Run ID: ERR1750929
Sample name:
Date: 31-03-2023 15:00:01
Number of reads: 1619732
Percentage reads mapped: 93.54
Strain: lineage4.1.1.3
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.1 | Euro-American (X-type) | X1;X2;X3 | None | 0.99 |
lineage4.1.1.3 | Euro-American (X-type) | X1;X3 | RD193 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7492 | p.Phe64Ser | missense_variant | 0.12 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7614 | c.313C>T | synonymous_variant | 0.17 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491298 | c.516C>T | synonymous_variant | 0.15 |
fgd1 | 491305 | p.Ala175Pro | missense_variant | 0.14 |
mshA | 576197 | p.Leu284Met | missense_variant | 0.14 |
mshA | 576318 | p.Arg324Pro | missense_variant | 0.12 |
mshA | 576480 | p.Pro378Arg | missense_variant | 0.17 |
ccsA | 619717 | c.-174G>C | upstream_gene_variant | 0.12 |
ccsA | 619760 | c.-131G>C | upstream_gene_variant | 0.13 |
ccsA | 620119 | p.Gly77Trp | missense_variant | 0.17 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.11 |
rpoC | 764551 | c.1182G>C | synonymous_variant | 0.12 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 779202 | c.-722G>A | upstream_gene_variant | 0.14 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801225 | c.417C>T | synonymous_variant | 0.15 |
Rv1258c | 1407485 | c.-145G>C | upstream_gene_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1471929 | n.84C>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1471930 | n.85G>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1471931 | n.86G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1471932 | n.87A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472168 | n.323G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472571 | n.726G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472606 | n.761C>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472623 | n.778A>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472645 | n.800G>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472660 | n.815T>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472666 | n.821G>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472680 | n.835C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472780 | n.935G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472837 | n.992C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472998 | n.1153C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473700 | n.43G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474354 | n.697C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474583 | n.926C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474601 | n.944C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474672 | n.1015C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474797 | n.1140G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475277 | n.1620G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475301 | n.1644T>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475814 | n.2157A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475963 | n.2306G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476384 | n.2727G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476540 | n.2883C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476566 | n.2909A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476608 | n.2951C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.67 |
inhA | 1674968 | p.Asp256Gly | missense_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918039 | p.Ile34Leu | missense_variant | 0.12 |
ndh | 2101668 | p.Ala459Pro | missense_variant | 0.15 |
ndh | 2102883 | c.160C>T | synonymous_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289903 | c.-662C>A | upstream_gene_variant | 0.15 |
eis | 2714871 | c.462G>T | synonymous_variant | 0.19 |
eis | 2714950 | p.Arg128Leu | missense_variant | 0.2 |
eis | 2714954 | p.Gly127Ser | missense_variant | 0.27 |
pepQ | 2860053 | c.366G>A | synonymous_variant | 0.2 |
pepQ | 2860082 | p.Ala113Ser | missense_variant | 0.15 |
Rv2752c | 3065603 | p.Asp197His | missense_variant | 0.12 |
Rv2752c | 3066299 | c.-109delG | upstream_gene_variant | 0.12 |
thyX | 3067209 | p.Leu246Ser | missense_variant | 0.15 |
thyX | 3067952 | c.-7G>A | upstream_gene_variant | 0.2 |
thyA | 3074427 | c.45T>C | synonymous_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339371 | p.Pro85Leu | missense_variant | 0.15 |
fbiD | 3339669 | c.552C>A | synonymous_variant | 0.2 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiA | 3641249 | p.Ala236Gly | missense_variant | 0.12 |
fbiA | 3641257 | p.Pro239Ala | missense_variant | 0.12 |
clpC1 | 4038201 | p.Ala835Asp | missense_variant | 0.18 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.18 |
clpC1 | 4040250 | p.Glu152Gly | missense_variant | 0.13 |
embC | 4242429 | p.Ala856Gly | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4243714 | p.Thr161Ser | missense_variant | 0.17 |
embA | 4246461 | p.Gly1077Cys | missense_variant | 0.15 |
embA | 4246489 | p.Arg1086Gln | missense_variant | 0.15 |
embA | 4246498 | p.Pro1089Gln | missense_variant | 0.18 |
embB | 4246980 | p.Gly156Asp | missense_variant | 0.17 |
embB | 4247037 | p.Gly175Asp | missense_variant | 0.25 |
embB | 4248315 | p.Ala601Asp | missense_variant | 0.16 |
embB | 4249268 | p.Asp919His | missense_variant | 0.13 |
embB | 4249408 | c.2895G>A | synonymous_variant | 1.0 |
ethA | 4326923 | p.Gly184Asp | missense_variant | 0.16 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407798 | c.405G>T | synonymous_variant | 1.0 |