Run ID: SRR16295792
Sample name:
Date: 03-04-2023 17:04:46
Number of reads: 4647863
Percentage reads mapped: 69.99
Strain: lineage2.2.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 1.0 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.34 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5405 | p.Glu56* | stop_gained | 0.25 |
gyrB | 5937 | p.Ala233Val | missense_variant | 0.12 |
gyrB | 7218 | p.Arg660His | missense_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8184 | p.Lys295Glu | missense_variant | 0.1 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491295 | c.513C>A | synonymous_variant | 0.13 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.63 |
mshA | 576111 | p.Ala255Gly | missense_variant | 0.29 |
rpoB | 759609 | c.-198C>A | upstream_gene_variant | 0.13 |
rpoB | 759614 | c.-193C>A | upstream_gene_variant | 0.14 |
rpoB | 760689 | p.Phe295Leu | missense_variant | 0.14 |
rpoB | 761152 | p.Leu449Gln | missense_variant | 0.25 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763167 | p.Glu1121* | stop_gained | 0.19 |
rpoB | 763264 | p.Ala1153Val | missense_variant | 0.15 |
rpoC | 764292 | p.Ser308* | stop_gained | 0.13 |
rpoC | 764583 | c.1215delG | frameshift_variant | 0.12 |
rpoC | 764828 | p.Leu487Phe | missense_variant | 0.14 |
rpoC | 765843 | p.Thr825Asn | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777918 | p.Gly188Asp | missense_variant | 0.15 |
mmpR5 | 779181 | c.198delG | frameshift_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781565 | c.6A>T | synonymous_variant | 0.12 |
fbiC | 1304477 | p.Ala516Val | missense_variant | 0.12 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1407518 | c.-178C>T | upstream_gene_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472101 | n.256G>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472665 | n.820G>A | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472669 | n.824_825insTGGA | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472678 | n.833T>G | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472679 | n.834T>C | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472682 | n.839_843delGGGAT | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472695 | n.850C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472701 | n.856T>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.37 |
rrs | 1473008 | n.1163C>A | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473009 | n.1164T>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474018 | n.361G>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476072 | n.2415T>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476141 | n.2484A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476195 | n.2538C>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476196 | n.2539C>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476204 | n.2547C>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476210 | n.2553G>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476211 | n.2554G>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476212 | n.2555T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476214 | n.2557G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476215 | n.2558C>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476229 | n.2572C>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476572 | n.2915G>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476577 | n.2920T>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476595 | n.2938C>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476602 | n.2945G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476614 | n.2957A>G | non_coding_transcript_exon_variant | 0.19 |
inhA | 1674779 | p.Pro193His | missense_variant | 0.12 |
inhA | 1674885 | c.684C>A | synonymous_variant | 0.12 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834274 | p.Ile245Leu | missense_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103038 | p.Ser2Ile | missense_variant | 0.15 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168036 | c.2577C>T | synonymous_variant | 0.14 |
PPE35 | 2170390 | p.Trp75Gly | missense_variant | 0.14 |
PPE35 | 2170415 | c.198A>G | synonymous_variant | 0.14 |
Rv1979c | 2222296 | p.Lys290Arg | missense_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289574 | c.-333T>C | upstream_gene_variant | 0.14 |
kasA | 2518180 | c.66G>A | synonymous_variant | 0.14 |
eis | 2714936 | p.Pro133Ser | missense_variant | 0.14 |
eis | 2715467 | c.-135A>G | upstream_gene_variant | 1.0 |
folC | 2746190 | p.Gly470Asp | missense_variant | 0.12 |
folC | 2747320 | c.279C>A | synonymous_variant | 0.17 |
pepQ | 2860144 | p.Val92Gly | missense_variant | 0.18 |
ribD | 2986709 | c.-130C>T | upstream_gene_variant | 0.12 |
ribD | 2986848 | p.Ser4Thr | missense_variant | 0.12 |
ribD | 2987447 | c.609C>T | synonymous_variant | 0.14 |
ribD | 2987530 | p.Pro231His | missense_variant | 0.14 |
ribD | 2987567 | c.729C>A | synonymous_variant | 0.18 |
thyX | 3067965 | c.-20C>T | upstream_gene_variant | 0.11 |
thyA | 3074211 | c.261A>T | synonymous_variant | 0.22 |
thyA | 3074420 | p.Lys18Gln | missense_variant | 0.14 |
thyA | 3074464 | p.Pro3Leu | missense_variant | 0.14 |
ald | 3086762 | c.-58C>A | upstream_gene_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339338 | p.Gly74Val | missense_variant | 0.2 |
Rv3083 | 3449477 | p.Thr325Asn | missense_variant | 0.14 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474717 | p.Asp237Glu | missense_variant | 0.12 |
fprA | 3474792 | c.786G>A | synonymous_variant | 0.12 |
Rv3236c | 3612272 | p.Val282Ala | missense_variant | 0.13 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiB | 3640879 | c.-656C>T | upstream_gene_variant | 1.0 |
fbiB | 3641457 | c.-78G>A | upstream_gene_variant | 0.13 |
rpoA | 3878569 | c.-62C>G | upstream_gene_variant | 0.21 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.17 |
rpoA | 3878648 | c.-141C>G | upstream_gene_variant | 0.13 |
embC | 4241452 | c.1590G>A | synonymous_variant | 0.11 |
embC | 4241933 | p.Ala691Thr | missense_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4243545 | p.Leu105Met | missense_variant | 0.11 |
embA | 4244144 | c.912C>T | synonymous_variant | 0.12 |
embA | 4244702 | c.1470C>T | synonymous_variant | 0.15 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.38 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.5 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.43 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.43 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.38 |
embB | 4247028 | p.Leu172Arg | missense_variant | 0.32 |
embB | 4248043 | c.1534delA | frameshift_variant | 0.12 |
embB | 4248958 | p.Trp815Cys | missense_variant | 0.12 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268506 | p.Arg111Trp | missense_variant | 0.2 |
ubiA | 4269155 | p.Thr227Pro | missense_variant | 0.23 |
ethA | 4326438 | p.Leu346Met | missense_variant | 0.12 |
ethA | 4326474 | p.Pro334Ala | missense_variant | 1.0 |
ethR | 4328149 | p.Asp201Asn | missense_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |