Run ID: ERR4816637
Sample name:
Date: 01-04-2023 14:32:37
Number of reads: 717514
Percentage reads mapped: 98.74
Strain: lineage4.3.3
Drug-resistance: HR-TB
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 | 1.0 |
lineage4.3.3 | Euro-American (LAM) | LAM;T | RD115 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2155064 | p.Ala350Ser | missense_variant | 0.22 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5512 | c.273C>A | synonymous_variant | 0.29 |
gyrB | 5627 | p.Ala130Ser | missense_variant | 0.12 |
gyrB | 5778 | p.Phe180Ser | missense_variant | 0.14 |
gyrB | 6590 | p.Arg451Ser | missense_variant | 0.15 |
gyrB | 6623 | p.Ser462Thr | missense_variant | 0.22 |
gyrB | 6912 | p.Asn558Ile | missense_variant | 0.18 |
gyrB | 6985 | p.Tyr582* | stop_gained | 0.11 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7804 | p.Ser168Thr | missense_variant | 0.15 |
gyrA | 8040 | p.Gly247Ser | missense_variant | 1.0 |
gyrA | 9036 | p.Ala579Ser | missense_variant | 0.17 |
gyrA | 9126 | p.Ala609Thr | missense_variant | 0.17 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9794 | p.Asn831Lys | missense_variant | 0.2 |
fgd1 | 490633 | c.-150C>A | upstream_gene_variant | 0.14 |
fgd1 | 491052 | c.270C>T | synonymous_variant | 0.15 |
fgd1 | 491401 | p.Leu207Met | missense_variant | 0.11 |
fgd1 | 491651 | p.Pro290His | missense_variant | 0.13 |
mshA | 576658 | c.1311G>T | synonymous_variant | 0.17 |
ccsA | 620315 | c.427delG | frameshift_variant | 0.15 |
ccsA | 620543 | p.Arg218Leu | missense_variant | 0.22 |
rpoB | 760590 | p.Val262Phe | missense_variant | 0.15 |
rpoB | 760723 | p.Gly306Val | missense_variant | 0.22 |
rpoB | 760862 | c.1056G>T | synonymous_variant | 0.18 |
rpoB | 760992 | p.Glu396* | stop_gained | 0.29 |
rpoB | 761418 | p.Ala538Thr | missense_variant | 0.18 |
rpoB | 762273 | p.Ala823Ser | missense_variant | 0.22 |
rpoC | 763442 | p.Tyr25His | missense_variant | 0.2 |
rpoC | 763771 | c.402C>T | synonymous_variant | 0.67 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 765097 | p.Met576Ile | missense_variant | 0.5 |
rpoC | 766265 | p.Leu966Met | missense_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776217 | c.2258_2263delGATCCG | disruptive_inframe_deletion | 0.14 |
mmpL5 | 776495 | c.1986G>T | synonymous_variant | 0.25 |
mmpL5 | 776947 | p.Glu512Lys | missense_variant | 0.18 |
mmpL5 | 777983 | c.498G>T | synonymous_variant | 0.13 |
mmpL5 | 778452 | p.Thr10Met | missense_variant | 0.17 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781697 | c.138C>T | synonymous_variant | 0.2 |
fbiC | 1303539 | c.609G>A | synonymous_variant | 0.18 |
fbiC | 1304373 | p.His481Gln | missense_variant | 0.15 |
fbiC | 1304400 | c.1470C>A | synonymous_variant | 0.18 |
fbiC | 1304572 | p.Val548Phe | missense_variant | 0.14 |
fbiC | 1304659 | p.Tyr577Asn | missense_variant | 0.17 |
fbiC | 1304736 | p.Gln602His | missense_variant | 0.12 |
Rv1258c | 1406124 | p.Ala406Glu | missense_variant | 0.25 |
embR | 1416387 | p.Asp321Tyr | missense_variant | 0.15 |
embR | 1417167 | p.Glu61Gln | missense_variant | 0.14 |
embR | 1417251 | p.Pro33Thr | missense_variant | 0.12 |
atpE | 1460915 | c.-130C>T | upstream_gene_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472494 | n.649A>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1473569 | n.-89A>G | upstream_gene_variant | 0.13 |
rrl | 1474122 | n.465C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474784 | n.1127C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474885 | n.1228G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474974 | n.1317G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475380 | n.1723C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475741 | n.2086delT | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475837 | n.2180C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475882 | n.2225C>A | non_coding_transcript_exon_variant | 0.13 |
inhA | 1673484 | c.-718C>A | upstream_gene_variant | 0.2 |
fabG1 | 1673585 | p.Ser49Phe | missense_variant | 0.33 |
fabG1 | 1673987 | p.Pro183Leu | missense_variant | 0.4 |
inhA | 1674261 | c.60G>T | synonymous_variant | 0.12 |
inhA | 1674700 | p.Ala167Ser | missense_variant | 0.12 |
inhA | 1674930 | p.Cys243* | stop_gained | 0.4 |
rpsA | 1833725 | p.Val62Leu | missense_variant | 0.22 |
rpsA | 1834315 | c.774C>A | synonymous_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1917998 | p.Arg20Leu | missense_variant | 0.14 |
ndh | 2101909 | c.1134G>T | synonymous_variant | 0.22 |
ndh | 2101919 | p.Arg375Met | missense_variant | 0.22 |
ndh | 2102627 | p.Lys139Arg | missense_variant | 0.18 |
ndh | 2102757 | p.Gly96Trp | missense_variant | 0.33 |
katG | 2154408 | c.1704C>A | synonymous_variant | 0.17 |
katG | 2154547 | p.Glu522Gly | missense_variant | 0.15 |
katG | 2154639 | c.1473C>A | synonymous_variant | 0.14 |
katG | 2154882 | c.1230G>A | synonymous_variant | 0.29 |
katG | 2155218 | p.Leu298Phe | missense_variant | 0.14 |
katG | 2156228 | c.-117T>C | upstream_gene_variant | 0.12 |
PPE35 | 2167661 | p.Ser984Arg | missense_variant | 0.17 |
PPE35 | 2167812 | c.2800delC | frameshift_variant | 0.18 |
PPE35 | 2168246 | c.2367C>T | synonymous_variant | 0.13 |
PPE35 | 2168776 | p.Pro613Thr | missense_variant | 0.17 |
PPE35 | 2170068 | p.Pro182Leu | missense_variant | 0.29 |
PPE35 | 2170787 | c.-175T>C | upstream_gene_variant | 0.15 |
Rv1979c | 2222366 | p.Tyr267Asn | missense_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv1979c | 2223301 | c.-138delG | upstream_gene_variant | 0.11 |
pncA | 2288759 | c.483G>T | synonymous_variant | 0.17 |
pncA | 2289476 | c.-235G>T | upstream_gene_variant | 0.18 |
pncA | 2289481 | c.-240G>T | upstream_gene_variant | 0.22 |
pncA | 2289654 | c.-413A>T | upstream_gene_variant | 0.17 |
pncA | 2290235 | c.-994G>T | upstream_gene_variant | 0.4 |
kasA | 2518559 | p.Gly149Cys | missense_variant | 0.2 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
kasA | 2519292 | c.1180delT | frameshift_variant | 0.14 |
eis | 2714487 | c.846C>G | synonymous_variant | 0.15 |
eis | 2715144 | c.189G>C | synonymous_variant | 0.14 |
ahpC | 2726576 | p.Asp128Glu | missense_variant | 0.12 |
ahpC | 2726630 | p.Phe146Leu | missense_variant | 0.15 |
ahpC | 2726691 | p.Ala167Ser | missense_variant | 0.29 |
ahpC | 2726743 | p.Thr184Met | missense_variant | 0.12 |
folC | 2746369 | c.1230G>A | synonymous_variant | 0.2 |
folC | 2746669 | p.Glu310Asp | missense_variant | 0.29 |
pepQ | 2859378 | c.1041G>T | synonymous_variant | 0.12 |
ribD | 2986661 | c.-178G>C | upstream_gene_variant | 0.17 |
ribD | 2986750 | c.-89G>T | upstream_gene_variant | 0.29 |
ribD | 2987246 | c.408C>A | synonymous_variant | 0.18 |
ribD | 2987515 | p.Arg226Leu | missense_variant | 0.18 |
Rv2752c | 3065226 | c.966G>A | synonymous_variant | 0.17 |
Rv2752c | 3065736 | p.Asp152Glu | missense_variant | 0.2 |
thyX | 3067751 | c.195C>A | synonymous_variant | 0.12 |
thyX | 3067790 | c.156C>T | synonymous_variant | 0.12 |
thyX | 3067911 | p.Ile12Thr | missense_variant | 0.15 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
thyA | 3074639 | c.-168G>A | upstream_gene_variant | 0.25 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086861 | p.Phe14Leu | missense_variant | 0.11 |
ald | 3086881 | p.Ala21Val | missense_variant | 0.12 |
ald | 3087131 | c.312C>A | synonymous_variant | 0.15 |
fbiD | 3338922 | c.-196G>A | upstream_gene_variant | 0.12 |
fbiD | 3339015 | c.-103T>C | upstream_gene_variant | 0.15 |
fbiD | 3339048 | c.-70C>G | upstream_gene_variant | 0.15 |
fbiD | 3339138 | c.21C>T | synonymous_variant | 0.2 |
fbiD | 3339747 | c.630G>T | synonymous_variant | 0.2 |
Rv3083 | 3448540 | p.Gly13Ser | missense_variant | 0.15 |
Rv3083 | 3449411 | p.Gly303Val | missense_variant | 0.14 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474261 | c.255C>A | synonymous_variant | 0.12 |
fprA | 3475066 | p.Glu354Lys | missense_variant | 0.12 |
fprA | 3475305 | c.1299C>A | synonymous_variant | 0.15 |
fprA | 3475361 | c.1357_1360delATTG | frameshift_variant | 0.18 |
whiB7 | 3568635 | p.Leu15Phe | missense_variant | 0.17 |
Rv3236c | 3612009 | p.Ala370Ser | missense_variant | 0.2 |
Rv3236c | 3612281 | p.Gly279Asp | missense_variant | 0.17 |
Rv3236c | 3612304 | c.813C>A | synonymous_variant | 0.17 |
Rv3236c | 3612450 | c.667C>T | synonymous_variant | 0.29 |
Rv3236c | 3612969 | p.Gly50Trp | missense_variant | 0.13 |
fbiA | 3640409 | c.-134C>A | upstream_gene_variant | 0.22 |
fbiB | 3641961 | p.Thr143Ala | missense_variant | 0.15 |
fbiB | 3642148 | p.Val205Ala | missense_variant | 0.33 |
fbiB | 3642618 | p.Asp362Asn | missense_variant | 0.2 |
fbiB | 3642707 | c.1173C>A | synonymous_variant | 0.18 |
alr | 3840271 | p.Gly384Cys | missense_variant | 0.5 |
alr | 3841054 | p.Ala123Ser | missense_variant | 0.14 |
alr | 3841238 | c.183G>A | synonymous_variant | 0.25 |
alr | 3841422 | c.-2C>A | upstream_gene_variant | 0.22 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4039247 | p.Glu486Asp | missense_variant | 0.29 |
panD | 4043897 | p.Gly129Ser | missense_variant | 0.15 |
embC | 4239719 | c.-144G>T | upstream_gene_variant | 0.2 |
embC | 4240066 | c.204C>A | synonymous_variant | 0.25 |
embC | 4240799 | p.Tyr313Asn | missense_variant | 0.14 |
embC | 4241034 | p.Pro391Leu | missense_variant | 0.33 |
embC | 4241506 | c.1644G>T | synonymous_variant | 0.11 |
embC | 4241739 | p.Val626Glu | missense_variant | 0.18 |
embC | 4241911 | c.2049C>A | synonymous_variant | 0.4 |
embC | 4242182 | p.Ala774Ser | missense_variant | 1.0 |
embC | 4242324 | p.Gly821Val | missense_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245332 | c.2100C>A | synonymous_variant | 0.12 |
embA | 4246069 | p.Pro946Gln | missense_variant | 0.25 |
embA | 4246129 | p.Ser966Tyr | missense_variant | 0.15 |
embB | 4246419 | c.-95C>T | upstream_gene_variant | 0.13 |
embA | 4246509 | p.Leu1093Met | missense_variant | 0.14 |
embB | 4246849 | p.Gln112His | missense_variant | 0.17 |
embB | 4247239 | p.Leu242Phe | missense_variant | 0.12 |
embB | 4248818 | p.Gly769Cys | missense_variant | 0.17 |
embB | 4248964 | c.2451G>A | synonymous_variant | 0.22 |
embB | 4249802 | p.Gly1097Cys | missense_variant | 0.25 |
aftB | 4266954 | c.1883G>A | splice_region_variant&stop_retained_variant | 0.18 |
aftB | 4267487 | p.Leu450Phe | missense_variant | 0.22 |
aftB | 4268040 | p.Leu266Pro | missense_variant | 1.0 |
aftB | 4268060 | p.Asn259Lys | missense_variant | 0.11 |
aftB | 4268135 | c.702G>T | synonymous_variant | 0.29 |
ubiA | 4269221 | p.Ala205Thr | missense_variant | 0.13 |
aftB | 4269516 | c.-680G>A | upstream_gene_variant | 0.15 |
aftB | 4269531 | c.-695G>A | upstream_gene_variant | 0.18 |
ethA | 4326297 | p.Leu393Met | missense_variant | 0.17 |
ethA | 4326701 | p.Arg258Gln | missense_variant | 0.17 |
ethR | 4327974 | p.Met142Ile | missense_variant | 0.15 |
ethA | 4328079 | c.-606C>A | upstream_gene_variant | 0.2 |
ethR | 4328114 | p.Gly189Val | missense_variant | 0.15 |
whiB6 | 4338479 | p.Phe15Ile | missense_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407902 | p.Leu101Ile | missense_variant | 0.22 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |
gid | 4408451 | c.-249T>C | upstream_gene_variant | 0.18 |