Run ID: ERR3077935
Sample name:
Date: 01-04-2023 00:11:35
Number of reads: 620664
Percentage reads mapped: 98.65
Strain: lineage4.2.2.2
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.2 | Euro-American | H;T;LAM | None | 0.99 |
lineage4.2.2 | Euro-American (Ural) | T;LAM7-TUR | None | 1.0 |
lineage4.2.2.2 | Euro-American (Ural) | T;LAM7-TUR | None | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
pncA | 2288823 | p.Arg140His | missense_variant | 0.12 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8688 | p.Ala463Ser | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9307 | p.Asp669Gly | missense_variant | 0.11 |
mshA | 575589 | p.Arg81His | missense_variant | 0.13 |
mshA | 576077 | c.730C>T | synonymous_variant | 1.0 |
ccsA | 619694 | c.-197C>T | upstream_gene_variant | 0.5 |
ccsA | 620228 | p.Phe113Ser | missense_variant | 0.14 |
rpoB | 761489 | c.1683G>A | synonymous_variant | 1.0 |
rpoB | 763147 | p.Ser1114Leu | missense_variant | 0.13 |
rpoC | 765468 | c.2101delG | frameshift_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776573 | c.1908G>T | synonymous_variant | 0.11 |
mmpL5 | 777087 | p.Ile465Asn | missense_variant | 0.11 |
mmpL5 | 777404 | c.1077C>G | synonymous_variant | 0.25 |
mmpL5 | 777888 | p.Gln198Arg | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781896 | p.Ala113Pro | missense_variant | 0.1 |
fbiC | 1303652 | p.Arg241Gln | missense_variant | 0.11 |
atpE | 1461075 | p.Ile11Val | missense_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475259 | n.1602T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475447 | n.1790A>G | non_coding_transcript_exon_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918136 | p.Gly66Val | missense_variant | 0.22 |
tlyA | 1918509 | c.570T>C | synonymous_variant | 0.11 |
ndh | 2102727 | p.His106Tyr | missense_variant | 0.11 |
ndh | 2103187 | c.-145G>A | upstream_gene_variant | 0.13 |
PPE35 | 2167945 | p.Ser890Pro | missense_variant | 0.11 |
Rv1979c | 2222517 | c.648C>T | synonymous_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518465 | c.351T>A | synonymous_variant | 0.18 |
kasA | 2518540 | c.426T>C | synonymous_variant | 0.13 |
kasA | 2518574 | p.Ile154Val | missense_variant | 0.18 |
eis | 2715223 | p.Arg37Gln | missense_variant | 0.13 |
eis | 2715367 | c.-35G>A | upstream_gene_variant | 0.11 |
pepQ | 2860075 | p.Glu115Gly | missense_variant | 0.11 |
ribD | 2986887 | p.Leu17Val | missense_variant | 0.17 |
Rv2752c | 3065553 | c.639A>T | synonymous_variant | 0.12 |
Rv2752c | 3066280 | c.-89C>T | upstream_gene_variant | 0.93 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087888 | p.Thr357Ala | missense_variant | 0.14 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475101 | c.1095C>G | synonymous_variant | 0.13 |
Rv3236c | 3612736 | c.381T>C | synonymous_variant | 0.11 |
fbiA | 3640979 | p.Thr146Ile | missense_variant | 0.12 |
alr | 3840503 | c.918T>C | synonymous_variant | 0.11 |
ddn | 3986723 | c.-121G>A | upstream_gene_variant | 0.12 |
ddn | 3987046 | p.Arg68His | missense_variant | 0.11 |
clpC1 | 4039590 | p.Val372Ala | missense_variant | 0.11 |
clpC1 | 4040688 | p.Thr6Ser | missense_variant | 0.11 |
panD | 4044429 | c.-148C>G | upstream_gene_variant | 0.15 |
embC | 4240646 | p.Phe262Val | missense_variant | 0.2 |
embC | 4242458 | p.Ser866Pro | missense_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4246386 | p.Arg1052Gly | missense_variant | 0.11 |
embB | 4247439 | p.Val309Asp | missense_variant | 0.1 |
aftB | 4268536 | p.Gly101Arg | missense_variant | 0.14 |
ubiA | 4269977 | c.-144C>A | upstream_gene_variant | 0.17 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |