Run ID: ERR2229810
Sample name:
Date: 31-03-2023 17:36:18
Number of reads: 98076
Percentage reads mapped: 61.76
Strain: lineage4.8
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 0.08 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.75 | kanamycin, capreomycin, aminoglycosides, amikacin |
tlyA | 1918322 | c.385delG | frameshift_variant | 0.67 | capreomycin |
panD | 4043900 | p.Ala128Ser | missense_variant | 1.0 | pyrazinamide |
ethR | 4327831 | p.Ala95Thr | missense_variant | 0.4 | ethionamide |
gid | 4408108 | c.94delG | frameshift_variant | 0.29 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5251 | c.17delA | frameshift_variant | 0.22 |
gyrA | 7993 | p.Ala231Val | missense_variant | 0.33 |
gyrA | 8211 | p.Asp304Tyr | missense_variant | 0.29 |
gyrA | 9639 | p.Gly780Ser | missense_variant | 0.5 |
fgd1 | 491407 | p.Pro209Thr | missense_variant | 0.67 |
mshA | 575830 | c.483C>A | synonymous_variant | 0.5 |
ccsA | 620820 | c.930T>C | synonymous_variant | 0.67 |
ccsA | 620837 | p.Gly316Val | missense_variant | 0.5 |
rpoB | 760751 | c.945G>T | synonymous_variant | 1.0 |
rpoC | 762899 | c.-471G>T | upstream_gene_variant | 1.0 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 1.0 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.5 |
rpoC | 762959 | c.-411G>T | upstream_gene_variant | 0.5 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 0.5 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 1.0 |
rpoC | 762989 | c.-381G>A | upstream_gene_variant | 1.0 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 1.0 |
rpoB | 763002 | c.3197dupA | frameshift_variant | 1.0 |
rpoB | 763006 | c.3201delC | frameshift_variant | 1.0 |
rpoB | 763017 | p.Gln1071Glu | missense_variant | 0.67 |
rpoC | 763537 | c.168C>G | synonymous_variant | 0.5 |
rpoC | 763546 | c.177A>G | synonymous_variant | 1.0 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.57 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.57 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.44 |
rpoC | 763622 | p.Ala85Ser | missense_variant | 0.29 |
rpoC | 763627 | p.Lys86Asn | missense_variant | 0.29 |
rpoC | 763730 | p.Ala121Thr | missense_variant | 1.0 |
rpoC | 765216 | p.Ala616Asp | missense_variant | 0.5 |
rpoC | 765844 | c.2475C>A | synonymous_variant | 0.67 |
rpoC | 766706 | p.Glu1113Lys | missense_variant | 0.5 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpR5 | 779357 | p.Arg123Met | missense_variant | 0.4 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.29 |
rpsL | 781658 | c.99A>G | synonymous_variant | 0.29 |
rplC | 801303 | c.495G>T | synonymous_variant | 0.25 |
rplC | 801318 | p.Met170Ile | missense_variant | 0.25 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304238 | p.Gln436His | missense_variant | 0.4 |
fbiC | 1305250 | p.Arg774Trp | missense_variant | 0.2 |
Rv1258c | 1406242 | p.Ala367Ser | missense_variant | 1.0 |
embR | 1416431 | p.Ala306Val | missense_variant | 0.29 |
embR | 1416642 | p.Ala236Ser | missense_variant | 1.0 |
atpE | 1460992 | c.-53A>T | upstream_gene_variant | 0.5 |
rrs | 1472225 | n.380C>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472251 | n.406G>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472279 | n.434T>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472368 | n.523A>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472396 | n.551A>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472412 | n.567A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472767 | n.922G>C | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472812 | n.967A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472954 | n.1110delC | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472958 | n.1113_1114insC | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472970 | n.1125C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472986 | n.1141_1142insA | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472989 | n.1145delA | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472996 | n.1151T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473164 | n.1319C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473226 | n.1381C>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473288 | n.1443C>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473292 | n.1447G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473294 | n.1449A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474202 | n.545T>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474218 | n.561T>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474253 | n.596A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474264 | n.607T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474265 | n.608G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474266 | n.609T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474269 | n.612C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474271 | n.614A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474275 | n.618T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474287 | n.631_649delCCTTTTCCTCTCCGGAGGA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474454 | n.797G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474467 | n.810A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474476 | n.819C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474488 | n.831G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474496 | n.839C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474516 | n.859C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474552 | n.895C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474558 | n.901G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474582 | n.925T>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474853 | n.1196A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475877 | n.2220C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475892 | n.2235A>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475991 | n.2334T>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475993 | n.2336C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475996 | n.2339T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476141 | n.2484A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476172 | n.2515G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476204 | n.2547C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476235 | n.2578A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476363 | n.2706A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476366 | n.2709A>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476368 | n.2711T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476374 | n.2717T>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.83 |
rpsA | 1834024 | c.483G>C | synonymous_variant | 0.67 |
rpsA | 1834034 | p.Ile165Val | missense_variant | 0.29 |
rpsA | 1834039 | c.498C>T | synonymous_variant | 0.29 |
rpsA | 1834040 | p.Lys167Gln | missense_variant | 0.29 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.4 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102084 | p.Val320Gly | missense_variant | 0.33 |
katG | 2154168 | p.Glu648Asp | missense_variant | 0.33 |
katG | 2154447 | c.1665A>G | synonymous_variant | 0.25 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2168948 | p.Leu555Phe | missense_variant | 0.29 |
PPE35 | 2169311 | c.1302G>T | synonymous_variant | 0.67 |
PPE35 | 2169325 | p.Gly430Cys | missense_variant | 0.67 |
PPE35 | 2170226 | c.387C>T | synonymous_variant | 0.67 |
PPE35 | 2170348 | p.Gln89* | stop_gained | 0.4 |
pncA | 2289355 | c.-114C>A | upstream_gene_variant | 0.25 |
pncA | 2289487 | c.-246C>A | upstream_gene_variant | 0.5 |
kasA | 2518638 | p.Ser175Leu | missense_variant | 0.5 |
eis | 2714934 | c.399C>A | synonymous_variant | 0.25 |
ahpC | 2726491 | p.His100Leu | missense_variant | 0.33 |
folC | 2746323 | p.Gly426Arg | missense_variant | 0.33 |
folC | 2746357 | c.1242C>A | synonymous_variant | 0.22 |
folC | 2746631 | p.Gly323Val | missense_variant | 1.0 |
folC | 2747215 | p.Glu128Asp | missense_variant | 0.67 |
pepQ | 2859744 | c.675G>T | synonymous_variant | 1.0 |
pepQ | 2860318 | p.Ser34Leu | missense_variant | 0.4 |
thyX | 3067321 | p.Arg209Trp | missense_variant | 1.0 |
thyX | 3067629 | c.316delC | frameshift_variant | 0.33 |
ald | 3087187 | p.Ala123Asp | missense_variant | 0.5 |
fprA | 3474568 | p.Pro188Thr | missense_variant | 0.5 |
whiB7 | 3568513 | p.Ala56Glu | missense_variant | 1.0 |
fbiB | 3640929 | c.-606C>T | upstream_gene_variant | 0.67 |
fbiB | 3640935 | c.-600C>A | upstream_gene_variant | 0.67 |
fbiA | 3640951 | p.Gln137Lys | missense_variant | 0.67 |
fbiA | 3641020 | p.Val160Ile | missense_variant | 0.25 |
fbiB | 3641539 | p.Thr2Asn | missense_variant | 0.67 |
alr | 3841443 | c.-23G>A | upstream_gene_variant | 0.2 |
alr | 3841454 | c.-34C>A | upstream_gene_variant | 0.15 |
rpoA | 3877816 | p.Gly231Val | missense_variant | 0.67 |
rpoA | 3877863 | c.645G>A | synonymous_variant | 0.4 |
embC | 4240256 | p.Leu132Ile | missense_variant | 0.29 |
embC | 4241891 | p.Ala677Ser | missense_variant | 0.33 |
embC | 4242426 | p.Arg855Leu | missense_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242676 | c.-557C>T | upstream_gene_variant | 1.0 |
embA | 4243265 | c.33G>T | synonymous_variant | 0.4 |
embA | 4243616 | c.384C>A | synonymous_variant | 0.67 |
embA | 4243717 | p.Leu162Gln | missense_variant | 0.5 |
embA | 4244206 | p.Arg325Leu | missense_variant | 0.5 |
embB | 4249092 | p.Ser860* | stop_gained | 0.67 |
aftB | 4268531 | c.306C>T | synonymous_variant | 0.2 |
aftB | 4268976 | c.-140G>T | upstream_gene_variant | 0.29 |
ethA | 4326677 | p.Ser266Ile | missense_variant | 0.33 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |