Run ID: ERR7821163
Sample name:
Date: 02-04-2023 06:23:09
Number of reads: 1551336
Percentage reads mapped: 75.74
Strain: lineage2.2.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 0.99 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472307 | n.462C>T | non_coding_transcript_exon_variant | 0.38 | streptomycin |
embB | 4247448 | p.His312Arg | missense_variant | 0.27 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6184 | c.945C>T | synonymous_variant | 0.24 |
gyrB | 6215 | p.Ser326Thr | missense_variant | 0.23 |
gyrB | 6223 | c.984G>C | synonymous_variant | 0.29 |
gyrB | 6238 | c.999G>A | synonymous_variant | 0.25 |
gyrB | 6242 | p.Arg335Lys | missense_variant | 0.22 |
gyrB | 6250 | c.1011A>C | synonymous_variant | 0.22 |
gyrB | 6253 | c.1014G>C | synonymous_variant | 0.21 |
gyrB | 6265 | c.1026C>T | synonymous_variant | 0.24 |
gyrB | 6268 | c.1029C>G | synonymous_variant | 0.25 |
gyrB | 6280 | c.1041T>C | synonymous_variant | 0.26 |
gyrB | 6286 | c.1047T>C | synonymous_variant | 0.27 |
gyrB | 6292 | c.1053G>C | synonymous_variant | 0.28 |
gyrB | 6295 | c.1056A>G | synonymous_variant | 0.28 |
gyrA | 6307 | c.-995T>G | upstream_gene_variant | 0.28 |
gyrA | 6319 | c.-983G>C | upstream_gene_variant | 0.25 |
gyrA | 6337 | c.-965G>A | upstream_gene_variant | 0.19 |
gyrA | 6362 | c.-940T>C | upstream_gene_variant | 0.15 |
gyrA | 6811 | c.-491C>T | upstream_gene_variant | 0.15 |
gyrA | 6838 | c.-464C>G | upstream_gene_variant | 0.17 |
gyrA | 6841 | c.-461T>C | upstream_gene_variant | 0.17 |
gyrA | 6844 | c.-458T>C | upstream_gene_variant | 0.17 |
gyrA | 6850 | c.-452C>T | upstream_gene_variant | 0.16 |
gyrA | 6878 | c.-424T>C | upstream_gene_variant | 0.19 |
gyrA | 6881 | c.-421T>C | upstream_gene_variant | 0.19 |
gyrA | 6904 | c.-398C>G | upstream_gene_variant | 0.16 |
gyrA | 6916 | c.-386G>A | upstream_gene_variant | 0.15 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7442 | c.141G>C | synonymous_variant | 0.16 |
gyrA | 7457 | c.156T>C | synonymous_variant | 0.16 |
gyrA | 7472 | c.171T>C | synonymous_variant | 0.18 |
gyrA | 7484 | c.183T>C | synonymous_variant | 0.21 |
gyrA | 7487 | c.186C>G | synonymous_variant | 0.23 |
gyrA | 7499 | c.198G>C | synonymous_variant | 0.26 |
gyrA | 7505 | c.204C>T | synonymous_variant | 0.26 |
gyrA | 7506 | p.Ser69Gly | missense_variant | 0.26 |
gyrA | 7514 | c.213C>G | synonymous_variant | 0.25 |
gyrA | 7526 | c.225G>C | synonymous_variant | 0.24 |
gyrA | 7529 | c.228G>C | synonymous_variant | 0.24 |
gyrA | 7532 | c.231T>C | synonymous_variant | 0.22 |
gyrA | 7541 | c.240C>G | synonymous_variant | 0.24 |
gyrA | 7569 | p.Ala90Ser | missense_variant | 0.17 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8121 | c.820T>C | synonymous_variant | 0.16 |
gyrA | 8126 | c.825G>T | synonymous_variant | 0.2 |
gyrA | 8129 | c.828T>C | synonymous_variant | 0.21 |
gyrA | 8135 | c.834C>G | synonymous_variant | 0.21 |
gyrA | 8156 | c.855T>C | synonymous_variant | 0.22 |
gyrA | 8168 | c.867A>G | synonymous_variant | 0.21 |
gyrA | 8177 | c.876A>C | synonymous_variant | 0.19 |
gyrA | 8180 | c.879C>T | synonymous_variant | 0.19 |
gyrA | 8198 | c.897T>C | synonymous_variant | 0.18 |
gyrA | 8201 | c.900C>G | synonymous_variant | 0.18 |
gyrA | 8207 | c.906T>C | synonymous_variant | 0.2 |
gyrA | 8210 | c.909G>A | synonymous_variant | 0.2 |
gyrA | 8225 | c.924T>C | synonymous_variant | 0.17 |
gyrA | 8228 | c.927G>T | synonymous_variant | 0.15 |
gyrA | 8267 | c.966G>C | synonymous_variant | 0.16 |
gyrA | 8283 | p.Ile328Leu | missense_variant | 0.2 |
gyrA | 8288 | c.987T>C | synonymous_variant | 0.2 |
gyrA | 8294 | c.993T>C | synonymous_variant | 0.2 |
gyrA | 8324 | c.1023T>C | synonymous_variant | 0.16 |
gyrA | 8330 | c.1029C>G | synonymous_variant | 0.17 |
gyrA | 8337 | c.1036_1038delCTAinsTTG | synonymous_variant | 0.17 |
gyrA | 8340 | p.Ala347Ser | missense_variant | 0.18 |
gyrA | 8375 | c.1074G>C | synonymous_variant | 0.23 |
gyrA | 8382 | p.Leu361Met | missense_variant | 0.22 |
gyrA | 8393 | c.1092T>C | synonymous_variant | 0.2 |
gyrA | 8442 | c.1141C>T | synonymous_variant | 0.16 |
gyrA | 8453 | c.1152A>G | synonymous_variant | 0.16 |
gyrA | 8531 | c.1230G>A | synonymous_variant | 0.16 |
gyrA | 8570 | p.Glu423Asp | missense_variant | 0.17 |
gyrA | 8672 | c.1371A>G | synonymous_variant | 0.18 |
gyrA | 8678 | c.1377G>A | synonymous_variant | 0.19 |
gyrA | 8693 | c.1392T>C | synonymous_variant | 0.19 |
gyrA | 8711 | c.1410A>C | synonymous_variant | 0.16 |
gyrA | 8897 | c.1596T>C | synonymous_variant | 0.18 |
gyrA | 8903 | c.1602T>C | synonymous_variant | 0.19 |
gyrA | 8930 | c.1629C>A | synonymous_variant | 0.27 |
gyrA | 8933 | c.1632G>C | synonymous_variant | 0.27 |
gyrA | 8939 | c.1638T>A | synonymous_variant | 0.25 |
gyrA | 8942 | c.1641G>C | synonymous_variant | 0.26 |
gyrA | 8966 | c.1665C>G | synonymous_variant | 0.22 |
gyrA | 8967 | p.Ala556Arg | missense_variant | 0.22 |
gyrA | 8978 | c.1677C>T | synonymous_variant | 0.21 |
gyrA | 8987 | c.1686C>G | synonymous_variant | 0.18 |
gyrA | 8990 | c.1689C>G | synonymous_variant | 0.18 |
gyrA | 8996 | c.1695T>C | synonymous_variant | 0.19 |
gyrA | 8998 | p.Leu566Trp | missense_variant | 0.19 |
gyrA | 9191 | c.1890G>T | synonymous_variant | 0.16 |
gyrA | 9197 | c.1896G>C | synonymous_variant | 0.16 |
gyrA | 9218 | c.1917C>T | synonymous_variant | 0.18 |
gyrA | 9230 | c.1929T>C | synonymous_variant | 0.23 |
gyrA | 9233 | c.1932C>G | synonymous_variant | 0.23 |
gyrA | 9242 | c.1941A>G | synonymous_variant | 0.27 |
gyrA | 9267 | p.Asn656Gly | missense_variant | 0.29 |
gyrA | 9293 | c.1992G>C | synonymous_variant | 0.37 |
gyrA | 9296 | c.1995T>C | synonymous_variant | 0.38 |
gyrA | 9299 | c.1998G>C | synonymous_variant | 0.4 |
gyrA | 9304 | p.Gly668Glu | missense_variant | 1.0 |
gyrA | 9329 | c.2028C>G | synonymous_variant | 0.42 |
gyrA | 9335 | c.2034G>C | synonymous_variant | 0.39 |
gyrA | 9345 | c.2044A>C | synonymous_variant | 0.33 |
gyrA | 9374 | c.2073G>C | synonymous_variant | 0.23 |
gyrA | 9377 | c.2076A>G | synonymous_variant | 0.21 |
gyrA | 9383 | c.2082T>C | synonymous_variant | 0.16 |
fgd1 | 490998 | c.216T>C | synonymous_variant | 0.19 |
fgd1 | 491010 | c.228C>G | synonymous_variant | 0.19 |
fgd1 | 491013 | c.231C>G | synonymous_variant | 0.21 |
fgd1 | 491022 | c.240C>G | synonymous_variant | 0.23 |
fgd1 | 491043 | c.261T>G | synonymous_variant | 0.19 |
fgd1 | 491049 | c.267T>G | synonymous_variant | 0.18 |
fgd1 | 491058 | c.276C>G | synonymous_variant | 0.19 |
fgd1 | 491064 | c.282A>T | synonymous_variant | 0.18 |
fgd1 | 491077 | p.Asn99Asp | missense_variant | 0.2 |
fgd1 | 491082 | c.300T>C | synonymous_variant | 0.21 |
fgd1 | 491083 | p.Val101Ile | missense_variant | 0.21 |
fgd1 | 491091 | c.309T>C | synonymous_variant | 0.2 |
fgd1 | 491097 | c.315G>C | synonymous_variant | 0.19 |
fgd1 | 491106 | c.324T>C | synonymous_variant | 0.2 |
fgd1 | 491110 | p.Ala110Ser | missense_variant | 0.2 |
fgd1 | 491115 | c.333G>C | synonymous_variant | 0.18 |
fgd1 | 491124 | c.342C>A | synonymous_variant | 0.19 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
ccsA | 620748 | c.858T>A | synonymous_variant | 0.17 |
rpoB | 760181 | c.375T>C | synonymous_variant | 0.17 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.18 |
rpoB | 760196 | c.390C>G | synonymous_variant | 0.19 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.23 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.24 |
rpoB | 760283 | c.477G>C | synonymous_variant | 0.23 |
rpoB | 760298 | c.492G>C | synonymous_variant | 0.26 |
rpoB | 760328 | c.522G>C | synonymous_variant | 0.27 |
rpoB | 760331 | c.525G>C | synonymous_variant | 0.25 |
rpoB | 760340 | c.534G>T | synonymous_variant | 0.23 |
rpoB | 760346 | c.540C>T | synonymous_variant | 0.22 |
rpoB | 760356 | p.Thr184Ser | missense_variant | 0.17 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.17 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.16 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.18 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.22 |
rpoB | 760670 | c.864G>C | synonymous_variant | 0.2 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.21 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.22 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.23 |
rpoB | 760724 | c.918T>C | synonymous_variant | 0.23 |
rpoB | 760730 | c.924T>C | synonymous_variant | 0.23 |
rpoB | 760751 | c.945G>C | synonymous_variant | 0.26 |
rpoB | 760757 | c.951T>C | synonymous_variant | 0.25 |
rpoB | 760758 | p.Val318Thr | missense_variant | 0.26 |
rpoB | 760769 | c.963C>G | synonymous_variant | 0.28 |
rpoB | 760793 | c.987A>G | synonymous_variant | 0.27 |
rpoB | 760805 | c.999G>C | synonymous_variant | 0.21 |
rpoB | 760820 | c.1014T>C | synonymous_variant | 0.17 |
rpoB | 760845 | p.Thr347Ala | missense_variant | 0.17 |
rpoB | 760859 | c.1053T>C | synonymous_variant | 0.18 |
rpoB | 760862 | c.1056G>C | synonymous_variant | 0.17 |
rpoB | 760919 | c.1113C>G | synonymous_variant | 0.19 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.22 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 0.22 |
rpoB | 760931 | c.1125C>G | synonymous_variant | 0.22 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.2 |
rpoB | 760968 | p.Ser388Thr | missense_variant | 0.16 |
rpoB | 760973 | c.1167G>C | synonymous_variant | 0.16 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.17 |
rpoB | 761006 | c.1200C>G | synonymous_variant | 0.2 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.2 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 0.2 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.21 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.18 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.17 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.2 |
rpoB | 761097 | p.Ser431Cys | missense_variant | 0.15 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.17 |
rpoB | 761129 | c.1323G>C | synonymous_variant | 0.22 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.21 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 0.22 |
rpoB | 761150 | c.1344A>T | synonymous_variant | 0.22 |
rpoB | 761153 | c.1347G>C | synonymous_variant | 0.28 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.19 |
rpoB | 761171 | c.1365C>T | synonymous_variant | 0.21 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.23 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.23 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.19 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.22 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.23 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.23 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.22 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.2 |
rpoB | 761258 | c.1452G>A | synonymous_variant | 0.2 |
rpoB | 761261 | c.1455G>C | synonymous_variant | 0.2 |
rpoB | 761264 | c.1458C>G | synonymous_variant | 0.21 |
rpoB | 761300 | c.1494G>C | synonymous_variant | 0.21 |
rpoB | 761324 | c.1518C>T | synonymous_variant | 0.17 |
rpoB | 761354 | c.1548C>T | synonymous_variant | 0.18 |
rpoB | 761384 | c.1578C>G | synonymous_variant | 0.17 |
rpoB | 761531 | c.1725C>G | synonymous_variant | 0.27 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.28 |
rpoB | 761552 | c.1746G>C | synonymous_variant | 0.31 |
rpoB | 761561 | c.1755C>G | synonymous_variant | 0.32 |
rpoB | 761564 | c.1758G>C | synonymous_variant | 0.34 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.35 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.36 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.34 |
rpoB | 761604 | c.1798_1800delCTCinsTTG | synonymous_variant | 0.27 |
rpoB | 761612 | c.1806G>T | synonymous_variant | 0.26 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.26 |
rpoB | 761633 | c.1827G>T | synonymous_variant | 0.26 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.26 |
rpoB | 761645 | c.1839C>G | synonymous_variant | 0.28 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.28 |
rpoB | 761657 | c.1851C>G | synonymous_variant | 0.29 |
rpoB | 761669 | c.1863C>T | synonymous_variant | 0.3 |
rpoB | 761675 | c.1869G>T | synonymous_variant | 0.31 |
rpoB | 761711 | c.1905C>G | synonymous_variant | 0.24 |
rpoB | 761717 | c.1911C>G | synonymous_variant | 0.21 |
rpoB | 761723 | p.Glu639Asp | missense_variant | 0.19 |
rpoB | 761724 | p.Glu640Lys | missense_variant | 0.19 |
rpoB | 761727 | p.Ser641Ala | missense_variant | 0.18 |
rpoB | 761732 | c.1926C>G | synonymous_variant | 0.2 |
rpoB | 761735 | c.1929C>G | synonymous_variant | 0.18 |
rpoB | 761747 | c.1941G>C | synonymous_variant | 0.19 |
rpoB | 761750 | c.1944G>C | synonymous_variant | 0.19 |
rpoB | 761828 | c.2022C>T | synonymous_variant | 0.15 |
rpoB | 761831 | c.2025C>A | synonymous_variant | 0.15 |
rpoB | 761885 | c.2079T>C | synonymous_variant | 0.19 |
rpoB | 761891 | c.2085G>C | synonymous_variant | 0.21 |
rpoB | 761909 | c.2103T>C | synonymous_variant | 0.19 |
rpoB | 761912 | c.2106T>C | synonymous_variant | 0.19 |
rpoB | 761915 | p.Asp703Glu | missense_variant | 0.2 |
rpoB | 761916 | p.Asp704Asn | missense_variant | 0.22 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.28 |
rpoB | 761954 | c.2148C>G | synonymous_variant | 0.3 |
rpoB | 761969 | c.2163G>A | synonymous_variant | 0.3 |
rpoB | 762008 | c.2202C>G | synonymous_variant | 0.34 |
rpoB | 762014 | c.2208C>T | synonymous_variant | 0.35 |
rpoB | 762017 | c.2211A>G | synonymous_variant | 0.36 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.4 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.39 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.39 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.39 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.38 |
rpoB | 762095 | c.2289C>A | synonymous_variant | 0.43 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.41 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.46 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 0.49 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.47 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.48 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.43 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.43 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.45 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.43 |
rpoB | 762284 | c.2478G>T | synonymous_variant | 0.38 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.35 |
rpoB | 762296 | c.2490G>A | synonymous_variant | 0.35 |
rpoB | 762314 | c.2508C>T | synonymous_variant | 0.3 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.3 |
rpoB | 762338 | c.2532T>C | synonymous_variant | 0.3 |
rpoB | 762347 | c.2541T>C | synonymous_variant | 0.29 |
rpoB | 762362 | p.Glu852Asp | missense_variant | 0.23 |
rpoC | 762410 | c.-960T>C | upstream_gene_variant | 0.18 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 0.22 |
rpoC | 762434 | c.-936T>C | upstream_gene_variant | 0.19 |
rpoC | 762443 | c.-927G>C | upstream_gene_variant | 0.2 |
rpoC | 762449 | c.-921C>A | upstream_gene_variant | 0.18 |
rpoC | 762452 | c.-918G>C | upstream_gene_variant | 0.2 |
rpoC | 762470 | c.-900G>C | upstream_gene_variant | 0.25 |
rpoB | 762489 | p.Val895Gln | missense_variant | 0.26 |
rpoC | 762509 | c.-861T>G | upstream_gene_variant | 0.29 |
rpoB | 762510 | p.Ala902Pro | missense_variant | 0.29 |
rpoC | 762521 | c.-849C>G | upstream_gene_variant | 0.32 |
rpoC | 762533 | c.-837T>C | upstream_gene_variant | 0.19 |
rpoC | 762536 | c.-834T>C | upstream_gene_variant | 0.18 |
rpoC | 762537 | c.-833T>C | upstream_gene_variant | 0.18 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.16 |
rpoC | 762947 | c.-423C>G | upstream_gene_variant | 0.23 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.22 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.22 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.23 |
rpoC | 763007 | c.-363C>T | upstream_gene_variant | 0.28 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.31 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 1.0 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.31 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.31 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.38 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.38 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.39 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.39 |
rpoC | 763139 | c.-231C>T | upstream_gene_variant | 0.33 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.29 |
rpoC | 763158 | c.-212C>T | upstream_gene_variant | 0.29 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.31 |
rpoC | 763169 | c.-201A>G | upstream_gene_variant | 0.27 |
rpoC | 763181 | c.-189G>C | upstream_gene_variant | 0.3 |
rpoC | 763202 | c.-168A>C | upstream_gene_variant | 0.22 |
rpoC | 763205 | c.-165G>C | upstream_gene_variant | 0.22 |
rpoC | 763206 | c.-164_-162delAGTinsTCG | upstream_gene_variant | 0.24 |
rpoC | 763226 | c.-144A>G | upstream_gene_variant | 0.27 |
rpoC | 763238 | c.-132T>C | upstream_gene_variant | 0.27 |
rpoC | 763253 | c.-117G>C | upstream_gene_variant | 0.27 |
rpoC | 763262 | c.-108C>A | upstream_gene_variant | 0.28 |
rpoC | 763265 | c.-105G>C | upstream_gene_variant | 0.22 |
rpoC | 763268 | c.-102C>G | upstream_gene_variant | 0.22 |
rpoC | 763283 | c.-87T>C | upstream_gene_variant | 0.15 |
rpoC | 763441 | c.72C>T | synonymous_variant | 0.18 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.21 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.16 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.27 |
rpoC | 763567 | c.198G>A | synonymous_variant | 0.26 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.26 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.28 |
rpoC | 763576 | c.207C>G | synonymous_variant | 0.32 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.35 |
rpoC | 763633 | c.264T>G | synonymous_variant | 0.33 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.33 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.27 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.28 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.34 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.31 |
rpoC | 763709 | c.340C>T | synonymous_variant | 0.29 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.23 |
rpoC | 763735 | c.366G>A | synonymous_variant | 0.26 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.27 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.27 |
rpoC | 763756 | c.387C>T | synonymous_variant | 0.28 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.32 |
rpoC | 763774 | c.405G>C | synonymous_variant | 0.29 |
rpoC | 763792 | p.Glu141Asp | missense_variant | 0.27 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.23 |
rpoC | 763816 | c.447C>G | synonymous_variant | 0.21 |
rpoC | 763835 | p.Ala156Met | missense_variant | 0.18 |
rpoC | 763858 | c.489A>G | synonymous_variant | 0.17 |
rpoC | 763894 | c.525A>G | synonymous_variant | 0.17 |
rpoC | 763900 | c.531G>C | synonymous_variant | 0.23 |
rpoC | 763909 | c.540C>T | synonymous_variant | 0.26 |
rpoC | 763945 | c.576T>C | synonymous_variant | 0.29 |
rpoC | 763951 | c.582G>C | synonymous_variant | 0.3 |
rpoC | 763960 | c.591T>C | synonymous_variant | 0.32 |
rpoC | 763987 | c.618C>T | synonymous_variant | 0.28 |
rpoC | 763991 | p.Ile208Leu | missense_variant | 0.24 |
rpoC | 763996 | c.627T>C | synonymous_variant | 0.26 |
rpoC | 764002 | c.633C>G | synonymous_variant | 0.27 |
rpoC | 764005 | c.636G>C | synonymous_variant | 0.28 |
rpoC | 764024 | c.655_657delTTGinsCTC | synonymous_variant | 0.21 |
rpoC | 764032 | p.Asp221Glu | missense_variant | 0.21 |
rpoC | 764040 | p.Ser224Thr | missense_variant | 0.23 |
rpoC | 764044 | c.675T>C | synonymous_variant | 0.26 |
rpoC | 764059 | c.690G>T | synonymous_variant | 0.3 |
rpoC | 764083 | c.714A>G | synonymous_variant | 0.29 |
rpoC | 764098 | c.729A>G | synonymous_variant | 0.3 |
rpoC | 764101 | c.732C>G | synonymous_variant | 0.3 |
rpoC | 764102 | p.Val245Ile | missense_variant | 0.3 |
rpoC | 764112 | p.Tyr248Phe | missense_variant | 0.29 |
rpoC | 764116 | c.747C>T | synonymous_variant | 0.29 |
rpoC | 764131 | c.762T>C | synonymous_variant | 0.31 |
rpoC | 764140 | c.771C>T | synonymous_variant | 0.32 |
rpoC | 764188 | c.819A>G | synonymous_variant | 0.27 |
rpoC | 764203 | c.834G>C | synonymous_variant | 0.2 |
rpoC | 764206 | c.837T>C | synonymous_variant | 0.19 |
rpoC | 764213 | p.Arg282Lys | missense_variant | 0.21 |
rpoC | 764245 | c.876C>G | synonymous_variant | 0.21 |
rpoC | 764266 | c.897T>C | synonymous_variant | 0.26 |
rpoC | 764269 | c.900G>C | synonymous_variant | 0.26 |
rpoC | 764272 | c.903G>C | synonymous_variant | 0.27 |
rpoC | 764278 | c.909A>G | synonymous_variant | 0.34 |
rpoC | 764293 | c.924G>C | synonymous_variant | 0.41 |
rpoC | 764338 | c.969G>A | synonymous_variant | 0.37 |
rpoC | 764359 | c.990C>G | synonymous_variant | 0.4 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.4 |
rpoC | 764383 | c.1014C>G | synonymous_variant | 0.42 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 0.39 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.35 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.36 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.35 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.34 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.33 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.34 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.36 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.39 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.4 |
rpoC | 764489 | c.1120C>T | synonymous_variant | 0.37 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.38 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.38 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.45 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.41 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.4 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.39 |
rpoC | 764554 | c.1185C>T | synonymous_variant | 0.44 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.43 |
rpoC | 764575 | c.1206T>C | synonymous_variant | 0.43 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 0.44 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.46 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.41 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.44 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.38 |
rpoC | 764659 | c.1290C>T | synonymous_variant | 0.34 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 0.38 |
rpoC | 764689 | c.1320G>A | synonymous_variant | 0.4 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.41 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.47 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.42 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.41 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.43 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.44 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.41 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.31 |
rpoC | 764923 | c.1554A>G | synonymous_variant | 0.22 |
rpoC | 764932 | c.1563C>G | synonymous_variant | 0.22 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.21 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.17 |
rpoC | 765454 | c.2085C>A | synonymous_variant | 0.16 |
rpoC | 765466 | c.2097C>T | synonymous_variant | 0.17 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.18 |
rpoC | 765493 | c.2124G>C | synonymous_variant | 0.22 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.21 |
rpoC | 765508 | c.2139C>G | synonymous_variant | 0.19 |
rpoC | 765529 | c.2160C>T | synonymous_variant | 0.19 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.17 |
rpoC | 765562 | c.2193G>C | synonymous_variant | 0.2 |
rpoC | 765580 | c.2211G>C | synonymous_variant | 0.21 |
rpoC | 765583 | c.2214G>C | synonymous_variant | 0.2 |
rpoC | 765613 | p.His748Gln | missense_variant | 0.2 |
rpoC | 765625 | c.2256C>G | synonymous_variant | 0.21 |
rpoC | 765628 | c.2259G>C | synonymous_variant | 0.21 |
rpoC | 765631 | p.Asp754Glu | missense_variant | 0.2 |
rpoC | 765658 | c.2289C>T | synonymous_variant | 0.22 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.21 |
rpoC | 765734 | c.2365T>C | synonymous_variant | 0.21 |
rpoC | 765739 | c.2370G>C | synonymous_variant | 0.22 |
rpoC | 765751 | c.2382C>G | synonymous_variant | 0.18 |
rpoC | 765753 | p.Asp795Ala | missense_variant | 0.17 |
rpoC | 765947 | c.2578T>C | synonymous_variant | 0.18 |
rpoC | 765979 | c.2610C>G | synonymous_variant | 0.16 |
rpoC | 765982 | c.2613C>T | synonymous_variant | 0.16 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.2 |
rpoC | 766009 | c.2640G>C | synonymous_variant | 0.19 |
rpoC | 766010 | c.2641_2642delTCinsAG | synonymous_variant | 0.18 |
rpoC | 766018 | c.2649C>T | synonymous_variant | 0.18 |
rpoC | 766021 | c.2652G>C | synonymous_variant | 0.22 |
rpoC | 766027 | c.2658G>C | synonymous_variant | 0.26 |
rpoC | 766043 | p.Gln892Glu | missense_variant | 0.3 |
rpoC | 766061 | p.Val898Ile | missense_variant | 0.27 |
rpoC | 766082 | p.Ala905Gln | missense_variant | 0.23 |
rpoC | 766087 | c.2718C>G | synonymous_variant | 0.24 |
rpoC | 766096 | c.2727G>C | synonymous_variant | 0.23 |
rpoC | 766105 | c.2736C>T | synonymous_variant | 0.23 |
rpoC | 766129 | c.2760C>G | synonymous_variant | 0.18 |
rpoC | 766312 | c.2943T>G | synonymous_variant | 0.17 |
rpoC | 766345 | c.2976T>C | synonymous_variant | 0.23 |
rpoC | 766348 | c.2979A>G | synonymous_variant | 0.22 |
rpoC | 766357 | c.2988C>T | synonymous_variant | 0.26 |
rpoC | 766363 | c.2994G>C | synonymous_variant | 0.25 |
rpoC | 766366 | c.2997C>G | synonymous_variant | 0.24 |
rpoC | 766369 | c.3000C>G | synonymous_variant | 0.24 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.24 |
rpoC | 766390 | c.3021C>T | synonymous_variant | 0.27 |
rpoC | 766402 | c.3033C>G | synonymous_variant | 0.25 |
rpoC | 766408 | c.3039C>T | synonymous_variant | 0.25 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.29 |
rpoC | 766447 | c.3078T>C | synonymous_variant | 0.33 |
rpoC | 766483 | c.3114G>C | synonymous_variant | 0.21 |
rpoC | 766484 | p.Val1039Ile | missense_variant | 0.2 |
rpoC | 766492 | c.3123T>C | synonymous_variant | 0.23 |
rpoC | 766522 | c.3153C>G | synonymous_variant | 0.21 |
rpoC | 766528 | c.3159T>G | synonymous_variant | 0.17 |
rpoC | 766531 | c.3162G>T | synonymous_variant | 0.16 |
rpoC | 766543 | c.3174C>T | synonymous_variant | 0.21 |
rpoC | 766573 | c.3204T>C | synonymous_variant | 0.29 |
rpoC | 766583 | p.Gly1072Ser | missense_variant | 0.27 |
rpoC | 766588 | c.3219G>A | synonymous_variant | 0.26 |
rpoC | 766591 | c.3222A>G | synonymous_variant | 0.27 |
rpoC | 766594 | c.3225G>C | synonymous_variant | 0.26 |
rpoC | 766597 | c.3228C>G | synonymous_variant | 0.26 |
rpoC | 766607 | p.Ile1080Leu | missense_variant | 0.28 |
rpoC | 766633 | c.3264G>C | synonymous_variant | 0.28 |
rpoC | 766657 | c.3288A>G | synonymous_variant | 0.19 |
rpoC | 766666 | c.3297C>G | synonymous_variant | 0.19 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.21 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.24 |
rpoC | 766783 | c.3414C>T | synonymous_variant | 0.22 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.2 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 0.29 |
rpoC | 766864 | c.3495G>C | synonymous_variant | 0.31 |
rpoC | 766894 | c.3525T>C | synonymous_variant | 0.27 |
rpoC | 766895 | c.3526T>C | synonymous_variant | 0.27 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.29 |
rpoC | 766918 | c.3549C>T | synonymous_variant | 0.31 |
rpoC | 766933 | c.3564A>G | synonymous_variant | 0.23 |
rpoC | 766945 | c.3576A>G | synonymous_variant | 0.33 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.34 |
rpoC | 766972 | c.3603G>C | synonymous_variant | 0.36 |
rpoC | 766978 | c.3609C>A | synonymous_variant | 0.37 |
rpoC | 766987 | c.3618G>C | synonymous_variant | 0.41 |
rpoC | 767033 | c.3664_3666delTCGinsAGT | synonymous_variant | 0.59 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.44 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.44 |
rpoC | 767074 | c.3705T>C | synonymous_variant | 0.46 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.45 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.44 |
rpoC | 767134 | c.3765C>A | synonymous_variant | 0.4 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.26 |
rpoC | 767191 | c.3822C>G | synonymous_variant | 0.29 |
rpoC | 767206 | c.3837C>G | synonymous_variant | 0.28 |
rpoC | 767209 | c.3840T>C | synonymous_variant | 0.27 |
rpoC | 767221 | c.3852C>G | synonymous_variant | 0.25 |
rpoC | 767230 | c.3861G>C | synonymous_variant | 0.23 |
rpoC | 767233 | c.3864T>C | synonymous_variant | 0.22 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775937 | c.2544G>C | synonymous_variant | 0.17 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781595 | c.36T>C | synonymous_variant | 0.18 |
rpsL | 781598 | c.39G>C | synonymous_variant | 0.17 |
rpsL | 781608 | p.Ser17Ala | missense_variant | 0.18 |
rpsL | 781628 | c.69T>C | synonymous_variant | 0.25 |
rpsL | 781649 | c.90T>C | synonymous_variant | 0.3 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.28 |
rpsL | 781682 | c.123T>C | synonymous_variant | 0.28 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.26 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.27 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.28 |
rpsL | 781742 | c.183C>T | synonymous_variant | 0.3 |
rpsL | 781751 | c.192G>C | synonymous_variant | 0.27 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.26 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.26 |
rpsL | 781769 | c.210G>A | synonymous_variant | 0.25 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.27 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.26 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.22 |
rpsL | 781835 | c.276T>C | synonymous_variant | 0.22 |
rpsL | 781838 | c.279G>C | synonymous_variant | 0.22 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.24 |
rpsL | 781859 | c.300T>A | synonymous_variant | 0.23 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.23 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.23 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.2 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.2 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.21 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.18 |
rplC | 800648 | c.-161A>T | upstream_gene_variant | 0.24 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.22 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.2 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.2 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.19 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.17 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.16 |
rplC | 801367 | p.Ala187Thr | missense_variant | 0.15 |
fbiC | 1303746 | c.816T>C | synonymous_variant | 0.16 |
fbiC | 1303761 | c.831T>C | synonymous_variant | 0.2 |
fbiC | 1303785 | c.855G>C | synonymous_variant | 0.17 |
fbiC | 1303788 | c.858T>C | synonymous_variant | 0.17 |
fbiC | 1303789 | p.Ile287Val | missense_variant | 0.17 |
fbiC | 1303794 | c.864A>G | synonymous_variant | 0.17 |
fbiC | 1303800 | c.870G>C | synonymous_variant | 0.21 |
fbiC | 1303818 | c.888C>G | synonymous_variant | 0.22 |
fbiC | 1303846 | p.Phe306Val | missense_variant | 0.16 |
fbiC | 1303851 | c.921C>A | synonymous_variant | 0.16 |
fbiC | 1303854 | c.924T>C | synonymous_variant | 0.16 |
fbiC | 1303860 | c.930A>C | synonymous_variant | 0.17 |
fbiC | 1304162 | p.Arg411Gln | missense_variant | 0.16 |
fbiC | 1304169 | c.1239T>C | synonymous_variant | 0.18 |
fbiC | 1304174 | p.Val415Ala | missense_variant | 0.21 |
fbiC | 1304184 | c.1254G>C | synonymous_variant | 0.22 |
fbiC | 1304199 | c.1269C>G | synonymous_variant | 0.22 |
fbiC | 1304757 | c.1827A>G | synonymous_variant | 0.19 |
fbiC | 1304763 | c.1833C>A | synonymous_variant | 0.19 |
fbiC | 1304778 | c.1848T>C | synonymous_variant | 0.2 |
fbiC | 1304784 | c.1854T>C | synonymous_variant | 0.21 |
fbiC | 1304787 | c.1857T>C | synonymous_variant | 0.2 |
fbiC | 1304796 | c.1866G>A | synonymous_variant | 0.19 |
fbiC | 1304808 | c.1878C>G | synonymous_variant | 0.18 |
fbiC | 1304811 | c.1881C>G | synonymous_variant | 0.19 |
fbiC | 1304817 | c.1887T>C | synonymous_variant | 0.22 |
fbiC | 1304829 | c.1899T>C | synonymous_variant | 0.25 |
fbiC | 1304853 | c.1923C>T | synonymous_variant | 0.22 |
fbiC | 1304856 | c.1926C>G | synonymous_variant | 0.22 |
fbiC | 1304869 | c.1939C>T | synonymous_variant | 0.21 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
atpE | 1461119 | c.75T>C | synonymous_variant | 0.21 |
atpE | 1461131 | c.87T>C | synonymous_variant | 0.21 |
atpE | 1461132 | p.Val30Ile | missense_variant | 0.21 |
atpE | 1461149 | c.105T>G | synonymous_variant | 0.2 |
atpE | 1461150 | p.Ile36Val | missense_variant | 0.2 |
atpE | 1461155 | c.111C>G | synonymous_variant | 0.2 |
atpE | 1461159 | p.Val39Ile | missense_variant | 0.2 |
atpE | 1461182 | c.138A>G | synonymous_variant | 0.19 |
atpE | 1461185 | c.141G>C | synonymous_variant | 0.19 |
atpE | 1461197 | c.153A>G | synonymous_variant | 0.19 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472044 | n.199G>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.34 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.34 |
rrl | 1473752 | n.95G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1473756 | n.99G>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473813 | n.156C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473839 | n.182G>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.34 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1473899 | n.242A>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1473943 | n.286G>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473944 | n.287G>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1473966 | n.309T>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1473971 | n.314G>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1473981 | n.324_325insT | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 0.34 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.37 |
rrl | 1474009 | n.352A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474012 | n.355C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474036 | n.379G>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474040 | n.383G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474054 | n.397T>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474093 | n.436G>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474099 | n.442G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474753 | n.1096A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474823 | n.1166C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475199 | n.1542G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475201 | n.1544G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475206 | n.1549C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475209 | n.1552G>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475267 | n.1610G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475291 | n.1634A>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475369 | n.1712G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475402 | n.1745C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475404 | n.1747A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475638 | n.1981C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475659 | n.2002G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476117 | n.2460G>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476689 | n.3032A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476693 | n.3036G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476695 | n.3038T>A | non_coding_transcript_exon_variant | 0.15 |
inhA | 1673547 | c.-655T>G | upstream_gene_variant | 0.18 |
inhA | 1673568 | c.-634C>T | upstream_gene_variant | 0.19 |
fabG1 | 1673569 | p.Val44Ile | missense_variant | 0.17 |
inhA | 1673580 | c.-622T>C | upstream_gene_variant | 0.16 |
inhA | 1673595 | c.-607A>G | upstream_gene_variant | 0.18 |
fabG1 | 1673596 | p.Lys53Glu | missense_variant | 0.19 |
inhA | 1673601 | c.-601G>A | upstream_gene_variant | 0.18 |
inhA | 1673607 | c.-595T>C | upstream_gene_variant | 0.17 |
inhA | 1673616 | c.-586A>G | upstream_gene_variant | 0.19 |
inhA | 1673664 | c.-538A>T | upstream_gene_variant | 0.17 |
fabG1 | 1674049 | p.Gln204Glu | missense_variant | 0.16 |
inhA | 1674054 | c.-148T>C | upstream_gene_variant | 0.21 |
inhA | 1674060 | c.-142A>C | upstream_gene_variant | 0.21 |
fabG1 | 1674079 | p.Pro214Ala | missense_variant | 0.19 |
inhA | 1674084 | c.-118C>G | upstream_gene_variant | 0.22 |
inhA | 1674096 | c.-106G>T | upstream_gene_variant | 0.22 |
inhA | 1674099 | c.-103G>A | upstream_gene_variant | 0.23 |
inhA | 1674114 | c.-88T>G | upstream_gene_variant | 0.22 |
inhA | 1674117 | c.-85C>A | upstream_gene_variant | 0.21 |
inhA | 1674123 | c.-79T>C | upstream_gene_variant | 0.21 |
inhA | 1674126 | c.-76G>C | upstream_gene_variant | 0.18 |
inhA | 1674132 | c.-70T>C | upstream_gene_variant | 0.17 |
fabG1 | 1674136 | p.Ser233Ala | missense_variant | 0.19 |
inhA | 1674141 | c.-61T>C | upstream_gene_variant | 0.2 |
inhA | 1674171 | c.-31T>C | upstream_gene_variant | 0.15 |
inhA | 1674480 | c.279T>C | synonymous_variant | 0.17 |
inhA | 1674486 | c.285T>C | synonymous_variant | 0.29 |
inhA | 1674561 | c.360C>T | synonymous_variant | 0.15 |
inhA | 1674570 | c.369G>A | synonymous_variant | 0.19 |
inhA | 1674582 | c.381T>C | synonymous_variant | 0.2 |
inhA | 1674585 | c.384T>A | synonymous_variant | 0.2 |
inhA | 1674589 | p.Met130Leu | missense_variant | 0.19 |
inhA | 1674601 | p.Leu134Ala | missense_variant | 0.19 |
inhA | 1674774 | c.573A>G | synonymous_variant | 0.16 |
inhA | 1674780 | c.579T>C | synonymous_variant | 0.18 |
inhA | 1674795 | c.594G>C | synonymous_variant | 0.22 |
inhA | 1674801 | c.600T>C | synonymous_variant | 0.23 |
inhA | 1674828 | c.627G>A | synonymous_variant | 0.25 |
inhA | 1674840 | c.639C>G | synonymous_variant | 0.25 |
inhA | 1674846 | p.Ile215Met | missense_variant | 0.24 |
inhA | 1674858 | c.657G>A | synonymous_variant | 0.19 |
inhA | 1674993 | c.792G>A | synonymous_variant | 0.2 |
inhA | 1674994 | p.His265Ser | missense_variant | 0.19 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.19 |
rpsA | 1833667 | c.126C>G | synonymous_variant | 0.18 |
rpsA | 1833703 | c.162C>T | synonymous_variant | 0.29 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.36 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.34 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.29 |
rpsA | 1833760 | c.219C>T | synonymous_variant | 0.28 |
rpsA | 1833772 | c.231C>T | synonymous_variant | 0.28 |
rpsA | 1833793 | c.252C>T | synonymous_variant | 0.24 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.22 |
rpsA | 1833811 | c.270G>C | synonymous_variant | 0.2 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.2 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.2 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.28 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.27 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.24 |
rpsA | 1834057 | c.516G>A | synonymous_variant | 0.25 |
rpsA | 1834099 | c.558C>G | synonymous_variant | 0.2 |
rpsA | 1834102 | c.561T>G | synonymous_variant | 0.21 |
rpsA | 1834108 | c.567C>G | synonymous_variant | 0.22 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.17 |
rpsA | 1834297 | c.756C>G | synonymous_variant | 0.23 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.22 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.26 |
rpsA | 1834369 | c.828C>G | synonymous_variant | 0.28 |
rpsA | 1834375 | c.834G>A | synonymous_variant | 0.28 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.28 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.25 |
rpsA | 1834423 | c.882G>T | synonymous_variant | 0.19 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.22 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.21 |
rpsA | 1834474 | c.933C>G | synonymous_variant | 0.21 |
rpsA | 1834477 | c.936C>T | synonymous_variant | 0.21 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.22 |
rpsA | 1834498 | c.957C>T | synonymous_variant | 0.22 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.22 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.27 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.32 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.32 |
rpsA | 1834636 | c.1095C>T | synonymous_variant | 0.33 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.35 |
rpsA | 1834690 | c.1149T>C | synonymous_variant | 0.39 |
rpsA | 1834693 | c.1152C>T | synonymous_variant | 0.38 |
rpsA | 1834723 | c.1182G>A | synonymous_variant | 0.31 |
rpsA | 1834732 | c.1191T>C | synonymous_variant | 0.31 |
rpsA | 1834733 | p.Ala398Ser | missense_variant | 0.31 |
rpsA | 1834738 | c.1197A>G | synonymous_variant | 0.31 |
rpsA | 1834753 | c.1212T>C | synonymous_variant | 0.29 |
rpsA | 1834765 | c.1224A>G | synonymous_variant | 0.29 |
rpsA | 1834775 | p.Ala412Asn | missense_variant | 0.29 |
rpsA | 1834780 | c.1239A>G | synonymous_variant | 0.28 |
rpsA | 1834789 | c.1248T>C | synonymous_variant | 0.26 |
rpsA | 1834792 | c.1251G>C | synonymous_variant | 0.26 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 0.98 |
ndh | 2101920 | c.1123A>C | synonymous_variant | 0.18 |
ndh | 2101924 | c.1119T>G | synonymous_variant | 0.18 |
ndh | 2101939 | c.1104A>C | synonymous_variant | 0.21 |
ndh | 2101960 | c.1083A>G | synonymous_variant | 0.18 |
ndh | 2101963 | c.1080G>A | synonymous_variant | 0.18 |
ndh | 2101966 | c.1077T>G | synonymous_variant | 0.17 |
ndh | 2101972 | c.1071G>C | synonymous_variant | 0.17 |
ndh | 2101988 | p.Ala352Gly | missense_variant | 0.24 |
ndh | 2101990 | c.1053G>C | synonymous_variant | 0.2 |
ndh | 2102005 | c.1038G>C | synonymous_variant | 0.2 |
ndh | 2102023 | c.1020G>C | synonymous_variant | 0.17 |
ndh | 2102026 | c.1017G>C | synonymous_variant | 0.17 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155017 | c.1095G>C | synonymous_variant | 0.18 |
katG | 2155037 | p.Ala359Thr | missense_variant | 0.17 |
katG | 2155614 | p.Val166Ile | missense_variant | 0.19 |
katG | 2155617 | c.495T>C | synonymous_variant | 0.19 |
katG | 2155623 | c.489C>T | synonymous_variant | 0.2 |
katG | 2155632 | c.480A>T | synonymous_variant | 0.24 |
katG | 2155637 | p.Leu159Ile | missense_variant | 0.25 |
katG | 2155641 | p.Lys157Asn | missense_variant | 0.24 |
katG | 2155647 | c.465C>T | synonymous_variant | 0.23 |
katG | 2155650 | c.462G>A | synonymous_variant | 0.23 |
katG | 2155680 | c.432G>C | synonymous_variant | 0.21 |
katG | 2155686 | c.426C>T | synonymous_variant | 0.21 |
katG | 2155704 | c.408C>G | synonymous_variant | 0.18 |
katG | 2155716 | c.396T>C | synonymous_variant | 0.17 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2517917 | c.-198G>T | upstream_gene_variant | 0.2 |
kasA | 2518618 | c.504G>C | synonymous_variant | 0.17 |
kasA | 2518627 | c.513T>C | synonymous_variant | 0.18 |
kasA | 2518636 | c.522C>T | synonymous_variant | 0.17 |
kasA | 2518642 | c.528A>G | synonymous_variant | 0.16 |
kasA | 2518672 | c.558G>C | synonymous_variant | 0.19 |
kasA | 2518705 | c.591T>G | synonymous_variant | 0.16 |
kasA | 2518747 | c.633C>G | synonymous_variant | 0.19 |
kasA | 2518777 | c.663C>T | synonymous_variant | 0.22 |
kasA | 2518783 | c.669T>C | synonymous_variant | 0.2 |
kasA | 2518789 | c.675G>C | synonymous_variant | 0.19 |
kasA | 2518792 | c.678C>A | synonymous_variant | 0.21 |
kasA | 2518795 | c.681C>G | synonymous_variant | 0.2 |
kasA | 2518825 | c.711T>C | synonymous_variant | 0.21 |
kasA | 2518828 | c.714G>A | synonymous_variant | 0.19 |
kasA | 2518834 | c.720C>T | synonymous_variant | 0.2 |
kasA | 2518843 | c.729T>G | synonymous_variant | 0.19 |
kasA | 2518847 | p.Leu245Met | missense_variant | 0.19 |
kasA | 2518853 | p.Leu247Ile | missense_variant | 0.21 |
kasA | 2518864 | c.750G>C | synonymous_variant | 0.21 |
kasA | 2518867 | c.753G>A | synonymous_variant | 0.21 |
kasA | 2518879 | c.765A>G | synonymous_variant | 0.21 |
folC | 2746915 | c.684G>C | synonymous_variant | 0.18 |
folC | 2746920 | p.Ser227Ala | missense_variant | 0.18 |
folC | 2746921 | c.678T>C | synonymous_variant | 0.21 |
folC | 2746948 | c.651G>C | synonymous_variant | 0.21 |
folC | 2746954 | c.645G>A | synonymous_variant | 0.2 |
folC | 2746960 | c.639C>A | synonymous_variant | 0.19 |
folC | 2747026 | c.573C>A | synonymous_variant | 0.17 |
folC | 2747343 | p.Val86Ile | missense_variant | 0.18 |
folC | 2747347 | c.252G>A | synonymous_variant | 0.18 |
folC | 2747350 | c.249C>T | synonymous_variant | 0.16 |
thyX | 3067349 | c.597G>C | synonymous_variant | 0.17 |
thyX | 3067355 | c.591A>G | synonymous_variant | 0.18 |
thyX | 3067394 | c.552G>C | synonymous_variant | 0.19 |
thyX | 3067412 | c.534C>G | synonymous_variant | 0.16 |
thyX | 3067427 | p.Ala173Ser | missense_variant | 0.21 |
thyX | 3067439 | c.507A>G | synonymous_variant | 0.18 |
thyX | 3067448 | c.498G>A | synonymous_variant | 0.15 |
thyX | 3067661 | c.285C>G | synonymous_variant | 0.15 |
thyX | 3067664 | c.282C>T | synonymous_variant | 0.15 |
thyX | 3067679 | c.267C>T | synonymous_variant | 0.17 |
thyX | 3067694 | c.252G>C | synonymous_variant | 0.18 |
thyX | 3067739 | c.207T>C | synonymous_variant | 0.2 |
thyX | 3067742 | c.204A>C | synonymous_variant | 0.18 |
thyX | 3067761 | p.Arg62Pro | missense_variant | 0.16 |
thyX | 3067765 | p.Leu61Ile | missense_variant | 0.17 |
thyX | 3067781 | c.165C>G | synonymous_variant | 0.2 |
thyX | 3067793 | c.153T>C | synonymous_variant | 0.21 |
thyX | 3067799 | c.147G>A | synonymous_variant | 0.2 |
thyX | 3067802 | c.144C>G | synonymous_variant | 0.22 |
thyX | 3067814 | c.132T>C | synonymous_variant | 0.19 |
thyX | 3067838 | c.108C>T | synonymous_variant | 0.23 |
thyX | 3067849 | p.Pro33Ala | missense_variant | 0.25 |
thyX | 3067850 | c.96A>C | synonymous_variant | 0.25 |
thyX | 3067869 | p.Thr26Asp | missense_variant | 0.23 |
thyX | 3067885 | p.Pro21Ala | missense_variant | 0.19 |
thyX | 3067886 | c.60A>C | synonymous_variant | 0.17 |
thyX | 3067889 | c.57C>G | synonymous_variant | 0.17 |
thyA | 3073920 | c.552C>G | synonymous_variant | 0.16 |
thyA | 3074097 | c.375C>G | synonymous_variant | 0.21 |
thyA | 3074100 | c.372T>C | synonymous_variant | 0.2 |
thyA | 3074106 | c.366T>C | synonymous_variant | 0.21 |
thyA | 3074334 | c.138T>C | synonymous_variant | 0.16 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339117 | c.-1C>A | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiA | 3641332 | p.Gly264Arg | missense_variant | 0.98 |
alr | 3840987 | p.Val145Ala | missense_variant | 0.15 |
alr | 3841017 | p.Leu135Glu | missense_variant | 0.16 |
alr | 3841022 | c.399C>G | synonymous_variant | 0.16 |
alr | 3841037 | p.Val128Ile | missense_variant | 0.17 |
alr | 3841043 | c.378C>T | synonymous_variant | 0.18 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.29 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.35 |
rpoA | 3877656 | c.852T>C | synonymous_variant | 0.37 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.37 |
rpoA | 3877677 | p.Ala277Ser | missense_variant | 0.33 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.32 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.33 |
rpoA | 3877704 | c.804G>T | synonymous_variant | 0.32 |
rpoA | 3877728 | c.780C>G | synonymous_variant | 0.29 |
rpoA | 3877731 | c.777G>C | synonymous_variant | 0.27 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.3 |
rpoA | 3877761 | c.747G>C | synonymous_variant | 0.29 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.3 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.31 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.31 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.29 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.23 |
rpoA | 3877848 | c.660C>T | synonymous_variant | 0.29 |
rpoA | 3877857 | c.651G>A | synonymous_variant | 0.3 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.3 |
rpoA | 3877872 | c.636C>T | synonymous_variant | 0.28 |
rpoA | 3877875 | c.633T>C | synonymous_variant | 0.28 |
rpoA | 3877900 | p.Ser203Asn | missense_variant | 0.22 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.23 |
rpoA | 3877908 | p.Asn200Ser | missense_variant | 0.23 |
rpoA | 3877920 | c.588G>C | synonymous_variant | 0.25 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.25 |
rpoA | 3877986 | c.522G>C | synonymous_variant | 0.32 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.3 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.3 |
rpoA | 3878022 | c.486T>C | synonymous_variant | 0.26 |
rpoA | 3878025 | c.483C>T | synonymous_variant | 0.28 |
rpoA | 3878028 | c.480G>C | synonymous_variant | 0.29 |
rpoA | 3878031 | c.477T>C | synonymous_variant | 0.28 |
rpoA | 3878043 | c.465G>C | synonymous_variant | 0.29 |
rpoA | 3878046 | c.462T>C | synonymous_variant | 0.29 |
rpoA | 3878049 | c.459G>C | synonymous_variant | 0.29 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.28 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.22 |
rpoA | 3878064 | c.444G>C | synonymous_variant | 0.22 |
rpoA | 3878067 | c.441C>G | synonymous_variant | 0.21 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.22 |
rpoA | 3878076 | c.432C>T | synonymous_variant | 0.23 |
rpoA | 3878082 | c.426T>C | synonymous_variant | 0.24 |
rpoA | 3878094 | c.414C>G | synonymous_variant | 0.24 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.25 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.27 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.24 |
rpoA | 3878130 | c.378C>G | synonymous_variant | 0.26 |
rpoA | 3878141 | p.Met123Leu | missense_variant | 0.26 |
rpoA | 3878143 | p.Gly122Asp | missense_variant | 0.22 |
rpoA | 3878163 | c.345C>T | synonymous_variant | 0.31 |
rpoA | 3878184 | c.324C>T | synonymous_variant | 0.36 |
rpoA | 3878187 | c.321C>G | synonymous_variant | 0.36 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.4 |
rpoA | 3878199 | c.309T>C | synonymous_variant | 0.41 |
rpoA | 3878205 | c.303T>C | synonymous_variant | 0.4 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.4 |
rpoA | 3878247 | c.261G>C | synonymous_variant | 0.43 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.42 |
rpoA | 3878276 | c.232C>T | synonymous_variant | 0.39 |
rpoA | 3878284 | p.Glu75Ala | missense_variant | 0.37 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.36 |
rpoA | 3878304 | c.204G>C | synonymous_variant | 0.38 |
rpoA | 3878307 | c.201C>G | synonymous_variant | 0.38 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 0.41 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.4 |
rpoA | 3878331 | c.177A>G | synonymous_variant | 0.31 |
rpoA | 3878334 | c.174T>C | synonymous_variant | 0.29 |
rpoA | 3878337 | c.171T>C | synonymous_variant | 0.33 |
rpoA | 3878346 | c.162T>C | synonymous_variant | 0.39 |
rpoA | 3878352 | c.156C>T | synonymous_variant | 0.36 |
rpoA | 3878364 | c.144A>T | synonymous_variant | 0.38 |
rpoA | 3878367 | c.141C>G | synonymous_variant | 0.36 |
rpoA | 3878376 | c.132G>C | synonymous_variant | 0.33 |
rpoA | 3878385 | c.123C>G | synonymous_variant | 0.36 |
rpoA | 3878388 | c.120C>G | synonymous_variant | 0.36 |
rpoA | 3878391 | c.117T>C | synonymous_variant | 0.35 |
rpoA | 3878396 | c.112C>T | synonymous_variant | 0.37 |
rpoA | 3878415 | c.93C>T | synonymous_variant | 0.34 |
rpoA | 3878436 | c.72A>G | synonymous_variant | 0.37 |
rpoA | 3878442 | c.66G>C | synonymous_variant | 0.32 |
rpoA | 3878454 | c.54A>T | synonymous_variant | 0.26 |
rpoA | 3878458 | p.Asn17Ser | missense_variant | 0.28 |
rpoA | 3878471 | p.Val13Ile | missense_variant | 0.25 |
rpoA | 3878472 | p.Asp12Glu | missense_variant | 0.25 |
rpoA | 3878478 | c.30C>G | synonymous_variant | 0.26 |
rpoA | 3878483 | c.25C>T | synonymous_variant | 0.26 |
rpoA | 3878484 | c.24C>A | synonymous_variant | 0.32 |
rpoA | 3878490 | c.18C>A | synonymous_variant | 0.28 |
rpoA | 3878496 | c.12A>T | synonymous_variant | 0.33 |
rpoA | 3878672 | c.-165A>T | upstream_gene_variant | 0.25 |
rpoA | 3878698 | c.-191A>G | upstream_gene_variant | 0.29 |
rpoA | 3878701 | c.-194C>G | upstream_gene_variant | 0.29 |
clpC1 | 4038359 | c.2346A>G | synonymous_variant | 0.16 |
clpC1 | 4038388 | c.2317T>C | synonymous_variant | 0.17 |
clpC1 | 4038398 | c.2307G>T | synonymous_variant | 0.2 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 0.2 |
clpC1 | 4038433 | c.2272C>T | synonymous_variant | 0.24 |
clpC1 | 4038444 | p.Ala754Lys | missense_variant | 0.2 |
clpC1 | 4038446 | c.2259T>C | synonymous_variant | 0.2 |
clpC1 | 4038456 | p.Val750Glu | missense_variant | 0.19 |
clpC1 | 4038458 | c.2247G>C | synonymous_variant | 0.19 |
clpC1 | 4038461 | c.2244G>C | synonymous_variant | 0.19 |
clpC1 | 4038486 | p.Gly740Ala | missense_variant | 0.16 |
clpC1 | 4038498 | p.Ser736Thr | missense_variant | 0.2 |
clpC1 | 4038506 | c.2199G>C | synonymous_variant | 0.21 |
clpC1 | 4038530 | p.Glu725Asp | missense_variant | 0.24 |
clpC1 | 4038533 | p.Arg724Lys | missense_variant | 0.24 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.23 |
clpC1 | 4038671 | c.2034T>C | synonymous_variant | 0.24 |
clpC1 | 4038683 | c.2022T>G | synonymous_variant | 0.28 |
clpC1 | 4038692 | c.2013C>G | synonymous_variant | 0.33 |
clpC1 | 4038701 | c.2004G>C | synonymous_variant | 0.33 |
clpC1 | 4038704 | c.2001T>C | synonymous_variant | 0.33 |
clpC1 | 4038707 | c.1998C>G | synonymous_variant | 0.32 |
clpC1 | 4038710 | c.1995G>C | synonymous_variant | 0.33 |
clpC1 | 4038713 | c.1992T>C | synonymous_variant | 0.35 |
clpC1 | 4038740 | c.1965G>C | synonymous_variant | 0.3 |
clpC1 | 4038755 | c.1950G>C | synonymous_variant | 0.27 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.29 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.29 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 0.29 |
clpC1 | 4038815 | c.1890G>C | synonymous_variant | 0.19 |
clpC1 | 4038821 | c.1884G>A | synonymous_variant | 0.19 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.19 |
clpC1 | 4038884 | c.1821C>T | synonymous_variant | 0.17 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.22 |
clpC1 | 4038911 | c.1794G>C | synonymous_variant | 0.2 |
clpC1 | 4038923 | c.1780_1782delCTAinsTTG | synonymous_variant | 0.21 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.22 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.21 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.2 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.2 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.27 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.3 |
clpC1 | 4039001 | c.1704C>T | synonymous_variant | 0.31 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.27 |
clpC1 | 4039064 | c.1641C>T | synonymous_variant | 0.29 |
clpC1 | 4039094 | c.1611C>G | synonymous_variant | 0.24 |
clpC1 | 4039103 | c.1602T>C | synonymous_variant | 0.24 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.22 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.22 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.22 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.23 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.23 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.21 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.23 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.24 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.22 |
clpC1 | 4039193 | c.1512C>G | synonymous_variant | 0.21 |
clpC1 | 4039241 | c.1464G>C | synonymous_variant | 0.17 |
clpC1 | 4039286 | c.1419T>C | synonymous_variant | 0.16 |
clpC1 | 4039338 | p.Thr456Lys | missense_variant | 0.16 |
clpC1 | 4039391 | c.1314T>G | synonymous_variant | 0.19 |
clpC1 | 4039409 | c.1296T>C | synonymous_variant | 0.17 |
clpC1 | 4039412 | c.1293T>G | synonymous_variant | 0.16 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.21 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.21 |
clpC1 | 4039454 | c.1251A>G | synonymous_variant | 0.22 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 0.22 |
clpC1 | 4039466 | c.1239T>G | synonymous_variant | 0.22 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.22 |
clpC1 | 4039481 | c.1224T>G | synonymous_variant | 0.25 |
clpC1 | 4039556 | c.1149G>C | synonymous_variant | 0.19 |
clpC1 | 4039559 | c.1146C>G | synonymous_variant | 0.19 |
clpC1 | 4039570 | c.1134_1135insCA | frameshift_variant | 0.19 |
clpC1 | 4039575 | c.1128_1129delTG | frameshift_variant | 0.19 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.19 |
clpC1 | 4039652 | c.1053G>C | synonymous_variant | 0.23 |
clpC1 | 4039661 | c.1044T>C | synonymous_variant | 0.24 |
clpC1 | 4039664 | c.1041G>C | synonymous_variant | 0.23 |
clpC1 | 4039691 | c.1014G>C | synonymous_variant | 0.22 |
clpC1 | 4039964 | c.741C>T | synonymous_variant | 0.18 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.18 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 0.18 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.18 |
clpC1 | 4040147 | c.558A>G | synonymous_variant | 0.18 |
clpC1 | 4040153 | c.552A>G | synonymous_variant | 0.15 |
clpC1 | 4040165 | c.540G>C | synonymous_variant | 0.16 |
clpC1 | 4040180 | c.525C>T | synonymous_variant | 0.21 |
clpC1 | 4040246 | c.459C>A | synonymous_variant | 0.18 |
clpC1 | 4040258 | c.447G>A | synonymous_variant | 0.18 |
clpC1 | 4040267 | c.438A>G | synonymous_variant | 0.25 |
clpC1 | 4040273 | c.432T>C | synonymous_variant | 0.24 |
clpC1 | 4040277 | c.427_428delTCinsAG | synonymous_variant | 0.22 |
clpC1 | 4040279 | c.426C>G | synonymous_variant | 0.22 |
clpC1 | 4040309 | c.396C>T | synonymous_variant | 0.21 |
clpC1 | 4040315 | c.390G>A | synonymous_variant | 0.17 |
clpC1 | 4040324 | c.381G>T | synonymous_variant | 0.17 |
clpC1 | 4040336 | c.369G>A | synonymous_variant | 0.17 |
clpC1 | 4040342 | c.363C>G | synonymous_variant | 0.17 |
embC | 4240726 | c.864G>C | synonymous_variant | 0.19 |
embC | 4240738 | c.876C>A | synonymous_variant | 0.2 |
embC | 4240771 | c.909G>A | synonymous_variant | 0.25 |
embC | 4240780 | c.918T>C | synonymous_variant | 0.27 |
embC | 4240786 | c.924C>T | synonymous_variant | 0.22 |
embC | 4240789 | c.927T>C | synonymous_variant | 0.22 |
embC | 4240805 | c.943_945delCGCinsAGG | synonymous_variant | 0.16 |
embC | 4240811 | p.Phe317Leu | missense_variant | 0.16 |
embC | 4241023 | c.1161T>C | synonymous_variant | 0.17 |
embC | 4241050 | c.1188T>G | synonymous_variant | 0.18 |
embC | 4241053 | c.1191G>C | synonymous_variant | 0.15 |
embC | 4241056 | c.1194C>G | synonymous_variant | 0.18 |
embC | 4241104 | c.1242G>A | synonymous_variant | 0.19 |
embC | 4241107 | c.1245G>C | synonymous_variant | 0.21 |
embC | 4241116 | c.1254C>G | synonymous_variant | 0.24 |
embC | 4241126 | c.1264C>T | synonymous_variant | 0.2 |
embC | 4241140 | c.1278A>G | synonymous_variant | 0.2 |
embC | 4241158 | c.1296T>G | synonymous_variant | 0.2 |
embC | 4241161 | c.1299C>G | synonymous_variant | 0.18 |
embC | 4241162 | c.1300T>C | synonymous_variant | 0.19 |
embC | 4241176 | c.1314C>G | synonymous_variant | 0.23 |
embC | 4241203 | c.1341T>C | synonymous_variant | 0.25 |
embC | 4241224 | c.1362G>A | synonymous_variant | 0.25 |
embC | 4241230 | c.1368A>G | synonymous_variant | 0.21 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 0.98 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4245074 | c.1842G>C | synonymous_variant | 0.17 |
embA | 4245078 | p.Trp616Gly | missense_variant | 0.17 |
embA | 4245083 | c.1851A>G | synonymous_variant | 0.19 |
embA | 4245089 | c.1857G>C | synonymous_variant | 0.19 |
embA | 4245093 | p.Ile621Val | missense_variant | 0.19 |
embA | 4245101 | c.1869G>C | synonymous_variant | 0.19 |
embA | 4245137 | c.1905T>C | synonymous_variant | 0.21 |
embA | 4245149 | c.1917C>G | synonymous_variant | 0.23 |
embA | 4245182 | c.1950T>C | synonymous_variant | 0.21 |
embA | 4245186 | p.Thr652Ala | missense_variant | 0.21 |
embA | 4245198 | p.Leu656Ala | missense_variant | 0.21 |
embA | 4245206 | c.1974A>C | synonymous_variant | 0.2 |
embA | 4245207 | c.1975T>C | synonymous_variant | 0.2 |
embA | 4245215 | c.1983A>C | synonymous_variant | 0.2 |
embA | 4245222 | p.Tyr664Gln | missense_variant | 0.18 |
embB | 4246034 | c.-480G>C | upstream_gene_variant | 0.17 |
embB | 4246040 | c.-474C>G | upstream_gene_variant | 0.18 |
embA | 4246041 | p.Asp937Asn | missense_variant | 0.18 |
embB | 4246055 | c.-459T>C | upstream_gene_variant | 0.19 |
embB | 4246064 | c.-450T>C | upstream_gene_variant | 0.2 |
embB | 4247375 | p.Leu288Val | missense_variant | 0.17 |
embB | 4247380 | c.867C>G | synonymous_variant | 0.2 |
embB | 4247386 | c.873T>C | synonymous_variant | 0.21 |
embB | 4247389 | c.876C>G | synonymous_variant | 0.23 |
embB | 4247395 | c.882C>G | synonymous_variant | 0.23 |
embB | 4247401 | c.888T>C | synonymous_variant | 0.23 |
embB | 4247404 | c.891G>C | synonymous_variant | 0.24 |
embB | 4247437 | c.924A>G | synonymous_variant | 0.3 |
embB | 4247446 | c.933C>T | synonymous_variant | 0.27 |
embB | 4247464 | c.951C>G | synonymous_variant | 0.26 |
embB | 4247470 | c.957T>C | synonymous_variant | 0.22 |
embB | 4247485 | c.972C>T | synonymous_variant | 0.23 |
embB | 4247491 | c.978G>C | synonymous_variant | 0.22 |
embB | 4247497 | c.984T>C | synonymous_variant | 0.22 |
embB | 4247512 | c.999T>C | synonymous_variant | 0.17 |
embB | 4249640 | c.3127T>C | synonymous_variant | 0.93 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268985 | c.-149A>G | upstream_gene_variant | 0.17 |
aftB | 4268991 | c.-155C>T | upstream_gene_variant | 0.21 |
aftB | 4268994 | c.-158T>G | upstream_gene_variant | 0.21 |
aftB | 4269006 | c.-170T>C | upstream_gene_variant | 0.21 |
aftB | 4269012 | c.-176G>C | upstream_gene_variant | 0.22 |
aftB | 4269015 | c.-179G>A | upstream_gene_variant | 0.21 |
aftB | 4269018 | c.-182G>C | upstream_gene_variant | 0.2 |
aftB | 4269027 | c.-191C>A | upstream_gene_variant | 0.2 |
aftB | 4269033 | c.-197T>C | upstream_gene_variant | 0.21 |
aftB | 4269036 | c.-200C>G | upstream_gene_variant | 0.22 |
aftB | 4269042 | c.-206G>C | upstream_gene_variant | 0.23 |
aftB | 4269048 | c.-212C>T | upstream_gene_variant | 0.24 |
aftB | 4269051 | c.-215C>T | upstream_gene_variant | 0.22 |
ubiA | 4269075 | p.Ile253Val | missense_variant | 0.25 |
aftB | 4269081 | c.-245G>C | upstream_gene_variant | 0.2 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |