Run ID: SRR069978
Sample name:
Date: 02-04-2023 14:18:09
Number of reads: 1711216
Percentage reads mapped: 76.54
Strain: lineage2.2.2
Drug-resistance: Pre-XDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.98 |
lineage2.2.2 | East-Asian (Beijing) | Beijing-RD105/RD207 | RD105;RD207 | 0.94 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7570 | p.Ala90Val | missense_variant | 0.9 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761098 | p.Ser431Thr | missense_variant | 0.13 | rifampicin |
rrs | 1472307 | n.462C>T | non_coding_transcript_exon_variant | 0.27 | streptomycin |
katG | 2155108 | c.1002_1003dupGA | frameshift_variant | 0.97 | isoniazid |
kasA | 2518310 | p.Asp66Asn | missense_variant | 1.0 | isoniazid |
embB | 4247448 | p.His312Arg | missense_variant | 0.17 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7710 | c.409T>C | synonymous_variant | 0.17 |
gyrA | 7715 | c.414G>C | synonymous_variant | 0.18 |
gyrA | 7728 | c.427_429delAGGinsCGC | synonymous_variant | 0.16 |
gyrA | 7859 | c.558A>C | synonymous_variant | 0.13 |
gyrA | 8111 | c.810G>C | synonymous_variant | 0.14 |
gyrA | 8156 | c.855T>C | synonymous_variant | 0.17 |
gyrA | 8168 | c.867A>G | synonymous_variant | 0.17 |
gyrA | 8174 | c.873C>G | synonymous_variant | 0.15 |
gyrA | 8177 | c.876A>C | synonymous_variant | 0.15 |
gyrA | 8619 | c.1318T>C | synonymous_variant | 0.14 |
gyrA | 8624 | c.1323G>C | synonymous_variant | 0.15 |
gyrA | 8627 | c.1326C>G | synonymous_variant | 0.2 |
gyrA | 8636 | c.1335A>C | synonymous_variant | 0.15 |
gyrA | 8645 | c.1344C>G | synonymous_variant | 0.14 |
gyrA | 8852 | c.1551T>C | synonymous_variant | 0.15 |
gyrA | 8867 | c.1566A>G | synonymous_variant | 0.15 |
gyrA | 8870 | c.1569G>C | synonymous_variant | 0.15 |
gyrA | 8873 | c.1572A>C | synonymous_variant | 0.15 |
gyrA | 8897 | c.1596T>C | synonymous_variant | 0.15 |
gyrA | 8903 | c.1602T>C | synonymous_variant | 0.16 |
gyrA | 8918 | c.1617C>G | synonymous_variant | 0.18 |
gyrA | 8966 | c.1665C>G | synonymous_variant | 0.17 |
gyrA | 8967 | p.Ala556Arg | missense_variant | 0.16 |
gyrA | 8987 | c.1686C>G | synonymous_variant | 0.14 |
gyrA | 8990 | c.1689C>G | synonymous_variant | 0.13 |
gyrA | 8996 | c.1695T>C | synonymous_variant | 0.14 |
gyrA | 8998 | p.Leu566Trp | missense_variant | 0.14 |
gyrA | 9191 | c.1890G>C | synonymous_variant | 0.13 |
gyrA | 9200 | c.1899A>G | synonymous_variant | 0.19 |
gyrA | 9204 | p.Ser635Thr | missense_variant | 0.19 |
gyrA | 9227 | c.1926C>G | synonymous_variant | 0.15 |
gyrA | 9230 | c.1929T>C | synonymous_variant | 0.15 |
gyrA | 9233 | c.1932C>T | synonymous_variant | 0.15 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9323 | c.2022C>G | synonymous_variant | 0.16 |
gyrA | 9335 | c.2034G>C | synonymous_variant | 0.15 |
gyrA | 9345 | c.2044A>C | synonymous_variant | 0.14 |
fgd1 | 490851 | c.69A>C | synonymous_variant | 0.18 |
fgd1 | 490887 | c.105G>C | synonymous_variant | 0.25 |
fgd1 | 490902 | c.120T>C | synonymous_variant | 0.16 |
fgd1 | 490905 | c.123T>C | synonymous_variant | 0.17 |
fgd1 | 490911 | c.129T>G | synonymous_variant | 0.13 |
fgd1 | 491286 | c.504G>C | synonymous_variant | 0.19 |
fgd1 | 491292 | c.510G>C | synonymous_variant | 0.14 |
fgd1 | 491319 | c.537G>C | synonymous_variant | 0.3 |
fgd1 | 491331 | c.549G>A | synonymous_variant | 0.23 |
fgd1 | 491583 | c.801G>A | synonymous_variant | 0.15 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575746 | c.399C>G | synonymous_variant | 0.14 |
mshA | 575767 | c.420G>A | synonymous_variant | 0.26 |
mshA | 575771 | p.Val142Ser | missense_variant | 0.26 |
mshA | 575779 | c.432A>G | synonymous_variant | 0.32 |
mshA | 575821 | c.474G>C | synonymous_variant | 0.36 |
mshA | 575824 | c.477T>G | synonymous_variant | 0.36 |
mshA | 575864 | c.517T>C | synonymous_variant | 0.19 |
ccsA | 619947 | c.57C>G | synonymous_variant | 0.19 |
ccsA | 619953 | c.63C>G | synonymous_variant | 0.23 |
ccsA | 619969 | p.Val27Ile | missense_variant | 0.16 |
ccsA | 619989 | c.99G>C | synonymous_variant | 0.15 |
ccsA | 620445 | c.555A>G | synonymous_variant | 0.14 |
ccsA | 620778 | c.888T>C | synonymous_variant | 0.18 |
ccsA | 620784 | c.894C>G | synonymous_variant | 0.21 |
ccsA | 620787 | c.897C>G | synonymous_variant | 0.21 |
ccsA | 620809 | c.919C>T | synonymous_variant | 0.28 |
ccsA | 620829 | c.939G>C | synonymous_variant | 0.21 |
ccsA | 620835 | c.945C>G | synonymous_variant | 0.14 |
ccsA | 620838 | c.948C>T | synonymous_variant | 0.15 |
ccsA | 620844 | c.954C>T | synonymous_variant | 0.16 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.16 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.16 |
rpoB | 760328 | c.522G>C | synonymous_variant | 0.14 |
rpoB | 760331 | c.525G>C | synonymous_variant | 0.13 |
rpoB | 760337 | c.531C>G | synonymous_variant | 0.15 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.15 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.29 |
rpoB | 760418 | c.612G>C | synonymous_variant | 0.32 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.32 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.3 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.17 |
rpoB | 760634 | c.828T>C | synonymous_variant | 0.15 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.15 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.21 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.18 |
rpoB | 760670 | c.864G>C | synonymous_variant | 0.13 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.13 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.15 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.17 |
rpoB | 760869 | p.Val355Ile | missense_variant | 0.14 |
rpoB | 760886 | c.1080A>G | synonymous_variant | 0.15 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.13 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 0.14 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.16 |
rpoB | 760970 | c.1164G>C | synonymous_variant | 0.18 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.23 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.23 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.17 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.19 |
rpoB | 761183 | c.1377T>G | synonymous_variant | 0.18 |
rpoB | 761189 | c.1383T>G | synonymous_variant | 0.16 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.17 |
rpoB | 761297 | c.1491C>T | synonymous_variant | 0.17 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.25 |
rpoB | 761360 | c.1554T>C | synonymous_variant | 0.25 |
rpoB | 761362 | p.Ser519Thr | missense_variant | 0.26 |
rpoB | 761373 | p.Val523Gln | missense_variant | 0.13 |
rpoB | 761492 | c.1686G>C | synonymous_variant | 0.18 |
rpoB | 761510 | c.1704T>C | synonymous_variant | 0.24 |
rpoB | 761531 | c.1725C>G | synonymous_variant | 0.19 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.18 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.22 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.26 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.21 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.15 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.14 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.15 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.16 |
rpoB | 761885 | c.2079T>C | synonymous_variant | 0.14 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.21 |
rpoB | 761954 | c.2148C>G | synonymous_variant | 0.21 |
rpoB | 761969 | c.2163G>A | synonymous_variant | 0.21 |
rpoB | 761999 | c.2193G>C | synonymous_variant | 0.24 |
rpoB | 762008 | c.2202C>G | synonymous_variant | 0.15 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.13 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.15 |
rpoB | 762218 | c.2412T>G | synonymous_variant | 0.24 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.23 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.22 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.22 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.19 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.17 |
rpoB | 762329 | c.2523G>C | synonymous_variant | 0.17 |
rpoB | 762338 | c.2532T>C | synonymous_variant | 0.15 |
rpoC | 762404 | c.-966T>C | upstream_gene_variant | 0.12 |
rpoC | 762836 | c.-534C>G | upstream_gene_variant | 0.18 |
rpoC | 762857 | c.-513C>G | upstream_gene_variant | 0.2 |
rpoC | 762860 | c.-510G>C | upstream_gene_variant | 0.18 |
rpoC | 762863 | c.-507T>C | upstream_gene_variant | 0.19 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.25 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.19 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.19 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.23 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.23 |
rpoC | 763076 | c.-294C>G | upstream_gene_variant | 0.26 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.26 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.16 |
rpoC | 763226 | c.-144A>G | upstream_gene_variant | 0.16 |
rpoC | 763238 | c.-132T>C | upstream_gene_variant | 0.19 |
rpoC | 763268 | c.-102C>G | upstream_gene_variant | 0.17 |
rpoC | 763402 | c.33C>G | synonymous_variant | 0.16 |
rpoC | 763411 | c.42T>G | synonymous_variant | 0.16 |
rpoC | 763414 | c.45T>C | synonymous_variant | 0.15 |
rpoC | 763441 | c.72C>G | synonymous_variant | 0.17 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.19 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.16 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.19 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.19 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.24 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.27 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.2 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.25 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.17 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.19 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.15 |
rpoC | 764040 | p.Ser224Asn | missense_variant | 0.14 |
rpoC | 764044 | c.675T>C | synonymous_variant | 0.16 |
rpoC | 764059 | c.690G>C | synonymous_variant | 0.18 |
rpoC | 764083 | c.714A>G | synonymous_variant | 0.21 |
rpoC | 764098 | c.729A>G | synonymous_variant | 0.2 |
rpoC | 764101 | c.732C>G | synonymous_variant | 0.17 |
rpoC | 764110 | c.741C>T | synonymous_variant | 0.14 |
rpoC | 764131 | c.762T>C | synonymous_variant | 0.13 |
rpoC | 764257 | c.888G>C | synonymous_variant | 0.21 |
rpoC | 764266 | c.897T>C | synonymous_variant | 0.22 |
rpoC | 764269 | c.900G>C | synonymous_variant | 0.26 |
rpoC | 764282 | c.913_915delTCGinsAGC | synonymous_variant | 0.24 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.25 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 0.14 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.2 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.16 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.15 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.17 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.16 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.14 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.14 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.14 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.24 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.2 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.14 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.14 |
rpoC | 764695 | c.1326T>C | synonymous_variant | 0.24 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.26 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.25 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.23 |
rpoC | 764791 | c.1422C>G | synonymous_variant | 0.18 |
rpoC | 765330 | p.Ser654Asn | missense_variant | 0.14 |
rpoC | 765349 | c.1980T>C | synonymous_variant | 0.22 |
rpoC | 765352 | c.1983G>C | synonymous_variant | 0.29 |
rpoC | 765383 | p.Met672Leu | missense_variant | 0.33 |
rpoC | 765404 | p.Leu679Val | missense_variant | 0.25 |
rpoC | 765409 | c.2040T>C | synonymous_variant | 0.27 |
rpoC | 765412 | c.2043T>C | synonymous_variant | 0.28 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.17 |
rpoC | 765451 | c.2082C>G | synonymous_variant | 0.22 |
rpoC | 765452 | p.Ala695Ser | missense_variant | 0.23 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.23 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.24 |
rpoC | 765508 | c.2139C>G | synonymous_variant | 0.19 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.29 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.25 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.22 |
rpoC | 765559 | c.2190G>C | synonymous_variant | 0.24 |
rpoC | 765578 | c.2209C>T | synonymous_variant | 0.28 |
rpoC | 765583 | c.2214G>T | synonymous_variant | 0.2 |
rpoC | 765613 | p.His748Gln | missense_variant | 0.14 |
rpoC | 765811 | c.2442T>C | synonymous_variant | 0.13 |
rpoC | 765814 | c.2445A>G | synonymous_variant | 0.14 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 0.14 |
rpoC | 765883 | c.2514C>G | synonymous_variant | 0.12 |
rpoC | 765928 | c.2559C>G | synonymous_variant | 0.19 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.2 |
rpoC | 765985 | c.2616C>T | synonymous_variant | 0.13 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.14 |
rpoC | 766096 | c.2727G>C | synonymous_variant | 0.17 |
rpoC | 766105 | c.2736C>T | synonymous_variant | 0.19 |
rpoC | 766141 | c.2772C>T | synonymous_variant | 0.15 |
rpoC | 766142 | c.2773C>T | synonymous_variant | 0.13 |
rpoC | 766543 | c.3174C>T | synonymous_variant | 0.18 |
rpoC | 766549 | c.3180G>C | synonymous_variant | 0.21 |
rpoC | 766573 | c.3204T>C | synonymous_variant | 0.2 |
rpoC | 766583 | p.Gly1072Ser | missense_variant | 0.16 |
rpoC | 766588 | c.3219G>A | synonymous_variant | 0.16 |
rpoC | 766591 | c.3222A>G | synonymous_variant | 0.2 |
rpoC | 766607 | p.Ile1080Leu | missense_variant | 0.19 |
rpoC | 766630 | c.3261G>C | synonymous_variant | 0.18 |
rpoC | 766645 | c.3276A>G | synonymous_variant | 0.17 |
rpoC | 766651 | c.3282T>C | synonymous_variant | 0.18 |
rpoC | 766657 | c.3288A>G | synonymous_variant | 0.17 |
rpoC | 766672 | c.3303T>C | synonymous_variant | 0.21 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.18 |
rpoC | 766738 | c.3369G>T | synonymous_variant | 0.16 |
rpoC | 766750 | c.3381C>G | synonymous_variant | 0.15 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 0.14 |
rpoC | 766864 | c.3495G>C | synonymous_variant | 0.15 |
rpoC | 766918 | c.3549C>T | synonymous_variant | 0.13 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.15 |
rpoC | 767074 | c.3705T>C | synonymous_variant | 0.14 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.22 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.21 |
rpoC | 767134 | c.3765C>G | synonymous_variant | 0.19 |
rpoC | 767191 | c.3822C>G | synonymous_variant | 0.16 |
rpoC | 767206 | c.3837C>G | synonymous_variant | 0.17 |
rpoC | 767209 | c.3840T>C | synonymous_variant | 0.17 |
rpoC | 767212 | c.3843G>C | synonymous_variant | 0.16 |
rpoC | 767221 | c.3852C>G | synonymous_variant | 0.16 |
rpoC | 767230 | c.3861G>C | synonymous_variant | 0.15 |
rpoC | 767233 | c.3864T>C | synonymous_variant | 0.17 |
rpoC | 767263 | c.3894T>C | synonymous_variant | 0.13 |
rpoC | 767264 | p.Ala1299Gln | missense_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775909 | p.Leu858Phe | missense_variant | 0.15 |
mmpL5 | 775916 | c.2565T>G | synonymous_variant | 0.17 |
mmpL5 | 775937 | c.2544G>C | synonymous_variant | 0.15 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776706 | p.Tyr592Phe | missense_variant | 0.17 |
mmpL5 | 776708 | c.1773C>T | synonymous_variant | 0.15 |
mmpL5 | 776717 | c.1764A>G | synonymous_variant | 0.14 |
mmpL5 | 776741 | c.1740C>G | synonymous_variant | 0.14 |
mmpL5 | 776744 | c.1737C>G | synonymous_variant | 0.23 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781631 | c.72G>C | synonymous_variant | 0.17 |
rpsL | 781649 | c.90T>C | synonymous_variant | 0.15 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.19 |
rpsL | 781682 | c.123T>C | synonymous_variant | 0.18 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.16 |
rpsL | 781793 | c.234G>C | synonymous_variant | 0.29 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.24 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.27 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.16 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.15 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.21 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.2 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.15 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.28 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.26 |
rplC | 800648 | c.-161A>C | upstream_gene_variant | 0.17 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.19 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.14 |
rplC | 800844 | c.36T>C | synonymous_variant | 0.17 |
rplC | 800865 | c.57A>G | synonymous_variant | 0.21 |
rplC | 800867 | p.Ser20Asn | missense_variant | 0.19 |
rplC | 800874 | c.66A>G | synonymous_variant | 0.2 |
rplC | 800877 | c.69A>C | synonymous_variant | 0.17 |
rplC | 800880 | c.72A>G | synonymous_variant | 0.17 |
fbiC | 1303818 | c.888C>G | synonymous_variant | 0.17 |
fbiC | 1303836 | c.906G>C | synonymous_variant | 0.17 |
fbiC | 1303845 | c.915C>G | synonymous_variant | 0.17 |
fbiC | 1303846 | p.Phe306Val | missense_variant | 0.18 |
fbiC | 1303854 | c.924T>C | synonymous_variant | 0.29 |
fbiC | 1303860 | c.930A>C | synonymous_variant | 0.29 |
fbiC | 1303881 | c.951G>C | synonymous_variant | 0.31 |
fbiC | 1303884 | c.954T>G | synonymous_variant | 0.31 |
fbiC | 1303911 | c.981G>C | synonymous_variant | 0.21 |
fbiC | 1303981 | p.Val351Ile | missense_variant | 0.19 |
fbiC | 1303995 | c.1065C>T | synonymous_variant | 0.29 |
fbiC | 1304001 | c.1071C>G | synonymous_variant | 0.2 |
fbiC | 1304008 | c.1078T>C | synonymous_variant | 0.19 |
fbiC | 1304034 | c.1104A>G | synonymous_variant | 0.2 |
fbiC | 1304040 | c.1110C>G | synonymous_variant | 0.2 |
fbiC | 1304046 | c.1116C>G | synonymous_variant | 0.15 |
fbiC | 1304049 | c.1119T>G | synonymous_variant | 0.17 |
fbiC | 1304080 | p.Ala384Ser | missense_variant | 0.18 |
fbiC | 1304091 | p.Asp387Glu | missense_variant | 0.18 |
fbiC | 1304092 | p.Met388Leu | missense_variant | 0.18 |
fbiC | 1304097 | c.1167G>C | synonymous_variant | 0.17 |
fbiC | 1304136 | c.1206C>T | synonymous_variant | 0.22 |
fbiC | 1304203 | c.1276delC | frameshift_variant | 0.2 |
fbiC | 1304715 | c.1785G>C | synonymous_variant | 0.18 |
fbiC | 1304724 | c.1794A>G | synonymous_variant | 0.25 |
fbiC | 1304727 | c.1797A>G | synonymous_variant | 0.25 |
fbiC | 1304742 | c.1812T>C | synonymous_variant | 0.19 |
fbiC | 1304748 | c.1818T>C | synonymous_variant | 0.16 |
fbiC | 1304754 | c.1824G>A | synonymous_variant | 0.16 |
fbiC | 1304757 | c.1827A>G | synonymous_variant | 0.19 |
fbiC | 1304808 | c.1878C>G | synonymous_variant | 0.16 |
fbiC | 1304811 | c.1881C>G | synonymous_variant | 0.15 |
fbiC | 1304817 | c.1887T>C | synonymous_variant | 0.14 |
fbiC | 1305303 | c.2373T>C | synonymous_variant | 0.14 |
fbiC | 1305311 | p.Arg794Gln | missense_variant | 0.16 |
fbiC | 1305381 | c.2451G>C | synonymous_variant | 0.16 |
fbiC | 1305397 | p.Glu823Gln | missense_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 0.35 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.32 |
rrs | 1471969 | n.124T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472028 | n.183A>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472030 | n.185G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472031 | n.186G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472034 | n.189T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472044 | n.199G>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1473756 | n.99G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1473813 | n.156C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1473839 | n.182G>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474009 | n.352A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474012 | n.355C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474051 | n.394T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474054 | n.397T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474056 | n.399T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474104 | n.447G>A | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474111 | n.454T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474112 | n.455T>A | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474376 | n.719T>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474904 | n.1247G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474956 | n.1299C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474959 | n.1302C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474962 | n.1306delG | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474970 | n.1313G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474991 | n.1334T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475006 | n.1349A>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475088 | n.1431A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475199 | n.1542G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475206 | n.1549C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475291 | n.1634A>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475313 | n.1656G>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475333 | n.1676T>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475369 | n.1712G>C | non_coding_transcript_exon_variant | 0.34 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475638 | n.1981C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475659 | n.2002G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476034 | n.2377C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476689 | n.3032A>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476716 | n.3059A>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476723 | n.3066T>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476725 | n.3068C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476726 | n.3069A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476732 | n.3075T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476755 | n.3098G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476759 | n.3102T>C | non_coding_transcript_exon_variant | 0.18 |
inhA | 1673646 | c.-556T>C | upstream_gene_variant | 0.24 |
inhA | 1673658 | c.-544G>A | upstream_gene_variant | 0.24 |
inhA | 1673660 | c.-542C>A | upstream_gene_variant | 0.24 |
inhA | 1673664 | c.-538A>G | upstream_gene_variant | 0.25 |
inhA | 1673667 | c.-535A>G | upstream_gene_variant | 0.25 |
inhA | 1673679 | c.-523T>G | upstream_gene_variant | 0.23 |
inhA | 1674507 | c.306G>C | synonymous_variant | 0.18 |
inhA | 1674537 | c.336C>G | synonymous_variant | 0.16 |
inhA | 1674542 | p.Ala114Glu | missense_variant | 0.14 |
inhA | 1674549 | c.348G>C | synonymous_variant | 0.15 |
inhA | 1674555 | c.354G>A | synonymous_variant | 0.16 |
inhA | 1674561 | c.360C>T | synonymous_variant | 0.15 |
inhA | 1674624 | c.423A>C | synonymous_variant | 0.14 |
inhA | 1674639 | c.438C>T | synonymous_variant | 0.15 |
inhA | 1674654 | c.453G>C | synonymous_variant | 0.19 |
inhA | 1674693 | c.492C>G | synonymous_variant | 0.17 |
rpsA | 1833541 | c.-1T>C | upstream_gene_variant | 0.13 |
rpsA | 1833568 | c.27G>C | synonymous_variant | 0.16 |
rpsA | 1833589 | c.48A>T | synonymous_variant | 0.19 |
rpsA | 1833595 | c.54T>C | synonymous_variant | 0.21 |
rpsA | 1833619 | c.78A>C | synonymous_variant | 0.3 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.21 |
rpsA | 1833667 | c.126C>G | synonymous_variant | 0.21 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.27 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.25 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.29 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.39 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.34 |
rpsA | 1833790 | c.249T>A | synonymous_variant | 0.35 |
rpsA | 1833799 | c.258C>G | synonymous_variant | 0.35 |
rpsA | 1833811 | c.270G>C | synonymous_variant | 0.31 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.24 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.25 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.22 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.15 |
rpsA | 1833862 | c.321G>T | synonymous_variant | 0.17 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.21 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.39 |
rpsA | 1833940 | c.399C>G | synonymous_variant | 0.3 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.36 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.36 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.26 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.25 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.26 |
rpsA | 1834097 | p.Ser186Thr | missense_variant | 0.16 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834225 | c.684C>G | synonymous_variant | 0.15 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.16 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.22 |
rpsA | 1834261 | c.720A>C | synonymous_variant | 0.23 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.23 |
rpsA | 1834297 | c.756C>G | synonymous_variant | 0.27 |
rpsA | 1834303 | c.762T>G | synonymous_variant | 0.27 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.3 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.25 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.2 |
rpsA | 1834375 | c.834G>A | synonymous_variant | 0.21 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.19 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.15 |
rpsA | 1834558 | c.1017C>G | synonymous_variant | 0.15 |
rpsA | 1834669 | c.1128G>C | synonymous_variant | 0.16 |
rpsA | 1834688 | p.Ser383Cys | missense_variant | 0.13 |
rpsA | 1834753 | c.1212T>C | synonymous_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101915 | c.1128T>C | synonymous_variant | 0.15 |
ndh | 2101918 | c.1123_1125delAGGinsCGC | synonymous_variant | 0.16 |
ndh | 2101924 | c.1119T>G | synonymous_variant | 0.17 |
ndh | 2101939 | c.1104A>C | synonymous_variant | 0.23 |
ndh | 2101960 | c.1083A>G | synonymous_variant | 0.27 |
ndh | 2101966 | c.1077T>G | synonymous_variant | 0.29 |
ndh | 2101972 | c.1071G>C | synonymous_variant | 0.21 |
ndh | 2101978 | p.Asn355Asp | missense_variant | 0.26 |
ndh | 2101988 | p.Ala352Gly | missense_variant | 0.33 |
ndh | 2102009 | p.Ser345Asn | missense_variant | 0.25 |
ndh | 2102020 | c.1023A>G | synonymous_variant | 0.21 |
ndh | 2102023 | c.1020G>C | synonymous_variant | 0.21 |
ndh | 2102026 | c.1017G>C | synonymous_variant | 0.2 |
ndh | 2102050 | c.993T>C | synonymous_variant | 0.14 |
ndh | 2102242 | c.801G>A | synonymous_variant | 0.14 |
ndh | 2102305 | c.738T>C | synonymous_variant | 0.17 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155590 | c.522A>G | synonymous_variant | 0.14 |
katG | 2155614 | p.Val166Ile | missense_variant | 0.21 |
katG | 2155617 | c.495T>C | synonymous_variant | 0.21 |
katG | 2155632 | c.480A>C | synonymous_variant | 0.21 |
katG | 2155637 | p.Leu159Ile | missense_variant | 0.21 |
katG | 2155641 | p.Lys157Asn | missense_variant | 0.22 |
katG | 2155677 | c.435C>G | synonymous_variant | 0.21 |
katG | 2155680 | c.432G>C | synonymous_variant | 0.23 |
katG | 2155691 | c.421T>C | synonymous_variant | 0.22 |
katG | 2155695 | p.Ala139Val | missense_variant | 0.23 |
katG | 2155716 | c.396T>C | synonymous_variant | 0.14 |
katG | 2155719 | c.393G>C | synonymous_variant | 0.14 |
katG | 2155722 | c.390G>C | synonymous_variant | 0.15 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170330 | p.Ala95Thr | missense_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290015 | c.-774A>C | upstream_gene_variant | 0.16 |
pncA | 2290027 | c.-786G>A | upstream_gene_variant | 0.12 |
kasA | 2517947 | c.-168C>T | upstream_gene_variant | 0.26 |
kasA | 2517974 | c.-141T>C | upstream_gene_variant | 0.19 |
kasA | 2517989 | c.-126T>C | upstream_gene_variant | 0.16 |
kasA | 2518190 | p.Ser26Ala | missense_variant | 0.17 |
kasA | 2518199 | p.Ile29Val | missense_variant | 0.17 |
kasA | 2518222 | c.108G>A | synonymous_variant | 0.14 |
kasA | 2518223 | c.109_111delTTGinsCTC | synonymous_variant | 0.14 |
kasA | 2518234 | c.120G>A | synonymous_variant | 0.13 |
kasA | 2518519 | c.405G>C | synonymous_variant | 0.2 |
kasA | 2518528 | c.414C>G | synonymous_variant | 0.2 |
kasA | 2518540 | c.426T>G | synonymous_variant | 0.25 |
kasA | 2518561 | c.447T>C | synonymous_variant | 0.13 |
kasA | 2518591 | c.477G>C | synonymous_variant | 0.13 |
kasA | 2518687 | c.573C>T | synonymous_variant | 0.14 |
kasA | 2518696 | c.582C>G | synonymous_variant | 0.14 |
kasA | 2518702 | c.588C>T | synonymous_variant | 0.15 |
kasA | 2518711 | c.597A>G | synonymous_variant | 0.14 |
kasA | 2518714 | c.600A>C | synonymous_variant | 0.17 |
kasA | 2518717 | c.603C>T | synonymous_variant | 0.14 |
kasA | 2518732 | c.618C>G | synonymous_variant | 0.16 |
kasA | 2518741 | c.627G>C | synonymous_variant | 0.17 |
kasA | 2518747 | c.633C>G | synonymous_variant | 0.18 |
kasA | 2518768 | c.654C>G | synonymous_variant | 0.18 |
kasA | 2518783 | c.669T>C | synonymous_variant | 0.18 |
kasA | 2518825 | c.711T>C | synonymous_variant | 0.13 |
kasA | 2518855 | c.741C>G | synonymous_variant | 0.15 |
kasA | 2519053 | c.939G>C | synonymous_variant | 0.14 |
kasA | 2519062 | c.948T>G | synonymous_variant | 0.25 |
kasA | 2519068 | c.954C>T | synonymous_variant | 0.22 |
kasA | 2519072 | p.Ala320Thr | missense_variant | 0.29 |
kasA | 2519077 | c.963G>C | synonymous_variant | 0.17 |
kasA | 2519125 | c.1011C>T | synonymous_variant | 0.15 |
kasA | 2519137 | c.1023T>C | synonymous_variant | 0.23 |
kasA | 2519146 | c.1032C>A | synonymous_variant | 0.2 |
kasA | 2519167 | c.1053T>C | synonymous_variant | 0.33 |
kasA | 2519173 | c.1059C>G | synonymous_variant | 0.33 |
kasA | 2519176 | c.1062G>A | synonymous_variant | 0.33 |
kasA | 2519197 | c.1083G>C | synonymous_variant | 0.23 |
kasA | 2519215 | c.1101C>T | synonymous_variant | 0.15 |
eis | 2715424 | c.-92C>G | upstream_gene_variant | 0.2 |
ahpC | 2726600 | c.408T>C | synonymous_variant | 0.13 |
ahpC | 2726612 | c.420C>G | synonymous_variant | 0.16 |
ahpC | 2726638 | p.Ala149Val | missense_variant | 0.2 |
ahpC | 2726645 | c.453C>G | synonymous_variant | 0.21 |
ahpC | 2726657 | c.465A>C | synonymous_variant | 0.19 |
ahpC | 2726669 | p.Asp159Glu | missense_variant | 0.16 |
ahpC | 2726672 | c.480G>A | synonymous_variant | 0.17 |
ahpC | 2726681 | c.489A>G | synonymous_variant | 0.24 |
ahpC | 2726687 | c.495C>G | synonymous_variant | 0.23 |
ahpC | 2726693 | c.501C>G | synonymous_variant | 0.23 |
ahpC | 2726696 | c.504C>G | synonymous_variant | 0.24 |
ahpC | 2726717 | c.525A>G | synonymous_variant | 0.2 |
ahpC | 2726735 | c.543C>T | synonymous_variant | 0.15 |
folC | 2746238 | p.Pro454Gln | missense_variant | 0.12 |
folC | 2747032 | c.567A>C | synonymous_variant | 0.17 |
folC | 2747040 | p.Ile187Val | missense_variant | 0.18 |
folC | 2747059 | c.540T>C | synonymous_variant | 0.2 |
folC | 2747065 | c.534C>G | synonymous_variant | 0.24 |
folC | 2747302 | c.297A>G | synonymous_variant | 0.15 |
folC | 2747317 | c.282C>G | synonymous_variant | 0.14 |
folC | 2747355 | p.Val82Ile | missense_variant | 0.21 |
folC | 2747359 | c.240C>G | synonymous_variant | 0.22 |
folC | 2747362 | c.237G>C | synonymous_variant | 0.18 |
folC | 2747394 | p.Ile69Val | missense_variant | 0.14 |
folC | 2747395 | c.204T>C | synonymous_variant | 0.14 |
folC | 2747401 | c.198G>C | synonymous_variant | 0.15 |
Rv2752c | 3064995 | c.1197C>G | synonymous_variant | 0.18 |
Rv2752c | 3064998 | c.1194A>G | synonymous_variant | 0.19 |
Rv2752c | 3065018 | p.Asn392His | missense_variant | 0.19 |
Rv2752c | 3065028 | c.1164G>C | synonymous_variant | 0.17 |
Rv2752c | 3065031 | c.1161G>C | synonymous_variant | 0.19 |
Rv2752c | 3065040 | c.1152C>G | synonymous_variant | 0.19 |
Rv2752c | 3065048 | c.1144C>T | synonymous_variant | 0.24 |
Rv2752c | 3065993 | p.Val67Ile | missense_variant | 0.12 |
Rv2752c | 3066024 | c.168T>C | synonymous_variant | 0.14 |
thyX | 3067284 | p.Ala221Asp | missense_variant | 0.12 |
thyX | 3067325 | c.621A>G | synonymous_variant | 0.15 |
thyX | 3067355 | c.591A>C | synonymous_variant | 0.17 |
thyX | 3067376 | c.570G>C | synonymous_variant | 0.15 |
thyX | 3067532 | c.414C>T | synonymous_variant | 0.12 |
thyX | 3067610 | p.Lys112Asn | missense_variant | 0.12 |
thyX | 3067613 | c.333G>A | synonymous_variant | 0.15 |
thyX | 3067619 | c.327A>C | synonymous_variant | 0.27 |
thyX | 3067640 | c.306G>C | synonymous_variant | 0.19 |
thyX | 3067643 | c.303C>T | synonymous_variant | 0.17 |
thyX | 3067652 | c.294T>C | synonymous_variant | 0.2 |
thyX | 3067661 | c.285C>G | synonymous_variant | 0.23 |
thyX | 3067682 | c.264G>C | synonymous_variant | 0.21 |
thyX | 3067685 | c.261A>G | synonymous_variant | 0.19 |
thyX | 3067688 | c.258G>C | synonymous_variant | 0.18 |
thyX | 3067694 | c.252G>C | synonymous_variant | 0.2 |
thyX | 3067718 | c.228C>G | synonymous_variant | 0.14 |
thyA | 3073953 | c.519T>C | synonymous_variant | 0.22 |
thyA | 3073977 | c.495A>G | synonymous_variant | 0.14 |
thyA | 3073989 | c.483T>C | synonymous_variant | 0.19 |
thyA | 3074001 | c.471C>G | synonymous_variant | 0.18 |
thyA | 3074004 | c.468T>C | synonymous_variant | 0.18 |
thyA | 3074010 | c.462C>G | synonymous_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339040 | c.-78T>C | upstream_gene_variant | 1.0 |
fprA | 3473809 | c.-198G>C | upstream_gene_variant | 0.31 |
fprA | 3473812 | c.-195G>A | upstream_gene_variant | 0.28 |
fprA | 3473836 | c.-171C>A | upstream_gene_variant | 0.26 |
fprA | 3473843 | c.-164C>G | upstream_gene_variant | 0.15 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474942 | c.936G>A | synonymous_variant | 0.17 |
fprA | 3474948 | c.942A>G | synonymous_variant | 0.18 |
fprA | 3474950 | p.Ala315Val | missense_variant | 0.18 |
fprA | 3474960 | c.954C>G | synonymous_variant | 0.18 |
fprA | 3474966 | c.960G>C | synonymous_variant | 0.19 |
fprA | 3474984 | c.978G>C | synonymous_variant | 0.17 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiA | 3640347 | c.-196A>G | upstream_gene_variant | 0.16 |
fbiA | 3640349 | c.-194A>G | upstream_gene_variant | 0.13 |
fbiA | 3640350 | c.-193C>T | upstream_gene_variant | 0.13 |
fbiA | 3640365 | c.-178C>G | upstream_gene_variant | 0.15 |
rpoA | 3877507 | p.Gly334Ala | missense_variant | 0.15 |
rpoA | 3877515 | c.993G>C | synonymous_variant | 0.24 |
rpoA | 3877542 | c.966C>T | synonymous_variant | 0.33 |
rpoA | 3877553 | p.Glu319Gln | missense_variant | 0.36 |
rpoA | 3877557 | c.951C>G | synonymous_variant | 0.35 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.25 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.21 |
rpoA | 3877704 | c.804G>T | synonymous_variant | 0.17 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.21 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.18 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.17 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.17 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.17 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.24 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.18 |
rpoA | 3877857 | c.651G>A | synonymous_variant | 0.16 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.14 |
rpoA | 3877986 | c.522G>C | synonymous_variant | 0.15 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.15 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.19 |
rpoA | 3878022 | c.486T>C | synonymous_variant | 0.13 |
rpoA | 3878082 | c.426T>C | synonymous_variant | 0.13 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.2 |
rpoA | 3878346 | c.162T>C | synonymous_variant | 0.13 |
rpoA | 3878376 | c.132G>C | synonymous_variant | 0.16 |
rpoA | 3878385 | c.123C>G | synonymous_variant | 0.15 |
rpoA | 3878391 | c.117T>C | synonymous_variant | 0.15 |
rpoA | 3878396 | c.112C>T | synonymous_variant | 0.14 |
rpoA | 3878436 | c.72A>G | synonymous_variant | 0.21 |
rpoA | 3878442 | c.66G>C | synonymous_variant | 0.24 |
rpoA | 3878454 | c.54A>C | synonymous_variant | 0.25 |
rpoA | 3878472 | p.Asp12Glu | missense_variant | 0.21 |
rpoA | 3878478 | c.30C>G | synonymous_variant | 0.22 |
rpoA | 3878490 | c.18C>A | synonymous_variant | 0.21 |
rpoA | 3878496 | c.12A>T | synonymous_variant | 0.23 |
rpoA | 3878672 | c.-165A>T | upstream_gene_variant | 0.2 |
rpoA | 3878698 | c.-191A>G | upstream_gene_variant | 0.23 |
rpoA | 3878701 | c.-194C>G | upstream_gene_variant | 0.22 |
ddn | 3986648 | c.-196C>G | upstream_gene_variant | 0.18 |
ddn | 3986655 | c.-189A>T | upstream_gene_variant | 0.14 |
ddn | 3986660 | c.-184C>T | upstream_gene_variant | 0.14 |
ddn | 3986665 | c.-179G>C | upstream_gene_variant | 0.14 |
ddn | 3986667 | c.-177C>A | upstream_gene_variant | 0.14 |
clpC1 | 4038317 | c.2388G>C | synonymous_variant | 0.16 |
clpC1 | 4038347 | c.2358G>C | synonymous_variant | 0.14 |
clpC1 | 4038368 | c.2337T>C | synonymous_variant | 0.14 |
clpC1 | 4038498 | p.Ser736Thr | missense_variant | 0.14 |
clpC1 | 4038536 | c.2169C>T | synonymous_variant | 0.13 |
clpC1 | 4038695 | c.2010C>G | synonymous_variant | 0.16 |
clpC1 | 4038701 | c.2004G>C | synonymous_variant | 0.13 |
clpC1 | 4038704 | c.2001T>C | synonymous_variant | 0.13 |
clpC1 | 4038740 | c.1965G>C | synonymous_variant | 0.19 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.3 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.46 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 0.42 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.36 |
clpC1 | 4038815 | c.1890G>T | synonymous_variant | 0.34 |
clpC1 | 4038851 | c.1854G>A | synonymous_variant | 0.25 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.64 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.38 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.33 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 0.29 |
clpC1 | 4038932 | c.1773G>C | synonymous_variant | 0.25 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.17 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.16 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.16 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.17 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.18 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.18 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.16 |
clpC1 | 4039025 | c.1680C>T | synonymous_variant | 0.82 |
clpC1 | 4039226 | c.1479T>C | synonymous_variant | 0.17 |
clpC1 | 4039268 | c.1437C>G | synonymous_variant | 0.16 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.15 |
clpC1 | 4039364 | c.1341C>G | synonymous_variant | 0.16 |
clpC1 | 4039388 | c.1317C>A | synonymous_variant | 0.26 |
clpC1 | 4039391 | c.1314T>G | synonymous_variant | 0.26 |
clpC1 | 4039409 | c.1296T>C | synonymous_variant | 0.23 |
clpC1 | 4039412 | c.1293T>G | synonymous_variant | 0.23 |
clpC1 | 4039424 | c.1281G>A | synonymous_variant | 0.3 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.26 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.16 |
clpC1 | 4039448 | c.1257A>G | synonymous_variant | 0.15 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.15 |
clpC1 | 4039526 | c.1179G>C | synonymous_variant | 0.16 |
clpC1 | 4039562 | c.1143C>G | synonymous_variant | 0.15 |
clpC1 | 4039565 | c.1140G>C | synonymous_variant | 0.22 |
clpC1 | 4039576 | p.Ala377Ser | missense_variant | 0.23 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.23 |
clpC1 | 4039586 | c.1119G>C | synonymous_variant | 0.19 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.2 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.17 |
clpC1 | 4039622 | c.1083C>G | synonymous_variant | 0.19 |
clpC1 | 4039682 | c.1023C>G | synonymous_variant | 0.14 |
clpC1 | 4039685 | c.1020C>T | synonymous_variant | 0.21 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.26 |
clpC1 | 4039733 | c.972G>A | synonymous_variant | 0.15 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 0.15 |
clpC1 | 4039832 | c.873C>G | synonymous_variant | 0.18 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.28 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.24 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.27 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.22 |
clpC1 | 4039928 | c.775_777delAGCinsTCG | synonymous_variant | 0.17 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.19 |
clpC1 | 4039946 | c.759A>T | synonymous_variant | 0.2 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.14 |
clpC1 | 4040105 | c.600C>G | synonymous_variant | 0.14 |
clpC1 | 4040354 | c.351A>G | synonymous_variant | 0.14 |
clpC1 | 4040363 | c.342A>C | synonymous_variant | 0.14 |
clpC1 | 4040369 | c.336C>G | synonymous_variant | 0.14 |
clpC1 | 4040411 | c.294T>C | synonymous_variant | 0.14 |
clpC1 | 4040444 | c.261C>G | synonymous_variant | 0.16 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 0.15 |
clpC1 | 4040528 | c.177G>C | synonymous_variant | 0.15 |
clpC1 | 4040644 | c.61A>C | synonymous_variant | 0.19 |
clpC1 | 4040654 | c.51G>A | synonymous_variant | 0.26 |
clpC1 | 4040657 | c.48T>G | synonymous_variant | 0.25 |
clpC1 | 4040662 | c.43C>T | synonymous_variant | 0.27 |
clpC1 | 4040699 | c.6C>T | synonymous_variant | 0.17 |
panD | 4044162 | c.120A>G | synonymous_variant | 0.14 |
panD | 4044165 | c.117G>C | synonymous_variant | 0.18 |
panD | 4044188 | c.94T>C | synonymous_variant | 0.19 |
embC | 4240657 | c.795G>C | synonymous_variant | 0.15 |
embC | 4240780 | c.918T>C | synonymous_variant | 0.17 |
embC | 4240783 | c.921G>C | synonymous_variant | 0.19 |
embC | 4240789 | c.927T>C | synonymous_variant | 0.22 |
embC | 4240819 | c.957A>G | synonymous_variant | 0.21 |
embC | 4240825 | c.963G>A | synonymous_variant | 0.21 |
embC | 4240831 | c.969T>G | synonymous_variant | 0.23 |
embC | 4240867 | c.1005T>G | synonymous_variant | 0.19 |
embC | 4240870 | c.1008T>C | synonymous_variant | 0.18 |
embC | 4240879 | c.1017G>C | synonymous_variant | 0.19 |
embC | 4240880 | p.Ala340Thr | missense_variant | 0.19 |
embC | 4240885 | c.1023T>C | synonymous_variant | 0.18 |
embC | 4240897 | c.1035C>G | synonymous_variant | 0.14 |
embC | 4241137 | c.1275G>C | synonymous_variant | 0.15 |
embC | 4241443 | c.1581C>G | synonymous_variant | 0.19 |
embC | 4241449 | c.1587C>G | synonymous_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4245083 | c.1851A>C | synonymous_variant | 0.15 |
embA | 4245089 | c.1857G>C | synonymous_variant | 0.14 |
embA | 4245092 | c.1860C>G | synonymous_variant | 0.13 |
embA | 4245101 | c.1869G>C | synonymous_variant | 0.14 |
embB | 4245848 | c.-666C>G | upstream_gene_variant | 0.17 |
embA | 4245885 | p.Asp885Thr | missense_variant | 0.17 |
embA | 4245892 | p.Ile887Thr | missense_variant | 0.19 |
embB | 4245905 | c.-609C>G | upstream_gene_variant | 0.15 |
embA | 4246041 | p.Asp937Asn | missense_variant | 0.14 |
embB | 4246064 | c.-450T>C | upstream_gene_variant | 0.14 |
embB | 4246373 | c.-141T>C | upstream_gene_variant | 0.13 |
embB | 4247326 | c.813A>G | synonymous_variant | 0.14 |
embB | 4247338 | c.825C>G | synonymous_variant | 0.13 |
embB | 4247348 | p.Thr279Ala | missense_variant | 0.15 |
embB | 4247437 | c.924A>G | synonymous_variant | 0.17 |
embB | 4247440 | c.927C>G | synonymous_variant | 0.17 |
embB | 4247464 | c.951C>G | synonymous_variant | 0.17 |
embB | 4247470 | c.957T>C | synonymous_variant | 0.17 |
embB | 4247491 | c.978G>C | synonymous_variant | 0.19 |
embB | 4247497 | c.984T>C | synonymous_variant | 0.14 |
embB | 4247500 | c.987C>G | synonymous_variant | 0.14 |
embB | 4247512 | c.999T>C | synonymous_variant | 0.16 |
embB | 4248097 | c.1584C>G | synonymous_variant | 0.14 |
embB | 4248118 | c.1605T>C | synonymous_variant | 0.3 |
embB | 4248127 | c.1614G>C | synonymous_variant | 0.25 |
embB | 4248133 | c.1620C>G | synonymous_variant | 0.25 |
embB | 4248142 | c.1629T>C | synonymous_variant | 0.23 |
embB | 4248143 | c.1630T>C | synonymous_variant | 0.23 |
embB | 4248157 | c.1644A>G | synonymous_variant | 0.19 |
embB | 4248206 | p.Ser565Gly | missense_variant | 0.14 |
embB | 4248220 | c.1707A>G | synonymous_variant | 0.2 |
embB | 4248241 | c.1728C>T | synonymous_variant | 0.21 |
embB | 4248265 | c.1752C>T | synonymous_variant | 0.15 |
embB | 4248266 | c.1753C>T | synonymous_variant | 0.15 |
embB | 4248902 | p.Thr797Pro | missense_variant | 1.0 |
embB | 4249469 | p.Leu986Met | missense_variant | 0.13 |
embB | 4249483 | c.2970C>G | synonymous_variant | 0.16 |
embB | 4249486 | c.2973T>G | synonymous_variant | 0.16 |
embB | 4249487 | c.2974T>C | synonymous_variant | 0.16 |
embB | 4249498 | c.2985G>C | synonymous_variant | 0.21 |
embB | 4249521 | p.Ala1003Val | missense_variant | 0.18 |
embB | 4249525 | c.3012T>C | synonymous_variant | 0.15 |
embB | 4249532 | p.Ala1007Thr | missense_variant | 0.12 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268117 | c.720G>C | synonymous_variant | 0.14 |
ubiA | 4269243 | p.His197Gln | missense_variant | 0.19 |
ubiA | 4269271 | p.Val188Ala | missense_variant | 0.17 |
ethA | 4328471 | c.-998A>G | upstream_gene_variant | 0.23 |
ethA | 4328473 | c.-1000G>C | upstream_gene_variant | 0.21 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |