Run ID: ERR502908
Sample name:
Date: 01-04-2023 21:58:47
Number of reads: 2450319
Percentage reads mapped: 83.84
Strain: lineage2.2.1
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.99 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 1.0 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472307 | n.462C>T | non_coding_transcript_exon_variant | 0.26 | streptomycin |
inhA | 1674048 | c.-154G>A | upstream_gene_variant | 0.98 | isoniazid, ethionamide |
panD | 4043869 | p.Val138Ala | missense_variant | 0.15 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6196 | c.957C>T | synonymous_variant | 0.19 |
gyrB | 6238 | c.999G>A | synonymous_variant | 0.18 |
gyrB | 6242 | p.Arg335Lys | missense_variant | 0.15 |
gyrB | 6250 | c.1011A>G | synonymous_variant | 0.16 |
gyrB | 6256 | c.1017G>A | synonymous_variant | 0.15 |
gyrB | 6268 | c.1029C>G | synonymous_variant | 0.16 |
gyrB | 6280 | c.1041T>C | synonymous_variant | 0.17 |
gyrB | 6286 | c.1047T>C | synonymous_variant | 0.16 |
gyrB | 6289 | c.1050C>T | synonymous_variant | 0.15 |
gyrA | 6655 | c.-647T>C | upstream_gene_variant | 0.15 |
gyrA | 6670 | c.-632G>C | upstream_gene_variant | 0.15 |
gyrA | 6673 | c.-629A>C | upstream_gene_variant | 0.16 |
gyrA | 6676 | c.-626T>G | upstream_gene_variant | 0.15 |
gyrA | 7006 | c.-296T>C | 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 |
gyrA | 7015 | c.-287G>A | upstream_gene_variant | 0.17 |
gyrA | 7018 | c.-284G>A | upstream_gene_variant | 0.17 |
gyrB | 7023 | p.Leu595Gln | missense_variant | 0.17 |
gyrA | 7033 | c.-269G>C | upstream_gene_variant | 0.18 |
gyrA | 7361 | c.60C>T | synonymous_variant | 0.14 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7391 | c.90C>T | synonymous_variant | 0.13 |
gyrA | 7394 | c.93T>C | synonymous_variant | 0.14 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7775 | c.474C>A | synonymous_variant | 0.13 |
gyrA | 8096 | c.795T>A | synonymous_variant | 0.16 |
gyrA | 8099 | c.798T>C | synonymous_variant | 0.16 |
gyrA | 8111 | c.810G>C | synonymous_variant | 0.17 |
gyrA | 8121 | c.820T>C | synonymous_variant | 0.2 |
gyrA | 8129 | c.828T>C | synonymous_variant | 0.23 |
gyrA | 8135 | c.834C>G | synonymous_variant | 0.24 |
gyrA | 8156 | c.855T>C | synonymous_variant | 0.24 |
gyrA | 8168 | c.867A>G | synonymous_variant | 0.23 |
gyrA | 8177 | c.876A>C | synonymous_variant | 0.21 |
gyrA | 8264 | c.963T>C | synonymous_variant | 0.15 |
gyrA | 8276 | c.975G>A | synonymous_variant | 0.15 |
gyrA | 8283 | p.Ile328Leu | missense_variant | 0.17 |
gyrA | 8294 | c.993T>C | synonymous_variant | 0.18 |
gyrA | 8324 | c.1023T>C | synonymous_variant | 0.18 |
gyrA | 8330 | c.1029C>G | synonymous_variant | 0.2 |
gyrA | 8339 | c.1038A>G | synonymous_variant | 0.18 |
gyrA | 8340 | p.Ala347Ser | missense_variant | 0.18 |
gyrA | 8372 | c.1071G>C | synonymous_variant | 0.14 |
gyrA | 8420 | c.1119T>C | synonymous_variant | 0.17 |
gyrA | 8576 | c.1275C>G | synonymous_variant | 0.15 |
gyrA | 8579 | c.1278C>T | synonymous_variant | 0.14 |
gyrA | 8588 | c.1287G>A | synonymous_variant | 0.15 |
gyrA | 8597 | c.1296C>G | synonymous_variant | 0.18 |
gyrA | 8603 | c.1302A>G | synonymous_variant | 0.19 |
gyrA | 8621 | c.1320G>A | synonymous_variant | 0.14 |
gyrA | 8636 | c.1335A>C | synonymous_variant | 0.17 |
gyrA | 8642 | c.1341A>G | synonymous_variant | 0.17 |
gyrA | 9204 | p.Ser635Thr | missense_variant | 0.13 |
gyrA | 9233 | c.1932C>G | synonymous_variant | 0.15 |
gyrA | 9239 | c.1938C>T | synonymous_variant | 0.17 |
gyrA | 9252 | p.Val651Ile | missense_variant | 0.18 |
gyrA | 9284 | c.1983T>C | synonymous_variant | 0.15 |
gyrA | 9291 | c.1990C>T | synonymous_variant | 0.15 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9323 | c.2022C>G | synonymous_variant | 0.16 |
gyrA | 9335 | c.2034G>C | synonymous_variant | 0.16 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575154 | c.-194_-192delGTGinsCTC | upstream_gene_variant | 0.18 |
mshA | 575161 | c.-187_-186delTTinsCG | upstream_gene_variant | 0.15 |
mshA | 575907 | p.Ala187Val | missense_variant | 0.96 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 760121 | c.315T>C | synonymous_variant | 0.14 |
rpoB | 760130 | p.Asp108Glu | missense_variant | 0.16 |
rpoB | 760139 | c.333A>G | synonymous_variant | 0.17 |
rpoB | 760142 | c.336C>G | synonymous_variant | 0.19 |
rpoB | 760181 | c.375T>C | synonymous_variant | 0.21 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.2 |
rpoB | 760196 | c.390C>G | synonymous_variant | 0.22 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.24 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.2 |
rpoB | 760283 | c.477G>C | synonymous_variant | 0.22 |
rpoB | 760298 | c.492G>C | synonymous_variant | 0.16 |
rpoB | 760307 | c.501T>C | synonymous_variant | 0.17 |
rpoB | 760310 | c.504G>C | synonymous_variant | 0.18 |
rpoB | 760328 | c.522G>C | synonymous_variant | 0.22 |
rpoB | 760331 | c.525G>C | synonymous_variant | 0.22 |
rpoB | 760340 | c.534G>T | synonymous_variant | 0.26 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.26 |
rpoB | 760370 | c.564C>G | synonymous_variant | 0.26 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.26 |
rpoB | 760380 | p.Thr192Leu | missense_variant | 0.25 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.25 |
rpoB | 760412 | c.606C>G | synonymous_variant | 0.26 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.23 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.23 |
rpoB | 760481 | c.675G>C | synonymous_variant | 0.15 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.14 |
rpoB | 760522 | p.Ser239Asn | missense_variant | 0.21 |
rpoB | 760532 | c.726T>C | synonymous_variant | 0.2 |
rpoB | 760533 | p.Val243Thr | missense_variant | 0.2 |
rpoB | 760541 | c.735G>C | synonymous_variant | 0.21 |
rpoB | 760547 | c.741G>C | synonymous_variant | 0.21 |
rpoB | 760563 | p.Arg253Met | missense_variant | 0.18 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.2 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.14 |
rpoB | 760793 | c.987A>G | synonymous_variant | 0.19 |
rpoB | 760805 | c.999G>C | synonymous_variant | 0.19 |
rpoB | 760817 | c.1011A>G | synonymous_variant | 0.21 |
rpoB | 760820 | c.1014T>C | synonymous_variant | 0.19 |
rpoB | 760826 | c.1020C>G | synonymous_variant | 0.19 |
rpoB | 760830 | c.1024T>C | synonymous_variant | 0.2 |
rpoB | 760841 | c.1035T>C | synonymous_variant | 0.23 |
rpoB | 760845 | p.Thr347Pro | missense_variant | 0.23 |
rpoB | 760859 | c.1053T>C | synonymous_variant | 0.21 |
rpoB | 760862 | c.1056G>C | synonymous_variant | 0.21 |
rpoB | 760869 | p.Val355Ile | missense_variant | 0.22 |
rpoB | 760886 | c.1080A>G | synonymous_variant | 0.18 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.18 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 0.15 |
rpoB | 760931 | c.1125C>G | synonymous_variant | 0.16 |
rpoB | 760934 | c.1128C>T | synonymous_variant | 0.16 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.23 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.23 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.24 |
rpoB | 761006 | c.1200C>G | synonymous_variant | 0.23 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.26 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 0.27 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.28 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.26 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.26 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.29 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.26 |
rpoB | 761129 | c.1323G>C | synonymous_variant | 0.29 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 0.29 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.29 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.28 |
rpoB | 761153 | c.1347G>C | synonymous_variant | 0.31 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.26 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.28 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.27 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.3 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.28 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.26 |
rpoB | 761219 | c.1413G>C | synonymous_variant | 0.25 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.27 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.29 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.26 |
rpoB | 761306 | c.1500C>G | synonymous_variant | 0.27 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.26 |
rpoB | 761330 | c.1524G>C | synonymous_variant | 0.23 |
rpoB | 761354 | c.1548C>T | synonymous_variant | 0.22 |
rpoB | 761360 | c.1554T>C | synonymous_variant | 0.23 |
rpoB | 761362 | p.Ser519Thr | missense_variant | 0.24 |
rpoB | 761373 | p.Val523His | missense_variant | 0.24 |
rpoB | 761510 | c.1704T>C | synonymous_variant | 0.17 |
rpoB | 761531 | c.1725C>G | synonymous_variant | 0.24 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.21 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.19 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.21 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.23 |
rpoB | 761588 | c.1782C>T | synonymous_variant | 0.23 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.18 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.15 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.15 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.15 |
rpoB | 761645 | c.1839C>G | synonymous_variant | 0.15 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.15 |
rpoB | 761657 | c.1851C>G | synonymous_variant | 0.15 |
rpoB | 761747 | c.1941G>C | synonymous_variant | 0.15 |
rpoB | 761750 | c.1944G>C | synonymous_variant | 0.15 |
rpoB | 761765 | c.1959T>C | synonymous_variant | 0.15 |
rpoB | 761873 | c.2067A>C | synonymous_variant | 0.15 |
rpoB | 761885 | c.2079T>C | synonymous_variant | 0.2 |
rpoB | 761906 | c.2100C>G | synonymous_variant | 0.17 |
rpoB | 761909 | c.2103T>C | synonymous_variant | 0.17 |
rpoB | 761912 | c.2106T>C | synonymous_variant | 0.17 |
rpoB | 761915 | p.Asp703Glu | missense_variant | 0.17 |
rpoB | 761916 | p.Asp704Asn | missense_variant | 0.17 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.19 |
rpoB | 761954 | c.2148C>G | synonymous_variant | 0.19 |
rpoB | 762008 | c.2202C>T | synonymous_variant | 0.24 |
rpoB | 762014 | c.2208C>T | synonymous_variant | 0.24 |
rpoB | 762017 | c.2211A>G | synonymous_variant | 0.24 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.26 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.19 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.15 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.19 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.17 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.15 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.15 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 0.19 |
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 | 0.19 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.18 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.21 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.22 |
rpoB | 762206 | c.2400C>G | synonymous_variant | 0.3 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.29 |
rpoB | 762246 | c.2440C>T | synonymous_variant | 0.27 |
rpoB | 762254 | c.2448T>G | synonymous_variant | 0.26 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.26 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.28 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.28 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.28 |
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 | 0.18 |
rpoB | 762338 | c.2532T>C | synonymous_variant | 0.2 |
rpoB | 762347 | c.2541T>C | synonymous_variant | 0.2 |
rpoB | 762362 | p.Glu852Asp | missense_variant | 0.19 |
rpoB | 762369 | c.2563T>C | synonymous_variant | 0.2 |
rpoC | 762395 | c.-975G>C | upstream_gene_variant | 0.17 |
rpoC | 762398 | c.-972T>C | upstream_gene_variant | 0.16 |
rpoC | 762401 | c.-969G>C | upstream_gene_variant | 0.16 |
rpoC | 762404 | c.-966T>C | upstream_gene_variant | 0.17 |
rpoC | 762410 | c.-960T>G | upstream_gene_variant | 0.17 |
rpoC | 762413 | c.-957G>A | upstream_gene_variant | 0.18 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 0.18 |
rpoC | 762419 | c.-951C>G | upstream_gene_variant | 0.17 |
rpoC | 762434 | c.-936T>C | upstream_gene_variant | 0.14 |
rpoC | 762857 | c.-513C>G | upstream_gene_variant | 0.14 |
rpoC | 762863 | c.-507T>C | upstream_gene_variant | 0.15 |
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 | 0.25 |
rpoC | 763013 | c.-357C>G | upstream_gene_variant | 0.24 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.2 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 1.0 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.22 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.24 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.2 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.21 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.15 |
rpoC | 763402 | c.33C>G | synonymous_variant | 0.16 |
rpoC | 763411 | c.42T>G | synonymous_variant | 0.16 |
rpoC | 763414 | c.45T>C | synonymous_variant | 0.17 |
rpoC | 763441 | c.72C>T | synonymous_variant | 0.22 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.2 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.23 |
rpoC | 763486 | c.117T>G | synonymous_variant | 0.26 |
rpoC | 763492 | c.123G>A | synonymous_variant | 0.25 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.23 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.25 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.17 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.18 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.21 |
rpoC | 763603 | c.234C>T | synonymous_variant | 0.21 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.24 |
rpoC | 763657 | c.288G>A | synonymous_variant | 0.27 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.28 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.29 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.31 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.28 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.28 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.26 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.23 |
rpoC | 763738 | c.369G>A | synonymous_variant | 0.21 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.21 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.21 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.23 |
rpoC | 763774 | c.405G>C | synonymous_variant | 0.19 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.17 |
rpoC | 763816 | c.447C>G | synonymous_variant | 0.14 |
rpoC | 763835 | p.Ala156Met | missense_variant | 0.15 |
rpoC | 763872 | p.Gly168Ala | missense_variant | 0.15 |
rpoC | 763876 | p.Glu169Asp | missense_variant | 0.14 |
rpoC | 763879 | c.510A>G | synonymous_variant | 0.17 |
rpoC | 763945 | c.576T>C | synonymous_variant | 0.17 |
rpoC | 763951 | c.582G>C | synonymous_variant | 0.17 |
rpoC | 763960 | c.591T>C | synonymous_variant | 0.2 |
rpoC | 763987 | c.618C>T | synonymous_variant | 0.16 |
rpoC | 763991 | p.Ile208Leu | missense_variant | 0.16 |
rpoC | 763996 | c.627T>C | synonymous_variant | 0.16 |
rpoC | 764002 | c.633C>G | synonymous_variant | 0.15 |
rpoC | 764005 | c.636G>C | synonymous_variant | 0.15 |
rpoC | 764059 | c.690G>T | synonymous_variant | 0.13 |
rpoC | 764083 | c.714A>G | synonymous_variant | 0.21 |
rpoC | 764098 | c.729A>G | synonymous_variant | 0.24 |
rpoC | 764101 | c.732C>G | synonymous_variant | 0.24 |
rpoC | 764102 | p.Val245Ile | missense_variant | 0.24 |
rpoC | 764112 | p.Tyr248Phe | missense_variant | 0.25 |
rpoC | 764116 | c.747C>T | synonymous_variant | 0.26 |
rpoC | 764131 | c.762T>C | synonymous_variant | 0.26 |
rpoC | 764188 | c.819A>G | synonymous_variant | 0.2 |
rpoC | 764195 | p.Ser276Ile | missense_variant | 0.16 |
rpoC | 764203 | c.834G>C | synonymous_variant | 0.2 |
rpoC | 764206 | c.837T>C | synonymous_variant | 0.22 |
rpoC | 764215 | c.846A>G | synonymous_variant | 0.23 |
rpoC | 764236 | c.867G>A | synonymous_variant | 0.25 |
rpoC | 764248 | c.879C>G | synonymous_variant | 0.25 |
rpoC | 764257 | c.888G>C | synonymous_variant | 0.22 |
rpoC | 764266 | c.897T>C | synonymous_variant | 0.23 |
rpoC | 764269 | c.900G>C | synonymous_variant | 0.22 |
rpoC | 764272 | c.903G>C | synonymous_variant | 0.21 |
rpoC | 764278 | c.909A>G | synonymous_variant | 0.23 |
rpoC | 764353 | c.984G>C | synonymous_variant | 0.14 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.13 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.14 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.14 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.15 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.17 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.18 |
rpoC | 764489 | c.1120C>T | synonymous_variant | 0.19 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.2 |
rpoC | 764510 | c.1141C>T | synonymous_variant | 0.2 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.19 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.18 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.18 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.19 |
rpoC | 764548 | c.1179G>A | synonymous_variant | 0.16 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.15 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.13 |
rpoC | 764650 | c.1281G>C | synonymous_variant | 0.16 |
rpoC | 764651 | c.1282_1284delTCGinsAGC | synonymous_variant | 0.16 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.21 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.23 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.25 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.28 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.29 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.2 |
rpoC | 764872 | c.1503A>G | synonymous_variant | 0.19 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.19 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.14 |
rpoC | 765034 | c.1665T>C | synonymous_variant | 0.15 |
rpoC | 765040 | c.1671T>C | synonymous_variant | 0.16 |
rpoC | 765041 | c.1672T>C | synonymous_variant | 0.17 |
rpoC | 765055 | c.1686C>G | synonymous_variant | 0.14 |
rpoC | 765300 | p.Val644Ala | missense_variant | 0.14 |
rpoC | 765319 | c.1950A>G | synonymous_variant | 0.16 |
rpoC | 765326 | p.His653Ala | missense_variant | 0.15 |
rpoC | 765330 | p.Ser654Asn | missense_variant | 0.15 |
rpoC | 765352 | c.1983G>C | synonymous_variant | 0.15 |
rpoC | 765383 | p.Met672Leu | missense_variant | 0.18 |
rpoC | 765404 | p.Leu679Val | missense_variant | 0.18 |
rpoC | 765409 | c.2040T>C | synonymous_variant | 0.17 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.23 |
rpoC | 765451 | c.2082C>A | synonymous_variant | 0.26 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.21 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.23 |
rpoC | 765529 | c.2160C>T | synonymous_variant | 0.18 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.2 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.18 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.17 |
rpoC | 765559 | c.2190G>C | synonymous_variant | 0.17 |
rpoC | 765580 | c.2211G>C | synonymous_variant | 0.21 |
rpoC | 765613 | p.His748Gln | missense_variant | 0.22 |
rpoC | 765625 | c.2256C>G | synonymous_variant | 0.21 |
rpoC | 765631 | p.Asp754Glu | missense_variant | 0.2 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.26 |
rpoC | 765734 | c.2365T>C | synonymous_variant | 0.23 |
rpoC | 765739 | c.2370G>T | synonymous_variant | 0.24 |
rpoC | 765751 | c.2382C>G | synonymous_variant | 0.21 |
rpoC | 765753 | p.Asp795Ala | missense_variant | 0.22 |
rpoC | 765772 | c.2403C>G | synonymous_variant | 0.24 |
rpoC | 765784 | c.2415C>G | synonymous_variant | 0.22 |
rpoC | 765787 | c.2418C>T | synonymous_variant | 0.22 |
rpoC | 765793 | c.2424C>G | synonymous_variant | 0.24 |
rpoC | 765796 | c.2427C>T | synonymous_variant | 0.24 |
rpoC | 765811 | c.2442T>C | synonymous_variant | 0.22 |
rpoC | 765814 | c.2445A>G | synonymous_variant | 0.22 |
rpoC | 765826 | c.2457T>C | synonymous_variant | 0.21 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 0.17 |
rpoC | 765850 | c.2481G>C | synonymous_variant | 0.18 |
rpoC | 765883 | c.2514C>G | synonymous_variant | 0.21 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.21 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.21 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.19 |
rpoC | 765947 | c.2578T>C | synonymous_variant | 0.2 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.2 |
rpoC | 765982 | c.2613C>G | synonymous_variant | 0.22 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.24 |
rpoC | 766010 | c.2641_2642delTCinsAG | synonymous_variant | 0.19 |
rpoC | 766021 | c.2652G>C | synonymous_variant | 0.2 |
rpoC | 766027 | c.2658G>C | synonymous_variant | 0.2 |
rpoC | 766043 | p.Gln892Glu | missense_variant | 0.2 |
rpoC | 766054 | c.2685C>G | synonymous_variant | 0.15 |
rpoC | 766082 | p.Ala905Gln | missense_variant | 0.16 |
rpoC | 766096 | c.2727G>C | synonymous_variant | 0.15 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.15 |
rpoC | 766390 | c.3021C>T | synonymous_variant | 0.15 |
rpoC | 766393 | c.3024C>G | synonymous_variant | 0.16 |
rpoC | 766411 | c.3042C>G | synonymous_variant | 0.14 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.19 |
rpoC | 766447 | c.3078T>C | synonymous_variant | 0.19 |
rpoC | 766462 | c.3093G>C | synonymous_variant | 0.17 |
rpoC | 766630 | c.3261G>C | synonymous_variant | 0.14 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.15 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.14 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.15 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.15 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 0.2 |
rpoC | 766864 | c.3495G>C | synonymous_variant | 0.19 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.2 |
rpoC | 766933 | c.3564A>G | synonymous_variant | 0.18 |
rpoC | 766945 | c.3576A>G | synonymous_variant | 0.17 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.16 |
rpoC | 766972 | c.3603G>C | synonymous_variant | 0.16 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.23 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.25 |
rpoC | 767134 | c.3765C>A | synonymous_variant | 0.25 |
rpoC | 767158 | c.3789T>C | synonymous_variant | 0.24 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.19 |
rpoC | 767191 | c.3822C>G | synonymous_variant | 0.15 |
rpoC | 767221 | c.3852C>G | synonymous_variant | 0.15 |
rpoC | 767233 | c.3864T>C | synonymous_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781628 | c.69T>C | synonymous_variant | 0.2 |
rpsL | 781631 | c.72G>C | synonymous_variant | 0.2 |
rpsL | 781649 | c.90T>C | synonymous_variant | 0.21 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.23 |
rpsL | 781682 | c.123T>C | synonymous_variant | 0.25 |
rpsL | 781700 | c.141G>C | synonymous_variant | 0.23 |
rpsL | 781703 | c.144G>T | synonymous_variant | 0.23 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.24 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.19 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.21 |
rpsL | 781742 | c.183C>T | synonymous_variant | 0.21 |
rpsL | 781748 | c.189C>G | synonymous_variant | 0.22 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.19 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.19 |
rpsL | 781772 | c.213C>A | synonymous_variant | 0.19 |
rpsL | 781808 | c.249C>T | synonymous_variant | 0.19 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.2 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.14 |
rpsL | 781838 | c.279G>C | synonymous_variant | 0.18 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.18 |
rpsL | 781865 | c.306G>C | synonymous_variant | 0.19 |
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 | 0.19 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.2 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.18 |
rpsL | 781916 | c.357T>C | synonymous_variant | 0.18 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.21 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.15 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.17 |
rplC | 800627 | c.-182C>T | upstream_gene_variant | 0.19 |
rplC | 800648 | c.-161A>T | upstream_gene_variant | 0.16 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.16 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.15 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.19 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.16 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.18 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.17 |
rplC | 800747 | c.-62C>G | upstream_gene_variant | 0.17 |
rplC | 800771 | c.-38C>T | upstream_gene_variant | 0.17 |
rplC | 800794 | c.-15A>G | upstream_gene_variant | 0.17 |
rplC | 800796 | c.-13A>G | upstream_gene_variant | 0.17 |
rplC | 800798 | c.-10_-9delGG | upstream_gene_variant | 0.17 |
rplC | 800814 | c.6A>G | synonymous_variant | 0.21 |
rplC | 800817 | c.9A>T | synonymous_variant | 0.22 |
rplC | 800844 | c.36T>C | synonymous_variant | 0.26 |
rplC | 800865 | c.57A>G | synonymous_variant | 0.18 |
rplC | 800867 | p.Ser20Asn | missense_variant | 0.16 |
rplC | 800874 | c.66A>G | synonymous_variant | 0.17 |
rplC | 800875 | p.Val23Ile | missense_variant | 0.17 |
rplC | 800880 | c.72A>G | synonymous_variant | 0.17 |
rplC | 800889 | c.81C>G | synonymous_variant | 0.17 |
rplC | 800892 | c.84G>C | synonymous_variant | 0.17 |
rplC | 801207 | c.399C>T | synonymous_variant | 0.13 |
rplC | 801348 | c.540T>G | synonymous_variant | 0.13 |
fbiC | 1303846 | p.Phe306Val | missense_variant | 0.14 |
fbiC | 1303854 | c.924T>C | synonymous_variant | 0.14 |
fbiC | 1303860 | c.930A>C | synonymous_variant | 0.15 |
fbiC | 1304161 | p.Arg411Ser | missense_variant | 0.21 |
fbiC | 1304169 | c.1239T>C | synonymous_variant | 0.18 |
fbiC | 1304174 | p.Val415Ala | missense_variant | 0.18 |
fbiC | 1304565 | c.1635C>G | synonymous_variant | 0.14 |
fbiC | 1304568 | c.1638T>C | synonymous_variant | 0.15 |
fbiC | 1304580 | c.1650T>C | synonymous_variant | 0.15 |
fbiC | 1304613 | c.1683T>C | synonymous_variant | 0.15 |
fbiC | 1304757 | c.1827A>G | synonymous_variant | 0.14 |
fbiC | 1304778 | c.1848T>C | synonymous_variant | 0.15 |
fbiC | 1304787 | c.1857T>G | synonymous_variant | 0.17 |
fbiC | 1304808 | c.1878C>G | synonymous_variant | 0.27 |
fbiC | 1304811 | c.1881C>G | synonymous_variant | 0.3 |
fbiC | 1304817 | c.1887T>C | synonymous_variant | 0.32 |
fbiC | 1304829 | c.1899T>C | synonymous_variant | 0.24 |
fbiC | 1304832 | c.1902C>T | synonymous_variant | 0.23 |
fbiC | 1304853 | c.1923C>T | synonymous_variant | 0.19 |
fbiC | 1304856 | c.1926C>G | synonymous_variant | 0.19 |
fbiC | 1304869 | c.1939C>T | synonymous_variant | 0.18 |
fbiC | 1304875 | p.Ile649Val | missense_variant | 0.16 |
fbiC | 1304883 | p.Glu651Asp | missense_variant | 0.18 |
fbiC | 1304891 | p.Ile654Thr | missense_variant | 0.15 |
fbiC | 1304893 | p.Gly655Ser | missense_variant | 0.14 |
fbiC | 1304937 | c.2007G>C | synonymous_variant | 0.17 |
fbiC | 1304958 | c.2028T>G | synonymous_variant | 0.22 |
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 | 0.19 |
fbiC | 1305015 | c.2085G>C | synonymous_variant | 0.2 |
fbiC | 1305021 | c.2091C>G | synonymous_variant | 0.2 |
fbiC | 1305030 | c.2100G>C | synonymous_variant | 0.25 |
fbiC | 1305033 | c.2103T>G | synonymous_variant | 0.22 |
fbiC | 1305042 | c.2112A>G | synonymous_variant | 0.2 |
fbiC | 1305063 | c.2133G>C | synonymous_variant | 0.21 |
fbiC | 1305066 | c.2136T>C | synonymous_variant | 0.2 |
fbiC | 1305069 | c.2139G>C | synonymous_variant | 0.17 |
fbiC | 1305114 | c.2184T>C | synonymous_variant | 0.18 |
fbiC | 1305117 | c.2187T>C | synonymous_variant | 0.16 |
fbiC | 1305252 | c.2322G>A | synonymous_variant | 0.17 |
fbiC | 1305276 | c.2346G>C | synonymous_variant | 0.2 |
fbiC | 1305279 | p.His783Gln | missense_variant | 0.2 |
fbiC | 1305282 | c.2352T>C | synonymous_variant | 0.2 |
fbiC | 1305331 | p.Glu801Asn | missense_variant | 0.17 |
fbiC | 1305336 | c.2406T>C | synonymous_variant | 0.18 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
atpE | 1460852 | c.-193C>G | upstream_gene_variant | 0.16 |
atpE | 1460855 | c.-190T>C | upstream_gene_variant | 0.16 |
atpE | 1460858 | c.-187C>G | upstream_gene_variant | 0.16 |
atpE | 1460861 | c.-184C>G | upstream_gene_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1471932 | n.87A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1471969 | n.124T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1473943 | n.286G>T | non_coding_transcript_exon_variant | 0.14 |
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 | 0.24 |
rrl | 1473987 | n.330G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474009 | n.352A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474012 | n.355C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474093 | n.436G>T | non_coding_transcript_exon_variant | 0.16 |
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 | 0.22 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474291 | n.635_649delTTCCTCTCCGGAGGA | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474376 | n.719T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474823 | n.1166C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474904 | n.1247G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474956 | n.1299C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474970 | n.1313G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475006 | n.1349A>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475088 | n.1431A>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475199 | n.1542G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475206 | n.1549C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475209 | n.1552G>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475249 | n.1592T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475252 | n.1595C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475266 | n.1609T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475267 | n.1610G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475275 | n.1618C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475291 | n.1634A>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475369 | n.1712G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475402 | n.1745C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475436 | n.1779C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475659 | n.2002G>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476117 | n.2460G>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476214 | n.2557G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476689 | n.3032A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476690 | n.3033C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476693 | n.3036G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476695 | n.3038T>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476716 | n.3059A>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476726 | n.3069A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476732 | n.3075T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476755 | n.3098G>A | non_coding_transcript_exon_variant | 0.12 |
inhA | 1674846 | p.Ile215Met | missense_variant | 0.17 |
inhA | 1674855 | c.654C>G | synonymous_variant | 0.17 |
inhA | 1674903 | c.702T>C | synonymous_variant | 0.15 |
inhA | 1674904 | p.Ala235Pro | missense_variant | 0.15 |
inhA | 1674909 | c.708G>A | synonymous_variant | 0.14 |
rpsA | 1833595 | c.54T>C | synonymous_variant | 0.14 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.17 |
rpsA | 1833667 | c.126C>G | synonymous_variant | 0.17 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.16 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.16 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.16 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.22 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.2 |
rpsA | 1833748 | c.207C>G | synonymous_variant | 0.18 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.16 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.16 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.16 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 0.2 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.21 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.24 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.23 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.22 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.24 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.16 |
rpsA | 1833940 | c.399C>G | synonymous_variant | 0.17 |
rpsA | 1833971 | c.430C>T | synonymous_variant | 0.15 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.16 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.15 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.14 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.14 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.14 |
rpsA | 1834333 | c.792C>T | synonymous_variant | 0.16 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.15 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.16 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155171 | p.Thr314Asn | missense_variant | 0.98 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2517950 | c.-165C>G | upstream_gene_variant | 0.2 |
kasA | 2518174 | c.60A>G | synonymous_variant | 0.17 |
kasA | 2518190 | p.Ser26Ala | missense_variant | 0.21 |
kasA | 2518199 | p.Ile29Val | missense_variant | 0.22 |
kasA | 2518220 | c.106C>T | synonymous_variant | 0.19 |
kasA | 2518234 | c.120G>A | synonymous_variant | 0.15 |
kasA | 2518248 | p.Ala45Val | missense_variant | 0.15 |
kasA | 2518459 | c.345T>C | synonymous_variant | 0.14 |
kasA | 2518462 | c.348A>C | synonymous_variant | 0.14 |
kasA | 2518468 | c.354A>C | synonymous_variant | 0.16 |
kasA | 2518474 | c.360G>A | synonymous_variant | 0.17 |
kasA | 2518480 | c.366T>C | synonymous_variant | 0.17 |
kasA | 2518483 | c.369C>G | synonymous_variant | 0.16 |
kasA | 2518519 | c.405G>C | synonymous_variant | 0.2 |
kasA | 2518528 | c.414C>G | synonymous_variant | 0.2 |
kasA | 2518540 | c.426T>C | synonymous_variant | 0.16 |
kasA | 2518696 | c.582C>G | synonymous_variant | 0.15 |
kasA | 2518702 | c.588C>T | synonymous_variant | 0.15 |
kasA | 2518744 | c.630C>T | synonymous_variant | 0.18 |
kasA | 2518747 | c.633C>G | synonymous_variant | 0.19 |
kasA | 2518768 | c.654C>T | synonymous_variant | 0.21 |
kasA | 2518777 | c.663C>T | synonymous_variant | 0.22 |
kasA | 2518783 | c.669T>C | synonymous_variant | 0.2 |
kasA | 2518789 | c.675G>C | synonymous_variant | 0.16 |
kasA | 2518792 | c.678C>A | synonymous_variant | 0.14 |
kasA | 2518795 | c.681C>G | synonymous_variant | 0.15 |
kasA | 2518825 | c.711T>C | synonymous_variant | 0.15 |
kasA | 2518864 | c.750G>C | synonymous_variant | 0.16 |
kasA | 2518879 | c.765A>G | synonymous_variant | 0.19 |
kasA | 2518885 | c.771T>C | synonymous_variant | 0.18 |
kasA | 2518898 | c.784T>C | synonymous_variant | 0.19 |
kasA | 2518906 | c.792A>G | synonymous_variant | 0.18 |
kasA | 2518910 | p.Leu266Met | missense_variant | 0.18 |
kasA | 2518921 | c.807T>C | synonymous_variant | 0.18 |
folC | 2747266 | c.333C>T | synonymous_variant | 0.13 |
folC | 2747275 | c.324T>C | synonymous_variant | 0.16 |
folC | 2747289 | p.Pro104Ala | missense_variant | 0.15 |
folC | 2747290 | c.309A>G | synonymous_variant | 0.15 |
folC | 2747293 | c.306G>A | synonymous_variant | 0.15 |
folC | 2747302 | c.297A>G | synonymous_variant | 0.18 |
folC | 2747314 | c.285A>C | synonymous_variant | 0.2 |
folC | 2747317 | c.282C>G | synonymous_variant | 0.19 |
folC | 2747343 | p.Val86Ile | missense_variant | 0.13 |
Rv2752c | 3065955 | p.Leu79Phe | missense_variant | 0.14 |
thyX | 3067379 | c.567C>T | synonymous_variant | 0.14 |
thyX | 3067691 | p.Ile85Met | missense_variant | 0.15 |
thyX | 3067694 | c.252G>C | synonymous_variant | 0.14 |
thyX | 3067702 | p.Ile82Val | missense_variant | 0.19 |
thyX | 3067718 | c.228C>G | synonymous_variant | 0.17 |
thyX | 3067721 | c.225T>C | synonymous_variant | 0.17 |
thyX | 3067727 | c.219A>C | synonymous_variant | 0.18 |
thyX | 3067736 | c.210C>T | synonymous_variant | 0.2 |
thyX | 3067761 | p.Arg62Lys | missense_variant | 0.19 |
thyX | 3067765 | p.Leu61Ile | missense_variant | 0.19 |
thyX | 3067781 | c.165C>G | synonymous_variant | 0.19 |
thyX | 3067793 | c.153T>C | synonymous_variant | 0.17 |
thyX | 3067799 | c.147G>A | synonymous_variant | 0.18 |
thyX | 3067802 | c.144C>G | synonymous_variant | 0.16 |
thyX | 3067814 | c.132T>C | synonymous_variant | 0.18 |
thyX | 3067850 | c.96A>C | synonymous_variant | 0.18 |
thyX | 3067869 | p.Thr26Ser | missense_variant | 0.28 |
thyX | 3067874 | c.72C>G | synonymous_variant | 0.27 |
thyX | 3067877 | c.69G>C | synonymous_variant | 0.26 |
thyX | 3067883 | c.63C>G | synonymous_variant | 0.25 |
thyX | 3067886 | c.60A>C | synonymous_variant | 0.22 |
thyX | 3067889 | c.57C>G | synonymous_variant | 0.23 |
thyX | 3067898 | p.Asp16Glu | missense_variant | 0.22 |
thyA | 3073839 | c.633T>C | synonymous_variant | 0.16 |
thyA | 3073860 | c.612C>G | synonymous_variant | 0.16 |
thyA | 3073863 | c.609T>C | synonymous_variant | 0.16 |
thyA | 3073866 | c.606C>G | synonymous_variant | 0.17 |
thyA | 3073872 | p.Ile200Val | missense_variant | 0.16 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiB | 3642668 | c.1134A>G | synonymous_variant | 0.15 |
rpoA | 3877494 | p.Glu338Asp | missense_variant | 0.14 |
rpoA | 3877503 | c.1005G>C | synonymous_variant | 0.16 |
rpoA | 3877507 | p.Gly334Ala | missense_variant | 0.17 |
rpoA | 3877515 | c.993G>C | synonymous_variant | 0.2 |
rpoA | 3877553 | p.Glu319Gln | missense_variant | 0.26 |
rpoA | 3877571 | p.Pro313Ala | missense_variant | 0.23 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.18 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.15 |
rpoA | 3877679 | p.Ala277Ser | missense_variant | 0.13 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.16 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.14 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.14 |
rpoA | 3878247 | c.261G>C | synonymous_variant | 0.2 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.16 |
rpoA | 3878284 | p.Glu75Ala | missense_variant | 0.17 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.2 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.2 |
rpoA | 3878304 | c.204G>C | synonymous_variant | 0.19 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 0.16 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.18 |
rpoA | 3878331 | c.177A>G | synonymous_variant | 0.16 |
rpoA | 3878346 | c.162T>C | synonymous_variant | 0.15 |
rpoA | 3878364 | c.144A>T | synonymous_variant | 0.21 |
rpoA | 3878367 | c.141C>G | synonymous_variant | 0.21 |
rpoA | 3878376 | c.132G>C | synonymous_variant | 0.15 |
rpoA | 3878385 | c.123C>G | synonymous_variant | 0.16 |
rpoA | 3878388 | c.120C>G | synonymous_variant | 0.16 |
rpoA | 3878391 | c.117T>C | synonymous_variant | 0.16 |
rpoA | 3878415 | c.93C>T | synonymous_variant | 0.2 |
rpoA | 3878424 | c.84G>C | synonymous_variant | 0.21 |
rpoA | 3878436 | c.72A>G | synonymous_variant | 0.23 |
rpoA | 3878442 | c.66G>C | synonymous_variant | 0.17 |
clpC1 | 4038255 | p.Val817Lys | missense_variant | 0.14 |
clpC1 | 4038278 | c.2427T>C | synonymous_variant | 0.17 |
clpC1 | 4038293 | c.2412G>C | synonymous_variant | 0.21 |
clpC1 | 4038302 | c.2403C>G | synonymous_variant | 0.26 |
clpC1 | 4038308 | c.2397G>T | synonymous_variant | 0.22 |
clpC1 | 4038314 | c.2391T>C | synonymous_variant | 0.22 |
clpC1 | 4038317 | c.2388G>C | synonymous_variant | 0.21 |
clpC1 | 4038320 | c.2385G>T | synonymous_variant | 0.21 |
clpC1 | 4038356 | c.2349T>C | synonymous_variant | 0.27 |
clpC1 | 4038359 | c.2346A>G | synonymous_variant | 0.27 |
clpC1 | 4038368 | c.2337T>C | synonymous_variant | 0.24 |
clpC1 | 4038388 | c.2317T>C | synonymous_variant | 0.22 |
clpC1 | 4038392 | c.2313C>T | synonymous_variant | 0.21 |
clpC1 | 4038398 | c.2307G>T | synonymous_variant | 0.2 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 0.18 |
clpC1 | 4038407 | c.2298G>C | synonymous_variant | 0.17 |
clpC1 | 4038419 | c.2286T>C | synonymous_variant | 0.17 |
clpC1 | 4038509 | c.2196C>T | synonymous_variant | 0.12 |
clpC1 | 4038530 | p.Glu725Asp | missense_variant | 0.15 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.26 |
clpC1 | 4038623 | c.2082A>G | synonymous_variant | 0.21 |
clpC1 | 4038640 | p.Asp689Asn | missense_variant | 0.25 |
clpC1 | 4038653 | c.2052C>T | synonymous_variant | 0.23 |
clpC1 | 4038658 | p.Lys683Gln | missense_variant | 0.19 |
clpC1 | 4038661 | p.Ser682Thr | missense_variant | 0.19 |
clpC1 | 4038662 | c.2043T>C | synonymous_variant | 0.19 |
clpC1 | 4038671 | c.2034T>C | synonymous_variant | 0.22 |
clpC1 | 4038683 | c.2022T>C | synonymous_variant | 0.21 |
clpC1 | 4038695 | c.2010C>G | synonymous_variant | 0.17 |
clpC1 | 4038755 | c.1950G>T | synonymous_variant | 0.13 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.24 |
clpC1 | 4038845 | c.1860G>C | synonymous_variant | 0.29 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 0.33 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.37 |
clpC1 | 4038893 | c.1812C>T | synonymous_variant | 0.38 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.33 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.31 |
clpC1 | 4038923 | c.1780_1782delCTAinsTTG | synonymous_variant | 0.3 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.3 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.31 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.3 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.3 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.27 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.19 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.25 |
clpC1 | 4039004 | c.1701C>G | synonymous_variant | 0.27 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.2 |
clpC1 | 4039064 | c.1641C>T | synonymous_variant | 0.17 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.15 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.14 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.14 |
clpC1 | 4039186 | c.1519C>T | synonymous_variant | 0.14 |
clpC1 | 4039226 | c.1479T>C | synonymous_variant | 0.17 |
clpC1 | 4039229 | c.1476C>G | synonymous_variant | 0.2 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.15 |
clpC1 | 4039286 | c.1419T>C | synonymous_variant | 0.16 |
clpC1 | 4039295 | c.1410A>C | synonymous_variant | 0.16 |
clpC1 | 4039298 | c.1407T>C | synonymous_variant | 0.14 |
clpC1 | 4039391 | c.1314T>G | synonymous_variant | 0.14 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.14 |
clpC1 | 4039454 | c.1251A>G | synonymous_variant | 0.18 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 0.17 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.14 |
clpC1 | 4039982 | c.723G>A | synonymous_variant | 0.13 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.15 |
clpC1 | 4040036 | c.669C>G | synonymous_variant | 0.14 |
clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 0.24 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.24 |
clpC1 | 4040105 | c.600C>G | synonymous_variant | 0.29 |
clpC1 | 4040147 | c.558A>G | synonymous_variant | 0.19 |
clpC1 | 4040162 | c.543G>C | synonymous_variant | 0.15 |
clpC1 | 4040201 | c.504C>G | synonymous_variant | 0.17 |
clpC1 | 4040225 | c.480A>C | synonymous_variant | 0.15 |
clpC1 | 4040228 | c.477G>T | synonymous_variant | 0.21 |
clpC1 | 4040237 | c.468C>T | synonymous_variant | 0.21 |
clpC1 | 4040246 | c.459C>G | synonymous_variant | 0.29 |
clpC1 | 4040249 | c.456A>G | synonymous_variant | 0.33 |
clpC1 | 4040267 | c.438A>G | synonymous_variant | 0.3 |
clpC1 | 4040273 | c.432T>C | synonymous_variant | 0.32 |
clpC1 | 4040276 | c.427_429delTCCinsAGT | synonymous_variant | 0.27 |
clpC1 | 4040279 | c.426C>G | synonymous_variant | 0.26 |
clpC1 | 4040291 | c.414G>C | synonymous_variant | 0.23 |
clpC1 | 4040318 | c.387C>G | synonymous_variant | 0.2 |
clpC1 | 4040330 | c.375C>G | synonymous_variant | 0.17 |
clpC1 | 4040477 | c.228G>C | synonymous_variant | 0.14 |
clpC1 | 4040480 | c.225T>G | synonymous_variant | 0.17 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 0.15 |
panD | 4043872 | p.Gly137Val | missense_variant | 0.15 |
panD | 4043876 | p.Leu136Ile | missense_variant | 0.15 |
embC | 4240726 | c.864G>C | synonymous_variant | 0.13 |
embC | 4240780 | c.918T>C | synonymous_variant | 0.16 |
embC | 4240783 | c.921G>C | synonymous_variant | 0.16 |
embC | 4240789 | c.927T>C | synonymous_variant | 0.16 |
embC | 4241053 | c.1191G>C | synonymous_variant | 0.15 |
embC | 4241089 | c.1227C>G | synonymous_variant | 0.23 |
embC | 4241095 | c.1233C>T | synonymous_variant | 0.24 |
embC | 4241107 | c.1245G>C | synonymous_variant | 0.22 |
embC | 4241140 | c.1278A>G | synonymous_variant | 0.17 |
embC | 4241453 | p.Ile531Val | missense_variant | 0.14 |
embC | 4241738 | p.Val626Leu | missense_variant | 0.95 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 0.98 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4245089 | c.1857G>C | synonymous_variant | 0.15 |
embA | 4245101 | c.1869G>C | synonymous_variant | 0.18 |
embA | 4245137 | c.1905T>C | synonymous_variant | 0.21 |
embA | 4245146 | c.1914G>A | synonymous_variant | 0.2 |
embA | 4245149 | c.1917C>G | synonymous_variant | 0.17 |
embA | 4245153 | p.Ile641Val | missense_variant | 0.17 |
embA | 4245182 | c.1950T>C | synonymous_variant | 0.25 |
embA | 4245189 | c.1957C>T | synonymous_variant | 0.25 |
embA | 4245198 | p.Leu656Ile | missense_variant | 0.22 |
embA | 4245207 | c.1975T>C | synonymous_variant | 0.19 |
embA | 4245215 | c.1983A>C | synonymous_variant | 0.2 |
embA | 4245222 | p.Tyr664Gln | missense_variant | 0.21 |
embA | 4245248 | c.2016G>C | synonymous_variant | 0.15 |
embB | 4245704 | c.-810G>C | upstream_gene_variant | 0.15 |
embB | 4245725 | c.-789A>G | upstream_gene_variant | 0.16 |
embB | 4245726 | c.-788T>C | upstream_gene_variant | 0.16 |
embB | 4245737 | c.-777A>C | upstream_gene_variant | 0.15 |
embB | 4245740 | c.-774T>C | upstream_gene_variant | 0.17 |
embB | 4245764 | c.-750G>C | upstream_gene_variant | 0.16 |
embB | 4245851 | c.-663G>C | upstream_gene_variant | 0.15 |
embB | 4245860 | c.-654C>G | upstream_gene_variant | 0.16 |
embA | 4245885 | p.Asp885Asn | missense_variant | 0.14 |
embB | 4245911 | c.-603A>G | upstream_gene_variant | 0.15 |
embB | 4245917 | c.-597G>A | upstream_gene_variant | 0.14 |
embB | 4247539 | c.1026T>C | synonymous_variant | 0.15 |
embB | 4247830 | c.1317A>G | synonymous_variant | 0.18 |
embB | 4247836 | c.1323A>G | synonymous_variant | 0.19 |
embB | 4247839 | c.1326G>C | synonymous_variant | 0.19 |
embB | 4247866 | c.1353G>C | synonymous_variant | 0.16 |
embB | 4247893 | c.1380C>T | synonymous_variant | 0.15 |
embB | 4247899 | p.Met462Ile | missense_variant | 0.21 |
embB | 4247905 | c.1392G>C | synonymous_variant | 0.19 |
embB | 4247909 | c.1396T>C | synonymous_variant | 0.21 |
embB | 4247914 | c.1401G>C | synonymous_variant | 0.23 |
embB | 4247932 | c.1419C>G | synonymous_variant | 0.23 |
embB | 4247940 | p.Leu476Trp | missense_variant | 0.24 |
embB | 4247945 | c.1432T>C | synonymous_variant | 0.24 |
embB | 4247951 | p.Ser480Ala | missense_variant | 0.22 |
embB | 4247956 | c.1443G>C | synonymous_variant | 0.21 |
embB | 4247974 | c.1461C>G | synonymous_variant | 0.2 |
embB | 4248007 | c.1494C>G | synonymous_variant | 0.16 |
embB | 4248011 | p.Ser500Arg | missense_variant | 0.16 |
embB | 4248014 | p.Thr501Ala | missense_variant | 0.15 |
embB | 4248035 | p.Val508Ile | missense_variant | 0.17 |
embB | 4248040 | c.1527C>G | synonymous_variant | 0.15 |
embB | 4248041 | p.Ala510Thr | missense_variant | 0.14 |
embB | 4248044 | p.Lys511Glu | missense_variant | 0.14 |
embB | 4248070 | c.1557T>C | synonymous_variant | 0.19 |
embB | 4248085 | c.1572T>C | synonymous_variant | 0.18 |
embB | 4248097 | c.1584C>G | synonymous_variant | 0.2 |
embB | 4248130 | c.1617G>C | synonymous_variant | 0.18 |
embB | 4248142 | c.1629T>C | synonymous_variant | 0.21 |
embB | 4248143 | c.1630T>C | synonymous_variant | 0.2 |
embB | 4248157 | c.1644A>G | synonymous_variant | 0.21 |
embB | 4248172 | c.1659G>C | synonymous_variant | 0.19 |
embB | 4248220 | c.1707A>C | synonymous_variant | 0.16 |
embB | 4248304 | c.1791G>C | synonymous_variant | 0.25 |
embB | 4248316 | c.1803C>G | synonymous_variant | 0.25 |
embB | 4248319 | c.1806A>G | synonymous_variant | 0.25 |
embB | 4248343 | c.1830G>C | synonymous_variant | 0.19 |
embB | 4248350 | c.1837T>C | synonymous_variant | 0.19 |
embB | 4249417 | c.2904A>G | synonymous_variant | 0.21 |
embB | 4249423 | p.Asp970Glu | missense_variant | 0.21 |
embB | 4249424 | p.Leu971Met | missense_variant | 0.21 |
embB | 4249429 | c.2916C>T | synonymous_variant | 0.18 |
embB | 4249432 | c.2919A>G | synonymous_variant | 0.2 |
embB | 4249441 | c.2928A>G | synonymous_variant | 0.21 |
embB | 4249444 | c.2931T>C | synonymous_variant | 0.21 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 0.98 |
aftB | 4268164 | p.Gln225Glu | missense_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |