Run ID: ERR216928
Sample name:
Date: 31-03-2023 15:56:01
Number of reads: 1047534
Percentage reads mapped: 55.9
Strain: lineage4.9.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
lineage4.9.1 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472122 | n.277G>C | non_coding_transcript_exon_variant | 0.32 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8978 | c.1677C>T | synonymous_variant | 1.0 |
fgd1 | 490751 | c.-32T>G | upstream_gene_variant | 0.29 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781717 | p.Ala53Val | missense_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472277 | n.432C>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472282 | n.437T>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472544 | n.699C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472549 | n.704G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472579 | n.734G>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472599 | n.754G>A | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472600 | n.755C>T | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472659 | n.814G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472705 | n.860G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472708 | n.863T>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472715 | n.870C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472779 | n.934G>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473001 | n.1156G>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473009 | n.1164T>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473062 | n.1217T>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473068 | n.1223A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473089 | n.1244A>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475843 | n.2186G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475853 | n.2196C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475874 | n.2217C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476523 | n.2866T>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476529 | n.2872A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.49 |
rrl | 1476572 | n.2915G>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476595 | n.2938C>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476602 | n.2945G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476614 | n.2957A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476621 | n.2964C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476625 | n.2968C>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476637 | n.2980C>A | non_coding_transcript_exon_variant | 0.19 |
inhA | 1674952 | p.Pro251Ala | missense_variant | 0.21 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155227 | p.Gln295His | missense_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289138 | p.Leu35Arg | missense_variant | 1.0 |
Rv2752c | 3064985 | c.1207C>T | synonymous_variant | 0.12 |
Rv2752c | 3065557 | p.Gly212Glu | missense_variant | 0.11 |
thyA | 3073806 | c.666C>G | synonymous_variant | 0.3 |
ald | 3086982 | p.Ala55Pro | missense_variant | 1.0 |
ald | 3086987 | p.Gln56His | missense_variant | 1.0 |
fbiD | 3339385 | p.Asp90Asn | missense_variant | 1.0 |
clpC1 | 4038857 | c.1848C>A | synonymous_variant | 0.21 |
embC | 4242422 | p.Trp854Gly | missense_variant | 0.22 |
embC | 4242425 | p.Arg855Gly | missense_variant | 0.36 |
embA | 4246144 | p.Ile971Asn | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |