Run ID: SRR11972436
Sample name:
Date: 03-04-2023 05:42:19
Number of reads: 758467
Percentage reads mapped: 83.6
Strain: lineage3.1.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
lineage3.1 | East-African-Indian | Non-CAS1-Delhi | RD750 | 1.0 |
lineage3.1.2 | East-African-Indian | CAS;CAS2 | 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 | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575162 | c.-186T>C | upstream_gene_variant | 0.12 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 761577 | c.1771C>T | synonymous_variant | 1.0 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 766821 | p.Asp1151Val | missense_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 | 781757 | p.Tyr66* | stop_gained | 0.12 |
fbiC | 1305307 | p.Val793Leu | missense_variant | 0.13 |
atpE | 1461186 | p.Arg48Trp | missense_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475115 | n.1458A>G | non_coding_transcript_exon_variant | 0.12 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.13 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.13 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.36 |
fabG1 | 1673990 | p.Gly184Asp | missense_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155717 | p.Leu132Pro | missense_variant | 0.18 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168604 | p.Pro670Leu | missense_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.31 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.31 |
PPE35 | 2170415 | c.198A>G | synonymous_variant | 0.12 |
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 |
pncA | 2289779 | c.-539delC | upstream_gene_variant | 0.2 |
eis | 2715060 | p.His91Lys | missense_variant | 0.1 |
eis | 2715065 | p.Thr90Ala | missense_variant | 0.11 |
ahpC | 2725929 | c.-264C>G | upstream_gene_variant | 1.0 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726213 | c.21C>G | synonymous_variant | 0.1 |
ahpC | 2726260 | p.Leu23Gln | missense_variant | 0.17 |
pepQ | 2859474 | c.945A>T | synonymous_variant | 0.18 |
pepQ | 2860092 | c.325_326dupGC | frameshift_variant | 0.11 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
ddn | 3987108 | p.Tyr89Asp | missense_variant | 0.14 |
clpC1 | 4039180 | p.Arg509Trp | missense_variant | 0.11 |
clpC1 | 4039406 | c.1299G>A | synonymous_variant | 0.14 |
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 | 4407806 | p.Ala133Pro | missense_variant | 0.17 |