Run ID: SRR17406743
Sample name:
Date: 03-04-2023 17:58:50
Number of reads: 2574535
Percentage reads mapped: 89.35
Strain: lineage1.1.2
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 1.0 |
lineage1.1 | Indo-Oceanic | EAI3;EAI4;EAI5;EAI6 | RD239 | 1.0 |
lineage1.1.2 | Indo-Oceanic | EAI3;EAI5 | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472362 | n.517C>T | non_coding_transcript_exon_variant | 1.0 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrB | 6124 | c.885C>T | synonymous_variant | 1.0 |
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 | 9047 | c.1746C>T | synonymous_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9443 | c.2142G>A | synonymous_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576000 | p.Asp218Ala | missense_variant | 1.0 |
rpoB | 760490 | c.684C>T | synonymous_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
rpoC | 765171 | p.Pro601Leu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776395 | p.Phe696Leu | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1407459 | c.-119T>C | upstream_gene_variant | 1.0 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472665 | n.820G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472678 | n.833T>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472679 | n.834T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472682 | n.839_843delGGGAT | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472689 | n.844C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472695 | n.850C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472733 | n.888G>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472742 | n.897C>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474790 | n.1133C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474802 | n.1145T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474844 | n.1187G>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476195 | n.2538C>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476196 | n.2539C>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476204 | n.2547C>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476210 | n.2553G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476211 | n.2554G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476212 | n.2555T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476215 | n.2558C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476229 | n.2572C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476573 | n.2916A>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476577 | n.2920T>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167983 | p.Gly877Asp | 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 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 0.99 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 1.0 |
Rv2752c | 3065305 | p.Ala296Val | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
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 | 0.97 |
Rv3236c | 3612709 | c.408G>T | synonymous_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 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243848 | p.Val206Met | missense_variant | 1.0 |
embA | 4245969 | p.Pro913Ser | missense_variant | 0.99 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_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 | 4407873 | c.330G>T | synonymous_variant | 1.0 |