Run ID: SRR11972435
Sample name:
Date: 03-04-2023 05:42:34
Number of reads: 1050318
Percentage reads mapped: 78.36
Strain: lineage1.1.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 0.98 |
lineage1.1 | Indo-Oceanic | EAI3;EAI4;EAI5;EAI6 | RD239 | 1.0 |
lineage1.1.1 | Indo-Oceanic | EAI4;EAI5 | RD239 | 0.97 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6112 | p.Met291Ile | missense_variant | 0.98 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9155 | c.1854C>T | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 761770 | p.Met655Thr | missense_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763884 | p.Ala172Val | missense_variant | 0.94 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
rpoC | 765171 | p.Pro601Leu | missense_variant | 1.0 |
rpoC | 767149 | c.3780C>T | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
embR | 1416771 | p.Glu193Lys | missense_variant | 0.95 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472596 | n.751G>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472614 | n.769G>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1473249 | n.1404T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473283 | n.1438T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474524 | n.867C>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474709 | n.1052G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476234 | n.2577G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476268 | n.2611A>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476275 | n.2618T>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.12 |
rpsA | 1834319 | p.Val260Ile | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103022 | c.21C>G | synonymous_variant | 1.0 |
ndh | 2103225 | c.-183A>C | upstream_gene_variant | 0.23 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167983 | p.Gly877Asp | missense_variant | 0.98 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.16 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.18 |
PPE35 | 2170159 | p.Ala152Ser | missense_variant | 0.12 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223144 | p.Arg7Ser | missense_variant | 0.96 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518123 | c.9G>A | synonymous_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 0.98 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339273 | c.156T>G | synonymous_variant | 0.3 |
Rv3083 | 3448642 | c.139T>C | synonymous_variant | 0.12 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
Rv3236c | 3612489 | p.Val210Leu | missense_variant | 1.0 |
rpoA | 3878630 | c.-124delC | 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 | 4242489 | p.Gln876Pro | missense_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243848 | p.Val206Met | missense_variant | 1.0 |
embA | 4244096 | c.864C>T | synonymous_variant | 1.0 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 0.95 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
whiB6 | 4338242 | p.Gln94Glu | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407591 | p.Phe204Leu | missense_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |