80C>A | upstream_gene_variant | 0.15 |
embC | 4240903 | c.1041C>A | synonymous_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244967 | p.Gly579Trp | missense_variant | 0.18 |
embA | 4245176 | c.1944G>T | synonymous_variant | 0.17 |
embA | 4245295 | p.Thr688Lys | missense_variant | 0.22 |
embB | 4245593 | c.-921C>A | upstream_gene_variant | 0.29 |
embA | 4245699 | c.2469_2476delGTCGCACG | frameshift_variant | 0.18 |
embA | 4246035 | p.Glu935* | stop_gained | 0.18 |
embB | 4246669 | c.156C>A | synonymous_variant | 0.14 |
embB | 4248857 | p.Gly782* | stop_gained | 0.29 |
embB | 4248930 | p.Pro806His | missense_variant | 0.29 |
embB | 4248959 | p.Asp816Tyr | missense_variant | 0.22 |
embB | 4249273 | p.Asp920Glu | missense_variant | 0.22 |
aftB | 4267607 | p.Glu410Asp | missense_variant | 0.14 |
aftB | 4268053 | c.784C>A | synonymous_variant | 0.22 |
aftB | 4268120 | c.717C>A | synonymous_variant | 0.18 |
aftB | 4268180 | p.Phe219Leu | missense_variant | 0.18 |
aftB | 4268250 | p.Ala196Val | missense_variant | 0.18 |
ubiA | 4269426 | p.Leu136Phe | missense_variant | 0.25 |
ethA | 4327060 | p.Ser138Arg | missense_variant | 0.15 |
ethR | 4327390 | c.-159C>A | upstream_gene_variant | 0.5 |
whiB6 | 4338549 | c.-28G>T | upstream_gene_variant | 0.25 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407539 | p.Gly222Trp | missense_variant | 0.18 |
gid | 4407606 | c.597C>A | synonymous_variant | 0.15 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |