Run ID: ERR4819723
Sample name:
Date: 01-04-2023 16:16:06
Number of reads: 349142
Percentage reads mapped: 94.31
Strain:
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.93 | streptomycin |
gid | 4407967 | p.Leu79Ser | missense_variant | 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 |
gyrA | 9596 | c.2295G>T | synonymous_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
ccsA | 620760 | c.872delA | frameshift_variant | 0.4 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoB | 762640 | p.Gly945Glu | missense_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763252 | p.Leu1149Pro | missense_variant | 0.29 |
rpoC | 764181 | p.Asp271Gly | missense_variant | 1.0 |
mmpL5 | 775610 | c.2870delC | frameshift_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776009 | c.2472A>G | synonymous_variant | 0.29 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776269 | p.Ile738Val | missense_variant | 0.17 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800904 | c.96G>A | synonymous_variant | 0.29 |
fbiC | 1303457 | p.Ala176Glu | missense_variant | 0.25 |
fbiC | 1304571 | c.1641G>T | synonymous_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472431 | n.586G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472438 | n.593T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472439 | n.594C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472447 | n.602C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472484 | n.639A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472574 | n.729T>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474130 | n.473C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474143 | n.486T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474275 | n.618T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.5 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.33 |
fabG1 | 1673572 | c.136delC | frameshift_variant | 0.4 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102079 | p.Asp322Asn | missense_variant | 0.15 |
katG | 2153964 | c.2148G>A | synonymous_variant | 0.22 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168513 | c.2100C>T | synonymous_variant | 0.25 |
PPE35 | 2170769 | c.-157C>T | upstream_gene_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
pncA | 2289376 | c.-135T>A | upstream_gene_variant | 0.33 |
kasA | 2518466 | p.Gly118* | stop_gained | 0.15 |
kasA | 2519348 | p.Ala412Thr | missense_variant | 0.2 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726221 | c.33delC | frameshift_variant | 0.67 |
ribD | 2987348 | c.510G>T | synonymous_variant | 0.25 |
Rv2752c | 3065806 | p.Arg129His | missense_variant | 0.22 |
thyA | 3073779 | c.690_692delACT | disruptive_inframe_deletion | 0.29 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086985 | p.Gln56Lys | missense_variant | 0.4 |
ald | 3087487 | p.Tyr223Cys | missense_variant | 0.4 |
ald | 3087835 | p.Leu339Pro | missense_variant | 0.25 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
alr | 3840687 | p.Asp245Ala | missense_variant | 0.2 |
clpC1 | 4040284 | c.421C>T | synonymous_variant | 0.25 |
embC | 4239685 | c.-178G>A | upstream_gene_variant | 1.0 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4249155 | p.Gly881Asp | missense_variant | 0.17 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |