Run ID: ERR2513470
Sample name:
Date: 31-03-2023 19:41:58
Number of reads: 2763595
Percentage reads mapped: 81.08
Strain: lineage4.2.2.2
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.98 |
La1.2.BCG | M.bovis | BCG | None | 0.06 |
lineage4.2 | Euro-American | H;T;LAM | None | 0.94 |
lineage4.2.2 | Euro-American (Ural) | T;LAM7-TUR | None | 1.0 |
lineage4.2.2.2 | Euro-American (Ural) | T;LAM7-TUR | None | 0.98 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472307 | n.462C>T | non_coding_transcript_exon_variant | 0.63 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6196 | c.957C>T | synonymous_variant | 0.16 |
gyrB | 6238 | c.999G>A | synonymous_variant | 0.19 |
gyrB | 6242 | p.Arg335Lys | missense_variant | 0.2 |
gyrB | 6250 | c.1011A>G | synonymous_variant | 0.18 |
gyrB | 6256 | c.1017G>A | synonymous_variant | 0.18 |
gyrB | 6268 | c.1029C>G | synonymous_variant | 0.17 |
gyrA | 6307 | c.-995T>G | upstream_gene_variant | 0.17 |
gyrA | 6319 | c.-983G>C | upstream_gene_variant | 0.16 |
gyrA | 6655 | c.-647T>C | upstream_gene_variant | 0.16 |
gyrA | 6670 | c.-632G>C | upstream_gene_variant | 0.2 |
gyrA | 6673 | c.-629A>C | upstream_gene_variant | 0.24 |
gyrA | 6676 | c.-626T>G | upstream_gene_variant | 0.23 |
gyrA | 6700 | c.-602T>C | upstream_gene_variant | 0.29 |
gyrA | 6703 | c.-599G>C | upstream_gene_variant | 0.32 |
gyrA | 6709 | c.-593A>G | upstream_gene_variant | 0.31 |
gyrA | 6712 | c.-590G>C | upstream_gene_variant | 0.32 |
gyrA | 6728 | c.-574_-572delCTAinsTTG | upstream_gene_variant | 0.31 |
gyrA | 6742 | c.-560A>G | upstream_gene_variant | 0.26 |
gyrA | 6745 | c.-557T>G | upstream_gene_variant | 0.26 |
gyrA | 6751 | c.-551G>C | upstream_gene_variant | 0.24 |
gyrA | 6760 | c.-542G>C | upstream_gene_variant | 0.22 |
gyrA | 6763 | c.-539G>C | upstream_gene_variant | 0.22 |
gyrA | 6775 | c.-527G>C | upstream_gene_variant | 0.22 |
gyrA | 6793 | c.-509T>C | upstream_gene_variant | 0.26 |
gyrB | 6797 | p.Gly520Thr | missense_variant | 0.24 |
gyrA | 6811 | c.-491C>T | upstream_gene_variant | 0.19 |
gyrA | 6949 | c.-353A>G | upstream_gene_variant | 0.18 |
gyrA | 6952 | c.-350C>G | upstream_gene_variant | 0.18 |
gyrA | 6967 | c.-335T>C | upstream_gene_variant | 0.19 |
gyrA | 6973 | c.-329G>C | upstream_gene_variant | 0.22 |
gyrA | 6982 | c.-320A>C | upstream_gene_variant | 0.2 |
gyrA | 7006 | c.-296T>C | upstream_gene_variant | 0.21 |
gyrA | 7007 | c.-295C>T | upstream_gene_variant | 0.21 |
gyrA | 7010 | c.-292C>T | upstream_gene_variant | 0.21 |
gyrA | 7015 | c.-287G>A | upstream_gene_variant | 0.21 |
gyrA | 7018 | c.-284G>A | upstream_gene_variant | 0.23 |
gyrB | 7023 | p.Leu595Gln | missense_variant | 0.23 |
gyrA | 7033 | c.-269G>C | upstream_gene_variant | 0.25 |
gyrB | 7051 | p.Glu604Asp | missense_variant | 0.23 |
gyrA | 7066 | c.-236G>C | upstream_gene_variant | 0.19 |
gyrA | 7075 | c.-227T>C | upstream_gene_variant | 0.17 |
gyrA | 7078 | c.-224A>C | upstream_gene_variant | 0.15 |
gyrA | 7084 | c.-218A>G | upstream_gene_variant | 0.16 |
gyrA | 7210 | c.-92C>T | upstream_gene_variant | 0.15 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7457 | c.156T>C | synonymous_variant | 0.15 |
gyrA | 7475 | c.174A>G | synonymous_variant | 0.17 |
gyrA | 7480 | p.Phe60Tyr | missense_variant | 0.16 |
gyrA | 7484 | c.183T>C | synonymous_variant | 0.16 |
gyrA | 7490 | c.189C>G | synonymous_variant | 0.16 |
gyrA | 7523 | c.222C>G | synonymous_variant | 0.16 |
gyrA | 7532 | c.231T>G | synonymous_variant | 0.16 |
gyrA | 7541 | c.240C>G | synonymous_variant | 0.18 |
gyrA | 7547 | c.246C>T | synonymous_variant | 0.19 |
gyrA | 7571 | c.270G>C | synonymous_variant | 0.22 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7595 | c.294C>G | synonymous_variant | 0.16 |
gyrA | 7637 | c.336C>G | synonymous_variant | 0.17 |
gyrA | 7652 | c.351C>T | synonymous_variant | 0.18 |
gyrA | 7658 | c.357A>C | synonymous_variant | 0.17 |
gyrA | 7670 | c.369A>G | synonymous_variant | 0.16 |
gyrA | 8219 | c.918T>C | synonymous_variant | 0.15 |
gyrA | 8225 | c.924T>C | synonymous_variant | 0.15 |
gyrA | 8237 | c.936A>G | synonymous_variant | 0.15 |
gyrA | 8247 | p.Ile316Val | missense_variant | 0.19 |
gyrA | 8264 | c.963T>C | synonymous_variant | 0.19 |
gyrA | 8267 | c.966G>C | synonymous_variant | 0.18 |
gyrA | 8270 | c.969G>C | synonymous_variant | 0.18 |
gyrA | 8276 | c.975G>A | synonymous_variant | 0.18 |
gyrA | 8283 | p.Ile328Leu | missense_variant | 0.18 |
gyrA | 8288 | c.987T>C | synonymous_variant | 0.17 |
gyrA | 8294 | c.993T>C | synonymous_variant | 0.18 |
gyrA | 8324 | c.1023T>C | synonymous_variant | 0.15 |
gyrA | 8330 | c.1029C>G | synonymous_variant | 0.16 |
gyrA | 8339 | c.1038A>G | synonymous_variant | 0.15 |
gyrA | 8543 | c.1242C>G | synonymous_variant | 0.17 |
gyrA | 8546 | c.1245T>C | synonymous_variant | 0.18 |
gyrA | 8552 | c.1251C>A | synonymous_variant | 0.17 |
gyrA | 8561 | c.1260A>G | synonymous_variant | 0.17 |
gyrA | 8576 | c.1275C>G | synonymous_variant | 0.16 |
gyrA | 8579 | c.1278C>T | synonymous_variant | 0.15 |
gyrA | 8588 | c.1287G>A | synonymous_variant | 0.15 |
gyrA | 8597 | c.1296C>G | synonymous_variant | 0.15 |
gyrA | 8603 | c.1302A>G | synonymous_variant | 0.17 |
gyrA | 8619 | c.1318_1320delTTGinsCTA | synonymous_variant | 0.16 |
gyrA | 8624 | c.1323G>C | synonymous_variant | 0.16 |
gyrA | 8688 | p.Ala463Ser | missense_variant | 0.92 |
gyrA | 8891 | c.1590G>A | synonymous_variant | 0.14 |
gyrA | 8897 | c.1596T>C | synonymous_variant | 0.16 |
gyrA | 8933 | c.1632G>C | synonymous_variant | 0.15 |
gyrA | 9204 | p.Ser635Thr | missense_variant | 0.15 |
gyrA | 9224 | c.1923C>T | synonymous_variant | 0.15 |
gyrA | 9230 | c.1929T>C | synonymous_variant | 0.16 |
gyrA | 9233 | c.1932C>G | synonymous_variant | 0.15 |
gyrA | 9239 | c.1938C>T | synonymous_variant | 0.16 |
gyrA | 9252 | p.Val651Ile | missense_variant | 0.17 |
gyrA | 9284 | c.1983T>C | synonymous_variant | 0.16 |
gyrA | 9300 | p.Ala667Ser | missense_variant | 0.16 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9308 | p.Asp669Glu | missense_variant | 0.17 |
gyrA | 9335 | c.2034G>C | synonymous_variant | 0.16 |
fgd1 | 490782 | c.-1G>C | upstream_gene_variant | 0.16 |
fgd1 | 490797 | c.15G>A | synonymous_variant | 0.16 |
fgd1 | 490800 | c.18A>C | synonymous_variant | 0.16 |
fgd1 | 490803 | c.21T>A | synonymous_variant | 0.16 |
fgd1 | 490812 | c.30A>G | synonymous_variant | 0.22 |
fgd1 | 490815 | c.33G>C | synonymous_variant | 0.22 |
fgd1 | 490827 | c.45C>T | synonymous_variant | 0.22 |
fgd1 | 490848 | c.66A>G | synonymous_variant | 0.24 |
fgd1 | 490851 | c.69A>T | synonymous_variant | 0.24 |
fgd1 | 490868 | p.Ala29Gly | missense_variant | 0.22 |
fgd1 | 490887 | c.105G>A | synonymous_variant | 0.17 |
fgd1 | 490890 | c.108C>G | synonymous_variant | 0.16 |
fgd1 | 490896 | c.114C>T | synonymous_variant | 0.16 |
fgd1 | 491130 | c.348C>G | synonymous_variant | 0.15 |
mshA | 575737 | c.390T>C | synonymous_variant | 0.15 |
mshA | 575770 | c.423G>A | synonymous_variant | 0.18 |
mshA | 575771 | p.Val142Ser | missense_variant | 0.17 |
mshA | 575779 | c.432A>G | synonymous_variant | 0.18 |
mshA | 575782 | c.435G>C | synonymous_variant | 0.18 |
mshA | 575809 | c.462C>T | synonymous_variant | 0.23 |
mshA | 575812 | c.465C>T | synonymous_variant | 0.2 |
mshA | 575821 | c.474G>C | synonymous_variant | 0.2 |
mshA | 575824 | c.477T>G | synonymous_variant | 0.2 |
mshA | 575830 | c.483C>G | synonymous_variant | 0.19 |
mshA | 575833 | c.486C>G | synonymous_variant | 0.19 |
mshA | 575845 | c.498C>T | synonymous_variant | 0.17 |
mshA | 576077 | c.730C>T | synonymous_variant | 1.0 |
ccsA | 620226 | c.336G>A | synonymous_variant | 0.18 |
ccsA | 620245 | c.355T>C | synonymous_variant | 0.18 |
ccsA | 620249 | p.Ser120Cys | missense_variant | 0.17 |
ccsA | 620254 | c.364_366delCTCinsTTG | synonymous_variant | 0.16 |
ccsA | 620265 | c.375C>G | synonymous_variant | 0.18 |
ccsA | 620268 | c.378G>C | synonymous_variant | 0.19 |
ccsA | 620283 | c.393T>C | synonymous_variant | 0.21 |
ccsA | 620284 | p.Ala132Pro | missense_variant | 0.2 |
ccsA | 620288 | p.Arg133Gln | missense_variant | 0.21 |
ccsA | 620295 | c.405G>T | synonymous_variant | 0.2 |
ccsA | 620298 | c.408G>C | synonymous_variant | 0.21 |
ccsA | 620310 | c.420C>T | synonymous_variant | 0.22 |
ccsA | 620317 | p.Val143Leu | missense_variant | 0.22 |
ccsA | 620340 | c.450C>G | synonymous_variant | 0.27 |
ccsA | 620346 | c.456C>G | synonymous_variant | 0.26 |
ccsA | 620362 | p.Ala158Thr | missense_variant | 0.25 |
ccsA | 620367 | c.477T>C | synonymous_variant | 0.23 |
ccsA | 620373 | c.483C>G | synonymous_variant | 0.22 |
ccsA | 620376 | c.486G>C | synonymous_variant | 0.21 |
ccsA | 620385 | c.495G>C | synonymous_variant | 0.19 |
ccsA | 620388 | c.498A>G | synonymous_variant | 0.18 |
ccsA | 620389 | c.499C>T | synonymous_variant | 0.17 |
ccsA | 620412 | c.522T>C | synonymous_variant | 0.17 |
ccsA | 620415 | c.525T>C | synonymous_variant | 0.16 |
rpoB | 760181 | c.375T>C | synonymous_variant | 0.16 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.16 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.16 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.18 |
rpoB | 760283 | c.477G>C | synonymous_variant | 0.22 |
rpoB | 760298 | c.492G>C | synonymous_variant | 0.2 |
rpoB | 760307 | c.501T>C | synonymous_variant | 0.2 |
rpoB | 760310 | c.504G>C | synonymous_variant | 0.2 |
rpoB | 760328 | c.522G>C | synonymous_variant | 0.23 |
rpoB | 760331 | c.525G>C | synonymous_variant | 0.23 |
rpoB | 760340 | c.534G>T | synonymous_variant | 0.22 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.22 |
rpoB | 760370 | c.564C>G | synonymous_variant | 0.21 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.2 |
rpoB | 760380 | p.Thr192Leu | missense_variant | 0.21 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.21 |
rpoB | 760412 | c.606C>G | synonymous_variant | 0.19 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.17 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.18 |
rpoB | 760522 | p.Ser239Asn | missense_variant | 0.17 |
rpoB | 760532 | c.726T>C | synonymous_variant | 0.17 |
rpoB | 760533 | p.Val243Thr | missense_variant | 0.16 |
rpoB | 760541 | c.735G>C | synonymous_variant | 0.16 |
rpoB | 760547 | c.741G>C | synonymous_variant | 0.19 |
rpoB | 760563 | p.Arg253Met | missense_variant | 0.19 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.24 |
rpoB | 760611 | c.805T>C | synonymous_variant | 0.21 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.17 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.17 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.17 |
rpoB | 760670 | c.864G>C | synonymous_variant | 0.16 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.17 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.17 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.17 |
rpoB | 760715 | c.909C>G | synonymous_variant | 0.2 |
rpoB | 760718 | c.912C>T | synonymous_variant | 0.18 |
rpoB | 760724 | c.918T>C | synonymous_variant | 0.16 |
rpoB | 760730 | c.924T>C | synonymous_variant | 0.16 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.17 |
rpoB | 760949 | c.1143C>T | synonymous_variant | 0.16 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.19 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.22 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.24 |
rpoB | 761006 | c.1200C>G | synonymous_variant | 0.22 |
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 | 0.24 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.2 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.2 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.22 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.22 |
rpoB | 761129 | c.1323G>C | synonymous_variant | 0.21 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 0.21 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.21 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.21 |
rpoB | 761153 | c.1347G>C | synonymous_variant | 0.23 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.22 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.21 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.24 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.22 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.22 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.23 |
rpoB | 761219 | c.1413G>C | synonymous_variant | 0.22 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.22 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.2 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.22 |
rpoB | 761489 | c.1683G>A | synonymous_variant | 0.87 |
rpoB | 761510 | c.1704T>C | synonymous_variant | 0.16 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.19 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.19 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.19 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.17 |
rpoB | 761588 | c.1782C>T | synonymous_variant | 0.2 |
rpoB | 761765 | c.1959T>C | synonymous_variant | 0.18 |
rpoB | 761773 | p.His656Pro | missense_variant | 0.15 |
rpoB | 761778 | p.Asn658Asp | missense_variant | 0.16 |
rpoB | 761791 | p.Arg662His | missense_variant | 0.16 |
rpoB | 761815 | p.Ala670Asp | missense_variant | 0.15 |
rpoB | 762008 | c.2202C>T | synonymous_variant | 0.19 |
rpoB | 762014 | c.2208C>T | synonymous_variant | 0.19 |
rpoB | 762017 | c.2211A>G | synonymous_variant | 0.19 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.17 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.17 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.16 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.16 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.18 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.2 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 0.18 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.17 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.17 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.17 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.16 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.19 |
rpoB | 762206 | c.2400C>G | synonymous_variant | 0.22 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.25 |
rpoB | 762246 | c.2440C>T | synonymous_variant | 0.21 |
rpoB | 762254 | c.2448T>G | synonymous_variant | 0.23 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.23 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.23 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.2 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.21 |
rpoB | 762314 | c.2508C>T | synonymous_variant | 0.21 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.2 |
rpoB | 762329 | c.2523G>C | synonymous_variant | 0.23 |
rpoB | 762338 | c.2532T>C | synonymous_variant | 0.24 |
rpoB | 762347 | c.2541T>C | synonymous_variant | 0.24 |
rpoB | 762362 | p.Glu852Asp | missense_variant | 0.22 |
rpoB | 762369 | c.2563T>C | synonymous_variant | 0.22 |
rpoC | 762398 | c.-972T>C | upstream_gene_variant | 0.21 |
rpoC | 762401 | c.-969G>C | upstream_gene_variant | 0.19 |
rpoC | 762404 | c.-966T>C | upstream_gene_variant | 0.2 |
rpoC | 762410 | c.-960T>C | upstream_gene_variant | 0.22 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 0.2 |
rpoC | 762419 | c.-951C>G | upstream_gene_variant | 0.19 |
rpoC | 762434 | c.-936T>C | upstream_gene_variant | 0.16 |
rpoC | 762449 | c.-921C>A | upstream_gene_variant | 0.16 |
rpoC | 762467 | c.-903C>T | upstream_gene_variant | 0.16 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.15 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.16 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.17 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.18 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.17 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.18 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.2 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.18 |
rpoC | 763158 | c.-212C>T | upstream_gene_variant | 0.21 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.2 |
rpoC | 763190 | c.-180C>T | upstream_gene_variant | 0.15 |
rpoC | 763411 | c.42T>G | synonymous_variant | 0.15 |
rpoC | 763414 | c.45T>C | synonymous_variant | 0.18 |
rpoC | 763441 | c.72C>T | synonymous_variant | 0.21 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.22 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.25 |
rpoC | 763486 | c.117T>G | synonymous_variant | 0.26 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.25 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.27 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.28 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.28 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.29 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.18 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.18 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.22 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.21 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.16 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.18 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.2 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.19 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.19 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.2 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.19 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.2 |
rpoC | 763774 | c.405G>C | synonymous_variant | 0.21 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.22 |
rpoC | 763816 | c.447C>G | synonymous_variant | 0.24 |
rpoC | 763835 | p.Ala156Met | missense_variant | 0.19 |
rpoC | 763853 | p.Val162Ile | missense_variant | 0.2 |
rpoC | 763858 | c.489A>G | synonymous_variant | 0.2 |
rpoC | 763872 | p.Gly168Ala | missense_variant | 0.17 |
rpoC | 763877 | c.508C>T | synonymous_variant | 0.14 |
rpoC | 763888 | c.519G>C | synonymous_variant | 0.16 |
rpoC | 763891 | c.522G>C | synonymous_variant | 0.16 |
rpoC | 763894 | c.525A>G | synonymous_variant | 0.17 |
rpoC | 763900 | c.531G>C | synonymous_variant | 0.17 |
rpoC | 763936 | c.567C>G | synonymous_variant | 0.18 |
rpoC | 763945 | c.576T>C | synonymous_variant | 0.18 |
rpoC | 763951 | c.582G>C | synonymous_variant | 0.18 |
rpoC | 763960 | c.591T>C | synonymous_variant | 0.16 |
rpoC | 764005 | c.636G>C | synonymous_variant | 0.17 |
rpoC | 764024 | c.655_657delTTGinsCTC | synonymous_variant | 0.17 |
rpoC | 764032 | p.Asp221Glu | missense_variant | 0.16 |
rpoC | 764041 | p.Ser224Arg | missense_variant | 0.15 |
rpoC | 764059 | c.690G>T | synonymous_variant | 0.16 |
rpoC | 764215 | c.846A>G | synonymous_variant | 0.18 |
rpoC | 764236 | c.867G>A | synonymous_variant | 0.2 |
rpoC | 764248 | c.879C>G | synonymous_variant | 0.2 |
rpoC | 764257 | c.888G>C | synonymous_variant | 0.2 |
rpoC | 764266 | c.897T>C | synonymous_variant | 0.19 |
rpoC | 764269 | c.900G>C | synonymous_variant | 0.19 |
rpoC | 764272 | c.903G>C | synonymous_variant | 0.2 |
rpoC | 764278 | c.909A>G | synonymous_variant | 0.23 |
rpoC | 764338 | c.969G>A | synonymous_variant | 0.27 |
rpoC | 764353 | c.984G>C | synonymous_variant | 0.29 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.21 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.16 |
rpoC | 764419 | c.1050C>G | synonymous_variant | 0.19 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.18 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.18 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.17 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.18 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.19 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.18 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.19 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.2 |
rpoC | 764489 | c.1120C>T | synonymous_variant | 0.22 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.19 |
rpoC | 764510 | c.1141C>T | synonymous_variant | 0.19 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.21 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.21 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.22 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.2 |
rpoC | 764554 | c.1185C>T | synonymous_variant | 0.17 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.15 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.16 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.16 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.16 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.23 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.22 |
rpoC | 764650 | c.1281G>C | synonymous_variant | 0.21 |
rpoC | 764651 | c.1282_1284delTCGinsAGC | synonymous_variant | 0.19 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.19 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.22 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.23 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.22 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.18 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.17 |
rpoC | 764872 | c.1503A>G | synonymous_variant | 0.17 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.22 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.25 |
rpoC | 764932 | c.1563C>A | synonymous_variant | 0.25 |
rpoC | 764935 | c.1566T>C | synonymous_variant | 0.25 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.25 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.25 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.26 |
rpoC | 765019 | c.1650A>G | synonymous_variant | 0.26 |
rpoC | 765034 | c.1665T>C | synonymous_variant | 0.21 |
rpoC | 765040 | c.1671T>C | synonymous_variant | 0.18 |
rpoC | 765041 | c.1672T>C | synonymous_variant | 0.18 |
rpoC | 765047 | c.1678T>C | synonymous_variant | 0.18 |
rpoC | 765053 | c.1684_1685delTCinsAG | synonymous_variant | 0.17 |
rpoC | 765383 | p.Met672Leu | missense_variant | 0.16 |
rpoC | 765404 | p.Leu679Val | missense_variant | 0.19 |
rpoC | 765409 | c.2040T>C | synonymous_variant | 0.18 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.2 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.24 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.24 |
rpoC | 765529 | c.2160C>T | synonymous_variant | 0.26 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.24 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.2 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.2 |
rpoC | 765559 | c.2190G>C | synonymous_variant | 0.2 |
rpoC | 765580 | c.2211G>C | synonymous_variant | 0.2 |
rpoC | 765613 | p.His748Gln | missense_variant | 0.17 |
rpoC | 765625 | c.2256C>G | synonymous_variant | 0.19 |
rpoC | 765631 | p.Asp754Glu | missense_variant | 0.17 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.19 |
rpoC | 765734 | c.2365T>C | synonymous_variant | 0.2 |
rpoC | 765739 | c.2370G>T | synonymous_variant | 0.23 |
rpoC | 765751 | c.2382C>G | synonymous_variant | 0.21 |
rpoC | 765753 | p.Asp795Ala | missense_variant | 0.2 |
rpoC | 765772 | c.2403C>G | synonymous_variant | 0.16 |
rpoC | 765787 | c.2418C>T | synonymous_variant | 0.15 |
rpoC | 765811 | c.2442T>C | synonymous_variant | 0.16 |
rpoC | 765826 | c.2457T>C | synonymous_variant | 0.15 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 0.15 |
rpoC | 765850 | c.2481G>C | synonymous_variant | 0.18 |
rpoC | 765883 | c.2514C>G | synonymous_variant | 0.2 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.2 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.19 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.23 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.26 |
rpoC | 765982 | c.2613C>G | synonymous_variant | 0.27 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.26 |
rpoC | 766010 | c.2641_2642delTCinsAG | synonymous_variant | 0.21 |
rpoC | 766021 | c.2652G>C | synonymous_variant | 0.26 |
rpoC | 766027 | c.2658G>C | synonymous_variant | 0.25 |
rpoC | 766030 | c.2661C>G | synonymous_variant | 0.25 |
rpoC | 766036 | c.2667C>T | synonymous_variant | 0.25 |
rpoC | 766043 | p.Gln892Glu | missense_variant | 0.24 |
rpoC | 766054 | c.2685C>G | synonymous_variant | 0.22 |
rpoC | 766082 | p.Ala905Gln | missense_variant | 0.2 |
rpoC | 766096 | c.2727G>C | synonymous_variant | 0.19 |
rpoC | 766129 | c.2760C>G | synonymous_variant | 0.21 |
rpoC | 766135 | c.2766G>A | synonymous_variant | 0.21 |
rpoC | 766141 | c.2772C>T | synonymous_variant | 0.16 |
rpoC | 766142 | c.2773C>T | synonymous_variant | 0.16 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.17 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.17 |
rpoC | 766408 | c.3039C>G | synonymous_variant | 0.17 |
rpoC | 766411 | c.3042C>G | synonymous_variant | 0.19 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.22 |
rpoC | 766447 | c.3078T>C | synonymous_variant | 0.18 |
rpoC | 766462 | c.3093G>C | synonymous_variant | 0.15 |
rpoC | 766483 | c.3114G>C | synonymous_variant | 0.16 |
rpoC | 766484 | p.Val1039Ile | missense_variant | 0.16 |
rpoC | 766492 | c.3123T>C | synonymous_variant | 0.18 |
rpoC | 766522 | c.3153C>G | synonymous_variant | 0.18 |
rpoC | 766528 | c.3159T>C | synonymous_variant | 0.18 |
rpoC | 766531 | c.3162G>C | synonymous_variant | 0.18 |
rpoC | 766540 | p.Asp1057Glu | missense_variant | 0.17 |
rpoC | 766549 | c.3180G>C | synonymous_variant | 0.16 |
rpoC | 766583 | p.Gly1072Ser | missense_variant | 0.14 |
rpoC | 766594 | c.3225G>C | synonymous_variant | 0.17 |
rpoC | 766597 | c.3228C>G | synonymous_variant | 0.18 |
rpoC | 766607 | p.Ile1080Leu | missense_variant | 0.2 |
rpoC | 766630 | c.3261G>C | synonymous_variant | 0.18 |
rpoC | 766657 | c.3288A>G | synonymous_variant | 0.15 |
rpoC | 766672 | c.3303T>C | synonymous_variant | 0.18 |
rpoC | 766673 | p.Gly1102Asn | missense_variant | 0.18 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.27 |
rpoC | 766738 | c.3369G>C | synonymous_variant | 0.29 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.36 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.38 |
rpoC | 766801 | c.3432C>G | synonymous_variant | 0.35 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.33 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 0.33 |
rpoC | 766864 | c.3495G>C | synonymous_variant | 0.33 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.39 |
rpoC | 766933 | c.3564A>G | synonymous_variant | 0.43 |
rpoC | 766945 | c.3576A>G | synonymous_variant | 0.43 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.37 |
rpoC | 766972 | c.3603G>C | synonymous_variant | 0.35 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.33 |
rpoC | 767009 | c.3640_3642delTCGinsAGC | synonymous_variant | 0.28 |
rpoC | 767014 | c.3645G>C | synonymous_variant | 0.26 |
rpoC | 767033 | c.3664_3666delTCGinsAGC | synonymous_variant | 0.26 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.23 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.23 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.17 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.2 |
rpoC | 767134 | c.3765C>A | synonymous_variant | 0.22 |
rpoC | 767158 | c.3789T>C | synonymous_variant | 0.23 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.23 |
rpoC | 767191 | c.3822C>G | synonymous_variant | 0.19 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776402 | c.2079C>G | synonymous_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781628 | c.69T>C | synonymous_variant | 0.16 |
rpsL | 781631 | c.72G>C | synonymous_variant | 0.18 |
rpsL | 781649 | c.90T>C | synonymous_variant | 0.22 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.23 |
rpsL | 781700 | c.141G>C | synonymous_variant | 0.27 |
rpsL | 781703 | c.144G>T | synonymous_variant | 0.27 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.25 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.23 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.24 |
rpsL | 781742 | c.183C>T | synonymous_variant | 0.23 |
rpsL | 781748 | c.189C>G | synonymous_variant | 0.21 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.23 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.23 |
rpsL | 781763 | c.204C>A | synonymous_variant | 0.21 |
rpsL | 781772 | c.213C>A | synonymous_variant | 0.22 |
rpsL | 781808 | c.249C>T | synonymous_variant | 0.21 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.2 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.19 |
rpsL | 781838 | c.279G>C | synonymous_variant | 0.2 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.2 |
rpsL | 781865 | c.306G>C | synonymous_variant | 0.16 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.15 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.15 |
rpsL | 781877 | c.318T>C | synonymous_variant | 0.15 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.16 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.16 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.16 |
rplC | 800648 | c.-161A>T | upstream_gene_variant | 0.19 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.18 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.18 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.16 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.17 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.17 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.17 |
rplC | 800747 | c.-62C>G | upstream_gene_variant | 0.15 |
rplC | 800771 | c.-38C>T | upstream_gene_variant | 0.15 |
rplC | 801246 | c.438C>T | synonymous_variant | 0.16 |
rplC | 801249 | c.441T>C | synonymous_variant | 0.16 |
rplC | 801255 | c.447C>T | synonymous_variant | 0.16 |
rplC | 801264 | c.456C>T | synonymous_variant | 0.15 |
rplC | 801300 | c.492C>G | synonymous_variant | 0.19 |
rplC | 801309 | c.501C>G | synonymous_variant | 0.18 |
rplC | 801312 | c.504G>C | synonymous_variant | 0.17 |
rplC | 801321 | c.513C>T | synonymous_variant | 0.16 |
rplC | 801324 | c.516T>C | synonymous_variant | 0.16 |
rplC | 801341 | p.Leu178His | missense_variant | 0.14 |
rplC | 801348 | c.540T>G | synonymous_variant | 0.15 |
rplC | 801357 | c.549T>C | synonymous_variant | 0.16 |
rplC | 801367 | p.Ala187Thr | missense_variant | 0.16 |
fbiC | 1303818 | c.888C>G | synonymous_variant | 0.18 |
fbiC | 1303836 | c.906G>C | synonymous_variant | 0.25 |
fbiC | 1303845 | c.915C>G | synonymous_variant | 0.25 |
fbiC | 1303846 | p.Phe306Val | missense_variant | 0.25 |
fbiC | 1303854 | c.924T>C | synonymous_variant | 0.27 |
fbiC | 1303860 | c.930A>C | synonymous_variant | 0.26 |
fbiC | 1303884 | c.954T>G | synonymous_variant | 0.25 |
fbiC | 1303905 | c.975G>C | synonymous_variant | 0.26 |
fbiC | 1303914 | c.984C>G | synonymous_variant | 0.28 |
fbiC | 1303920 | c.990C>T | synonymous_variant | 0.25 |
fbiC | 1304004 | c.1074A>G | synonymous_variant | 0.17 |
fbiC | 1304008 | c.1078T>C | synonymous_variant | 0.17 |
fbiC | 1304022 | c.1092T>C | synonymous_variant | 0.2 |
fbiC | 1304031 | c.1101C>G | synonymous_variant | 0.2 |
fbiC | 1304034 | c.1104A>G | synonymous_variant | 0.19 |
fbiC | 1304040 | c.1110C>G | synonymous_variant | 0.16 |
fbiC | 1304046 | c.1116C>G | synonymous_variant | 0.16 |
fbiC | 1304049 | c.1119T>C | synonymous_variant | 0.15 |
fbiC | 1304058 | c.1128G>A | synonymous_variant | 0.17 |
fbiC | 1304059 | c.1129C>T | synonymous_variant | 0.17 |
fbiC | 1304064 | c.1134G>C | synonymous_variant | 0.19 |
fbiC | 1304067 | c.1137G>C | synonymous_variant | 0.19 |
fbiC | 1304085 | c.1155C>T | synonymous_variant | 0.18 |
fbiC | 1304091 | p.Asp387Glu | missense_variant | 0.18 |
fbiC | 1304092 | p.Met388Leu | missense_variant | 0.18 |
fbiC | 1304097 | c.1167G>C | synonymous_variant | 0.18 |
fbiC | 1304127 | c.1197A>G | synonymous_variant | 0.16 |
fbiC | 1304634 | c.1704C>G | synonymous_variant | 0.16 |
fbiC | 1304640 | c.1710A>C | synonymous_variant | 0.16 |
fbiC | 1304646 | c.1716T>C | synonymous_variant | 0.16 |
fbiC | 1304703 | c.1773C>G | synonymous_variant | 0.17 |
fbiC | 1304711 | p.Ala594Asp | missense_variant | 0.15 |
fbiC | 1304724 | c.1794A>G | synonymous_variant | 0.17 |
fbiC | 1304727 | c.1797A>G | synonymous_variant | 0.18 |
fbiC | 1304742 | c.1812T>C | synonymous_variant | 0.17 |
fbiC | 1304748 | c.1818T>C | synonymous_variant | 0.15 |
fbiC | 1304757 | c.1827A>G | synonymous_variant | 0.15 |
fbiC | 1304778 | c.1848T>C | synonymous_variant | 0.17 |
fbiC | 1304784 | c.1854T>C | synonymous_variant | 0.18 |
fbiC | 1304787 | c.1857T>G | synonymous_variant | 0.19 |
fbiC | 1304808 | c.1878C>G | synonymous_variant | 0.21 |
fbiC | 1304811 | c.1881C>G | synonymous_variant | 0.21 |
fbiC | 1304817 | c.1887T>C | synonymous_variant | 0.24 |
fbiC | 1304829 | c.1899T>C | synonymous_variant | 0.26 |
fbiC | 1304832 | c.1902C>T | synonymous_variant | 0.27 |
fbiC | 1304853 | c.1923C>T | synonymous_variant | 0.26 |
fbiC | 1304856 | c.1926C>G | synonymous_variant | 0.28 |
fbiC | 1304869 | c.1939C>T | synonymous_variant | 0.29 |
fbiC | 1304875 | p.Ile649Val | missense_variant | 0.27 |
fbiC | 1304883 | p.Glu651Asp | missense_variant | 0.27 |
fbiC | 1304891 | p.Ile654Thr | missense_variant | 0.27 |
fbiC | 1304893 | p.Gly655Ser | missense_variant | 0.25 |
fbiC | 1304907 | c.1977C>G | synonymous_variant | 0.24 |
fbiC | 1304910 | c.1980G>C | synonymous_variant | 0.25 |
fbiC | 1304916 | c.1986T>C | synonymous_variant | 0.24 |
fbiC | 1304928 | c.1998T>C | synonymous_variant | 0.25 |
fbiC | 1304937 | c.2007G>C | synonymous_variant | 0.25 |
fbiC | 1304958 | c.2028T>G | synonymous_variant | 0.27 |
fbiC | 1304983 | c.2053C>T | synonymous_variant | 0.25 |
fbiC | 1304994 | c.2064A>G | synonymous_variant | 0.22 |
fbiC | 1304995 | p.Leu689Met | missense_variant | 0.22 |
fbiC | 1305006 | c.2076A>G | synonymous_variant | 0.2 |
fbiC | 1305012 | c.2082G>C | synonymous_variant | 0.18 |
fbiC | 1305015 | c.2085G>C | synonymous_variant | 0.17 |
atpE | 1461113 | c.69C>T | synonymous_variant | 0.18 |
atpE | 1461132 | p.Val30Ile | missense_variant | 0.17 |
atpE | 1461149 | c.105T>G | synonymous_variant | 0.16 |
atpE | 1461150 | p.Ile36Val | missense_variant | 0.16 |
atpE | 1461159 | p.Val39Ile | missense_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1471932 | n.87A>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1471969 | n.124T>C | non_coding_transcript_exon_variant | 0.32 |
rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472044 | n.199G>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472045 | n.200T>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.37 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473668 | n.11C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473756 | n.99G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.59 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1473943 | n.286G>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1473945 | n.288T>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1473946 | n.289A>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473986 | n.329T>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1473987 | n.330G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474009 | n.352A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474012 | n.355C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474291 | n.635_649delTTCCTCTCCGGAGGA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474823 | n.1166C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475199 | n.1542G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475249 | n.1592T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475252 | n.1595C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475266 | n.1609T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475267 | n.1610G>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475275 | n.1618C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475276 | n.1619T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475291 | n.1634A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475369 | n.1712G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475402 | n.1745C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475573 | n.1916G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 0.55 |
rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475659 | n.2002G>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475765 | n.2111delG | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476031 | n.2374C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476033 | n.2376T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476034 | n.2377C>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476048 | n.2391G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476089 | n.2432T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476095 | n.2438C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476105 | n.2448G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476106 | n.2449A>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476689 | n.3032A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476690 | n.3033C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476693 | n.3036G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476695 | n.3038T>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476716 | n.3059A>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476717 | n.3060C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476723 | n.3066T>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476726 | n.3069A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476755 | n.3098G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476759 | n.3102T>C | non_coding_transcript_exon_variant | 0.14 |
inhA | 1674780 | c.579T>G | synonymous_variant | 0.16 |
inhA | 1674789 | c.588G>T | synonymous_variant | 0.16 |
inhA | 1674795 | c.594G>C | synonymous_variant | 0.15 |
inhA | 1674801 | c.600T>C | synonymous_variant | 0.15 |
inhA | 1674813 | c.612C>T | synonymous_variant | 0.15 |
inhA | 1674816 | c.615T>C | synonymous_variant | 0.16 |
inhA | 1674819 | c.618G>A | synonymous_variant | 0.16 |
inhA | 1674828 | p.Glu209Asp | missense_variant | 0.18 |
inhA | 1674846 | p.Ile215Met | missense_variant | 0.19 |
inhA | 1674870 | c.669T>C | synonymous_variant | 0.16 |
inhA | 1674903 | c.702T>C | synonymous_variant | 0.16 |
inhA | 1674904 | p.Ala235Pro | missense_variant | 0.16 |
inhA | 1674909 | c.708G>A | synonymous_variant | 0.17 |
inhA | 1674924 | c.723G>C | synonymous_variant | 0.16 |
rpsA | 1833568 | c.27G>C | synonymous_variant | 0.17 |
rpsA | 1833589 | c.48A>T | synonymous_variant | 0.17 |
rpsA | 1833595 | c.54T>C | synonymous_variant | 0.19 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.18 |
rpsA | 1833667 | c.126C>G | synonymous_variant | 0.19 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.18 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.18 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.18 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.18 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.2 |
rpsA | 1833748 | c.207C>G | synonymous_variant | 0.2 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.15 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.15 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 0.17 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.17 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.17 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.21 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.2 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.2 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.24 |
rpsA | 1833940 | c.399C>G | synonymous_variant | 0.2 |
rpsA | 1833971 | c.430C>T | synonymous_variant | 0.18 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.16 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.17 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.19 |
rpsA | 1834096 | c.555G>C | synonymous_variant | 0.17 |
rpsA | 1834099 | c.558C>G | synonymous_variant | 0.17 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.17 |
rpsA | 1834105 | c.564C>G | synonymous_variant | 0.17 |
rpsA | 1834108 | c.567C>G | synonymous_variant | 0.17 |
rpsA | 1834123 | c.582C>G | synonymous_variant | 0.18 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.15 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.15 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.16 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.16 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918036 | p.Arg33Ser | missense_variant | 0.15 |
tlyA | 1918048 | p.Leu37Met | missense_variant | 0.15 |
katG | 2155695 | c.417C>G | synonymous_variant | 0.16 |
katG | 2155704 | c.408C>G | synonymous_variant | 0.2 |
katG | 2155722 | c.390G>C | synonymous_variant | 0.16 |
katG | 2155728 | c.384G>C | synonymous_variant | 0.16 |
katG | 2155740 | p.Gly124Gln | missense_variant | 0.16 |
katG | 2155743 | c.369G>C | synonymous_variant | 0.16 |
katG | 2155746 | c.366C>T | synonymous_variant | 0.16 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2517950 | c.-165C>G | upstream_gene_variant | 0.3 |
kasA | 2517989 | c.-126T>C | upstream_gene_variant | 0.2 |
kasA | 2517993 | c.-122G>T | upstream_gene_variant | 0.2 |
kasA | 2518019 | c.-96A>G | upstream_gene_variant | 0.15 |
kasA | 2518504 | c.390T>C | synonymous_variant | 0.18 |
kasA | 2518506 | p.Ala131Glu | missense_variant | 0.18 |
kasA | 2518519 | c.405G>C | synonymous_variant | 0.17 |
kasA | 2518528 | c.414C>G | synonymous_variant | 0.19 |
kasA | 2518540 | c.426T>C | synonymous_variant | 0.19 |
kasA | 2518588 | c.474T>C | synonymous_variant | 0.18 |
kasA | 2518591 | c.477G>C | synonymous_variant | 0.16 |
kasA | 2518609 | p.Met165Ile | missense_variant | 0.16 |
kasA | 2518624 | c.510C>G | synonymous_variant | 0.16 |
kasA | 2518777 | c.663C>T | synonymous_variant | 0.14 |
kasA | 2518783 | c.669T>C | synonymous_variant | 0.16 |
kasA | 2518789 | c.675G>C | synonymous_variant | 0.15 |
kasA | 2518792 | c.678C>A | synonymous_variant | 0.15 |
kasA | 2518795 | c.681C>G | synonymous_variant | 0.15 |
kasA | 2518825 | c.711T>C | synonymous_variant | 0.16 |
kasA | 2518879 | c.765A>G | synonymous_variant | 0.18 |
kasA | 2518885 | c.771T>C | synonymous_variant | 0.17 |
kasA | 2518898 | c.784T>C | synonymous_variant | 0.17 |
kasA | 2518906 | c.792A>G | synonymous_variant | 0.16 |
kasA | 2518910 | p.Leu266Met | missense_variant | 0.16 |
folC | 2747302 | c.297A>C | synonymous_variant | 0.15 |
folC | 2747314 | c.285A>C | synonymous_variant | 0.16 |
folC | 2747317 | c.282C>G | synonymous_variant | 0.16 |
folC | 2747343 | p.Val86Ile | missense_variant | 0.22 |
folC | 2747355 | p.Val82Ile | missense_variant | 0.2 |
folC | 2747362 | c.237G>C | synonymous_variant | 0.22 |
Rv2752c | 3066280 | c.-89C>T | upstream_gene_variant | 0.97 |
thyX | 3067373 | c.573C>G | synonymous_variant | 0.15 |
thyX | 3067391 | c.555G>C | synonymous_variant | 0.16 |
thyX | 3067439 | c.507A>G | synonymous_variant | 0.23 |
thyX | 3067445 | c.501C>G | synonymous_variant | 0.24 |
thyX | 3067457 | c.489C>G | synonymous_variant | 0.23 |
thyX | 3067465 | p.Ile161Val | missense_variant | 0.22 |
thyX | 3067466 | c.480G>C | synonymous_variant | 0.2 |
thyX | 3067475 | c.471A>G | synonymous_variant | 0.2 |
thyX | 3067490 | c.456C>G | synonymous_variant | 0.21 |
thyX | 3067493 | c.453A>G | synonymous_variant | 0.21 |
thyX | 3067515 | p.Ser144Thr | missense_variant | 0.23 |
thyX | 3067530 | p.Ala139Ser | missense_variant | 0.21 |
thyX | 3067545 | p.Glu134Ala | missense_variant | 0.21 |
thyX | 3067549 | p.Thr133Ala | missense_variant | 0.17 |
thyX | 3067685 | c.261A>C | synonymous_variant | 0.18 |
thyX | 3067691 | p.Ile85Leu | missense_variant | 0.18 |
thyX | 3067694 | c.252G>C | synonymous_variant | 0.18 |
thyX | 3067718 | c.228C>G | synonymous_variant | 0.16 |
thyX | 3067721 | c.225T>C | synonymous_variant | 0.16 |
thyX | 3067736 | c.210C>T | synonymous_variant | 0.15 |
thyX | 3067772 | c.174C>G | synonymous_variant | 0.15 |
thyX | 3067793 | c.153T>C | synonymous_variant | 0.17 |
thyX | 3067799 | c.147G>A | synonymous_variant | 0.15 |
thyX | 3067814 | c.132T>C | synonymous_variant | 0.16 |
thyA | 3074181 | c.291A>G | synonymous_variant | 0.16 |
thyA | 3074187 | c.285T>C | synonymous_variant | 0.16 |
thyA | 3074205 | p.Glu89Asp | missense_variant | 0.19 |
thyA | 3074214 | c.258T>C | synonymous_variant | 0.19 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 0.98 |
fprA | 3475015 | p.Gln337Lys | missense_variant | 0.14 |
fbiB | 3642587 | p.Met351Ile | missense_variant | 0.15 |
fbiB | 3642593 | c.1059G>T | synonymous_variant | 0.15 |
fbiB | 3642614 | c.1080C>T | synonymous_variant | 0.15 |
fbiB | 3642617 | c.1083C>G | synonymous_variant | 0.16 |
fbiB | 3642620 | c.1086T>C | synonymous_variant | 0.16 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.16 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.22 |
rpoA | 3877656 | c.852T>G | synonymous_variant | 0.21 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.19 |
rpoA | 3877679 | p.Ala277Ser | missense_variant | 0.18 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.16 |
rpoA | 3877737 | c.771G>C | synonymous_variant | 0.16 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.16 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.16 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.17 |
rpoA | 3877791 | c.717C>G | synonymous_variant | 0.17 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.18 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.22 |
rpoA | 3877857 | c.651G>A | synonymous_variant | 0.31 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.33 |
rpoA | 3877875 | c.633T>G | synonymous_variant | 0.31 |
rpoA | 3877878 | c.630G>C | synonymous_variant | 0.3 |
rpoA | 3877890 | c.618C>T | synonymous_variant | 0.35 |
rpoA | 3877896 | c.612G>C | synonymous_variant | 0.35 |
rpoA | 3877900 | p.Ser203Asn | missense_variant | 0.35 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.35 |
rpoA | 3877908 | p.Asn200Ser | missense_variant | 0.34 |
rpoA | 3877920 | c.588G>C | synonymous_variant | 0.37 |
rpoA | 3877926 | c.582G>C | synonymous_variant | 0.34 |
rpoA | 3877962 | c.546G>C | synonymous_variant | 0.27 |
rpoA | 3877986 | c.522G>C | synonymous_variant | 0.22 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.19 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.17 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.15 |
rpoA | 3878199 | c.309T>C | synonymous_variant | 0.16 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.16 |
rpoA | 3878226 | c.282C>G | synonymous_variant | 0.15 |
rpoA | 3878232 | c.276G>C | synonymous_variant | 0.18 |
rpoA | 3878247 | c.261G>C | synonymous_variant | 0.23 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.23 |
rpoA | 3878284 | p.Glu75Ala | missense_variant | 0.2 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.19 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.19 |
rpoA | 3878304 | c.204G>C | synonymous_variant | 0.2 |
rpoA | 3878310 | c.198G>C | synonymous_variant | 0.19 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 0.2 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.24 |
rpoA | 3878331 | c.177A>G | synonymous_variant | 0.19 |
rpoA | 3878334 | c.174T>C | synonymous_variant | 0.19 |
rpoA | 3878337 | c.171T>C | synonymous_variant | 0.21 |
rpoA | 3878346 | c.162T>C | synonymous_variant | 0.21 |
rpoA | 3878364 | c.144A>C | synonymous_variant | 0.22 |
rpoA | 3878367 | c.141C>G | synonymous_variant | 0.23 |
rpoA | 3878376 | c.132G>C | synonymous_variant | 0.25 |
rpoA | 3878385 | c.123C>G | synonymous_variant | 0.25 |
rpoA | 3878388 | c.120C>G | synonymous_variant | 0.25 |
rpoA | 3878391 | c.117T>C | synonymous_variant | 0.25 |
rpoA | 3878415 | c.93C>T | synonymous_variant | 0.22 |
rpoA | 3878424 | c.84G>C | synonymous_variant | 0.24 |
rpoA | 3878436 | c.72A>G | synonymous_variant | 0.25 |
rpoA | 3878442 | c.66G>C | synonymous_variant | 0.25 |
rpoA | 3878454 | c.54A>C | synonymous_variant | 0.23 |
rpoA | 3878463 | c.45C>A | synonymous_variant | 0.17 |
rpoA | 3878472 | p.Asp12Glu | missense_variant | 0.16 |
rpoA | 3878478 | c.30C>G | synonymous_variant | 0.16 |
rpoA | 3878484 | c.24C>A | synonymous_variant | 0.16 |
rpoA | 3878496 | c.12A>T | synonymous_variant | 0.13 |
clpC1 | 4038456 | p.Val750Glu | missense_variant | 0.17 |
clpC1 | 4038460 | p.Leu749Met | missense_variant | 0.17 |
clpC1 | 4038486 | p.Gly740Asn | missense_variant | 0.17 |
clpC1 | 4038489 | p.Ala739Gly | missense_variant | 0.17 |
clpC1 | 4038494 | c.2211G>C | synonymous_variant | 0.17 |
clpC1 | 4038497 | p.Ser736Gln | missense_variant | 0.17 |
clpC1 | 4038509 | c.2196C>T | synonymous_variant | 0.19 |
clpC1 | 4038530 | p.Glu725Asp | missense_variant | 0.22 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.2 |
clpC1 | 4038640 | p.Asp689Asn | missense_variant | 0.14 |
clpC1 | 4038653 | c.2052C>T | synonymous_variant | 0.15 |
clpC1 | 4038671 | c.2034T>C | synonymous_variant | 0.19 |
clpC1 | 4038683 | c.2022T>C | synonymous_variant | 0.2 |
clpC1 | 4038695 | c.2010C>G | synonymous_variant | 0.17 |
clpC1 | 4038701 | c.2004G>C | synonymous_variant | 0.18 |
clpC1 | 4038704 | c.2001T>C | synonymous_variant | 0.18 |
clpC1 | 4038707 | c.1998C>G | synonymous_variant | 0.19 |
clpC1 | 4038710 | c.1995G>C | synonymous_variant | 0.18 |
clpC1 | 4038713 | c.1992T>C | synonymous_variant | 0.18 |
clpC1 | 4038749 | c.1956C>A | synonymous_variant | 0.21 |
clpC1 | 4038755 | c.1950G>T | synonymous_variant | 0.21 |
clpC1 | 4038770 | c.1935C>T | synonymous_variant | 0.21 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.21 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.19 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.18 |
clpC1 | 4038845 | c.1860G>C | synonymous_variant | 0.2 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 0.2 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.24 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.23 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.23 |
clpC1 | 4038923 | c.1780_1782delCTAinsTTG | synonymous_variant | 0.2 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.21 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.22 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.21 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.21 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.22 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.19 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.2 |
clpC1 | 4039004 | c.1701C>G | synonymous_variant | 0.2 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.19 |
clpC1 | 4039064 | c.1641C>T | synonymous_variant | 0.18 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.22 |
clpC1 | 4039103 | c.1602T>C | synonymous_variant | 0.21 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.2 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.21 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.22 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.26 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.25 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.22 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.23 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.22 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.21 |
clpC1 | 4039186 | c.1519C>T | synonymous_variant | 0.21 |
clpC1 | 4039190 | c.1515C>G | synonymous_variant | 0.2 |
clpC1 | 4039226 | c.1479T>C | synonymous_variant | 0.16 |
clpC1 | 4039229 | c.1476C>G | synonymous_variant | 0.16 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.18 |
clpC1 | 4039286 | c.1419T>C | synonymous_variant | 0.17 |
clpC1 | 4039319 | c.1386T>C | synonymous_variant | 0.16 |
clpC1 | 4039338 | p.Thr456Gln | missense_variant | 0.14 |
clpC1 | 4039349 | c.1356C>T | synonymous_variant | 0.17 |
clpC1 | 4039352 | c.1353C>G | synonymous_variant | 0.17 |
clpC1 | 4039364 | c.1341C>G | synonymous_variant | 0.17 |
clpC1 | 4039391 | c.1314T>G | synonymous_variant | 0.16 |
clpC1 | 4039661 | c.1044T>G | synonymous_variant | 0.17 |
clpC1 | 4039664 | c.1041G>C | synonymous_variant | 0.15 |
clpC1 | 4039790 | c.915C>G | synonymous_variant | 0.15 |
clpC1 | 4039817 | c.888A>C | synonymous_variant | 0.18 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.17 |
clpC1 | 4039826 | c.879C>G | synonymous_variant | 0.2 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 0.21 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.22 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.2 |
clpC1 | 4039928 | c.775_777delAGCinsTCG | synonymous_variant | 0.19 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.18 |
clpC1 | 4039937 | c.768G>C | synonymous_variant | 0.18 |
clpC1 | 4039946 | c.759A>C | synonymous_variant | 0.2 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.19 |
clpC1 | 4039982 | c.723G>A | synonymous_variant | 0.19 |
clpC1 | 4039988 | c.717C>G | synonymous_variant | 0.18 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 0.19 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.24 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.25 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.24 |
clpC1 | 4040036 | c.669C>G | synonymous_variant | 0.26 |
clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 0.18 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.17 |
clpC1 | 4040105 | c.600C>G | synonymous_variant | 0.18 |
clpC1 | 4040147 | c.558A>G | synonymous_variant | 0.18 |
clpC1 | 4040162 | c.543G>C | synonymous_variant | 0.19 |
clpC1 | 4040165 | c.540G>C | synonymous_variant | 0.19 |
clpC1 | 4040171 | c.534C>G | synonymous_variant | 0.19 |
clpC1 | 4040246 | c.459C>G | synonymous_variant | 0.18 |
clpC1 | 4040249 | c.456A>G | synonymous_variant | 0.18 |
clpC1 | 4040267 | c.438A>G | synonymous_variant | 0.16 |
clpC1 | 4040279 | c.426C>G | synonymous_variant | 0.15 |
clpC1 | 4040291 | c.414G>C | synonymous_variant | 0.17 |
clpC1 | 4040318 | c.387C>G | synonymous_variant | 0.16 |
clpC1 | 4040363 | c.342A>T | synonymous_variant | 0.15 |
clpC1 | 4040369 | c.336C>G | synonymous_variant | 0.15 |
embC | 4240669 | c.807G>C | synonymous_variant | 0.21 |
embC | 4240671 | p.Thr270Ile | missense_variant | 0.21 |
embC | 4240677 | p.Gly272Ala | missense_variant | 0.19 |
embC | 4240685 | p.Thr275Ala | missense_variant | 0.19 |
embC | 4240693 | c.831T>G | synonymous_variant | 0.16 |
embC | 4240699 | c.837C>G | synonymous_variant | 0.18 |
embC | 4240726 | c.864G>C | synonymous_variant | 0.21 |
embC | 4240780 | c.918T>C | synonymous_variant | 0.22 |
embC | 4240783 | c.921G>C | synonymous_variant | 0.23 |
embC | 4240789 | c.927T>C | synonymous_variant | 0.22 |
embC | 4240819 | c.957A>G | synonymous_variant | 0.2 |
embC | 4240828 | c.966G>A | synonymous_variant | 0.18 |
embC | 4240831 | c.969T>G | synonymous_variant | 0.18 |
embC | 4240867 | c.1005T>C | synonymous_variant | 0.15 |
embC | 4241089 | c.1227C>G | synonymous_variant | 0.15 |
embC | 4241095 | c.1233C>T | synonymous_variant | 0.17 |
embC | 4241107 | c.1245G>C | synonymous_variant | 0.21 |
embC | 4241140 | c.1278A>G | synonymous_variant | 0.21 |
embC | 4241146 | c.1284C>G | synonymous_variant | 0.18 |
embC | 4241173 | c.1311C>T | synonymous_variant | 0.15 |
embC | 4241218 | c.1356G>C | synonymous_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245146 | c.1914G>A | synonymous_variant | 0.16 |
embA | 4245149 | c.1917C>G | synonymous_variant | 0.16 |
embA | 4245153 | p.Ile641Val | missense_variant | 0.16 |
embA | 4245182 | c.1950T>C | synonymous_variant | 0.19 |
embA | 4245189 | c.1957C>T | synonymous_variant | 0.18 |
embA | 4245198 | p.Leu656Ile | missense_variant | 0.16 |
embA | 4245207 | c.1975T>C | synonymous_variant | 0.16 |
embA | 4245215 | c.1983A>C | synonymous_variant | 0.16 |
embB | 4247491 | c.978G>C | synonymous_variant | 0.17 |
embB | 4247497 | c.984T>C | synonymous_variant | 0.19 |
embB | 4247512 | c.999T>C | synonymous_variant | 0.19 |
embB | 4247539 | c.1026T>C | synonymous_variant | 0.21 |
embB | 4247554 | c.1041T>C | synonymous_variant | 0.19 |
embB | 4247566 | c.1053C>A | synonymous_variant | 0.2 |
embB | 4247572 | c.1059A>G | synonymous_variant | 0.18 |
embB | 4247603 | c.1090C>T | synonymous_variant | 0.15 |
embB | 4247761 | c.1248T>C | synonymous_variant | 0.16 |
embB | 4247773 | c.1260G>A | synonymous_variant | 0.14 |
embB | 4247776 | c.1263G>T | synonymous_variant | 0.16 |
embB | 4247797 | c.1284C>G | synonymous_variant | 0.18 |
embB | 4247800 | c.1287A>T | synonymous_variant | 0.17 |
embB | 4247803 | c.1290G>C | synonymous_variant | 0.18 |
embB | 4247815 | c.1302C>G | synonymous_variant | 0.18 |
embB | 4247819 | p.Val436Ile | missense_variant | 0.18 |
embB | 4247830 | c.1317A>C | synonymous_variant | 0.19 |
embB | 4247836 | c.1323A>G | synonymous_variant | 0.2 |
embB | 4247839 | c.1326G>C | synonymous_variant | 0.2 |
embB | 4247866 | c.1353G>C | synonymous_variant | 0.22 |
embB | 4247875 | c.1362G>C | synonymous_variant | 0.24 |
embB | 4247876 | c.1363C>T | synonymous_variant | 0.23 |
embB | 4247881 | c.1368G>C | synonymous_variant | 0.24 |
embB | 4247887 | c.1374C>T | synonymous_variant | 0.25 |
embB | 4247899 | p.Met462Ile | missense_variant | 0.22 |
embB | 4247905 | c.1392G>C | synonymous_variant | 0.18 |
embB | 4247909 | c.1396T>C | synonymous_variant | 0.2 |
embB | 4247914 | c.1401G>C | synonymous_variant | 0.21 |
embB | 4247932 | c.1419C>G | synonymous_variant | 0.16 |
embB | 4247956 | c.1443G>C | synonymous_variant | 0.15 |
embB | 4248130 | c.1617G>C | synonymous_variant | 0.16 |
embB | 4248133 | c.1620C>G | synonymous_variant | 0.16 |
embB | 4248139 | c.1626C>G | synonymous_variant | 0.16 |
embB | 4248142 | c.1629T>C | synonymous_variant | 0.16 |
embB | 4248143 | c.1630T>C | synonymous_variant | 0.16 |
embB | 4248157 | c.1644A>G | synonymous_variant | 0.16 |
embB | 4248172 | c.1659G>C | synonymous_variant | 0.16 |
embB | 4248199 | c.1686A>G | synonymous_variant | 0.15 |
embB | 4248200 | p.Ile563Val | missense_variant | 0.15 |
embB | 4248205 | c.1692C>G | synonymous_variant | 0.16 |
embB | 4248206 | p.Ser565Gly | missense_variant | 0.16 |
embB | 4248220 | c.1707A>C | synonymous_variant | 0.19 |
embB | 4248304 | c.1791G>C | synonymous_variant | 0.15 |
embB | 4249469 | p.Leu986Met | missense_variant | 0.19 |
embB | 4249486 | c.2973T>G | synonymous_variant | 0.18 |
embB | 4249498 | c.2985G>C | synonymous_variant | 0.18 |
embB | 4249521 | p.Ala1003Val | missense_variant | 0.16 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |