Run ID: SRR8692863
Sample name:
Date: 13-08-2023 21:25:30
Number of reads: NA
Percentage reads mapped: NA
Strain: lineage4;lineage2.2
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.05 |
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.89 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 0.11 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rplC | 801268 | p.Cys154Arg | missense_variant | 0.42 | linezolid |
embB | 4247431 | p.Met306Ile | missense_variant | 0.23 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6083 | p.Gly282Cys | missense_variant | 0.18 |
gyrB | 6223 | c.984G>C | synonymous_variant | 0.15 |
gyrB | 6242 | p.Arg335Lys | missense_variant | 0.18 |
gyrB | 6250 | c.1011A>G | synonymous_variant | 0.2 |
gyrB | 6253 | c.1014G>C | synonymous_variant | 0.2 |
gyrB | 6265 | c.1026C>T | synonymous_variant | 0.2 |
gyrB | 6268 | c.1029C>G | synonymous_variant | 0.22 |
gyrB | 6280 | c.1041T>C | synonymous_variant | 0.22 |
gyrB | 6286 | c.1047T>C | synonymous_variant | 0.18 |
gyrB | 6295 | c.1056A>G | synonymous_variant | 0.2 |
gyrB | 6298 | c.1059C>T | synonymous_variant | 0.18 |
gyrB | 6301 | c.1062G>T | synonymous_variant | 0.17 |
gyrA | 6307 | c.-995T>G | upstream_gene_variant | 0.17 |
gyrA | 6310 | c.-992G>C | upstream_gene_variant | 0.17 |
gyrB | 6322 | p.Lys361Asn | missense_variant | 0.17 |
gyrB | 6324 | c.1086dupC | frameshift_variant | 0.17 |
gyrB | 6328 | c.1090delG | frameshift_variant | 0.17 |
gyrA | 6331 | c.-971A>G | upstream_gene_variant | 0.17 |
gyrB | 6343 | p.Glu368Asp | missense_variant | 0.17 |
gyrA | 6361 | c.-941G>A | upstream_gene_variant | 0.25 |
gyrA | 6832 | c.-470C>A | upstream_gene_variant | 0.18 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 0.43 |
gyrA | 7433 | c.132G>C | synonymous_variant | 0.12 |
gyrA | 7451 | c.150C>G | synonymous_variant | 0.15 |
gyrA | 7457 | c.156T>C | synonymous_variant | 0.14 |
gyrA | 7475 | c.174A>C | synonymous_variant | 0.14 |
gyrA | 7484 | c.183T>C | synonymous_variant | 0.14 |
gyrA | 7487 | c.186C>G | synonymous_variant | 0.15 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 0.2 |
gyrA | 7589 | c.288G>C | synonymous_variant | 0.18 |
gyrA | 7607 | c.306C>G | synonymous_variant | 0.18 |
gyrA | 7631 | c.330G>C | synonymous_variant | 0.23 |
gyrA | 7637 | c.336C>T | synonymous_variant | 0.23 |
gyrA | 7658 | c.357A>G | synonymous_variant | 0.17 |
gyrA | 7664 | c.363T>C | synonymous_variant | 0.17 |
gyrA | 7700 | c.399G>T | synonymous_variant | 0.15 |
gyrA | 7710 | c.409T>C | synonymous_variant | 0.14 |
gyrA | 7715 | c.414G>C | synonymous_variant | 0.2 |
gyrA | 7728 | c.427_429delAGGinsCGT | synonymous_variant | 0.19 |
gyrA | 7752 | p.Asp151Asn | missense_variant | 0.2 |
gyrA | 7763 | c.462T>C | synonymous_variant | 0.21 |
gyrA | 7769 | c.468C>T | synonymous_variant | 0.21 |
gyrA | 7775 | c.474C>G | synonymous_variant | 0.21 |
gyrA | 7778 | c.477G>C | synonymous_variant | 0.2 |
gyrA | 7784 | c.483A>G | synonymous_variant | 0.2 |
gyrA | 7796 | c.495G>C | synonymous_variant | 0.21 |
gyrA | 7799 | c.498A>G | synonymous_variant | 0.2 |
gyrA | 7802 | c.501C>G | synonymous_variant | 0.2 |
gyrA | 7814 | c.513C>G | synonymous_variant | 0.21 |
gyrA | 7832 | c.531G>T | synonymous_variant | 0.23 |
gyrA | 7835 | c.534A>G | synonymous_variant | 0.25 |
gyrA | 7841 | c.540C>T | synonymous_variant | 0.23 |
gyrA | 7853 | c.552C>T | synonymous_variant | 0.18 |
gyrA | 8069 | c.768T>C | synonymous_variant | 0.12 |
gyrA | 8078 | c.777A>C | synonymous_variant | 0.12 |
gyrA | 8090 | c.789C>G | synonymous_variant | 0.19 |
gyrA | 8096 | c.795T>G | synonymous_variant | 0.19 |
gyrA | 8099 | c.798T>C | synonymous_variant | 0.19 |
gyrA | 8106 | p.Leu269Ile | missense_variant | 0.17 |
gyrA | 8129 | c.828T>C | synonymous_variant | 0.17 |
gyrA | 8135 | c.834C>G | synonymous_variant | 0.21 |
gyrA | 8156 | c.855T>C | synonymous_variant | 0.2 |
gyrA | 8168 | c.867A>G | synonymous_variant | 0.26 |
gyrA | 8177 | c.876A>C | synonymous_variant | 0.21 |
gyrA | 8189 | c.888G>C | synonymous_variant | 0.22 |
gyrA | 8190 | p.Ala297Thr | missense_variant | 0.18 |
gyrA | 8198 | c.897T>C | synonymous_variant | 0.2 |
gyrA | 8207 | c.906T>C | synonymous_variant | 0.21 |
gyrA | 8210 | c.909G>A | synonymous_variant | 0.21 |
gyrA | 8219 | c.918T>C | synonymous_variant | 0.17 |
gyrA | 8283 | p.Ile328Leu | missense_variant | 0.18 |
gyrA | 8288 | c.987T>C | synonymous_variant | 0.17 |
gyrA | 8294 | c.993T>C | synonymous_variant | 0.17 |
gyrA | 8486 | c.1185T>C | synonymous_variant | 0.13 |
gyrA | 8489 | c.1188A>G | synonymous_variant | 0.19 |
gyrA | 8504 | c.1203G>C | synonymous_variant | 0.33 |
gyrA | 8516 | c.1215T>C | synonymous_variant | 0.3 |
gyrA | 8520 | c.1219C>T | synonymous_variant | 0.3 |
gyrA | 8531 | c.1230G>C | synonymous_variant | 0.33 |
gyrA | 8536 | p.Glu412Ala | missense_variant | 0.33 |
gyrA | 8539 | p.Thr413Asn | missense_variant | 0.33 |
gyrA | 8542 | p.Val414Ala | missense_variant | 0.33 |
gyrA | 8547 | p.Ile416Val | missense_variant | 0.33 |
gyrA | 8555 | c.1254G>C | synonymous_variant | 0.33 |
gyrA | 8556 | p.Ala419Ser | missense_variant | 0.33 |
gyrA | 8561 | c.1260A>C | synonymous_variant | 0.37 |
gyrA | 8567 | p.Ile422Met | missense_variant | 0.37 |
gyrA | 8580 | p.Ile427Val | missense_variant | 0.35 |
gyrA | 8603 | c.1302A>C | synonymous_variant | 0.44 |
gyrA | 8609 | c.1308G>C | synonymous_variant | 0.44 |
gyrA | 8619 | c.1318T>C | synonymous_variant | 0.35 |
gyrA | 8624 | c.1323G>T | synonymous_variant | 0.38 |
gyrA | 8627 | c.1326C>A | synonymous_variant | 0.33 |
gyrA | 8636 | c.1335A>T | synonymous_variant | 0.25 |
gyrA | 8645 | c.1344C>T | synonymous_variant | 0.21 |
gyrA | 8655 | p.Ile452Val | missense_variant | 0.12 |
gyrA | 8690 | c.1389C>G | synonymous_variant | 0.14 |
gyrA | 8693 | c.1392T>C | synonymous_variant | 0.14 |
gyrA | 8696 | c.1395G>C | synonymous_variant | 0.14 |
gyrA | 8699 | c.1398A>G | synonymous_variant | 0.13 |
gyrA | 9230 | c.1929T>C | synonymous_variant | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 0.3 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.23 |
mshA | 575626 | c.279C>A | synonymous_variant | 0.17 |
mshA | 575907 | p.Ala187Val | missense_variant | 0.2 |
ccsA | 619782 | c.-109C>A | upstream_gene_variant | 0.17 |
rpoB | 760091 | c.285G>C | synonymous_variant | 0.14 |
rpoB | 760106 | c.300G>C | synonymous_variant | 0.19 |
rpoB | 760112 | c.306T>C | synonymous_variant | 0.19 |
rpoB | 760118 | c.312T>G | synonymous_variant | 0.2 |
rpoB | 760121 | c.315T>C | synonymous_variant | 0.2 |
rpoB | 760130 | p.Asp108Glu | missense_variant | 0.19 |
rpoB | 760139 | c.333A>G | synonymous_variant | 0.17 |
rpoB | 760142 | c.336C>G | synonymous_variant | 0.16 |
rpoB | 760145 | c.339C>G | synonymous_variant | 0.17 |
rpoB | 760331 | c.525G>T | synonymous_variant | 0.14 |
rpoB | 760337 | c.531C>G | synonymous_variant | 0.15 |
rpoB | 760340 | c.534G>C | synonymous_variant | 0.16 |
rpoB | 760354 | p.Glu183Ala | missense_variant | 0.14 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.16 |
rpoB | 760368 | p.Ser188Ala | missense_variant | 0.18 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.2 |
rpoB | 760380 | p.Thr192Asp | missense_variant | 0.25 |
rpoB | 760400 | c.594G>C | synonymous_variant | 0.24 |
rpoB | 760407 | p.Ser201Gly | missense_variant | 0.24 |
rpoB | 760415 | c.609C>T | synonymous_variant | 0.24 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.17 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.18 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.12 |
rpoB | 760502 | c.696C>G | synonymous_variant | 0.2 |
rpoB | 760508 | c.702G>C | synonymous_variant | 0.21 |
rpoB | 760511 | c.705G>C | synonymous_variant | 0.21 |
rpoB | 760522 | p.Ser239Asn | missense_variant | 0.22 |
rpoB | 760532 | c.726T>C | synonymous_variant | 0.29 |
rpoB | 760535 | c.729C>G | synonymous_variant | 0.27 |
rpoB | 760541 | c.735G>C | synonymous_variant | 0.25 |
rpoB | 760547 | c.741G>C | synonymous_variant | 0.24 |
rpoB | 760567 | p.Ser254Trp | missense_variant | 0.13 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.15 |
rpoB | 760625 | c.819C>G | synonymous_variant | 0.13 |
rpoB | 760796 | c.990A>G | synonymous_variant | 0.17 |
rpoB | 760805 | c.999G>C | synonymous_variant | 0.18 |
rpoB | 760808 | c.1002C>G | synonymous_variant | 0.18 |
rpoB | 760811 | c.1005C>G | synonymous_variant | 0.18 |
rpoB | 760817 | c.1011A>G | synonymous_variant | 0.18 |
rpoB | 760820 | c.1014T>C | synonymous_variant | 0.18 |
rpoB | 760826 | c.1020C>G | synonymous_variant | 0.31 |
rpoB | 760830 | c.1024T>C | synonymous_variant | 0.23 |
rpoB | 760841 | c.1035T>C | synonymous_variant | 0.23 |
rpoB | 760858 | p.Val351Ala | missense_variant | 0.15 |
rpoB | 760862 | c.1056G>C | synonymous_variant | 0.18 |
rpoB | 760919 | c.1113C>T | synonymous_variant | 0.16 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.16 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 0.19 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.15 |
rpoB | 760965 | p.Met387Leu | missense_variant | 0.16 |
rpoB | 760970 | c.1164G>C | synonymous_variant | 0.15 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.13 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.15 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.17 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.17 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.17 |
rpoB | 761198 | c.1392G>T | synonymous_variant | 0.17 |
rpoB | 761219 | c.1413G>C | synonymous_variant | 0.15 |
rpoB | 761221 | p.Ser472Cys | missense_variant | 0.14 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.18 |
rpoB | 761261 | c.1455G>C | synonymous_variant | 0.19 |
rpoB | 761273 | c.1467T>C | synonymous_variant | 0.14 |
rpoB | 761282 | c.1476C>T | synonymous_variant | 0.13 |
rpoB | 761300 | c.1494G>C | synonymous_variant | 0.15 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.18 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.15 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.14 |
rpoB | 761636 | c.1830G>C | synonymous_variant | 0.15 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.16 |
rpoB | 761666 | c.1860G>C | synonymous_variant | 0.16 |
rpoB | 761669 | c.1863C>T | synonymous_variant | 0.16 |
rpoB | 761675 | c.1869G>T | synonymous_variant | 0.15 |
rpoB | 761687 | c.1881C>T | synonymous_variant | 0.17 |
rpoB | 761892 | p.Ile696Leu | missense_variant | 0.14 |
rpoB | 761903 | c.2097T>C | synonymous_variant | 0.15 |
rpoB | 761909 | c.2103T>C | synonymous_variant | 0.14 |
rpoB | 761912 | c.2106T>C | synonymous_variant | 0.14 |
rpoB | 761915 | p.Asp703Glu | missense_variant | 0.14 |
rpoB | 761930 | c.2124G>C | synonymous_variant | 0.24 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.32 |
rpoB | 761954 | c.2148C>G | synonymous_variant | 0.33 |
rpoB | 761990 | c.2184G>C | synonymous_variant | 0.44 |
rpoB | 761999 | c.2193G>C | synonymous_variant | 0.42 |
rpoB | 762002 | c.2196C>G | synonymous_variant | 0.4 |
rpoB | 762047 | c.2241G>A | synonymous_variant | 0.38 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.36 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.38 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.33 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.33 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.26 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.32 |
rpoB | 762122 | c.2316C>T | synonymous_variant | 0.29 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 0.31 |
rpoB | 762137 | c.2331C>T | synonymous_variant | 0.31 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.31 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.29 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.29 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.29 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.29 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.24 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.27 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.33 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.3 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.36 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.21 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.21 |
rpoB | 762296 | c.2490G>C | synonymous_variant | 0.21 |
rpoB | 762314 | c.2508C>T | synonymous_variant | 0.19 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.18 |
rpoB | 762329 | c.2523G>C | synonymous_variant | 0.17 |
rpoB | 762338 | c.2532T>C | synonymous_variant | 0.2 |
rpoB | 762347 | c.2541T>C | synonymous_variant | 0.21 |
rpoB | 762362 | p.Glu852Asp | missense_variant | 0.14 |
rpoB | 762369 | c.2563T>C | synonymous_variant | 0.15 |
rpoC | 762434 | c.-936T>C | upstream_gene_variant | 0.2 |
rpoC | 762443 | c.-927G>C | upstream_gene_variant | 0.23 |
rpoC | 762449 | c.-921C>G | upstream_gene_variant | 0.23 |
rpoC | 762452 | c.-918G>C | upstream_gene_variant | 0.23 |
rpoC | 762470 | c.-900G>C | upstream_gene_variant | 0.24 |
rpoC | 762488 | c.-882G>C | upstream_gene_variant | 0.14 |
rpoC | 762491 | c.-879T>C | upstream_gene_variant | 0.13 |
rpoC | 762533 | c.-837T>C | upstream_gene_variant | 0.15 |
rpoC | 762536 | c.-834T>C | upstream_gene_variant | 0.15 |
rpoC | 762537 | c.-833T>C | upstream_gene_variant | 0.16 |
rpoC | 762551 | c.-819C>T | upstream_gene_variant | 0.2 |
rpoC | 762560 | c.-810A>T | upstream_gene_variant | 0.21 |
rpoC | 762563 | c.-807G>T | upstream_gene_variant | 0.2 |
rpoB | 762576 | p.Gln924Glu | missense_variant | 0.17 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.14 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.18 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 0.24 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.24 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.26 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.24 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.25 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.25 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.33 |
rpoC | 762989 | c.-381G>A | upstream_gene_variant | 0.31 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.31 |
rpoC | 763004 | c.-366G>A | upstream_gene_variant | 0.32 |
rpoC | 763007 | c.-363C>T | upstream_gene_variant | 0.33 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.34 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.47 |
rpoC | 763049 | c.-321G>A | upstream_gene_variant | 0.35 |
rpoC | 763053 | c.-317_-315delTTGinsCTC | upstream_gene_variant | 0.32 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.31 |
rpoC | 763076 | c.-294C>G | upstream_gene_variant | 0.3 |
rpoC | 763079 | c.-291C>G | upstream_gene_variant | 0.3 |
rpoC | 763082 | c.-288C>T | upstream_gene_variant | 0.3 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.3 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.31 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.29 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.2 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.17 |
rpoC | 763158 | c.-212C>T | upstream_gene_variant | 0.23 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.22 |
rpoC | 763169 | c.-201A>G | upstream_gene_variant | 0.22 |
rpoC | 763181 | c.-189G>C | upstream_gene_variant | 0.17 |
rpoC | 763187 | c.-183C>G | upstream_gene_variant | 0.17 |
rpoC | 763190 | c.-180C>T | upstream_gene_variant | 0.17 |
rpoC | 763202 | c.-168A>G | upstream_gene_variant | 0.17 |
rpoC | 763205 | c.-165G>C | upstream_gene_variant | 0.17 |
rpoC | 763206 | c.-164_-162delAGTinsTCG | upstream_gene_variant | 0.17 |
rpoC | 763214 | c.-156T>C | upstream_gene_variant | 0.17 |
rpoB | 763227 | p.Leu1141Met | missense_variant | 0.18 |
rpoC | 763232 | c.-138C>T | upstream_gene_variant | 0.19 |
rpoB | 763235 | p.Glu1143Asp | missense_variant | 0.19 |
rpoB | 763241 | p.Glu1145Asp | missense_variant | 0.2 |
rpoC | 763250 | c.-120C>T | upstream_gene_variant | 0.19 |
rpoC | 763259 | c.-111G>C | upstream_gene_variant | 0.18 |
rpoC | 763265 | c.-105G>T | upstream_gene_variant | 0.18 |
rpoC | 763274 | c.-96G>C | upstream_gene_variant | 0.17 |
rpoC | 763283 | c.-87T>C | upstream_gene_variant | 0.16 |
rpoC | 763411 | c.42T>C | synonymous_variant | 0.12 |
rpoC | 763414 | c.45T>G | synonymous_variant | 0.13 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.13 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.22 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.24 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.17 |
rpoC | 763712 | p.Gly115Trp | missense_variant | 0.15 |
rpoC | 763844 | p.Arg159Ser | missense_variant | 0.17 |
rpoC | 764032 | p.Asp221Glu | missense_variant | 0.13 |
rpoC | 764040 | p.Ser224Thr | missense_variant | 0.16 |
rpoC | 764044 | c.675T>C | synonymous_variant | 0.17 |
rpoC | 764059 | c.690G>T | synonymous_variant | 0.19 |
rpoC | 764071 | c.702G>C | synonymous_variant | 0.17 |
rpoC | 764077 | c.708C>G | synonymous_variant | 0.19 |
rpoC | 764083 | c.714A>G | synonymous_variant | 0.16 |
rpoC | 764084 | p.Asn239Val | missense_variant | 0.16 |
rpoC | 764098 | c.729A>G | synonymous_variant | 0.2 |
rpoC | 764320 | c.951C>T | synonymous_variant | 0.25 |
rpoC | 764353 | c.984G>T | synonymous_variant | 0.31 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.29 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 0.29 |
rpoC | 764377 | c.1008C>G | synonymous_variant | 0.29 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.29 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 0.31 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.42 |
rpoC | 764410 | c.1041G>C | synonymous_variant | 0.42 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.56 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.56 |
rpoC | 764435 | c.1066_1068delAGGinsCGA | synonymous_variant | 0.5 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.36 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.3 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.33 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.2 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.21 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.2 |
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 | 0.23 |
rpoC | 764530 | c.1161C>T | synonymous_variant | 0.22 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.21 |
rpoC | 764548 | c.1179G>T | synonymous_variant | 0.15 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.15 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.16 |
rpoC | 764869 | c.1500C>T | synonymous_variant | 0.17 |
rpoC | 764878 | c.1509C>G | synonymous_variant | 0.13 |
rpoC | 764887 | c.1518G>C | synonymous_variant | 0.14 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.14 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.14 |
rpoC | 764912 | p.Met515Leu | missense_variant | 0.14 |
rpoC | 764923 | c.1554A>G | synonymous_variant | 0.14 |
rpoC | 765136 | c.1767C>A | synonymous_variant | 0.15 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.15 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.15 |
rpoC | 765898 | c.2529C>T | synonymous_variant | 0.15 |
rpoC | 765934 | c.2565C>T | synonymous_variant | 0.15 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.15 |
rpoC | 765940 | c.2571A>T | synonymous_variant | 0.16 |
rpoC | 766345 | c.2976T>C | synonymous_variant | 0.22 |
rpoC | 766690 | c.3321G>C | synonymous_variant | 0.13 |
rpoC | 766702 | c.3333G>C | synonymous_variant | 0.18 |
rpoC | 766712 | p.Ser1115Ala | missense_variant | 0.12 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.13 |
rpoC | 766738 | c.3369G>T | synonymous_variant | 0.18 |
rpoC | 766750 | c.3381C>G | synonymous_variant | 0.2 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.2 |
rpoC | 766771 | c.3402G>C | synonymous_variant | 0.2 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.2 |
rpoC | 766775 | p.Arg1136Lys | missense_variant | 0.2 |
rpoC | 766798 | c.3429C>G | synonymous_variant | 0.25 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.24 |
rpoC | 766807 | c.3438T>C | synonymous_variant | 0.24 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.22 |
rpoC | 767104 | c.3735C>G | synonymous_variant | 0.2 |
rpoC | 767106 | p.Asn1246Met | missense_variant | 0.22 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.36 |
rpoC | 767155 | c.3786C>G | synonymous_variant | 0.19 |
rpoC | 767162 | p.Asn1265Ala | missense_variant | 0.19 |
rpoC | 767173 | c.3804C>G | synonymous_variant | 0.19 |
rpoC | 767174 | p.Asn1269Asp | missense_variant | 0.19 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.19 |
rpoC | 767185 | c.3816G>C | synonymous_variant | 0.2 |
rpoC | 767186 | p.Gln1273Asn | missense_variant | 0.2 |
rpoC | 767191 | c.3822C>G | synonymous_variant | 0.21 |
rpoC | 767197 | c.3828G>A | synonymous_variant | 0.18 |
rpoC | 767221 | c.3852C>G | synonymous_variant | 0.16 |
mmpL5 | 775814 | c.2667C>G | synonymous_variant | 0.12 |
mmpL5 | 775835 | c.2646C>G | synonymous_variant | 0.31 |
mmpL5 | 775847 | c.2634G>T | synonymous_variant | 0.36 |
mmpL5 | 775851 | p.Ser877Thr | missense_variant | 0.36 |
mmpL5 | 775856 | c.2625T>C | synonymous_variant | 0.33 |
mmpL5 | 775862 | c.2619G>C | synonymous_variant | 0.33 |
mmpL5 | 775865 | c.2616T>C | synonymous_variant | 0.38 |
mmpL5 | 775885 | p.Ile866Leu | missense_variant | 0.43 |
mmpL5 | 775886 | c.2595A>T | synonymous_variant | 0.43 |
mmpL5 | 775889 | c.2592C>G | synonymous_variant | 0.46 |
mmpL5 | 775905 | p.Lys859Arg | missense_variant | 0.55 |
mmpL5 | 775909 | p.Leu858Ile | missense_variant | 0.64 |
mmpL5 | 775916 | c.2565T>C | synonymous_variant | 0.67 |
mmpL5 | 775949 | c.2532G>C | synonymous_variant | 0.39 |
mmpL5 | 775955 | p.Ile842Val | missense_variant | 0.38 |
mmpL5 | 775961 | c.2520C>G | synonymous_variant | 0.35 |
mmpL5 | 775975 | p.Leu836Met | missense_variant | 0.31 |
mmpL5 | 775981 | p.Leu834Met | missense_variant | 0.31 |
mmpL5 | 775982 | p.Trp833Phe | missense_variant | 0.19 |
mmpL5 | 775990 | c.2491C>T | synonymous_variant | 0.16 |
mmpL5 | 775997 | c.2484T>C | synonymous_variant | 0.21 |
mmpL5 | 776039 | c.2442C>G | synonymous_variant | 0.14 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.14 |
mmpL5 | 777289 | p.Val398Leu | missense_variant | 0.18 |
mmpS5 | 778872 | p.Leu12Met | missense_variant | 0.14 |
mmpL5 | 779124 | c.-644C>T | upstream_gene_variant | 0.2 |
mmpL5 | 779145 | c.-665G>T | upstream_gene_variant | 0.2 |
mmpR5 | 779171 | p.Ala61Glu | missense_variant | 0.15 |
mmpR5 | 779185 | p.Gly66Trp | missense_variant | 0.14 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 0.25 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 0.47 |
rpsL | 781595 | c.36T>C | synonymous_variant | 0.17 |
rpsL | 781598 | c.39G>C | synonymous_variant | 0.18 |
rpsL | 781605 | p.Ile16Val | missense_variant | 0.19 |
rpsL | 781608 | p.Ser17Ala | missense_variant | 0.19 |
rpsL | 781616 | c.57C>G | synonymous_variant | 0.2 |
rpsL | 781628 | c.69T>C | synonymous_variant | 0.25 |
rpsL | 781631 | c.72G>C | synonymous_variant | 0.31 |
rpsL | 781652 | c.93T>C | synonymous_variant | 0.29 |
rpsL | 781658 | c.99A>G | synonymous_variant | 0.25 |
rpsL | 781664 | c.105C>T | synonymous_variant | 0.27 |
rpsL | 781682 | c.123T>C | synonymous_variant | 0.25 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.15 |
rpsL | 781739 | p.Gln60His | missense_variant | 0.17 |
rpsL | 781743 | p.Glu62* | stop_gained | 0.18 |
rpsL | 781769 | p.Glu70Asp | missense_variant | 0.15 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.16 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.17 |
rplC | 800633 | c.-176T>C | upstream_gene_variant | 0.19 |
rplC | 800651 | c.-158G>C | upstream_gene_variant | 0.15 |
rplC | 800693 | c.-116A>C | upstream_gene_variant | 0.14 |
rplC | 800702 | c.-107G>C | upstream_gene_variant | 0.14 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.14 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.14 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.15 |
rplC | 800744 | c.-65G>C | upstream_gene_variant | 0.14 |
rplC | 800955 | c.147C>A | synonymous_variant | 0.18 |
rplC | 800992 | p.Val62Ile | missense_variant | 0.2 |
rplC | 801041 | p.Arg78Leu | missense_variant | 0.18 |
fbiC | 1303605 | c.675C>G | synonymous_variant | 0.12 |
fbiC | 1303606 | p.Lys226Arg | missense_variant | 0.13 |
fbiC | 1303614 | c.684C>G | synonymous_variant | 0.13 |
fbiC | 1305118 | p.Gln730Lys | missense_variant | 0.17 |
Rv1258c | 1406686 | p.Val219Ile | missense_variant | 0.78 |
embR | 1416494 | p.Gly285Val | missense_variant | 0.15 |
embR | 1416594 | p.Glu252* | stop_gained | 0.15 |
atpE | 1460917 | c.-128C>A | upstream_gene_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471922 | n.78delT | non_coding_transcript_exon_variant | 0.21 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1471931 | n.87delA | non_coding_transcript_exon_variant | 0.2 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1471979 | n.134T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472019 | n.174G>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472023 | n.178G>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472029 | n.184C>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472030 | n.185G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472033 | n.188A>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472035 | n.190G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472040 | n.195T>G | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472043 | n.198T>G | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472289 | n.444T>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472290 | n.445C>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472297 | n.453_465delGTCCGGGTTCTCT | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472324 | n.479G>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472337 | n.492C>G | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472380 | n.535G>C | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472847 | n.1002G>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472848 | n.1003T>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472849 | n.1004C>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472850 | n.1005T>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472857 | n.1012A>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472858 | n.1013G>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472859 | n.1014G>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472860 | n.1015C>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.66 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.54 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1473390 | n.-268A>T | upstream_gene_variant | 0.17 |
rrl | 1473500 | n.-158C>A | upstream_gene_variant | 0.18 |
rrl | 1473697 | n.40C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473699 | n.42A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473717 | n.60G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473731 | n.74T>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473746 | n.89T>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473811 | n.154C>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473814 | n.157A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473815 | n.158T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473816 | n.159C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473828 | n.171G>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1473829 | n.172G>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1473830 | n.173T>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1473831 | n.174G>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1473887 | n.230T>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1473888 | n.231T>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473925 | n.268G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474134 | n.477G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474185 | n.528G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474188 | n.531G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474439 | n.782A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474446 | n.789C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474498 | n.841G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474505 | n.848C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474552 | n.895C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474709 | n.1053delT | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474714 | n.1058delT | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474753 | n.1096A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474974 | n.1317G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475108 | n.1451C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475202 | n.1545G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475206 | n.1549C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475209 | n.1552G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475221 | n.1564C>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475286 | n.1629T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475291 | n.1634A>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475296 | n.1639G>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475343 | n.1686A>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475358 | n.1701T>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1475363 | n.1706C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475369 | n.1712G>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475380 | n.1723C>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475381 | n.1724G>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475382 | n.1725A>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475395 | n.1738T>G | non_coding_transcript_exon_variant | 0.61 |
rrl | 1475396 | n.1739C>G | non_coding_transcript_exon_variant | 0.61 |
rrl | 1475397 | n.1740G>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1475402 | n.1745C>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.69 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 0.66 |
rrl | 1475460 | n.1803A>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1475479 | n.1822C>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.74 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475544 | n.1887A>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1475759 | n.2102C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1475764 | n.2107A>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.74 |
rrl | 1475775 | n.2118G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.59 |
rrl | 1475991 | n.2334T>C | non_coding_transcript_exon_variant | 0.59 |
rrl | 1475995 | n.2338G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476056 | n.2399G>A | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476088 | n.2431A>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476095 | n.2438C>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476103 | n.2446C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476105 | n.2448G>A | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476106 | n.2449A>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476251 | n.2594T>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476529 | n.2872A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476583 | n.2926G>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476684 | n.3027C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476761 | n.3104G>T | non_coding_transcript_exon_variant | 0.17 |
inhA | 1673544 | c.-658G>T | upstream_gene_variant | 0.25 |
inhA | 1673778 | c.-424C>A | upstream_gene_variant | 0.27 |
inhA | 1673973 | c.-229G>C | upstream_gene_variant | 0.17 |
fabG1 | 1674006 | p.Asp189Glu | missense_variant | 0.17 |
inhA | 1674774 | c.573A>G | synonymous_variant | 0.13 |
inhA | 1674780 | c.579T>G | synonymous_variant | 0.14 |
inhA | 1674789 | c.588G>C | synonymous_variant | 0.14 |
inhA | 1674795 | c.594G>C | synonymous_variant | 0.14 |
inhA | 1674801 | c.600T>C | synonymous_variant | 0.15 |
inhA | 1674804 | c.603G>C | synonymous_variant | 0.19 |
inhA | 1674810 | c.609C>G | synonymous_variant | 0.23 |
inhA | 1674822 | c.621C>G | synonymous_variant | 0.2 |
inhA | 1674827 | p.Glu209Ala | missense_variant | 0.17 |
inhA | 1674839 | p.Ala213Asp | missense_variant | 0.17 |
inhA | 1674846 | p.Ile215Met | missense_variant | 0.18 |
inhA | 1674848 | p.Gln216Arg | missense_variant | 0.18 |
inhA | 1674858 | c.657G>A | synonymous_variant | 0.2 |
inhA | 1674879 | c.678T>A | synonymous_variant | 0.22 |
inhA | 1674883 | p.Ile228Val | missense_variant | 0.21 |
inhA | 1674904 | p.Ala235Pro | missense_variant | 0.18 |
inhA | 1674909 | c.708G>C | synonymous_variant | 0.12 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.15 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.15 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.17 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.17 |
rpsA | 1833862 | c.321G>T | synonymous_variant | 0.17 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.17 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.13 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.17 |
rpsA | 1833991 | c.450C>A | synonymous_variant | 0.17 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.13 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.13 |
rpsA | 1834108 | c.567C>G | synonymous_variant | 0.17 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.2 |
rpsA | 1834213 | c.672G>C | synonymous_variant | 0.31 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 0.31 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.31 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.37 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.32 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.37 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.37 |
rpsA | 1834279 | c.738C>T | synonymous_variant | 0.38 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.4 |
rpsA | 1834298 | p.Gln253Thr | missense_variant | 0.36 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.39 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.39 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.24 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.17 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.14 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.14 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.13 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.13 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.13 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.12 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.13 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.14 |
rpsA | 1834513 | c.972C>G | synonymous_variant | 0.15 |
rpsA | 1834520 | p.Ala327Ser | missense_variant | 0.15 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.15 |
tlyA | 1917927 | c.-13G>T | upstream_gene_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 0.39 |
ndh | 2102089 | p.Phe318Leu | missense_variant | 0.18 |
ndh | 2102991 | p.Val18Leu | missense_variant | 0.13 |
ndh | 2103147 | c.-105G>T | upstream_gene_variant | 0.14 |
katG | 2153974 | p.Ala713Val | missense_variant | 0.14 |
katG | 2154059 | p.Gly685Cys | missense_variant | 0.17 |
katG | 2154170 | p.Glu648Lys | missense_variant | 0.22 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.16 |
katG | 2155936 | p.Gly59Val | missense_variant | 0.14 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 0.17 |
PPE35 | 2168802 | p.Gly604Val | missense_variant | 0.19 |
PPE35 | 2169275 | c.1338G>T | synonymous_variant | 0.2 |
PPE35 | 2169929 | c.684C>A | synonymous_variant | 0.17 |
Rv1979c | 2222422 | p.Pro248Gln | missense_variant | 0.22 |
Rv1979c | 2222861 | p.Ala102Thr | missense_variant | 0.14 |
Rv1979c | 2222868 | c.297C>A | synonymous_variant | 0.15 |
Rv1979c | 2222873 | p.His98Asn | missense_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 0.33 |
pncA | 2288710 | p.Ala178Thr | missense_variant | 0.18 |
pncA | 2289620 | c.-379G>A | upstream_gene_variant | 0.14 |
pncA | 2290165 | c.-924C>A | upstream_gene_variant | 0.14 |
kasA | 2517941 | c.-174C>G | upstream_gene_variant | 0.18 |
kasA | 2517950 | c.-165C>G | upstream_gene_variant | 0.18 |
kasA | 2517962 | c.-153C>G | upstream_gene_variant | 0.2 |
kasA | 2517968 | c.-147T>C | upstream_gene_variant | 0.19 |
kasA | 2517974 | c.-141T>C | upstream_gene_variant | 0.15 |
kasA | 2518711 | c.597A>G | synonymous_variant | 0.17 |
kasA | 2518714 | c.600A>T | synonymous_variant | 0.17 |
kasA | 2518715 | p.Pro201Ala | missense_variant | 0.19 |
kasA | 2518732 | c.618C>G | synonymous_variant | 0.19 |
kasA | 2518747 | c.633C>G | synonymous_variant | 0.16 |
kasA | 2518756 | c.642G>T | synonymous_variant | 0.17 |
kasA | 2518759 | c.645C>G | synonymous_variant | 0.17 |
kasA | 2518780 | p.Glu222Asp | missense_variant | 0.21 |
kasA | 2518783 | c.669T>G | synonymous_variant | 0.18 |
kasA | 2518787 | p.Arg225Gly | missense_variant | 0.2 |
kasA | 2518792 | c.678C>G | synonymous_variant | 0.18 |
kasA | 2518795 | c.681C>G | synonymous_variant | 0.19 |
kasA | 2518798 | c.684G>T | synonymous_variant | 0.18 |
kasA | 2518813 | c.699C>T | synonymous_variant | 0.23 |
kasA | 2518816 | c.702C>T | synonymous_variant | 0.25 |
kasA | 2518822 | c.708C>G | synonymous_variant | 0.24 |
kasA | 2518825 | c.711T>C | synonymous_variant | 0.24 |
kasA | 2518828 | c.714G>C | synonymous_variant | 0.25 |
kasA | 2518849 | c.735G>C | synonymous_variant | 0.17 |
kasA | 2518853 | p.Leu247Ile | missense_variant | 0.17 |
kasA | 2519275 | c.1161C>A | synonymous_variant | 0.17 |
eis | 2715276 | c.57G>T | synonymous_variant | 0.15 |
folC | 2746428 | p.Leu391Met | missense_variant | 0.17 |
folC | 2747074 | c.525G>T | synonymous_variant | 0.14 |
folC | 2747520 | p.Leu27Met | missense_variant | 0.22 |
ribD | 2986659 | c.-180G>T | upstream_gene_variant | 0.15 |
Rv2752c | 3064944 | c.1248G>A | synonymous_variant | 0.17 |
Rv2752c | 3065567 | p.Pro209Thr | missense_variant | 0.14 |
Rv2752c | 3065735 | p.Ala153Ser | missense_variant | 0.14 |
Rv2752c | 3065951 | p.His81Asn | missense_variant | 0.22 |
thyA | 3073947 | c.525G>C | synonymous_variant | 0.14 |
thyA | 3073953 | c.519T>C | synonymous_variant | 0.15 |
thyA | 3073956 | c.516G>C | synonymous_variant | 0.17 |
thyA | 3073959 | c.513T>C | synonymous_variant | 0.18 |
thyA | 3073968 | c.504C>G | synonymous_variant | 0.2 |
thyA | 3073977 | c.495A>G | synonymous_variant | 0.22 |
thyA | 3073983 | c.489C>G | synonymous_variant | 0.22 |
thyA | 3073989 | c.483T>C | synonymous_variant | 0.25 |
thyA | 3073993 | c.478_479delAGinsTC | synonymous_variant | 0.25 |
thyA | 3073999 | p.Arg158Lys | missense_variant | 0.22 |
thyA | 3074004 | c.468T>C | synonymous_variant | 0.2 |
thyA | 3074031 | c.441T>C | synonymous_variant | 0.2 |
thyA | 3074034 | c.438T>C | synonymous_variant | 0.2 |
thyA | 3074037 | c.435C>G | synonymous_variant | 0.2 |
thyA | 3074046 | c.426G>C | synonymous_variant | 0.18 |
ald | 3086668 | c.-152G>T | upstream_gene_variant | 0.18 |
ald | 3086699 | c.-121C>T | upstream_gene_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.35 |
ald | 3086814 | c.-6G>A | upstream_gene_variant | 0.14 |
ald | 3087348 | p.Gly177Cys | missense_variant | 0.2 |
ald | 3087423 | p.Asp202Tyr | missense_variant | 0.25 |
Rv3083 | 3449484 | p.Lys327Asn | missense_variant | 0.2 |
Rv3083 | 3449515 | p.Glu338Tyr | missense_variant | 0.2 |
Rv3083 | 3449521 | p.Asp340Tyr | missense_variant | 0.2 |
Rv3083 | 3449538 | c.1035G>T | synonymous_variant | 0.18 |
Rv3083 | 3449938 | p.Asp479Asn | missense_variant | 0.15 |
Rv3083 | 3449984 | p.Ala494Glu | missense_variant | 0.18 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 0.23 |
fprA | 3474365 | p.Pro120Gln | missense_variant | 0.17 |
fprA | 3474517 | p.Asp171Tyr | missense_variant | 0.15 |
fprA | 3475228 | p.Asp408Tyr | missense_variant | 0.22 |
Rv3236c | 3613017 | p.Pro34Thr | missense_variant | 0.17 |
fbiB | 3640617 | c.-918G>T | upstream_gene_variant | 0.17 |
fbiA | 3640721 | p.Pro60Gln | missense_variant | 0.17 |
fbiA | 3641468 | p.Leu309Pro | missense_variant | 0.14 |
fbiB | 3641561 | c.27C>A | synonymous_variant | 0.18 |
fbiB | 3641582 | c.48C>A | synonymous_variant | 0.15 |
fbiB | 3641604 | p.Arg24Ser | missense_variant | 0.17 |
fbiB | 3641832 | p.Gly100Trp | missense_variant | 0.2 |
alr | 3841135 | p.Glu96* | stop_gained | 0.15 |
alr | 3841137 | p.Asp95Gly | missense_variant | 0.14 |
rpoA | 3877617 | c.891G>C | synonymous_variant | 0.17 |
rpoA | 3877638 | c.870T>G | synonymous_variant | 0.22 |
rpoA | 3877647 | c.861C>T | synonymous_variant | 0.22 |
rpoA | 3877656 | c.852T>C | synonymous_variant | 0.25 |
rpoA | 3877662 | c.846C>T | synonymous_variant | 0.25 |
rpoA | 3877665 | c.843C>G | synonymous_variant | 0.27 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.25 |
rpoA | 3877674 | c.834C>T | synonymous_variant | 0.27 |
rpoA | 3877679 | p.Ala277Ser | missense_variant | 0.27 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.18 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.2 |
rpoA | 3877704 | c.804G>T | synonymous_variant | 0.19 |
rpoA | 3877728 | c.780C>G | synonymous_variant | 0.14 |
rpoA | 3877734 | c.774G>C | synonymous_variant | 0.14 |
rpoA | 3877737 | c.771G>C | synonymous_variant | 0.14 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.13 |
rpoA | 3877875 | c.633T>C | synonymous_variant | 0.18 |
rpoA | 3877881 | c.627G>C | synonymous_variant | 0.18 |
rpoA | 3877887 | c.621G>C | synonymous_variant | 0.18 |
rpoA | 3877893 | c.615C>T | synonymous_variant | 0.19 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.2 |
rpoA | 3877908 | c.600T>C | synonymous_variant | 0.19 |
rpoA | 3877920 | c.588G>C | synonymous_variant | 0.19 |
rpoA | 3877926 | c.582G>C | synonymous_variant | 0.18 |
rpoA | 3878157 | c.351C>G | synonymous_variant | 0.21 |
rpoA | 3878160 | c.348C>G | synonymous_variant | 0.21 |
rpoA | 3878163 | c.345C>T | synonymous_variant | 0.22 |
rpoA | 3878184 | c.324C>T | synonymous_variant | 0.24 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.25 |
rpoA | 3878197 | p.Glu104Ala | missense_variant | 0.24 |
rpoA | 3878205 | c.303T>C | synonymous_variant | 0.21 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.23 |
rpoA | 3878244 | c.264G>A | synonymous_variant | 0.2 |
rpoA | 3878253 | c.255G>C | synonymous_variant | 0.2 |
rpoA | 3878256 | c.252G>C | synonymous_variant | 0.16 |
rpoA | 3878262 | p.Ser82Gly | missense_variant | 0.15 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.16 |
rpoA | 3878283 | p.Glu75Asp | missense_variant | 0.16 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.15 |
rpoA | 3878575 | c.-68C>T | upstream_gene_variant | 0.18 |
rpoA | 3878621 | c.-114C>A | upstream_gene_variant | 0.22 |
clpC1 | 4038263 | p.Glu814Asp | missense_variant | 0.21 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.14 |
clpC1 | 4038605 | c.2100G>A | synonymous_variant | 0.15 |
clpC1 | 4038613 | p.Asn698His | missense_variant | 0.16 |
clpC1 | 4038620 | p.Gln695His | missense_variant | 0.15 |
clpC1 | 4038623 | c.2082A>G | synonymous_variant | 0.15 |
clpC1 | 4038647 | c.2058T>C | synonymous_variant | 0.15 |
clpC1 | 4038704 | c.2001T>C | synonymous_variant | 0.15 |
clpC1 | 4038707 | c.1998C>G | synonymous_variant | 0.15 |
clpC1 | 4038710 | c.1995G>C | synonymous_variant | 0.18 |
clpC1 | 4038713 | c.1992T>C | synonymous_variant | 0.18 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.13 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 0.15 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.14 |
clpC1 | 4038881 | c.1824C>G | synonymous_variant | 0.14 |
clpC1 | 4038890 | c.1815G>A | synonymous_variant | 0.16 |
clpC1 | 4038905 | c.1800A>C | synonymous_variant | 0.17 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.17 |
clpC1 | 4038911 | c.1794G>T | synonymous_variant | 0.16 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.17 |
clpC1 | 4038917 | c.1788C>T | synonymous_variant | 0.16 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 0.16 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.16 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.16 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.17 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.15 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.13 |
clpC1 | 4039064 | c.1641C>T | synonymous_variant | 0.2 |
clpC1 | 4039067 | c.1638G>C | synonymous_variant | 0.2 |
clpC1 | 4039079 | c.1626C>G | synonymous_variant | 0.19 |
clpC1 | 4039085 | c.1620A>G | synonymous_variant | 0.16 |
clpC1 | 4039091 | c.1614G>C | synonymous_variant | 0.16 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.16 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.15 |
clpC1 | 4039118 | c.1587C>G | synonymous_variant | 0.15 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.15 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.2 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.21 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.24 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.16 |
clpC1 | 4039187 | c.1518G>C | synonymous_variant | 0.16 |
clpC1 | 4039262 | p.Asp481Glu | missense_variant | 0.18 |
clpC1 | 4039267 | p.Asp480Asn | missense_variant | 0.15 |
clpC1 | 4039832 | c.873C>G | synonymous_variant | 0.13 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.16 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.21 |
clpC1 | 4039934 | c.771G>C | synonymous_variant | 0.21 |
clpC1 | 4039937 | c.768G>C | synonymous_variant | 0.21 |
clpC1 | 4039946 | c.759A>C | synonymous_variant | 0.19 |
clpC1 | 4039949 | c.756G>C | synonymous_variant | 0.2 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.19 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.19 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 0.2 |
clpC1 | 4040015 | c.690G>C | synonymous_variant | 0.26 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.23 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.23 |
clpC1 | 4040030 | c.675C>G | synonymous_variant | 0.23 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.25 |
clpC1 | 4040042 | c.663C>T | synonymous_variant | 0.29 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.26 |
clpC1 | 4040087 | c.618G>C | synonymous_variant | 0.22 |
clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 0.22 |
clpC1 | 4040093 | c.612C>T | synonymous_variant | 0.21 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.24 |
clpC1 | 4040147 | c.558A>G | synonymous_variant | 0.22 |
clpC1 | 4040153 | c.552A>G | synonymous_variant | 0.18 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 0.14 |
clpC1 | 4040531 | c.174T>C | synonymous_variant | 0.14 |
clpC1 | 4040537 | c.168G>C | synonymous_variant | 0.15 |
panD | 4043876 | p.Leu136Ile | missense_variant | 0.18 |
panD | 4044324 | c.-43C>G | upstream_gene_variant | 0.18 |
panD | 4044341 | c.-60C>A | upstream_gene_variant | 0.2 |
panD | 4044376 | c.-95C>A | upstream_gene_variant | 0.25 |
embC | 4240665 | p.Trp268Leu | missense_variant | 0.14 |
embC | 4240699 | c.837C>T | synonymous_variant | 0.17 |
embC | 4240774 | c.912C>G | synonymous_variant | 0.15 |
embC | 4240777 | p.Glu305Asp | missense_variant | 0.15 |
embC | 4240780 | c.918T>C | synonymous_variant | 0.15 |
embC | 4240783 | c.921G>C | synonymous_variant | 0.15 |
embC | 4240789 | c.927T>C | synonymous_variant | 0.18 |
embC | 4240819 | c.957A>C | synonymous_variant | 0.3 |
embC | 4240822 | c.960C>G | synonymous_variant | 0.3 |
embC | 4240831 | c.969T>G | synonymous_variant | 0.3 |
embC | 4240855 | c.993G>C | synonymous_variant | 0.2 |
embC | 4240857 | p.Ala332Gly | missense_variant | 0.2 |
embC | 4241880 | p.Leu673Pro | missense_variant | 0.15 |
embA | 4244061 | p.Leu277Ile | missense_variant | 0.15 |
embA | 4244183 | c.951G>T | synonymous_variant | 0.17 |
embA | 4244408 | c.1176G>T | synonymous_variant | 0.18 |
embA | 4244631 | p.Thr467Ala | missense_variant | 0.12 |
embB | 4245662 | c.-852G>T | upstream_gene_variant | 0.18 |
embB | 4245842 | c.-672G>C | upstream_gene_variant | 0.18 |
embB | 4246448 | c.-66C>A | upstream_gene_variant | 0.2 |
embB | 4248202 | c.1689T>A | synonymous_variant | 0.17 |
embB | 4248311 | p.Ala600Ser | missense_variant | 0.15 |
embB | 4248506 | p.Gly665Trp | missense_variant | 0.25 |
embB | 4248630 | p.Pro706Leu | missense_variant | 0.15 |
embB | 4248853 | c.2340G>T | synonymous_variant | 0.22 |
embB | 4248880 | c.2367G>T | synonymous_variant | 0.2 |
embB | 4249019 | p.Gly836Leu | missense_variant | 0.2 |
embB | 4249154 | p.Gly881Ser | missense_variant | 0.18 |
embB | 4249189 | p.Tyr892* | stop_gained | 0.15 |
embB | 4249319 | c.2806C>A | synonymous_variant | 0.15 |
embB | 4249497 | p.Pro995Gln | missense_variant | 0.3 |
aftB | 4267528 | p.Ala437Ser | missense_variant | 0.18 |
aftB | 4267755 | p.Lys361Met | missense_variant | 0.14 |
aftB | 4269123 | c.-287T>G | upstream_gene_variant | 0.16 |
aftB | 4269129 | c.-293G>C | upstream_gene_variant | 0.15 |
aftB | 4269141 | c.-307_-305delTTGinsCTC | upstream_gene_variant | 0.15 |
aftB | 4269144 | c.-308C>G | upstream_gene_variant | 0.14 |
ubiA | 4269149 | p.Val229Leu | missense_variant | 0.15 |
aftB | 4269171 | c.-335C>G | upstream_gene_variant | 0.21 |
aftB | 4269177 | c.-341G>C | upstream_gene_variant | 0.2 |
ubiA | 4269186 | p.Thr216Ser | missense_variant | 0.2 |
ubiA | 4269199 | p.Ser212Asn | missense_variant | 0.18 |
aftB | 4269201 | c.-365A>G | upstream_gene_variant | 0.18 |
aftB | 4269210 | c.-374G>A | upstream_gene_variant | 0.17 |
ubiA | 4269220 | p.Ala205Lys | missense_variant | 0.19 |
aftB | 4269222 | c.-386T>C | upstream_gene_variant | 0.19 |
aftB | 4269234 | c.-398A>G | upstream_gene_variant | 0.22 |
ubiA | 4269238 | p.Ala199Val | missense_variant | 0.23 |
aftB | 4269240 | c.-404G>C | upstream_gene_variant | 0.23 |
ubiA | 4269243 | p.His197Gln | missense_variant | 0.23 |
aftB | 4269249 | c.-413G>A | upstream_gene_variant | 0.24 |
aftB | 4269258 | c.-422C>T | upstream_gene_variant | 0.25 |
aftB | 4269264 | c.-428C>T | upstream_gene_variant | 0.21 |
ubiA | 4269297 | p.Ile179Met | missense_variant | 0.15 |
ubiA | 4269623 | p.Leu71Ile | missense_variant | 0.14 |
ethA | 4327296 | p.Tyr60His | missense_variant | 0.14 |
ethA | 4328223 | c.-750C>T | upstream_gene_variant | 0.15 |
ethA | 4328243 | c.-770C>A | upstream_gene_variant | 0.18 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 0.29 |
gid | 4407923 | p.Leu94Ile | missense_variant | 0.17 |
gid | 4407927 | p.Glu92Asp | missense_variant | 0.17 |
gid | 4407951 | c.252G>A | synonymous_variant | 0.15 |
gid | 4407964 | p.Ala80Glu | missense_variant | 0.14 |