Run ID: ERR2514821
Sample name:
Date: 31-03-2023 20:35:07
Number of reads: 556988
Percentage reads mapped: 70.38
Strain: lineage2.2.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.97 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 0.95 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
embB | 4247448 | p.His312Arg | missense_variant | 0.18 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5997 | p.Tyr253Cys | missense_variant | 0.15 |
gyrA | 6334 | c.-968G>C | upstream_gene_variant | 0.23 |
gyrA | 6361 | c.-941G>A | upstream_gene_variant | 0.2 |
gyrA | 6362 | c.-940T>C | upstream_gene_variant | 0.2 |
gyrA | 6376 | c.-926G>A | upstream_gene_variant | 0.33 |
gyrA | 6379 | c.-923C>G | upstream_gene_variant | 0.31 |
gyrA | 6382 | c.-920A>G | upstream_gene_variant | 0.31 |
gyrA | 6403 | c.-899T>C | upstream_gene_variant | 0.45 |
gyrA | 6412 | c.-890G>A | upstream_gene_variant | 0.5 |
gyrA | 6415 | c.-887G>C | upstream_gene_variant | 0.5 |
gyrA | 6418 | c.-884C>G | upstream_gene_variant | 0.38 |
gyrA | 6427 | c.-875T>C | upstream_gene_variant | 0.38 |
gyrA | 6430 | c.-872A>G | upstream_gene_variant | 0.38 |
gyrA | 6811 | c.-491C>T | upstream_gene_variant | 0.36 |
gyrA | 6841 | c.-461T>C | upstream_gene_variant | 0.45 |
gyrA | 6853 | c.-449A>G | upstream_gene_variant | 0.45 |
gyrA | 6856 | c.-446T>C | upstream_gene_variant | 0.45 |
gyrA | 6859 | c.-443T>C | upstream_gene_variant | 0.45 |
gyrA | 6862 | c.-440C>G | upstream_gene_variant | 0.45 |
gyrA | 6866 | c.-436C>T | upstream_gene_variant | 0.45 |
gyrA | 6878 | c.-424T>C | upstream_gene_variant | 0.45 |
gyrA | 6881 | c.-421_-419delTTGinsCTA | upstream_gene_variant | 0.45 |
gyrA | 6892 | c.-410C>T | upstream_gene_variant | 0.56 |
gyrA | 6901 | c.-401G>C | upstream_gene_variant | 0.56 |
gyrA | 6904 | c.-398C>G | upstream_gene_variant | 0.5 |
gyrB | 6911 | p.Asn558His | missense_variant | 0.44 |
gyrA | 6919 | c.-383T>C | upstream_gene_variant | 0.44 |
gyrA | 6931 | c.-371A>G | upstream_gene_variant | 0.36 |
gyrA | 6934 | c.-368A>G | upstream_gene_variant | 0.27 |
gyrA | 7334 | c.33G>C | synonymous_variant | 0.17 |
gyrA | 7335 | p.Leu12Val | missense_variant | 0.17 |
gyrA | 7347 | p.Glu16Gln | missense_variant | 0.17 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7391 | c.90C>T | synonymous_variant | 0.2 |
gyrA | 7394 | c.93T>C | synonymous_variant | 0.2 |
gyrA | 7427 | c.126G>C | synonymous_variant | 0.21 |
gyrA | 7442 | c.141G>T | synonymous_variant | 0.38 |
gyrA | 7451 | c.150C>G | synonymous_variant | 0.26 |
gyrA | 7457 | c.156T>C | synonymous_variant | 0.25 |
gyrA | 7475 | c.174A>G | synonymous_variant | 0.3 |
gyrA | 7480 | p.Phe60Tyr | missense_variant | 0.32 |
gyrA | 7484 | c.183T>C | synonymous_variant | 0.32 |
gyrA | 7490 | c.189C>G | synonymous_variant | 0.32 |
gyrA | 7523 | c.222C>G | synonymous_variant | 0.18 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7763 | c.462T>C | synonymous_variant | 0.19 |
gyrA | 7784 | c.483A>G | synonymous_variant | 0.22 |
gyrA | 7787 | c.486G>A | synonymous_variant | 0.24 |
gyrA | 7790 | c.489G>C | synonymous_variant | 0.25 |
gyrA | 7793 | c.492G>C | synonymous_variant | 0.25 |
gyrA | 7796 | c.495G>C | synonymous_variant | 0.25 |
gyrA | 7797 | c.496_498delCTAinsTTG | synonymous_variant | 0.24 |
gyrA | 7829 | c.528C>T | synonymous_variant | 0.22 |
gyrA | 7835 | c.534A>C | synonymous_variant | 0.22 |
gyrA | 7838 | c.537C>T | synonymous_variant | 0.22 |
gyrA | 7847 | c.546G>C | synonymous_variant | 0.23 |
gyrA | 7853 | c.552C>A | synonymous_variant | 0.2 |
gyrA | 7859 | c.558A>G | synonymous_variant | 0.17 |
gyrA | 8111 | c.810G>C | synonymous_variant | 0.27 |
gyrA | 8121 | c.820T>C | synonymous_variant | 0.23 |
gyrA | 8129 | c.828T>C | synonymous_variant | 0.28 |
gyrA | 8135 | c.834C>G | synonymous_variant | 0.29 |
gyrA | 8156 | c.855T>C | synonymous_variant | 0.39 |
gyrA | 8168 | c.867A>G | synonymous_variant | 0.29 |
gyrA | 8177 | c.876A>C | synonymous_variant | 0.25 |
gyrA | 8189 | c.888G>C | synonymous_variant | 0.27 |
gyrA | 8198 | c.897T>C | synonymous_variant | 0.27 |
gyrA | 8207 | c.906T>C | synonymous_variant | 0.28 |
gyrA | 8219 | c.918T>C | synonymous_variant | 0.18 |
gyrA | 8225 | c.924T>C | synonymous_variant | 0.21 |
gyrA | 8453 | c.1152A>C | synonymous_variant | 0.31 |
gyrA | 8459 | c.1158G>A | synonymous_variant | 0.31 |
gyrA | 8462 | c.1161A>C | synonymous_variant | 0.33 |
gyrA | 8465 | c.1164C>G | synonymous_variant | 0.33 |
gyrA | 8471 | c.1170T>C | synonymous_variant | 0.33 |
gyrA | 8472 | c.1171C>T | synonymous_variant | 0.33 |
gyrA | 8480 | c.1179C>T | synonymous_variant | 0.47 |
gyrA | 8486 | c.1185T>C | synonymous_variant | 0.47 |
gyrA | 8516 | c.1215T>C | synonymous_variant | 0.58 |
gyrA | 8519 | c.1218A>G | synonymous_variant | 0.47 |
gyrA | 8528 | c.1227G>C | synonymous_variant | 0.21 |
gyrA | 8543 | c.1242C>G | synonymous_variant | 0.24 |
gyrA | 8546 | c.1245T>C | synonymous_variant | 0.22 |
gyrA | 8552 | c.1251C>G | synonymous_variant | 0.22 |
gyrA | 8555 | c.1254G>T | synonymous_variant | 0.22 |
gyrA | 8561 | c.1260A>C | synonymous_variant | 0.22 |
gyrA | 8570 | p.Glu423Asp | missense_variant | 0.25 |
gyrA | 8576 | c.1275C>G | synonymous_variant | 0.25 |
gyrA | 8579 | c.1278C>T | synonymous_variant | 0.25 |
gyrA | 8588 | c.1287G>A | synonymous_variant | 0.25 |
gyrA | 8818 | p.Ser506Asn | missense_variant | 0.13 |
gyrA | 8852 | c.1551T>C | synonymous_variant | 0.19 |
gyrA | 8858 | c.1557T>C | synonymous_variant | 0.19 |
gyrA | 8867 | c.1566A>G | synonymous_variant | 0.19 |
gyrA | 8870 | c.1569G>C | synonymous_variant | 0.23 |
gyrA | 8873 | c.1572A>C | synonymous_variant | 0.22 |
gyrA | 8882 | c.1581G>A | synonymous_variant | 0.22 |
gyrA | 8897 | c.1596T>C | synonymous_variant | 0.19 |
gyrA | 8933 | c.1632G>C | synonymous_variant | 0.2 |
gyrA | 8939 | c.1638T>C | synonymous_variant | 0.2 |
gyrA | 8946 | c.1645T>C | synonymous_variant | 0.19 |
gyrA | 9080 | c.1779G>T | synonymous_variant | 0.14 |
gyrA | 9089 | c.1788G>C | synonymous_variant | 0.17 |
gyrA | 9104 | c.1803C>T | synonymous_variant | 0.23 |
gyrA | 9119 | c.1818A>G | synonymous_variant | 0.22 |
gyrA | 9153 | p.Thr618Ala | missense_variant | 0.18 |
gyrA | 9230 | c.1929T>C | synonymous_variant | 0.14 |
gyrA | 9233 | c.1932C>G | synonymous_variant | 0.15 |
gyrA | 9284 | c.1983T>C | synonymous_variant | 0.33 |
gyrA | 9296 | c.1995T>C | synonymous_variant | 0.27 |
gyrA | 9299 | c.1998G>C | synonymous_variant | 0.27 |
gyrA | 9300 | p.Ala667Ser | missense_variant | 0.27 |
gyrA | 9304 | p.Gly668Glu | missense_variant | 1.0 |
gyrA | 9308 | p.Asp669Glu | missense_variant | 0.29 |
gyrA | 9323 | c.2022C>G | synonymous_variant | 0.26 |
gyrA | 9329 | c.2028C>G | synonymous_variant | 0.26 |
gyrA | 9335 | c.2034G>C | synonymous_variant | 0.26 |
gyrA | 9365 | c.2064G>A | synonymous_variant | 0.29 |
gyrA | 9374 | c.2073G>C | synonymous_variant | 0.25 |
gyrA | 9377 | c.2076A>G | synonymous_variant | 0.24 |
gyrA | 9383 | c.2082T>A | synonymous_variant | 0.23 |
gyrA | 9386 | c.2085T>C | synonymous_variant | 0.23 |
gyrA | 9395 | c.2094G>C | synonymous_variant | 0.17 |
gyrA | 9398 | c.2097T>C | synonymous_variant | 0.17 |
gyrA | 9413 | c.2112G>C | synonymous_variant | 0.19 |
fgd1 | 490751 | c.-32T>G | upstream_gene_variant | 0.23 |
fgd1 | 491620 | p.Ile280Val | missense_variant | 0.19 |
fgd1 | 491643 | c.861G>C | synonymous_variant | 0.2 |
fgd1 | 491649 | c.867C>T | synonymous_variant | 0.2 |
fgd1 | 491658 | c.876A>G | synonymous_variant | 0.2 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575629 | c.282A>G | synonymous_variant | 0.16 |
mshA | 575641 | c.294A>G | synonymous_variant | 0.2 |
mshA | 575649 | p.Val101Ala | missense_variant | 0.2 |
mshA | 575659 | c.312A>G | synonymous_variant | 0.23 |
mshA | 575674 | c.327G>C | synonymous_variant | 0.21 |
mshA | 575713 | c.366G>A | synonymous_variant | 0.23 |
mshA | 575878 | c.531A>G | synonymous_variant | 0.21 |
mshA | 575907 | p.Ala187Val | missense_variant | 0.93 |
mshA | 575965 | c.618C>G | synonymous_variant | 0.14 |
mshA | 575980 | c.633T>C | synonymous_variant | 0.17 |
mshA | 575983 | c.636G>C | synonymous_variant | 0.17 |
ccsA | 620362 | p.Ala158Thr | missense_variant | 0.15 |
ccsA | 620412 | c.522T>C | synonymous_variant | 0.15 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
ccsA | 620718 | c.828G>C | synonymous_variant | 0.16 |
ccsA | 620733 | c.843G>C | synonymous_variant | 0.18 |
ccsA | 620734 | c.844C>A | synonymous_variant | 0.18 |
ccsA | 620739 | c.849A>G | synonymous_variant | 0.18 |
ccsA | 620742 | c.852G>C | synonymous_variant | 0.18 |
ccsA | 620745 | c.855G>C | synonymous_variant | 0.19 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.2 |
ccsA | 620778 | c.888T>C | synonymous_variant | 0.23 |
ccsA | 620784 | c.894C>G | synonymous_variant | 0.23 |
ccsA | 620787 | c.897C>G | synonymous_variant | 0.23 |
ccsA | 620796 | c.906C>G | synonymous_variant | 0.2 |
rpoB | 759620 | c.-187A>C | upstream_gene_variant | 0.36 |
rpoB | 760091 | c.285G>C | synonymous_variant | 0.35 |
rpoB | 760101 | c.295T>C | synonymous_variant | 0.35 |
rpoB | 760112 | c.306T>C | synonymous_variant | 0.42 |
rpoB | 760118 | c.312T>G | synonymous_variant | 0.42 |
rpoB | 760121 | c.315T>C | synonymous_variant | 0.42 |
rpoB | 760130 | p.Asp108Glu | missense_variant | 0.47 |
rpoB | 760139 | c.333A>C | synonymous_variant | 0.45 |
rpoB | 760142 | c.336C>G | synonymous_variant | 0.45 |
rpoB | 760181 | c.375T>C | synonymous_variant | 0.55 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.52 |
rpoB | 760196 | c.390C>G | synonymous_variant | 0.5 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.46 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.52 |
rpoB | 760283 | c.477G>C | synonymous_variant | 0.53 |
rpoB | 760298 | c.492G>C | synonymous_variant | 0.47 |
rpoB | 760307 | c.501T>C | synonymous_variant | 0.35 |
rpoB | 760310 | c.504G>C | synonymous_variant | 0.31 |
rpoB | 760328 | c.522G>C | synonymous_variant | 0.47 |
rpoB | 760331 | c.525G>C | synonymous_variant | 0.42 |
rpoB | 760340 | c.534G>T | synonymous_variant | 0.4 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.36 |
rpoB | 760370 | c.564C>G | synonymous_variant | 0.33 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.35 |
rpoB | 760380 | p.Thr192Leu | missense_variant | 0.33 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.19 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.18 |
rpoB | 760519 | p.Thr238Ser | missense_variant | 0.2 |
rpoB | 760522 | p.Ser239Asn | missense_variant | 0.21 |
rpoB | 760532 | c.726T>C | synonymous_variant | 0.2 |
rpoB | 760533 | p.Val243Thr | missense_variant | 0.19 |
rpoB | 760541 | c.735G>C | synonymous_variant | 0.2 |
rpoB | 760547 | c.741G>C | synonymous_variant | 0.2 |
rpoB | 760563 | p.Arg253Met | missense_variant | 0.22 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.17 |
rpoB | 760611 | c.805T>C | synonymous_variant | 0.35 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.38 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.47 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.33 |
rpoB | 760670 | c.864G>C | synonymous_variant | 0.31 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.31 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.29 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.36 |
rpoB | 760718 | c.912C>T | synonymous_variant | 0.36 |
rpoB | 760724 | c.918T>C | synonymous_variant | 0.4 |
rpoB | 760730 | c.924T>C | synonymous_variant | 0.36 |
rpoB | 760751 | c.945G>C | synonymous_variant | 0.27 |
rpoB | 760757 | c.951T>C | synonymous_variant | 0.27 |
rpoB | 760759 | p.Val318Ala | missense_variant | 0.3 |
rpoB | 760769 | c.963C>G | synonymous_variant | 0.3 |
rpoB | 760775 | c.969G>C | synonymous_variant | 0.3 |
rpoB | 760776 | c.970_972delTCGinsAGC | synonymous_variant | 0.3 |
rpoB | 760793 | c.987A>G | synonymous_variant | 0.27 |
rpoB | 760805 | c.999G>C | synonymous_variant | 0.3 |
rpoB | 760808 | c.1002C>G | synonymous_variant | 0.3 |
rpoB | 760820 | c.1014T>C | synonymous_variant | 0.4 |
rpoB | 760826 | c.1020C>G | synonymous_variant | 0.44 |
rpoB | 760830 | c.1024T>C | synonymous_variant | 0.44 |
rpoB | 760845 | p.Thr347Pro | missense_variant | 0.33 |
rpoB | 760859 | c.1053T>C | synonymous_variant | 0.27 |
rpoB | 760862 | c.1056G>C | synonymous_variant | 0.27 |
rpoB | 760869 | p.Val355Ile | missense_variant | 0.29 |
rpoB | 760886 | c.1080A>G | synonymous_variant | 0.25 |
rpoB | 760910 | c.1104C>T | synonymous_variant | 0.2 |
rpoB | 760934 | c.1128C>T | synonymous_variant | 0.2 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.29 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.29 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.29 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.27 |
rpoB | 761006 | c.1200C>G | synonymous_variant | 0.2 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.27 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 0.29 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.29 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.29 |
rpoB | 761042 | c.1236C>T | synonymous_variant | 0.29 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.31 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.25 |
rpoB | 761129 | c.1323G>C | synonymous_variant | 0.22 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.23 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.19 |
rpoB | 761153 | c.1347G>C | synonymous_variant | 0.19 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.21 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.27 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.29 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.29 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.32 |
rpoB | 761306 | c.1500C>G | synonymous_variant | 0.3 |
rpoB | 761318 | c.1512G>C | synonymous_variant | 0.26 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.2 |
rpoB | 761330 | c.1524G>C | synonymous_variant | 0.17 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.17 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.18 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.17 |
rpoB | 761675 | c.1869G>C | synonymous_variant | 0.19 |
