Run ID: ERR4831739
Sample name:
Date: 01-04-2023 21:05:29
Number of reads: 819079
Percentage reads mapped: 93.95
Strain: lineage2.2.1
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 0.97 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.95 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761161 | p.Leu452Pro | missense_variant | 0.2 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 0.92 | streptomycin |
inhA | 1674048 | c.-154G>A | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
katG | 2154227 | c.1884delA | frameshift_variant | 0.33 | isoniazid |
katG | 2155169 | p.Ser315Gly | missense_variant | 1.0 | isoniazid |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
embB | 4247730 | p.Gly406Asp | missense_variant | 0.17 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6917 | p.His560Asn | missense_variant | 0.18 |
gyrB | 6946 | p.Tyr569* | stop_gained | 0.13 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7750 | p.Val150Ala | missense_variant | 0.12 |
gyrA | 8852 | c.1551T>C | synonymous_variant | 0.11 |
gyrA | 8858 | c.1557T>C | synonymous_variant | 0.19 |
gyrA | 8870 | c.1569G>C | synonymous_variant | 0.17 |
gyrA | 8873 | c.1572A>G | synonymous_variant | 0.17 |
gyrA | 8897 | c.1596T>C | synonymous_variant | 0.12 |
gyrA | 8903 | c.1602T>C | synonymous_variant | 0.12 |
gyrA | 8915 | c.1614A>G | synonymous_variant | 0.11 |
gyrA | 8957 | c.1656C>T | synonymous_variant | 0.13 |
gyrA | 8967 | p.Ala556Lys | missense_variant | 0.14 |
gyrA | 9026 | c.1725G>C | synonymous_variant | 0.12 |
gyrA | 9029 | c.1728T>C | synonymous_variant | 0.12 |
gyrA | 9035 | c.1734G>C | synonymous_variant | 0.11 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490835 | p.Arg18Leu | missense_variant | 0.22 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575575 | c.228G>T | synonymous_variant | 0.17 |
mshA | 575850 | p.Arg168His | missense_variant | 0.25 |
mshA | 575894 | p.Val183Met | missense_variant | 0.15 |
mshA | 576045 | p.Ala233Glu | missense_variant | 0.15 |
mshA | 576077 | p.Leu244Met | missense_variant | 0.18 |
mshA | 576114 | p.Arg256Leu | missense_variant | 0.17 |
mshA | 576755 | p.Arg470Ser | missense_variant | 0.29 |
ccsA | 619738 | c.-153T>C | upstream_gene_variant | 0.25 |
ccsA | 619944 | p.Phe18Leu | missense_variant | 0.14 |
ccsA | 619973 | c.94_96delCTG | conservative_inframe_deletion | 0.33 |
ccsA | 619992 | c.102C>T | synonymous_variant | 0.2 |
ccsA | 619993 | p.Glu35Lys | missense_variant | 0.2 |
ccsA | 620183 | p.Arg98Leu | missense_variant | 0.15 |
ccsA | 620388 | c.498A>C | synonymous_variant | 0.13 |
ccsA | 620397 | c.507C>G | synonymous_variant | 0.13 |
ccsA | 620412 | c.522T>C | synonymous_variant | 0.17 |
ccsA | 620415 | c.525T>C | synonymous_variant | 0.17 |
ccsA | 620421 | c.531G>C | synonymous_variant | 0.17 |
ccsA | 620430 | c.540C>T | synonymous_variant | 0.14 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 759615 | c.-192A>C | upstream_gene_variant | 0.25 |
rpoB | 760415 | c.609C>A | synonymous_variant | 0.2 |
rpoB | 760460 | c.654G>C | synonymous_variant | 0.17 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.2 |
rpoB | 760481 | c.675G>C | synonymous_variant | 0.2 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.22 |
rpoB | 760749 | p.Gly315Trp | missense_variant | 0.14 |
rpoB | 761184 | p.Glu460* | stop_gained | 0.14 |
rpoB | 761343 | p.Val513Leu | missense_variant | 0.13 |
rpoB | 761405 | p.His533Gln | missense_variant | 0.22 |
rpoB | 762158 | c.2352G>C | synonymous_variant | 0.12 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.11 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.12 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.12 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 0.13 |
rpoB | 762329 | c.2523G>C | synonymous_variant | 0.11 |
rpoB | 762362 | p.Glu852Asp | missense_variant | 0.11 |
rpoB | 762369 | c.2563T>C | synonymous_variant | 0.11 |
rpoC | 762383 | c.-987C>G | upstream_gene_variant | 0.11 |
rpoC | 762392 | c.-978G>C | upstream_gene_variant | 0.24 |
rpoC | 762395 | c.-975G>T | upstream_gene_variant | 0.24 |
rpoC | 762398 | c.-972T>C | upstream_gene_variant | 0.25 |
rpoC | 762404 | c.-966T>C | upstream_gene_variant | 0.25 |
rpoC | 762410 | c.-960T>G | upstream_gene_variant | 0.31 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 0.27 |
rpoC | 762449 | c.-921C>A | upstream_gene_variant | 0.14 |
rpoC | 762452 | c.-918G>C | upstream_gene_variant | 0.14 |
rpoC | 762470 | c.-900G>C | upstream_gene_variant | 0.14 |
rpoC | 762485 | c.-885G>A | upstream_gene_variant | 0.14 |
rpoC | 762488 | c.-882G>C | upstream_gene_variant | 0.14 |
rpoC | 762491 | c.-879T>C | upstream_gene_variant | 0.14 |
rpoC | 762509 | c.-861T>G | upstream_gene_variant | 0.25 |
rpoB | 762510 | p.Ala902Pro | missense_variant | 0.25 |
rpoC | 762515 | c.-855C>T | upstream_gene_variant | 0.25 |
rpoB | 762633 | p.Ala943Ser | missense_variant | 0.33 |
rpoB | 762660 | p.Arg952Trp | missense_variant | 0.2 |
rpoC | 762761 | c.-609C>T | upstream_gene_variant | 0.13 |
rpoB | 762852 | p.Pro1016Thr | missense_variant | 0.13 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763102 | p.Ala1099Glu | missense_variant | 0.13 |
rpoC | 763380 | p.Val4Ala | missense_variant | 0.12 |
rpoC | 763981 | p.Glu204Asp | missense_variant | 0.17 |
rpoC | 764546 | p.Gly393Trp | missense_variant | 0.17 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.19 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.19 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.17 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.24 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 0.29 |
rpoC | 764692 | c.1323C>T | synonymous_variant | 0.22 |
rpoC | 764713 | c.1344G>T | synonymous_variant | 0.2 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.2 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.14 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.13 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.12 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.12 |
rpoC | 764791 | c.1422C>G | synonymous_variant | 0.13 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.12 |
rpoC | 764810 | p.Pro481Ala | missense_variant | 0.11 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.11 |
rpoC | 765244 | c.1875T>G | synonymous_variant | 0.14 |
rpoC | 765285 | p.Gln639Pro | missense_variant | 0.12 |
rpoC | 765295 | c.1926G>A | synonymous_variant | 0.17 |
rpoC | 765343 | c.1974G>A | synonymous_variant | 0.14 |
rpoC | 765352 | c.1983G>C | synonymous_variant | 0.17 |
rpoC | 765356 | p.Met663Val | missense_variant | 0.17 |
rpoC | 765370 | c.2001G>C | synonymous_variant | 0.18 |
rpoC | 765379 | c.2010G>C | synonymous_variant | 0.33 |
rpoC | 765382 | c.2013G>T | synonymous_variant | 0.25 |
rpoC | 765383 | p.Met672Leu | missense_variant | 0.25 |
rpoC | 765398 | c.2030_2031delTG | frameshift_variant | 0.18 |
rpoC | 765403 | c.2034G>C | synonymous_variant | 0.18 |
rpoC | 765405 | p.Leu679His | missense_variant | 0.18 |
rpoC | 765409 | c.2040T>G | synonymous_variant | 0.15 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.15 |
rpoC | 766042 | c.2673C>T | synonymous_variant | 0.4 |
rpoC | 766668 | c.3301_3309delGATGGCGAC | conservative_inframe_deletion | 0.13 |
rpoC | 766724 | p.His1119Asn | missense_variant | 0.14 |
rpoC | 766942 | c.3573C>T | synonymous_variant | 0.22 |
rpoC | 766945 | c.3576A>C | synonymous_variant | 0.22 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.33 |
rpoC | 766983 | p.Pro1205Gln | missense_variant | 0.2 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.22 |
rpoC | 767002 | c.3633G>C | synonymous_variant | 0.22 |
rpoC | 767008 | c.3639G>A | synonymous_variant | 0.25 |
rpoC | 767023 | c.3654C>T | synonymous_variant | 0.22 |
rpoC | 767044 | c.3675G>C | synonymous_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775835 | c.2646C>A | synonymous_variant | 0.2 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776639 | c.1842C>T | synonymous_variant | 0.17 |
mmpL5 | 776747 | p.Phe578Leu | missense_variant | 0.13 |
mmpL5 | 777655 | p.Asp276Tyr | missense_variant | 0.13 |
mmpL5 | 778282 | p.Asp67Tyr | missense_variant | 0.15 |
mmpL5 | 779172 | c.-692C>T | upstream_gene_variant | 0.25 |
mmpL5 | 779436 | c.-956G>A | upstream_gene_variant | 0.15 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 0.94 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781684 | p.Pro42Gln | missense_variant | 0.17 |
rpsL | 781762 | p.Pro68His | missense_variant | 0.12 |
rpsL | 781897 | p.Ala113Glu | missense_variant | 0.15 |
rplC | 800703 | c.-106_-104delTTGinsCTC | upstream_gene_variant | 0.13 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.12 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.13 |
rplC | 800735 | c.-74C>G | upstream_gene_variant | 0.13 |
fbiC | 1303207 | p.Pro93Ser | missense_variant | 0.18 |
fbiC | 1303216 | c.286C>A | synonymous_variant | 0.15 |
fbiC | 1303417 | p.Gly163Cys | missense_variant | 0.17 |
fbiC | 1303711 | p.Val261Ile | missense_variant | 0.12 |
fbiC | 1304335 | p.Ala469Ser | missense_variant | 0.2 |
fbiC | 1304592 | p.Phe554Leu | missense_variant | 0.12 |
fbiC | 1304623 | p.Cys565Gly | missense_variant | 0.13 |
fbiC | 1304640 | c.1710A>C | synonymous_variant | 0.11 |
fbiC | 1304646 | c.1716T>C | synonymous_variant | 0.11 |
fbiC | 1304676 | c.1746A>C | synonymous_variant | 0.1 |
fbiC | 1304819 | p.Val630Ala | missense_variant | 0.11 |
fbiC | 1304938 | p.Glu670* | stop_gained | 0.25 |
fbiC | 1304985 | c.2055G>T | synonymous_variant | 0.2 |
fbiC | 1305407 | p.Ser826Leu | missense_variant | 0.33 |
Rv1258c | 1406292 | p.Gly350Val | missense_variant | 0.17 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1407227 | p.Glu38Asp | missense_variant | 0.22 |
embR | 1416759 | p.Leu197Met | missense_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471670 | n.-176G>T | upstream_gene_variant | 0.13 |
rrs | 1471678 | n.-168A>G | upstream_gene_variant | 0.12 |
rrs | 1472111 | n.266C>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472848 | n.1003T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474585 | n.928G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474593 | n.936T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474622 | n.965G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474639 | n.982G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474640 | n.983C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475009 | n.1352G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475764 | n.2107A>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475766 | n.2109G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475775 | n.2118G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476392 | n.2735A>G | non_coding_transcript_exon_variant | 0.12 |
fabG1 | 1673344 | c.-96C>T | upstream_gene_variant | 0.12 |
inhA | 1674212 | p.Leu4Pro | missense_variant | 0.11 |
inhA | 1674737 | p.Ala179Asp | missense_variant | 0.2 |
inhA | 1674777 | c.576C>A | synonymous_variant | 0.13 |
inhA | 1674867 | p.Trp222Cys | missense_variant | 0.14 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.11 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.11 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.11 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.14 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.17 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.14 |
rpsA | 1834645 | c.1104C>T | synonymous_variant | 0.11 |
rpsA | 1834666 | c.1125G>C | synonymous_variant | 0.13 |
rpsA | 1834667 | p.Ala376Ser | missense_variant | 0.13 |
rpsA | 1834690 | c.1149T>C | synonymous_variant | 0.17 |
rpsA | 1834700 | p.Gln387* | stop_gained | 0.14 |
rpsA | 1834838 | p.Glu433* | stop_gained | 0.17 |
rpsA | 1834860 | p.Ala440Val | missense_variant | 0.2 |
rpsA | 1834896 | p.Ser452Ile | missense_variant | 0.14 |
rpsA | 1834958 | p.Leu473Met | missense_variant | 0.22 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918351 | p.Gly138Cys | missense_variant | 0.14 |
tlyA | 1918406 | p.Ser156* | stop_gained | 0.15 |
ndh | 2101699 | c.1344G>T | synonymous_variant | 0.17 |
ndh | 2101980 | p.Asn355Asp | missense_variant | 0.17 |
ndh | 2102281 | c.762C>T | synonymous_variant | 0.13 |
ndh | 2102302 | c.741G>C | synonymous_variant | 0.18 |
ndh | 2102305 | p.Gly246Ser | missense_variant | 0.18 |
ndh | 2102308 | c.735G>C | synonymous_variant | 0.17 |
ndh | 2102320 | c.723G>C | synonymous_variant | 0.15 |
ndh | 2103191 | c.-149G>T | upstream_gene_variant | 0.14 |
katG | 2154642 | c.1470C>A | synonymous_variant | 0.12 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2154827 | p.Pro429Thr | missense_variant | 0.12 |
katG | 2154904 | p.Glu403Val | missense_variant | 0.17 |
katG | 2155723 | p.Ala130Val | missense_variant | 0.18 |
katG | 2155879 | p.Arg78Leu | missense_variant | 0.4 |
katG | 2156430 | c.-319G>T | upstream_gene_variant | 0.2 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169101 | c.1512G>T | synonymous_variant | 0.13 |
PPE35 | 2169607 | p.Asn336Asp | missense_variant | 0.11 |
PPE35 | 2169634 | p.Ala327Thr | missense_variant | 0.12 |
PPE35 | 2170262 | c.351C>T | synonymous_variant | 0.22 |
PPE35 | 2170583 | c.30C>A | synonymous_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289884 | c.-643G>T | upstream_gene_variant | 0.14 |
pncA | 2290131 | c.-890G>A | upstream_gene_variant | 0.14 |
kasA | 2518084 | c.-31A>G | upstream_gene_variant | 0.12 |
kasA | 2518487 | p.Ser125Arg | missense_variant | 0.13 |
kasA | 2518675 | p.Met187Ile | missense_variant | 0.17 |
kasA | 2518805 | p.Asp231Tyr | missense_variant | 0.14 |
kasA | 2519225 | p.Leu371Met | missense_variant | 0.22 |
kasA | 2519272 | c.1158C>T | synonymous_variant | 0.15 |
kasA | 2519364 | c.1250G>A | splice_region_variant&stop_retained_variant | 0.17 |
eis | 2714287 | p.Ile349Thr | missense_variant | 0.11 |
eis | 2714544 | p.Glu263Asp | missense_variant | 0.15 |
eis | 2715532 | c.-200G>T | upstream_gene_variant | 0.2 |
eis | 2715557 | c.-225C>A | upstream_gene_variant | 0.25 |
folC | 2746432 | c.1167C>T | synonymous_variant | 0.14 |
folC | 2746436 | p.Asp388Gly | missense_variant | 0.12 |
folC | 2746758 | p.Gly281Ser | missense_variant | 0.14 |
folC | 2746867 | c.732G>T | synonymous_variant | 0.18 |
folC | 2746995 | p.Val202Ile | missense_variant | 0.13 |
folC | 2747033 | p.Ala189Glu | missense_variant | 0.12 |
pepQ | 2859558 | c.861C>A | synonymous_variant | 0.13 |
pepQ | 2860262 | p.Val53Leu | missense_variant | 0.2 |
pepQ | 2860589 | c.-171G>T | upstream_gene_variant | 0.14 |
ribD | 2986916 | c.78C>T | synonymous_variant | 0.17 |
ribD | 2986997 | c.159T>G | synonymous_variant | 0.12 |
ribD | 2987027 | c.189C>A | synonymous_variant | 0.15 |
ribD | 2987048 | c.210C>A | synonymous_variant | 0.12 |
ribD | 2987134 | p.Gly99Val | missense_variant | 0.18 |
ribD | 2987537 | p.Gln233His | missense_variant | 0.15 |
Rv2752c | 3065129 | c.1063C>T | synonymous_variant | 0.96 |
Rv2752c | 3065496 | c.696G>C | synonymous_variant | 0.15 |
Rv2752c | 3065948 | p.Gly82Trp | missense_variant | 0.12 |
thyX | 3067340 | p.Glu202Asp | missense_variant | 0.2 |
thyA | 3074048 | p.Ala142Ser | missense_variant | 0.12 |
thyA | 3074430 | c.42G>T | synonymous_variant | 0.15 |
thyA | 3074435 | p.Glu13* | stop_gained | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086848 | p.Lys10Arg | missense_variant | 0.18 |
fbiD | 3339112 | c.-6G>T | upstream_gene_variant | 0.25 |
fbiD | 3339556 | p.Gly147Cys | missense_variant | 0.2 |
fbiD | 3339628 | p.Arg171Ser | missense_variant | 0.4 |
Rv3083 | 3448642 | c.139T>C | synonymous_variant | 0.18 |
Rv3083 | 3448874 | p.Ala124Glu | missense_variant | 0.17 |
Rv3083 | 3449063 | p.Ala187Glu | missense_variant | 0.2 |
fprA | 3473860 | c.-146delT | upstream_gene_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474000 | c.-7C>A | upstream_gene_variant | 0.18 |
fprA | 3474594 | c.588C>A | synonymous_variant | 0.13 |
fprA | 3474862 | p.Arg286Trp | missense_variant | 0.15 |
fprA | 3475043 | p.Gly346Asp | missense_variant | 0.22 |
fprA | 3475090 | p.Arg362Cys | missense_variant | 0.22 |
fprA | 3475182 | c.1176C>T | synonymous_variant | 0.18 |
fprA | 3475196 | p.Ser397Ile | missense_variant | 0.18 |
Rv3236c | 3612037 | p.Phe360Leu | missense_variant | 1.0 |
Rv3236c | 3612427 | c.690G>A | synonymous_variant | 0.13 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiA | 3640538 | c.-5G>A | upstream_gene_variant | 0.17 |
fbiA | 3640913 | p.Pro124His | missense_variant | 0.12 |
fbiA | 3641161 | p.Asp207Tyr | missense_variant | 0.18 |
fbiB | 3641382 | c.-153C>T | upstream_gene_variant | 0.25 |
fbiB | 3641807 | c.273C>A | synonymous_variant | 0.14 |
fbiB | 3642037 | p.Ala168Asp | missense_variant | 0.33 |
fbiB | 3642125 | p.Glu197Asp | missense_variant | 0.15 |
fbiB | 3642416 | c.882G>T | synonymous_variant | 0.15 |
alr | 3840430 | p.Asn331Tyr | missense_variant | 0.14 |
alr | 3840689 | c.732C>A | synonymous_variant | 0.22 |
rpoA | 3877524 | c.984C>A | synonymous_variant | 0.12 |
rpoA | 3877542 | c.966C>A | synonymous_variant | 0.12 |
rpoA | 3877545 | c.963G>T | synonymous_variant | 0.14 |
rpoA | 3877554 | c.954G>A | synonymous_variant | 0.13 |
rpoA | 3877560 | c.948C>T | synonymous_variant | 0.13 |
rpoA | 3877563 | c.945C>T | synonymous_variant | 0.14 |
rpoA | 3877569 | p.Pro313Thr | missense_variant | 0.17 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.11 |
rpoA | 3877638 | c.870T>C | synonymous_variant | 0.12 |
rpoA | 3877656 | c.852T>G | synonymous_variant | 0.12 |
rpoA | 3877729 | p.Ser260Tyr | missense_variant | 0.14 |
rpoA | 3877763 | p.Leu249Met | missense_variant | 0.17 |
rpoA | 3877765 | p.Ala248Val | missense_variant | 0.17 |
rpoA | 3878142 | p.Gly122Asp | missense_variant | 0.14 |
rpoA | 3878160 | c.348C>G | synonymous_variant | 0.18 |
rpoA | 3878163 | c.345C>T | synonymous_variant | 0.18 |
rpoA | 3878169 | c.339G>C | synonymous_variant | 0.18 |
rpoA | 3878184 | c.324C>T | synonymous_variant | 0.18 |
ddn | 3986949 | p.Gly36Arg | missense_variant | 0.11 |
ddn | 3987045 | p.Arg68Cys | missense_variant | 0.12 |
clpC1 | 4038354 | p.Gln784Leu | missense_variant | 0.15 |
clpC1 | 4038526 | p.Ile727Val | missense_variant | 0.14 |
clpC1 | 4039044 | p.Pro554Gln | missense_variant | 0.15 |
clpC1 | 4039085 | c.1620A>G | synonymous_variant | 0.17 |
clpC1 | 4039091 | c.1614G>T | synonymous_variant | 0.17 |
clpC1 | 4039097 | c.1608G>T | synonymous_variant | 0.17 |
clpC1 | 4039103 | c.1602T>C | synonymous_variant | 0.17 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.14 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.21 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.21 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.19 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.17 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.17 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.18 |
clpC1 | 4039190 | c.1515C>T | synonymous_variant | 0.18 |
clpC1 | 4039196 | c.1509G>A | synonymous_variant | 0.14 |
clpC1 | 4039199 | p.Ala502Glu | missense_variant | 0.14 |
clpC1 | 4039208 | c.1497C>G | synonymous_variant | 0.14 |
clpC1 | 4039220 | c.1485G>C | synonymous_variant | 0.14 |
clpC1 | 4039625 | p.Lys360Asn | missense_variant | 0.17 |
clpC1 | 4039882 | p.Glu275Gln | missense_variant | 0.33 |
clpC1 | 4039890 | p.Val272Ala | missense_variant | 0.25 |
clpC1 | 4039913 | c.792C>T | synonymous_variant | 0.31 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.31 |
clpC1 | 4039934 | c.771G>C | synonymous_variant | 0.29 |
clpC1 | 4039943 | c.762G>C | synonymous_variant | 0.15 |
clpC1 | 4039946 | c.759A>G | synonymous_variant | 0.12 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.13 |
clpC1 | 4039957 | c.748C>T | synonymous_variant | 0.13 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.13 |
clpC1 | 4039964 | c.741C>G | synonymous_variant | 0.11 |
clpC1 | 4040779 | c.-75C>T | upstream_gene_variant | 0.14 |
panD | 4044059 | p.Ala75Thr | missense_variant | 0.14 |
panD | 4044155 | p.Gln43* | stop_gained | 0.12 |
panD | 4044232 | p.Cys17His | missense_variant | 0.17 |
panD | 4044234 | c.48C>G | synonymous_variant | 0.14 |
panD | 4044249 | c.33C>T | synonymous_variant | 0.12 |
panD | 4044266 | p.Leu6Met | missense_variant | 0.13 |
panD | 4044388 | c.-107G>T | upstream_gene_variant | 0.12 |
embC | 4239898 | c.36C>A | synonymous_variant | 0.18 |
embC | 4239904 | c.42A>G | synonymous_variant | 0.18 |
embC | 4239958 | c.96C>T | synonymous_variant | 0.12 |
embC | 4240015 | c.153G>C | synonymous_variant | 0.14 |
embC | 4240916 | p.Ala352Ser | missense_variant | 0.2 |
embC | 4240963 | c.1101G>T | synonymous_variant | 0.2 |
embC | 4241042 | p.Asn394Asp | missense_variant | 0.12 |
embC | 4241259 | p.Arg466Leu | missense_variant | 0.15 |
embC | 4241924 | p.Arg688Gly | missense_variant | 0.12 |
embC | 4242175 | c.2313G>T | synonymous_variant | 0.25 |
embC | 4242459 | p.Ser866Leu | missense_variant | 0.17 |
embC | 4242536 | p.Asp892Tyr | missense_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4243737 | p.Gln169* | stop_gained | 0.22 |
embA | 4243779 | p.Pro183Ser | missense_variant | 0.15 |
embA | 4243893 | p.Leu221Met | missense_variant | 0.13 |
embA | 4244903 | c.1671G>T | synonymous_variant | 0.67 |
embA | 4244941 | p.Trp570Leu | missense_variant | 0.2 |
embA | 4244966 | c.1734C>T | synonymous_variant | 0.2 |
embA | 4244976 | p.Gly582Arg | missense_variant | 0.2 |
embA | 4245090 | p.Gly620Ser | missense_variant | 0.12 |
embA | 4245456 | p.Glu742Lys | missense_variant | 0.5 |
embA | 4245558 | p.Gly776Cys | missense_variant | 0.13 |
embB | 4245713 | c.-801G>T | upstream_gene_variant | 0.29 |
embB | 4245716 | c.-798G>A | upstream_gene_variant | 0.29 |
embA | 4245966 | p.Phe912Leu | missense_variant | 0.13 |
embA | 4246096 | p.Ala955Asp | missense_variant | 0.22 |
embA | 4246146 | p.Gly972Arg | missense_variant | 0.18 |
embB | 4247695 | c.1182G>T | synonymous_variant | 0.4 |
embB | 4247790 | p.Ser426Ile | missense_variant | 0.22 |
embB | 4248045 | p.Lys511Arg | missense_variant | 0.12 |
embB | 4248321 | p.Gly603Val | missense_variant | 0.33 |
embB | 4248762 | p.Ala750Val | missense_variant | 0.2 |
embB | 4249037 | p.Val842Ile | missense_variant | 0.2 |
embB | 4249041 | p.Pro843Gln | missense_variant | 0.2 |
embB | 4249260 | p.Met916Thr | missense_variant | 0.13 |
embB | 4249340 | p.Ala943Ser | missense_variant | 0.12 |
embB | 4249683 | p.Trp1057* | stop_gained | 0.25 |
aftB | 4267409 | c.1428C>A | synonymous_variant | 0.13 |
aftB | 4267505 | p.Asn444Lys | missense_variant | 0.22 |
aftB | 4267518 | p.Thr440Lys | missense_variant | 0.29 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4267786 | p.Gly351Trp | missense_variant | 0.17 |
aftB | 4267977 | p.Pro287Gln | missense_variant | 0.2 |
aftB | 4268295 | p.Cys181Phe | missense_variant | 0.17 |
aftB | 4268302 | p.Ala179Ser | missense_variant | 0.17 |
aftB | 4268477 | c.360C>G | synonymous_variant | 0.12 |
aftB | 4268527 | c.310C>A | synonymous_variant | 0.15 |
aftB | 4268551 | p.Val96Leu | missense_variant | 0.12 |
aftB | 4268695 | p.Val48Ile | missense_variant | 0.13 |
aftB | 4269783 | c.-947G>T | upstream_gene_variant | 0.12 |
ubiA | 4269809 | p.Pro9Ser | missense_variant | 0.17 |
ethA | 4326676 | p.Ser266Arg | missense_variant | 0.9 |
ethA | 4326870 | p.Val202Phe | missense_variant | 0.12 |
ethA | 4327905 | c.-432C>T | upstream_gene_variant | 0.14 |
ethR | 4328096 | p.Leu183Arg | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 0.93 |
gid | 4407557 | c.639_645delAGGGTCG | frameshift_variant | 0.13 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407854 | p.Gly117Trp | missense_variant | 0.2 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |