Run ID: SRR1173767
Sample name:
Date: 03-04-2023 03:31:18
Number of reads: 1366691
Percentage reads mapped: 75.06
Strain: lineage4.4.1.1
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.98 |
lineage4.4 | Euro-American | S;T | None | 0.93 |
lineage4.4.1 | Euro-American (S-type) | S;T | None | 0.92 |
lineage4.4.1.1 | Euro-American | S;Orphans | None | 0.95 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472307 | n.462C>T | non_coding_transcript_exon_variant | 0.4 | streptomycin |
katG | 2155108 | p.Ile335Thr | missense_variant | 0.16 | isoniazid |
katG | 2155810 | c.300_301delGC | frameshift_variant | 0.25 | isoniazid |
katG | 2155815 | c.296_297insTG | frameshift_variant | 0.25 | isoniazid |
embB | 4247708 | p.Asn399Asp | missense_variant | 0.15 | ethambutol |
gid | 4408087 | c.115delC | frameshift_variant | 1.0 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5815 | c.576C>G | synonymous_variant | 0.17 |
gyrB | 5824 | c.585A>G | synonymous_variant | 0.16 |
gyrB | 5827 | c.588G>A | synonymous_variant | 0.16 |
gyrB | 6115 | c.876A>G | synonymous_variant | 0.19 |
gyrB | 6123 | p.Ala295Gly | missense_variant | 0.19 |
gyrB | 6127 | c.888G>C | synonymous_variant | 0.21 |
gyrB | 6133 | c.894G>C | synonymous_variant | 0.19 |
gyrB | 6136 | c.897G>A | synonymous_variant | 0.19 |
gyrB | 6148 | c.909C>G | synonymous_variant | 0.19 |
gyrB | 6169 | c.930C>G | synonymous_variant | 0.24 |
gyrB | 6190 | c.951A>G | synonymous_variant | 0.27 |
gyrB | 6209 | c.970C>T | synonymous_variant | 0.23 |
gyrB | 6214 | c.975G>C | synonymous_variant | 0.22 |
gyrB | 6217 | c.978G>C | synonymous_variant | 0.21 |
gyrB | 6223 | c.984G>C | synonymous_variant | 0.19 |
gyrB | 6242 | p.Arg335Lys | missense_variant | 0.23 |
gyrB | 6250 | c.1011A>G | synonymous_variant | 0.22 |
gyrB | 6253 | c.1014G>C | synonymous_variant | 0.23 |
gyrB | 6280 | c.1041T>C | synonymous_variant | 0.29 |
gyrB | 6286 | c.1047T>C | synonymous_variant | 0.26 |
gyrB | 6292 | c.1053G>C | synonymous_variant | 0.22 |
gyrB | 6295 | c.1056A>G | synonymous_variant | 0.2 |
gyrB | 6298 | c.1059C>T | synonymous_variant | 0.21 |
gyrB | 6299 | c.1060C>T | synonymous_variant | 0.21 |
gyrA | 6307 | c.-995T>G | upstream_gene_variant | 0.26 |
gyrA | 6319 | c.-983G>C | upstream_gene_variant | 0.3 |
gyrA | 6325 | c.-977C>G | upstream_gene_variant | 0.35 |
gyrA | 6361 | c.-941G>A | upstream_gene_variant | 0.32 |
gyrA | 6362 | c.-940T>C | upstream_gene_variant | 0.3 |
gyrA | 6379 | c.-923C>G | upstream_gene_variant | 0.32 |
gyrA | 6382 | c.-920A>G | upstream_gene_variant | 0.32 |
gyrA | 6388 | c.-914T>C | upstream_gene_variant | 0.3 |
gyrA | 6400 | c.-902C>G | upstream_gene_variant | 0.24 |
gyrA | 6403 | c.-899T>C | upstream_gene_variant | 0.23 |
gyrA | 6415 | c.-887G>C | upstream_gene_variant | 0.15 |
gyrA | 6670 | c.-632G>C | upstream_gene_variant | 0.18 |
gyrA | 6673 | c.-629A>C | upstream_gene_variant | 0.18 |
gyrA | 6745 | c.-557T>G | upstream_gene_variant | 0.14 |
gyrA | 6778 | c.-524C>T | upstream_gene_variant | 0.15 |
gyrA | 6793 | c.-509T>C | upstream_gene_variant | 0.2 |
gyrB | 6797 | p.Gly520Thr | missense_variant | 0.2 |
gyrA | 6824 | c.-478C>T | upstream_gene_variant | 0.29 |
gyrA | 6841 | c.-461T>C | upstream_gene_variant | 0.24 |
gyrA | 6844 | c.-458T>G | upstream_gene_variant | 0.23 |
gyrA | 6853 | c.-449A>G | upstream_gene_variant | 0.19 |
gyrA | 6856 | c.-446T>C | upstream_gene_variant | 0.2 |
gyrA | 6859 | c.-443T>C | upstream_gene_variant | 0.2 |
gyrA | 6862 | c.-440C>G | upstream_gene_variant | 0.2 |
gyrA | 6878 | c.-424T>C | upstream_gene_variant | 0.2 |
gyrA | 6881 | c.-421T>C | upstream_gene_variant | 0.17 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7427 | c.126G>C | synonymous_variant | 0.22 |
gyrA | 7442 | c.141G>C | synonymous_variant | 0.19 |
gyrA | 7472 | c.171T>C | synonymous_variant | 0.16 |
gyrA | 7480 | p.Phe60Tyr | missense_variant | 0.15 |
gyrA | 7487 | c.186C>G | synonymous_variant | 0.16 |
gyrA | 7490 | c.189C>T | synonymous_variant | 0.15 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7607 | c.306C>G | synonymous_variant | 0.15 |
gyrA | 7622 | c.321C>T | synonymous_variant | 0.2 |
gyrA | 7626 | c.325C>T | synonymous_variant | 0.21 |
gyrA | 7631 | c.330G>C | synonymous_variant | 0.19 |
gyrA | 7637 | c.336C>G | synonymous_variant | 0.17 |
gyrA | 7664 | c.363T>C | synonymous_variant | 0.17 |
gyrA | 7670 | c.369A>G | synonymous_variant | 0.17 |
gyrA | 7676 | c.375G>C | synonymous_variant | 0.17 |
gyrA | 7763 | c.462T>C | synonymous_variant | 0.17 |
gyrA | 7799 | c.498A>G | synonymous_variant | 0.15 |
gyrA | 7892 | c.591G>C | synonymous_variant | 0.15 |
gyrA | 7898 | p.Asp199Glu | missense_variant | 0.17 |
gyrA | 7919 | p.Glu206Asp | missense_variant | 0.2 |
gyrA | 7923 | p.His208Tyr | missense_variant | 0.22 |
gyrA | 7928 | p.Asp209Glu | missense_variant | 0.18 |
gyrA | 8078 | c.777A>G | synonymous_variant | 0.19 |
gyrA | 8090 | c.789C>G | synonymous_variant | 0.26 |
gyrA | 8099 | c.798T>C | synonymous_variant | 0.27 |
gyrA | 8111 | c.810G>C | synonymous_variant | 0.29 |
gyrA | 8156 | c.855T>C | synonymous_variant | 0.31 |
gyrA | 8168 | c.867A>G | synonymous_variant | 0.34 |
gyrA | 8174 | c.873C>G | synonymous_variant | 0.28 |
gyrA | 8177 | c.876A>C | synonymous_variant | 0.23 |
gyrA | 8198 | c.897T>C | synonymous_variant | 0.16 |
gyrA | 8207 | c.906T>C | synonymous_variant | 0.16 |
gyrA | 8219 | c.918T>C | synonymous_variant | 0.17 |
gyrA | 8225 | c.924T>C | synonymous_variant | 0.17 |
gyrA | 8234 | c.933T>G | synonymous_variant | 0.17 |
gyrA | 8235 | c.934_936delTTAinsCTG | synonymous_variant | 0.17 |
gyrA | 8253 | p.Ile318Leu | missense_variant | 0.18 |
gyrA | 8264 | c.963T>C | synonymous_variant | 0.22 |
gyrA | 8267 | c.966G>C | synonymous_variant | 0.18 |
gyrA | 8270 | c.969G>C | synonymous_variant | 0.18 |
gyrA | 8283 | p.Ile328Leu | missense_variant | 0.21 |
gyrA | 8288 | c.987T>C | synonymous_variant | 0.21 |
gyrA | 8294 | c.993T>C | synonymous_variant | 0.2 |
gyrA | 8324 | c.1023T>C | synonymous_variant | 0.16 |
gyrA | 8399 | c.1098T>C | synonymous_variant | 0.18 |
gyrA | 8420 | c.1119T>C | synonymous_variant | 0.2 |
gyrA | 8423 | c.1122G>C | synonymous_variant | 0.21 |
gyrA | 8442 | c.1141C>T | synonymous_variant | 0.18 |
gyrA | 8453 | c.1152A>C | synonymous_variant | 0.22 |
gyrA | 8462 | c.1161A>G | synonymous_variant | 0.21 |
gyrA | 8471 | c.1170T>C | synonymous_variant | 0.23 |
gyrA | 8480 | c.1179C>T | synonymous_variant | 0.18 |
gyrA | 8486 | c.1185T>C | synonymous_variant | 0.2 |
gyrA | 8489 | c.1188A>G | synonymous_variant | 0.2 |
gyrA | 8498 | c.1197C>T | synonymous_variant | 0.19 |
gyrA | 8504 | c.1203G>C | synonymous_variant | 0.15 |
gyrA | 8516 | c.1215T>C | synonymous_variant | 0.18 |
gyrA | 8519 | c.1218A>C | synonymous_variant | 0.15 |
gyrA | 8537 | c.1236G>A | synonymous_variant | 0.16 |
gyrA | 8672 | c.1371A>G | synonymous_variant | 0.18 |
gyrA | 8693 | c.1392T>C | synonymous_variant | 0.18 |
gyrA | 8711 | c.1410A>C | synonymous_variant | 0.19 |
gyrA | 8714 | c.1413A>G | synonymous_variant | 0.2 |
gyrA | 8732 | c.1431G>C | synonymous_variant | 0.17 |
gyrA | 8747 | c.1446A>G | synonymous_variant | 0.21 |
gyrA | 8756 | c.1455A>G | synonymous_variant | 0.21 |
gyrA | 8762 | c.1461G>C | synonymous_variant | 0.21 |
gyrA | 8765 | p.Asp488Glu | missense_variant | 0.17 |
gyrA | 8767 | p.Arg489Lys | missense_variant | 0.17 |
gyrA | 9252 | p.Val651Ile | missense_variant | 0.14 |
gyrA | 9275 | c.1974G>A | synonymous_variant | 0.18 |
gyrA | 9278 | c.1977G>C | synonymous_variant | 0.19 |
gyrA | 9281 | c.1980C>G | synonymous_variant | 0.18 |
gyrA | 9284 | c.1983T>C | synonymous_variant | 0.19 |
gyrA | 9291 | c.1990C>T | synonymous_variant | 0.18 |
gyrA | 9296 | c.1995T>C | synonymous_variant | 0.21 |
gyrA | 9304 | p.Gly668Glu | missense_variant | 1.0 |
gyrA | 9311 | c.2010C>T | synonymous_variant | 0.23 |
gyrA | 9323 | c.2022C>G | synonymous_variant | 0.24 |
gyrA | 9335 | c.2034G>C | synonymous_variant | 0.24 |
gyrA | 9345 | c.2044A>C | synonymous_variant | 0.23 |
fgd1 | 490851 | c.69A>C | synonymous_variant | 0.15 |
fgd1 | 490887 | c.105G>C | synonymous_variant | 0.21 |
fgd1 | 490902 | c.120T>C | synonymous_variant | 0.19 |
fgd1 | 490905 | c.123T>C | synonymous_variant | 0.18 |
fgd1 | 490911 | c.129T>G | synonymous_variant | 0.18 |
fgd1 | 490917 | c.135C>G | synonymous_variant | 0.16 |
fgd1 | 490921 | p.Gln47Glu | missense_variant | 0.16 |
fgd1 | 491106 | c.324T>C | synonymous_variant | 0.17 |
fgd1 | 491166 | c.384G>C | synonymous_variant | 0.18 |
fgd1 | 491181 | c.399T>C | synonymous_variant | 0.15 |
fgd1 | 491191 | p.Gly137Arg | missense_variant | 0.16 |
fgd1 | 491196 | c.414A>G | synonymous_variant | 0.17 |
fgd1 | 491202 | c.420G>C | synonymous_variant | 0.17 |
fgd1 | 491208 | c.426G>A | synonymous_variant | 0.14 |
fgd1 | 491241 | p.Asp153Glu | missense_variant | 0.18 |
fgd1 | 491244 | c.462T>C | synonymous_variant | 0.18 |
fgd1 | 491259 | c.477T>C | synonymous_variant | 0.18 |
fgd1 | 491319 | c.537G>C | synonymous_variant | 0.21 |
fgd1 | 491331 | c.549G>A | synonymous_variant | 0.17 |
fgd1 | 491388 | c.606C>G | synonymous_variant | 0.17 |
fgd1 | 491393 | p.Thr204Lys | missense_variant | 0.17 |
fgd1 | 491397 | p.Glu205Asp | missense_variant | 0.18 |
fgd1 | 491502 | c.720G>A | synonymous_variant | 0.24 |
fgd1 | 491508 | c.726A>G | synonymous_variant | 0.22 |
fgd1 | 491509 | c.727T>C | synonymous_variant | 0.22 |
fgd1 | 491512 | p.Asn244Glu | missense_variant | 0.23 |
fgd1 | 491526 | c.744T>C | synonymous_variant | 0.35 |
fgd1 | 491542 | c.760T>C | synonymous_variant | 0.39 |
fgd1 | 491547 | c.765A>C | synonymous_variant | 0.41 |
fgd1 | 491550 | c.768T>C | synonymous_variant | 0.41 |
fgd1 | 491583 | c.801G>A | synonymous_variant | 0.22 |
mshA | 575623 | c.276C>G | synonymous_variant | 0.17 |
mshA | 575695 | c.348C>G | synonymous_variant | 0.15 |
mshA | 575704 | c.357T>C | synonymous_variant | 0.17 |
mshA | 575705 | c.358T>C | synonymous_variant | 0.18 |
mshA | 575713 | c.366G>A | synonymous_variant | 0.16 |
mshA | 575719 | c.372C>T | synonymous_variant | 0.15 |
mshA | 575734 | c.387T>G | synonymous_variant | 0.25 |
mshA | 575737 | c.390T>C | synonymous_variant | 0.25 |
mshA | 575746 | c.399C>G | synonymous_variant | 0.27 |
mshA | 575767 | c.420G>A | synonymous_variant | 0.26 |
mshA | 575771 | p.Val142Ser | missense_variant | 0.24 |
mshA | 575779 | c.432A>G | synonymous_variant | 0.29 |
mshA | 575821 | c.474G>C | synonymous_variant | 0.36 |
mshA | 575824 | c.477T>G | synonymous_variant | 0.35 |
mshA | 575827 | c.480G>A | synonymous_variant | 0.3 |
mshA | 575864 | c.517T>C | synonymous_variant | 0.33 |
mshA | 575878 | c.531A>G | synonymous_variant | 0.3 |
mshA | 575884 | c.537G>C | synonymous_variant | 0.3 |
mshA | 575893 | c.546C>G | synonymous_variant | 0.25 |
ccsA | 620241 | c.351C>T | synonymous_variant | 0.71 |
ccsA | 620362 | p.Ala158Thr | missense_variant | 0.14 |
ccsA | 620367 | c.477T>C | synonymous_variant | 0.15 |
ccsA | 620373 | c.483C>G | synonymous_variant | 0.16 |
ccsA | 620385 | c.495G>C | synonymous_variant | 0.17 |
ccsA | 620388 | c.498A>G | synonymous_variant | 0.21 |
ccsA | 620412 | c.522T>C | synonymous_variant | 0.35 |
ccsA | 620415 | c.525T>C | synonymous_variant | 0.35 |
ccsA | 620433 | c.543C>G | synonymous_variant | 0.32 |
ccsA | 620436 | c.546T>C | synonymous_variant | 0.32 |
ccsA | 620439 | c.549T>C | synonymous_variant | 0.33 |
ccsA | 620445 | c.555A>G | synonymous_variant | 0.29 |
ccsA | 620460 | c.570T>C | synonymous_variant | 0.29 |
ccsA | 620461 | p.Val191Ile | missense_variant | 0.29 |
ccsA | 620481 | c.591T>G | synonymous_variant | 0.24 |
ccsA | 620482 | p.Val198Leu | missense_variant | 0.24 |
ccsA | 620490 | c.600A>C | synonymous_variant | 0.18 |
ccsA | 620495 | p.Arg202Pro | missense_variant | 0.17 |
ccsA | 620646 | c.756G>A | synonymous_variant | 0.15 |
ccsA | 620661 | c.771C>G | synonymous_variant | 0.16 |
ccsA | 620718 | c.828G>C | synonymous_variant | 0.18 |
ccsA | 620721 | c.831G>C | synonymous_variant | 0.17 |
ccsA | 620730 | c.840C>T | synonymous_variant | 0.17 |
ccsA | 620734 | c.844C>A | synonymous_variant | 0.16 |
ccsA | 620739 | c.849A>G | synonymous_variant | 0.17 |
ccsA | 620748 | c.858T>A | synonymous_variant | 0.17 |
ccsA | 620778 | c.888T>C | synonymous_variant | 0.21 |
ccsA | 620784 | c.894C>G | synonymous_variant | 0.18 |
rpoB | 760181 | c.375T>C | synonymous_variant | 0.17 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.19 |
rpoB | 760196 | c.390C>G | synonymous_variant | 0.22 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.15 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.16 |
rpoB | 760283 | c.477G>C | synonymous_variant | 0.2 |
rpoB | 760307 | c.501T>C | synonymous_variant | 0.17 |
rpoB | 760328 | c.522G>C | synonymous_variant | 0.26 |
rpoB | 760331 | c.525G>C | synonymous_variant | 0.26 |
rpoB | 760337 | c.531C>G | synonymous_variant | 0.28 |
rpoB | 760340 | c.534G>C | synonymous_variant | 0.26 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.33 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.3 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.34 |
rpoB | 760418 | c.612G>C | synonymous_variant | 0.25 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.24 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.25 |
rpoB | 760522 | p.Ser239Asn | missense_variant | 0.15 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.21 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.16 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.16 |
rpoB | 760718 | c.912C>G | synonymous_variant | 0.15 |
rpoB | 760721 | c.915C>G | synonymous_variant | 0.16 |
rpoB | 760724 | c.918T>C | synonymous_variant | 0.16 |
rpoB | 760730 | c.924T>C | synonymous_variant | 0.18 |
rpoB | 760845 | p.Thr347Pro | missense_variant | 0.2 |
rpoB | 760859 | c.1053T>C | synonymous_variant | 0.17 |
rpoB | 760862 | c.1056G>C | synonymous_variant | 0.21 |
rpoB | 760869 | p.Val355Ile | missense_variant | 0.19 |
rpoB | 760886 | c.1080A>G | synonymous_variant | 0.17 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 0.22 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.24 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.26 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.26 |
rpoB | 761051 | c.1245G>T | synonymous_variant | 0.28 |
rpoB | 761054 | c.1248G>A | synonymous_variant | 0.27 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.29 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.29 |
rpoB | 761063 | c.1257C>G | synonymous_variant | 0.27 |
rpoB | 761097 | c.1291_1292delAGinsTC | synonymous_variant | 0.33 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.34 |
rpoB | 761133 | c.1327_1329delTTGinsCTC | synonymous_variant | 0.21 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.23 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.26 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.29 |
rpoB | 761171 | c.1365C>T | synonymous_variant | 0.27 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.26 |
rpoB | 761183 | c.1377T>G | synonymous_variant | 0.25 |
rpoB | 761189 | c.1383T>G | synonymous_variant | 0.29 |
rpoB | 761222 | c.1416G>C | synonymous_variant | 0.25 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.31 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.32 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.3 |
rpoB | 761297 | c.1491C>T | synonymous_variant | 0.36 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.36 |
rpoB | 761360 | c.1554T>C | synonymous_variant | 0.21 |
rpoB | 761362 | p.Ser519Thr | missense_variant | 0.21 |
rpoB | 761373 | p.Val523His | missense_variant | 0.19 |
rpoB | 761531 | c.1725C>G | synonymous_variant | 0.24 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.24 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.26 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.27 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.25 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.25 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.24 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.19 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.22 |
rpoB | 761645 | c.1839C>G | synonymous_variant | 0.22 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.25 |
rpoB | 761657 | c.1851C>G | synonymous_variant | 0.19 |
rpoB | 761873 | c.2067A>G | synonymous_variant | 0.21 |
rpoB | 761882 | c.2076C>G | synonymous_variant | 0.22 |
rpoB | 761885 | c.2079T>C | synonymous_variant | 0.21 |
rpoB | 761891 | c.2085G>C | synonymous_variant | 0.24 |
rpoB | 761906 | c.2100C>G | synonymous_variant | 0.22 |
rpoB | 761909 | c.2103T>C | synonymous_variant | 0.23 |
rpoB | 761912 | c.2106T>C | synonymous_variant | 0.22 |
rpoB | 761915 | p.Asp703Glu | missense_variant | 0.21 |
rpoB | 761916 | p.Asp704Asn | missense_variant | 0.21 |
rpoB | 761924 | c.2118G>A | synonymous_variant | 0.28 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.31 |
rpoB | 761954 | c.2148C>G | synonymous_variant | 0.33 |
rpoB | 761969 | c.2163G>A | synonymous_variant | 0.27 |
rpoB | 761999 | c.2193G>C | synonymous_variant | 0.28 |
rpoB | 762008 | c.2202C>G | synonymous_variant | 0.3 |
rpoB | 762014 | c.2208C>T | synonymous_variant | 0.31 |
rpoB | 762017 | c.2211A>G | synonymous_variant | 0.32 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.27 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.26 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.24 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.28 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.22 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.26 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.28 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 0.33 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.32 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.35 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.35 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.48 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.48 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.41 |
rpoB | 762218 | c.2412T>G | synonymous_variant | 0.42 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.26 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.2 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.2 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.19 |
rpoC | 762395 | c.-975G>C | upstream_gene_variant | 0.24 |
rpoC | 762398 | c.-972T>C | upstream_gene_variant | 0.22 |
rpoC | 762401 | c.-969G>C | upstream_gene_variant | 0.22 |
rpoC | 762404 | c.-966T>C | upstream_gene_variant | 0.24 |
rpoC | 762410 | c.-960T>C | upstream_gene_variant | 0.29 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 0.28 |
rpoC | 762443 | c.-927G>T | upstream_gene_variant | 0.24 |
rpoC | 762470 | c.-900G>C | upstream_gene_variant | 0.24 |
rpoB | 762490 | p.Val895Asp | missense_variant | 0.15 |
rpoC | 762509 | c.-861T>G | upstream_gene_variant | 0.17 |
rpoB | 762510 | p.Ala902Pro | missense_variant | 0.14 |
rpoC | 762521 | c.-849C>G | upstream_gene_variant | 0.2 |
rpoC | 762533 | c.-837T>C | upstream_gene_variant | 0.21 |
rpoC | 762536 | c.-834T>C | upstream_gene_variant | 0.2 |
rpoC | 762537 | c.-833T>C | upstream_gene_variant | 0.2 |
rpoC | 762551 | c.-819C>T | upstream_gene_variant | 0.21 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.29 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.2 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.15 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 0.19 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.19 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.18 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.21 |
rpoC | 763076 | c.-294C>G | upstream_gene_variant | 0.26 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.31 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.32 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.3 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.29 |
rpoC | 763158 | c.-212C>T | upstream_gene_variant | 0.24 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.29 |
rpoC | 763169 | c.-201A>G | upstream_gene_variant | 0.3 |
rpoC | 763202 | c.-168A>C | upstream_gene_variant | 0.25 |
rpoC | 763205 | c.-165G>C | upstream_gene_variant | 0.25 |
rpoC | 763206 | c.-164_-162delAGTinsTCC | upstream_gene_variant | 0.26 |
rpoC | 763214 | c.-156T>C | upstream_gene_variant | 0.27 |
rpoC | 763226 | c.-144A>G | upstream_gene_variant | 0.28 |
rpoC | 763238 | c.-132T>C | upstream_gene_variant | 0.35 |
rpoC | 763268 | c.-102C>G | upstream_gene_variant | 0.31 |
rpoC | 763402 | c.33C>G | synonymous_variant | 0.23 |
rpoC | 763411 | c.42T>G | synonymous_variant | 0.23 |
rpoC | 763414 | c.45T>C | synonymous_variant | 0.23 |
rpoC | 763441 | c.72C>G | synonymous_variant | 0.36 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.41 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.42 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.33 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.32 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.24 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.2 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.21 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.23 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.31 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.3 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.3 |
rpoC | 763658 | c.289_291delCTTinsTTG | synonymous_variant | 0.25 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.21 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.21 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.2 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.16 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.16 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.16 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.19 |
rpoC | 763735 | c.366G>C | synonymous_variant | 0.24 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.25 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.28 |
rpoC | 763768 | c.399C>G | synonymous_variant | 0.29 |
rpoC | 763780 | c.411C>G | synonymous_variant | 0.34 |
rpoC | 763783 | c.414G>C | synonymous_variant | 0.31 |
rpoC | 763801 | c.432C>G | synonymous_variant | 0.27 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.3 |
rpoC | 763819 | c.450G>C | synonymous_variant | 0.29 |
rpoC | 763831 | c.462A>G | synonymous_variant | 0.23 |
rpoC | 763835 | p.Ala156Met | missense_variant | 0.2 |
rpoC | 763858 | c.489A>G | synonymous_variant | 0.23 |
rpoC | 763872 | p.Gly168Ala | missense_variant | 0.19 |
rpoC | 763876 | p.Glu169Asp | missense_variant | 0.19 |
rpoC | 763879 | c.510A>G | synonymous_variant | 0.17 |
rpoC | 763885 | c.516C>G | synonymous_variant | 0.17 |
rpoC | 763888 | c.519G>C | synonymous_variant | 0.2 |
rpoC | 763891 | c.522G>C | synonymous_variant | 0.22 |
rpoC | 763894 | c.525A>G | synonymous_variant | 0.21 |
rpoC | 763945 | c.576T>C | synonymous_variant | 0.35 |
rpoC | 763960 | c.591T>C | synonymous_variant | 0.32 |
rpoC | 763967 | p.Gly200Ser | missense_variant | 0.29 |
rpoC | 763978 | c.609C>G | synonymous_variant | 0.29 |
rpoC | 763996 | c.627T>C | synonymous_variant | 0.31 |
rpoC | 764005 | c.636G>C | synonymous_variant | 0.34 |
rpoC | 764011 | c.642T>C | synonymous_variant | 0.33 |
rpoC | 764024 | c.655T>C | synonymous_variant | 0.33 |
rpoC | 764040 | p.Ser224Asn | missense_variant | 0.31 |
rpoC | 764044 | c.675T>C | synonymous_variant | 0.29 |
rpoC | 764059 | c.690G>C | synonymous_variant | 0.33 |
rpoC | 764083 | c.714A>G | synonymous_variant | 0.37 |
rpoC | 764098 | c.729A>G | synonymous_variant | 0.36 |
rpoC | 764101 | c.732C>G | synonymous_variant | 0.37 |
rpoC | 764110 | c.741C>T | synonymous_variant | 0.35 |
rpoC | 764131 | c.762T>C | synonymous_variant | 0.37 |
rpoC | 764161 | c.792G>C | synonymous_variant | 0.31 |
rpoC | 764188 | c.819A>G | synonymous_variant | 0.26 |
rpoC | 764195 | p.Ser276Gln | missense_variant | 0.24 |
rpoC | 764203 | c.834G>T | synonymous_variant | 0.23 |
rpoC | 764206 | c.837T>C | synonymous_variant | 0.23 |
rpoC | 764257 | c.888G>C | synonymous_variant | 0.23 |
rpoC | 764266 | c.897T>C | synonymous_variant | 0.19 |
rpoC | 764282 | c.913_915delTCGinsAGC | synonymous_variant | 0.17 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.23 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.19 |
rpoC | 764381 | c.1012_1013delTCinsAG | synonymous_variant | 0.19 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 0.18 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.17 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.23 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.21 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.19 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.21 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.2 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.22 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.21 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.27 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.3 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.24 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.19 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.24 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.17 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.17 |
rpoC | 764573 | c.1204_1206delCTTinsTTG | synonymous_variant | 0.15 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.21 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.29 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.38 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.3 |
rpoC | 764695 | c.1326T>C | synonymous_variant | 0.39 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.34 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.5 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.45 |
rpoC | 764791 | c.1422C>G | synonymous_variant | 0.42 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.39 |
rpoC | 764812 | c.1443C>G | synonymous_variant | 0.39 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.38 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 0.35 |
rpoC | 764830 | c.1461C>G | synonymous_variant | 0.33 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.27 |
rpoC | 764872 | c.1503A>G | synonymous_variant | 0.27 |
rpoC | 764878 | c.1509C>G | synonymous_variant | 0.22 |
rpoC | 764893 | c.1524T>C | synonymous_variant | 0.26 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.27 |
rpoC | 764923 | c.1554A>G | synonymous_variant | 0.25 |
rpoC | 764932 | c.1563C>A | synonymous_variant | 0.24 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.21 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.18 |
rpoC | 765007 | c.1638T>G | synonymous_variant | 0.16 |
rpoC | 765034 | c.1665T>C | synonymous_variant | 0.15 |
rpoC | 765300 | p.Val644Ala | missense_variant | 0.15 |
rpoC | 765319 | c.1950A>G | synonymous_variant | 0.17 |
rpoC | 765325 | c.1956C>T | synonymous_variant | 0.17 |
rpoC | 765326 | p.His653Ala | missense_variant | 0.17 |
rpoC | 765330 | p.Ser654Asn | missense_variant | 0.17 |
rpoC | 765349 | c.1980T>C | synonymous_variant | 0.21 |
rpoC | 765352 | c.1983G>C | synonymous_variant | 0.21 |
rpoC | 765383 | p.Met672Leu | missense_variant | 0.25 |
rpoC | 765404 | p.Leu679Val | missense_variant | 0.18 |
rpoC | 765409 | c.2040T>C | synonymous_variant | 0.17 |
rpoC | 765412 | c.2043T>C | synonymous_variant | 0.17 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.22 |
rpoC | 765451 | c.2082C>G | synonymous_variant | 0.19 |
rpoC | 765452 | p.Ala695Ser | missense_variant | 0.16 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.17 |
rpoC | 765493 | c.2124G>C | synonymous_variant | 0.25 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.26 |
rpoC | 765508 | c.2139C>G | synonymous_variant | 0.28 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.36 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.28 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.31 |
rpoC | 765559 | c.2190G>C | synonymous_variant | 0.31 |
rpoC | 765577 | c.2208G>C | synonymous_variant | 0.26 |
rpoC | 765578 | c.2209C>T | synonymous_variant | 0.29 |
rpoC | 765583 | c.2214G>T | synonymous_variant | 0.31 |
rpoC | 765613 | p.His748Gln | missense_variant | 0.33 |
rpoC | 765625 | c.2256C>G | synonymous_variant | 0.31 |
rpoC | 765628 | c.2259G>C | synonymous_variant | 0.29 |
rpoC | 765631 | p.Asp754Glu | missense_variant | 0.27 |
rpoC | 765658 | c.2289C>T | synonymous_variant | 0.27 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.18 |
rpoC | 765772 | c.2403C>G | synonymous_variant | 0.24 |
rpoC | 765784 | c.2415C>G | synonymous_variant | 0.25 |
rpoC | 765796 | c.2427C>T | synonymous_variant | 0.24 |
rpoC | 765811 | c.2442T>C | synonymous_variant | 0.26 |
rpoC | 765814 | c.2445A>G | synonymous_variant | 0.26 |
rpoC | 765826 | c.2457T>C | synonymous_variant | 0.22 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 0.24 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.19 |
rpoC | 765928 | c.2559C>G | synonymous_variant | 0.23 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.3 |
rpoC | 765979 | c.2610C>G | synonymous_variant | 0.28 |
rpoC | 765982 | c.2613C>T | synonymous_variant | 0.29 |
rpoC | 765985 | c.2616C>T | synonymous_variant | 0.28 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.25 |
rpoC | 766043 | p.Gln892Glu | missense_variant | 0.22 |
rpoC | 766054 | c.2685C>G | synonymous_variant | 0.24 |
rpoC | 766069 | c.2700G>A | synonymous_variant | 0.26 |
rpoC | 766082 | p.Ala905Gln | missense_variant | 0.23 |
rpoC | 766096 | c.2727G>C | synonymous_variant | 0.23 |
rpoC | 766105 | c.2736C>T | synonymous_variant | 0.23 |
rpoC | 766129 | c.2760C>G | synonymous_variant | 0.19 |
rpoC | 766135 | c.2766G>A | synonymous_variant | 0.15 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.14 |
rpoC | 766645 | c.3276A>G | synonymous_variant | 0.17 |
rpoC | 766651 | c.3282T>C | synonymous_variant | 0.18 |
rpoC | 766657 | c.3288A>G | synonymous_variant | 0.22 |
rpoC | 766672 | c.3303T>C | synonymous_variant | 0.38 |
rpoC | 766738 | c.3369G>T | synonymous_variant | 0.44 |
rpoC | 766750 | c.3381C>G | synonymous_variant | 0.35 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.22 |
rpoC | 766769 | c.3400C>T | synonymous_variant | 0.22 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.24 |
rpoC | 766801 | c.3432C>G | synonymous_variant | 0.21 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.24 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 0.3 |
rpoC | 766864 | c.3495G>C | synonymous_variant | 0.33 |
rpoC | 766894 | c.3525T>C | synonymous_variant | 0.29 |
rpoC | 766895 | c.3526T>C | synonymous_variant | 0.29 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.31 |
rpoC | 766933 | c.3564A>G | synonymous_variant | 0.16 |
rpoC | 766945 | c.3576A>G | synonymous_variant | 0.16 |
rpoC | 767009 | c.3640_3642delTCGinsAGC | synonymous_variant | 0.22 |
rpoC | 767014 | c.3645G>C | synonymous_variant | 0.25 |
rpoC | 767033 | c.3664_3666delTCGinsAGC | synonymous_variant | 0.35 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.38 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.38 |
rpoC | 767074 | c.3705T>C | synonymous_variant | 0.38 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.31 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.29 |
rpoC | 767134 | c.3765C>G | synonymous_variant | 0.33 |
rpoC | 767158 | c.3789T>G | synonymous_variant | 0.37 |
rpoC | 767167 | c.3798C>G | synonymous_variant | 0.33 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.22 |
rpoC | 767191 | c.3822C>G | synonymous_variant | 0.25 |
rpoC | 767206 | c.3837C>G | synonymous_variant | 0.27 |
rpoC | 767209 | c.3840T>C | synonymous_variant | 0.27 |
rpoC | 767212 | c.3843G>C | synonymous_variant | 0.24 |
rpoC | 767221 | c.3852C>G | synonymous_variant | 0.35 |
rpoC | 767230 | c.3861G>C | synonymous_variant | 0.24 |
rpoC | 767233 | c.3864T>C | synonymous_variant | 0.19 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775966 | p.Ala839Ser | missense_variant | 0.16 |
mmpL5 | 775970 | c.2511G>C | synonymous_variant | 0.17 |
mmpL5 | 775975 | c.2506T>C | synonymous_variant | 0.25 |
mmpL5 | 775981 | p.Leu834Met | missense_variant | 0.25 |
mmpL5 | 775991 | c.2490G>A | synonymous_variant | 0.17 |
mmpL5 | 775997 | c.2484T>C | synonymous_variant | 0.15 |
mmpL5 | 776009 | c.2472A>G | synonymous_variant | 0.17 |
mmpS5 | 778605 | p.Pro101Thr | missense_variant | 0.17 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781631 | c.72G>C | synonymous_variant | 0.18 |
rpsL | 781649 | c.90T>C | synonymous_variant | 0.21 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.2 |
rpsL | 781682 | c.123T>C | synonymous_variant | 0.32 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.33 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.3 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.32 |
rpsL | 781751 | c.192G>C | synonymous_variant | 0.28 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.32 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.36 |
rpsL | 781793 | c.234G>C | synonymous_variant | 0.37 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.35 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.4 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.42 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.42 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.42 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.36 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.35 |
rpsL | 781916 | c.357T>C | synonymous_variant | 0.29 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.27 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.26 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.27 |
rplC | 800648 | c.-161A>C | upstream_gene_variant | 0.32 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.38 |
rplC | 800690 | c.-119C>T | upstream_gene_variant | 0.35 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.32 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.36 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.33 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.33 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.36 |
rplC | 800738 | c.-71T>C | upstream_gene_variant | 0.33 |
rplC | 800747 | c.-62C>G | upstream_gene_variant | 0.29 |
rplC | 800771 | c.-38C>T | upstream_gene_variant | 0.24 |
rplC | 800814 | c.6A>G | synonymous_variant | 0.15 |
rplC | 800817 | c.9A>T | synonymous_variant | 0.15 |
rplC | 800844 | c.36T>C | synonymous_variant | 0.16 |
rplC | 800907 | c.99C>G | synonymous_variant | 0.18 |
rplC | 800916 | c.108A>G | synonymous_variant | 0.26 |
rplC | 800937 | c.129A>G | synonymous_variant | 0.2 |
rplC | 800939 | p.Arg44Gln | missense_variant | 0.17 |
rplC | 800946 | c.138T>C | synonymous_variant | 0.16 |
rplC | 800949 | c.141T>C | synonymous_variant | 0.17 |
rplC | 800955 | c.147C>G | synonymous_variant | 0.17 |
rplC | 800967 | c.159C>G | synonymous_variant | 0.16 |
rplC | 801222 | c.414T>C | synonymous_variant | 0.17 |
rplC | 801228 | c.420T>C | synonymous_variant | 0.15 |
rplC | 801246 | c.438C>G | synonymous_variant | 0.18 |
rplC | 801249 | c.441T>G | synonymous_variant | 0.19 |
rplC | 801255 | c.447C>T | synonymous_variant | 0.19 |
rplC | 801267 | c.459A>C | synonymous_variant | 0.24 |
rplC | 801270 | c.462T>C | synonymous_variant | 0.21 |
rplC | 801276 | c.468G>C | synonymous_variant | 0.2 |
rplC | 801279 | c.471G>C | synonymous_variant | 0.21 |
rplC | 801282 | c.474G>C | synonymous_variant | 0.21 |
rplC | 801301 | c.493C>A | synonymous_variant | 0.15 |
fbiC | 1303480 | p.Gln184Glu | missense_variant | 0.19 |
fbiC | 1303509 | c.579G>C | synonymous_variant | 0.22 |
fbiC | 1303512 | c.582T>C | synonymous_variant | 0.26 |
fbiC | 1303534 | p.Ser202Ala | missense_variant | 0.27 |
fbiC | 1303545 | c.615A>G | synonymous_variant | 0.24 |
fbiC | 1303560 | c.630G>C | synonymous_variant | 0.27 |
fbiC | 1303575 | c.645G>C | synonymous_variant | 0.26 |
fbiC | 1303584 | c.654C>G | synonymous_variant | 0.18 |
fbiC | 1303590 | c.660A>G | synonymous_variant | 0.22 |
fbiC | 1303602 | c.672A>G | synonymous_variant | 0.26 |
fbiC | 1303605 | c.675C>G | synonymous_variant | 0.25 |
fbiC | 1303608 | c.678G>A | synonymous_variant | 0.25 |
fbiC | 1303611 | c.681G>C | synonymous_variant | 0.24 |
fbiC | 1303614 | c.684C>T | synonymous_variant | 0.24 |
fbiC | 1303617 | c.687C>G | synonymous_variant | 0.24 |
fbiC | 1303632 | c.702T>G | synonymous_variant | 0.29 |
fbiC | 1303638 | c.708A>G | synonymous_variant | 0.27 |
fbiC | 1303686 | c.756C>G | synonymous_variant | 0.15 |
fbiC | 1303716 | c.786C>T | synonymous_variant | 0.16 |
fbiC | 1303728 | c.798G>A | synonymous_variant | 0.16 |
fbiC | 1303737 | c.807G>A | synonymous_variant | 0.19 |
fbiC | 1303746 | c.816T>C | synonymous_variant | 0.19 |
fbiC | 1303749 | c.819G>C | synonymous_variant | 0.19 |
fbiC | 1303752 | c.822A>G | synonymous_variant | 0.19 |
fbiC | 1303755 | c.825T>C | synonymous_variant | 0.19 |
fbiC | 1303785 | c.855G>C | synonymous_variant | 0.18 |
fbiC | 1303789 | p.Ile287Val | missense_variant | 0.17 |
fbiC | 1303818 | c.888C>G | synonymous_variant | 0.15 |
fbiC | 1303860 | c.930A>C | synonymous_variant | 0.17 |
fbiC | 1303911 | c.981G>C | synonymous_variant | 0.21 |
fbiC | 1303914 | c.984C>G | synonymous_variant | 0.21 |
fbiC | 1303920 | c.990C>G | synonymous_variant | 0.19 |
fbiC | 1303923 | c.993C>T | synonymous_variant | 0.19 |
fbiC | 1303929 | c.999G>C | synonymous_variant | 0.22 |
fbiC | 1303947 | c.1017T>C | synonymous_variant | 0.21 |
fbiC | 1303948 | p.Gly340Arg | missense_variant | 0.21 |
fbiC | 1303969 | p.Val347Ile | missense_variant | 0.19 |
fbiC | 1303973 | p.Gly348Ala | missense_variant | 0.19 |
fbiC | 1303981 | p.Val351Ile | missense_variant | 0.15 |
fbiC | 1303995 | c.1065C>T | synonymous_variant | 0.18 |
fbiC | 1304001 | c.1071C>G | synonymous_variant | 0.16 |
fbiC | 1304008 | c.1078T>C | synonymous_variant | 0.17 |
fbiC | 1304040 | c.1110C>G | synonymous_variant | 0.16 |
fbiC | 1304046 | c.1116C>G | synonymous_variant | 0.17 |
fbiC | 1304049 | c.1119T>G | synonymous_variant | 0.18 |
fbiC | 1304080 | p.Ala384Ser | missense_variant | 0.14 |
fbiC | 1304464 | p.Gly512Ser | missense_variant | 0.18 |
fbiC | 1304469 | c.1539G>A | synonymous_variant | 0.22 |
fbiC | 1304472 | c.1542T>C | synonymous_variant | 0.22 |
fbiC | 1304476 | p.Ala516Ser | missense_variant | 0.22 |
fbiC | 1304481 | c.1551T>G | synonymous_variant | 0.23 |
fbiC | 1304520 | c.1590A>C | synonymous_variant | 0.29 |
fbiC | 1304523 | c.1593G>T | synonymous_variant | 0.29 |
fbiC | 1304526 | c.1596T>A | synonymous_variant | 0.29 |
fbiC | 1304544 | c.1614T>C | synonymous_variant | 0.29 |
fbiC | 1304545 | p.Val539Thr | missense_variant | 0.29 |
fbiC | 1304559 | p.Glu543Asp | missense_variant | 0.24 |
fbiC | 1304565 | c.1635C>G | synonymous_variant | 0.24 |
fbiC | 1304568 | c.1638T>C | synonymous_variant | 0.22 |
fbiC | 1304574 | c.1644C>G | synonymous_variant | 0.27 |
fbiC | 1304580 | c.1650T>C | synonymous_variant | 0.26 |
fbiC | 1304613 | c.1683T>C | synonymous_variant | 0.25 |
fbiC | 1304628 | c.1698G>C | synonymous_variant | 0.22 |
fbiC | 1304634 | c.1704C>G | synonymous_variant | 0.22 |
fbiC | 1304640 | c.1710A>C | synonymous_variant | 0.31 |
fbiC | 1304646 | c.1716T>C | synonymous_variant | 0.24 |
fbiC | 1304658 | c.1728C>G | synonymous_variant | 0.29 |
fbiC | 1304691 | c.1761G>C | synonymous_variant | 0.24 |
fbiC | 1304694 | c.1764A>C | synonymous_variant | 0.25 |
fbiC | 1304703 | c.1773C>G | synonymous_variant | 0.28 |
fbiC | 1304715 | c.1785G>C | synonymous_variant | 0.3 |
fbiC | 1304724 | c.1794A>G | synonymous_variant | 0.25 |
fbiC | 1304727 | c.1797A>G | synonymous_variant | 0.26 |
fbiC | 1304742 | c.1812T>C | synonymous_variant | 0.3 |
fbiC | 1304748 | c.1818T>C | synonymous_variant | 0.32 |
fbiC | 1304754 | c.1824G>A | synonymous_variant | 0.35 |
fbiC | 1304757 | c.1827A>G | synonymous_variant | 0.39 |
fbiC | 1304784 | c.1854T>C | synonymous_variant | 0.43 |
fbiC | 1304787 | c.1857T>C | synonymous_variant | 0.38 |
fbiC | 1304790 | c.1860C>G | synonymous_variant | 0.38 |
fbiC | 1304808 | c.1878C>G | synonymous_variant | 0.27 |
fbiC | 1304811 | c.1881C>G | synonymous_variant | 0.32 |
fbiC | 1304817 | c.1887T>C | synonymous_variant | 0.38 |
fbiC | 1304829 | c.1899T>C | synonymous_variant | 0.44 |
fbiC | 1304832 | c.1902C>G | synonymous_variant | 0.46 |
fbiC | 1304853 | c.1923C>G | synonymous_variant | 0.46 |
fbiC | 1304856 | c.1926C>G | synonymous_variant | 0.46 |
fbiC | 1304872 | c.1942_1944delAGCinsTCG | synonymous_variant | 0.29 |
fbiC | 1304877 | c.1947T>C | synonymous_variant | 0.29 |
fbiC | 1304878 | c.1948_1950delCGCinsAGG | synonymous_variant | 0.28 |
fbiC | 1304893 | p.Gly655Ser | missense_variant | 0.34 |
fbiC | 1304916 | c.1986T>C | synonymous_variant | 0.45 |
fbiC | 1304925 | c.1995G>C | synonymous_variant | 0.39 |
fbiC | 1304928 | c.1998T>C | synonymous_variant | 0.36 |
fbiC | 1304934 | c.2004C>G | synonymous_variant | 0.28 |
fbiC | 1304937 | c.2007G>C | synonymous_variant | 0.27 |
fbiC | 1304940 | c.2010A>G | synonymous_variant | 0.27 |
fbiC | 1304946 | c.2016G>C | synonymous_variant | 0.24 |
fbiC | 1304958 | c.2028T>G | synonymous_variant | 0.25 |
fbiC | 1304961 | c.2031C>T | synonymous_variant | 0.26 |
fbiC | 1304991 | c.2061G>C | synonymous_variant | 0.21 |
fbiC | 1304994 | c.2064A>G | synonymous_variant | 0.19 |
fbiC | 1304995 | c.2065T>C | synonymous_variant | 0.18 |
fbiC | 1305006 | c.2076A>G | synonymous_variant | 0.18 |
fbiC | 1305381 | c.2451G>C | synonymous_variant | 0.22 |
fbiC | 1305393 | c.2463T>C | synonymous_variant | 0.22 |
fbiC | 1305405 | c.2475A>G | synonymous_variant | 0.21 |
fbiC | 1305420 | c.2490C>G | synonymous_variant | 0.26 |
fbiC | 1305423 | c.2493T>C | synonymous_variant | 0.25 |
fbiC | 1305430 | p.Val834Thr | missense_variant | 0.26 |
fbiC | 1305444 | c.2514A>G | synonymous_variant | 0.25 |
fbiC | 1305453 | c.2523C>G | synonymous_variant | 0.24 |
atpE | 1460855 | c.-190T>C | upstream_gene_variant | 0.16 |
atpE | 1460858 | c.-187C>G | upstream_gene_variant | 0.15 |
atpE | 1461185 | c.141G>C | synonymous_variant | 0.18 |
atpE | 1461189 | c.145C>T | synonymous_variant | 0.17 |
atpE | 1461194 | c.150C>T | synonymous_variant | 0.18 |
atpE | 1461197 | c.153A>G | synonymous_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472028 | n.183A>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472030 | n.185G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472031 | n.186G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472034 | n.189T>C | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472044 | n.199G>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473756 | n.99G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473813 | n.156C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1473839 | n.182G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473899 | n.242A>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473937 | n.280C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1473944 | n.287G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473945 | n.288T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474009 | n.352A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474012 | n.355C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474051 | n.394T>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474054 | n.397T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474056 | n.399T>C | non_coding_transcript_exon_variant | 0.34 |
rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474104 | n.447G>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474111 | n.454T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474112 | n.455T>A | non_coding_transcript_exon_variant | 0.41 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474823 | n.1166C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474904 | n.1247G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474956 | n.1299C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474959 | n.1302C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474962 | n.1306delG | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474970 | n.1313G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474991 | n.1334T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475006 | n.1349A>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475088 | n.1431A>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1475199 | n.1542G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475206 | n.1549C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475209 | n.1552G>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475313 | n.1656G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475333 | n.1676T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475369 | n.1712G>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475659 | n.2002G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476025 | n.2368G>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476033 | n.2376T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476034 | n.2377C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476089 | n.2432T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476095 | n.2438C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476117 | n.2460G>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.27 |
inhA | 1673408 | c.-794G>T | upstream_gene_variant | 0.17 |
inhA | 1673547 | c.-655T>C | upstream_gene_variant | 0.18 |
inhA | 1673574 | c.-628C>G | upstream_gene_variant | 0.15 |
inhA | 1673580 | c.-622T>C | upstream_gene_variant | 0.23 |
fabG1 | 1673710 | p.Leu91Ile | missense_variant | 0.15 |
inhA | 1674452 | p.Ala84Glu | missense_variant | 0.14 |
inhA | 1674480 | c.279T>C | synonymous_variant | 0.27 |
inhA | 1674486 | c.285T>C | synonymous_variant | 0.25 |
inhA | 1674489 | c.288G>C | synonymous_variant | 0.25 |
inhA | 1674507 | c.306G>C | synonymous_variant | 0.24 |
inhA | 1674537 | c.336C>G | synonymous_variant | 0.28 |
inhA | 1674542 | p.Ala114Glu | missense_variant | 0.28 |
inhA | 1674549 | c.348G>C | synonymous_variant | 0.32 |
inhA | 1674555 | c.354G>A | synonymous_variant | 0.26 |
inhA | 1674561 | c.360C>T | synonymous_variant | 0.22 |
inhA | 1674582 | c.381T>C | synonymous_variant | 0.19 |
inhA | 1674585 | c.384T>C | synonymous_variant | 0.17 |
inhA | 1674589 | p.Met130Leu | missense_variant | 0.15 |
rpsA | 1833589 | c.48A>T | synonymous_variant | 0.15 |
rpsA | 1833595 | c.54T>C | synonymous_variant | 0.17 |
rpsA | 1833619 | c.78A>C | synonymous_variant | 0.27 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.36 |
rpsA | 1833667 | c.126C>G | synonymous_variant | 0.36 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.3 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.27 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.29 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.26 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.31 |
rpsA | 1833790 | c.249T>A | synonymous_variant | 0.3 |
rpsA | 1833799 | c.258C>G | synonymous_variant | 0.27 |
rpsA | 1833811 | c.270G>C | synonymous_variant | 0.32 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.36 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.4 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.39 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.33 |
rpsA | 1833862 | c.321G>T | synonymous_variant | 0.36 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.29 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.21 |
rpsA | 1833940 | c.399C>G | synonymous_variant | 0.23 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.25 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.23 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.27 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.23 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.29 |
rpsA | 1834097 | c.556_557delTCinsAG | synonymous_variant | 0.2 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.19 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.16 |
rpsA | 1834186 | c.645C>G | synonymous_variant | 0.18 |
rpsA | 1834189 | c.648G>C | synonymous_variant | 0.17 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 0.19 |
rpsA | 1834201 | c.660C>T | synonymous_variant | 0.23 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.23 |
rpsA | 1834225 | c.684C>G | synonymous_variant | 0.2 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.26 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.27 |
rpsA | 1834261 | c.720A>C | synonymous_variant | 0.32 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.34 |
rpsA | 1834297 | c.756C>G | synonymous_variant | 0.24 |
rpsA | 1834303 | c.762T>G | synonymous_variant | 0.23 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.21 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.18 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.16 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.16 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.17 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.17 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.19 |
rpsA | 1834474 | c.933C>G | synonymous_variant | 0.15 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.21 |
rpsA | 1834498 | c.957C>T | synonymous_variant | 0.23 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.29 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.24 |
rpsA | 1834555 | c.1014T>C | synonymous_variant | 0.24 |
rpsA | 1834558 | c.1017C>G | synonymous_variant | 0.26 |
rpsA | 1834594 | c.1053C>T | synonymous_variant | 0.22 |
rpsA | 1834606 | c.1065C>G | synonymous_variant | 0.21 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.21 |
rpsA | 1834622 | c.1081_1083delTCGinsAGC | synonymous_variant | 0.23 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.24 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.24 |
rpsA | 1834666 | c.1125G>C | synonymous_variant | 0.28 |
rpsA | 1834669 | c.1128G>C | synonymous_variant | 0.26 |
rpsA | 1834688 | c.1147_1149delAGTinsTCC | synonymous_variant | 0.27 |
rpsA | 1834726 | c.1185C>A | synonymous_variant | 0.3 |
rpsA | 1834732 | c.1191T>C | synonymous_variant | 0.32 |
rpsA | 1834733 | p.Ala398Pro | missense_variant | 0.32 |
rpsA | 1834753 | c.1212T>C | synonymous_variant | 0.39 |
rpsA | 1834765 | c.1224A>G | synonymous_variant | 0.32 |
rpsA | 1834780 | c.1239A>G | synonymous_variant | 0.36 |
rpsA | 1834786 | c.1245A>G | synonymous_variant | 0.34 |
rpsA | 1834789 | c.1248T>C | synonymous_variant | 0.34 |
rpsA | 1834792 | c.1251G>C | synonymous_variant | 0.31 |
tlyA | 1917945 | c.6A>T | synonymous_variant | 0.18 |
tlyA | 1917951 | c.12T>C | synonymous_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101939 | c.1104A>C | synonymous_variant | 0.17 |
ndh | 2101960 | c.1083A>G | synonymous_variant | 0.24 |
ndh | 2101966 | c.1077T>G | synonymous_variant | 0.24 |
ndh | 2101972 | c.1071G>C | synonymous_variant | 0.24 |
ndh | 2101978 | p.Asn355Asp | missense_variant | 0.27 |
ndh | 2101988 | p.Ala352Gly | missense_variant | 0.25 |
ndh | 2101990 | c.1053G>T | synonymous_variant | 0.25 |
ndh | 2102009 | p.Ser345Asn | missense_variant | 0.26 |
ndh | 2102020 | c.1023A>G | synonymous_variant | 0.31 |
ndh | 2102023 | c.1020G>C | synonymous_variant | 0.31 |
ndh | 2102026 | c.1017G>C | synonymous_variant | 0.29 |
ndh | 2102050 | c.993T>C | synonymous_variant | 0.35 |
ndh | 2102053 | c.990G>C | synonymous_variant | 0.33 |
ndh | 2102059 | c.984T>C | synonymous_variant | 0.33 |
ndh | 2102065 | c.978G>C | synonymous_variant | 0.29 |
ndh | 2102068 | c.975T>C | synonymous_variant | 0.29 |
ndh | 2102076 | p.Met323Leu | missense_variant | 0.25 |
ndh | 2102077 | c.966T>C | synonymous_variant | 0.25 |
ndh | 2102083 | p.Val320Ile | missense_variant | 0.2 |
ndh | 2102092 | c.951G>C | synonymous_variant | 0.2 |
ndh | 2102098 | c.945G>C | synonymous_variant | 0.2 |
ndh | 2102103 | p.Tyr314His | missense_variant | 0.22 |
ndh | 2102104 | c.939G>C | synonymous_variant | 0.17 |
ndh | 2102110 | c.933T>C | synonymous_variant | 0.15 |
ndh | 2102212 | c.831G>C | synonymous_variant | 0.17 |
ndh | 2102218 | c.825C>G | synonymous_variant | 0.19 |
ndh | 2102233 | c.810G>A | synonymous_variant | 0.21 |
ndh | 2102242 | c.801G>A | synonymous_variant | 0.21 |
ndh | 2102305 | c.738T>C | synonymous_variant | 0.14 |
ndh | 2102990 | p.Val18Ala | missense_variant | 0.93 |
katG | 2155113 | c.999C>G | synonymous_variant | 0.17 |
katG | 2155120 | p.Ser331Thr | missense_variant | 0.15 |
katG | 2155614 | p.Val166Ile | missense_variant | 0.17 |
katG | 2155617 | c.495T>C | synonymous_variant | 0.17 |
katG | 2155632 | c.480A>C | synonymous_variant | 0.17 |
katG | 2155637 | p.Leu159Ile | missense_variant | 0.21 |
katG | 2155641 | p.Lys157Asn | missense_variant | 0.23 |
katG | 2155782 | c.330C>G | synonymous_variant | 0.27 |
katG | 2155785 | c.327T>C | synonymous_variant | 0.27 |
katG | 2155788 | c.324C>T | synonymous_variant | 0.27 |
katG | 2155794 | p.Ala106Ser | missense_variant | 0.24 |
katG | 2155806 | c.306T>C | synonymous_variant | 0.25 |
katG | 2155845 | p.Pro89Asp | missense_variant | 0.17 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.16 |
PPE35 | 2169840 | p.Gly258Asp | missense_variant | 0.95 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2517947 | c.-168C>T | upstream_gene_variant | 0.31 |
kasA | 2517974 | c.-141T>C | upstream_gene_variant | 0.36 |
kasA | 2517989 | c.-126T>C | upstream_gene_variant | 0.29 |
kasA | 2517992 | c.-123C>G | upstream_gene_variant | 0.28 |
kasA | 2518019 | c.-96A>G | upstream_gene_variant | 0.17 |
kasA | 2518025 | c.-90G>C | upstream_gene_variant | 0.17 |
kasA | 2518035 | c.-80C>G | upstream_gene_variant | 0.15 |
kasA | 2518450 | c.336C>G | synonymous_variant | 0.16 |
kasA | 2518459 | c.345T>C | synonymous_variant | 0.2 |
kasA | 2518462 | c.348A>C | synonymous_variant | 0.19 |
kasA | 2518468 | c.354A>T | synonymous_variant | 0.22 |
kasA | 2518475 | c.361A>C | synonymous_variant | 0.27 |
kasA | 2518480 | c.366T>C | synonymous_variant | 0.28 |
kasA | 2518483 | c.369C>G | synonymous_variant | 0.28 |
kasA | 2518504 | c.390T>C | synonymous_variant | 0.32 |
kasA | 2518506 | p.Ala131Glu | missense_variant | 0.33 |
kasA | 2518519 | c.405G>C | synonymous_variant | 0.32 |
kasA | 2518528 | c.414C>G | synonymous_variant | 0.35 |
kasA | 2518540 | c.426T>G | synonymous_variant | 0.42 |
kasA | 2518561 | c.447T>C | synonymous_variant | 0.35 |
kasA | 2518567 | c.453G>C | synonymous_variant | 0.32 |
kasA | 2518570 | c.456G>C | synonymous_variant | 0.28 |
kasA | 2518574 | p.Ile154Val | missense_variant | 0.28 |
kasA | 2518588 | c.474T>C | synonymous_variant | 0.3 |
kasA | 2518591 | c.477G>C | synonymous_variant | 0.33 |
kasA | 2518609 | p.Met165Ile | missense_variant | 0.28 |
kasA | 2518621 | c.507G>A | synonymous_variant | 0.29 |
kasA | 2518642 | c.528A>G | synonymous_variant | 0.33 |
kasA | 2518663 | c.549T>C | synonymous_variant | 0.33 |
kasA | 2518672 | c.558G>C | synonymous_variant | 0.35 |
kasA | 2518687 | c.573C>T | synonymous_variant | 0.29 |
kasA | 2518696 | c.582C>G | synonymous_variant | 0.24 |
kasA | 2518702 | c.588C>T | synonymous_variant | 0.28 |
kasA | 2518711 | c.597A>G | synonymous_variant | 0.22 |
kasA | 2518714 | c.600A>C | synonymous_variant | 0.23 |
kasA | 2518717 | c.603C>T | synonymous_variant | 0.27 |
kasA | 2518732 | c.618C>G | synonymous_variant | 0.17 |
kasA | 2518741 | c.627G>C | synonymous_variant | 0.17 |
kasA | 2518747 | c.633C>G | synonymous_variant | 0.16 |
kasA | 2518768 | c.654C>G | synonymous_variant | 0.19 |
kasA | 2518783 | c.669T>C | synonymous_variant | 0.17 |
kasA | 2518792 | c.678C>G | synonymous_variant | 0.15 |
kasA | 2518795 | c.681C>G | synonymous_variant | 0.15 |
kasA | 2518816 | c.702C>A | synonymous_variant | 0.27 |
kasA | 2518822 | c.708C>G | synonymous_variant | 0.27 |
kasA | 2518825 | c.711T>C | synonymous_variant | 0.3 |
kasA | 2518855 | c.741C>G | synonymous_variant | 0.25 |
kasA | 2518864 | c.750G>C | synonymous_variant | 0.25 |
kasA | 2518879 | c.765A>G | synonymous_variant | 0.22 |
kasA | 2518885 | c.771T>C | synonymous_variant | 0.24 |
kasA | 2518888 | c.774C>T | synonymous_variant | 0.25 |
kasA | 2518898 | c.784T>C | synonymous_variant | 0.23 |
kasA | 2518906 | c.792A>G | synonymous_variant | 0.23 |
kasA | 2519072 | p.Ala320Thr | missense_variant | 0.13 |
kasA | 2519146 | c.1032C>A | synonymous_variant | 0.19 |
ahpC | 2726612 | c.420C>G | synonymous_variant | 0.15 |
ahpC | 2726638 | p.Ala149Val | missense_variant | 0.23 |
ahpC | 2726645 | c.453C>G | synonymous_variant | 0.24 |
ahpC | 2726657 | c.465A>C | synonymous_variant | 0.24 |
ahpC | 2726669 | p.Asp159Glu | missense_variant | 0.23 |
ahpC | 2726672 | c.480G>A | synonymous_variant | 0.23 |
ahpC | 2726681 | c.489A>G | synonymous_variant | 0.21 |
ahpC | 2726687 | c.495C>G | synonymous_variant | 0.18 |
ahpC | 2726693 | c.501C>G | synonymous_variant | 0.17 |
folC | 2746576 | c.1023C>A | synonymous_variant | 0.17 |
folC | 2746582 | c.1015_1017delTTGinsCTT | synonymous_variant | 0.17 |
folC | 2746594 | c.1005T>C | synonymous_variant | 0.18 |
folC | 2746597 | c.1002C>A | synonymous_variant | 0.18 |
folC | 2746609 | c.990T>C | synonymous_variant | 0.17 |
folC | 2746612 | c.987C>T | synonymous_variant | 0.17 |
folC | 2746618 | c.981G>T | synonymous_variant | 0.16 |
folC | 2746621 | c.978C>T | synonymous_variant | 0.15 |
folC | 2747302 | c.297A>G | synonymous_variant | 0.22 |
folC | 2747314 | c.285A>C | synonymous_variant | 0.22 |
folC | 2747317 | c.282C>G | synonymous_variant | 0.23 |
folC | 2747355 | p.Val82Ile | missense_variant | 0.22 |
folC | 2747359 | c.240C>G | synonymous_variant | 0.19 |
folC | 2747362 | c.237G>C | synonymous_variant | 0.19 |
pepQ | 2860257 | p.Leu54Phe | missense_variant | 0.13 |
ribD | 2987560 | p.Ala241Asp | missense_variant | 0.96 |
Rv2752c | 3064980 | c.1212C>G | synonymous_variant | 0.21 |
Rv2752c | 3064995 | c.1197C>G | synonymous_variant | 0.21 |
Rv2752c | 3064998 | c.1194A>G | synonymous_variant | 0.23 |
Rv2752c | 3065018 | p.Asn392His | missense_variant | 0.21 |
Rv2752c | 3065028 | c.1164G>C | synonymous_variant | 0.2 |
Rv2752c | 3065031 | c.1161G>C | synonymous_variant | 0.2 |
Rv2752c | 3065048 | c.1144C>T | synonymous_variant | 0.17 |
Rv2752c | 3065947 | p.Gly82Ala | missense_variant | 0.2 |
Rv2752c | 3065955 | c.235_237delTTGinsCTC | synonymous_variant | 0.19 |
Rv2752c | 3065979 | c.213T>C | synonymous_variant | 0.19 |
Rv2752c | 3065993 | p.Val67Ile | missense_variant | 0.14 |
Rv2752c | 3065997 | c.195C>G | synonymous_variant | 0.17 |
Rv2752c | 3066002 | p.Met64Leu | missense_variant | 0.19 |
Rv2752c | 3066024 | c.168T>C | synonymous_variant | 0.21 |
Rv2752c | 3066040 | p.Gly51Thr | missense_variant | 0.2 |
Rv2752c | 3066042 | c.150T>C | synonymous_variant | 0.19 |
Rv2752c | 3066050 | p.Leu48Met | missense_variant | 0.22 |
Rv2752c | 3066054 | c.138T>G | synonymous_variant | 0.21 |
Rv2752c | 3066066 | c.126T>C | synonymous_variant | 0.21 |
Rv2752c | 3066075 | c.117A>G | synonymous_variant | 0.21 |
Rv2752c | 3066087 | c.105A>G | synonymous_variant | 0.17 |
Rv2752c | 3066257 | c.-66G>A | upstream_gene_variant | 0.15 |
Rv2752c | 3066279 | c.-88A>G | upstream_gene_variant | 0.15 |
Rv2752c | 3066294 | c.-103C>G | upstream_gene_variant | 0.17 |
Rv2752c | 3066300 | c.-109G>A | upstream_gene_variant | 0.17 |
Rv2752c | 3066303 | c.-112C>G | upstream_gene_variant | 0.18 |
Rv2752c | 3066306 | c.-115T>C | upstream_gene_variant | 0.17 |
Rv2752c | 3066309 | c.-118T>C | upstream_gene_variant | 0.2 |
Rv2752c | 3066335 | c.-144T>C | upstream_gene_variant | 0.19 |
Rv2752c | 3066336 | c.-145C>G | upstream_gene_variant | 0.19 |
Rv2752c | 3066342 | c.-151G>A | upstream_gene_variant | 0.21 |
Rv2752c | 3066345 | c.-154C>G | upstream_gene_variant | 0.21 |
Rv2752c | 3066350 | c.-159T>A | upstream_gene_variant | 0.2 |
thyX | 3067277 | c.669C>G | synonymous_variant | 0.18 |
thyX | 3067280 | c.666G>C | synonymous_variant | 0.17 |
thyX | 3067284 | p.Ala221Asp | missense_variant | 0.17 |
thyX | 3067286 | c.660C>G | synonymous_variant | 0.17 |
thyX | 3067289 | c.657C>G | synonymous_variant | 0.17 |
thyX | 3067293 | p.Gln218Arg | missense_variant | 0.15 |
thyX | 3067304 | c.642A>G | synonymous_variant | 0.22 |
thyX | 3067316 | c.630A>G | synonymous_variant | 0.18 |
thyX | 3067325 | c.621A>G | synonymous_variant | 0.18 |
thyX | 3067355 | c.591A>C | synonymous_variant | 0.24 |
thyX | 3067367 | c.579G>C | synonymous_variant | 0.23 |
thyX | 3067376 | c.570G>C | synonymous_variant | 0.22 |
thyX | 3067391 | c.555G>C | synonymous_variant | 0.2 |
thyX | 3067394 | c.552G>C | synonymous_variant | 0.22 |
thyX | 3067412 | c.534C>G | synonymous_variant | 0.2 |
thyX | 3067439 | c.507A>G | synonymous_variant | 0.17 |
thyX | 3067451 | c.495G>A | synonymous_variant | 0.16 |
thyX | 3067850 | c.96A>C | synonymous_variant | 0.19 |
thyX | 3067874 | c.72C>G | synonymous_variant | 0.18 |
thyX | 3067883 | c.63C>G | synonymous_variant | 0.2 |
thyX | 3067886 | c.60A>C | synonymous_variant | 0.2 |
thyX | 3067889 | c.57C>G | synonymous_variant | 0.2 |
thyX | 3067894 | c.52T>C | synonymous_variant | 0.19 |
thyA | 3073812 | c.660C>G | synonymous_variant | 0.16 |
thyA | 3073824 | c.648A>C | synonymous_variant | 0.17 |
thyA | 3073827 | c.645A>G | synonymous_variant | 0.17 |
thyA | 3073839 | c.633T>C | synonymous_variant | 0.21 |
thyA | 3073872 | p.Ile200Val | missense_variant | 0.25 |
thyA | 3073878 | c.594G>A | synonymous_variant | 0.26 |
thyA | 3073892 | c.580T>C | synonymous_variant | 0.24 |
thyA | 3073893 | c.579C>G | synonymous_variant | 0.22 |
thyA | 3073925 | c.547T>C | synonymous_variant | 0.17 |
thyA | 3073926 | c.546G>C | synonymous_variant | 0.17 |
thyA | 3073929 | c.543T>C | synonymous_variant | 0.17 |
thyA | 3073953 | c.519T>C | synonymous_variant | 0.17 |
thyA | 3073977 | c.495A>G | synonymous_variant | 0.17 |
thyA | 3073989 | c.483T>C | synonymous_variant | 0.25 |
thyA | 3074001 | c.471C>G | synonymous_variant | 0.24 |
thyA | 3074004 | c.468T>C | synonymous_variant | 0.24 |
thyA | 3074010 | c.462C>A | synonymous_variant | 0.2 |
thyA | 3074031 | c.441T>C | synonymous_variant | 0.17 |
thyA | 3074037 | c.435C>G | synonymous_variant | 0.19 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.97 |
ald | 3086964 | p.Asp49Tyr | missense_variant | 0.14 |
fbiD | 3339665 | p.Pro183Leu | missense_variant | 0.15 |
Rv3083 | 3448608 | c.105G>A | synonymous_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474165 | c.159C>G | synonymous_variant | 0.16 |
fprA | 3474177 | c.171C>T | synonymous_variant | 0.16 |
Rv3236c | 3612621 | c.496T>C | synonymous_variant | 0.17 |
Rv3236c | 3612628 | c.489G>C | synonymous_variant | 0.17 |
Rv3236c | 3612643 | c.474A>G | synonymous_variant | 0.22 |
Rv3236c | 3612665 | p.Val151Ala | missense_variant | 0.69 |
Rv3236c | 3612667 | c.450T>G | synonymous_variant | 0.25 |
Rv3236c | 3612673 | c.444G>C | synonymous_variant | 0.27 |
Rv3236c | 3612676 | c.441A>G | synonymous_variant | 0.27 |
Rv3236c | 3612685 | c.432C>T | synonymous_variant | 0.28 |
Rv3236c | 3612694 | c.423T>C | synonymous_variant | 0.27 |
rpoA | 3877503 | c.1005G>C | synonymous_variant | 0.21 |
rpoA | 3877507 | p.Gly334Ala | missense_variant | 0.19 |
rpoA | 3877515 | c.993G>C | synonymous_variant | 0.19 |
rpoA | 3877542 | c.966C>T | synonymous_variant | 0.19 |
rpoA | 3877553 | p.Glu319Gln | missense_variant | 0.28 |
rpoA | 3877557 | c.951C>G | synonymous_variant | 0.25 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.29 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.24 |
rpoA | 3877638 | c.870T>C | synonymous_variant | 0.26 |
rpoA | 3877656 | c.852T>C | synonymous_variant | 0.17 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.17 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.16 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.18 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.19 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.16 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.24 |
rpoA | 3877857 | c.651G>A | synonymous_variant | 0.28 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.27 |
rpoA | 3877872 | c.636C>T | synonymous_variant | 0.23 |
rpoA | 3877875 | c.633T>G | synonymous_variant | 0.23 |
rpoA | 3877899 | p.Ser203Thr | missense_variant | 0.24 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.23 |
rpoA | 3877908 | p.Asn200Ser | missense_variant | 0.23 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.22 |
rpoA | 3877986 | c.522G>C | synonymous_variant | 0.17 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.17 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.18 |
rpoA | 3878040 | c.468T>C | synonymous_variant | 0.15 |
rpoA | 3878046 | c.462T>C | synonymous_variant | 0.15 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.15 |
rpoA | 3878082 | c.426T>C | synonymous_variant | 0.2 |
rpoA | 3878094 | c.414C>G | synonymous_variant | 0.24 |
rpoA | 3878100 | c.408C>G | synonymous_variant | 0.28 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.27 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.28 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.3 |
rpoA | 3878141 | p.Met123Leu | missense_variant | 0.26 |
rpoA | 3878142 | p.Gly122Glu | missense_variant | 0.26 |
rpoA | 3878169 | c.339G>C | synonymous_variant | 0.29 |
rpoA | 3878184 | c.324C>T | synonymous_variant | 0.26 |
rpoA | 3878187 | c.321C>G | synonymous_variant | 0.25 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.19 |
rpoA | 3878199 | c.309T>C | synonymous_variant | 0.19 |
rpoA | 3878202 | c.306G>C | synonymous_variant | 0.21 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.18 |
rpoA | 3878220 | c.288C>T | synonymous_variant | 0.15 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.27 |
rpoA | 3878284 | p.Glu75Ala | missense_variant | 0.22 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.24 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.24 |
rpoA | 3878304 | c.204G>C | synonymous_variant | 0.18 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 0.19 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.23 |
rpoA | 3878331 | c.177A>G | synonymous_variant | 0.21 |
rpoA | 3878334 | c.174T>C | synonymous_variant | 0.21 |
rpoA | 3878337 | c.171T>C | synonymous_variant | 0.2 |
rpoA | 3878346 | c.162T>C | synonymous_variant | 0.2 |
rpoA | 3878391 | c.117T>C | synonymous_variant | 0.16 |
rpoA | 3878396 | c.112C>T | synonymous_variant | 0.16 |
rpoA | 3878436 | c.72A>G | synonymous_variant | 0.18 |
rpoA | 3878442 | c.66G>C | synonymous_variant | 0.18 |
rpoA | 3878454 | c.54A>C | synonymous_variant | 0.18 |
rpoA | 3878490 | c.18C>A | synonymous_variant | 0.15 |
rpoA | 3878496 | c.12A>T | synonymous_variant | 0.14 |
rpoA | 3878698 | c.-191A>G | upstream_gene_variant | 0.15 |
rpoA | 3878701 | c.-194C>G | upstream_gene_variant | 0.15 |
ddn | 3986648 | c.-196C>G | upstream_gene_variant | 0.33 |
ddn | 3986655 | c.-189A>T | upstream_gene_variant | 0.32 |
ddn | 3986660 | c.-184C>T | upstream_gene_variant | 0.29 |
ddn | 3986665 | c.-179G>C | upstream_gene_variant | 0.29 |
ddn | 3986667 | c.-177_-176delCTinsAC | upstream_gene_variant | 0.29 |
ddn | 3986681 | c.-163C>G | upstream_gene_variant | 0.23 |
ddn | 3986690 | c.-154C>G | upstream_gene_variant | 0.2 |
clpC1 | 4038278 | c.2427T>C | synonymous_variant | 0.17 |
clpC1 | 4038293 | c.2412G>C | synonymous_variant | 0.21 |
clpC1 | 4038302 | c.2403C>G | synonymous_variant | 0.21 |
clpC1 | 4038308 | p.Val799Ile | missense_variant | 0.21 |
clpC1 | 4038317 | c.2388G>C | synonymous_variant | 0.22 |
clpC1 | 4038347 | c.2358G>C | synonymous_variant | 0.2 |
clpC1 | 4038368 | c.2337T>C | synonymous_variant | 0.15 |
clpC1 | 4038388 | c.2317T>C | synonymous_variant | 0.15 |
clpC1 | 4038498 | p.Ser736Thr | missense_variant | 0.16 |
clpC1 | 4038530 | p.Glu725Asp | missense_variant | 0.22 |
clpC1 | 4038536 | c.2169C>T | synonymous_variant | 0.22 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.26 |
clpC1 | 4038623 | c.2082A>G | synonymous_variant | 0.21 |
clpC1 | 4038640 | p.Asp689Asn | missense_variant | 0.22 |
clpC1 | 4038653 | c.2052C>T | synonymous_variant | 0.2 |
clpC1 | 4038658 | p.Lys683Gln | missense_variant | 0.19 |
clpC1 | 4038661 | p.Ser682Thr | missense_variant | 0.19 |
clpC1 | 4038662 | c.2043T>C | synonymous_variant | 0.2 |
clpC1 | 4038671 | c.2034T>C | synonymous_variant | 0.18 |
clpC1 | 4038683 | c.2022T>C | synonymous_variant | 0.18 |
clpC1 | 4038740 | c.1965G>C | synonymous_variant | 0.23 |
clpC1 | 4038755 | c.1950G>C | synonymous_variant | 0.24 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.29 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.29 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 0.28 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.33 |
clpC1 | 4038815 | c.1890G>T | synonymous_variant | 0.33 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 0.16 |
clpC1 | 4038932 | c.1773G>C | synonymous_variant | 0.16 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.18 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.2 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.21 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.2 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.19 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.22 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.24 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.19 |
clpC1 | 4039073 | c.1632C>G | synonymous_variant | 0.23 |
clpC1 | 4039085 | c.1620A>G | synonymous_variant | 0.22 |
clpC1 | 4039090 | c.1615C>T | synonymous_variant | 0.21 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.17 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.17 |
clpC1 | 4039124 | c.1581C>G | synonymous_variant | 0.17 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.14 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.17 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.18 |
clpC1 | 4039187 | c.1518G>C | synonymous_variant | 0.16 |
clpC1 | 4039190 | c.1515C>G | synonymous_variant | 0.16 |
clpC1 | 4039208 | c.1497C>G | synonymous_variant | 0.19 |
clpC1 | 4039226 | c.1479T>C | synonymous_variant | 0.19 |
clpC1 | 4039484 | c.1221T>G | synonymous_variant | 0.17 |
clpC1 | 4039493 | c.1212C>T | synonymous_variant | 0.16 |
clpC1 | 4039682 | c.1023C>G | synonymous_variant | 0.17 |
clpC1 | 4039685 | c.1020C>T | synonymous_variant | 0.18 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.23 |
clpC1 | 4039760 | c.945T>C | synonymous_variant | 0.15 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.17 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.2 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.19 |
clpC1 | 4039946 | c.759A>T | synonymous_variant | 0.14 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.17 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.16 |
clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 0.28 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.28 |
clpC1 | 4040105 | c.600C>G | synonymous_variant | 0.32 |
clpC1 | 4040147 | c.558A>G | synonymous_variant | 0.27 |
clpC1 | 4040153 | c.552A>G | synonymous_variant | 0.2 |
clpC1 | 4040225 | c.480A>C | synonymous_variant | 0.18 |
clpC1 | 4040228 | c.477G>C | synonymous_variant | 0.17 |
clpC1 | 4040234 | c.471C>G | synonymous_variant | 0.16 |
clpC1 | 4040237 | c.468C>T | synonymous_variant | 0.16 |
clpC1 | 4040264 | c.441C>T | synonymous_variant | 0.15 |
clpC1 | 4040267 | c.438A>G | synonymous_variant | 0.17 |
clpC1 | 4040273 | c.432T>C | synonymous_variant | 0.2 |
clpC1 | 4040354 | c.351A>G | synonymous_variant | 0.38 |
clpC1 | 4040363 | c.342A>C | synonymous_variant | 0.37 |
clpC1 | 4040369 | c.336C>G | synonymous_variant | 0.37 |
clpC1 | 4040380 | c.325T>C | synonymous_variant | 0.26 |
clpC1 | 4040387 | c.318A>G | synonymous_variant | 0.21 |
clpC1 | 4040393 | c.312G>C | synonymous_variant | 0.21 |
clpC1 | 4040411 | c.294T>C | synonymous_variant | 0.17 |
clpC1 | 4040450 | c.255A>G | synonymous_variant | 0.16 |
clpC1 | 4040459 | c.246C>G | synonymous_variant | 0.19 |
clpC1 | 4040465 | c.240T>C | synonymous_variant | 0.26 |
clpC1 | 4040471 | c.234T>C | synonymous_variant | 0.25 |
clpC1 | 4040477 | c.228G>A | synonymous_variant | 0.24 |
clpC1 | 4040480 | c.225T>C | synonymous_variant | 0.26 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 0.24 |
clpC1 | 4040528 | c.177G>C | synonymous_variant | 0.25 |
clpC1 | 4040531 | c.174T>C | synonymous_variant | 0.25 |
clpC1 | 4040534 | c.171A>G | synonymous_variant | 0.25 |
clpC1 | 4040546 | c.159G>C | synonymous_variant | 0.19 |
clpC1 | 4040644 | c.61A>C | synonymous_variant | 0.2 |
clpC1 | 4040654 | c.51G>A | synonymous_variant | 0.21 |
clpC1 | 4040657 | c.48T>G | synonymous_variant | 0.2 |
clpC1 | 4040662 | c.43C>T | synonymous_variant | 0.2 |
clpC1 | 4040699 | c.6C>T | synonymous_variant | 0.26 |
clpC1 | 4040711 | c.-7G>A | upstream_gene_variant | 0.23 |
panD | 4044057 | c.225C>A | synonymous_variant | 0.14 |
panD | 4044096 | c.186C>T | synonymous_variant | 0.14 |
panD | 4044195 | c.87T>C | synonymous_variant | 0.15 |
embC | 4240444 | c.582C>G | synonymous_variant | 0.14 |
embC | 4240462 | c.600G>C | synonymous_variant | 0.21 |
embC | 4240475 | p.Ala205Ser | missense_variant | 0.23 |
embC | 4240480 | c.618G>A | synonymous_variant | 0.22 |
embC | 4240489 | c.627A>G | synonymous_variant | 0.22 |
embC | 4240495 | c.633T>C | synonymous_variant | 0.24 |
embC | 4240512 | p.Ser217Thr | missense_variant | 0.26 |
embC | 4240514 | p.Val218Ile | missense_variant | 0.25 |
embC | 4240519 | c.657T>C | synonymous_variant | 0.25 |
embC | 4240543 | c.681G>C | synonymous_variant | 0.17 |
embC | 4240561 | c.699C>G | synonymous_variant | 0.17 |
embC | 4240573 | c.711G>C | synonymous_variant | 0.18 |
embC | 4240574 | p.Val238Leu | missense_variant | 0.18 |
embC | 4240578 | p.Ala239Val | missense_variant | 0.19 |
embC | 4240582 | c.720C>G | synonymous_variant | 0.21 |
embC | 4240591 | c.729C>G | synonymous_variant | 0.21 |
embC | 4240594 | c.732C>G | synonymous_variant | 0.21 |
embC | 4240600 | c.738G>C | synonymous_variant | 0.21 |
embC | 4240632 | p.Met257Thr | missense_variant | 0.25 |
embC | 4240642 | c.780G>C | synonymous_variant | 0.3 |
embC | 4240645 | c.783G>C | synonymous_variant | 0.36 |
embC | 4240654 | c.792C>T | synonymous_variant | 0.38 |
embC | 4240657 | c.795G>C | synonymous_variant | 0.33 |
embC | 4240671 | p.Thr270Ile | missense_variant | 0.29 |
embC | 4240678 | c.816T>G | synonymous_variant | 0.25 |
embC | 4240685 | p.Thr275Ala | missense_variant | 0.26 |
embC | 4240693 | c.831T>C | synonymous_variant | 0.28 |
embC | 4240706 | p.Val282Thr | missense_variant | 0.26 |
embC | 4240726 | c.864G>C | synonymous_variant | 0.24 |
embC | 4240780 | c.918T>C | synonymous_variant | 0.35 |
embC | 4240783 | c.921G>C | synonymous_variant | 0.35 |
embC | 4240789 | c.927T>C | synonymous_variant | 0.35 |
embC | 4240819 | c.957A>G | synonymous_variant | 0.48 |
embC | 4240831 | c.969T>G | synonymous_variant | 0.54 |
embC | 4240867 | c.1005T>G | synonymous_variant | 0.57 |
embC | 4240870 | c.1008T>C | synonymous_variant | 0.59 |
embC | 4240879 | c.1017G>C | synonymous_variant | 0.5 |
embC | 4240880 | p.Ala340Thr | missense_variant | 0.5 |
embC | 4240885 | c.1023T>C | synonymous_variant | 0.48 |
embC | 4240897 | c.1035C>G | synonymous_variant | 0.32 |
embC | 4240900 | c.1038A>G | synonymous_variant | 0.32 |
embC | 4240919 | c.1057_1059delCTCinsTTG | synonymous_variant | 0.23 |
embC | 4240936 | c.1074A>G | synonymous_variant | 0.27 |
embC | 4240945 | c.1083T>C | synonymous_variant | 0.33 |
embC | 4240951 | c.1089C>G | synonymous_variant | 0.26 |
embC | 4240954 | p.Ile364Met | missense_variant | 0.25 |
embC | 4240957 | c.1095C>G | synonymous_variant | 0.24 |
embC | 4240966 | c.1104G>T | synonymous_variant | 0.25 |
embC | 4240979 | p.Thr373Gln | missense_variant | 0.29 |
embC | 4240983 | p.Ser374Asn | missense_variant | 0.29 |
embC | 4240990 | c.1128A>G | synonymous_variant | 0.33 |
embC | 4240996 | c.1134G>C | synonymous_variant | 0.39 |
embC | 4241017 | c.1155T>C | synonymous_variant | 0.44 |
embC | 4241023 | c.1161T>G | synonymous_variant | 0.4 |
embC | 4241026 | c.1164C>G | synonymous_variant | 0.38 |
embC | 4241035 | c.1173G>A | synonymous_variant | 0.31 |
embC | 4241050 | c.1188T>G | synonymous_variant | 0.18 |
embC | 4241104 | c.1242G>A | synonymous_variant | 0.29 |
embC | 4241107 | c.1245G>C | synonymous_variant | 0.28 |
embC | 4241137 | c.1275G>C | synonymous_variant | 0.36 |
embC | 4241140 | c.1278A>G | synonymous_variant | 0.35 |
embC | 4241141 | p.Ile427Val | missense_variant | 0.38 |
embC | 4241158 | c.1296T>C | synonymous_variant | 0.35 |
embC | 4241161 | c.1299C>G | synonymous_variant | 0.35 |
embC | 4241162 | c.1300T>C | synonymous_variant | 0.35 |
embC | 4241657 | p.Ser599Pro | missense_variant | 0.15 |
embC | 4241665 | c.1803G>T | synonymous_variant | 0.14 |
embC | 4241671 | c.1809T>G | synonymous_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 0.88 |
embC | 4242656 | p.Pro932Ser | missense_variant | 0.14 |
embA | 4244276 | c.1044A>C | synonymous_variant | 0.2 |
embA | 4244284 | p.Pro351Arg | missense_variant | 0.19 |
embA | 4244919 | c.1687_1689delCTCinsTTG | synonymous_variant | 0.2 |
embA | 4244933 | c.1701A>G | synonymous_variant | 0.17 |
embA | 4245083 | c.1851A>C | synonymous_variant | 0.18 |
embA | 4245089 | c.1857G>C | synonymous_variant | 0.19 |
embA | 4245092 | c.1860C>G | synonymous_variant | 0.19 |
embA | 4245101 | c.1869G>C | synonymous_variant | 0.18 |
embA | 4245137 | c.1905T>C | synonymous_variant | 0.21 |
embA | 4245149 | c.1917C>G | synonymous_variant | 0.24 |
embA | 4245182 | c.1950T>C | synonymous_variant | 0.2 |
embA | 4245194 | c.1962G>C | synonymous_variant | 0.19 |
embA | 4245198 | p.Leu656Ile | missense_variant | 0.19 |
embA | 4245206 | c.1974A>G | synonymous_variant | 0.17 |
embA | 4245207 | c.1975T>C | synonymous_variant | 0.17 |
embA | 4245215 | c.1983A>G | synonymous_variant | 0.15 |
embA | 4245222 | p.Tyr664Gln | missense_variant | 0.15 |
embB | 4245764 | c.-750G>C | upstream_gene_variant | 0.15 |
embA | 4245821 | p.Ser863Arg | missense_variant | 0.17 |
embB | 4245830 | c.-684G>C | upstream_gene_variant | 0.24 |
embB | 4245845 | c.-669T>G | upstream_gene_variant | 0.27 |
embB | 4245848 | c.-666C>G | upstream_gene_variant | 0.26 |
embB | 4245860 | c.-654C>G | upstream_gene_variant | 0.17 |
embA | 4245885 | p.Asp885Thr | missense_variant | 0.2 |
embA | 4245892 | p.Ile887Thr | missense_variant | 0.19 |
embB | 4245905 | c.-609C>G | upstream_gene_variant | 0.29 |
embA | 4246041 | p.Asp937Asn | missense_variant | 0.15 |
embB | 4246367 | c.-147C>T | upstream_gene_variant | 0.15 |
embB | 4246373 | c.-141T>C | upstream_gene_variant | 0.16 |
embB | 4246376 | c.-138G>C | upstream_gene_variant | 0.16 |
embA | 4246413 | p.His1061Phe | missense_variant | 0.14 |
embB | 4246419 | c.-95C>T | upstream_gene_variant | 0.14 |
embB | 4247338 | c.825C>G | synonymous_variant | 0.18 |
embB | 4247348 | p.Thr279Ala | missense_variant | 0.19 |
embB | 4247355 | p.Ala281Val | missense_variant | 0.18 |
embB | 4247358 | p.Val282Ala | missense_variant | 0.19 |
embB | 4247365 | c.852A>C | synonymous_variant | 0.17 |
embB | 4247371 | c.858C>G | synonymous_variant | 0.21 |
embB | 4247375 | p.Leu288Val | missense_variant | 0.19 |
embB | 4247386 | c.873T>C | synonymous_variant | 0.17 |
embB | 4247389 | c.876C>G | synonymous_variant | 0.22 |
embB | 4247395 | c.882C>G | synonymous_variant | 0.21 |
embB | 4247401 | c.888T>C | synonymous_variant | 0.2 |
embB | 4247464 | c.951C>G | synonymous_variant | 0.19 |
embB | 4247470 | c.957T>C | synonymous_variant | 0.22 |
embB | 4247491 | c.978G>C | synonymous_variant | 0.18 |
embB | 4247500 | c.987C>G | synonymous_variant | 0.18 |
embB | 4247512 | c.999T>C | synonymous_variant | 0.21 |
embB | 4247536 | c.1023C>G | synonymous_variant | 0.2 |
embB | 4247554 | c.1041T>C | synonymous_variant | 0.22 |
embB | 4247603 | c.1090C>T | synonymous_variant | 0.17 |
embB | 4247611 | c.1098G>C | synonymous_variant | 0.13 |
embB | 4247683 | c.1170C>G | synonymous_variant | 0.15 |
embB | 4247716 | c.1203C>G | synonymous_variant | 0.16 |
embB | 4247722 | c.1209G>C | synonymous_variant | 0.18 |
embB | 4247725 | c.1212G>C | synonymous_variant | 0.19 |
embB | 4247729 | p.Gly406Pro | missense_variant | 0.18 |
embB | 4247743 | c.1230C>G | synonymous_variant | 0.22 |
embB | 4247746 | c.1233C>A | synonymous_variant | 0.22 |
embB | 4247819 | p.Val436Ile | missense_variant | 0.19 |
embB | 4247824 | c.1311C>G | synonymous_variant | 0.19 |
embB | 4247876 | c.1363C>T | synonymous_variant | 0.25 |
embB | 4247881 | c.1368G>C | synonymous_variant | 0.25 |
embB | 4247887 | c.1374C>T | synonymous_variant | 0.25 |
embB | 4247890 | c.1377C>T | synonymous_variant | 0.27 |
embB | 4247929 | c.1416G>A | synonymous_variant | 0.15 |
embB | 4248007 | c.1494C>G | synonymous_variant | 0.17 |
embB | 4248011 | p.Ser500Ala | missense_variant | 0.17 |
embB | 4248035 | p.Val508Ile | missense_variant | 0.35 |
embB | 4248041 | p.Ala510Thr | missense_variant | 0.32 |
embB | 4248044 | p.Lys511Ala | missense_variant | 0.33 |
embB | 4248052 | c.1539G>A | synonymous_variant | 0.35 |
embB | 4248055 | c.1542G>A | synonymous_variant | 0.35 |
embB | 4248064 | c.1551G>C | synonymous_variant | 0.46 |
embB | 4248070 | c.1557T>C | synonymous_variant | 0.44 |
embB | 4248085 | c.1572T>C | synonymous_variant | 0.45 |
embB | 4248097 | c.1584C>G | synonymous_variant | 0.54 |
embB | 4248118 | c.1605T>C | synonymous_variant | 0.61 |
embB | 4248127 | c.1614G>C | synonymous_variant | 0.5 |
embB | 4248133 | c.1620C>G | synonymous_variant | 0.48 |
embB | 4248142 | c.1629T>C | synonymous_variant | 0.48 |
embB | 4248143 | c.1630T>C | synonymous_variant | 0.5 |
embB | 4248157 | c.1644A>G | synonymous_variant | 0.43 |
embB | 4248206 | p.Ser565Gly | missense_variant | 0.33 |
embB | 4248220 | c.1707A>G | synonymous_variant | 0.25 |
embB | 4248241 | c.1728C>T | synonymous_variant | 0.28 |
embB | 4248265 | c.1752C>T | synonymous_variant | 0.27 |
embB | 4248266 | c.1753C>T | synonymous_variant | 0.23 |
embB | 4248277 | c.1764G>C | synonymous_variant | 0.29 |
embB | 4248304 | c.1791G>C | synonymous_variant | 0.25 |
embB | 4248316 | c.1803C>G | synonymous_variant | 0.3 |
embB | 4248319 | c.1806A>G | synonymous_variant | 0.26 |
embB | 4248322 | c.1809G>C | synonymous_variant | 0.24 |
embB | 4248840 | p.Pro776His | missense_variant | 0.14 |
embB | 4249322 | p.Ala937Ser | missense_variant | 0.14 |
embB | 4249369 | c.2856T>C | synonymous_variant | 0.24 |
embB | 4249381 | c.2868A>G | synonymous_variant | 0.38 |
embB | 4249417 | c.2904A>G | synonymous_variant | 0.24 |
embB | 4249420 | c.2907G>C | synonymous_variant | 0.24 |
embB | 4249423 | p.Asp970Glu | missense_variant | 0.23 |
embB | 4249424 | p.Leu971Met | missense_variant | 0.23 |
embB | 4249432 | c.2919A>G | synonymous_variant | 0.25 |
embB | 4249441 | c.2928A>G | synonymous_variant | 0.25 |
embB | 4249444 | c.2931T>C | synonymous_variant | 0.28 |
embB | 4249447 | c.2934G>C | synonymous_variant | 0.29 |
embB | 4249456 | c.2943G>C | synonymous_variant | 0.22 |
embB | 4249469 | p.Leu986Met | missense_variant | 0.22 |
aftB | 4268384 | p.Leu151Phe | missense_variant | 0.94 |
aftB | 4269123 | c.-287T>C | upstream_gene_variant | 0.19 |
ubiA | 4269141 | p.Leu231Val | missense_variant | 0.19 |
aftB | 4269144 | c.-308C>G | upstream_gene_variant | 0.2 |
ubiA | 4269149 | p.Val229Leu | missense_variant | 0.18 |
aftB | 4269183 | c.-347T>C | upstream_gene_variant | 0.33 |
aftB | 4269201 | c.-365A>G | upstream_gene_variant | 0.37 |
ubiA | 4269209 | p.Ser209Ala | missense_variant | 0.31 |
ubiA | 4269220 | p.Ala205Lys | missense_variant | 0.23 |
aftB | 4269222 | c.-386T>G | upstream_gene_variant | 0.23 |
aftB | 4269225 | c.-389C>G | upstream_gene_variant | 0.23 |
aftB | 4269231 | c.-395C>G | upstream_gene_variant | 0.25 |
aftB | 4269234 | c.-398A>G | upstream_gene_variant | 0.25 |
ubiA | 4269243 | p.His197Gln | missense_variant | 0.21 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 0.17 |
ubiA | 4269610 | p.Val75Ala | missense_variant | 0.17 |
aftB | 4269612 | c.-776T>C | upstream_gene_variant | 0.17 |
aftB | 4269621 | c.-785C>G | upstream_gene_variant | 0.19 |
ubiA | 4269627 | p.Val69Ile | missense_variant | 0.21 |
ubiA | 4269632 | p.Ala68Ser | missense_variant | 0.19 |
ubiA | 4269841 | c.-8G>A | upstream_gene_variant | 0.89 |
ethA | 4328441 | c.-968G>T | upstream_gene_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |