Run ID: ERR2245276
Sample name:
Date: 31-03-2023 17:36:52
Number of reads: 1953858
Percentage reads mapped: 98.82
Strain: lineage3.1
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3.1 | East-African-Indian | Non-CAS1-Delhi | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
tlyA | 1918739 | c.803delC | frameshift_variant | 0.4 | capreomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
embB | 4247431 | p.Met306Ile | missense_variant | 1.0 | ethambutol |
ethA | 4327222 | c.251delA | frameshift_variant | 0.13 | ethionamide |
gid | 4407796 | p.Ser136* | stop_gained | 0.17 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5840 | p.Asn201Tyr | missense_variant | 0.4 |
gyrB | 6053 | p.His272Tyr | missense_variant | 0.33 |
gyrB | 6421 | p.His394Gln | missense_variant | 0.14 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9557 | c.2256G>T | synonymous_variant | 0.29 |
gyrA | 9774 | p.Asp825Tyr | missense_variant | 0.38 |
fgd1 | 491326 | p.Ala182Ser | missense_variant | 0.29 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575254 | c.-94C>T | upstream_gene_variant | 0.2 |
mshA | 575972 | p.Glu209Lys | missense_variant | 0.33 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.35 |
ccsA | 620679 | c.789C>A | synonymous_variant | 0.25 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 760631 | c.825G>T | synonymous_variant | 0.22 |
rpoB | 761587 | p.Asp594Val | missense_variant | 0.25 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763796 | p.Met143Leu | missense_variant | 0.25 |
rpoC | 764101 | c.732C>T | synonymous_variant | 0.22 |
rpoC | 764208 | p.Val280Gly | missense_variant | 0.29 |
rpoC | 764456 | p.Pro363Thr | missense_variant | 0.22 |
rpoC | 764610 | p.Arg414Gln | missense_variant | 0.2 |
rpoC | 764866 | c.1497C>T | synonymous_variant | 0.25 |
rpoC | 765545 | p.Arg726Ser | missense_variant | 0.15 |
rpoC | 766415 | p.His1016Tyr | missense_variant | 0.4 |
rpoC | 766795 | p.Tyr1142* | stop_gained | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776711 | p.His590Gln | missense_variant | 0.22 |
mmpL5 | 777676 | p.Leu269Met | missense_variant | 0.33 |
mmpR5 | 778451 | c.-539C>T | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781404 | c.-156G>T | upstream_gene_variant | 0.5 |
rplC | 801113 | p.Thr102Asn | missense_variant | 0.2 |
fbiC | 1303391 | p.Arg154Leu | missense_variant | 0.5 |
fbiC | 1303576 | p.Glu216* | stop_gained | 0.2 |
fbiC | 1304270 | p.Val447Gly | missense_variant | 0.67 |
fbiC | 1304707 | p.Val593Ile | missense_variant | 0.5 |
fbiC | 1305177 | c.2249dupC | frameshift_variant | 0.22 |
fbiC | 1305197 | p.Ala756Val | missense_variant | 0.12 |
fbiC | 1305361 | p.Leu811Met | missense_variant | 0.17 |
Rv1258c | 1406599 | p.Pro248Thr | missense_variant | 0.22 |
Rv1258c | 1407266 | c.75C>A | synonymous_variant | 0.4 |
embR | 1416493 | c.855C>A | synonymous_variant | 0.22 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1476461 | n.2804A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476736 | n.3079A>C | non_coding_transcript_exon_variant | 0.18 |
fabG1 | 1674091 | p.Ala218Ser | missense_variant | 0.22 |
inhA | 1674997 | p.Thr266Pro | missense_variant | 0.29 |
rpsA | 1833982 | p.Phe147Leu | missense_variant | 0.18 |
rpsA | 1834039 | c.498C>A | synonymous_variant | 0.17 |
rpsA | 1834735 | c.1194C>T | synonymous_variant | 0.18 |
rpsA | 1834806 | p.Glu422Val | missense_variant | 0.33 |
rpsA | 1834822 | p.Met427Ile | missense_variant | 0.29 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918428 | c.489G>T | synonymous_variant | 0.2 |
tlyA | 1918607 | p.Val223Gly | missense_variant | 0.67 |
ndh | 2102054 | p.Pro330Leu | missense_variant | 0.17 |
ndh | 2102128 | c.915G>T | synonymous_variant | 0.67 |
ndh | 2102733 | p.Leu104Ile | missense_variant | 0.18 |
katG | 2154489 | c.1623C>A | synonymous_variant | 0.22 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2154871 | p.Lys414Arg | missense_variant | 0.19 |
katG | 2155033 | p.Gly360Asp | missense_variant | 0.29 |
katG | 2155706 | p.Pro136Thr | missense_variant | 0.33 |
katG | 2156356 | c.-245G>T | upstream_gene_variant | 0.27 |
katG | 2156415 | c.-304C>G | upstream_gene_variant | 0.14 |
PPE35 | 2167740 | p.Thr958Ile | missense_variant | 0.29 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168843 | c.1770G>A | synonymous_variant | 0.17 |
PPE35 | 2169049 | p.Ile522Phe | missense_variant | 0.15 |
PPE35 | 2169125 | c.1488T>A | synonymous_variant | 0.15 |
PPE35 | 2169237 | p.Asp459Val | missense_variant | 0.17 |
PPE35 | 2169417 | p.Thr399Lys | missense_variant | 0.25 |
PPE35 | 2169838 | p.Ile259Leu | missense_variant | 0.13 |
Rv1979c | 2222113 | p.Val351Gly | missense_variant | 0.25 |
Rv1979c | 2222371 | p.Ala265Glu | missense_variant | 0.2 |
Rv1979c | 2223126 | p.Lys13Asn | missense_variant | 0.33 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289352 | c.-112delG | upstream_gene_variant | 0.25 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
kasA | 2518307 | p.Lys65* | stop_gained | 0.29 |
kasA | 2518531 | c.417G>A | synonymous_variant | 0.22 |
eis | 2714410 | p.Arg308Leu | missense_variant | 0.29 |
ahpC | 2726061 | c.-132G>T | upstream_gene_variant | 0.15 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
folC | 2746395 | p.Val402Phe | missense_variant | 0.4 |
pepQ | 2859751 | p.Gly223Val | missense_variant | 0.25 |
pepQ | 2859811 | p.Pro203Leu | missense_variant | 0.5 |
pepQ | 2860296 | c.123C>A | synonymous_variant | 0.2 |
ribD | 2987213 | c.375C>A | synonymous_variant | 0.67 |
ribD | 2987541 | c.703C>T | synonymous_variant | 0.67 |
thyX | 3067276 | p.Pro224Thr | missense_variant | 0.5 |
thyX | 3067533 | p.Ala138Val | missense_variant | 0.29 |
thyX | 3068065 | c.-120G>C | upstream_gene_variant | 0.29 |
thyA | 3074235 | c.237C>A | synonymous_variant | 0.13 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087394 | p.Ala192Val | missense_variant | 0.18 |
fbiD | 3339171 | c.54C>A | synonymous_variant | 0.17 |
Rv3083 | 3449258 | p.Arg252Gln | missense_variant | 1.0 |
Rv3083 | 3449841 | c.1338C>A | synonymous_variant | 0.15 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474052 | p.Phe16Ile | missense_variant | 0.4 |
fprA | 3474320 | p.Gly105Asp | missense_variant | 0.18 |
fprA | 3474634 | p.Leu210Val | missense_variant | 0.2 |
fprA | 3475110 | c.1104C>T | synonymous_variant | 0.5 |
fprA | 3475250 | p.Pro415Arg | missense_variant | 0.33 |
Rv3236c | 3612581 | p.Leu179Arg | missense_variant | 0.33 |
Rv3236c | 3612637 | p.Phe160Leu | missense_variant | 0.4 |
fbiB | 3641912 | p.Asp126Glu | missense_variant | 0.29 |
fbiB | 3642666 | p.Gly378Arg | missense_variant | 0.4 |
fbiB | 3642673 | p.Ala380Asp | missense_variant | 0.33 |
fbiB | 3642728 | c.1194C>T | synonymous_variant | 0.4 |
alr | 3840631 | p.Pro264Ser | missense_variant | 0.29 |
alr | 3840688 | p.Asp245Tyr | missense_variant | 0.22 |
rpoA | 3877935 | p.Lys191Asn | missense_variant | 0.15 |
ddn | 3987061 | p.Val73Gly | missense_variant | 0.29 |
clpC1 | 4038212 | p.Asp831Glu | missense_variant | 0.4 |
clpC1 | 4039166 | p.Glu513Asp | missense_variant | 0.15 |
clpC1 | 4039626 | p.Lys360Met | missense_variant | 0.33 |
clpC1 | 4040249 | p.Glu152Asp | missense_variant | 0.33 |
clpC1 | 4040262 | p.Lys148Met | missense_variant | 0.4 |
clpC1 | 4040457 | p.Arg83Leu | missense_variant | 0.15 |
embC | 4239879 | p.Ala6Gly | missense_variant | 0.27 |
embC | 4240172 | p.Val104Met | missense_variant | 1.0 |
embC | 4240239 | p.Ala126Asp | missense_variant | 0.25 |
embC | 4241187 | p.Gly442Asp | missense_variant | 0.4 |
embC | 4241562 | p.Arg567His | missense_variant | 1.0 |
embC | 4241679 | p.Val606Gly | missense_variant | 0.33 |
embC | 4242075 | p.Arg738Gln | missense_variant | 0.92 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242851 | p.Phe997Ile | missense_variant | 0.29 |
embA | 4243212 | c.-21C>A | upstream_gene_variant | 0.25 |
embA | 4243235 | c.3G>A | synonymous_variant | 0.29 |
embA | 4243253 | p.Glu7Asp | missense_variant | 0.33 |
embA | 4243448 | c.216C>A | synonymous_variant | 0.67 |
embA | 4244715 | p.Trp495Arg | missense_variant | 0.29 |
embA | 4244781 | p.Arg517Ser | missense_variant | 0.33 |
embA | 4244989 | p.Ala586Val | missense_variant | 0.2 |
embA | 4245160 | p.Ser643Ile | missense_variant | 0.15 |
embB | 4247024 | p.Pro171Ala | missense_variant | 1.0 |
embB | 4247438 | p.Val309Phe | missense_variant | 0.15 |
embB | 4247458 | p.Tyr315* | stop_gained | 0.14 |
embB | 4247625 | p.Pro371His | missense_variant | 0.25 |
embB | 4248897 | p.Glu795Val | missense_variant | 0.17 |
embB | 4249586 | p.Thr1025Ser | missense_variant | 0.25 |
aftB | 4268619 | p.Val73Gly | missense_variant | 0.5 |
aftB | 4268689 | p.Asn50Asp | missense_variant | 0.33 |
ubiA | 4269230 | p.Thr202Ala | missense_variant | 0.25 |
aftB | 4269348 | c.-512C>A | upstream_gene_variant | 0.14 |
ubiA | 4269781 | p.Val18Gly | missense_variant | 0.29 |
ubiA | 4269793 | p.Val14Gly | missense_variant | 0.22 |
ubiA | 4269959 | c.-126C>A | upstream_gene_variant | 0.33 |
ethA | 4327543 | c.-70C>A | upstream_gene_variant | 0.22 |
ethR | 4328041 | p.Thr165Pro | missense_variant | 0.27 |
ethA | 4328436 | c.-963G>T | upstream_gene_variant | 0.29 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407553 | p.Arg217Gln | missense_variant | 0.4 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4408321 | c.-119C>T | upstream_gene_variant | 0.33 |
gid | 4408396 | c.-194G>T | upstream_gene_variant | 0.22 |