Run ID: ERR3994122
Sample name:
Date: 01-04-2023 03:43:06
Number of reads: 2338174
Percentage reads mapped: 99.97
Strain: lineage4.3.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3.2 | Euro-American (LAM) | LAM3 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8456 | p.Asn385Lys | missense_variant | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491540 | p.Ser253Leu | missense_variant | 0.13 |
ccsA | 620465 | p.Ala192Asp | missense_variant | 0.25 |
ccsA | 620651 | p.Ala254Val | missense_variant | 0.17 |
rpoC | 762686 | c.-684G>A | upstream_gene_variant | 0.14 |
rpoB | 762881 | p.Met1025Ile | missense_variant | 0.2 |
rpoC | 764913 | p.Met515Thr | missense_variant | 0.12 |
rpoC | 764964 | p.Phe532Ser | missense_variant | 0.12 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 767133 | p.Gly1255Asp | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776953 | p.Leu510Met | missense_variant | 0.13 |
mmpL5 | 777795 | p.Ser229Trp | missense_variant | 0.1 |
mmpL5 | 777996 | p.Ala162Gly | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800639 | c.-170C>A | upstream_gene_variant | 0.12 |
fbiC | 1304184 | c.1254G>C | synonymous_variant | 0.17 |
fbiC | 1304243 | p.Pro438Arg | missense_variant | 0.18 |
Rv1258c | 1406205 | p.Thr379Met | missense_variant | 0.29 |
embR | 1416334 | p.Asn338Lys | missense_variant | 0.11 |
embR | 1416810 | p.Ala180Ser | missense_variant | 0.14 |
embR | 1417045 | p.Tyr101* | stop_gained | 0.12 |
atpE | 1461118 | p.Gly25Asp | missense_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472337 | n.492C>T | non_coding_transcript_exon_variant | 1.0 |
inhA | 1674283 | p.Val28Ile | missense_variant | 0.13 |
rpsA | 1833369 | c.-173C>G | upstream_gene_variant | 0.18 |
rpsA | 1833441 | c.-101C>T | upstream_gene_variant | 0.12 |
rpsA | 1834190 | p.Ser217Thr | missense_variant | 0.11 |
rpsA | 1834307 | p.Asp256Asn | missense_variant | 0.15 |
rpsA | 1834337 | p.Asp266Asn | missense_variant | 0.14 |
rpsA | 1834488 | p.Gly316Ala | missense_variant | 0.13 |
rpsA | 1834939 | c.1398C>T | synonymous_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154520 | p.Ala531Val | missense_variant | 0.15 |
katG | 2154674 | p.Ala480Pro | missense_variant | 0.11 |
katG | 2155318 | p.Leu265Pro | missense_variant | 0.17 |
PPE35 | 2169545 | c.1058_1067delACCCCGGACA | frameshift_variant | 0.14 |
PPE35 | 2170588 | p.Glu9Lys | missense_variant | 0.17 |
Rv1979c | 2222229 | p.Met312Ile | missense_variant | 0.13 |
Rv1979c | 2222274 | p.Asn297Lys | missense_variant | 0.13 |
Rv1979c | 2222412 | p.Asn251Lys | missense_variant | 0.11 |
Rv1979c | 2222420 | p.Asp249Asn | missense_variant | 0.12 |
Rv1979c | 2222852 | p.Ala105Thr | missense_variant | 0.18 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289324 | c.-83C>G | upstream_gene_variant | 0.12 |
kasA | 2518193 | p.Pro27Thr | missense_variant | 0.12 |
kasA | 2519015 | p.Ser301Thr | missense_variant | 0.12 |
eis | 2714477 | p.Arg286Ser | missense_variant | 0.12 |
eis | 2715137 | p.Asp66Tyr | missense_variant | 0.25 |
eis | 2715240 | p.Glu31Asp | missense_variant | 0.12 |
eis | 2715556 | c.-224C>T | upstream_gene_variant | 0.12 |
ahpC | 2725930 | c.-263C>G | upstream_gene_variant | 0.14 |
ahpC | 2726043 | c.-150C>T | upstream_gene_variant | 0.11 |
folC | 2746224 | p.Asp459Tyr | missense_variant | 0.47 |
folC | 2747796 | c.-198C>T | upstream_gene_variant | 0.2 |
pepQ | 2860085 | p.Gly112Arg | missense_variant | 0.2 |
pepQ | 2860177 | p.Arg81His | missense_variant | 0.13 |
pepQ | 2860436 | c.-18C>T | upstream_gene_variant | 1.0 |
ribD | 2986916 | c.78C>T | synonymous_variant | 0.13 |
ribD | 2987297 | c.459C>G | synonymous_variant | 0.17 |
thyX | 3068094 | c.-149A>G | upstream_gene_variant | 0.12 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
thyA | 3074481 | c.-10C>T | upstream_gene_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086810 | c.-10_-9insG | upstream_gene_variant | 0.18 |
ald | 3086856 | p.Glu13Lys | missense_variant | 0.14 |
ald | 3087889 | p.Thr357Asn | missense_variant | 0.12 |
ald | 3087902 | c.1083G>T | synonymous_variant | 0.16 |
Rv3083 | 3448717 | p.Val72Met | missense_variant | 0.13 |
Rv3083 | 3448737 | c.234C>T | synonymous_variant | 0.12 |
Rv3083 | 3448853 | p.Thr117Asn | missense_variant | 0.12 |
Rv3083 | 3449666 | p.Ile388Asn | missense_variant | 0.11 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474107 | c.103delG | frameshift_variant | 0.12 |
whiB7 | 3568427 | p.Arg85Cys | missense_variant | 0.12 |
whiB7 | 3568777 | c.-98C>A | upstream_gene_variant | 0.12 |
Rv3236c | 3612817 | c.300C>T | synonymous_variant | 0.12 |
fbiB | 3641927 | c.393C>G | synonymous_variant | 0.2 |
fbiB | 3641990 | p.Met152Ile | missense_variant | 0.18 |
fbiB | 3642365 | p.Glu277Asp | missense_variant | 0.2 |
alr | 3840955 | p.Val156Phe | missense_variant | 0.18 |
rpoA | 3878234 | p.Pro92Ala | missense_variant | 0.12 |
rpoA | 3878275 | p.Leu78Pro | missense_variant | 0.14 |
ddn | 3986868 | c.25C>T | synonymous_variant | 0.11 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4038717 | p.Ile663Thr | missense_variant | 0.12 |
clpC1 | 4040502 | p.Gly68Ala | missense_variant | 0.12 |
panD | 4044072 | c.210C>T | synonymous_variant | 0.12 |
embC | 4239885 | p.Pro8His | missense_variant | 0.15 |
embC | 4239899 | p.Arg13Trp | missense_variant | 0.15 |
embA | 4242425 | c.-808C>A | upstream_gene_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244596 | p.Pro455Arg | missense_variant | 0.2 |
embA | 4244871 | p.Gly547Arg | missense_variant | 0.17 |
embA | 4244986 | p.Gly585Asp | missense_variant | 0.33 |
embB | 4248078 | p.Asn522Ser | missense_variant | 0.11 |
embB | 4248794 | p.Ala761Thr | missense_variant | 0.13 |
embB | 4249255 | c.2742G>C | synonymous_variant | 0.25 |
embB | 4249643 | p.Leu1044Val | missense_variant | 0.11 |
aftB | 4267134 | p.Cys568Phe | missense_variant | 0.11 |
aftB | 4267914 | p.Pro308Gln | missense_variant | 0.2 |
ethA | 4327003 | p.Phe157Leu | missense_variant | 0.33 |
ethA | 4327239 | p.Lys79Glu | missense_variant | 0.1 |
ethR | 4327444 | c.-105C>G | upstream_gene_variant | 0.13 |
ethA | 4327608 | c.-135C>T | upstream_gene_variant | 0.13 |
ethR | 4327742 | p.Phe65Tyr | missense_variant | 0.4 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |