Run ID: ERR9786986
Sample name:
Date: 02-04-2023 12:54:53
Number of reads: 895210
Percentage reads mapped: 77.16
Strain: lineage4.1.2.1
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.96 |
lineage4.1 | Euro-American | T;X;H | None | 0.94 |
lineage4.1.2 | Euro-American | T;H | None | 0.99 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 0.98 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
folC | 2747141 | p.Glu153Ala | missense_variant | 0.98 | para-aminosalicylic_acid |
gid | 4408100 | c.102delG | frameshift_variant | 1.0 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6190 | c.951A>G | synonymous_variant | 0.19 |
gyrB | 6214 | c.975G>C | synonymous_variant | 0.21 |
gyrB | 6238 | c.999G>A | synonymous_variant | 0.19 |
gyrB | 6242 | p.Arg335Lys | missense_variant | 0.19 |
gyrB | 6250 | c.1011A>G | synonymous_variant | 0.17 |
gyrB | 6280 | c.1041T>C | synonymous_variant | 0.17 |
gyrB | 6292 | c.1053G>T | synonymous_variant | 0.16 |
gyrB | 6299 | c.1060C>T | synonymous_variant | 0.16 |
gyrA | 6403 | c.-899T>C | upstream_gene_variant | 0.18 |
gyrA | 6559 | c.-743C>A | upstream_gene_variant | 0.15 |
gyrA | 6571 | c.-731T>C | upstream_gene_variant | 0.18 |
gyrA | 6577 | c.-725T>C | upstream_gene_variant | 0.18 |
gyrA | 6778 | c.-524C>T | upstream_gene_variant | 0.17 |
gyrA | 6793 | c.-509T>C | upstream_gene_variant | 0.19 |
gyrB | 6797 | p.Gly520Thr | missense_variant | 0.19 |
gyrA | 6841 | c.-461T>C | upstream_gene_variant | 0.2 |
gyrA | 6844 | c.-458T>G | upstream_gene_variant | 0.2 |
gyrA | 6973 | c.-329G>C | upstream_gene_variant | 0.18 |
gyrA | 6976 | c.-326A>G | upstream_gene_variant | 0.19 |
gyrA | 6982 | c.-320A>C | upstream_gene_variant | 0.18 |
gyrA | 6988 | c.-314C>G | upstream_gene_variant | 0.2 |
gyrA | 6997 | c.-305G>A | upstream_gene_variant | 0.21 |
gyrA | 7006 | c.-296T>C | upstream_gene_variant | 0.21 |
gyrA | 7012 | c.-290G>C | upstream_gene_variant | 0.22 |
gyrA | 7018 | c.-284G>C | upstream_gene_variant | 0.22 |
gyrA | 7021 | c.-281G>T | upstream_gene_variant | 0.18 |
gyrA | 7024 | c.-278G>C | upstream_gene_variant | 0.19 |
gyrA | 7156 | c.-146C>T | upstream_gene_variant | 0.16 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7433 | c.132G>C | synonymous_variant | 0.19 |
gyrA | 7442 | c.141G>C | synonymous_variant | 0.23 |
gyrA | 7451 | c.150C>G | synonymous_variant | 0.23 |
gyrA | 7457 | c.156T>C | synonymous_variant | 0.22 |
gyrA | 7463 | c.162G>C | synonymous_variant | 0.21 |
gyrA | 7469 | c.168C>G | synonymous_variant | 0.2 |
gyrA | 7475 | c.174A>G | synonymous_variant | 0.21 |
gyrA | 7480 | p.Phe60Tyr | missense_variant | 0.21 |
gyrA | 7484 | c.183T>C | synonymous_variant | 0.21 |
gyrA | 7487 | c.186C>G | synonymous_variant | 0.21 |
gyrA | 7490 | c.189C>T | synonymous_variant | 0.21 |
gyrA | 7496 | c.195C>A | synonymous_variant | 0.21 |
gyrA | 7520 | c.219G>C | synonymous_variant | 0.19 |
gyrA | 7523 | c.222C>G | synonymous_variant | 0.19 |
gyrA | 7532 | c.231T>C | synonymous_variant | 0.19 |
gyrA | 7559 | c.258G>C | synonymous_variant | 0.21 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8337 | c.1036C>T | synonymous_variant | 0.16 |
gyrA | 8340 | p.Ala347Ser | missense_variant | 0.16 |
gyrA | 8382 | p.Leu361Met | missense_variant | 0.17 |
gyrA | 8453 | c.1152A>C | synonymous_variant | 0.17 |
gyrA | 8459 | c.1158G>A | synonymous_variant | 0.18 |
gyrA | 8510 | c.1209G>A | synonymous_variant | 0.18 |
gyrA | 8537 | c.1236G>A | synonymous_variant | 0.17 |
gyrA | 8588 | c.1287G>A | synonymous_variant | 0.21 |
gyrA | 8591 | c.1290C>T | synonymous_variant | 0.23 |
gyrA | 8603 | c.1302A>C | synonymous_variant | 0.21 |
gyrA | 8619 | c.1318T>C | synonymous_variant | 0.2 |
gyrA | 8633 | c.1332C>G | synonymous_variant | 0.23 |
gyrA | 8636 | c.1335A>C | synonymous_variant | 0.23 |
gyrA | 8642 | c.1341A>G | synonymous_variant | 0.23 |
gyrA | 8645 | c.1344C>G | synonymous_variant | 0.23 |
gyrA | 8672 | c.1371A>G | synonymous_variant | 0.24 |
gyrA | 8678 | c.1377G>A | synonymous_variant | 0.25 |
gyrA | 8693 | c.1392T>C | synonymous_variant | 0.24 |
gyrA | 8696 | c.1395G>C | synonymous_variant | 0.23 |
gyrA | 8711 | c.1410A>C | synonymous_variant | 0.24 |
gyrA | 8714 | c.1413A>G | synonymous_variant | 0.24 |
gyrA | 8717 | c.1416C>G | synonymous_variant | 0.24 |
gyrA | 8720 | c.1419G>A | synonymous_variant | 0.22 |
gyrA | 8729 | c.1428T>C | synonymous_variant | 0.22 |
gyrA | 8732 | c.1431G>C | synonymous_variant | 0.21 |
gyrA | 8747 | c.1446A>G | synonymous_variant | 0.22 |
gyrA | 8751 | p.Ala484Thr | missense_variant | 0.22 |
gyrA | 8756 | c.1455A>G | synonymous_variant | 0.2 |
gyrA | 8767 | p.Arg489Lys | missense_variant | 0.19 |
gyrA | 8790 | c.1489C>A | synonymous_variant | 0.17 |
gyrA | 8796 | p.Ile499Val | missense_variant | 0.18 |
gyrA | 8810 | c.1509A>T | synonymous_variant | 0.17 |
gyrA | 8873 | c.1572A>C | synonymous_variant | 0.2 |
gyrA | 8882 | c.1581G>A | synonymous_variant | 0.21 |
gyrA | 8894 | c.1593C>G | synonymous_variant | 0.26 |
gyrA | 8900 | c.1599G>C | synonymous_variant | 0.29 |
gyrA | 8903 | c.1602T>C | synonymous_variant | 0.29 |
gyrA | 8939 | c.1638T>C | synonymous_variant | 0.29 |
gyrA | 8942 | c.1641G>C | synonymous_variant | 0.29 |
gyrA | 8945 | c.1644G>C | synonymous_variant | 0.28 |
gyrA | 8946 | c.1645_1647delTTGinsCTC | synonymous_variant | 0.29 |
gyrA | 8967 | p.Ala556Arg | missense_variant | 0.23 |
gyrA | 8981 | c.1680G>C | synonymous_variant | 0.24 |
gyrA | 8982 | p.Cys561Ser | missense_variant | 0.24 |
gyrA | 8990 | c.1689C>G | synonymous_variant | 0.23 |
gyrA | 8996 | c.1695T>C | synonymous_variant | 0.23 |
gyrA | 8998 | p.Leu566Trp | missense_variant | 0.24 |
gyrA | 9002 | c.1701C>T | synonymous_variant | 0.24 |
gyrA | 9017 | c.1716C>G | synonymous_variant | 0.21 |
gyrA | 9023 | c.1722A>C | synonymous_variant | 0.21 |
gyrA | 9029 | c.1728T>G | synonymous_variant | 0.23 |
gyrA | 9032 | c.1731T>C | synonymous_variant | 0.23 |
gyrA | 9038 | c.1737C>G | synonymous_variant | 0.23 |
gyrA | 9050 | p.Asp583Glu | missense_variant | 0.24 |
gyrA | 9051 | c.1750T>C | synonymous_variant | 0.24 |
gyrA | 9062 | c.1761C>G | synonymous_variant | 0.24 |
gyrA | 9066 | c.1765C>A | synonymous_variant | 0.24 |
gyrA | 9071 | c.1770G>C | synonymous_variant | 0.22 |
gyrA | 9074 | c.1773G>C | synonymous_variant | 0.22 |
gyrA | 9080 | c.1779G>T | synonymous_variant | 0.21 |
gyrA | 9083 | c.1782G>A | synonymous_variant | 0.2 |
gyrA | 9089 | c.1788G>C | synonymous_variant | 0.2 |
gyrA | 9095 | c.1794C>T | synonymous_variant | 0.2 |
gyrA | 9099 | c.1798_1800delTTAinsCTG | synonymous_variant | 0.2 |
gyrA | 9134 | c.1833C>G | synonymous_variant | 0.18 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 0.19 |
gyrA | 9153 | p.Thr618Asp | missense_variant | 0.18 |
gyrA | 9161 | c.1860C>G | synonymous_variant | 0.18 |
gyrA | 9182 | c.1881T>C | synonymous_variant | 0.19 |
gyrA | 9191 | c.1890G>C | synonymous_variant | 0.21 |
gyrA | 9200 | c.1899A>G | synonymous_variant | 0.21 |
gyrA | 9204 | p.Ser635Thr | missense_variant | 0.18 |
gyrA | 9218 | c.1917C>T | synonymous_variant | 0.16 |
gyrA | 9230 | c.1929T>C | synonymous_variant | 0.17 |
gyrA | 9233 | c.1932C>A | synonymous_variant | 0.21 |
gyrA | 9242 | c.1941A>C | synonymous_variant | 0.2 |
gyrA | 9248 | c.1947G>C | synonymous_variant | 0.21 |
gyrA | 9252 | p.Val651Ile | missense_variant | 0.21 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9527 | c.2226A>G | synonymous_variant | 0.17 |
gyrA | 9542 | c.2241T>C | synonymous_variant | 0.19 |
gyrA | 9545 | c.2244A>G | synonymous_variant | 0.19 |
gyrA | 9548 | c.2247T>C | synonymous_variant | 0.18 |
gyrA | 9554 | c.2253G>C | synonymous_variant | 0.18 |
gyrA | 9557 | c.2256G>C | synonymous_variant | 0.18 |
gyrA | 9565 | p.Tyr755Phe | missense_variant | 0.16 |
gyrA | 9583 | p.Arg761Lys | missense_variant | 0.17 |
gyrA | 9593 | c.2292G>C | synonymous_variant | 0.18 |
gyrA | 9602 | c.2301T>C | synonymous_variant | 0.2 |
gyrA | 9626 | c.2325T>C | synonymous_variant | 0.2 |
gyrA | 9630 | p.Val777Ile | missense_variant | 0.21 |
gyrA | 9635 | c.2334T>C | synonymous_variant | 0.21 |
gyrA | 9641 | c.2340C>G | synonymous_variant | 0.23 |
gyrA | 9644 | c.2343T>C | synonymous_variant | 0.23 |
gyrA | 9661 | p.Ala787Asp | missense_variant | 0.21 |
gyrA | 9665 | c.2364A>G | synonymous_variant | 0.21 |
gyrA | 9674 | c.2373T>C | synonymous_variant | 0.2 |
fgd1 | 491022 | c.240C>G | synonymous_variant | 0.19 |
fgd1 | 491340 | c.558C>G | synonymous_variant | 0.21 |
fgd1 | 491343 | c.561C>G | synonymous_variant | 0.21 |
fgd1 | 491349 | c.567T>C | synonymous_variant | 0.2 |
fgd1 | 491364 | c.582T>C | synonymous_variant | 0.17 |
fgd1 | 491379 | c.597C>T | synonymous_variant | 0.16 |
fgd1 | 491496 | c.714C>T | synonymous_variant | 0.19 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 0.93 |
mshA | 575561 | p.Met72Val | missense_variant | 0.19 |
mshA | 575571 | p.Ser75Thr | missense_variant | 0.21 |
mshA | 575576 | c.229C>T | synonymous_variant | 0.23 |
mshA | 575587 | c.240C>G | synonymous_variant | 0.26 |
mshA | 575590 | c.243T>G | synonymous_variant | 0.25 |
mshA | 575629 | c.282A>G | synonymous_variant | 0.28 |
mshA | 575632 | c.285G>C | synonymous_variant | 0.28 |
mshA | 575635 | c.288A>C | synonymous_variant | 0.28 |
mshA | 575638 | c.291T>C | synonymous_variant | 0.29 |
mshA | 575641 | c.294A>G | synonymous_variant | 0.29 |
mshA | 575649 | p.Val101Ala | missense_variant | 0.31 |
mshA | 575659 | c.312A>G | synonymous_variant | 0.36 |
mshA | 575665 | c.318G>C | synonymous_variant | 0.39 |
mshA | 575679 | p.Asn111Ser | missense_variant | 0.61 |
mshA | 575695 | c.348C>G | synonymous_variant | 0.37 |
mshA | 575704 | c.357T>C | synonymous_variant | 0.35 |
mshA | 575705 | c.358T>C | synonymous_variant | 0.35 |
mshA | 575713 | c.366G>A | synonymous_variant | 0.36 |
mshA | 575728 | c.381C>T | synonymous_variant | 0.28 |
mshA | 575734 | c.387T>G | synonymous_variant | 0.25 |
mshA | 575737 | c.390T>C | synonymous_variant | 0.26 |
mshA | 575764 | c.417C>G | synonymous_variant | 0.27 |
mshA | 575771 | p.Val142Ser | missense_variant | 0.24 |
mshA | 575785 | c.438T>C | synonymous_variant | 0.21 |
mshA | 575786 | p.Tyr147His | missense_variant | 0.21 |
mshA | 575864 | c.517T>C | synonymous_variant | 0.23 |
mshA | 575878 | c.531A>G | synonymous_variant | 0.24 |
mshA | 575893 | c.546C>G | synonymous_variant | 0.21 |
mshA | 575896 | c.549G>C | synonymous_variant | 0.2 |
mshA | 575902 | c.555C>T | synonymous_variant | 0.2 |
mshA | 575908 | c.561A>G | synonymous_variant | 0.19 |
mshA | 575914 | c.567C>G | synonymous_variant | 0.19 |
mshA | 575916 | p.Asp190Ala | missense_variant | 0.2 |
mshA | 575925 | p.Gly193Ala | missense_variant | 0.19 |
mshA | 575944 | c.597T>C | synonymous_variant | 0.23 |
mshA | 575953 | c.606G>C | synonymous_variant | 0.21 |
mshA | 575959 | c.612G>A | synonymous_variant | 0.2 |
mshA | 575980 | c.633T>C | synonymous_variant | 0.18 |
mshA | 575984 | c.637T>C | synonymous_variant | 0.18 |
rpoB | 760115 | c.309C>T | synonymous_variant | 0.93 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.17 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.17 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.25 |
rpoB | 760481 | c.675G>C | synonymous_variant | 0.24 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.24 |
rpoB | 760522 | p.Ser239Asn | missense_variant | 0.3 |
rpoB | 760532 | c.726T>C | synonymous_variant | 0.3 |
rpoB | 760533 | p.Val243His | missense_variant | 0.31 |
rpoB | 760547 | c.741G>C | synonymous_variant | 0.3 |
rpoB | 760561 | c.757_758delCG | frameshift_variant | 0.28 |
rpoB | 760567 | p.Ser254Trp | missense_variant | 0.28 |
rpoB | 760568 | c.762_763insGC | frameshift_variant | 0.28 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.29 |
rpoB | 760611 | c.805T>C | synonymous_variant | 0.29 |
rpoB | 760634 | c.828T>C | synonymous_variant | 0.27 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.27 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.25 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.26 |
rpoB | 760670 | c.864G>C | synonymous_variant | 0.24 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.23 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.24 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.22 |
rpoB | 760724 | c.918T>C | synonymous_variant | 0.18 |
rpoB | 760730 | c.924T>C | synonymous_variant | 0.18 |
rpoB | 760748 | c.942C>G | synonymous_variant | 0.21 |
rpoB | 760751 | c.945G>C | synonymous_variant | 0.2 |
rpoB | 760757 | c.951T>C | synonymous_variant | 0.19 |
rpoB | 760759 | p.Val318Ala | missense_variant | 0.19 |
rpoB | 760769 | c.963C>G | synonymous_variant | 0.19 |
rpoB | 760781 | c.975G>C | synonymous_variant | 0.18 |
rpoB | 760805 | c.999G>C | synonymous_variant | 0.17 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.22 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.27 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.29 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.29 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.29 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.35 |
rpoB | 761096 | c.1290G>C | synonymous_variant | 0.33 |
rpoB | 761097 | c.1291_1292delAGinsTC | synonymous_variant | 0.33 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.31 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 0.31 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.3 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.28 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.24 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.24 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.22 |
rpoB | 761189 | c.1383T>G | synonymous_variant | 0.24 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.23 |
rpoB | 761198 | c.1392G>C | synonymous_variant | 0.24 |
rpoB | 761204 | c.1398C>G | synonymous_variant | 0.22 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.2 |
rpoB | 761345 | c.1539G>C | synonymous_variant | 0.24 |
rpoB | 761354 | c.1548C>T | synonymous_variant | 0.24 |
rpoB | 761360 | c.1554T>C | synonymous_variant | 0.24 |
rpoB | 761362 | p.Ser519Thr | missense_variant | 0.23 |
rpoB | 761373 | p.Val523His | missense_variant | 0.24 |
rpoB | 761408 | c.1602G>C | synonymous_variant | 0.26 |
rpoB | 761414 | c.1608A>G | synonymous_variant | 0.26 |
rpoB | 761423 | c.1617T>C | synonymous_variant | 0.28 |
rpoB | 761435 | c.1629T>C | synonymous_variant | 0.23 |
rpoB | 761439 | p.Asp545Ser | missense_variant | 0.23 |
rpoB | 761444 | c.1638T>C | synonymous_variant | 0.23 |
rpoB | 761447 | c.1641C>G | synonymous_variant | 0.23 |
rpoB | 761452 | p.Val549Glu | missense_variant | 0.23 |
rpoB | 761457 | p.Pro551Ser | missense_variant | 0.23 |
rpoB | 761477 | c.1671C>G | synonymous_variant | 0.22 |
rpoB | 761483 | c.1677G>C | synonymous_variant | 0.24 |
rpoB | 761492 | c.1686G>C | synonymous_variant | 0.27 |
rpoB | 761504 | c.1698C>G | synonymous_variant | 0.26 |
rpoB | 761510 | c.1704T>C | synonymous_variant | 0.25 |
rpoB | 761531 | c.1725C>G | synonymous_variant | 0.2 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.21 |
rpoB | 761564 | c.1758G>C | synonymous_variant | 0.27 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.27 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.24 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.26 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.24 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.21 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.21 |
rpoB | 761636 | c.1830G>C | synonymous_variant | 0.24 |
rpoB | 761645 | c.1839C>G | synonymous_variant | 0.24 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.24 |
rpoB | 761657 | c.1851C>G | synonymous_variant | 0.24 |
rpoB | 761675 | c.1869G>C | synonymous_variant | 0.22 |
rpoB | 761682 | c.1876C>T | synonymous_variant | 0.21 |
rpoB | 761690 | c.1884G>C | synonymous_variant | 0.23 |
rpoB | 761705 | c.1899C>T | synonymous_variant | 0.24 |
rpoB | 761720 | c.1914C>G | synonymous_variant | 0.2 |
rpoB | 761732 | c.1926C>G | synonymous_variant | 0.2 |
rpoB | 761735 | c.1929C>G | synonymous_variant | 0.2 |
rpoB | 761747 | c.1941G>C | synonymous_variant | 0.19 |
rpoB | 761765 | c.1959T>C | synonymous_variant | 0.22 |
rpoB | 761772 | p.His656Ala | missense_variant | 0.21 |
rpoB | 761778 | p.Asn658Asp | missense_variant | 0.23 |
rpoB | 761791 | p.Arg662His | missense_variant | 0.21 |
rpoB | 761815 | p.Ala670Asp | missense_variant | 0.17 |
rpoB | 761819 | c.2013G>C | synonymous_variant | 0.19 |
rpoB | 761834 | c.2028T>G | synonymous_variant | 0.2 |
rpoB | 761848 | p.Cys681Ser | missense_variant | 0.2 |
rpoB | 761852 | c.2046C>G | synonymous_variant | 0.2 |
rpoB | 761873 | c.2067A>G | synonymous_variant | 0.21 |
rpoB | 761885 | c.2079T>C | synonymous_variant | 0.21 |
rpoB | 761891 | c.2085G>C | synonymous_variant | 0.21 |
rpoB | 761906 | c.2100C>G | synonymous_variant | 0.19 |
rpoB | 761909 | c.2103T>C | synonymous_variant | 0.19 |
rpoB | 761916 | p.Asp704Asn | missense_variant | 0.18 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.26 |
rpoB | 761954 | c.2148C>G | synonymous_variant | 0.27 |
rpoB | 761999 | c.2193G>C | synonymous_variant | 0.29 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.34 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.33 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.31 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.31 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.3 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.31 |
rpoB | 762122 | c.2316C>T | synonymous_variant | 0.34 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 0.3 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.31 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.29 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.32 |
rpoB | 762158 | c.2352G>C | synonymous_variant | 0.3 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.27 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.28 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.28 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.33 |
rpoB | 762248 | c.2442G>C | synonymous_variant | 0.3 |
rpoB | 762254 | c.2448T>G | synonymous_variant | 0.32 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.33 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.35 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.38 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.35 |
rpoB | 762329 | c.2523G>C | synonymous_variant | 0.33 |
rpoB | 762338 | c.2532T>C | synonymous_variant | 0.31 |
rpoB | 762347 | c.2541T>C | synonymous_variant | 0.3 |
rpoB | 762362 | p.Glu852Asp | missense_variant | 0.29 |
rpoB | 762369 | c.2563T>C | synonymous_variant | 0.29 |
rpoC | 762389 | c.-981G>A | upstream_gene_variant | 0.24 |
rpoC | 762395 | c.-975G>C | upstream_gene_variant | 0.2 |
rpoC | 762398 | c.-972T>C | upstream_gene_variant | 0.2 |
rpoC | 762401 | c.-969G>C | upstream_gene_variant | 0.19 |
rpoC | 762404 | c.-966T>C | upstream_gene_variant | 0.19 |
rpoC | 762410 | c.-960T>C | upstream_gene_variant | 0.21 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 0.21 |
rpoC | 762434 | c.-936T>C | upstream_gene_variant | 0.23 |
rpoC | 762446 | c.-924C>G | upstream_gene_variant | 0.23 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.25 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.27 |
rpoC | 762995 | c.-375G>C | upstream_gene_variant | 0.35 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.3 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.29 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.28 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.32 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.37 |
rpoC | 763076 | c.-294C>G | upstream_gene_variant | 0.35 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.33 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.38 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.32 |
rpoC | 763142 | c.-228C>G | upstream_gene_variant | 0.28 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.29 |
rpoC | 763169 | c.-201A>G | upstream_gene_variant | 0.28 |
rpoC | 763187 | c.-183C>G | upstream_gene_variant | 0.26 |
rpoC | 763202 | c.-168A>C | upstream_gene_variant | 0.19 |
rpoB | 763206 | p.Ser1134Cys | missense_variant | 0.16 |
rpoC | 763227 | c.-143C>T | upstream_gene_variant | 0.19 |
rpoC | 763238 | c.-132T>C | upstream_gene_variant | 0.22 |
rpoC | 763253 | c.-117G>C | upstream_gene_variant | 0.2 |
rpoC | 763262 | c.-108C>A | upstream_gene_variant | 0.17 |
rpoC | 763272 | c.-98C>T | upstream_gene_variant | 0.18 |
rpoC | 763283 | c.-87T>C | upstream_gene_variant | 0.17 |
rpoC | 763310 | c.-60C>T | upstream_gene_variant | 0.17 |
rpoC | 763316 | c.-54T>C | upstream_gene_variant | 0.17 |
rpoC | 763319 | c.-51T>G | upstream_gene_variant | 0.17 |
rpoC | 763322 | c.-48G>T | upstream_gene_variant | 0.15 |
rpoC | 763351 | c.-19T>C | upstream_gene_variant | 0.2 |
rpoC | 763352 | c.-18T>A | upstream_gene_variant | 0.2 |
rpoC | 763402 | c.33C>T | synonymous_variant | 0.28 |
rpoC | 763408 | c.39T>C | synonymous_variant | 0.28 |
rpoC | 763411 | c.42T>G | synonymous_variant | 0.28 |
rpoC | 763414 | c.45T>C | synonymous_variant | 0.28 |
rpoC | 763441 | c.72C>T | synonymous_variant | 0.32 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.32 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.32 |
rpoC | 763486 | c.117T>G | synonymous_variant | 0.31 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.31 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.34 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.34 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.35 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.33 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.33 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.3 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.31 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.33 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.35 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.4 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.35 |
rpoC | 763729 | c.360G>C | synonymous_variant | 0.34 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.32 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.33 |
rpoC | 763765 | c.396T>G | synonymous_variant | 0.37 |
rpoC | 763768 | c.399C>G | synonymous_variant | 0.36 |
rpoC | 763780 | c.411C>G | synonymous_variant | 0.36 |
rpoC | 763792 | p.Glu141Asp | missense_variant | 0.38 |
rpoC | 763801 | c.432C>G | synonymous_variant | 0.35 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.34 |
rpoC | 763813 | c.444C>G | synonymous_variant | 0.34 |
rpoC | 763835 | p.Ala156Met | missense_variant | 0.33 |
rpoC | 763855 | c.486C>T | synonymous_variant | 0.37 |
rpoC | 763858 | c.489A>G | synonymous_variant | 0.37 |
rpoC | 763872 | p.Gly168Ala | missense_variant | 0.42 |
rpoC | 763876 | p.Glu169Asp | missense_variant | 0.39 |
rpoC | 763879 | c.510A>G | synonymous_variant | 0.4 |
rpoC | 763888 | c.519G>C | synonymous_variant | 0.39 |
rpoC | 763894 | c.525A>G | synonymous_variant | 0.4 |
rpoC | 763945 | c.576T>C | synonymous_variant | 0.38 |
rpoC | 763951 | c.582G>C | synonymous_variant | 0.38 |
rpoC | 763960 | c.591T>C | synonymous_variant | 0.35 |
rpoC | 763978 | c.609C>G | synonymous_variant | 0.35 |
rpoC | 763991 | p.Ile208Leu | missense_variant | 0.37 |
rpoC | 763996 | c.627T>C | synonymous_variant | 0.37 |
rpoC | 764005 | c.636G>C | synonymous_variant | 0.34 |
rpoC | 764011 | c.642T>C | synonymous_variant | 0.35 |
rpoC | 764024 | c.655_657delTTGinsCTC | synonymous_variant | 0.3 |
rpoC | 764044 | c.675T>C | synonymous_variant | 0.35 |
rpoC | 764059 | c.690G>C | synonymous_variant | 0.38 |
rpoC | 764083 | c.714A>G | synonymous_variant | 0.38 |
rpoC | 764098 | c.729A>G | synonymous_variant | 0.34 |
rpoC | 764101 | c.732C>G | synonymous_variant | 0.34 |
rpoC | 764131 | c.762T>C | synonymous_variant | 0.3 |
rpoC | 764161 | c.792G>C | synonymous_variant | 0.3 |
rpoC | 764188 | c.819A>G | synonymous_variant | 0.36 |
rpoC | 764194 | p.Glu275Asp | missense_variant | 0.36 |
rpoC | 764203 | c.834G>C | synonymous_variant | 0.37 |
rpoC | 764206 | c.837T>C | synonymous_variant | 0.36 |
rpoC | 764215 | c.846A>G | synonymous_variant | 0.36 |
rpoC | 764245 | c.876C>A | synonymous_variant | 0.39 |
rpoC | 764266 | c.897T>C | synonymous_variant | 0.39 |
rpoC | 764269 | c.900G>C | synonymous_variant | 0.39 |
rpoC | 764272 | c.903G>C | synonymous_variant | 0.38 |
rpoC | 764278 | c.909A>G | synonymous_variant | 0.38 |
rpoC | 764344 | c.975C>G | synonymous_variant | 0.33 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.31 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.29 |
rpoC | 764381 | c.1012_1013delTCinsAG | synonymous_variant | 0.28 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 0.25 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.31 |
rpoC | 764410 | c.1041G>C | synonymous_variant | 0.33 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.29 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.29 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.29 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.29 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.29 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.31 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.32 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.32 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.31 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.29 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.24 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.24 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.28 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 0.28 |
rpoC | 764585 | c.1216_1218delCTCinsTTG | synonymous_variant | 0.26 |
rpoC | 764611 | c.1242G>C | synonymous_variant | 0.27 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.26 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.27 |
rpoC | 764644 | c.1275G>C | synonymous_variant | 0.26 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.27 |
rpoC | 764695 | c.1326T>G | synonymous_variant | 0.27 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.27 |
rpoC | 764749 | c.1380G>C | synonymous_variant | 0.26 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.26 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.25 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.24 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.24 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 0.23 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.25 |
rpoC | 764830 | c.1461C>G | synonymous_variant | 0.23 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.23 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.26 |
rpoC | 764893 | c.1524T>C | synonymous_variant | 0.26 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.26 |
rpoC | 764923 | c.1554A>G | synonymous_variant | 0.25 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.22 |
rpoC | 764962 | c.1593G>C | synonymous_variant | 0.23 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.22 |
rpoC | 764983 | c.1614T>C | synonymous_variant | 0.2 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.2 |
rpoC | 764998 | c.1629G>A | synonymous_variant | 0.2 |
rpoC | 765008 | c.1639T>C | synonymous_variant | 0.19 |
rpoC | 765016 | c.1647C>G | synonymous_variant | 0.19 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765467 | c.2098C>T | synonymous_variant | 0.22 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.27 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.33 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.27 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.35 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.35 |
rpoC | 765559 | c.2190G>C | synonymous_variant | 0.35 |
rpoC | 765583 | c.2214G>T | synonymous_variant | 0.38 |
rpoC | 765625 | c.2256C>G | synonymous_variant | 0.39 |
rpoC | 765631 | p.Asp754Glu | missense_variant | 0.38 |
rpoC | 765658 | c.2289C>T | synonymous_variant | 0.43 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.44 |
rpoC | 765734 | c.2365T>C | synonymous_variant | 0.43 |
rpoC | 765739 | c.2370G>C | synonymous_variant | 0.43 |
rpoC | 765751 | c.2382C>G | synonymous_variant | 0.43 |
rpoC | 765752 | p.Asp795Ser | missense_variant | 0.43 |
rpoC | 765772 | c.2403C>G | synonymous_variant | 0.4 |
rpoC | 765784 | c.2415C>G | synonymous_variant | 0.38 |
rpoC | 765796 | c.2427C>T | synonymous_variant | 0.37 |
rpoC | 765811 | c.2442T>C | synonymous_variant | 0.35 |
rpoC | 765814 | c.2445A>G | synonymous_variant | 0.34 |
rpoC | 765826 | c.2457T>C | synonymous_variant | 0.31 |
rpoC | 765883 | c.2514C>G | synonymous_variant | 0.24 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.23 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.23 |
rpoC | 765928 | c.2559C>G | synonymous_variant | 0.19 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.21 |
rpoC | 765947 | c.2578T>C | synonymous_variant | 0.2 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.2 |
rpoC | 765979 | c.2610C>G | synonymous_variant | 0.23 |
rpoC | 765982 | c.2613C>T | synonymous_variant | 0.23 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.21 |
rpoC | 766010 | c.2641_2642delTCinsAG | synonymous_variant | 0.18 |
rpoC | 766027 | c.2658G>C | synonymous_variant | 0.23 |
rpoC | 766043 | p.Gln892Glu | missense_variant | 0.22 |
rpoC | 766054 | c.2685C>T | synonymous_variant | 0.23 |
rpoC | 766061 | p.Val898Leu | missense_variant | 0.23 |
rpoC | 766081 | c.2712T>C | synonymous_variant | 0.21 |
rpoC | 766082 | p.Ala905Gln | missense_variant | 0.21 |
rpoC | 766129 | c.2760C>G | synonymous_variant | 0.17 |
rpoC | 766141 | c.2772C>T | synonymous_variant | 0.16 |
rpoC | 766142 | c.2773C>T | synonymous_variant | 0.16 |
rpoC | 766168 | c.2799C>G | synonymous_variant | 0.18 |
rpoC | 766393 | c.3024C>G | synonymous_variant | 0.17 |
rpoC | 766408 | c.3039C>T | synonymous_variant | 0.19 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.21 |
rpoC | 766447 | c.3078T>C | synonymous_variant | 0.24 |
rpoC | 766456 | c.3087C>G | synonymous_variant | 0.25 |
rpoC | 766471 | c.3102G>C | synonymous_variant | 0.24 |
rpoC | 766486 | c.3117A>G | synonymous_variant | 0.25 |
rpoC | 766492 | c.3123T>C | synonymous_variant | 0.24 |
rpoC | 766522 | c.3153C>G | synonymous_variant | 0.24 |
rpoC | 766528 | c.3159T>C | synonymous_variant | 0.2 |
rpoC | 766530 | p.Arg1054Gln | missense_variant | 0.2 |
rpoC | 766573 | c.3204T>C | synonymous_variant | 0.2 |
rpoC | 766582 | c.3213C>G | synonymous_variant | 0.17 |
rpoC | 766583 | p.Gly1072Ser | missense_variant | 0.17 |
rpoC | 766594 | c.3225G>C | synonymous_variant | 0.17 |
rpoC | 766607 | p.Ile1080Leu | missense_variant | 0.22 |
rpoC | 766630 | c.3261G>T | synonymous_variant | 0.24 |
rpoC | 766633 | c.3264G>C | synonymous_variant | 0.24 |
rpoC | 766645 | c.3276A>G | synonymous_variant | 0.25 |
rpoC | 766651 | c.3282T>G | synonymous_variant | 0.25 |
rpoC | 766657 | c.3288A>G | synonymous_variant | 0.23 |
rpoC | 766666 | c.3297C>G | synonymous_variant | 0.23 |
rpoC | 766672 | c.3303T>C | synonymous_variant | 0.23 |
rpoC | 766708 | c.3339A>G | synonymous_variant | 0.21 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.22 |
rpoC | 766738 | c.3369G>C | synonymous_variant | 0.23 |
rpoC | 766750 | c.3381C>G | synonymous_variant | 0.23 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.29 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.27 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.25 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 0.18 |
rpoC | 766864 | c.3495G>C | synonymous_variant | 0.17 |
rpoC | 766894 | c.3525T>C | synonymous_variant | 0.17 |
rpoC | 766895 | c.3526T>C | synonymous_variant | 0.17 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.17 |
rpoC | 766933 | c.3564A>G | synonymous_variant | 0.25 |
rpoC | 766942 | c.3573C>T | synonymous_variant | 0.19 |
rpoC | 766945 | c.3576A>G | synonymous_variant | 0.2 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.21 |
rpoC | 767035 | c.3666G>C | synonymous_variant | 0.21 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.17 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.16 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.17 |
rpoC | 767134 | c.3765C>A | synonymous_variant | 0.16 |
rpoC | 767158 | c.3789T>C | synonymous_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.18 |
rpsL | 781658 | c.99A>G | synonymous_variant | 0.18 |
rpsL | 781682 | c.123T>C | synonymous_variant | 0.22 |
rpsL | 781703 | c.144G>T | synonymous_variant | 0.23 |
rpsL | 781706 | c.147T>G | synonymous_variant | 0.28 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.28 |
rpsL | 781718 | c.159C>G | synonymous_variant | 0.28 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.29 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.3 |
rpsL | 781751 | c.192G>C | synonymous_variant | 0.32 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.33 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.33 |
rpsL | 781763 | c.204C>G | synonymous_variant | 0.33 |
rpsL | 781808 | c.249C>T | synonymous_variant | 0.29 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.29 |
rpsL | 781820 | c.261G>C | synonymous_variant | 0.3 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.29 |
rpsL | 781835 | c.276T>C | synonymous_variant | 0.3 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.3 |
rpsL | 781865 | c.306G>C | synonymous_variant | 0.23 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.23 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.23 |
rpsL | 781877 | c.318T>G | synonymous_variant | 0.24 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.19 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.19 |
rpsL | 781916 | c.357T>C | synonymous_variant | 0.21 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.21 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.2 |
rplC | 800648 | c.-161A>T | upstream_gene_variant | 0.22 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.22 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.21 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.24 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.24 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.24 |
rplC | 800738 | c.-71T>C | upstream_gene_variant | 0.24 |
rplC | 800747 | c.-62C>G | upstream_gene_variant | 0.25 |
rplC | 800771 | c.-38C>T | upstream_gene_variant | 0.23 |
rplC | 800793 | c.-15_-11delAGATT | upstream_gene_variant | 0.24 |
rplC | 800803 | c.-6A>C | upstream_gene_variant | 0.25 |
rplC | 800804 | c.-4delA | upstream_gene_variant | 0.23 |
rplC | 800815 | c.7C>A | synonymous_variant | 0.23 |
rplC | 800820 | c.12G>A | synonymous_variant | 0.23 |
rplC | 800829 | c.21C>G | synonymous_variant | 0.23 |
rplC | 800844 | c.36T>C | synonymous_variant | 0.22 |
rplC | 800856 | c.48A>G | synonymous_variant | 0.23 |
rplC | 800865 | c.57A>G | synonymous_variant | 0.21 |
rplC | 800867 | p.Ser20Asn | missense_variant | 0.21 |
rplC | 800872 | c.64_66delAGAinsCGG | synonymous_variant | 0.2 |
rplC | 800875 | p.Val23Ile | missense_variant | 0.19 |
rplC | 800880 | c.72A>C | synonymous_variant | 0.19 |
rplC | 800889 | c.81C>G | synonymous_variant | 0.2 |
rplC | 800901 | c.93C>G | synonymous_variant | 0.22 |
rplC | 800916 | c.108A>C | synonymous_variant | 0.2 |
fbiC | 1303812 | c.882C>T | synonymous_variant | 0.18 |
fbiC | 1303842 | c.912C>G | synonymous_variant | 0.19 |
fbiC | 1303846 | p.Phe306Val | missense_variant | 0.19 |
fbiC | 1303851 | c.921C>G | synonymous_variant | 0.19 |
fbiC | 1303854 | c.924T>C | synonymous_variant | 0.2 |
fbiC | 1303855 | p.Ala309Thr | missense_variant | 0.19 |
fbiC | 1303860 | c.930A>C | synonymous_variant | 0.22 |
fbiC | 1303869 | c.939T>C | synonymous_variant | 0.2 |
fbiC | 1303881 | c.951G>C | synonymous_variant | 0.19 |
fbiC | 1303884 | c.954T>G | synonymous_variant | 0.19 |
fbiC | 1303887 | c.957G>C | synonymous_variant | 0.19 |
fbiC | 1303897 | c.967C>T | synonymous_variant | 0.19 |
fbiC | 1303905 | c.975G>C | synonymous_variant | 0.19 |
fbiC | 1303908 | c.978C>G | synonymous_variant | 0.19 |
fbiC | 1303935 | c.1005G>C | synonymous_variant | 0.18 |
fbiC | 1303938 | c.1008C>T | synonymous_variant | 0.2 |
fbiC | 1303947 | c.1017T>C | synonymous_variant | 0.19 |
fbiC | 1303948 | p.Gly340Arg | missense_variant | 0.19 |
fbiC | 1303961 | p.Arg344Leu | missense_variant | 0.18 |
fbiC | 1303971 | c.1041T>G | synonymous_variant | 0.17 |
fbiC | 1303974 | c.1044C>T | synonymous_variant | 0.17 |
fbiC | 1304875 | p.Ile649Val | missense_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472030 | n.185G>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472031 | n.186G>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473839 | n.182G>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1473899 | n.242A>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1473937 | n.280C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473944 | n.287G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474009 | n.352A>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474012 | n.355C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474051 | n.394T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474054 | n.397T>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474056 | n.399T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474071 | n.414G>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474099 | n.442G>A | non_coding_transcript_exon_variant | 0.34 |
rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 0.34 |
rrl | 1474111 | n.454T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474112 | n.455T>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.34 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474376 | n.719T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474409 | n.756_766delACCCACACGCG | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474427 | n.770A>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474429 | n.772G>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474435 | n.780_783delGAAT | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474627 | n.970G>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474717 | n.1060A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474753 | n.1096A>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474952 | n.1296_1300delCATCC | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474961 | n.1304T>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474962 | n.1305T>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474963 | n.1306G>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474964 | n.1307T>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474967 | n.1311_1315delGGGTG | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474991 | n.1334T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474995 | n.1338T>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475005 | n.1348C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475013 | n.1356G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475027 | n.1370G>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475028 | n.1371G>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475088 | n.1431A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475202 | n.1545G>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475206 | n.1549C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475209 | n.1552G>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475249 | n.1592T>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475252 | n.1595C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475266 | n.1609T>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475275 | n.1618C>T | non_coding_transcript_exon_variant | 0.34 |
rrl | 1475276 | n.1619T>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475291 | n.1634A>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475387 | n.1730C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475402 | n.1745C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475436 | n.1779C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475504 | n.1847C>A | non_coding_transcript_exon_variant | 0.65 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 0.37 |
rrl | 1475603 | n.1946G>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475638 | n.1981C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475659 | n.2002G>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475765 | n.2111delG | non_coding_transcript_exon_variant | 0.37 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476033 | n.2376T>C | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476035 | n.2378G>A | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476089 | n.2432T>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476095 | n.2438C>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.49 |
rrl | 1476117 | n.2460G>C | non_coding_transcript_exon_variant | 0.49 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.16 |
inhA | 1673772 | c.-430C>G | upstream_gene_variant | 0.2 |
inhA | 1673799 | c.-403T>C | upstream_gene_variant | 0.21 |
inhA | 1673802 | c.-400A>G | upstream_gene_variant | 0.21 |
inhA | 1674331 | c.130C>T | synonymous_variant | 0.3 |
inhA | 1674342 | c.141T>C | synonymous_variant | 0.3 |
inhA | 1674352 | p.Thr51Ala | missense_variant | 0.29 |
inhA | 1674368 | p.Ala56Glu | missense_variant | 0.3 |
inhA | 1674382 | p.Leu61Ile | missense_variant | 0.35 |
inhA | 1674399 | c.198A>G | synonymous_variant | 0.26 |
inhA | 1674415 | p.Ala72Asn | missense_variant | 0.25 |
inhA | 1674421 | c.220T>C | synonymous_variant | 0.26 |
inhA | 1674428 | p.Gly76Glu | missense_variant | 0.26 |
inhA | 1674435 | c.234G>C | synonymous_variant | 0.19 |
inhA | 1674440 | p.Glu80Ala | missense_variant | 0.21 |
inhA | 1674443 | p.Ala81Glu | missense_variant | 0.21 |
inhA | 1674450 | c.249G>T | synonymous_variant | 0.27 |
inhA | 1674465 | c.264C>G | synonymous_variant | 0.35 |
inhA | 1674471 | c.270G>C | synonymous_variant | 0.32 |
inhA | 1674480 | c.279T>C | synonymous_variant | 0.29 |
inhA | 1674483 | c.282G>C | synonymous_variant | 0.28 |
inhA | 1674486 | c.285T>C | synonymous_variant | 0.28 |
inhA | 1674489 | c.288G>C | synonymous_variant | 0.28 |
inhA | 1674507 | c.306G>C | synonymous_variant | 0.29 |
inhA | 1674542 | p.Ala114Glu | missense_variant | 0.32 |
inhA | 1674546 | c.345T>C | synonymous_variant | 0.31 |
inhA | 1674549 | c.348G>C | synonymous_variant | 0.29 |
inhA | 1674576 | c.375T>C | synonymous_variant | 0.32 |
inhA | 1674582 | c.381T>C | synonymous_variant | 0.33 |
inhA | 1674585 | c.384T>C | synonymous_variant | 0.33 |
inhA | 1674589 | p.Met130Leu | missense_variant | 0.33 |
inhA | 1674624 | c.423A>C | synonymous_variant | 0.41 |
inhA | 1674627 | c.426T>G | synonymous_variant | 0.41 |
inhA | 1674639 | c.438C>G | synonymous_variant | 0.41 |
inhA | 1674654 | c.453G>C | synonymous_variant | 0.41 |
inhA | 1674660 | c.459G>C | synonymous_variant | 0.41 |
inhA | 1674663 | c.462G>C | synonymous_variant | 0.42 |
inhA | 1674669 | c.468G>C | synonymous_variant | 0.39 |
inhA | 1674690 | c.489C>G | synonymous_variant | 0.37 |
inhA | 1674703 | c.502T>C | synonymous_variant | 0.38 |
inhA | 1674708 | c.507G>A | synonymous_variant | 0.38 |
inhA | 1674718 | c.517A>C | synonymous_variant | 0.3 |
inhA | 1674726 | c.525G>C | synonymous_variant | 0.33 |
inhA | 1674729 | c.528G>C | synonymous_variant | 0.36 |
inhA | 1674750 | c.549T>G | synonymous_variant | 0.4 |
inhA | 1674759 | c.558G>C | synonymous_variant | 0.4 |
inhA | 1674771 | c.570C>G | synonymous_variant | 0.38 |
inhA | 1674774 | c.573A>G | synonymous_variant | 0.38 |
inhA | 1674780 | c.579T>C | synonymous_variant | 0.38 |
inhA | 1674799 | c.598_600delAGTinsTCG | synonymous_variant | 0.27 |
inhA | 1674846 | p.Ile215Met | missense_variant | 0.27 |
inhA | 1674858 | c.657G>A | synonymous_variant | 0.25 |
inhA | 1674870 | c.669T>C | synonymous_variant | 0.25 |
inhA | 1674879 | c.678T>G | synonymous_variant | 0.25 |
inhA | 1674903 | c.702T>C | synonymous_variant | 0.25 |
inhA | 1674904 | p.Ala235Pro | missense_variant | 0.25 |
inhA | 1674912 | c.711G>C | synonymous_variant | 0.25 |
inhA | 1674933 | c.732G>C | synonymous_variant | 0.23 |
inhA | 1674934 | p.Leu245Val | missense_variant | 0.23 |
inhA | 1674939 | c.738G>C | synonymous_variant | 0.21 |
inhA | 1674942 | c.741T>G | synonymous_variant | 0.21 |
inhA | 1674954 | c.753G>C | synonymous_variant | 0.21 |
inhA | 1674957 | c.756G>C | synonymous_variant | 0.25 |
inhA | 1674963 | c.762G>C | synonymous_variant | 0.25 |
inhA | 1674966 | c.765T>C | synonymous_variant | 0.25 |
inhA | 1674967 | p.Asp256Thr | missense_variant | 0.23 |
inhA | 1674977 | p.Tyr259Phe | missense_variant | 0.25 |
inhA | 1674994 | p.His265Asn | missense_variant | 0.15 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.18 |
rpsA | 1833664 | c.123C>G | synonymous_variant | 0.18 |
rpsA | 1833667 | c.126C>G | synonymous_variant | 0.18 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.2 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.19 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.2 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.2 |
rpsA | 1833754 | c.213G>A | synonymous_variant | 0.23 |
rpsA | 1833760 | c.219C>T | synonymous_variant | 0.21 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.26 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.26 |
rpsA | 1833793 | c.252C>T | synonymous_variant | 0.26 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.27 |
rpsA | 1833805 | c.264C>T | synonymous_variant | 0.27 |
rpsA | 1833808 | c.267G>C | synonymous_variant | 0.27 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 0.27 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.33 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.33 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.37 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.35 |
rpsA | 1833871 | c.330G>A | synonymous_variant | 0.29 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.28 |
rpsA | 1833895 | c.354G>C | synonymous_variant | 0.26 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.25 |
rpsA | 1833940 | c.399C>G | synonymous_variant | 0.22 |
rpsA | 1833949 | c.408T>G | synonymous_variant | 0.23 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.18 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.18 |
rpsA | 1834102 | c.561T>G | synonymous_variant | 0.18 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.17 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.19 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.31 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.35 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.36 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.36 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.4 |
rpsA | 1834303 | c.762T>G | synonymous_variant | 0.39 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.39 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.45 |
rpsA | 1834351 | c.810G>A | synonymous_variant | 0.45 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.47 |
rpsA | 1834375 | c.834G>A | synonymous_variant | 0.48 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.48 |
rpsA | 1834411 | c.870T>G | synonymous_variant | 0.53 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.49 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.49 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.46 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.44 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.46 |
rpsA | 1834465 | c.924T>C | synonymous_variant | 0.46 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.44 |
rpsA | 1834474 | c.933C>G | synonymous_variant | 0.43 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.41 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.48 |
rpsA | 1834540 | c.999G>C | synonymous_variant | 0.43 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.4 |
rpsA | 1834555 | c.1014T>C | synonymous_variant | 0.4 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.32 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.3 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.3 |
rpsA | 1834690 | c.1149T>C | synonymous_variant | 0.24 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289945 | c.-704T>C | upstream_gene_variant | 0.17 |
kasA | 2517974 | c.-141T>C | upstream_gene_variant | 0.17 |
kasA | 2517993 | c.-122G>T | upstream_gene_variant | 0.15 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 0.85 |
kasA | 2518444 | c.330T>C | synonymous_variant | 0.18 |
kasA | 2518447 | c.333T>G | synonymous_variant | 0.18 |
kasA | 2518459 | c.345T>G | synonymous_variant | 0.22 |
kasA | 2518462 | c.348A>C | synonymous_variant | 0.24 |
kasA | 2518468 | c.354A>C | synonymous_variant | 0.26 |
kasA | 2518475 | c.361A>C | synonymous_variant | 0.29 |
kasA | 2518480 | c.366T>C | synonymous_variant | 0.29 |
kasA | 2518504 | c.390T>C | synonymous_variant | 0.35 |
kasA | 2518506 | p.Ala131Glu | missense_variant | 0.36 |
kasA | 2518513 | c.399C>G | synonymous_variant | 0.38 |
kasA | 2518519 | c.405G>C | synonymous_variant | 0.38 |
kasA | 2518528 | c.414C>G | synonymous_variant | 0.42 |
kasA | 2518534 | c.420G>C | synonymous_variant | 0.41 |
kasA | 2518561 | c.447T>C | synonymous_variant | 0.4 |
kasA | 2518570 | c.456G>C | synonymous_variant | 0.41 |
kasA | 2518574 | p.Ile154Val | missense_variant | 0.42 |
kasA | 2518579 | c.465T>C | synonymous_variant | 0.41 |
kasA | 2518588 | c.474T>C | synonymous_variant | 0.43 |
kasA | 2518594 | c.480C>G | synonymous_variant | 0.42 |
kasA | 2518597 | c.483C>G | synonymous_variant | 0.41 |
kasA | 2518609 | p.Met165Ile | missense_variant | 0.45 |
kasA | 2518639 | c.525G>C | synonymous_variant | 0.43 |
kasA | 2518657 | c.543G>C | synonymous_variant | 0.38 |
kasA | 2518663 | c.549T>C | synonymous_variant | 0.38 |
kasA | 2518672 | c.558G>C | synonymous_variant | 0.42 |
kasA | 2518678 | c.564C>T | synonymous_variant | 0.45 |
kasA | 2518684 | c.570C>G | synonymous_variant | 0.42 |
kasA | 2518702 | c.588C>T | synonymous_variant | 0.38 |
kasA | 2518705 | c.591T>C | synonymous_variant | 0.42 |
kasA | 2518711 | c.597A>G | synonymous_variant | 0.41 |
kasA | 2518714 | c.600A>C | synonymous_variant | 0.41 |
kasA | 2518747 | c.633C>G | synonymous_variant | 0.38 |
kasA | 2518783 | c.669T>C | synonymous_variant | 0.33 |
kasA | 2518789 | c.675G>C | synonymous_variant | 0.34 |
kasA | 2518792 | c.678C>G | synonymous_variant | 0.33 |
kasA | 2518795 | c.681C>G | synonymous_variant | 0.32 |
kasA | 2518807 | c.693C>T | synonymous_variant | 0.32 |
kasA | 2518822 | c.708C>G | synonymous_variant | 0.3 |
kasA | 2518825 | c.711T>C | synonymous_variant | 0.31 |
kasA | 2518843 | c.729T>G | synonymous_variant | 0.23 |
kasA | 2518846 | c.732G>C | synonymous_variant | 0.23 |
kasA | 2518847 | p.Leu245Met | missense_variant | 0.23 |
kasA | 2518864 | c.750G>C | synonymous_variant | 0.22 |
kasA | 2518879 | c.765A>G | synonymous_variant | 0.22 |
kasA | 2518885 | c.771T>C | synonymous_variant | 0.22 |
kasA | 2518898 | c.784T>C | synonymous_variant | 0.18 |
kasA | 2518910 | p.Leu266Met | missense_variant | 0.16 |
Rv2752c | 3065659 | p.Pro178Leu | missense_variant | 0.15 |
Rv2752c | 3066075 | c.117A>G | synonymous_variant | 0.19 |
Rv2752c | 3066081 | c.111G>C | synonymous_variant | 0.22 |
Rv2752c | 3066087 | c.105A>G | synonymous_variant | 0.22 |
Rv2752c | 3066114 | c.78A>G | synonymous_variant | 0.26 |
Rv2752c | 3066118 | p.Asn25Ser | missense_variant | 0.24 |
Rv2752c | 3066150 | c.42C>T | synonymous_variant | 0.25 |
Rv2752c | 3066155 | p.Ser13Thr | missense_variant | 0.2 |
Rv2752c | 3066168 | c.24A>C | synonymous_variant | 0.2 |
Rv2752c | 3066171 | c.21G>T | synonymous_variant | 0.2 |
Rv2752c | 3066176 | p.Pro6Ala | missense_variant | 0.2 |
Rv2752c | 3066177 | c.15T>C | synonymous_variant | 0.2 |
Rv2752c | 3066194 | c.-3G>T | upstream_gene_variant | 0.2 |
Rv2752c | 3066195 | c.-4A>G | upstream_gene_variant | 0.2 |
Rv2752c | 3066206 | c.-15A>G | upstream_gene_variant | 0.21 |
Rv2752c | 3066210 | c.-30_-20delTCTAAAGGTGA | upstream_gene_variant | 0.21 |
Rv2752c | 3066228 | c.-37T>C | upstream_gene_variant | 0.24 |
Rv2752c | 3066237 | c.-46C>G | upstream_gene_variant | 0.25 |
Rv2752c | 3066260 | c.-69T>C | upstream_gene_variant | 0.25 |
Rv2752c | 3066264 | c.-73C>T | upstream_gene_variant | 0.27 |
Rv2752c | 3066276 | c.-85G>C | upstream_gene_variant | 0.21 |
Rv2752c | 3066279 | c.-88A>G | upstream_gene_variant | 0.18 |
Rv2752c | 3066285 | c.-96_-94delGCCinsCCG | upstream_gene_variant | 0.18 |
Rv2752c | 3066290 | c.-99G>A | upstream_gene_variant | 0.17 |
Rv2752c | 3066309 | c.-118T>C | upstream_gene_variant | 0.17 |
Rv2752c | 3066312 | c.-121C>T | upstream_gene_variant | 0.19 |
Rv2752c | 3066320 | c.-129A>G | upstream_gene_variant | 0.18 |
Rv2752c | 3066330 | c.-139G>C | upstream_gene_variant | 0.2 |
Rv2752c | 3066335 | c.-144T>C | upstream_gene_variant | 0.18 |
Rv2752c | 3066350 | c.-159T>A | upstream_gene_variant | 0.18 |
thyA | 3073959 | c.513T>C | synonymous_variant | 0.2 |
thyA | 3073977 | c.495A>G | synonymous_variant | 0.24 |
thyA | 3073980 | c.492C>T | synonymous_variant | 0.23 |
thyA | 3073983 | c.489C>G | synonymous_variant | 0.23 |
thyA | 3073989 | c.483T>C | synonymous_variant | 0.26 |
thyA | 3074004 | c.468T>C | synonymous_variant | 0.26 |
thyA | 3074010 | c.462C>G | synonymous_variant | 0.25 |
thyA | 3074031 | c.441T>C | synonymous_variant | 0.2 |
thyA | 3074037 | c.435C>G | synonymous_variant | 0.2 |
thyA | 3074053 | p.Arg140Gln | missense_variant | 0.19 |
thyA | 3074056 | p.Glu139Pro | missense_variant | 0.19 |
thyA | 3074061 | c.411A>G | synonymous_variant | 0.19 |
thyA | 3074064 | c.408C>G | synonymous_variant | 0.18 |
thyA | 3074076 | c.396C>G | synonymous_variant | 0.2 |
thyA | 3074097 | c.375C>G | synonymous_variant | 0.2 |
thyA | 3074100 | p.Asp124Asn | missense_variant | 0.2 |
thyA | 3074103 | c.369C>G | synonymous_variant | 0.21 |
thyA | 3074106 | c.366T>C | synonymous_variant | 0.21 |
thyA | 3074121 | p.Asp117Glu | missense_variant | 0.2 |
thyA | 3074130 | c.342G>C | synonymous_variant | 0.21 |
thyA | 3074147 | p.Ile109Val | missense_variant | 0.19 |
thyA | 3074154 | c.318T>C | synonymous_variant | 0.18 |
thyA | 3074165 | p.Ala103Thr | missense_variant | 0.16 |
thyA | 3074205 | p.Glu89Asp | missense_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiA | 3641351 | p.Ala270Asp | missense_variant | 0.15 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.18 |
rpoA | 3877656 | c.852T>C | synonymous_variant | 0.24 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.23 |
rpoA | 3877677 | p.Ala277Ser | missense_variant | 0.19 |
rpoA | 3877680 | c.828G>C | synonymous_variant | 0.2 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.22 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.23 |
rpoA | 3877695 | c.813C>G | synonymous_variant | 0.22 |
rpoA | 3877704 | c.804G>C | synonymous_variant | 0.22 |
rpoA | 3877728 | c.780C>G | synonymous_variant | 0.27 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.29 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.29 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.27 |
rpoA | 3877773 | c.735G>C | synonymous_variant | 0.25 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.26 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.27 |
rpoA | 3877803 | c.705G>C | synonymous_variant | 0.28 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.29 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.26 |
rpoA | 3877848 | c.660C>G | synonymous_variant | 0.27 |
rpoA | 3877857 | c.651G>A | synonymous_variant | 0.23 |
rpoA | 3877875 | c.633T>C | synonymous_variant | 0.21 |
rpoA | 3877920 | c.588G>C | synonymous_variant | 0.2 |
rpoA | 3877934 | c.574C>T | synonymous_variant | 0.22 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.22 |
rpoA | 3877968 | c.540C>G | synonymous_variant | 0.21 |
rpoA | 3877974 | c.534G>C | synonymous_variant | 0.2 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.19 |
rpoA | 3878019 | c.489A>G | synonymous_variant | 0.26 |
rpoA | 3878022 | c.486T>C | synonymous_variant | 0.27 |
rpoA | 3878031 | c.477T>C | synonymous_variant | 0.27 |
rpoA | 3878040 | c.468T>C | synonymous_variant | 0.26 |
rpoA | 3878043 | c.465G>C | synonymous_variant | 0.26 |
rpoA | 3878046 | c.462T>A | synonymous_variant | 0.26 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.26 |
rpoA | 3878067 | c.441C>T | synonymous_variant | 0.23 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.23 |
rpoA | 3878073 | c.435C>T | synonymous_variant | 0.24 |
rpoA | 3878082 | c.426T>G | synonymous_variant | 0.25 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.27 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.28 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.33 |
rpoA | 3878130 | c.378C>G | synonymous_variant | 0.36 |
rpoA | 3878142 | p.Gly122Glu | missense_variant | 0.36 |
rpoA | 3878157 | c.351C>G | synonymous_variant | 0.36 |
rpoA | 3878163 | c.345C>T | synonymous_variant | 0.39 |
rpoA | 3878169 | c.339G>C | synonymous_variant | 0.39 |
rpoA | 3878184 | c.324C>T | synonymous_variant | 0.38 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.38 |
rpoA | 3878197 | p.Glu104Ala | missense_variant | 0.37 |
rpoA | 3878199 | c.309T>C | synonymous_variant | 0.38 |
rpoA | 3878205 | c.303T>C | synonymous_variant | 0.38 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.39 |
rpoA | 3878264 | p.Ser82Gly | missense_variant | 0.45 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.43 |
rpoA | 3878284 | p.Glu75Ala | missense_variant | 0.4 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.38 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.39 |
rpoA | 3878301 | c.207C>G | synonymous_variant | 0.39 |
rpoA | 3878309 | p.Pro67Ala | missense_variant | 0.39 |
rpoA | 3878310 | c.198G>C | synonymous_variant | 0.39 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 0.41 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.42 |
rpoA | 3878331 | c.177A>G | synonymous_variant | 0.41 |
rpoA | 3878334 | c.174T>C | synonymous_variant | 0.41 |
rpoA | 3878337 | c.171T>C | synonymous_variant | 0.42 |
rpoA | 3878346 | c.162T>C | synonymous_variant | 0.44 |
rpoA | 3878364 | c.144A>C | synonymous_variant | 0.38 |
rpoA | 3878367 | c.141C>G | synonymous_variant | 0.38 |
rpoA | 3878370 | c.138T>C | synonymous_variant | 0.38 |
rpoA | 3878385 | c.123C>G | synonymous_variant | 0.42 |
rpoA | 3878388 | c.120C>G | synonymous_variant | 0.42 |
rpoA | 3878391 | c.117T>C | synonymous_variant | 0.42 |
rpoA | 3878415 | c.93C>T | synonymous_variant | 0.41 |
rpoA | 3878424 | c.84G>C | synonymous_variant | 0.43 |
rpoA | 3878430 | c.78G>C | synonymous_variant | 0.41 |
rpoA | 3878433 | c.75G>C | synonymous_variant | 0.41 |
rpoA | 3878436 | c.72A>G | synonymous_variant | 0.41 |
rpoA | 3878442 | c.66G>C | synonymous_variant | 0.41 |
rpoA | 3878454 | c.54A>C | synonymous_variant | 0.42 |
rpoA | 3878472 | p.Asp12Glu | missense_variant | 0.39 |
rpoA | 3878478 | c.30C>G | synonymous_variant | 0.39 |
rpoA | 3878490 | c.18C>A | synonymous_variant | 0.28 |
rpoA | 3878496 | c.12A>T | synonymous_variant | 0.23 |
rpoA | 3878665 | c.-158A>G | upstream_gene_variant | 0.25 |
rpoA | 3878672 | c.-165A>T | upstream_gene_variant | 0.22 |
rpoA | 3878694 | c.-187A>G | upstream_gene_variant | 0.18 |
ddn | 3986648 | c.-196C>G | upstream_gene_variant | 0.18 |
ddn | 3986665 | c.-179G>C | upstream_gene_variant | 0.16 |
clpC1 | 4038347 | c.2358G>C | synonymous_variant | 0.21 |
clpC1 | 4038356 | c.2349T>C | synonymous_variant | 0.19 |
clpC1 | 4038359 | c.2346A>G | synonymous_variant | 0.19 |
clpC1 | 4038368 | c.2337T>C | synonymous_variant | 0.2 |
clpC1 | 4038398 | c.2307G>T | synonymous_variant | 0.24 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 0.24 |
clpC1 | 4038419 | c.2286T>C | synonymous_variant | 0.26 |
clpC1 | 4038433 | c.2272C>T | synonymous_variant | 0.33 |
clpC1 | 4038444 | p.Ala754Lys | missense_variant | 0.35 |
clpC1 | 4038446 | c.2259T>C | synonymous_variant | 0.35 |
clpC1 | 4038456 | p.Val750Glu | missense_variant | 0.33 |
clpC1 | 4038460 | p.Leu749Met | missense_variant | 0.31 |
clpC1 | 4038461 | c.2244G>T | synonymous_variant | 0.31 |
clpC1 | 4038474 | p.Ser744Ala | missense_variant | 0.27 |
clpC1 | 4038486 | p.Gly740Asn | missense_variant | 0.27 |
clpC1 | 4038489 | p.Ala739Gly | missense_variant | 0.26 |
clpC1 | 4038498 | p.Ser736Thr | missense_variant | 0.29 |
clpC1 | 4038530 | p.Glu725Asp | missense_variant | 0.35 |
clpC1 | 4038533 | p.Arg724Lys | missense_variant | 0.35 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.25 |
clpC1 | 4038623 | c.2082A>G | synonymous_variant | 0.26 |
clpC1 | 4038640 | p.Asp689Asn | missense_variant | 0.27 |
clpC1 | 4038658 | p.Lys683Gln | missense_variant | 0.26 |
clpC1 | 4038661 | p.Ser682Thr | missense_variant | 0.27 |
clpC1 | 4038662 | c.2043T>C | synonymous_variant | 0.27 |
clpC1 | 4038683 | c.2022T>C | synonymous_variant | 0.2 |
clpC1 | 4038695 | c.2010C>G | synonymous_variant | 0.19 |
clpC1 | 4038698 | c.2007C>T | synonymous_variant | 0.2 |
clpC1 | 4038701 | c.2004G>C | synonymous_variant | 0.2 |
clpC1 | 4038704 | c.2001T>C | synonymous_variant | 0.19 |
clpC1 | 4038707 | c.1998C>G | synonymous_variant | 0.19 |
clpC1 | 4038713 | c.1992T>C | synonymous_variant | 0.19 |
clpC1 | 4038755 | c.1950G>C | synonymous_variant | 0.2 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.2 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 0.19 |
clpC1 | 4038860 | c.1845G>A | synonymous_variant | 0.17 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.18 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.18 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.19 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.19 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.21 |
clpC1 | 4039043 | c.1662G>C | synonymous_variant | 0.21 |
clpC1 | 4039064 | c.1641C>T | synonymous_variant | 0.21 |
clpC1 | 4039085 | c.1620A>G | synonymous_variant | 0.23 |
clpC1 | 4039090 | c.1615C>T | synonymous_variant | 0.22 |
clpC1 | 4039118 | c.1587C>G | synonymous_variant | 0.19 |
clpC1 | 4039133 | c.1572C>G | synonymous_variant | 0.2 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.19 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.19 |
clpC1 | 4039166 | c.1539G>A | synonymous_variant | 0.19 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.19 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.19 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.2 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.21 |
clpC1 | 4039187 | c.1518G>C | synonymous_variant | 0.2 |
clpC1 | 4039190 | c.1515C>G | synonymous_variant | 0.2 |
clpC1 | 4039208 | c.1497C>G | synonymous_variant | 0.19 |
clpC1 | 4039226 | c.1479T>C | synonymous_variant | 0.19 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.21 |
clpC1 | 4039283 | c.1422C>T | synonymous_variant | 0.17 |
clpC1 | 4039292 | c.1413C>T | synonymous_variant | 0.16 |
clpC1 | 4039409 | c.1296T>C | synonymous_variant | 0.19 |
clpC1 | 4039412 | c.1293T>G | synonymous_variant | 0.19 |
clpC1 | 4039415 | p.Glu430Asp | missense_variant | 0.19 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.2 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.2 |
clpC1 | 4039454 | c.1251A>G | synonymous_variant | 0.2 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.21 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.23 |
clpC1 | 4039481 | c.1224T>G | synonymous_variant | 0.25 |
clpC1 | 4039484 | c.1221T>C | synonymous_variant | 0.24 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.31 |
clpC1 | 4039532 | c.1173C>T | synonymous_variant | 0.32 |
clpC1 | 4039541 | c.1164C>G | synonymous_variant | 0.37 |
clpC1 | 4039556 | c.1149G>C | synonymous_variant | 0.4 |
clpC1 | 4039570 | p.Met379Leu | missense_variant | 0.41 |
clpC1 | 4039582 | p.Thr375Ser | missense_variant | 0.4 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.4 |
clpC1 | 4039622 | c.1083C>G | synonymous_variant | 0.41 |
clpC1 | 4039661 | c.1044T>G | synonymous_variant | 0.34 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.3 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.24 |
clpC1 | 4039733 | c.972G>C | synonymous_variant | 0.26 |
clpC1 | 4039748 | c.957G>C | synonymous_variant | 0.24 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.24 |
clpC1 | 4039760 | c.945T>G | synonymous_variant | 0.22 |
clpC1 | 4039766 | c.939T>C | synonymous_variant | 0.18 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.18 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.17 |
clpC1 | 4039789 | p.Ser306Thr | missense_variant | 0.15 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.16 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.18 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.18 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.21 |
clpC1 | 4039988 | c.717C>G | synonymous_variant | 0.2 |
clpC1 | 4039996 | p.Glu237Gln | missense_variant | 0.22 |
clpC1 | 4040009 | c.696C>G | synonymous_variant | 0.2 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.2 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.2 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.21 |
clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 0.2 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.2 |
clpC1 | 4040108 | c.597G>C | synonymous_variant | 0.2 |
clpC1 | 4040129 | c.576C>G | synonymous_variant | 0.26 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.24 |
clpC1 | 4040147 | c.558A>G | synonymous_variant | 0.26 |
clpC1 | 4040162 | c.543G>C | synonymous_variant | 0.29 |
clpC1 | 4040165 | c.540G>C | synonymous_variant | 0.29 |
clpC1 | 4040171 | c.534C>G | synonymous_variant | 0.25 |
clpC1 | 4040180 | c.525C>G | synonymous_variant | 0.25 |
clpC1 | 4040201 | c.504C>G | synonymous_variant | 0.22 |
clpC1 | 4040207 | c.498T>C | synonymous_variant | 0.23 |
clpC1 | 4040213 | c.492T>G | synonymous_variant | 0.22 |
clpC1 | 4040228 | c.477G>C | synonymous_variant | 0.23 |
clpC1 | 4040231 | c.474C>G | synonymous_variant | 0.23 |
clpC1 | 4040234 | c.471C>G | synonymous_variant | 0.23 |
clpC1 | 4040240 | c.465C>G | synonymous_variant | 0.23 |
clpC1 | 4040249 | c.456A>G | synonymous_variant | 0.25 |
clpC1 | 4040267 | c.438A>G | synonymous_variant | 0.28 |
clpC1 | 4040273 | c.432T>C | synonymous_variant | 0.28 |
clpC1 | 4040277 | c.427_428delTCinsAG | synonymous_variant | 0.25 |
clpC1 | 4040279 | c.426C>G | synonymous_variant | 0.26 |
clpC1 | 4040291 | c.414G>C | synonymous_variant | 0.24 |
clpC1 | 4040330 | c.375C>G | synonymous_variant | 0.24 |
clpC1 | 4040335 | c.370C>T | synonymous_variant | 0.25 |
clpC1 | 4040354 | c.351A>G | synonymous_variant | 0.22 |
clpC1 | 4040387 | c.318A>G | synonymous_variant | 0.21 |
clpC1 | 4040393 | c.312G>C | synonymous_variant | 0.23 |
clpC1 | 4040411 | c.294T>C | synonymous_variant | 0.19 |
clpC1 | 4040423 | c.282A>G | synonymous_variant | 0.2 |
clpC1 | 4040431 | c.274T>C | synonymous_variant | 0.2 |
clpC1 | 4040441 | c.264C>G | synonymous_variant | 0.23 |
clpC1 | 4040450 | c.255A>G | synonymous_variant | 0.22 |
clpC1 | 4040459 | c.246C>G | synonymous_variant | 0.22 |
clpC1 | 4040462 | c.243C>G | synonymous_variant | 0.22 |
clpC1 | 4040465 | c.240T>C | synonymous_variant | 0.21 |
clpC1 | 4040471 | c.234T>C | synonymous_variant | 0.22 |
clpC1 | 4040480 | c.225T>G | synonymous_variant | 0.23 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 0.2 |
clpC1 | 4040528 | c.177G>C | synonymous_variant | 0.2 |
clpC1 | 4040531 | c.174T>C | synonymous_variant | 0.2 |
clpC1 | 4040534 | c.171A>G | synonymous_variant | 0.21 |
clpC1 | 4040537 | c.168G>C | synonymous_variant | 0.21 |
clpC1 | 4040546 | c.159G>C | synonymous_variant | 0.21 |
clpC1 | 4040551 | c.154T>C | synonymous_variant | 0.21 |
clpC1 | 4040561 | c.144A>G | synonymous_variant | 0.21 |
clpC1 | 4040567 | c.138C>G | synonymous_variant | 0.21 |
clpC1 | 4040570 | c.135C>G | synonymous_variant | 0.21 |
clpC1 | 4040573 | c.132T>C | synonymous_variant | 0.2 |
clpC1 | 4040594 | c.111G>T | synonymous_variant | 0.18 |
clpC1 | 4040597 | c.108C>T | synonymous_variant | 0.18 |
clpC1 | 4040600 | c.105A>G | synonymous_variant | 0.2 |
clpC1 | 4040603 | c.102T>G | synonymous_variant | 0.2 |
clpC1 | 4040606 | c.99T>C | synonymous_variant | 0.2 |
panD | 4044120 | c.162A>C | synonymous_variant | 0.19 |
panD | 4044123 | c.159T>C | synonymous_variant | 0.19 |
panD | 4044126 | c.156T>C | synonymous_variant | 0.19 |
panD | 4044138 | c.144T>C | synonymous_variant | 0.19 |
panD | 4044150 | c.132A>G | synonymous_variant | 0.18 |
embC | 4240495 | c.633T>C | synonymous_variant | 0.17 |
embC | 4240514 | p.Val218Met | missense_variant | 0.17 |
embC | 4240543 | c.681G>C | synonymous_variant | 0.19 |
embC | 4240545 | p.Pro228Gln | missense_variant | 0.19 |
embC | 4240558 | c.696C>G | synonymous_variant | 0.21 |
embC | 4240561 | c.699C>G | synonymous_variant | 0.21 |
embC | 4240576 | c.714A>G | synonymous_variant | 0.23 |
embC | 4240578 | p.Ala239Val | missense_variant | 0.22 |
embC | 4240587 | p.Gly242Ala | missense_variant | 0.22 |
embC | 4240598 | p.Val246Ile | missense_variant | 0.22 |
embC | 4240610 | p.Ile250Leu | missense_variant | 0.26 |
embC | 4240615 | c.753G>C | synonymous_variant | 0.26 |
embC | 4240632 | p.Met257Thr | missense_variant | 0.21 |
embC | 4240645 | c.783G>C | synonymous_variant | 0.21 |
embC | 4240654 | c.792C>G | synonymous_variant | 0.21 |
embC | 4240655 | p.Ala265Ser | missense_variant | 0.21 |
embC | 4240670 | p.Thr270Leu | missense_variant | 0.2 |
embC | 4240673 | p.Gly271Ser | missense_variant | 0.2 |
embC | 4240678 | c.816T>G | synonymous_variant | 0.2 |
embC | 4240685 | p.Thr275Ala | missense_variant | 0.21 |
embC | 4240693 | c.831T>C | synonymous_variant | 0.19 |
embC | 4240694 | p.Ile278Val | missense_variant | 0.19 |
embC | 4240729 | c.867C>G | synonymous_variant | 0.18 |
embC | 4240735 | c.873C>G | synonymous_variant | 0.2 |
embC | 4240822 | c.960C>G | synonymous_variant | 0.19 |
embC | 4240831 | c.969T>G | synonymous_variant | 0.2 |
embC | 4240867 | c.1005T>G | synonymous_variant | 0.29 |
embC | 4240870 | c.1008T>C | synonymous_variant | 0.33 |
embC | 4240885 | c.1023T>C | synonymous_variant | 0.33 |
embC | 4240897 | c.1035C>G | synonymous_variant | 0.35 |
embC | 4240898 | c.1036_1038delCTAinsTTG | synonymous_variant | 0.35 |
embC | 4240911 | p.Ala350Val | missense_variant | 0.31 |
embC | 4240924 | c.1062C>G | synonymous_variant | 0.33 |
embC | 4240936 | c.1074A>G | synonymous_variant | 0.33 |
embC | 4240945 | c.1083T>C | synonymous_variant | 0.33 |
embC | 4240951 | c.1089C>G | synonymous_variant | 0.29 |
embC | 4240954 | p.Ile364Met | missense_variant | 0.29 |
embC | 4240957 | c.1095C>G | synonymous_variant | 0.28 |
embC | 4240960 | c.1098G>C | synonymous_variant | 0.3 |
embC | 4240978 | c.1116G>A | synonymous_variant | 0.24 |
embC | 4240979 | p.Thr373Gln | missense_variant | 0.24 |
embC | 4240983 | p.Ser374Asn | missense_variant | 0.24 |
embC | 4240987 | c.1125G>C | synonymous_variant | 0.24 |
embC | 4240989 | p.Ala376Gly | missense_variant | 0.23 |
embC | 4241005 | c.1143G>C | synonymous_variant | 0.26 |
embC | 4241008 | c.1146G>C | synonymous_variant | 0.26 |
embC | 4241011 | c.1149C>A | synonymous_variant | 0.27 |
embC | 4241017 | c.1155T>C | synonymous_variant | 0.26 |
embC | 4241023 | c.1161T>C | synonymous_variant | 0.27 |
embC | 4241026 | c.1164C>G | synonymous_variant | 0.29 |
embC | 4241038 | c.1176G>C | synonymous_variant | 0.28 |
embC | 4241039 | p.Asp393Asn | missense_variant | 0.28 |
embC | 4241047 | c.1185C>G | synonymous_variant | 0.28 |
embC | 4241050 | c.1188T>G | synonymous_variant | 0.29 |
embC | 4241071 | c.1209C>G | synonymous_variant | 0.26 |
embC | 4241074 | c.1212G>C | synonymous_variant | 0.24 |
embC | 4241104 | c.1242G>A | synonymous_variant | 0.22 |
embC | 4241107 | c.1245G>C | synonymous_variant | 0.24 |
embC | 4241116 | c.1254C>G | synonymous_variant | 0.24 |
embC | 4241140 | c.1278A>G | synonymous_variant | 0.24 |
embC | 4241141 | p.Ile427Ala | missense_variant | 0.24 |
embC | 4241158 | c.1296T>C | synonymous_variant | 0.21 |
embC | 4241161 | c.1299C>G | synonymous_variant | 0.19 |
embC | 4241162 | c.1300T>C | synonymous_variant | 0.2 |
embC | 4241230 | c.1368A>G | synonymous_variant | 0.19 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 0.9 |
embA | 4244298 | p.Ser356Ala | missense_variant | 0.2 |
embA | 4244312 | c.1080T>C | synonymous_variant | 0.2 |
embA | 4244324 | c.1092T>G | synonymous_variant | 0.19 |
embA | 4244327 | c.1095T>C | synonymous_variant | 0.19 |
embA | 4244337 | p.Leu369Val | missense_variant | 0.19 |
embA | 4244340 | p.Ser370Ala | missense_variant | 0.19 |
embA | 4244366 | c.1134C>G | synonymous_variant | 0.18 |
embA | 4244372 | c.1140T>C | synonymous_variant | 0.18 |
embA | 4244390 | c.1158G>C | synonymous_variant | 0.19 |
embA | 4244393 | c.1161G>C | synonymous_variant | 0.18 |
embA | 4245194 | c.1962G>C | synonymous_variant | 0.23 |
embA | 4245206 | c.1974A>G | synonymous_variant | 0.21 |
embA | 4245207 | c.1975T>C | synonymous_variant | 0.21 |
embA | 4245215 | c.1983A>C | synonymous_variant | 0.21 |
embA | 4245218 | c.1986C>G | synonymous_variant | 0.21 |
embA | 4245222 | p.Tyr664Gln | missense_variant | 0.21 |
embA | 4245233 | c.2001G>C | synonymous_variant | 0.21 |
embA | 4245261 | p.Lys677Glu | missense_variant | 0.2 |
embA | 4245281 | c.2049C>G | synonymous_variant | 0.21 |
embA | 4245282 | p.Ile684Val | missense_variant | 0.21 |
embA | 4245285 | c.2053_2055delTTGinsCTC | synonymous_variant | 0.21 |
embA | 4245290 | c.2058C>G | synonymous_variant | 0.22 |
embA | 4245293 | c.2061T>G | synonymous_variant | 0.21 |
embA | 4245299 | c.2067A>C | synonymous_variant | 0.22 |
embA | 4245315 | p.Val695Thr | missense_variant | 0.26 |
embA | 4245327 | p.Ala699Ile | missense_variant | 0.26 |
embA | 4245345 | p.Met705Leu | missense_variant | 0.32 |
embA | 4245355 | p.Ala708Gly | missense_variant | 0.23 |
embA | 4245362 | c.2130G>C | synonymous_variant | 0.26 |
embA | 4245368 | c.2136T>C | synonymous_variant | 0.23 |
embA | 4245377 | c.2145T>C | synonymous_variant | 0.2 |
embA | 4245650 | p.Ile806Met | missense_variant | 0.17 |
embB | 4245665 | c.-849C>G | upstream_gene_variant | 0.16 |
embB | 4245674 | c.-840A>C | upstream_gene_variant | 0.19 |
embB | 4245680 | c.-834G>A | upstream_gene_variant | 0.16 |
embA | 4245693 | p.Ile821Val | missense_variant | 0.16 |
embA | 4245834 | p.Leu868Met | missense_variant | 0.15 |
embB | 4249296 | p.Ala928Val | missense_variant | 0.16 |
embB | 4249316 | p.Ala935Pro | missense_variant | 0.22 |
embB | 4249321 | c.2808A>C | synonymous_variant | 0.22 |
embB | 4249322 | p.Ala937Ser | missense_variant | 0.22 |
embB | 4249325 | p.Lys938Gln | missense_variant | 0.22 |
embB | 4249330 | p.Met939Ile | missense_variant | 0.23 |
embB | 4249339 | c.2826T>C | synonymous_variant | 0.27 |
embB | 4249351 | c.2838C>G | synonymous_variant | 0.29 |
embB | 4249360 | c.2847G>C | synonymous_variant | 0.32 |
embB | 4249369 | c.2856T>C | synonymous_variant | 0.33 |
embB | 4249375 | c.2862G>C | synonymous_variant | 0.32 |
embB | 4249381 | c.2868A>G | synonymous_variant | 0.32 |
embB | 4249387 | p.Glu958Asp | missense_variant | 0.32 |
embB | 4249394 | p.Ile961Val | missense_variant | 0.32 |
embB | 4249399 | c.2886G>C | synonymous_variant | 0.3 |
embB | 4249400 | p.Val963Leu | missense_variant | 0.3 |
embB | 4249411 | c.2898G>C | synonymous_variant | 0.26 |
embB | 4249414 | c.2901G>C | synonymous_variant | 0.25 |
embB | 4249417 | c.2904A>G | synonymous_variant | 0.25 |
embB | 4249423 | p.Asp970Glu | missense_variant | 0.27 |
embB | 4249432 | c.2919A>G | synonymous_variant | 0.27 |
embB | 4249441 | c.2928A>G | synonymous_variant | 0.21 |
embB | 4249444 | c.2931T>C | synonymous_variant | 0.19 |
embB | 4249447 | c.2934G>C | synonymous_variant | 0.19 |
embB | 4249450 | c.2937C>T | synonymous_variant | 0.19 |
embB | 4249456 | c.2943G>A | synonymous_variant | 0.17 |
embB | 4249465 | c.2952G>C | synonymous_variant | 0.19 |
embB | 4249469 | p.Leu986Met | missense_variant | 0.18 |
embB | 4249486 | c.2973T>G | synonymous_variant | 0.19 |
embB | 4249487 | c.2974T>C | synonymous_variant | 0.19 |
embB | 4249492 | c.2979C>A | synonymous_variant | 0.19 |
aftB | 4268138 | c.699A>C | synonymous_variant | 0.17 |
aftB | 4268162 | p.Gln225Glu | missense_variant | 0.2 |
aftB | 4268169 | p.Ala223Gly | missense_variant | 0.25 |
aftB | 4268171 | c.666G>C | synonymous_variant | 0.25 |
aftB | 4268179 | c.658T>C | synonymous_variant | 0.25 |
aftB | 4268180 | p.Phe219Leu | missense_variant | 0.25 |
aftB | 4268186 | c.651C>G | synonymous_variant | 0.25 |
aftB | 4268189 | c.648C>G | synonymous_variant | 0.25 |
aftB | 4268194 | p.Leu215Val | missense_variant | 0.25 |
aftB | 4268200 | p.Ile213Val | missense_variant | 0.33 |
aftB | 4268207 | c.630C>G | synonymous_variant | 0.33 |
aftB | 4268213 | c.624T>G | synonymous_variant | 0.33 |
aftB | 4268219 | c.618C>G | synonymous_variant | 0.25 |
aftB | 4268236 | c.601T>C | synonymous_variant | 0.23 |
aftB | 4268295 | p.Cys181Phe | missense_variant | 0.15 |
aftB | 4268386 | c.451T>C | synonymous_variant | 0.2 |
aftB | 4268393 | c.444G>C | synonymous_variant | 0.2 |
aftB | 4268404 | c.433T>C | synonymous_variant | 0.17 |
aftB | 4268407 | p.Val144Met | missense_variant | 0.17 |
aftB | 4268423 | c.414C>T | synonymous_variant | 0.18 |
aftB | 4268426 | c.411C>G | synonymous_variant | 0.18 |
aftB | 4268591 | c.246G>C | synonymous_variant | 0.29 |
aftB | 4268597 | c.240G>A | synonymous_variant | 0.29 |
aftB | 4268602 | p.Leu79Met | missense_variant | 0.29 |
aftB | 4269042 | c.-206G>C | upstream_gene_variant | 0.19 |
aftB | 4269096 | c.-260C>G | upstream_gene_variant | 0.21 |
aftB | 4269099 | c.-263G>A | upstream_gene_variant | 0.19 |
aftB | 4269103 | c.-268_-267delAGinsTC | upstream_gene_variant | 0.18 |
ubiA | 4269107 | p.Tyr243His | missense_variant | 0.19 |
ubiA | 4269110 | p.Gly242Arg | missense_variant | 0.19 |
aftB | 4269114 | c.-278C>T | upstream_gene_variant | 0.19 |
aftB | 4269123 | c.-287T>G | upstream_gene_variant | 0.2 |
aftB | 4269131 | c.-295C>T | upstream_gene_variant | 0.19 |
aftB | 4269144 | c.-308C>G | upstream_gene_variant | 0.19 |
ubiA | 4269164 | p.Leu224Met | missense_variant | 0.21 |
aftB | 4269165 | c.-329G>C | upstream_gene_variant | 0.19 |
aftB | 4269201 | c.-365A>G | upstream_gene_variant | 0.2 |
aftB | 4269207 | c.-371G>C | upstream_gene_variant | 0.19 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |