Run ID: ERR5864916
Sample name:
Date: 01-04-2023 23:40:51
Number of reads: 1027117
Percentage reads mapped: 99.43
Strain: lineage4.1.2.1
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 |
lineage4.1 | Euro-American | T;X;H | None | 0.99 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761139 | p.His445Tyr | missense_variant | 1.0 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 0.96 | isoniazid |
gid | 4407830 | p.Gln125* | stop_gained | 1.0 | streptomycin |
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 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
mshA | 576491 | p.Arg382Ser | missense_variant | 0.12 |
ccsA | 620554 | c.667dupC | frameshift_variant | 0.13 |
ccsA | 620851 | p.Ala321Ser | missense_variant | 0.12 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1407464 | c.-124G>T | upstream_gene_variant | 0.12 |
embR | 1416253 | c.1095C>T | synonymous_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475030 | n.1373G>T | non_coding_transcript_exon_variant | 0.17 |
rpsA | 1833630 | p.Ile30Ser | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2518280 | p.Leu56Ile | missense_variant | 0.12 |
kasA | 2518967 | p.Val285Phe | missense_variant | 0.13 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3338996 | c.-122C>A | upstream_gene_variant | 0.13 |
fbiD | 3339342 | c.225G>T | synonymous_variant | 0.15 |
fbiD | 3339596 | p.Pro160Leu | missense_variant | 0.12 |
Rv3083 | 3449636 | p.Leu378Arg | missense_variant | 0.97 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiB | 3642138 | p.Ala202Thr | missense_variant | 0.13 |
clpC1 | 4038848 | p.Phe619Leu | missense_variant | 0.4 |
embC | 4241030 | p.Leu390Met | missense_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4244273 | c.1041G>T | synonymous_variant | 0.14 |
embB | 4246996 | p.Phe161Leu | missense_variant | 0.14 |
embB | 4249714 | c.3201C>T | synonymous_variant | 0.12 |
aftB | 4267938 | p.Arg300Leu | missense_variant | 0.13 |
aftB | 4268002 | p.Leu279Met | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |