Run ID: ERR4972550
Sample name:
Date: 01-04-2023 21:46:23
Number of reads: 331921
Percentage reads mapped: 89.87
Strain: lineage4.3
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 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
katG | 2154799 | p.Trp438* | stop_gained | 0.33 | isoniazid |
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 |
---|---|---|---|---|
gyrB | 5947 | c.708C>T | synonymous_variant | 0.13 |
gyrA | 6406 | c.-896C>T | upstream_gene_variant | 0.22 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9417 | p.Asn706Tyr | missense_variant | 0.14 |
fgd1 | 490757 | c.-26T>A | upstream_gene_variant | 1.0 |
fgd1 | 491351 | p.Asp190Val | missense_variant | 0.4 |
rpoB | 760133 | c.327C>A | synonymous_variant | 0.15 |
rpoB | 761075 | c.1271delT | frameshift_variant | 0.22 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 765889 | c.2521_2522dupCG | frameshift_variant | 0.22 |
rpoC | 766649 | p.Gly1094Ser | missense_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775855 | p.Gly876Arg | missense_variant | 0.5 |
mmpL5 | 777682 | p.Val267Met | missense_variant | 0.33 |
mmpL5 | 778345 | p.Leu46Phe | missense_variant | 0.17 |
mmpL5 | 778951 | c.-471G>T | upstream_gene_variant | 0.15 |
mmpR5 | 779137 | p.Arg50Trp | missense_variant | 0.2 |
mmpR5 | 779303 | c.315delT | frameshift_variant | 0.14 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303752 | c.822A>G | synonymous_variant | 0.17 |
fbiC | 1303787 | p.His286Leu | missense_variant | 0.22 |
fbiC | 1304826 | c.1900delT | frameshift_variant | 0.18 |
Rv1258c | 1406570 | c.771G>A | synonymous_variant | 0.18 |
embR | 1417517 | c.-170T>A | upstream_gene_variant | 0.29 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472337 | n.492C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476669 | n.3012C>A | non_coding_transcript_exon_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918034 | p.Val32Gly | missense_variant | 0.22 |
ndh | 2102403 | p.Leu214Phe | missense_variant | 0.11 |
katG | 2154962 | c.1150C>T | synonymous_variant | 0.25 |
katG | 2155454 | p.Leu220Val | missense_variant | 0.25 |
PPE35 | 2168260 | c.2352delT | frameshift_variant | 0.25 |
PPE35 | 2169691 | p.Gly308Cys | missense_variant | 0.13 |
PPE35 | 2170545 | p.Pro23Leu | missense_variant | 0.25 |
PPE35 | 2170698 | c.-86G>A | upstream_gene_variant | 0.11 |
Rv1979c | 2221794 | c.1371C>A | synonymous_variant | 0.29 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288969 | p.Glu91Asp | missense_variant | 0.22 |
eis | 2714438 | p.Met299Leu | missense_variant | 0.18 |
eis | 2715056 | p.Arg93Trp | missense_variant | 0.2 |
ahpC | 2726306 | c.114C>T | synonymous_variant | 0.22 |
folC | 2746687 | c.912C>A | synonymous_variant | 0.15 |
folC | 2747639 | c.-41C>A | upstream_gene_variant | 0.18 |
ribD | 2986903 | c.67_69delCTC | conservative_inframe_deletion | 0.17 |
Rv2752c | 3065953 | p.Thr80Ile | missense_variant | 1.0 |
thyX | 3067606 | p.Ser114Thr | missense_variant | 0.5 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087686 | c.867C>A | synonymous_variant | 0.4 |
Rv3083 | 3449484 | c.981G>A | synonymous_variant | 0.15 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474224 | c.223delC | frameshift_variant | 0.14 |
fprA | 3474517 | p.Asp171Asn | missense_variant | 0.2 |
Rv3236c | 3612332 | c.784dupG | frameshift_variant | 0.18 |
rpoA | 3877527 | c.981C>T | synonymous_variant | 0.22 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
panD | 4044387 | c.-106G>A | upstream_gene_variant | 0.22 |
embC | 4241861 | p.Glu667Lys | missense_variant | 0.2 |
embC | 4242402 | p.Arg847His | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244637 | p.Val469Met | missense_variant | 0.13 |
embB | 4249620 | c.3108delG | frameshift_variant | 0.12 |
aftB | 4267596 | p.Tyr414Cys | missense_variant | 0.33 |
aftB | 4268083 | p.Gln252* | stop_gained | 0.33 |
aftB | 4268741 | c.96G>A | synonymous_variant | 0.25 |
aftB | 4268779 | p.Gly20Arg | missense_variant | 0.22 |
ubiA | 4269319 | p.Leu172Pro | missense_variant | 1.0 |
ethR | 4326568 | c.-981G>A | upstream_gene_variant | 0.33 |
ethA | 4327491 | c.-18C>G | upstream_gene_variant | 0.18 |
ethR | 4327680 | p.Asp44Glu | missense_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |