Run ID: ERR2229503
Sample name:
Date: 18-08-2022 10:31:27
Number of reads: 996773
Percentage reads mapped: 99.28
Strain: lineage4.8
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6114 | p.Gln292Arg | missense_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7416 | p.Arg39Ser | missense_variant | 0.15 |
gyrA | 7423 | p.Leu41Arg | missense_variant | 0.14 |
gyrA | 9507 | p.Ala736Ser | missense_variant | 0.14 |
rpoB | 759775 | c.-32G>A | upstream_gene_variant | 0.14 |
rpoB | 760575 | p.Glu257* | stop_gained | 0.16 |
rpoB | 761960 | p.Met718Ile | missense_variant | 0.12 |
rpoC | 763540 | c.171C>T | synonymous_variant | 0.2 |
rpoC | 764343 | p.Arg325His | missense_variant | 0.18 |
rpoC | 764352 | p.Val328Ala | missense_variant | 0.12 |
rpoC | 766028 | p.Arg887Cys | missense_variant | 0.18 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800636 | c.-173C>A | upstream_gene_variant | 0.12 |
fbiC | 1303618 | p.His230Asn | missense_variant | 0.14 |
atpE | 1461096 | p.Ala18Ser | missense_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1476150 | n.2493G>T | non_coding_transcript_exon_variant | 0.17 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.44 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.42 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.17 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.17 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.17 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.23 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
eis | 2714753 | p.Gln194Lys | missense_variant | 0.12 |
folC | 2747204 | p.Ala132Glu | missense_variant | 0.15 |
folC | 2747252 | p.Ser116Ile | missense_variant | 0.15 |
pepQ | 2859601 | c.817delG | frameshift_variant | 0.18 |
pepQ | 2859807 | p.His204Gln | missense_variant | 0.12 |
thyX | 3068063 | c.-118C>T | upstream_gene_variant | 0.14 |
fbiD | 3339517 | p.His134Asn | missense_variant | 0.14 |
fbiA | 3641450 | p.Val303Glu | missense_variant | 0.13 |
alr | 3840232 | p.Arg397Cys | missense_variant | 0.12 |
alr | 3840269 | c.1152C>T | synonymous_variant | 0.14 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.17 |
panD | 4044088 | p.Gly65Val | missense_variant | 0.12 |
panD | 4044125 | p.Ala53Thr | missense_variant | 0.15 |
embC | 4241825 | p.Pro655Ala | missense_variant | 0.15 |
embA | 4246381 | p.Trp1050* | stop_gained | 0.18 |
embB | 4247181 | p.Ile223Ser | missense_variant | 0.11 |
embB | 4249151 | p.Ala880Ser | missense_variant | 0.13 |
ethR | 4328118 | p.Glu190Asp | missense_variant | 0.18 |