Run ID: ERR2229166
Sample name:
Date: 31-03-2023 16:46:12
Number of reads: 325253
Percentage reads mapped: 98.9
Strain: lineage4
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5493 | p.Pro85Gln | missense_variant | 0.33 |
gyrB | 6627 | p.Ala463Asp | missense_variant | 0.15 |
gyrA | 7341 | p.Arg14Trp | missense_variant | 0.17 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8287 | p.Asn329Ile | missense_variant | 0.2 |
gyrA | 9733 | p.Thr811Ile | missense_variant | 0.4 |
fgd1 | 491087 | p.Phe102Tyr | missense_variant | 0.22 |
rpoC | 767198 | p.Glu1277* | stop_gained | 0.5 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775662 | p.Pro940Leu | missense_variant | 0.4 |
mmpL5 | 775727 | c.2754C>T | synonymous_variant | 0.4 |
mmpL5 | 776729 | c.1752C>T | synonymous_variant | 0.33 |
mmpS5 | 778578 | p.Thr110Ser | missense_variant | 0.29 |
mmpS5 | 778854 | p.Val18Leu | missense_variant | 0.67 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1303855 | p.Ala309Thr | missense_variant | 0.5 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472354 | n.509C>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473435 | n.-223C>T | upstream_gene_variant | 0.2 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474310 | n.653T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474739 | n.1082G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475610 | n.1953G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475904 | n.2247G>A | non_coding_transcript_exon_variant | 0.15 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.29 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.29 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.57 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.57 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.57 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.71 |
rpsA | 1833703 | p.Asp54Glu | missense_variant | 0.14 |
tlyA | 1917848 | c.-92G>A | upstream_gene_variant | 0.29 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102625 | p.Ser140Thr | missense_variant | 0.29 |
ndh | 2102632 | c.411C>A | synonymous_variant | 0.25 |
ndh | 2102753 | p.Gln97Arg | missense_variant | 0.25 |
PPE35 | 2167814 | c.2799C>T | synonymous_variant | 0.4 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.33 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.33 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169185 | c.1428C>T | synonymous_variant | 0.33 |
PPE35 | 2169191 | c.1422G>C | synonymous_variant | 0.4 |
PPE35 | 2169581 | c.1032C>G | synonymous_variant | 0.29 |
PPE35 | 2169587 | c.1026G>A | synonymous_variant | 0.15 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.14 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 1.0 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 1.0 |
PPE35 | 2170188 | p.Glu142Leu | missense_variant | 0.29 |
PPE35 | 2170403 | c.210C>G | synonymous_variant | 0.67 |
PPE35 | 2170406 | c.207A>G | synonymous_variant | 0.67 |
PPE35 | 2170592 | c.21G>A | synonymous_variant | 0.29 |
Rv1979c | 2222991 | c.174G>A | synonymous_variant | 0.22 |
Rv1979c | 2223182 | c.-18C>A | upstream_gene_variant | 0.29 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289191 | c.51C>A | synonymous_variant | 0.5 |
pncA | 2289885 | c.-644C>A | upstream_gene_variant | 0.5 |
pncA | 2290058 | c.-817G>A | upstream_gene_variant | 0.29 |
kasA | 2518879 | c.765A>G | synonymous_variant | 0.67 |
eis | 2714990 | p.Val115Phe | missense_variant | 0.67 |
folC | 2746654 | c.945C>T | synonymous_variant | 0.5 |
pepQ | 2859711 | c.708C>A | synonymous_variant | 0.4 |
Rv2752c | 3065112 | c.1080C>A | synonymous_variant | 0.15 |
Rv2752c | 3065422 | p.Arg257Gln | missense_variant | 0.33 |
Rv2752c | 3065451 | c.741G>A | synonymous_variant | 0.33 |
Rv2752c | 3066212 | c.-21G>A | upstream_gene_variant | 1.0 |
Rv2752c | 3067161 | c.-970C>A | upstream_gene_variant | 0.33 |
thyX | 3067736 | p.Phe70Leu | missense_variant | 0.25 |
ald | 3087469 | p.Thr217Asn | missense_variant | 0.2 |
fprA | 3475092 | c.1086C>A | synonymous_variant | 0.29 |
whiB7 | 3568704 | c.-25G>A | upstream_gene_variant | 0.2 |
Rv3236c | 3613017 | p.Pro34Thr | missense_variant | 0.5 |
fbiA | 3640979 | p.Thr146Asn | missense_variant | 0.25 |
alr | 3840450 | p.Gly324Glu | missense_variant | 0.33 |
alr | 3840808 | p.Asp205Tyr | missense_variant | 0.67 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.36 |
rpoA | 3878490 | c.18C>A | synonymous_variant | 1.0 |
ddn | 3987195 | p.Glu118* | stop_gained | 0.15 |
ddn | 3987278 | c.435G>T | synonymous_variant | 0.12 |
clpC1 | 4039714 | p.Tyr331His | missense_variant | 0.2 |
clpC1 | 4039730 | c.975C>G | synonymous_variant | 0.15 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.25 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.4 |
embC | 4240148 | p.Gly96Arg | missense_variant | 0.18 |
embC | 4240306 | c.444C>A | synonymous_variant | 0.4 |
embC | 4240435 | p.Tyr191* | stop_gained | 0.22 |
embC | 4241728 | c.1866C>T | synonymous_variant | 0.4 |
embB | 4246820 | p.Pro103Thr | missense_variant | 1.0 |
embB | 4247593 | c.1080G>T | synonymous_variant | 0.33 |
embB | 4248033 | p.Arg507Met | missense_variant | 0.2 |
embB | 4248051 | p.Gly513Val | missense_variant | 0.22 |
embB | 4248738 | p.Ala742Glu | missense_variant | 0.67 |
aftB | 4269627 | c.-791G>T | upstream_gene_variant | 0.5 |
ethA | 4327151 | p.Asp108Val | missense_variant | 0.14 |
ethA | 4327774 | c.-301G>A | upstream_gene_variant | 0.22 |
ethR | 4328008 | p.Asp154Asn | missense_variant | 0.5 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |