Run ID: SRR6824572
Sample name:
Date: 04-04-2023 16:47:19
Number of reads: 2669112
Percentage reads mapped: 83.13
Strain: lineage2.2.1
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.99 |
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 |
---|---|---|---|---|---|
rpoB | 761139 | p.His445Asn | missense_variant | 0.97 | rifampicin |
rpoB | 761154 | p.Ser450Ala | missense_variant | 0.5 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 0.95 | isoniazid |
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 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
ccsA | 620625 | p.Ile245Met | missense_variant | 0.98 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472953 | n.1111_1112delTC | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472959 | n.1114_1115insTA | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472969 | n.1125delC | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472974 | n.1129A>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472975 | n.1130T>G | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472982 | n.1137G>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472987 | n.1142G>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472988 | n.1143T>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472990 | n.1145A>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473004 | n.1159T>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475866 | n.2209T>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475876 | n.2220_2221delCT | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476141 | n.2484A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476165 | n.2508T>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476196 | n.2539C>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476197 | n.2540T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476204 | n.2547C>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476209 | n.2552A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476210 | n.2553G>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476212 | n.2555T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476214 | n.2557G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476215 | n.2558C>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476229 | n.2572C>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476251 | n.2594T>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.29 |
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 | 0.3 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.49 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.49 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476411 | n.2754G>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476463 | n.2806C>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476536 | n.2879G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476572 | n.2915G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.16 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.98 |
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 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv2752c | 3066194 | c.-3G>T | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449504 | p.Gly334Ala | missense_variant | 0.93 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
rpoA | 3878620 | c.-113C>T | upstream_gene_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
ethA | 4326676 | p.Ser266Arg | missense_variant | 1.0 |
whiB6 | 4338537 | c.-16T>C | upstream_gene_variant | 0.97 |
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 |