Run ID: ERR4814881
Sample name:
Date: 01-04-2023 13:32:43
Number of reads: 1681532
Percentage reads mapped: 98.28
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 |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8933 | c.1632G>C | synonymous_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 |
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 |
Rv1258c | 1407228 | c.103_112delTTGCAGCGCG | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472674 | n.829T>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.61 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475751 | n.2094C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475752 | n.2095C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475758 | n.2101A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476134 | n.2477G>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.12 |
inhA | 1674210 | c.9A>C | synonymous_variant | 1.0 |
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 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ahpC | 2726153 | c.-40G>A | 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 |