Run ID: SRR17658565
Sample name:
Date: 03-04-2023 18:04:37
Number of reads: 3942034
Percentage reads mapped: 77.57
Strain: lineage3
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 0.96 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7570 | p.Ala90Val | missense_variant | 0.91 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6217 | c.978G>A | synonymous_variant | 0.14 |
gyrA | 6673 | c.-629A>T | upstream_gene_variant | 0.16 |
gyrA | 6676 | c.-626T>G | upstream_gene_variant | 0.16 |
gyrA | 6700 | c.-602T>C | upstream_gene_variant | 0.17 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7502 | c.201C>T | synonymous_variant | 0.14 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8324 | c.1023T>C | synonymous_variant | 0.24 |
gyrA | 8330 | c.1029C>G | synonymous_variant | 0.24 |
gyrA | 8337 | c.1036_1038delCTAinsTTG | synonymous_variant | 0.23 |
gyrA | 8340 | p.Ala347Ser | missense_variant | 0.24 |
gyrA | 8375 | c.1074G>C | synonymous_variant | 0.19 |
gyrA | 8382 | p.Leu361Met | missense_variant | 0.17 |
gyrA | 8390 | c.1089C>G | synonymous_variant | 0.17 |
gyrA | 8391 | p.Tyr364His | missense_variant | 0.18 |
gyrA | 8399 | c.1098T>C | synonymous_variant | 0.18 |
gyrA | 8401 | p.Asp367Ala | missense_variant | 0.18 |
gyrA | 8420 | c.1119T>C | synonymous_variant | 0.18 |
gyrA | 8423 | c.1122G>C | synonymous_variant | 0.18 |
gyrA | 8426 | c.1125G>C | synonymous_variant | 0.18 |
gyrA | 8501 | c.1200G>C | synonymous_variant | 0.18 |
gyrA | 8510 | c.1209G>A | synonymous_variant | 0.18 |
gyrA | 8516 | c.1215T>C | synonymous_variant | 0.19 |
gyrA | 8519 | c.1218A>C | synonymous_variant | 0.2 |
gyrA | 8537 | c.1236G>A | synonymous_variant | 0.22 |
gyrA | 8546 | c.1245T>C | synonymous_variant | 0.27 |
gyrA | 8555 | c.1254G>C | synonymous_variant | 0.26 |
gyrA | 8561 | c.1260A>C | synonymous_variant | 0.28 |
gyrA | 8588 | c.1287G>A | synonymous_variant | 0.25 |
gyrA | 8591 | c.1290C>T | synonymous_variant | 0.25 |
gyrA | 8603 | c.1302A>C | synonymous_variant | 0.23 |
gyrA | 8619 | c.1318T>C | synonymous_variant | 0.23 |
gyrA | 8633 | c.1332C>G | synonymous_variant | 0.24 |
gyrA | 8636 | c.1335A>C | synonymous_variant | 0.25 |
gyrA | 8642 | c.1341A>G | synonymous_variant | 0.26 |
gyrA | 8645 | c.1344C>G | synonymous_variant | 0.26 |
gyrA | 8672 | c.1371A>G | synonymous_variant | 0.24 |
gyrA | 8678 | c.1377G>A | synonymous_variant | 0.23 |
gyrA | 8693 | c.1392T>C | synonymous_variant | 0.16 |
gyrA | 8720 | c.1419G>A | synonymous_variant | 0.16 |
gyrA | 8747 | c.1446A>G | synonymous_variant | 0.17 |
gyrA | 8751 | p.Ala484Thr | missense_variant | 0.16 |
gyrA | 8756 | c.1455A>G | synonymous_variant | 0.17 |
gyrA | 8762 | c.1461G>C | synonymous_variant | 0.17 |
gyrA | 8767 | p.Arg489Lys | missense_variant | 0.17 |
gyrA | 8852 | c.1551T>C | synonymous_variant | 0.17 |
gyrA | 8873 | c.1572A>C | synonymous_variant | 0.17 |
gyrA | 8882 | c.1581G>A | synonymous_variant | 0.17 |
gyrA | 8894 | c.1593C>G | synonymous_variant | 0.22 |
gyrA | 8900 | c.1599G>C | synonymous_variant | 0.21 |
gyrA | 8903 | c.1602T>C | synonymous_variant | 0.21 |
gyrA | 8939 | c.1638T>C | synonymous_variant | 0.18 |
gyrA | 8982 | p.Cys561Ser | missense_variant | 0.14 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 0.16 |
gyrA | 9154 | p.Thr618Asn | missense_variant | 0.15 |
gyrA | 9218 | c.1917C>T | synonymous_variant | 0.16 |
gyrA | 9233 | c.1932C>A | synonymous_variant | 0.15 |
gyrA | 9242 | c.1941A>C | synonymous_variant | 0.18 |
gyrA | 9252 | p.Val651Ile | missense_variant | 0.16 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491043 | c.261T>G | synonymous_variant | 0.17 |
fgd1 | 491049 | c.267T>G | synonymous_variant | 0.16 |
fgd1 | 491063 | p.Gly94Ala | missense_variant | 0.16 |
fgd1 | 491077 | p.Asn99Asp | missense_variant | 0.17 |
fgd1 | 491082 | c.300T>G | synonymous_variant | 0.17 |
fgd1 | 491083 | p.Val101Ile | missense_variant | 0.16 |
fgd1 | 491091 | c.309T>C | synonymous_variant | 0.19 |
fgd1 | 491097 | c.315G>C | synonymous_variant | 0.18 |
fgd1 | 491106 | c.324T>G | synonymous_variant | 0.19 |
fgd1 | 491121 | c.339A>G | synonymous_variant | 0.23 |
fgd1 | 491133 | c.351A>C | synonymous_variant | 0.24 |
fgd1 | 491144 | p.Ala121Glu | missense_variant | 0.26 |
fgd1 | 491166 | c.384G>C | synonymous_variant | 0.22 |
fgd1 | 491181 | c.399T>C | synonymous_variant | 0.21 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575576 | c.229C>T | synonymous_variant | 0.16 |
mshA | 575587 | c.240C>G | synonymous_variant | 0.16 |
mshA | 575590 | c.243T>G | synonymous_variant | 0.17 |
mshA | 575629 | c.282A>G | synonymous_variant | 0.22 |
mshA | 575632 | c.285G>C | synonymous_variant | 0.22 |
mshA | 575635 | c.288A>C | synonymous_variant | 0.23 |
mshA | 575638 | c.291T>C | synonymous_variant | 0.22 |
mshA | 575641 | c.294A>G | synonymous_variant | 0.22 |
mshA | 575649 | p.Val101Ala | missense_variant | 0.24 |
mshA | 575659 | c.312A>G | synonymous_variant | 0.25 |
mshA | 575665 | c.318G>C | synonymous_variant | 0.23 |
mshA | 575695 | c.348C>G | synonymous_variant | 0.17 |
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 | 0.2 |
mshA | 575728 | c.381C>T | synonymous_variant | 0.22 |
mshA | 575734 | c.387T>G | synonymous_variant | 0.2 |
mshA | 575737 | c.390T>C | synonymous_variant | 0.2 |
mshA | 575764 | c.417C>G | synonymous_variant | 0.23 |
mshA | 575770 | c.423G>C | synonymous_variant | 0.21 |
mshA | 575771 | p.Val142Ser | missense_variant | 0.22 |
mshA | 575785 | c.438T>C | synonymous_variant | 0.22 |
mshA | 575786 | p.Tyr147His | missense_variant | 0.22 |
mshA | 575821 | c.474G>C | synonymous_variant | 0.24 |
mshA | 575824 | c.477T>A | synonymous_variant | 0.25 |
mshA | 575842 | c.495G>C | synonymous_variant | 0.28 |
mshA | 575864 | c.517T>C | synonymous_variant | 0.31 |
mshA | 575878 | c.531A>G | synonymous_variant | 0.32 |
mshA | 575893 | c.546C>G | synonymous_variant | 0.28 |
mshA | 575896 | c.549G>C | synonymous_variant | 0.28 |
mshA | 575902 | c.555C>T | synonymous_variant | 0.27 |
mshA | 575908 | c.561A>G | synonymous_variant | 0.27 |
mshA | 575914 | c.567C>G | synonymous_variant | 0.27 |
mshA | 575916 | p.Asp190Ala | missense_variant | 0.28 |
mshA | 575925 | p.Gly193Ala | missense_variant | 0.26 |
mshA | 575944 | c.597T>C | synonymous_variant | 0.29 |
mshA | 575953 | c.606G>C | synonymous_variant | 0.3 |
mshA | 575959 | c.612G>A | synonymous_variant | 0.28 |
mshA | 575980 | c.633T>C | synonymous_variant | 0.19 |
mshA | 575984 | c.637T>C | synonymous_variant | 0.17 |
mshA | 576311 | p.Ser322Ala | missense_variant | 0.16 |
ccsA | 619697 | c.-194_-192delAGGinsCGC | upstream_gene_variant | 0.19 |
ccsA | 619714 | c.-177G>C | upstream_gene_variant | 0.2 |
ccsA | 619715 | c.-176C>A | upstream_gene_variant | 0.2 |
ccsA | 619718 | c.-173A>C | upstream_gene_variant | 0.2 |
ccsA | 619723 | c.-168G>C | upstream_gene_variant | 0.19 |
ccsA | 619727 | c.-164A>G | upstream_gene_variant | 0.19 |
ccsA | 619729 | c.-161_-159delACC | upstream_gene_variant | 0.19 |
ccsA | 619735 | c.-156G>C | upstream_gene_variant | 0.18 |
ccsA | 619744 | c.-147A>G | upstream_gene_variant | 0.17 |
ccsA | 619748 | c.-143G>A | upstream_gene_variant | 0.18 |
ccsA | 619753 | c.-138G>A | upstream_gene_variant | 0.18 |
ccsA | 619762 | c.-129C>G | upstream_gene_variant | 0.18 |
ccsA | 619766 | c.-125A>G | upstream_gene_variant | 0.18 |
ccsA | 620245 | p.Leu119Met | missense_variant | 0.14 |
ccsA | 620288 | p.Arg133Gln | missense_variant | 0.14 |
ccsA | 620362 | p.Ala158Thr | missense_variant | 0.16 |
ccsA | 620643 | c.753C>G | synonymous_variant | 0.18 |
ccsA | 620649 | c.759A>G | synonymous_variant | 0.17 |
ccsA | 620652 | c.762C>G | synonymous_variant | 0.18 |
ccsA | 620661 | c.771C>G | synonymous_variant | 0.18 |
ccsA | 620688 | c.798G>C | synonymous_variant | 0.22 |
ccsA | 620703 | c.813G>C | synonymous_variant | 0.19 |
ccsA | 620710 | p.Val274Ile | missense_variant | 0.19 |
ccsA | 620721 | c.831G>C | synonymous_variant | 0.19 |
ccsA | 620734 | c.844C>A | synonymous_variant | 0.16 |
ccsA | 620758 | p.Arg290Ser | missense_variant | 0.15 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 760307 | c.501T>G | synonymous_variant | 0.17 |
rpoB | 760310 | c.504G>C | synonymous_variant | 0.17 |
rpoB | 760313 | c.507G>C | synonymous_variant | 0.19 |
rpoB | 760340 | c.534G>C | synonymous_variant | 0.18 |
rpoB | 760343 | c.537G>C | synonymous_variant | 0.19 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.18 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.18 |
rpoB | 760380 | p.Thr192Leu | missense_variant | 0.18 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.17 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.19 |
rpoB | 760481 | c.675G>C | synonymous_variant | 0.19 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.2 |
rpoB | 760522 | p.Ser239Asn | missense_variant | 0.26 |
rpoB | 760532 | c.726T>C | synonymous_variant | 0.25 |
rpoB | 760533 | p.Val243His | missense_variant | 0.25 |
rpoB | 760547 | c.741G>C | synonymous_variant | 0.27 |
rpoB | 760561 | c.757_758delCG | frameshift_variant | 0.2 |
rpoB | 760567 | p.Ser254Trp | missense_variant | 0.21 |
rpoB | 760568 | c.762_763insGC | frameshift_variant | 0.21 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.24 |
rpoB | 760611 | c.805T>C | synonymous_variant | 0.25 |
rpoB | 760634 | c.828T>C | synonymous_variant | 0.26 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.26 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.24 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.26 |
rpoB | 760670 | c.864G>C | synonymous_variant | 0.25 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.26 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.28 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.29 |
rpoB | 760724 | c.918T>C | synonymous_variant | 0.31 |
rpoB | 760730 | c.924T>C | synonymous_variant | 0.3 |
rpoB | 760748 | c.942C>G | synonymous_variant | 0.25 |
rpoB | 760751 | c.945G>C | synonymous_variant | 0.23 |
rpoB | 760757 | c.951T>C | synonymous_variant | 0.21 |
rpoB | 760759 | p.Val318Ala | missense_variant | 0.21 |
rpoB | 760769 | c.963C>G | synonymous_variant | 0.18 |
rpoB | 760781 | c.975G>C | synonymous_variant | 0.17 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.16 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.21 |
rpoB | 761018 | c.1212G>A | synonymous_variant | 0.2 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.19 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.19 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.19 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.2 |
rpoB | 761097 | p.Ser431Cys | missense_variant | 0.16 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 0.16 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.22 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.22 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.24 |
rpoB | 761273 | c.1467T>C | synonymous_variant | 0.24 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.25 |
rpoB | 761345 | c.1539G>C | synonymous_variant | 0.21 |
rpoB | 761354 | c.1548C>T | synonymous_variant | 0.26 |
rpoB | 761360 | c.1554T>C | synonymous_variant | 0.2 |
rpoB | 761362 | p.Ser519Thr | missense_variant | 0.2 |
rpoB | 761373 | p.Val523His | missense_variant | 0.18 |
rpoB | 761408 | c.1602G>C | synonymous_variant | 0.25 |
rpoB | 761414 | c.1608A>G | synonymous_variant | 0.24 |
rpoB | 761423 | c.1617T>C | synonymous_variant | 0.25 |
rpoB | 761435 | c.1629T>C | synonymous_variant | 0.25 |
rpoB | 761439 | p.Asp545Ser | missense_variant | 0.24 |
rpoB | 761444 | c.1638T>C | synonymous_variant | 0.25 |
rpoB | 761447 | c.1641C>G | synonymous_variant | 0.24 |
rpoB | 761452 | p.Val549Glu | missense_variant | 0.24 |
rpoB | 761457 | p.Pro551Ser | missense_variant | 0.24 |
rpoB | 761477 | c.1671C>G | synonymous_variant | 0.24 |
rpoB | 761483 | c.1677G>C | synonymous_variant | 0.25 |
rpoB | 761492 | c.1686G>C | synonymous_variant | 0.26 |
rpoB | 761504 | c.1698C>G | synonymous_variant | 0.26 |
rpoB | 761510 | c.1704T>C | synonymous_variant | 0.28 |
rpoB | 761531 | c.1725C>G | synonymous_variant | 0.29 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.26 |
rpoB | 761564 | c.1758G>C | synonymous_variant | 0.29 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.29 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.3 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.34 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.34 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.32 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.32 |
rpoB | 761636 | c.1830G>C | synonymous_variant | 0.31 |
rpoB | 761645 | c.1839C>G | synonymous_variant | 0.28 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.29 |
rpoB | 761657 | c.1851C>G | synonymous_variant | 0.27 |
rpoB | 761675 | c.1869G>C | synonymous_variant | 0.24 |
rpoB | 761682 | c.1876C>T | synonymous_variant | 0.21 |
rpoB | 761690 | c.1884G>C | synonymous_variant | 0.24 |
rpoB | 761705 | c.1899C>T | synonymous_variant | 0.16 |
rpoB | 761765 | c.1959T>C | synonymous_variant | 0.18 |
rpoB | 761772 | p.His656Ala | missense_variant | 0.17 |
rpoB | 761778 | p.Asn658Asp | missense_variant | 0.17 |
rpoB | 761791 | p.Arg662His | missense_variant | 0.16 |
rpoB | 761815 | p.Ala670Asp | missense_variant | 0.15 |
rpoB | 761834 | c.2028T>G | synonymous_variant | 0.16 |
rpoB | 761873 | c.2067A>G | synonymous_variant | 0.22 |
rpoB | 761885 | c.2079T>C | synonymous_variant | 0.22 |
rpoB | 761891 | c.2085G>C | synonymous_variant | 0.22 |
rpoB | 761906 | c.2100C>G | synonymous_variant | 0.27 |
rpoB | 761909 | c.2103T>C | synonymous_variant | 0.25 |
rpoB | 761912 | c.2106T>C | synonymous_variant | 0.24 |
rpoB | 761915 | p.Asp703Glu | missense_variant | 0.25 |
rpoB | 761916 | p.Asp704Asn | missense_variant | 0.25 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.24 |
rpoB | 761954 | c.2148C>G | synonymous_variant | 0.23 |
rpoB | 761999 | c.2193G>C | synonymous_variant | 0.25 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.29 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.4 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.47 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.49 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.48 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.48 |
rpoB | 762122 | c.2316C>T | synonymous_variant | 0.47 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 0.51 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.51 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.51 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.51 |
rpoB | 762158 | c.2352G>C | synonymous_variant | 0.49 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.51 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.52 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.5 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.37 |
rpoB | 762254 | c.2448T>G | synonymous_variant | 0.36 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.34 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.36 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.3 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.27 |
rpoB | 762329 | c.2523G>C | synonymous_variant | 0.28 |
rpoB | 762338 | c.2532T>C | synonymous_variant | 0.26 |
rpoB | 762347 | c.2541T>C | synonymous_variant | 0.28 |
rpoB | 762362 | p.Glu852Asp | missense_variant | 0.27 |
rpoB | 762369 | c.2563T>C | synonymous_variant | 0.28 |
rpoC | 762389 | c.-981G>A | upstream_gene_variant | 0.24 |
rpoC | 762395 | c.-975G>C | upstream_gene_variant | 0.24 |
rpoC | 762398 | c.-972T>C | upstream_gene_variant | 0.23 |
rpoC | 762401 | c.-969G>C | upstream_gene_variant | 0.23 |
rpoC | 762404 | c.-966T>C | upstream_gene_variant | 0.23 |
rpoC | 762410 | c.-960T>C | upstream_gene_variant | 0.24 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 0.25 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 762446 | c.-924C>G | upstream_gene_variant | 0.22 |
rpoB | 762490 | p.Val895Asp | missense_variant | 0.16 |
rpoC | 762749 | c.-621C>G | upstream_gene_variant | 0.18 |
rpoC | 762753 | c.-617T>C | upstream_gene_variant | 0.19 |
rpoC | 762758 | c.-612G>C | upstream_gene_variant | 0.18 |
rpoC | 762776 | c.-594C>G | upstream_gene_variant | 0.22 |
rpoB | 762780 | p.Gly992Asn | missense_variant | 0.22 |
rpoB | 762785 | p.Asp993Glu | missense_variant | 0.22 |
rpoB | 762789 | p.Leu995Met | missense_variant | 0.24 |
rpoB | 762799 | p.Ala998Gly | missense_variant | 0.24 |
rpoC | 762812 | c.-558C>G | upstream_gene_variant | 0.27 |
rpoB | 762813 | p.Met1003Val | missense_variant | 0.26 |
rpoC | 762818 | c.-552C>G | upstream_gene_variant | 0.27 |
rpoC | 762827 | c.-543G>C | upstream_gene_variant | 0.28 |
rpoC | 762836 | c.-534C>T | upstream_gene_variant | 0.27 |
rpoC | 762857 | c.-513C>G | upstream_gene_variant | 0.24 |
rpoC | 762860 | c.-510G>C | upstream_gene_variant | 0.25 |
rpoC | 762863 | c.-507T>C | upstream_gene_variant | 0.28 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.21 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.17 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.16 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.18 |
rpoC | 763049 | c.-321G>A | upstream_gene_variant | 0.2 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.2 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.2 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.23 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.25 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.25 |
rpoC | 763169 | c.-201A>G | upstream_gene_variant | 0.24 |
rpoC | 763187 | c.-183C>G | upstream_gene_variant | 0.23 |
rpoC | 763202 | c.-168A>C | upstream_gene_variant | 0.19 |
rpoC | 763206 | c.-164_-162delAGTinsTCG | upstream_gene_variant | 0.19 |
rpoC | 763214 | c.-156T>C | upstream_gene_variant | 0.18 |
rpoC | 763227 | c.-143C>T | upstream_gene_variant | 0.19 |
rpoC | 763402 | c.33C>T | synonymous_variant | 0.22 |
rpoC | 763408 | c.39T>C | synonymous_variant | 0.22 |
rpoC | 763411 | c.42T>G | synonymous_variant | 0.24 |
rpoC | 763414 | c.45T>C | synonymous_variant | 0.23 |
rpoC | 763426 | c.57C>T | synonymous_variant | 0.25 |
rpoC | 763441 | c.72C>T | synonymous_variant | 0.29 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.3 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.3 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.29 |
rpoC | 763504 | c.135C>G | synonymous_variant | 0.24 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.22 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.21 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.19 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.19 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.2 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.19 |
rpoC | 763636 | c.267T>G | synonymous_variant | 0.18 |
rpoC | 763657 | c.288G>A | synonymous_variant | 0.17 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.18 |
rpoC | 763666 | c.297G>C | synonymous_variant | 0.18 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.19 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.16 |
rpoC | 763729 | c.360G>C | synonymous_variant | 0.17 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.15 |
rpoC | 763792 | p.Glu141Asp | missense_variant | 0.18 |
rpoC | 763801 | c.432C>G | synonymous_variant | 0.19 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.2 |
rpoC | 763813 | c.444C>G | synonymous_variant | 0.18 |
rpoC | 763835 | p.Ala156Met | missense_variant | 0.19 |
rpoC | 763855 | c.486C>T | synonymous_variant | 0.18 |
rpoC | 763858 | c.489A>G | synonymous_variant | 0.17 |
rpoC | 763996 | c.627T>G | synonymous_variant | 0.16 |
rpoC | 764011 | c.642T>C | synonymous_variant | 0.16 |
rpoC | 764040 | p.Ser224Asn | missense_variant | 0.17 |
rpoC | 764044 | c.675T>C | synonymous_variant | 0.18 |
rpoC | 764059 | c.690G>C | synonymous_variant | 0.18 |
rpoC | 764083 | c.714A>G | synonymous_variant | 0.17 |
rpoC | 764098 | c.729A>G | synonymous_variant | 0.17 |
rpoC | 764110 | c.741C>T | synonymous_variant | 0.18 |
rpoC | 764188 | c.819A>G | synonymous_variant | 0.2 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.15 |
rpoC | 764381 | p.Ser338Thr | missense_variant | 0.15 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.2 |
rpoC | 764410 | c.1041G>C | synonymous_variant | 0.21 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.23 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.22 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.18 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.18 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.2 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.21 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.22 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.22 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.23 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.2 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.21 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.22 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.19 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 0.19 |
rpoC | 764585 | c.1216_1218delCTCinsTTG | synonymous_variant | 0.2 |
rpoC | 764611 | c.1242G>C | synonymous_variant | 0.2 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.19 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.19 |
rpoC | 764644 | c.1275G>C | synonymous_variant | 0.23 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.24 |
rpoC | 764695 | c.1326T>G | synonymous_variant | 0.26 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.26 |
rpoC | 764749 | c.1380G>C | synonymous_variant | 0.29 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.27 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.29 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.21 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 0.17 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.17 |
rpoC | 764830 | c.1461C>G | synonymous_variant | 0.19 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.23 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.2 |
rpoC | 764893 | c.1524T>C | synonymous_variant | 0.2 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.17 |
rpoC | 764923 | c.1554A>G | synonymous_variant | 0.2 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.22 |
rpoC | 764962 | c.1593G>C | synonymous_variant | 0.24 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.22 |
rpoC | 764983 | c.1614T>C | synonymous_variant | 0.2 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.23 |
rpoC | 765007 | c.1638T>G | synonymous_variant | 0.2 |
rpoC | 765008 | c.1639T>C | synonymous_variant | 0.19 |
rpoC | 765016 | c.1647C>G | synonymous_variant | 0.19 |
rpoC | 765019 | c.1650A>G | synonymous_variant | 0.19 |
rpoC | 765034 | c.1665T>G | synonymous_variant | 0.17 |
rpoC | 765040 | c.1671T>C | synonymous_variant | 0.17 |
rpoC | 765053 | p.Ser562Thr | missense_variant | 0.16 |
rpoC | 765103 | c.1734G>T | synonymous_variant | 0.15 |
rpoC | 765349 | c.1980T>C | synonymous_variant | 0.15 |
rpoC | 765352 | c.1983G>C | synonymous_variant | 0.16 |
rpoC | 765364 | p.Glu665Asp | missense_variant | 0.21 |
rpoC | 765383 | p.Met672Leu | missense_variant | 0.2 |
rpoC | 765394 | c.2025G>A | synonymous_variant | 0.23 |
rpoC | 765404 | p.Leu679Val | missense_variant | 0.2 |
rpoC | 765409 | c.2040T>C | synonymous_variant | 0.19 |
rpoC | 765412 | c.2043T>C | synonymous_variant | 0.18 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.19 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.28 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.29 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.26 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.29 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.31 |
rpoC | 765559 | c.2190G>C | synonymous_variant | 0.31 |
rpoC | 765583 | c.2214G>T | synonymous_variant | 0.34 |
rpoC | 765625 | c.2256C>G | synonymous_variant | 0.27 |
rpoC | 765631 | p.Asp754Glu | missense_variant | 0.26 |
rpoC | 765658 | c.2289C>T | synonymous_variant | 0.25 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.27 |
rpoC | 765734 | c.2365T>C | synonymous_variant | 0.24 |
rpoC | 765739 | c.2370G>C | synonymous_variant | 0.25 |
rpoC | 765751 | c.2382C>G | synonymous_variant | 0.25 |
rpoC | 765752 | p.Asp795Ser | missense_variant | 0.26 |
rpoC | 765772 | c.2403C>G | synonymous_variant | 0.26 |
rpoC | 765784 | c.2415C>G | synonymous_variant | 0.28 |
rpoC | 765796 | c.2427C>T | synonymous_variant | 0.31 |
rpoC | 765811 | c.2442T>C | synonymous_variant | 0.29 |
rpoC | 765814 | c.2445A>G | synonymous_variant | 0.29 |
rpoC | 765826 | c.2457T>C | synonymous_variant | 0.29 |
rpoC | 765883 | c.2514C>G | synonymous_variant | 0.24 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.25 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.25 |
rpoC | 765899 | c.2530C>T | synonymous_variant | 0.24 |
rpoC | 765928 | c.2559C>G | synonymous_variant | 0.23 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.25 |
rpoC | 765947 | c.2578T>C | synonymous_variant | 0.22 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.22 |
rpoC | 765979 | c.2610C>G | synonymous_variant | 0.22 |
rpoC | 765982 | c.2613C>T | synonymous_variant | 0.22 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.21 |
rpoC | 766010 | c.2641_2642delTCinsAG | synonymous_variant | 0.23 |
rpoC | 766021 | c.2652G>C | synonymous_variant | 0.23 |
rpoC | 766027 | c.2658G>C | synonymous_variant | 0.24 |
rpoC | 766043 | p.Gln892Glu | missense_variant | 0.22 |
rpoC | 766061 | p.Val898Leu | missense_variant | 0.2 |
rpoC | 766083 | p.Ala905Glu | missense_variant | 0.15 |
rpoC | 766300 | c.2931C>G | synonymous_variant | 0.16 |
rpoC | 766321 | c.2952C>G | synonymous_variant | 0.17 |
rpoC | 766345 | c.2976T>C | synonymous_variant | 0.24 |
rpoC | 766348 | c.2979A>G | synonymous_variant | 0.24 |
rpoC | 766357 | c.2988C>T | synonymous_variant | 0.27 |
rpoC | 766363 | c.2994G>C | synonymous_variant | 0.27 |
rpoC | 766369 | c.3000C>G | synonymous_variant | 0.29 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.29 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.29 |
rpoC | 766387 | c.3018C>G | synonymous_variant | 0.29 |
rpoC | 766393 | c.3024C>G | synonymous_variant | 0.3 |
rpoC | 766402 | c.3033C>G | synonymous_variant | 0.33 |
rpoC | 766408 | c.3039C>T | synonymous_variant | 0.33 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.36 |
rpoC | 766447 | c.3078T>C | synonymous_variant | 0.33 |
rpoC | 766456 | c.3087C>G | synonymous_variant | 0.3 |
rpoC | 766471 | c.3102G>C | synonymous_variant | 0.33 |
rpoC | 766486 | c.3117A>G | synonymous_variant | 0.34 |
rpoC | 766492 | c.3123T>C | synonymous_variant | 0.32 |
rpoC | 766522 | c.3153C>G | synonymous_variant | 0.29 |
rpoC | 766528 | c.3159T>C | synonymous_variant | 0.28 |
rpoC | 766530 | p.Arg1054Gln | missense_variant | 0.28 |
rpoC | 766573 | c.3204T>C | synonymous_variant | 0.24 |
rpoC | 766582 | c.3213C>G | synonymous_variant | 0.22 |
rpoC | 766583 | p.Gly1072Ser | missense_variant | 0.22 |
rpoC | 766591 | c.3222A>G | synonymous_variant | 0.22 |
rpoC | 766594 | c.3225G>C | synonymous_variant | 0.22 |
rpoC | 766607 | p.Ile1080Leu | missense_variant | 0.24 |
rpoC | 766630 | c.3261G>T | synonymous_variant | 0.25 |
rpoC | 766633 | c.3264G>C | synonymous_variant | 0.26 |
rpoC | 766645 | c.3276A>G | synonymous_variant | 0.29 |
rpoC | 766651 | c.3282T>G | synonymous_variant | 0.27 |
rpoC | 766657 | c.3288A>G | synonymous_variant | 0.27 |
rpoC | 766666 | c.3297C>G | synonymous_variant | 0.29 |
rpoC | 766672 | c.3303T>C | synonymous_variant | 0.27 |
rpoC | 766708 | c.3339A>G | synonymous_variant | 0.27 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.24 |
rpoC | 766738 | c.3369G>C | synonymous_variant | 0.25 |
rpoC | 766750 | c.3381C>G | synonymous_variant | 0.27 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.23 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.22 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.22 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 0.29 |
rpoC | 766864 | c.3495G>C | synonymous_variant | 0.3 |
rpoC | 766894 | c.3525T>C | synonymous_variant | 0.31 |
rpoC | 766895 | c.3526T>C | synonymous_variant | 0.31 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.3 |
rpoC | 766933 | c.3564A>G | synonymous_variant | 0.34 |
rpoC | 766942 | c.3573C>T | synonymous_variant | 0.33 |
rpoC | 766945 | c.3576A>G | synonymous_variant | 0.33 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.32 |
rpoC | 766972 | c.3603G>C | synonymous_variant | 0.31 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.35 |
rpoC | 767035 | c.3666G>C | synonymous_variant | 0.33 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.31 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.31 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.26 |
rpoC | 767110 | c.3741T>C | synonymous_variant | 0.26 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.27 |
rpoC | 767134 | c.3765C>A | synonymous_variant | 0.21 |
rpoC | 767152 | c.3783T>G | synonymous_variant | 0.2 |
rpoC | 767158 | c.3789T>C | synonymous_variant | 0.17 |
rpoC | 767167 | c.3798C>G | synonymous_variant | 0.16 |
rpoC | 767181 | p.Ala1271Glu | missense_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775909 | p.Leu858Phe | missense_variant | 0.15 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776181 | p.Asp767Ala | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781568 | c.9C>G | synonymous_variant | 0.16 |
rpsL | 781571 | c.12C>T | synonymous_variant | 0.16 |
rpsL | 781595 | c.36T>C | synonymous_variant | 0.22 |
rpsL | 781598 | c.39G>C | synonymous_variant | 0.22 |
rpsL | 781608 | p.Ser17Ala | missense_variant | 0.21 |
rpsL | 781628 | c.69T>C | synonymous_variant | 0.27 |
rpsL | 781649 | c.90T>C | synonymous_variant | 0.28 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.27 |
rpsL | 781658 | c.99A>G | synonymous_variant | 0.28 |
rpsL | 781682 | c.123T>C | synonymous_variant | 0.28 |
rpsL | 781703 | c.144G>T | synonymous_variant | 0.28 |
rpsL | 781706 | c.147T>G | synonymous_variant | 0.29 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.24 |
rpsL | 781718 | c.159C>G | synonymous_variant | 0.23 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.2 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.21 |
rpsL | 781751 | c.192G>C | synonymous_variant | 0.23 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.23 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.24 |
rpsL | 781763 | c.204C>G | synonymous_variant | 0.25 |
rpsL | 781772 | c.213C>T | synonymous_variant | 0.25 |
rpsL | 781808 | c.249C>T | synonymous_variant | 0.27 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.26 |
rpsL | 781820 | c.261G>C | synonymous_variant | 0.25 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.24 |
rpsL | 781835 | c.276T>C | synonymous_variant | 0.25 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.28 |
rpsL | 781865 | c.306G>C | synonymous_variant | 0.24 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.24 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.24 |
rpsL | 781877 | c.318T>G | synonymous_variant | 0.23 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.22 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.24 |
rpsL | 781916 | c.357T>C | synonymous_variant | 0.24 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.23 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.21 |
rplC | 800648 | c.-161A>T | upstream_gene_variant | 0.27 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.27 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.26 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.24 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.24 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.22 |
rplC | 800738 | c.-71T>C | upstream_gene_variant | 0.21 |
rplC | 800747 | c.-62C>G | upstream_gene_variant | 0.2 |
rplC | 800771 | c.-38C>T | upstream_gene_variant | 0.14 |
rplC | 800937 | c.129A>G | synonymous_variant | 0.17 |
rplC | 800946 | c.138T>C | synonymous_variant | 0.17 |
rplC | 800949 | c.141T>C | synonymous_variant | 0.17 |
fbiC | 1303812 | c.882C>T | synonymous_variant | 0.15 |
fbiC | 1303842 | c.912C>T | synonymous_variant | 0.15 |
fbiC | 1303855 | p.Ala309Thr | missense_variant | 0.15 |
fbiC | 1303869 | c.939T>C | synonymous_variant | 0.16 |
fbiC | 1303881 | c.951G>C | synonymous_variant | 0.17 |
fbiC | 1303884 | c.954T>G | synonymous_variant | 0.19 |
fbiC | 1303887 | c.957G>C | synonymous_variant | 0.19 |
fbiC | 1303897 | c.967C>T | synonymous_variant | 0.2 |
fbiC | 1303905 | c.975G>C | synonymous_variant | 0.18 |
fbiC | 1303908 | c.978C>G | synonymous_variant | 0.19 |
fbiC | 1303938 | c.1008C>T | synonymous_variant | 0.14 |
fbiC | 1304481 | c.1551T>G | synonymous_variant | 0.18 |
fbiC | 1304484 | c.1554C>G | synonymous_variant | 0.2 |
fbiC | 1304493 | p.Asp521Glu | missense_variant | 0.24 |
fbiC | 1304496 | c.1566T>G | synonymous_variant | 0.23 |
fbiC | 1304499 | c.1569T>C | synonymous_variant | 0.23 |
fbiC | 1304520 | c.1590A>G | synonymous_variant | 0.25 |
fbiC | 1304526 | c.1596T>G | synonymous_variant | 0.24 |
fbiC | 1304530 | p.Ser534Ala | missense_variant | 0.25 |
fbiC | 1304533 | c.1603T>C | synonymous_variant | 0.24 |
fbiC | 1304538 | c.1608C>G | synonymous_variant | 0.24 |
fbiC | 1304544 | c.1614T>C | synonymous_variant | 0.22 |
fbiC | 1304546 | p.Val539Ala | missense_variant | 0.22 |
fbiC | 1304559 | p.Glu543Asp | missense_variant | 0.23 |
fbiC | 1304565 | c.1635C>G | synonymous_variant | 0.24 |
fbiC | 1304568 | c.1638T>C | synonymous_variant | 0.24 |
fbiC | 1304580 | c.1650T>C | synonymous_variant | 0.27 |
fbiC | 1304604 | c.1674C>T | synonymous_variant | 0.24 |
fbiC | 1304634 | c.1704C>G | synonymous_variant | 0.17 |
fbiC | 1304817 | c.1887T>C | synonymous_variant | 0.16 |
fbiC | 1304856 | c.1926C>G | synonymous_variant | 0.17 |
fbiC | 1304875 | p.Ile649Val | missense_variant | 0.18 |
fbiC | 1304916 | c.1986T>C | synonymous_variant | 0.28 |
fbiC | 1304928 | c.1998T>C | synonymous_variant | 0.24 |
fbiC | 1304931 | c.2001C>G | synonymous_variant | 0.24 |
fbiC | 1304937 | c.2007G>C | synonymous_variant | 0.23 |
fbiC | 1304940 | c.2010A>G | synonymous_variant | 0.25 |
fbiC | 1304955 | c.2025G>A | synonymous_variant | 0.23 |
fbiC | 1304958 | c.2028T>G | synonymous_variant | 0.23 |
fbiC | 1304991 | c.2061G>A | synonymous_variant | 0.21 |
fbiC | 1304994 | c.2064A>G | synonymous_variant | 0.21 |
fbiC | 1304995 | p.Leu689Glu | missense_variant | 0.21 |
fbiC | 1305006 | p.Glu692Asp | missense_variant | 0.24 |
fbiC | 1305015 | c.2085G>C | synonymous_variant | 0.24 |
fbiC | 1305021 | c.2091C>A | synonymous_variant | 0.25 |
fbiC | 1305033 | c.2103T>G | synonymous_variant | 0.24 |
fbiC | 1305042 | c.2112A>G | synonymous_variant | 0.23 |
fbiC | 1305045 | c.2115A>G | synonymous_variant | 0.24 |
fbiC | 1305066 | c.2136T>C | synonymous_variant | 0.24 |
fbiC | 1305069 | c.2139G>C | synonymous_variant | 0.24 |
fbiC | 1305075 | c.2145T>C | synonymous_variant | 0.23 |
fbiC | 1305093 | c.2163C>G | synonymous_variant | 0.2 |
fbiC | 1305096 | c.2166T>C | synonymous_variant | 0.2 |
fbiC | 1305099 | c.2169T>C | synonymous_variant | 0.2 |
fbiC | 1305113 | p.Asp728Gly | missense_variant | 0.17 |
fbiC | 1305117 | c.2187T>C | synonymous_variant | 0.17 |
fbiC | 1305126 | c.2196T>C | synonymous_variant | 0.16 |
fbiC | 1305331 | p.Glu801Lys | missense_variant | 0.14 |
fbiC | 1305348 | c.2418C>T | synonymous_variant | 0.2 |
atpE | 1460855 | c.-190T>C | upstream_gene_variant | 0.2 |
atpE | 1460858 | c.-187C>G | upstream_gene_variant | 0.2 |
atpE | 1460861 | c.-184C>G | upstream_gene_variant | 0.2 |
atpE | 1460879 | c.-166C>G | upstream_gene_variant | 0.2 |
atpE | 1460882 | c.-163T>C | upstream_gene_variant | 0.19 |
atpE | 1461132 | p.Val30Ile | missense_variant | 0.15 |
atpE | 1461150 | p.Ile36Val | missense_variant | 0.16 |
atpE | 1461159 | p.Val39Ile | missense_variant | 0.16 |
atpE | 1461197 | c.153A>G | synonymous_variant | 0.17 |
atpE | 1461219 | c.175T>C | synonymous_variant | 0.22 |
atpE | 1461224 | c.180T>C | synonymous_variant | 0.2 |
atpE | 1461233 | c.189A>C | synonymous_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473937 | n.280C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473944 | n.287G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474009 | n.352A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474012 | n.355C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474051 | n.394T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474054 | n.397T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474071 | n.414G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474099 | n.442G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474627 | n.970G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474717 | n.1060A>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474991 | n.1334T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474995 | n.1338T>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475005 | n.1348C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475013 | n.1356G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475027 | n.1370G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475028 | n.1371G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475088 | n.1431A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475249 | n.1592T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475252 | n.1595C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475266 | n.1609T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475275 | n.1618C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475276 | n.1619T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475291 | n.1634A>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475369 | n.1712G>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475387 | n.1730C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475402 | n.1745C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475436 | n.1779C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475603 | n.1946G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476035 | n.2378G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.17 |
inhA | 1673799 | c.-403T>C | upstream_gene_variant | 0.2 |
inhA | 1673802 | c.-400A>G | upstream_gene_variant | 0.19 |
inhA | 1673808 | c.-394A>G | upstream_gene_variant | 0.19 |
inhA | 1673838 | c.-364T>C | upstream_gene_variant | 0.15 |
inhA | 1673841 | c.-361A>C | upstream_gene_variant | 0.15 |
fabG1 | 1673844 | p.Met135Ile | missense_variant | 0.16 |
inhA | 1673856 | c.-346T>G | upstream_gene_variant | 0.15 |
fabG1 | 1673870 | p.Ser144Ile | missense_variant | 0.14 |
inhA | 1673901 | c.-301A>G | upstream_gene_variant | 0.21 |
fabG1 | 1673905 | p.Ser156Ala | missense_variant | 0.21 |
inhA | 1673916 | c.-286A>C | upstream_gene_variant | 0.17 |
fabG1 | 1673917 | p.Val160Leu | missense_variant | 0.17 |
inhA | 1673922 | c.-280T>C | upstream_gene_variant | 0.16 |
inhA | 1673988 | c.-214G>C | upstream_gene_variant | 0.16 |
fabG1 | 1674006 | p.Asp189Glu | missense_variant | 0.17 |
inhA | 1674399 | c.198A>G | synonymous_variant | 0.15 |
inhA | 1674450 | c.249G>T | synonymous_variant | 0.14 |
inhA | 1674471 | c.270G>C | synonymous_variant | 0.16 |
inhA | 1674483 | c.282G>C | synonymous_variant | 0.17 |
inhA | 1674507 | c.306G>C | synonymous_variant | 0.19 |
inhA | 1674542 | p.Ala114Glu | missense_variant | 0.23 |
inhA | 1674546 | c.345T>C | synonymous_variant | 0.22 |
inhA | 1674549 | c.348G>C | synonymous_variant | 0.2 |
inhA | 1674576 | c.375T>C | synonymous_variant | 0.22 |
inhA | 1674582 | c.381T>C | synonymous_variant | 0.25 |
inhA | 1674585 | c.384T>C | synonymous_variant | 0.25 |
inhA | 1674589 | p.Met130Leu | missense_variant | 0.24 |
inhA | 1674624 | c.423A>C | synonymous_variant | 0.25 |
inhA | 1674627 | c.426T>G | synonymous_variant | 0.25 |
inhA | 1674639 | c.438C>G | synonymous_variant | 0.26 |
inhA | 1674654 | c.453G>C | synonymous_variant | 0.23 |
inhA | 1674660 | c.459G>C | synonymous_variant | 0.23 |
inhA | 1674663 | c.462G>C | synonymous_variant | 0.23 |
inhA | 1674669 | c.468G>C | synonymous_variant | 0.24 |
inhA | 1674690 | c.489C>G | synonymous_variant | 0.2 |
inhA | 1674703 | c.502T>C | synonymous_variant | 0.21 |
inhA | 1674708 | c.507G>A | synonymous_variant | 0.22 |
inhA | 1674718 | c.517A>C | synonymous_variant | 0.22 |
inhA | 1674726 | c.525G>C | synonymous_variant | 0.22 |
inhA | 1674729 | c.528G>C | synonymous_variant | 0.23 |
inhA | 1674750 | c.549T>G | synonymous_variant | 0.25 |
inhA | 1674759 | c.558G>C | synonymous_variant | 0.22 |
inhA | 1674771 | c.570C>G | synonymous_variant | 0.23 |
inhA | 1674774 | c.573A>G | synonymous_variant | 0.23 |
inhA | 1674780 | c.579T>C | synonymous_variant | 0.22 |
inhA | 1674783 | c.582C>T | synonymous_variant | 0.23 |
inhA | 1674790 | c.589C>T | synonymous_variant | 0.23 |
inhA | 1674799 | c.598_600delAGTinsTCG | synonymous_variant | 0.22 |
inhA | 1674846 | p.Ile215Met | missense_variant | 0.22 |
inhA | 1674858 | c.657G>A | synonymous_variant | 0.2 |
inhA | 1674870 | c.669T>C | synonymous_variant | 0.21 |
inhA | 1674879 | c.678T>G | synonymous_variant | 0.21 |
inhA | 1674924 | c.723G>A | synonymous_variant | 0.15 |
rpsA | 1833589 | c.48A>T | synonymous_variant | 0.14 |
rpsA | 1833604 | c.63C>T | synonymous_variant | 0.16 |
rpsA | 1833610 | c.69C>T | synonymous_variant | 0.2 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.24 |
rpsA | 1833664 | c.123C>G | synonymous_variant | 0.23 |
rpsA | 1833667 | c.126C>G | synonymous_variant | 0.24 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.32 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.31 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.32 |
rpsA | 1833760 | c.219C>T | synonymous_variant | 0.31 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.24 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.24 |
rpsA | 1833793 | c.252C>T | synonymous_variant | 0.24 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.24 |
rpsA | 1833805 | c.264C>T | synonymous_variant | 0.23 |
rpsA | 1833808 | c.267G>C | synonymous_variant | 0.23 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 0.23 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.23 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.22 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.2 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.18 |
rpsA | 1833895 | c.354G>C | synonymous_variant | 0.17 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.21 |
rpsA | 1833940 | c.399C>G | synonymous_variant | 0.21 |
rpsA | 1833949 | c.408T>G | synonymous_variant | 0.22 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.21 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.22 |
rpsA | 1833991 | c.450C>G | synonymous_variant | 0.19 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.22 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.21 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.21 |
rpsA | 1834099 | c.558C>G | synonymous_variant | 0.18 |
rpsA | 1834102 | c.561T>G | synonymous_variant | 0.17 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.19 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.18 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.17 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.23 |
rpsA | 1834303 | c.762T>G | synonymous_variant | 0.25 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.27 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.29 |
rpsA | 1834351 | c.810G>A | synonymous_variant | 0.3 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.26 |
rpsA | 1834375 | c.834G>A | synonymous_variant | 0.27 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.28 |
rpsA | 1834411 | c.870T>G | synonymous_variant | 0.33 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.31 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.3 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.27 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.24 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.24 |
rpsA | 1834459 | c.918G>C | synonymous_variant | 0.24 |
rpsA | 1834465 | c.924T>C | synonymous_variant | 0.22 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.24 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.24 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.27 |
rpsA | 1834540 | c.999G>C | synonymous_variant | 0.3 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.29 |
rpsA | 1834555 | c.1014T>C | synonymous_variant | 0.28 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.42 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.4 |
rpsA | 1834636 | c.1095C>G | synonymous_variant | 0.43 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.43 |
rpsA | 1834690 | c.1149T>C | synonymous_variant | 0.37 |
rpsA | 1834732 | c.1191T>C | synonymous_variant | 0.26 |
rpsA | 1834738 | c.1197A>G | synonymous_variant | 0.23 |
rpsA | 1834753 | c.1212T>C | synonymous_variant | 0.18 |
rpsA | 1834759 | c.1218A>G | synonymous_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
kasA | 2517941 | c.-174C>G | upstream_gene_variant | 0.18 |
kasA | 2518439 | p.Ala109Ser | missense_variant | 0.14 |
kasA | 2518480 | c.366T>C | synonymous_variant | 0.18 |
kasA | 2518504 | c.390T>C | synonymous_variant | 0.22 |
kasA | 2518506 | p.Ala131Glu | missense_variant | 0.22 |
kasA | 2518519 | c.405G>C | synonymous_variant | 0.22 |
kasA | 2518528 | c.414C>G | synonymous_variant | 0.21 |
kasA | 2518534 | c.420G>C | synonymous_variant | 0.21 |
kasA | 2518561 | c.447T>C | synonymous_variant | 0.23 |
kasA | 2518570 | c.456G>C | synonymous_variant | 0.22 |
kasA | 2518574 | p.Ile154Val | missense_variant | 0.23 |
kasA | 2518579 | c.465T>C | synonymous_variant | 0.23 |
kasA | 2518588 | c.474T>C | synonymous_variant | 0.24 |
kasA | 2518594 | c.480C>G | synonymous_variant | 0.26 |
kasA | 2518597 | c.483C>G | synonymous_variant | 0.26 |
kasA | 2518609 | p.Met165Ile | missense_variant | 0.26 |
kasA | 2518639 | c.525G>C | synonymous_variant | 0.28 |
kasA | 2518657 | c.543G>C | synonymous_variant | 0.24 |
kasA | 2518663 | c.549T>C | synonymous_variant | 0.24 |
kasA | 2518672 | c.558G>C | synonymous_variant | 0.27 |
kasA | 2518678 | c.564C>T | synonymous_variant | 0.27 |
kasA | 2518684 | c.570C>G | synonymous_variant | 0.27 |
kasA | 2518702 | c.588C>T | synonymous_variant | 0.23 |
kasA | 2518705 | c.591T>C | synonymous_variant | 0.23 |
kasA | 2518711 | c.597A>G | synonymous_variant | 0.22 |
kasA | 2518714 | c.600A>C | synonymous_variant | 0.19 |
kasA | 2518717 | c.603C>T | synonymous_variant | 0.2 |
kasA | 2518747 | c.633C>G | synonymous_variant | 0.2 |
kasA | 2518783 | c.669T>C | synonymous_variant | 0.18 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
folC | 2746999 | c.600T>C | synonymous_variant | 0.16 |
folC | 2747002 | c.597T>C | synonymous_variant | 0.16 |
folC | 2747007 | p.Ser198Gly | missense_variant | 0.18 |
folC | 2747010 | p.Ile197Val | missense_variant | 0.22 |
folC | 2747023 | c.576C>G | synonymous_variant | 0.25 |
folC | 2747026 | c.573C>G | synonymous_variant | 0.24 |
folC | 2747032 | c.567A>G | synonymous_variant | 0.23 |
folC | 2747040 | p.Ile187Val | missense_variant | 0.23 |
folC | 2747041 | c.558G>C | synonymous_variant | 0.23 |
folC | 2747053 | c.546C>T | synonymous_variant | 0.22 |
folC | 2747059 | c.540T>G | synonymous_variant | 0.21 |
folC | 2747062 | c.537A>C | synonymous_variant | 0.21 |
folC | 2747074 | c.525G>C | synonymous_variant | 0.22 |
folC | 2747083 | c.516G>C | synonymous_variant | 0.21 |
folC | 2747086 | c.513A>G | synonymous_variant | 0.19 |
folC | 2747089 | c.510G>C | synonymous_variant | 0.19 |
folC | 2747110 | c.489T>C | synonymous_variant | 0.18 |
folC | 2747113 | c.486C>G | synonymous_variant | 0.18 |
folC | 2747116 | c.483G>C | synonymous_variant | 0.17 |
pepQ | 2859873 | c.546T>C | synonymous_variant | 0.15 |
pepQ | 2859885 | c.534C>G | synonymous_variant | 0.18 |
pepQ | 2859908 | p.Gln171Glu | missense_variant | 0.21 |
pepQ | 2859909 | c.510G>C | synonymous_variant | 0.21 |
pepQ | 2859921 | c.498C>G | synonymous_variant | 0.22 |
pepQ | 2859924 | c.495G>C | synonymous_variant | 0.22 |
pepQ | 2859933 | c.486C>T | synonymous_variant | 0.23 |
pepQ | 2859939 | c.480C>G | synonymous_variant | 0.21 |
pepQ | 2859942 | p.Ala159Glu | missense_variant | 0.22 |
pepQ | 2859950 | c.469T>C | synonymous_variant | 0.2 |
pepQ | 2859956 | p.Thr155Ala | missense_variant | 0.21 |
pepQ | 2859957 | c.462G>C | synonymous_variant | 0.21 |
pepQ | 2859966 | c.453T>C | synonymous_variant | 0.22 |
pepQ | 2859972 | c.447A>G | synonymous_variant | 0.22 |
pepQ | 2859975 | c.444A>G | synonymous_variant | 0.21 |
pepQ | 2859984 | c.435A>G | synonymous_variant | 0.2 |
pepQ | 2859987 | c.432A>G | synonymous_variant | 0.17 |
Rv2752c | 3065866 | p.Leu109Trp | missense_variant | 0.87 |
thyX | 3067532 | c.414C>G | synonymous_variant | 0.17 |
thyX | 3067553 | c.393C>T | synonymous_variant | 0.17 |
thyX | 3067586 | c.360C>A | synonymous_variant | 0.16 |
thyX | 3067619 | c.327A>G | synonymous_variant | 0.18 |
thyX | 3067622 | c.324C>T | synonymous_variant | 0.19 |
thyX | 3067661 | c.285C>G | synonymous_variant | 0.27 |
thyX | 3067680 | p.Cys89Leu | missense_variant | 0.27 |
thyX | 3067685 | c.261A>C | synonymous_variant | 0.27 |
thyX | 3067688 | c.258G>C | synonymous_variant | 0.28 |
thyX | 3067694 | c.252G>C | synonymous_variant | 0.27 |
thyX | 3067718 | c.228C>G | synonymous_variant | 0.29 |
thyX | 3067721 | c.225T>C | synonymous_variant | 0.29 |
thyX | 3067727 | c.219A>C | synonymous_variant | 0.3 |
thyX | 3067733 | c.213G>C | synonymous_variant | 0.28 |
thyX | 3067742 | c.204A>G | synonymous_variant | 0.28 |
thyX | 3067745 | c.201C>G | synonymous_variant | 0.28 |
thyX | 3067761 | p.Arg62Lys | missense_variant | 0.27 |
thyX | 3067765 | p.Leu61Ile | missense_variant | 0.28 |
thyX | 3067781 | c.165C>G | synonymous_variant | 0.28 |
thyX | 3067784 | c.162C>G | synonymous_variant | 0.26 |
thyX | 3067790 | c.156C>G | synonymous_variant | 0.25 |
thyX | 3067793 | c.153T>C | synonymous_variant | 0.25 |
thyX | 3067796 | c.150C>G | synonymous_variant | 0.26 |
thyX | 3067823 | c.123G>C | synonymous_variant | 0.2 |
thyX | 3067826 | c.120C>G | synonymous_variant | 0.19 |
thyX | 3067839 | p.Val36Thr | missense_variant | 0.17 |
thyX | 3067841 | c.105G>C | synonymous_variant | 0.17 |
thyX | 3067850 | c.96A>C | synonymous_variant | 0.16 |
thyX | 3067853 | c.93C>T | synonymous_variant | 0.15 |
thyA | 3073892 | c.580T>C | synonymous_variant | 0.17 |
thyA | 3073896 | c.576C>G | synonymous_variant | 0.18 |
thyA | 3073929 | c.543T>C | synonymous_variant | 0.2 |
thyA | 3073959 | c.513T>C | synonymous_variant | 0.21 |
thyA | 3073977 | c.495A>G | synonymous_variant | 0.2 |
thyA | 3073980 | c.492C>T | synonymous_variant | 0.19 |
thyA | 3073983 | c.489C>G | synonymous_variant | 0.18 |
thyA | 3073989 | c.483T>C | synonymous_variant | 0.19 |
thyA | 3074004 | c.468T>C | synonymous_variant | 0.18 |
thyA | 3074010 | c.462C>G | synonymous_variant | 0.18 |
thyA | 3074031 | c.441T>C | synonymous_variant | 0.16 |
thyA | 3074037 | c.435C>G | synonymous_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474174 | c.168T>C | synonymous_variant | 0.15 |
fprA | 3474180 | c.174C>G | synonymous_variant | 0.17 |
fbiB | 3640914 | c.-621C>G | upstream_gene_variant | 0.16 |
fbiA | 3640930 | p.Glu130Lys | missense_variant | 0.15 |
fbiB | 3640944 | c.-591T>C | upstream_gene_variant | 0.16 |
fbiB | 3641286 | c.-249C>T | upstream_gene_variant | 0.17 |
fbiA | 3641288 | p.Glu249Gly | missense_variant | 0.17 |
fbiB | 3641292 | c.-243G>A | upstream_gene_variant | 0.17 |
fbiB | 3641295 | c.-240G>C | upstream_gene_variant | 0.17 |
fbiA | 3641314 | p.Thr258Ala | missense_variant | 0.17 |
fbiB | 3641322 | c.-213T>G | upstream_gene_variant | 0.16 |
fbiA | 3641340 | p.Asp266Glu | missense_variant | 0.15 |
fbiA | 3641351 | p.Ala270Asp | missense_variant | 0.15 |
fbiB | 3641373 | c.-162C>G | upstream_gene_variant | 0.18 |
fbiB | 3641379 | c.-156G>C | upstream_gene_variant | 0.19 |
fbiA | 3641380 | p.Cys280Arg | missense_variant | 0.19 |
fbiA | 3641384 | p.Ala281Gly | missense_variant | 0.19 |
fbiB | 3641394 | c.-141A>C | upstream_gene_variant | 0.19 |
fbiB | 3641609 | c.75C>A | synonymous_variant | 0.14 |
alr | 3841001 | c.420A>G | synonymous_variant | 0.16 |
alr | 3841017 | p.Leu135Gln | missense_variant | 0.16 |
alr | 3841022 | c.399C>G | synonymous_variant | 0.17 |
alr | 3841028 | c.393G>C | synonymous_variant | 0.17 |
alr | 3841033 | p.Val130Ile | missense_variant | 0.17 |
alr | 3841036 | p.Gln129Glu | missense_variant | 0.17 |
alr | 3841058 | p.Gly121Arg | missense_variant | 0.17 |
alr | 3841590 | c.-170G>A | upstream_gene_variant | 1.0 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.18 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.23 |
rpoA | 3877656 | c.852T>C | synonymous_variant | 0.25 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.21 |
rpoA | 3877677 | p.Ala277Ser | missense_variant | 0.21 |
rpoA | 3877680 | c.828G>C | synonymous_variant | 0.21 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.2 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.21 |
rpoA | 3877695 | c.813C>G | synonymous_variant | 0.21 |
rpoA | 3877704 | c.804G>C | synonymous_variant | 0.21 |
rpoA | 3877728 | c.780C>G | synonymous_variant | 0.2 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.15 |
rpoA | 3877746 | c.762G>T | synonymous_variant | 0.15 |
rpoA | 3877920 | c.588G>C | synonymous_variant | 0.21 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.26 |
rpoA | 3877968 | c.540C>G | synonymous_variant | 0.26 |
rpoA | 3877974 | c.534G>C | synonymous_variant | 0.22 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.25 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.3 |
rpoA | 3878019 | c.489A>G | synonymous_variant | 0.31 |
rpoA | 3878022 | c.486T>C | synonymous_variant | 0.32 |
rpoA | 3878031 | c.477T>C | synonymous_variant | 0.35 |
rpoA | 3878040 | c.468T>C | synonymous_variant | 0.35 |
rpoA | 3878043 | c.465G>C | synonymous_variant | 0.34 |
rpoA | 3878046 | c.462T>A | synonymous_variant | 0.34 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.37 |
rpoA | 3878067 | c.441C>T | synonymous_variant | 0.35 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.36 |
rpoA | 3878073 | c.435C>T | synonymous_variant | 0.36 |
rpoA | 3878082 | c.426T>G | synonymous_variant | 0.37 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.36 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.37 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.37 |
rpoA | 3878130 | c.378C>G | synonymous_variant | 0.36 |
rpoA | 3878142 | p.Gly122Glu | missense_variant | 0.3 |
rpoA | 3878157 | c.351C>G | synonymous_variant | 0.29 |
rpoA | 3878163 | c.345C>T | synonymous_variant | 0.32 |
rpoA | 3878169 | c.339G>C | synonymous_variant | 0.31 |
rpoA | 3878184 | c.324C>T | synonymous_variant | 0.26 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.29 |
rpoA | 3878197 | p.Glu104Ala | missense_variant | 0.28 |
rpoA | 3878199 | c.309T>C | synonymous_variant | 0.28 |
rpoA | 3878205 | c.303T>C | synonymous_variant | 0.26 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.25 |
rpoA | 3878264 | p.Ser82Gly | missense_variant | 0.2 |
rpoA | 3878284 | p.Glu75Ala | missense_variant | 0.24 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.23 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.23 |
rpoA | 3878301 | c.207C>G | synonymous_variant | 0.24 |
rpoA | 3878309 | p.Pro67Ala | missense_variant | 0.22 |
rpoA | 3878310 | c.198G>C | synonymous_variant | 0.22 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 0.22 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.21 |
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 | 0.23 |
rpoA | 3878364 | c.144A>C | synonymous_variant | 0.22 |
rpoA | 3878367 | c.141C>G | synonymous_variant | 0.21 |
rpoA | 3878370 | c.138T>C | synonymous_variant | 0.22 |
rpoA | 3878385 | c.123C>G | synonymous_variant | 0.23 |
rpoA | 3878388 | c.120C>G | synonymous_variant | 0.23 |
rpoA | 3878391 | c.117T>C | synonymous_variant | 0.23 |
rpoA | 3878415 | c.93C>T | synonymous_variant | 0.19 |
rpoA | 3878430 | c.78G>C | synonymous_variant | 0.17 |
rpoA | 3878442 | c.66G>C | synonymous_variant | 0.18 |
clpC1 | 4038299 | c.2406C>A | synonymous_variant | 0.14 |
clpC1 | 4038310 | p.Val799Met | missense_variant | 0.17 |
clpC1 | 4038314 | c.2391T>A | synonymous_variant | 0.17 |
clpC1 | 4038320 | c.2385G>A | synonymous_variant | 0.15 |
clpC1 | 4038347 | c.2358G>C | synonymous_variant | 0.17 |
clpC1 | 4038368 | c.2337T>C | synonymous_variant | 0.17 |
clpC1 | 4038398 | c.2307G>T | synonymous_variant | 0.17 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 0.17 |
clpC1 | 4038419 | c.2286T>C | synonymous_variant | 0.16 |
clpC1 | 4038433 | c.2272C>T | synonymous_variant | 0.18 |
clpC1 | 4038444 | p.Ala754Lys | missense_variant | 0.17 |
clpC1 | 4038446 | c.2259T>C | synonymous_variant | 0.16 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.16 |
clpC1 | 4038623 | c.2082A>G | synonymous_variant | 0.22 |
clpC1 | 4038640 | p.Asp689Asn | missense_variant | 0.25 |
clpC1 | 4038658 | p.Lys683Gln | missense_variant | 0.25 |
clpC1 | 4038661 | p.Ser682Thr | missense_variant | 0.23 |
clpC1 | 4038662 | c.2043T>C | synonymous_variant | 0.23 |
clpC1 | 4038683 | c.2022T>C | synonymous_variant | 0.23 |
clpC1 | 4038695 | c.2010C>G | synonymous_variant | 0.22 |
clpC1 | 4038698 | c.2007C>T | synonymous_variant | 0.22 |
clpC1 | 4038701 | c.2004G>C | synonymous_variant | 0.22 |
clpC1 | 4038704 | c.2001T>C | synonymous_variant | 0.22 |
clpC1 | 4038707 | c.1998C>G | synonymous_variant | 0.22 |
clpC1 | 4038710 | c.1995G>C | synonymous_variant | 0.22 |
clpC1 | 4038713 | c.1992T>C | synonymous_variant | 0.22 |
clpC1 | 4038755 | c.1950G>C | synonymous_variant | 0.26 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.21 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.19 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 0.18 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.16 |
clpC1 | 4038845 | c.1860G>C | synonymous_variant | 0.25 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.25 |
clpC1 | 4038884 | c.1821C>T | synonymous_variant | 0.27 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.26 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.26 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 0.26 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.28 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.28 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.28 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.27 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.27 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.27 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.29 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.33 |
clpC1 | 4039043 | c.1662G>C | synonymous_variant | 0.29 |
clpC1 | 4039064 | c.1641C>T | synonymous_variant | 0.31 |
clpC1 | 4039085 | c.1620A>G | synonymous_variant | 0.3 |
clpC1 | 4039090 | c.1615C>T | synonymous_variant | 0.3 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.28 |
clpC1 | 4039100 | c.1605C>G | synonymous_variant | 0.28 |
clpC1 | 4039103 | c.1602T>C | synonymous_variant | 0.28 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.28 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.27 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.27 |
clpC1 | 4039133 | c.1572C>G | synonymous_variant | 0.25 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.25 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.23 |
clpC1 | 4039166 | c.1539G>A | synonymous_variant | 0.17 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.16 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.16 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.17 |
clpC1 | 4039283 | c.1422C>T | synonymous_variant | 0.16 |
clpC1 | 4039286 | c.1419T>C | synonymous_variant | 0.16 |
clpC1 | 4039292 | c.1413C>T | synonymous_variant | 0.15 |
clpC1 | 4039316 | c.1389G>A | synonymous_variant | 0.15 |
clpC1 | 4039322 | c.1383T>G | synonymous_variant | 0.18 |
clpC1 | 4039328 | c.1377A>C | synonymous_variant | 0.2 |
clpC1 | 4039338 | p.Thr456Gln | missense_variant | 0.22 |
clpC1 | 4039382 | c.1323C>G | synonymous_variant | 0.23 |
clpC1 | 4039391 | c.1314T>G | synonymous_variant | 0.23 |
clpC1 | 4039394 | c.1311G>C | synonymous_variant | 0.21 |
clpC1 | 4039397 | c.1308A>G | synonymous_variant | 0.22 |
clpC1 | 4039409 | c.1296T>C | synonymous_variant | 0.23 |
clpC1 | 4039412 | c.1293T>G | synonymous_variant | 0.24 |
clpC1 | 4039415 | p.Glu430Asp | missense_variant | 0.25 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.36 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.38 |
clpC1 | 4039454 | c.1251A>G | synonymous_variant | 0.39 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.41 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.4 |
clpC1 | 4039481 | c.1224T>G | synonymous_variant | 0.37 |
clpC1 | 4039484 | c.1221T>C | synonymous_variant | 0.37 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.36 |
clpC1 | 4039541 | c.1164C>G | synonymous_variant | 0.36 |
clpC1 | 4039556 | c.1149G>C | synonymous_variant | 0.38 |
clpC1 | 4039570 | p.Met379Leu | missense_variant | 0.39 |
clpC1 | 4039582 | p.Thr375Ser | missense_variant | 0.36 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.31 |
clpC1 | 4039622 | c.1083C>G | synonymous_variant | 0.32 |
clpC1 | 4039661 | c.1044T>G | synonymous_variant | 0.32 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.29 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.23 |
clpC1 | 4039733 | c.972G>C | synonymous_variant | 0.23 |
clpC1 | 4039748 | c.957G>C | synonymous_variant | 0.22 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.23 |
clpC1 | 4039760 | c.945T>G | synonymous_variant | 0.2 |
clpC1 | 4039766 | c.939T>C | synonymous_variant | 0.19 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.19 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.18 |
clpC1 | 4039781 | c.924G>C | synonymous_variant | 0.17 |
clpC1 | 4039787 | c.916_918delTCGinsAGC | synonymous_variant | 0.17 |
clpC1 | 4039793 | c.912C>G | synonymous_variant | 0.17 |
clpC1 | 4039796 | c.909C>T | synonymous_variant | 0.19 |
clpC1 | 4039814 | c.891C>G | synonymous_variant | 0.19 |
clpC1 | 4039817 | c.888A>C | synonymous_variant | 0.19 |
clpC1 | 4039820 | c.885T>C | synonymous_variant | 0.18 |
clpC1 | 4039832 | c.873C>G | synonymous_variant | 0.17 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.15 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.18 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.18 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.21 |
clpC1 | 4039919 | c.786C>A | synonymous_variant | 0.21 |
clpC1 | 4039929 | c.775_776delAGinsTC | synonymous_variant | 0.21 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.21 |
clpC1 | 4039934 | c.771G>C | synonymous_variant | 0.21 |
clpC1 | 4039946 | c.759A>C | synonymous_variant | 0.2 |
clpC1 | 4039949 | c.756G>C | synonymous_variant | 0.2 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.21 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.2 |
clpC1 | 4039988 | c.717C>G | synonymous_variant | 0.19 |
clpC1 | 4039996 | p.Glu237Gln | missense_variant | 0.2 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.17 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.19 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.2 |
clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 0.2 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.2 |
clpC1 | 4040108 | c.597G>C | synonymous_variant | 0.22 |
clpC1 | 4040129 | c.576C>G | synonymous_variant | 0.23 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.24 |
clpC1 | 4040147 | c.558A>G | synonymous_variant | 0.24 |
clpC1 | 4040162 | c.543G>C | synonymous_variant | 0.27 |
clpC1 | 4040165 | c.540G>C | synonymous_variant | 0.27 |
clpC1 | 4040171 | c.534C>G | synonymous_variant | 0.3 |
clpC1 | 4040180 | c.525C>G | synonymous_variant | 0.32 |
clpC1 | 4040201 | c.504C>G | synonymous_variant | 0.32 |
clpC1 | 4040207 | c.498T>C | synonymous_variant | 0.29 |
clpC1 | 4040213 | c.492T>G | synonymous_variant | 0.31 |
clpC1 | 4040228 | c.477G>C | synonymous_variant | 0.31 |
clpC1 | 4040231 | c.474C>G | synonymous_variant | 0.31 |
clpC1 | 4040234 | c.471C>G | synonymous_variant | 0.31 |
clpC1 | 4040240 | c.465C>G | synonymous_variant | 0.31 |
clpC1 | 4040249 | c.456A>G | synonymous_variant | 0.3 |
clpC1 | 4040267 | c.438A>G | synonymous_variant | 0.31 |
clpC1 | 4040273 | c.432T>C | synonymous_variant | 0.3 |
clpC1 | 4040277 | c.427_428delTCinsAG | synonymous_variant | 0.3 |
clpC1 | 4040279 | c.426C>G | synonymous_variant | 0.3 |
clpC1 | 4040291 | c.414G>C | synonymous_variant | 0.31 |
clpC1 | 4040330 | c.375C>G | synonymous_variant | 0.21 |
clpC1 | 4040335 | c.370C>T | synonymous_variant | 0.22 |
clpC1 | 4040354 | c.351A>G | synonymous_variant | 0.22 |
clpC1 | 4040363 | c.342A>C | synonymous_variant | 0.22 |
clpC1 | 4040372 | c.333C>G | synonymous_variant | 0.18 |
clpC1 | 4040375 | c.330G>C | synonymous_variant | 0.18 |
clpC1 | 4040380 | c.325T>C | synonymous_variant | 0.18 |
clpC1 | 4040381 | c.324T>C | synonymous_variant | 0.18 |
clpC1 | 4040387 | c.318A>G | synonymous_variant | 0.17 |
clpC1 | 4040393 | c.312G>C | synonymous_variant | 0.17 |
clpC1 | 4040411 | c.294T>C | synonymous_variant | 0.16 |
clpC1 | 4040423 | c.282A>G | synonymous_variant | 0.19 |
clpC1 | 4040431 | c.274T>C | synonymous_variant | 0.18 |
clpC1 | 4040441 | c.264C>G | synonymous_variant | 0.17 |
clpC1 | 4040480 | c.225T>G | synonymous_variant | 0.2 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 0.17 |
clpC1 | 4040528 | c.177G>C | synonymous_variant | 0.17 |
clpC1 | 4040531 | c.174T>C | synonymous_variant | 0.16 |
clpC1 | 4040537 | c.168G>C | synonymous_variant | 0.16 |
clpC1 | 4040546 | c.159G>C | synonymous_variant | 0.16 |
panD | 4044150 | c.132A>G | synonymous_variant | 0.18 |
embC | 4240819 | c.957A>G | synonymous_variant | 0.16 |
embC | 4240831 | c.969T>G | synonymous_variant | 0.19 |
embC | 4240870 | c.1008T>C | synonymous_variant | 0.16 |
embC | 4240898 | c.1036C>T | synonymous_variant | 0.15 |
embC | 4240911 | p.Ala350Val | missense_variant | 0.15 |
embC | 4240924 | c.1062C>G | synonymous_variant | 0.2 |
embC | 4240936 | c.1074A>G | synonymous_variant | 0.21 |
embC | 4240945 | c.1083T>C | synonymous_variant | 0.16 |
embC | 4241071 | c.1209C>G | synonymous_variant | 0.16 |
embC | 4241074 | c.1212G>C | synonymous_variant | 0.16 |
embC | 4241104 | c.1242G>A | synonymous_variant | 0.18 |
embC | 4241107 | c.1245G>C | synonymous_variant | 0.19 |
embC | 4241116 | c.1254C>G | synonymous_variant | 0.22 |
embC | 4241140 | c.1278A>G | synonymous_variant | 0.24 |
embC | 4241141 | p.Ile427Ala | missense_variant | 0.23 |
embC | 4241158 | c.1296T>C | synonymous_variant | 0.23 |
embC | 4241161 | c.1299C>G | synonymous_variant | 0.22 |
embC | 4241162 | c.1300T>C | synonymous_variant | 0.22 |
embC | 4241203 | c.1341T>C | synonymous_variant | 0.19 |
embC | 4241206 | c.1344G>C | synonymous_variant | 0.18 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 0.99 |
embB | 4245665 | c.-849C>G | upstream_gene_variant | 0.19 |
embB | 4245668 | c.-846C>G | upstream_gene_variant | 0.2 |
embB | 4245674 | c.-840A>C | upstream_gene_variant | 0.2 |
embB | 4245680 | c.-834G>A | upstream_gene_variant | 0.23 |
embA | 4245688 | p.Val819Ala | missense_variant | 0.23 |
embB | 4245692 | c.-822G>C | upstream_gene_variant | 0.23 |
embA | 4245693 | p.Ile821Val | missense_variant | 0.23 |
embB | 4245701 | c.-813G>C | upstream_gene_variant | 0.22 |
embB | 4245725 | c.-789A>C | upstream_gene_variant | 0.2 |
embB | 4245726 | c.-788_-786delTTGinsCTC | upstream_gene_variant | 0.2 |
embB | 4245737 | c.-777A>C | upstream_gene_variant | 0.19 |
embB | 4245740 | c.-774T>G | upstream_gene_variant | 0.2 |
embB | 4245755 | c.-759C>G | upstream_gene_variant | 0.18 |
embB | 4245764 | c.-750G>C | upstream_gene_variant | 0.16 |
embA | 4245771 | p.Asn847Tyr | missense_variant | 0.15 |
embB | 4247455 | c.942C>T | synonymous_variant | 0.15 |
embB | 4247857 | c.1344C>G | synonymous_variant | 0.17 |
embB | 4247858 | c.1345C>T | synonymous_variant | 0.16 |
embB | 4247881 | c.1368G>C | synonymous_variant | 0.24 |
embB | 4247887 | c.1374C>T | synonymous_variant | 0.24 |
embB | 4247896 | c.1383G>C | synonymous_variant | 0.24 |
embB | 4247899 | p.Met462Ile | missense_variant | 0.23 |
embB | 4247905 | c.1392G>A | synonymous_variant | 0.22 |
embB | 4247909 | c.1396_1398delTTGinsCTC | synonymous_variant | 0.21 |
embB | 4247914 | c.1401G>C | synonymous_variant | 0.21 |
embB | 4247920 | c.1407T>G | synonymous_variant | 0.21 |
embB | 4247923 | c.1410T>C | synonymous_variant | 0.21 |
embB | 4247926 | c.1413C>G | synonymous_variant | 0.21 |
embB | 4247938 | c.1425G>C | synonymous_variant | 0.23 |
embB | 4247940 | p.Leu476Trp | missense_variant | 0.23 |
embB | 4247951 | p.Ser480Ala | missense_variant | 0.27 |
embB | 4247956 | c.1443G>C | synonymous_variant | 0.28 |
embB | 4247962 | c.1449G>C | synonymous_variant | 0.28 |
embB | 4247974 | c.1461C>G | synonymous_variant | 0.29 |
embB | 4248001 | c.1488C>T | synonymous_variant | 0.23 |
embB | 4248007 | c.1494C>G | synonymous_variant | 0.22 |
embB | 4248019 | c.1506G>C | synonymous_variant | 0.19 |
embB | 4248025 | c.1512A>G | synonymous_variant | 0.18 |
embB | 4248035 | p.Val508Ile | missense_variant | 0.16 |
embB | 4248041 | p.Ala510Thr | missense_variant | 0.16 |
embB | 4248055 | c.1542G>C | synonymous_variant | 0.19 |
embB | 4248064 | c.1551G>C | synonymous_variant | 0.18 |
embB | 4248070 | c.1557T>C | synonymous_variant | 0.18 |
embB | 4248085 | c.1572T>C | synonymous_variant | 0.18 |
embB | 4248265 | c.1752C>T | synonymous_variant | 0.2 |
embB | 4248266 | c.1753C>T | synonymous_variant | 0.2 |
embB | 4248277 | c.1764G>C | synonymous_variant | 0.2 |
embB | 4248313 | c.1800C>G | synonymous_variant | 0.17 |
embB | 4248316 | c.1803C>G | synonymous_variant | 0.17 |
embB | 4248319 | c.1806A>G | synonymous_variant | 0.17 |
embB | 4248322 | c.1809G>C | synonymous_variant | 0.17 |
embB | 4248325 | c.1812G>C | synonymous_variant | 0.17 |
embB | 4248334 | c.1821C>G | synonymous_variant | 0.17 |
embB | 4248346 | c.1833G>C | synonymous_variant | 0.16 |
embB | 4248362 | p.Ser617Lys | missense_variant | 0.14 |
embB | 4248382 | c.1869C>G | synonymous_variant | 0.17 |
aftB | 4268719 | p.Asn40Asp | missense_variant | 0.94 |
ubiA | 4269075 | p.Ile253Val | missense_variant | 0.15 |
aftB | 4269096 | c.-260C>G | upstream_gene_variant | 0.17 |
aftB | 4269099 | c.-263G>A | upstream_gene_variant | 0.17 |
aftB | 4269103 | c.-268_-267delAGinsTC | upstream_gene_variant | 0.17 |
ubiA | 4269107 | p.Tyr243His | missense_variant | 0.17 |
ubiA | 4269110 | p.Gly242Arg | missense_variant | 0.17 |
aftB | 4269114 | c.-278C>T | upstream_gene_variant | 0.18 |
aftB | 4269123 | c.-287T>G | upstream_gene_variant | 0.18 |
aftB | 4269131 | c.-295C>T | upstream_gene_variant | 0.19 |
aftB | 4269143 | c.-307T>C | upstream_gene_variant | 0.18 |
aftB | 4269144 | c.-308C>G | upstream_gene_variant | 0.19 |
ubiA | 4269164 | p.Leu224Met | missense_variant | 0.17 |
aftB | 4269165 | c.-329G>C | upstream_gene_variant | 0.17 |
aftB | 4269174 | c.-338C>T | upstream_gene_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |