Run ID: ERR2513121
Sample name:
Date: 31-03-2023 19:28:37
Number of reads: 1658248
Percentage reads mapped: 73.65
Strain: lineage3.1.3
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
lineage3.1.3 | East-African-Indian | CAS | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6175 | c.936G>A | synonymous_variant | 0.15 |
gyrB | 6187 | c.948C>T | synonymous_variant | 0.14 |
gyrB | 6203 | c.964_966delAGCinsTCG | synonymous_variant | 0.13 |
gyrB | 6215 | p.Ser326Thr | missense_variant | 0.12 |
gyrB | 6242 | p.Arg335Lys | missense_variant | 0.24 |
gyrB | 6250 | c.1011A>T | synonymous_variant | 0.22 |
gyrB | 6253 | c.1014G>C | synonymous_variant | 0.2 |
gyrB | 6265 | c.1026C>T | synonymous_variant | 0.22 |
gyrB | 6268 | c.1029C>G | synonymous_variant | 0.22 |
gyrB | 6280 | c.1041T>C | synonymous_variant | 0.18 |
gyrB | 6286 | c.1047T>C | synonymous_variant | 0.18 |
gyrB | 6292 | c.1053G>T | synonymous_variant | 0.16 |
gyrA | 6727 | c.-575G>T | upstream_gene_variant | 0.13 |
gyrA | 6730 | c.-572A>G | upstream_gene_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7424 | c.123G>A | synonymous_variant | 0.21 |
gyrA | 7433 | c.132G>C | synonymous_variant | 0.23 |
gyrA | 7436 | c.135C>T | synonymous_variant | 0.22 |
gyrA | 7442 | c.141G>C | synonymous_variant | 0.23 |
gyrA | 7457 | c.156T>C | synonymous_variant | 0.26 |
gyrA | 7460 | c.159C>G | synonymous_variant | 0.26 |
gyrA | 7463 | c.162G>C | synonymous_variant | 0.26 |
gyrA | 7472 | c.171T>C | synonymous_variant | 0.21 |
gyrA | 7475 | c.174A>G | synonymous_variant | 0.23 |
gyrA | 7480 | p.Phe60Tyr | missense_variant | 0.25 |
gyrA | 7484 | c.183T>C | synonymous_variant | 0.24 |
gyrA | 7487 | c.186C>G | synonymous_variant | 0.24 |
gyrA | 7499 | c.198G>A | synonymous_variant | 0.3 |
gyrA | 7523 | c.222C>A | synonymous_variant | 0.32 |
gyrA | 7526 | c.225G>T | synonymous_variant | 0.32 |
gyrA | 7532 | c.231T>C | synonymous_variant | 0.32 |
gyrA | 7541 | c.240C>G | synonymous_variant | 0.3 |
gyrA | 7547 | c.246C>T | synonymous_variant | 0.26 |
gyrA | 7569 | p.Ala90Ser | missense_variant | 0.22 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7859 | c.558A>C | synonymous_variant | 0.14 |
gyrA | 7865 | c.564T>C | synonymous_variant | 0.12 |
gyrA | 7886 | c.585T>C | synonymous_variant | 0.13 |
gyrA | 7889 | c.588G>A | synonymous_variant | 0.12 |
gyrA | 7890 | c.589C>T | synonymous_variant | 0.12 |
gyrA | 7898 | p.Asp199Glu | missense_variant | 0.13 |
gyrA | 8375 | c.1074G>C | synonymous_variant | 0.13 |
gyrA | 8471 | c.1170T>C | synonymous_variant | 0.15 |
gyrA | 8477 | c.1176C>T | synonymous_variant | 0.15 |
gyrA | 8486 | c.1185T>G | synonymous_variant | 0.17 |
gyrA | 8489 | c.1188A>G | synonymous_variant | 0.16 |
gyrA | 8501 | c.1200G>A | synonymous_variant | 0.16 |
gyrA | 8504 | c.1203G>C | synonymous_variant | 0.16 |
gyrA | 8513 | c.1212C>G | synonymous_variant | 0.16 |
gyrA | 8516 | c.1215T>C | synonymous_variant | 0.16 |
gyrA | 8519 | c.1218A>C | synonymous_variant | 0.16 |
gyrA | 8520 | c.1219C>T | synonymous_variant | 0.16 |
gyrA | 8528 | c.1227G>C | synonymous_variant | 0.15 |
gyrA | 8535 | p.Glu412Gln | missense_variant | 0.16 |
gyrA | 8540 | c.1239C>G | synonymous_variant | 0.16 |
gyrA | 8546 | p.Asp415Glu | missense_variant | 0.16 |
gyrA | 8555 | c.1254G>C | synonymous_variant | 0.18 |
gyrA | 8561 | c.1260A>C | synonymous_variant | 0.16 |
gyrA | 8588 | c.1287G>A | synonymous_variant | 0.15 |
gyrA | 8603 | c.1302A>C | synonymous_variant | 0.13 |
gyrA | 8897 | c.1596T>C | synonymous_variant | 0.19 |
gyrA | 8903 | c.1602T>C | synonymous_variant | 0.19 |
gyrA | 8915 | c.1614A>G | synonymous_variant | 0.21 |
gyrA | 8939 | c.1638T>C | synonymous_variant | 0.18 |
gyrA | 8942 | c.1641G>A | synonymous_variant | 0.18 |
gyrA | 8946 | c.1645T>C | synonymous_variant | 0.18 |
gyrA | 8952 | p.Gln551Ala | missense_variant | 0.18 |
gyrA | 8967 | p.Ala556Asn | missense_variant | 0.19 |
gyrA | 8981 | c.1680G>C | synonymous_variant | 0.18 |
gyrA | 8996 | c.1695T>C | synonymous_variant | 0.19 |
gyrA | 8998 | p.Leu566Trp | missense_variant | 0.19 |
gyrA | 9017 | c.1716C>G | synonymous_variant | 0.17 |
gyrA | 9023 | c.1722A>C | synonymous_variant | 0.17 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 760151 | c.345G>A | synonymous_variant | 0.13 |
rpoB | 760196 | c.390C>G | synonymous_variant | 0.14 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.13 |
rpoB | 760244 | c.438G>C | synonymous_variant | 0.15 |
rpoB | 760283 | c.477G>C | synonymous_variant | 0.15 |
rpoB | 760298 | c.492G>C | synonymous_variant | 0.16 |
rpoB | 760310 | c.504G>C | synonymous_variant | 0.17 |
rpoB | 760316 | c.510C>G | synonymous_variant | 0.18 |
rpoB | 760325 | c.519G>C | synonymous_variant | 0.2 |
rpoB | 760331 | c.525G>C | synonymous_variant | 0.19 |
rpoB | 760334 | c.528G>T | synonymous_variant | 0.2 |
rpoB | 760340 | c.534G>T | synonymous_variant | 0.19 |
rpoB | 760357 | p.Thr184Ser | missense_variant | 0.26 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.27 |
rpoB | 760370 | c.564C>G | synonymous_variant | 0.26 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.25 |
rpoB | 760407 | p.Ser201Gly | missense_variant | 0.22 |
rpoB | 760415 | c.609C>T | synonymous_variant | 0.19 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.2 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.19 |
rpoB | 760784 | c.978G>C | synonymous_variant | 0.12 |
rpoB | 760793 | c.987A>G | synonymous_variant | 0.13 |
rpoB | 760805 | c.999G>C | synonymous_variant | 0.13 |
rpoB | 760817 | c.1011A>G | synonymous_variant | 0.15 |
rpoB | 760820 | c.1014T>C | synonymous_variant | 0.15 |
rpoB | 760826 | c.1020C>G | synonymous_variant | 0.17 |
rpoB | 760829 | c.1023C>T | synonymous_variant | 0.17 |
rpoB | 760830 | c.1024T>C | synonymous_variant | 0.17 |
rpoB | 760841 | c.1035T>C | synonymous_variant | 0.15 |
rpoB | 760848 | p.Thr348Ser | missense_variant | 0.14 |
rpoB | 760859 | c.1053T>C | synonymous_variant | 0.14 |
rpoB | 760862 | c.1056G>C | synonymous_variant | 0.14 |
rpoB | 760865 | c.1059C>T | synonymous_variant | 0.13 |
rpoB | 760877 | c.1071G>T | synonymous_variant | 0.13 |
rpoB | 760883 | c.1077G>C | synonymous_variant | 0.12 |
rpoB | 760916 | c.1110C>T | synonymous_variant | 0.16 |
rpoB | 760919 | c.1113C>T | synonymous_variant | 0.15 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.13 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 0.13 |
rpoB | 760934 | c.1128C>T | synonymous_variant | 0.15 |
rpoB | 760997 | c.1191G>C | synonymous_variant | 0.13 |
rpoB | 761027 | c.1221A>C | synonymous_variant | 0.17 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.16 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.16 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 0.13 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.14 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.15 |
rpoB | 761300 | c.1494G>C | synonymous_variant | 0.13 |
rpoB | 761318 | c.1512G>C | synonymous_variant | 0.14 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.14 |
rpoB | 761333 | c.1527G>T | synonymous_variant | 0.14 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.13 |
rpoB | 761999 | c.2193G>C | synonymous_variant | 0.22 |
rpoB | 762002 | c.2196C>G | synonymous_variant | 0.22 |
rpoB | 762038 | c.2232C>T | synonymous_variant | 0.22 |
rpoB | 762047 | c.2241G>A | synonymous_variant | 0.22 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.24 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.24 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.23 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.23 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.22 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.23 |
rpoB | 762122 | c.2316C>T | synonymous_variant | 0.24 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 0.18 |
rpoB | 762137 | c.2331C>T | synonymous_variant | 0.17 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.19 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.18 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.2 |
rpoB | 762158 | c.2352G>C | synonymous_variant | 0.24 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.22 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.21 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.2 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.24 |
rpoB | 762239 | c.2433G>A | synonymous_variant | 0.22 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.23 |
rpoB | 762284 | c.2478G>T | synonymous_variant | 0.27 |
rpoB | 762293 | c.2487T>G | synonymous_variant | 0.26 |
rpoB | 762308 | c.2502G>C | synonymous_variant | 0.2 |
rpoB | 762314 | c.2508C>T | synonymous_variant | 0.19 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.19 |
rpoB | 762329 | c.2523G>C | synonymous_variant | 0.18 |
rpoB | 762338 | c.2532T>C | synonymous_variant | 0.18 |
rpoB | 762341 | c.2535G>C | synonymous_variant | 0.17 |
rpoB | 762347 | c.2541T>C | synonymous_variant | 0.24 |
rpoB | 762353 | c.2547C>T | synonymous_variant | 0.26 |
rpoB | 762362 | p.Glu852Asp | missense_variant | 0.27 |
rpoB | 762369 | c.2563T>C | synonymous_variant | 0.27 |
rpoC | 762374 | c.-996G>C | upstream_gene_variant | 0.29 |
rpoC | 762380 | c.-990T>C | upstream_gene_variant | 0.29 |
rpoC | 762395 | c.-975G>C | upstream_gene_variant | 0.22 |
rpoC | 762398 | c.-972T>C | upstream_gene_variant | 0.21 |
rpoC | 762401 | c.-969G>C | upstream_gene_variant | 0.19 |
rpoC | 762404 | c.-966T>C | upstream_gene_variant | 0.2 |
rpoC | 762410 | c.-960T>C | upstream_gene_variant | 0.28 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 0.28 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 0.72 |
rpoC | 762443 | c.-927G>C | upstream_gene_variant | 0.3 |
rpoC | 762449 | c.-921C>A | upstream_gene_variant | 0.26 |
rpoC | 762452 | c.-918G>C | upstream_gene_variant | 0.27 |
rpoC | 762470 | c.-900G>C | upstream_gene_variant | 0.24 |
rpoC | 762488 | c.-882G>C | upstream_gene_variant | 0.16 |
rpoC | 762491 | c.-879T>C | upstream_gene_variant | 0.18 |
rpoC | 762509 | c.-861T>G | upstream_gene_variant | 0.14 |
rpoB | 762510 | p.Ala902Pro | missense_variant | 0.14 |
rpoC | 762515 | c.-855C>T | upstream_gene_variant | 0.14 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.15 |
rpoC | 762911 | c.-459C>T | upstream_gene_variant | 0.22 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.21 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.2 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.22 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.24 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.26 |
rpoC | 762989 | c.-381G>A | upstream_gene_variant | 0.24 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.24 |
rpoC | 763004 | c.-366G>A | upstream_gene_variant | 0.23 |
rpoC | 763007 | c.-363C>T | upstream_gene_variant | 0.23 |
rpoC | 763022 | c.-348C>G | upstream_gene_variant | 0.26 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.26 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.75 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.3 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.31 |
rpoC | 763076 | c.-294C>G | upstream_gene_variant | 0.33 |
rpoC | 763088 | c.-282C>G | upstream_gene_variant | 0.31 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.3 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.26 |
rpoC | 763127 | c.-243G>T | upstream_gene_variant | 0.24 |
rpoC | 763130 | c.-240G>A | upstream_gene_variant | 0.24 |
rpoC | 763133 | c.-237G>C | upstream_gene_variant | 0.25 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.27 |
rpoC | 763160 | c.-210G>T | upstream_gene_variant | 0.26 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.26 |
rpoC | 763169 | c.-201A>G | upstream_gene_variant | 0.24 |
rpoC | 763193 | c.-177C>T | upstream_gene_variant | 0.18 |
rpoC | 763202 | c.-168A>C | upstream_gene_variant | 0.16 |
rpoC | 763205 | c.-165G>C | upstream_gene_variant | 0.15 |
rpoC | 763208 | c.-162T>C | upstream_gene_variant | 0.14 |
rpoC | 763214 | c.-156T>C | upstream_gene_variant | 0.14 |
rpoC | 763465 | c.96G>A | synonymous_variant | 0.16 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.18 |
rpoC | 763486 | c.117T>G | synonymous_variant | 0.22 |
rpoC | 763492 | c.123G>T | synonymous_variant | 0.21 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.28 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.23 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.23 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.22 |
rpoC | 763576 | c.207C>G | synonymous_variant | 0.22 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.25 |
rpoC | 763621 | c.252C>G | synonymous_variant | 0.14 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.12 |
rpoC | 763747 | c.378G>A | synonymous_variant | 0.15 |
rpoC | 763765 | c.396T>G | synonymous_variant | 0.13 |
rpoC | 763781 | p.Ser138Ala | missense_variant | 0.14 |
rpoC | 763792 | p.Glu141Asp | missense_variant | 0.16 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.16 |
rpoC | 763813 | c.444C>G | synonymous_variant | 0.17 |
rpoC | 763816 | c.447C>G | synonymous_variant | 0.17 |
rpoC | 763831 | c.462A>G | synonymous_variant | 0.16 |
rpoC | 763837 | c.468G>C | synonymous_variant | 0.14 |
rpoC | 763840 | c.471G>C | synonymous_variant | 0.16 |
rpoC | 763861 | c.492C>T | synonymous_variant | 0.13 |
rpoC | 763872 | p.Gly168Ala | missense_variant | 0.16 |
rpoC | 763876 | p.Glu169Asp | missense_variant | 0.16 |
rpoC | 763879 | c.510A>G | synonymous_variant | 0.15 |
rpoC | 763891 | c.522G>C | synonymous_variant | 0.15 |
rpoC | 763894 | c.525A>G | synonymous_variant | 0.15 |
rpoC | 763900 | c.531G>C | synonymous_variant | 0.14 |
rpoC | 764227 | c.858G>C | synonymous_variant | 0.13 |
rpoC | 764239 | c.870T>G | synonymous_variant | 0.14 |
rpoC | 764254 | c.885G>C | synonymous_variant | 0.19 |
rpoC | 764263 | c.894G>C | synonymous_variant | 0.16 |
rpoC | 764266 | c.897T>C | synonymous_variant | 0.17 |
rpoC | 764272 | c.903G>C | synonymous_variant | 0.17 |
rpoC | 764278 | c.909A>G | synonymous_variant | 0.17 |
rpoC | 764293 | c.924G>C | synonymous_variant | 0.21 |
rpoC | 764297 | p.Met310Leu | missense_variant | 0.23 |
rpoC | 764344 | c.975C>T | synonymous_variant | 0.2 |
rpoC | 764353 | c.984G>T | synonymous_variant | 0.2 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.19 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 0.15 |
rpoC | 764374 | c.1005C>T | synonymous_variant | 0.15 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.17 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 0.17 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.13 |
rpoC | 764435 | c.1066A>C | synonymous_variant | 0.12 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.18 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.18 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.18 |
rpoC | 764500 | c.1131C>G | synonymous_variant | 0.2 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.23 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.2 |
rpoC | 764530 | c.1161C>T | synonymous_variant | 0.15 |
rpoC | 764536 | c.1167G>T | synonymous_variant | 0.15 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.19 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.21 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.25 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 0.32 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.35 |
rpoC | 764623 | c.1254C>G | synonymous_variant | 0.27 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.27 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.28 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.26 |
rpoC | 764692 | c.1323C>T | synonymous_variant | 0.19 |
rpoC | 764701 | c.1332C>G | synonymous_variant | 0.19 |
rpoC | 764713 | c.1344G>T | synonymous_variant | 0.2 |
rpoC | 764719 | c.1350G>A | synonymous_variant | 0.21 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.15 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.15 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.13 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.13 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.13 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.13 |
rpoC | 764851 | c.1482C>T | synonymous_variant | 0.16 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.16 |
rpoC | 764869 | c.1500C>T | synonymous_variant | 0.15 |
rpoC | 764875 | c.1506C>T | synonymous_variant | 0.13 |
rpoC | 765466 | c.2097C>T | synonymous_variant | 0.13 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 0.15 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.13 |
rpoC | 767020 | c.3651C>G | synonymous_variant | 0.13 |
rpoC | 767023 | c.3654C>T | synonymous_variant | 0.13 |
rpoC | 767068 | c.3699G>T | synonymous_variant | 0.21 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.16 |
rpoC | 767104 | c.3735C>G | synonymous_variant | 0.14 |
rpoC | 767105 | p.Asn1246Gln | missense_variant | 0.14 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.18 |
rpoC | 767134 | c.3765C>T | synonymous_variant | 0.16 |
rpoC | 767138 | c.3769C>T | synonymous_variant | 0.19 |
rpoC | 767162 | p.Asn1265Ala | missense_variant | 0.15 |
rpoC | 767167 | c.3798C>T | synonymous_variant | 0.15 |
rpoC | 767174 | p.Asn1269Asp | missense_variant | 0.15 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.15 |
rpoC | 767191 | c.3822C>G | synonymous_variant | 0.14 |
rpoC | 767197 | c.3828G>A | synonymous_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.14 |
rpsL | 781829 | c.270G>T | synonymous_variant | 0.16 |
rpsL | 781832 | c.273T>G | synonymous_variant | 0.15 |
rpsL | 781838 | c.279G>C | synonymous_variant | 0.16 |
rpsL | 781841 | c.282C>T | synonymous_variant | 0.16 |
rpsL | 781859 | c.300T>G | synonymous_variant | 0.16 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.17 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.17 |
rpsL | 781877 | c.318T>C | synonymous_variant | 0.19 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.17 |
rpsL | 781898 | c.339A>C | synonymous_variant | 0.16 |
rpsL | 781901 | c.342C>T | synonymous_variant | 0.15 |
rpsL | 781907 | c.348T>C | synonymous_variant | 0.15 |
rpsL | 781916 | c.357T>C | synonymous_variant | 0.16 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.14 |
fbiC | 1304571 | c.1641G>C | synonymous_variant | 0.13 |
fbiC | 1304580 | c.1650T>C | synonymous_variant | 0.14 |
atpE | 1461116 | c.72C>T | synonymous_variant | 0.19 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471922 | n.78delT | non_coding_transcript_exon_variant | 0.14 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472019 | n.174G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472023 | n.178G>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472028 | n.183A>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472031 | n.186G>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472032 | n.187G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472033 | n.188A>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472035 | n.190G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472037 | n.192A>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472040 | n.195T>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472041 | n.196C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472042 | n.197T>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472337 | n.492C>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472380 | n.535G>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472847 | n.1002G>C | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472848 | n.1003T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472849 | n.1004C>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472858 | n.1013G>T | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472859 | n.1014G>T | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472860 | n.1015C>G | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472953 | n.1108G>A | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.47 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.51 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.49 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.49 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1473291 | n.1446_1447insT | non_coding_transcript_exon_variant | 0.51 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.49 |
rrl | 1473657 | n.-1T>G | upstream_gene_variant | 0.2 |
rrl | 1473668 | n.11C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1473696 | n.39T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473697 | n.40C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473699 | n.42A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473717 | n.60G>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473746 | n.89T>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 0.46 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473812 | n.155G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473814 | n.157A>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1473815 | n.158T>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1473823 | n.166T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473829 | n.172G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473830 | n.173T>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1473832 | n.175C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473836 | n.179A>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474034 | n.377G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474044 | n.387C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474045 | n.388C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474054 | n.397T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474083 | n.426C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474091 | n.434C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474093 | n.436G>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474096 | n.439C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474102 | n.445_446insTGAAC | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474135 | n.478G>A | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.46 |
rrl | 1474185 | n.528G>A | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474186 | n.529A>G | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474266 | n.609T>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474305 | n.648G>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474306 | n.649A>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.39 |
rrl | 1474432 | n.775C>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1474439 | n.782A>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474446 | n.789C>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474627 | n.970G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474629 | n.972G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474639 | n.982G>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474640 | n.983C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1474710 | n.1053T>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474711 | n.1054G>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474712 | n.1055G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474713 | n.1056T>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474753 | n.1096A>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474803 | n.1146G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.49 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475061 | n.1404C>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475062 | n.1405A>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475120 | n.1463G>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475353 | n.1696A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475354 | n.1697A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475363 | n.1706C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475379 | n.1722G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475380 | n.1723C>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475381 | n.1724G>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475382 | n.1725A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475394 | n.1738delT | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475398 | n.1741C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475400 | n.1743C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475401 | n.1744A>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475402 | n.1745C>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475405 | n.1748A>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475429 | n.1772G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475479 | n.1822C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475544 | n.1887A>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475602 | n.1945G>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475603 | n.1946G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475604 | n.1947A>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475612 | n.1955G>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475615 | n.1958C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475616 | n.1959A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475618 | n.1961C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475629 | n.1972G>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475637 | n.1980T>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475638 | n.1981C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475639 | n.1982C>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1475643 | n.1986C>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475647 | n.1990G>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1475764 | n.2107A>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475775 | n.2118G>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.37 |
rrl | 1475991 | n.2334T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475995 | n.2338G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476033 | n.2376T>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476046 | n.2389G>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476088 | n.2431A>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476103 | n.2446C>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476105 | n.2448G>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476106 | n.2449A>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476251 | n.2594T>G | non_coding_transcript_exon_variant | 0.49 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476529 | n.2872A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476540 | n.2883C>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476664 | n.3007T>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476665 | n.3008T>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476674 | n.3017T>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476679 | n.3022T>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476689 | n.3032A>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476690 | n.3033C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476693 | n.3036G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476695 | n.3038T>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476716 | n.3059A>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476723 | n.3066T>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476725 | n.3068C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476726 | n.3069A>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476731 | n.3074G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476732 | n.3075T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476746 | n.3089T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476750 | n.3093T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476759 | n.3102T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476770 | n.3113T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476771 | n.3114G>A | non_coding_transcript_exon_variant | 0.13 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.13 |
rpsA | 1833709 | c.168C>T | synonymous_variant | 0.15 |
rpsA | 1833724 | c.183C>T | synonymous_variant | 0.13 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.13 |
rpsA | 1833730 | c.189C>T | synonymous_variant | 0.13 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.13 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.16 |
rpsA | 1833760 | c.219C>T | synonymous_variant | 0.21 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.19 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.18 |
rpsA | 1833793 | c.252C>T | synonymous_variant | 0.18 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.21 |
rpsA | 1833808 | c.267G>C | synonymous_variant | 0.22 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 0.2 |
rpsA | 1833829 | c.288A>G | synonymous_variant | 0.22 |
rpsA | 1833832 | c.291G>A | synonymous_variant | 0.18 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.17 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.17 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.18 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.19 |
rpsA | 1833862 | c.321G>T | synonymous_variant | 0.18 |
rpsA | 1833894 | p.Ala118Glu | missense_variant | 0.14 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.14 |
rpsA | 1833976 | c.435C>T | synonymous_variant | 0.12 |
rpsA | 1834012 | c.471G>T | synonymous_variant | 0.13 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.14 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.14 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.14 |
rpsA | 1834097 | c.556_557delTCinsAG | synonymous_variant | 0.17 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.18 |
rpsA | 1834150 | c.609G>C | synonymous_variant | 0.17 |
rpsA | 1834153 | c.612T>C | synonymous_variant | 0.16 |
rpsA | 1834154 | p.Asn205Gln | missense_variant | 0.15 |
rpsA | 1834157 | c.616_618delTTGinsCTA | synonymous_variant | 0.16 |
rpsA | 1834162 | c.621A>G | synonymous_variant | 0.16 |
rpsA | 1834165 | c.624A>G | synonymous_variant | 0.16 |
rpsA | 1834168 | c.627C>T | synonymous_variant | 0.16 |
rpsA | 1834169 | p.Thr210Ala | missense_variant | 0.18 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.21 |
rpsA | 1834213 | c.672G>C | synonymous_variant | 0.23 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 0.19 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.18 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.19 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.22 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.18 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.18 |
rpsA | 1834279 | c.738C>T | synonymous_variant | 0.16 |
rpsA | 1834297 | c.756C>T | synonymous_variant | 0.13 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.17 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.17 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.16 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.23 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.23 |
rpsA | 1834423 | c.882G>T | synonymous_variant | 0.28 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.25 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.26 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.25 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.19 |
rpsA | 1834498 | c.957C>T | synonymous_variant | 0.22 |
rpsA | 1834513 | c.972C>G | synonymous_variant | 0.22 |
rpsA | 1834520 | p.Ala327Ser | missense_variant | 0.22 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.2 |
rpsA | 1834540 | c.999G>C | synonymous_variant | 0.14 |
rpsA | 1834543 | c.1002C>G | synonymous_variant | 0.14 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.14 |
rpsA | 1834554 | c.1014_1015delTG | frameshift_variant | 0.15 |
rpsA | 1834558 | c.1017_1018insAG | frameshift_variant | 0.14 |
rpsA | 1834606 | c.1065C>T | synonymous_variant | 0.14 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.14 |
rpsA | 1834619 | c.1078T>C | synonymous_variant | 0.13 |
rpsA | 1834622 | c.1081_1083delTCGinsAGC | synonymous_variant | 0.14 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.15 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.16 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918474 | p.Pro179Ser | missense_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2222732 | c.432delT | frameshift_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.28 |
Rv2752c | 3066008 | p.Pro62Ser | missense_variant | 0.93 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3877857 | c.651G>A | synonymous_variant | 0.12 |
rpoA | 3877875 | c.633T>C | synonymous_variant | 0.13 |
rpoA | 3877878 | c.630G>A | synonymous_variant | 0.15 |
rpoA | 3877887 | c.621G>C | synonymous_variant | 0.17 |
rpoA | 3877893 | c.615C>T | synonymous_variant | 0.17 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.16 |
rpoA | 3877908 | c.600T>C | synonymous_variant | 0.17 |
rpoA | 3877920 | c.588G>C | synonymous_variant | 0.17 |
rpoA | 3877923 | c.585C>T | synonymous_variant | 0.16 |
rpoA | 3877926 | c.582G>C | synonymous_variant | 0.16 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.14 |
rpoA | 3877965 | c.543C>G | synonymous_variant | 0.15 |
rpoA | 3877971 | p.Asp179Glu | missense_variant | 0.14 |
rpoA | 3878143 | p.Gly122Asp | missense_variant | 0.13 |
rpoA | 3878145 | c.363C>G | synonymous_variant | 0.14 |
rpoA | 3878157 | c.351C>G | synonymous_variant | 0.14 |
rpoA | 3878160 | c.348C>G | synonymous_variant | 0.15 |
rpoA | 3878163 | c.345C>T | synonymous_variant | 0.14 |
rpoA | 3878172 | c.336G>C | synonymous_variant | 0.14 |
rpoA | 3878184 | c.324C>T | synonymous_variant | 0.17 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.12 |
rpoA | 3878250 | c.258C>G | synonymous_variant | 0.13 |
rpoA | 3878256 | c.252G>C | synonymous_variant | 0.15 |
rpoA | 3878264 | p.Ser82Gly | missense_variant | 0.17 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.16 |
rpoA | 3878283 | p.Glu75Asp | missense_variant | 0.17 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.16 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.15 |
rpoA | 3878310 | c.198G>C | synonymous_variant | 0.14 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 0.14 |
clpC1 | 4038519 | p.Arg729Gln | missense_variant | 0.16 |
clpC1 | 4038623 | c.2082A>G | synonymous_variant | 0.14 |
clpC1 | 4038640 | p.Asp689Asn | missense_variant | 0.16 |
clpC1 | 4038647 | c.2058T>C | synonymous_variant | 0.16 |
clpC1 | 4038653 | c.2052C>T | synonymous_variant | 0.15 |
clpC1 | 4038695 | c.2010C>G | synonymous_variant | 0.13 |
clpC1 | 4038721 | c.1984C>T | synonymous_variant | 0.13 |
clpC1 | 4038725 | c.1980C>G | synonymous_variant | 0.15 |
clpC1 | 4038740 | c.1965G>C | synonymous_variant | 0.15 |
clpC1 | 4038767 | c.1938G>C | synonymous_variant | 0.13 |
clpC1 | 4038770 | c.1935C>T | synonymous_variant | 0.13 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.13 |
clpC1 | 4038776 | c.1929G>A | synonymous_variant | 0.13 |
clpC1 | 4038779 | c.1926C>G | synonymous_variant | 0.13 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.12 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 0.15 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.19 |
clpC1 | 4038815 | c.1890G>T | synonymous_variant | 0.2 |
clpC1 | 4038842 | c.1863G>C | synonymous_variant | 0.21 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.24 |
clpC1 | 4038884 | c.1821C>T | synonymous_variant | 0.25 |
clpC1 | 4038890 | c.1815G>A | synonymous_variant | 0.3 |
clpC1 | 4038905 | c.1800A>C | synonymous_variant | 0.28 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.26 |
clpC1 | 4038911 | c.1794G>T | synonymous_variant | 0.26 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.26 |
clpC1 | 4038917 | c.1788C>T | synonymous_variant | 0.26 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 0.25 |
clpC1 | 4038941 | c.1764G>C | synonymous_variant | 0.24 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.28 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.27 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.29 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.29 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.27 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.25 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.26 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.26 |
clpC1 | 4039064 | c.1641C>T | synonymous_variant | 0.28 |
clpC1 | 4039067 | c.1638G>C | synonymous_variant | 0.28 |
clpC1 | 4039079 | c.1626C>G | synonymous_variant | 0.25 |
clpC1 | 4039085 | c.1620A>G | synonymous_variant | 0.28 |
clpC1 | 4039091 | c.1614G>T | synonymous_variant | 0.28 |
clpC1 | 4039097 | c.1608G>T | synonymous_variant | 0.27 |
clpC1 | 4039106 | c.1599G>T | synonymous_variant | 0.26 |
clpC1 | 4039109 | c.1596C>T | synonymous_variant | 0.25 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.25 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.25 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.24 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.26 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.22 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.22 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.22 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.21 |
clpC1 | 4039187 | c.1518G>C | synonymous_variant | 0.21 |
clpC1 | 4039190 | c.1515C>G | synonymous_variant | 0.21 |
clpC1 | 4039208 | c.1497C>G | synonymous_variant | 0.25 |
clpC1 | 4039220 | c.1485G>C | synonymous_variant | 0.23 |
clpC1 | 4039226 | c.1479T>C | synonymous_variant | 0.25 |
clpC1 | 4039241 | c.1464G>C | synonymous_variant | 0.26 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.2 |
clpC1 | 4039280 | c.1425G>T | synonymous_variant | 0.2 |
clpC1 | 4039283 | c.1422C>T | synonymous_variant | 0.19 |
clpC1 | 4039286 | c.1419T>C | synonymous_variant | 0.19 |
clpC1 | 4039298 | c.1407T>C | synonymous_variant | 0.16 |
clpC1 | 4039310 | c.1395A>G | synonymous_variant | 0.17 |
clpC1 | 4039313 | c.1392C>T | synonymous_variant | 0.16 |
clpC1 | 4039320 | p.Ala462Gly | missense_variant | 0.18 |
clpC1 | 4039328 | c.1377A>T | synonymous_variant | 0.16 |
clpC1 | 4039337 | c.1368A>C | synonymous_variant | 0.16 |
clpC1 | 4039592 | c.1113G>C | synonymous_variant | 0.15 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.16 |
clpC1 | 4039622 | c.1083C>T | synonymous_variant | 0.2 |
clpC1 | 4039649 | c.1056G>C | synonymous_variant | 0.19 |
clpC1 | 4039673 | c.1032G>A | synonymous_variant | 0.18 |
clpC1 | 4039682 | c.1023C>G | synonymous_variant | 0.2 |
clpC1 | 4039685 | c.1020C>T | synonymous_variant | 0.19 |
clpC1 | 4039694 | c.1011G>T | synonymous_variant | 0.19 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.15 |
clpC1 | 4039733 | c.972G>C | synonymous_variant | 0.14 |
clpC1 | 4039907 | c.798G>A | synonymous_variant | 0.14 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 0.14 |
clpC1 | 4040015 | c.690G>C | synonymous_variant | 0.14 |
clpC1 | 4040021 | c.684A>T | synonymous_variant | 0.12 |
clpC1 | 4040444 | c.261C>G | synonymous_variant | 0.13 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4249195 | c.2682C>A | synonymous_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4408175 | p.Ala10Pro | missense_variant | 1.0 |