Run ID: ERR4815394
Sample name:
Date: 01-04-2023 13:50:21
Number of reads: 453359
Percentage reads mapped: 87.79
Strain: lineage4.2.1
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.2 | Euro-American | H;T;LAM | None | 1.0 |
lineage4.2.1 | Euro-American (TUR) | H3;H4 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761127 | p.Ser441Ala | missense_variant | 0.12 | rifampicin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.12 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.12 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.12 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.12 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.13 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.17 |
rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 0.15 |
rpoB | 761096 | c.1290G>C | synonymous_variant | 0.13 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.13 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.13 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 0.12 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.12 |
rpoB | 761159 | c.1353G>C | synonymous_variant | 0.11 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.11 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.11 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.14 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.12 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.12 |
rpoC | 764503 | c.1134G>T | synonymous_variant | 0.12 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.12 |
rpoC | 764512 | c.1143G>C | synonymous_variant | 0.12 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.11 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.12 |
rpoC | 764543 | p.Thr392Ala | missense_variant | 0.16 |
rpoC | 764548 | c.1179G>T | synonymous_variant | 0.16 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.25 |
rpoC | 764573 | p.Leu402Ile | missense_variant | 0.23 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 0.23 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.22 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.22 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.19 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 0.19 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.21 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.17 |
rpoC | 764647 | c.1278C>T | synonymous_variant | 0.18 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.18 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.18 |
rpoC | 764656 | c.1287C>T | synonymous_variant | 0.18 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.17 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.17 |
rpoC | 764678 | p.Lys437Gln | missense_variant | 0.17 |
rpoC | 766321 | c.2953delA | frameshift_variant | 0.17 |
rpoC | 766951 | c.3582G>A | synonymous_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
atpE | 1460871 | c.-174T>C | upstream_gene_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472513 | n.668T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472549 | n.704G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472686 | n.841G>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472690 | n.845C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.32 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.37 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.32 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.32 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.32 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.41 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.41 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.32 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.34 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476523 | n.2866T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476542 | n.2885T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.11 |
inhA | 1674648 | c.447C>T | synonymous_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102401 | c.642T>C | synonymous_variant | 1.0 |
PPE35 | 2168435 | c.2178C>T | synonymous_variant | 0.11 |
PPE35 | 2169879 | p.Phe245Cys | missense_variant | 1.0 |
Rv1979c | 2222012 | p.Gln385* | stop_gained | 1.0 |
Rv1979c | 2222040 | c.1125C>T | synonymous_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.27 |
folC | 2746669 | p.Glu310Asp | missense_variant | 0.22 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246310 | c.-204C>T | upstream_gene_variant | 1.0 |
embB | 4248153 | p.Ala547Val | missense_variant | 0.15 |
embB | 4249594 | c.3081G>A | synonymous_variant | 1.0 |
ethA | 4328376 | c.-903G>C | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |