Run ID: SRR13861386
Sample name:
Date: 03-04-2023 09:30:25
Number of reads: 506920
Percentage reads mapped: 16.91
Strain: lineage4.9
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.99 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472307 | n.462C>T | non_coding_transcript_exon_variant | 0.2 | streptomycin |
katG | 2154411 | c.1700delT | frameshift_variant | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7585 | p.Ser95Thr | missense_variant | 0.14 |
gyrA | 7676 | c.375G>C | synonymous_variant | 0.13 |
gyrA | 7683 | c.382A>C | synonymous_variant | 0.2 |
gyrA | 7694 | c.393A>G | synonymous_variant | 0.19 |
gyrA | 7697 | c.396C>G | synonymous_variant | 0.19 |
gyrA | 7710 | c.409T>C | synonymous_variant | 0.13 |
gyrA | 7760 | c.459C>T | synonymous_variant | 0.14 |
gyrA | 7763 | c.462T>C | synonymous_variant | 0.15 |
gyrA | 7799 | c.498A>G | synonymous_variant | 0.17 |
gyrA | 7949 | c.648G>T | synonymous_variant | 1.0 |
gyrA | 8123 | p.Leu274Phe | missense_variant | 0.9 |
gyrA | 8198 | c.897T>C | synonymous_variant | 0.14 |
gyrA | 8204 | c.903C>T | synonymous_variant | 0.14 |
gyrA | 8207 | c.906T>C | synonymous_variant | 0.16 |
gyrA | 8216 | c.915G>A | synonymous_variant | 0.18 |
gyrA | 8219 | c.918T>C | synonymous_variant | 0.16 |
gyrA | 8225 | c.924T>C | synonymous_variant | 0.16 |
gyrA | 8253 | p.Ile318Leu | missense_variant | 0.2 |
gyrA | 8264 | c.963T>C | synonymous_variant | 0.21 |
gyrA | 8267 | c.966G>C | synonymous_variant | 0.21 |
gyrA | 8270 | c.969G>C | synonymous_variant | 0.21 |
gyrA | 8283 | p.Ile328Leu | missense_variant | 0.19 |
gyrA | 8288 | c.987T>C | synonymous_variant | 0.19 |
gyrA | 8294 | c.993T>C | synonymous_variant | 0.33 |
gyrA | 8324 | c.1023T>C | synonymous_variant | 0.22 |
gyrA | 8339 | c.1038A>G | synonymous_variant | 0.16 |
gyrA | 8342 | c.1041G>C | synonymous_variant | 0.17 |
gyrA | 8366 | c.1065G>C | synonymous_variant | 0.22 |
gyrA | 8375 | c.1074G>C | synonymous_variant | 0.22 |
gyrA | 8391 | p.Tyr364His | missense_variant | 0.29 |
gyrA | 8399 | c.1098T>C | synonymous_variant | 0.29 |
gyrA | 8420 | c.1119T>C | synonymous_variant | 0.26 |
gyrA | 8423 | c.1122G>C | synonymous_variant | 0.31 |
gyrA | 8442 | c.1141C>T | synonymous_variant | 0.16 |
gyrA | 8453 | c.1152A>C | synonymous_variant | 0.16 |
gyrA | 8462 | c.1161A>G | synonymous_variant | 0.15 |
gyrA | 8471 | c.1170T>C | synonymous_variant | 0.15 |
gyrA | 8480 | c.1179C>T | synonymous_variant | 0.15 |
gyrA | 8486 | c.1185T>C | synonymous_variant | 0.14 |
gyrA | 8489 | c.1188A>G | synonymous_variant | 0.15 |
gyrA | 8498 | c.1197C>T | synonymous_variant | 0.15 |
gyrA | 8796 | p.Ile499Val | missense_variant | 0.15 |
gyrA | 8801 | c.1500G>C | synonymous_variant | 0.17 |
gyrA | 8810 | c.1509A>C | synonymous_variant | 0.15 |
gyrA | 8816 | c.1515C>T | synonymous_variant | 0.14 |
gyrA | 8837 | c.1536C>T | synonymous_variant | 0.14 |
gyrA | 8858 | c.1557T>C | synonymous_variant | 0.16 |
gyrA | 8915 | c.1614A>G | synonymous_variant | 0.13 |
gyrA | 9626 | c.2325T>C | synonymous_variant | 0.13 |
gyrA | 9629 | c.2328C>G | synonymous_variant | 0.13 |
gyrA | 9630 | p.Val777Ile | missense_variant | 0.13 |
gyrA | 9635 | c.2334T>C | synonymous_variant | 0.13 |
gyrA | 9647 | c.2346C>T | synonymous_variant | 0.12 |
gyrA | 9768 | p.Gly823Cys | missense_variant | 1.0 |
fgd1 | 491166 | c.384G>C | synonymous_variant | 0.2 |
fgd1 | 491181 | c.399T>C | synonymous_variant | 0.18 |
fgd1 | 491191 | p.Gly137Arg | missense_variant | 0.2 |
fgd1 | 491194 | c.412_414delCTAinsTTG | synonymous_variant | 0.18 |
fgd1 | 491202 | c.420G>C | synonymous_variant | 0.18 |
fgd1 | 491203 | p.Gln141Glu | missense_variant | 0.17 |
fgd1 | 491212 | p.Ser144Arg | missense_variant | 0.17 |
fgd1 | 491217 | c.435T>C | synonymous_variant | 0.17 |
fgd1 | 491232 | c.450T>C | synonymous_variant | 0.17 |
fgd1 | 491241 | p.Asp153Glu | missense_variant | 0.18 |
fgd1 | 491244 | c.462T>C | synonymous_variant | 0.18 |
fgd1 | 491259 | c.477T>C | synonymous_variant | 0.15 |
fgd1 | 491286 | c.504G>C | synonymous_variant | 0.13 |
fgd1 | 491292 | c.510G>C | synonymous_variant | 0.13 |
fgd1 | 491295 | c.513C>G | synonymous_variant | 0.13 |
fgd1 | 491296 | p.Val172Ile | missense_variant | 0.13 |
mshA | 575587 | c.240C>A | synonymous_variant | 0.13 |
mshA | 575590 | c.243T>C | synonymous_variant | 0.12 |
mshA | 575623 | c.276C>G | synonymous_variant | 0.19 |
mshA | 575629 | c.282A>C | synonymous_variant | 0.2 |
mshA | 575635 | c.288A>C | synonymous_variant | 0.16 |
mshA | 575638 | c.291T>C | synonymous_variant | 0.17 |
mshA | 575641 | c.294A>G | synonymous_variant | 0.17 |
mshA | 575648 | p.Val101Gln | missense_variant | 0.16 |
mshA | 575659 | c.312A>G | synonymous_variant | 0.19 |
mshA | 575665 | c.318G>C | synonymous_variant | 0.2 |
mshA | 575689 | c.342G>C | synonymous_variant | 0.16 |
mshA | 575695 | c.348C>G | synonymous_variant | 0.17 |
mshA | 575704 | c.357T>C | synonymous_variant | 0.18 |
mshA | 575705 | c.358T>C | synonymous_variant | 0.18 |
mshA | 575713 | c.366G>A | synonymous_variant | 0.19 |
mshA | 575719 | c.372C>T | synonymous_variant | 0.18 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.13 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.13 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 0.14 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.13 |
rpoB | 761094 | c.1288C>T | synonymous_variant | 0.21 |
rpoB | 761097 | c.1291_1292delAGinsTC | synonymous_variant | 0.14 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.19 |
rpoB | 761133 | c.1327_1329delTTGinsCTC | synonymous_variant | 0.19 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.21 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.19 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.19 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.23 |
rpoB | 761183 | c.1377T>G | synonymous_variant | 0.14 |
rpoB | 761222 | c.1416G>C | synonymous_variant | 0.22 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.15 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.15 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.13 |
rpoB | 761954 | c.2148C>G | synonymous_variant | 0.15 |
rpoB | 761999 | c.2193G>C | synonymous_variant | 0.15 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.13 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.13 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.13 |
rpoB | 762218 | c.2412T>G | synonymous_variant | 0.19 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.19 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.19 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.2 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.19 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.16 |
rpoB | 762329 | c.2523G>C | synonymous_variant | 0.17 |
rpoB | 762338 | c.2532T>C | synonymous_variant | 0.17 |
rpoC | 762374 | c.-996G>C | upstream_gene_variant | 0.13 |
rpoC | 762380 | c.-990T>G | upstream_gene_variant | 0.12 |
rpoC | 762443 | c.-927G>C | upstream_gene_variant | 0.14 |
rpoC | 762470 | c.-900G>C | upstream_gene_variant | 0.15 |
rpoB | 762489 | p.Val895Gln | missense_variant | 0.15 |
rpoC | 762509 | c.-861T>A | upstream_gene_variant | 0.16 |
rpoB | 762510 | p.Ala902Pro | missense_variant | 0.16 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.12 |
rpoC | 763734 | p.Pro122Leu | missense_variant | 0.94 |
rpoC | 763858 | c.489A>G | synonymous_variant | 0.17 |
rpoC | 763872 | p.Gly168Ala | missense_variant | 0.17 |
rpoC | 763876 | p.Glu169Asp | missense_variant | 0.15 |
rpoC | 763879 | c.510A>G | synonymous_variant | 0.16 |
rpoC | 763888 | c.519G>C | synonymous_variant | 0.13 |
rpoC | 763891 | c.522G>C | synonymous_variant | 0.13 |
rpoC | 763894 | c.525A>G | synonymous_variant | 0.13 |
rpoC | 763933 | c.564C>T | synonymous_variant | 0.21 |
rpoC | 763945 | c.576T>C | synonymous_variant | 0.18 |
rpoC | 763978 | c.609C>G | synonymous_variant | 0.14 |
rpoC | 763996 | c.627T>C | synonymous_variant | 0.14 |
rpoC | 764059 | c.690G>C | synonymous_variant | 0.14 |
rpoC | 764131 | c.762T>C | synonymous_variant | 0.2 |
rpoC | 764161 | c.792G>C | synonymous_variant | 0.22 |
rpoC | 764188 | c.819A>G | synonymous_variant | 0.21 |
rpoC | 764195 | p.Ser276Gln | missense_variant | 0.17 |
rpoC | 764203 | c.834G>T | synonymous_variant | 0.17 |
rpoC | 764206 | c.837T>C | synonymous_variant | 0.17 |
rpoC | 764257 | c.888G>C | synonymous_variant | 0.23 |
rpoC | 764266 | c.897T>C | synonymous_variant | 0.21 |
rpoC | 764269 | c.900G>C | synonymous_variant | 0.21 |
rpoC | 764278 | c.909A>G | synonymous_variant | 0.15 |
rpoC | 764282 | c.913_915delTCGinsAGC | synonymous_variant | 0.15 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.13 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 0.19 |
rpoC | 764401 | c.1032C>T | synonymous_variant | 0.18 |
rpoC | 764404 | c.1035C>T | synonymous_variant | 0.18 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.24 |
rpoC | 764419 | c.1050C>T | synonymous_variant | 0.16 |
rpoC | 764428 | c.1059G>T | synonymous_variant | 0.15 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.2 |
rpoC | 764435 | c.1066_1068delAGGinsCGC | synonymous_variant | 0.15 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.2 |
rpoC | 764451 | p.Gly361Ala | missense_variant | 0.15 |
rpoC | 764461 | p.Glu364Asp | missense_variant | 0.17 |
rpoC | 764471 | p.Asn368Arg | missense_variant | 0.14 |
rpoC | 764479 | c.1110G>A | synonymous_variant | 0.14 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 0.14 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.15 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.13 |
rpoC | 764513 | p.Phe382Leu | missense_variant | 0.13 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.21 |
rpoC | 765249 | p.Leu627Ser | missense_variant | 0.14 |
rpoC | 765250 | c.1882_1884delAGC | conservative_inframe_deletion | 0.15 |
rpoC | 765287 | c.1918C>T | synonymous_variant | 0.14 |
rpoC | 765292 | c.1923G>T | synonymous_variant | 0.14 |
rpoC | 765298 | c.1929G>C | synonymous_variant | 0.14 |
rpoC | 765300 | p.Val644Ala | missense_variant | 0.14 |
rpoC | 765319 | c.1950A>G | synonymous_variant | 0.17 |
rpoC | 765326 | p.His653Ala | missense_variant | 0.15 |
rpoC | 765330 | p.Ser654Asn | missense_variant | 0.15 |
rpoC | 765349 | c.1980T>C | synonymous_variant | 0.18 |
rpoC | 765404 | p.Leu679Val | missense_variant | 0.12 |
rpoC | 765412 | c.2043T>C | synonymous_variant | 0.13 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.17 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.13 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.17 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.18 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.16 |
rpoC | 765559 | c.2190G>C | synonymous_variant | 0.16 |
rpoC | 765578 | c.2209C>T | synonymous_variant | 0.18 |
rpoC | 765583 | c.2214G>T | synonymous_variant | 0.18 |
rpoC | 765613 | p.His748Gln | missense_variant | 0.19 |
rpoC | 765625 | c.2256C>G | synonymous_variant | 0.14 |
rpoC | 765628 | c.2259G>C | synonymous_variant | 0.14 |
rpoC | 765631 | p.Asp754Glu | missense_variant | 0.14 |
rpoC | 765658 | c.2289C>T | synonymous_variant | 0.18 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.15 |
rpoC | 765734 | c.2365T>C | synonymous_variant | 0.18 |
rpoC | 765739 | c.2370G>C | synonymous_variant | 0.18 |
rpoC | 765751 | c.2382C>G | synonymous_variant | 0.2 |
rpoC | 765753 | p.Asp795Ala | missense_variant | 0.2 |
rpoC | 765772 | c.2403C>G | synonymous_variant | 0.18 |
rpoC | 765784 | c.2415C>G | synonymous_variant | 0.23 |
rpoC | 765796 | c.2427C>T | synonymous_variant | 0.17 |
rpoC | 765814 | c.2445A>G | synonymous_variant | 0.13 |
rpoC | 766327 | c.2958C>G | synonymous_variant | 0.12 |
rpoC | 766345 | c.2976T>C | synonymous_variant | 0.13 |
rpoC | 766363 | c.2994G>C | synonymous_variant | 0.13 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.17 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.16 |
rpoC | 766390 | c.3021C>T | synonymous_variant | 0.17 |
rpoC | 766408 | c.3039C>T | synonymous_variant | 0.17 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.21 |
rpoC | 766447 | c.3078T>C | synonymous_variant | 0.18 |
rpoC | 766484 | p.Val1039Ile | missense_variant | 0.13 |
rpoC | 766495 | c.3126C>T | synonymous_variant | 0.13 |
rpoC | 766522 | c.3153C>G | synonymous_variant | 0.12 |
rpoC | 766549 | c.3180G>C | synonymous_variant | 0.15 |
rpoC | 766573 | c.3204T>C | synonymous_variant | 0.18 |
rpoC | 766583 | p.Gly1072Ser | missense_variant | 0.17 |
rpoC | 766588 | c.3219G>A | synonymous_variant | 0.15 |
rpoC | 766594 | c.3225G>C | synonymous_variant | 0.14 |
rpoC | 766607 | p.Ile1080Leu | missense_variant | 0.18 |
rpoC | 766630 | c.3261G>C | synonymous_variant | 0.25 |
rpoC | 766645 | c.3276A>G | synonymous_variant | 0.29 |
rpoC | 766651 | c.3282T>C | synonymous_variant | 0.22 |
rpoC | 766657 | c.3288A>G | synonymous_variant | 0.17 |
rpoC | 766672 | c.3303T>C | synonymous_variant | 0.15 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.12 |
rpoC | 766738 | c.3369G>T | synonymous_variant | 0.19 |
rpoC | 766750 | c.3381C>G | synonymous_variant | 0.19 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.17 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.16 |
rpoC | 766801 | c.3432C>A | synonymous_variant | 0.2 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.22 |
rpoC | 766843 | c.3474T>C | synonymous_variant | 0.19 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 0.15 |
rpoC | 766864 | c.3495G>C | synonymous_variant | 0.15 |
mmpL5 | 775832 | p.Ala883Ser | missense_variant | 0.18 |
mmpL5 | 775847 | c.2634G>C | synonymous_variant | 0.19 |
mmpL5 | 775851 | p.Ser877Thr | missense_variant | 0.18 |
mmpL5 | 775856 | c.2625T>C | synonymous_variant | 0.18 |
mmpL5 | 775864 | p.Ala873Ser | missense_variant | 0.19 |
mmpL5 | 775865 | c.2616T>G | synonymous_variant | 0.19 |
mmpL5 | 775883 | p.Ile866Leu | missense_variant | 0.23 |
mmpL5 | 775886 | c.2595A>C | synonymous_variant | 0.27 |
mmpL5 | 775898 | c.2583G>A | synonymous_variant | 0.21 |
mmpL5 | 775901 | c.2580G>A | synonymous_variant | 0.2 |
mmpL5 | 775904 | c.2577G>A | synonymous_variant | 0.19 |
mmpL5 | 775909 | p.Leu858Phe | missense_variant | 0.19 |
mmpL5 | 775912 | c.2569C>A | synonymous_variant | 0.19 |
mmpL5 | 775916 | c.2565T>G | synonymous_variant | 0.18 |
mmpL5 | 775937 | c.2544G>C | synonymous_variant | 0.18 |
mmpL5 | 775966 | p.Ala839Ser | missense_variant | 0.22 |
mmpL5 | 775970 | c.2511G>C | synonymous_variant | 0.16 |
rpsL | 781631 | c.72G>C | synonymous_variant | 0.17 |
rpsL | 781649 | c.90T>C | synonymous_variant | 0.2 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.2 |
rpsL | 781682 | c.123T>C | synonymous_variant | 0.15 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.17 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.17 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.18 |
rpsL | 781751 | c.192G>C | synonymous_variant | 0.19 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.19 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.19 |
rpsL | 781793 | c.234G>C | synonymous_variant | 0.18 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.16 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.16 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.17 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.18 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.18 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.17 |
rpsL | 781916 | c.357T>C | synonymous_variant | 0.17 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.18 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.19 |
rplC | 800648 | c.-161A>C | upstream_gene_variant | 0.24 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.24 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.21 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.2 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.21 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.17 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.17 |
rplC | 800738 | c.-71T>C | upstream_gene_variant | 0.15 |
rplC | 800747 | c.-62C>G | upstream_gene_variant | 0.17 |
rplC | 800817 | c.9A>T | synonymous_variant | 0.21 |
rplC | 800844 | c.36T>C | synonymous_variant | 0.27 |
rplC | 800865 | c.57A>G | synonymous_variant | 0.24 |
rplC | 800867 | p.Ser20Asn | missense_variant | 0.24 |
rplC | 800874 | c.66A>G | synonymous_variant | 0.24 |
rplC | 800877 | c.69A>C | synonymous_variant | 0.24 |
rplC | 800880 | c.72A>G | synonymous_variant | 0.24 |
rplC | 800889 | c.81C>G | synonymous_variant | 0.24 |
rplC | 800907 | c.99C>G | synonymous_variant | 0.27 |
rplC | 800916 | c.108A>G | synonymous_variant | 0.31 |
rplC | 800937 | c.129A>G | synonymous_variant | 0.18 |
rplC | 800939 | p.Arg44Gln | missense_variant | 0.18 |
rplC | 800946 | c.138T>C | synonymous_variant | 0.17 |
rplC | 800949 | c.141T>C | synonymous_variant | 0.16 |
rplC | 800955 | c.147C>G | synonymous_variant | 0.14 |
fbiC | 1303995 | c.1065C>T | synonymous_variant | 0.14 |
fbiC | 1304001 | c.1071C>G | synonymous_variant | 0.17 |
fbiC | 1304008 | c.1078T>C | synonymous_variant | 0.15 |
fbiC | 1304049 | c.1119T>G | synonymous_variant | 0.13 |
fbiC | 1304058 | c.1128G>A | synonymous_variant | 0.2 |
fbiC | 1304059 | c.1129C>T | synonymous_variant | 0.13 |
fbiC | 1304634 | c.1704C>G | synonymous_variant | 0.12 |
fbiC | 1304640 | c.1710A>C | synonymous_variant | 0.13 |
fbiC | 1304691 | c.1761G>C | synonymous_variant | 0.15 |
fbiC | 1304703 | c.1773C>G | synonymous_variant | 0.21 |
fbiC | 1304715 | c.1785G>C | synonymous_variant | 0.27 |
fbiC | 1304724 | c.1794A>G | synonymous_variant | 0.25 |
fbiC | 1304727 | c.1797A>G | synonymous_variant | 0.22 |
fbiC | 1304742 | c.1812T>C | synonymous_variant | 0.21 |
fbiC | 1304748 | c.1818T>C | synonymous_variant | 0.21 |
fbiC | 1304754 | c.1824G>A | synonymous_variant | 0.2 |
fbiC | 1304757 | c.1827A>G | synonymous_variant | 0.2 |
fbiC | 1304784 | c.1854T>C | synonymous_variant | 0.2 |
fbiC | 1304787 | c.1857T>C | synonymous_variant | 0.21 |
fbiC | 1304790 | c.1860C>G | synonymous_variant | 0.2 |
fbiC | 1304808 | c.1878C>G | synonymous_variant | 0.19 |
fbiC | 1304811 | c.1881C>G | synonymous_variant | 0.19 |
fbiC | 1304817 | c.1887T>C | synonymous_variant | 0.19 |
fbiC | 1304829 | c.1899T>C | synonymous_variant | 0.16 |
fbiC | 1304832 | c.1902C>G | synonymous_variant | 0.2 |
fbiC | 1304853 | c.1923C>G | synonymous_variant | 0.17 |
fbiC | 1304856 | c.1926C>G | synonymous_variant | 0.17 |
fbiC | 1304872 | c.1942_1944delAGCinsTCG | synonymous_variant | 0.16 |
fbiC | 1304877 | c.1947T>C | synonymous_variant | 0.16 |
fbiC | 1304878 | c.1948_1950delCGCinsAGG | synonymous_variant | 0.16 |
fbiC | 1304893 | p.Gly655Ser | missense_variant | 0.17 |
fbiC | 1304940 | c.2010A>G | synonymous_variant | 0.14 |
fbiC | 1304958 | c.2028T>G | synonymous_variant | 0.14 |
atpE | 1461150 | p.Ile36Val | missense_variant | 0.19 |
atpE | 1461194 | c.150C>T | synonymous_variant | 0.13 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472936 | n.1091C>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472958 | n.1113A>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472959 | n.1114T>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472963 | n.1118G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472971 | n.1126G>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472982 | n.1137G>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472987 | n.1142G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472988 | n.1143T>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473002 | n.1157G>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473004 | n.1159T>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473008 | n.1163C>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473009 | n.1164T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473044 | n.1199C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473813 | n.156C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473839 | n.182G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473899 | n.242A>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473945 | n.288T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475638 | n.1981C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475659 | n.2002G>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476025 | n.2368G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476033 | n.2376T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476034 | n.2377C>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476089 | n.2432T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476117 | n.2460G>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476512 | n.2855C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476640 | n.2983C>A | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476725 | n.3068C>T | non_coding_transcript_exon_variant | 0.12 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.16 |
rpsA | 1834375 | c.834G>A | synonymous_variant | 0.15 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.17 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.17 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.21 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.21 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.23 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.17 |
rpsA | 1834465 | c.924T>C | synonymous_variant | 0.22 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.22 |
rpsA | 1834474 | c.933C>G | synonymous_variant | 0.23 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.26 |
rpsA | 1834498 | c.957C>T | synonymous_variant | 0.25 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.21 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.21 |
rpsA | 1834555 | c.1014T>C | synonymous_variant | 0.22 |
rpsA | 1834558 | c.1017C>G | synonymous_variant | 0.21 |
rpsA | 1834606 | c.1065C>G | synonymous_variant | 0.29 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.27 |
rpsA | 1834622 | c.1081_1083delTCGinsAGC | synonymous_variant | 0.25 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.21 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.21 |
rpsA | 1834666 | c.1125G>C | synonymous_variant | 0.17 |
rpsA | 1834669 | c.1128G>C | synonymous_variant | 0.15 |
rpsA | 1834688 | c.1147_1149delAGTinsTCC | synonymous_variant | 0.18 |
rpsA | 1834732 | c.1191T>C | synonymous_variant | 0.2 |
rpsA | 1834733 | p.Ala398Pro | missense_variant | 0.2 |
rpsA | 1834753 | c.1212T>C | synonymous_variant | 0.2 |
tlyA | 1918034 | p.Val32Ala | missense_variant | 1.0 |
katG | 2155918 | p.Ala65Val | missense_variant | 1.0 |
PPE35 | 2168767 | p.Ser616Gly | missense_variant | 1.0 |
Rv1979c | 2222377 | p.Val263Gly | missense_variant | 1.0 |
kasA | 2517947 | c.-168C>T | upstream_gene_variant | 0.24 |
kasA | 2517974 | c.-141T>C | upstream_gene_variant | 0.18 |
kasA | 2517989 | c.-126T>C | upstream_gene_variant | 0.17 |
kasA | 2517992 | c.-123C>G | upstream_gene_variant | 0.17 |
kasA | 2517998 | c.-117C>T | upstream_gene_variant | 0.17 |
kasA | 2518019 | c.-96A>G | upstream_gene_variant | 0.17 |
kasA | 2518025 | c.-90G>C | upstream_gene_variant | 0.22 |
folC | 2747355 | p.Val82Ile | missense_variant | 0.14 |
folC | 2747359 | c.240C>G | synonymous_variant | 0.14 |
folC | 2747362 | c.237G>C | synonymous_variant | 0.14 |
ribD | 2986993 | p.Gly52Val | missense_variant | 1.0 |
Rv2752c | 3065787 | c.405G>C | synonymous_variant | 1.0 |
thyA | 3074001 | c.471C>G | synonymous_variant | 0.14 |
thyA | 3074010 | c.462C>G | synonymous_variant | 0.18 |
thyA | 3074031 | c.441T>C | synonymous_variant | 0.18 |
thyA | 3074037 | c.435C>G | synonymous_variant | 0.18 |
thyA | 3074056 | p.Glu139Pro | missense_variant | 0.19 |
thyA | 3074061 | c.411A>G | synonymous_variant | 0.19 |
thyA | 3074076 | c.396C>G | synonymous_variant | 0.18 |
thyA | 3074097 | c.375C>G | synonymous_variant | 0.18 |
thyA | 3074100 | c.372T>C | synonymous_variant | 0.18 |
thyA | 3074106 | c.366T>C | synonymous_variant | 0.17 |
thyA | 3074117 | c.355C>T | synonymous_variant | 0.17 |
thyA | 3074120 | c.352T>C | synonymous_variant | 0.17 |
thyA | 3074130 | c.342G>C | synonymous_variant | 0.16 |
Rv3083 | 3448649 | p.Arg49Pro | missense_variant | 1.0 |
fprA | 3473812 | c.-195G>A | upstream_gene_variant | 0.12 |
Rv3236c | 3613067 | p.Val17Gly | missense_variant | 1.0 |
Rv3236c | 3613315 | c.-199T>G | upstream_gene_variant | 1.0 |
fbiA | 3640435 | c.-108A>C | upstream_gene_variant | 1.0 |
fbiB | 3642614 | c.1080C>T | synonymous_variant | 0.2 |
fbiB | 3642620 | c.1086T>C | synonymous_variant | 0.19 |
fbiB | 3642656 | c.1122G>C | synonymous_variant | 0.2 |
fbiB | 3642659 | c.1125C>G | synonymous_variant | 0.17 |
fbiB | 3642662 | c.1128C>G | synonymous_variant | 0.18 |
fbiB | 3642668 | c.1134A>C | synonymous_variant | 0.25 |
fbiB | 3642677 | c.1143A>G | synonymous_variant | 0.13 |
fbiB | 3642696 | c.1162C>T | synonymous_variant | 0.13 |
fbiB | 3642734 | c.1200G>C | synonymous_variant | 0.14 |
fbiB | 3642743 | c.1209T>C | synonymous_variant | 0.14 |
clpC1 | 4038308 | p.Val799Ile | missense_variant | 0.14 |
clpC1 | 4038317 | c.2388G>C | synonymous_variant | 0.18 |
clpC1 | 4038398 | c.2307G>T | synonymous_variant | 0.12 |
clpC1 | 4038740 | c.1965G>C | synonymous_variant | 0.14 |
clpC1 | 4038748 | p.Arg653Cys | missense_variant | 0.14 |
clpC1 | 4038851 | c.1854G>A | synonymous_variant | 0.19 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.14 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.14 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 0.14 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.15 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.14 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.16 |
clpC1 | 4039553 | c.1152C>G | synonymous_variant | 0.12 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.2 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.2 |
clpC1 | 4039622 | c.1083C>G | synonymous_variant | 0.19 |
clpC1 | 4039682 | c.1023C>G | synonymous_variant | 0.14 |
clpC1 | 4039685 | c.1020C>T | synonymous_variant | 0.14 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.14 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.14 |
clpC1 | 4039748 | c.957G>C | synonymous_variant | 0.17 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.15 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.15 |
clpC1 | 4039842 | c.862_863insT | frameshift_variant | 0.91 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.2 |
clpC1 | 4039928 | c.775_777delAGCinsTCG | synonymous_variant | 0.17 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.18 |
clpC1 | 4039946 | c.759A>T | synonymous_variant | 0.18 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.19 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.19 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.18 |
clpC1 | 4039996 | p.Glu237Gln | missense_variant | 0.19 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.21 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.21 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.17 |
clpC1 | 4040036 | c.669C>G | synonymous_variant | 0.17 |
clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 0.17 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.18 |
clpC1 | 4040105 | c.600C>G | synonymous_variant | 0.16 |
clpC1 | 4040153 | c.552A>G | synonymous_variant | 0.16 |
clpC1 | 4040201 | c.504C>G | synonymous_variant | 0.18 |
clpC1 | 4040207 | c.498T>C | synonymous_variant | 0.12 |
clpC1 | 4040215 | p.Ser164Thr | missense_variant | 0.12 |
clpC1 | 4040225 | c.480A>C | synonymous_variant | 0.14 |
clpC1 | 4040228 | c.477G>C | synonymous_variant | 0.14 |
clpC1 | 4040234 | c.471C>G | synonymous_variant | 0.13 |
clpC1 | 4040237 | c.468C>T | synonymous_variant | 0.12 |
clpC1 | 4040249 | c.456A>G | synonymous_variant | 0.18 |
clpC1 | 4040273 | c.432T>C | synonymous_variant | 0.21 |
clpC1 | 4040354 | c.351A>G | synonymous_variant | 0.25 |
clpC1 | 4040363 | c.342A>C | synonymous_variant | 0.27 |
clpC1 | 4040369 | c.336C>G | synonymous_variant | 0.25 |
clpC1 | 4040380 | c.325T>C | synonymous_variant | 0.21 |
clpC1 | 4040381 | c.324T>C | synonymous_variant | 0.21 |
clpC1 | 4040387 | c.318A>G | synonymous_variant | 0.25 |
clpC1 | 4040393 | c.312G>C | synonymous_variant | 0.17 |
clpC1 | 4040411 | c.294T>C | synonymous_variant | 0.25 |
clpC1 | 4040423 | c.282A>G | synonymous_variant | 0.23 |
clpC1 | 4040426 | c.279T>C | synonymous_variant | 0.23 |
clpC1 | 4040431 | c.274T>C | synonymous_variant | 0.21 |
clpC1 | 4040441 | c.264C>G | synonymous_variant | 0.18 |
clpC1 | 4040444 | c.261C>G | synonymous_variant | 0.18 |
panD | 4044103 | p.Ile60Ser | missense_variant | 1.0 |
embA | 4244298 | p.Ser356Ala | missense_variant | 0.12 |
embA | 4244309 | c.1077C>G | synonymous_variant | 0.13 |
embA | 4244312 | c.1080T>G | synonymous_variant | 0.13 |
embA | 4244315 | c.1083G>C | synonymous_variant | 0.15 |
embA | 4244324 | c.1092T>G | synonymous_variant | 0.17 |
embA | 4244327 | c.1095T>C | synonymous_variant | 0.18 |
embA | 4244337 | p.Leu369Val | missense_variant | 0.17 |
embA | 4244340 | p.Ser370Ala | missense_variant | 0.17 |
embA | 4244366 | c.1134C>G | synonymous_variant | 0.2 |
embA | 4244372 | c.1140T>G | synonymous_variant | 0.17 |
embA | 4244378 | c.1146G>A | synonymous_variant | 0.17 |
embA | 4245031 | p.Arg600Gln | missense_variant | 1.0 |
embB | 4247773 | c.1260G>A | synonymous_variant | 0.15 |
embB | 4247776 | c.1263G>T | synonymous_variant | 0.13 |
embB | 4247779 | c.1266C>G | synonymous_variant | 0.13 |
embB | 4247819 | p.Val436Ile | missense_variant | 0.12 |
embB | 4247836 | c.1323A>G | synonymous_variant | 0.14 |
embB | 4247842 | c.1329T>C | synonymous_variant | 0.14 |
embB | 4247876 | c.1363C>T | synonymous_variant | 0.17 |
embB | 4247986 | c.1473C>G | synonymous_variant | 0.17 |
embB | 4248007 | c.1494C>G | synonymous_variant | 0.17 |
embB | 4248011 | p.Ser500Ala | missense_variant | 0.17 |
gid | 4408218 | c.-16G>T | upstream_gene_variant | 1.0 |