Run ID: ERR3806850
Sample name:
Date: 01-04-2023 03:27:37
Number of reads: 655457
Percentage reads mapped: 66.53
Strain: lineage4.1.2.1
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 0.98 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrB | 6738 | p.Thr500Asn | missense_variant | 0.17 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
katG | 2153909 | p.Asp735Asn | missense_variant | 0.12 | isoniazid |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6178 | c.939C>T | synonymous_variant | 0.3 |
gyrB | 6181 | c.942C>T | synonymous_variant | 0.32 |
gyrB | 6184 | c.945C>G | synonymous_variant | 0.3 |
gyrB | 6193 | c.954G>A | synonymous_variant | 0.31 |
gyrB | 6203 | p.Ser322Ala | missense_variant | 0.3 |
gyrB | 6214 | c.975G>C | synonymous_variant | 0.31 |
gyrB | 6215 | p.Ser326Thr | missense_variant | 0.28 |
gyrB | 6223 | c.984G>C | synonymous_variant | 0.26 |
gyrB | 6234 | c.995_996insGCGCGA | disruptive_inframe_insertion | 0.25 |
gyrB | 6238 | c.1000_1005delGACCGC | conservative_inframe_deletion | 0.28 |
gyrB | 6250 | c.1011A>G | synonymous_variant | 0.26 |
gyrB | 6259 | p.Asp340Glu | missense_variant | 0.26 |
gyrB | 6265 | p.Asp342Glu | missense_variant | 0.26 |
gyrB | 6266 | p.Pro343Ala | missense_variant | 0.26 |
gyrB | 6286 | c.1047T>C | synonymous_variant | 0.31 |
gyrB | 6292 | c.1053G>T | synonymous_variant | 0.21 |
gyrB | 6301 | c.1062G>C | synonymous_variant | 0.25 |
gyrA | 6304 | c.-998C>G | upstream_gene_variant | 0.2 |
gyrA | 6307 | c.-995T>C | upstream_gene_variant | 0.21 |
gyrA | 6310 | c.-992G>C | upstream_gene_variant | 0.21 |
gyrB | 6311 | p.Ile358Val | missense_variant | 0.21 |
gyrB | 6326 | p.Ser363Arg | missense_variant | 0.27 |
gyrB | 6329 | p.Glu364Gln | missense_variant | 0.27 |
gyrA | 6334 | c.-968G>C | upstream_gene_variant | 0.27 |
gyrA | 6362 | c.-940T>C | upstream_gene_variant | 0.24 |
gyrA | 6382 | c.-920A>G | upstream_gene_variant | 0.19 |
gyrA | 6388 | c.-914T>C | upstream_gene_variant | 0.2 |
gyrA | 6508 | c.-794A>G | upstream_gene_variant | 0.2 |
gyrA | 6511 | c.-791A>T | upstream_gene_variant | 0.16 |
gyrA | 6535 | c.-767C>G | upstream_gene_variant | 0.14 |
gyrA | 6551 | c.-751T>C | upstream_gene_variant | 0.21 |
gyrA | 6673 | c.-629A>C | upstream_gene_variant | 0.14 |
gyrA | 6676 | c.-626T>G | upstream_gene_variant | 0.15 |
gyrA | 6730 | c.-572A>G | upstream_gene_variant | 0.19 |
gyrA | 6742 | c.-560A>G | upstream_gene_variant | 0.16 |
gyrA | 6745 | c.-557T>C | upstream_gene_variant | 0.16 |
gyrA | 6763 | c.-539G>C | upstream_gene_variant | 0.19 |
gyrA | 6775 | c.-527G>T | upstream_gene_variant | 0.14 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7397 | c.96G>C | synonymous_variant | 0.14 |
gyrA | 7406 | c.105G>C | synonymous_variant | 0.14 |
gyrA | 7412 | c.111C>G | synonymous_variant | 0.19 |
gyrA | 7421 | c.120G>C | synonymous_variant | 0.18 |
gyrA | 7424 | c.123G>C | synonymous_variant | 0.18 |
gyrA | 7427 | c.126G>C | synonymous_variant | 0.18 |
gyrA | 7433 | c.132G>C | synonymous_variant | 0.19 |
gyrA | 7442 | c.141G>C | synonymous_variant | 0.18 |
gyrA | 7451 | c.150C>G | synonymous_variant | 0.2 |
gyrA | 7457 | c.156T>C | synonymous_variant | 0.21 |
gyrA | 7463 | c.162G>C | synonymous_variant | 0.2 |
gyrA | 7472 | c.171T>C | synonymous_variant | 0.2 |
gyrA | 7475 | c.174A>C | synonymous_variant | 0.22 |
gyrA | 7480 | p.Phe60Tyr | missense_variant | 0.32 |
gyrA | 7484 | c.183T>C | synonymous_variant | 0.29 |
gyrA | 7490 | c.189C>G | synonymous_variant | 0.29 |
gyrA | 7496 | c.195C>G | synonymous_variant | 0.27 |
gyrA | 7506 | c.205_207delAGCinsTCG | synonymous_variant | 0.29 |
gyrA | 7523 | c.222C>G | synonymous_variant | 0.32 |
gyrA | 7526 | c.225G>T | synonymous_variant | 0.35 |
gyrA | 7532 | c.231T>C | synonymous_variant | 0.35 |
gyrA | 7547 | c.246C>T | synonymous_variant | 0.3 |
gyrA | 7565 | c.264C>T | synonymous_variant | 0.31 |
gyrA | 7571 | c.270G>C | synonymous_variant | 0.36 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7592 | c.291G>C | synonymous_variant | 0.38 |
gyrA | 7622 | c.321C>T | synonymous_variant | 0.27 |
gyrA | 7631 | c.330G>C | synonymous_variant | 0.28 |
gyrA | 7637 | c.336C>T | synonymous_variant | 0.3 |
gyrA | 7658 | c.357A>G | synonymous_variant | 0.26 |
gyrA | 7661 | c.360C>T | synonymous_variant | 0.23 |
gyrA | 7664 | c.363T>C | synonymous_variant | 0.23 |
gyrA | 7670 | c.369A>C | synonymous_variant | 0.22 |
gyrA | 7671 | p.Pro124Ala | missense_variant | 0.22 |
gyrA | 7676 | c.375G>C | synonymous_variant | 0.23 |
gyrA | 7679 | c.378G>C | synonymous_variant | 0.23 |
gyrA | 7683 | c.382_384delAGGinsCGT | synonymous_variant | 0.23 |
gyrA | 7694 | c.393A>G | synonymous_variant | 0.25 |
gyrA | 7703 | c.402G>C | synonymous_variant | 0.23 |
gyrA | 7710 | c.409T>C | synonymous_variant | 0.22 |
gyrA | 7715 | c.414G>C | synonymous_variant | 0.22 |
gyrA | 7730 | p.Arg143Ser | missense_variant | 0.15 |
gyrA | 8121 | c.820T>C | synonymous_variant | 0.18 |
gyrA | 8129 | c.828T>C | synonymous_variant | 0.17 |
gyrA | 8156 | c.855T>C | synonymous_variant | 0.22 |
gyrA | 8168 | c.867A>G | synonymous_variant | 0.17 |
gyrA | 8174 | c.873C>G | synonymous_variant | 0.21 |
gyrA | 8177 | c.876A>C | synonymous_variant | 0.21 |
gyrA | 8187 | p.Leu296Ile | missense_variant | 0.14 |
gyrA | 8191 | p.Ala297Gly | missense_variant | 0.13 |
gyrA | 8339 | c.1038A>G | synonymous_variant | 0.14 |
gyrA | 8340 | p.Ala347Ser | missense_variant | 0.14 |
gyrA | 8619 | c.1318T>C | synonymous_variant | 0.17 |
gyrA | 8624 | c.1323G>T | synonymous_variant | 0.16 |
gyrA | 8693 | c.1392T>C | synonymous_variant | 0.17 |
gyrA | 8696 | c.1395G>C | synonymous_variant | 0.17 |
gyrA | 8699 | c.1398A>G | synonymous_variant | 0.17 |
gyrA | 8711 | c.1410A>C | synonymous_variant | 0.16 |
gyrA | 8714 | c.1413A>G | synonymous_variant | 0.16 |
gyrA | 8731 | p.Gly477Ala | missense_variant | 0.15 |
gyrA | 8747 | c.1446A>G | synonymous_variant | 0.15 |
gyrA | 8751 | p.Ala484Lys | missense_variant | 0.15 |
gyrA | 8756 | c.1455A>G | synonymous_variant | 0.15 |
gyrA | 8757 | p.Ile486Leu | missense_variant | 0.16 |
gyrA | 8761 | p.Val487Ala | missense_variant | 0.17 |
gyrA | 8767 | p.Arg489Lys | missense_variant | 0.2 |
gyrA | 8769 | p.His490Tyr | missense_variant | 0.21 |
gyrA | 8783 | c.1482G>T | synonymous_variant | 0.22 |
gyrA | 8810 | c.1509A>C | synonymous_variant | 0.35 |
gyrA | 8818 | p.Ser506Thr | missense_variant | 0.35 |
gyrA | 8828 | c.1527T>C | synonymous_variant | 0.3 |
gyrA | 8829 | c.1528T>C | synonymous_variant | 0.3 |
gyrA | 8835 | p.Ala512Gln | missense_variant | 0.3 |
gyrA | 8852 | c.1551T>C | synonymous_variant | 0.33 |
gyrA | 8858 | c.1557T>C | synonymous_variant | 0.36 |
gyrA | 8867 | c.1566A>G | synonymous_variant | 0.32 |
gyrA | 8870 | c.1569G>C | synonymous_variant | 0.32 |
gyrA | 8873 | c.1572A>C | synonymous_variant | 0.31 |
gyrA | 8897 | c.1596T>C | synonymous_variant | 0.42 |
gyrA | 8900 | c.1599G>C | synonymous_variant | 0.41 |
gyrA | 8903 | c.1602T>C | synonymous_variant | 0.41 |
gyrA | 8912 | c.1611G>A | synonymous_variant | 0.42 |
gyrA | 8915 | c.1614A>G | synonymous_variant | 0.42 |
gyrA | 8924 | c.1623C>T | synonymous_variant | 0.44 |
gyrA | 8939 | c.1638T>C | synonymous_variant | 0.38 |
gyrA | 8942 | c.1641G>C | synonymous_variant | 0.38 |
gyrA | 8946 | c.1645_1647delTTGinsCTC | synonymous_variant | 0.38 |
gyrA | 8967 | p.Ala556Asn | missense_variant | 0.4 |
gyrA | 8990 | c.1689C>G | synonymous_variant | 0.39 |
gyrA | 8996 | c.1695T>C | synonymous_variant | 0.36 |
gyrA | 8998 | p.Leu566Trp | missense_variant | 0.36 |
gyrA | 9014 | c.1713C>G | synonymous_variant | 0.33 |
gyrA | 9017 | c.1716C>G | synonymous_variant | 0.31 |
gyrA | 9023 | c.1722A>C | synonymous_variant | 0.31 |
gyrA | 9029 | c.1728T>G | synonymous_variant | 0.32 |
gyrA | 9032 | c.1731T>C | synonymous_variant | 0.32 |
gyrA | 9051 | c.1750T>C | synonymous_variant | 0.24 |
gyrA | 9065 | c.1764C>G | synonymous_variant | 0.22 |
gyrA | 9071 | c.1770G>C | synonymous_variant | 0.2 |
gyrA | 9080 | c.1779G>T | synonymous_variant | 0.21 |
gyrA | 9092 | c.1791C>G | synonymous_variant | 0.21 |
gyrA | 9099 | c.1798_1800delTTAinsCTG | synonymous_variant | 0.19 |
gyrA | 9113 | c.1812C>G | synonymous_variant | 0.14 |
gyrA | 9119 | c.1818A>G | synonymous_variant | 0.17 |
gyrA | 9176 | c.1875G>C | synonymous_variant | 0.16 |
gyrA | 9182 | c.1881T>C | synonymous_variant | 0.17 |
gyrA | 9191 | c.1890G>T | synonymous_variant | 0.17 |
gyrA | 9200 | c.1899A>G | synonymous_variant | 0.17 |
gyrA | 9213 | p.Thr638Ala | missense_variant | 0.16 |
gyrA | 9227 | c.1926C>G | synonymous_variant | 0.15 |
gyrA | 9230 | c.1929T>C | synonymous_variant | 0.19 |
gyrA | 9236 | c.1935G>C | synonymous_variant | 0.19 |
gyrA | 9242 | c.1941A>C | synonymous_variant | 0.19 |
gyrA | 9248 | c.1947G>C | synonymous_variant | 0.19 |
gyrA | 9252 | p.Val651Ile | missense_variant | 0.18 |
gyrA | 9267 | p.Asn656Gly | missense_variant | 0.16 |
gyrA | 9275 | c.1974G>A | synonymous_variant | 0.16 |
gyrA | 9278 | c.1977G>C | synonymous_variant | 0.17 |
gyrA | 9287 | c.1986G>C | synonymous_variant | 0.15 |
gyrA | 9296 | c.1995T>C | synonymous_variant | 0.17 |
gyrA | 9299 | c.1998G>C | synonymous_variant | 0.17 |
gyrA | 9304 | p.Gly668Glu | missense_variant | 1.0 |
gyrA | 9308 | p.Asp669Glu | missense_variant | 0.16 |
gyrA | 9323 | c.2022C>G | synonymous_variant | 0.14 |
gyrA | 9326 | c.2025G>C | synonymous_variant | 0.14 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
rpoB | 760115 | c.309C>T | synonymous_variant | 0.96 |
rpoB | 760382 | c.576G>C | synonymous_variant | 0.14 |
rpoB | 760400 | c.594G>C | synonymous_variant | 0.14 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.19 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.2 |
rpoB | 760457 | c.651C>T | synonymous_variant | 0.17 |
rpoB | 760460 | c.654G>C | synonymous_variant | 0.17 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.17 |
rpoB | 760481 | c.675G>C | synonymous_variant | 0.17 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.17 |
rpoB | 760487 | c.681G>C | synonymous_variant | 0.17 |
rpoB | 760508 | c.702G>A | synonymous_variant | 0.14 |
rpoB | 760511 | c.705G>C | synonymous_variant | 0.14 |
rpoB | 760522 | p.Ser239Asn | missense_variant | 0.13 |
rpoB | 761051 | c.1245G>T | synonymous_variant | 0.15 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.15 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.15 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.15 |
rpoB | 761063 | c.1257C>G | synonymous_variant | 0.14 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.14 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 0.16 |
rpoB | 761150 | c.1344A>T | synonymous_variant | 0.16 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.19 |
rpoB | 761171 | c.1365C>T | synonymous_variant | 0.2 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.21 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.21 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.2 |
rpoB | 761198 | c.1392G>C | synonymous_variant | 0.21 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.21 |
rpoB | 761217 | p.Pro471Ser | missense_variant | 0.2 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.17 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.15 |
rpoB | 761258 | c.1452G>A | synonymous_variant | 0.16 |
rpoB | 761261 | c.1455G>C | synonymous_variant | 0.15 |
rpoB | 761306 | c.1500C>G | synonymous_variant | 0.17 |
rpoB | 761936 | c.2130C>T | synonymous_variant | 0.14 |
rpoB | 761969 | c.2163G>A | synonymous_variant | 0.17 |
rpoB | 761999 | c.2193G>C | synonymous_variant | 0.19 |
rpoB | 762002 | c.2196C>G | synonymous_variant | 0.19 |
rpoB | 762003 | p.Asn733Gln | missense_variant | 0.19 |
rpoB | 762014 | c.2208C>G | synonymous_variant | 0.19 |
rpoB | 762017 | c.2211A>G | synonymous_variant | 0.19 |
rpoB | 762018 | p.Glu738Gln | missense_variant | 0.19 |
rpoB | 762026 | c.2220G>T | synonymous_variant | 0.19 |
rpoB | 762029 | c.2223C>G | synonymous_variant | 0.19 |
rpoB | 762032 | c.2226C>G | synonymous_variant | 0.18 |
rpoB | 762035 | c.2229G>C | synonymous_variant | 0.17 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.25 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.24 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.22 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.21 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.23 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.25 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 0.22 |
rpoB | 762134 | c.2328C>T | synonymous_variant | 0.22 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.22 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.22 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.22 |
rpoB | 762158 | c.2352G>C | synonymous_variant | 0.26 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.23 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.26 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.22 |
rpoB | 762239 | c.2433G>A | synonymous_variant | 0.25 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.25 |
rpoB | 762249 | c.2443C>T | synonymous_variant | 0.26 |
rpoB | 762278 | c.2472C>T | synonymous_variant | 0.2 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.18 |
rpoC | 762374 | c.-996G>C | upstream_gene_variant | 0.2 |
rpoC | 762395 | c.-975G>C | upstream_gene_variant | 0.19 |
rpoC | 762398 | c.-972T>C | upstream_gene_variant | 0.17 |
rpoC | 762401 | c.-969G>C | upstream_gene_variant | 0.17 |
rpoC | 762404 | c.-966T>C | upstream_gene_variant | 0.17 |
rpoC | 762410 | c.-960T>C | upstream_gene_variant | 0.19 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 0.18 |
rpoC | 762443 | c.-927G>C | upstream_gene_variant | 0.19 |
rpoC | 762452 | c.-918G>C | upstream_gene_variant | 0.19 |
rpoC | 762470 | c.-900G>C | upstream_gene_variant | 0.2 |
rpoB | 762489 | p.Val895Ile | missense_variant | 0.15 |
rpoB | 762507 | p.Leu901Ile | missense_variant | 0.13 |
rpoB | 762795 | p.Asp997Asn | missense_variant | 0.14 |
rpoB | 762814 | p.Met1003Thr | missense_variant | 0.17 |
rpoC | 762818 | c.-552C>G | upstream_gene_variant | 0.17 |
rpoC | 762827 | c.-543G>T | upstream_gene_variant | 0.17 |
rpoC | 762830 | c.-540C>T | upstream_gene_variant | 0.17 |
rpoC | 762831 | c.-539_-538delAGinsTC | upstream_gene_variant | 0.17 |
rpoC | 762863 | c.-507T>C | upstream_gene_variant | 0.18 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.19 |
rpoC | 762911 | c.-459C>T | upstream_gene_variant | 0.16 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 0.17 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.17 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.17 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.19 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.26 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.24 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.16 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.15 |
rpoC | 763082 | c.-288C>T | upstream_gene_variant | 0.15 |
rpoC | 763088 | c.-282C>G | upstream_gene_variant | 0.14 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.14 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.19 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.18 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.17 |
rpoC | 763142 | c.-228C>G | upstream_gene_variant | 0.18 |
rpoC | 763495 | c.126G>A | synonymous_variant | 0.15 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.2 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.2 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.2 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.2 |
rpoC | 763589 | p.Ile74Val | missense_variant | 0.22 |
rpoC | 763603 | c.234C>T | synonymous_variant | 0.24 |
rpoC | 763618 | c.249C>T | synonymous_variant | 0.21 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.15 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.17 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.16 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.14 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.14 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.14 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.14 |
rpoC | 763709 | c.340C>T | synonymous_variant | 0.14 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.14 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.14 |
rpoC | 764239 | c.870T>G | synonymous_variant | 0.16 |
rpoC | 764254 | c.885G>T | synonymous_variant | 0.19 |
rpoC | 764263 | c.894G>C | synonymous_variant | 0.18 |
rpoC | 764266 | c.897T>C | synonymous_variant | 0.19 |
rpoC | 764269 | c.900G>C | synonymous_variant | 0.19 |
rpoC | 764278 | c.909A>G | synonymous_variant | 0.17 |
rpoC | 764284 | c.915G>C | synonymous_variant | 0.17 |
rpoC | 764296 | c.927G>C | synonymous_variant | 0.16 |
rpoC | 764320 | c.951C>T | synonymous_variant | 0.21 |
rpoC | 764353 | c.984G>T | synonymous_variant | 0.24 |
rpoC | 764359 | c.990C>G | synonymous_variant | 0.25 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.21 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 0.21 |
rpoC | 764377 | c.1008C>G | synonymous_variant | 0.21 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.21 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 0.23 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.19 |
rpoC | 764410 | c.1041G>C | synonymous_variant | 0.24 |
rpoC | 764429 | c.1060C>T | synonymous_variant | 0.28 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.28 |
rpoC | 764435 | c.1066_1068delAGGinsCGA | synonymous_variant | 0.28 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.25 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.24 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.29 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.29 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.3 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.24 |
rpoC | 764500 | c.1131C>G | synonymous_variant | 0.26 |
rpoC | 764506 | c.1137C>T | synonymous_variant | 0.31 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.31 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.34 |
rpoC | 764530 | c.1161C>T | synonymous_variant | 0.31 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.27 |
rpoC | 764548 | c.1179G>C | synonymous_variant | 0.26 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.25 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.27 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 0.23 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.23 |
rpoC | 764623 | c.1254C>G | synonymous_variant | 0.24 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.24 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.22 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.24 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.22 |
rpoC | 764692 | c.1323C>T | synonymous_variant | 0.19 |
rpoC | 764701 | c.1332C>G | synonymous_variant | 0.18 |
rpoC | 764707 | c.1338G>C | synonymous_variant | 0.17 |
rpoC | 764713 | c.1344G>C | synonymous_variant | 0.17 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.17 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.14 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.17 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.17 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.15 |
rpoC | 764797 | c.1428G>C | synonymous_variant | 0.14 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.14 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.15 |
rpoC | 764875 | c.1506C>T | synonymous_variant | 0.13 |
rpoC | 764913 | p.Met515Lys | missense_variant | 0.14 |
rpoC | 764935 | c.1566T>C | synonymous_variant | 0.16 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.16 |
rpoC | 765007 | c.1638T>G | synonymous_variant | 0.14 |
rpoC | 765011 | p.Ser548Trp | missense_variant | 0.14 |
rpoC | 765016 | c.1647C>G | synonymous_variant | 0.15 |
rpoC | 765019 | c.1650A>G | synonymous_variant | 0.15 |
rpoC | 765034 | c.1665T>G | synonymous_variant | 0.15 |
rpoC | 765040 | c.1671T>C | synonymous_variant | 0.15 |
rpoC | 765041 | c.1672T>C | synonymous_variant | 0.15 |
rpoC | 765052 | c.1683C>G | synonymous_variant | 0.15 |
rpoC | 765055 | c.1686C>G | synonymous_variant | 0.15 |
rpoC | 765076 | c.1707A>G | synonymous_variant | 0.15 |
rpoC | 765079 | c.1710T>G | synonymous_variant | 0.15 |
rpoC | 765082 | c.1713G>C | synonymous_variant | 0.15 |
rpoC | 765085 | c.1716T>C | synonymous_variant | 0.14 |
rpoC | 765103 | c.1734G>T | synonymous_variant | 0.15 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 766801 | c.3432C>A | synonymous_variant | 0.15 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.15 |
rpoC | 766837 | c.3468G>C | synonymous_variant | 0.18 |
rpoC | 766858 | c.3489C>T | synonymous_variant | 0.14 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.14 |
rpoC | 766911 | p.Ile1181Thr | missense_variant | 0.14 |
rpoC | 766915 | p.Asp1182Glu | missense_variant | 0.14 |
rpoC | 766919 | p.Ala1184Thr | missense_variant | 0.14 |
rpoC | 766931 | p.Ala1188Thr | missense_variant | 0.15 |
rpoC | 766942 | c.3573C>T | synonymous_variant | 0.15 |
rpoC | 766945 | c.3576A>C | synonymous_variant | 0.15 |
rpoC | 766960 | c.3591C>T | synonymous_variant | 0.19 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.16 |
rpoC | 766978 | c.3609C>A | synonymous_variant | 0.21 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.22 |
rpoC | 767008 | c.3639G>A | synonymous_variant | 0.18 |
rpoC | 767020 | c.3651C>G | synonymous_variant | 0.22 |
rpoC | 767092 | c.3723C>T | synonymous_variant | 0.26 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.28 |
rpoC | 767104 | c.3735C>G | synonymous_variant | 0.26 |
rpoC | 767105 | p.Asn1246Gln | missense_variant | 0.26 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.25 |
rpoC | 767134 | c.3765C>T | synonymous_variant | 0.24 |
rpoC | 767138 | c.3769C>T | synonymous_variant | 0.24 |
rpoC | 767149 | c.3780C>T | synonymous_variant | 0.26 |
rpoC | 767155 | c.3786C>G | synonymous_variant | 0.23 |
rpoC | 767158 | c.3789T>C | synonymous_variant | 0.23 |
rpoC | 767167 | c.3798C>G | synonymous_variant | 0.26 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.29 |
rpoC | 767185 | c.3816G>C | synonymous_variant | 0.28 |
rpoC | 767191 | c.3822C>G | synonymous_variant | 0.28 |
rpoC | 767200 | c.3831G>A | synonymous_variant | 0.29 |
rpoC | 767221 | c.3852C>G | synonymous_variant | 0.28 |
rpoC | 767230 | c.3861G>T | synonymous_variant | 0.21 |
rpoC | 767233 | c.3864T>C | synonymous_variant | 0.21 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775955 | p.Ile842Met | missense_variant | 0.14 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781572 | p.Gln5Lys | missense_variant | 0.13 |
rpsL | 781628 | c.69T>G | synonymous_variant | 0.17 |
rpsL | 781631 | c.72G>C | synonymous_variant | 0.16 |
rpsL | 781658 | c.99A>G | synonymous_variant | 0.24 |
rpsL | 781682 | c.123T>C | synonymous_variant | 0.19 |
rpsL | 781685 | c.126G>C | synonymous_variant | 0.2 |
rpsL | 781706 | c.147T>G | synonymous_variant | 0.22 |
rpsL | 781709 | c.150G>C | synonymous_variant | 0.22 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.21 |
rpsL | 781721 | c.162C>T | synonymous_variant | 0.17 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.17 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.2 |
rpsL | 781742 | c.183C>T | synonymous_variant | 0.19 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.2 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.2 |
rpsL | 781763 | c.204C>G | synonymous_variant | 0.18 |
rpsL | 781766 | c.207C>T | synonymous_variant | 0.18 |
rpsL | 781769 | c.210G>A | synonymous_variant | 0.18 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.19 |
rpsL | 781808 | c.249C>T | synonymous_variant | 0.19 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.19 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.19 |
rpsL | 781829 | c.270G>C | synonymous_variant | 0.24 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.25 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.24 |
rpsL | 781865 | c.306G>C | synonymous_variant | 0.23 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.23 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.23 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.19 |
rplC | 800651 | c.-158G>C | upstream_gene_variant | 0.17 |
rplC | 800678 | c.-131C>T | upstream_gene_variant | 0.17 |
rplC | 800684 | c.-125G>A | upstream_gene_variant | 0.17 |
rplC | 800690 | c.-119C>T | upstream_gene_variant | 0.16 |
rplC | 800693 | c.-116A>C | upstream_gene_variant | 0.16 |
rplC | 800702 | c.-107G>C | upstream_gene_variant | 0.16 |
rplC | 800703 | c.-106_-104delTTGinsCTT | upstream_gene_variant | 0.16 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.18 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.18 |
rplC | 800744 | c.-65G>C | upstream_gene_variant | 0.17 |
rplC | 800745 | c.-64_-62delCTCinsTTG | upstream_gene_variant | 0.17 |
rplC | 800759 | c.-50C>T | upstream_gene_variant | 0.19 |
rplC | 800762 | c.-47T>G | upstream_gene_variant | 0.19 |
rplC | 800768 | c.-41C>G | upstream_gene_variant | 0.17 |
fbiC | 1304508 | p.Glu526Asp | missense_variant | 0.16 |
fbiC | 1304511 | c.1581C>T | synonymous_variant | 0.16 |
fbiC | 1304520 | c.1590A>G | synonymous_variant | 0.15 |
fbiC | 1304556 | c.1626C>T | synonymous_variant | 0.15 |
fbiC | 1304559 | p.Glu543Asp | missense_variant | 0.15 |
fbiC | 1304565 | c.1635C>G | synonymous_variant | 0.16 |
fbiC | 1304568 | c.1638T>C | synonymous_variant | 0.15 |
fbiC | 1304574 | c.1644C>G | synonymous_variant | 0.15 |
fbiC | 1304580 | c.1650T>G | synonymous_variant | 0.15 |
fbiC | 1304634 | c.1704C>G | synonymous_variant | 0.16 |
fbiC | 1304640 | c.1710A>C | synonymous_variant | 0.16 |
fbiC | 1304652 | c.1722C>T | synonymous_variant | 0.17 |
fbiC | 1304655 | c.1725C>T | synonymous_variant | 0.16 |
fbiC | 1304675 | p.Gly582Asp | missense_variant | 0.16 |
fbiC | 1304694 | c.1764A>G | synonymous_variant | 0.15 |
fbiC | 1304703 | c.1773C>G | synonymous_variant | 0.14 |
fbiC | 1304706 | c.1776C>T | synonymous_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471922 | n.78delT | non_coding_transcript_exon_variant | 0.17 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1471931 | n.87delA | non_coding_transcript_exon_variant | 0.17 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472019 | n.174G>A | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472031 | n.186G>C | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472033 | n.188A>C | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472035 | n.190G>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472040 | n.195T>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472041 | n.196C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472042 | n.197T>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472672 | n.830delT | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472847 | n.1002G>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472848 | n.1003T>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472849 | n.1004C>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472850 | n.1005T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472857 | n.1012A>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472858 | n.1013G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472859 | n.1014G>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472860 | n.1015C>G | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.48 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.48 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.49 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473291 | n.1446_1447insT | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1473717 | n.60G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473731 | n.74T>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1473743 | n.86C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1473746 | n.89T>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.37 |
rrl | 1473815 | n.158T>C | non_coding_transcript_exon_variant | 0.37 |
rrl | 1473832 | n.175C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1473839 | n.182G>T | non_coding_transcript_exon_variant | 0.34 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473922 | n.265A>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1473923 | n.266C>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473935 | n.278C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1473937 | n.280C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1473943 | n.286G>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1473945 | n.288T>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1473946 | n.289A>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474022 | n.365G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474034 | n.377G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474045 | n.388C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474054 | n.397T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474065 | n.408C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474074 | n.417C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474077 | n.420G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474093 | n.436G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474094 | n.437C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474096 | n.439C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474104 | n.448_452delTATCA | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474135 | n.478G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474156 | n.499G>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474163 | n.506C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474178 | n.522dupC | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474183 | n.527delC | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474306 | n.649A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474308 | n.653_654delTG | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474376 | n.719T>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474436 | n.779T>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474447 | n.790G>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.51 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.49 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.49 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.49 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.49 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.37 |
rrl | 1474676 | n.1019T>C | non_coding_transcript_exon_variant | 0.37 |
rrl | 1474709 | n.1053_1056delTGGT | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474715 | n.1060_1061insGACAAA | non_coding_transcript_exon_variant | 0.41 |
rrl | 1474753 | n.1096A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.39 |
rrl | 1474783 | n.1126G>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474945 | n.1288C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474950 | n.1296_1297delCA | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474990 | n.1333C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474991 | n.1334T>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474995 | n.1338T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474997 | n.1340A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474999 | n.1342C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475005 | n.1348C>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475006 | n.1349A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475010 | n.1353G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475015 | n.1358C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475017 | n.1360_1361insA | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475020 | n.1363G>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475031 | n.1374G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475061 | n.1404C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475062 | n.1405A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475108 | n.1451C>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475343 | n.1686A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475358 | n.1701T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475363 | n.1706C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475369 | n.1712G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475375 | n.1718G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475376 | n.1719A>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475379 | n.1722G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475398 | n.1741C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475402 | n.1746_1747delTA | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475430 | n.1773T>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475479 | n.1822C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1475480 | n.1823A>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1475487 | n.1830C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475544 | n.1887A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475602 | n.1945G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475603 | n.1946G>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475604 | n.1947A>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475612 | n.1955G>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475615 | n.1958C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475616 | n.1959A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475618 | n.1961C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475620 | n.1963T>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475637 | n.1980T>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475638 | n.1981C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475639 | n.1982C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475643 | n.1986C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475647 | n.1990G>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.58 |
rrl | 1475989 | n.2332T>A | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476088 | n.2431A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476103 | n.2446C>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476105 | n.2448G>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476106 | n.2449A>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476114 | n.2457T>C | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476251 | n.2594T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476583 | n.2926G>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476665 | n.3008T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476666 | n.3009C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476674 | n.3017T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476689 | n.3032A>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476690 | n.3033C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476693 | n.3036G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476695 | n.3038T>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476723 | n.3066T>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476726 | n.3069A>G | non_coding_transcript_exon_variant | 0.19 |
inhA | 1674304 | p.Gln35Glu | missense_variant | 0.16 |
inhA | 1674384 | c.183C>G | synonymous_variant | 0.13 |
inhA | 1674387 | c.186A>G | synonymous_variant | 0.13 |
inhA | 1674399 | c.198A>G | synonymous_variant | 0.13 |
inhA | 1674422 | p.Leu74Ser | missense_variant | 0.17 |
inhA | 1674429 | c.228C>G | synonymous_variant | 0.17 |
inhA | 1674432 | c.231G>C | synonymous_variant | 0.17 |
inhA | 1674435 | c.234G>C | synonymous_variant | 0.15 |
inhA | 1674443 | p.Ala81Val | missense_variant | 0.15 |
inhA | 1674450 | c.249G>C | synonymous_variant | 0.17 |
inhA | 1674534 | c.333G>A | synonymous_variant | 0.2 |
inhA | 1674542 | p.Ala114Glu | missense_variant | 0.25 |
inhA | 1674550 | p.Ser117Ala | missense_variant | 0.19 |
inhA | 1674573 | c.372G>C | synonymous_variant | 0.2 |
inhA | 1674576 | c.375T>C | synonymous_variant | 0.17 |
inhA | 1674582 | c.381T>C | synonymous_variant | 0.23 |
inhA | 1674585 | c.384T>C | synonymous_variant | 0.23 |
inhA | 1674589 | p.Met130Leu | missense_variant | 0.27 |
inhA | 1674600 | c.399G>C | synonymous_variant | 0.24 |
inhA | 1674619 | p.Pro140Glu | missense_variant | 0.21 |
inhA | 1674624 | c.423A>C | synonymous_variant | 0.2 |
inhA | 1674627 | c.426T>C | synonymous_variant | 0.21 |
inhA | 1674628 | p.Ser143Gly | missense_variant | 0.21 |
inhA | 1674669 | c.468G>C | synonymous_variant | 0.18 |
inhA | 1674702 | c.501G>C | synonymous_variant | 0.18 |
inhA | 1674703 | c.502_504delTTGinsCTC | synonymous_variant | 0.18 |
inhA | 1674718 | c.517A>C | synonymous_variant | 0.18 |
inhA | 1674750 | c.549T>C | synonymous_variant | 0.16 |
inhA | 1674756 | c.555T>C | synonymous_variant | 0.16 |
inhA | 1674759 | c.558G>C | synonymous_variant | 0.15 |
inhA | 1674771 | c.570C>G | synonymous_variant | 0.18 |
inhA | 1674780 | c.579T>C | synonymous_variant | 0.17 |
inhA | 1674789 | c.588G>C | synonymous_variant | 0.19 |
inhA | 1674795 | c.594G>C | synonymous_variant | 0.21 |
inhA | 1674801 | c.600T>C | synonymous_variant | 0.18 |
inhA | 1674804 | c.603G>C | synonymous_variant | 0.18 |
inhA | 1674819 | c.618G>C | synonymous_variant | 0.17 |
inhA | 1674828 | p.Glu209Asp | missense_variant | 0.17 |
inhA | 1674838 | p.Ala213Gln | missense_variant | 0.14 |
inhA | 1674846 | p.Ile215Met | missense_variant | 0.14 |
inhA | 1674858 | c.657G>A | synonymous_variant | 0.14 |
inhA | 1674870 | c.669T>C | synonymous_variant | 0.15 |
rpsA | 1833628 | c.87G>C | synonymous_variant | 0.15 |
rpsA | 1833664 | c.123C>G | synonymous_variant | 0.19 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.22 |
rpsA | 1833685 | c.144G>T | synonymous_variant | 0.24 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.21 |
rpsA | 1833697 | c.156C>G | synonymous_variant | 0.21 |
rpsA | 1833724 | c.183C>T | synonymous_variant | 0.22 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.22 |
rpsA | 1833730 | c.189C>T | synonymous_variant | 0.23 |
rpsA | 1833733 | c.192C>T | synonymous_variant | 0.23 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.23 |
rpsA | 1833745 | c.204G>T | synonymous_variant | 0.22 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.16 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.16 |
rpsA | 1833793 | c.252C>T | synonymous_variant | 0.16 |
rpsA | 1833808 | c.267G>C | synonymous_variant | 0.16 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 0.16 |
rpsA | 1833829 | c.288A>G | synonymous_variant | 0.15 |
rpsA | 1833832 | c.291G>A | synonymous_variant | 0.16 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.16 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.16 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.15 |
rpsA | 1833894 | p.Ala118Glu | missense_variant | 0.17 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.17 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.14 |
rpsA | 1833976 | c.435C>G | synonymous_variant | 0.15 |
rpsA | 1833991 | c.450C>A | synonymous_variant | 0.17 |
rpsA | 1833997 | c.456G>C | synonymous_variant | 0.16 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.15 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.14 |
rpsA | 1834099 | c.558C>G | synonymous_variant | 0.14 |
rpsA | 1834108 | c.567C>T | synonymous_variant | 0.14 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.15 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.16 |
rpsA | 1834255 | c.714C>G | synonymous_variant | 0.23 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.23 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.23 |
rpsA | 1834279 | c.738C>T | synonymous_variant | 0.3 |
rpsA | 1834297 | c.756C>T | synonymous_variant | 0.31 |
rpsA | 1834303 | c.762T>G | synonymous_variant | 0.29 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.3 |
rpsA | 1834330 | c.789C>G | synonymous_variant | 0.32 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.25 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.26 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.25 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.26 |
rpsA | 1834408 | c.867C>T | synonymous_variant | 0.24 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.26 |
rpsA | 1834423 | c.882G>T | synonymous_variant | 0.22 |
rpsA | 1834432 | c.891G>C | synonymous_variant | 0.21 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.21 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.24 |
rpsA | 1834483 | c.942G>A | synonymous_variant | 0.24 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.23 |
rpsA | 1834520 | p.Ala327Ser | missense_variant | 0.21 |
rpsA | 1834540 | c.999G>C | synonymous_variant | 0.21 |
rpsA | 1834543 | c.1002C>G | synonymous_variant | 0.21 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.21 |
rpsA | 1834554 | c.1014_1015delTG | frameshift_variant | 0.24 |
rpsA | 1834558 | c.1017_1018insAG | frameshift_variant | 0.24 |
rpsA | 1834606 | c.1065C>T | synonymous_variant | 0.15 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.15 |
rpsA | 1834612 | c.1071G>C | synonymous_variant | 0.15 |
rpsA | 1834619 | c.1078T>C | synonymous_variant | 0.16 |
rpsA | 1834622 | c.1081_1083delTCGinsAGC | synonymous_variant | 0.16 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.15 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.17 |
rpsA | 1834667 | p.Ala376Ser | missense_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155716 | c.396T>C | synonymous_variant | 0.14 |
katG | 2155722 | c.390G>C | synonymous_variant | 0.15 |
katG | 2155728 | c.384G>C | synonymous_variant | 0.15 |
katG | 2155743 | c.369G>C | synonymous_variant | 0.14 |
katG | 2155769 | p.Ile115Val | missense_variant | 0.15 |
katG | 2155785 | c.327T>C | synonymous_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2517917 | c.-198G>C | upstream_gene_variant | 0.23 |
kasA | 2517941 | c.-174C>G | upstream_gene_variant | 0.22 |
kasA | 2517950 | c.-165C>G | upstream_gene_variant | 0.21 |
kasA | 2517968 | c.-147T>C | upstream_gene_variant | 0.14 |
kasA | 2517980 | c.-135C>T | upstream_gene_variant | 0.14 |
kasA | 2517989 | c.-126T>C | upstream_gene_variant | 0.17 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2518756 | c.642G>C | synonymous_variant | 0.13 |
ribD | 2986827 | c.-12G>A | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3877728 | c.780C>G | synonymous_variant | 0.16 |
rpoA | 3877737 | c.771G>C | synonymous_variant | 0.16 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.15 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.15 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.16 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.16 |
rpoA | 3877785 | c.723C>A | synonymous_variant | 0.16 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.17 |
rpoA | 3878010 | c.498C>G | synonymous_variant | 0.17 |
rpoA | 3878013 | c.495T>C | synonymous_variant | 0.17 |
rpoA | 3878019 | c.489A>G | synonymous_variant | 0.17 |
rpoA | 3878022 | c.486T>C | synonymous_variant | 0.15 |
rpoA | 3878025 | c.483C>T | synonymous_variant | 0.15 |
rpoA | 3878028 | c.480G>C | synonymous_variant | 0.15 |
rpoA | 3878031 | c.477T>C | synonymous_variant | 0.15 |
rpoA | 3878034 | c.474A>G | synonymous_variant | 0.19 |
rpoA | 3878046 | c.462T>G | synonymous_variant | 0.2 |
rpoA | 3878050 | p.Arg153Lys | missense_variant | 0.2 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.2 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.21 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.21 |
rpoA | 3878073 | c.435C>T | synonymous_variant | 0.21 |
rpoA | 3878082 | c.426T>C | synonymous_variant | 0.21 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.14 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.14 |
rpoA | 3878127 | c.381G>C | synonymous_variant | 0.18 |
rpoA | 3878143 | p.Gly122Asp | missense_variant | 0.25 |
rpoA | 3878145 | c.363C>G | synonymous_variant | 0.26 |
rpoA | 3878154 | c.354G>C | synonymous_variant | 0.24 |
rpoA | 3878157 | c.351C>G | synonymous_variant | 0.25 |
rpoA | 3878160 | c.348C>G | synonymous_variant | 0.25 |
rpoA | 3878163 | c.345C>T | synonymous_variant | 0.31 |
rpoA | 3878172 | c.336G>C | synonymous_variant | 0.33 |
rpoA | 3878184 | c.324C>T | synonymous_variant | 0.37 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.33 |
rpoA | 3878196 | p.Glu104Ala | missense_variant | 0.33 |
rpoA | 3878205 | c.303T>C | synonymous_variant | 0.33 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.38 |
rpoA | 3878244 | c.264G>A | synonymous_variant | 0.43 |
rpoA | 3878256 | c.252G>C | synonymous_variant | 0.45 |
rpoA | 3878264 | p.Ser82Gly | missense_variant | 0.48 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.56 |
rpoA | 3878283 | p.Glu75Asp | missense_variant | 0.5 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.47 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.32 |
rpoA | 3878310 | c.198G>C | synonymous_variant | 0.24 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 0.2 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.18 |
rpoA | 3878331 | c.177A>C | synonymous_variant | 0.2 |
rpoA | 3878337 | c.171T>C | synonymous_variant | 0.21 |
rpoA | 3878346 | c.162T>C | synonymous_variant | 0.19 |
rpoA | 3878358 | c.150C>G | synonymous_variant | 0.19 |
rpoA | 3878361 | c.147G>A | synonymous_variant | 0.19 |
rpoA | 3878364 | c.144A>C | synonymous_variant | 0.17 |
rpoA | 3878367 | c.141C>G | synonymous_variant | 0.17 |
rpoA | 3878370 | c.138T>C | synonymous_variant | 0.17 |
rpoA | 3878373 | c.135G>C | synonymous_variant | 0.17 |
rpoA | 3878385 | c.123C>G | synonymous_variant | 0.17 |
rpoA | 3878400 | c.108T>C | synonymous_variant | 0.19 |
rpoA | 3878403 | c.105C>T | synonymous_variant | 0.17 |
rpoA | 3878415 | c.93C>T | synonymous_variant | 0.12 |
rpoA | 3878454 | c.54A>G | synonymous_variant | 0.13 |
rpoA | 3878465 | p.Thr15Ala | missense_variant | 0.14 |
rpoA | 3878466 | c.42C>G | synonymous_variant | 0.14 |
rpoA | 3878469 | c.39C>G | synonymous_variant | 0.14 |
rpoA | 3878490 | c.18C>A | synonymous_variant | 0.2 |
rpoA | 3878496 | c.12A>T | synonymous_variant | 0.25 |
clpC1 | 4038410 | c.2295C>T | synonymous_variant | 0.14 |
clpC1 | 4038445 | p.Ala754Thr | missense_variant | 0.14 |
clpC1 | 4038485 | p.Gly740Lys | missense_variant | 0.15 |
clpC1 | 4038490 | p.Ala739Ser | missense_variant | 0.15 |
clpC1 | 4038491 | c.2214C>G | synonymous_variant | 0.15 |
clpC1 | 4038499 | p.Ser736Gly | missense_variant | 0.16 |
clpC1 | 4038917 | c.1788C>T | synonymous_variant | 0.16 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 0.16 |
clpC1 | 4038941 | c.1764G>C | synonymous_variant | 0.15 |
clpC1 | 4039001 | p.Asn568Glu | missense_variant | 0.16 |
clpC1 | 4039016 | c.1689C>G | synonymous_variant | 0.15 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.18 |
clpC1 | 4039073 | c.1632C>T | synonymous_variant | 0.18 |
clpC1 | 4039079 | c.1626C>G | synonymous_variant | 0.18 |
clpC1 | 4039085 | c.1620A>G | synonymous_variant | 0.2 |
clpC1 | 4039091 | c.1614G>C | synonymous_variant | 0.21 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.19 |
clpC1 | 4039139 | p.Glu522Val | missense_variant | 0.15 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.15 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.15 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.2 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.24 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.25 |
clpC1 | 4039187 | c.1518G>T | synonymous_variant | 0.25 |
clpC1 | 4039190 | c.1515C>G | synonymous_variant | 0.25 |
clpC1 | 4039208 | c.1497C>G | synonymous_variant | 0.27 |
clpC1 | 4039217 | c.1488G>C | synonymous_variant | 0.26 |
clpC1 | 4039244 | c.1461G>C | synonymous_variant | 0.25 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.3 |
clpC1 | 4039286 | c.1419T>G | synonymous_variant | 0.27 |
clpC1 | 4039292 | c.1413C>T | synonymous_variant | 0.26 |
clpC1 | 4039295 | c.1410A>G | synonymous_variant | 0.2 |
clpC1 | 4039310 | c.1395A>G | synonymous_variant | 0.18 |
clpC1 | 4039313 | c.1392C>G | synonymous_variant | 0.18 |
clpC1 | 4039319 | c.1386T>G | synonymous_variant | 0.18 |
clpC1 | 4039322 | c.1383T>C | synonymous_variant | 0.18 |
clpC1 | 4039328 | c.1377A>C | synonymous_variant | 0.18 |
clpC1 | 4039337 | c.1368A>G | synonymous_variant | 0.21 |
clpC1 | 4039391 | c.1314T>C | synonymous_variant | 0.15 |
clpC1 | 4039409 | c.1296T>C | synonymous_variant | 0.15 |
clpC1 | 4039415 | p.Glu430Asp | missense_variant | 0.15 |
clpC1 | 4039610 | c.1095G>T | synonymous_variant | 0.17 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.19 |
clpC1 | 4039622 | c.1083C>T | synonymous_variant | 0.19 |
clpC1 | 4039646 | c.1059G>A | synonymous_variant | 0.16 |
clpC1 | 4039649 | c.1056G>C | synonymous_variant | 0.16 |
clpC1 | 4039652 | c.1053G>C | synonymous_variant | 0.17 |
clpC1 | 4039661 | c.1044T>C | synonymous_variant | 0.18 |
clpC1 | 4039670 | c.1035G>C | synonymous_variant | 0.15 |
clpC1 | 4039682 | c.1023C>G | synonymous_variant | 0.16 |
clpC1 | 4039691 | c.1014G>C | synonymous_variant | 0.16 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.16 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.17 |
clpC1 | 4039733 | c.972G>C | synonymous_variant | 0.17 |
clpC1 | 4039748 | c.957G>C | synonymous_variant | 0.15 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.16 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.14 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 0.13 |
embC | 4241168 | c.1306C>T | synonymous_variant | 0.14 |
embC | 4241179 | c.1317G>C | synonymous_variant | 0.15 |
embC | 4241195 | p.Ser445Ala | missense_variant | 0.15 |
embC | 4241602 | p.Met580Ile | missense_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |