Run ID: ERR4815257
Sample name:
Date: 01-04-2023 13:45:38
Number of reads: 199998
Percentage reads mapped: 72.43
Strain: lineage4.4.1.1
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 |
lineage4.4 | Euro-American | S;T | None | 1.0 |
lineage4.4.1 | Euro-American (S-type) | S;T | None | 1.0 |
lineage4.4.1.1 | Euro-American | S;Orphans | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.18 | kanamycin, capreomycin, aminoglycosides, amikacin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5570 | p.Ser111Thr | missense_variant | 0.29 |
gyrB | 5826 | p.Glu196Gly | missense_variant | 0.5 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8587 | p.Glu429Ala | missense_variant | 0.29 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 575582 | c.236_237delTG | frameshift_variant | 0.22 |
rpoB | 760907 | c.1101C>T | synonymous_variant | 0.29 |
rpoC | 763353 | c.-17A>G | upstream_gene_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775682 | c.2799C>T | synonymous_variant | 0.2 |
mmpL5 | 777879 | p.Asp201Gly | missense_variant | 0.29 |
mmpL5 | 778270 | p.Ser71Thr | missense_variant | 0.22 |
mmpS5 | 778841 | p.Gly22Asp | missense_variant | 0.4 |
rpsL | 781379 | c.-181G>T | upstream_gene_variant | 0.5 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303433 | p.Asp168Val | missense_variant | 0.15 |
Rv1258c | 1406973 | p.Ala123Asp | missense_variant | 0.25 |
embR | 1417338 | p.Ser4Cys | missense_variant | 0.14 |
atpE | 1461033 | c.-12G>C | upstream_gene_variant | 0.2 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471876 | n.31G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472171 | n.326A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472342 | n.499delC | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473150 | n.1305T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473161 | n.1316A>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473164 | n.1319C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473201 | n.1356A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473202 | n.1357C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473215 | n.1370A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473734 | n.77C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473993 | n.336G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474551 | n.894G>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474552 | n.895C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474558 | n.901G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474837 | n.1180A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474862 | n.1205C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475224 | n.1567T>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475751 | n.2094C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475765 | n.2108A>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475772 | n.2115A>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475892 | n.2235A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475897 | n.2240T>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475900 | n.2243A>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475938 | n.2281C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476359 | n.2702C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476443 | n.2786G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476455 | n.2798C>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476501 | n.2844C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476520 | n.2863G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476529 | n.2872A>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476539 | n.2882A>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476544 | n.2887T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476547 | n.2890C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476563 | n.2906G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476566 | n.2909A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.33 |
inhA | 1673859 | c.-343G>T | upstream_gene_variant | 0.29 |
fabG1 | 1673873 | p.Trp145* | stop_gained | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918092 | c.153G>A | synonymous_variant | 0.25 |
ndh | 2102326 | c.717G>C | synonymous_variant | 0.33 |
ndh | 2102990 | p.Val18Ala | missense_variant | 1.0 |
katG | 2154397 | p.Thr572Met | missense_variant | 0.29 |
PPE35 | 2168928 | p.Ser562* | stop_gained | 0.33 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714581 | c.750_751delTG | frameshift_variant | 0.4 |
folC | 2747603 | c.-5C>A | upstream_gene_variant | 0.22 |
Rv2752c | 3065404 | p.Gly263Asp | missense_variant | 0.22 |
thyA | 3074100 | c.372T>C | synonymous_variant | 0.29 |
ald | 3086694 | c.-126C>A | upstream_gene_variant | 0.33 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087288 | c.473_474dupTG | frameshift_variant | 0.29 |
Rv3083 | 3448608 | c.105G>A | synonymous_variant | 1.0 |
Rv3083 | 3449865 | c.1362G>A | synonymous_variant | 0.2 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474464 | p.Ile153Thr | missense_variant | 0.25 |
fprA | 3474643 | p.Arg213Cys | missense_variant | 0.22 |
whiB7 | 3568689 | c.-10G>T | upstream_gene_variant | 0.15 |
Rv3236c | 3612665 | p.Val151Ala | missense_variant | 1.0 |
Rv3236c | 3613114 | c.3G>A | synonymous_variant | 0.22 |
fbiA | 3641504 | p.Arg321His | missense_variant | 0.5 |
alr | 3840723 | p.His233Leu | missense_variant | 0.2 |
alr | 3841501 | c.-81G>C | upstream_gene_variant | 0.22 |
rpoA | 3878436 | c.72A>G | synonymous_variant | 0.4 |
ddn | 3986650 | c.-194A>C | upstream_gene_variant | 0.4 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 1.0 |
panD | 4044223 | p.Leu20Gln | missense_variant | 0.29 |
embC | 4241717 | p.Arg619Trp | missense_variant | 0.33 |
embC | 4241972 | p.Val704Ile | missense_variant | 0.33 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243484 | c.252C>T | synonymous_variant | 0.33 |
embB | 4248647 | p.Gly712Ser | missense_variant | 0.29 |
embB | 4248840 | p.Pro776His | missense_variant | 0.4 |
aftB | 4268368 | p.Cys157Ser | missense_variant | 0.67 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |