Run ID: ERR2514535
Sample name:
Date: 31-03-2023 20:23:55
Number of reads: 1345486
Percentage reads mapped: 95.3
Strain: lineage3
Drug-resistance: Sensitive
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 |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8172 | p.Val291Phe | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.17 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.14 |
rpoB | 760380 | p.Thr192Leu | missense_variant | 0.14 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.14 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.14 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.12 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.13 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 766573 | c.3204T>C | synonymous_variant | 0.12 |
rpoC | 766582 | c.3213C>G | synonymous_variant | 0.12 |
rpoC | 766583 | p.Gly1072Ser | missense_variant | 0.12 |
rpoC | 766933 | c.3564A>G | synonymous_variant | 0.16 |
rpoC | 766942 | c.3573C>T | synonymous_variant | 0.14 |
rpoC | 766945 | c.3576A>G | synonymous_variant | 0.14 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.14 |
rpoC | 766972 | c.3603G>C | synonymous_variant | 0.14 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.14 |
rpoC | 767035 | c.3666G>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 |
fbiC | 1304817 | c.1887T>C | synonymous_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473756 | n.99G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475739 | n.2082A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476033 | n.2376T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476035 | n.2378G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.12 |
inhA | 1674243 | c.42A>G | synonymous_variant | 0.14 |
inhA | 1674279 | c.78A>C | synonymous_variant | 0.18 |
inhA | 1674280 | p.Arg27Lys | missense_variant | 0.19 |
inhA | 1674284 | p.Val28Ala | missense_variant | 0.19 |
inhA | 1674301 | c.102_103delCC | frameshift_variant | 0.16 |
inhA | 1674331 | c.130C>T | synonymous_variant | 0.14 |
inhA | 1674603 | c.402G>A | synonymous_variant | 0.12 |
inhA | 1674627 | c.426T>G | synonymous_variant | 0.14 |
inhA | 1674639 | c.438C>G | synonymous_variant | 0.14 |
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 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
kasA | 2517980 | c.-135C>T | upstream_gene_variant | 0.14 |
kasA | 2518594 | c.480C>G | synonymous_variant | 0.12 |
kasA | 2518597 | c.483C>G | synonymous_variant | 0.13 |
kasA | 2518609 | p.Met165Ile | missense_variant | 0.12 |
kasA | 2518672 | c.558G>C | synonymous_variant | 0.12 |
kasA | 2518678 | c.564C>T | synonymous_variant | 0.12 |
kasA | 2518684 | c.570C>G | synonymous_variant | 0.12 |
kasA | 2518783 | c.669T>C | synonymous_variant | 0.13 |
kasA | 2518789 | c.675G>C | synonymous_variant | 0.13 |
kasA | 2518792 | c.678C>G | synonymous_variant | 0.13 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
Rv2752c | 3066197 | c.-6C>T | upstream_gene_variant | 0.95 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.14 |
embC | 4240069 | c.207T>C | synonymous_variant | 1.0 |
embC | 4240780 | c.918T>C | synonymous_variant | 0.13 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4408163 | p.Pro14Ser | missense_variant | 1.0 |