Run ID: SRR5709967
Sample name:
Date: 04-04-2023 11:09:01
Number of reads: 1293017
Percentage reads mapped: 82.61
Strain: lineage2.2.1
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.95 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 0.98 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.97 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761110 | p.Asp435Val | missense_variant | 0.67 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 0.7 | streptomycin |
rrs | 1472307 | n.462C>T | non_coding_transcript_exon_variant | 0.19 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 0.96 | isoniazid |
embB | 4248003 | p.Gln497Pro | missense_variant | 0.91 | ethambutol |
ethA | 4326833 | c.639_640delGT | frameshift_variant | 1.0 | ethionamide, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6209 | c.970C>T | synonymous_variant | 0.16 |
gyrB | 6217 | c.978G>C | synonymous_variant | 0.17 |
gyrB | 6223 | c.984G>C | synonymous_variant | 0.17 |
gyrB | 6242 | p.Arg335Lys | missense_variant | 0.18 |
gyrB | 6250 | c.1011A>G | synonymous_variant | 0.2 |
gyrB | 6253 | c.1014G>C | synonymous_variant | 0.19 |
gyrB | 6280 | c.1041T>C | synonymous_variant | 0.19 |
gyrB | 6286 | c.1047T>C | synonymous_variant | 0.17 |
gyrB | 6298 | c.1059C>A | synonymous_variant | 0.16 |
gyrB | 6299 | c.1060C>T | synonymous_variant | 0.15 |
gyrA | 6307 | c.-995T>G | upstream_gene_variant | 0.2 |
gyrA | 6700 | c.-602T>C | upstream_gene_variant | 0.17 |
gyrA | 6727 | c.-575G>T | upstream_gene_variant | 0.15 |
gyrA | 6778 | c.-524C>T | upstream_gene_variant | 0.17 |
gyrA | 6793 | c.-509T>C | upstream_gene_variant | 0.16 |
gyrB | 6797 | p.Gly520Thr | missense_variant | 0.17 |
gyrA | 6824 | c.-478C>T | upstream_gene_variant | 0.19 |
gyrA | 6841 | c.-461T>C | upstream_gene_variant | 0.17 |
gyrA | 6844 | c.-458T>G | upstream_gene_variant | 0.16 |
gyrA | 6856 | c.-446T>C | upstream_gene_variant | 0.15 |
gyrA | 6904 | c.-398C>G | upstream_gene_variant | 0.17 |
gyrA | 6910 | c.-392G>A | upstream_gene_variant | 0.16 |
gyrB | 6911 | p.Asn558His | missense_variant | 0.17 |
gyrA | 6919 | c.-383T>C | upstream_gene_variant | 0.2 |
gyrA | 6925 | c.-377T>C | upstream_gene_variant | 0.18 |
gyrA | 6931 | c.-371A>C | upstream_gene_variant | 0.16 |
gyrA | 6937 | c.-365G>A | upstream_gene_variant | 0.16 |
gyrA | 6967 | c.-335T>C | upstream_gene_variant | 0.17 |
gyrA | 6970 | c.-332C>T | upstream_gene_variant | 0.17 |
gyrA | 7000 | c.-302C>G | upstream_gene_variant | 0.2 |
gyrA | 7006 | c.-296T>G | upstream_gene_variant | 0.2 |
gyrA | 7012 | c.-290G>C | upstream_gene_variant | 0.2 |
gyrA | 7018 | c.-284G>C | upstream_gene_variant | 0.17 |
gyrA | 7021 | c.-281G>C | upstream_gene_variant | 0.17 |
gyrA | 7033 | c.-269G>C | upstream_gene_variant | 0.16 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7694 | c.393A>G | synonymous_variant | 0.18 |
gyrA | 7697 | c.396C>G | synonymous_variant | 0.2 |
gyrA | 7710 | c.409T>C | synonymous_variant | 0.21 |
gyrA | 7715 | c.414G>C | synonymous_variant | 0.22 |
gyrA | 7728 | c.427_429delAGGinsCGC | synonymous_variant | 0.23 |
gyrA | 7760 | c.459C>T | synonymous_variant | 0.24 |
gyrA | 7763 | c.462T>C | synonymous_variant | 0.22 |
gyrA | 8057 | c.756A>G | synonymous_variant | 0.16 |
gyrA | 8069 | c.768T>C | synonymous_variant | 0.17 |
gyrA | 8078 | c.777A>G | synonymous_variant | 0.19 |
gyrA | 8090 | c.789C>G | synonymous_variant | 0.19 |
gyrA | 8096 | c.795T>C | synonymous_variant | 0.19 |
gyrA | 8099 | c.798T>C | synonymous_variant | 0.21 |
gyrA | 8174 | c.873C>G | synonymous_variant | 0.17 |
gyrA | 8177 | c.876A>C | synonymous_variant | 0.18 |
gyrA | 8198 | c.897T>C | synonymous_variant | 0.23 |
gyrA | 8207 | c.906T>C | synonymous_variant | 0.25 |
gyrA | 8219 | c.918T>C | synonymous_variant | 0.28 |
gyrA | 8225 | c.924T>C | synonymous_variant | 0.3 |
gyrA | 8234 | c.933T>G | synonymous_variant | 0.26 |
gyrA | 8235 | c.934_936delTTAinsCTG | synonymous_variant | 0.26 |
gyrA | 8253 | p.Ile318Leu | missense_variant | 0.27 |
gyrA | 8264 | c.963T>C | synonymous_variant | 0.28 |
gyrA | 8267 | c.966G>C | synonymous_variant | 0.29 |
gyrA | 8270 | c.969G>C | synonymous_variant | 0.27 |
gyrA | 8283 | p.Ile328Leu | missense_variant | 0.26 |
gyrA | 8288 | c.987T>C | synonymous_variant | 0.26 |
gyrA | 8294 | c.993T>C | synonymous_variant | 0.26 |
gyrA | 8324 | c.1023T>C | synonymous_variant | 0.22 |
gyrA | 8339 | c.1038A>G | synonymous_variant | 0.23 |
gyrA | 8342 | c.1041G>C | synonymous_variant | 0.2 |
gyrA | 8366 | c.1065G>C | synonymous_variant | 0.16 |
gyrA | 8375 | c.1074G>C | synonymous_variant | 0.18 |
gyrA | 8391 | p.Tyr364His | missense_variant | 0.17 |
gyrA | 8399 | c.1098T>C | synonymous_variant | 0.17 |
gyrA | 8414 | c.1113C>T | synonymous_variant | 0.2 |
gyrA | 8420 | c.1119T>C | synonymous_variant | 0.2 |
gyrA | 8423 | c.1122G>C | synonymous_variant | 0.19 |
gyrA | 8442 | c.1141C>T | synonymous_variant | 0.17 |
gyrA | 8453 | c.1152A>C | synonymous_variant | 0.17 |
gyrA | 8462 | c.1161A>G | synonymous_variant | 0.17 |
gyrA | 8471 | c.1170T>C | synonymous_variant | 0.19 |
gyrA | 8480 | c.1179C>T | synonymous_variant | 0.19 |
gyrA | 8486 | c.1185T>C | synonymous_variant | 0.18 |
gyrA | 8489 | c.1188A>G | synonymous_variant | 0.18 |
gyrA | 8498 | c.1197C>T | synonymous_variant | 0.15 |
gyrA | 8504 | c.1203G>C | synonymous_variant | 0.16 |
gyrA | 8903 | c.1602T>C | synonymous_variant | 0.17 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490827 | c.45C>T | synonymous_variant | 0.24 |
fgd1 | 490833 | c.51G>C | synonymous_variant | 0.24 |
fgd1 | 490842 | c.60C>G | synonymous_variant | 0.23 |
fgd1 | 490851 | c.69A>C | synonymous_variant | 0.27 |
fgd1 | 490887 | c.105G>C | synonymous_variant | 0.29 |
fgd1 | 490902 | c.120T>C | synonymous_variant | 0.24 |
fgd1 | 490905 | c.123T>C | synonymous_variant | 0.23 |
fgd1 | 490911 | c.129T>G | synonymous_variant | 0.24 |
fgd1 | 490917 | c.135C>A | synonymous_variant | 0.23 |
fgd1 | 490921 | p.Gln47Glu | missense_variant | 0.22 |
fgd1 | 490932 | c.150T>C | synonymous_variant | 0.18 |
fgd1 | 490948 | p.Ser56Ala | missense_variant | 0.18 |
fgd1 | 491232 | c.450T>C | synonymous_variant | 0.24 |
fgd1 | 491241 | p.Asp153Glu | missense_variant | 0.23 |
fgd1 | 491244 | c.462T>C | synonymous_variant | 0.23 |
fgd1 | 491259 | c.477T>C | synonymous_variant | 0.26 |
fgd1 | 491286 | c.504G>C | synonymous_variant | 0.23 |
fgd1 | 491292 | c.510G>C | synonymous_variant | 0.24 |
fgd1 | 491295 | c.513C>G | synonymous_variant | 0.24 |
fgd1 | 491296 | p.Val172Ile | missense_variant | 0.24 |
fgd1 | 491319 | c.537G>C | synonymous_variant | 0.2 |
fgd1 | 491331 | c.549G>A | synonymous_variant | 0.21 |
fgd1 | 491343 | c.561C>G | synonymous_variant | 0.17 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575542 | c.195C>G | synonymous_variant | 0.2 |
mshA | 575561 | p.Met72Val | missense_variant | 0.24 |
mshA | 575569 | c.222A>G | synonymous_variant | 0.24 |
mshA | 575571 | p.Ser75Thr | missense_variant | 0.24 |
mshA | 575575 | c.228G>C | synonymous_variant | 0.28 |
mshA | 575587 | c.240C>A | synonymous_variant | 0.28 |
mshA | 575590 | c.243T>C | synonymous_variant | 0.29 |
mshA | 575593 | c.246G>C | synonymous_variant | 0.29 |
mshA | 575623 | c.276C>G | synonymous_variant | 0.29 |
mshA | 575629 | c.282A>C | synonymous_variant | 0.22 |
mshA | 575635 | c.288A>C | synonymous_variant | 0.22 |
mshA | 575638 | c.291T>C | synonymous_variant | 0.21 |
mshA | 575641 | c.294A>G | synonymous_variant | 0.18 |
mshA | 575648 | p.Val101Gln | missense_variant | 0.23 |
mshA | 575659 | c.312A>G | synonymous_variant | 0.25 |
mshA | 575665 | c.318G>C | synonymous_variant | 0.24 |
mshA | 575689 | c.342G>C | synonymous_variant | 0.33 |
mshA | 575695 | c.348C>G | synonymous_variant | 0.32 |
mshA | 575704 | c.357T>C | synonymous_variant | 0.32 |
mshA | 575705 | c.358T>C | synonymous_variant | 0.32 |
mshA | 575713 | c.366G>A | synonymous_variant | 0.31 |
mshA | 575719 | c.372C>T | synonymous_variant | 0.31 |
mshA | 575734 | c.387T>G | synonymous_variant | 0.31 |
mshA | 575737 | c.390T>C | synonymous_variant | 0.32 |
mshA | 575746 | c.399C>G | synonymous_variant | 0.33 |
mshA | 575752 | c.405G>A | synonymous_variant | 0.34 |
mshA | 575767 | c.420G>A | synonymous_variant | 0.35 |
mshA | 575771 | p.Val142Ser | missense_variant | 0.35 |
mshA | 575779 | c.432A>G | synonymous_variant | 0.39 |
mshA | 575821 | c.474G>C | synonymous_variant | 0.39 |
mshA | 575864 | c.517T>C | synonymous_variant | 0.23 |
mshA | 575878 | c.531A>G | synonymous_variant | 0.2 |
mshA | 575884 | c.537G>C | synonymous_variant | 0.16 |
mshA | 575907 | p.Ala187Val | missense_variant | 0.94 |
ccsA | 620269 | p.Val127Ile | missense_variant | 0.15 |
ccsA | 620307 | c.417C>G | synonymous_variant | 0.17 |
ccsA | 620340 | c.450C>G | synonymous_variant | 0.15 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
ccsA | 620739 | c.849A>G | synonymous_variant | 0.17 |
ccsA | 620745 | c.855G>T | synonymous_variant | 0.16 |
ccsA | 620748 | c.858T>A | synonymous_variant | 0.16 |
rpoB | 760101 | c.295T>C | synonymous_variant | 0.18 |
rpoB | 760106 | c.300G>T | synonymous_variant | 0.19 |
rpoB | 760112 | c.306T>C | synonymous_variant | 0.2 |
rpoB | 760118 | c.312T>C | synonymous_variant | 0.19 |
rpoB | 760121 | c.315T>C | synonymous_variant | 0.2 |
rpoB | 760130 | p.Asp108Glu | missense_variant | 0.2 |
rpoB | 760139 | c.333A>G | synonymous_variant | 0.23 |
rpoB | 760142 | c.336C>G | synonymous_variant | 0.22 |
rpoB | 760181 | c.375T>C | synonymous_variant | 0.22 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.23 |
rpoB | 760196 | c.390C>G | synonymous_variant | 0.19 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.23 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.18 |
rpoB | 760283 | c.477G>C | synonymous_variant | 0.18 |
rpoB | 760307 | c.501T>C | synonymous_variant | 0.23 |
rpoB | 760328 | c.522G>C | synonymous_variant | 0.24 |
rpoB | 760331 | c.525G>C | synonymous_variant | 0.25 |
rpoB | 760337 | c.531C>G | synonymous_variant | 0.24 |
rpoB | 760340 | c.534G>C | synonymous_variant | 0.24 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.2 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.23 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.26 |
rpoB | 760418 | c.612G>C | synonymous_variant | 0.23 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.22 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.2 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.22 |
rpoB | 760481 | c.675G>C | synonymous_variant | 0.23 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.23 |
rpoB | 760522 | p.Ser239Asn | missense_variant | 0.23 |
rpoB | 760533 | p.Val243Thr | missense_variant | 0.16 |
rpoB | 760547 | c.741G>C | synonymous_variant | 0.18 |
rpoB | 760563 | p.Arg253Met | missense_variant | 0.19 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.2 |
rpoB | 760611 | c.805T>C | synonymous_variant | 0.2 |
rpoB | 760634 | c.828T>C | synonymous_variant | 0.19 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.19 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.2 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.21 |
rpoB | 760670 | c.864G>C | synonymous_variant | 0.21 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.2 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.23 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.25 |
rpoB | 760718 | c.912C>G | synonymous_variant | 0.28 |
rpoB | 760721 | c.915C>G | synonymous_variant | 0.28 |
rpoB | 760724 | c.918T>C | synonymous_variant | 0.29 |
rpoB | 760730 | c.924T>C | synonymous_variant | 0.26 |
rpoB | 760751 | c.945G>C | synonymous_variant | 0.26 |
rpoB | 760757 | c.951T>C | synonymous_variant | 0.25 |
rpoB | 760759 | p.Val318Ala | missense_variant | 0.25 |
rpoB | 760763 | c.957C>T | synonymous_variant | 0.25 |
rpoB | 760769 | c.963C>G | synonymous_variant | 0.23 |
rpoB | 760775 | c.969G>C | synonymous_variant | 0.21 |
rpoB | 760776 | c.970_972delTCGinsAGC | synonymous_variant | 0.21 |
rpoB | 760793 | c.987A>G | synonymous_variant | 0.18 |
rpoB | 760805 | c.999G>C | synonymous_variant | 0.17 |
rpoB | 760817 | c.1011A>G | synonymous_variant | 0.17 |
rpoB | 760820 | c.1014T>C | synonymous_variant | 0.18 |
rpoB | 760826 | c.1020C>G | synonymous_variant | 0.18 |
rpoB | 760835 | c.1029C>T | synonymous_variant | 0.17 |
rpoB | 760845 | p.Thr347Pro | missense_variant | 0.19 |
rpoB | 760859 | c.1053T>C | synonymous_variant | 0.19 |
rpoB | 760869 | p.Val355Ile | missense_variant | 0.18 |
rpoB | 760886 | c.1080A>G | synonymous_variant | 0.2 |
rpoB | 760919 | c.1113C>G | synonymous_variant | 0.26 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.26 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 0.28 |
rpoB | 760934 | c.1128C>T | synonymous_variant | 0.32 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.34 |
rpoB | 760970 | c.1164G>C | synonymous_variant | 0.32 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.35 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.31 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.33 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.33 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 0.33 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.32 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.3 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.3 |
rpoB | 761051 | c.1245G>T | synonymous_variant | 0.3 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.29 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.29 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.29 |
rpoB | 761063 | c.1257C>G | synonymous_variant | 0.32 |
rpoB | 761097 | c.1291_1292delAGinsTC | synonymous_variant | 0.28 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.29 |
rpoB | 761133 | c.1327_1329delTTGinsCTC | synonymous_variant | 0.31 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.28 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.25 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.24 |
rpoB | 761171 | c.1365C>T | synonymous_variant | 0.24 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.27 |
rpoB | 761183 | c.1377T>G | synonymous_variant | 0.27 |
rpoB | 761189 | c.1383T>G | synonymous_variant | 0.26 |
rpoB | 761222 | c.1416G>C | synonymous_variant | 0.25 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.26 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.26 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.29 |
rpoB | 761306 | c.1500C>G | synonymous_variant | 0.19 |
rpoB | 761492 | c.1686G>C | synonymous_variant | 0.17 |
rpoB | 761510 | c.1704T>C | synonymous_variant | 0.18 |
rpoB | 761531 | c.1725C>G | synonymous_variant | 0.19 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.17 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.2 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.2 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.2 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.22 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.22 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.22 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.18 |
rpoB | 761645 | c.1839C>G | synonymous_variant | 0.2 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.18 |
rpoB | 761657 | c.1851C>G | synonymous_variant | 0.2 |
rpoB | 761675 | c.1869G>C | synonymous_variant | 0.16 |
rpoB | 761687 | c.1881C>T | synonymous_variant | 0.15 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.18 |
rpoB | 761954 | c.2148C>G | synonymous_variant | 0.18 |
rpoB | 761999 | c.2193G>C | synonymous_variant | 0.16 |
rpoB | 762008 | c.2202C>G | synonymous_variant | 0.15 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.18 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.24 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.22 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.19 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.18 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.16 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.17 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 0.21 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.26 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.26 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.24 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.26 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.24 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.22 |
rpoB | 762218 | c.2412T>G | synonymous_variant | 0.17 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.2 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.19 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.21 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.2 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.22 |
rpoB | 762329 | c.2523G>C | synonymous_variant | 0.22 |
rpoB | 762338 | c.2532T>C | synonymous_variant | 0.22 |
rpoB | 762347 | c.2541T>C | synonymous_variant | 0.2 |
rpoB | 762362 | p.Glu852Asp | missense_variant | 0.2 |
rpoB | 762369 | c.2563T>C | synonymous_variant | 0.18 |
rpoC | 762395 | c.-975G>C | upstream_gene_variant | 0.17 |
rpoC | 762398 | c.-972T>C | upstream_gene_variant | 0.18 |
rpoC | 762401 | c.-969G>C | upstream_gene_variant | 0.18 |
rpoC | 762404 | c.-966T>C | upstream_gene_variant | 0.18 |
rpoC | 762410 | c.-960T>C | upstream_gene_variant | 0.18 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 0.18 |
rpoC | 762443 | c.-927G>C | upstream_gene_variant | 0.17 |
rpoC | 762470 | c.-900G>C | upstream_gene_variant | 0.16 |
rpoB | 762490 | p.Val895Asp | missense_variant | 0.16 |
rpoB | 762510 | p.Ala902Pro | missense_variant | 0.17 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.16 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.33 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.34 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.3 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 1.0 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.3 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.32 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.32 |
rpoC | 763076 | c.-294C>G | upstream_gene_variant | 0.32 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.27 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.27 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.26 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.25 |
rpoC | 763158 | c.-212C>T | upstream_gene_variant | 0.23 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.24 |
rpoC | 763169 | c.-201A>G | upstream_gene_variant | 0.24 |
rpoC | 763202 | c.-168A>C | upstream_gene_variant | 0.21 |
rpoC | 763205 | c.-165G>C | upstream_gene_variant | 0.21 |
rpoC | 763206 | c.-164_-162delAGTinsTCC | upstream_gene_variant | 0.22 |
rpoC | 763214 | c.-156T>C | upstream_gene_variant | 0.21 |
rpoC | 763220 | c.-150G>C | upstream_gene_variant | 0.21 |
rpoC | 763226 | c.-144A>G | upstream_gene_variant | 0.19 |
rpoC | 763238 | c.-132T>C | upstream_gene_variant | 0.19 |
rpoC | 763402 | c.33C>G | synonymous_variant | 0.16 |
rpoC | 763441 | c.72C>G | synonymous_variant | 0.18 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.18 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.24 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.24 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.36 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.33 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.36 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.33 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.24 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.26 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.25 |
rpoC | 763658 | c.289_291delCTTinsTTG | synonymous_variant | 0.26 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.22 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.19 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.17 |
rpoC | 763801 | c.432C>G | synonymous_variant | 0.18 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.18 |
rpoC | 763819 | c.450G>C | synonymous_variant | 0.17 |
rpoC | 763835 | p.Ala156Met | missense_variant | 0.15 |
rpoC | 763858 | c.489A>G | synonymous_variant | 0.21 |
rpoC | 763872 | p.Gly168Ala | missense_variant | 0.2 |
rpoC | 763876 | p.Glu169Asp | missense_variant | 0.22 |
rpoC | 763879 | c.510A>G | synonymous_variant | 0.23 |
rpoC | 763888 | c.519G>C | synonymous_variant | 0.22 |
rpoC | 763891 | c.522G>C | synonymous_variant | 0.23 |
rpoC | 763894 | c.525A>G | synonymous_variant | 0.23 |
rpoC | 763903 | c.534G>A | synonymous_variant | 0.23 |
rpoC | 763945 | c.576T>C | synonymous_variant | 0.2 |
rpoC | 763960 | c.591T>C | synonymous_variant | 0.18 |
rpoC | 763967 | p.Gly200Ser | missense_variant | 0.18 |
rpoC | 763978 | c.609C>G | synonymous_variant | 0.22 |
rpoC | 763996 | c.627T>C | synonymous_variant | 0.24 |
rpoC | 764005 | c.636G>C | synonymous_variant | 0.25 |
rpoC | 764011 | c.642T>C | synonymous_variant | 0.25 |
rpoC | 764024 | c.655T>C | synonymous_variant | 0.28 |
rpoC | 764040 | p.Ser224Asn | missense_variant | 0.3 |
rpoC | 764044 | c.675T>C | synonymous_variant | 0.31 |
rpoC | 764059 | c.690G>C | synonymous_variant | 0.32 |
rpoC | 764083 | c.714A>G | synonymous_variant | 0.32 |
rpoC | 764098 | c.729A>G | synonymous_variant | 0.3 |
rpoC | 764101 | c.732C>G | synonymous_variant | 0.31 |
rpoC | 764116 | c.747C>T | synonymous_variant | 0.3 |
rpoC | 764131 | c.762T>C | synonymous_variant | 0.29 |
rpoC | 764161 | c.792G>C | synonymous_variant | 0.23 |
rpoC | 764188 | c.819A>G | synonymous_variant | 0.18 |
rpoC | 764195 | p.Ser276Gln | missense_variant | 0.17 |
rpoC | 764203 | c.834G>T | synonymous_variant | 0.16 |
rpoC | 764257 | c.888G>C | synonymous_variant | 0.23 |
rpoC | 764266 | c.897T>C | synonymous_variant | 0.24 |
rpoC | 764269 | c.900G>C | synonymous_variant | 0.23 |
rpoC | 764278 | c.909A>G | synonymous_variant | 0.22 |
rpoC | 764282 | c.913_915delTCGinsAGC | synonymous_variant | 0.22 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.21 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.19 |
rpoC | 764381 | c.1012_1013delTCinsAG | synonymous_variant | 0.2 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 0.2 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.18 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.18 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.17 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.21 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.22 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.26 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.25 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.23 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.24 |
rpoC | 764573 | c.1204_1206delCTTinsTTG | synonymous_variant | 0.2 |
rpoC | 764576 | c.1207_1208delTCinsAG | synonymous_variant | 0.19 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.19 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.19 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.19 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.21 |
rpoC | 764681 | c.1312C>T | synonymous_variant | 0.2 |
rpoC | 764695 | c.1326T>C | synonymous_variant | 0.21 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.19 |
rpoC | 764746 | c.1377G>C | synonymous_variant | 0.22 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.23 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.21 |
rpoC | 764779 | c.1410G>A | synonymous_variant | 0.16 |
rpoC | 764791 | c.1422C>G | synonymous_variant | 0.2 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.17 |
rpoC | 764812 | c.1443C>G | synonymous_variant | 0.17 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.18 |
rpoC | 765404 | p.Leu679Val | missense_variant | 0.18 |
rpoC | 765409 | c.2040T>C | synonymous_variant | 0.17 |
rpoC | 765412 | c.2043T>C | synonymous_variant | 0.17 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.21 |
rpoC | 765451 | c.2082C>G | synonymous_variant | 0.23 |
rpoC | 765452 | p.Ala695Ser | missense_variant | 0.21 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.22 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.2 |
rpoC | 765508 | c.2139C>G | synonymous_variant | 0.18 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.2 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.2 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.2 |
rpoC | 765559 | c.2190G>C | synonymous_variant | 0.19 |
rpoC | 765578 | c.2209C>T | synonymous_variant | 0.17 |
rpoC | 765583 | c.2214G>T | synonymous_variant | 0.18 |
rpoC | 765613 | p.His748Gln | missense_variant | 0.17 |
rpoC | 765625 | c.2256C>G | synonymous_variant | 0.2 |
rpoC | 765628 | c.2259G>C | synonymous_variant | 0.2 |
rpoC | 765631 | p.Asp754Glu | missense_variant | 0.23 |
rpoC | 765649 | c.2280C>T | synonymous_variant | 0.26 |
rpoC | 765658 | c.2289C>T | synonymous_variant | 0.29 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.25 |
rpoC | 765734 | c.2365T>C | synonymous_variant | 0.22 |
rpoC | 765739 | c.2370G>C | synonymous_variant | 0.2 |
rpoC | 765751 | c.2382C>G | synonymous_variant | 0.21 |
rpoC | 765753 | p.Asp795Ala | missense_variant | 0.21 |
rpoC | 765772 | c.2403C>G | synonymous_variant | 0.2 |
rpoC | 765784 | c.2415C>G | synonymous_variant | 0.2 |
rpoC | 765796 | c.2427C>T | synonymous_variant | 0.19 |
rpoC | 765811 | c.2442T>C | synonymous_variant | 0.19 |
rpoC | 765814 | c.2445A>G | synonymous_variant | 0.19 |
rpoC | 765826 | c.2457T>C | synonymous_variant | 0.22 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 0.2 |
rpoC | 765871 | c.2502T>C | synonymous_variant | 0.2 |
rpoC | 765883 | c.2514C>G | synonymous_variant | 0.22 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.21 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.2 |
rpoC | 765928 | c.2559C>G | synonymous_variant | 0.17 |
rpoC | 766484 | p.Val1039Ile | missense_variant | 0.16 |
rpoC | 766492 | c.3123T>C | synonymous_variant | 0.18 |
rpoC | 766495 | c.3126C>T | synonymous_variant | 0.19 |
rpoC | 766528 | c.3159T>G | synonymous_variant | 0.22 |
rpoC | 766543 | c.3174C>T | synonymous_variant | 0.22 |
rpoC | 766573 | c.3204T>C | synonymous_variant | 0.2 |
rpoC | 766583 | p.Gly1072Ser | missense_variant | 0.15 |
rpoC | 766607 | p.Ile1080Leu | missense_variant | 0.21 |
rpoC | 766645 | c.3276A>G | synonymous_variant | 0.18 |
rpoC | 766651 | c.3282T>C | synonymous_variant | 0.19 |
rpoC | 766657 | c.3288A>G | synonymous_variant | 0.19 |
rpoC | 766672 | c.3303T>C | synonymous_variant | 0.16 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.17 |
rpoC | 766738 | c.3369G>T | synonymous_variant | 0.21 |
rpoC | 766750 | c.3381C>G | synonymous_variant | 0.22 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.19 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.19 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 0.18 |
rpoC | 766864 | c.3495G>C | synonymous_variant | 0.19 |
rpoC | 766978 | c.3609C>G | synonymous_variant | 0.15 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.15 |
rpoC | 767033 | c.3664_3666delTCGinsAGT | synonymous_variant | 0.22 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.29 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.3 |
rpoC | 767074 | c.3705T>C | synonymous_variant | 0.29 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.3 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.31 |
rpoC | 767134 | c.3765C>G | synonymous_variant | 0.3 |
rpoC | 767158 | c.3789T>C | synonymous_variant | 0.32 |
rpoC | 767167 | c.3798C>G | synonymous_variant | 0.24 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.22 |
rpoC | 767191 | c.3822C>G | synonymous_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781649 | c.90T>C | synonymous_variant | 0.2 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.2 |
rpsL | 781682 | c.123T>C | synonymous_variant | 0.29 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.28 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.3 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.31 |
rpsL | 781751 | c.192G>C | synonymous_variant | 0.3 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.3 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.27 |
rpsL | 781793 | c.234G>C | synonymous_variant | 0.26 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.21 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.21 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.17 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.17 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.17 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.17 |
rpsL | 781916 | c.357T>C | synonymous_variant | 0.22 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.2 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.24 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.25 |
rplC | 800648 | c.-161A>C | upstream_gene_variant | 0.24 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.24 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.21 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.21 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.18 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.19 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.19 |
rplC | 800738 | c.-71T>C | upstream_gene_variant | 0.16 |
rplC | 800771 | c.-38C>T | upstream_gene_variant | 0.13 |
rplC | 801156 | c.348T>A | synonymous_variant | 0.12 |
fbiC | 1303312 | p.Ile128Val | missense_variant | 1.0 |
fbiC | 1303534 | p.Ser202Ala | missense_variant | 0.17 |
fbiC | 1303545 | c.615A>G | synonymous_variant | 0.21 |
fbiC | 1303560 | c.630G>C | synonymous_variant | 0.26 |
fbiC | 1303575 | c.645G>C | synonymous_variant | 0.26 |
fbiC | 1303584 | c.654C>G | synonymous_variant | 0.27 |
fbiC | 1303590 | c.660A>G | synonymous_variant | 0.3 |
fbiC | 1303602 | c.672A>G | synonymous_variant | 0.28 |
fbiC | 1303605 | c.675C>G | synonymous_variant | 0.28 |
fbiC | 1303608 | c.678G>A | synonymous_variant | 0.28 |
fbiC | 1303611 | c.681G>C | synonymous_variant | 0.27 |
fbiC | 1303614 | c.684C>T | synonymous_variant | 0.27 |
fbiC | 1303617 | c.687C>G | synonymous_variant | 0.29 |
fbiC | 1303632 | c.702T>G | synonymous_variant | 0.31 |
fbiC | 1303638 | c.708A>G | synonymous_variant | 0.31 |
fbiC | 1303659 | c.729T>C | synonymous_variant | 0.18 |
fbiC | 1303661 | p.Val244Ala | missense_variant | 0.18 |
fbiC | 1303674 | c.744C>G | synonymous_variant | 0.19 |
fbiC | 1303686 | c.756C>G | synonymous_variant | 0.21 |
fbiC | 1303695 | c.765T>C | synonymous_variant | 0.22 |
fbiC | 1303701 | c.771C>G | synonymous_variant | 0.24 |
fbiC | 1303708 | c.778T>C | synonymous_variant | 0.22 |
fbiC | 1303722 | c.792C>G | synonymous_variant | 0.23 |
fbiC | 1303728 | c.798G>A | synonymous_variant | 0.22 |
fbiC | 1303731 | c.801A>C | synonymous_variant | 0.22 |
fbiC | 1303732 | p.Ser268Ala | missense_variant | 0.22 |
fbiC | 1303737 | c.807G>A | synonymous_variant | 0.22 |
fbiC | 1303746 | c.816T>C | synonymous_variant | 0.22 |
fbiC | 1303749 | c.819G>C | synonymous_variant | 0.22 |
fbiC | 1303752 | c.822A>G | synonymous_variant | 0.22 |
fbiC | 1303755 | c.825T>C | synonymous_variant | 0.21 |
fbiC | 1303785 | c.855G>C | synonymous_variant | 0.2 |
fbiC | 1303789 | p.Ile287Val | missense_variant | 0.19 |
fbiC | 1303818 | c.888C>G | synonymous_variant | 0.28 |
fbiC | 1303836 | c.906G>C | synonymous_variant | 0.25 |
fbiC | 1303845 | c.915C>G | synonymous_variant | 0.17 |
fbiC | 1303846 | p.Phe306Val | missense_variant | 0.19 |
fbiC | 1303854 | c.924T>C | synonymous_variant | 0.2 |
fbiC | 1303860 | c.930A>C | synonymous_variant | 0.2 |
fbiC | 1303884 | c.954T>G | synonymous_variant | 0.26 |
fbiC | 1303911 | c.981G>C | synonymous_variant | 0.24 |
fbiC | 1303914 | c.984C>G | synonymous_variant | 0.25 |
fbiC | 1303920 | c.990C>G | synonymous_variant | 0.22 |
fbiC | 1303923 | c.993C>T | synonymous_variant | 0.19 |
fbiC | 1303929 | c.999G>C | synonymous_variant | 0.19 |
fbiC | 1303932 | c.1002G>A | synonymous_variant | 0.19 |
fbiC | 1303947 | c.1017T>C | synonymous_variant | 0.2 |
fbiC | 1303948 | p.Gly340Arg | missense_variant | 0.19 |
fbiC | 1303969 | p.Val347Ile | missense_variant | 0.17 |
fbiC | 1303973 | p.Gly348Ala | missense_variant | 0.17 |
fbiC | 1303995 | c.1065C>T | synonymous_variant | 0.15 |
fbiC | 1304008 | c.1078T>C | synonymous_variant | 0.19 |
fbiC | 1304034 | c.1104A>G | synonymous_variant | 0.17 |
fbiC | 1304040 | c.1110C>G | synonymous_variant | 0.17 |
fbiC | 1304046 | c.1116C>G | synonymous_variant | 0.18 |
fbiC | 1304049 | c.1119T>G | synonymous_variant | 0.19 |
fbiC | 1304058 | c.1128G>A | synonymous_variant | 0.18 |
fbiC | 1304059 | c.1129C>T | synonymous_variant | 0.18 |
fbiC | 1304064 | c.1134G>C | synonymous_variant | 0.17 |
fbiC | 1304067 | c.1137G>C | synonymous_variant | 0.17 |
fbiC | 1304097 | c.1167G>C | synonymous_variant | 0.16 |
fbiC | 1304136 | c.1206C>T | synonymous_variant | 0.14 |
fbiC | 1304784 | c.1854T>C | synonymous_variant | 0.16 |
fbiC | 1304787 | c.1857T>C | synonymous_variant | 0.16 |
fbiC | 1304893 | p.Gly655Ser | missense_variant | 0.19 |
fbiC | 1304916 | c.1986T>C | synonymous_variant | 0.19 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
atpE | 1461132 | p.Val30Ile | missense_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473813 | n.156C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473839 | n.182G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473899 | n.242A>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473937 | n.280C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1473944 | n.287G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474012 | n.355C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474376 | n.719T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474409 | n.756_766delACCCACACGCG | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474427 | n.770A>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474429 | n.772G>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474823 | n.1166C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474904 | n.1247G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474956 | n.1299C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474959 | n.1302C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474962 | n.1306delG | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474970 | n.1313G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474991 | n.1334T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475006 | n.1349A>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476089 | n.2432T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476095 | n.2438C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476689 | n.3032A>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476690 | n.3033C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476693 | n.3036G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476695 | n.3038T>A | non_coding_transcript_exon_variant | 0.19 |
inhA | 1674382 | p.Leu61Ile | missense_variant | 0.14 |
inhA | 1674507 | c.306G>C | synonymous_variant | 0.26 |
inhA | 1674537 | c.336C>G | synonymous_variant | 0.28 |
inhA | 1674542 | p.Ala114Glu | missense_variant | 0.25 |
inhA | 1674549 | c.348G>C | synonymous_variant | 0.23 |
inhA | 1674555 | c.354G>A | synonymous_variant | 0.19 |
inhA | 1674558 | c.357C>A | synonymous_variant | 0.19 |
inhA | 1674561 | c.360C>T | synonymous_variant | 0.19 |
inhA | 1674582 | c.381T>C | synonymous_variant | 0.19 |
inhA | 1674585 | c.384T>C | synonymous_variant | 0.19 |
inhA | 1674589 | p.Met130Leu | missense_variant | 0.2 |
inhA | 1674624 | c.423A>C | synonymous_variant | 0.21 |
inhA | 1674627 | c.426T>G | synonymous_variant | 0.2 |
inhA | 1674630 | c.429C>G | synonymous_variant | 0.2 |
inhA | 1674636 | c.435C>G | synonymous_variant | 0.19 |
inhA | 1674654 | c.453G>C | synonymous_variant | 0.19 |
inhA | 1674693 | c.492C>G | synonymous_variant | 0.16 |
inhA | 1674703 | c.502T>C | synonymous_variant | 0.17 |
rpsA | 1833589 | c.48A>T | synonymous_variant | 0.18 |
rpsA | 1833595 | c.54T>C | synonymous_variant | 0.18 |
rpsA | 1833619 | c.78A>C | synonymous_variant | 0.2 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.23 |
rpsA | 1833667 | c.126C>G | synonymous_variant | 0.23 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.17 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.16 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.2 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.2 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.21 |
rpsA | 1833790 | c.249T>A | synonymous_variant | 0.22 |
rpsA | 1833799 | c.258C>G | synonymous_variant | 0.23 |
rpsA | 1833811 | c.270G>C | synonymous_variant | 0.21 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.21 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.19 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.18 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.23 |
rpsA | 1833862 | c.321G>T | synonymous_variant | 0.24 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.24 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.23 |
rpsA | 1833940 | c.399C>G | synonymous_variant | 0.24 |
rpsA | 1833952 | c.411C>A | synonymous_variant | 0.25 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.22 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.22 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.22 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.19 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.2 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834186 | c.645C>G | synonymous_variant | 0.18 |
rpsA | 1834189 | c.648G>C | synonymous_variant | 0.19 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 0.18 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.18 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.17 |
rpsA | 1834375 | c.834G>A | synonymous_variant | 0.18 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.21 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.25 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.27 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.26 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.24 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.29 |
rpsA | 1834465 | c.924T>C | synonymous_variant | 0.32 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.32 |
rpsA | 1834474 | c.933C>G | synonymous_variant | 0.33 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.31 |
rpsA | 1834498 | c.957C>T | synonymous_variant | 0.29 |
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 | 0.28 |
rpsA | 1834558 | c.1017C>G | synonymous_variant | 0.25 |
rpsA | 1834606 | c.1065C>G | synonymous_variant | 0.2 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.19 |
rpsA | 1834622 | c.1081_1083delTCGinsAGC | synonymous_variant | 0.19 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.19 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.19 |
rpsA | 1834666 | c.1125G>C | synonymous_variant | 0.16 |
rpsA | 1834669 | c.1128G>A | synonymous_variant | 0.15 |
rpsA | 1834688 | p.Ser383Cys | missense_variant | 0.14 |
rpsA | 1834726 | c.1185C>A | synonymous_variant | 0.16 |
rpsA | 1834733 | p.Ala398Pro | missense_variant | 0.16 |
tlyA | 1917929 | c.-11T>C | upstream_gene_variant | 0.17 |
tlyA | 1917943 | p.Ala2Ser | missense_variant | 0.19 |
tlyA | 1917951 | c.12T>C | synonymous_variant | 0.19 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1917981 | c.42G>C | synonymous_variant | 0.17 |
tlyA | 1917990 | c.51G>C | synonymous_variant | 0.18 |
tlyA | 1917993 | c.54A>G | synonymous_variant | 0.18 |
tlyA | 1917996 | c.57A>G | synonymous_variant | 0.17 |
tlyA | 1917999 | c.60T>C | synonymous_variant | 0.17 |
tlyA | 1918002 | c.63A>G | synonymous_variant | 0.18 |
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 |
kasA | 2517947 | c.-168C>T | upstream_gene_variant | 0.21 |
kasA | 2518609 | p.Met165Ile | missense_variant | 0.2 |
kasA | 2518621 | c.507G>A | synonymous_variant | 0.24 |
kasA | 2518642 | c.528A>G | synonymous_variant | 0.25 |
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 | 0.21 |
kasA | 2518696 | c.582C>G | synonymous_variant | 0.22 |
kasA | 2518702 | c.588C>T | synonymous_variant | 0.22 |
kasA | 2518711 | c.597A>G | synonymous_variant | 0.17 |
kasA | 2518714 | c.600A>C | synonymous_variant | 0.17 |
kasA | 2518717 | c.603C>T | synonymous_variant | 0.18 |
kasA | 2518732 | c.618C>G | synonymous_variant | 0.18 |
kasA | 2518741 | c.627G>C | synonymous_variant | 0.19 |
kasA | 2518747 | c.633C>G | synonymous_variant | 0.17 |
kasA | 2518783 | c.669T>C | synonymous_variant | 0.19 |
kasA | 2518792 | c.678C>G | synonymous_variant | 0.24 |
kasA | 2518795 | c.681C>G | synonymous_variant | 0.22 |
kasA | 2518816 | c.702C>A | synonymous_variant | 0.27 |
kasA | 2518822 | c.708C>G | synonymous_variant | 0.27 |
kasA | 2518825 | c.711T>C | synonymous_variant | 0.28 |
kasA | 2518855 | c.741C>G | synonymous_variant | 0.25 |
kasA | 2518864 | c.750G>C | synonymous_variant | 0.26 |
kasA | 2518879 | c.765A>G | synonymous_variant | 0.22 |
kasA | 2518885 | c.771T>C | synonymous_variant | 0.2 |
kasA | 2518888 | c.774C>T | synonymous_variant | 0.21 |
kasA | 2518898 | c.784T>C | synonymous_variant | 0.2 |
kasA | 2518906 | c.792A>G | synonymous_variant | 0.18 |
kasA | 2519068 | c.954C>T | synonymous_variant | 0.15 |
kasA | 2519072 | p.Ala320Thr | missense_variant | 0.17 |
kasA | 2519077 | c.963G>C | synonymous_variant | 0.16 |
kasA | 2519095 | c.981C>G | synonymous_variant | 0.17 |
kasA | 2519098 | c.984C>G | synonymous_variant | 0.18 |
kasA | 2519104 | c.990T>A | synonymous_variant | 0.19 |
kasA | 2519108 | p.Asp332Gln | missense_variant | 0.19 |
kasA | 2519111 | p.Gln333Glu | missense_variant | 0.19 |
kasA | 2519116 | c.1002C>G | synonymous_variant | 0.18 |
kasA | 2519125 | c.1011C>T | synonymous_variant | 0.18 |
kasA | 2519137 | c.1023T>C | synonymous_variant | 0.17 |
kasA | 2519146 | c.1032C>A | synonymous_variant | 0.18 |
kasA | 2519173 | c.1059C>G | synonymous_variant | 0.18 |
kasA | 2519176 | c.1062G>A | synonymous_variant | 0.16 |
folC | 2747355 | p.Val82Ile | missense_variant | 0.18 |
folC | 2747359 | c.240C>G | synonymous_variant | 0.18 |
folC | 2747362 | c.237G>C | synonymous_variant | 0.18 |
Rv2752c | 3065993 | p.Val67Ile | missense_variant | 0.18 |
Rv2752c | 3065994 | c.198T>C | synonymous_variant | 0.18 |
Rv2752c | 3065997 | c.195C>G | synonymous_variant | 0.17 |
Rv2752c | 3066024 | c.168T>C | synonymous_variant | 0.16 |
Rv2752c | 3066040 | p.Gly51Thr | missense_variant | 0.16 |
Rv2752c | 3066042 | c.150T>C | synonymous_variant | 0.17 |
Rv2752c | 3066050 | p.Leu48Met | missense_variant | 0.19 |
Rv2752c | 3066054 | c.138T>G | synonymous_variant | 0.18 |
Rv2752c | 3066066 | c.126T>C | synonymous_variant | 0.19 |
Rv2752c | 3066075 | c.117A>G | synonymous_variant | 0.17 |
Rv2752c | 3066087 | c.105A>G | synonymous_variant | 0.16 |
Rv2752c | 3066118 | p.Asn25Ser | missense_variant | 0.17 |
thyX | 3067293 | p.Gln218Arg | missense_variant | 0.2 |
thyX | 3067304 | c.642A>G | synonymous_variant | 0.22 |
thyX | 3067316 | c.630A>G | synonymous_variant | 0.26 |
thyX | 3067325 | c.621A>G | synonymous_variant | 0.27 |
thyX | 3067355 | c.591A>C | synonymous_variant | 0.26 |
thyX | 3067367 | c.579G>C | synonymous_variant | 0.27 |
thyX | 3067376 | c.570G>C | synonymous_variant | 0.25 |
thyX | 3067391 | c.555G>C | synonymous_variant | 0.23 |
thyX | 3067394 | c.552G>C | synonymous_variant | 0.24 |
thyX | 3067412 | c.534C>G | synonymous_variant | 0.29 |
thyX | 3067439 | c.507A>G | synonymous_variant | 0.31 |
thyX | 3067445 | c.501C>G | synonymous_variant | 0.27 |
thyX | 3067451 | c.495G>A | synonymous_variant | 0.25 |
thyX | 3067457 | c.489C>G | synonymous_variant | 0.24 |
thyX | 3067463 | p.Ile161Val | missense_variant | 0.22 |
thyX | 3067466 | c.480G>C | synonymous_variant | 0.22 |
thyX | 3067470 | p.Asn159Ser | missense_variant | 0.21 |
thyX | 3067493 | c.453A>G | synonymous_variant | 0.22 |
thyX | 3067500 | p.Lys149Arg | missense_variant | 0.22 |
thyX | 3067515 | p.Ser144Thr | missense_variant | 0.2 |
thyX | 3067531 | p.Ala139Thr | missense_variant | 0.14 |
thyX | 3067685 | c.261A>G | synonymous_variant | 0.17 |
thyX | 3067688 | c.258G>C | synonymous_variant | 0.18 |
thyX | 3067694 | c.252G>C | synonymous_variant | 0.18 |
thyX | 3067718 | c.228C>G | synonymous_variant | 0.18 |
thyX | 3067721 | c.225T>C | synonymous_variant | 0.18 |
thyX | 3067724 | c.222G>A | synonymous_variant | 0.18 |
thyX | 3067727 | c.219A>C | synonymous_variant | 0.18 |
thyX | 3067742 | c.204A>C | synonymous_variant | 0.16 |
thyX | 3067762 | c.184C>A | synonymous_variant | 0.14 |
thyX | 3067765 | p.Leu61Ile | missense_variant | 0.16 |
thyX | 3067781 | c.165C>G | synonymous_variant | 0.21 |
thyX | 3067787 | c.159G>A | synonymous_variant | 0.19 |
thyX | 3067793 | c.153T>C | synonymous_variant | 0.19 |
thyX | 3067799 | c.147G>A | synonymous_variant | 0.18 |
thyX | 3067802 | c.144C>G | synonymous_variant | 0.19 |
thyA | 3073872 | p.Ile200Val | missense_variant | 0.17 |
thyA | 3073878 | c.594G>A | synonymous_variant | 0.17 |
thyA | 3073892 | c.580T>C | synonymous_variant | 0.22 |
thyA | 3073893 | c.579C>G | synonymous_variant | 0.22 |
thyA | 3073899 | c.573G>A | synonymous_variant | 0.24 |
thyA | 3073925 | c.547T>C | synonymous_variant | 0.25 |
thyA | 3073926 | c.546G>C | synonymous_variant | 0.25 |
thyA | 3073929 | c.543T>C | synonymous_variant | 0.25 |
thyA | 3073953 | c.519T>C | synonymous_variant | 0.26 |
thyA | 3073977 | c.495A>G | synonymous_variant | 0.27 |
thyA | 3073989 | c.483T>C | synonymous_variant | 0.26 |
thyA | 3074001 | c.471C>G | synonymous_variant | 0.17 |
thyA | 3074004 | c.468T>C | synonymous_variant | 0.17 |
thyA | 3074010 | c.462C>G | synonymous_variant | 0.17 |
thyA | 3074031 | c.441T>C | synonymous_variant | 0.18 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473809 | c.-198G>C | upstream_gene_variant | 0.19 |
fprA | 3473812 | c.-195G>A | upstream_gene_variant | 0.19 |
fprA | 3473836 | c.-171C>A | upstream_gene_variant | 0.17 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475015 | p.Gln337Lys | missense_variant | 0.18 |
fprA | 3475036 | p.Val344Thr | missense_variant | 0.16 |
fprA | 3475047 | c.1041A>G | synonymous_variant | 0.16 |
fprA | 3475048 | p.Ile348Val | missense_variant | 0.16 |
fprA | 3475061 | p.Pro352Arg | missense_variant | 0.17 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiB | 3642668 | c.1134A>C | synonymous_variant | 0.17 |
fbiB | 3642677 | c.1143A>G | synonymous_variant | 0.18 |
fbiB | 3642680 | c.1146A>G | synonymous_variant | 0.19 |
fbiB | 3642684 | c.1150T>C | synonymous_variant | 0.19 |
alr | 3840435 | p.Leu329Ser | missense_variant | 0.16 |
alr | 3840442 | p.Glu327Gln | missense_variant | 0.17 |
alr | 3840467 | p.Val318Ile | missense_variant | 0.18 |
alr | 3840476 | c.945A>C | synonymous_variant | 0.18 |
alr | 3840482 | c.939T>C | synonymous_variant | 0.17 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.16 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.18 |
rpoA | 3877638 | c.870T>C | synonymous_variant | 0.24 |
rpoA | 3877677 | p.Ala277Thr | missense_variant | 0.16 |
rpoA | 3877680 | c.828G>C | synonymous_variant | 0.18 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.21 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.21 |
rpoA | 3877704 | c.804G>T | synonymous_variant | 0.22 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.2 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.19 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.19 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.2 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.17 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.23 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.23 |
rpoA | 3877857 | c.651G>A | synonymous_variant | 0.2 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.18 |
rpoA | 3877872 | c.636C>T | synonymous_variant | 0.17 |
rpoA | 3877875 | c.633T>G | synonymous_variant | 0.24 |
rpoA | 3877899 | p.Ser203Thr | missense_variant | 0.22 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.21 |
rpoA | 3877908 | p.Asn200Ser | missense_variant | 0.2 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.15 |
rpoA | 3878082 | c.426T>C | synonymous_variant | 0.17 |
rpoA | 3878094 | c.414C>G | synonymous_variant | 0.17 |
rpoA | 3878100 | c.408C>G | synonymous_variant | 0.17 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.17 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.17 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.17 |
rpoA | 3878143 | p.Gly122Asp | missense_variant | 0.17 |
rpoA | 3878184 | c.324C>T | synonymous_variant | 0.16 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.17 |
rpoA | 3878199 | c.309T>C | synonymous_variant | 0.2 |
rpoA | 3878202 | c.306G>C | synonymous_variant | 0.18 |
rpoA | 3878261 | c.247C>T | synonymous_variant | 0.17 |
rpoA | 3878262 | c.246C>T | synonymous_variant | 0.17 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.17 |
rpoA | 3878284 | p.Glu75Ala | missense_variant | 0.17 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.18 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.17 |
rpoA | 3878304 | c.204G>C | synonymous_variant | 0.2 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 0.2 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.27 |
rpoA | 3878331 | c.177A>G | synonymous_variant | 0.23 |
rpoA | 3878334 | c.174T>C | synonymous_variant | 0.22 |
rpoA | 3878337 | c.171T>C | synonymous_variant | 0.22 |
rpoA | 3878346 | c.162T>C | synonymous_variant | 0.24 |
rpoA | 3878364 | c.144A>G | synonymous_variant | 0.18 |
rpoA | 3878367 | c.141C>G | synonymous_variant | 0.18 |
rpoA | 3878370 | c.138T>C | synonymous_variant | 0.2 |
rpoA | 3878376 | c.132G>C | synonymous_variant | 0.23 |
rpoA | 3878385 | c.123C>G | synonymous_variant | 0.24 |
rpoA | 3878391 | c.117T>C | synonymous_variant | 0.25 |
rpoA | 3878396 | c.112C>T | synonymous_variant | 0.26 |
rpoA | 3878436 | c.72A>G | synonymous_variant | 0.32 |
rpoA | 3878442 | c.66G>C | synonymous_variant | 0.33 |
rpoA | 3878454 | c.54A>C | synonymous_variant | 0.26 |
rpoA | 3878472 | p.Asp12Glu | missense_variant | 0.24 |
rpoA | 3878478 | c.30C>G | synonymous_variant | 0.25 |
rpoA | 3878490 | c.18C>A | synonymous_variant | 0.25 |
rpoA | 3878496 | c.12A>T | synonymous_variant | 0.15 |
rpoA | 3878665 | c.-158A>G | upstream_gene_variant | 0.15 |
rpoA | 3878672 | c.-165A>T | upstream_gene_variant | 0.14 |
rpoA | 3878698 | c.-191A>G | upstream_gene_variant | 0.22 |
rpoA | 3878701 | c.-194C>G | upstream_gene_variant | 0.23 |
ddn | 3986655 | c.-189A>T | upstream_gene_variant | 0.17 |
ddn | 3986660 | c.-184C>T | upstream_gene_variant | 0.17 |
ddn | 3986665 | c.-179G>C | upstream_gene_variant | 0.17 |
ddn | 3986667 | c.-177_-176delCTinsAC | upstream_gene_variant | 0.18 |
ddn | 3986681 | c.-163C>G | upstream_gene_variant | 0.2 |
ddn | 3986690 | c.-154C>G | upstream_gene_variant | 0.2 |
ddn | 3986696 | c.-148G>T | upstream_gene_variant | 0.2 |
ddn | 3986699 | c.-145C>G | upstream_gene_variant | 0.19 |
clpC1 | 4038212 | c.2493T>C | synonymous_variant | 0.17 |
clpC1 | 4038271 | p.Pro812Ala | missense_variant | 0.19 |
clpC1 | 4038274 | p.Gly811Ser | missense_variant | 0.17 |
clpC1 | 4038278 | c.2427T>C | synonymous_variant | 0.19 |
clpC1 | 4038293 | c.2412G>C | synonymous_variant | 0.24 |
clpC1 | 4038302 | c.2403C>A | synonymous_variant | 0.24 |
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 | 0.19 |
clpC1 | 4038359 | c.2346A>G | synonymous_variant | 0.2 |
clpC1 | 4038368 | c.2337T>C | synonymous_variant | 0.19 |
clpC1 | 4038388 | c.2317T>C | synonymous_variant | 0.19 |
clpC1 | 4038398 | c.2307G>T | synonymous_variant | 0.21 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 0.21 |
clpC1 | 4038419 | c.2286T>C | synonymous_variant | 0.18 |
clpC1 | 4038434 | c.2271G>C | synonymous_variant | 0.17 |
clpC1 | 4038498 | p.Ser736Thr | missense_variant | 0.15 |
clpC1 | 4038530 | p.Glu725Asp | missense_variant | 0.19 |
clpC1 | 4038536 | c.2169C>T | synonymous_variant | 0.22 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.29 |
clpC1 | 4038623 | c.2082A>G | synonymous_variant | 0.19 |
clpC1 | 4038640 | p.Asp689Asn | missense_variant | 0.18 |
clpC1 | 4038653 | c.2052C>T | synonymous_variant | 0.18 |
clpC1 | 4038661 | p.Ser682Thr | missense_variant | 0.15 |
clpC1 | 4038671 | c.2034T>C | synonymous_variant | 0.18 |
clpC1 | 4038683 | c.2022T>C | synonymous_variant | 0.16 |
clpC1 | 4038755 | c.1950G>C | synonymous_variant | 0.15 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.18 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 0.21 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.23 |
clpC1 | 4038815 | c.1890G>T | synonymous_variant | 0.23 |
clpC1 | 4038860 | c.1845G>A | synonymous_variant | 0.29 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.31 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.29 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.29 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 0.33 |
clpC1 | 4038932 | c.1773G>C | synonymous_variant | 0.27 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.23 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.22 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.2 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.18 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.18 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.22 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.22 |
clpC1 | 4039073 | c.1632C>G | synonymous_variant | 0.22 |
clpC1 | 4039085 | c.1620A>G | synonymous_variant | 0.19 |
clpC1 | 4039090 | c.1615C>T | synonymous_variant | 0.19 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.2 |
clpC1 | 4039103 | c.1602T>C | synonymous_variant | 0.21 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.19 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.21 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.22 |
clpC1 | 4039124 | c.1581C>G | synonymous_variant | 0.22 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.17 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.19 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.2 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.2 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.2 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.21 |
clpC1 | 4039187 | c.1518G>C | synonymous_variant | 0.2 |
clpC1 | 4039190 | c.1515C>G | synonymous_variant | 0.2 |
clpC1 | 4039268 | c.1437C>G | synonymous_variant | 0.18 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.19 |
clpC1 | 4039286 | c.1419T>C | synonymous_variant | 0.22 |
clpC1 | 4039289 | c.1416T>C | synonymous_variant | 0.22 |
clpC1 | 4039295 | c.1410A>C | synonymous_variant | 0.22 |
clpC1 | 4039298 | c.1407T>C | synonymous_variant | 0.22 |
clpC1 | 4039319 | c.1386T>C | synonymous_variant | 0.18 |
clpC1 | 4039328 | c.1377A>G | synonymous_variant | 0.17 |
clpC1 | 4039391 | c.1314T>G | synonymous_variant | 0.19 |
clpC1 | 4039409 | c.1296T>C | synonymous_variant | 0.18 |
clpC1 | 4039412 | c.1293T>G | synonymous_variant | 0.16 |
clpC1 | 4039484 | c.1221T>G | synonymous_variant | 0.17 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.2 |
clpC1 | 4039524 | p.Phe394Tyr | missense_variant | 0.16 |
clpC1 | 4039526 | c.1179G>C | synonymous_variant | 0.17 |
clpC1 | 4039547 | c.1158C>G | synonymous_variant | 0.16 |
clpC1 | 4039586 | c.1119G>C | synonymous_variant | 0.16 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.17 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.17 |
clpC1 | 4039622 | c.1083C>G | synonymous_variant | 0.17 |
clpC1 | 4039682 | c.1023C>G | synonymous_variant | 0.2 |
clpC1 | 4039685 | c.1020C>T | synonymous_variant | 0.21 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.23 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.27 |
clpC1 | 4039748 | c.957G>C | synonymous_variant | 0.27 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.27 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.28 |
clpC1 | 4039760 | c.945T>C | synonymous_variant | 0.28 |
clpC1 | 4039766 | c.939T>C | synonymous_variant | 0.27 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.27 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.26 |
clpC1 | 4039781 | c.924G>C | synonymous_variant | 0.23 |
clpC1 | 4039787 | c.916_918delTCGinsAGC | synonymous_variant | 0.25 |
clpC1 | 4039793 | c.912C>G | synonymous_variant | 0.26 |
clpC1 | 4039817 | c.888A>T | synonymous_variant | 0.22 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.23 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 0.22 |
clpC1 | 4039832 | c.873C>G | synonymous_variant | 0.22 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.24 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.22 |
clpC1 | 4039886 | c.819C>G | synonymous_variant | 0.24 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.26 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.27 |
clpC1 | 4039928 | c.775_777delAGCinsTCG | synonymous_variant | 0.25 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.25 |
clpC1 | 4039946 | c.759A>T | synonymous_variant | 0.25 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.23 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.23 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.2 |
clpC1 | 4039996 | p.Glu237Gln | missense_variant | 0.17 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.18 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.18 |
clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 0.17 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.17 |
clpC1 | 4040105 | c.600C>G | synonymous_variant | 0.21 |
clpC1 | 4040123 | c.582G>A | synonymous_variant | 0.26 |
clpC1 | 4040147 | c.558A>G | synonymous_variant | 0.24 |
clpC1 | 4040153 | c.552A>G | synonymous_variant | 0.25 |
clpC1 | 4040162 | c.543G>C | synonymous_variant | 0.22 |
clpC1 | 4040165 | c.540G>C | synonymous_variant | 0.21 |
clpC1 | 4040168 | c.537G>C | synonymous_variant | 0.21 |
clpC1 | 4040171 | c.534C>G | synonymous_variant | 0.21 |
clpC1 | 4040201 | c.504C>G | synonymous_variant | 0.16 |
clpC1 | 4040237 | c.468C>T | synonymous_variant | 0.14 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 0.16 |
embC | 4240561 | c.699C>G | synonymous_variant | 0.16 |
embC | 4240591 | c.729C>G | synonymous_variant | 0.16 |
embC | 4240594 | c.732C>G | synonymous_variant | 0.18 |
embC | 4240600 | c.738G>C | synonymous_variant | 0.17 |
embC | 4240632 | p.Met257Thr | missense_variant | 0.16 |
embC | 4240642 | c.780G>C | synonymous_variant | 0.17 |
embC | 4240645 | c.783G>C | synonymous_variant | 0.17 |
embC | 4240657 | c.795G>C | synonymous_variant | 0.2 |
embC | 4240671 | p.Thr270Ile | missense_variant | 0.26 |
embC | 4240678 | c.816T>G | synonymous_variant | 0.25 |
embC | 4240685 | p.Thr275Ala | missense_variant | 0.24 |
embC | 4240693 | c.831T>C | synonymous_variant | 0.24 |
embC | 4240706 | p.Val282Thr | missense_variant | 0.2 |
embC | 4240726 | c.864G>C | synonymous_variant | 0.18 |
embC | 4240780 | c.918T>C | synonymous_variant | 0.17 |
embC | 4240783 | c.921G>C | synonymous_variant | 0.18 |
embC | 4240789 | c.927T>C | synonymous_variant | 0.2 |
embC | 4240819 | c.957A>G | synonymous_variant | 0.25 |
embC | 4240831 | c.969T>G | synonymous_variant | 0.24 |
embC | 4240867 | c.1005T>G | synonymous_variant | 0.24 |
embC | 4240870 | c.1008T>C | synonymous_variant | 0.24 |
embC | 4240879 | c.1017G>C | synonymous_variant | 0.23 |
embC | 4240880 | p.Ala340Thr | missense_variant | 0.24 |
embC | 4240885 | c.1023T>C | synonymous_variant | 0.23 |
embC | 4240897 | c.1035C>G | synonymous_variant | 0.21 |
embC | 4240900 | c.1038A>G | synonymous_variant | 0.22 |
embC | 4240919 | c.1057_1059delCTCinsTTG | synonymous_variant | 0.21 |
embC | 4240936 | c.1074A>G | synonymous_variant | 0.23 |
embC | 4240945 | c.1083T>C | synonymous_variant | 0.18 |
embC | 4240951 | c.1089C>G | synonymous_variant | 0.2 |
embC | 4240954 | p.Ile364Met | missense_variant | 0.17 |
embC | 4240957 | c.1095C>G | synonymous_variant | 0.18 |
embC | 4240980 | p.Thr373Lys | missense_variant | 0.16 |
embC | 4240983 | p.Ser374Asn | missense_variant | 0.17 |
embC | 4240990 | c.1128A>G | synonymous_variant | 0.16 |
embC | 4241104 | c.1242G>A | synonymous_variant | 0.17 |
embC | 4241107 | c.1245G>C | synonymous_variant | 0.17 |
embC | 4241137 | c.1275G>C | synonymous_variant | 0.19 |
embC | 4241140 | c.1278A>G | synonymous_variant | 0.19 |
embC | 4241141 | p.Ile427Val | missense_variant | 0.19 |
embC | 4241158 | c.1296T>C | synonymous_variant | 0.18 |
embC | 4241161 | c.1299C>G | synonymous_variant | 0.19 |
embC | 4241162 | c.1300T>C | synonymous_variant | 0.19 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 0.97 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4245137 | c.1905T>C | synonymous_variant | 0.16 |
embA | 4245185 | c.1953G>T | synonymous_variant | 0.14 |
embA | 4245194 | c.1962G>C | synonymous_variant | 0.17 |
embA | 4245198 | p.Leu656Ile | missense_variant | 0.17 |
embA | 4245408 | p.Leu726Ile | missense_variant | 0.14 |
embA | 4245461 | c.2229C>G | synonymous_variant | 0.18 |
embA | 4245465 | p.Pro745Ala | missense_variant | 0.17 |
embA | 4245470 | c.2238T>C | synonymous_variant | 0.18 |
embB | 4245674 | c.-840A>C | upstream_gene_variant | 0.18 |
embB | 4245677 | c.-837G>C | upstream_gene_variant | 0.18 |
embB | 4245683 | c.-831C>G | upstream_gene_variant | 0.17 |
embB | 4245689 | c.-825C>G | upstream_gene_variant | 0.18 |
embB | 4245692 | c.-822G>C | upstream_gene_variant | 0.18 |
embA | 4245693 | p.Ile821Val | missense_variant | 0.17 |
embB | 4245701 | c.-813G>C | upstream_gene_variant | 0.18 |
embB | 4245725 | c.-789A>C | upstream_gene_variant | 0.23 |
embB | 4245726 | c.-788_-786delTTGinsCTC | upstream_gene_variant | 0.23 |
embB | 4245737 | c.-777A>C | upstream_gene_variant | 0.26 |
embB | 4245740 | c.-774T>C | upstream_gene_variant | 0.26 |
embB | 4245764 | c.-750G>C | upstream_gene_variant | 0.26 |
embA | 4245771 | p.Asn847Ser | missense_variant | 0.25 |
embB | 4245807 | c.-707_-705delTTAinsCTG | upstream_gene_variant | 0.2 |
embA | 4245820 | p.Ser863Thr | missense_variant | 0.17 |
embB | 4245830 | c.-684G>C | upstream_gene_variant | 0.18 |
embB | 4245845 | c.-669T>G | upstream_gene_variant | 0.15 |
embB | 4245848 | c.-666C>G | upstream_gene_variant | 0.17 |
embB | 4248085 | c.1572T>C | synonymous_variant | 0.18 |
embB | 4248097 | c.1584C>G | synonymous_variant | 0.17 |
embB | 4248118 | c.1605T>C | synonymous_variant | 0.16 |
embB | 4248127 | c.1614G>C | synonymous_variant | 0.16 |
embB | 4248133 | c.1620C>G | synonymous_variant | 0.15 |
embB | 4248142 | c.1629T>C | synonymous_variant | 0.16 |
embB | 4248265 | c.1752C>T | synonymous_variant | 0.15 |
embB | 4248266 | c.1753C>T | synonymous_variant | 0.15 |
embB | 4248277 | c.1764G>C | synonymous_variant | 0.15 |
embB | 4248343 | c.1830G>C | synonymous_variant | 0.19 |
embB | 4248346 | c.1833G>C | synonymous_variant | 0.18 |
embB | 4248350 | c.1837T>C | synonymous_variant | 0.19 |
embB | 4248355 | c.1842A>G | synonymous_variant | 0.19 |
embB | 4248358 | c.1845C>G | synonymous_variant | 0.19 |
embB | 4248361 | c.1848A>G | synonymous_variant | 0.21 |
embB | 4248362 | p.Ser617Ala | missense_variant | 0.21 |
embB | 4248398 | c.1885C>T | synonymous_variant | 0.21 |
embB | 4248403 | c.1890G>C | synonymous_variant | 0.18 |
embB | 4249381 | c.2868A>G | synonymous_variant | 0.16 |
embB | 4249469 | p.Leu986Met | missense_variant | 0.15 |
embB | 4249486 | c.2973T>G | synonymous_variant | 0.16 |
embB | 4249521 | p.Ala1003Val | missense_variant | 0.15 |
aftB | 4267571 | c.1266T>C | synonymous_variant | 0.18 |
aftB | 4267580 | c.1257G>C | synonymous_variant | 0.25 |
aftB | 4267607 | c.1230G>A | synonymous_variant | 0.26 |
aftB | 4267619 | c.1218C>G | synonymous_variant | 0.19 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 0.88 |
aftB | 4269183 | c.-347T>C | upstream_gene_variant | 0.17 |
aftB | 4269201 | c.-365A>G | upstream_gene_variant | 0.18 |
ubiA | 4269220 | p.Ala205Lys | missense_variant | 0.15 |
aftB | 4269231 | c.-395C>G | upstream_gene_variant | 0.16 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |