Run ID: ERR4972584
Sample name:
Date: 01-04-2023 21:47:47
Number of reads: 646773
Percentage reads mapped: 99.44
Strain: lineage4.3.2
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 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.2 | Euro-American (LAM) | LAM3 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288930 | p.Ser104Arg | 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 |
fgd1 | 490757 | c.-26T>A | upstream_gene_variant | 1.0 |
mshA | 575672 | p.Val109Met | missense_variant | 0.12 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.2 |
ccsA | 620461 | p.Val191Ile | missense_variant | 0.14 |
rpoB | 761607 | p.Met601Val | missense_variant | 0.11 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 766337 | p.Asp990Asn | missense_variant | 0.13 |
rpoC | 766933 | c.3564A>C | synonymous_variant | 0.13 |
rpoC | 767041 | c.3672G>A | synonymous_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801440 | c.633dupG | frameshift_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472337 | n.492C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472881 | n.1036C>T | non_coding_transcript_exon_variant | 0.25 |
rpsA | 1834551 | p.Val337Glu | missense_variant | 0.11 |
tlyA | 1917926 | c.-14G>T | upstream_gene_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2170147 | p.Ser156Ala | missense_variant | 0.14 |
PPE35 | 2170157 | p.Ala152Ser | missense_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2715473 | c.-141A>G | upstream_gene_variant | 0.12 |
Rv2752c | 3065453 | p.Gln247* | stop_gained | 1.0 |
Rv2752c | 3066212 | c.-22delT | upstream_gene_variant | 0.1 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087830 | c.1011G>A | synonymous_variant | 0.15 |
Rv3083 | 3449376 | c.873G>A | synonymous_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
alr | 3841072 | p.Gly117Ser | missense_variant | 0.15 |
clpC1 | 4038245 | p.Phe820Leu | missense_variant | 0.29 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4039306 | c.1398dupG | frameshift_variant | 0.12 |
clpC1 | 4039968 | p.Gln246Leu | missense_variant | 0.11 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.17 |
embC | 4242252 | p.Asp797Gly | missense_variant | 0.14 |
embC | 4242402 | p.Arg847His | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243651 | p.His140Leu | missense_variant | 0.11 |
embB | 4245803 | c.-711C>T | upstream_gene_variant | 0.14 |
embB | 4248324 | p.Ala604Gly | missense_variant | 0.2 |
ubiA | 4269734 | p.Ala34Thr | missense_variant | 0.12 |
ethR | 4327441 | c.-108G>A | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407980 | p.Pro75Ser | missense_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |