Run ID: ERR4276853
Sample name:
Date: 01-04-2023 05:38:14
Number of reads: 743678
Percentage reads mapped: 83.5
Strain: lineage4.2.1
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 |
lineage4.2 | Euro-American | H;T;LAM | None | 1.0 |
lineage4.2.1 | Euro-American (TUR) | H3;H4 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761109 | p.Asp435Tyr | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289057 | p.Pro62Leu | missense_variant | 1.0 | pyrazinamide |
embB | 4248002 | p.Gln497Lys | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7822 | p.Leu174Gln | missense_variant | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491247 | c.465C>T | synonymous_variant | 1.0 |
mshA | 575480 | p.Arg45Cys | missense_variant | 0.22 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.23 |
mshA | 576431 | p.Ala362Thr | missense_variant | 0.15 |
mshA | 576720 | c.1375delG | frameshift_variant | 0.22 |
rpoB | 760306 | p.Arg167His | missense_variant | 1.0 |
rpoB | 762037 | p.Ile744Thr | missense_variant | 0.11 |
rpoC | 766340 | p.Ile991Val | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303701 | c.771C>T | synonymous_variant | 0.15 |
embR | 1417083 | p.Asp89Asn | missense_variant | 0.15 |
atpE | 1461143 | c.99C>T | synonymous_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472924 | n.1079G>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1473934 | n.277G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473946 | n.289A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474003 | n.346G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474558 | n.901G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.19 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.17 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.16 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.13 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.13 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.14 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.61 |
inhA | 1673883 | c.-319C>T | upstream_gene_variant | 0.12 |
inhA | 1674780 | c.580delA | frameshift_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102367 | p.Ala226Pro | missense_variant | 0.13 |
ndh | 2102368 | c.675C>T | synonymous_variant | 0.13 |
PPE35 | 2167814 | c.2799C>T | synonymous_variant | 0.18 |
PPE35 | 2168003 | p.His870Gln | missense_variant | 0.12 |
PPE35 | 2168145 | p.Pro823Arg | missense_variant | 0.12 |
PPE35 | 2169879 | p.Phe245Cys | missense_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.26 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.26 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518451 | p.Gly113Ser | missense_variant | 0.14 |
eis | 2715030 | c.303C>T | synonymous_variant | 0.14 |
ahpC | 2726142 | c.-51G>A | upstream_gene_variant | 1.0 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339364 | p.Pro83Ala | missense_variant | 0.12 |
fprA | 3473890 | c.-117C>A | upstream_gene_variant | 0.14 |
fprA | 3473959 | c.-47delT | upstream_gene_variant | 0.14 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474336 | c.330C>A | synonymous_variant | 0.15 |
rpoA | 3878535 | c.-28G>T | upstream_gene_variant | 0.29 |
embC | 4239860 | c.-3G>T | upstream_gene_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244511 | p.Ile427Val | missense_variant | 0.12 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.22 |
embB | 4247138 | c.627delG | frameshift_variant | 0.12 |
embB | 4249594 | c.3081G>A | synonymous_variant | 1.0 |
aftB | 4268497 | p.Arg114Trp | missense_variant | 0.18 |
aftB | 4268619 | p.Val73Gly | missense_variant | 0.67 |
ethA | 4327346 | p.Gly43Val | missense_variant | 1.0 |
ethA | 4328376 | c.-903G>C | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |