Run ID: ERR1633781
Sample name:
Date: 18-08-2022 14:46:30
Number of reads: 1245560
Percentage reads mapped: 99.62
Strain: lineage4.1.1.3
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 0.99 |
lineage4.1.1 | Euro-American (X-type) | X1;X2;X3 | None | 1.0 |
lineage4.1.1.3 | Euro-American (X-type) | X1;X3 | RD193 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
pncA | 2288775 | p.Leu156Pro | missense_variant | 0.18 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6216 | p.Ser326* | stop_gained | 0.14 |
gyrA | 7332 | p.Ser11Thr | missense_variant | 0.15 |
gyrA | 7335 | p.Leu12Phe | missense_variant | 0.15 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8164 | p.Ala288Asp | missense_variant | 0.14 |
gyrA | 8342 | c.1041G>A | synonymous_variant | 0.14 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoB | 759621 | c.-186C>T | upstream_gene_variant | 0.14 |
rpoB | 760274 | c.468G>A | synonymous_variant | 0.18 |
rpoB | 761465 | c.1659G>T | synonymous_variant | 0.14 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765505 | c.2136C>T | synonymous_variant | 0.17 |
rpoC | 766845 | p.Arg1159His | missense_variant | 0.15 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781458 | c.-102C>T | upstream_gene_variant | 0.13 |
embR | 1416795 | p.Gly185Trp | missense_variant | 0.13 |
atpE | 1461232 | p.Ala63Val | missense_variant | 0.2 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475490 | n.1833C>T | non_coding_transcript_exon_variant | 0.18 |
rpsA | 1834220 | p.Asp227Tyr | missense_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155324 | p.Ala263Glu | missense_variant | 0.17 |
katG | 2155898 | p.Asp72Asn | missense_variant | 0.14 |
pncA | 2288822 | c.420C>T | synonymous_variant | 0.2 |
pncA | 2288966 | c.276G>A | synonymous_variant | 0.2 |
folC | 2746455 | c.1144C>T | synonymous_variant | 0.2 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339119 | c.4_5delAG | frameshift_variant | 0.17 |
fbiB | 3641658 | p.Asp42Asn | missense_variant | 0.15 |
fbiB | 3641807 | c.273C>G | synonymous_variant | 1.0 |
fbiB | 3642112 | p.Ala193Val | missense_variant | 0.18 |
ddn | 3986956 | p.Gly38Asp | missense_variant | 0.15 |
panD | 4044114 | c.168C>A | synonymous_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4245855 | p.Gly875Cys | missense_variant | 0.2 |
embB | 4248846 | p.Gly778Asp | missense_variant | 0.17 |
embB | 4249408 | c.2895G>A | synonymous_variant | 1.0 |
ethR | 4327691 | p.Asp48Gly | missense_variant | 1.0 |