Run ID: SRR1159158
Sample name:
Date: 02-04-2023 21:49:18
Number of reads: 2891132
Percentage reads mapped: 75.63
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 | 0.73 | streptomycin |
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 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 576450 | c.1109_1111dupTGG | disruptive_inframe_insertion | 0.12 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | 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 | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472122 | n.277G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472128 | n.283G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472378 | n.533G>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472379 | n.534T>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472389 | n.544G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472415 | n.570T>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472596 | n.751G>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472614 | n.769G>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.41 |
rrs | 1473147 | n.1302G>T | non_coding_transcript_exon_variant | 0.41 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 0.41 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1473164 | n.1319C>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1473172 | n.1327T>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473191 | n.1346C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473206 | n.1361G>A | non_coding_transcript_exon_variant | 0.58 |
rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1473248 | n.1403G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473249 | n.1404T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473255 | n.1410A>G | non_coding_transcript_exon_variant | 0.34 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473260 | n.1415G>T | non_coding_transcript_exon_variant | 0.34 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.39 |
rrl | 1475866 | n.2209T>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476268 | n.2611A>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.36 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
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 | 2169221 | c.1392T>C | synonymous_variant | 1.0 |
PPE35 | 2170623 | c.-11G>A | upstream_gene_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714955 | c.378C>T | synonymous_variant | 1.0 |
eis | 2715123 | c.210G>T | synonymous_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
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 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338711 | c.-190C>A | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 0.98 |