Run ID: ERR2229496
Sample name:
Date: 31-03-2023 17:15:27
Number of reads: 366995
Percentage reads mapped: 99.26
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 |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
rpoB | 759620 | c.-187A>C | upstream_gene_variant | 0.33 |
rpoC | 765031 | p.Glu554Asp | missense_variant | 0.4 |
mmpL5 | 777482 | c.999G>A | synonymous_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801277 | p.Pro157Thr | missense_variant | 0.33 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1305264 | c.2334C>T | synonymous_variant | 0.22 |
Rv1258c | 1406797 | p.Gly182Arg | missense_variant | 0.25 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472124 | n.279C>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472312 | n.467G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474328 | n.675_677dupGAA | non_coding_transcript_exon_variant | 0.67 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.14 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.14 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.14 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.14 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.14 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.57 |
rpsA | 1833440 | c.-102G>T | upstream_gene_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102074 | p.Met323Lys | missense_variant | 0.3 |
ndh | 2103225 | c.-183A>C | upstream_gene_variant | 0.5 |
katG | 2155318 | p.Leu265Pro | missense_variant | 0.22 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.25 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.25 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169386 | c.1227C>A | synonymous_variant | 0.14 |
PPE35 | 2169394 | p.Ala407Ser | missense_variant | 0.14 |
PPE35 | 2169397 | p.Gly406Ser | missense_variant | 0.14 |
PPE35 | 2169866 | c.747G>A | synonymous_variant | 0.13 |
PPE35 | 2169879 | p.Phe245Ser | missense_variant | 0.26 |
PPE35 | 2169882 | p.Ser244Asn | missense_variant | 0.27 |
PPE35 | 2169890 | c.723C>T | synonymous_variant | 0.2 |
PPE35 | 2169893 | c.720C>A | synonymous_variant | 0.21 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.54 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.55 |
PPE35 | 2170157 | p.Ala152Ser | missense_variant | 0.2 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
whiB7 | 3568501 | p.Ala60Asp | missense_variant | 0.25 |
ddn | 3987144 | p.Gln101* | stop_gained | 0.2 |
embC | 4240757 | p.Thr299Gly | missense_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.4 |
embB | 4248569 | c.2056C>T | synonymous_variant | 0.15 |
ethR | 4326961 | c.-588G>C | upstream_gene_variant | 0.4 |
ethR | 4326964 | c.-585G>A | upstream_gene_variant | 0.4 |
ethR | 4326970 | c.-579G>T | upstream_gene_variant | 0.5 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |