Run ID: SRR18213958
Sample name:
Date: 03-04-2023 19:36:25
Number of reads: 2441352
Percentage reads mapped: 99.43
Strain: lineage4.4
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.4 | Euro-American | S;T | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5509 | c.270C>T | synonymous_variant | 1.0 |
gyrB | 5779 | p.Phe180Leu | missense_variant | 0.17 |
gyrB | 5821 | c.582G>T | synonymous_variant | 0.14 |
gyrB | 5848 | c.609G>T | synonymous_variant | 0.14 |
gyrB | 5915 | p.Val226Ile | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8829 | c.1528T>C | synonymous_variant | 0.18 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490777 | c.-6G>T | upstream_gene_variant | 0.12 |
fgd1 | 491337 | c.555C>G | synonymous_variant | 1.0 |
ccsA | 620361 | p.Tyr157* | stop_gained | 0.13 |
ccsA | 620376 | c.486G>A | synonymous_variant | 0.15 |
rpoB | 760604 | c.798G>A | synonymous_variant | 0.14 |
rpoB | 760633 | p.Arg276Leu | missense_variant | 0.11 |
rpoB | 761157 | p.Ala451Ser | missense_variant | 0.17 |
rpoB | 762952 | p.Gln1049Arg | missense_variant | 0.13 |
rpoC | 763666 | c.297G>A | synonymous_variant | 0.25 |
rpoC | 764550 | p.Pro394Leu | missense_variant | 0.2 |
rpoC | 764890 | c.1521G>A | synonymous_variant | 0.12 |
rpoC | 765546 | p.Arg726His | missense_variant | 0.13 |
rpoC | 767145 | p.Pro1259Gln | missense_variant | 0.12 |
mmpL5 | 775633 | p.Gln950Lys | missense_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776177 | p.Leu768Phe | missense_variant | 0.13 |
mmpL5 | 777795 | p.Ser229Trp | missense_variant | 0.11 |
mmpS5 | 778491 | c.414delT | frameshift_variant | 0.2 |
mmpS5 | 778642 | p.Trp88Cys | missense_variant | 0.29 |
mmpS5 | 778753 | p.Phe51Leu | missense_variant | 0.2 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800902 | p.Gly32Trp | missense_variant | 0.12 |
fbiC | 1302875 | c.-56C>A | upstream_gene_variant | 0.15 |
fbiC | 1302880 | c.-51C>A | upstream_gene_variant | 0.14 |
fbiC | 1302956 | p.Ser9Tyr | missense_variant | 0.18 |
fbiC | 1303497 | c.567G>T | synonymous_variant | 0.15 |
Rv1258c | 1407228 | p.Glu38Ala | missense_variant | 1.0 |
Rv1258c | 1407305 | c.36C>A | synonymous_variant | 0.14 |
embR | 1416605 | p.Arg248Leu | missense_variant | 0.12 |
atpE | 1460931 | c.-113delT | upstream_gene_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473600 | n.-57_-56delCG | upstream_gene_variant | 0.18 |
inhA | 1674189 | c.-13C>A | upstream_gene_variant | 0.12 |
rpsA | 1833799 | c.258C>A | synonymous_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103151 | c.-109G>T | upstream_gene_variant | 0.13 |
katG | 2154587 | p.Asp509Tyr | missense_variant | 0.12 |
katG | 2155936 | p.Gly59Asp | missense_variant | 0.12 |
PPE35 | 2167879 | p.Ser912Gly | missense_variant | 0.17 |
PPE35 | 2168073 | p.Pro847Gln | missense_variant | 0.2 |
PPE35 | 2170220 | c.393C>A | synonymous_variant | 0.12 |
Rv1979c | 2221857 | p.Cys436* | stop_gained | 0.13 |
Rv1979c | 2222224 | p.Gly314Val | missense_variant | 0.18 |
Rv1979c | 2223037 | p.Ala43Val | missense_variant | 0.18 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289911 | c.-670G>A | upstream_gene_variant | 0.13 |
kasA | 2518243 | c.129C>A | synonymous_variant | 0.18 |
kasA | 2518469 | p.Ala119Pro | missense_variant | 0.11 |
eis | 2715432 | c.-100C>T | upstream_gene_variant | 0.12 |
eis | 2715436 | c.-104G>A | upstream_gene_variant | 0.12 |
eis | 2715440 | c.-108A>C | upstream_gene_variant | 0.12 |
eis | 2715445 | c.-113C>T | upstream_gene_variant | 0.12 |
eis | 2715447 | c.-115T>A | upstream_gene_variant | 0.12 |
eis | 2715450 | c.-118T>C | upstream_gene_variant | 0.12 |
eis | 2715451 | c.-119C>A | upstream_gene_variant | 0.11 |
eis | 2715454 | c.-122T>G | upstream_gene_variant | 0.11 |
eis | 2715458 | c.-126T>A | upstream_gene_variant | 0.11 |
eis | 2715460 | c.-128A>G | upstream_gene_variant | 0.11 |
eis | 2715469 | c.-137T>C | upstream_gene_variant | 0.12 |
eis | 2715473 | c.-141A>G | upstream_gene_variant | 0.12 |
ahpC | 2726556 | p.Ala122Thr | missense_variant | 0.12 |
folC | 2746185 | p.Val472Phe | missense_variant | 0.14 |
folC | 2746319 | p.Pro427Arg | missense_variant | 0.13 |
folC | 2746555 | c.1044G>T | synonymous_variant | 0.2 |
folC | 2747153 | p.Met149Thr | missense_variant | 0.17 |
pepQ | 2859519 | c.900G>T | synonymous_variant | 0.14 |
pepQ | 2859665 | p.Leu252Met | missense_variant | 0.14 |
pepQ | 2860052 | c.367C>A | synonymous_variant | 0.14 |
ribD | 2986733 | c.-106C>T | upstream_gene_variant | 0.12 |
ribD | 2987168 | c.330C>T | synonymous_variant | 0.4 |
ribD | 2987378 | c.540C>G | synonymous_variant | 0.1 |
ribD | 2987583 | p.Gly249Ser | missense_variant | 0.13 |
Rv2752c | 3065265 | c.927C>T | synonymous_variant | 0.4 |
Rv2752c | 3066099 | p.Met31Ile | missense_variant | 1.0 |
Rv2752c | 3066127 | p.Gly22Val | missense_variant | 0.17 |
thyX | 3068073 | c.-128C>A | upstream_gene_variant | 0.12 |
thyA | 3074483 | c.-12C>T | upstream_gene_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087399 | p.Val194Phe | missense_variant | 0.13 |
fbiD | 3339126 | c.9C>A | synonymous_variant | 0.18 |
fbiD | 3339200 | p.Pro28Gln | missense_variant | 0.12 |
Rv3083 | 3448759 | p.Ala86Thr | missense_variant | 0.18 |
Rv3083 | 3449110 | p.Ser203Gly | missense_variant | 0.11 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3611997 | p.Gly374Cys | missense_variant | 0.12 |
Rv3236c | 3613224 | c.-108C>G | upstream_gene_variant | 0.1 |
fbiA | 3640941 | p.Cys133* | stop_gained | 0.13 |
fbiA | 3641179 | p.Pro213Thr | missense_variant | 0.18 |
fbiB | 3642189 | p.Gly219Arg | missense_variant | 0.38 |
fbiB | 3642621 | p.Ala363Thr | missense_variant | 0.12 |
rpoA | 3877648 | p.Arg287Leu | missense_variant | 0.14 |
rpoA | 3878099 | p.Glu137Lys | missense_variant | 0.17 |
clpC1 | 4039250 | c.1455C>T | synonymous_variant | 0.14 |
clpC1 | 4040173 | p.Leu178Ile | missense_variant | 0.18 |
clpC1 | 4040545 | p.Ile54Val | missense_variant | 0.14 |
embC | 4241111 | p.Val417Leu | missense_variant | 0.13 |
embC | 4241197 | c.1335G>C | synonymous_variant | 0.18 |
embC | 4241361 | p.Asn500Ser | missense_variant | 0.1 |
embC | 4241752 | p.Leu630Phe | missense_variant | 0.17 |
embC | 4241889 | p.Ala676Val | missense_variant | 0.17 |
embC | 4242105 | p.Thr748Asn | missense_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243910 | c.678G>A | synonymous_variant | 0.22 |
embA | 4244635 | c.1405delG | frameshift_variant | 0.14 |
embB | 4245917 | c.-597G>A | upstream_gene_variant | 0.12 |
embA | 4246008 | p.Arg926Trp | missense_variant | 0.17 |
embB | 4246508 | c.-6G>A | upstream_gene_variant | 1.0 |
embB | 4249465 | c.2952G>T | synonymous_variant | 0.11 |
aftB | 4267536 | p.Arg434Gln | missense_variant | 0.2 |
aftB | 4268277 | p.Pro187Leu | missense_variant | 0.14 |
aftB | 4268513 | c.324C>A | synonymous_variant | 0.12 |
aftB | 4268928 | c.-92C>T | upstream_gene_variant | 1.0 |
aftB | 4269375 | c.-539G>A | upstream_gene_variant | 1.0 |
ubiA | 4269827 | p.Glu3* | stop_gained | 0.18 |
ubiA | 4269879 | c.-46C>G | upstream_gene_variant | 0.17 |
ethA | 4327590 | c.-117G>A | upstream_gene_variant | 0.13 |
ethA | 4327671 | c.-198C>T | upstream_gene_variant | 0.15 |
ethA | 4328115 | c.-642G>T | upstream_gene_variant | 0.22 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408185 | c.18C>T | synonymous_variant | 0.22 |