Run ID: ERR1023502
Sample name:
Date: 31-03-2023 09:24:34
Number of reads: 233512
Percentage reads mapped: 4.48
Strain: lineage2.2.1
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 0.17 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.1 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761127 | p.Ser441Ala | missense_variant | 0.64 | rifampicin |
rpoB | 761139 | p.His445Tyr | missense_variant | 0.36 | rifampicin |
rpoB | 761196 | p.Leu464Met | missense_variant | 0.79 | rifampicin |
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.99 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.98 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.96 | kanamycin, capreomycin, aminoglycosides, amikacin |
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
katG | 2155693 | p.Ser140Asn | missense_variant | 0.91 | isoniazid |
ethR | 4327831 | p.Ala95Thr | missense_variant | 1.0 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6266 | p.Pro343Asp | missense_variant | 0.73 |
gyrB | 6280 | c.1041T>C | synonymous_variant | 0.79 |
gyrB | 6283 | p.Asp348Glu | missense_variant | 0.79 |
gyrB | 6286 | c.1047T>C | synonymous_variant | 0.79 |
gyrB | 6292 | c.1053G>C | synonymous_variant | 0.79 |
gyrB | 6295 | c.1056A>G | synonymous_variant | 0.79 |
gyrB | 6298 | c.1059C>T | synonymous_variant | 0.85 |
gyrB | 6302 | p.Ala355Thr | missense_variant | 0.86 |
gyrA | 6307 | c.-995T>G | upstream_gene_variant | 0.86 |
gyrA | 6310 | c.-992G>C | upstream_gene_variant | 0.8 |
gyrA | 6319 | c.-983G>C | upstream_gene_variant | 0.8 |
gyrB | 6326 | p.Ser363Gly | missense_variant | 0.8 |
gyrA | 6331 | c.-971A>G | upstream_gene_variant | 0.8 |
gyrA | 6362 | c.-940_-938delTTGinsCTC | upstream_gene_variant | 0.81 |
gyrB | 6371 | p.Thr378Ser | missense_variant | 0.87 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8279 | c.978G>C | synonymous_variant | 0.67 |
gyrA | 8283 | p.Ile328Leu | missense_variant | 0.67 |
gyrA | 8288 | c.987T>C | synonymous_variant | 0.67 |
gyrA | 8294 | c.993T>C | synonymous_variant | 0.67 |
gyrA | 8315 | c.1015_1016delAC | frameshift_variant | 1.0 |
gyrA | 8324 | c.1023T>C | synonymous_variant | 1.0 |
gyrA | 8330 | c.1029C>G | synonymous_variant | 0.67 |
gyrA | 8339 | c.1038A>C | synonymous_variant | 0.67 |
gyrA | 8343 | p.Ile348Leu | missense_variant | 0.67 |
gyrA | 8351 | p.Asp350Glu | missense_variant | 0.67 |
gyrA | 8354 | c.1053G>T | synonymous_variant | 0.67 |
fgd1 | 491295 | c.513C>G | synonymous_variant | 0.67 |
fgd1 | 491310 | c.528C>G | synonymous_variant | 0.67 |
fgd1 | 491316 | c.534C>G | synonymous_variant | 0.67 |
fgd1 | 491320 | p.Ala180Gln | missense_variant | 0.67 |
fgd1 | 491325 | c.543G>C | synonymous_variant | 0.75 |
fgd1 | 491328 | c.546C>G | synonymous_variant | 0.75 |
fgd1 | 491344 | p.Ala188Met | missense_variant | 0.75 |
fgd1 | 491349 | c.567T>C | synonymous_variant | 0.75 |
fgd1 | 491356 | p.Phe192Val | missense_variant | 0.75 |
fgd1 | 491364 | c.582T>C | synonymous_variant | 0.75 |
fgd1 | 491367 | c.585G>C | synonymous_variant | 0.75 |
fgd1 | 491380 | p.Glu200Met | missense_variant | 0.75 |
fgd1 | 491394 | c.612C>G | synonymous_variant | 0.75 |
fgd1 | 491397 | p.Glu205Asp | missense_variant | 0.75 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
rpoB | 760143 | p.Val113Ile | missense_variant | 0.67 |
rpoB | 760148 | p.Asp114Glu | missense_variant | 0.86 |
rpoB | 760157 | c.351A>G | synonymous_variant | 0.92 |
rpoB | 760160 | p.Asp118Glu | missense_variant | 0.92 |
rpoB | 760172 | c.366G>C | synonymous_variant | 0.92 |
rpoB | 760176 | p.Ala124Ser | missense_variant | 0.92 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.88 |
rpoB | 760196 | c.390C>G | synonymous_variant | 0.89 |
rpoB | 760199 | c.393C>G | synonymous_variant | 0.89 |
rpoB | 760208 | p.Ile134Met | missense_variant | 0.89 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.89 |
rpoB | 760263 | p.Met153Leu | missense_variant | 0.89 |
rpoB | 760274 | p.Glu156Asp | missense_variant | 0.5 |
rpoB | 760390 | p.Ser195Thr | missense_variant | 0.5 |
rpoB | 760393 | p.Val196Ala | missense_variant | 0.71 |
rpoB | 760400 | c.594G>C | synonymous_variant | 0.89 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.91 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.87 |
rpoB | 760433 | p.Asp209Glu | missense_variant | 0.87 |
rpoB | 760434 | p.Val210Ile | missense_variant | 0.87 |
rpoB | 760450 | p.Thr215Ile | missense_variant | 0.83 |
rpoB | 760464 | p.Ile220Val | missense_variant | 0.87 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.87 |
rpoB | 760479 | p.Arg225Lys | missense_variant | 0.87 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.87 |
rpoB | 760485 | p.Pro227Ser | missense_variant | 0.87 |
rpoB | 760502 | c.696C>G | synonymous_variant | 0.8 |
rpoB | 760508 | c.702G>C | synonymous_variant | 0.83 |
rpoB | 760584 | p.Asn260His | missense_variant | 0.33 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.33 |
rpoB | 760596 | p.Thr264Gln | missense_variant | 0.33 |
rpoB | 760607 | c.801G>C | synonymous_variant | 0.33 |
rpoB | 760611 | c.805_807delTTGinsCTC | synonymous_variant | 0.33 |
rpoB | 760634 | c.828T>C | synonymous_variant | 0.85 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.91 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.9 |
rpoB | 760659 | p.Ser285Ala | missense_variant | 0.9 |
rpoB | 760664 | c.858G>C | synonymous_variant | 0.9 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.8 |
rpoB | 760679 | p.Glu291Asp | missense_variant | 0.8 |
rpoB | 760683 | c.877_879delTTGinsCTT | synonymous_variant | 0.73 |
rpoB | 760687 | p.Phe294Tyr | missense_variant | 0.8 |
rpoB | 760694 | p.Lys296Asn | missense_variant | 0.8 |
rpoB | 760696 | p.Glu297Gly | missense_variant | 0.8 |
rpoB | 760703 | c.897C>G | synonymous_variant | 0.8 |
rpoB | 760716 | p.Arg304Lys | missense_variant | 0.78 |
rpoB | 760730 | c.924T>C | synonymous_variant | 0.78 |
rpoB | 760734 | p.Val310Ile | missense_variant | 0.7 |
rpoB | 760916 | c.1110C>T | synonymous_variant | 0.9 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.9 |
rpoB | 760927 | p.Thr374Ser | missense_variant | 0.9 |
rpoB | 760940 | c.1134G>C | synonymous_variant | 0.9 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.9 |
rpoB | 760953 | p.Ile383Val | missense_variant | 0.94 |
rpoB | 760958 | c.1152G>C | synonymous_variant | 0.94 |
rpoB | 760959 | p.Val385Thr | missense_variant | 0.94 |
rpoB | 760965 | p.Met387Leu | missense_variant | 0.94 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.97 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.97 |
rpoB | 760988 | c.1182C>G | synonymous_variant | 0.97 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.97 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.95 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 0.96 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.96 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.96 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.96 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.95 |
rpoB | 761064 | p.Ala420Ser | missense_variant | 0.95 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.91 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.91 |
rpoB | 761123 | c.1317G>C | synonymous_variant | 0.76 |
rpoB | 761126 | c.1320G>C | synonymous_variant | 0.64 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.64 |
rpoB | 761138 | c.1332C>G | synonymous_variant | 0.64 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 0.33 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.4 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.67 |
rpoB | 761171 | c.1365C>T | synonymous_variant | 0.75 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.75 |
rpoB | 761186 | p.Glu460Asp | missense_variant | 0.75 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.67 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.67 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.88 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.88 |
rpoB | 761220 | c.1414_1416delTCGinsAGC | synonymous_variant | 0.88 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.91 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.91 |
rpoB | 761255 | c.1449T>C | synonymous_variant | 0.94 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.94 |
rpoB | 761289 | p.Ser495Ala | missense_variant | 0.94 |
rpoB | 761292 | p.Val496Ser | missense_variant | 0.91 |
rpoB | 761299 | p.Ala498Gly | missense_variant | 0.91 |
rpoB | 761304 | p.Val500Ile | missense_variant | 0.88 |
rpoB | 761322 | p.Ile506Val | missense_variant | 0.83 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.83 |
rpoB | 761330 | c.1524G>T | synonymous_variant | 0.83 |
rpoB | 761333 | c.1527G>C | synonymous_variant | 0.83 |
rpoB | 761345 | c.1539G>C | synonymous_variant | 0.8 |
rpoB | 761349 | p.Asp515Lys | missense_variant | 0.67 |
rpoB | 761355 | p.Val517Lys | missense_variant | 0.75 |
rpoB | 761360 | c.1554T>G | synonymous_variant | 0.75 |
rpoB | 761362 | p.Ser519Thr | missense_variant | 0.75 |
rpoB | 761370 | p.Ile522Val | missense_variant | 0.75 |
rpoB | 761375 | c.1569G>C | synonymous_variant | 0.75 |
rpoB | 761382 | p.Thr526Ser | missense_variant | 0.67 |
rpoB | 761516 | c.1710G>C | synonymous_variant | 0.9 |
rpoB | 761534 | c.1728G>C | synonymous_variant | 0.97 |
rpoB | 761535 | p.Pro577Ala | missense_variant | 0.97 |
rpoB | 761554 | p.Val583Ala | missense_variant | 0.94 |
rpoB | 761558 | c.1752C>G | synonymous_variant | 0.94 |
rpoB | 761565 | p.Met587Leu | missense_variant | 0.94 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.94 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.94 |
rpoB | 761596 | p.Asn597Ser | missense_variant | 0.97 |
rpoB | 761600 | c.1794T>C | synonymous_variant | 0.97 |
rpoB | 761603 | c.1797C>G | synonymous_variant | 0.97 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.97 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.97 |
rpoB | 761627 | c.1821C>T | synonymous_variant | 0.97 |
rpoB | 761633 | c.1827G>C | synonymous_variant | 1.0 |
rpoB | 761645 | c.1839C>G | synonymous_variant | 1.0 |
rpoB | 761933 | c.2127G>C | synonymous_variant | 0.71 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.95 |
rpoB | 761954 | c.2148C>G | synonymous_variant | 0.96 |
rpoB | 761955 | p.Ile717Phe | missense_variant | 0.96 |
rpoB | 762002 | c.2196C>G | synonymous_variant | 0.97 |
rpoB | 762003 | p.Asn733Gln | missense_variant | 0.97 |
rpoB | 762011 | c.2205G>C | synonymous_variant | 0.97 |
rpoB | 762014 | c.2208C>G | synonymous_variant | 0.97 |
rpoB | 762015 | p.Glu737Gln | missense_variant | 0.97 |
rpoB | 762020 | p.Glu738Asp | missense_variant | 0.97 |
rpoB | 762029 | c.2223C>G | synonymous_variant | 0.97 |
rpoB | 762030 | p.Thr742Ser | missense_variant | 0.97 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.96 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.96 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.95 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.93 |
rpoB | 762084 | p.Ala760Pro | missense_variant | 0.93 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.94 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.95 |
rpoB | 762122 | p.Asp772Glu | missense_variant | 0.95 |
rpoB | 762128 | c.2322G>C | synonymous_variant | 0.95 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 0.95 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.95 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.95 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.93 |
rpoB | 762156 | p.Val784Met | missense_variant | 0.6 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.78 |
rpoB | 762170 | c.2364C>G | synonymous_variant | 0.85 |
rpoB | 762176 | c.2370T>G | synonymous_variant | 0.89 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.92 |
rpoB | 762189 | p.Ile795Leu | missense_variant | 0.93 |
rpoB | 762209 | c.2403C>G | synonymous_variant | 0.95 |
rpoB | 762212 | c.2406G>C | synonymous_variant | 0.96 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.96 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.96 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.96 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.96 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.98 |
rpoB | 762287 | c.2481C>T | synonymous_variant | 1.0 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 1.0 |
rpoB | 762297 | p.Leu831Met | missense_variant | 1.0 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 1.0 |
rpoB | 762318 | p.Ser838Thr | missense_variant | 1.0 |
rpoB | 762325 | p.Lys840Thr | missense_variant | 0.92 |
rpoB | 762329 | c.2523G>C | synonymous_variant | 0.92 |
rpoB | 762336 | p.Ile844Val | missense_variant | 0.83 |
rpoB | 762339 | p.Arg845Lys | missense_variant | 0.83 |
rpoB | 762347 | c.2541T>C | synonymous_variant | 0.83 |
rpoB | 762348 | p.Ser848Asp | missense_variant | 0.83 |
rpoB | 762362 | p.Glu852Asp | missense_variant | 0.83 |
rpoB | 762369 | c.2563T>C | synonymous_variant | 0.83 |
rpoB | 762375 | p.Ala857Pro | missense_variant | 0.83 |
rpoC | 762380 | c.-990T>C | upstream_gene_variant | 0.83 |
rpoB | 762387 | p.Glu861Gln | missense_variant | 0.83 |
rpoB | 762849 | p.Tyr1015Asp | missense_variant | 0.9 |
rpoB | 762858 | p.Thr1018Ala | missense_variant | 0.94 |
rpoC | 762863 | c.-507T>C | upstream_gene_variant | 0.91 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.95 |
rpoC | 762887 | c.-483G>C | upstream_gene_variant | 0.96 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.98 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 0.98 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.98 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.98 |
rpoC | 762947 | c.-423C>G | upstream_gene_variant | 0.98 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 0.93 |
rpoC | 762995 | c.-375G>C | upstream_gene_variant | 0.83 |
rpoB | 763005 | p.Cys1067Gly | missense_variant | 0.5 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.38 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.81 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.88 |
rpoC | 763483 | c.114G>C | synonymous_variant | 0.93 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.93 |
rpoC | 763492 | c.123G>C | synonymous_variant | 0.93 |
rpoC | 763507 | c.138G>C | synonymous_variant | 0.96 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.96 |
rpoC | 763531 | c.162G>C | synonymous_variant | 0.96 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.96 |
rpoC | 763537 | c.168C>G | synonymous_variant | 0.96 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.97 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.99 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.97 |
rpoC | 763622 | p.Ala85Ser | missense_variant | 0.95 |
rpoC | 763627 | p.Lys86Asn | missense_variant | 0.94 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.94 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.95 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.95 |
rpoC | 763666 | c.297G>C | synonymous_variant | 0.95 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.95 |
rpoC | 763699 | c.330G>C | synonymous_variant | 0.9 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.91 |
rpoC | 763703 | c.334_336delTCGinsAGC | synonymous_variant | 0.91 |
rpoC | 763711 | c.342G>C | synonymous_variant | 0.93 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.93 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.91 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.91 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.91 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.93 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.93 |
rpoC | 763765 | c.396T>G | synonymous_variant | 0.91 |
rpoC | 763772 | p.Val135Met | missense_variant | 0.88 |
rpoC | 764308 | c.939G>C | synonymous_variant | 0.71 |
rpoC | 764311 | c.942C>G | synonymous_variant | 0.71 |
rpoC | 764315 | p.Ala316Cys | missense_variant | 0.71 |
rpoC | 764320 | c.951C>G | synonymous_variant | 0.8 |
rpoC | 764326 | c.957G>C | synonymous_variant | 0.8 |
rpoC | 764338 | p.Glu323Asp | missense_variant | 0.83 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.91 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 0.91 |
rpoC | 764377 | c.1008C>G | synonymous_variant | 0.91 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.91 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 0.91 |
rpoC | 764398 | c.1029G>C | synonymous_variant | 0.92 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.83 |
rpoC | 764410 | c.1041G>C | synonymous_variant | 1.0 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.6 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.5 |
rpoC | 764435 | c.1066_1068delAGGinsCGA | synonymous_variant | 0.5 |
rpoC | 764441 | p.Ile358Leu | missense_variant | 0.5 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.4 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.4 |
rpoC | 764452 | c.1083T>G | synonymous_variant | 0.4 |
rpoC | 764455 | c.1086G>C | synonymous_variant | 0.4 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.57 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.73 |
rpoC | 764470 | c.1101C>G | synonymous_variant | 0.8 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.88 |
rpoC | 764500 | c.1131C>G | synonymous_variant | 0.88 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.88 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.92 |
rpoC | 764527 | c.1158C>G | synonymous_variant | 0.93 |
rpoC | 764533 | c.1164C>T | synonymous_variant | 0.93 |
rpoC | 764536 | c.1167G>T | synonymous_variant | 0.93 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.93 |
rpoC | 764548 | c.1179G>C | synonymous_variant | 0.95 |
rpoC | 764551 | c.1182G>C | synonymous_variant | 0.95 |
rpoC | 764560 | c.1191T>G | synonymous_variant | 0.97 |
rpoC | 764561 | p.Pro398Ala | missense_variant | 0.97 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.98 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.99 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.99 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.99 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 1.0 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 1.0 |
rpoC | 764644 | c.1275G>C | synonymous_variant | 1.0 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 1.0 |
rpoC | 764651 | c.1282_1284delTCGinsAGC | synonymous_variant | 1.0 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 1.0 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 1.0 |
rpoC | 764713 | c.1344G>C | synonymous_variant | 1.0 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 1.0 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.98 |
rpoC | 764759 | p.Asn464Asp | missense_variant | 0.98 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.98 |
rpoC | 764780 | c.1411_1413delAGCinsTCG | synonymous_variant | 0.97 |
rpoC | 764797 | c.1428G>C | synonymous_variant | 0.96 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.69 |
rpoC | 764812 | c.1443C>G | synonymous_variant | 0.9 |
rpoC | 764813 | p.Gln482Val | missense_variant | 0.9 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 0.9 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.82 |
rpoC | 764843 | p.Ala492Thr | missense_variant | 0.9 |
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 | 778979 | c.-74G>T | upstream_gene_variant | 1.0 |
rpsL | 781670 | c.111G>C | synonymous_variant | 0.5 |
rpsL | 781682 | c.123T>C | synonymous_variant | 0.7 |
rpsL | 781700 | c.141G>C | synonymous_variant | 0.82 |
rpsL | 781706 | c.147T>G | synonymous_variant | 0.82 |
rpsL | 781709 | c.150G>C | synonymous_variant | 0.82 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.82 |
rpsL | 781718 | c.159C>G | synonymous_variant | 0.82 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.82 |
rpsL | 781738 | p.Gln60Arg | missense_variant | 0.69 |
rpsL | 781740 | c.181_182insCA | frameshift_variant | 0.69 |
rpsL | 781751 | c.192G>C | synonymous_variant | 0.71 |
rpsL | 781754 | c.195G>T | synonymous_variant | 0.71 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.67 |
rpsL | 781763 | c.204C>G | synonymous_variant | 0.67 |
rpsL | 781766 | c.207C>T | synonymous_variant | 0.67 |
rpsL | 781768 | p.Glu70Val | missense_variant | 0.67 |
rpsL | 781796 | p.Met79Ile | missense_variant | 0.81 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.78 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.82 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.83 |
rpsL | 781832 | c.273T>G | synonymous_variant | 0.83 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.85 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.9 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.9 |
rpsL | 781884 | p.Asn109Gly | missense_variant | 0.88 |
rpsL | 781890 | p.Lys111Gln | missense_variant | 0.88 |
rpsL | 781898 | c.339A>C | synonymous_variant | 0.88 |
rpsL | 781901 | c.342C>T | synonymous_variant | 0.88 |
rpsL | 781916 | c.357T>G | synonymous_variant | 0.81 |
rpsL | 781929 | p.Gly124Lys | missense_variant | 0.6 |
rpsL | 781933 | c.374G>A | splice_region_variant&stop_retained_variant | 0.5 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.55 |
rplC | 800618 | c.-191T>G | upstream_gene_variant | 0.6 |
rplC | 800630 | c.-179G>C | upstream_gene_variant | 0.6 |
rplC | 800632 | c.-177_-176delATinsTC | upstream_gene_variant | 0.6 |
rplC | 800645 | c.-164C>G | upstream_gene_variant | 0.6 |
rplC | 800648 | c.-161A>G | upstream_gene_variant | 0.6 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.67 |
rplC | 800667 | c.-142_-140delTCGinsAGC | upstream_gene_variant | 0.55 |
rplC | 800672 | c.-137G>C | upstream_gene_variant | 0.55 |
rplC | 800693 | c.-116A>C | upstream_gene_variant | 0.6 |
rplC | 800702 | c.-107G>C | upstream_gene_variant | 0.44 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.5 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472107 | n.262A>G | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472123 | n.278A>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472148 | n.303T>C | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472278 | n.433C>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472279 | n.434T>C | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472290 | n.445C>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472297 | n.453_454delGT | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472301 | n.457_461delGGGTT | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472308 | n.464delC | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472314 | n.469A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472345 | n.500A>G | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472416 | n.571C>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472476 | n.631A>G | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472495 | n.650C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472496 | n.651T>G | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472582 | n.737G>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472597 | n.752G>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472673 | n.828T>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472840 | n.995A>C | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472846 | n.1001C>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472847 | n.1002G>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472849 | n.1004C>G | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472850 | n.1005T>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472857 | n.1012A>G | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472858 | n.1013G>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472860 | n.1015C>G | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472861 | n.1016G>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472866 | n.1023dupT | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472874 | n.1029C>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472875 | n.1030T>G | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472879 | n.1034T>C | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473099 | n.1254T>G | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473129 | n.1284C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473165 | n.1320C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.98 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473294 | n.1449A>G | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473300 | n.1455C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473768 | n.111A>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1473793 | n.136G>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1473794 | n.137A>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1473797 | n.140G>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1473801 | n.144T>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1473802 | n.145C>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1473832 | n.175C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1473833 | n.176_177insT | non_coding_transcript_exon_variant | 0.96 |
rrl | 1473844 | n.187C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1473870 | n.213G>A | non_coding_transcript_exon_variant | 0.98 |
rrl | 1473871 | n.214T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473887 | n.230_231insA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473922 | n.265A>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1473923 | n.266C>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1473934 | n.277G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474201 | n.544T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474263 | n.606G>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474283 | n.626A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474310 | n.655dupG | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1474450 | n.793T>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474454 | n.797G>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474676 | n.1019T>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474708 | n.1053_1054delTG | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474713 | n.1056_1057insAA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474716 | n.1059A>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474790 | n.1133C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474830 | n.1173A>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474832 | n.1175A>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474869 | n.1212G>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474936 | n.1279C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474938 | n.1281G>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474946 | n.1289C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474948 | n.1291C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475060 | n.1403_1404insAT | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475063 | n.1406A>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475065 | n.1409_1411delCAA | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475080 | n.1425_1426delCC | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475091 | n.1434G>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475104 | n.1447T>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475108 | n.1451C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475111 | n.1454G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475116 | n.1459G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475119 | n.1462C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475124 | n.1467A>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475129 | n.1472G>A | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475173 | n.1516A>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475175 | n.1518G>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475508 | n.1851A>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475517 | n.1860C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475518 | n.1861A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475538 | n.1881T>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475544 | n.1887A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475548 | n.1891C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475549 | n.1892T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475550 | n.1893A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475562 | n.1905C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475649 | n.1992A>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475655 | n.1998T>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475696 | n.2039T>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475697 | n.2040C>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475702 | n.2045G>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475703 | n.2046A>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475740 | n.2083G>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1475747 | n.2090A>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475759 | n.2103_2107delCCGCA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475767 | n.2110G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475780 | n.2123A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475781 | n.2124T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475788 | n.2131C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.99 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476022 | n.2366delC | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476049 | n.2392C>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476076 | n.2419A>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476081 | n.2424A>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476082 | n.2425T>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476088 | n.2431A>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476089 | n.2432T>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476095 | n.2438C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476103 | n.2446C>A | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476105 | n.2450delA | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476110 | n.2453G>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476251 | n.2594T>A | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476287 | n.2631_2639delTCCGGCACC | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476301 | n.2644_2645insCGGTGGCTT | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476368 | n.2711T>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476529 | n.2872A>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476586 | n.2929C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476596 | n.2939C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476601 | n.2944G>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476613 | n.2956G>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476631 | n.2974G>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476661 | n.3004A>G | non_coding_transcript_exon_variant | 0.67 |
rpsA | 1833635 | p.Tyr32His | missense_variant | 0.77 |
rpsA | 1833643 | c.102C>T | synonymous_variant | 0.8 |
rpsA | 1833646 | c.105T>C | synonymous_variant | 0.86 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.89 |
rpsA | 1833664 | c.123C>T | synonymous_variant | 0.89 |
rpsA | 1833665 | p.Thr42Val | missense_variant | 0.89 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.91 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 0.92 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.96 |
rpsA | 1833697 | c.156C>G | synonymous_variant | 0.96 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.96 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.96 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.96 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.97 |
rpsA | 1833748 | c.207C>G | synonymous_variant | 0.97 |
rpsA | 1833781 | c.240T>C | synonymous_variant | 0.99 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.99 |
rpsA | 1833796 | p.Glu85Asp | missense_variant | 0.99 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 1.0 |
rpsA | 1833811 | c.270G>C | synonymous_variant | 1.0 |
rpsA | 1833815 | p.Thr92Gln | missense_variant | 1.0 |
rpsA | 1833829 | c.288A>G | synonymous_variant | 1.0 |
rpsA | 1833832 | c.291G>A | synonymous_variant | 1.0 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 1.0 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 1.0 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 1.0 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 1.0 |
rpsA | 1833859 | c.318C>T | synonymous_variant | 1.0 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 1.0 |
rpsA | 1833893 | p.Ala118Gln | missense_variant | 0.98 |
rpsA | 1833896 | p.Leu119Ile | missense_variant | 0.97 |
rpsA | 1833905 | p.Lys122Asp | missense_variant | 0.97 |
rpsA | 1833912 | p.Glu124Gly | missense_variant | 0.97 |
rpsA | 1833915 | p.Ala125Val | missense_variant | 0.97 |
rpsA | 1833921 | p.Lys127Thr | missense_variant | 0.96 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.97 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.98 |
rpsA | 1833955 | c.414G>C | synonymous_variant | 0.97 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.98 |
rpsA | 1833976 | c.435C>T | synonymous_variant | 0.98 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.98 |
rpsA | 1833991 | c.450C>G | synonymous_variant | 0.98 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.98 |
rpsA | 1834009 | c.468C>T | synonymous_variant | 0.97 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.98 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.98 |
rpsA | 1834024 | c.483G>C | synonymous_variant | 0.99 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.99 |
rpsA | 1834034 | p.Ile165Val | missense_variant | 0.98 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.98 |
rpsA | 1834096 | c.555G>C | synonymous_variant | 0.94 |
rpsA | 1834099 | c.558C>T | synonymous_variant | 0.94 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.94 |
rpsA | 1834108 | c.567C>G | synonymous_variant | 0.93 |
rpsA | 1834114 | c.573G>C | synonymous_variant | 0.93 |
rpsA | 1834210 | c.669C>T | synonymous_variant | 0.92 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.94 |
rpsA | 1834228 | c.687C>T | synonymous_variant | 0.94 |
rpsA | 1834231 | c.690T>A | synonymous_variant | 0.95 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.95 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.96 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.96 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.96 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.96 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.96 |
rpsA | 1834303 | c.762T>G | synonymous_variant | 0.96 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.96 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.96 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.98 |
rpsA | 1834354 | c.813G>T | synonymous_variant | 0.96 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 0.96 |
rpsA | 1834360 | c.819G>C | synonymous_variant | 0.95 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.96 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.95 |
rpsA | 1834369 | c.828C>G | synonymous_variant | 0.95 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.96 |
rpsA | 1834384 | c.843A>G | synonymous_variant | 0.96 |
rpsA | 1834395 | p.Arg285Gln | missense_variant | 0.96 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.96 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.96 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.96 |
rpsA | 1834427 | p.Ile296Val | missense_variant | 0.96 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.97 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.96 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.95 |
rpsA | 1834474 | c.933C>G | synonymous_variant | 0.93 |
rpsA | 1834483 | p.Glu314Asp | missense_variant | 0.94 |
rpsA | 1834486 | p.Glu315Asp | missense_variant | 0.94 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.95 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.93 |
rpsA | 1834534 | c.993C>G | synonymous_variant | 0.91 |
rpsA | 1834538 | p.Val333Leu | missense_variant | 0.91 |
rpsA | 1834546 | p.Asp335Glu | missense_variant | 0.89 |
rpsA | 1834552 | c.1011G>C | synonymous_variant | 0.86 |
rpsA | 1834555 | c.1014T>C | synonymous_variant | 0.79 |
rpsA | 1834556 | p.Ala339Thr | missense_variant | 0.79 |
rpsA | 1834564 | c.1024_1028delGACGA | frameshift_variant | 0.79 |
rpsA | 1834572 | p.Ala344Val | missense_variant | 0.79 |
rpsA | 1834606 | c.1065C>T | synonymous_variant | 0.88 |
rpsA | 1834612 | c.1071G>C | synonymous_variant | 0.87 |
rpsA | 1834619 | c.1078T>C | synonymous_variant | 0.75 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155410 | c.702G>C | synonymous_variant | 0.67 |
katG | 2155416 | c.696G>C | synonymous_variant | 0.6 |
katG | 2155422 | c.690G>C | synonymous_variant | 0.67 |
katG | 2155434 | c.678G>T | synonymous_variant | 0.67 |
katG | 2155443 | c.669G>C | synonymous_variant | 0.67 |
katG | 2155467 | c.645T>C | synonymous_variant | 0.67 |
katG | 2155470 | c.642G>C | synonymous_variant | 0.67 |
katG | 2155475 | p.Lys213Glu | missense_variant | 0.6 |
katG | 2155480 | p.Ser211Thr | missense_variant | 0.6 |
katG | 2155485 | c.627T>C | synonymous_variant | 0.6 |
katG | 2155490 | p.Glu208Lys | missense_variant | 0.6 |
katG | 2155491 | c.621T>C | synonymous_variant | 0.6 |
katG | 2155677 | c.435C>G | synonymous_variant | 0.91 |
katG | 2155680 | c.432G>C | synonymous_variant | 0.91 |
katG | 2155689 | c.421_423delTTGinsCTC | synonymous_variant | 0.91 |
katG | 2155696 | p.Ala139Gly | missense_variant | 0.93 |
katG | 2155716 | c.396T>C | synonymous_variant | 1.0 |
katG | 2155722 | c.390G>C | synonymous_variant | 1.0 |
katG | 2155735 | p.Met126Gln | missense_variant | 1.0 |
katG | 2155741 | p.Gly124Thr | missense_variant | 1.0 |
katG | 2155743 | c.369G>C | synonymous_variant | 1.0 |
katG | 2155758 | c.354C>T | synonymous_variant | 1.0 |
katG | 2155765 | p.His116Ala | missense_variant | 1.0 |
katG | 2155768 | p.Ile115Thr | missense_variant | 1.0 |
katG | 2155785 | p.Ala109Ser | missense_variant | 1.0 |
katG | 2155794 | c.318G>C | synonymous_variant | 1.0 |
katG | 2155806 | p.Phe102Met | missense_variant | 1.0 |
katG | 2155815 | c.297G>C | synonymous_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3877638 | c.870T>G | synonymous_variant | 0.33 |
rpoA | 3877656 | c.852T>C | synonymous_variant | 0.75 |
rpoA | 3877667 | p.Ser281Ala | missense_variant | 0.75 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.75 |
rpoA | 3877672 | p.Thr279Ser | missense_variant | 0.75 |
rpoA | 3877677 | p.Ala277Gly | missense_variant | 0.75 |
rpoA | 3877683 | c.825G>C | synonymous_variant | 0.75 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.75 |
rpoA | 3877689 | c.819C>T | synonymous_variant | 0.75 |
rpoA | 3877696 | p.Thr271Ser | missense_variant | 0.86 |
rpoA | 3877701 | p.Val269Ile | missense_variant | 0.86 |
rpoA | 3877704 | c.804G>C | synonymous_variant | 0.86 |
rpoA | 3877737 | c.771G>C | synonymous_variant | 0.8 |
rpoA | 3877743 | p.Asp255Glu | missense_variant | 0.77 |
rpoA | 3877746 | c.762G>C | synonymous_variant | 0.77 |
rpoA | 3877752 | p.Asp252Glu | missense_variant | 0.83 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.71 |
rpoA | 3877836 | c.672A>G | synonymous_variant | 0.57 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.57 |
rpoA | 3877842 | c.666A>C | synonymous_variant | 0.75 |
rpoA | 3877856 | c.652T>C | synonymous_variant | 0.87 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.9 |
rpoA | 3877875 | c.633T>C | synonymous_variant | 0.87 |
rpoA | 3877878 | c.630G>C | synonymous_variant | 0.87 |
rpoA | 3877881 | c.627G>C | synonymous_variant | 0.87 |
rpoA | 3877886 | p.Leu208Met | missense_variant | 0.87 |
rpoA | 3877893 | c.615C>T | synonymous_variant | 0.87 |
rpoA | 3877900 | p.Ser203Ala | missense_variant | 0.87 |
rpoA | 3877902 | p.Ile202Met | missense_variant | 0.87 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.87 |
rpoA | 3877908 | c.600T>C | synonymous_variant | 0.87 |
rpoA | 3877920 | c.588G>C | synonymous_variant | 0.87 |
rpoA | 3877926 | p.Leu194Val | missense_variant | 0.87 |
rpoA | 3877932 | c.576G>C | synonymous_variant | 0.91 |
rpoA | 3877962 | c.546G>A | synonymous_variant | 0.94 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.33 |
rpoA | 3878226 | p.Thr94Val | missense_variant | 0.33 |
rpoA | 3878241 | p.Glu89His | missense_variant | 0.33 |
rpoA | 3878253 | c.255G>C | synonymous_variant | 0.4 |
rpoA | 3878256 | c.252G>C | synonymous_variant | 0.4 |
rpoA | 3878264 | p.Ser82Gly | missense_variant | 0.4 |
rpoA | 3878270 | p.Leu80Ile | missense_variant | 0.4 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.4 |
rpoA | 3878274 | c.234G>C | synonymous_variant | 0.4 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.4 |
rpoA | 3878295 | c.213A>G | synonymous_variant | 0.4 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.5 |
rpoA | 3878310 | c.198G>C | synonymous_variant | 0.67 |
rpoA | 3878318 | p.Thr64Ser | missense_variant | 0.67 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.67 |
clpC1 | 4038499 | p.Ser736Gly | missense_variant | 0.67 |
clpC1 | 4038515 | p.Met730Ile | missense_variant | 0.9 |
clpC1 | 4038519 | p.Arg729Gln | missense_variant | 0.9 |
clpC1 | 4038523 | p.Ile728Val | missense_variant | 0.9 |
clpC1 | 4038531 | c.2173delG | frameshift_variant | 0.9 |
clpC1 | 4038536 | c.2168_2169insG | frameshift_variant | 0.9 |
clpC1 | 4038539 | c.2166G>C | synonymous_variant | 0.9 |
clpC1 | 4038545 | p.His720Pro | missense_variant | 0.9 |
clpC1 | 4038558 | p.Ile716Thr | missense_variant | 0.9 |
clpC1 | 4038568 | p.Ile713Val | missense_variant | 0.9 |
clpC1 | 4038569 | c.2136C>G | synonymous_variant | 0.9 |
clpC1 | 4038587 | c.2118C>G | synonymous_variant | 1.0 |
clpC1 | 4038596 | p.Lys703Gln | missense_variant | 1.0 |
clpC1 | 4038826 | p.Ile627Val | missense_variant | 1.0 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 1.0 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.94 |
clpC1 | 4038881 | c.1824C>T | synonymous_variant | 0.94 |
clpC1 | 4038890 | p.Glu605Asp | missense_variant | 0.94 |
clpC1 | 4038905 | c.1800A>G | synonymous_variant | 0.89 |
clpC1 | 4038911 | c.1794G>C | synonymous_variant | 0.88 |
clpC1 | 4038914 | p.Ala597Ser | missense_variant | 0.88 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 0.88 |
clpC1 | 4038933 | p.Ala591Val | missense_variant | 0.86 |
clpC1 | 4039418 | c.1287C>G | synonymous_variant | 0.4 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.73 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.73 |
clpC1 | 4039448 | c.1257A>G | synonymous_variant | 0.73 |
clpC1 | 4039454 | c.1251A>T | synonymous_variant | 0.79 |
clpC1 | 4039457 | c.1248C>G | synonymous_variant | 0.79 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 0.79 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.85 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.85 |
clpC1 | 4039472 | c.1233G>C | synonymous_variant | 0.79 |
clpC1 | 4039477 | p.Met410Leu | missense_variant | 0.73 |
clpC1 | 4039478 | c.1227G>A | synonymous_variant | 0.73 |
clpC1 | 4039481 | c.1224T>G | synonymous_variant | 0.69 |
clpC1 | 4039484 | c.1221T>C | synonymous_variant | 0.74 |
clpC1 | 4039499 | c.1206G>C | synonymous_variant | 0.85 |
clpC1 | 4039524 | p.Phe394His | missense_variant | 0.88 |
clpC1 | 4039549 | p.Ala386Ser | missense_variant | 0.87 |
clpC1 | 4039552 | p.Leu385Met | missense_variant | 0.87 |
clpC1 | 4039554 | p.Thr384Asn | missense_variant | 0.87 |
clpC1 | 4039556 | p.Ala383Val | missense_variant | 0.87 |
clpC1 | 4039559 | c.1146C>G | synonymous_variant | 0.87 |
clpC1 | 4039563 | p.Ala381Gly | missense_variant | 0.88 |
clpC1 | 4039565 | c.1140G>C | synonymous_variant | 0.88 |
clpC1 | 4039570 | p.Met379Leu | missense_variant | 0.89 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.89 |
clpC1 | 4039588 | p.Ser373Thr | missense_variant | 0.9 |
clpC1 | 4039589 | c.1116G>C | synonymous_variant | 0.91 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.95 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.95 |
clpC1 | 4039622 | c.1083C>G | synonymous_variant | 0.95 |
clpC1 | 4039642 | p.Thr355Ala | missense_variant | 0.96 |
clpC1 | 4039647 | p.Glu353Pro | missense_variant | 0.95 |
clpC1 | 4039649 | p.Val352Ile | missense_variant | 0.95 |
clpC1 | 4039661 | p.Gly348Ala | missense_variant | 0.95 |
clpC1 | 4039670 | p.Val345Ile | missense_variant | 0.95 |
clpC1 | 4039685 | c.1020C>G | synonymous_variant | 0.96 |
clpC1 | 4039691 | c.1014G>C | synonymous_variant | 0.95 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.94 |
clpC1 | 4039697 | c.1008C>T | synonymous_variant | 0.94 |
clpC1 | 4039714 | p.Tyr331His | missense_variant | 0.95 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.95 |
clpC1 | 4039733 | c.972G>C | synonymous_variant | 0.95 |
clpC1 | 4039736 | c.969C>G | synonymous_variant | 0.92 |
clpC1 | 4039739 | c.966C>G | synonymous_variant | 0.92 |
clpC1 | 4039742 | c.963C>T | synonymous_variant | 0.92 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.92 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.92 |
clpC1 | 4039760 | c.945T>C | synonymous_variant | 0.92 |
clpC1 | 4039763 | c.942C>G | synonymous_variant | 0.92 |
clpC1 | 4039766 | c.939T>G | synonymous_variant | 0.92 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.92 |
clpC1 | 4039773 | p.Lys311Met | missense_variant | 0.93 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.93 |
clpC1 | 4039781 | c.924G>C | synonymous_variant | 0.94 |
clpC1 | 4039802 | c.903G>C | synonymous_variant | 0.95 |
clpC1 | 4039817 | c.888A>T | synonymous_variant | 0.94 |
clpC1 | 4039820 | c.885T>C | synonymous_variant | 0.94 |
clpC1 | 4039823 | c.882T>C | synonymous_variant | 0.95 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 0.95 |
clpC1 | 4039838 | p.Leu289Ile | missense_variant | 0.94 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.95 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.96 |
clpC1 | 4039875 | p.Asn277Arg | missense_variant | 0.96 |
clpC1 | 4039886 | c.819C>G | synonymous_variant | 0.96 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.95 |
clpC1 | 4039925 | c.780C>T | synonymous_variant | 0.94 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.93 |
clpC1 | 4039934 | c.771G>C | synonymous_variant | 0.93 |
clpC1 | 4039946 | c.759A>G | synonymous_variant | 0.94 |
clpC1 | 4039949 | c.756G>C | synonymous_variant | 0.93 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.93 |
clpC1 | 4039955 | c.750G>C | synonymous_variant | 0.93 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.93 |
clpC1 | 4039964 | c.741C>G | synonymous_variant | 0.94 |
clpC1 | 4039994 | p.Glu237Asp | missense_variant | 0.94 |
clpC1 | 4040001 | p.His235Arg | missense_variant | 0.93 |
clpC1 | 4040010 | p.Ala232Asp | missense_variant | 0.93 |
clpC1 | 4040012 | p.Gln231Ala | missense_variant | 0.93 |
clpC1 | 4040018 | c.687G>C | synonymous_variant | 0.93 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.93 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.93 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.94 |
clpC1 | 4040036 | c.669C>G | synonymous_variant | 0.94 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.93 |
clpC1 | 4040063 | c.642G>C | synonymous_variant | 0.92 |
clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 0.87 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.85 |
clpC1 | 4040105 | c.600C>G | synonymous_variant | 0.85 |
clpC1 | 4040108 | c.597G>C | synonymous_variant | 0.85 |
clpC1 | 4040117 | c.588A>G | synonymous_variant | 0.79 |
clpC1 | 4040129 | p.Gly192Met | missense_variant | 0.75 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.7 |
clpC1 | 4040147 | c.558A>G | synonymous_variant | 0.57 |
clpC1 | 4040255 | p.Ala150Pro | missense_variant | 0.67 |
clpC1 | 4040267 | c.438A>G | synonymous_variant | 0.86 |
clpC1 | 4040273 | c.432T>A | synonymous_variant | 0.84 |
clpC1 | 4040278 | p.Ser143Ala | missense_variant | 0.88 |
clpC1 | 4040291 | c.414G>C | synonymous_variant | 0.92 |
clpC1 | 4040300 | c.405C>G | synonymous_variant | 0.93 |
clpC1 | 4040306 | p.Arg133Ser | missense_variant | 0.91 |
clpC1 | 4040311 | p.Thr132Ser | missense_variant | 0.91 |
clpC1 | 4040315 | p.Glu130Asp | missense_variant | 0.91 |
clpC1 | 4040354 | c.351A>G | synonymous_variant | 0.89 |
clpC1 | 4040363 | c.342A>C | synonymous_variant | 0.89 |
clpC1 | 4040369 | c.336C>G | synonymous_variant | 0.89 |
clpC1 | 4040375 | c.330G>C | synonymous_variant | 0.89 |
clpC1 | 4040380 | c.325T>C | synonymous_variant | 0.87 |
clpC1 | 4040381 | c.324T>C | synonymous_variant | 0.89 |
clpC1 | 4040387 | c.318A>G | synonymous_variant | 0.89 |
clpC1 | 4040393 | c.312G>C | synonymous_variant | 0.9 |
clpC1 | 4040403 | p.Asn101Ser | missense_variant | 0.89 |
clpC1 | 4040411 | c.294T>G | synonymous_variant | 0.7 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |