Run ID: SRR5535705
Sample name:
Date: 04-04-2023 10:38:32
Number of reads: 1040120
Percentage reads mapped: 99.26
Strain:
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5167 | c.-73C>T | upstream_gene_variant | 0.15 |
gyrB | 5707 | c.468G>T | synonymous_variant | 0.4 |
gyrB | 5806 | c.567C>A | synonymous_variant | 0.2 |
gyrA | 6475 | c.-827C>A | upstream_gene_variant | 0.25 |
gyrA | 6589 | c.-713G>A | upstream_gene_variant | 0.4 |
gyrB | 6782 | p.Asp515His | missense_variant | 0.22 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7538 | p.Glu79Asp | missense_variant | 0.17 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7725 | p.Leu142Met | missense_variant | 0.25 |
gyrA | 8123 | p.Leu274Phe | missense_variant | 0.67 |
gyrA | 8960 | p.Asp553Glu | missense_variant | 0.22 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491660 | p.Ala293Asp | missense_variant | 0.4 |
fgd1 | 491719 | p.Pro313Thr | missense_variant | 0.5 |
mshA | 575360 | p.Arg5Trp | missense_variant | 0.15 |
mshA | 575907 | p.Ala187Val | missense_variant | 0.86 |
mshA | 575946 | p.Thr200Met | missense_variant | 0.25 |
ccsA | 620506 | p.Pro206Thr | missense_variant | 0.67 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 759947 | c.141C>A | synonymous_variant | 0.5 |
rpoB | 760177 | p.Ala124Val | missense_variant | 0.2 |
rpoB | 760394 | c.588C>A | synonymous_variant | 0.25 |
rpoB | 760648 | p.Pro281Leu | missense_variant | 0.5 |
rpoB | 762321 | p.Gly839Ser | missense_variant | 0.2 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 766244 | c.2876delA | frameshift_variant | 0.29 |
rpoC | 767053 | p.Glu1228Asp | missense_variant | 0.22 |
rpoC | 767088 | p.Cys1240Phe | missense_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776002 | p.Leu827Met | missense_variant | 0.5 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 776204 | c.2277C>A | synonymous_variant | 0.4 |
mmpL5 | 776498 | c.1983G>A | synonymous_variant | 0.33 |
mmpL5 | 777697 | p.Ala262Thr | missense_variant | 0.33 |
mmpL5 | 778035 | p.Val149Asp | missense_variant | 0.18 |
mmpR5 | 778271 | c.-719C>T | upstream_gene_variant | 0.4 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
mmpS5 | 779630 | c.-725T>C | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801138 | p.Ser110Arg | missense_variant | 0.22 |
rplC | 801159 | c.351C>A | synonymous_variant | 0.29 |
fbiC | 1303776 | p.Lys282Asn | missense_variant | 0.67 |
fbiC | 1303892 | p.Ala321Glu | missense_variant | 0.17 |
fbiC | 1303978 | p.Gly350Arg | missense_variant | 0.17 |
fbiC | 1305003 | c.2073C>A | synonymous_variant | 0.5 |
Rv1258c | 1406242 | p.Ala367Ser | missense_variant | 0.13 |
Rv1258c | 1406256 | p.Leu362Trp | missense_variant | 0.12 |
Rv1258c | 1406402 | c.939C>A | synonymous_variant | 0.29 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1407163 | p.Leu60Val | missense_variant | 0.11 |
Rv1258c | 1407200 | c.141G>C | synonymous_variant | 0.12 |
embR | 1416985 | c.363G>T | synonymous_variant | 0.29 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475714 | n.2057G>T | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673257 | c.-183C>A | upstream_gene_variant | 0.18 |
fabG1 | 1673515 | p.Gly26Trp | missense_variant | 0.67 |
fabG1 | 1673840 | p.Arg134Leu | missense_variant | 0.33 |
inhA | 1674643 | p.Asp148Tyr | missense_variant | 0.33 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834480 | c.939C>A | synonymous_variant | 0.33 |
rpsA | 1834751 | p.Leu404Phe | missense_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101711 | c.1332G>A | synonymous_variant | 0.22 |
ndh | 2102275 | c.768C>T | synonymous_variant | 0.25 |
ndh | 2103016 | c.27G>T | synonymous_variant | 0.67 |
katG | 2154303 | c.1809G>A | synonymous_variant | 0.4 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155216 | p.Gly299Val | missense_variant | 0.4 |
katG | 2156499 | c.-388C>T | upstream_gene_variant | 0.25 |
PPE35 | 2167825 | p.Gly930Cys | missense_variant | 0.5 |
PPE35 | 2169370 | p.Gly415* | stop_gained | 0.29 |
PPE35 | 2169374 | c.1239C>T | synonymous_variant | 0.29 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.25 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.25 |
PPE35 | 2170282 | p.Ala111Ser | missense_variant | 0.22 |
Rv1979c | 2223112 | p.Ser18Ile | missense_variant | 0.25 |
Rv1979c | 2223123 | c.42G>T | synonymous_variant | 0.33 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289063 | p.Gly60Val | missense_variant | 0.25 |
pncA | 2289172 | p.Gly24Cys | missense_variant | 0.4 |
kasA | 2518047 | c.-68G>T | upstream_gene_variant | 0.22 |
kasA | 2518782 | p.Pro223His | missense_variant | 0.2 |
eis | 2715358 | c.-26C>T | upstream_gene_variant | 0.25 |
eis | 2715481 | c.-149G>A | upstream_gene_variant | 0.22 |
ahpC | 2726271 | p.Asp27Tyr | missense_variant | 0.25 |
pepQ | 2859718 | p.Thr234Ile | missense_variant | 0.17 |
pepQ | 2860537 | c.-119C>A | upstream_gene_variant | 0.22 |
ribD | 2986802 | c.-37C>A | upstream_gene_variant | 0.4 |
Rv2752c | 3064571 | p.Val541Leu | missense_variant | 0.25 |
Rv2752c | 3064682 | p.Leu504Ile | missense_variant | 0.22 |
Rv2752c | 3066233 | c.-42G>A | upstream_gene_variant | 0.18 |
Rv2752c | 3067039 | c.-848T>C | upstream_gene_variant | 1.0 |
thyA | 3073897 | p.Ala192Asp | missense_variant | 0.5 |
ald | 3086650 | c.-170C>A | upstream_gene_variant | 0.2 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087329 | p.Asp170Glu | missense_variant | 0.25 |
ald | 3087755 | c.936G>T | synonymous_variant | 1.0 |
ald | 3087824 | c.1005G>A | synonymous_variant | 0.25 |
fbiD | 3339262 | p.Ala49Ser | missense_variant | 0.29 |
fbiD | 3339664 | p.Pro183Ala | missense_variant | 0.11 |
Rv3083 | 3449660 | p.Trp386Leu | missense_variant | 0.29 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475293 | c.1287C>T | synonymous_variant | 0.25 |
whiB7 | 3568482 | p.Trp66Cys | missense_variant | 0.25 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 0.75 |
fbiA | 3640561 | p.Ala7Ser | missense_variant | 0.33 |
fbiA | 3641422 | p.Asp294Tyr | missense_variant | 0.18 |
fbiA | 3641518 | p.Leu326Val | missense_variant | 0.2 |
alr | 3840629 | c.792C>T | synonymous_variant | 0.29 |
alr | 3840822 | p.Ala200Val | missense_variant | 0.15 |
rpoA | 3877788 | p.Glu240Asp | missense_variant | 0.33 |
rpoA | 3878646 | c.-139G>T | upstream_gene_variant | 0.67 |
clpC1 | 4039843 | p.Glu288* | stop_gained | 0.29 |
clpC1 | 4039864 | p.Asp281Tyr | missense_variant | 0.33 |
clpC1 | 4040395 | p.Gly104Trp | missense_variant | 0.15 |
clpC1 | 4040417 | c.288G>T | synonymous_variant | 0.2 |
panD | 4044125 | p.Ala53Ser | missense_variant | 0.33 |
embC | 4240482 | p.Pro207Gln | missense_variant | 0.15 |
embC | 4241319 | p.Pro486Gln | missense_variant | 0.15 |
embC | 4241359 | c.1497C>G | synonymous_variant | 0.18 |
embC | 4241435 | p.Ala525Pro | missense_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242773 | p.Leu971Met | missense_variant | 0.14 |
embA | 4243455 | p.Pro75Thr | missense_variant | 0.13 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4244702 | c.1470C>T | synonymous_variant | 0.29 |
embA | 4244720 | p.Tyr496* | stop_gained | 0.29 |
embA | 4244795 | c.1563G>T | synonymous_variant | 0.33 |
embA | 4245253 | p.Thr674Asn | missense_variant | 0.33 |
embA | 4245606 | p.Leu792Met | missense_variant | 0.17 |
embA | 4246332 | p.Gln1034Lys | missense_variant | 0.25 |
embB | 4247536 | c.1023C>A | synonymous_variant | 0.33 |
embB | 4247899 | p.Met462Ile | missense_variant | 0.14 |
aftB | 4267547 | c.1290C>A | synonymous_variant | 0.67 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268019 | p.Ser273* | stop_gained | 0.5 |
aftB | 4268032 | p.Pro269Ser | missense_variant | 0.5 |
aftB | 4268190 | p.Ala216Asp | missense_variant | 0.25 |
ethA | 4326133 | c.1341C>A | synonymous_variant | 0.25 |
ethA | 4326433 | p.Gln347His | missense_variant | 0.67 |
ethA | 4326720 | p.Ala252Ser | missense_variant | 0.33 |
ethA | 4328378 | c.-905G>T | upstream_gene_variant | 0.17 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407532 | p.Ala224Val | missense_variant | 0.4 |
gid | 4407563 | p.Gly214Trp | missense_variant | 0.22 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407636 | c.567G>T | synonymous_variant | 0.29 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |