Run ID: ERR4831745
Sample name:
Date: 01-04-2023 21:05:47
Number of reads: 1887064
Percentage reads mapped: 96.22
Strain: lineage2.2.1.1
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 0.99 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.99 |
lineage2.2.1.1 | East-Asian (Beijing) | Beijing-RD150 | RD105;RD207;RD181;RD150 | 0.98 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761140 | p.His445Pro | missense_variant | 0.8 | rifampicin |
rpoB | 761155 | p.Ser450Leu | missense_variant | 0.13 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288751 | p.Ser164* | stop_gained | 1.0 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6824 | c.-478C>T | upstream_gene_variant | 0.12 |
gyrA | 6841 | c.-461T>C | upstream_gene_variant | 0.1 |
gyrA | 6889 | c.-413G>A | upstream_gene_variant | 0.14 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8784 | p.Arg495Ser | missense_variant | 0.17 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575580 | c.235delC | frameshift_variant | 0.12 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 576302 | p.Leu319Met | missense_variant | 0.14 |
ccsA | 620010 | c.120C>A | synonymous_variant | 0.12 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 759615 | c.-192A>C | upstream_gene_variant | 0.23 |
rpoB | 760541 | c.735G>C | synonymous_variant | 0.12 |
rpoB | 760561 | c.757_758delCG | frameshift_variant | 0.13 |
rpoB | 760567 | p.Ser254Trp | missense_variant | 0.11 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.14 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.17 |
rpoC | 762728 | c.-642C>G | upstream_gene_variant | 0.11 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763088 | c.-282C>G | upstream_gene_variant | 0.12 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.11 |
rpoC | 764331 | p.Pro321Gln | missense_variant | 0.12 |
rpoC | 764542 | c.1173C>T | synonymous_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 777776 | p.Met235Ile | missense_variant | 0.11 |
mmpL5 | 777841 | p.Val214Leu | missense_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 0.94 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303144 | p.Ser72Pro | missense_variant | 0.12 |
fbiC | 1303155 | c.225G>A | synonymous_variant | 0.11 |
fbiC | 1304000 | p.Val357Ala | missense_variant | 0.1 |
fbiC | 1304451 | c.1521C>T | synonymous_variant | 0.18 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1407005 | c.336G>C | synonymous_variant | 0.13 |
Rv1258c | 1407179 | c.162G>T | synonymous_variant | 0.14 |
Rv1258c | 1407399 | c.-59C>T | upstream_gene_variant | 0.33 |
embR | 1416523 | c.825G>T | synonymous_variant | 0.15 |
embR | 1416534 | p.Gly272Ser | missense_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472162 | n.317G>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472712 | n.867G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474980 | n.1323G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475075 | n.1418A>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475136 | n.1479G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475337 | n.1680C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475343 | n.1686A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475346 | n.1689C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475353 | n.1696A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475358 | n.1701T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475361 | n.1704G>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476504 | n.2847T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.11 |
rpsA | 1833353 | c.-189C>T | upstream_gene_variant | 0.12 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.1 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.96 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918572 | c.633C>A | synonymous_variant | 0.18 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170028 | p.Met195Ile | missense_variant | 0.11 |
PPE35 | 2170123 | p.Ala164Ser | missense_variant | 0.14 |
PPE35 | 2170292 | c.321G>C | synonymous_variant | 0.1 |
PPE35 | 2170395 | p.Ala73Val | missense_variant | 0.22 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518905 | p.Arg264Gln | missense_variant | 0.15 |
kasA | 2518918 | c.804C>G | synonymous_variant | 0.12 |
kasA | 2519032 | c.918C>T | synonymous_variant | 0.17 |
kasA | 2519202 | p.Arg363Leu | missense_variant | 0.12 |
eis | 2714846 | p.Val163Ile | missense_variant | 1.0 |
ahpC | 2726350 | p.Trp53Leu | missense_variant | 0.21 |
folC | 2746244 | p.Ala452Asp | missense_variant | 0.12 |
folC | 2746309 | c.1290G>T | synonymous_variant | 0.25 |
folC | 2746588 | c.1011C>T | synonymous_variant | 0.14 |
folC | 2746883 | p.Pro239Gln | missense_variant | 0.14 |
folC | 2747053 | c.546C>T | synonymous_variant | 0.2 |
folC | 2747631 | c.-33C>A | upstream_gene_variant | 0.12 |
Rv2752c | 3065669 | p.Gln175Lys | missense_variant | 0.11 |
Rv2752c | 3067155 | c.-964C>T | upstream_gene_variant | 0.17 |
thyX | 3067388 | c.558C>T | synonymous_variant | 0.2 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449142 | c.639C>A | synonymous_variant | 0.14 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612161 | p.Ala319Gly | missense_variant | 0.12 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 0.94 |
fbiA | 3640407 | c.-136G>A | upstream_gene_variant | 1.0 |
fbiB | 3642197 | c.663C>G | synonymous_variant | 0.2 |
alr | 3840498 | p.Ala308Glu | missense_variant | 0.12 |
rpoA | 3878637 | c.-130G>A | upstream_gene_variant | 1.0 |
clpC1 | 4039032 | p.Gly558Asp | missense_variant | 0.22 |
clpC1 | 4039096 | p.Ala537Ser | missense_variant | 0.14 |
clpC1 | 4040078 | p.Lys209Asn | missense_variant | 0.14 |
embC | 4240671 | p.Thr270Ile | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4243488 | p.Gly86Ser | missense_variant | 0.12 |
embA | 4244899 | p.Thr556Met | missense_variant | 0.13 |
embA | 4245597 | p.Lys789Glu | missense_variant | 0.13 |
embA | 4246009 | p.Arg926Gln | missense_variant | 0.15 |
embA | 4246018 | p.Leu929Pro | missense_variant | 0.15 |
embB | 4246861 | c.348C>A | synonymous_variant | 0.15 |
embB | 4246977 | p.Ala155Val | missense_variant | 0.17 |
embB | 4248115 | c.1602C>T | synonymous_variant | 1.0 |
embB | 4249286 | p.Gln925Lys | missense_variant | 0.14 |
embB | 4249475 | p.Trp988Arg | missense_variant | 0.12 |
embB | 4249650 | p.Ala1046Val | missense_variant | 0.12 |
embB | 4249753 | p.Leu1080Phe | missense_variant | 0.11 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
ethA | 4328043 | c.-570G>T | upstream_gene_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.94 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |