Run ID: ERR4817735
Sample name:
Date: 01-04-2023 15:10:00
Number of reads: 2100820
Percentage reads mapped: 69.56
Strain: lineage4.8
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.97 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 0.97 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.57 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.15 | kanamycin, capreomycin, aminoglycosides, amikacin |
embB | 4247448 | p.His312Arg | missense_variant | 0.16 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5078 | c.-162_-161insG | upstream_gene_variant | 0.85 |
gyrB | 5827 | c.588G>A | synonymous_variant | 0.15 |
gyrB | 6115 | c.876A>G | synonymous_variant | 0.22 |
gyrB | 6123 | p.Ala295Gly | missense_variant | 0.28 |
gyrB | 6127 | c.888G>C | synonymous_variant | 0.28 |
gyrB | 6130 | c.891T>C | synonymous_variant | 0.3 |
gyrB | 6136 | c.897G>A | synonymous_variant | 0.32 |
gyrB | 6139 | c.900G>C | synonymous_variant | 0.4 |
gyrB | 6196 | c.957C>T | synonymous_variant | 0.35 |
gyrB | 6238 | c.999G>A | synonymous_variant | 0.15 |
gyrB | 6242 | p.Arg335Lys | missense_variant | 0.17 |
gyrB | 6250 | c.1011A>G | synonymous_variant | 0.23 |
gyrB | 6256 | c.1017G>A | synonymous_variant | 0.24 |
gyrB | 6268 | c.1029C>G | synonymous_variant | 0.24 |
gyrB | 6280 | c.1041T>C | synonymous_variant | 0.21 |
gyrB | 6286 | c.1047T>C | synonymous_variant | 0.17 |
gyrB | 6289 | c.1050C>T | synonymous_variant | 0.18 |
gyrB | 6292 | c.1053G>C | synonymous_variant | 0.18 |
gyrA | 6307 | c.-995T>G | upstream_gene_variant | 0.23 |
gyrA | 6319 | c.-983G>C | upstream_gene_variant | 0.26 |
gyrA | 6362 | c.-940T>C | upstream_gene_variant | 0.21 |
gyrA | 6376 | c.-926G>A | upstream_gene_variant | 0.2 |
gyrA | 6379 | c.-923C>G | upstream_gene_variant | 0.2 |
gyrA | 6382 | c.-920A>G | upstream_gene_variant | 0.21 |
gyrA | 6388 | c.-914T>C | upstream_gene_variant | 0.21 |
gyrA | 6403 | c.-899T>C | upstream_gene_variant | 0.18 |
gyrA | 6613 | c.-689A>G | upstream_gene_variant | 0.17 |
gyrA | 6616 | c.-686A>G | upstream_gene_variant | 0.16 |
gyrA | 6622 | c.-680C>T | upstream_gene_variant | 0.16 |
gyrA | 6634 | c.-668T>C | upstream_gene_variant | 0.19 |
gyrA | 6637 | c.-665T>G | upstream_gene_variant | 0.18 |
gyrA | 6640 | c.-662A>G | upstream_gene_variant | 0.18 |
gyrA | 6643 | c.-659A>G | upstream_gene_variant | 0.17 |
gyrA | 6649 | c.-653T>C | upstream_gene_variant | 0.18 |
gyrA | 6655 | c.-647T>C | upstream_gene_variant | 0.18 |
gyrA | 6670 | c.-632G>C | upstream_gene_variant | 0.21 |
gyrA | 6673 | c.-629A>C | upstream_gene_variant | 0.23 |
gyrA | 6676 | c.-626T>G | upstream_gene_variant | 0.23 |
gyrA | 6700 | c.-602T>C | upstream_gene_variant | 0.21 |
gyrA | 6703 | c.-599G>C | upstream_gene_variant | 0.22 |
gyrA | 6709 | c.-593A>G | upstream_gene_variant | 0.24 |
gyrA | 6712 | c.-590G>C | upstream_gene_variant | 0.21 |
gyrA | 6751 | c.-551G>C | upstream_gene_variant | 0.21 |
gyrA | 6760 | c.-542G>C | upstream_gene_variant | 0.23 |
gyrA | 6763 | c.-539G>C | upstream_gene_variant | 0.2 |
gyrA | 6775 | c.-527G>C | upstream_gene_variant | 0.16 |
gyrA | 6793 | c.-509T>C | upstream_gene_variant | 0.18 |
gyrB | 6797 | p.Gly520Thr | missense_variant | 0.18 |
gyrA | 6811 | c.-491C>T | upstream_gene_variant | 0.17 |
gyrA | 6841 | c.-461T>C | upstream_gene_variant | 0.25 |
gyrA | 6844 | c.-458T>C | upstream_gene_variant | 0.23 |
gyrA | 6901 | c.-401G>C | upstream_gene_variant | 0.15 |
gyrA | 6904 | c.-398C>G | upstream_gene_variant | 0.17 |
gyrA | 6910 | c.-392G>A | upstream_gene_variant | 0.17 |
gyrA | 6967 | c.-335T>C | upstream_gene_variant | 0.27 |
gyrA | 6973 | c.-329G>C | upstream_gene_variant | 0.33 |
gyrA | 6982 | c.-320A>C | upstream_gene_variant | 0.29 |
gyrA | 7006 | c.-296T>C | upstream_gene_variant | 0.27 |
gyrA | 7007 | c.-295C>T | upstream_gene_variant | 0.26 |
gyrA | 7010 | c.-292C>T | upstream_gene_variant | 0.25 |
gyrA | 7015 | c.-287G>A | upstream_gene_variant | 0.25 |
gyrA | 7018 | c.-284G>A | upstream_gene_variant | 0.29 |
gyrB | 7023 | p.Leu595Gln | missense_variant | 0.27 |
gyrA | 7033 | c.-269G>C | upstream_gene_variant | 0.29 |
gyrB | 7051 | p.Glu604Asp | missense_variant | 0.21 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7391 | c.90C>T | synonymous_variant | 0.21 |
gyrA | 7394 | c.93T>C | synonymous_variant | 0.21 |
gyrA | 7427 | c.126G>C | synonymous_variant | 0.24 |
gyrA | 7442 | c.141G>C | synonymous_variant | 0.24 |
gyrA | 7451 | c.150C>G | synonymous_variant | 0.28 |
gyrA | 7457 | c.156T>C | synonymous_variant | 0.3 |
gyrA | 7475 | c.174A>G | synonymous_variant | 0.23 |
gyrA | 7477 | p.Met59Thr | missense_variant | 0.78 |
gyrA | 7480 | p.Phe60Tyr | missense_variant | 0.21 |
gyrA | 7484 | c.183T>C | synonymous_variant | 0.22 |
gyrA | 7490 | c.189C>G | synonymous_variant | 0.24 |
gyrA | 7523 | c.222C>G | synonymous_variant | 0.25 |
gyrA | 7532 | c.231T>G | synonymous_variant | 0.24 |
gyrA | 7541 | c.240C>G | synonymous_variant | 0.24 |
gyrA | 7547 | c.246C>T | synonymous_variant | 0.24 |
gyrA | 7571 | c.270G>C | synonymous_variant | 0.23 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 0.23 |
gyrA | 7595 | c.294C>G | synonymous_variant | 0.17 |
gyrA | 7601 | c.300C>G | synonymous_variant | 0.16 |
gyrA | 7607 | c.306C>T | synonymous_variant | 0.15 |
gyrA | 7622 | c.321C>T | synonymous_variant | 0.16 |
gyrA | 7625 | c.324G>C | synonymous_variant | 0.17 |
gyrA | 7631 | c.330G>C | synonymous_variant | 0.17 |
gyrA | 7637 | c.336C>G | synonymous_variant | 0.18 |
gyrA | 7658 | c.357A>C | synonymous_variant | 0.18 |
gyrA | 7664 | c.363T>C | synonymous_variant | 0.16 |
gyrA | 7670 | c.369A>G | synonymous_variant | 0.16 |
gyrA | 7679 | c.378G>C | synonymous_variant | 0.17 |
gyrA | 7763 | c.462T>C | synonymous_variant | 0.15 |
gyrA | 7775 | c.474C>A | synonymous_variant | 0.17 |
gyrA | 7781 | c.480G>C | synonymous_variant | 0.16 |
gyrA | 7784 | c.483A>G | synonymous_variant | 0.16 |
gyrA | 7790 | c.489G>C | synonymous_variant | 0.18 |
gyrA | 7793 | c.492G>C | synonymous_variant | 0.19 |
gyrA | 7796 | c.495G>C | synonymous_variant | 0.21 |
gyrA | 7799 | c.498A>G | synonymous_variant | 0.21 |
gyrA | 7814 | c.513C>G | synonymous_variant | 0.23 |
gyrA | 7823 | c.522G>C | synonymous_variant | 0.26 |
gyrA | 7832 | c.531G>T | synonymous_variant | 0.22 |
gyrA | 7835 | c.534A>C | synonymous_variant | 0.19 |
gyrA | 8121 | c.820T>C | synonymous_variant | 0.17 |
gyrA | 8129 | c.828T>C | synonymous_variant | 0.16 |
gyrA | 8135 | c.834C>G | synonymous_variant | 0.19 |
gyrA | 8156 | c.855T>C | synonymous_variant | 0.32 |
gyrA | 8168 | c.867A>G | synonymous_variant | 0.31 |
gyrA | 8177 | c.876A>C | synonymous_variant | 0.3 |
gyrA | 8198 | c.897T>C | synonymous_variant | 0.22 |
gyrA | 8207 | c.906T>C | synonymous_variant | 0.19 |
gyrA | 8219 | c.918T>C | synonymous_variant | 0.2 |
gyrA | 8225 | c.924T>C | synonymous_variant | 0.2 |
gyrA | 8234 | c.933T>C | synonymous_variant | 0.2 |
gyrA | 8237 | c.936A>G | synonymous_variant | 0.21 |
gyrA | 8247 | p.Ile316Val | missense_variant | 0.21 |
gyrA | 8264 | c.963T>C | synonymous_variant | 0.16 |
gyrA | 8267 | c.966G>C | synonymous_variant | 0.16 |
gyrA | 8270 | c.969G>C | synonymous_variant | 0.17 |
gyrA | 8276 | c.975G>A | synonymous_variant | 0.19 |
gyrA | 8283 | p.Ile328Leu | missense_variant | 0.21 |
gyrA | 8288 | c.987T>C | synonymous_variant | 0.19 |
gyrA | 8294 | c.993T>C | synonymous_variant | 0.26 |
gyrA | 8324 | c.1023T>C | synonymous_variant | 0.27 |
gyrA | 8330 | c.1029C>G | synonymous_variant | 0.3 |
gyrA | 8339 | c.1038A>G | synonymous_variant | 0.27 |
gyrA | 8340 | p.Ala347Ser | missense_variant | 0.25 |
gyrA | 8372 | c.1071G>C | synonymous_variant | 0.29 |
gyrA | 8375 | c.1074G>C | synonymous_variant | 0.31 |
gyrA | 8382 | p.Leu361Met | missense_variant | 0.35 |
gyrA | 8387 | c.1086C>T | synonymous_variant | 0.33 |
gyrA | 8391 | p.Tyr364His | missense_variant | 0.27 |
gyrA | 8399 | c.1098T>G | synonymous_variant | 0.26 |
gyrA | 8401 | p.Asp367Ala | missense_variant | 0.26 |
gyrA | 8405 | c.1104C>T | synonymous_variant | 0.25 |
gyrA | 8420 | c.1119T>C | synonymous_variant | 0.17 |
gyrA | 8504 | c.1203G>C | synonymous_variant | 0.16 |
gyrA | 8576 | c.1275C>G | synonymous_variant | 0.15 |
gyrA | 8579 | c.1278C>T | synonymous_variant | 0.18 |
gyrA | 8588 | c.1287G>A | synonymous_variant | 0.15 |
gyrA | 8619 | c.1318_1320delTTGinsCTA | synonymous_variant | 0.24 |
gyrA | 8624 | c.1323G>C | synonymous_variant | 0.24 |
gyrA | 8636 | c.1335A>C | synonymous_variant | 0.25 |
gyrA | 8642 | c.1341A>G | synonymous_variant | 0.24 |
gyrA | 8672 | c.1371A>G | synonymous_variant | 0.21 |
gyrA | 8678 | c.1377G>A | synonymous_variant | 0.17 |
gyrA | 8693 | c.1392T>C | synonymous_variant | 0.17 |
gyrA | 8699 | c.1398A>G | synonymous_variant | 0.18 |
gyrA | 8828 | c.1527T>C | synonymous_variant | 0.15 |
gyrA | 8837 | c.1536C>T | synonymous_variant | 0.15 |
gyrA | 8852 | c.1551T>C | synonymous_variant | 0.16 |
gyrA | 8858 | c.1557T>C | synonymous_variant | 0.19 |
gyrA | 8867 | c.1566A>G | synonymous_variant | 0.18 |
gyrA | 8870 | c.1569G>C | synonymous_variant | 0.19 |
gyrA | 8873 | c.1572A>C | synonymous_variant | 0.18 |
gyrA | 8891 | c.1590G>A | synonymous_variant | 0.21 |
gyrA | 8897 | c.1596T>C | synonymous_variant | 0.22 |
gyrA | 8903 | c.1602T>C | synonymous_variant | 0.22 |
gyrA | 8933 | c.1632G>C | synonymous_variant | 0.24 |
gyrA | 8939 | c.1638T>C | synonymous_variant | 0.22 |
gyrA | 8942 | c.1641G>C | synonymous_variant | 0.22 |
gyrA | 8946 | c.1645_1647delTTGinsCTC | synonymous_variant | 0.2 |
gyrA | 8996 | c.1695T>C | synonymous_variant | 0.16 |
gyrA | 8998 | p.Leu566Trp | missense_variant | 0.16 |
gyrA | 9119 | c.1818A>G | synonymous_variant | 0.17 |
gyrA | 9122 | c.1821C>G | synonymous_variant | 0.17 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 0.2 |
gyrA | 9152 | c.1851C>T | synonymous_variant | 0.15 |
gyrA | 9158 | c.1857C>T | synonymous_variant | 0.15 |
gyrA | 9191 | c.1890G>C | synonymous_variant | 0.15 |
gyrA | 9204 | p.Ser635Thr | missense_variant | 0.13 |
gyrA | 9323 | c.2022C>G | synonymous_variant | 0.17 |
gyrA | 9335 | c.2034G>C | synonymous_variant | 0.16 |
fgd1 | 490803 | c.21T>A | synonymous_variant | 0.13 |
fgd1 | 490827 | c.45C>T | synonymous_variant | 0.16 |
fgd1 | 490848 | c.66A>G | synonymous_variant | 0.17 |
fgd1 | 490851 | c.69A>T | synonymous_variant | 0.17 |
fgd1 | 490868 | p.Ala29Gly | missense_variant | 0.19 |
fgd1 | 491173 | c.391C>A | synonymous_variant | 0.14 |
fgd1 | 491241 | p.Asp153Glu | missense_variant | 0.16 |
fgd1 | 491244 | c.462T>C | synonymous_variant | 0.16 |
mshA | 575674 | c.327G>C | synonymous_variant | 0.17 |
mshA | 575812 | c.465C>T | synonymous_variant | 0.26 |
mshA | 575821 | c.474G>C | synonymous_variant | 0.23 |
mshA | 575824 | c.477T>G | synonymous_variant | 0.24 |
mshA | 575830 | c.483C>G | synonymous_variant | 0.26 |
mshA | 575833 | c.486C>G | synonymous_variant | 0.26 |
mshA | 575845 | c.498C>T | synonymous_variant | 0.26 |
mshA | 575884 | c.537G>C | synonymous_variant | 0.23 |
mshA | 575887 | c.540G>C | synonymous_variant | 0.23 |
mshA | 575893 | c.546C>G | synonymous_variant | 0.21 |
mshA | 575896 | c.549G>C | synonymous_variant | 0.21 |
ccsA | 620362 | p.Ala158Thr | missense_variant | 0.15 |
ccsA | 620373 | c.483C>G | synonymous_variant | 0.16 |
ccsA | 620376 | c.486G>C | synonymous_variant | 0.19 |
ccsA | 620389 | c.499C>T | synonymous_variant | 0.16 |
ccsA | 620412 | c.522T>C | synonymous_variant | 0.19 |
ccsA | 620415 | c.525T>C | synonymous_variant | 0.19 |
rpoB | 760181 | c.375T>C | synonymous_variant | 0.17 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.17 |
rpoB | 760328 | c.522G>C | synonymous_variant | 0.16 |
rpoB | 760331 | c.525G>C | synonymous_variant | 0.17 |
rpoB | 760340 | c.534G>T | synonymous_variant | 0.17 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.19 |
rpoB | 760412 | c.606C>G | synonymous_variant | 0.16 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.17 |
rpoB | 760522 | p.Ser239Asn | missense_variant | 0.22 |
rpoB | 760532 | c.726T>C | synonymous_variant | 0.21 |
rpoB | 760533 | p.Val243Thr | missense_variant | 0.21 |
rpoB | 760541 | c.735G>C | synonymous_variant | 0.25 |
rpoB | 760547 | c.741G>C | synonymous_variant | 0.25 |
rpoB | 760563 | p.Arg253Met | missense_variant | 0.31 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.3 |
rpoB | 760595 | c.789C>T | synonymous_variant | 0.28 |
rpoB | 760598 | c.792C>A | synonymous_variant | 0.25 |
rpoB | 760611 | c.805T>C | synonymous_variant | 0.28 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.24 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.21 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.2 |
rpoB | 760670 | c.864G>C | synonymous_variant | 0.21 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.19 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.2 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.18 |
rpoB | 760886 | c.1080A>G | synonymous_variant | 0.24 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.23 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 0.23 |
rpoB | 760931 | c.1125C>G | synonymous_variant | 0.25 |
rpoB | 760934 | c.1128C>T | synonymous_variant | 0.25 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.21 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.22 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.17 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.19 |
rpoB | 761006 | c.1200C>G | synonymous_variant | 0.21 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.23 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 0.24 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.22 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.2 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.21 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.18 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.23 |
rpoB | 761129 | c.1323G>C | synonymous_variant | 0.21 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 0.2 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.2 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.22 |
rpoB | 761153 | c.1347G>C | synonymous_variant | 0.25 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.25 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.23 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.22 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.21 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.23 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.27 |
rpoB | 761219 | c.1413G>C | synonymous_variant | 0.29 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.29 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.24 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.25 |
rpoB | 761306 | c.1500C>G | synonymous_variant | 0.22 |
rpoB | 761312 | c.1506G>C | synonymous_variant | 0.19 |
rpoB | 761354 | c.1548C>T | synonymous_variant | 0.16 |
rpoB | 761510 | c.1704T>C | synonymous_variant | 0.19 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.3 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.3 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.28 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.27 |
rpoB | 761588 | c.1782C>T | synonymous_variant | 0.26 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.27 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.29 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.3 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.24 |
rpoB | 761645 | c.1839C>G | synonymous_variant | 0.2 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.19 |
rpoB | 761657 | c.1851C>G | synonymous_variant | 0.21 |
rpoB | 761675 | c.1869G>C | synonymous_variant | 0.23 |
rpoB | 761873 | c.2067A>C | synonymous_variant | 0.19 |
rpoB | 762008 | c.2202C>T | synonymous_variant | 0.15 |
rpoB | 762014 | c.2208C>T | synonymous_variant | 0.15 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.16 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.16 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.15 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.2 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.31 |
rpoB | 762314 | c.2508C>T | synonymous_variant | 0.28 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.28 |
rpoB | 762329 | c.2523G>C | synonymous_variant | 0.26 |
rpoB | 762338 | c.2532T>C | synonymous_variant | 0.26 |
rpoB | 762347 | c.2541T>C | synonymous_variant | 0.24 |
rpoB | 762362 | p.Glu852Asp | missense_variant | 0.23 |
rpoB | 762369 | c.2563T>C | synonymous_variant | 0.2 |
rpoC | 762398 | c.-972T>C | upstream_gene_variant | 0.21 |
rpoC | 762401 | c.-969G>C | upstream_gene_variant | 0.21 |
rpoC | 762404 | c.-966T>C | upstream_gene_variant | 0.22 |
rpoC | 762410 | c.-960T>C | upstream_gene_variant | 0.23 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 0.23 |
rpoC | 762419 | c.-951C>G | upstream_gene_variant | 0.22 |
rpoC | 762434 | c.-936T>C | upstream_gene_variant | 0.19 |
rpoC | 762449 | c.-921C>A | upstream_gene_variant | 0.25 |
rpoC | 762467 | c.-903C>T | upstream_gene_variant | 0.22 |
rpoC | 762509 | c.-861T>G | upstream_gene_variant | 0.19 |
rpoB | 762510 | p.Ala902Pro | missense_variant | 0.19 |
rpoC | 762521 | c.-849C>T | upstream_gene_variant | 0.19 |
rpoC | 762533 | c.-837T>C | upstream_gene_variant | 0.21 |
rpoC | 762536 | c.-834T>C | upstream_gene_variant | 0.19 |
rpoC | 762537 | c.-833T>C | upstream_gene_variant | 0.2 |
rpoC | 762551 | c.-819C>G | upstream_gene_variant | 0.16 |
rpoC | 762857 | c.-513C>G | upstream_gene_variant | 0.16 |
rpoC | 762860 | c.-510G>C | upstream_gene_variant | 0.16 |
rpoC | 762863 | c.-507T>C | upstream_gene_variant | 0.15 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.33 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.27 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.3 |
rpoC | 763013 | c.-357C>G | upstream_gene_variant | 0.29 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.2 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 0.2 |
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 | 0.29 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.26 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.31 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.32 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.28 |
rpoC | 763158 | c.-212C>T | upstream_gene_variant | 0.22 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.21 |
rpoC | 763190 | c.-180C>T | upstream_gene_variant | 0.22 |
rpoC | 763202 | c.-168A>G | upstream_gene_variant | 0.22 |
rpoC | 763205 | c.-165G>C | upstream_gene_variant | 0.17 |
rpoC | 763206 | c.-164_-162delAGTinsTCG | upstream_gene_variant | 0.19 |
rpoC | 763214 | c.-156T>C | upstream_gene_variant | 0.23 |
rpoC | 763226 | c.-144A>G | upstream_gene_variant | 0.23 |
rpoC | 763227 | c.-143C>T | upstream_gene_variant | 0.23 |
rpoC | 763238 | c.-132T>C | upstream_gene_variant | 0.21 |
rpoC | 763253 | c.-117G>C | upstream_gene_variant | 0.17 |
rpoC | 763402 | c.33C>G | synonymous_variant | 0.16 |
rpoC | 763411 | c.42T>G | synonymous_variant | 0.24 |
rpoC | 763414 | c.45T>C | synonymous_variant | 0.24 |
rpoC | 763441 | c.72C>T | synonymous_variant | 0.31 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.31 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.36 |
rpoC | 763486 | c.117T>G | synonymous_variant | 0.35 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.36 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.34 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.3 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.3 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.24 |
rpoC | 763603 | c.234C>T | synonymous_variant | 0.19 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.21 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.22 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.17 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.18 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.17 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.2 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.18 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.2 |
rpoC | 763774 | c.405G>C | synonymous_variant | 0.16 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.18 |
rpoC | 763816 | c.447C>G | synonymous_variant | 0.2 |
rpoC | 763825 | c.456G>A | synonymous_variant | 0.21 |
rpoC | 763835 | p.Ala156Met | missense_variant | 0.21 |
rpoC | 763853 | p.Val162Ile | missense_variant | 0.21 |
rpoC | 763858 | c.489A>G | synonymous_variant | 0.21 |
rpoC | 763987 | c.618C>T | synonymous_variant | 0.16 |
rpoC | 763996 | c.627T>C | synonymous_variant | 0.18 |
rpoC | 764002 | c.633C>G | synonymous_variant | 0.19 |
rpoC | 764005 | c.636G>C | synonymous_variant | 0.21 |
rpoC | 764024 | c.655_657delTTGinsCTC | synonymous_variant | 0.19 |
rpoC | 764032 | p.Asp221Glu | missense_variant | 0.25 |
rpoC | 764040 | p.Ser224Thr | missense_variant | 0.24 |
rpoC | 764044 | c.675T>C | synonymous_variant | 0.27 |
rpoC | 764059 | c.690G>T | synonymous_variant | 0.14 |
rpoC | 764083 | c.714A>G | synonymous_variant | 0.17 |
rpoC | 764098 | c.729A>G | synonymous_variant | 0.17 |
rpoC | 764101 | c.732C>G | synonymous_variant | 0.17 |
rpoC | 764102 | p.Val245Ile | missense_variant | 0.17 |
rpoC | 764112 | p.Tyr248Phe | missense_variant | 0.14 |
rpoC | 764131 | c.762T>C | synonymous_variant | 0.22 |
rpoC | 764140 | c.771C>T | synonymous_variant | 0.18 |
rpoC | 764188 | c.819A>G | synonymous_variant | 0.21 |
rpoC | 764195 | p.Ser276Ile | missense_variant | 0.21 |
rpoC | 764203 | c.834G>C | synonymous_variant | 0.22 |
rpoC | 764206 | c.837T>C | synonymous_variant | 0.24 |
rpoC | 764215 | c.846A>G | synonymous_variant | 0.3 |
rpoC | 764236 | c.867G>A | synonymous_variant | 0.33 |
rpoC | 764248 | c.879C>G | synonymous_variant | 0.39 |
rpoC | 764257 | c.888G>C | synonymous_variant | 0.38 |
rpoC | 764266 | c.897T>C | synonymous_variant | 0.41 |
rpoC | 764269 | c.900G>C | synonymous_variant | 0.4 |
rpoC | 764272 | c.903G>C | synonymous_variant | 0.36 |
rpoC | 764278 | c.909A>G | synonymous_variant | 0.34 |
rpoC | 764338 | c.969G>A | synonymous_variant | 0.16 |
rpoC | 764554 | c.1185C>T | synonymous_variant | 0.16 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.16 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.15 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.15 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.3 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.32 |
rpoC | 764650 | c.1281G>C | synonymous_variant | 0.3 |
rpoC | 764651 | c.1282_1284delTCGinsAGC | synonymous_variant | 0.31 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.31 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.29 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.26 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.25 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.25 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.24 |
rpoC | 764872 | c.1503A>G | synonymous_variant | 0.28 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.3 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.3 |
rpoC | 764932 | c.1563C>A | synonymous_variant | 0.27 |
rpoC | 764935 | c.1566T>C | synonymous_variant | 0.32 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.29 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.19 |
rpoC | 765292 | c.1923G>C | synonymous_variant | 0.13 |
rpoC | 765349 | c.1980T>C | synonymous_variant | 0.15 |
rpoC | 765352 | c.1983G>C | synonymous_variant | 0.18 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.18 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.16 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.19 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.17 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.17 |
rpoC | 765559 | c.2190G>C | synonymous_variant | 0.18 |
rpoC | 765580 | c.2211G>C | synonymous_variant | 0.23 |
rpoC | 765613 | p.His748Gln | missense_variant | 0.21 |
rpoC | 765625 | c.2256C>G | synonymous_variant | 0.21 |
rpoC | 765631 | p.Asp754Glu | missense_variant | 0.2 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.25 |
rpoC | 765734 | c.2365T>C | synonymous_variant | 0.26 |
rpoC | 765739 | c.2370G>T | synonymous_variant | 0.22 |
rpoC | 765751 | c.2382C>G | synonymous_variant | 0.24 |
rpoC | 765753 | p.Asp795Ala | missense_variant | 0.24 |
rpoC | 765772 | c.2403C>G | synonymous_variant | 0.26 |
rpoC | 765784 | c.2415C>G | synonymous_variant | 0.28 |
rpoC | 765787 | c.2418C>T | synonymous_variant | 0.23 |
rpoC | 765793 | c.2424C>G | synonymous_variant | 0.23 |
rpoC | 765796 | c.2427C>T | synonymous_variant | 0.23 |
rpoC | 765811 | c.2442T>C | synonymous_variant | 0.24 |
rpoC | 765814 | c.2445A>G | synonymous_variant | 0.24 |
rpoC | 765826 | c.2457T>C | synonymous_variant | 0.3 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 0.35 |
rpoC | 765850 | c.2481G>C | synonymous_variant | 0.35 |
rpoC | 765883 | c.2514C>G | synonymous_variant | 0.25 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.25 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.22 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.19 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.22 |
rpoC | 765982 | c.2613C>G | synonymous_variant | 0.23 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.22 |
rpoC | 766010 | c.2641_2642delTCinsAG | synonymous_variant | 0.18 |
rpoC | 766027 | c.2658G>C | synonymous_variant | 0.17 |
rpoC | 766043 | p.Gln892Glu | missense_variant | 0.17 |
rpoC | 766082 | p.Ala905Gln | missense_variant | 0.21 |
rpoC | 766096 | c.2727G>C | synonymous_variant | 0.23 |
rpoC | 766129 | c.2760C>G | synonymous_variant | 0.16 |
rpoC | 766135 | c.2766G>A | synonymous_variant | 0.14 |
rpoC | 766303 | c.2934C>T | synonymous_variant | 0.22 |
rpoC | 766312 | c.2943T>G | synonymous_variant | 0.19 |
rpoC | 766327 | c.2958C>A | synonymous_variant | 0.17 |
rpoC | 766348 | c.2979A>G | synonymous_variant | 0.17 |
rpoC | 766357 | c.2988C>T | synonymous_variant | 0.17 |
rpoC | 766363 | c.2994G>C | synonymous_variant | 0.17 |
rpoC | 766366 | c.2997C>G | synonymous_variant | 0.17 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.17 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.18 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.16 |
rpoC | 766447 | c.3078T>C | synonymous_variant | 0.22 |
rpoC | 766462 | c.3093G>C | synonymous_variant | 0.22 |
rpoC | 766483 | c.3114G>C | synonymous_variant | 0.15 |
rpoC | 766484 | p.Val1039Ile | missense_variant | 0.15 |
rpoC | 766492 | c.3123T>C | synonymous_variant | 0.17 |
rpoC | 766522 | c.3153C>G | synonymous_variant | 0.23 |
rpoC | 766528 | c.3159T>C | synonymous_variant | 0.25 |
rpoC | 766531 | c.3162G>C | synonymous_variant | 0.27 |
rpoC | 766540 | p.Asp1057Glu | missense_variant | 0.22 |
rpoC | 766549 | c.3180G>C | synonymous_variant | 0.19 |
rpoC | 766573 | c.3204T>C | synonymous_variant | 0.17 |
rpoC | 766583 | p.Gly1072Ser | missense_variant | 0.15 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.14 |
rpoC | 766747 | c.3378C>T | synonymous_variant | 0.15 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.19 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.16 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 0.15 |
rpoC | 766885 | c.3516G>A | synonymous_variant | 0.19 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.18 |
rpoC | 766933 | c.3564A>G | synonymous_variant | 0.17 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.16 |
rpoC | 766972 | c.3603G>C | synonymous_variant | 0.19 |
rpoC | 766987 | c.3618G>C | synonymous_variant | 0.16 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.17 |
rpoC | 767033 | c.3664_3666delTCGinsAGC | synonymous_variant | 0.21 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.19 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.21 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.22 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.17 |
rpoC | 767158 | c.3789T>C | synonymous_variant | 0.21 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.19 |
rpoC | 767191 | c.3822C>G | synonymous_variant | 0.16 |
rpoC | 767206 | c.3837C>G | synonymous_variant | 0.16 |
rpoC | 767212 | c.3843G>C | synonymous_variant | 0.16 |
rpoC | 767221 | c.3852C>G | synonymous_variant | 0.18 |
rpoC | 767230 | c.3861G>C | synonymous_variant | 0.2 |
rpoC | 767233 | c.3864T>C | synonymous_variant | 0.21 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777173 | c.1308C>G | synonymous_variant | 0.14 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781595 | c.36T>C | synonymous_variant | 0.15 |
rpsL | 781608 | p.Ser17Ala | missense_variant | 0.16 |
rpsL | 781628 | c.69T>C | synonymous_variant | 0.24 |
rpsL | 781631 | c.72G>C | synonymous_variant | 0.25 |
rpsL | 781649 | c.90T>C | synonymous_variant | 0.24 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.24 |
rpsL | 781700 | c.141G>C | synonymous_variant | 0.21 |
rpsL | 781703 | c.144G>T | synonymous_variant | 0.2 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.18 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.2 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.19 |
rpsL | 781742 | c.183C>T | synonymous_variant | 0.21 |
rpsL | 781748 | c.189C>G | synonymous_variant | 0.23 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.22 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.25 |
rpsL | 781772 | c.213C>A | synonymous_variant | 0.28 |
rpsL | 781808 | c.249C>T | synonymous_variant | 0.21 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.22 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.21 |
rpsL | 781838 | c.279G>C | synonymous_variant | 0.21 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.19 |
rpsL | 781865 | c.306G>C | synonymous_variant | 0.17 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.16 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.16 |
rpsL | 781877 | c.318T>C | synonymous_variant | 0.19 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.21 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.2 |
rpsL | 781916 | c.357T>C | synonymous_variant | 0.18 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.16 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.26 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.26 |
rplC | 800627 | c.-182C>T | upstream_gene_variant | 0.27 |
rplC | 800648 | c.-161A>T | upstream_gene_variant | 0.33 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.3 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.31 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.28 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.27 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.27 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.25 |
rplC | 800747 | c.-62C>G | upstream_gene_variant | 0.22 |
rplC | 800771 | c.-38C>T | upstream_gene_variant | 0.2 |
rplC | 800817 | c.9A>T | synonymous_variant | 0.15 |
rplC | 801195 | c.387G>C | synonymous_variant | 0.19 |
rplC | 801207 | c.399C>T | synonymous_variant | 0.28 |
rplC | 801246 | c.438C>T | synonymous_variant | 0.28 |
rplC | 801249 | c.441T>C | synonymous_variant | 0.28 |
rplC | 801255 | c.447C>T | synonymous_variant | 0.26 |
rplC | 801264 | c.456C>T | synonymous_variant | 0.21 |
rplC | 801267 | c.459A>T | synonymous_variant | 0.21 |
rplC | 801270 | c.462T>C | synonymous_variant | 0.18 |
rplC | 801276 | c.468G>C | synonymous_variant | 0.18 |
rplC | 801279 | c.471G>A | synonymous_variant | 0.18 |
rplC | 801282 | c.474G>C | synonymous_variant | 0.18 |
rplC | 801285 | c.477G>C | synonymous_variant | 0.18 |
rplC | 801367 | p.Ala187Thr | missense_variant | 0.16 |
rplC | 801442 | p.Ile212Val | missense_variant | 0.15 |
fbiC | 1303920 | c.990C>T | synonymous_variant | 0.15 |
fbiC | 1304535 | c.1605G>A | synonymous_variant | 0.17 |
fbiC | 1304544 | c.1614T>C | synonymous_variant | 0.17 |
fbiC | 1304545 | p.Val539Thr | missense_variant | 0.16 |
fbiC | 1304553 | c.1623C>T | synonymous_variant | 0.18 |
fbiC | 1304559 | p.Glu543Asp | missense_variant | 0.18 |
fbiC | 1304565 | c.1635C>G | synonymous_variant | 0.16 |
fbiC | 1304568 | c.1638T>C | synonymous_variant | 0.17 |
fbiC | 1304580 | c.1650T>C | synonymous_variant | 0.15 |
fbiC | 1304784 | c.1854T>C | synonymous_variant | 0.16 |
fbiC | 1304787 | c.1857T>G | synonymous_variant | 0.16 |
fbiC | 1304808 | c.1878C>G | synonymous_variant | 0.18 |
fbiC | 1304811 | c.1881C>G | synonymous_variant | 0.22 |
fbiC | 1304817 | c.1887T>C | synonymous_variant | 0.24 |
fbiC | 1304829 | c.1899T>C | synonymous_variant | 0.39 |
fbiC | 1304832 | c.1902C>T | synonymous_variant | 0.41 |
fbiC | 1304856 | c.1926C>G | synonymous_variant | 0.52 |
fbiC | 1304869 | c.1939C>T | synonymous_variant | 0.3 |
fbiC | 1304875 | p.Ile649Val | missense_variant | 0.29 |
fbiC | 1304883 | p.Glu651Asp | missense_variant | 0.27 |
fbiC | 1304891 | p.Ile654Thr | missense_variant | 0.23 |
fbiC | 1304893 | p.Gly655Ser | missense_variant | 0.23 |
fbiC | 1304907 | c.1977C>G | synonymous_variant | 0.18 |
fbiC | 1304910 | c.1980G>C | synonymous_variant | 0.18 |
fbiC | 1304916 | c.1986T>C | synonymous_variant | 0.22 |
fbiC | 1304928 | c.1998T>C | synonymous_variant | 0.21 |
fbiC | 1304937 | c.2007G>C | synonymous_variant | 0.18 |
fbiC | 1304958 | c.2028T>G | synonymous_variant | 0.18 |
fbiC | 1304983 | c.2053C>T | synonymous_variant | 0.16 |
fbiC | 1304995 | p.Leu689Met | missense_variant | 0.14 |
fbiC | 1305372 | c.2442G>A | synonymous_variant | 0.17 |
fbiC | 1305384 | c.2454G>C | synonymous_variant | 0.16 |
fbiC | 1305396 | c.2466C>G | synonymous_variant | 0.17 |
fbiC | 1305405 | c.2475A>G | synonymous_variant | 0.18 |
atpE | 1460852 | c.-193C>G | upstream_gene_variant | 0.21 |
atpE | 1460855 | c.-190T>C | upstream_gene_variant | 0.2 |
atpE | 1460858 | c.-187C>G | upstream_gene_variant | 0.2 |
atpE | 1460861 | c.-184C>G | upstream_gene_variant | 0.2 |
atpE | 1460882 | c.-163T>C | upstream_gene_variant | 0.2 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1471932 | n.87A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472396 | n.551A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472426 | n.581T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472574 | n.729T>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473148 | n.1303G>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473163 | n.1318C>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.7 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473270 | n.1425G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473305 | n.1460G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473408 | n.-250C>T | upstream_gene_variant | 0.23 |
rrl | 1473417 | n.-241C>T | upstream_gene_variant | 0.23 |
rrl | 1473419 | n.-239T>C | upstream_gene_variant | 0.23 |
rrl | 1473420 | n.-238A>G | upstream_gene_variant | 0.23 |
rrl | 1473421 | n.-237G>A | upstream_gene_variant | 0.23 |
rrl | 1473437 | n.-221T>C | upstream_gene_variant | 0.15 |
rrl | 1473756 | n.99G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473899 | n.242A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473943 | n.286G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474315 | n.658A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474355 | n.698A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474393 | n.736A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474402 | n.745T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474448 | n.791T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474558 | n.901G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474584 | n.927C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474634 | n.977T>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474658 | n.1001A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475104 | n.1447T>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475124 | n.1467A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475171 | n.1514C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475172 | n.1515A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475902 | n.2245T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476179 | n.2522C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476204 | n.2547C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476580 | n.2923G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476600 | n.2943A>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476633 | n.2976A>G | non_coding_transcript_exon_variant | 0.36 |
fabG1 | 1673941 | p.Ala168Ser | missense_variant | 0.15 |
inhA | 1673955 | c.-247G>C | upstream_gene_variant | 0.16 |
inhA | 1674549 | c.348G>C | synonymous_variant | 0.16 |
inhA | 1674555 | c.354G>A | synonymous_variant | 0.16 |
inhA | 1674561 | c.360C>T | synonymous_variant | 0.22 |
inhA | 1674582 | c.381T>C | synonymous_variant | 0.28 |
inhA | 1674585 | c.384T>C | synonymous_variant | 0.29 |
inhA | 1674589 | p.Met130Leu | missense_variant | 0.32 |
inhA | 1674601 | p.Leu134Ala | missense_variant | 0.24 |
inhA | 1674624 | c.423A>C | synonymous_variant | 0.17 |
inhA | 1674636 | c.435C>G | synonymous_variant | 0.22 |
inhA | 1674660 | c.459G>C | synonymous_variant | 0.28 |
inhA | 1674703 | c.502T>C | synonymous_variant | 0.23 |
inhA | 1674708 | c.507G>A | synonymous_variant | 0.23 |
inhA | 1674718 | c.517A>C | synonymous_variant | 0.21 |
inhA | 1674729 | c.528G>C | synonymous_variant | 0.27 |
inhA | 1674732 | c.531C>T | synonymous_variant | 0.21 |
inhA | 1674738 | c.537C>G | synonymous_variant | 0.18 |
inhA | 1674816 | c.615T>G | synonymous_variant | 0.15 |
inhA | 1674846 | p.Ile215Met | missense_variant | 0.23 |
inhA | 1674864 | c.663C>T | synonymous_variant | 0.2 |
inhA | 1674870 | c.669T>C | synonymous_variant | 0.21 |
inhA | 1674879 | c.678T>C | synonymous_variant | 0.2 |
inhA | 1674904 | p.Ala235Pro | missense_variant | 0.21 |
inhA | 1674909 | c.708G>C | synonymous_variant | 0.21 |
rpsA | 1833589 | c.48A>T | synonymous_variant | 0.17 |
rpsA | 1833595 | c.54T>C | synonymous_variant | 0.21 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.17 |
rpsA | 1833667 | c.126C>G | synonymous_variant | 0.17 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.19 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.21 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.2 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.2 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.21 |
rpsA | 1833748 | c.207C>G | synonymous_variant | 0.2 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.28 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.27 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.29 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 0.36 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.38 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.38 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.41 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.44 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.34 |
rpsA | 1833886 | c.345C>G | synonymous_variant | 0.32 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.23 |
rpsA | 1833940 | c.399C>G | synonymous_variant | 0.22 |
rpsA | 1833971 | c.430C>T | synonymous_variant | 0.31 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.28 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.3 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.29 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.26 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 0.15 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.15 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.18 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.2 |
rpsA | 1834262 | p.Ser241Thr | missense_variant | 0.16 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.21 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.25 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.37 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.36 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.34 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.35 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.32 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.33 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.29 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.26 |
rpsA | 1834465 | c.924T>C | synonymous_variant | 0.23 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.25 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.31 |
rpsA | 1834513 | c.972C>G | synonymous_variant | 0.41 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.41 |
rpsA | 1834540 | c.999G>C | synonymous_variant | 0.41 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.33 |
rpsA | 1834555 | c.1014T>G | synonymous_variant | 0.35 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.29 |
rpsA | 1834618 | c.1077G>C | synonymous_variant | 0.31 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.32 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.31 |
rpsA | 1834654 | p.Glu371Asp | missense_variant | 0.29 |
rpsA | 1834690 | c.1149T>C | synonymous_variant | 0.2 |
rpsA | 1834753 | c.1212T>C | synonymous_variant | 0.16 |
rpsA | 1834765 | p.Glu408Asp | missense_variant | 0.17 |
rpsA | 1834775 | p.Ala412Thr | missense_variant | 0.2 |
rpsA | 1834780 | c.1239A>G | synonymous_variant | 0.18 |
rpsA | 1834789 | c.1248T>C | synonymous_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101744 | p.Asp433Glu | missense_variant | 0.16 |
ndh | 2101756 | c.1287G>C | synonymous_variant | 0.16 |
ndh | 2101765 | c.1278C>G | synonymous_variant | 0.18 |
ndh | 2101768 | c.1275C>A | synonymous_variant | 0.17 |
ndh | 2101771 | c.1272T>G | synonymous_variant | 0.16 |
ndh | 2101774 | c.1269T>C | synonymous_variant | 0.16 |
ndh | 2101777 | c.1266C>G | synonymous_variant | 0.17 |
ndh | 2101783 | c.1260T>A | synonymous_variant | 0.15 |
ndh | 2101939 | c.1104A>G | synonymous_variant | 0.16 |
ndh | 2101960 | c.1083A>G | synonymous_variant | 0.18 |
ndh | 2101963 | c.1080G>A | synonymous_variant | 0.18 |
ndh | 2101966 | c.1077T>G | synonymous_variant | 0.18 |
ndh | 2101972 | c.1071G>C | synonymous_variant | 0.18 |
ndh | 2101988 | p.Ala352Asp | missense_variant | 0.17 |
ndh | 2102014 | c.1029C>G | synonymous_variant | 0.17 |
katG | 2155677 | c.435C>G | synonymous_variant | 0.18 |
katG | 2155680 | c.432G>C | synonymous_variant | 0.18 |
katG | 2155716 | c.396T>G | synonymous_variant | 0.18 |
katG | 2155722 | c.390G>C | synonymous_variant | 0.18 |
katG | 2155794 | p.Ala106Thr | missense_variant | 0.16 |
katG | 2155806 | c.306T>C | synonymous_variant | 0.17 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289997 | c.-756G>C | upstream_gene_variant | 0.16 |
kasA | 2517950 | c.-165C>G | upstream_gene_variant | 0.21 |
kasA | 2518506 | p.Ala131Glu | missense_variant | 0.18 |
kasA | 2518519 | c.405G>C | synonymous_variant | 0.2 |
kasA | 2518528 | c.414C>G | synonymous_variant | 0.19 |
kasA | 2518540 | c.426T>C | synonymous_variant | 0.25 |
kasA | 2518561 | c.447T>C | synonymous_variant | 0.23 |
kasA | 2518567 | c.453G>C | synonymous_variant | 0.24 |
kasA | 2518570 | c.456G>C | synonymous_variant | 0.25 |
kasA | 2518574 | p.Ile154Val | missense_variant | 0.24 |
kasA | 2518579 | c.465T>C | synonymous_variant | 0.24 |
kasA | 2518588 | c.474T>C | synonymous_variant | 0.24 |
kasA | 2518591 | c.477G>C | synonymous_variant | 0.24 |
kasA | 2518609 | p.Met165Ile | missense_variant | 0.27 |
kasA | 2518768 | c.654C>T | synonymous_variant | 0.17 |
kasA | 2518777 | c.663C>T | synonymous_variant | 0.17 |
kasA | 2518783 | c.669T>C | synonymous_variant | 0.19 |
kasA | 2518789 | c.675G>C | synonymous_variant | 0.18 |
kasA | 2518792 | c.678C>A | synonymous_variant | 0.18 |
kasA | 2518795 | c.681C>G | synonymous_variant | 0.18 |
kasA | 2518825 | c.711T>C | synonymous_variant | 0.21 |
kasA | 2519068 | c.954C>T | synonymous_variant | 0.14 |
kasA | 2519072 | p.Ala320Thr | missense_variant | 0.14 |
kasA | 2519107 | c.993T>C | synonymous_variant | 0.18 |
kasA | 2519108 | p.Asp332Gln | missense_variant | 0.17 |
kasA | 2519116 | c.1002C>G | synonymous_variant | 0.21 |
kasA | 2519122 | c.1008G>C | synonymous_variant | 0.21 |
kasA | 2519137 | c.1023T>G | synonymous_variant | 0.21 |
kasA | 2519158 | c.1044C>T | synonymous_variant | 0.2 |
kasA | 2519167 | c.1053T>G | synonymous_variant | 0.17 |
kasA | 2519173 | c.1059C>G | synonymous_variant | 0.18 |
Rv2752c | 3064831 | p.Ala454Asn | missense_variant | 0.19 |
Rv2752c | 3064838 | c.1354T>C | synonymous_variant | 0.21 |
Rv2752c | 3064860 | c.1332G>C | synonymous_variant | 0.18 |
Rv2752c | 3064863 | c.1329G>C | synonymous_variant | 0.19 |
Rv2752c | 3064872 | c.1320T>G | synonymous_variant | 0.18 |
Rv2752c | 3064877 | p.Ser439Ala | missense_variant | 0.18 |
Rv2752c | 3064883 | p.Ser437Gly | missense_variant | 0.18 |
Rv2752c | 3064887 | c.1305A>G | synonymous_variant | 0.19 |
Rv2752c | 3064893 | c.1299C>G | synonymous_variant | 0.19 |
Rv2752c | 3064896 | c.1296T>C | synonymous_variant | 0.19 |
Rv2752c | 3065241 | c.951A>G | synonymous_variant | 0.19 |
Rv2752c | 3065412 | c.780G>A | synonymous_variant | 0.15 |
Rv2752c | 3066339 | c.-148G>C | upstream_gene_variant | 0.16 |
thyX | 3067325 | c.621A>G | synonymous_variant | 0.17 |
thyX | 3067349 | c.597G>C | synonymous_variant | 0.2 |
thyX | 3067355 | c.591A>C | synonymous_variant | 0.21 |
thyX | 3067367 | c.579G>C | synonymous_variant | 0.21 |
thyX | 3067373 | c.573C>G | synonymous_variant | 0.21 |
thyX | 3067376 | c.570G>A | synonymous_variant | 0.22 |
thyX | 3067391 | c.555G>C | synonymous_variant | 0.28 |
thyX | 3067394 | c.552G>C | synonymous_variant | 0.27 |
thyX | 3067439 | c.507A>G | synonymous_variant | 0.33 |
thyX | 3067445 | c.501C>G | synonymous_variant | 0.33 |
thyX | 3067457 | c.489C>G | synonymous_variant | 0.3 |
thyX | 3067465 | p.Ile161Val | missense_variant | 0.25 |
thyX | 3067475 | c.471A>G | synonymous_variant | 0.27 |
thyX | 3067490 | c.456C>G | synonymous_variant | 0.26 |
thyX | 3067493 | c.453A>G | synonymous_variant | 0.27 |
thyX | 3067515 | p.Ser144Thr | missense_variant | 0.29 |
thyX | 3067530 | p.Ala139Ser | missense_variant | 0.16 |
thyX | 3067545 | p.Glu134Ala | missense_variant | 0.16 |
thyX | 3067565 | p.Asp127Glu | missense_variant | 0.16 |
thyX | 3067583 | c.363C>G | synonymous_variant | 0.2 |
thyX | 3067602 | p.Arg115Gln | missense_variant | 0.15 |
thyX | 3067611 | p.Lys112Thr | missense_variant | 0.17 |
thyX | 3067619 | c.327A>C | synonymous_variant | 0.19 |
thyX | 3067631 | c.315C>G | synonymous_variant | 0.19 |
thyX | 3067634 | c.312C>G | synonymous_variant | 0.18 |
thyX | 3067652 | c.294T>C | synonymous_variant | 0.21 |
thyX | 3067661 | c.285C>G | synonymous_variant | 0.21 |
thyX | 3067685 | c.261A>C | synonymous_variant | 0.22 |
thyX | 3067691 | p.Ile85Leu | missense_variant | 0.2 |
thyX | 3067694 | c.252G>C | synonymous_variant | 0.19 |
thyX | 3067718 | c.228C>G | synonymous_variant | 0.19 |
thyX | 3067721 | c.225T>C | synonymous_variant | 0.16 |
thyX | 3067736 | c.210C>T | synonymous_variant | 0.15 |
thyX | 3067781 | c.165C>A | synonymous_variant | 0.14 |
thyX | 3067793 | c.153T>C | synonymous_variant | 0.16 |
thyX | 3067799 | c.147G>A | synonymous_variant | 0.15 |
thyX | 3067850 | c.96A>C | synonymous_variant | 0.18 |
thyX | 3067869 | p.Thr26Ser | missense_variant | 0.16 |
thyX | 3067874 | c.72C>G | synonymous_variant | 0.15 |
thyA | 3073815 | c.657G>A | synonymous_variant | 0.15 |
thyA | 3073824 | c.648A>G | synonymous_variant | 0.14 |
thyA | 3073827 | c.645A>G | synonymous_variant | 0.17 |
thyA | 3073836 | c.636C>T | synonymous_variant | 0.22 |
thyA | 3073839 | c.633T>C | synonymous_variant | 0.27 |
thyA | 3073860 | c.612C>G | synonymous_variant | 0.36 |
thyA | 3073863 | c.609T>C | synonymous_variant | 0.33 |
thyA | 3073866 | c.606C>G | synonymous_variant | 0.33 |
thyA | 3073872 | p.Ile200Val | missense_variant | 0.33 |
thyA | 3073892 | c.580T>C | synonymous_variant | 0.4 |
thyA | 3073898 | p.Ala192Ser | missense_variant | 0.38 |
thyA | 3073917 | c.555C>G | synonymous_variant | 0.36 |
thyA | 3073920 | c.552C>G | synonymous_variant | 0.37 |
thyA | 3073925 | c.547T>C | synonymous_variant | 0.38 |
thyA | 3073929 | c.543T>C | synonymous_variant | 0.37 |
thyA | 3073953 | c.519T>C | synonymous_variant | 0.29 |
thyA | 3073956 | c.516G>C | synonymous_variant | 0.27 |
thyA | 3073959 | c.513T>C | synonymous_variant | 0.26 |
thyA | 3073977 | c.495A>G | synonymous_variant | 0.26 |
thyA | 3073989 | c.483T>C | synonymous_variant | 0.2 |
thyA | 3074004 | c.468T>C | synonymous_variant | 0.17 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
alr | 3841059 | p.Gly121Ala | missense_variant | 0.15 |
alr | 3841069 | p.Ile118Phe | missense_variant | 0.16 |
alr | 3841079 | c.342T>C | synonymous_variant | 0.16 |
rpoA | 3877515 | c.993G>C | synonymous_variant | 0.16 |
rpoA | 3877553 | p.Glu319Gln | missense_variant | 0.21 |
rpoA | 3877571 | p.Pro313Ala | missense_variant | 0.2 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.16 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.19 |
rpoA | 3877656 | c.852T>G | synonymous_variant | 0.2 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.2 |
rpoA | 3877679 | p.Ala277Ser | missense_variant | 0.16 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.17 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.2 |
rpoA | 3877704 | c.804G>C | synonymous_variant | 0.19 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.26 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.29 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.25 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.28 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.29 |
rpoA | 3877791 | c.717C>G | synonymous_variant | 0.29 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.26 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.19 |
rpoA | 3877848 | c.660C>T | synonymous_variant | 0.21 |
rpoA | 3877857 | c.651G>A | synonymous_variant | 0.19 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.22 |
rpoA | 3877875 | c.633T>G | synonymous_variant | 0.24 |
rpoA | 3877878 | c.630G>C | synonymous_variant | 0.23 |
rpoA | 3877890 | c.618C>T | synonymous_variant | 0.25 |
rpoA | 3877896 | c.612G>C | synonymous_variant | 0.26 |
rpoA | 3877900 | p.Ser203Asn | missense_variant | 0.23 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.23 |
rpoA | 3877909 | p.Asn200Ser | missense_variant | 0.21 |
rpoA | 3877920 | c.588G>C | synonymous_variant | 0.23 |
rpoA | 3877923 | c.585C>T | synonymous_variant | 0.24 |
rpoA | 3877926 | c.582G>C | synonymous_variant | 0.25 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.36 |
rpoA | 3877986 | c.522G>C | synonymous_variant | 0.21 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.23 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.23 |
rpoA | 3878022 | c.486T>C | synonymous_variant | 0.16 |
rpoA | 3878094 | c.414C>G | synonymous_variant | 0.18 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.17 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.19 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.24 |
rpoA | 3878130 | c.378C>G | synonymous_variant | 0.2 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.16 |
rpoA | 3878340 | c.168C>T | synonymous_variant | 0.15 |
rpoA | 3878346 | c.162T>C | synonymous_variant | 0.18 |
rpoA | 3878364 | c.144A>T | synonymous_variant | 0.23 |
rpoA | 3878367 | c.141C>G | synonymous_variant | 0.23 |
rpoA | 3878376 | c.132G>C | synonymous_variant | 0.24 |
rpoA | 3878385 | c.123C>G | synonymous_variant | 0.2 |
rpoA | 3878388 | c.120C>G | synonymous_variant | 0.2 |
rpoA | 3878391 | c.117T>C | synonymous_variant | 0.21 |
rpoA | 3878415 | c.93C>T | synonymous_variant | 0.21 |
rpoA | 3878424 | c.84G>C | synonymous_variant | 0.26 |
rpoA | 3878436 | c.72A>G | synonymous_variant | 0.23 |
rpoA | 3878442 | c.66G>C | synonymous_variant | 0.22 |
rpoA | 3878672 | c.-165A>T | upstream_gene_variant | 0.15 |
clpC1 | 4038407 | c.2298G>C | synonymous_variant | 0.18 |
clpC1 | 4038419 | c.2286T>C | synonymous_variant | 0.18 |
clpC1 | 4038530 | p.Glu725Asp | missense_variant | 0.17 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.18 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.3 |
clpC1 | 4038821 | c.1884G>A | synonymous_variant | 0.3 |
clpC1 | 4038845 | c.1860G>C | synonymous_variant | 0.31 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 0.29 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.29 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.24 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.24 |
clpC1 | 4038923 | c.1780_1782delCTAinsTTG | synonymous_variant | 0.25 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.27 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.25 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.23 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.15 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.15 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.17 |
clpC1 | 4039004 | c.1701C>G | synonymous_variant | 0.17 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.18 |
clpC1 | 4039064 | c.1641C>T | synonymous_variant | 0.2 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.18 |
clpC1 | 4039103 | c.1602T>C | synonymous_variant | 0.2 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.2 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.17 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.18 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.21 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.21 |
clpC1 | 4039226 | c.1479T>C | synonymous_variant | 0.2 |
clpC1 | 4039229 | c.1476C>G | synonymous_variant | 0.24 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.22 |
clpC1 | 4039286 | c.1419T>C | synonymous_variant | 0.21 |
clpC1 | 4039295 | c.1410A>C | synonymous_variant | 0.27 |
clpC1 | 4039298 | c.1407T>C | synonymous_variant | 0.28 |
clpC1 | 4039319 | c.1386T>C | synonymous_variant | 0.22 |
clpC1 | 4039322 | c.1383T>C | synonymous_variant | 0.19 |
clpC1 | 4039328 | c.1377A>C | synonymous_variant | 0.17 |
clpC1 | 4039331 | c.1374C>G | synonymous_variant | 0.17 |
clpC1 | 4039338 | p.Thr456Gln | missense_variant | 0.14 |
clpC1 | 4039349 | c.1356C>T | synonymous_variant | 0.19 |
clpC1 | 4039352 | c.1353C>G | synonymous_variant | 0.19 |
clpC1 | 4039364 | c.1341C>G | synonymous_variant | 0.29 |
clpC1 | 4039391 | c.1314T>G | synonymous_variant | 0.36 |
clpC1 | 4039397 | c.1308A>G | synonymous_variant | 0.32 |
clpC1 | 4039409 | c.1296T>C | synonymous_variant | 0.33 |
clpC1 | 4039412 | c.1293T>G | synonymous_variant | 0.35 |
clpC1 | 4039415 | p.Glu430Asp | missense_variant | 0.33 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.35 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.36 |
clpC1 | 4039454 | c.1251A>G | synonymous_variant | 0.34 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 0.26 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.26 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.23 |
clpC1 | 4039480 | c.1225C>A | synonymous_variant | 0.2 |
clpC1 | 4039481 | c.1224T>G | synonymous_variant | 0.2 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.25 |
clpC1 | 4039556 | c.1149G>C | synonymous_variant | 0.15 |
clpC1 | 4039559 | c.1146C>G | synonymous_variant | 0.15 |
clpC1 | 4039562 | c.1143C>G | synonymous_variant | 0.16 |
clpC1 | 4039565 | c.1140G>C | synonymous_variant | 0.16 |
clpC1 | 4039576 | p.Ala377Pro | missense_variant | 0.16 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.16 |
clpC1 | 4039589 | c.1116G>C | synonymous_variant | 0.18 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.18 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.18 |
clpC1 | 4039622 | c.1083C>T | synonymous_variant | 0.15 |
clpC1 | 4039625 | c.1080G>A | synonymous_variant | 0.17 |
clpC1 | 4039661 | c.1044T>G | synonymous_variant | 0.31 |
clpC1 | 4039664 | c.1041G>C | synonymous_variant | 0.3 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.2 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.4 |
clpC1 | 4039729 | p.Asp326Asn | missense_variant | 0.59 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.36 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.24 |
clpC1 | 4039760 | c.945T>C | synonymous_variant | 0.31 |
clpC1 | 4039766 | c.939T>C | synonymous_variant | 0.29 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.29 |
clpC1 | 4039775 | c.930G>C | synonymous_variant | 0.3 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.3 |
clpC1 | 4039781 | c.924G>C | synonymous_variant | 0.31 |
clpC1 | 4039790 | c.915C>G | synonymous_variant | 0.28 |
clpC1 | 4039817 | c.888A>C | synonymous_variant | 0.3 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.31 |
clpC1 | 4039826 | c.879C>G | synonymous_variant | 0.28 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 0.3 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.22 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.19 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.16 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.15 |
clpC1 | 4039988 | c.717C>G | synonymous_variant | 0.18 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 0.18 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.24 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.24 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.25 |
clpC1 | 4040036 | c.669C>G | synonymous_variant | 0.25 |
clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 0.2 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.17 |
clpC1 | 4040105 | c.600C>G | synonymous_variant | 0.25 |
clpC1 | 4040147 | c.558A>G | synonymous_variant | 0.17 |
clpC1 | 4040165 | c.540G>C | synonymous_variant | 0.14 |
clpC1 | 4040171 | c.534C>G | synonymous_variant | 0.17 |
clpC1 | 4040228 | c.477G>T | synonymous_variant | 0.14 |
clpC1 | 4040231 | c.474C>T | synonymous_variant | 0.14 |
clpC1 | 4040237 | c.468C>T | synonymous_variant | 0.14 |
clpC1 | 4040246 | c.459C>G | synonymous_variant | 0.15 |
clpC1 | 4040291 | c.414G>C | synonymous_variant | 0.2 |
clpC1 | 4040318 | c.387C>G | synonymous_variant | 0.23 |
clpC1 | 4040330 | c.375C>G | synonymous_variant | 0.19 |
clpC1 | 4040342 | c.363C>G | synonymous_variant | 0.17 |
clpC1 | 4040471 | c.234T>C | synonymous_variant | 0.18 |
clpC1 | 4040477 | c.228G>C | synonymous_variant | 0.18 |
clpC1 | 4040480 | c.225T>G | synonymous_variant | 0.18 |
clpC1 | 4040501 | c.204C>T | synonymous_variant | 0.14 |
embC | 4240780 | c.918T>C | synonymous_variant | 0.22 |
embC | 4240783 | c.921G>C | synonymous_variant | 0.22 |
embC | 4240789 | c.927T>C | synonymous_variant | 0.22 |
embC | 4240819 | c.957A>G | synonymous_variant | 0.15 |
embC | 4240828 | c.966G>A | synonymous_variant | 0.16 |
embC | 4240831 | c.969T>G | synonymous_variant | 0.15 |
embC | 4241032 | c.1170G>C | synonymous_variant | 0.17 |
embC | 4241038 | c.1176G>C | synonymous_variant | 0.19 |
embC | 4241047 | c.1185C>G | synonymous_variant | 0.2 |
embC | 4241050 | c.1188T>G | synonymous_variant | 0.2 |
embC | 4241053 | c.1191G>C | synonymous_variant | 0.2 |
embC | 4241089 | c.1227C>G | synonymous_variant | 0.25 |
embC | 4241095 | c.1233C>T | synonymous_variant | 0.24 |
embC | 4241107 | c.1245G>C | synonymous_variant | 0.21 |
embC | 4241146 | c.1284C>G | synonymous_variant | 0.2 |
embC | 4241158 | c.1296T>C | synonymous_variant | 0.22 |
embC | 4241161 | c.1299C>G | synonymous_variant | 0.21 |
embC | 4241162 | c.1300T>C | synonymous_variant | 0.21 |
embC | 4241170 | c.1308G>C | synonymous_variant | 0.2 |
embC | 4241173 | c.1311C>T | synonymous_variant | 0.2 |
embC | 4241179 | c.1317G>A | synonymous_variant | 0.2 |
embC | 4241203 | c.1341T>C | synonymous_variant | 0.19 |
embC | 4241206 | c.1344G>C | synonymous_variant | 0.19 |
embC | 4241218 | c.1356G>C | synonymous_variant | 0.17 |
embC | 4241233 | c.1371G>C | synonymous_variant | 0.15 |
embC | 4241449 | c.1587C>G | synonymous_variant | 0.22 |
embC | 4241453 | p.Ile531Val | missense_variant | 0.2 |
embC | 4241479 | c.1617C>G | synonymous_variant | 0.18 |
embC | 4241480 | c.1618T>C | synonymous_variant | 0.17 |
embC | 4241488 | c.1626G>C | synonymous_variant | 0.22 |
embC | 4241496 | p.Ala545Gly | missense_variant | 0.21 |
embC | 4241500 | c.1638A>C | synonymous_variant | 0.19 |
embC | 4241501 | p.Ser547Thr | missense_variant | 0.2 |
embC | 4241506 | c.1644G>C | synonymous_variant | 0.19 |
embC | 4241518 | c.1656A>G | synonymous_variant | 0.18 |
embC | 4241530 | c.1668C>G | synonymous_variant | 0.15 |
embC | 4241572 | c.1710C>G | synonymous_variant | 0.16 |
embC | 4241584 | c.1722T>C | synonymous_variant | 0.16 |
embC | 4241587 | c.1725C>G | synonymous_variant | 0.18 |
embC | 4241591 | p.Leu577Val | missense_variant | 0.22 |
embC | 4241611 | c.1749G>C | synonymous_variant | 0.21 |
embC | 4241614 | c.1752A>C | synonymous_variant | 0.2 |
embC | 4241626 | c.1764T>C | synonymous_variant | 0.22 |
embC | 4241635 | c.1773G>C | synonymous_variant | 0.22 |
embC | 4241644 | c.1782G>C | synonymous_variant | 0.22 |
embC | 4241648 | c.1786_1788delTTGinsCTC | synonymous_variant | 0.22 |
embC | 4241657 | p.Ser599Pro | missense_variant | 0.17 |
embC | 4241665 | c.1803G>C | synonymous_variant | 0.17 |
embC | 4241755 | c.1893C>G | synonymous_variant | 0.15 |
embC | 4241770 | c.1908T>C | synonymous_variant | 0.19 |
embC | 4241791 | c.1929G>C | synonymous_variant | 0.17 |
embC | 4241794 | c.1932C>G | synonymous_variant | 0.16 |
embC | 4241797 | c.1935C>T | synonymous_variant | 0.17 |
embC | 4241809 | c.1947A>C | synonymous_variant | 0.16 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 0.94 |
embA | 4245053 | c.1821G>C | synonymous_variant | 0.16 |
embA | 4245060 | c.1828T>C | synonymous_variant | 0.16 |
embA | 4245083 | c.1851A>C | synonymous_variant | 0.22 |
embA | 4245089 | c.1857G>C | synonymous_variant | 0.22 |
embA | 4245101 | c.1869G>C | synonymous_variant | 0.21 |
embA | 4245137 | c.1905T>C | synonymous_variant | 0.24 |
embA | 4245146 | c.1914G>A | synonymous_variant | 0.2 |
embA | 4245149 | c.1917C>G | synonymous_variant | 0.18 |
embA | 4245153 | p.Ile641Val | missense_variant | 0.2 |
embA | 4245182 | c.1950T>C | synonymous_variant | 0.25 |
embA | 4245189 | c.1957C>T | synonymous_variant | 0.27 |
embA | 4245198 | p.Leu656Ile | missense_variant | 0.26 |
embA | 4245207 | c.1975T>C | synonymous_variant | 0.25 |
embA | 4245215 | c.1983A>C | synonymous_variant | 0.25 |
embA | 4245222 | p.Tyr664Gln | missense_variant | 0.24 |
embA | 4245248 | c.2016G>C | synonymous_variant | 0.22 |
embA | 4245257 | c.2025A>G | synonymous_variant | 0.17 |
embB | 4245725 | c.-789A>G | upstream_gene_variant | 0.15 |
embB | 4245737 | c.-777A>C | upstream_gene_variant | 0.18 |
embB | 4245740 | c.-774T>C | upstream_gene_variant | 0.17 |
embB | 4246292 | c.-222A>G | upstream_gene_variant | 0.17 |
embA | 4246305 | p.Ser1025Glu | missense_variant | 0.16 |
embA | 4246308 | p.Thr1026Ala | missense_variant | 0.16 |
embB | 4246316 | c.-198T>G | upstream_gene_variant | 0.2 |
embB | 4246319 | c.-195G>C | upstream_gene_variant | 0.2 |
embA | 4246329 | p.Thr1033Ala | missense_variant | 0.22 |
embB | 4246349 | c.-165C>G | upstream_gene_variant | 0.2 |
embA | 4246359 | p.Ala1043Ser | missense_variant | 0.17 |
embB | 4246367 | c.-147C>T | upstream_gene_variant | 0.16 |
embB | 4246373 | c.-141T>C | upstream_gene_variant | 0.15 |
embB | 4246376 | c.-138G>C | upstream_gene_variant | 0.15 |
embB | 4246379 | c.-135C>T | upstream_gene_variant | 0.15 |
embB | 4247425 | c.912G>C | synonymous_variant | 0.15 |
embB | 4247434 | c.921C>G | synonymous_variant | 0.16 |
embB | 4247437 | c.924A>G | synonymous_variant | 0.16 |
embB | 4247440 | c.927C>G | synonymous_variant | 0.16 |
embB | 4247446 | c.933C>T | synonymous_variant | 0.16 |
embB | 4247464 | c.951C>G | synonymous_variant | 0.2 |
embB | 4247470 | c.957T>C | synonymous_variant | 0.2 |
embB | 4247491 | c.978G>C | synonymous_variant | 0.23 |
embB | 4247497 | c.984T>C | synonymous_variant | 0.26 |
embB | 4247512 | c.999T>C | synonymous_variant | 0.23 |
embB | 4247539 | c.1026T>C | synonymous_variant | 0.18 |
embB | 4247815 | c.1302C>G | synonymous_variant | 0.16 |
embB | 4247819 | p.Val436Ile | missense_variant | 0.16 |
embB | 4247830 | c.1317A>G | synonymous_variant | 0.17 |
embB | 4247836 | c.1323A>G | synonymous_variant | 0.18 |
embB | 4247839 | c.1326G>C | synonymous_variant | 0.2 |
embB | 4247866 | c.1353G>C | synonymous_variant | 0.3 |
embB | 4247875 | c.1362G>C | synonymous_variant | 0.29 |
embB | 4247876 | c.1363C>T | synonymous_variant | 0.3 |
embB | 4247881 | c.1368G>C | synonymous_variant | 0.3 |
embB | 4247887 | c.1374C>T | synonymous_variant | 0.31 |
embB | 4247893 | c.1380C>T | synonymous_variant | 0.32 |
embB | 4247899 | p.Met462Ile | missense_variant | 0.32 |
embB | 4247905 | c.1392G>C | synonymous_variant | 0.32 |
embB | 4247909 | c.1396T>C | synonymous_variant | 0.3 |
embB | 4247932 | c.1419C>G | synonymous_variant | 0.25 |
embB | 4247940 | p.Leu476Trp | missense_variant | 0.22 |
embB | 4247945 | c.1432T>C | synonymous_variant | 0.19 |
embB | 4247951 | p.Ser480Ala | missense_variant | 0.18 |
embB | 4247956 | c.1443G>C | synonymous_variant | 0.18 |
embB | 4247974 | c.1461C>G | synonymous_variant | 0.16 |
embB | 4248035 | p.Val508Ile | missense_variant | 0.16 |
embB | 4248040 | c.1527C>G | synonymous_variant | 0.16 |
embB | 4248041 | p.Ala510Thr | missense_variant | 0.15 |
embB | 4248070 | c.1557T>C | synonymous_variant | 0.22 |
embB | 4248085 | c.1572T>C | synonymous_variant | 0.24 |
embB | 4248097 | c.1584C>G | synonymous_variant | 0.26 |
embB | 4248130 | c.1617G>C | synonymous_variant | 0.25 |
embB | 4248133 | c.1620C>G | synonymous_variant | 0.25 |
embB | 4248139 | c.1626C>G | synonymous_variant | 0.24 |
embB | 4248142 | c.1629T>C | synonymous_variant | 0.24 |
embB | 4248143 | c.1630T>C | synonymous_variant | 0.24 |
embB | 4248157 | c.1644A>G | synonymous_variant | 0.24 |
embB | 4248220 | c.1707A>C | synonymous_variant | 0.16 |
embB | 4248457 | c.1944T>C | synonymous_variant | 0.15 |
embB | 4249375 | c.2862G>C | synonymous_variant | 0.16 |
embB | 4249381 | c.2868A>G | synonymous_variant | 0.17 |
embB | 4249384 | c.2871G>T | synonymous_variant | 0.19 |
embB | 4249417 | c.2904A>G | synonymous_variant | 0.24 |
embB | 4249423 | p.Asp970Glu | missense_variant | 0.26 |
embB | 4249424 | p.Leu971Met | missense_variant | 0.27 |
embB | 4249429 | c.2916C>T | synonymous_variant | 0.27 |
embB | 4249432 | c.2919A>G | synonymous_variant | 0.26 |
embB | 4249441 | c.2928A>G | synonymous_variant | 0.26 |
embB | 4249444 | c.2931T>C | synonymous_variant | 0.31 |
embB | 4249447 | c.2934G>A | synonymous_variant | 0.29 |
embB | 4249469 | p.Leu986Met | missense_variant | 0.28 |
embB | 4249486 | c.2973T>G | synonymous_variant | 0.26 |
embB | 4249498 | c.2985G>C | synonymous_variant | 0.21 |
embB | 4249521 | p.Ala1003Val | missense_variant | 0.21 |
embB | 4249525 | c.3012T>C | synonymous_variant | 0.21 |
embB | 4249529 | p.Ile1006Val | missense_variant | 0.21 |
embB | 4249532 | p.Ala1007Thr | missense_variant | 0.22 |
embB | 4249537 | c.3024A>G | synonymous_variant | 0.21 |
embB | 4249543 | c.3030G>C | synonymous_variant | 0.22 |
embB | 4249546 | c.3033G>A | synonymous_variant | 0.21 |
embB | 4249558 | c.3045A>C | synonymous_variant | 0.16 |
embB | 4249568 | p.Ser1019Thr | missense_variant | 0.15 |
embB | 4249756 | c.3243C>T | synonymous_variant | 1.0 |
aftB | 4267580 | c.1257G>T | synonymous_variant | 0.17 |
aftB | 4267604 | c.1233C>G | synonymous_variant | 0.2 |
aftB | 4267607 | c.1230G>A | synonymous_variant | 0.2 |
aftB | 4267622 | c.1215G>C | synonymous_variant | 0.21 |
aftB | 4267625 | c.1212T>C | synonymous_variant | 0.21 |
aftB | 4267628 | c.1209C>G | synonymous_variant | 0.21 |
aftB | 4267634 | p.Arg401His | missense_variant | 0.22 |
aftB | 4267649 | c.1188T>C | synonymous_variant | 0.24 |
aftB | 4268164 | p.Gln225Glu | missense_variant | 0.2 |
aftB | 4268169 | p.Ala223Gly | missense_variant | 0.19 |
aftB | 4268171 | c.666G>C | synonymous_variant | 0.19 |
aftB | 4268179 | c.658T>C | synonymous_variant | 0.2 |
aftB | 4268182 | p.Phe219Leu | missense_variant | 0.2 |
aftB | 4268183 | c.654A>T | synonymous_variant | 0.2 |
aftB | 4268193 | p.Leu215Ala | missense_variant | 0.19 |
aftB | 4268225 | c.612G>C | synonymous_variant | 0.15 |
aftB | 4268236 | p.Leu201Met | missense_variant | 0.15 |
aftB | 4269012 | c.-176G>C | upstream_gene_variant | 0.18 |
aftB | 4269027 | c.-191C>T | upstream_gene_variant | 0.16 |
aftB | 4269201 | c.-365A>G | upstream_gene_variant | 0.24 |
ubiA | 4269220 | p.Ala205Lys | missense_variant | 0.24 |
aftB | 4269222 | c.-386T>C | upstream_gene_variant | 0.24 |
aftB | 4269242 | c.-406C>T | upstream_gene_variant | 0.28 |
ubiA | 4269243 | p.His197Gln | missense_variant | 0.26 |
aftB | 4269249 | c.-413G>A | upstream_gene_variant | 0.3 |
aftB | 4269258 | c.-422C>T | upstream_gene_variant | 0.3 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |