Run ID: ERR4817377
Sample name:
Date: 01-04-2023 14:57:34
Number of reads: 475605
Percentage reads mapped: 99.5
Strain: lineage3
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5322 | p.Lys28Arg | missense_variant | 0.11 |
gyrB | 5640 | p.Arg134Leu | missense_variant | 0.11 |
gyrB | 6804 | p.Leu522Pro | missense_variant | 0.12 |
gyrA | 6922 | c.-380G>T | upstream_gene_variant | 0.2 |
gyrA | 7010 | c.-292C>T | upstream_gene_variant | 0.13 |
gyrB | 7118 | p.Asp627Tyr | missense_variant | 0.25 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7406 | c.105G>A | synonymous_variant | 0.11 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7696 | p.Ala132Val | missense_variant | 0.12 |
gyrA | 8763 | p.Asp488Tyr | missense_variant | 0.29 |
gyrA | 8801 | c.1500G>A | synonymous_variant | 0.18 |
gyrA | 8873 | c.1572A>G | synonymous_variant | 0.2 |
gyrA | 9121 | p.Arg607Leu | missense_variant | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
fgd1 | 491774 | p.Arg331Met | missense_variant | 0.11 |
mshA | 575950 | c.607delG | frameshift_variant | 0.5 |
mshA | 576463 | c.1116G>A | synonymous_variant | 0.13 |
mshA | 576517 | c.1170G>A | synonymous_variant | 0.18 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763063 | p.Lys1086Arg | missense_variant | 0.15 |
rpoC | 765571 | c.2202C>G | synonymous_variant | 0.2 |
rpoC | 766126 | c.2757G>A | synonymous_variant | 0.22 |
rpoC | 766582 | c.3213C>A | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776605 | p.Arg626Ser | missense_variant | 0.11 |
mmpL5 | 777032 | c.1449C>G | synonymous_variant | 0.12 |
mmpL5 | 777035 | c.1446G>A | synonymous_variant | 0.12 |
mmpL5 | 777157 | c.1324C>A | synonymous_variant | 0.15 |
mmpL5 | 777164 | c.1317C>T | synonymous_variant | 0.15 |
mmpL5 | 777767 | c.714C>T | synonymous_variant | 0.18 |
mmpL5 | 777811 | p.Arg224Trp | missense_variant | 0.14 |
mmpR5 | 778349 | c.-641G>T | upstream_gene_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800640 | c.-169A>G | upstream_gene_variant | 0.2 |
rplC | 800856 | c.48A>G | synonymous_variant | 0.25 |
rplC | 800955 | c.147C>A | synonymous_variant | 0.2 |
fbiC | 1303817 | p.Arg296His | missense_variant | 0.11 |
fbiC | 1304113 | p.Gln395Lys | missense_variant | 0.18 |
fbiC | 1305232 | p.Ala768Ser | missense_variant | 0.2 |
embR | 1416408 | p.His314Tyr | missense_variant | 0.12 |
embR | 1417093 | c.255C>A | synonymous_variant | 0.11 |
embR | 1417528 | c.-181C>A | upstream_gene_variant | 0.14 |
atpE | 1461036 | c.-9G>T | upstream_gene_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673738 | p.Met100Thr | missense_variant | 0.18 |
fabG1 | 1674020 | p.Leu194Pro | missense_variant | 0.29 |
fabG1 | 1674152 | p.Pro238Gln | missense_variant | 0.17 |
inhA | 1674767 | p.Val189Ala | missense_variant | 0.33 |
tlyA | 1917828 | c.-112G>T | upstream_gene_variant | 0.29 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918034 | p.Val32Gly | missense_variant | 0.5 |
ndh | 2102077 | c.966T>C | synonymous_variant | 0.25 |
ndh | 2102631 | p.Met138Val | missense_variant | 0.12 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168260 | c.2352delT | frameshift_variant | 0.33 |
PPE35 | 2169162 | p.Ser484* | stop_gained | 0.17 |
Rv1979c | 2222540 | p.Gly209Cys | missense_variant | 0.14 |
Rv1979c | 2222556 | c.609C>T | synonymous_variant | 0.12 |
Rv1979c | 2222982 | c.183G>A | synonymous_variant | 0.12 |
Rv1979c | 2223078 | c.87C>T | synonymous_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
pncA | 2289786 | c.-545G>T | upstream_gene_variant | 0.22 |
pncA | 2289833 | c.-592T>G | upstream_gene_variant | 0.29 |
pncA | 2289887 | c.-649_-647delCCG | upstream_gene_variant | 0.2 |
pncA | 2290132 | c.-891C>T | upstream_gene_variant | 0.12 |
ahpC | 2726022 | c.-171C>A | upstream_gene_variant | 0.12 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726257 | p.Asp22Val | missense_variant | 0.25 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.38 |
ahpC | 2726583 | p.Ala131Thr | missense_variant | 0.5 |
pepQ | 2859372 | c.1047G>A | synonymous_variant | 0.13 |
ribD | 2986798 | c.-41C>G | upstream_gene_variant | 0.12 |
ribD | 2987096 | c.258C>T | synonymous_variant | 0.15 |
ribD | 2987127 | p.Arg97Trp | missense_variant | 0.12 |
Rv2752c | 3065586 | p.Asp202Glu | missense_variant | 0.22 |
Rv2752c | 3065995 | p.His66Arg | missense_variant | 0.18 |
Rv2752c | 3066157 | p.Thr12Ile | missense_variant | 0.22 |
thyA | 3074116 | p.Leu119Pro | missense_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3338993 | c.-125C>T | upstream_gene_variant | 0.12 |
Rv3083 | 3449223 | p.Tyr240* | stop_gained | 0.11 |
Rv3083 | 3449796 | c.1293G>A | synonymous_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475358 | p.Leu451* | stop_gained | 0.22 |
whiB7 | 3568574 | p.Leu36Val | missense_variant | 0.1 |
fbiB | 3640674 | c.-861C>T | upstream_gene_variant | 0.29 |
fbiB | 3641573 | p.Glu13Asp | missense_variant | 0.22 |
fbiB | 3641850 | p.Ala106Ser | missense_variant | 0.25 |
fbiB | 3642370 | p.Ala279Val | missense_variant | 0.11 |
fbiB | 3642833 | c.1299C>T | synonymous_variant | 0.17 |
alr | 3841151 | c.270C>A | synonymous_variant | 0.13 |
alr | 3841473 | c.-53G>A | upstream_gene_variant | 1.0 |
rpoA | 3877850 | p.Gly220Ser | missense_variant | 0.22 |
ddn | 3987108 | p.Tyr89Asp | missense_variant | 0.12 |
clpC1 | 4038588 | p.Arg706Leu | missense_variant | 0.2 |
clpC1 | 4039597 | p.His370Asn | missense_variant | 0.22 |
clpC1 | 4040724 | c.-20G>T | upstream_gene_variant | 0.12 |
embC | 4240133 | p.Ala91Ser | missense_variant | 0.2 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embC | 4242249 | p.Ala796Val | missense_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244780 | c.1548C>A | synonymous_variant | 0.17 |
embA | 4245313 | p.Ala694Glu | missense_variant | 0.22 |
embB | 4248563 | p.Ala684Thr | missense_variant | 0.17 |
aftB | 4267623 | p.Ser405* | stop_gained | 0.22 |
aftB | 4268418 | p.Glu140Gly | missense_variant | 0.2 |
ubiA | 4269032 | p.Gly268Ser | missense_variant | 0.15 |
aftB | 4269366 | c.-530G>A | upstream_gene_variant | 0.15 |
ethA | 4326011 | p.Gly488Val | missense_variant | 0.11 |
ethA | 4326548 | p.Lys309Arg | missense_variant | 0.15 |
ethA | 4326743 | p.Leu244Pro | missense_variant | 0.17 |
ethR | 4327042 | c.-507G>A | upstream_gene_variant | 0.14 |
ethA | 4327306 | p.Asp56Glu | missense_variant | 0.18 |
ethR | 4328047 | p.Pro167Ser | missense_variant | 1.0 |
ethA | 4328292 | c.-819A>G | upstream_gene_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4408436 | c.-234C>T | upstream_gene_variant | 0.2 |