Run ID: ERR11081864
Sample name:
Date: 09-04-2023 13:37:01
Number of reads: 5867255
Percentage reads mapped: 95.62
Strain: lineage3
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472307 | n.462C>T | non_coding_transcript_exon_variant | 0.14 | 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 |
gyrA | 9596 | c.2295G>T | synonymous_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.32 |
mshA | 576482 | p.Val379Leu | missense_variant | 0.17 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 759875 | c.69T>C | synonymous_variant | 1.0 |
rpoB | 761306 | c.1500C>G | synonymous_variant | 0.11 |
rpoB | 762206 | c.2400C>G | synonymous_variant | 0.12 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 0.99 |
rpoC | 762926 | c.-444C>T | upstream_gene_variant | 0.14 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.13 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.13 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.13 |
rpoC | 763013 | c.-357C>G | upstream_gene_variant | 0.15 |
rpoC | 763025 | c.-345C>T | upstream_gene_variant | 0.13 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.14 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.13 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.14 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.13 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.12 |
rpoC | 763486 | c.117T>G | synonymous_variant | 0.14 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.13 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.12 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.12 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.13 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.13 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.14 |
rpoC | 764181 | p.Asp271Gly | missense_variant | 0.91 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.13 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.14 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.13 |
rpoC | 764872 | c.1503A>G | synonymous_variant | 0.15 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.14 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.15 |
rpoC | 764932 | c.1563C>A | synonymous_variant | 0.14 |
rpoC | 764935 | c.1566T>C | synonymous_variant | 0.14 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.13 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.13 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.15 |
rpoC | 765019 | c.1650A>G | synonymous_variant | 0.15 |
rpoC | 765034 | c.1665T>C | synonymous_variant | 0.16 |
rpoC | 765040 | c.1671T>C | synonymous_variant | 0.14 |
rpoC | 765041 | c.1672T>C | synonymous_variant | 0.13 |
rpoC | 765047 | c.1678T>C | synonymous_variant | 0.13 |
rpoC | 765053 | c.1684_1685delTCinsAG | synonymous_variant | 0.13 |
rpoC | 765073 | c.1704G>C | synonymous_variant | 0.12 |
rpoC | 765076 | c.1707A>G | synonymous_variant | 0.12 |
rpoC | 765079 | c.1710T>G | synonymous_variant | 0.12 |
rpoC | 765082 | c.1713G>C | synonymous_variant | 0.12 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.14 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.13 |
rpoC | 765625 | c.2256C>G | synonymous_variant | 0.12 |
rpoC | 765811 | c.2442T>C | synonymous_variant | 0.12 |
rpoC | 765814 | c.2445A>G | synonymous_variant | 0.12 |
rpoC | 765826 | c.2457T>C | synonymous_variant | 0.12 |
rpoC | 765850 | c.2481G>C | synonymous_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.12 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.15 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.15 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.16 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.16 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.17 |
rplC | 800747 | c.-62C>G | upstream_gene_variant | 0.15 |
rplC | 800771 | c.-38C>T | upstream_gene_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472300 | n.455C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.2 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.16 |
rpsA | 1833667 | c.126C>G | synonymous_variant | 0.18 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.13 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.12 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.12 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.15 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.14 |
rpsA | 1833748 | c.207C>G | synonymous_variant | 0.14 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.12 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.13 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 0.13 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.13 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.13 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.14 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.14 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.13 |
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 | 2170769 | c.-157C>T | upstream_gene_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
kasA | 2517950 | c.-165C>G | upstream_gene_variant | 0.12 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
Rv2752c | 3065678 | p.Lys172Glu | missense_variant | 0.99 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.14 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.16 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.16 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.15 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.14 |
rpoA | 3877791 | c.717C>G | synonymous_variant | 0.13 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.14 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.13 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.13 |
rpoA | 3877986 | c.522G>C | synonymous_variant | 0.12 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.14 |
rpoA | 3878022 | c.486T>C | synonymous_variant | 0.13 |
rpoA | 3878028 | c.480G>C | synonymous_variant | 0.12 |
rpoA | 3878031 | c.477T>C | synonymous_variant | 0.12 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.12 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.12 |
rpoA | 3878346 | c.162T>C | synonymous_variant | 0.13 |
rpoA | 3878364 | c.144A>T | synonymous_variant | 0.13 |
rpoA | 3878367 | c.141C>G | synonymous_variant | 0.13 |
rpoA | 3878376 | c.132G>C | synonymous_variant | 0.13 |
rpoA | 3878385 | c.123C>G | synonymous_variant | 0.13 |
rpoA | 3878388 | c.120C>G | synonymous_variant | 0.13 |
rpoA | 3878391 | c.117T>C | synonymous_variant | 0.13 |
clpC1 | 4039004 | c.1701C>G | synonymous_variant | 0.12 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.36 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4408002 | p.Asp67Glu | missense_variant | 1.0 |