Run ID: ERR027293
Sample name:
Date: 31-03-2023 08:20:28
Number of reads: 180602
Percentage reads mapped: 61.32
Strain:
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472307 | n.462C>T | non_coding_transcript_exon_variant | 0.22 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5671 | c.432C>T | synonymous_variant | 1.0 |
gyrB | 6446 | p.Ala403Ser | missense_variant | 1.0 |
gyrA | 6535 | c.-767C>A | upstream_gene_variant | 0.5 |
gyrA | 6541 | c.-761C>T | upstream_gene_variant | 0.67 |
gyrB | 6542 | p.Ile435Leu | missense_variant | 0.67 |
gyrA | 6550 | c.-752A>G | upstream_gene_variant | 0.5 |
gyrA | 6551 | c.-751T>C | upstream_gene_variant | 0.5 |
gyrA | 6563 | c.-739C>T | upstream_gene_variant | 0.5 |
gyrA | 6571 | c.-731T>C | upstream_gene_variant | 0.4 |
gyrA | 6577 | c.-725T>C | upstream_gene_variant | 0.4 |
gyrA | 6580 | c.-722C>G | upstream_gene_variant | 0.33 |
gyrA | 6583 | c.-719G>A | upstream_gene_variant | 0.33 |
gyrA | 6589 | c.-713G>A | upstream_gene_variant | 0.33 |
gyrA | 6592 | c.-710C>T | upstream_gene_variant | 0.29 |
gyrA | 6598 | c.-704C>G | upstream_gene_variant | 0.29 |
gyrA | 6610 | c.-692C>G | upstream_gene_variant | 0.25 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8247 | p.Ile316Val | missense_variant | 0.33 |
gyrA | 8258 | c.957G>A | synonymous_variant | 0.22 |
gyrA | 8264 | c.963T>C | synonymous_variant | 0.22 |
gyrA | 8267 | c.966G>C | synonymous_variant | 0.18 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575732 | c.385_387delCTTinsTTG | synonymous_variant | 0.67 |
mshA | 575746 | c.399C>G | synonymous_variant | 0.67 |
mshA | 575764 | c.417C>G | synonymous_variant | 0.5 |
mshA | 575767 | c.420G>A | synonymous_variant | 0.5 |
mshA | 575770 | c.423G>C | synonymous_variant | 0.5 |
mshA | 575772 | p.Val142Ala | missense_variant | 0.5 |
mshA | 575782 | c.435G>C | synonymous_variant | 0.5 |
mshA | 575785 | c.438T>G | synonymous_variant | 0.5 |
mshA | 575786 | p.Tyr147His | missense_variant | 0.4 |
mshA | 575812 | c.465C>T | synonymous_variant | 0.33 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.4 |
rpoB | 761195 | c.1389G>T | synonymous_variant | 0.5 |
rpoB | 761201 | c.1395G>A | synonymous_variant | 0.5 |
rpoB | 761204 | c.1398C>T | synonymous_variant | 0.5 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.5 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.5 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.5 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.5 |
rpoB | 761588 | c.1782C>T | synonymous_variant | 0.5 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.33 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.25 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.25 |
rpoC | 763721 | c.352C>T | synonymous_variant | 0.4 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.33 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.33 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.33 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.33 |
rpoC | 763768 | c.399C>A | synonymous_variant | 0.29 |
rpoC | 763790 | p.Glu141Asn | missense_variant | 0.29 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.25 |
rpoC | 765454 | c.2085C>G | synonymous_variant | 0.2 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.33 |
rpoC | 765562 | c.2193G>C | synonymous_variant | 0.4 |
rpoC | 765611 | p.His748Ser | missense_variant | 0.5 |
rpoC | 765625 | c.2256C>G | synonymous_variant | 0.5 |
rpoC | 765631 | p.Asp754Glu | missense_variant | 0.67 |
rpoC | 765640 | c.2271A>G | synonymous_variant | 0.75 |
rpoC | 765658 | c.2289C>T | synonymous_variant | 0.33 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.33 |
rpoC | 765850 | c.2481G>C | synonymous_variant | 0.22 |
rpoC | 765868 | c.2499G>A | synonymous_variant | 0.22 |
rpoC | 765871 | c.2502T>C | synonymous_variant | 0.22 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.22 |
rpoC | 766309 | c.2940G>A | synonymous_variant | 0.33 |
rpoC | 766315 | c.2946C>G | synonymous_variant | 0.4 |
rpoC | 766321 | c.2952C>G | synonymous_variant | 0.4 |
rpoC | 766348 | c.2979A>G | synonymous_variant | 0.4 |
rpoC | 766351 | c.2982C>A | synonymous_variant | 0.4 |
rpoC | 766363 | c.2994G>C | synonymous_variant | 0.4 |
rpoC | 766372 | c.3003G>A | synonymous_variant | 0.4 |
rpoC | 766528 | c.3159T>C | synonymous_variant | 0.5 |
rpoC | 766543 | c.3174C>T | synonymous_variant | 0.33 |
rpoC | 766549 | c.3180G>C | synonymous_variant | 0.33 |
rpoC | 766570 | c.3201T>C | synonymous_variant | 0.25 |
rpoC | 766573 | c.3204T>C | synonymous_variant | 0.33 |
rpoC | 766579 | c.3210C>T | synonymous_variant | 0.33 |
rpoC | 766585 | c.3216T>C | synonymous_variant | 0.3 |
rpoC | 766594 | c.3225G>C | synonymous_variant | 0.2 |
rpoC | 766607 | p.Ile1080Leu | missense_variant | 0.3 |
rpoC | 766645 | c.3276A>G | synonymous_variant | 0.22 |
rpoC | 766651 | c.3282T>C | synonymous_variant | 0.29 |
rpoC | 766654 | c.3285C>G | synonymous_variant | 0.22 |
rpoC | 766657 | c.3288A>G | synonymous_variant | 0.22 |
rpoC | 766666 | c.3297C>T | synonymous_variant | 0.29 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.4 |
rpoC | 766738 | c.3369G>T | synonymous_variant | 0.33 |
rpoC | 766750 | c.3381C>G | synonymous_variant | 0.4 |
rpoC | 766753 | c.3384C>T | synonymous_variant | 0.4 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.4 |
rpoC | 766769 | c.3400C>T | synonymous_variant | 0.4 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.4 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776132 | c.2349A>G | synonymous_variant | 0.4 |
mmpL5 | 776141 | c.2340A>C | synonymous_variant | 0.4 |
mmpL5 | 776198 | c.2283C>G | synonymous_variant | 0.29 |
mmpL5 | 776207 | c.2274G>C | synonymous_variant | 0.29 |
mmpL5 | 776459 | p.Ala674Ser | missense_variant | 0.4 |
mmpL5 | 777028 | p.Thr485Pro | missense_variant | 0.4 |
mmpL5 | 777826 | c.655T>C | synonymous_variant | 0.29 |
mmpL5 | 777842 | c.639C>G | synonymous_variant | 0.25 |
mmpL5 | 779064 | c.-584G>T | upstream_gene_variant | 0.29 |
mmpR5 | 779079 | p.Arg30Ser | missense_variant | 0.5 |
mmpR5 | 779080 | p.Ser31Gly | missense_variant | 0.5 |
mmpL5 | 779083 | c.-603A>G | upstream_gene_variant | 0.4 |
mmpL5 | 779100 | c.-620A>G | upstream_gene_variant | 0.5 |
mmpL5 | 779107 | c.-627A>G | upstream_gene_variant | 0.5 |
mmpL5 | 779118 | c.-638C>T | upstream_gene_variant | 0.5 |
mmpL5 | 779119 | c.-639G>A | upstream_gene_variant | 0.5 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800690 | c.-119C>T | upstream_gene_variant | 0.67 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.67 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 1.0 |
rplC | 800735 | c.-74C>G | upstream_gene_variant | 0.67 |
rplC | 800744 | c.-65G>A | upstream_gene_variant | 0.67 |
rplC | 801205 | p.Arg133Ser | missense_variant | 0.22 |
rplC | 801210 | c.402T>C | synonymous_variant | 0.44 |
rplC | 801222 | c.414T>C | synonymous_variant | 0.33 |
rplC | 801249 | c.441T>G | synonymous_variant | 0.5 |
rplC | 801255 | c.447C>T | synonymous_variant | 0.43 |
rplC | 801264 | c.456C>T | synonymous_variant | 0.43 |
rplC | 801267 | c.459A>C | synonymous_variant | 0.33 |
rplC | 801312 | c.504G>C | synonymous_variant | 0.67 |
rplC | 801396 | c.588T>C | synonymous_variant | 0.4 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 1.0 |
Rv1258c | 1407299 | p.Phe14Leu | missense_variant | 0.5 |
embR | 1417338 | p.Ser4Gly | missense_variant | 0.25 |
atpE | 1461219 | c.175T>C | synonymous_variant | 0.5 |
atpE | 1461230 | c.186G>C | synonymous_variant | 0.4 |
atpE | 1461233 | c.189A>C | synonymous_variant | 0.4 |
atpE | 1461239 | c.195C>T | synonymous_variant | 0.4 |
atpE | 1461275 | c.231T>C | synonymous_variant | 0.5 |
atpE | 1461278 | c.234A>G | synonymous_variant | 0.5 |
atpE | 1461284 | c.240C>T | synonymous_variant | 0.5 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472300 | n.455C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473079 | n.1234G>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473571 | n.-87C>T | upstream_gene_variant | 0.4 |
rrl | 1473594 | n.-64_-63insT | upstream_gene_variant | 0.5 |
rrl | 1473600 | n.-58A>G | upstream_gene_variant | 0.33 |
rrl | 1473627 | n.-31_-30insG | upstream_gene_variant | 0.29 |
rrl | 1473635 | n.-23_-22insTTT | upstream_gene_variant | 0.25 |
rrl | 1473752 | n.95G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473815 | n.158T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473836 | n.179A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473923 | n.266C>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1473924 | n.267_268insT | non_coding_transcript_exon_variant | 0.43 |
rrl | 1473943 | n.286G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473944 | n.287G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474028 | n.371T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474029 | n.372G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474034 | n.377G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474040 | n.383G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474083 | n.426C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.4 |
fabG1 | 1673449 | p.Thr4Pro | missense_variant | 0.67 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.4 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 0.5 |
rpsA | 1833820 | c.279G>A | synonymous_variant | 0.5 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.6 |
rpsA | 1833862 | c.321G>A | synonymous_variant | 0.6 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.5 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.4 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.5 |
rpsA | 1834369 | c.828C>G | synonymous_variant | 0.5 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.75 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.67 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.67 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.67 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.8 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.8 |
rpsA | 1834459 | c.918G>C | synonymous_variant | 0.8 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.75 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155503 | c.609C>T | synonymous_variant | 1.0 |
katG | 2155605 | c.507C>A | synonymous_variant | 0.5 |
katG | 2156056 | p.Gly19Val | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168460 | p.Asn718Ser | missense_variant | 1.0 |
PPE35 | 2168726 | c.1887C>A | synonymous_variant | 0.33 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.4 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2518765 | c.651G>C | synonymous_variant | 0.67 |
kasA | 2518780 | c.666G>A | synonymous_variant | 0.67 |
kasA | 2518783 | c.669T>C | synonymous_variant | 0.67 |
kasA | 2518789 | c.675G>C | synonymous_variant | 0.67 |
kasA | 2518795 | c.681C>G | synonymous_variant | 0.4 |
eis | 2714215 | p.Asn373Ser | missense_variant | 0.33 |
eis | 2714835 | c.498C>T | synonymous_variant | 0.5 |
eis | 2715185 | p.Asp50Tyr | missense_variant | 0.67 |
ahpC | 2726408 | c.216T>C | synonymous_variant | 0.33 |
ahpC | 2726432 | c.240C>G | synonymous_variant | 0.4 |
ahpC | 2726436 | p.Ile82Val | missense_variant | 0.4 |
ahpC | 2726444 | c.252G>T | synonymous_variant | 0.33 |
ahpC | 2726447 | c.255T>C | synonymous_variant | 0.33 |
ahpC | 2726453 | c.261T>C | synonymous_variant | 0.33 |
pepQ | 2859381 | c.1038C>G | synonymous_variant | 0.67 |
pepQ | 2859974 | p.Ala149Pro | missense_variant | 0.5 |
Rv2752c | 3065187 | c.1005G>T | synonymous_variant | 0.15 |
Rv2752c | 3065202 | c.990T>C | synonymous_variant | 0.27 |
Rv2752c | 3065210 | c.982T>C | synonymous_variant | 0.3 |
Rv2752c | 3065223 | c.969T>C | synonymous_variant | 0.27 |
Rv2752c | 3065229 | c.963G>T | synonymous_variant | 0.33 |
Rv2752c | 3065232 | c.960T>C | synonymous_variant | 0.33 |
Rv2752c | 3065241 | c.951A>G | synonymous_variant | 0.27 |
Rv2752c | 3065262 | c.930G>A | synonymous_variant | 0.3 |
Rv2752c | 3065268 | c.924A>G | synonymous_variant | 0.22 |
Rv2752c | 3065283 | c.909C>T | synonymous_variant | 0.25 |
ald | 3086728 | c.-92C>T | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087084 | c.266delA | frameshift_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474123 | c.117G>A | synonymous_variant | 1.0 |
fbiA | 3641258 | p.Pro239Leu | missense_variant | 0.67 |
fbiB | 3642772 | p.Asp413Ala | missense_variant | 0.75 |
ddn | 3987111 | p.Leu90Val | missense_variant | 0.67 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.67 |
clpC1 | 4039133 | c.1572C>G | synonymous_variant | 0.5 |
clpC1 | 4039139 | c.1566G>A | synonymous_variant | 0.33 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.33 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.33 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.4 |
clpC1 | 4039507 | p.Ile400Val | missense_variant | 0.33 |
clpC1 | 4039553 | c.1152C>G | synonymous_variant | 0.4 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 0.5 |
embC | 4239719 | c.-144G>C | upstream_gene_variant | 0.33 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241182 | c.1320G>T | synonymous_variant | 0.5 |
embC | 4241185 | c.1323G>C | synonymous_variant | 0.5 |
embC | 4241197 | c.1335G>C | synonymous_variant | 0.67 |
embC | 4241203 | c.1341T>C | synonymous_variant | 0.67 |
embC | 4241230 | c.1368A>G | synonymous_variant | 0.4 |
embC | 4241233 | c.1371G>C | synonymous_variant | 0.4 |
embA | 4244220 | c.988C>T | synonymous_variant | 1.0 |
embB | 4246828 | c.315A>G | synonymous_variant | 0.5 |
embB | 4246843 | c.330T>C | synonymous_variant | 0.5 |
embB | 4246844 | c.331T>C | synonymous_variant | 0.5 |
embB | 4246853 | c.340T>C | synonymous_variant | 0.5 |
embB | 4246864 | c.351C>T | synonymous_variant | 0.67 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4247948 | p.Val479Leu | missense_variant | 0.5 |
embB | 4247965 | c.1452C>G | synonymous_variant | 0.67 |
embB | 4247975 | p.Val488Ile | missense_variant | 0.5 |
embB | 4248070 | c.1557T>C | synonymous_variant | 0.67 |
embB | 4248085 | c.1572T>G | synonymous_variant | 0.67 |
embB | 4248097 | c.1584C>G | synonymous_variant | 0.5 |
embB | 4248118 | c.1605T>G | synonymous_variant | 0.5 |
aftB | 4267305 | p.Val511Ala | missense_variant | 0.29 |
aftB | 4267310 | c.1527G>T | synonymous_variant | 0.43 |
aftB | 4267316 | c.1521A>G | synonymous_variant | 0.29 |
aftB | 4269189 | c.-353C>T | upstream_gene_variant | 0.33 |
aftB | 4269192 | c.-356C>G | upstream_gene_variant | 0.33 |
aftB | 4269195 | c.-359C>T | upstream_gene_variant | 0.33 |
aftB | 4269222 | c.-386T>G | upstream_gene_variant | 0.25 |
aftB | 4269225 | c.-389C>T | upstream_gene_variant | 0.25 |
aftB | 4269234 | c.-398A>G | upstream_gene_variant | 0.22 |
aftB | 4269240 | c.-404G>C | upstream_gene_variant | 0.22 |
ubiA | 4269243 | p.His197Gln | missense_variant | 0.22 |
aftB | 4269351 | c.-515C>T | upstream_gene_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |