Run ID: SRR6045264
Sample name:
Date: 04-04-2023 11:55:54
Number of reads: 496523
Percentage reads mapped: 13.1
Strain: lineage2.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.99 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 0.99 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5661 | p.Arg141Leu | missense_variant | 0.18 |
gyrB | 6061 | c.822C>T | synonymous_variant | 0.18 |
gyrA | 6673 | c.-629A>C | upstream_gene_variant | 0.17 |
gyrA | 6676 | c.-626T>C | upstream_gene_variant | 0.17 |
gyrA | 6685 | c.-617C>T | upstream_gene_variant | 0.15 |
gyrA | 6700 | c.-602T>C | upstream_gene_variant | 0.15 |
gyrA | 6703 | c.-599G>C | upstream_gene_variant | 0.15 |
gyrA | 6709 | c.-593A>G | upstream_gene_variant | 0.18 |
gyrA | 6730 | c.-572A>G | upstream_gene_variant | 0.18 |
gyrA | 7033 | c.-269G>T | upstream_gene_variant | 0.18 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491466 | p.Met228Ile | missense_variant | 0.2 |
fgd1 | 491610 | c.828A>G | synonymous_variant | 0.16 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575649 | p.Val101Glu | missense_variant | 0.17 |
mshA | 575907 | p.Ala187Val | missense_variant | 0.92 |
mshA | 576645 | p.Thr433Asn | missense_variant | 0.14 |
ccsA | 620020 | p.Leu44Phe | missense_variant | 0.14 |
ccsA | 620583 | c.693G>C | synonymous_variant | 0.15 |
ccsA | 620589 | c.699G>C | synonymous_variant | 0.15 |
ccsA | 620598 | c.708C>G | synonymous_variant | 0.15 |
ccsA | 620604 | c.714C>G | synonymous_variant | 0.15 |
ccsA | 620607 | c.717T>A | synonymous_variant | 0.15 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.14 |
rpoB | 761253 | p.Pro483Ser | missense_variant | 0.14 |
rpoB | 761276 | c.1470G>A | synonymous_variant | 0.14 |
rpoB | 762834 | p.Gly1010Ser | missense_variant | 0.22 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763052 | c.-318G>C | upstream_gene_variant | 0.21 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.3 |
rpoC | 763076 | c.-294C>G | upstream_gene_variant | 0.3 |
rpoC | 763082 | c.-288C>G | upstream_gene_variant | 0.3 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.3 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.36 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.42 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.4 |
rpoC | 763169 | c.-201A>G | upstream_gene_variant | 0.33 |
rpoC | 763184 | c.-186C>T | upstream_gene_variant | 0.31 |
rpoC | 763202 | c.-168A>G | upstream_gene_variant | 0.29 |
rpoC | 763206 | c.-164_-162delAGTinsTCC | upstream_gene_variant | 0.27 |
rpoC | 763226 | c.-144A>G | upstream_gene_variant | 0.31 |
rpoC | 763238 | c.-132T>C | upstream_gene_variant | 0.36 |
rpoC | 763268 | c.-102C>A | upstream_gene_variant | 0.22 |
rpoC | 763441 | c.72C>T | synonymous_variant | 0.19 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.19 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.22 |
rpoC | 763486 | c.117T>G | synonymous_variant | 0.29 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.33 |
rpoC | 763537 | c.168C>G | synonymous_variant | 0.29 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.28 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.19 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.13 |
rpoC | 763822 | c.453C>A | synonymous_variant | 0.15 |
rpoC | 763836 | p.Ala156Val | missense_variant | 0.15 |
rpoC | 763851 | p.Ala161Gly | missense_variant | 0.2 |
rpoC | 763855 | c.486C>T | synonymous_variant | 0.2 |
rpoC | 763858 | c.489A>G | synonymous_variant | 0.2 |
rpoC | 763871 | p.Gly168Thr | missense_variant | 0.25 |
rpoC | 763879 | c.510A>G | synonymous_variant | 0.22 |
rpoC | 763888 | c.519G>T | synonymous_variant | 0.2 |
rpoC | 763894 | c.525A>G | synonymous_variant | 0.18 |
rpoC | 764044 | c.675T>C | synonymous_variant | 0.15 |
rpoC | 764059 | c.690G>C | synonymous_variant | 0.31 |
rpoC | 764071 | c.702G>C | synonymous_variant | 0.33 |
rpoC | 764083 | c.714A>G | synonymous_variant | 0.4 |
rpoC | 764098 | c.729A>G | synonymous_variant | 0.33 |
rpoC | 764101 | c.732C>G | synonymous_variant | 0.36 |
rpoC | 764110 | c.741C>T | synonymous_variant | 0.46 |
rpoC | 764320 | c.951C>G | synonymous_variant | 0.22 |
rpoC | 764338 | c.969G>A | synonymous_variant | 0.25 |
rpoC | 764339 | c.970C>T | synonymous_variant | 0.25 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.22 |
rpoC | 764381 | c.1012_1013delTCinsAG | synonymous_variant | 0.22 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 0.29 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.15 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.17 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 0.17 |
rpoC | 764830 | c.1461C>G | synonymous_variant | 0.16 |
rpoC | 764858 | c.1489_1491delTTGinsCTA | synonymous_variant | 0.14 |
rpoC | 764861 | c.1492C>T | synonymous_variant | 0.14 |
rpoC | 764867 | c.1498_1500delCGCinsAGG | synonymous_variant | 0.14 |
rpoC | 764878 | c.1509C>G | synonymous_variant | 0.12 |
rpoC | 764881 | c.1512G>C | synonymous_variant | 0.12 |
rpoC | 765029 | p.Glu554* | stop_gained | 0.15 |
rpoC | 766345 | c.2976T>C | synonymous_variant | 0.19 |
rpoC | 766348 | c.2979A>G | synonymous_variant | 0.15 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.17 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.15 |
rpoC | 766393 | c.3024C>G | synonymous_variant | 0.14 |
rpoC | 766408 | c.3039C>G | synonymous_variant | 0.18 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.25 |
rpoC | 766447 | c.3078T>C | synonymous_variant | 0.13 |
rpoC | 766456 | c.3087C>G | synonymous_variant | 0.18 |
rpoC | 766522 | c.3153C>G | synonymous_variant | 0.15 |
rpoC | 766528 | c.3159T>C | synonymous_variant | 0.15 |
rpoC | 766540 | p.Asp1057Glu | missense_variant | 0.12 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 0.93 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.27 |
rpoC | 766861 | c.3492G>A | synonymous_variant | 0.43 |
rpoC | 766864 | c.3495G>C | synonymous_variant | 0.43 |
rpoC | 766883 | p.Ser1172Ala | missense_variant | 0.4 |
rpoC | 766894 | c.3525T>C | synonymous_variant | 0.4 |
rpoC | 766895 | c.3526T>C | synonymous_variant | 0.4 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.4 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775883 | p.Ile866Leu | missense_variant | 0.16 |
mmpL5 | 775909 | p.Leu858Phe | missense_variant | 0.21 |
mmpL5 | 775913 | p.Ala856Ser | missense_variant | 0.21 |
mmpL5 | 775916 | c.2565T>G | synonymous_variant | 0.21 |
mmpL5 | 775937 | c.2544G>C | synonymous_variant | 0.2 |
mmpL5 | 775961 | c.2520C>G | synonymous_variant | 0.17 |
mmpL5 | 775966 | p.Ala839Ser | missense_variant | 0.18 |
mmpL5 | 775991 | c.2490G>A | synonymous_variant | 0.12 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 777775 | p.Val236Leu | missense_variant | 0.14 |
mmpL5 | 778209 | p.Ala91Val | missense_variant | 0.33 |
mmpL5 | 778287 | p.Ser65Asn | missense_variant | 0.2 |
mmpS5 | 778588 | p.Gln106His | missense_variant | 0.56 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801222 | c.414T>C | synonymous_variant | 0.14 |
rplC | 801270 | c.462T>C | synonymous_variant | 0.14 |
rplC | 801276 | c.468G>T | synonymous_variant | 0.13 |
rplC | 801288 | c.480G>C | synonymous_variant | 0.14 |
fbiC | 1303575 | c.645G>C | synonymous_variant | 0.14 |
fbiC | 1303584 | c.654C>G | synonymous_variant | 0.14 |
fbiC | 1303990 | c.1064delG | frameshift_variant | 0.2 |
fbiC | 1304580 | c.1650T>C | synonymous_variant | 0.17 |
fbiC | 1304613 | c.1683T>C | synonymous_variant | 0.19 |
fbiC | 1304640 | c.1710A>C | synonymous_variant | 0.12 |
fbiC | 1304646 | c.1716T>C | synonymous_variant | 0.2 |
fbiC | 1304670 | c.1740G>C | synonymous_variant | 0.23 |
fbiC | 1304671 | p.Val581Thr | missense_variant | 0.23 |
fbiC | 1304675 | p.Gly582Glu | missense_variant | 0.23 |
fbiC | 1304691 | c.1761G>C | synonymous_variant | 0.23 |
fbiC | 1304694 | c.1764A>C | synonymous_variant | 0.23 |
fbiC | 1304703 | c.1773C>G | synonymous_variant | 0.27 |
fbiC | 1304715 | c.1785G>C | synonymous_variant | 0.29 |
fbiC | 1304724 | c.1794A>G | synonymous_variant | 0.24 |
fbiC | 1304727 | c.1797A>G | synonymous_variant | 0.17 |
fbiC | 1304757 | c.1827A>G | synonymous_variant | 0.17 |
fbiC | 1304778 | c.1848T>C | synonymous_variant | 0.17 |
fbiC | 1304784 | c.1854T>G | synonymous_variant | 0.13 |
fbiC | 1304787 | c.1857T>C | synonymous_variant | 0.15 |
fbiC | 1304799 | c.1869G>C | synonymous_variant | 0.15 |
fbiC | 1304808 | c.1878C>G | synonymous_variant | 0.18 |
fbiC | 1304811 | c.1881C>G | synonymous_variant | 0.17 |
fbiC | 1304817 | c.1887T>C | synonymous_variant | 0.23 |
fbiC | 1304823 | c.1893C>T | synonymous_variant | 0.21 |
fbiC | 1304829 | c.1899T>C | synonymous_variant | 0.2 |
fbiC | 1304853 | c.1923C>T | synonymous_variant | 0.19 |
fbiC | 1304856 | c.1926C>G | synonymous_variant | 0.18 |
fbiC | 1304869 | c.1939C>T | synonymous_variant | 0.17 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1406978 | p.Met121Ile | missense_variant | 0.18 |
embR | 1417062 | c.285delC | frameshift_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472574 | n.729T>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472591 | n.746G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472970 | n.1125C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1473234 | n.1389A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473389 | n.-269C>A | upstream_gene_variant | 0.17 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473813 | n.156C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473899 | n.242A>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474009 | n.352A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474012 | n.355C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474040 | n.383G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474089 | n.432C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474111 | n.454T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474249 | n.592G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474552 | n.895C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474837 | n.1180A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474950 | n.1293G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474952 | n.1296_1300delCATCC | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474961 | n.1304T>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474962 | n.1305T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474963 | n.1306G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474964 | n.1307T>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474967 | n.1311_1315delGGGTG | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474997 | n.1340A>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475006 | n.1349A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475252 | n.1595C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475253 | n.1596T>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475606 | n.1949T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475616 | n.1959A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475617 | n.1960C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475625 | n.1968G>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475626 | n.1969T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475639 | n.1982C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475883 | n.2226A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476226 | n.2569G>T | non_coding_transcript_exon_variant | 0.29 |
inhA | 1674333 | c.132G>A | synonymous_variant | 0.18 |
inhA | 1674792 | c.591G>C | synonymous_variant | 0.14 |
inhA | 1674801 | c.600T>C | synonymous_variant | 0.15 |
inhA | 1674816 | c.615T>A | synonymous_variant | 0.14 |
inhA | 1674822 | c.621C>G | synonymous_variant | 0.15 |
inhA | 1674825 | c.624C>T | synonymous_variant | 0.19 |
inhA | 1674846 | c.645C>A | synonymous_variant | 0.29 |
inhA | 1674849 | p.Gln216His | missense_variant | 0.29 |
inhA | 1674870 | c.669T>C | synonymous_variant | 0.31 |
inhA | 1674876 | c.675C>G | synonymous_variant | 0.31 |
inhA | 1674879 | c.678T>G | synonymous_variant | 0.27 |
inhA | 1674883 | p.Ile228Leu | missense_variant | 0.25 |
inhA | 1674903 | c.702T>C | synonymous_variant | 0.24 |
inhA | 1674904 | p.Ala235Pro | missense_variant | 0.24 |
inhA | 1674933 | c.732G>C | synonymous_variant | 0.27 |
inhA | 1674939 | c.738G>C | synonymous_variant | 0.15 |
inhA | 1674942 | c.741T>G | synonymous_variant | 0.14 |
inhA | 1674945 | p.Asp248Glu | missense_variant | 0.2 |
inhA | 1674957 | c.756G>A | synonymous_variant | 0.14 |
rpsA | 1833517 | c.-24delC | upstream_gene_variant | 0.18 |
rpsA | 1833541 | c.-1T>C | upstream_gene_variant | 0.21 |
rpsA | 1833554 | p.Thr5Ala | missense_variant | 0.25 |
rpsA | 1833578 | p.Val13Ile | missense_variant | 0.17 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.14 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.18 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.18 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.2 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.19 |
rpsA | 1834465 | c.924T>C | synonymous_variant | 0.15 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.2 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.17 |
tlyA | 1917798 | c.-142C>A | upstream_gene_variant | 0.22 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2156354 | c.-243G>T | upstream_gene_variant | 0.25 |
katG | 2156545 | c.-434G>T | upstream_gene_variant | 0.12 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169484 | p.Ala377Ser | missense_variant | 0.25 |
PPE35 | 2170031 | c.582C>A | synonymous_variant | 0.25 |
Rv1979c | 2222385 | c.780C>A | synonymous_variant | 0.18 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290104 | c.-863G>T | upstream_gene_variant | 0.2 |
kasA | 2518567 | c.453G>C | synonymous_variant | 0.14 |
kasA | 2518571 | p.Val153Thr | missense_variant | 0.14 |
kasA | 2518574 | p.Ile154Val | missense_variant | 0.15 |
kasA | 2518579 | c.465T>G | synonymous_variant | 0.17 |
kasA | 2518588 | c.474T>G | synonymous_variant | 0.18 |
kasA | 2518594 | c.480C>G | synonymous_variant | 0.23 |
kasA | 2518603 | c.489G>A | synonymous_variant | 0.25 |
kasA | 2518627 | c.513T>C | synonymous_variant | 0.23 |
kasA | 2518642 | c.528A>G | synonymous_variant | 0.17 |
kasA | 2518645 | c.531G>C | synonymous_variant | 0.17 |
kasA | 2519239 | c.1125A>C | synonymous_variant | 0.2 |
kasA | 2519272 | c.1158C>G | synonymous_variant | 0.14 |
eis | 2715427 | c.-95T>C | upstream_gene_variant | 0.15 |
ahpC | 2726265 | p.Lys25Gln | missense_variant | 0.33 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.29 |
ahpC | 2726450 | c.258G>T | synonymous_variant | 0.17 |
folC | 2746527 | p.Gly358Trp | missense_variant | 0.2 |
folC | 2746816 | c.783C>A | synonymous_variant | 0.14 |
folC | 2747302 | c.297A>G | synonymous_variant | 0.16 |
folC | 2747335 | c.264G>A | synonymous_variant | 0.13 |
folC | 2747338 | c.261C>G | synonymous_variant | 0.13 |
folC | 2747341 | p.Val86Leu | missense_variant | 0.2 |
folC | 2747344 | c.255G>C | synonymous_variant | 0.14 |
folC | 2747355 | p.Val82Ile | missense_variant | 0.13 |
folC | 2747359 | c.238_240delCGCinsAGG | synonymous_variant | 0.2 |
folC | 2747362 | p.Ala79Thr | missense_variant | 0.13 |
pepQ | 2859825 | p.Ala198Pro | missense_variant | 0.17 |
pepQ | 2859834 | c.585T>C | synonymous_variant | 0.15 |
ribD | 2986995 | p.Ala53Ser | missense_variant | 0.14 |
thyX | 3067883 | c.63C>G | synonymous_variant | 0.13 |
thyX | 3067886 | c.60A>G | synonymous_variant | 0.13 |
thyX | 3067894 | c.52T>C | synonymous_variant | 0.14 |
thyX | 3067898 | p.Asp16Glu | missense_variant | 0.14 |
thyA | 3074367 | c.105C>A | synonymous_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087578 | c.759A>G | synonymous_variant | 0.14 |
ald | 3087587 | c.768G>A | synonymous_variant | 0.14 |
ald | 3087641 | c.822T>C | synonymous_variant | 0.13 |
ald | 3087647 | c.828A>G | synonymous_variant | 0.13 |
ald | 3087649 | p.Gly277Asp | missense_variant | 0.13 |
ald | 3087653 | c.834A>C | synonymous_variant | 0.13 |
ald | 3087656 | c.837A>G | synonymous_variant | 0.14 |
ald | 3087659 | c.840G>C | synonymous_variant | 0.15 |
ald | 3087666 | p.Tyr283His | missense_variant | 0.15 |
ald | 3087671 | c.852C>T | synonymous_variant | 0.21 |
ald | 3087698 | c.879G>C | synonymous_variant | 0.15 |
ald | 3087704 | c.885T>C | synonymous_variant | 0.14 |
fbiD | 3339744 | c.627A>T | synonymous_variant | 0.18 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474237 | c.231C>A | synonymous_variant | 0.12 |
fprA | 3475032 | c.1026C>T | synonymous_variant | 0.15 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiB | 3641073 | c.-462T>G | upstream_gene_variant | 0.13 |
fbiB | 3641097 | c.-438T>C | upstream_gene_variant | 0.13 |
fbiB | 3641100 | c.-435T>A | upstream_gene_variant | 0.13 |
fbiB | 3641112 | c.-423T>C | upstream_gene_variant | 0.13 |
fbiA | 3641118 | p.Lys192Asn | missense_variant | 0.13 |
fbiA | 3641119 | p.Ser193Ala | missense_variant | 0.13 |
alr | 3840864 | p.Asp186Val | missense_variant | 0.14 |
rpoA | 3877494 | p.Glu338Asp | missense_variant | 0.14 |
rpoA | 3877503 | c.1005G>C | synonymous_variant | 0.15 |
rpoA | 3877515 | c.993G>C | synonymous_variant | 0.15 |
rpoA | 3877557 | c.951C>G | synonymous_variant | 0.14 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.19 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.25 |
rpoA | 3877638 | c.870T>C | synonymous_variant | 0.2 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.19 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.14 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.12 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.15 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.14 |
rpoA | 3878046 | c.462T>C | synonymous_variant | 0.17 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.16 |
rpoA | 3878067 | c.441C>G | synonymous_variant | 0.22 |
rpoA | 3878094 | c.414C>G | synonymous_variant | 0.15 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.15 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.16 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.22 |
rpoA | 3878130 | c.378C>G | synonymous_variant | 0.22 |
rpoA | 3878160 | c.348C>G | synonymous_variant | 0.27 |
rpoA | 3878163 | c.345C>T | synonymous_variant | 0.38 |
rpoA | 3878169 | c.339G>C | synonymous_variant | 0.19 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 0.18 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.18 |
rpoA | 3878331 | c.177A>G | synonymous_variant | 0.14 |
rpoA | 3878361 | c.147G>C | synonymous_variant | 0.15 |
rpoA | 3878364 | c.144A>C | synonymous_variant | 0.15 |
rpoA | 3878385 | c.123C>G | synonymous_variant | 0.18 |
rpoA | 3878409 | c.99C>G | synonymous_variant | 0.18 |
rpoA | 3878488 | p.Pro7His | missense_variant | 0.29 |
clpC1 | 4038368 | c.2337T>C | synonymous_variant | 0.14 |
clpC1 | 4038395 | c.2310C>T | synonymous_variant | 0.13 |
clpC1 | 4038398 | c.2307G>C | synonymous_variant | 0.13 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 0.13 |
clpC1 | 4038433 | c.2272C>T | synonymous_variant | 0.18 |
clpC1 | 4038444 | p.Ala754Lys | missense_variant | 0.15 |
clpC1 | 4038446 | c.2259T>C | synonymous_variant | 0.15 |
clpC1 | 4038456 | p.Val750Glu | missense_variant | 0.16 |
clpC1 | 4038494 | c.2211G>C | synonymous_variant | 0.23 |
clpC1 | 4038499 | p.Ser736Gly | missense_variant | 0.21 |
clpC1 | 4038530 | p.Glu725Asp | missense_variant | 0.17 |
clpC1 | 4038559 | p.Ile716Val | missense_variant | 0.15 |
clpC1 | 4038560 | p.Asp715Glu | missense_variant | 0.15 |
clpC1 | 4038755 | c.1950G>C | synonymous_variant | 0.18 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.29 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.31 |
clpC1 | 4038815 | c.1890G>A | synonymous_variant | 0.25 |
clpC1 | 4039345 | p.Glu454* | stop_gained | 0.13 |
clpC1 | 4039346 | c.1359G>C | synonymous_variant | 0.13 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 0.18 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.18 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.18 |
clpC1 | 4039481 | c.1224T>C | synonymous_variant | 0.2 |
clpC1 | 4039484 | c.1221T>C | synonymous_variant | 0.16 |
clpC1 | 4039574 | p.Ala377Ser | missense_variant | 0.16 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.18 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.18 |
clpC1 | 4039661 | c.1044T>C | synonymous_variant | 0.24 |
clpC1 | 4039664 | c.1041G>C | synonymous_variant | 0.22 |
clpC1 | 4039679 | c.1026C>T | synonymous_variant | 0.22 |
clpC1 | 4039682 | c.1023C>G | synonymous_variant | 0.33 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.25 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.14 |
clpC1 | 4039760 | c.945T>C | synonymous_variant | 0.15 |
clpC1 | 4039766 | c.939T>C | synonymous_variant | 0.15 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.15 |
clpC1 | 4039775 | c.930G>C | synonymous_variant | 0.15 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.13 |
clpC1 | 4039790 | c.915C>G | synonymous_variant | 0.14 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.18 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.17 |
clpC1 | 4039913 | c.792C>T | synonymous_variant | 0.15 |
clpC1 | 4039916 | c.789T>C | synonymous_variant | 0.15 |
clpC1 | 4039925 | c.780C>T | synonymous_variant | 0.14 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.15 |
clpC1 | 4039934 | c.771G>C | synonymous_variant | 0.15 |
clpC1 | 4039937 | c.768G>C | synonymous_variant | 0.13 |
clpC1 | 4040354 | c.351A>G | synonymous_variant | 0.13 |
clpC1 | 4040363 | c.342A>T | synonymous_variant | 0.14 |
clpC1 | 4040381 | c.324T>C | synonymous_variant | 0.14 |
clpC1 | 4040387 | c.318A>G | synonymous_variant | 0.2 |
clpC1 | 4040393 | c.312G>C | synonymous_variant | 0.18 |
clpC1 | 4040411 | c.294T>C | synonymous_variant | 0.15 |
clpC1 | 4040423 | c.282A>G | synonymous_variant | 0.16 |
clpC1 | 4040426 | c.279T>C | synonymous_variant | 0.16 |
clpC1 | 4040431 | c.274T>C | synonymous_variant | 0.16 |
clpC1 | 4040872 | c.-168C>G | upstream_gene_variant | 0.18 |
embC | 4240111 | c.249C>T | synonymous_variant | 0.19 |
embC | 4240120 | c.258C>G | synonymous_variant | 0.19 |
embC | 4240141 | c.279A>G | synonymous_variant | 0.16 |
embC | 4240154 | c.293_301delAGAACACCG | disruptive_inframe_deletion | 0.17 |
embC | 4240165 | c.305_307delAGA | disruptive_inframe_deletion | 0.16 |
embC | 4240178 | c.316T>C | synonymous_variant | 0.21 |
embC | 4240183 | c.321A>G | synonymous_variant | 0.22 |
embC | 4240201 | c.339G>C | synonymous_variant | 0.24 |
embC | 4240204 | c.342T>G | synonymous_variant | 0.24 |
embC | 4240211 | p.Val117Ile | missense_variant | 0.13 |
embC | 4240216 | c.354T>C | synonymous_variant | 0.13 |
embC | 4240228 | c.366G>C | synonymous_variant | 0.13 |
embC | 4240229 | p.Leu123Ile | missense_variant | 0.14 |
embC | 4240234 | c.372A>G | synonymous_variant | 0.17 |
embC | 4240237 | c.375G>C | synonymous_variant | 0.15 |
embC | 4240258 | c.396T>G | synonymous_variant | 0.12 |
embC | 4240828 | c.966G>C | synonymous_variant | 0.13 |
embC | 4240831 | c.969T>G | synonymous_variant | 0.13 |
embC | 4240879 | c.1017G>C | synonymous_variant | 0.2 |
embC | 4240885 | c.1023T>C | synonymous_variant | 0.2 |
embC | 4240897 | c.1035C>G | synonymous_variant | 0.31 |
embC | 4240898 | c.1036C>T | synonymous_variant | 0.31 |
embC | 4240911 | p.Ala350Val | missense_variant | 0.27 |
embC | 4240921 | c.1059C>G | synonymous_variant | 0.29 |
embC | 4240936 | c.1074A>G | synonymous_variant | 0.21 |
embC | 4240957 | c.1095C>G | synonymous_variant | 0.2 |
embC | 4240960 | c.1098G>C | synonymous_variant | 0.2 |
embC | 4240966 | c.1104G>T | synonymous_variant | 0.2 |
embC | 4240969 | c.1107C>T | synonymous_variant | 0.2 |
embC | 4240979 | p.Thr373Gln | missense_variant | 0.18 |
embC | 4240990 | c.1128A>C | synonymous_variant | 0.18 |
embC | 4241002 | c.1140G>C | synonymous_variant | 0.18 |
embC | 4241715 | p.Asn618Ile | missense_variant | 0.15 |
embC | 4241717 | p.Arg619Trp | missense_variant | 0.15 |
embC | 4242059 | p.Ala733Ser | missense_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243024 | c.-209T>C | upstream_gene_variant | 0.13 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4244708 | c.1476C>G | synonymous_variant | 0.3 |
embA | 4244726 | p.Asp498Glu | missense_variant | 0.3 |
embA | 4244728 | p.Phe499Trp | missense_variant | 0.33 |
embA | 4244747 | c.1515T>C | synonymous_variant | 0.43 |
embA | 4244756 | c.1524G>A | synonymous_variant | 0.5 |
embA | 4244764 | p.Val511Ala | missense_variant | 0.43 |
embA | 4244771 | c.1539G>T | synonymous_variant | 0.43 |
embA | 4244780 | c.1548C>G | synonymous_variant | 0.38 |
embA | 4244783 | c.1551C>G | synonymous_variant | 0.38 |
embA | 4244792 | c.1560G>C | synonymous_variant | 0.38 |
embA | 4244802 | p.Leu524Met | missense_variant | 0.33 |
embA | 4244808 | p.Phe526Leu | missense_variant | 0.33 |
embA | 4244823 | p.Val531Met | missense_variant | 0.33 |
embA | 4244829 | p.Phe533Val | missense_variant | 0.33 |
embA | 4244843 | c.1611G>C | synonymous_variant | 0.25 |
embA | 4244996 | c.1764C>A | synonymous_variant | 0.18 |
embB | 4246268 | c.-246G>A | upstream_gene_variant | 0.13 |
embB | 4246277 | c.-237G>C | upstream_gene_variant | 0.14 |
embB | 4246280 | c.-234G>C | upstream_gene_variant | 0.14 |
embB | 4246292 | c.-222A>G | upstream_gene_variant | 0.12 |
embA | 4246305 | p.Ser1025Ala | missense_variant | 0.12 |
embB | 4246316 | c.-198T>C | upstream_gene_variant | 0.13 |
embB | 4246922 | p.Arg137Ser | missense_variant | 0.15 |
embB | 4247269 | c.756C>A | synonymous_variant | 0.13 |
embB | 4248867 | p.Pro785Gln | missense_variant | 0.13 |
embB | 4249757 | p.Thr1082Ala | missense_variant | 0.5 |
aftB | 4267018 | p.Arg607Ser | missense_variant | 0.17 |
aftB | 4267271 | c.1566G>A | synonymous_variant | 0.14 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4269573 | c.-737A>G | upstream_gene_variant | 0.14 |
aftB | 4269594 | c.-758A>C | upstream_gene_variant | 0.21 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 0.19 |
aftB | 4269612 | c.-776T>C | upstream_gene_variant | 0.21 |
aftB | 4269621 | c.-785C>G | upstream_gene_variant | 0.21 |
ubiA | 4269627 | p.Val69Thr | missense_variant | 0.19 |
ubiA | 4269632 | p.Ala68Ser | missense_variant | 0.2 |
aftB | 4269639 | c.-803C>G | upstream_gene_variant | 0.2 |
ubiA | 4269647 | p.Ser63Cys | missense_variant | 0.23 |
aftB | 4269660 | c.-824C>T | upstream_gene_variant | 0.27 |
ubiA | 4269665 | p.Met57Val | missense_variant | 0.27 |
aftB | 4269666 | c.-830G>C | upstream_gene_variant | 0.3 |
whiB6 | 4338446 | p.Leu26Met | missense_variant | 0.29 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407745 | p.Ile153Thr | missense_variant | 0.17 |
gid | 4407774 | p.Asp143Glu | missense_variant | 0.18 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |