Run ID: SRR12882155
Sample name:
Date: 03-04-2023 07:13:47
Number of reads: 898465
Percentage reads mapped: 97.0
Strain: lineage1.2.2.2
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 0.98 |
lineage1.2.2 | Indo-Oceanic | EAI1 | RD239 | 1.0 |
lineage1.2.2.2 | Indo-Oceanic | NA | RD239 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761122 | p.Pro439Leu | missense_variant | 0.17 | rifampicin |
rpsA | 1834962 | p.Arg474Leu | missense_variant | 0.18 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5075 | c.-165C>T | upstream_gene_variant | 1.0 |
gyrB | 5630 | c.391C>T | synonymous_variant | 1.0 |
gyrB | 5878 | c.639G>T | synonymous_variant | 0.17 |
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrA | 7268 | c.-34C>T | upstream_gene_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8141 | c.840C>T | synonymous_variant | 0.15 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491075 | p.Pro98Gln | missense_variant | 0.17 |
fgd1 | 491144 | p.Ala121Asp | missense_variant | 0.17 |
fgd1 | 491170 | p.Ala130Ser | missense_variant | 0.15 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575482 | c.135C>A | synonymous_variant | 0.17 |
mshA | 576104 | p.Arg253Ser | missense_variant | 0.18 |
mshA | 576111 | p.Ala255Asp | missense_variant | 0.2 |
mshA | 576186 | p.Pro280His | missense_variant | 0.18 |
mshA | 576241 | c.894C>A | synonymous_variant | 0.17 |
mshA | 576290 | p.Leu315Ile | missense_variant | 0.15 |
ccsA | 619699 | c.-192G>T | upstream_gene_variant | 0.2 |
ccsA | 619805 | c.-86C>T | upstream_gene_variant | 0.17 |
ccsA | 620016 | c.126C>A | synonymous_variant | 0.15 |
ccsA | 620424 | c.534G>T | synonymous_variant | 0.22 |
ccsA | 620782 | p.Ala298Ser | missense_variant | 0.18 |
ccsA | 620864 | c.974G>T | stop_lost&splice_region_variant | 0.2 |
rpoB | 760109 | p.Phe101Leu | missense_variant | 0.4 |
rpoB | 760864 | p.Gly353Val | missense_variant | 0.15 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763058 | c.-312C>A | upstream_gene_variant | 0.15 |
rpoC | 763711 | c.342G>T | synonymous_variant | 0.25 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
rpoC | 764593 | c.1224C>A | synonymous_variant | 0.18 |
rpoC | 764939 | p.Leu524Met | missense_variant | 0.17 |
rpoC | 765358 | p.Met663Ile | missense_variant | 0.5 |
rpoC | 765484 | c.2115G>A | synonymous_variant | 0.4 |
rpoC | 765500 | p.Gln711Lys | missense_variant | 0.4 |
rpoC | 765541 | c.2172C>A | synonymous_variant | 0.29 |
rpoC | 766917 | p.Arg1183His | missense_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775682 | c.2799C>A | synonymous_variant | 0.22 |
mmpL5 | 775751 | c.2730C>T | synonymous_variant | 0.2 |
mmpL5 | 776030 | c.2451G>T | synonymous_variant | 0.17 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776260 | p.Ala741Thr | missense_variant | 0.15 |
mmpL5 | 776789 | c.1692C>A | synonymous_variant | 0.25 |
mmpL5 | 777174 | p.Arg436His | missense_variant | 0.17 |
mmpL5 | 777185 | c.1296G>T | synonymous_variant | 0.17 |
mmpL5 | 777702 | p.Thr260Asn | missense_variant | 0.17 |
mmpL5 | 778201 | p.Val94Met | missense_variant | 0.17 |
mmpL5 | 779118 | c.-638C>T | upstream_gene_variant | 0.4 |
mmpL5 | 779361 | c.-881C>T | upstream_gene_variant | 0.25 |
mmpL5 | 779397 | c.-917C>T | upstream_gene_variant | 0.25 |
mmpS5 | 779506 | c.-601C>A | upstream_gene_variant | 0.22 |
mmpS5 | 779510 | c.-605C>A | upstream_gene_variant | 0.22 |
rpsL | 781382 | c.-178T>A | upstream_gene_variant | 0.18 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781556 | c.-4G>T | upstream_gene_variant | 0.18 |
rpsL | 781667 | c.108C>A | synonymous_variant | 0.2 |
rplC | 800669 | c.-140G>T | upstream_gene_variant | 0.23 |
rplC | 800853 | p.Gln15His | missense_variant | 0.11 |
rplC | 801235 | p.Ala143Ser | missense_variant | 0.15 |
fbiC | 1303701 | c.771C>T | synonymous_variant | 0.18 |
fbiC | 1303705 | p.Leu259Met | missense_variant | 0.17 |
fbiC | 1304449 | p.Ala507Thr | missense_variant | 0.33 |
fbiC | 1304911 | p.Leu661Met | missense_variant | 0.29 |
fbiC | 1304924 | p.Pro665Gln | missense_variant | 0.25 |
Rv1258c | 1406710 | p.Gly211Arg | missense_variant | 0.25 |
Rv1258c | 1406954 | c.387C>A | synonymous_variant | 0.17 |
embR | 1416952 | c.396A>G | synonymous_variant | 0.12 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
embR | 1417343 | p.Ala2Asp | missense_variant | 0.17 |
embR | 1417456 | c.-109G>T | upstream_gene_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471720 | n.-126G>T | upstream_gene_variant | 0.18 |
rrs | 1471793 | n.-53G>A | upstream_gene_variant | 0.15 |
rrs | 1472019 | n.174G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472920 | n.1075G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1473605 | n.-53G>A | upstream_gene_variant | 0.2 |
rrl | 1474307 | n.650G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474409 | n.752G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474701 | n.1044C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474948 | n.1291C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475186 | n.1529C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475397 | n.1740G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475523 | n.1866G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475726 | n.2069G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475749 | n.2092G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475892 | n.2235A>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.14 |
fabG1 | 1673437 | c.-3G>T | upstream_gene_variant | 0.2 |
inhA | 1674255 | p.Asp18Glu | missense_variant | 0.22 |
inhA | 1674424 | p.Ala75Ser | missense_variant | 0.25 |
inhA | 1674474 | c.273G>A | synonymous_variant | 0.18 |
inhA | 1674495 | p.Met98Ile | missense_variant | 0.18 |
rpsA | 1833478 | c.-64G>T | upstream_gene_variant | 0.22 |
rpsA | 1834402 | c.861C>T | synonymous_variant | 0.5 |
rpsA | 1834478 | p.Val313Phe | missense_variant | 0.2 |
rpsA | 1834512 | p.Ser324Tyr | missense_variant | 0.18 |
rpsA | 1834684 | c.1143C>A | synonymous_variant | 0.18 |
tlyA | 1917758 | c.-182G>T | upstream_gene_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101870 | c.1173C>T | synonymous_variant | 0.18 |
ndh | 2101961 | p.Pro361Gln | missense_variant | 0.22 |
ndh | 2102240 | p.Arg268His | missense_variant | 1.0 |
ndh | 2102422 | c.621C>A | synonymous_variant | 0.17 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2154941 | p.Glu391* | stop_gained | 0.2 |
katG | 2154971 | p.Asp381Tyr | missense_variant | 0.22 |
katG | 2154987 | c.1125G>T | synonymous_variant | 0.25 |
katG | 2155018 | p.Pro365Gln | missense_variant | 0.22 |
katG | 2155029 | c.1083C>A | synonymous_variant | 0.22 |
katG | 2155223 | p.Gly297Cys | missense_variant | 0.29 |
katG | 2155757 | p.Arg119Ser | missense_variant | 0.18 |
katG | 2155993 | p.Pro40His | missense_variant | 0.22 |
katG | 2156042 | p.Gly24Cys | missense_variant | 0.22 |
PPE35 | 2167857 | p.Trp919Leu | missense_variant | 0.18 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168742 | p.Gly624Asp | missense_variant | 1.0 |
PPE35 | 2169023 | c.1590G>T | synonymous_variant | 0.4 |
PPE35 | 2169668 | c.945C>A | synonymous_variant | 0.17 |
PPE35 | 2170013 | c.600C>A | synonymous_variant | 0.2 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.3 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.29 |
Rv1979c | 2221975 | p.Ala397Glu | missense_variant | 0.2 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223026 | p.Ala47Ser | missense_variant | 0.18 |
Rv1979c | 2223045 | c.120C>A | synonymous_variant | 0.18 |
Rv1979c | 2223145 | p.Arg7Ile | missense_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288861 | p.Glu127Asp | missense_variant | 0.15 |
pncA | 2289500 | c.-260delG | upstream_gene_variant | 0.17 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2518757 | p.Ala215Thr | missense_variant | 0.25 |
kasA | 2518769 | p.Arg219Ser | missense_variant | 0.22 |
kasA | 2519355 | p.Gly414Glu | missense_variant | 0.17 |
eis | 2714149 | p.Pro395Arg | missense_variant | 0.11 |
ahpC | 2726029 | c.-164G>C | upstream_gene_variant | 0.22 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
ahpC | 2726088 | c.-105G>A | upstream_gene_variant | 0.2 |
ahpC | 2726377 | p.Pro62His | missense_variant | 0.25 |
ahpC | 2726442 | p.Gly84Trp | missense_variant | 0.18 |
ahpC | 2726659 | p.Arg156Leu | missense_variant | 0.15 |
pepQ | 2859547 | p.Gly291Asp | missense_variant | 0.22 |
pepQ | 2859586 | p.Arg278Leu | missense_variant | 0.17 |
ribD | 2986979 | c.141C>T | synonymous_variant | 0.25 |
ribD | 2987261 | p.Leu141Phe | missense_variant | 0.21 |
Rv2752c | 3064810 | p.Thr461Ile | missense_variant | 0.2 |
Rv2752c | 3065020 | p.Arg391His | missense_variant | 0.18 |
Rv2752c | 3065389 | p.Arg268His | missense_variant | 0.29 |
Rv2752c | 3065519 | p.Leu225Ile | missense_variant | 0.14 |
Rv2752c | 3065790 | c.402C>A | synonymous_variant | 0.18 |
thyX | 3067346 | c.600C>A | synonymous_variant | 0.22 |
thyX | 3067773 | p.Ala58Val | missense_variant | 0.22 |
thyA | 3073687 | p.Ala262Val | missense_variant | 0.22 |
thyA | 3073937 | p.Ala179Thr | missense_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087601 | p.Gly261Val | missense_variant | 1.0 |
fbiD | 3339288 | c.171C>A | synonymous_variant | 0.18 |
fbiD | 3339434 | p.Gly106Val | missense_variant | 0.18 |
fbiD | 3339438 | c.321C>T | synonymous_variant | 0.18 |
Rv3083 | 3448707 | c.204G>A | synonymous_variant | 0.18 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
Rv3083 | 3449286 | p.Trp261Cys | missense_variant | 0.15 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474027 | c.21C>T | synonymous_variant | 0.29 |
fprA | 3474089 | p.Thr28Met | missense_variant | 0.17 |
fprA | 3474282 | p.Glu92Asp | missense_variant | 0.14 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3475071 | c.1065C>T | synonymous_variant | 0.14 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
whiB7 | 3568691 | c.-12G>T | upstream_gene_variant | 0.13 |
whiB7 | 3568702 | c.-23C>T | upstream_gene_variant | 0.15 |
Rv3236c | 3612034 | c.1083C>A | synonymous_variant | 0.22 |
Rv3236c | 3612070 | c.1047G>T | synonymous_variant | 0.18 |
Rv3236c | 3612651 | p.Val156Leu | missense_variant | 0.15 |
Rv3236c | 3612822 | p.Leu99Ile | missense_variant | 0.15 |
Rv3236c | 3612968 | p.Gly50Glu | missense_variant | 0.22 |
Rv3236c | 3613254 | c.-138T>C | upstream_gene_variant | 0.12 |
fbiB | 3641978 | c.444C>T | synonymous_variant | 0.17 |
fbiB | 3642359 | c.825C>A | synonymous_variant | 0.2 |
alr | 3840296 | c.1125G>T | synonymous_variant | 0.18 |
alr | 3840349 | p.Ala358Ser | missense_variant | 0.17 |
alr | 3840452 | c.969C>T | synonymous_variant | 0.19 |
rpoA | 3877798 | p.Ser237* | stop_gained | 0.2 |
rpoA | 3878058 | c.450G>T | synonymous_variant | 0.17 |
rpoA | 3878174 | p.Pro112Ser | missense_variant | 0.2 |
rpoA | 3878177 | p.Val111Met | missense_variant | 0.2 |
rpoA | 3878178 | p.Ile110Thr | missense_variant | 0.2 |
rpoA | 3878182 | p.Asp109Gly | missense_variant | 0.2 |
ddn | 3987044 | c.201G>A | synonymous_variant | 0.18 |
ddn | 3987054 | p.Gly71Arg | missense_variant | 0.2 |
clpC1 | 4038171 | p.Pro845Leu | missense_variant | 0.18 |
clpC1 | 4038344 | p.Glu787Asp | missense_variant | 0.15 |
clpC1 | 4039100 | c.1605C>T | synonymous_variant | 0.2 |
clpC1 | 4039372 | p.Glu445* | stop_gained | 0.2 |
clpC1 | 4039550 | c.1155G>T | synonymous_variant | 0.18 |
clpC1 | 4039564 | p.Ala381Ser | missense_variant | 0.22 |
clpC1 | 4040071 | p.Pro212Thr | missense_variant | 0.29 |
clpC1 | 4040491 | p.Gln72* | stop_gained | 0.17 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
clpC1 | 4040719 | c.-15A>G | upstream_gene_variant | 0.92 |
clpC1 | 4040894 | c.-190G>A | upstream_gene_variant | 0.2 |
panD | 4044380 | c.-99C>A | upstream_gene_variant | 0.18 |
panD | 4044431 | c.-150G>T | upstream_gene_variant | 0.2 |
panD | 4044474 | c.-193C>T | upstream_gene_variant | 0.18 |
embC | 4240391 | p.Ala177Ser | missense_variant | 0.17 |
embC | 4240639 | c.777C>T | synonymous_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embC | 4241291 | p.Leu477Met | missense_variant | 0.17 |
embC | 4241717 | c.1855C>A | synonymous_variant | 0.18 |
embC | 4241982 | p.Pro707Arg | missense_variant | 0.2 |
embC | 4242095 | p.Ala745Ser | missense_variant | 0.2 |
embA | 4242367 | c.-866C>A | upstream_gene_variant | 0.22 |
embA | 4242385 | c.-848C>T | upstream_gene_variant | 0.18 |
embC | 4242399 | p.Ala846Asp | missense_variant | 0.18 |
embC | 4242419 | p.Ser853Gly | missense_variant | 0.15 |
embA | 4242433 | c.-800C>A | upstream_gene_variant | 0.17 |
embC | 4242473 | p.Leu871Met | missense_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243661 | c.429C>A | synonymous_variant | 0.22 |
embA | 4243707 | p.Ala159Ser | missense_variant | 0.18 |
embA | 4245088 | p.Ser619* | stop_gained | 0.21 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4247790 | p.Ser426Ile | missense_variant | 0.18 |
embB | 4247846 | p.Gln445Lys | missense_variant | 0.29 |
embB | 4248382 | c.1869C>A | synonymous_variant | 0.18 |
embB | 4249528 | c.3015C>A | synonymous_variant | 0.29 |
aftB | 4267035 | p.Arg601His | missense_variant | 0.25 |
aftB | 4267939 | p.Arg300Trp | missense_variant | 0.22 |
aftB | 4268201 | c.636G>T | synonymous_variant | 0.18 |
aftB | 4268617 | p.Gly74Cys | missense_variant | 0.25 |
aftB | 4268886 | c.-50G>T | upstream_gene_variant | 0.2 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 0.94 |
ethA | 4326012 | p.Gly488Trp | missense_variant | 0.27 |
ethA | 4326136 | c.1338G>T | synonymous_variant | 0.17 |
ethA | 4326148 | c.1326G>T | synonymous_variant | 1.0 |
ethA | 4326439 | p.Asn345Lys | missense_variant | 1.0 |
ethA | 4327511 | c.-38C>T | upstream_gene_variant | 0.18 |
whiB6 | 4338203 | p.Arg107Cys | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.94 |
gid | 4407848 | p.Ala119Thr | missense_variant | 1.0 |
gid | 4407856 | p.Arg116Leu | missense_variant | 0.2 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |