Run ID: ERR9896153
Sample name:
Date: 02-04-2023 13:29:26
Number of reads: 651537
Percentage reads mapped: 62.97
Strain: lineage4.4.1.1
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 |
lineage4.4 | Euro-American | S;T | None | 1.0 |
lineage4.4.1 | Euro-American (S-type) | S;T | None | 1.0 |
lineage4.4.1.1 | Euro-American | S;Orphans | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761127 | p.Ser441Ala | missense_variant | 0.2 | rifampicin |
rpoB | 761196 | p.Leu464Met | missense_variant | 0.17 | 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 |
mshA | 575920 | c.573C>G | synonymous_variant | 0.13 |
mshA | 575932 | c.585G>A | synonymous_variant | 0.12 |
mshA | 575944 | c.597T>C | synonymous_variant | 0.13 |
ccsA | 619801 | c.-90C>A | upstream_gene_variant | 0.22 |
ccsA | 619936 | p.Trp16Arg | missense_variant | 0.17 |
rpoB | 760859 | c.1053T>C | synonymous_variant | 0.14 |
rpoB | 760862 | c.1056G>C | synonymous_variant | 0.13 |
rpoB | 760869 | p.Val355Thr | missense_variant | 0.14 |
rpoB | 760886 | c.1080A>G | synonymous_variant | 0.15 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.21 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.17 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.17 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.16 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.17 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.2 |
rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 0.19 |
rpoB | 761096 | c.1290G>C | synonymous_variant | 0.19 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.29 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.28 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 0.2 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.3 |
rpoB | 761150 | c.1344A>T | synonymous_variant | 0.21 |
rpoB | 761159 | c.1353G>C | synonymous_variant | 0.18 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.26 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.26 |
rpoB | 761186 | p.Glu460Asp | missense_variant | 0.17 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.27 |
rpoB | 761192 | c.1386C>G | synonymous_variant | 0.17 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.28 |
rpoB | 761201 | c.1395G>A | synonymous_variant | 0.17 |
rpoB | 761204 | c.1398C>T | synonymous_variant | 0.18 |
rpoB | 761207 | c.1401C>A | synonymous_variant | 0.19 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.29 |
rpoB | 761219 | c.1413G>C | synonymous_variant | 0.18 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.14 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.19 |
rpoB | 763014 | p.Met1070Leu | missense_variant | 0.13 |
rpoB | 763017 | p.Gln1071Glu | missense_variant | 0.13 |
rpoC | 763022 | c.-348C>T | upstream_gene_variant | 0.19 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.2 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.18 |
rpoB | 763038 | p.Thr1078Ala | missense_variant | 0.17 |
rpoC | 763043 | c.-327G>C | upstream_gene_variant | 0.17 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.18 |
rpoC | 763067 | c.-303C>G | upstream_gene_variant | 0.16 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.19 |
rpoB | 763077 | p.Val1091Thr | missense_variant | 0.15 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.15 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.19 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.14 |
rpoC | 763648 | c.279C>T | synonymous_variant | 0.14 |
rpoC | 763657 | p.Glu96Asp | missense_variant | 0.14 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.14 |
rpoC | 763666 | c.297G>C | synonymous_variant | 0.14 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.14 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.18 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.21 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.15 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.15 |
rpoC | 763718 | p.Leu117Val | missense_variant | 0.14 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.14 |
rpoC | 763729 | c.360G>C | synonymous_variant | 0.16 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.16 |
rpoC | 763735 | c.366G>C | synonymous_variant | 0.16 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.15 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.15 |
rpoC | 764140 | c.771C>T | synonymous_variant | 0.13 |
rpoC | 764266 | c.897T>C | synonymous_variant | 0.13 |
rpoC | 764269 | c.900G>C | synonymous_variant | 0.13 |
rpoC | 764278 | c.909A>G | synonymous_variant | 0.14 |
rpoC | 764293 | c.924G>C | synonymous_variant | 0.15 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.21 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.18 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.17 |
rpoC | 764503 | c.1134G>T | synonymous_variant | 0.19 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.19 |
rpoC | 764512 | c.1143G>C | synonymous_variant | 0.18 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.22 |
rpoC | 764530 | c.1161C>T | synonymous_variant | 0.17 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.21 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.15 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.15 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.14 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.14 |
rpoC | 766918 | c.3549C>T | synonymous_variant | 0.15 |
rpoC | 766933 | c.3564A>G | synonymous_variant | 0.17 |
rpoC | 766945 | c.3576A>G | synonymous_variant | 0.17 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.16 |
rpoC | 766972 | c.3603G>C | synonymous_variant | 0.17 |
rpoC | 766978 | c.3609C>A | synonymous_variant | 0.16 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.19 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.14 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.14 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.13 |
fbiC | 1304137 | p.Ala403Ser | missense_variant | 0.13 |
fbiC | 1304142 | c.1212G>C | synonymous_variant | 0.13 |
fbiC | 1305021 | c.2091C>A | synonymous_variant | 0.14 |
fbiC | 1305033 | c.2103T>G | synonymous_variant | 0.14 |
fbiC | 1305321 | c.2391G>A | synonymous_variant | 0.96 |
Rv1258c | 1406938 | p.Ala135Thr | missense_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472286 | n.441_442insT | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472292 | n.447A>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472293 | n.449delG | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472297 | n.453_454delGT | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472308 | n.464_466delCTC | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472313 | n.469_470delAT | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472319 | n.474C>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472325 | n.480G>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472326 | n.481T>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472329 | n.484A>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472338 | n.493A>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472412 | n.567A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472416 | n.571C>T | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472427 | n.582T>G | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472436 | n.591G>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472437 | n.592T>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472438 | n.593T>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472449 | n.604C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472450 | n.605A>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472451 | n.606C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472462 | n.617T>G | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472473 | n.628G>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472474 | n.629C>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472476 | n.631A>G | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472484 | n.639A>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472496 | n.651T>G | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472513 | n.668T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472549 | n.704G>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472686 | n.841G>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472690 | n.845C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472840 | n.995A>G | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472841 | n.996_997insC | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472845 | n.1000G>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472846 | n.1002delG | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472849 | n.1004C>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472850 | n.1005T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472868 | n.1023T>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472874 | n.1029C>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472875 | n.1030_1031insTTAGTTGGTC | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.41 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.46 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.47 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.45 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.45 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.45 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.52 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.54 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.41 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.41 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.34 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.34 |
rrs | 1473288 | n.1443C>G | non_coding_transcript_exon_variant | 0.32 |
rrs | 1473289 | n.1444_1445insTTTTG | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473293 | n.1449delA | non_coding_transcript_exon_variant | 0.34 |
rrs | 1473300 | n.1455C>T | non_coding_transcript_exon_variant | 0.34 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.34 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473384 | n.-274A>G | upstream_gene_variant | 0.2 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474483 | n.826C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474497 | n.840G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474506 | n.849C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474528 | n.871T>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474529 | n.872A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474540 | n.883T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474541 | n.884G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474551 | n.894G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.39 |
rrl | 1474634 | n.977T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474640 | n.983C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474674 | n.1018delC | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 0.49 |
rrl | 1474709 | n.1052G>A | non_coding_transcript_exon_variant | 0.49 |
rrl | 1474722 | n.1065T>C | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.49 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.51 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.46 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474801 | n.1144G>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474802 | n.1145T>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.39 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.39 |
rrl | 1474832 | n.1175A>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474901 | n.1244A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475686 | n.2029C>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475696 | n.2039T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475703 | n.2046A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475715 | n.2058G>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475756 | n.2099T>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475767 | n.2110_2111insT | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.37 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.53 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.54 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 0.49 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475995 | n.2338G>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475998 | n.2341C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476000 | n.2343G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476179 | n.2522C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476204 | n.2547C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476255 | n.2598A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476267 | n.2610G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476268 | n.2611A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476275 | n.2618T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476276 | n.2619C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476290 | n.2636_2637insCATGGC | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476295 | n.2639_2644delCCCCGA | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476306 | n.2649A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476307 | n.2650A>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476311 | n.2654G>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476312 | n.2655T>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.13 |
inhA | 1674501 | p.Gln100His | missense_variant | 0.13 |
rpsA | 1834228 | c.687C>T | synonymous_variant | 0.19 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.22 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.19 |
rpsA | 1834246 | c.705G>T | synonymous_variant | 0.19 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.14 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.15 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.15 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.17 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.15 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.17 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.15 |
rpsA | 1834312 | c.771G>A | synonymous_variant | 0.15 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.14 |
rpsA | 1834345 | c.804C>T | synonymous_variant | 0.14 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.18 |
rpsA | 1834354 | c.813G>C | synonymous_variant | 0.15 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 0.15 |
rpsA | 1834360 | c.819G>C | synonymous_variant | 0.15 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.15 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.19 |
rpsA | 1834375 | c.834G>C | synonymous_variant | 0.14 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.14 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.15 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.17 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.15 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.14 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.13 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102990 | p.Val18Ala | missense_variant | 1.0 |
katG | 2155538 | p.Glu192* | stop_gained | 0.17 |
PPE35 | 2169840 | p.Gly258Asp | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518532 | p.Leu140Met | missense_variant | 0.12 |
kasA | 2518627 | c.513T>C | synonymous_variant | 0.13 |
kasA | 2518636 | c.522C>T | synonymous_variant | 0.13 |
kasA | 2518642 | c.528A>G | synonymous_variant | 0.14 |
kasA | 2518672 | c.558G>C | synonymous_variant | 0.18 |
kasA | 2518678 | c.564C>T | synonymous_variant | 0.18 |
kasA | 2518684 | c.570C>G | synonymous_variant | 0.2 |
kasA | 2518687 | c.573C>T | synonymous_variant | 0.18 |
kasA | 2518688 | p.Val192Phe | missense_variant | 0.18 |
kasA | 2518705 | c.591T>G | synonymous_variant | 0.18 |
kasA | 2518711 | c.597A>G | synonymous_variant | 0.18 |
kasA | 2518714 | c.600A>T | synonymous_variant | 0.2 |
kasA | 2518717 | c.603C>T | synonymous_variant | 0.18 |
kasA | 2518723 | c.609G>A | synonymous_variant | 0.18 |
kasA | 2518747 | c.633C>G | synonymous_variant | 0.13 |
kasA | 2518768 | c.654C>G | synonymous_variant | 0.15 |
kasA | 2518789 | c.675G>C | synonymous_variant | 0.12 |
kasA | 2518792 | c.678C>A | synonymous_variant | 0.12 |
folC | 2746393 | c.1206C>G | synonymous_variant | 0.13 |
folC | 2746401 | p.Ser400Ala | missense_variant | 0.13 |
folC | 2746402 | c.1197T>C | synonymous_variant | 0.13 |
folC | 2746416 | p.Glu395Gln | missense_variant | 0.14 |
folC | 2746420 | c.1179A>C | synonymous_variant | 0.13 |
thyX | 3067619 | c.327A>C | synonymous_variant | 0.14 |
thyX | 3067634 | c.312C>G | synonymous_variant | 0.14 |
thyX | 3067643 | c.303C>T | synonymous_variant | 0.14 |
thyX | 3067652 | c.294T>C | synonymous_variant | 0.14 |
thyX | 3067661 | c.285C>G | synonymous_variant | 0.18 |
thyX | 3067685 | c.261A>C | synonymous_variant | 0.17 |
thyX | 3067694 | c.252G>C | synonymous_variant | 0.17 |
thyX | 3067718 | c.228C>G | synonymous_variant | 0.18 |
thyX | 3067721 | c.225T>C | synonymous_variant | 0.19 |
thyX | 3067724 | c.222G>A | synonymous_variant | 0.2 |
thyX | 3067727 | c.219A>C | synonymous_variant | 0.25 |
thyX | 3067736 | c.210C>T | synonymous_variant | 0.25 |
thyX | 3067739 | c.207T>C | synonymous_variant | 0.25 |
thyX | 3067742 | c.204A>C | synonymous_variant | 0.25 |
thyX | 3067762 | c.184C>A | synonymous_variant | 0.21 |
thyX | 3067765 | p.Leu61Ile | missense_variant | 0.21 |
thyX | 3067781 | c.165C>G | synonymous_variant | 0.21 |
thyX | 3067793 | c.153T>C | synonymous_variant | 0.13 |
thyX | 3067799 | c.147G>A | synonymous_variant | 0.17 |
thyX | 3067802 | c.144C>G | synonymous_variant | 0.17 |
thyX | 3067811 | c.135G>A | synonymous_variant | 0.13 |
thyX | 3067937 | p.Glu3Asp | missense_variant | 0.25 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339689 | p.Thr191Asn | missense_variant | 0.14 |
Rv3083 | 3448608 | c.105G>A | synonymous_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612665 | p.Val151Ala | missense_variant | 1.0 |
clpC1 | 4039364 | c.1341C>G | synonymous_variant | 0.15 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.14 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.13 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.13 |
clpC1 | 4039760 | c.945T>C | synonymous_variant | 0.14 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.14 |
clpC1 | 4039775 | c.930G>C | synonymous_variant | 0.14 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.14 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 0.15 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.14 |
embC | 4240780 | c.918T>C | synonymous_variant | 0.13 |
embC | 4240783 | c.921G>C | synonymous_variant | 0.13 |
embC | 4240789 | c.927T>C | synonymous_variant | 0.13 |
embC | 4240811 | p.Phe317Leu | missense_variant | 0.14 |
embC | 4240819 | c.957A>G | synonymous_variant | 0.14 |
embC | 4240831 | c.969T>G | synonymous_variant | 0.14 |
embC | 4240867 | c.1005T>G | synonymous_variant | 0.17 |
embC | 4240870 | c.1008T>C | synonymous_variant | 0.18 |
embC | 4240873 | c.1011C>G | synonymous_variant | 0.18 |
embC | 4240880 | p.Ala340Thr | missense_variant | 0.2 |
embC | 4240885 | c.1023T>C | synonymous_variant | 0.2 |
embC | 4240897 | c.1035C>G | synonymous_variant | 0.18 |
embC | 4240898 | c.1036_1038delCTAinsTTG | synonymous_variant | 0.18 |
embC | 4240921 | c.1059C>G | synonymous_variant | 0.12 |
embC | 4240924 | c.1062C>G | synonymous_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246764 | p.Pro84Gln | missense_variant | 0.14 |
ethA | 4328384 | c.-911A>G | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |