Run ID: ERR4820043
Sample name:
Date: 01-04-2023 16:27:11
Number of reads: 2528389
Percentage reads mapped: 85.0
Strain: lineage4.1.2.1
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 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6061 | c.822C>T | synonymous_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7394 | c.93T>C | synonymous_variant | 0.12 |
gyrA | 7397 | c.96G>C | synonymous_variant | 0.13 |
gyrA | 7553 | c.252C>T | synonymous_variant | 0.12 |
gyrA | 7559 | c.258G>C | synonymous_variant | 0.14 |
gyrA | 7565 | c.264C>T | synonymous_variant | 0.12 |
gyrA | 7574 | c.273G>C | synonymous_variant | 0.13 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7589 | c.288G>C | synonymous_variant | 0.11 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
rpoB | 760115 | c.309C>T | synonymous_variant | 0.97 |
rpoB | 760841 | c.1035T>C | synonymous_variant | 0.11 |
rpoB | 760858 | p.Val351Ala | missense_variant | 0.12 |
rpoB | 760862 | c.1056G>C | synonymous_variant | 0.12 |
rpoB | 760865 | c.1059C>T | synonymous_variant | 0.14 |
rpoB | 760886 | p.Glu360Asp | missense_variant | 0.13 |
rpoB | 760887 | p.Thr361Val | missense_variant | 0.13 |
rpoB | 760910 | c.1104C>T | synonymous_variant | 0.13 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.11 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.11 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.11 |
rpoB | 761063 | c.1257C>G | synonymous_variant | 0.11 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.14 |
rpoB | 761198 | c.1392G>C | synonymous_variant | 0.11 |
rpoB | 761219 | c.1413G>C | synonymous_variant | 0.15 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.15 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.12 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.11 |
rpoB | 761258 | c.1452G>A | synonymous_variant | 0.11 |
rpoB | 761261 | c.1455G>C | synonymous_variant | 0.11 |
rpoB | 761264 | c.1458C>G | synonymous_variant | 0.11 |
rpoB | 762014 | c.2208C>G | synonymous_variant | 0.12 |
rpoB | 762038 | c.2232C>T | synonymous_variant | 0.11 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.12 |
rpoB | 762236 | c.2430G>C | synonymous_variant | 0.12 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.11 |
rpoB | 762275 | c.2469C>T | synonymous_variant | 0.12 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.14 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.17 |
rpoB | 762296 | c.2490G>C | synonymous_variant | 0.14 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.11 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.12 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 0.14 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.11 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.11 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.15 |
rpoC | 763082 | c.-288C>T | upstream_gene_variant | 0.17 |
rpoC | 763088 | c.-282C>G | upstream_gene_variant | 0.16 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.15 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.14 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.13 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.11 |
rpoC | 763492 | c.123G>C | synonymous_variant | 0.12 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.18 |
rpoC | 763531 | c.162G>T | synonymous_variant | 0.18 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.21 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.22 |
rpoC | 764098 | c.729A>G | synonymous_variant | 0.1 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 0.11 |
rpoC | 764377 | c.1008C>G | synonymous_variant | 0.11 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.11 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 0.12 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.12 |
rpoC | 764524 | c.1155C>G | synonymous_variant | 0.14 |
rpoC | 764530 | c.1161C>G | synonymous_variant | 0.14 |
rpoC | 764534 | c.1165C>A | synonymous_variant | 0.15 |
rpoC | 764539 | c.1170C>T | synonymous_variant | 0.15 |
rpoC | 764542 | c.1173C>T | synonymous_variant | 0.15 |
rpoC | 764545 | c.1176C>A | synonymous_variant | 0.15 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.19 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.18 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.21 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.18 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.18 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.16 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 0.17 |
rpoC | 764692 | c.1323C>T | synonymous_variant | 0.17 |
rpoC | 764713 | c.1344G>T | synonymous_variant | 0.18 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.18 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.18 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.17 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.17 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.16 |
rpoC | 764791 | c.1422C>G | synonymous_variant | 0.16 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.14 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.13 |
rpoC | 764810 | p.Pro481Ala | missense_variant | 0.14 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.15 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 0.12 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.14 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.14 |
rpoC | 764869 | c.1500C>T | synonymous_variant | 0.14 |
rpoC | 764875 | c.1506C>A | synonymous_variant | 0.12 |
rpoC | 764887 | c.1518G>C | synonymous_variant | 0.12 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.11 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765409 | c.2040T>G | synonymous_variant | 0.1 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.11 |
rpoC | 765449 | p.Ala694Ser | missense_variant | 0.11 |
rpoC | 765454 | c.2085C>G | synonymous_variant | 0.11 |
rpoC | 765469 | c.2100G>C | synonymous_variant | 0.11 |
rpoC | 765478 | c.2109T>G | synonymous_variant | 0.11 |
rpoC | 767008 | c.3639G>A | synonymous_variant | 0.11 |
rpoC | 767044 | c.3675G>C | synonymous_variant | 0.14 |
rpoC | 767080 | c.3711G>C | synonymous_variant | 0.13 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.16 |
rpoC | 767104 | c.3735C>G | synonymous_variant | 0.15 |
rpoC | 767107 | c.3738C>T | synonymous_variant | 0.15 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.17 |
rpoC | 767125 | c.3756G>C | synonymous_variant | 0.16 |
rpoC | 767149 | c.3780C>T | synonymous_variant | 0.13 |
rpoC | 767158 | c.3789T>C | synonymous_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777404 | c.1077C>T | synonymous_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472846 | n.1001C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472847 | n.1002G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472848 | n.1003T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472860 | n.1015C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472861 | n.1016G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473129 | n.1284C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473288 | n.1443C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1473707 | n.50T>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1473717 | n.60G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1473731 | n.74T>A | non_coding_transcript_exon_variant | 0.32 |
rrl | 1473746 | n.89T>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1473756 | n.99G>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1473770 | n.113T>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473812 | n.155G>A | non_coding_transcript_exon_variant | 0.47 |
rrl | 1473814 | n.157A>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1473815 | n.158T>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1473829 | n.172G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473831 | n.174G>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1473832 | n.175C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473839 | n.182G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473887 | n.230T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473888 | n.231T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474181 | n.524_525insT | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474184 | n.527C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474185 | n.529delA | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474263 | n.606G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474490 | n.833G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474507 | n.850G>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475076 | n.1419C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475120 | n.1463G>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475129 | n.1472G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475202 | n.1545G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475475 | n.1818C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475479 | n.1822C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475760 | n.2105_2106delGC | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475764 | n.2107A>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475765 | n.2108A>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475989 | n.2332T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475993 | n.2336C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.11 |
rpsA | 1833874 | c.333T>G | synonymous_variant | 0.11 |
rpsA | 1833886 | c.345C>G | synonymous_variant | 0.11 |
rpsA | 1833894 | p.Ala118Glu | missense_variant | 0.12 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.16 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2518768 | c.654C>G | synonymous_variant | 0.11 |
kasA | 2518771 | c.657C>G | synonymous_variant | 0.12 |
kasA | 2518783 | c.669T>G | synonymous_variant | 0.12 |
kasA | 2518787 | p.Arg225Lys | missense_variant | 0.12 |
kasA | 2518792 | c.678C>T | synonymous_variant | 0.12 |
kasA | 2518795 | c.681C>T | synonymous_variant | 0.12 |
kasA | 2518798 | c.684G>C | synonymous_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448432 | c.-72C>A | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3877638 | c.870T>C | synonymous_variant | 0.11 |
rpoA | 3877656 | c.852T>G | synonymous_variant | 0.12 |
rpoA | 3877665 | c.843C>G | synonymous_variant | 0.11 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.11 |
rpoA | 3878196 | p.Glu104Ala | missense_variant | 0.11 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.12 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.1 |
clpC1 | 4039097 | c.1608G>T | synonymous_variant | 0.12 |
clpC1 | 4039103 | c.1602T>C | synonymous_variant | 0.12 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.12 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.12 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.1 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.12 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.12 |
clpC1 | 4039472 | c.1233G>C | synonymous_variant | 0.12 |
clpC1 | 4039478 | c.1227G>C | synonymous_variant | 0.12 |
clpC1 | 4039481 | c.1224T>C | synonymous_variant | 0.13 |
clpC1 | 4039487 | c.1218G>C | synonymous_variant | 0.14 |
clpC1 | 4039522 | c.1183C>T | synonymous_variant | 0.11 |
clpC1 | 4039541 | c.1164C>G | synonymous_variant | 0.11 |
clpC1 | 4039661 | c.1044T>C | synonymous_variant | 0.12 |
clpC1 | 4039682 | c.1023C>G | synonymous_variant | 0.1 |
clpC1 | 4040546 | c.159G>C | synonymous_variant | 0.1 |
clpC1 | 4040561 | c.144A>G | synonymous_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |