Run ID: SRR1169313
Sample name:
Date: 03-04-2023 02:51:16
Number of reads: 691586
Percentage reads mapped: 97.59
Strain: lineage4.1.1
Drug-resistance: MDR-TB
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 | 1.0 |
lineage4.1.1 | Euro-American (X-type) | X1;X2;X3 | None | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761110 | p.Asp435Val | missense_variant | 1.0 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288953 | p.Gly97Cys | missense_variant | 1.0 | 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 | 9304 | p.Gly668Asp | missense_variant | 1.0 |
ccsA | 619812 | c.-79C>A | upstream_gene_variant | 0.33 |
rpoC | 763669 | c.300C>A | synonymous_variant | 0.13 |
rpoC | 764923 | c.1554A>G | synonymous_variant | 0.15 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765359 | p.Ala664Ser | missense_variant | 0.17 |
rpoC | 765608 | p.Asp747Asn | missense_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776094 | p.Arg796Pro | missense_variant | 0.22 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304484 | c.1554C>A | synonymous_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473263 | n.1418A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475324 | n.1667G>A | non_coding_transcript_exon_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103150 | c.-108T>C | upstream_gene_variant | 0.11 |
Rv1979c | 2222401 | p.Ala255Val | missense_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288723 | p.Glu173Asp | missense_variant | 0.2 |
pncA | 2289160 | p.Ala28Thr | missense_variant | 0.17 |
eis | 2714933 | p.Ala134Ser | missense_variant | 0.13 |
ahpC | 2726210 | c.18T>C | synonymous_variant | 1.0 |
ribD | 2986865 | c.27C>A | synonymous_variant | 0.15 |
Rv2752c | 3067099 | c.-908C>A | upstream_gene_variant | 0.18 |
Rv2752c | 3067179 | c.-988T>C | upstream_gene_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiA | 3641447 | p.Thr302Met | missense_variant | 1.0 |
rpoA | 3877553 | p.Glu319Lys | missense_variant | 1.0 |
embC | 4240897 | c.1035C>G | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4243267 | p.Ile12Thr | missense_variant | 0.11 |
embA | 4246318 | p.Pro1029Gln | missense_variant | 0.11 |
embB | 4247495 | p.Asp328His | missense_variant | 1.0 |
embB | 4248073 | c.1560C>G | synonymous_variant | 1.0 |
embB | 4249408 | c.2895G>A | synonymous_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407935 | p.Leu90Phe | missense_variant | 0.94 |
gid | 4408142 | c.61C>A | synonymous_variant | 0.14 |