Run ID: SRR11972208
Sample name:
Date: 03-04-2023 05:32:02
Number of reads: 115396
Percentage reads mapped: 97.02
Strain:
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1.2.1 | Indo-Oceanic | EAI2 | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5879 | p.Thr214Ser | missense_variant | 0.29 |
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8417 | c.1116C>T | synonymous_variant | 1.0 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9260 | c.1959G>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575368 | c.21T>C | synonymous_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763531 | c.162G>C | synonymous_variant | 1.0 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
rpoC | 763921 | c.552G>A | synonymous_variant | 0.33 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777792 | p.Ala230Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781619 | c.60G>A | synonymous_variant | 0.14 |
rplC | 800906 | p.Pro33His | missense_variant | 0.18 |
fbiC | 1303525 | p.Ser199Thr | missense_variant | 0.25 |
Rv1258c | 1406312 | c.1029T>C | synonymous_variant | 1.0 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
atpE | 1460907 | c.-138T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472009 | n.164T>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472665 | n.820G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472669 | n.824_825insTAGG | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472695 | n.850C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473048 | n.1203T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473127 | n.1282G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.38 |
inhA | 1674162 | c.-40C>T | upstream_gene_variant | 1.0 |
rpsA | 1833843 | p.Ile101Thr | missense_variant | 0.29 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2519048 | p.Gly312Ser | missense_variant | 1.0 |
eis | 2714499 | c.834G>A | synonymous_variant | 0.15 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
ribD | 2986898 | c.60G>A | synonymous_variant | 1.0 |
Rv2752c | 3066171 | c.21G>A | synonymous_variant | 0.4 |
thyX | 3067796 | c.150C>T | synonymous_variant | 0.29 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087106 | p.His96Leu | missense_variant | 0.22 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568488 | c.191delG | frameshift_variant | 1.0 |
fbiA | 3640405 | c.-138G>T | upstream_gene_variant | 0.25 |
fbiB | 3640557 | c.-978T>C | upstream_gene_variant | 1.0 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embC | 4241496 | p.Ala545Glu | missense_variant | 0.33 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243580 | c.348G>A | synonymous_variant | 1.0 |
embA | 4243845 | p.Ala205Thr | missense_variant | 0.22 |
embA | 4244420 | c.1188G>C | synonymous_variant | 1.0 |
embA | 4245829 | p.Arg866Gln | missense_variant | 1.0 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4247578 | c.1065G>A | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
aftB | 4269120 | c.-284C>T | upstream_gene_variant | 0.29 |
ubiA | 4269126 | p.Trp236* | stop_gained | 0.29 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ubiA | 4269864 | c.-32delG | upstream_gene_variant | 1.0 |
whiB6 | 4338308 | p.Ala72Thr | missense_variant | 0.2 |
whiB6 | 4338361 | p.Arg54Gln | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |