Run ID: ERR9786627
Sample name:
Date: 02-04-2023 12:37:28
Number of reads: 2764976
Percentage reads mapped: 83.78
Strain: lineage4.1.2.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.97 |
lineage4.1 | Euro-American | T;X;H | None | 0.96 |
lineage4.1.2 | Euro-American | T;H | None | 0.99 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
embB | 4247676 | p.Ala388Gly | missense_variant | 0.16 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6403 | c.-899T>C | upstream_gene_variant | 0.16 |
gyrA | 6931 | c.-371A>G | upstream_gene_variant | 0.16 |
gyrA | 6952 | c.-350C>G | upstream_gene_variant | 0.17 |
gyrA | 7007 | c.-295C>T | upstream_gene_variant | 0.17 |
gyrA | 7010 | c.-292C>T | upstream_gene_variant | 0.17 |
gyrB | 7023 | p.Leu595Gln | missense_variant | 0.14 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7541 | c.240C>G | synonymous_variant | 0.16 |
gyrA | 7547 | c.246C>T | synonymous_variant | 0.17 |
gyrA | 7562 | c.261C>T | synonymous_variant | 0.16 |
gyrA | 7571 | c.270G>C | synonymous_variant | 0.17 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7595 | c.294C>G | synonymous_variant | 0.19 |
gyrA | 7601 | c.300C>G | synonymous_variant | 0.19 |
gyrA | 7607 | c.306C>A | synonymous_variant | 0.18 |
gyrA | 7622 | c.321C>T | synonymous_variant | 0.2 |
gyrA | 7625 | c.324G>C | synonymous_variant | 0.2 |
gyrA | 7631 | c.330G>C | synonymous_variant | 0.19 |
gyrA | 7637 | c.336C>G | synonymous_variant | 0.21 |
gyrA | 7652 | c.351C>T | synonymous_variant | 0.22 |
gyrA | 7658 | c.357A>G | synonymous_variant | 0.22 |
gyrA | 7664 | c.363T>C | synonymous_variant | 0.22 |
gyrA | 7673 | c.372G>A | synonymous_variant | 0.21 |
gyrA | 7683 | c.382_384delAGGinsCGC | synonymous_variant | 0.21 |
gyrA | 7694 | c.393A>G | synonymous_variant | 0.2 |
gyrA | 7697 | c.396C>G | synonymous_variant | 0.2 |
gyrA | 7710 | c.409_411delTTGinsCTC | synonymous_variant | 0.18 |
gyrA | 7715 | c.414G>C | synonymous_variant | 0.17 |
gyrA | 7721 | c.420G>A | synonymous_variant | 0.17 |
gyrA | 7725 | c.424C>T | synonymous_variant | 0.17 |
gyrA | 7728 | c.427_429delAGGinsCGC | synonymous_variant | 0.17 |
gyrA | 7739 | c.438C>T | synonymous_variant | 0.18 |
gyrA | 7763 | c.462T>C | synonymous_variant | 0.19 |
gyrA | 7772 | c.471C>T | synonymous_variant | 0.18 |
gyrA | 8767 | p.Arg489Lys | missense_variant | 0.15 |
gyrA | 8870 | c.1569G>C | synonymous_variant | 0.17 |
gyrA | 8897 | c.1596T>C | synonymous_variant | 0.16 |
gyrA | 8903 | c.1602T>C | synonymous_variant | 0.17 |
gyrA | 9182 | c.1881T>C | synonymous_variant | 0.17 |
gyrA | 9191 | c.1890G>C | synonymous_variant | 0.16 |
gyrA | 9204 | p.Ser635Thr | missense_variant | 0.16 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490984 | p.Leu68Met | missense_variant | 0.14 |
fgd1 | 491007 | c.225G>C | synonymous_variant | 0.18 |
fgd1 | 491043 | c.261T>G | synonymous_variant | 0.17 |
fgd1 | 491202 | c.420G>C | synonymous_variant | 0.16 |
fgd1 | 491217 | c.435T>C | synonymous_variant | 0.16 |
fgd1 | 491232 | c.450T>C | synonymous_variant | 0.16 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 0.94 |
mshA | 575665 | c.318G>A | synonymous_variant | 0.15 |
mshA | 575674 | c.327G>C | synonymous_variant | 0.17 |
mshA | 575679 | p.Asn111Ser | missense_variant | 0.84 |
mshA | 575695 | c.348C>G | synonymous_variant | 0.16 |
mshA | 575701 | c.354G>A | synonymous_variant | 0.16 |
mshA | 575713 | c.366G>A | synonymous_variant | 0.16 |
mshA | 575719 | c.372C>T | synonymous_variant | 0.17 |
mshA | 575734 | c.387T>G | synonymous_variant | 0.18 |
mshA | 575737 | c.390T>C | synonymous_variant | 0.19 |
mshA | 575755 | c.408G>A | synonymous_variant | 0.16 |
mshA | 575756 | c.409C>T | synonymous_variant | 0.16 |
mshA | 575770 | c.423G>A | synonymous_variant | 0.16 |
mshA | 575771 | p.Val142Ser | missense_variant | 0.16 |
ccsA | 620340 | c.450C>G | synonymous_variant | 0.16 |
ccsA | 620346 | c.456C>G | synonymous_variant | 0.17 |
ccsA | 620362 | p.Ala158Thr | missense_variant | 0.16 |
rpoB | 760115 | c.309C>T | synonymous_variant | 0.85 |
rpoB | 760139 | c.333A>G | synonymous_variant | 0.16 |
rpoB | 760142 | c.336C>G | synonymous_variant | 0.16 |
rpoB | 760181 | c.375T>C | synonymous_variant | 0.22 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.23 |
rpoB | 760196 | c.390C>G | synonymous_variant | 0.24 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.24 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.23 |
rpoB | 760283 | c.477G>C | synonymous_variant | 0.25 |
rpoB | 760298 | c.492G>C | synonymous_variant | 0.21 |
rpoB | 760307 | c.501T>C | synonymous_variant | 0.23 |
rpoB | 760310 | c.504G>C | synonymous_variant | 0.23 |
rpoB | 760319 | c.513C>T | synonymous_variant | 0.23 |
rpoB | 760328 | c.522G>C | synonymous_variant | 0.22 |
rpoB | 760331 | c.525G>C | synonymous_variant | 0.21 |
rpoB | 760340 | c.534G>T | synonymous_variant | 0.21 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.22 |
rpoB | 760370 | c.564C>G | synonymous_variant | 0.22 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.21 |
rpoB | 760380 | p.Thr192Leu | missense_variant | 0.21 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.22 |
rpoB | 760412 | c.606C>G | synonymous_variant | 0.22 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.23 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.23 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.18 |
rpoB | 760481 | c.675G>C | synonymous_variant | 0.18 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.17 |
rpoB | 760541 | c.735G>C | synonymous_variant | 0.17 |
rpoB | 760547 | c.741G>C | synonymous_variant | 0.18 |
rpoB | 760563 | p.Arg253Met | missense_variant | 0.17 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.19 |
rpoB | 760634 | c.828T>C | synonymous_variant | 0.17 |
rpoB | 760670 | c.864G>C | synonymous_variant | 0.16 |
rpoB | 760718 | c.912C>T | synonymous_variant | 0.19 |
rpoB | 760724 | c.918T>C | synonymous_variant | 0.17 |
rpoB | 760934 | c.1128C>T | synonymous_variant | 0.15 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.19 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.2 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.19 |
rpoB | 761006 | c.1200C>G | synonymous_variant | 0.22 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.22 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 0.23 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.23 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.23 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.23 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.24 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.25 |
rpoB | 761123 | c.1317G>C | synonymous_variant | 0.24 |
rpoB | 761129 | c.1323G>C | synonymous_variant | 0.23 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 0.23 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.24 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.28 |
rpoB | 761153 | c.1347G>C | synonymous_variant | 0.28 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.25 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.25 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.24 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.25 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.26 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.24 |
rpoB | 761219 | c.1413G>C | synonymous_variant | 0.23 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.19 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.19 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.21 |
rpoB | 761306 | c.1500C>G | synonymous_variant | 0.23 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.24 |
rpoB | 761330 | c.1524G>C | synonymous_variant | 0.24 |
rpoB | 761354 | c.1548C>T | synonymous_variant | 0.26 |
rpoB | 761360 | c.1554T>C | synonymous_variant | 0.24 |
rpoB | 761362 | p.Ser519Thr | missense_variant | 0.24 |
rpoB | 761373 | p.Val523His | missense_variant | 0.2 |
rpoB | 761408 | c.1602G>C | synonymous_variant | 0.22 |
rpoB | 761414 | c.1608A>G | synonymous_variant | 0.22 |
rpoB | 761423 | c.1617T>C | synonymous_variant | 0.22 |
rpoB | 761435 | c.1629T>C | synonymous_variant | 0.21 |
rpoB | 761438 | c.1632G>C | synonymous_variant | 0.21 |
rpoB | 761439 | p.Asp545Lys | missense_variant | 0.21 |
rpoB | 761444 | c.1638T>C | synonymous_variant | 0.22 |
rpoB | 761447 | c.1641C>G | synonymous_variant | 0.21 |
rpoB | 761452 | p.Val549Glu | missense_variant | 0.21 |
rpoB | 761457 | p.Pro551Ser | missense_variant | 0.21 |
rpoB | 761477 | c.1671C>G | synonymous_variant | 0.22 |
rpoB | 761492 | c.1686G>C | synonymous_variant | 0.22 |
rpoB | 761510 | c.1704T>C | synonymous_variant | 0.23 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.2 |
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 | 0.2 |
rpoB | 761588 | c.1782C>T | synonymous_variant | 0.22 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.19 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.18 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.18 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.2 |
rpoB | 761645 | c.1839C>G | synonymous_variant | 0.2 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.2 |
rpoB | 761657 | c.1851C>G | synonymous_variant | 0.19 |
rpoB | 761675 | c.1869G>C | synonymous_variant | 0.2 |
rpoB | 761727 | p.Ser641Gly | missense_variant | 0.21 |
rpoB | 761728 | c.1923dupC | frameshift_variant | 0.22 |
rpoB | 761732 | c.1926C>G | synonymous_variant | 0.22 |
rpoB | 761735 | c.1929C>G | synonymous_variant | 0.21 |
rpoB | 761747 | c.1941G>C | synonymous_variant | 0.22 |
rpoB | 761750 | c.1944G>C | synonymous_variant | 0.22 |
rpoB | 761765 | c.1959T>C | synonymous_variant | 0.23 |
rpoB | 761772 | p.His656Ala | missense_variant | 0.21 |
rpoB | 761778 | p.Asn658Asp | missense_variant | 0.21 |
rpoB | 761791 | p.Arg662His | missense_variant | 0.2 |
rpoB | 761813 | c.2007T>C | synonymous_variant | 0.18 |
rpoB | 761815 | p.Ala670Glu | missense_variant | 0.18 |
rpoB | 761834 | c.2028T>C | synonymous_variant | 0.21 |
rpoB | 761848 | p.Cys681Ser | missense_variant | 0.18 |
rpoB | 761852 | c.2046C>G | synonymous_variant | 0.19 |
rpoB | 761858 | c.2052G>C | synonymous_variant | 0.19 |
rpoB | 761873 | c.2067A>C | synonymous_variant | 0.22 |
rpoB | 761885 | c.2079T>C | synonymous_variant | 0.22 |
rpoB | 761906 | c.2100C>G | synonymous_variant | 0.2 |
rpoB | 761909 | c.2103T>C | synonymous_variant | 0.19 |
rpoB | 761912 | c.2106T>C | synonymous_variant | 0.2 |
rpoB | 761915 | p.Asp703Glu | missense_variant | 0.2 |
rpoB | 761916 | p.Asp704Asn | missense_variant | 0.2 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.2 |
rpoB | 761954 | c.2148C>G | synonymous_variant | 0.22 |
rpoB | 762008 | c.2202C>T | synonymous_variant | 0.19 |
rpoB | 762014 | c.2208C>T | synonymous_variant | 0.18 |
rpoB | 762017 | c.2211A>G | synonymous_variant | 0.18 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.19 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.19 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.19 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.19 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.19 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.2 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.2 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 0.21 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.23 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.22 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.23 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.24 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.22 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.21 |
rpoB | 762206 | c.2400C>G | synonymous_variant | 0.19 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.22 |
rpoB | 762246 | c.2440C>T | synonymous_variant | 0.2 |
rpoB | 762254 | c.2448T>G | synonymous_variant | 0.19 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.18 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.17 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.16 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.18 |
rpoB | 762329 | c.2523G>C | synonymous_variant | 0.17 |
rpoB | 762338 | c.2532T>C | synonymous_variant | 0.18 |
rpoB | 762347 | c.2541T>C | synonymous_variant | 0.18 |
rpoB | 762362 | p.Glu852Asp | missense_variant | 0.18 |
rpoB | 762369 | c.2563T>C | synonymous_variant | 0.19 |
rpoC | 762398 | c.-972T>C | upstream_gene_variant | 0.2 |
rpoC | 762401 | c.-969G>C | upstream_gene_variant | 0.2 |
rpoC | 762404 | c.-966T>C | upstream_gene_variant | 0.21 |
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 | 0.23 |
rpoC | 762434 | c.-936T>C | upstream_gene_variant | 0.22 |
rpoC | 762449 | c.-921C>A | upstream_gene_variant | 0.22 |
rpoC | 762467 | c.-903C>T | upstream_gene_variant | 0.21 |
rpoB | 762490 | p.Val895Asp | missense_variant | 0.16 |
rpoC | 762509 | c.-861T>G | upstream_gene_variant | 0.17 |
rpoB | 762510 | p.Ala902Pro | missense_variant | 0.17 |
rpoC | 762521 | c.-849C>T | upstream_gene_variant | 0.18 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.25 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.25 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.24 |
rpoC | 763013 | c.-357C>G | upstream_gene_variant | 0.24 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.26 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 0.26 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.25 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.25 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.24 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.21 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.17 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.17 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.17 |
rpoC | 763190 | c.-180C>T | upstream_gene_variant | 0.16 |
rpoC | 763402 | c.33C>G | synonymous_variant | 0.19 |
rpoC | 763411 | c.42T>G | synonymous_variant | 0.21 |
rpoC | 763414 | c.45T>C | synonymous_variant | 0.21 |
rpoC | 763441 | c.72C>T | synonymous_variant | 0.25 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.25 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.29 |
rpoC | 763486 | c.117T>G | synonymous_variant | 0.29 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.3 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.31 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.29 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.29 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.28 |
rpoC | 763603 | c.234C>T | synonymous_variant | 0.29 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.28 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.27 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.27 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.25 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.25 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.25 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.23 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.23 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.25 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.26 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.26 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.26 |
rpoC | 763774 | c.405G>C | synonymous_variant | 0.26 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.24 |
rpoC | 763816 | c.447C>G | synonymous_variant | 0.23 |
rpoC | 763835 | p.Ala156Met | missense_variant | 0.19 |
rpoC | 763853 | p.Val162Ile | missense_variant | 0.19 |
rpoC | 763858 | c.489A>G | synonymous_variant | 0.19 |
rpoC | 763872 | p.Gly168Ala | missense_variant | 0.19 |
rpoC | 763876 | p.Glu169Asp | missense_variant | 0.19 |
rpoC | 763879 | c.510A>G | synonymous_variant | 0.19 |
rpoC | 763888 | c.519G>C | synonymous_variant | 0.18 |
rpoC | 763891 | c.522G>C | synonymous_variant | 0.18 |
rpoC | 763894 | c.525A>G | synonymous_variant | 0.18 |
rpoC | 763900 | c.531G>C | synonymous_variant | 0.19 |
rpoC | 763936 | c.567C>G | synonymous_variant | 0.2 |
rpoC | 763939 | c.570G>A | synonymous_variant | 0.2 |
rpoC | 763942 | c.573C>G | synonymous_variant | 0.2 |
rpoC | 763945 | c.576T>C | synonymous_variant | 0.2 |
rpoC | 763948 | c.579G>A | synonymous_variant | 0.2 |
rpoC | 763949 | c.580C>A | synonymous_variant | 0.2 |
rpoC | 763954 | c.585C>G | synonymous_variant | 0.21 |
rpoC | 763963 | c.594C>T | synonymous_variant | 0.22 |
rpoC | 763987 | c.618C>T | synonymous_variant | 0.22 |
rpoC | 763991 | p.Ile208Leu | missense_variant | 0.19 |
rpoC | 763996 | c.627T>C | synonymous_variant | 0.2 |
rpoC | 764002 | c.633C>G | synonymous_variant | 0.22 |
rpoC | 764005 | c.636G>C | synonymous_variant | 0.22 |
rpoC | 764024 | c.655_657delTTGinsCTC | synonymous_variant | 0.2 |
rpoC | 764032 | p.Asp221Glu | missense_variant | 0.2 |
rpoC | 764040 | p.Ser224Thr | missense_variant | 0.2 |
rpoC | 764044 | c.675T>C | synonymous_variant | 0.2 |
rpoC | 764059 | c.690G>T | synonymous_variant | 0.21 |
rpoC | 764083 | c.714A>G | synonymous_variant | 0.22 |
rpoC | 764098 | c.729A>G | synonymous_variant | 0.2 |
rpoC | 764101 | c.732C>G | synonymous_variant | 0.2 |
rpoC | 764102 | p.Val245Ile | missense_variant | 0.19 |
rpoC | 764107 | c.738C>T | synonymous_variant | 0.18 |
rpoC | 764112 | p.Tyr248Phe | missense_variant | 0.18 |
rpoC | 764116 | c.747C>T | synonymous_variant | 0.19 |
rpoC | 764131 | c.762T>C | synonymous_variant | 0.2 |
rpoC | 764140 | c.771C>T | synonymous_variant | 0.2 |
rpoC | 764195 | p.Ser276Thr | missense_variant | 0.16 |
rpoC | 764203 | c.834G>C | synonymous_variant | 0.16 |
rpoC | 764215 | c.846A>G | synonymous_variant | 0.19 |
rpoC | 764236 | c.867G>A | synonymous_variant | 0.21 |
rpoC | 764248 | c.879C>G | synonymous_variant | 0.21 |
rpoC | 764257 | c.888G>C | synonymous_variant | 0.18 |
rpoC | 764338 | c.969G>A | synonymous_variant | 0.19 |
rpoC | 764353 | c.984G>C | synonymous_variant | 0.19 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.18 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.17 |
rpoC | 764381 | p.Ser338Thr | missense_variant | 0.16 |
rpoC | 764389 | p.Leu340Phe | missense_variant | 0.17 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.21 |
rpoC | 764419 | c.1050C>G | synonymous_variant | 0.24 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.25 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.24 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.23 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.23 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.23 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.24 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.24 |
rpoC | 764489 | c.1120C>T | synonymous_variant | 0.29 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.3 |
rpoC | 764510 | c.1141C>T | synonymous_variant | 0.3 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.3 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.31 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.31 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.3 |
rpoC | 764554 | c.1185C>T | synonymous_variant | 0.3 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.29 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.3 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.32 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.31 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.31 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.31 |
rpoC | 764650 | c.1281G>C | synonymous_variant | 0.28 |
rpoC | 764651 | c.1282_1284delTCGinsAGC | synonymous_variant | 0.28 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.29 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.31 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.28 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.28 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.31 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.26 |
rpoC | 764872 | c.1503A>G | synonymous_variant | 0.25 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.24 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.25 |
rpoC | 764932 | c.1563C>A | synonymous_variant | 0.2 |
rpoC | 764935 | c.1566T>C | synonymous_variant | 0.2 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.2 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.2 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.21 |
rpoC | 765019 | c.1650A>G | synonymous_variant | 0.19 |
rpoC | 765034 | c.1665T>C | synonymous_variant | 0.18 |
rpoC | 765040 | c.1671T>C | synonymous_variant | 0.17 |
rpoC | 765041 | c.1672T>C | synonymous_variant | 0.17 |
rpoC | 765047 | c.1678T>C | synonymous_variant | 0.19 |
rpoC | 765053 | c.1684_1685delTCinsAG | synonymous_variant | 0.19 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 0.96 |
rpoC | 765383 | p.Met672Leu | missense_variant | 0.22 |
rpoC | 765404 | p.Leu679Val | missense_variant | 0.24 |
rpoC | 765409 | c.2040T>C | synonymous_variant | 0.23 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.22 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.29 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.32 |
rpoC | 765529 | c.2160C>T | synonymous_variant | 0.34 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.34 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.3 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.31 |
rpoC | 765559 | c.2190G>C | synonymous_variant | 0.29 |
rpoC | 765580 | c.2211G>C | synonymous_variant | 0.3 |
rpoC | 765613 | p.His748Gln | missense_variant | 0.3 |
rpoC | 765625 | c.2256C>G | synonymous_variant | 0.27 |
rpoC | 765631 | p.Asp754Glu | missense_variant | 0.27 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.31 |
rpoC | 765734 | c.2365T>C | synonymous_variant | 0.29 |
rpoC | 765739 | c.2370G>T | synonymous_variant | 0.28 |
rpoC | 765751 | c.2382C>G | synonymous_variant | 0.26 |
rpoC | 765753 | p.Asp795Ala | missense_variant | 0.26 |
rpoC | 765772 | c.2403C>G | synonymous_variant | 0.3 |
rpoC | 765784 | c.2415C>G | synonymous_variant | 0.3 |
rpoC | 765787 | c.2418C>T | synonymous_variant | 0.3 |
rpoC | 765793 | c.2424C>G | synonymous_variant | 0.3 |
rpoC | 765796 | c.2427C>T | synonymous_variant | 0.3 |
rpoC | 765811 | c.2442T>C | synonymous_variant | 0.31 |
rpoC | 765814 | c.2445A>G | synonymous_variant | 0.33 |
rpoC | 765826 | c.2457T>C | synonymous_variant | 0.32 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 0.31 |
rpoC | 765850 | c.2481G>C | synonymous_variant | 0.34 |
rpoC | 765883 | c.2514C>G | synonymous_variant | 0.3 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.3 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.31 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.33 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.32 |
rpoC | 765982 | c.2613C>G | synonymous_variant | 0.3 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.29 |
rpoC | 766010 | c.2641_2642delTCinsAG | synonymous_variant | 0.26 |
rpoC | 766021 | c.2652G>C | synonymous_variant | 0.27 |
rpoC | 766027 | c.2658G>C | synonymous_variant | 0.28 |
rpoC | 766030 | c.2661C>G | synonymous_variant | 0.28 |
rpoC | 766043 | p.Gln892Glu | missense_variant | 0.27 |
rpoC | 766054 | c.2685C>G | synonymous_variant | 0.28 |
rpoC | 766082 | p.Ala905Gln | missense_variant | 0.26 |
rpoC | 766096 | c.2727G>C | synonymous_variant | 0.27 |
rpoC | 766129 | c.2760C>G | synonymous_variant | 0.22 |
rpoC | 766135 | c.2766G>A | synonymous_variant | 0.21 |
rpoC | 766141 | c.2772C>T | synonymous_variant | 0.2 |
rpoC | 766142 | c.2773C>T | synonymous_variant | 0.2 |
rpoC | 766357 | c.2988C>T | synonymous_variant | 0.17 |
rpoC | 766363 | c.2994G>C | synonymous_variant | 0.18 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.21 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.22 |
rpoC | 766408 | c.3039C>G | synonymous_variant | 0.22 |
rpoC | 766411 | c.3042C>G | synonymous_variant | 0.23 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.28 |
rpoC | 766447 | c.3078T>C | synonymous_variant | 0.28 |
rpoC | 766462 | c.3093G>C | synonymous_variant | 0.27 |
rpoC | 766483 | c.3114G>C | synonymous_variant | 0.26 |
rpoC | 766484 | p.Val1039Ile | missense_variant | 0.26 |
rpoC | 766492 | c.3123T>C | synonymous_variant | 0.28 |
rpoC | 766522 | c.3153C>G | synonymous_variant | 0.26 |
rpoC | 766528 | c.3159T>C | synonymous_variant | 0.25 |
rpoC | 766531 | c.3162G>C | synonymous_variant | 0.27 |
rpoC | 766540 | p.Asp1057Glu | missense_variant | 0.28 |
rpoC | 766549 | c.3180G>C | synonymous_variant | 0.25 |
rpoC | 766573 | c.3204T>C | synonymous_variant | 0.27 |
rpoC | 766582 | c.3213C>G | synonymous_variant | 0.26 |
rpoC | 766583 | p.Gly1072Ser | missense_variant | 0.26 |
rpoC | 766591 | c.3222A>G | synonymous_variant | 0.26 |
rpoC | 766594 | c.3225G>C | synonymous_variant | 0.26 |
rpoC | 766597 | c.3228C>G | synonymous_variant | 0.27 |
rpoC | 766607 | p.Ile1080Leu | missense_variant | 0.3 |
rpoC | 766625 | c.3256C>T | synonymous_variant | 0.26 |
rpoC | 766630 | c.3261G>C | synonymous_variant | 0.25 |
rpoC | 766657 | c.3288A>G | synonymous_variant | 0.23 |
rpoC | 766672 | c.3303T>C | synonymous_variant | 0.2 |
rpoC | 766673 | p.Gly1102Asn | missense_variant | 0.2 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.23 |
rpoC | 766738 | c.3369G>C | synonymous_variant | 0.22 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.21 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.21 |
rpoC | 766801 | c.3432C>G | synonymous_variant | 0.23 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.25 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 0.25 |
rpoC | 766864 | c.3495G>C | synonymous_variant | 0.25 |
rpoC | 766876 | c.3507C>T | synonymous_variant | 0.27 |
rpoC | 766882 | c.3513C>T | synonymous_variant | 0.27 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.29 |
rpoC | 766933 | c.3564A>G | synonymous_variant | 0.26 |
rpoC | 766945 | c.3576A>G | synonymous_variant | 0.3 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.31 |
rpoC | 766972 | c.3603G>C | synonymous_variant | 0.3 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.28 |
rpoC | 767009 | c.3640_3642delTCGinsAGC | synonymous_variant | 0.28 |
rpoC | 767014 | c.3645G>C | synonymous_variant | 0.28 |
rpoC | 767033 | c.3664_3666delTCGinsAGC | synonymous_variant | 0.3 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.31 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.31 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.26 |
rpoC | 767111 | c.3742C>T | synonymous_variant | 0.25 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.25 |
rpoC | 767134 | c.3765C>A | synonymous_variant | 0.25 |
rpoC | 767158 | c.3789T>G | synonymous_variant | 0.21 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.16 |
rpoC | 767206 | c.3837C>G | synonymous_variant | 0.18 |
rpoC | 767209 | c.3840T>C | synonymous_variant | 0.17 |
rpoC | 767212 | c.3843G>C | synonymous_variant | 0.17 |
rpoC | 767221 | c.3852C>G | synonymous_variant | 0.18 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781700 | c.141G>C | synonymous_variant | 0.18 |
rpsL | 781703 | c.144G>T | synonymous_variant | 0.18 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.19 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.19 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.19 |
rpsL | 781742 | c.183C>T | synonymous_variant | 0.2 |
rpsL | 781748 | c.189C>G | synonymous_variant | 0.2 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.2 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.2 |
rpsL | 781772 | c.213C>A | synonymous_variant | 0.2 |
rpsL | 781808 | c.249C>T | synonymous_variant | 0.23 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.22 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.22 |
rpsL | 781838 | c.279G>C | synonymous_variant | 0.21 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.22 |
rpsL | 781865 | c.306G>C | synonymous_variant | 0.2 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.19 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.19 |
rpsL | 781877 | c.318T>C | synonymous_variant | 0.2 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.2 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.2 |
rpsL | 781916 | c.357T>C | synonymous_variant | 0.21 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.24 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.16 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.15 |
rplC | 800627 | c.-182C>T | upstream_gene_variant | 0.17 |
rplC | 800648 | c.-161A>T | upstream_gene_variant | 0.21 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.22 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.21 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.23 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.23 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.23 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.23 |
rplC | 800747 | c.-62C>G | upstream_gene_variant | 0.24 |
rplC | 800771 | c.-38C>T | upstream_gene_variant | 0.23 |
rplC | 800794 | c.-15A>G | upstream_gene_variant | 0.22 |
rplC | 800796 | c.-13A>G | upstream_gene_variant | 0.22 |
rplC | 800798 | c.-10_-9delGG | upstream_gene_variant | 0.22 |
rplC | 800814 | c.6A>G | synonymous_variant | 0.26 |
rplC | 800817 | c.9A>T | synonymous_variant | 0.25 |
rplC | 800844 | c.36T>C | synonymous_variant | 0.23 |
rplC | 800865 | c.57A>G | synonymous_variant | 0.21 |
rplC | 800867 | p.Ser20Asn | missense_variant | 0.2 |
rplC | 800874 | c.66A>G | synonymous_variant | 0.19 |
rplC | 800875 | p.Val23Ile | missense_variant | 0.18 |
rplC | 800880 | c.72A>G | synonymous_variant | 0.18 |
rplC | 800889 | c.81C>G | synonymous_variant | 0.19 |
rplC | 800892 | c.84G>C | synonymous_variant | 0.19 |
rplC | 801367 | p.Ala187Thr | missense_variant | 0.14 |
rplC | 801402 | c.594T>C | synonymous_variant | 0.17 |
rplC | 801405 | c.597T>C | synonymous_variant | 0.17 |
rplC | 801427 | p.Met207Val | missense_variant | 0.16 |
rplC | 801438 | c.630T>C | synonymous_variant | 0.17 |
rplC | 801442 | p.Ile212Val | missense_variant | 0.18 |
fbiC | 1303884 | c.954T>G | synonymous_variant | 0.17 |
fbiC | 1303905 | c.975G>C | synonymous_variant | 0.19 |
fbiC | 1303920 | c.990C>T | synonymous_variant | 0.16 |
fbiC | 1303932 | c.1002G>T | synonymous_variant | 0.16 |
fbiC | 1303961 | p.Arg344Leu | missense_variant | 0.15 |
fbiC | 1303971 | c.1041T>C | synonymous_variant | 0.16 |
fbiC | 1303980 | c.1050G>A | synonymous_variant | 0.17 |
fbiC | 1304008 | c.1078T>C | synonymous_variant | 0.17 |
fbiC | 1304727 | c.1797A>G | synonymous_variant | 0.16 |
fbiC | 1304742 | c.1812T>C | synonymous_variant | 0.19 |
fbiC | 1304757 | c.1827A>G | synonymous_variant | 0.2 |
fbiC | 1304778 | c.1848T>C | synonymous_variant | 0.22 |
fbiC | 1304784 | c.1854T>C | synonymous_variant | 0.22 |
fbiC | 1304787 | c.1857T>G | synonymous_variant | 0.22 |
fbiC | 1304808 | c.1878C>G | synonymous_variant | 0.2 |
fbiC | 1304811 | c.1881C>G | synonymous_variant | 0.2 |
fbiC | 1304817 | c.1887T>C | synonymous_variant | 0.21 |
fbiC | 1304829 | c.1899T>C | synonymous_variant | 0.21 |
fbiC | 1304832 | c.1902C>T | synonymous_variant | 0.2 |
fbiC | 1304856 | c.1926C>G | synonymous_variant | 0.22 |
fbiC | 1304862 | c.1932G>A | synonymous_variant | 0.2 |
fbiC | 1304869 | c.1939C>T | synonymous_variant | 0.21 |
fbiC | 1304875 | p.Ile649Val | missense_variant | 0.2 |
fbiC | 1304883 | p.Glu651Asp | missense_variant | 0.21 |
fbiC | 1304891 | p.Ile654Thr | missense_variant | 0.21 |
fbiC | 1304893 | p.Gly655Ser | missense_variant | 0.21 |
fbiC | 1304907 | c.1977C>G | synonymous_variant | 0.22 |
fbiC | 1304910 | c.1980G>C | synonymous_variant | 0.22 |
fbiC | 1304916 | c.1986T>C | synonymous_variant | 0.23 |
fbiC | 1304928 | c.1998T>C | synonymous_variant | 0.22 |
fbiC | 1304937 | c.2007G>C | synonymous_variant | 0.21 |
fbiC | 1304958 | c.2028T>G | synonymous_variant | 0.2 |
fbiC | 1304983 | c.2053C>T | synonymous_variant | 0.16 |
fbiC | 1304995 | p.Leu689Met | missense_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473832 | n.175C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473945 | n.288T>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473946 | n.289A>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473986 | n.329T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473987 | n.330G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474009 | n.352A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474012 | n.355C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474093 | n.436G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474099 | n.442G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474376 | n.719T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474823 | n.1166C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474904 | n.1247G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474956 | n.1299C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474960 | n.1303C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474963 | n.1306G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474964 | n.1307T>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474965 | n.1308G>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474970 | n.1313G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475006 | n.1349A>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475088 | n.1431A>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475199 | n.1542G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475206 | n.1549C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475209 | n.1552G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475249 | n.1592T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475252 | n.1595C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475266 | n.1609T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475267 | n.1610G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475275 | n.1618C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475276 | n.1619T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475291 | n.1634A>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475313 | n.1656G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475369 | n.1712G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475402 | n.1745C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475436 | n.1779C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.15 |
fabG1 | 1673710 | p.Leu91Ile | missense_variant | 0.15 |
inhA | 1673716 | c.-486G>A | upstream_gene_variant | 0.16 |
fabG1 | 1673733 | p.Met98Ile | missense_variant | 0.18 |
inhA | 1673748 | c.-454A>G | upstream_gene_variant | 0.18 |
fabG1 | 1673749 | p.Lys104Gln | missense_variant | 0.17 |
fabG1 | 1673758 | p.Lys107Glu | missense_variant | 0.17 |
inhA | 1674368 | p.Ala56Glu | missense_variant | 0.16 |
inhA | 1674382 | p.Leu61Ile | missense_variant | 0.15 |
inhA | 1674419 | p.Ser73Asn | missense_variant | 0.15 |
inhA | 1674428 | p.Gly76Asp | missense_variant | 0.16 |
inhA | 1674440 | p.Glu80Ala | missense_variant | 0.16 |
inhA | 1674443 | p.Ala81Glu | missense_variant | 0.16 |
inhA | 1674452 | p.Ala84Glu | missense_variant | 0.16 |
inhA | 1674471 | c.270G>C | synonymous_variant | 0.18 |
inhA | 1674480 | c.279T>C | synonymous_variant | 0.18 |
inhA | 1674486 | c.285T>C | synonymous_variant | 0.18 |
inhA | 1674504 | c.303C>G | synonymous_variant | 0.21 |
inhA | 1674507 | c.306G>C | synonymous_variant | 0.21 |
inhA | 1674537 | c.336C>G | synonymous_variant | 0.21 |
inhA | 1674542 | p.Ala114Glu | missense_variant | 0.2 |
inhA | 1674546 | c.345T>C | synonymous_variant | 0.2 |
inhA | 1674549 | c.348G>C | synonymous_variant | 0.19 |
inhA | 1674555 | c.354G>A | synonymous_variant | 0.18 |
inhA | 1674561 | c.360C>T | synonymous_variant | 0.2 |
inhA | 1674846 | p.Ile215Met | missense_variant | 0.16 |
inhA | 1674864 | c.663C>T | synonymous_variant | 0.17 |
inhA | 1674870 | c.669T>C | synonymous_variant | 0.17 |
inhA | 1674879 | c.678T>C | synonymous_variant | 0.18 |
inhA | 1674888 | c.687C>G | synonymous_variant | 0.17 |
inhA | 1674903 | c.702T>C | synonymous_variant | 0.16 |
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 | 0.23 |
rpsA | 1833667 | c.126C>G | synonymous_variant | 0.22 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.26 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.26 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.27 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.28 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.28 |
rpsA | 1833748 | c.207C>G | synonymous_variant | 0.28 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.31 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.3 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.31 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 0.31 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.29 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.29 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.32 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.32 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.29 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.25 |
rpsA | 1833940 | c.399C>G | synonymous_variant | 0.24 |
rpsA | 1833971 | c.430C>T | synonymous_variant | 0.22 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.22 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.22 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.23 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.24 |
rpsA | 1834096 | c.555G>C | synonymous_variant | 0.18 |
rpsA | 1834099 | c.558C>G | synonymous_variant | 0.17 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.18 |
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 | 0.19 |
rpsA | 1834153 | c.612T>C | synonymous_variant | 0.16 |
rpsA | 1834154 | p.Asn205His | missense_variant | 0.16 |
rpsA | 1834169 | p.Thr210Ala | missense_variant | 0.17 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.17 |
rpsA | 1834189 | c.648G>C | synonymous_variant | 0.21 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 0.22 |
rpsA | 1834210 | c.669C>T | synonymous_variant | 0.2 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.18 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 0.19 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.18 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.22 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.19 |
rpsA | 1834262 | c.721_723delTCGinsAGC | synonymous_variant | 0.18 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.27 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.27 |
rpsA | 1834333 | c.792C>T | synonymous_variant | 0.3 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.3 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.27 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.29 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.31 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.3 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.3 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.31 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.29 |
rpsA | 1834465 | c.924T>C | synonymous_variant | 0.32 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.31 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.29 |
rpsA | 1834513 | c.972C>G | synonymous_variant | 0.29 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.27 |
rpsA | 1834540 | c.999G>C | synonymous_variant | 0.28 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.29 |
rpsA | 1834555 | c.1014T>G | synonymous_variant | 0.3 |
rpsA | 1834606 | c.1065C>G | synonymous_variant | 0.27 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.27 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.24 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.24 |
rpsA | 1834654 | p.Glu371Asp | missense_variant | 0.21 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101838 | p.Ala402Val | missense_variant | 0.16 |
ndh | 2101873 | p.Phe390Leu | missense_variant | 0.16 |
ndh | 2101885 | c.1158G>A | synonymous_variant | 0.16 |
ndh | 2101920 | c.1123A>C | synonymous_variant | 0.17 |
ndh | 2101924 | c.1119T>G | synonymous_variant | 0.17 |
ndh | 2101939 | c.1104A>G | synonymous_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2517950 | c.-165C>G | upstream_gene_variant | 0.25 |
kasA | 2517989 | c.-126T>C | upstream_gene_variant | 0.21 |
kasA | 2517993 | c.-122G>T | upstream_gene_variant | 0.22 |
kasA | 2518019 | c.-96A>G | upstream_gene_variant | 0.17 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2518624 | c.510C>G | synonymous_variant | 0.18 |
kasA | 2518639 | c.525G>C | synonymous_variant | 0.2 |
kasA | 2518657 | c.543G>C | synonymous_variant | 0.22 |
kasA | 2518672 | c.558G>C | synonymous_variant | 0.27 |
kasA | 2518678 | c.564C>T | synonymous_variant | 0.24 |
kasA | 2518684 | c.570C>G | synonymous_variant | 0.25 |
kasA | 2518693 | c.579C>G | synonymous_variant | 0.24 |
kasA | 2518696 | c.582C>G | synonymous_variant | 0.24 |
kasA | 2518702 | c.588C>T | synonymous_variant | 0.26 |
kasA | 2518705 | c.591T>C | synonymous_variant | 0.26 |
kasA | 2518711 | c.597A>G | synonymous_variant | 0.25 |
kasA | 2518714 | c.600A>C | synonymous_variant | 0.24 |
kasA | 2518732 | c.618C>G | synonymous_variant | 0.23 |
kasA | 2518744 | c.630C>T | synonymous_variant | 0.22 |
kasA | 2518747 | c.633C>G | synonymous_variant | 0.21 |
kasA | 2518768 | c.654C>T | synonymous_variant | 0.23 |
kasA | 2518777 | c.663C>T | synonymous_variant | 0.23 |
kasA | 2518783 | c.669T>C | synonymous_variant | 0.22 |
kasA | 2518789 | c.675G>C | synonymous_variant | 0.21 |
kasA | 2518792 | c.678C>A | synonymous_variant | 0.21 |
kasA | 2518795 | c.681C>G | synonymous_variant | 0.21 |
kasA | 2518819 | c.705C>T | synonymous_variant | 0.22 |
kasA | 2518825 | c.711T>C | synonymous_variant | 0.22 |
kasA | 2518864 | c.750G>C | synonymous_variant | 0.19 |
kasA | 2518910 | p.Leu266Met | missense_variant | 0.15 |
kasA | 2518999 | c.885G>A | synonymous_variant | 0.14 |
Rv2752c | 3065040 | c.1152C>G | synonymous_variant | 0.18 |
Rv2752c | 3065196 | c.996T>C | synonymous_variant | 0.15 |
Rv2752c | 3065202 | c.990T>G | synonymous_variant | 0.16 |
Rv2752c | 3065205 | c.987T>C | synonymous_variant | 0.16 |
Rv2752c | 3065223 | c.969T>C | synonymous_variant | 0.16 |
Rv2752c | 3065232 | c.960T>C | synonymous_variant | 0.15 |
Rv2752c | 3065241 | c.951A>G | synonymous_variant | 0.15 |
thyX | 3067325 | c.621A>G | synonymous_variant | 0.17 |
thyX | 3067349 | c.597G>C | synonymous_variant | 0.21 |
thyX | 3067355 | c.591A>C | synonymous_variant | 0.21 |
thyX | 3067367 | c.579G>C | synonymous_variant | 0.26 |
thyX | 3067373 | c.573C>G | synonymous_variant | 0.26 |
thyX | 3067391 | c.555G>C | synonymous_variant | 0.25 |
thyX | 3067394 | c.552G>C | synonymous_variant | 0.26 |
thyX | 3067439 | c.507A>G | synonymous_variant | 0.26 |
thyX | 3067445 | c.501C>G | synonymous_variant | 0.26 |
thyX | 3067457 | c.489C>G | synonymous_variant | 0.27 |
thyX | 3067465 | p.Ile161Val | missense_variant | 0.27 |
thyX | 3067475 | c.471A>G | synonymous_variant | 0.23 |
thyX | 3067490 | c.456C>G | synonymous_variant | 0.23 |
thyX | 3067493 | c.453A>G | synonymous_variant | 0.23 |
thyX | 3067515 | p.Ser144Thr | missense_variant | 0.25 |
thyX | 3067530 | p.Ala139Ser | missense_variant | 0.26 |
thyX | 3067545 | p.Glu134Ala | missense_variant | 0.25 |
thyX | 3067549 | p.Thr133Ala | missense_variant | 0.24 |
thyX | 3067556 | p.His130Gln | missense_variant | 0.26 |
thyX | 3067559 | c.387C>G | synonymous_variant | 0.26 |
thyX | 3067565 | p.Asp127Glu | missense_variant | 0.26 |
thyX | 3067570 | p.Ala126Pro | missense_variant | 0.26 |
thyX | 3067577 | c.369G>A | synonymous_variant | 0.29 |
thyX | 3067601 | p.Arg115His | missense_variant | 0.26 |
thyX | 3067611 | p.Lys112Thr | missense_variant | 0.25 |
thyX | 3067619 | c.327A>C | synonymous_variant | 0.23 |
thyX | 3067631 | c.315C>G | synonymous_variant | 0.24 |
thyX | 3067634 | c.312C>G | synonymous_variant | 0.24 |
thyX | 3067652 | c.294T>C | synonymous_variant | 0.24 |
thyX | 3067661 | c.285C>G | synonymous_variant | 0.22 |
thyX | 3067685 | c.261A>C | synonymous_variant | 0.19 |
thyX | 3067691 | p.Ile85Leu | missense_variant | 0.18 |
thyX | 3067694 | c.252G>C | synonymous_variant | 0.18 |
thyA | 3073872 | p.Ile200Met | missense_variant | 0.16 |
thyA | 3073892 | c.580T>C | synonymous_variant | 0.17 |
thyA | 3073898 | p.Ala192Ser | missense_variant | 0.17 |
thyA | 3073917 | c.555C>G | synonymous_variant | 0.16 |
thyA | 3073920 | c.552C>G | synonymous_variant | 0.17 |
thyA | 3073977 | c.495A>G | synonymous_variant | 0.19 |
thyA | 3073989 | c.483T>C | synonymous_variant | 0.18 |
thyA | 3074004 | c.468T>C | synonymous_variant | 0.2 |
thyA | 3074010 | c.462C>G | synonymous_variant | 0.21 |
thyA | 3074028 | c.444G>C | synonymous_variant | 0.2 |
thyA | 3074031 | c.441T>C | synonymous_variant | 0.19 |
thyA | 3074034 | c.438T>C | synonymous_variant | 0.19 |
thyA | 3074037 | c.435C>G | synonymous_variant | 0.19 |
thyA | 3074053 | p.Arg140Gln | missense_variant | 0.19 |
thyA | 3074055 | p.Glu139Pro | missense_variant | 0.18 |
thyA | 3074061 | c.411A>G | synonymous_variant | 0.18 |
thyA | 3074079 | c.393G>C | synonymous_variant | 0.17 |
thyA | 3074097 | c.375C>A | synonymous_variant | 0.16 |
thyA | 3074102 | p.Asp124Asn | missense_variant | 0.16 |
thyA | 3074106 | c.366T>C | synonymous_variant | 0.16 |
thyA | 3074127 | c.345G>C | synonymous_variant | 0.16 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.18 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.21 |
rpoA | 3877617 | c.891G>C | synonymous_variant | 0.21 |
rpoA | 3877656 | c.852T>G | synonymous_variant | 0.25 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.25 |
rpoA | 3877679 | p.Ala277Ser | missense_variant | 0.28 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.28 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.29 |
rpoA | 3877704 | c.804G>C | synonymous_variant | 0.28 |
rpoA | 3877737 | c.771G>C | synonymous_variant | 0.25 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.26 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.23 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.23 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.25 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.26 |
rpoA | 3877791 | c.717C>G | synonymous_variant | 0.26 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.29 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.29 |
rpoA | 3877848 | c.660C>T | synonymous_variant | 0.29 |
rpoA | 3877857 | c.651G>A | synonymous_variant | 0.28 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.28 |
rpoA | 3877875 | c.633T>G | synonymous_variant | 0.28 |
rpoA | 3877878 | c.630G>C | synonymous_variant | 0.27 |
rpoA | 3877890 | c.618C>T | synonymous_variant | 0.3 |
rpoA | 3877896 | c.612G>C | synonymous_variant | 0.28 |
rpoA | 3877900 | p.Ser203Asn | missense_variant | 0.3 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.29 |
rpoA | 3877908 | p.Asn200Ser | missense_variant | 0.29 |
rpoA | 3877920 | c.588G>C | synonymous_variant | 0.28 |
rpoA | 3877923 | c.585C>T | synonymous_variant | 0.28 |
rpoA | 3877926 | c.582G>C | synonymous_variant | 0.28 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.3 |
rpoA | 3877986 | c.522G>C | synonymous_variant | 0.28 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.28 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.29 |
rpoA | 3878022 | c.486T>C | synonymous_variant | 0.28 |
rpoA | 3878028 | c.480G>C | synonymous_variant | 0.26 |
rpoA | 3878031 | c.477T>C | synonymous_variant | 0.26 |
rpoA | 3878040 | c.468T>C | synonymous_variant | 0.27 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.29 |
rpoA | 3878058 | c.450G>T | synonymous_variant | 0.27 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.26 |
rpoA | 3878067 | c.441C>G | synonymous_variant | 0.26 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.26 |
rpoA | 3878076 | c.432C>T | synonymous_variant | 0.27 |
rpoA | 3878094 | c.414C>G | synonymous_variant | 0.28 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.27 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.28 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.28 |
rpoA | 3878130 | c.378C>G | synonymous_variant | 0.29 |
rpoA | 3878141 | p.Met123Leu | missense_variant | 0.25 |
rpoA | 3878143 | p.Gly122Asp | missense_variant | 0.25 |
rpoA | 3878157 | c.351C>G | synonymous_variant | 0.26 |
rpoA | 3878163 | c.345C>T | synonymous_variant | 0.27 |
rpoA | 3878169 | c.339G>C | synonymous_variant | 0.26 |
rpoA | 3878172 | c.336G>C | synonymous_variant | 0.25 |
rpoA | 3878187 | c.321C>G | synonymous_variant | 0.28 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.3 |
rpoA | 3878199 | c.309T>C | synonymous_variant | 0.3 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.29 |
rpoA | 3878226 | c.282C>G | synonymous_variant | 0.28 |
rpoA | 3878232 | c.276G>C | synonymous_variant | 0.3 |
rpoA | 3878247 | c.261G>C | synonymous_variant | 0.33 |
rpoA | 3878250 | c.258C>G | synonymous_variant | 0.33 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.31 |
rpoA | 3878284 | p.Glu75Ala | missense_variant | 0.31 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.3 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.32 |
rpoA | 3878304 | c.204G>C | synonymous_variant | 0.31 |
rpoA | 3878310 | c.198G>C | synonymous_variant | 0.3 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 0.31 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.3 |
rpoA | 3878331 | c.177A>G | synonymous_variant | 0.29 |
rpoA | 3878334 | c.174T>C | synonymous_variant | 0.29 |
rpoA | 3878337 | c.171T>C | synonymous_variant | 0.3 |
rpoA | 3878346 | c.162T>C | synonymous_variant | 0.33 |
rpoA | 3878364 | c.144A>C | synonymous_variant | 0.27 |
rpoA | 3878367 | c.141C>G | synonymous_variant | 0.27 |
rpoA | 3878376 | c.132G>C | synonymous_variant | 0.27 |
rpoA | 3878385 | c.123C>G | synonymous_variant | 0.25 |
rpoA | 3878388 | c.120C>G | synonymous_variant | 0.24 |
rpoA | 3878391 | c.117T>C | synonymous_variant | 0.25 |
rpoA | 3878415 | c.93C>T | synonymous_variant | 0.26 |
rpoA | 3878424 | c.84G>C | synonymous_variant | 0.27 |
rpoA | 3878436 | c.72A>G | synonymous_variant | 0.23 |
rpoA | 3878442 | c.66G>C | synonymous_variant | 0.23 |
rpoA | 3878454 | c.54A>C | synonymous_variant | 0.22 |
rpoA | 3878472 | p.Asp12Glu | missense_variant | 0.21 |
rpoA | 3878478 | c.30C>G | synonymous_variant | 0.23 |
rpoA | 3878484 | c.24C>A | synonymous_variant | 0.2 |
rpoA | 3878490 | c.18C>A | synonymous_variant | 0.19 |
rpoA | 3878496 | c.12A>T | synonymous_variant | 0.19 |
rpoA | 3878578 | c.-71C>A | upstream_gene_variant | 0.67 |
rpoA | 3878683 | c.-176G>C | upstream_gene_variant | 0.22 |
rpoA | 3878698 | c.-191A>G | upstream_gene_variant | 0.24 |
clpC1 | 4038356 | c.2349T>C | synonymous_variant | 0.2 |
clpC1 | 4038359 | c.2346A>G | synonymous_variant | 0.21 |
clpC1 | 4038368 | c.2337T>C | synonymous_variant | 0.23 |
clpC1 | 4038388 | c.2317T>C | synonymous_variant | 0.21 |
clpC1 | 4038392 | c.2313C>T | synonymous_variant | 0.21 |
clpC1 | 4038398 | c.2307G>T | synonymous_variant | 0.22 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 0.22 |
clpC1 | 4038407 | c.2298G>C | synonymous_variant | 0.23 |
clpC1 | 4038419 | c.2286T>C | synonymous_variant | 0.2 |
clpC1 | 4038433 | c.2272C>T | synonymous_variant | 0.19 |
clpC1 | 4038434 | c.2271G>A | synonymous_variant | 0.2 |
clpC1 | 4038444 | p.Ala754Lys | missense_variant | 0.19 |
clpC1 | 4038446 | c.2259T>C | synonymous_variant | 0.19 |
clpC1 | 4038456 | p.Val750Glu | missense_variant | 0.21 |
clpC1 | 4038460 | p.Leu749Met | missense_variant | 0.21 |
clpC1 | 4038486 | p.Gly740Asn | missense_variant | 0.2 |
clpC1 | 4038489 | p.Ala739Gly | missense_variant | 0.2 |
clpC1 | 4038494 | c.2211G>C | synonymous_variant | 0.2 |
clpC1 | 4038497 | p.Ser736Gln | missense_variant | 0.2 |
clpC1 | 4038530 | p.Glu725Asp | missense_variant | 0.2 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.22 |
clpC1 | 4038623 | c.2082A>G | synonymous_variant | 0.19 |
clpC1 | 4038640 | p.Asp689Asn | missense_variant | 0.21 |
clpC1 | 4038653 | c.2052C>T | synonymous_variant | 0.19 |
clpC1 | 4038658 | p.Lys683Gln | missense_variant | 0.18 |
clpC1 | 4038661 | p.Ser682Thr | missense_variant | 0.17 |
clpC1 | 4038662 | c.2043T>C | synonymous_variant | 0.17 |
clpC1 | 4038671 | c.2034T>C | synonymous_variant | 0.18 |
clpC1 | 4038683 | c.2022T>C | synonymous_variant | 0.18 |
clpC1 | 4038695 | c.2010C>G | synonymous_variant | 0.18 |
clpC1 | 4038704 | c.2001T>C | synonymous_variant | 0.16 |
clpC1 | 4038713 | c.1992T>C | synonymous_variant | 0.17 |
clpC1 | 4038749 | c.1956C>G | synonymous_variant | 0.22 |
clpC1 | 4038755 | c.1950G>T | synonymous_variant | 0.22 |
clpC1 | 4038770 | c.1935C>T | synonymous_variant | 0.22 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.23 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.21 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.22 |
clpC1 | 4038821 | c.1884G>A | synonymous_variant | 0.19 |
clpC1 | 4038845 | c.1860G>C | synonymous_variant | 0.26 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 0.3 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.31 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.36 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.37 |
clpC1 | 4038923 | c.1780_1782delCTAinsTTG | synonymous_variant | 0.35 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.35 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.36 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.32 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.3 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.3 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.33 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.31 |
clpC1 | 4039004 | c.1701C>G | synonymous_variant | 0.34 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.33 |
clpC1 | 4039064 | c.1641C>T | synonymous_variant | 0.34 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.31 |
clpC1 | 4039103 | c.1602T>C | synonymous_variant | 0.3 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.28 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.28 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.28 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.29 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.29 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.28 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.28 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.28 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.28 |
clpC1 | 4039186 | c.1519C>T | synonymous_variant | 0.29 |
clpC1 | 4039226 | c.1479T>C | synonymous_variant | 0.25 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.21 |
clpC1 | 4039286 | c.1419T>C | synonymous_variant | 0.23 |
clpC1 | 4039295 | c.1410A>C | synonymous_variant | 0.23 |
clpC1 | 4039298 | c.1407T>C | synonymous_variant | 0.23 |
clpC1 | 4039319 | c.1386T>C | synonymous_variant | 0.21 |
clpC1 | 4039322 | c.1383T>C | synonymous_variant | 0.21 |
clpC1 | 4039328 | c.1377A>C | synonymous_variant | 0.21 |
clpC1 | 4039331 | c.1374C>G | synonymous_variant | 0.21 |
clpC1 | 4039337 | p.Thr456Gln | missense_variant | 0.22 |
clpC1 | 4039349 | c.1356C>T | synonymous_variant | 0.22 |
clpC1 | 4039352 | c.1353C>G | synonymous_variant | 0.24 |
clpC1 | 4039364 | c.1341C>G | synonymous_variant | 0.24 |
clpC1 | 4039391 | c.1314T>G | synonymous_variant | 0.21 |
clpC1 | 4039409 | c.1296T>C | synonymous_variant | 0.22 |
clpC1 | 4039412 | c.1293T>G | synonymous_variant | 0.2 |
clpC1 | 4039415 | p.Glu430Asp | missense_variant | 0.19 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.21 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.21 |
clpC1 | 4039454 | c.1251A>G | synonymous_variant | 0.22 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 0.24 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.24 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.24 |
clpC1 | 4039480 | c.1225C>A | synonymous_variant | 0.24 |
clpC1 | 4039481 | c.1224T>G | synonymous_variant | 0.24 |
clpC1 | 4039484 | c.1221T>C | synonymous_variant | 0.24 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.24 |
clpC1 | 4039556 | c.1149G>C | synonymous_variant | 0.22 |
clpC1 | 4039559 | c.1146C>G | synonymous_variant | 0.22 |
clpC1 | 4039562 | c.1143C>G | synonymous_variant | 0.22 |
clpC1 | 4039565 | c.1140G>C | synonymous_variant | 0.22 |
clpC1 | 4039570 | p.Met379Leu | missense_variant | 0.22 |
clpC1 | 4039576 | p.Ala377Pro | missense_variant | 0.22 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.22 |
clpC1 | 4039589 | c.1116G>C | synonymous_variant | 0.23 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.22 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.22 |
clpC1 | 4039622 | c.1083C>T | synonymous_variant | 0.22 |
clpC1 | 4039661 | c.1044T>G | synonymous_variant | 0.25 |
clpC1 | 4039664 | c.1041G>C | synonymous_variant | 0.25 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.24 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.21 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.17 |
clpC1 | 4039760 | c.945T>C | synonymous_variant | 0.17 |
clpC1 | 4039766 | c.939T>C | synonymous_variant | 0.17 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.17 |
clpC1 | 4039775 | c.930G>C | synonymous_variant | 0.17 |
clpC1 | 4039781 | c.924G>C | synonymous_variant | 0.17 |
clpC1 | 4039790 | c.915C>G | synonymous_variant | 0.18 |
clpC1 | 4039805 | c.900C>T | synonymous_variant | 0.19 |
clpC1 | 4039817 | c.888A>C | synonymous_variant | 0.2 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.2 |
clpC1 | 4039826 | c.879C>G | synonymous_variant | 0.22 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 0.22 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.19 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.18 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.21 |
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 | 0.18 |
clpC1 | 4039951 | c.754C>T | synonymous_variant | 0.2 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.2 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.22 |
clpC1 | 4039988 | c.717C>G | synonymous_variant | 0.22 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 0.22 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.22 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.21 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.2 |
clpC1 | 4040036 | c.669C>G | synonymous_variant | 0.2 |
clpC1 | 4040090 | p.Ser205Thr | missense_variant | 0.16 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.16 |
clpC1 | 4040105 | c.600C>G | synonymous_variant | 0.2 |
clpC1 | 4040147 | c.558A>G | synonymous_variant | 0.27 |
clpC1 | 4040162 | c.543G>C | synonymous_variant | 0.23 |
clpC1 | 4040165 | c.540G>C | synonymous_variant | 0.23 |
clpC1 | 4040171 | c.534C>G | synonymous_variant | 0.25 |
clpC1 | 4040201 | c.504C>G | synonymous_variant | 0.24 |
clpC1 | 4040204 | c.501G>C | synonymous_variant | 0.22 |
clpC1 | 4040207 | c.498T>G | synonymous_variant | 0.23 |
clpC1 | 4040210 | c.495G>C | synonymous_variant | 0.23 |
clpC1 | 4040213 | c.490_492delTCTinsAGC | synonymous_variant | 0.23 |
clpC1 | 4040225 | c.480A>C | synonymous_variant | 0.22 |
clpC1 | 4040228 | c.477G>T | synonymous_variant | 0.23 |
clpC1 | 4040231 | c.474C>T | synonymous_variant | 0.23 |
clpC1 | 4040237 | c.468C>T | synonymous_variant | 0.27 |
clpC1 | 4040246 | c.459C>G | synonymous_variant | 0.27 |
clpC1 | 4040249 | c.456A>G | synonymous_variant | 0.27 |
clpC1 | 4040267 | c.438A>G | synonymous_variant | 0.27 |
clpC1 | 4040273 | c.432T>C | synonymous_variant | 0.28 |
clpC1 | 4040277 | c.427_428delTCinsAG | synonymous_variant | 0.25 |
clpC1 | 4040279 | c.426C>G | synonymous_variant | 0.25 |
clpC1 | 4040291 | c.414G>C | synonymous_variant | 0.28 |
clpC1 | 4040318 | c.387C>G | synonymous_variant | 0.22 |
clpC1 | 4040330 | c.375C>G | synonymous_variant | 0.21 |
clpC1 | 4040342 | c.363C>G | synonymous_variant | 0.23 |
clpC1 | 4040354 | c.351A>G | synonymous_variant | 0.23 |
clpC1 | 4040363 | c.342A>T | synonymous_variant | 0.2 |
clpC1 | 4040369 | c.336C>G | synonymous_variant | 0.19 |
clpC1 | 4040381 | c.324T>C | synonymous_variant | 0.17 |
clpC1 | 4040393 | c.312G>C | synonymous_variant | 0.17 |
clpC1 | 4040411 | c.294T>C | synonymous_variant | 0.16 |
clpC1 | 4040471 | c.234T>C | synonymous_variant | 0.17 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 0.17 |
clpC1 | 4040528 | c.177G>C | synonymous_variant | 0.16 |
embC | 4240726 | c.864G>C | synonymous_variant | 0.2 |
embC | 4240819 | c.957A>T | synonymous_variant | 0.16 |
embC | 4240828 | c.966G>A | synonymous_variant | 0.16 |
embC | 4240880 | p.Ala340Thr | missense_variant | 0.15 |
embC | 4240945 | c.1083T>G | synonymous_variant | 0.16 |
embC | 4241032 | c.1170G>C | synonymous_variant | 0.15 |
embC | 4241449 | c.1587C>G | synonymous_variant | 0.18 |
embC | 4241453 | p.Ile531Val | missense_variant | 0.19 |
embC | 4241479 | c.1617C>G | synonymous_variant | 0.18 |
embC | 4241480 | c.1618T>C | synonymous_variant | 0.18 |
embC | 4241496 | p.Ala545Gly | missense_variant | 0.2 |
embC | 4241500 | c.1638A>C | synonymous_variant | 0.19 |
embC | 4241501 | p.Ser547Thr | missense_variant | 0.2 |
embC | 4241506 | c.1644G>C | synonymous_variant | 0.2 |
embC | 4241518 | c.1656A>G | synonymous_variant | 0.21 |
embC | 4241521 | c.1659T>C | synonymous_variant | 0.21 |
embC | 4241530 | c.1668C>A | synonymous_variant | 0.23 |
embC | 4241536 | c.1674A>G | synonymous_variant | 0.2 |
embC | 4241539 | c.1677T>C | synonymous_variant | 0.2 |
embC | 4241545 | c.1683T>C | synonymous_variant | 0.2 |
embC | 4241548 | c.1686T>C | synonymous_variant | 0.2 |
embC | 4241551 | c.1689A>G | synonymous_variant | 0.2 |
embC | 4241567 | p.Ile569Val | missense_variant | 0.22 |
embC | 4241572 | c.1710C>G | synonymous_variant | 0.22 |
embC | 4241578 | c.1716G>C | synonymous_variant | 0.21 |
embC | 4241584 | c.1722T>C | synonymous_variant | 0.21 |
embC | 4241587 | c.1725C>G | synonymous_variant | 0.21 |
embC | 4241591 | p.Leu577Val | missense_variant | 0.21 |
embC | 4241611 | c.1749G>C | synonymous_variant | 0.21 |
embC | 4241614 | c.1752A>C | synonymous_variant | 0.21 |
embC | 4241626 | c.1764T>C | synonymous_variant | 0.17 |
embC | 4241635 | c.1773G>C | synonymous_variant | 0.18 |
embC | 4241650 | p.Leu596Phe | missense_variant | 0.16 |
embC | 4241657 | p.Ser599Pro | missense_variant | 0.18 |
embC | 4241665 | c.1803G>C | synonymous_variant | 0.16 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 0.99 |
embC | 4242803 | p.Val981Leu | missense_variant | 0.96 |
embA | 4245189 | c.1957C>T | synonymous_variant | 0.16 |
embA | 4245198 | p.Leu656Ile | missense_variant | 0.18 |
embA | 4245207 | c.1975T>C | synonymous_variant | 0.19 |
embA | 4245222 | p.Tyr664Gln | missense_variant | 0.19 |
embA | 4245248 | c.2016G>C | synonymous_variant | 0.22 |
embA | 4245257 | c.2025A>G | synonymous_variant | 0.24 |
embA | 4245263 | c.2031A>G | synonymous_variant | 0.22 |
embA | 4245282 | p.Ile684Val | missense_variant | 0.19 |
embA | 4245285 | c.2053T>C | synonymous_variant | 0.19 |
embA | 4245290 | c.2058C>G | synonymous_variant | 0.19 |
embA | 4245293 | c.2061T>G | synonymous_variant | 0.19 |
embA | 4245296 | c.2064G>C | synonymous_variant | 0.2 |
embA | 4245299 | c.2067A>G | synonymous_variant | 0.19 |
embA | 4245315 | p.Val695Thr | missense_variant | 0.17 |
embB | 4247611 | c.1098G>T | synonymous_variant | 0.15 |
embB | 4247629 | c.1116C>G | synonymous_variant | 0.18 |
embB | 4247632 | c.1119C>G | synonymous_variant | 0.17 |
embB | 4247638 | c.1125G>C | synonymous_variant | 0.17 |
embB | 4247646 | p.Glu378Ala | missense_variant | 0.17 |
embB | 4247683 | c.1170C>G | synonymous_variant | 0.17 |
embB | 4247761 | c.1248T>C | synonymous_variant | 0.18 |
embB | 4247773 | c.1260G>A | synonymous_variant | 0.18 |
embB | 4247776 | c.1263G>T | synonymous_variant | 0.18 |
embB | 4247800 | c.1287A>T | synonymous_variant | 0.15 |
embB | 4247819 | p.Val436Ile | missense_variant | 0.15 |
embB | 4247830 | c.1317A>C | synonymous_variant | 0.17 |
embB | 4247836 | c.1323A>G | synonymous_variant | 0.17 |
embB | 4247839 | c.1326G>C | synonymous_variant | 0.17 |
embB | 4247866 | c.1353G>C | synonymous_variant | 0.2 |
embB | 4247875 | c.1362G>C | synonymous_variant | 0.22 |
embB | 4247876 | c.1363C>T | synonymous_variant | 0.22 |
embB | 4247881 | c.1368G>C | synonymous_variant | 0.22 |
embB | 4247887 | c.1374C>T | synonymous_variant | 0.23 |
embB | 4247893 | c.1380C>T | synonymous_variant | 0.24 |
embB | 4247899 | p.Met462Ile | missense_variant | 0.24 |
embB | 4247905 | c.1392G>C | synonymous_variant | 0.23 |
embB | 4247909 | c.1396T>C | synonymous_variant | 0.25 |
embB | 4247914 | c.1401G>C | synonymous_variant | 0.25 |
embB | 4247926 | c.1413C>T | synonymous_variant | 0.25 |
embB | 4247932 | c.1419C>G | synonymous_variant | 0.26 |
embB | 4247940 | p.Leu476Trp | missense_variant | 0.25 |
embB | 4247945 | c.1432T>C | synonymous_variant | 0.25 |
embB | 4247951 | p.Ser480Ala | missense_variant | 0.24 |
embB | 4247956 | c.1443G>C | synonymous_variant | 0.23 |
embB | 4247974 | c.1461C>G | synonymous_variant | 0.22 |
embB | 4248007 | c.1494C>G | synonymous_variant | 0.22 |
embB | 4248011 | p.Ser500Arg | missense_variant | 0.21 |
embB | 4248014 | p.Thr501Ala | missense_variant | 0.21 |
embB | 4248035 | p.Val508Ile | missense_variant | 0.22 |
embB | 4248040 | c.1527C>G | synonymous_variant | 0.22 |
embB | 4248041 | p.Ala510Thr | missense_variant | 0.22 |
embB | 4248044 | p.Lys511Ala | missense_variant | 0.22 |
embB | 4248070 | c.1557T>C | synonymous_variant | 0.24 |
embB | 4248085 | c.1572T>C | synonymous_variant | 0.21 |
embB | 4248097 | c.1584C>G | synonymous_variant | 0.23 |
embB | 4248130 | c.1617G>C | synonymous_variant | 0.22 |
embB | 4248133 | c.1620C>G | synonymous_variant | 0.22 |
embB | 4248139 | c.1626C>G | synonymous_variant | 0.22 |
embB | 4248142 | c.1629T>C | synonymous_variant | 0.22 |
embB | 4248143 | c.1630T>C | synonymous_variant | 0.22 |
embB | 4248157 | c.1644A>G | synonymous_variant | 0.24 |
embB | 4248199 | c.1686A>G | synonymous_variant | 0.19 |
embB | 4248200 | p.Ile563Val | missense_variant | 0.19 |
embB | 4248205 | c.1692C>G | synonymous_variant | 0.19 |
embB | 4248206 | p.Ser565Gly | missense_variant | 0.19 |
embB | 4248220 | c.1707A>C | synonymous_variant | 0.21 |
embB | 4248304 | c.1791G>C | synonymous_variant | 0.17 |
embB | 4249411 | c.2898G>A | synonymous_variant | 0.18 |
embB | 4249417 | c.2904A>G | synonymous_variant | 0.18 |
embB | 4249424 | p.Leu971Met | missense_variant | 0.16 |
embB | 4249429 | c.2916C>T | synonymous_variant | 0.17 |
embB | 4249432 | c.2919A>G | synonymous_variant | 0.17 |
embB | 4249441 | c.2928A>G | synonymous_variant | 0.18 |
embB | 4249444 | c.2931T>C | synonymous_variant | 0.19 |
embB | 4249447 | c.2934G>C | synonymous_variant | 0.2 |
embB | 4249469 | p.Leu986Met | missense_variant | 0.2 |
embB | 4249486 | c.2973T>G | synonymous_variant | 0.21 |
embB | 4249498 | c.2985G>C | synonymous_variant | 0.24 |
embB | 4249521 | p.Ala1003Val | missense_variant | 0.23 |
embB | 4249525 | c.3012T>C | synonymous_variant | 0.23 |
embB | 4249529 | p.Ile1006Val | missense_variant | 0.23 |
embB | 4249532 | p.Ala1007Thr | missense_variant | 0.23 |
embB | 4249537 | c.3024A>G | synonymous_variant | 0.23 |
embB | 4249543 | c.3030G>C | synonymous_variant | 0.23 |
embB | 4249546 | c.3033G>A | synonymous_variant | 0.23 |
embB | 4249558 | c.3045A>C | synonymous_variant | 0.22 |
embB | 4249568 | p.Ser1019Thr | missense_variant | 0.21 |
embB | 4249573 | c.3060T>C | synonymous_variant | 0.2 |
embB | 4249579 | c.3066G>A | synonymous_variant | 0.18 |
embB | 4249580 | p.Leu1023Met | missense_variant | 0.18 |
embB | 4249594 | c.3081G>C | synonymous_variant | 0.17 |
embB | 4249606 | c.3093C>A | synonymous_variant | 0.16 |
aftB | 4269201 | c.-365A>G | upstream_gene_variant | 0.18 |
aftB | 4269206 | c.-370C>T | upstream_gene_variant | 0.18 |
ubiA | 4269220 | p.Ala205Lys | missense_variant | 0.16 |
aftB | 4269222 | c.-386T>C | upstream_gene_variant | 0.17 |
aftB | 4269242 | c.-406C>T | upstream_gene_variant | 0.17 |
ubiA | 4269243 | p.His197Gln | missense_variant | 0.17 |
aftB | 4269249 | c.-413G>A | upstream_gene_variant | 0.18 |
aftB | 4269258 | c.-422C>T | upstream_gene_variant | 0.18 |
aftB | 4269312 | c.-476G>A | upstream_gene_variant | 0.16 |
ubiA | 4269329 | p.Lys169Glu | missense_variant | 0.18 |
aftB | 4269342 | c.-506G>C | upstream_gene_variant | 0.2 |
ubiA | 4269380 | p.Val152Ile | missense_variant | 0.22 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 0.2 |
ubiA | 4269390 | p.Val148Leu | missense_variant | 0.19 |
aftB | 4269402 | c.-566T>C | upstream_gene_variant | 0.19 |
aftB | 4269405 | c.-569G>A | upstream_gene_variant | 0.18 |
aftB | 4269411 | c.-575T>G | upstream_gene_variant | 0.17 |
aftB | 4269414 | c.-578T>C | upstream_gene_variant | 0.18 |
aftB | 4269420 | c.-584T>C | upstream_gene_variant | 0.18 |
aftB | 4269428 | c.-592T>C | upstream_gene_variant | 0.18 |
ubiA | 4269436 | p.Ala133Gly | missense_variant | 0.17 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |