Run ID: SRR1169017
Sample name:
Date: 03-04-2023 02:38:14
Number of reads: 1588225
Percentage reads mapped: 58.42
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 | 0.99 |
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 |
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 |
mmpL5 | 776517 | p.Met655Thr | 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 | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472701 | n.856T>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474839 | n.1182C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474844 | n.1187G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474866 | n.1209C>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474869 | n.1212G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474892 | n.1235G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 0.1 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.1 |
rrl | 1475776 | n.2119G>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475783 | n.2126T>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475866 | n.2209T>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.49 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476572 | n.2915G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476577 | n.2920T>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.15 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102161 | c.882G>T | synonymous_variant | 0.11 |
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 |
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 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |