Run ID: SRR1510066
Sample name:
Date: 03-04-2023 12:40:49
Number of reads: 5480616
Percentage reads mapped: 78.59
Strain: lineage1.2.1.2.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 0.93 |
lineage1.2.1 | Indo-Oceanic | EAI2 | RD239 | 0.99 |
lineage1.2.1.2 | Indo-Oceanic | NA | RD239 | 0.94 |
lineage1.2.1.2.1 | Indo-Oceanic | NA | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472307 | n.462C>T | non_coding_transcript_exon_variant | 0.23 | streptomycin |
embB | 4247448 | p.His312Arg | missense_variant | 0.15 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6112 | p.Met291Ile | missense_variant | 0.97 |
gyrB | 6169 | c.930C>G | synonymous_variant | 0.15 |
gyrB | 6190 | c.951A>G | synonymous_variant | 0.18 |
gyrB | 6209 | c.970C>T | synonymous_variant | 0.15 |
gyrB | 6217 | c.978G>C | synonymous_variant | 0.14 |
gyrB | 6223 | c.984G>C | synonymous_variant | 0.15 |
gyrB | 6242 | p.Arg335Asn | missense_variant | 0.14 |
gyrB | 6250 | c.1011A>G | synonymous_variant | 0.14 |
gyrB | 6280 | c.1041T>C | synonymous_variant | 0.16 |
gyrB | 6286 | c.1047T>C | synonymous_variant | 0.14 |
gyrA | 6307 | c.-995T>G | upstream_gene_variant | 0.15 |
gyrA | 6319 | c.-983G>C | upstream_gene_variant | 0.16 |
gyrA | 6325 | c.-977C>G | upstream_gene_variant | 0.16 |
gyrA | 6361 | c.-941G>A | upstream_gene_variant | 0.14 |
gyrA | 6706 | c.-596G>A | upstream_gene_variant | 0.14 |
gyrA | 6712 | c.-590G>C | upstream_gene_variant | 0.15 |
gyrA | 6727 | c.-575G>T | upstream_gene_variant | 0.18 |
gyrA | 6730 | c.-572A>G | upstream_gene_variant | 0.18 |
gyrA | 6745 | c.-557T>G | upstream_gene_variant | 0.22 |
gyrA | 6760 | c.-542G>C | upstream_gene_variant | 0.22 |
gyrA | 6778 | c.-524C>T | upstream_gene_variant | 0.17 |
gyrA | 6793 | c.-509T>C | upstream_gene_variant | 0.17 |
gyrB | 6797 | p.Gly520Thr | missense_variant | 0.18 |
gyrA | 6824 | c.-478C>T | upstream_gene_variant | 0.23 |
gyrA | 6841 | c.-461T>C | upstream_gene_variant | 0.24 |
gyrA | 6844 | c.-458T>G | upstream_gene_variant | 0.25 |
gyrA | 6853 | c.-449A>G | upstream_gene_variant | 0.19 |
gyrA | 6856 | c.-446T>C | upstream_gene_variant | 0.19 |
gyrA | 6859 | c.-443T>C | upstream_gene_variant | 0.19 |
gyrA | 6862 | c.-440C>G | upstream_gene_variant | 0.21 |
gyrA | 6878 | c.-424T>C | upstream_gene_variant | 0.21 |
gyrA | 6881 | c.-421T>C | upstream_gene_variant | 0.21 |
gyrA | 6904 | c.-398C>G | upstream_gene_variant | 0.17 |
gyrA | 6910 | c.-392G>A | upstream_gene_variant | 0.15 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7457 | c.156T>C | synonymous_variant | 0.15 |
gyrA | 7490 | c.189C>T | synonymous_variant | 0.14 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 0.98 |
gyrA | 7799 | c.498A>G | synonymous_variant | 0.14 |
gyrA | 8099 | c.798T>C | synonymous_variant | 0.14 |
gyrA | 8111 | c.810G>C | synonymous_variant | 0.17 |
gyrA | 8174 | c.873C>G | synonymous_variant | 0.14 |
gyrA | 8177 | c.876A>C | synonymous_variant | 0.15 |
gyrA | 8294 | c.993T>C | synonymous_variant | 0.16 |
gyrA | 8324 | c.1023T>C | synonymous_variant | 0.17 |
gyrA | 8339 | c.1038A>G | synonymous_variant | 0.17 |
gyrA | 8342 | c.1041G>C | synonymous_variant | 0.16 |
gyrA | 8351 | c.1050C>T | synonymous_variant | 0.2 |
gyrA | 8366 | c.1065G>C | synonymous_variant | 0.2 |
gyrA | 8375 | c.1074G>C | synonymous_variant | 0.18 |
gyrA | 8391 | p.Tyr364His | missense_variant | 0.16 |
gyrA | 8399 | c.1098T>C | synonymous_variant | 0.19 |
gyrA | 8420 | c.1119T>C | synonymous_variant | 0.16 |
gyrA | 8423 | c.1122G>C | synonymous_variant | 0.16 |
gyrA | 8442 | c.1141C>T | synonymous_variant | 0.16 |
gyrA | 8452 | p.Ala384Val | missense_variant | 0.84 |
gyrA | 8462 | c.1161A>G | synonymous_variant | 0.16 |
gyrA | 8498 | c.1197C>T | synonymous_variant | 0.14 |
gyrA | 8519 | c.1218A>C | synonymous_variant | 0.14 |
gyrA | 8619 | c.1318T>C | synonymous_variant | 0.16 |
gyrA | 8624 | c.1323G>C | synonymous_variant | 0.16 |
gyrA | 8627 | c.1326C>G | synonymous_variant | 0.16 |
gyrA | 8636 | c.1335A>C | synonymous_variant | 0.17 |
gyrA | 8642 | c.1341A>G | synonymous_variant | 0.16 |
gyrA | 8645 | c.1344C>G | synonymous_variant | 0.17 |
gyrA | 8672 | c.1371A>G | synonymous_variant | 0.15 |
gyrA | 8810 | c.1509A>C | synonymous_variant | 0.18 |
gyrA | 8829 | c.1528T>C | synonymous_variant | 0.23 |
gyrA | 8852 | c.1551T>C | synonymous_variant | 0.2 |
gyrA | 8858 | c.1557T>C | synonymous_variant | 0.19 |
gyrA | 8867 | c.1566A>G | synonymous_variant | 0.2 |
gyrA | 8870 | c.1569G>C | synonymous_variant | 0.2 |
gyrA | 8873 | c.1572A>C | synonymous_variant | 0.21 |
gyrA | 8897 | c.1596T>C | synonymous_variant | 0.18 |
gyrA | 8903 | c.1602T>C | synonymous_variant | 0.19 |
gyrA | 8915 | c.1614A>G | synonymous_variant | 0.15 |
gyrA | 8918 | c.1617C>G | synonymous_variant | 0.14 |
gyrA | 8966 | c.1665C>G | synonymous_variant | 0.14 |
gyrA | 8967 | p.Ala556Arg | missense_variant | 0.15 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9233 | c.1932C>T | synonymous_variant | 0.14 |
gyrA | 9242 | c.1941A>C | synonymous_variant | 0.16 |
gyrA | 9252 | p.Val651Ile | missense_variant | 0.16 |
gyrA | 9260 | c.1959G>C | synonymous_variant | 0.87 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491144 | p.Ala121Glu | missense_variant | 0.16 |
fgd1 | 491166 | c.384G>C | synonymous_variant | 0.2 |
fgd1 | 491181 | c.399T>C | synonymous_variant | 0.2 |
fgd1 | 491191 | p.Gly137Arg | missense_variant | 0.18 |
fgd1 | 491196 | c.414A>G | synonymous_variant | 0.18 |
fgd1 | 491202 | c.420G>C | synonymous_variant | 0.18 |
fgd1 | 491203 | p.Gln141Glu | missense_variant | 0.18 |
fgd1 | 491212 | p.Ser144Arg | missense_variant | 0.19 |
fgd1 | 491217 | c.435T>C | synonymous_variant | 0.18 |
fgd1 | 491232 | c.450T>C | synonymous_variant | 0.17 |
fgd1 | 491259 | c.477T>C | synonymous_variant | 0.2 |
fgd1 | 491286 | c.504G>C | synonymous_variant | 0.21 |
fgd1 | 491292 | c.510G>C | synonymous_variant | 0.23 |
fgd1 | 491295 | c.513C>G | synonymous_variant | 0.21 |
fgd1 | 491296 | p.Val172Ile | missense_variant | 0.21 |
fgd1 | 491319 | c.537G>C | synonymous_variant | 0.15 |
fgd1 | 491532 | c.750G>T | synonymous_variant | 0.13 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575368 | c.21T>C | synonymous_variant | 1.0 |
ccsA | 620340 | c.450C>G | synonymous_variant | 0.19 |
ccsA | 620349 | c.459A>G | synonymous_variant | 0.2 |
ccsA | 620362 | p.Ala158Thr | missense_variant | 0.21 |
ccsA | 620367 | c.477T>C | synonymous_variant | 0.22 |
ccsA | 620373 | c.483C>G | synonymous_variant | 0.23 |
ccsA | 620385 | c.495G>C | synonymous_variant | 0.22 |
ccsA | 620388 | c.498A>G | synonymous_variant | 0.21 |
ccsA | 620412 | c.522T>C | synonymous_variant | 0.18 |
ccsA | 620415 | c.525T>C | synonymous_variant | 0.18 |
ccsA | 620433 | c.543C>G | synonymous_variant | 0.16 |
ccsA | 620631 | c.741T>C | synonymous_variant | 0.15 |
ccsA | 620646 | c.756G>A | synonymous_variant | 0.15 |
ccsA | 620661 | c.771C>G | synonymous_variant | 0.17 |
rpoB | 760181 | c.375T>C | synonymous_variant | 0.15 |
rpoB | 760196 | c.390C>G | synonymous_variant | 0.14 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.15 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.14 |
rpoB | 760253 | c.447T>C | synonymous_variant | 0.14 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.18 |
rpoB | 760418 | c.612G>C | synonymous_variant | 0.18 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.16 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.17 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.18 |
rpoB | 760481 | c.675G>C | synonymous_variant | 0.17 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.18 |
rpoB | 760522 | p.Ser239Asn | missense_variant | 0.19 |
rpoB | 760532 | c.726T>C | synonymous_variant | 0.16 |
rpoB | 760533 | p.Val243Thr | missense_variant | 0.15 |
rpoB | 760547 | c.741G>C | synonymous_variant | 0.17 |
rpoB | 760563 | p.Arg253Met | missense_variant | 0.17 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.17 |
rpoB | 760611 | c.805T>C | synonymous_variant | 0.17 |
rpoB | 760634 | c.828T>C | synonymous_variant | 0.18 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.16 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.15 |
rpoB | 760670 | c.864G>C | synonymous_variant | 0.16 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.15 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.15 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.16 |
rpoB | 760869 | p.Val355Ile | missense_variant | 0.15 |
rpoB | 760886 | c.1080A>G | synonymous_variant | 0.15 |
rpoB | 760919 | c.1113C>G | synonymous_variant | 0.17 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.17 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 0.17 |
rpoB | 760934 | c.1128C>T | synonymous_variant | 0.18 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.19 |
rpoB | 760970 | c.1164G>C | synonymous_variant | 0.19 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.18 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.17 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.18 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.16 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 0.17 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.18 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.16 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.16 |
rpoB | 761051 | c.1245G>T | synonymous_variant | 0.24 |
rpoB | 761054 | c.1248G>A | synonymous_variant | 0.24 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.23 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.23 |
rpoB | 761063 | c.1257C>G | synonymous_variant | 0.24 |
rpoB | 761097 | c.1291_1292delAGinsTC | synonymous_variant | 0.22 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.23 |
rpoB | 761133 | c.1327_1329delTTGinsCTC | synonymous_variant | 0.17 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.16 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.16 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.16 |
rpoB | 761171 | c.1365C>T | synonymous_variant | 0.18 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.19 |
rpoB | 761183 | c.1377T>G | synonymous_variant | 0.19 |
rpoB | 761189 | c.1383T>G | synonymous_variant | 0.21 |
rpoB | 761222 | c.1416G>C | synonymous_variant | 0.26 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.23 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.25 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.25 |
rpoB | 761297 | c.1491C>T | synonymous_variant | 0.25 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.24 |
rpoB | 761360 | c.1554T>C | synonymous_variant | 0.2 |
rpoB | 761362 | p.Ser519Thr | missense_variant | 0.2 |
rpoB | 761373 | p.Val523His | missense_variant | 0.18 |
rpoB | 761510 | c.1704T>C | synonymous_variant | 0.16 |
rpoB | 761531 | c.1725C>G | synonymous_variant | 0.18 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.19 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.2 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.18 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.19 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.18 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.2 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.22 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.21 |
rpoB | 761645 | c.1839C>G | synonymous_variant | 0.19 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.19 |
rpoB | 761657 | c.1851C>G | synonymous_variant | 0.18 |
rpoB | 761675 | c.1869G>C | synonymous_variant | 0.14 |
rpoB | 761924 | c.2118G>A | synonymous_variant | 0.13 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.15 |
rpoB | 761954 | c.2148C>G | synonymous_variant | 0.17 |
rpoB | 761969 | c.2163G>A | synonymous_variant | 0.19 |
rpoB | 761999 | c.2193G>C | synonymous_variant | 0.17 |
rpoB | 762008 | c.2202C>G | synonymous_variant | 0.17 |
rpoB | 762014 | c.2208C>T | synonymous_variant | 0.17 |
rpoB | 762017 | c.2211A>G | synonymous_variant | 0.17 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.15 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.15 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.15 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.16 |
rpoB | 762218 | c.2412T>G | synonymous_variant | 0.16 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.17 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.2 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.21 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.21 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.16 |
rpoB | 762329 | c.2523G>C | synonymous_variant | 0.16 |
rpoB | 762338 | c.2532T>C | synonymous_variant | 0.14 |
rpoB | 762347 | c.2541T>C | synonymous_variant | 0.15 |
rpoC | 762395 | c.-975G>C | upstream_gene_variant | 0.14 |
rpoC | 762410 | c.-960T>C | upstream_gene_variant | 0.15 |
rpoC | 762443 | c.-927G>T | upstream_gene_variant | 0.13 |
rpoC | 762533 | c.-837T>C | upstream_gene_variant | 0.14 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.31 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.2 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.2 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.18 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.19 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.2 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.28 |
rpoC | 763076 | c.-294C>G | upstream_gene_variant | 0.28 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.29 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.24 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.19 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.19 |
rpoC | 763158 | c.-212C>T | upstream_gene_variant | 0.2 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.21 |
rpoC | 763169 | c.-201A>G | upstream_gene_variant | 0.2 |
rpoC | 763206 | c.-164_-162delAGTinsTCC | upstream_gene_variant | 0.15 |
rpoC | 763214 | c.-156T>C | upstream_gene_variant | 0.2 |
rpoC | 763226 | c.-144A>G | upstream_gene_variant | 0.2 |
rpoC | 763238 | c.-132T>C | upstream_gene_variant | 0.19 |
rpoC | 763402 | c.33C>G | synonymous_variant | 0.17 |
rpoC | 763411 | c.42T>G | synonymous_variant | 0.17 |
rpoC | 763414 | c.45T>C | synonymous_variant | 0.16 |
rpoC | 763441 | c.72C>G | synonymous_variant | 0.2 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.19 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.22 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.21 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.19 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.23 |
rpoC | 763531 | c.162G>C | synonymous_variant | 0.77 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.26 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.27 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.26 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.22 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.22 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.21 |
rpoC | 763658 | c.289_291delCTTinsTTG | synonymous_variant | 0.2 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.2 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.21 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.2 |
rpoC | 763708 | c.339G>A | synonymous_variant | 0.18 |
rpoC | 763709 | c.340C>T | synonymous_variant | 0.18 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.19 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.2 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.21 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.21 |
rpoC | 763735 | c.366G>C | synonymous_variant | 0.23 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.21 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.19 |
rpoC | 763768 | c.399C>G | synonymous_variant | 0.19 |
rpoC | 763780 | c.411C>G | synonymous_variant | 0.17 |
rpoC | 763783 | c.414G>C | synonymous_variant | 0.18 |
rpoC | 763801 | c.432C>G | synonymous_variant | 0.15 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.15 |
rpoC | 763819 | c.450G>C | synonymous_variant | 0.17 |
rpoC | 763831 | c.462A>G | synonymous_variant | 0.15 |
rpoC | 763884 | p.Ala172Val | missense_variant | 0.9 |
rpoC | 763886 | c.517C>A | synonymous_variant | 0.9 |
rpoC | 763960 | c.591T>C | synonymous_variant | 0.16 |
rpoC | 763967 | p.Gly200Ser | missense_variant | 0.18 |
rpoC | 763978 | c.609C>G | synonymous_variant | 0.2 |
rpoC | 763996 | c.627T>C | synonymous_variant | 0.22 |
rpoC | 764005 | c.636G>C | synonymous_variant | 0.23 |
rpoC | 764011 | c.642T>C | synonymous_variant | 0.22 |
rpoC | 764015 | c.646C>T | synonymous_variant | 0.23 |
rpoC | 764024 | c.655T>C | synonymous_variant | 0.25 |
rpoC | 764040 | p.Ser224Asn | missense_variant | 0.24 |
rpoC | 764044 | c.675T>C | synonymous_variant | 0.25 |
rpoC | 764059 | c.690G>C | synonymous_variant | 0.25 |
rpoC | 764083 | c.714A>G | synonymous_variant | 0.26 |
rpoC | 764098 | c.729A>G | synonymous_variant | 0.23 |
rpoC | 764101 | c.732C>G | synonymous_variant | 0.22 |
rpoC | 764110 | c.741C>T | synonymous_variant | 0.2 |
rpoC | 764131 | c.762T>C | synonymous_variant | 0.17 |
rpoC | 764161 | c.792G>C | synonymous_variant | 0.16 |
rpoC | 764188 | c.819A>G | synonymous_variant | 0.17 |
rpoC | 764195 | p.Ser276Gln | missense_variant | 0.17 |
rpoC | 764203 | c.834G>T | synonymous_variant | 0.18 |
rpoC | 764206 | c.837T>C | synonymous_variant | 0.18 |
rpoC | 764257 | c.888G>C | synonymous_variant | 0.19 |
rpoC | 764269 | c.900G>C | synonymous_variant | 0.16 |
rpoC | 764282 | c.913_915delTCGinsAGC | synonymous_variant | 0.17 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.18 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.16 |
rpoC | 764381 | c.1012_1013delTCinsAG | synonymous_variant | 0.15 |
rpoC | 764389 | p.Leu340Phe | missense_variant | 0.14 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.15 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.15 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.16 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.15 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.15 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.18 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.19 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.21 |
rpoC | 764695 | c.1326T>C | synonymous_variant | 0.15 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.16 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.16 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.17 |
rpoC | 764791 | c.1422C>G | synonymous_variant | 0.23 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.2 |
rpoC | 764812 | c.1443C>G | synonymous_variant | 0.2 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.2 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 0.19 |
rpoC | 764830 | c.1461C>G | synonymous_variant | 0.2 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.19 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.14 |
rpoC | 764923 | c.1554A>G | synonymous_variant | 0.16 |
rpoC | 764932 | c.1563C>A | synonymous_variant | 0.16 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.15 |
rpoC | 765404 | p.Leu679Val | missense_variant | 0.14 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.17 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.16 |
rpoC | 765508 | c.2139C>G | synonymous_variant | 0.19 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.17 |
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 | 0.18 |
rpoC | 765578 | c.2209C>T | synonymous_variant | 0.19 |
rpoC | 765583 | c.2214G>T | synonymous_variant | 0.2 |
rpoC | 765613 | p.His748Gln | missense_variant | 0.16 |
rpoC | 765625 | c.2256C>G | synonymous_variant | 0.17 |
rpoC | 765628 | c.2259G>C | synonymous_variant | 0.16 |
rpoC | 765631 | p.Asp754Glu | missense_variant | 0.16 |
rpoC | 765658 | c.2289C>T | synonymous_variant | 0.2 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.19 |
rpoC | 765734 | c.2365T>C | synonymous_variant | 0.18 |
rpoC | 765739 | c.2370G>C | synonymous_variant | 0.16 |
rpoC | 765772 | c.2403C>G | synonymous_variant | 0.14 |
rpoC | 765796 | c.2427C>T | synonymous_variant | 0.13 |
rpoC | 765814 | c.2445A>G | synonymous_variant | 0.13 |
rpoC | 765826 | c.2457T>C | synonymous_variant | 0.15 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 0.16 |
rpoC | 765883 | c.2514C>G | synonymous_variant | 0.17 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.18 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.2 |
rpoC | 765928 | c.2559C>G | synonymous_variant | 0.15 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.15 |
rpoC | 766069 | c.2700G>A | synonymous_variant | 0.14 |
rpoC | 766082 | p.Ala905Gln | missense_variant | 0.16 |
rpoC | 766096 | c.2727G>C | synonymous_variant | 0.16 |
rpoC | 766105 | c.2736C>T | synonymous_variant | 0.14 |
rpoC | 766135 | c.2766G>A | synonymous_variant | 0.13 |
rpoC | 766345 | c.2976T>C | synonymous_variant | 0.14 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.17 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.16 |
rpoC | 766390 | c.3021C>T | synonymous_variant | 0.16 |
rpoC | 766408 | c.3039C>T | synonymous_variant | 0.14 |
rpoC | 766444 | c.3075C>G | synonymous_variant | 0.21 |
rpoC | 766447 | c.3078T>C | synonymous_variant | 0.21 |
rpoC | 766484 | p.Val1039Ile | missense_variant | 0.13 |
rpoC | 766489 | c.3120G>T | synonymous_variant | 0.13 |
rpoC | 766495 | c.3126C>T | synonymous_variant | 0.15 |
rpoC | 766522 | c.3153C>G | synonymous_variant | 0.16 |
rpoC | 766573 | c.3204T>C | synonymous_variant | 0.16 |
rpoC | 766583 | p.Gly1072Ser | missense_variant | 0.15 |
rpoC | 766588 | c.3219G>A | synonymous_variant | 0.15 |
rpoC | 766591 | c.3222A>G | synonymous_variant | 0.16 |
rpoC | 766607 | p.Ile1080Leu | missense_variant | 0.19 |
rpoC | 766630 | c.3261G>C | synonymous_variant | 0.2 |
rpoC | 766645 | c.3276A>G | synonymous_variant | 0.25 |
rpoC | 766651 | c.3282T>C | synonymous_variant | 0.24 |
rpoC | 766657 | c.3288A>G | synonymous_variant | 0.22 |
rpoC | 766672 | c.3303T>C | synonymous_variant | 0.18 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.18 |
rpoC | 766738 | c.3369G>T | synonymous_variant | 0.21 |
rpoC | 766750 | c.3381C>G | synonymous_variant | 0.22 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.24 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.28 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.29 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 0.19 |
rpoC | 766864 | c.3495G>C | synonymous_variant | 0.19 |
rpoC | 766894 | c.3525T>C | synonymous_variant | 0.2 |
rpoC | 766895 | c.3526T>C | synonymous_variant | 0.19 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.2 |
rpoC | 766903 | c.3534C>T | synonymous_variant | 0.19 |
rpoC | 766918 | c.3549C>T | synonymous_variant | 0.21 |
rpoC | 766933 | c.3564A>G | synonymous_variant | 0.18 |
rpoC | 766942 | c.3573C>T | synonymous_variant | 0.17 |
rpoC | 766945 | c.3576A>G | synonymous_variant | 0.16 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.14 |
rpoC | 766972 | c.3603G>C | synonymous_variant | 0.18 |
rpoC | 766978 | c.3609C>G | synonymous_variant | 0.19 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.23 |
rpoC | 767009 | c.3640_3642delTCGinsAGC | synonymous_variant | 0.23 |
rpoC | 767014 | c.3645G>C | synonymous_variant | 0.24 |
rpoC | 767033 | c.3664_3666delTCGinsAGT | synonymous_variant | 0.29 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.31 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.32 |
rpoC | 767074 | c.3705T>C | synonymous_variant | 0.29 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.28 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.26 |
rpoC | 767134 | c.3765C>G | synonymous_variant | 0.2 |
rpoC | 767158 | c.3789T>G | synonymous_variant | 0.14 |
rpoC | 767167 | c.3798C>G | synonymous_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775981 | p.Leu834Met | missense_variant | 0.15 |
mmpL5 | 776009 | c.2472A>G | synonymous_variant | 0.14 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781631 | c.72G>C | synonymous_variant | 0.17 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.14 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.16 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.16 |
rpsL | 781751 | c.192G>C | synonymous_variant | 0.19 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.18 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.18 |
rpsL | 781793 | c.234G>C | synonymous_variant | 0.22 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.19 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.19 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.17 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.15 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.15 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.16 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.16 |
rpsL | 781916 | c.357T>C | synonymous_variant | 0.15 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.15 |
rplC | 800648 | c.-161A>C | upstream_gene_variant | 0.17 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.17 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.22 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.22 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.21 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.19 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.21 |
rplC | 800738 | c.-71T>C | upstream_gene_variant | 0.18 |
rplC | 800747 | c.-62C>G | upstream_gene_variant | 0.18 |
rplC | 800771 | c.-38C>T | upstream_gene_variant | 0.16 |
rplC | 800817 | c.9A>T | synonymous_variant | 0.14 |
rplC | 800844 | c.36T>C | synonymous_variant | 0.15 |
rplC | 800889 | c.81C>G | synonymous_variant | 0.15 |
rplC | 800907 | c.99C>G | synonymous_variant | 0.18 |
rplC | 800916 | c.108A>G | synonymous_variant | 0.18 |
rplC | 800939 | p.Arg44His | missense_variant | 0.13 |
rplC | 800955 | c.147C>G | synonymous_variant | 0.15 |
rplC | 800967 | c.159C>G | synonymous_variant | 0.14 |
rplC | 800982 | c.174C>T | synonymous_variant | 0.14 |
rplC | 801222 | c.414T>C | synonymous_variant | 0.15 |
fbiC | 1303836 | c.906G>C | synonymous_variant | 0.14 |
fbiC | 1303854 | c.924T>C | synonymous_variant | 0.15 |
fbiC | 1303860 | c.930A>C | synonymous_variant | 0.15 |
fbiC | 1303923 | c.993C>T | synonymous_variant | 0.14 |
fbiC | 1303929 | c.999G>C | synonymous_variant | 0.17 |
fbiC | 1303947 | c.1017T>C | synonymous_variant | 0.16 |
fbiC | 1303948 | p.Gly340Arg | missense_variant | 0.16 |
fbiC | 1303969 | p.Val347Ile | missense_variant | 0.17 |
fbiC | 1303973 | p.Gly348Ala | missense_variant | 0.17 |
fbiC | 1303981 | p.Val351Ile | missense_variant | 0.16 |
fbiC | 1303995 | c.1065C>T | synonymous_variant | 0.16 |
Rv1258c | 1406312 | c.1029T>C | synonymous_variant | 1.0 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
atpE | 1460907 | c.-138T>C | upstream_gene_variant | 0.99 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1471969 | n.124T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473756 | n.99G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473813 | n.156C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1473839 | n.182G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1473899 | n.242A>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1473937 | n.280C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1473944 | n.287G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473945 | n.288T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474009 | n.352A>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474012 | n.355C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474051 | n.394T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474054 | n.397T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474056 | n.399T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474104 | n.447G>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474111 | n.454T>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474112 | n.455T>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474376 | n.719T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.34 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474823 | n.1166C>T | non_coding_transcript_exon_variant | 0.34 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474904 | n.1247G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474956 | n.1299C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474959 | n.1302C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474962 | n.1306delG | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474970 | n.1313G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474991 | n.1334T>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475006 | n.1349A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475088 | n.1431A>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475199 | n.1542G>A | non_coding_transcript_exon_variant | 0.37 |
rrl | 1475206 | n.1549C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475209 | n.1552G>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475249 | n.1592T>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475252 | n.1595C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475266 | n.1609T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475271 | n.1614A>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475273 | n.1616T>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475275 | n.1618C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475276 | n.1619T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475291 | n.1634A>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475313 | n.1656G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475333 | n.1676T>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475369 | n.1712G>C | non_coding_transcript_exon_variant | 0.34 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.37 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475638 | n.1981C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 0.34 |
rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 0.34 |
rrl | 1475659 | n.2002G>T | non_coding_transcript_exon_variant | 0.34 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475819 | n.2162C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476025 | n.2368G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476033 | n.2376T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476034 | n.2377C>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476089 | n.2432T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476095 | n.2438C>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476117 | n.2460G>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476693 | n.3036G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476695 | n.3038T>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476716 | n.3059A>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476723 | n.3066T>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476725 | n.3068C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476726 | n.3069A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476732 | n.3075T>C | non_coding_transcript_exon_variant | 0.17 |
inhA | 1674162 | c.-40C>T | upstream_gene_variant | 1.0 |
inhA | 1674321 | c.120G>C | synonymous_variant | 0.15 |
inhA | 1674537 | c.336C>G | synonymous_variant | 0.15 |
inhA | 1674542 | p.Ala114Glu | missense_variant | 0.15 |
inhA | 1674555 | c.354G>A | synonymous_variant | 0.14 |
inhA | 1674561 | c.360C>T | synonymous_variant | 0.14 |
inhA | 1674564 | c.363C>T | synonymous_variant | 0.15 |
inhA | 1674636 | c.435C>G | synonymous_variant | 0.15 |
inhA | 1674639 | c.438C>T | synonymous_variant | 0.15 |
inhA | 1674654 | c.453G>C | synonymous_variant | 0.17 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.16 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.15 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.15 |
rpsA | 1833790 | c.249T>A | synonymous_variant | 0.13 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.14 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.14 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.16 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.17 |
rpsA | 1833862 | c.321G>T | synonymous_variant | 0.19 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.17 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.17 |
rpsA | 1833940 | c.399C>G | synonymous_variant | 0.2 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.2 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.21 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.19 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.2 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.21 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.15 |
rpsA | 1834297 | c.756C>G | synonymous_variant | 0.19 |
rpsA | 1834303 | c.762T>G | synonymous_variant | 0.2 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.2 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.19 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.15 |
rpsA | 1834375 | c.834G>A | synonymous_variant | 0.14 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.15 |
rpsA | 1834465 | c.924T>C | synonymous_variant | 0.14 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.15 |
rpsA | 1834474 | c.933C>G | synonymous_variant | 0.15 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.15 |
rpsA | 1834498 | c.957C>T | synonymous_variant | 0.16 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.17 |
rpsA | 1834555 | c.1014T>C | synonymous_variant | 0.14 |
rpsA | 1834624 | c.1083G>C | synonymous_variant | 0.14 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.14 |
rpsA | 1834753 | c.1212T>C | synonymous_variant | 0.15 |
rpsA | 1834765 | c.1224A>G | synonymous_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102050 | c.993T>C | synonymous_variant | 0.17 |
ndh | 2102053 | c.990G>C | synonymous_variant | 0.17 |
ndh | 2102059 | c.984T>C | synonymous_variant | 0.15 |
ndh | 2102242 | c.801G>A | synonymous_variant | 0.13 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2517947 | c.-168C>T | upstream_gene_variant | 0.13 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2519048 | p.Gly312Ser | missense_variant | 0.99 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
ahpC | 2726657 | c.465A>C | synonymous_variant | 0.14 |
folC | 2747065 | c.534C>G | synonymous_variant | 0.14 |
Rv2752c | 3066066 | c.126T>C | synonymous_variant | 0.14 |
thyX | 3067316 | c.630A>G | synonymous_variant | 0.16 |
thyA | 3073872 | p.Ile200Val | missense_variant | 0.15 |
thyA | 3073878 | c.594G>A | synonymous_variant | 0.15 |
thyA | 3073902 | c.570C>G | synonymous_variant | 0.15 |
thyA | 3073925 | c.547T>C | synonymous_variant | 0.14 |
thyA | 3073926 | c.546G>C | synonymous_variant | 0.14 |
thyA | 3073929 | c.543T>C | synonymous_variant | 0.16 |
thyA | 3073953 | c.519T>C | synonymous_variant | 0.19 |
thyA | 3073977 | c.495A>G | synonymous_variant | 0.18 |
thyA | 3073989 | c.483T>C | synonymous_variant | 0.17 |
thyA | 3074001 | c.471C>G | synonymous_variant | 0.16 |
thyA | 3074004 | c.468T>C | synonymous_variant | 0.16 |
thyA | 3074010 | c.462C>G | synonymous_variant | 0.17 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339417 | c.300A>G | synonymous_variant | 1.0 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
fprA | 3473809 | c.-198G>C | upstream_gene_variant | 0.19 |
fprA | 3473812 | c.-195G>A | upstream_gene_variant | 0.19 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
whiB7 | 3568488 | c.191delG | frameshift_variant | 1.0 |
fbiB | 3640557 | c.-978T>C | upstream_gene_variant | 0.99 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.17 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.16 |
rpoA | 3877638 | c.870T>C | synonymous_variant | 0.16 |
rpoA | 3877656 | c.852T>C | synonymous_variant | 0.15 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.14 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.19 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.19 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.19 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.2 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.2 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.2 |
rpoA | 3877830 | c.678C>T | synonymous_variant | 0.19 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.16 |
rpoA | 3877857 | c.651G>A | synonymous_variant | 0.16 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.16 |
rpoA | 3877872 | c.636C>T | synonymous_variant | 0.15 |
rpoA | 3877953 | c.555G>A | synonymous_variant | 0.14 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.15 |
rpoA | 3877986 | c.522G>C | synonymous_variant | 0.16 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.17 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.19 |
rpoA | 3878022 | c.486T>C | synonymous_variant | 0.16 |
rpoA | 3878025 | c.483C>T | synonymous_variant | 0.17 |
rpoA | 3878028 | c.480G>C | synonymous_variant | 0.17 |
rpoA | 3878031 | c.477T>C | synonymous_variant | 0.17 |
rpoA | 3878040 | c.468T>C | synonymous_variant | 0.17 |
rpoA | 3878046 | c.462T>C | synonymous_variant | 0.16 |
rpoA | 3878049 | c.459G>C | synonymous_variant | 0.15 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.16 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.16 |
rpoA | 3878067 | c.441C>G | synonymous_variant | 0.16 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.16 |
rpoA | 3878082 | c.426T>C | synonymous_variant | 0.18 |
rpoA | 3878094 | c.414C>G | synonymous_variant | 0.18 |
rpoA | 3878100 | c.408C>G | synonymous_variant | 0.16 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.16 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.17 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.16 |
rpoA | 3878141 | p.Met123Leu | missense_variant | 0.17 |
rpoA | 3878142 | p.Gly122Glu | missense_variant | 0.17 |
rpoA | 3878169 | c.339G>C | synonymous_variant | 0.15 |
rpoA | 3878220 | c.288C>T | synonymous_variant | 0.13 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.2 |
rpoA | 3878284 | p.Glu75Ala | missense_variant | 0.17 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.18 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.19 |
rpoA | 3878304 | c.204G>C | synonymous_variant | 0.18 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 0.18 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.24 |
rpoA | 3878331 | c.177A>G | synonymous_variant | 0.23 |
rpoA | 3878334 | c.174T>C | synonymous_variant | 0.23 |
rpoA | 3878337 | c.171T>C | synonymous_variant | 0.24 |
rpoA | 3878346 | c.162T>C | synonymous_variant | 0.3 |
rpoA | 3878364 | c.144A>G | synonymous_variant | 0.31 |
rpoA | 3878367 | c.141C>G | synonymous_variant | 0.31 |
rpoA | 3878370 | c.138T>C | synonymous_variant | 0.31 |
rpoA | 3878376 | c.132G>C | synonymous_variant | 0.35 |
rpoA | 3878385 | c.123C>G | synonymous_variant | 0.36 |
rpoA | 3878391 | c.117T>C | synonymous_variant | 0.35 |
rpoA | 3878396 | c.112C>T | synonymous_variant | 0.34 |
rpoA | 3878436 | c.72A>G | synonymous_variant | 0.34 |
rpoA | 3878442 | c.66G>C | synonymous_variant | 0.29 |
rpoA | 3878454 | c.54A>C | synonymous_variant | 0.25 |
rpoA | 3878472 | p.Asp12Glu | missense_variant | 0.2 |
rpoA | 3878478 | c.30C>G | synonymous_variant | 0.17 |
rpoA | 3878490 | c.18C>A | synonymous_variant | 0.15 |
rpoA | 3878496 | c.12A>T | synonymous_variant | 0.14 |
rpoA | 3878665 | c.-158A>G | upstream_gene_variant | 0.17 |
rpoA | 3878672 | c.-165A>T | upstream_gene_variant | 0.18 |
rpoA | 3878698 | c.-191A>G | upstream_gene_variant | 0.17 |
rpoA | 3878701 | c.-194C>G | upstream_gene_variant | 0.17 |
clpC1 | 4038302 | c.2403C>G | synonymous_variant | 0.16 |
clpC1 | 4038347 | c.2358G>C | synonymous_variant | 0.17 |
clpC1 | 4038356 | c.2349T>C | synonymous_variant | 0.15 |
clpC1 | 4038398 | c.2307G>T | synonymous_variant | 0.14 |
clpC1 | 4038419 | c.2286T>C | synonymous_variant | 0.16 |
clpC1 | 4038434 | c.2271G>C | synonymous_variant | 0.17 |
clpC1 | 4038444 | p.Ala754Lys | missense_variant | 0.16 |
clpC1 | 4038446 | c.2259T>C | synonymous_variant | 0.15 |
clpC1 | 4038452 | c.2253G>C | synonymous_variant | 0.15 |
clpC1 | 4038461 | p.Ala748Asp | missense_variant | 0.16 |
clpC1 | 4038498 | p.Ser736Thr | missense_variant | 0.21 |
clpC1 | 4038530 | p.Glu725Asp | missense_variant | 0.18 |
clpC1 | 4038536 | c.2169C>T | synonymous_variant | 0.19 |
clpC1 | 4038611 | c.2094C>T | synonymous_variant | 0.14 |
clpC1 | 4038640 | p.Asp689Asn | missense_variant | 0.13 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.15 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 0.15 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.19 |
clpC1 | 4038815 | c.1890G>T | synonymous_variant | 0.19 |
clpC1 | 4038851 | c.1854G>A | synonymous_variant | 0.2 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.15 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.15 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.15 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.15 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.18 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.17 |
clpC1 | 4039090 | c.1615C>T | synonymous_variant | 0.14 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.15 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.16 |
clpC1 | 4039124 | c.1581C>G | synonymous_variant | 0.17 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.16 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.16 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.16 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.16 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.19 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.18 |
clpC1 | 4039187 | c.1518G>C | synonymous_variant | 0.18 |
clpC1 | 4039190 | c.1515C>G | synonymous_variant | 0.16 |
clpC1 | 4039208 | c.1497C>G | synonymous_variant | 0.17 |
clpC1 | 4039226 | c.1479T>C | synonymous_variant | 0.14 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.15 |
clpC1 | 4039524 | p.Phe394Tyr | missense_variant | 0.14 |
clpC1 | 4039547 | c.1158C>G | synonymous_variant | 0.16 |
clpC1 | 4039553 | c.1152C>G | synonymous_variant | 0.17 |
clpC1 | 4039562 | c.1143C>G | synonymous_variant | 0.17 |
clpC1 | 4039565 | c.1140G>C | synonymous_variant | 0.17 |
clpC1 | 4039576 | p.Ala377Ser | missense_variant | 0.17 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.18 |
clpC1 | 4039586 | c.1119G>C | synonymous_variant | 0.2 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.19 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.16 |
clpC1 | 4039622 | c.1083C>G | synonymous_variant | 0.18 |
clpC1 | 4039682 | c.1023C>G | synonymous_variant | 0.18 |
clpC1 | 4039685 | c.1020C>T | synonymous_variant | 0.17 |
clpC1 | 4039733 | c.972G>A | synonymous_variant | 0.13 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.14 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.18 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.16 |
clpC1 | 4039928 | c.775_777delAGCinsTCG | synonymous_variant | 0.16 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.16 |
clpC1 | 4039946 | c.759A>T | synonymous_variant | 0.18 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.19 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.2 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.15 |
clpC1 | 4039996 | p.Glu237Gln | missense_variant | 0.15 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.17 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.17 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.19 |
clpC1 | 4040036 | c.669C>G | synonymous_variant | 0.19 |
clpC1 | 4040090 | p.Ser205Thr | missense_variant | 0.14 |
clpC1 | 4040267 | c.438A>G | synonymous_variant | 0.21 |
clpC1 | 4040273 | c.432T>C | synonymous_variant | 0.21 |
clpC1 | 4040354 | c.351A>G | synonymous_variant | 0.17 |
clpC1 | 4040450 | c.255A>G | synonymous_variant | 0.14 |
clpC1 | 4040459 | c.246C>G | synonymous_variant | 0.15 |
clpC1 | 4040465 | c.240T>C | synonymous_variant | 0.18 |
clpC1 | 4040471 | c.234T>C | synonymous_variant | 0.19 |
clpC1 | 4040477 | c.228G>A | synonymous_variant | 0.18 |
clpC1 | 4040480 | c.225T>C | synonymous_variant | 0.19 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 0.89 |
clpC1 | 4040699 | c.6C>T | synonymous_variant | 0.13 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4240780 | c.918T>C | synonymous_variant | 0.21 |
embC | 4240783 | c.921G>C | synonymous_variant | 0.21 |
embC | 4240789 | c.927T>C | synonymous_variant | 0.19 |
embC | 4240819 | c.957A>G | synonymous_variant | 0.24 |
embC | 4240825 | c.963G>A | synonymous_variant | 0.26 |
embC | 4240831 | c.969T>G | synonymous_variant | 0.27 |
embC | 4240867 | c.1005T>G | synonymous_variant | 0.2 |
embC | 4240870 | c.1008T>C | synonymous_variant | 0.2 |
embC | 4240879 | c.1017G>C | synonymous_variant | 0.19 |
embC | 4240880 | p.Ala340Thr | missense_variant | 0.18 |
embC | 4240885 | c.1023T>C | synonymous_variant | 0.16 |
embC | 4240897 | c.1035C>G | synonymous_variant | 0.14 |
embC | 4240990 | c.1128A>G | synonymous_variant | 0.15 |
embC | 4241017 | c.1155T>C | synonymous_variant | 0.19 |
embC | 4241023 | c.1161T>G | synonymous_variant | 0.17 |
embC | 4241026 | c.1164C>G | synonymous_variant | 0.14 |
embC | 4241035 | c.1173G>A | synonymous_variant | 0.19 |
embC | 4241042 | p.Asn394Asp | missense_variant | 0.83 |
embC | 4241050 | c.1188T>G | synonymous_variant | 0.18 |
embC | 4241104 | c.1242G>A | synonymous_variant | 0.17 |
embC | 4241107 | c.1245G>C | synonymous_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243580 | c.348G>A | synonymous_variant | 1.0 |
embA | 4244420 | c.1188G>C | synonymous_variant | 0.98 |
embA | 4245089 | c.1857G>C | synonymous_variant | 0.15 |
embA | 4245092 | c.1860C>G | synonymous_variant | 0.16 |
embA | 4245101 | c.1869G>C | synonymous_variant | 0.18 |
embA | 4245137 | c.1905T>C | synonymous_variant | 0.16 |
embA | 4245149 | c.1917C>G | synonymous_variant | 0.17 |
embA | 4245182 | c.1950T>C | synonymous_variant | 0.15 |
embB | 4245845 | c.-669T>G | upstream_gene_variant | 0.15 |
embB | 4245848 | c.-666C>G | upstream_gene_variant | 0.18 |
embB | 4245860 | c.-654C>G | upstream_gene_variant | 0.16 |
embA | 4245885 | p.Asp885Asn | missense_variant | 0.15 |
embA | 4245969 | p.Pro913Ser | missense_variant | 0.99 |
embB | 4247437 | c.924A>G | synonymous_variant | 0.15 |
embB | 4247440 | c.927C>G | synonymous_variant | 0.15 |
embB | 4247464 | c.951C>G | synonymous_variant | 0.15 |
embB | 4247470 | c.957T>C | synonymous_variant | 0.15 |
embB | 4247491 | c.978G>C | synonymous_variant | 0.15 |
embB | 4247497 | c.984T>C | synonymous_variant | 0.14 |
embB | 4247578 | c.1065G>A | synonymous_variant | 0.93 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4247776 | c.1263G>T | synonymous_variant | 0.14 |
embB | 4247779 | c.1266C>G | synonymous_variant | 0.14 |
embB | 4248085 | c.1572T>C | synonymous_variant | 0.19 |
embB | 4248097 | c.1584C>G | synonymous_variant | 0.21 |
embB | 4248118 | c.1605T>C | synonymous_variant | 0.22 |
embB | 4248127 | c.1614G>C | synonymous_variant | 0.21 |
embB | 4248133 | c.1620C>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 | 0.23 |
embB | 4248206 | p.Ser565Gly | missense_variant | 0.2 |
embB | 4248220 | c.1707A>G | synonymous_variant | 0.21 |
embB | 4248241 | c.1728C>T | synonymous_variant | 0.2 |
embB | 4248304 | c.1791G>C | synonymous_variant | 0.15 |
embB | 4248316 | c.1803C>G | synonymous_variant | 0.14 |
embB | 4248322 | c.1809G>C | synonymous_variant | 0.14 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ubiA | 4269864 | c.-32delG | upstream_gene_variant | 0.99 |
whiB6 | 4338361 | p.Arg54Gln | missense_variant | 1.0 |
whiB6 | 4338592 | c.-71G>A | upstream_gene_variant | 0.32 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407735 | c.467delA | frameshift_variant | 0.15 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |