Run ID: ERR4817692
Sample name:
Date: 01-04-2023 15:08:21
Number of reads: 2835646
Percentage reads mapped: 68.34
Strain: lineage4;lineage1.1.2
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.12 |
lineage1 | Indo-Oceanic | EAI | RD239 | 0.77 |
lineage1.1 | Indo-Oceanic | EAI3;EAI4;EAI5;EAI6 | RD239 | 0.85 |
lineage1.1.2 | Indo-Oceanic | EAI3;EAI5 | RD239 | 0.81 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472307 | n.462C>T | non_coding_transcript_exon_variant | 0.17 | streptomycin |
katG | 2155108 | p.Ile335Thr | missense_variant | 0.24 | isoniazid |
embB | 4247448 | p.His312Arg | missense_variant | 0.23 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5788 | c.549G>C | synonymous_variant | 0.18 |
gyrB | 5806 | c.567C>G | synonymous_variant | 0.19 |
gyrB | 5809 | c.570C>G | synonymous_variant | 0.22 |
gyrB | 5824 | c.585A>G | synonymous_variant | 0.24 |
gyrB | 5827 | c.588G>A | synonymous_variant | 0.24 |
gyrB | 5863 | c.624G>C | synonymous_variant | 0.17 |
gyrB | 5873 | c.634A>C | synonymous_variant | 0.17 |
gyrB | 6112 | p.Met291Ile | missense_variant | 0.77 |
gyrB | 6124 | c.885C>T | synonymous_variant | 0.76 |
gyrB | 6280 | c.1041T>C | synonymous_variant | 0.18 |
gyrB | 6286 | c.1047T>C | synonymous_variant | 0.17 |
gyrB | 6292 | c.1053G>C | synonymous_variant | 0.18 |
gyrA | 6319 | c.-983G>C | upstream_gene_variant | 0.18 |
gyrA | 6325 | c.-977C>G | upstream_gene_variant | 0.17 |
gyrA | 6649 | c.-653T>C | upstream_gene_variant | 0.18 |
gyrA | 6655 | c.-647T>C | upstream_gene_variant | 0.17 |
gyrA | 6670 | c.-632G>C | upstream_gene_variant | 0.25 |
gyrA | 6673 | c.-629A>C | upstream_gene_variant | 0.26 |
gyrA | 6700 | c.-602T>C | upstream_gene_variant | 0.25 |
gyrA | 6703 | c.-599G>C | upstream_gene_variant | 0.22 |
gyrA | 6706 | c.-596G>A | upstream_gene_variant | 0.21 |
gyrA | 6709 | c.-593A>G | upstream_gene_variant | 0.23 |
gyrA | 6712 | c.-590G>C | upstream_gene_variant | 0.24 |
gyrA | 6727 | c.-575G>T | upstream_gene_variant | 0.25 |
gyrA | 6730 | c.-572A>G | upstream_gene_variant | 0.29 |
gyrA | 6745 | c.-557T>G | upstream_gene_variant | 0.31 |
gyrA | 6760 | c.-542G>C | upstream_gene_variant | 0.33 |
gyrA | 6778 | c.-524C>T | upstream_gene_variant | 0.18 |
gyrA | 6793 | c.-509T>C | upstream_gene_variant | 0.23 |
gyrB | 6797 | p.Gly520Thr | missense_variant | 0.23 |
gyrA | 6824 | c.-478C>T | upstream_gene_variant | 0.28 |
gyrA | 6841 | c.-461T>C | upstream_gene_variant | 0.27 |
gyrA | 6844 | c.-458T>G | upstream_gene_variant | 0.23 |
gyrA | 6853 | c.-449A>G | upstream_gene_variant | 0.22 |
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 | 0.22 |
gyrA | 6878 | c.-424T>C | upstream_gene_variant | 0.26 |
gyrA | 6881 | c.-421T>C | upstream_gene_variant | 0.26 |
gyrA | 6904 | c.-398C>G | upstream_gene_variant | 0.21 |
gyrA | 6910 | c.-392G>A | upstream_gene_variant | 0.15 |
gyrA | 7033 | c.-269G>C | upstream_gene_variant | 0.17 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 0.98 |
gyrA | 7457 | c.156T>C | synonymous_variant | 0.18 |
gyrA | 7532 | c.231T>C | synonymous_variant | 0.21 |
gyrA | 7541 | c.240C>G | synonymous_variant | 0.18 |
gyrA | 7571 | c.270G>C | synonymous_variant | 0.2 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7607 | c.306C>G | synonymous_variant | 0.2 |
gyrA | 7631 | c.330G>C | synonymous_variant | 0.19 |
gyrA | 7637 | c.336C>G | synonymous_variant | 0.18 |
gyrA | 7658 | c.357A>G | synonymous_variant | 0.21 |
gyrA | 7664 | c.363T>C | synonymous_variant | 0.24 |
gyrA | 7670 | c.369A>G | synonymous_variant | 0.24 |
gyrA | 7676 | c.375G>C | synonymous_variant | 0.24 |
gyrA | 7683 | c.382A>C | synonymous_variant | 0.26 |
gyrA | 7694 | c.393A>G | synonymous_variant | 0.27 |
gyrA | 7697 | c.396C>G | synonymous_variant | 0.23 |
gyrA | 7710 | c.409T>C | synonymous_variant | 0.25 |
gyrA | 7715 | c.414G>C | synonymous_variant | 0.25 |
gyrA | 7727 | c.426G>C | synonymous_variant | 0.26 |
gyrA | 7728 | c.427_429delAGGinsCGC | synonymous_variant | 0.28 |
gyrA | 7760 | c.459C>T | synonymous_variant | 0.28 |
gyrA | 7763 | c.462T>C | synonymous_variant | 0.25 |
gyrA | 7799 | c.498A>G | synonymous_variant | 0.24 |
gyrA | 7835 | c.534A>G | synonymous_variant | 0.29 |
gyrA | 7838 | c.537C>G | synonymous_variant | 0.26 |
gyrA | 7859 | c.558A>C | synonymous_variant | 0.25 |
gyrA | 7862 | c.561C>G | synonymous_variant | 0.24 |
gyrA | 7865 | c.564T>C | synonymous_variant | 0.26 |
gyrA | 7883 | c.582G>C | synonymous_variant | 0.23 |
gyrA | 7884 | p.Arg195Gly | missense_variant | 0.23 |
gyrA | 7892 | c.591G>C | synonymous_variant | 0.22 |
gyrA | 7898 | p.Asp199Glu | missense_variant | 0.23 |
gyrA | 7919 | p.Glu206Asp | missense_variant | 0.19 |
gyrA | 7923 | p.His208Tyr | missense_variant | 0.17 |
gyrA | 8090 | c.789C>A | synonymous_variant | 0.22 |
gyrA | 8129 | c.828T>C | synonymous_variant | 0.3 |
gyrA | 8156 | c.855T>C | synonymous_variant | 0.31 |
gyrA | 8168 | c.867A>G | synonymous_variant | 0.29 |
gyrA | 8177 | c.876A>C | synonymous_variant | 0.28 |
gyrA | 8198 | c.897T>C | synonymous_variant | 0.21 |
gyrA | 8207 | c.906T>C | synonymous_variant | 0.17 |
gyrA | 8219 | c.918T>C | synonymous_variant | 0.18 |
gyrA | 8225 | c.924T>C | synonymous_variant | 0.21 |
gyrA | 8234 | c.933T>G | synonymous_variant | 0.16 |
gyrA | 8237 | c.936A>G | synonymous_variant | 0.18 |
gyrA | 8253 | p.Ile318Leu | missense_variant | 0.23 |
gyrA | 8264 | c.963T>C | synonymous_variant | 0.23 |
gyrA | 8267 | c.966G>C | synonymous_variant | 0.24 |
gyrA | 8270 | c.969G>C | synonymous_variant | 0.23 |
gyrA | 8283 | p.Ile328Leu | missense_variant | 0.22 |
gyrA | 8288 | c.987T>C | synonymous_variant | 0.23 |
gyrA | 8294 | c.993T>C | synonymous_variant | 0.27 |
gyrA | 8324 | c.1023T>C | synonymous_variant | 0.26 |
gyrA | 8339 | c.1038A>G | synonymous_variant | 0.23 |
gyrA | 8342 | c.1041G>C | synonymous_variant | 0.24 |
gyrA | 8375 | c.1074G>C | synonymous_variant | 0.22 |
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 | 0.2 |
gyrA | 8435 | c.1134C>G | synonymous_variant | 0.63 |
gyrA | 8438 | c.1137C>T | synonymous_variant | 0.15 |
gyrA | 8452 | p.Ala384Val | missense_variant | 0.69 |
gyrA | 8486 | c.1185T>C | synonymous_variant | 0.21 |
gyrA | 8489 | c.1188A>G | synonymous_variant | 0.19 |
gyrA | 8498 | c.1197C>T | synonymous_variant | 0.18 |
gyrA | 8504 | c.1203G>C | synonymous_variant | 0.2 |
gyrA | 8519 | c.1218A>C | synonymous_variant | 0.18 |
gyrA | 8546 | c.1245T>C | synonymous_variant | 0.26 |
gyrA | 8561 | c.1260A>C | synonymous_variant | 0.34 |
gyrA | 8603 | c.1302A>G | synonymous_variant | 0.3 |
gyrA | 8619 | c.1318T>C | synonymous_variant | 0.29 |
gyrA | 8624 | c.1323G>C | synonymous_variant | 0.26 |
gyrA | 8636 | c.1335A>C | synonymous_variant | 0.25 |
gyrA | 8642 | c.1341A>G | synonymous_variant | 0.19 |
gyrA | 8693 | c.1392T>C | synonymous_variant | 0.16 |
gyrA | 8801 | c.1500G>C | synonymous_variant | 0.16 |
gyrA | 8810 | c.1509A>C | synonymous_variant | 0.17 |
gyrA | 8829 | c.1528T>C | synonymous_variant | 0.22 |
gyrA | 8852 | c.1551T>C | synonymous_variant | 0.22 |
gyrA | 8867 | c.1566A>G | synonymous_variant | 0.26 |
gyrA | 8870 | c.1569G>C | synonymous_variant | 0.27 |
gyrA | 8873 | c.1572A>C | synonymous_variant | 0.27 |
gyrA | 8897 | c.1596T>C | synonymous_variant | 0.29 |
gyrA | 8903 | c.1602T>C | synonymous_variant | 0.27 |
gyrA | 8946 | c.1645_1647delTTGinsCTC | synonymous_variant | 0.2 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 0.89 |
gyrA | 9182 | c.1881T>C | synonymous_variant | 0.18 |
gyrA | 9191 | c.1890G>C | synonymous_variant | 0.19 |
gyrA | 9200 | c.1899A>G | synonymous_variant | 0.19 |
gyrA | 9204 | p.Ser635Thr | missense_variant | 0.18 |
gyrA | 9227 | c.1926C>G | synonymous_variant | 0.2 |
gyrA | 9230 | c.1929T>C | synonymous_variant | 0.2 |
gyrA | 9242 | c.1941A>C | synonymous_variant | 0.17 |
gyrA | 9252 | p.Val651Ile | missense_variant | 0.19 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9323 | c.2022C>G | synonymous_variant | 0.17 |
gyrA | 9666 | p.Arg789Gly | missense_variant | 0.2 |
gyrA | 9674 | c.2373T>C | synonymous_variant | 0.2 |
fgd1 | 490803 | c.21T>A | synonymous_variant | 0.16 |
fgd1 | 490812 | c.30A>G | synonymous_variant | 0.18 |
fgd1 | 490815 | c.33G>C | synonymous_variant | 0.18 |
fgd1 | 490827 | c.45C>T | synonymous_variant | 0.24 |
fgd1 | 490851 | c.69A>C | synonymous_variant | 0.19 |
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 | 0.25 |
fgd1 | 490911 | c.129T>G | synonymous_variant | 0.22 |
fgd1 | 490917 | c.135C>A | synonymous_variant | 0.16 |
fgd1 | 490921 | p.Gln47Glu | missense_variant | 0.18 |
fgd1 | 491137 | p.Glu119Gln | missense_variant | 0.18 |
fgd1 | 491144 | p.Ala121Glu | missense_variant | 0.2 |
fgd1 | 491166 | c.384G>C | synonymous_variant | 0.19 |
fgd1 | 491181 | c.399T>C | synonymous_variant | 0.24 |
fgd1 | 491191 | p.Gly137Arg | missense_variant | 0.26 |
fgd1 | 491196 | c.414A>G | synonymous_variant | 0.24 |
fgd1 | 491202 | c.420G>C | synonymous_variant | 0.2 |
fgd1 | 491203 | p.Gln141Glu | missense_variant | 0.21 |
fgd1 | 491212 | p.Ser144Arg | missense_variant | 0.21 |
fgd1 | 491217 | c.435T>C | synonymous_variant | 0.23 |
fgd1 | 491232 | c.450T>C | synonymous_variant | 0.28 |
fgd1 | 491241 | p.Asp153Glu | missense_variant | 0.26 |
fgd1 | 491244 | c.462T>C | synonymous_variant | 0.29 |
fgd1 | 491259 | c.477T>C | synonymous_variant | 0.33 |
fgd1 | 491286 | c.504G>C | synonymous_variant | 0.38 |
fgd1 | 491292 | c.510G>C | synonymous_variant | 0.38 |
fgd1 | 491295 | c.513C>G | synonymous_variant | 0.37 |
fgd1 | 491296 | p.Val172Ile | missense_variant | 0.37 |
fgd1 | 491319 | c.537G>C | synonymous_variant | 0.36 |
fgd1 | 491331 | c.549G>A | synonymous_variant | 0.23 |
fgd1 | 491349 | c.567T>C | synonymous_variant | 0.22 |
fgd1 | 491472 | c.690A>G | synonymous_variant | 0.2 |
fgd1 | 491502 | c.720G>A | synonymous_variant | 0.29 |
fgd1 | 491508 | c.726A>G | synonymous_variant | 0.29 |
fgd1 | 491509 | c.727T>C | synonymous_variant | 0.3 |
fgd1 | 491512 | p.Asn244Glu | missense_variant | 0.29 |
fgd1 | 491526 | c.744T>C | synonymous_variant | 0.36 |
fgd1 | 491542 | c.760T>C | synonymous_variant | 0.38 |
fgd1 | 491547 | c.765A>C | synonymous_variant | 0.37 |
fgd1 | 491550 | c.768T>C | synonymous_variant | 0.37 |
fgd1 | 491583 | c.801G>A | synonymous_variant | 0.24 |
fgd1 | 491601 | c.819T>C | synonymous_variant | 0.22 |
fgd1 | 491610 | c.828A>C | synonymous_variant | 0.17 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.86 |
mshA | 575376 | p.Ser10Leu | missense_variant | 0.89 |
mshA | 575659 | c.312A>G | synonymous_variant | 0.18 |
mshA | 575665 | c.318G>C | synonymous_variant | 0.21 |
mshA | 575669 | p.Leu108Val | missense_variant | 0.2 |
mshA | 575689 | c.342G>C | synonymous_variant | 0.22 |
mshA | 575695 | c.348C>G | synonymous_variant | 0.25 |
mshA | 575704 | c.357T>C | synonymous_variant | 0.22 |
mshA | 575705 | c.358T>C | synonymous_variant | 0.25 |
mshA | 575713 | c.366G>A | synonymous_variant | 0.26 |
mshA | 575719 | c.372C>T | synonymous_variant | 0.27 |
mshA | 575734 | c.387T>G | synonymous_variant | 0.3 |
mshA | 575737 | c.390T>C | synonymous_variant | 0.3 |
mshA | 575746 | c.399C>G | synonymous_variant | 0.31 |
mshA | 575767 | c.420G>A | synonymous_variant | 0.23 |
mshA | 575771 | p.Val142Ser | missense_variant | 0.22 |
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 | 575864 | c.517T>C | synonymous_variant | 0.24 |
mshA | 575878 | c.531A>G | synonymous_variant | 0.17 |
mshA | 575884 | c.537G>C | synonymous_variant | 0.25 |
ccsA | 620362 | p.Ala158Thr | missense_variant | 0.21 |
ccsA | 620367 | c.477T>C | synonymous_variant | 0.22 |
ccsA | 620373 | c.483C>G | synonymous_variant | 0.23 |
ccsA | 620385 | c.495G>C | synonymous_variant | 0.22 |
ccsA | 620388 | c.498A>G | synonymous_variant | 0.22 |
ccsA | 620412 | c.522T>C | synonymous_variant | 0.21 |
ccsA | 620415 | c.525T>C | synonymous_variant | 0.22 |
ccsA | 620433 | c.543C>G | synonymous_variant | 0.19 |
ccsA | 620439 | c.549T>C | synonymous_variant | 0.19 |
ccsA | 620445 | c.555A>G | synonymous_variant | 0.16 |
ccsA | 620622 | c.732G>C | synonymous_variant | 0.17 |
ccsA | 620646 | c.756G>A | synonymous_variant | 0.2 |
ccsA | 620661 | c.771C>G | synonymous_variant | 0.21 |
rpoB | 759644 | c.-163T>A | upstream_gene_variant | 0.16 |
rpoB | 759647 | c.-160T>C | upstream_gene_variant | 0.17 |
rpoB | 760091 | c.285G>C | synonymous_variant | 0.17 |
rpoB | 760101 | c.295T>C | synonymous_variant | 0.19 |
rpoB | 760112 | c.306T>C | synonymous_variant | 0.18 |
rpoB | 760130 | p.Asp108Glu | missense_variant | 0.19 |
rpoB | 760181 | c.375T>C | synonymous_variant | 0.21 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.21 |
rpoB | 760196 | c.390C>G | synonymous_variant | 0.24 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.27 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.27 |
rpoB | 760283 | c.477G>C | synonymous_variant | 0.2 |
rpoB | 760307 | c.501T>C | synonymous_variant | 0.21 |
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 | 0.19 |
rpoB | 760340 | c.534G>C | synonymous_variant | 0.23 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.29 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.26 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.3 |
rpoB | 760418 | c.612G>C | synonymous_variant | 0.24 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.29 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.32 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.32 |
rpoB | 760481 | c.675G>C | synonymous_variant | 0.32 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.31 |
rpoB | 760522 | p.Ser239Asn | missense_variant | 0.17 |
rpoB | 760563 | p.Arg253Met | missense_variant | 0.18 |
rpoB | 760611 | c.805T>C | synonymous_variant | 0.21 |
rpoB | 760634 | c.828T>C | synonymous_variant | 0.2 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.2 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.21 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.26 |
rpoB | 760670 | c.864G>C | synonymous_variant | 0.3 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.3 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.29 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.3 |
rpoB | 760724 | c.918T>C | synonymous_variant | 0.2 |
rpoB | 760730 | c.924T>C | synonymous_variant | 0.19 |
rpoB | 760751 | c.945G>C | synonymous_variant | 0.22 |
rpoB | 760859 | c.1053T>C | synonymous_variant | 0.2 |
rpoB | 760862 | c.1056G>C | synonymous_variant | 0.2 |
rpoB | 760886 | c.1080A>G | synonymous_variant | 0.25 |
rpoB | 760919 | c.1113C>G | synonymous_variant | 0.2 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.27 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 0.25 |
rpoB | 760934 | c.1128C>T | synonymous_variant | 0.24 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.28 |
rpoB | 760970 | c.1164G>C | synonymous_variant | 0.24 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.3 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.3 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.27 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.28 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 0.28 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.31 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.31 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.28 |
rpoB | 761051 | c.1245G>T | synonymous_variant | 0.21 |
rpoB | 761054 | c.1248G>A | synonymous_variant | 0.17 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.24 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.19 |
rpoB | 761063 | c.1257C>G | synonymous_variant | 0.2 |
rpoB | 761097 | c.1291_1292delAGinsTC | synonymous_variant | 0.2 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.23 |
rpoB | 761133 | c.1327_1329delTTGinsCTC | synonymous_variant | 0.26 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.28 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.29 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.24 |
rpoB | 761171 | c.1365C>T | synonymous_variant | 0.23 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.3 |
rpoB | 761183 | c.1377T>G | synonymous_variant | 0.25 |
rpoB | 761189 | c.1383T>G | synonymous_variant | 0.28 |
rpoB | 761222 | c.1416G>C | synonymous_variant | 0.24 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.27 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.27 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.28 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.19 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.22 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.25 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.24 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.23 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.23 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.2 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.18 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.17 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.21 |
rpoB | 761954 | c.2148C>G | synonymous_variant | 0.21 |
rpoB | 761969 | c.2163G>A | synonymous_variant | 0.16 |
rpoB | 762008 | c.2202C>G | synonymous_variant | 0.18 |
rpoB | 762014 | c.2208C>T | synonymous_variant | 0.23 |
rpoB | 762017 | c.2211A>G | synonymous_variant | 0.23 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.23 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.22 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.23 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.22 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.22 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.17 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.18 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 0.16 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.24 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.25 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.25 |
rpoC | 762509 | c.-861T>G | upstream_gene_variant | 0.17 |
rpoB | 762510 | p.Ala902Pro | missense_variant | 0.17 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.28 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.35 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.35 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.35 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 0.97 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.33 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.37 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.28 |
rpoC | 763076 | c.-294C>G | upstream_gene_variant | 0.21 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.22 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.21 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.2 |
rpoC | 763158 | c.-212C>T | upstream_gene_variant | 0.21 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.21 |
rpoC | 763169 | c.-201A>G | upstream_gene_variant | 0.2 |
rpoC | 763202 | c.-168A>C | upstream_gene_variant | 0.19 |
rpoC | 763205 | c.-165G>C | upstream_gene_variant | 0.21 |
rpoC | 763206 | c.-164_-162delAGTinsTCC | upstream_gene_variant | 0.21 |
rpoC | 763214 | c.-156T>C | upstream_gene_variant | 0.22 |
rpoC | 763226 | c.-144A>G | upstream_gene_variant | 0.21 |
rpoC | 763238 | c.-132T>C | upstream_gene_variant | 0.2 |
rpoC | 763402 | c.33C>G | synonymous_variant | 0.21 |
rpoC | 763411 | c.42T>G | synonymous_variant | 0.22 |
rpoC | 763414 | c.45T>C | synonymous_variant | 0.22 |
rpoC | 763441 | c.72C>G | synonymous_variant | 0.22 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.26 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.31 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.21 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.2 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.34 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.36 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.47 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.44 |
rpoC | 763603 | c.234C>T | synonymous_variant | 0.17 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.17 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.3 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.18 |
rpoC | 763658 | c.289_291delCTTinsTTG | synonymous_variant | 0.17 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.23 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.21 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.22 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.21 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.21 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.2 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.2 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.27 |
rpoC | 763768 | c.399C>G | synonymous_variant | 0.17 |
rpoC | 763780 | c.411C>G | synonymous_variant | 0.2 |
rpoC | 763783 | c.414G>C | synonymous_variant | 0.2 |
rpoC | 763801 | c.432C>G | synonymous_variant | 0.22 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.26 |
rpoC | 763819 | c.450G>C | synonymous_variant | 0.2 |
rpoC | 763831 | c.462A>G | synonymous_variant | 0.18 |
rpoC | 763835 | p.Ala156Met | missense_variant | 0.24 |
rpoC | 763858 | c.489A>G | synonymous_variant | 0.25 |
rpoC | 763872 | p.Gly168Ala | missense_variant | 0.21 |
rpoC | 763876 | p.Glu169Asp | missense_variant | 0.22 |
rpoC | 763879 | c.510A>G | synonymous_variant | 0.22 |
rpoC | 763884 | p.Ala172Val | missense_variant | 0.67 |
rpoC | 763886 | p.Arg173Ser | missense_variant | 0.67 |
rpoC | 763891 | c.522G>C | synonymous_variant | 0.22 |
rpoC | 763894 | c.525A>G | synonymous_variant | 0.26 |
rpoC | 763919 | c.550C>T | synonymous_variant | 0.18 |
rpoC | 763933 | c.564C>T | synonymous_variant | 0.17 |
rpoC | 763960 | c.591T>C | synonymous_variant | 0.18 |
rpoC | 763967 | p.Gly200Ser | missense_variant | 0.22 |
rpoC | 763978 | c.609C>G | synonymous_variant | 0.23 |
rpoC | 763996 | c.627T>C | synonymous_variant | 0.31 |
rpoC | 764005 | c.636G>C | synonymous_variant | 0.33 |
rpoC | 764011 | c.642T>C | synonymous_variant | 0.21 |
rpoC | 764024 | c.655T>C | synonymous_variant | 0.33 |
rpoC | 764040 | p.Ser224Asn | missense_variant | 0.31 |
rpoC | 764044 | c.675T>C | synonymous_variant | 0.34 |
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 | 0.34 |
rpoC | 764101 | c.732C>G | synonymous_variant | 0.34 |
rpoC | 764131 | c.762T>C | synonymous_variant | 0.31 |
rpoC | 764161 | c.792G>C | synonymous_variant | 0.22 |
rpoC | 764188 | c.819A>G | synonymous_variant | 0.19 |
rpoC | 764196 | p.Ser276* | stop_gained | 0.15 |
rpoC | 764203 | c.834G>T | synonymous_variant | 0.21 |
rpoC | 764206 | c.837T>C | synonymous_variant | 0.22 |
rpoC | 764257 | c.888G>C | synonymous_variant | 0.31 |
rpoC | 764266 | c.897T>C | synonymous_variant | 0.29 |
rpoC | 764269 | c.900G>C | synonymous_variant | 0.26 |
rpoC | 764278 | c.909A>G | synonymous_variant | 0.22 |
rpoC | 764282 | c.913_915delTCGinsAGC | synonymous_variant | 0.22 |
rpoC | 764320 | c.951C>G | synonymous_variant | 0.19 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.25 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.22 |
rpoC | 764381 | c.1012_1013delTCinsAG | synonymous_variant | 0.2 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 0.24 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.29 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.34 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.34 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.34 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.36 |
rpoC | 764455 | c.1086G>C | synonymous_variant | 0.29 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.35 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.36 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.34 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.28 |
rpoC | 764530 | c.1161C>G | synonymous_variant | 0.2 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.31 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.29 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.27 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.26 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.24 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.23 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.24 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.23 |
rpoC | 764644 | c.1275G>C | synonymous_variant | 0.24 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.32 |
rpoC | 764714 | c.1345C>T | synonymous_variant | 0.27 |
rpoC | 764720 | c.1351C>T | synonymous_variant | 0.22 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.28 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.33 |
rpoC | 764791 | c.1422C>G | synonymous_variant | 0.16 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.21 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.21 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.25 |
rpoC | 764872 | c.1503A>G | synonymous_variant | 0.26 |
rpoC | 764893 | c.1524T>C | synonymous_variant | 0.19 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.29 |
rpoC | 764923 | c.1554A>G | synonymous_variant | 0.19 |
rpoC | 764932 | c.1563C>A | synonymous_variant | 0.28 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.29 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.3 |
rpoC | 765007 | c.1638T>G | synonymous_variant | 0.2 |
rpoC | 765019 | c.1650A>G | synonymous_variant | 0.32 |
rpoC | 765022 | c.1653G>C | synonymous_variant | 0.21 |
rpoC | 765034 | c.1665T>C | synonymous_variant | 0.32 |
rpoC | 765040 | c.1671T>C | synonymous_variant | 0.3 |
rpoC | 765041 | c.1672T>C | synonymous_variant | 0.29 |
rpoC | 765047 | c.1678T>C | synonymous_variant | 0.31 |
rpoC | 765073 | c.1704G>C | synonymous_variant | 0.24 |
rpoC | 765076 | c.1707A>G | synonymous_variant | 0.23 |
rpoC | 765079 | c.1710T>G | synonymous_variant | 0.23 |
rpoC | 765082 | c.1713G>C | synonymous_variant | 0.22 |
rpoC | 765089 | c.1720T>C | synonymous_variant | 0.23 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 0.16 |
rpoC | 765171 | p.Pro601Leu | missense_variant | 0.77 |
rpoC | 765287 | c.1918C>T | synonymous_variant | 0.21 |
rpoC | 765292 | c.1923G>T | synonymous_variant | 0.23 |
rpoC | 765298 | c.1929G>C | synonymous_variant | 0.31 |
rpoC | 765300 | p.Val644Ala | missense_variant | 0.32 |
rpoC | 765319 | c.1950A>G | synonymous_variant | 0.28 |
rpoC | 765326 | p.His653Ala | missense_variant | 0.29 |
rpoC | 765346 | c.1977C>G | synonymous_variant | 0.19 |
rpoC | 765349 | c.1980T>C | synonymous_variant | 0.38 |
rpoC | 765352 | c.1983G>C | synonymous_variant | 0.37 |
rpoC | 765383 | p.Met672Leu | missense_variant | 0.34 |
rpoC | 765404 | p.Leu679Val | missense_variant | 0.32 |
rpoC | 765409 | c.2040T>C | synonymous_variant | 0.32 |
rpoC | 765412 | c.2043T>C | synonymous_variant | 0.18 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.36 |
rpoC | 765451 | c.2082C>G | synonymous_variant | 0.21 |
rpoC | 765452 | p.Ala695Ser | missense_variant | 0.22 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.36 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.34 |
rpoC | 765508 | c.2139C>G | synonymous_variant | 0.27 |
rpoC | 765517 | c.2148C>G | synonymous_variant | 0.27 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.35 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.34 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.32 |
rpoC | 765559 | c.2190G>C | synonymous_variant | 0.33 |
rpoC | 765578 | c.2209C>T | synonymous_variant | 0.26 |
rpoC | 765583 | c.2214G>T | synonymous_variant | 0.27 |
rpoC | 765613 | p.His748Gln | missense_variant | 0.38 |
rpoC | 765625 | c.2256C>G | synonymous_variant | 0.38 |
rpoC | 765628 | c.2259G>C | synonymous_variant | 0.26 |
rpoC | 765631 | p.Asp754Glu | missense_variant | 0.3 |
rpoC | 765658 | c.2289C>T | synonymous_variant | 0.23 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.39 |
rpoC | 765734 | c.2365T>C | synonymous_variant | 0.35 |
rpoC | 765739 | c.2370G>C | synonymous_variant | 0.32 |
rpoC | 765751 | c.2382C>G | synonymous_variant | 0.36 |
rpoC | 765753 | p.Asp795Ala | missense_variant | 0.34 |
rpoC | 765772 | c.2403C>G | synonymous_variant | 0.34 |
rpoC | 765784 | c.2415C>G | synonymous_variant | 0.28 |
rpoC | 765796 | c.2427C>T | synonymous_variant | 0.29 |
rpoC | 765811 | c.2442T>C | synonymous_variant | 0.32 |
rpoC | 765814 | c.2445A>G | synonymous_variant | 0.33 |
rpoC | 765826 | c.2457T>C | synonymous_variant | 0.32 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 0.3 |
rpoC | 765883 | c.2514C>G | synonymous_variant | 0.33 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.32 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.29 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.28 |
rpoC | 765970 | c.2601C>T | synonymous_variant | 0.18 |
rpoC | 765982 | c.2613C>T | synonymous_variant | 0.18 |
rpoC | 765985 | c.2616C>T | synonymous_variant | 0.16 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.3 |
rpoC | 766009 | c.2640G>C | synonymous_variant | 0.18 |
rpoC | 766010 | c.2641_2642delTCinsAG | synonymous_variant | 0.25 |
rpoC | 766021 | c.2652G>C | synonymous_variant | 0.29 |
rpoC | 766043 | p.Gln892Glu | missense_variant | 0.27 |
rpoC | 766054 | c.2685C>G | synonymous_variant | 0.3 |
rpoC | 766069 | c.2700G>A | synonymous_variant | 0.23 |
rpoC | 766082 | p.Ala905Gln | missense_variant | 0.29 |
rpoC | 766096 | c.2727G>C | synonymous_variant | 0.33 |
rpoC | 766105 | c.2736C>T | synonymous_variant | 0.24 |
rpoC | 766129 | c.2760C>G | synonymous_variant | 0.23 |
rpoC | 766135 | c.2766G>A | synonymous_variant | 0.21 |
rpoC | 766141 | c.2772C>T | synonymous_variant | 0.2 |
rpoC | 766142 | c.2773C>T | synonymous_variant | 0.2 |
rpoC | 766363 | c.2994G>C | synonymous_variant | 0.18 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.17 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.17 |
rpoC | 766390 | c.3021C>T | synonymous_variant | 0.19 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.25 |
rpoC | 766447 | c.3078T>C | synonymous_variant | 0.32 |
rpoC | 766483 | c.3114G>C | synonymous_variant | 0.28 |
rpoC | 766484 | p.Val1039Ile | missense_variant | 0.28 |
rpoC | 766492 | c.3123T>C | synonymous_variant | 0.28 |
rpoC | 766495 | c.3126C>T | synonymous_variant | 0.19 |
rpoC | 766573 | c.3204T>C | synonymous_variant | 0.18 |
rpoC | 766583 | p.Gly1072Ser | missense_variant | 0.21 |
rpoC | 766591 | c.3222A>G | synonymous_variant | 0.2 |
rpoC | 766594 | c.3225G>C | synonymous_variant | 0.21 |
rpoC | 766597 | c.3228C>G | synonymous_variant | 0.22 |
rpoC | 766607 | p.Ile1080Leu | missense_variant | 0.25 |
rpoC | 766630 | c.3261G>C | synonymous_variant | 0.28 |
rpoC | 766645 | c.3276A>G | synonymous_variant | 0.23 |
rpoC | 766651 | c.3282T>C | synonymous_variant | 0.23 |
rpoC | 766657 | c.3288A>G | synonymous_variant | 0.28 |
rpoC | 766672 | c.3303T>C | synonymous_variant | 0.25 |
rpoC | 766738 | c.3369G>T | synonymous_variant | 0.31 |
rpoC | 766750 | c.3381C>G | synonymous_variant | 0.3 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.34 |
rpoC | 766769 | c.3400C>T | synonymous_variant | 0.26 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.36 |
rpoC | 766801 | c.3432C>G | synonymous_variant | 0.4 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.41 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 0.37 |
rpoC | 766864 | c.3495G>C | synonymous_variant | 0.39 |
rpoC | 766894 | c.3525T>C | synonymous_variant | 0.27 |
rpoC | 766895 | c.3526T>C | synonymous_variant | 0.28 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.27 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.2 |
rpoC | 767009 | p.Ser1214Thr | missense_variant | 0.16 |
rpoC | 767014 | c.3645G>C | synonymous_variant | 0.2 |
rpoC | 767033 | c.3664_3666delTCGinsAGC | synonymous_variant | 0.29 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.28 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.26 |
rpoC | 767074 | c.3705T>C | synonymous_variant | 0.21 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.27 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.39 |
rpoC | 767134 | c.3765C>G | synonymous_variant | 0.23 |
rpoC | 767158 | c.3789T>G | synonymous_variant | 0.22 |
rpoC | 767167 | c.3798C>G | synonymous_variant | 0.23 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.3 |
rpoC | 767191 | c.3822C>G | synonymous_variant | 0.28 |
rpoC | 767206 | c.3837C>G | synonymous_variant | 0.24 |
rpoC | 767209 | c.3840T>C | synonymous_variant | 0.23 |
rpoC | 767212 | c.3843G>C | synonymous_variant | 0.21 |
rpoC | 767221 | c.3852C>G | synonymous_variant | 0.24 |
rpoC | 767230 | c.3861G>C | synonymous_variant | 0.23 |
rpoC | 767233 | c.3864T>C | synonymous_variant | 0.23 |
rpoC | 767263 | c.3894T>C | synonymous_variant | 0.19 |
rpoC | 767264 | p.Ala1299Gln | missense_variant | 0.19 |
rpoC | 767275 | c.3906T>C | synonymous_variant | 0.18 |
rpoC | 767278 | c.3909T>C | synonymous_variant | 0.18 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.93 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 0.98 |
rpsL | 781421 | c.-139C>A | upstream_gene_variant | 0.17 |
rpsL | 781631 | c.72G>C | synonymous_variant | 0.21 |
rpsL | 781649 | c.90T>C | synonymous_variant | 0.27 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.31 |
rpsL | 781682 | c.123T>C | synonymous_variant | 0.26 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.34 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.31 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.3 |
rpsL | 781751 | c.192G>C | synonymous_variant | 0.22 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.28 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.26 |
rpsL | 781793 | c.234G>C | synonymous_variant | 0.23 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.32 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.33 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.29 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.39 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.4 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.42 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.42 |
rpsL | 781916 | c.357T>C | synonymous_variant | 0.38 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.4 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.17 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.19 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.19 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.19 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.2 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.2 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.19 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.18 |
rplC | 800747 | c.-62C>G | upstream_gene_variant | 0.17 |
rplC | 800771 | c.-38C>T | upstream_gene_variant | 0.2 |
rplC | 800814 | c.6A>G | synonymous_variant | 0.25 |
rplC | 800817 | c.9A>T | synonymous_variant | 0.27 |
rplC | 800844 | c.36T>C | synonymous_variant | 0.28 |
rplC | 800865 | c.57A>G | synonymous_variant | 0.23 |
rplC | 800867 | p.Ser20Asn | missense_variant | 0.22 |
rplC | 800874 | c.66A>G | synonymous_variant | 0.2 |
rplC | 800877 | c.69A>C | synonymous_variant | 0.2 |
rplC | 800880 | c.72A>G | synonymous_variant | 0.21 |
rplC | 800889 | c.81C>G | synonymous_variant | 0.25 |
rplC | 800907 | c.99C>G | synonymous_variant | 0.2 |
rplC | 800916 | c.108A>G | synonymous_variant | 0.18 |
rplC | 801312 | c.504G>C | synonymous_variant | 0.17 |
rplC | 801324 | c.516T>C | synonymous_variant | 0.19 |
rplC | 801341 | p.Leu178His | missense_variant | 0.16 |
rplC | 801348 | c.540T>G | synonymous_variant | 0.18 |
rplC | 801357 | c.549T>C | synonymous_variant | 0.2 |
rplC | 801367 | p.Ala187Thr | missense_variant | 0.26 |
rplC | 801396 | c.588T>C | synonymous_variant | 0.19 |
rplC | 801402 | c.594T>C | synonymous_variant | 0.21 |
rplC | 801405 | c.597T>C | synonymous_variant | 0.2 |
rplC | 801438 | c.630T>C | synonymous_variant | 0.18 |
rplC | 801442 | p.Ile212Val | missense_variant | 0.19 |
fbiC | 1303509 | c.579G>C | synonymous_variant | 0.24 |
fbiC | 1303512 | c.582T>C | synonymous_variant | 0.24 |
fbiC | 1303534 | p.Ser202Ala | missense_variant | 0.26 |
fbiC | 1303545 | c.615A>G | synonymous_variant | 0.26 |
fbiC | 1303560 | c.630G>C | synonymous_variant | 0.22 |
fbiC | 1303575 | c.645G>C | synonymous_variant | 0.23 |
fbiC | 1303590 | c.660A>G | synonymous_variant | 0.19 |
fbiC | 1303602 | c.672A>G | synonymous_variant | 0.18 |
fbiC | 1303614 | c.684C>T | synonymous_variant | 0.15 |
fbiC | 1303632 | c.702T>G | synonymous_variant | 0.23 |
fbiC | 1303686 | c.756C>G | synonymous_variant | 0.16 |
fbiC | 1303701 | c.771C>G | synonymous_variant | 0.17 |
fbiC | 1303708 | c.778T>C | synonymous_variant | 0.19 |
fbiC | 1303716 | c.786C>T | synonymous_variant | 0.2 |
fbiC | 1303728 | c.798G>A | synonymous_variant | 0.18 |
fbiC | 1303737 | c.807G>A | synonymous_variant | 0.18 |
fbiC | 1303746 | c.816T>C | synonymous_variant | 0.19 |
fbiC | 1303752 | c.822A>G | synonymous_variant | 0.18 |
fbiC | 1303755 | c.825T>C | synonymous_variant | 0.19 |
fbiC | 1303785 | c.855G>C | synonymous_variant | 0.23 |
fbiC | 1303789 | p.Ile287Val | missense_variant | 0.23 |
fbiC | 1303818 | c.888C>G | synonymous_variant | 0.23 |
fbiC | 1303836 | c.906G>C | synonymous_variant | 0.28 |
fbiC | 1303845 | c.915C>G | synonymous_variant | 0.3 |
fbiC | 1303846 | p.Phe306Val | missense_variant | 0.3 |
fbiC | 1303854 | c.924T>C | synonymous_variant | 0.32 |
fbiC | 1303860 | c.930A>C | synonymous_variant | 0.32 |
fbiC | 1303881 | c.951G>C | synonymous_variant | 0.25 |
fbiC | 1303884 | c.954T>G | synonymous_variant | 0.29 |
fbiC | 1303911 | c.981G>C | synonymous_variant | 0.3 |
fbiC | 1303914 | c.984C>G | synonymous_variant | 0.36 |
fbiC | 1303920 | c.990C>G | synonymous_variant | 0.3 |
fbiC | 1303923 | c.993C>T | synonymous_variant | 0.26 |
fbiC | 1303929 | c.999G>C | synonymous_variant | 0.3 |
fbiC | 1303947 | c.1017T>C | synonymous_variant | 0.28 |
fbiC | 1303948 | p.Gly340Arg | missense_variant | 0.3 |
fbiC | 1303969 | p.Val347Ile | missense_variant | 0.26 |
fbiC | 1303973 | p.Gly348Ala | missense_variant | 0.26 |
fbiC | 1303981 | p.Val351Ile | missense_variant | 0.22 |
fbiC | 1303995 | c.1065C>T | synonymous_variant | 0.24 |
fbiC | 1304001 | c.1071C>G | synonymous_variant | 0.23 |
fbiC | 1304008 | c.1078T>C | synonymous_variant | 0.21 |
fbiC | 1304034 | c.1104A>G | synonymous_variant | 0.21 |
fbiC | 1304040 | c.1110C>G | synonymous_variant | 0.23 |
fbiC | 1304046 | c.1116C>G | synonymous_variant | 0.21 |
fbiC | 1304049 | c.1119T>G | synonymous_variant | 0.2 |
fbiC | 1304058 | c.1128G>A | synonymous_variant | 0.19 |
fbiC | 1304059 | c.1129C>T | synonymous_variant | 0.19 |
fbiC | 1304064 | c.1134G>C | synonymous_variant | 0.18 |
fbiC | 1304067 | c.1137G>C | synonymous_variant | 0.17 |
fbiC | 1304080 | p.Ala384Ser | missense_variant | 0.17 |
fbiC | 1304559 | p.Glu543Asp | missense_variant | 0.17 |
fbiC | 1304565 | c.1635C>G | synonymous_variant | 0.19 |
fbiC | 1304568 | c.1638T>C | synonymous_variant | 0.18 |
fbiC | 1304580 | c.1650T>C | synonymous_variant | 0.19 |
fbiC | 1304613 | c.1683T>C | synonymous_variant | 0.18 |
fbiC | 1304634 | c.1704C>G | synonymous_variant | 0.2 |
fbiC | 1304640 | c.1710A>C | synonymous_variant | 0.22 |
fbiC | 1304646 | c.1716T>C | synonymous_variant | 0.19 |
fbiC | 1304658 | c.1728C>G | synonymous_variant | 0.18 |
fbiC | 1304703 | c.1773C>G | synonymous_variant | 0.21 |
fbiC | 1304715 | c.1785G>C | synonymous_variant | 0.21 |
fbiC | 1304742 | c.1812T>C | synonymous_variant | 0.19 |
fbiC | 1304754 | c.1824G>A | synonymous_variant | 0.17 |
fbiC | 1304757 | c.1827A>G | synonymous_variant | 0.24 |
fbiC | 1304784 | c.1854T>C | synonymous_variant | 0.32 |
fbiC | 1304787 | c.1857T>C | synonymous_variant | 0.24 |
fbiC | 1304790 | c.1860C>G | synonymous_variant | 0.21 |
fbiC | 1304808 | c.1878C>G | synonymous_variant | 0.31 |
fbiC | 1304811 | c.1881C>G | synonymous_variant | 0.32 |
fbiC | 1304817 | c.1887T>C | synonymous_variant | 0.39 |
fbiC | 1304829 | c.1899T>C | synonymous_variant | 0.55 |
fbiC | 1304832 | c.1902C>T | synonymous_variant | 0.36 |
fbiC | 1304853 | c.1923C>G | synonymous_variant | 0.36 |
fbiC | 1304856 | c.1926C>G | synonymous_variant | 0.68 |
fbiC | 1304862 | c.1932G>A | synonymous_variant | 0.25 |
fbiC | 1304869 | c.1939C>T | synonymous_variant | 0.28 |
fbiC | 1304875 | p.Ile649Val | missense_variant | 0.26 |
fbiC | 1304883 | p.Glu651Asp | missense_variant | 0.23 |
fbiC | 1304891 | p.Ile654Thr | missense_variant | 0.21 |
fbiC | 1304893 | p.Gly655Ser | missense_variant | 0.38 |
fbiC | 1304907 | c.1977C>G | synonymous_variant | 0.21 |
fbiC | 1304910 | c.1980G>C | synonymous_variant | 0.19 |
fbiC | 1304916 | c.1986T>C | synonymous_variant | 0.32 |
fbiC | 1304928 | c.1998T>C | synonymous_variant | 0.23 |
fbiC | 1304937 | c.2007G>C | synonymous_variant | 0.22 |
fbiC | 1304958 | c.2028T>G | synonymous_variant | 0.24 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 0.86 |
atpE | 1461132 | p.Val30Ile | missense_variant | 0.18 |
atpE | 1461159 | p.Val39Ile | missense_variant | 0.18 |
atpE | 1461185 | c.141G>C | synonymous_variant | 0.21 |
atpE | 1461189 | c.145C>T | synonymous_variant | 0.2 |
atpE | 1461194 | c.150C>T | synonymous_variant | 0.21 |
atpE | 1461197 | c.153A>G | synonymous_variant | 0.24 |
atpE | 1461219 | c.175T>C | synonymous_variant | 0.2 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473123 | n.1278A>G | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473660 | n.3G>A | non_coding_transcript_exon_variant | 0.68 |
rrl | 1473668 | n.11C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473756 | n.99G>A | non_coding_transcript_exon_variant | 0.32 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473813 | n.156C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1473839 | n.182G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1473899 | n.242A>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1473937 | n.280C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1473944 | n.287G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473945 | n.288T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474009 | n.352A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474012 | n.355C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474051 | n.394T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474054 | n.397T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474056 | n.399T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474093 | n.436G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474099 | n.442G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474104 | n.447G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474111 | n.454T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474112 | n.455T>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475249 | n.1592T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475252 | n.1595C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475266 | n.1609T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475275 | n.1618C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475276 | n.1619T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475291 | n.1634A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475313 | n.1656G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475638 | n.1981C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475659 | n.2002G>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476025 | n.2368G>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476033 | n.2376T>C | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476034 | n.2377C>A | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476089 | n.2432T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476095 | n.2438C>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476117 | n.2460G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476214 | n.2557G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476689 | n.3032A>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476690 | n.3033C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476693 | n.3036G>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476695 | n.3038T>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476716 | n.3059A>C | non_coding_transcript_exon_variant | 0.17 |
inhA | 1674280 | c.79C>A | synonymous_variant | 0.15 |
inhA | 1674315 | c.114C>G | synonymous_variant | 0.23 |
inhA | 1674321 | c.120G>C | synonymous_variant | 0.29 |
inhA | 1674342 | c.141T>C | synonymous_variant | 0.28 |
inhA | 1674352 | p.Thr51Val | missense_variant | 0.25 |
inhA | 1674368 | p.Ala56Glu | missense_variant | 0.21 |
inhA | 1674379 | c.178C>T | synonymous_variant | 0.21 |
inhA | 1674382 | p.Leu61Ile | missense_variant | 0.2 |
inhA | 1674387 | c.186A>G | synonymous_variant | 0.23 |
inhA | 1674399 | c.198A>G | synonymous_variant | 0.22 |
inhA | 1674507 | c.306G>C | synonymous_variant | 0.24 |
inhA | 1674537 | c.336C>G | synonymous_variant | 0.25 |
inhA | 1674542 | p.Ala114Glu | missense_variant | 0.26 |
inhA | 1674549 | c.348G>C | synonymous_variant | 0.25 |
inhA | 1674555 | c.354G>A | synonymous_variant | 0.26 |
inhA | 1674561 | c.360C>T | synonymous_variant | 0.27 |
inhA | 1674582 | c.381T>C | synonymous_variant | 0.31 |
inhA | 1674585 | c.384T>C | synonymous_variant | 0.3 |
inhA | 1674589 | p.Met130Leu | missense_variant | 0.3 |
inhA | 1674624 | c.423A>C | synonymous_variant | 0.36 |
inhA | 1674627 | c.426T>G | synonymous_variant | 0.27 |
inhA | 1674630 | c.429C>G | synonymous_variant | 0.27 |
inhA | 1674636 | c.435C>G | synonymous_variant | 0.33 |
inhA | 1674654 | c.453G>C | synonymous_variant | 0.33 |
inhA | 1674693 | c.492C>G | synonymous_variant | 0.23 |
inhA | 1674703 | c.502T>C | synonymous_variant | 0.23 |
rpsA | 1833541 | c.-1T>C | upstream_gene_variant | 0.17 |
rpsA | 1833554 | p.Thr5Ala | missense_variant | 0.21 |
rpsA | 1833568 | c.27G>C | synonymous_variant | 0.22 |
rpsA | 1833589 | c.48A>T | synonymous_variant | 0.18 |
rpsA | 1833595 | c.54T>C | synonymous_variant | 0.2 |
rpsA | 1833619 | c.78A>C | synonymous_variant | 0.16 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.2 |
rpsA | 1833667 | c.126C>G | synonymous_variant | 0.21 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.32 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.33 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.37 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.36 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.4 |
rpsA | 1833790 | c.249T>A | synonymous_variant | 0.32 |
rpsA | 1833799 | c.258C>G | synonymous_variant | 0.29 |
rpsA | 1833811 | c.270G>C | synonymous_variant | 0.31 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.34 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.35 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.38 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.37 |
rpsA | 1833862 | c.321G>T | synonymous_variant | 0.3 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.34 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.37 |
rpsA | 1833940 | c.399C>G | synonymous_variant | 0.35 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.24 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.33 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.32 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.22 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.24 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.22 |
rpsA | 1834186 | c.645C>G | synonymous_variant | 0.28 |
rpsA | 1834189 | c.648G>C | synonymous_variant | 0.33 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 0.33 |
rpsA | 1834201 | c.660C>T | synonymous_variant | 0.29 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.29 |
rpsA | 1834225 | c.684C>G | synonymous_variant | 0.25 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.25 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.3 |
rpsA | 1834261 | c.720A>C | synonymous_variant | 0.3 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.32 |
rpsA | 1834297 | c.756C>G | synonymous_variant | 0.26 |
rpsA | 1834303 | c.762T>G | synonymous_variant | 0.29 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.28 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.34 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.36 |
rpsA | 1834375 | c.834G>A | synonymous_variant | 0.24 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.33 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.31 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.34 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.31 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.33 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.34 |
rpsA | 1834465 | c.924T>C | synonymous_variant | 0.29 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.32 |
rpsA | 1834474 | c.933C>G | synonymous_variant | 0.21 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.3 |
rpsA | 1834498 | c.957C>T | synonymous_variant | 0.25 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.32 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.25 |
rpsA | 1834555 | c.1014T>C | synonymous_variant | 0.24 |
rpsA | 1834558 | c.1017C>G | synonymous_variant | 0.23 |
rpsA | 1834594 | c.1053C>T | synonymous_variant | 0.15 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.19 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.19 |
rpsA | 1834726 | c.1185C>A | synonymous_variant | 0.2 |
rpsA | 1834732 | c.1191T>C | synonymous_variant | 0.26 |
rpsA | 1834733 | p.Ala398Pro | missense_variant | 0.22 |
rpsA | 1834753 | c.1212T>C | synonymous_variant | 0.29 |
rpsA | 1834765 | c.1224A>G | synonymous_variant | 0.25 |
rpsA | 1834780 | c.1239A>G | synonymous_variant | 0.32 |
rpsA | 1834786 | c.1245A>G | synonymous_variant | 0.32 |
rpsA | 1834789 | c.1248T>C | synonymous_variant | 0.33 |
rpsA | 1834792 | c.1251G>C | synonymous_variant | 0.33 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 0.98 |
ndh | 2102212 | c.831G>C | synonymous_variant | 0.18 |
ndh | 2102218 | c.825C>G | synonymous_variant | 0.22 |
ndh | 2102233 | c.810G>A | synonymous_variant | 0.31 |
ndh | 2102242 | c.801G>A | synonymous_variant | 0.26 |
ndh | 2102644 | c.399A>G | synonymous_variant | 0.17 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.75 |
katG | 2155054 | p.Tyr353Phe | missense_variant | 0.19 |
katG | 2155056 | c.1056A>G | synonymous_variant | 0.2 |
katG | 2155062 | c.1050T>C | synonymous_variant | 0.2 |
katG | 2155065 | c.1047C>G | synonymous_variant | 0.2 |
katG | 2155068 | c.1044T>C | synonymous_variant | 0.2 |
katG | 2155071 | c.1041T>C | synonymous_variant | 0.2 |
katG | 2155080 | c.1032G>C | synonymous_variant | 0.25 |
katG | 2155113 | c.999C>G | synonymous_variant | 0.22 |
katG | 2155632 | c.480A>C | synonymous_variant | 0.21 |
katG | 2155637 | p.Leu159Ile | missense_variant | 0.23 |
katG | 2155641 | p.Lys157Asn | missense_variant | 0.24 |
katG | 2155691 | c.421T>C | synonymous_variant | 0.2 |
katG | 2155695 | c.417C>G | synonymous_variant | 0.19 |
katG | 2155704 | c.408C>G | synonymous_variant | 0.2 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 0.84 |
PPE35 | 2167983 | p.Gly877Asp | missense_variant | 0.83 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 0.76 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289991 | c.-750G>C | upstream_gene_variant | 0.22 |
pncA | 2289994 | c.-753A>G | upstream_gene_variant | 0.21 |
pncA | 2289997 | c.-756G>C | upstream_gene_variant | 0.18 |
pncA | 2290015 | c.-774A>C | upstream_gene_variant | 0.19 |
pncA | 2290027 | c.-786G>A | upstream_gene_variant | 0.17 |
pncA | 2290030 | c.-791_-789delAATinsCAC | upstream_gene_variant | 0.22 |
pncA | 2290033 | c.-792C>G | upstream_gene_variant | 0.22 |
pncA | 2290038 | c.-797G>T | upstream_gene_variant | 0.18 |
pncA | 2290042 | c.-801T>C | upstream_gene_variant | 0.2 |
kasA | 2517947 | c.-168C>T | upstream_gene_variant | 0.24 |
kasA | 2517974 | c.-141T>C | upstream_gene_variant | 0.24 |
kasA | 2517989 | c.-126T>C | upstream_gene_variant | 0.18 |
kasA | 2518132 | c.18C>T | synonymous_variant | 0.88 |
kasA | 2518146 | p.Phe11Tyr | missense_variant | 0.15 |
kasA | 2518162 | c.48G>A | synonymous_variant | 0.22 |
kasA | 2518174 | c.60A>G | synonymous_variant | 0.22 |
kasA | 2518190 | p.Ser26Ala | missense_variant | 0.23 |
kasA | 2518199 | p.Ile29Val | missense_variant | 0.19 |
kasA | 2518561 | c.447T>C | synonymous_variant | 0.19 |
kasA | 2518567 | c.453G>C | synonymous_variant | 0.19 |
kasA | 2518574 | p.Ile154Val | missense_variant | 0.18 |
kasA | 2518588 | c.474T>C | synonymous_variant | 0.19 |
kasA | 2518609 | p.Met165Ile | missense_variant | 0.22 |
kasA | 2518621 | c.507G>A | synonymous_variant | 0.18 |
kasA | 2518642 | c.528A>G | synonymous_variant | 0.21 |
kasA | 2518663 | c.549T>C | synonymous_variant | 0.21 |
kasA | 2518672 | c.558G>C | synonymous_variant | 0.21 |
kasA | 2518687 | c.573C>T | synonymous_variant | 0.18 |
kasA | 2518696 | c.582C>G | synonymous_variant | 0.2 |
kasA | 2518702 | c.588C>T | synonymous_variant | 0.18 |
kasA | 2518714 | c.600A>C | synonymous_variant | 0.17 |
kasA | 2518732 | c.618C>G | synonymous_variant | 0.17 |
kasA | 2518768 | c.654C>G | synonymous_variant | 0.21 |
kasA | 2518783 | c.669T>C | synonymous_variant | 0.24 |
kasA | 2518792 | c.678C>G | synonymous_variant | 0.22 |
kasA | 2518795 | c.681C>G | synonymous_variant | 0.25 |
kasA | 2518816 | c.702C>A | synonymous_variant | 0.25 |
kasA | 2518822 | c.708C>G | synonymous_variant | 0.23 |
kasA | 2518825 | c.711T>C | synonymous_variant | 0.25 |
kasA | 2518855 | c.741C>G | synonymous_variant | 0.2 |
kasA | 2518864 | c.750G>C | synonymous_variant | 0.17 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 0.91 |
ahpC | 2726336 | c.144G>C | synonymous_variant | 0.17 |
ahpC | 2726348 | c.156T>C | synonymous_variant | 0.21 |
ahpC | 2726354 | c.162G>C | synonymous_variant | 0.21 |
ahpC | 2726357 | c.165A>G | synonymous_variant | 0.19 |
ahpC | 2726579 | c.387T>C | synonymous_variant | 0.18 |
ahpC | 2726591 | c.399C>G | synonymous_variant | 0.2 |
ahpC | 2726593 | p.Val134Ala | missense_variant | 0.2 |
ahpC | 2726600 | c.408T>C | synonymous_variant | 0.2 |
ahpC | 2726612 | c.420C>G | synonymous_variant | 0.18 |
ahpC | 2726638 | p.Ala149Val | missense_variant | 0.24 |
ahpC | 2726645 | c.453C>G | synonymous_variant | 0.26 |
ahpC | 2726657 | c.465A>C | synonymous_variant | 0.24 |
ahpC | 2726669 | p.Asp159Glu | missense_variant | 0.2 |
ahpC | 2726672 | c.480G>A | synonymous_variant | 0.19 |
ahpC | 2726696 | c.504C>G | synonymous_variant | 0.17 |
folC | 2747059 | c.540T>C | synonymous_variant | 0.2 |
folC | 2747065 | c.534C>G | synonymous_variant | 0.2 |
folC | 2747086 | c.513A>C | synonymous_variant | 0.25 |
folC | 2747089 | c.510G>C | synonymous_variant | 0.25 |
folC | 2747098 | c.501C>G | synonymous_variant | 0.22 |
folC | 2747101 | c.498G>C | synonymous_variant | 0.25 |
folC | 2747107 | c.492G>C | synonymous_variant | 0.24 |
folC | 2747110 | c.489T>C | synonymous_variant | 0.23 |
folC | 2747113 | c.486C>G | synonymous_variant | 0.21 |
folC | 2747116 | c.483G>C | synonymous_variant | 0.21 |
folC | 2747314 | c.285A>C | synonymous_variant | 0.17 |
folC | 2747317 | c.282C>G | synonymous_variant | 0.16 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 0.9 |
Rv2752c | 3064995 | c.1197C>G | synonymous_variant | 0.18 |
Rv2752c | 3064998 | c.1194A>G | synonymous_variant | 0.19 |
Rv2752c | 3065018 | p.Asn392His | missense_variant | 0.2 |
Rv2752c | 3065028 | c.1164G>C | synonymous_variant | 0.19 |
Rv2752c | 3065925 | p.Ala89Gly | missense_variant | 0.18 |
Rv2752c | 3065928 | c.264G>C | synonymous_variant | 0.18 |
Rv2752c | 3065947 | p.Gly82Ala | missense_variant | 0.23 |
Rv2752c | 3065955 | c.235_237delTTGinsCTC | synonymous_variant | 0.21 |
Rv2752c | 3065979 | c.213T>C | synonymous_variant | 0.25 |
Rv2752c | 3065993 | p.Val67Ile | missense_variant | 0.2 |
Rv2752c | 3065994 | c.198T>C | synonymous_variant | 0.2 |
Rv2752c | 3065997 | c.195C>G | synonymous_variant | 0.18 |
Rv2752c | 3066002 | p.Met64Leu | missense_variant | 0.23 |
Rv2752c | 3066024 | c.168T>C | synonymous_variant | 0.21 |
Rv2752c | 3066040 | p.Gly51Thr | missense_variant | 0.24 |
Rv2752c | 3066042 | c.150T>C | synonymous_variant | 0.25 |
Rv2752c | 3066050 | p.Leu48Met | missense_variant | 0.28 |
Rv2752c | 3066054 | c.138T>G | synonymous_variant | 0.32 |
Rv2752c | 3066066 | c.126T>C | synonymous_variant | 0.3 |
Rv2752c | 3066075 | c.117A>G | synonymous_variant | 0.29 |
Rv2752c | 3066087 | c.105A>G | synonymous_variant | 0.2 |
Rv2752c | 3066117 | p.Asn25Ser | missense_variant | 0.21 |
Rv2752c | 3066294 | c.-103C>G | upstream_gene_variant | 0.18 |
Rv2752c | 3066300 | c.-109G>A | upstream_gene_variant | 0.18 |
Rv2752c | 3066303 | c.-112C>G | upstream_gene_variant | 0.19 |
Rv2752c | 3066309 | c.-118T>C | upstream_gene_variant | 0.2 |
Rv2752c | 3066336 | c.-145C>G | upstream_gene_variant | 0.2 |
Rv2752c | 3066345 | c.-154C>G | upstream_gene_variant | 0.17 |
Rv2752c | 3066350 | c.-159T>A | upstream_gene_variant | 0.18 |
thyX | 3067316 | c.630A>G | synonymous_variant | 0.19 |
thyX | 3067325 | c.621A>G | synonymous_variant | 0.25 |
thyX | 3067355 | c.591A>C | synonymous_variant | 0.28 |
thyX | 3067367 | c.579G>C | synonymous_variant | 0.32 |
thyX | 3067376 | c.570G>C | synonymous_variant | 0.26 |
thyX | 3067391 | c.555G>C | synonymous_variant | 0.38 |
thyX | 3067394 | c.552G>C | synonymous_variant | 0.37 |
thyX | 3067412 | c.534C>G | synonymous_variant | 0.23 |
thyX | 3067439 | c.507A>G | synonymous_variant | 0.3 |
thyX | 3067457 | c.489C>G | synonymous_variant | 0.3 |
thyX | 3067465 | p.Ile161Val | missense_variant | 0.28 |
thyX | 3067490 | c.456C>G | synonymous_variant | 0.17 |
thyX | 3067493 | c.453A>G | synonymous_variant | 0.27 |
thyX | 3067515 | p.Ser144Thr | missense_variant | 0.25 |
thyX | 3067531 | p.Ala139Thr | missense_variant | 0.16 |
thyX | 3067652 | c.294T>C | synonymous_variant | 0.2 |
thyX | 3067661 | c.285C>G | synonymous_variant | 0.23 |
thyX | 3067682 | c.264G>C | synonymous_variant | 0.18 |
thyX | 3067685 | c.261A>G | synonymous_variant | 0.19 |
thyX | 3067688 | c.258G>C | synonymous_variant | 0.18 |
thyX | 3067694 | c.252G>C | synonymous_variant | 0.21 |
thyX | 3067793 | c.153T>C | synonymous_variant | 0.17 |
thyX | 3067814 | c.132T>C | synonymous_variant | 0.17 |
thyX | 3067826 | c.120C>G | synonymous_variant | 0.2 |
thyX | 3067850 | c.96A>C | synonymous_variant | 0.26 |
thyX | 3067869 | p.Thr26Ser | missense_variant | 0.18 |
thyX | 3067874 | c.72C>G | synonymous_variant | 0.19 |
thyA | 3073863 | c.609T>C | synonymous_variant | 0.19 |
thyA | 3073872 | p.Ile200Val | missense_variant | 0.19 |
thyA | 3073878 | c.594G>A | synonymous_variant | 0.21 |
thyA | 3073892 | c.580T>C | synonymous_variant | 0.25 |
thyA | 3073893 | c.579C>G | synonymous_variant | 0.22 |
thyA | 3073925 | c.547T>C | synonymous_variant | 0.27 |
thyA | 3073929 | c.543T>C | synonymous_variant | 0.28 |
thyA | 3073953 | c.519T>C | synonymous_variant | 0.3 |
thyA | 3073977 | c.495A>G | synonymous_variant | 0.26 |
thyA | 3073989 | c.483T>C | synonymous_variant | 0.28 |
thyA | 3074001 | c.471C>G | synonymous_variant | 0.22 |
thyA | 3074004 | c.468T>C | synonymous_variant | 0.29 |
thyA | 3074010 | c.462C>G | synonymous_variant | 0.28 |
thyA | 3074031 | c.441T>C | synonymous_variant | 0.3 |
thyA | 3074037 | c.435C>G | synonymous_variant | 0.27 |
thyA | 3074056 | p.Glu139Pro | missense_variant | 0.28 |
thyA | 3074061 | c.411A>G | synonymous_variant | 0.26 |
thyA | 3074076 | c.396C>G | synonymous_variant | 0.21 |
thyA | 3074082 | c.390G>C | synonymous_variant | 0.2 |
thyA | 3074205 | p.Glu89Asp | missense_variant | 0.16 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 0.91 |
fprA | 3473809 | c.-198G>C | upstream_gene_variant | 0.21 |
fprA | 3473812 | c.-195G>A | upstream_gene_variant | 0.21 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 0.98 |
fprA | 3474141 | c.135C>G | synonymous_variant | 0.17 |
fprA | 3474177 | c.171C>T | synonymous_variant | 0.17 |
fprA | 3474597 | c.591C>A | synonymous_variant | 0.84 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 0.9 |
Rv3236c | 3612643 | c.474A>G | synonymous_variant | 0.21 |
Rv3236c | 3612667 | c.450T>G | synonymous_variant | 0.21 |
Rv3236c | 3612673 | c.444G>C | synonymous_variant | 0.17 |
fbiB | 3642614 | c.1080C>T | synonymous_variant | 0.22 |
fbiB | 3642620 | c.1086T>C | synonymous_variant | 0.24 |
fbiB | 3642656 | c.1122G>C | synonymous_variant | 0.18 |
fbiB | 3642662 | c.1128C>G | synonymous_variant | 0.18 |
fbiB | 3642677 | c.1143A>G | synonymous_variant | 0.17 |
fbiB | 3642680 | c.1146A>G | synonymous_variant | 0.17 |
fbiB | 3642684 | c.1150T>C | synonymous_variant | 0.18 |
rpoA | 3877503 | c.1005G>C | synonymous_variant | 0.2 |
rpoA | 3877507 | p.Gly334Ala | missense_variant | 0.21 |
rpoA | 3877515 | c.993G>C | synonymous_variant | 0.26 |
rpoA | 3877542 | c.966C>T | synonymous_variant | 0.2 |
rpoA | 3877553 | p.Glu319Gln | missense_variant | 0.28 |
rpoA | 3877557 | c.951C>G | synonymous_variant | 0.22 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.31 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.2 |
rpoA | 3877638 | c.870T>C | synonymous_variant | 0.2 |
rpoA | 3877656 | c.852T>C | synonymous_variant | 0.23 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.27 |
rpoA | 3877677 | p.Ala277Thr | missense_variant | 0.18 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.25 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.24 |
rpoA | 3877704 | c.804G>T | synonymous_variant | 0.22 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.31 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.37 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.37 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.38 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.4 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.38 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.33 |
rpoA | 3877848 | c.660C>T | synonymous_variant | 0.19 |
rpoA | 3877857 | c.651G>A | synonymous_variant | 0.3 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.27 |
rpoA | 3877872 | c.636C>T | synonymous_variant | 0.2 |
rpoA | 3877875 | c.633T>G | synonymous_variant | 0.33 |
rpoA | 3877890 | c.618C>T | synonymous_variant | 0.16 |
rpoA | 3877899 | p.Ser203Thr | missense_variant | 0.18 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.32 |
rpoA | 3877908 | p.Asn200Ser | missense_variant | 0.19 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.37 |
rpoA | 3877986 | c.522G>C | synonymous_variant | 0.32 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.29 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.3 |
rpoA | 3878022 | c.486T>C | synonymous_variant | 0.29 |
rpoA | 3878025 | c.483C>T | synonymous_variant | 0.25 |
rpoA | 3878028 | c.480G>C | synonymous_variant | 0.31 |
rpoA | 3878031 | c.477T>C | synonymous_variant | 0.31 |
rpoA | 3878040 | c.468T>C | synonymous_variant | 0.32 |
rpoA | 3878046 | c.462T>C | synonymous_variant | 0.28 |
rpoA | 3878049 | c.459G>C | synonymous_variant | 0.25 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.27 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.25 |
rpoA | 3878067 | c.441C>G | synonymous_variant | 0.22 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.2 |
rpoA | 3878082 | c.426T>C | synonymous_variant | 0.19 |
rpoA | 3878094 | c.414C>G | synonymous_variant | 0.21 |
rpoA | 3878100 | c.408C>G | synonymous_variant | 0.2 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.2 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.2 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.23 |
rpoA | 3878141 | p.Met123Leu | missense_variant | 0.23 |
rpoA | 3878142 | p.Gly122Glu | missense_variant | 0.2 |
rpoA | 3878169 | c.339G>C | synonymous_variant | 0.29 |
rpoA | 3878184 | c.324C>T | synonymous_variant | 0.25 |
rpoA | 3878187 | c.321C>G | synonymous_variant | 0.28 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.26 |
rpoA | 3878199 | c.309T>C | synonymous_variant | 0.25 |
rpoA | 3878202 | c.306G>C | synonymous_variant | 0.2 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.24 |
rpoA | 3878220 | c.288C>T | synonymous_variant | 0.25 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.27 |
rpoA | 3878284 | p.Glu75Ala | missense_variant | 0.19 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.21 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.2 |
rpoA | 3878304 | c.204G>C | synonymous_variant | 0.21 |
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 | 0.2 |
rpoA | 3878334 | c.174T>C | synonymous_variant | 0.2 |
rpoA | 3878337 | c.171T>C | synonymous_variant | 0.21 |
rpoA | 3878346 | c.162T>C | synonymous_variant | 0.23 |
rpoA | 3878367 | c.141C>G | synonymous_variant | 0.2 |
rpoA | 3878376 | c.132G>C | synonymous_variant | 0.22 |
rpoA | 3878385 | c.123C>G | synonymous_variant | 0.22 |
rpoA | 3878391 | c.117T>C | synonymous_variant | 0.24 |
rpoA | 3878396 | c.112C>T | synonymous_variant | 0.2 |
rpoA | 3878436 | c.72A>G | synonymous_variant | 0.3 |
rpoA | 3878442 | c.66G>C | synonymous_variant | 0.28 |
rpoA | 3878454 | c.54A>C | synonymous_variant | 0.24 |
rpoA | 3878472 | p.Asp12Glu | missense_variant | 0.23 |
rpoA | 3878478 | c.30C>G | synonymous_variant | 0.2 |
rpoA | 3878490 | c.18C>A | synonymous_variant | 0.2 |
rpoA | 3878496 | c.12A>T | synonymous_variant | 0.18 |
rpoA | 3878672 | c.-165A>T | upstream_gene_variant | 0.15 |
ddn | 3986648 | c.-196C>G | upstream_gene_variant | 0.24 |
ddn | 3986655 | c.-189A>T | upstream_gene_variant | 0.15 |
ddn | 3986665 | c.-179G>C | upstream_gene_variant | 0.2 |
ddn | 3986667 | c.-177_-176delCTinsAC | upstream_gene_variant | 0.19 |
clpC1 | 4038271 | p.Pro812Ala | missense_variant | 0.25 |
clpC1 | 4038272 | p.Gly811Ser | missense_variant | 0.25 |
clpC1 | 4038278 | c.2427T>C | synonymous_variant | 0.24 |
clpC1 | 4038293 | c.2412G>C | synonymous_variant | 0.27 |
clpC1 | 4038302 | c.2403C>G | synonymous_variant | 0.3 |
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 | 4038356 | c.2349T>C | synonymous_variant | 0.25 |
clpC1 | 4038359 | c.2346A>G | synonymous_variant | 0.24 |
clpC1 | 4038368 | c.2337T>C | synonymous_variant | 0.24 |
clpC1 | 4038388 | c.2317T>C | synonymous_variant | 0.21 |
clpC1 | 4038398 | c.2307G>T | synonymous_variant | 0.22 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 0.21 |
clpC1 | 4038419 | c.2286T>C | synonymous_variant | 0.24 |
clpC1 | 4038445 | p.Ala754Thr | missense_variant | 0.15 |
clpC1 | 4038462 | p.Ala748Glu | missense_variant | 0.16 |
clpC1 | 4038498 | p.Ser736Thr | missense_variant | 0.29 |
clpC1 | 4038530 | p.Glu725Asp | missense_variant | 0.39 |
clpC1 | 4038536 | c.2169C>T | synonymous_variant | 0.29 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.41 |
clpC1 | 4038623 | c.2082A>G | synonymous_variant | 0.29 |
clpC1 | 4038640 | p.Asp689Asn | missense_variant | 0.24 |
clpC1 | 4038653 | c.2052C>T | synonymous_variant | 0.2 |
clpC1 | 4038661 | p.Ser682Thr | missense_variant | 0.17 |
clpC1 | 4038671 | c.2034T>C | synonymous_variant | 0.2 |
clpC1 | 4038683 | c.2022T>C | synonymous_variant | 0.23 |
clpC1 | 4038695 | c.2010C>G | synonymous_variant | 0.19 |
clpC1 | 4038701 | c.2004G>C | synonymous_variant | 0.2 |
clpC1 | 4038704 | c.2001T>C | synonymous_variant | 0.2 |
clpC1 | 4038707 | c.1998C>G | synonymous_variant | 0.19 |
clpC1 | 4038710 | c.1995G>C | synonymous_variant | 0.2 |
clpC1 | 4038713 | c.1992T>C | synonymous_variant | 0.22 |
clpC1 | 4038740 | c.1965G>C | synonymous_variant | 0.23 |
clpC1 | 4038755 | c.1950G>C | synonymous_variant | 0.25 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.28 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.26 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 0.21 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.32 |
clpC1 | 4038815 | c.1890G>T | synonymous_variant | 0.25 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.37 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.41 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.43 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 0.4 |
clpC1 | 4038932 | c.1773G>C | synonymous_variant | 0.29 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.38 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.37 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.38 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.34 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.36 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.36 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.34 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.34 |
clpC1 | 4039073 | c.1632C>G | synonymous_variant | 0.32 |
clpC1 | 4039085 | c.1620A>G | synonymous_variant | 0.27 |
clpC1 | 4039090 | c.1615C>T | synonymous_variant | 0.27 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.35 |
clpC1 | 4039103 | c.1602T>C | synonymous_variant | 0.32 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.31 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.33 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.35 |
clpC1 | 4039124 | c.1581C>G | synonymous_variant | 0.21 |
clpC1 | 4039127 | c.1578G>A | synonymous_variant | 0.21 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.3 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.28 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.3 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.29 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.3 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.29 |
clpC1 | 4039187 | c.1518G>C | synonymous_variant | 0.21 |
clpC1 | 4039190 | c.1515C>G | synonymous_variant | 0.23 |
clpC1 | 4039208 | c.1497C>G | synonymous_variant | 0.2 |
clpC1 | 4039226 | c.1479T>C | synonymous_variant | 0.29 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.27 |
clpC1 | 4039286 | c.1419T>C | synonymous_variant | 0.25 |
clpC1 | 4039295 | c.1410A>C | synonymous_variant | 0.24 |
clpC1 | 4039298 | c.1407T>C | synonymous_variant | 0.24 |
clpC1 | 4039319 | c.1386T>C | synonymous_variant | 0.25 |
clpC1 | 4039322 | c.1383T>C | synonymous_variant | 0.24 |
clpC1 | 4039328 | c.1377A>G | synonymous_variant | 0.19 |
clpC1 | 4039337 | p.Thr456Gln | missense_variant | 0.19 |
clpC1 | 4039364 | c.1341C>G | synonymous_variant | 0.25 |
clpC1 | 4039391 | c.1314T>G | synonymous_variant | 0.19 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.18 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.2 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 0.19 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.19 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.2 |
clpC1 | 4039481 | c.1224T>G | synonymous_variant | 0.17 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.27 |
clpC1 | 4039524 | p.Phe394Tyr | missense_variant | 0.17 |
clpC1 | 4039532 | c.1173C>T | synonymous_variant | 0.19 |
clpC1 | 4039547 | c.1158C>G | synonymous_variant | 0.26 |
clpC1 | 4039553 | c.1152C>G | synonymous_variant | 0.26 |
clpC1 | 4039562 | c.1143C>G | synonymous_variant | 0.37 |
clpC1 | 4039576 | p.Ala377Ser | missense_variant | 0.28 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.37 |
clpC1 | 4039586 | c.1119G>C | synonymous_variant | 0.27 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.4 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.42 |
clpC1 | 4039622 | c.1083C>G | synonymous_variant | 0.36 |
clpC1 | 4039682 | c.1023C>G | synonymous_variant | 0.33 |
clpC1 | 4039685 | c.1020C>T | synonymous_variant | 0.34 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.3 |
clpC1 | 4039748 | c.957G>C | synonymous_variant | 0.2 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.25 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.24 |
clpC1 | 4039760 | c.945T>C | synonymous_variant | 0.23 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.26 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.23 |
clpC1 | 4039781 | c.924G>C | synonymous_variant | 0.21 |
clpC1 | 4039789 | p.Ser306Thr | missense_variant | 0.15 |
clpC1 | 4039793 | c.912C>G | synonymous_variant | 0.18 |
clpC1 | 4039817 | c.888A>T | synonymous_variant | 0.17 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.24 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 0.32 |
clpC1 | 4039832 | c.873C>G | synonymous_variant | 0.18 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.31 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.38 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.37 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.31 |
clpC1 | 4039928 | c.775_777delAGCinsTCG | synonymous_variant | 0.27 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.28 |
clpC1 | 4039946 | c.759A>T | synonymous_variant | 0.21 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.3 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.23 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.34 |
clpC1 | 4039996 | p.Glu237Gln | missense_variant | 0.28 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.3 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.3 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.33 |
clpC1 | 4040036 | c.669C>G | synonymous_variant | 0.32 |
clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 0.21 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.21 |
clpC1 | 4040105 | c.600C>G | synonymous_variant | 0.24 |
clpC1 | 4040147 | c.558A>G | synonymous_variant | 0.24 |
clpC1 | 4040171 | c.534C>G | synonymous_variant | 0.2 |
clpC1 | 4040201 | c.504C>G | synonymous_variant | 0.24 |
clpC1 | 4040213 | c.490_492delTCTinsAGC | synonymous_variant | 0.2 |
clpC1 | 4040225 | c.480A>C | synonymous_variant | 0.24 |
clpC1 | 4040237 | c.468C>T | synonymous_variant | 0.29 |
clpC1 | 4040249 | c.456A>G | synonymous_variant | 0.33 |
clpC1 | 4040264 | c.441C>T | synonymous_variant | 0.24 |
clpC1 | 4040267 | c.438A>G | synonymous_variant | 0.32 |
clpC1 | 4040273 | c.432T>C | synonymous_variant | 0.29 |
clpC1 | 4040354 | c.351A>G | synonymous_variant | 0.32 |
clpC1 | 4040363 | c.342A>C | synonymous_variant | 0.28 |
clpC1 | 4040369 | c.336C>G | synonymous_variant | 0.28 |
clpC1 | 4040380 | c.325T>C | synonymous_variant | 0.24 |
clpC1 | 4040387 | c.318A>G | synonymous_variant | 0.21 |
clpC1 | 4040393 | c.312G>C | synonymous_variant | 0.17 |
clpC1 | 4040411 | c.294T>C | synonymous_variant | 0.21 |
clpC1 | 4040423 | c.282A>G | synonymous_variant | 0.25 |
clpC1 | 4040426 | c.279T>C | synonymous_variant | 0.25 |
clpC1 | 4040431 | c.274T>C | synonymous_variant | 0.26 |
clpC1 | 4040444 | c.261C>G | synonymous_variant | 0.23 |
clpC1 | 4040450 | c.255A>G | synonymous_variant | 0.29 |
clpC1 | 4040459 | c.246C>G | synonymous_variant | 0.33 |
clpC1 | 4040465 | c.240T>C | synonymous_variant | 0.38 |
clpC1 | 4040471 | c.234T>C | synonymous_variant | 0.39 |
clpC1 | 4040477 | c.228G>A | synonymous_variant | 0.32 |
clpC1 | 4040480 | c.225T>C | synonymous_variant | 0.34 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 0.64 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 0.22 |
clpC1 | 4040528 | c.177G>C | synonymous_variant | 0.2 |
clpC1 | 4040531 | c.174T>C | synonymous_variant | 0.19 |
clpC1 | 4040546 | c.159G>C | synonymous_variant | 0.18 |
clpC1 | 4040644 | c.61A>C | synonymous_variant | 0.22 |
clpC1 | 4040654 | c.51G>A | synonymous_variant | 0.21 |
clpC1 | 4040657 | c.48T>G | synonymous_variant | 0.19 |
clpC1 | 4040662 | c.43C>T | synonymous_variant | 0.16 |
clpC1 | 4040699 | c.6C>T | synonymous_variant | 0.19 |
clpC1 | 4040711 | c.-7G>A | upstream_gene_variant | 0.18 |
panD | 4044138 | c.144T>C | synonymous_variant | 0.19 |
panD | 4044150 | c.132A>G | synonymous_variant | 0.2 |
embC | 4240543 | c.681G>C | synonymous_variant | 0.17 |
embC | 4240671 | p.Thr270Ile | missense_variant | 0.91 |
embC | 4240678 | c.816T>G | synonymous_variant | 0.17 |
embC | 4240685 | p.Thr275Ala | missense_variant | 0.18 |
embC | 4240726 | c.864G>C | synonymous_variant | 0.26 |
embC | 4240780 | c.918T>C | synonymous_variant | 0.28 |
embC | 4240783 | c.921G>C | synonymous_variant | 0.28 |
embC | 4240789 | c.927T>C | synonymous_variant | 0.27 |
embC | 4240819 | c.957A>G | synonymous_variant | 0.27 |
embC | 4240831 | c.969T>G | synonymous_variant | 0.27 |
embC | 4240867 | c.1005T>G | synonymous_variant | 0.18 |
embC | 4240870 | c.1008T>C | synonymous_variant | 0.2 |
embC | 4240879 | c.1017G>C | synonymous_variant | 0.21 |
embC | 4240880 | p.Ala340Thr | missense_variant | 0.2 |
embC | 4240885 | c.1023T>C | synonymous_variant | 0.19 |
embC | 4240897 | c.1035C>G | synonymous_variant | 0.19 |
embC | 4240900 | c.1038A>G | synonymous_variant | 0.17 |
embC | 4240936 | c.1074A>G | synonymous_variant | 0.18 |
embC | 4241017 | c.1155T>C | synonymous_variant | 0.18 |
embC | 4241023 | c.1161T>G | synonymous_variant | 0.17 |
embC | 4241042 | p.Asn394Asp | missense_variant | 0.8 |
embC | 4241050 | c.1188T>G | synonymous_variant | 0.19 |
embC | 4241104 | c.1242G>A | synonymous_variant | 0.2 |
embC | 4241107 | c.1245G>C | synonymous_variant | 0.21 |
embC | 4241137 | c.1275G>C | synonymous_variant | 0.18 |
embC | 4241140 | c.1278A>G | synonymous_variant | 0.21 |
embC | 4241141 | p.Ile427Val | missense_variant | 0.18 |
embC | 4241158 | c.1296T>C | synonymous_variant | 0.25 |
embC | 4241161 | c.1299C>G | synonymous_variant | 0.25 |
embC | 4241162 | c.1300T>C | synonymous_variant | 0.26 |
embC | 4241203 | c.1341T>C | synonymous_variant | 0.18 |
embC | 4241380 | c.1518A>C | synonymous_variant | 0.17 |
embC | 4241394 | p.Lys511Ser | missense_variant | 0.21 |
embC | 4241443 | c.1581C>G | synonymous_variant | 0.23 |
embC | 4241449 | c.1587C>G | synonymous_variant | 0.26 |
embC | 4241453 | p.Ile531Val | missense_variant | 0.24 |
embC | 4241473 | c.1611G>A | synonymous_variant | 0.17 |
embC | 4241479 | c.1617C>G | synonymous_variant | 0.17 |
embC | 4241587 | c.1725C>G | synonymous_variant | 0.17 |
embC | 4241591 | p.Leu577Val | missense_variant | 0.18 |
embC | 4241611 | c.1749G>C | synonymous_variant | 0.22 |
embC | 4241614 | c.1752A>C | synonymous_variant | 0.23 |
embC | 4241617 | c.1755G>A | synonymous_variant | 0.21 |
embC | 4241623 | c.1761C>G | synonymous_variant | 0.2 |
embC | 4241626 | c.1764T>C | synonymous_variant | 0.23 |
embC | 4241644 | c.1782G>C | synonymous_variant | 0.27 |
embC | 4241648 | c.1786T>C | synonymous_variant | 0.29 |
embC | 4241657 | p.Ser599Pro | missense_variant | 0.23 |
embC | 4241665 | c.1803G>T | synonymous_variant | 0.15 |
embC | 4241750 | p.Leu630Val | missense_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 0.96 |
embA | 4243848 | p.Val206Met | missense_variant | 0.91 |
embA | 4245083 | c.1851A>C | synonymous_variant | 0.27 |
embA | 4245089 | c.1857G>C | synonymous_variant | 0.26 |
embA | 4245092 | c.1860C>G | synonymous_variant | 0.26 |
embA | 4245101 | c.1869G>C | synonymous_variant | 0.28 |
embA | 4245137 | c.1905T>C | synonymous_variant | 0.32 |
embA | 4245149 | c.1917C>G | synonymous_variant | 0.32 |
embA | 4245182 | c.1950T>C | synonymous_variant | 0.27 |
embA | 4245194 | c.1962G>C | synonymous_variant | 0.26 |
embA | 4245198 | p.Leu656Ile | missense_variant | 0.28 |
embA | 4245206 | c.1974A>G | synonymous_variant | 0.2 |
embA | 4245207 | c.1975T>C | synonymous_variant | 0.23 |
embA | 4245215 | c.1983A>G | synonymous_variant | 0.2 |
embA | 4245222 | p.Tyr664Gln | missense_variant | 0.23 |
embB | 4245587 | c.-927G>C | upstream_gene_variant | 0.21 |
embB | 4245593 | c.-921C>G | upstream_gene_variant | 0.21 |
embA | 4245594 | p.Ser788Thr | missense_variant | 0.21 |
embB | 4245599 | c.-915A>G | upstream_gene_variant | 0.21 |
embB | 4245620 | c.-894T>C | upstream_gene_variant | 0.23 |
embB | 4245623 | c.-891G>C | upstream_gene_variant | 0.22 |
embB | 4245626 | c.-888G>C | upstream_gene_variant | 0.23 |
embA | 4245643 | p.Ala804Val | missense_variant | 0.23 |
embA | 4245648 | p.Ile806Tyr | missense_variant | 0.19 |
embA | 4245652 | p.Thr807Ser | missense_variant | 0.17 |
embB | 4245659 | c.-855C>G | upstream_gene_variant | 0.19 |
embB | 4245740 | c.-774T>C | upstream_gene_variant | 0.17 |
embB | 4245764 | c.-750G>C | upstream_gene_variant | 0.19 |
embA | 4245771 | p.Asn847Ser | missense_variant | 0.15 |
embB | 4245807 | c.-707_-705delTTAinsCTG | upstream_gene_variant | 0.19 |
embA | 4245820 | p.Ser863Thr | missense_variant | 0.22 |
embB | 4245830 | c.-684G>C | upstream_gene_variant | 0.25 |
embB | 4245845 | c.-669T>G | upstream_gene_variant | 0.24 |
embB | 4245848 | c.-666C>G | upstream_gene_variant | 0.24 |
embB | 4245860 | c.-654C>G | upstream_gene_variant | 0.23 |
embA | 4245969 | p.Pro913Ser | missense_variant | 0.78 |
embB | 4247356 | c.843C>T | synonymous_variant | 0.82 |
embB | 4247395 | c.882C>G | synonymous_variant | 0.17 |
embB | 4247401 | c.888T>C | synonymous_variant | 0.19 |
embB | 4247437 | c.924A>G | synonymous_variant | 0.22 |
embB | 4247440 | c.927C>G | synonymous_variant | 0.22 |
embB | 4247464 | c.951C>G | synonymous_variant | 0.25 |
embB | 4247470 | c.957T>C | synonymous_variant | 0.24 |
embB | 4247491 | c.978G>C | synonymous_variant | 0.28 |
embB | 4247497 | c.984T>C | synonymous_variant | 0.24 |
embB | 4247500 | c.987C>G | synonymous_variant | 0.21 |
embB | 4247512 | c.999T>C | synonymous_variant | 0.23 |
embB | 4247646 | p.Glu378Ala | missense_variant | 0.94 |
embB | 4247819 | p.Val436Ile | missense_variant | 0.22 |
embB | 4247836 | c.1323A>G | synonymous_variant | 0.2 |
embB | 4248035 | p.Val508Ile | missense_variant | 0.17 |
embB | 4248041 | p.Ala510Thr | missense_variant | 0.16 |
embB | 4248070 | c.1557T>C | synonymous_variant | 0.21 |
embB | 4248085 | c.1572T>C | synonymous_variant | 0.26 |
embB | 4248097 | c.1584C>G | synonymous_variant | 0.26 |
embB | 4248127 | c.1614G>C | synonymous_variant | 0.18 |
embB | 4248133 | c.1620C>G | synonymous_variant | 0.25 |
embB | 4248142 | c.1629T>C | synonymous_variant | 0.27 |
embB | 4248143 | c.1630T>C | synonymous_variant | 0.27 |
embB | 4248157 | c.1644A>G | synonymous_variant | 0.29 |
embB | 4248206 | p.Ser565Gly | missense_variant | 0.34 |
embB | 4248220 | c.1707A>G | synonymous_variant | 0.29 |
embB | 4248241 | c.1728C>T | synonymous_variant | 0.22 |
embB | 4248277 | c.1764G>C | synonymous_variant | 0.17 |
embB | 4248304 | c.1791G>C | synonymous_variant | 0.3 |
embB | 4248316 | c.1803C>G | synonymous_variant | 0.2 |
embB | 4248319 | c.1806A>G | synonymous_variant | 0.33 |
embB | 4248322 | c.1809G>C | synonymous_variant | 0.17 |
embB | 4248343 | c.1830G>C | synonymous_variant | 0.27 |
embB | 4248346 | c.1833G>C | synonymous_variant | 0.17 |
embB | 4248350 | c.1837T>C | synonymous_variant | 0.2 |
embB | 4248355 | c.1842A>G | synonymous_variant | 0.19 |
embB | 4248358 | c.1845C>G | synonymous_variant | 0.2 |
embB | 4248362 | p.Ser617Ala | missense_variant | 0.2 |
embB | 4249469 | p.Leu986Met | missense_variant | 0.16 |
embB | 4249498 | c.2985G>C | synonymous_variant | 0.18 |
embB | 4249521 | p.Ala1003Val | missense_variant | 0.19 |
embB | 4249525 | c.3012T>C | synonymous_variant | 0.2 |
embB | 4249529 | p.Ile1006Val | missense_variant | 0.19 |
embB | 4249532 | p.Ala1007Thr | missense_variant | 0.19 |
embB | 4249537 | c.3024A>G | synonymous_variant | 0.21 |
embB | 4249543 | c.3030G>C | synonymous_variant | 0.23 |
embB | 4249558 | c.3045A>C | synonymous_variant | 0.23 |
embB | 4249564 | c.3051C>T | synonymous_variant | 0.15 |
embB | 4249568 | p.Ser1019Thr | missense_variant | 0.2 |
embB | 4249573 | c.3060T>C | synonymous_variant | 0.19 |
embB | 4249580 | p.Leu1023Met | missense_variant | 0.2 |
aftB | 4269006 | c.-170T>C | upstream_gene_variant | 0.17 |
aftB | 4269012 | c.-176G>C | upstream_gene_variant | 0.18 |
aftB | 4269033 | c.-197T>C | upstream_gene_variant | 0.18 |
aftB | 4269036 | c.-200C>G | upstream_gene_variant | 0.19 |
aftB | 4269042 | c.-206G>C | upstream_gene_variant | 0.18 |
aftB | 4269183 | c.-347T>C | upstream_gene_variant | 0.18 |
aftB | 4269201 | c.-365A>G | upstream_gene_variant | 0.24 |
ubiA | 4269209 | p.Ser209Ala | missense_variant | 0.25 |
ubiA | 4269220 | p.Ala205Lys | missense_variant | 0.17 |
ubiA | 4269243 | p.His197Gln | missense_variant | 0.17 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 0.88 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 0.89 |
whiB6 | 4338441 | p.Tyr27* | stop_gained | 0.84 |
whiB6 | 4338449 | p.Ala25Pro | missense_variant | 0.83 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 0.88 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.82 |
gid | 4407873 | c.330G>T | synonymous_variant | 0.87 |