Run ID: ERR4813502
Sample name:
Date: 01-04-2023 12:47:48
Number of reads: 2767675
Percentage reads mapped: 99.27
Strain:
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
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 | 491288 | p.Gly169Asp | missense_variant | 0.22 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.3 |
ccsA | 620196 | c.306C>T | synonymous_variant | 0.29 |
ccsA | 620220 | p.Met110Ile | missense_variant | 0.2 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 766957 | c.3588G>A | synonymous_variant | 0.18 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406145 | p.Ala399Val | missense_variant | 0.18 |
embR | 1416858 | p.Thr164Ala | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472552 | n.707A>G | non_coding_transcript_exon_variant | 0.1 |
PPE35 | 2170020 | p.Phe198Ser | missense_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
folC | 2746565 | p.Ala345Val | missense_variant | 0.33 |
pepQ | 2859819 | c.600G>T | synonymous_variant | 0.11 |
thyX | 3068035 | c.-90G>A | upstream_gene_variant | 0.11 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339263 | p.Ala49Val | missense_variant | 0.17 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 0.98 |
alr | 3841001 | p.Glu140Asp | missense_variant | 1.0 |
clpC1 | 4040192 | c.513C>T | synonymous_variant | 0.11 |
clpC1 | 4040254 | p.Ala151Thr | missense_variant | 0.13 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embB | 4248522 | p.Thr670Lys | missense_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407967 | p.Leu79Trp | missense_variant | 1.0 |