rpoB | 761708 | c.1902C>T | synonymous_variant | 0.19 |
rpoB | 761732 | c.1926C>G | synonymous_variant | 0.16 |
rpoB | 761735 | c.1929C>G | synonymous_variant | 0.16 |
rpoB | 761747 | c.1941G>C | synonymous_variant | 0.2 |
rpoB | 761750 | c.1944G>C | synonymous_variant | 0.2 |
rpoB | 761765 | c.1959T>C | synonymous_variant | 0.2 |
rpoB | 761772 | p.His656Ala | missense_variant | 0.19 |
rpoB | 761778 | p.Asn658Asp | missense_variant | 0.19 |
rpoB | 761815 | p.Ala670Asp | missense_variant | 0.15 |
rpoB | 761834 | c.2028T>C | synonymous_variant | 0.19 |
rpoB | 761867 | c.2061C>T | synonymous_variant | 0.22 |
rpoB | 761873 | c.2067A>C | synonymous_variant | 0.19 |
rpoB | 761885 | c.2079T>C | synonymous_variant | 0.2 |
rpoB | 761909 | c.2103T>C | synonymous_variant | 0.21 |
rpoB | 761912 | c.2106T>C | synonymous_variant | 0.22 |
rpoB | 761915 | p.Asp703Glu | missense_variant | 0.23 |
rpoB | 761916 | p.Asp704Asn | missense_variant | 0.23 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.25 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.25 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.44 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 1.0 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.41 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.47 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.47 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.42 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.45 |
rpoC | 763145 | c.-225G>A | upstream_gene_variant | 0.43 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.45 |
rpoC | 763158 | c.-212C>T | upstream_gene_variant | 0.42 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.44 |
rpoC | 763193 | c.-177C>G | upstream_gene_variant | 0.27 |
rpoC | 763202 | c.-168A>C | upstream_gene_variant | 0.25 |
rpoC | 763205 | c.-165G>C | upstream_gene_variant | 0.25 |
rpoC | 763206 | c.-164_-162delAGTinsTCG | upstream_gene_variant | 0.25 |
rpoC | 763214 | c.-156T>C | upstream_gene_variant | 0.25 |
rpoC | 763226 | c.-144A>G | upstream_gene_variant | 0.3 |
rpoC | 763227 | c.-143C>T | upstream_gene_variant | 0.3 |
rpoC | 763238 | c.-132T>C | upstream_gene_variant | 0.27 |
rpoC | 763253 | c.-117G>C | upstream_gene_variant | 0.27 |
rpoC | 763256 | c.-114G>A | upstream_gene_variant | 0.27 |
rpoC | 763351 | c.-19T>C | upstream_gene_variant | 0.5 |
rpoC | 763352 | c.-18T>A | upstream_gene_variant | 0.5 |
rpoC | 763402 | c.33C>A | synonymous_variant | 0.44 |
rpoC | 763411 | c.42T>G | synonymous_variant | 0.44 |
rpoC | 763414 | c.45T>C | synonymous_variant | 0.4 |
rpoC | 763441 | c.72C>T | synonymous_variant | 0.4 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.4 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.44 |
rpoC | 763486 | c.117T>G | synonymous_variant | 0.25 |
rpoC | 763492 | c.123G>C | synonymous_variant | 0.24 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.22 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.29 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.31 |
rpoC | 763576 | c.207C>G | synonymous_variant | 0.31 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.25 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.19 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.2 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.16 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.17 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.17 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.17 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.19 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.19 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.18 |
rpoC | 763774 | c.405G>C | synonymous_variant | 0.18 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.15 |
rpoC | 763872 | p.Gly168Ala | missense_variant | 0.23 |
rpoC | 763876 | p.Glu169Asp | missense_variant | 0.21 |
rpoC | 763879 | c.510A>G | synonymous_variant | 0.2 |
rpoC | 763888 | c.519G>C | synonymous_variant | 0.18 |
rpoC | 763891 | c.522G>C | synonymous_variant | 0.19 |
rpoC | 763936 | c.567C>G | synonymous_variant | 0.17 |
rpoC | 763939 | c.570G>A | synonymous_variant | 0.18 |
rpoC | 763942 | c.573C>G | synonymous_variant | 0.18 |
rpoC | 763945 | c.576T>C | synonymous_variant | 0.18 |
rpoC | 763948 | c.579G>A | synonymous_variant | 0.19 |
rpoC | 763954 | c.585C>G | synonymous_variant | 0.19 |
rpoC | 763963 | c.594C>G | synonymous_variant | 0.19 |
rpoC | 763969 | c.600C>T | synonymous_variant | 0.19 |
rpoC | 763978 | c.609C>T | synonymous_variant | 0.15 |
rpoC | 763996 | c.627T>C | synonymous_variant | 0.15 |
rpoC | 764026 | p.Leu219Phe | missense_variant | 0.17 |
rpoC | 764040 | p.Ser224Thr | missense_variant | 0.17 |
rpoC | 764044 | c.675T>C | synonymous_variant | 0.22 |
rpoC | 764059 | c.690G>C | synonymous_variant | 0.21 |
rpoC | 764098 | c.729A>G | synonymous_variant | 0.17 |
rpoC | 764188 | c.819A>G | synonymous_variant | 0.21 |
rpoC | 764206 | c.837T>C | synonymous_variant | 0.19 |
rpoC | 764215 | c.846A>G | synonymous_variant | 0.3 |
rpoC | 764236 | c.867G>A | synonymous_variant | 0.3 |
rpoC | 764237 | p.Leu290Ile | missense_variant | 0.3 |
rpoC | 764257 | c.888G>C | synonymous_variant | 0.22 |
rpoC | 764266 | c.897T>C | synonymous_variant | 0.29 |
rpoC | 764269 | c.900G>C | synonymous_variant | 0.29 |
rpoC | 764272 | c.903G>C | synonymous_variant | 0.29 |
rpoC | 764278 | c.909A>G | synonymous_variant | 0.3 |
rpoC | 764293 | c.924G>C | synonymous_variant | 0.3 |
rpoC | 764317 | c.948C>G | synonymous_variant | 0.31 |
rpoC | 764329 | c.960C>T | synonymous_variant | 0.27 |
rpoC | 764338 | c.969G>A | synonymous_variant | 0.27 |
rpoC | 764353 | c.984G>T | synonymous_variant | 0.31 |
rpoC | 764419 | c.1050C>G | synonymous_variant | 0.21 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.21 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.18 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.18 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.17 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.17 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.17 |
rpoC | 764489 | c.1120C>T | synonymous_variant | 0.17 |
rpoC | 764554 | c.1185C>T | synonymous_variant | 0.14 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.18 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.35 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.35 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.3 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 0.32 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.24 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.23 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.24 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.24 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.23 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.19 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.18 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.18 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.17 |
rpoC | 765383 | p.Met672Leu | missense_variant | 0.26 |
rpoC | 765404 | p.Leu679Val | missense_variant | 0.32 |
rpoC | 765409 | c.2040T>C | synonymous_variant | 0.27 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.23 |
rpoC | 765454 | c.2085C>G | synonymous_variant | 0.25 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.21 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.29 |
rpoC | 765508 | c.2139C>G | synonymous_variant | 0.29 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.32 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.25 |
rpoC | 765559 | c.2190G>C | synonymous_variant | 0.27 |
rpoC | 765580 | c.2211G>C | synonymous_variant | 0.17 |
rpoC | 765613 | p.His748Gln | missense_variant | 0.15 |
rpoC | 765625 | c.2256C>G | synonymous_variant | 0.18 |
rpoC | 765628 | c.2259G>C | synonymous_variant | 0.18 |
rpoC | 765631 | p.Asp754Glu | missense_variant | 0.31 |
rpoC | 765658 | c.2289C>T | synonymous_variant | 0.4 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.33 |
rpoC | 765734 | c.2365T>C | synonymous_variant | 0.29 |
rpoC | 765739 | c.2370G>T | synonymous_variant | 0.21 |
rpoC | 765751 | c.2382C>G | synonymous_variant | 0.21 |
rpoC | 765753 | p.Asp795Ala | missense_variant | 0.19 |
rpoC | 765883 | c.2514C>G | synonymous_variant | 0.37 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.37 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.3 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.48 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.56 |
rpoC | 765982 | c.2613C>G | synonymous_variant | 0.4 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.45 |
rpoC | 766010 | c.2641_2642delTCinsAG | synonymous_variant | 0.46 |
rpoC | 766021 | c.2652G>C | synonymous_variant | 0.35 |
rpoC | 766027 | c.2658G>C | synonymous_variant | 0.35 |
rpoC | 766043 | p.Gln892Glu | missense_variant | 0.38 |
rpoC | 766061 | p.Val898Ile | missense_variant | 0.29 |
rpoC | 766081 | c.2712T>C | synonymous_variant | 0.21 |
rpoC | 766082 | p.Ala905Gln | missense_variant | 0.21 |
rpoC | 766096 | c.2727G>C | synonymous_variant | 0.18 |
rpoC | 766288 | c.2919C>G | synonymous_variant | 0.2 |
rpoC | 766303 | c.2934C>T | synonymous_variant | 0.17 |
rpoC | 766312 | c.2943T>G | synonymous_variant | 0.25 |
rpoC | 766327 | c.2958C>A | synonymous_variant | 0.26 |
rpoC | 766345 | c.2976T>C | synonymous_variant | 0.35 |
rpoC | 766348 | c.2979A>G | synonymous_variant | 0.35 |
rpoC | 766357 | c.2988C>T | synonymous_variant | 0.38 |
rpoC | 766363 | c.2994G>C | synonymous_variant | 0.39 |
rpoC | 766366 | c.2997C>G | synonymous_variant | 0.39 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.42 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.44 |
rpoC | 766408 | c.3039C>G | synonymous_variant | 0.5 |
rpoC | 766411 | c.3042C>G | synonymous_variant | 0.5 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.45 |
rpoC | 766447 | c.3078T>C | synonymous_variant | 0.62 |
rpoC | 766483 | c.3114G>C | synonymous_variant | 0.67 |
rpoC | 766484 | p.Val1039Ile | missense_variant | 0.67 |
rpoC | 766492 | c.3123T>C | synonymous_variant | 0.67 |
rpoC | 766495 | c.3126C>T | synonymous_variant | 0.56 |
rpoC | 766522 | c.3153C>G | synonymous_variant | 0.57 |
rpoC | 766528 | c.3159T>C | synonymous_variant | 0.53 |
rpoC | 766531 | c.3162G>C | synonymous_variant | 0.53 |
rpoC | 766540 | p.Asp1057Glu | missense_variant | 0.42 |
rpoC | 766543 | c.3174C>T | synonymous_variant | 0.42 |
rpoC | 766549 | c.3180G>C | synonymous_variant | 0.36 |
rpoC | 766573 | c.3204T>C | synonymous_variant | 0.27 |
rpoC | 766582 | c.3213C>G | synonymous_variant | 0.23 |
rpoC | 766583 | p.Gly1072Ser | missense_variant | 0.23 |
rpoC | 766591 | c.3222A>G | synonymous_variant | 0.23 |
rpoC | 766594 | c.3225G>C | synonymous_variant | 0.27 |
rpoC | 766597 | c.3228C>G | synonymous_variant | 0.36 |
rpoC | 766607 | p.Ile1080Leu | missense_variant | 0.36 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 0.87 |
rpoC | 766657 | c.3288A>G | synonymous_variant | 0.25 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.17 |
rpoC | 766801 | c.3432C>G | synonymous_variant | 0.17 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.17 |
rpoC | 766843 | c.3474T>C | synonymous_variant | 0.26 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 0.17 |
rpoC | 766864 | c.3495G>C | synonymous_variant | 0.17 |
rpoC | 766894 | c.3525T>C | synonymous_variant | 0.2 |
rpoC | 766895 | c.3526T>C | synonymous_variant | 0.2 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.2 |
rpoC | 766933 | c.3564A>G | synonymous_variant | 0.2 |
rpoC | 766945 | c.3576A>G | synonymous_variant | 0.17 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.19 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.18 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.18 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.19 |
rpoC | 767134 | c.3765C>A | synonymous_variant | 0.22 |
rpoC | 767158 | c.3789T>C | synonymous_variant | 0.29 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.29 |
rpoC | 767206 | c.3837C>G | synonymous_variant | 0.17 |
rpoC | 767209 | c.3840T>C | synonymous_variant | 0.17 |
rpoC | 767212 | c.3843G>C | synonymous_variant | 0.17 |
rpoC | 767221 | c.3852C>G | synonymous_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775939 | p.Ala848Ser | missense_variant | 0.18 |
mmpL5 | 775940 | c.2541C>G | synonymous_variant | 0.18 |
mmpL5 | 775946 | c.2535C>G | synonymous_variant | 0.18 |
mmpL5 | 775957 | p.Ile842Val | missense_variant | 0.19 |
mmpL5 | 775964 | p.Ala839Ser | missense_variant | 0.2 |
mmpL5 | 775972 | p.Ala837Pro | missense_variant | 0.19 |
mmpL5 | 775975 | c.2506T>C | synonymous_variant | 0.18 |
mmpL5 | 775994 | c.2487C>T | synonymous_variant | 0.25 |
mmpL5 | 776042 | c.2439C>A | synonymous_variant | 0.17 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 776308 | p.Asp725Asn | missense_variant | 0.14 |
mmpL5 | 776693 | p.Val596Ile | missense_variant | 0.22 |
mmpL5 | 776705 | c.1776C>T | synonymous_variant | 0.18 |
mmpL5 | 776963 | c.1518C>T | synonymous_variant | 0.14 |
mmpL5 | 778321 | p.Glu54* | stop_gained | 0.15 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.18 |
rpsL | 781658 | c.99A>G | synonymous_variant | 0.25 |
rpsL | 781700 | c.141G>C | synonymous_variant | 0.3 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.29 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.27 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.31 |
rpsL | 781742 | c.183C>T | synonymous_variant | 0.31 |
rpsL | 781748 | c.189C>G | synonymous_variant | 0.31 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.33 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.31 |
rpsL | 781769 | c.210G>A | synonymous_variant | 0.33 |
rpsL | 781772 | c.213C>G | synonymous_variant | 0.33 |
rpsL | 781808 | c.249C>T | synonymous_variant | 0.29 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.29 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.29 |
rpsL | 781838 | c.279G>C | synonymous_variant | 0.29 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.23 |
rpsL | 781865 | c.306G>C | synonymous_variant | 0.17 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.17 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.17 |
rpsL | 781877 | c.318T>C | synonymous_variant | 0.17 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.17 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.17 |
rplC | 801207 | c.399C>T | synonymous_variant | 0.15 |
rplC | 801246 | c.438C>T | synonymous_variant | 0.21 |
fbiC | 1303200 | c.270G>C | synonymous_variant | 0.17 |
fbiC | 1303217 | p.Arg96His | missense_variant | 0.21 |
fbiC | 1303219 | c.289_291delTTAinsCTG | synonymous_variant | 0.19 |
fbiC | 1303227 | c.297G>C | synonymous_variant | 0.2 |
fbiC | 1303233 | c.303T>C | synonymous_variant | 0.2 |
fbiC | 1303239 | c.309C>T | synonymous_variant | 0.18 |
fbiC | 1303501 | c.571C>T | synonymous_variant | 0.18 |
fbiC | 1303509 | c.579G>C | synonymous_variant | 0.21 |
fbiC | 1303530 | c.600G>A | synonymous_variant | 0.21 |
fbiC | 1303534 | p.Ser202Ala | missense_variant | 0.21 |
fbiC | 1303545 | c.615A>G | synonymous_variant | 0.24 |
fbiC | 1303575 | c.645G>C | synonymous_variant | 0.24 |
fbiC | 1303590 | c.660A>G | synonymous_variant | 0.22 |
fbiC | 1303605 | c.675C>G | synonymous_variant | 0.17 |
fbiC | 1303608 | c.678G>A | synonymous_variant | 0.17 |
fbiC | 1303614 | c.684C>T | synonymous_variant | 0.24 |
fbiC | 1303617 | c.687C>G | synonymous_variant | 0.24 |
fbiC | 1303632 | c.702T>G | synonymous_variant | 0.22 |
fbiC | 1303681 | c.751T>C | synonymous_variant | 0.2 |
fbiC | 1303686 | c.756C>G | synonymous_variant | 0.27 |
fbiC | 1303695 | c.765T>C | synonymous_variant | 0.24 |
fbiC | 1303704 | c.774T>G | synonymous_variant | 0.25 |
fbiC | 1303708 | c.778T>C | synonymous_variant | 0.24 |
fbiC | 1303728 | c.798G>A | synonymous_variant | 0.25 |
fbiC | 1303731 | c.801A>G | synonymous_variant | 0.18 |
fbiC | 1303732 | p.Ser268Glu | missense_variant | 0.18 |
fbiC | 1303737 | c.807G>A | synonymous_variant | 0.21 |
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 | 0.28 |
fbiC | 1303755 | c.825T>C | synonymous_variant | 0.21 |
fbiC | 1303785 | c.855G>T | synonymous_variant | 0.32 |
fbiC | 1303789 | p.Ile287Val | missense_variant | 0.3 |
fbiC | 1303812 | c.882C>T | synonymous_variant | 0.23 |
fbiC | 1303818 | c.888C>G | synonymous_variant | 0.29 |
fbiC | 1303836 | c.906G>C | synonymous_variant | 0.22 |
fbiC | 1303845 | c.915C>G | synonymous_variant | 0.22 |
fbiC | 1303846 | p.Phe306Val | missense_variant | 0.22 |
fbiC | 1303854 | c.924T>C | synonymous_variant | 0.24 |
fbiC | 1303860 | c.930A>C | synonymous_variant | 0.29 |
fbiC | 1303884 | c.954T>G | synonymous_variant | 0.29 |
fbiC | 1303905 | c.975G>C | synonymous_variant | 0.24 |
fbiC | 1303911 | c.981G>C | synonymous_variant | 0.24 |
fbiC | 1303920 | c.990C>T | synonymous_variant | 0.26 |
fbiC | 1303948 | p.Gly340Arg | missense_variant | 0.17 |
fbiC | 1303953 | p.Asp341Glu | missense_variant | 0.19 |
fbiC | 1303956 | c.1026A>G | synonymous_variant | 0.18 |
fbiC | 1303961 | p.Arg344Leu | missense_variant | 0.18 |
fbiC | 1303971 | c.1041T>C | synonymous_variant | 0.22 |
fbiC | 1303980 | c.1050G>A | synonymous_variant | 0.25 |
fbiC | 1304004 | c.1074A>G | synonymous_variant | 0.27 |
fbiC | 1304008 | c.1078T>C | synonymous_variant | 0.26 |
fbiC | 1304022 | c.1092T>C | synonymous_variant | 0.24 |
fbiC | 1304031 | c.1101C>G | synonymous_variant | 0.23 |
fbiC | 1304034 | c.1104A>G | synonymous_variant | 0.23 |
fbiC | 1304040 | c.1110C>G | synonymous_variant | 0.24 |
fbiC | 1304046 | c.1116C>G | synonymous_variant | 0.26 |
fbiC | 1304049 | c.1119T>C | synonymous_variant | 0.25 |
fbiC | 1304050 | c.1120T>C | synonymous_variant | 0.25 |
fbiC | 1304058 | c.1128G>A | synonymous_variant | 0.24 |
fbiC | 1304059 | c.1129C>T | synonymous_variant | 0.24 |
fbiC | 1304064 | c.1134G>C | synonymous_variant | 0.22 |
fbiC | 1304067 | c.1137G>C | synonymous_variant | 0.21 |
fbiC | 1304104 | c.1174C>T | synonymous_variant | 0.16 |
fbiC | 1304499 | c.1569T>C | synonymous_variant | 0.18 |
fbiC | 1304526 | c.1596T>G | synonymous_variant | 0.3 |
fbiC | 1304535 | c.1605G>A | synonymous_variant | 0.33 |
fbiC | 1304541 | c.1611C>T | synonymous_variant | 0.33 |
fbiC | 1304544 | c.1614T>C | synonymous_variant | 0.3 |
fbiC | 1304545 | p.Val539Thr | missense_variant | 0.3 |
fbiC | 1304553 | c.1623C>T | synonymous_variant | 0.25 |
fbiC | 1304559 | p.Glu543Asp | missense_variant | 0.25 |
fbiC | 1304565 | c.1635C>G | synonymous_variant | 0.27 |
fbiC | 1304568 | c.1638T>C | synonymous_variant | 0.25 |
fbiC | 1304571 | c.1641G>C | synonymous_variant | 0.25 |
fbiC | 1304580 | c.1650T>C | synonymous_variant | 0.25 |
fbiC | 1304613 | c.1683T>G | synonymous_variant | 0.27 |
fbiC | 1304625 | c.1695C>T | synonymous_variant | 0.25 |
fbiC | 1304634 | c.1704C>G | synonymous_variant | 0.18 |
fbiC | 1304703 | c.1773C>G | synonymous_variant | 0.23 |
fbiC | 1304711 | p.Ala594Glu | missense_variant | 0.19 |
fbiC | 1304715 | c.1785G>C | synonymous_variant | 0.19 |
fbiC | 1304724 | c.1794A>G | synonymous_variant | 0.21 |
fbiC | 1304727 | c.1797A>G | synonymous_variant | 0.25 |
fbiC | 1304742 | c.1812T>C | synonymous_variant | 0.31 |
fbiC | 1304748 | c.1818T>C | synonymous_variant | 0.3 |
fbiC | 1304757 | c.1827A>G | synonymous_variant | 0.31 |
fbiC | 1304760 | c.1830G>C | synonymous_variant | 0.31 |
fbiC | 1304769 | c.1839C>T | synonymous_variant | 0.32 |
fbiC | 1304778 | c.1848T>C | synonymous_variant | 0.33 |
fbiC | 1304784 | c.1854T>C | synonymous_variant | 0.34 |
fbiC | 1304787 | c.1857T>C | synonymous_variant | 0.39 |
fbiC | 1304808 | c.1878C>G | synonymous_variant | 0.37 |
fbiC | 1304811 | c.1881C>G | synonymous_variant | 0.37 |
fbiC | 1304817 | c.1887T>C | synonymous_variant | 0.4 |
fbiC | 1304829 | c.1899T>C | synonymous_variant | 0.5 |
fbiC | 1304832 | c.1902C>T | synonymous_variant | 0.48 |
fbiC | 1304853 | c.1923C>G | synonymous_variant | 0.43 |
fbiC | 1304856 | c.1926C>G | synonymous_variant | 0.38 |
fbiC | 1304869 | c.1939C>T | synonymous_variant | 0.37 |
fbiC | 1304875 | p.Ile649Val | missense_variant | 0.37 |
fbiC | 1304889 | c.1959G>C | synonymous_variant | 0.18 |
fbiC | 1304891 | p.Ile654Thr | missense_variant | 0.17 |
fbiC | 1304893 | p.Gly655Ser | missense_variant | 0.17 |
fbiC | 1304904 | c.1974G>A | synonymous_variant | 0.15 |
fbiC | 1304907 | c.1977C>G | synonymous_variant | 0.15 |
fbiC | 1304910 | c.1981dupC | frameshift_variant | 0.15 |
fbiC | 1304916 | c.1986T>C | synonymous_variant | 0.31 |
fbiC | 1304925 | c.1995G>C | synonymous_variant | 0.31 |
fbiC | 1304928 | c.1998T>C | synonymous_variant | 0.35 |
fbiC | 1304937 | c.2007G>C | synonymous_variant | 0.38 |
fbiC | 1304940 | c.2010A>G | synonymous_variant | 0.43 |
fbiC | 1304946 | c.2016G>C | synonymous_variant | 0.5 |
fbiC | 1304955 | c.2025G>A | synonymous_variant | 0.46 |
fbiC | 1304958 | c.2028T>G | synonymous_variant | 0.46 |
fbiC | 1304991 | c.2061G>C | synonymous_variant | 0.45 |
fbiC | 1304994 | c.2064A>G | synonymous_variant | 0.45 |
fbiC | 1304995 | p.Leu689Met | missense_variant | 0.45 |
fbiC | 1305006 | c.2076A>G | synonymous_variant | 0.42 |
fbiC | 1305012 | c.2082G>C | synonymous_variant | 0.33 |
fbiC | 1305015 | c.2085G>C | synonymous_variant | 0.33 |
fbiC | 1305016 | p.Thr696Ala | missense_variant | 0.33 |
fbiC | 1305021 | c.2091C>G | synonymous_variant | 0.3 |
fbiC | 1305033 | c.2103T>G | synonymous_variant | 0.3 |
fbiC | 1305042 | c.2112A>G | synonymous_variant | 0.33 |
fbiC | 1305045 | c.2115A>G | synonymous_variant | 0.33 |
fbiC | 1305051 | c.2121G>C | synonymous_variant | 0.38 |
fbiC | 1305063 | c.2133G>C | synonymous_variant | 0.25 |
fbiC | 1305066 | c.2136T>C | synonymous_variant | 0.22 |
fbiC | 1305075 | c.2145T>C | synonymous_variant | 0.27 |
fbiC | 1305078 | c.2148A>G | synonymous_variant | 0.2 |
fbiC | 1305092 | p.Ala721Gly | missense_variant | 0.22 |
fbiC | 1305096 | c.2166T>C | synonymous_variant | 0.25 |
fbiC | 1305099 | c.2169T>C | synonymous_variant | 0.25 |
fbiC | 1305114 | c.2184T>C | synonymous_variant | 0.33 |
fbiC | 1305117 | c.2187T>C | synonymous_variant | 0.36 |
fbiC | 1305126 | c.2196T>C | synonymous_variant | 0.33 |
fbiC | 1305135 | c.2205C>T | synonymous_variant | 0.36 |
fbiC | 1305150 | c.2220C>G | synonymous_variant | 0.6 |
fbiC | 1305173 | p.Asn748Ser | missense_variant | 0.47 |
fbiC | 1305177 | c.2247A>G | synonymous_variant | 0.47 |
fbiC | 1305181 | c.2251T>C | synonymous_variant | 0.47 |
fbiC | 1305195 | c.2265T>C | synonymous_variant | 0.32 |
fbiC | 1305201 | c.2271G>C | synonymous_variant | 0.3 |
fbiC | 1305204 | c.2274C>G | synonymous_variant | 0.26 |
fbiC | 1305215 | p.Ser762Thr | missense_variant | 0.24 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1407215 | c.126G>T | synonymous_variant | 0.18 |
embR | 1416355 | c.993C>A | synonymous_variant | 0.22 |
embR | 1416431 | p.Ala306Glu | missense_variant | 0.18 |
embR | 1416971 | p.Ala126Asp | missense_variant | 0.17 |
atpE | 1460861 | c.-184C>G | upstream_gene_variant | 0.2 |
atpE | 1460882 | c.-163T>C | upstream_gene_variant | 0.18 |
atpE | 1460897 | c.-148A>C | upstream_gene_variant | 0.18 |
atpE | 1460900 | c.-145T>C | upstream_gene_variant | 0.18 |
atpE | 1460915 | c.-130C>G | upstream_gene_variant | 0.2 |
atpE | 1460918 | c.-127A>G | upstream_gene_variant | 0.2 |
atpE | 1461113 | c.69C>T | synonymous_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472244 | n.399C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473767 | n.110G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475091 | n.1434G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475175 | n.1518G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476031 | n.2374C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476033 | n.2376T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476034 | n.2377C>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476048 | n.2391G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476089 | n.2432T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476095 | n.2438C>G | non_coding_transcript_exon_variant | 0.29 |
fabG1 | 1673890 | p.Ala151Ser | missense_variant | 0.25 |
inhA | 1673901 | c.-301A>C | upstream_gene_variant | 0.24 |
fabG1 | 1673905 | p.Ser156Ala | missense_variant | 0.22 |
inhA | 1673916 | c.-286A>C | upstream_gene_variant | 0.22 |
fabG1 | 1673917 | p.Val160Leu | missense_variant | 0.22 |
inhA | 1673922 | c.-280T>C | upstream_gene_variant | 0.21 |
inhA | 1673946 | c.-256C>G | upstream_gene_variant | 0.18 |
inhA | 1673955 | c.-247G>C | upstream_gene_variant | 0.18 |
inhA | 1673961 | c.-241A>C | upstream_gene_variant | 0.17 |
inhA | 1673985 | c.-217C>G | upstream_gene_variant | 0.17 |
inhA | 1674123 | c.-79T>C | upstream_gene_variant | 0.15 |
inhA | 1674489 | c.288G>C | synonymous_variant | 0.18 |
inhA | 1674542 | p.Ala114Glu | missense_variant | 0.25 |
inhA | 1674546 | c.345T>C | synonymous_variant | 0.33 |
inhA | 1674549 | c.348G>C | synonymous_variant | 0.27 |
inhA | 1674552 | c.351C>G | synonymous_variant | 0.27 |
inhA | 1674555 | c.354G>A | synonymous_variant | 0.27 |
inhA | 1674561 | c.360C>T | synonymous_variant | 0.25 |
inhA | 1674582 | c.381T>C | synonymous_variant | 0.27 |
inhA | 1674585 | c.384T>C | synonymous_variant | 0.35 |
inhA | 1674589 | p.Met130Leu | missense_variant | 0.33 |
inhA | 1674601 | p.Leu134Ala | missense_variant | 0.26 |
inhA | 1674609 | c.408G>C | synonymous_variant | 0.26 |
inhA | 1674621 | c.420C>G | synonymous_variant | 0.19 |
inhA | 1674624 | c.423A>T | synonymous_variant | 0.19 |
inhA | 1674669 | c.468G>C | synonymous_variant | 0.19 |
inhA | 1674703 | c.502T>C | synonymous_variant | 0.27 |
inhA | 1674708 | c.507G>A | synonymous_variant | 0.3 |
inhA | 1674714 | c.513C>G | synonymous_variant | 0.3 |
inhA | 1674718 | c.517A>C | synonymous_variant | 0.3 |
inhA | 1674723 | c.522C>T | synonymous_variant | 0.27 |
inhA | 1674726 | c.525G>C | synonymous_variant | 0.27 |
inhA | 1674732 | c.531C>T | synonymous_variant | 0.27 |
inhA | 1674738 | c.537C>G | synonymous_variant | 0.29 |
inhA | 1674746 | p.Tyr182Phe | missense_variant | 0.29 |
inhA | 1674750 | c.549T>C | synonymous_variant | 0.29 |
inhA | 1674756 | c.555T>C | synonymous_variant | 0.29 |
inhA | 1674759 | c.558G>C | synonymous_variant | 0.29 |
inhA | 1674774 | c.573A>G | synonymous_variant | 0.29 |
inhA | 1674780 | c.579T>G | synonymous_variant | 0.44 |
inhA | 1674789 | c.588G>C | synonymous_variant | 0.44 |
inhA | 1674795 | c.594G>C | synonymous_variant | 0.3 |
inhA | 1674801 | c.600T>C | synonymous_variant | 0.25 |
inhA | 1674813 | c.612C>T | synonymous_variant | 0.33 |
inhA | 1674816 | c.615T>C | synonymous_variant | 0.33 |
inhA | 1674840 | c.639C>G | synonymous_variant | 0.36 |
inhA | 1674846 | p.Ile215Met | missense_variant | 0.36 |
inhA | 1674870 | c.669T>C | synonymous_variant | 0.33 |
inhA | 1674879 | c.678T>C | synonymous_variant | 0.31 |
inhA | 1674903 | c.702T>C | synonymous_variant | 0.23 |
inhA | 1674904 | p.Ala235Pro | missense_variant | 0.23 |
rpsA | 1833413 | c.-129G>A | upstream_gene_variant | 0.18 |
rpsA | 1833556 | c.15C>A | synonymous_variant | 0.2 |
rpsA | 1833589 | c.48A>T | synonymous_variant | 0.21 |
rpsA | 1833595 | c.54T>C | synonymous_variant | 0.21 |
rpsA | 1833667 | c.126C>G | synonymous_variant | 0.25 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.18 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.18 |
rpsA | 1833799 | c.258C>T | synonymous_variant | 0.2 |
rpsA | 1833805 | c.264C>G | synonymous_variant | 0.19 |
rpsA | 1833811 | c.270G>C | synonymous_variant | 0.19 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.22 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.21 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.2 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.19 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.32 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.24 |
rpsA | 1833931 | c.390C>T | synonymous_variant | 0.22 |
rpsA | 1833940 | c.399C>G | synonymous_variant | 0.18 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.17 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.23 |
rpsA | 1834099 | c.558C>G | synonymous_variant | 0.29 |
rpsA | 1834105 | c.564C>G | synonymous_variant | 0.27 |
rpsA | 1834108 | c.567C>G | synonymous_variant | 0.29 |
rpsA | 1834123 | c.582C>G | synonymous_variant | 0.39 |
rpsA | 1834150 | c.609G>C | synonymous_variant | 0.32 |
rpsA | 1834153 | c.612T>C | synonymous_variant | 0.32 |
rpsA | 1834154 | p.Asn205Gln | missense_variant | 0.32 |
rpsA | 1834157 | c.616T>C | synonymous_variant | 0.33 |
rpsA | 1834162 | c.621A>G | synonymous_variant | 0.32 |
rpsA | 1834165 | c.624A>G | synonymous_variant | 0.35 |
rpsA | 1834169 | p.Thr210Ala | missense_variant | 0.35 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834189 | c.648G>C | synonymous_variant | 0.43 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 0.45 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.41 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.37 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.36 |
rpsA | 1834262 | c.721_723delTCGinsAGT | synonymous_variant | 0.36 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.3 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.29 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.21 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.18 |
rpsA | 1834396 | c.855G>T | synonymous_variant | 0.18 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.18 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.19 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.2 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.25 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.19 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.17 |
rpsA | 1834654 | p.Glu371Asp | missense_variant | 0.27 |
rpsA | 1834690 | c.1149T>C | synonymous_variant | 0.32 |
rpsA | 1834732 | c.1191T>C | synonymous_variant | 0.28 |
rpsA | 1834733 | p.Ala398Ser | missense_variant | 0.29 |
rpsA | 1834753 | c.1212T>C | synonymous_variant | 0.29 |
rpsA | 1834765 | p.Glu408Asp | missense_variant | 0.35 |
rpsA | 1834775 | p.Ala412Thr | missense_variant | 0.33 |
rpsA | 1834780 | c.1239A>G | synonymous_variant | 0.33 |
rpsA | 1834786 | c.1245A>G | synonymous_variant | 0.25 |
rpsA | 1834789 | c.1248T>C | synonymous_variant | 0.25 |
rpsA | 1834792 | c.1251G>C | synonymous_variant | 0.21 |
rpsA | 1834902 | p.Ala454Glu | missense_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101831 | c.1212G>A | synonymous_variant | 0.14 |
ndh | 2102227 | c.816C>T | synonymous_variant | 0.2 |
ndh | 2102230 | c.813G>C | synonymous_variant | 0.18 |
ndh | 2102233 | c.810G>A | synonymous_variant | 0.18 |
ndh | 2102248 | c.795C>G | synonymous_variant | 0.2 |
katG | 2154470 | p.Gly548Cys | missense_variant | 0.14 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155632 | c.480A>C | synonymous_variant | 0.22 |
katG | 2155638 | c.474G>A | synonymous_variant | 0.22 |
katG | 2155641 | p.Lys157Asn | missense_variant | 0.2 |
katG | 2155661 | p.Val151Ile | missense_variant | 0.25 |
katG | 2155668 | c.444G>C | synonymous_variant | 0.22 |
katG | 2155677 | c.435C>A | synonymous_variant | 0.22 |
katG | 2155680 | c.432G>C | synonymous_variant | 0.22 |
katG | 2155852 | p.Ser87* | stop_gained | 0.15 |
katG | 2156153 | c.-42C>A | upstream_gene_variant | 0.14 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169084 | p.Ser510Leu | missense_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289991 | c.-750G>C | upstream_gene_variant | 0.29 |
pncA | 2289994 | c.-753A>G | upstream_gene_variant | 0.29 |
pncA | 2289997 | c.-756G>C | upstream_gene_variant | 0.29 |
pncA | 2290009 | c.-768A>G | upstream_gene_variant | 0.22 |
pncA | 2290015 | c.-774A>C | upstream_gene_variant | 0.2 |
pncA | 2290024 | c.-783C>G | upstream_gene_variant | 0.18 |
pncA | 2290030 | c.-791_-789delAATinsCAC | upstream_gene_variant | 0.2 |
pncA | 2290033 | c.-794_-792delGCCinsACG | upstream_gene_variant | 0.18 |
pncA | 2290042 | c.-801T>C | upstream_gene_variant | 0.18 |
kasA | 2517923 | c.-192C>G | upstream_gene_variant | 0.18 |
kasA | 2518190 | p.Ser26Ala | missense_variant | 0.15 |
kasA | 2518196 | p.Asp28Tyr | missense_variant | 0.15 |
kasA | 2518248 | p.Ala45Val | missense_variant | 0.14 |
kasA | 2518282 | c.168A>G | synonymous_variant | 0.15 |
kasA | 2518283 | p.Ala57Pro | missense_variant | 0.15 |
kasA | 2518459 | c.345T>C | synonymous_variant | 0.38 |
kasA | 2518462 | c.348A>C | synonymous_variant | 0.38 |
kasA | 2518468 | c.354A>C | synonymous_variant | 0.43 |
kasA | 2518474 | c.360G>A | synonymous_variant | 0.56 |
kasA | 2518480 | c.366T>C | synonymous_variant | 0.5 |
kasA | 2518483 | c.369C>G | synonymous_variant | 0.5 |
kasA | 2518504 | c.390T>C | synonymous_variant | 0.42 |
kasA | 2518506 | p.Ala131Glu | missense_variant | 0.42 |
kasA | 2518519 | c.405G>C | synonymous_variant | 0.42 |
kasA | 2518528 | c.414C>G | synonymous_variant | 0.42 |
kasA | 2518540 | c.426T>G | synonymous_variant | 0.42 |
kasA | 2518561 | c.447T>C | synonymous_variant | 0.36 |
kasA | 2518564 | c.450C>G | synonymous_variant | 0.22 |
kasA | 2518567 | c.453G>C | synonymous_variant | 0.2 |
kasA | 2518570 | c.456G>C | synonymous_variant | 0.2 |
kasA | 2518574 | p.Ile154Val | missense_variant | 0.22 |
kasA | 2518588 | c.474T>C | synonymous_variant | 0.2 |
kasA | 2518591 | c.477G>C | synonymous_variant | 0.2 |
kasA | 2518885 | c.771T>C | synonymous_variant | 0.15 |
kasA | 2518898 | c.784T>C | synonymous_variant | 0.17 |
kasA | 2518906 | c.792A>G | synonymous_variant | 0.17 |
kasA | 2518910 | p.Leu266Met | missense_variant | 0.18 |
kasA | 2518915 | c.801T>C | synonymous_variant | 0.18 |
kasA | 2518936 | c.822C>G | synonymous_variant | 0.17 |
kasA | 2518951 | c.837G>C | synonymous_variant | 0.18 |
kasA | 2518963 | c.849T>C | synonymous_variant | 0.18 |
kasA | 2519095 | c.981C>G | synonymous_variant | 0.15 |
kasA | 2519158 | c.1044C>T | synonymous_variant | 0.15 |
kasA | 2519170 | c.1056G>T | synonymous_variant | 0.14 |
ahpC | 2726561 | c.369T>C | synonymous_variant | 0.23 |
ahpC | 2726564 | c.372C>G | synonymous_variant | 0.29 |
ahpC | 2726579 | c.387T>C | synonymous_variant | 0.28 |
ahpC | 2726591 | c.399C>G | synonymous_variant | 0.35 |
ahpC | 2726593 | p.Val134Ala | missense_variant | 0.35 |
ahpC | 2726600 | c.408T>C | synonymous_variant | 0.37 |
ahpC | 2726601 | p.Ile137Leu | missense_variant | 0.35 |
ahpC | 2726633 | c.441C>T | synonymous_variant | 0.24 |
ahpC | 2726638 | p.Ala149Val | missense_variant | 0.22 |
ahpC | 2726645 | c.453C>G | synonymous_variant | 0.19 |
ahpC | 2726657 | c.465A>C | synonymous_variant | 0.21 |
ahpC | 2726669 | p.Asp159Glu | missense_variant | 0.17 |
ahpC | 2726672 | c.480G>A | synonymous_variant | 0.16 |
ahpC | 2726675 | c.483A>G | synonymous_variant | 0.17 |
ahpC | 2726681 | c.489A>C | synonymous_variant | 0.19 |
ahpC | 2726693 | c.501C>A | synonymous_variant | 0.25 |
ahpC | 2726696 | c.504C>G | synonymous_variant | 0.24 |
ahpC | 2726709 | c.517C>T | synonymous_variant | 0.16 |
folC | 2746948 | c.651G>C | synonymous_variant | 0.15 |
folC | 2746957 | c.642G>A | synonymous_variant | 0.15 |
folC | 2746966 | c.633G>C | synonymous_variant | 0.18 |
folC | 2746974 | p.Ile209Leu | missense_variant | 0.22 |
folC | 2746975 | c.624T>C | synonymous_variant | 0.22 |
folC | 2746979 | p.Ala207Asp | missense_variant | 0.22 |
folC | 2746981 | c.618T>C | synonymous_variant | 0.22 |
folC | 2746984 | c.615C>G | synonymous_variant | 0.2 |
folC | 2746987 | c.612T>C | synonymous_variant | 0.2 |
folC | 2746999 | c.600T>C | synonymous_variant | 0.18 |
folC | 2747002 | c.597T>C | synonymous_variant | 0.18 |
folC | 2747006 | p.Ser198Ala | missense_variant | 0.2 |
folC | 2747032 | c.567A>G | synonymous_variant | 0.14 |
folC | 2747053 | c.546C>T | synonymous_variant | 0.18 |
folC | 2747059 | c.540T>C | synonymous_variant | 0.19 |
folC | 2747071 | c.528C>G | synonymous_variant | 0.19 |
folC | 2747239 | c.360T>C | synonymous_variant | 0.21 |
folC | 2747264 | p.Gly112Ala | missense_variant | 0.27 |
folC | 2747266 | c.333C>T | synonymous_variant | 0.27 |
folC | 2747281 | c.318A>G | synonymous_variant | 0.24 |
folC | 2747284 | c.315G>C | synonymous_variant | 0.24 |
folC | 2747289 | p.Pro104Ala | missense_variant | 0.23 |
folC | 2747290 | c.309A>G | synonymous_variant | 0.23 |
folC | 2747293 | c.306G>A | synonymous_variant | 0.22 |
folC | 2747299 | c.300C>T | synonymous_variant | 0.22 |
folC | 2747302 | c.297A>C | synonymous_variant | 0.23 |
folC | 2747314 | c.285A>G | synonymous_variant | 0.27 |
folC | 2747317 | c.282C>G | synonymous_variant | 0.29 |
folC | 2747329 | c.270C>T | synonymous_variant | 0.27 |
folC | 2747332 | c.267G>A | synonymous_variant | 0.26 |
folC | 2747338 | c.261C>G | synonymous_variant | 0.21 |
folC | 2747343 | p.Val86Ile | missense_variant | 0.2 |
folC | 2747355 | p.Val82Ile | missense_variant | 0.16 |
folC | 2747368 | c.231G>A | synonymous_variant | 0.14 |
pepQ | 2859438 | c.981T>C | synonymous_variant | 0.17 |
pepQ | 2860121 | p.His100Asn | missense_variant | 0.14 |
Rv2752c | 3064797 | c.1395G>C | synonymous_variant | 0.25 |
Rv2752c | 3064803 | c.1389C>T | synonymous_variant | 0.25 |
Rv2752c | 3064809 | c.1383C>G | synonymous_variant | 0.22 |
Rv2752c | 3064815 | c.1377T>C | synonymous_variant | 0.3 |
Rv2752c | 3064831 | p.Ala454Asn | missense_variant | 0.27 |
Rv2752c | 3064838 | c.1354T>C | synonymous_variant | 0.22 |
Rv2752c | 3064860 | c.1332G>C | synonymous_variant | 0.24 |
Rv2752c | 3064872 | c.1320T>G | synonymous_variant | 0.25 |
Rv2752c | 3064877 | p.Ser439Ala | missense_variant | 0.25 |
Rv2752c | 3064878 | c.1314C>A | synonymous_variant | 0.17 |
Rv2752c | 3064881 | p.Ser437Ala | missense_variant | 0.18 |
Rv2752c | 3064914 | c.1278T>G | synonymous_variant | 0.2 |
Rv2752c | 3064926 | c.1264_1266delTTGinsCTC | synonymous_variant | 0.16 |
Rv2752c | 3064932 | c.1260T>C | synonymous_variant | 0.16 |
Rv2752c | 3064956 | p.Ser412Arg | missense_variant | 0.2 |
Rv2752c | 3064962 | c.1230C>G | synonymous_variant | 0.21 |
Rv2752c | 3064973 | p.Ala407Ser | missense_variant | 0.24 |
Rv2752c | 3064974 | c.1218T>C | synonymous_variant | 0.3 |
Rv2752c | 3064995 | c.1197C>G | synonymous_variant | 0.31 |
Rv2752c | 3064998 | c.1194A>G | synonymous_variant | 0.3 |
Rv2752c | 3065007 | c.1185G>C | synonymous_variant | 0.29 |
Rv2752c | 3065013 | c.1179G>C | synonymous_variant | 0.29 |
Rv2752c | 3065018 | p.Asn392His | missense_variant | 0.3 |
Rv2752c | 3065022 | c.1170G>C | synonymous_variant | 0.3 |
Rv2752c | 3065028 | p.Val388Ile | missense_variant | 0.33 |
Rv2752c | 3065040 | c.1152C>G | synonymous_variant | 0.32 |
Rv2752c | 3065048 | c.1144C>T | synonymous_variant | 0.32 |
Rv2752c | 3065064 | c.1128G>C | synonymous_variant | 0.22 |
Rv2752c | 3066330 | c.-139G>C | upstream_gene_variant | 0.16 |
Rv2752c | 3066336 | c.-145C>T | upstream_gene_variant | 0.16 |
Rv2752c | 3066369 | c.-180_-178delAGCinsGGG | upstream_gene_variant | 0.17 |
thyX | 3067223 | c.723G>C | synonymous_variant | 0.18 |
thyX | 3067232 | c.714C>G | synonymous_variant | 0.2 |
thyX | 3067421 | c.525G>C | synonymous_variant | 0.17 |
thyX | 3067427 | c.519G>C | synonymous_variant | 0.18 |
thyX | 3067718 | c.228C>G | synonymous_variant | 0.22 |
thyX | 3067721 | c.225T>C | synonymous_variant | 0.21 |
thyX | 3067727 | c.219A>C | synonymous_variant | 0.18 |
thyX | 3067736 | c.210C>T | synonymous_variant | 0.19 |
thyX | 3067793 | c.153T>C | synonymous_variant | 0.28 |
thyX | 3067802 | c.144C>G | synonymous_variant | 0.28 |
thyX | 3067835 | c.111G>A | synonymous_variant | 0.19 |
thyX | 3067838 | c.108C>G | synonymous_variant | 0.19 |
thyX | 3067850 | c.96A>C | synonymous_variant | 0.21 |
thyX | 3067853 | c.93C>T | synonymous_variant | 0.22 |
thyX | 3067869 | p.Thr26Ser | missense_variant | 0.24 |
thyX | 3067874 | c.72C>G | synonymous_variant | 0.22 |
thyA | 3073839 | c.633T>C | synonymous_variant | 0.15 |
thyA | 3073860 | c.612C>G | synonymous_variant | 0.18 |
thyA | 3073863 | c.609T>C | synonymous_variant | 0.18 |
thyA | 3073866 | c.606C>G | synonymous_variant | 0.18 |
thyA | 3073872 | p.Ile200Val | missense_variant | 0.18 |
thyA | 3073878 | c.594G>A | synonymous_variant | 0.18 |
thyA | 3073892 | c.580T>C | synonymous_variant | 0.18 |
thyA | 3073893 | c.579C>T | synonymous_variant | 0.18 |
thyA | 3073898 | p.Ala192Ser | missense_variant | 0.25 |
thyA | 3073902 | c.570C>G | synonymous_variant | 0.25 |
thyA | 3073917 | c.555C>A | synonymous_variant | 0.4 |
thyA | 3073920 | c.552C>G | synonymous_variant | 0.43 |
thyA | 3073925 | c.547T>C | synonymous_variant | 0.38 |
thyA | 3073929 | c.543T>C | synonymous_variant | 0.25 |
thyA | 3073953 | c.519T>C | synonymous_variant | 0.29 |
thyA | 3073977 | c.495A>G | synonymous_variant | 0.31 |
thyA | 3073989 | c.483T>C | synonymous_variant | 0.43 |
thyA | 3074001 | c.471C>G | synonymous_variant | 0.43 |
thyA | 3074004 | c.468T>C | synonymous_variant | 0.43 |
thyA | 3074010 | c.462C>G | synonymous_variant | 0.43 |
thyA | 3074028 | c.444G>C | synonymous_variant | 0.33 |
thyA | 3074031 | c.441T>C | synonymous_variant | 0.33 |
thyA | 3074045 | c.427C>T | synonymous_variant | 0.41 |
thyA | 3074053 | p.Arg140Gln | missense_variant | 0.36 |
thyA | 3074056 | p.Glu139Pro | missense_variant | 0.38 |
thyA | 3074079 | c.393G>C | synonymous_variant | 0.31 |
thyA | 3074097 | c.375C>G | synonymous_variant | 0.15 |
thyA | 3074100 | c.372T>C | synonymous_variant | 0.21 |
thyA | 3074106 | c.366T>C | synonymous_variant | 0.2 |
thyA | 3074118 | c.354G>A | synonymous_variant | 0.25 |
thyA | 3074127 | c.345G>C | synonymous_variant | 0.25 |
thyA | 3074214 | c.258T>C | synonymous_variant | 0.21 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087608 | c.789A>G | synonymous_variant | 0.16 |
ald | 3087617 | c.798T>C | synonymous_variant | 0.18 |
ald | 3087620 | c.801A>C | synonymous_variant | 0.18 |
ald | 3087621 | p.Ala268Ser | missense_variant | 0.17 |
ald | 3087641 | c.822T>C | synonymous_variant | 0.29 |
ald | 3087647 | c.828A>G | synonymous_variant | 0.27 |
ald | 3087649 | p.Gly277Asp | missense_variant | 0.27 |
ald | 3087653 | c.834A>G | synonymous_variant | 0.29 |
ald | 3087656 | c.837A>G | synonymous_variant | 0.29 |
ald | 3087665 | c.846C>G | synonymous_variant | 0.29 |
ald | 3087666 | p.Tyr283His | missense_variant | 0.29 |
ald | 3087672 | p.His285Asp | missense_variant | 0.31 |
ald | 3087680 | c.861G>C | synonymous_variant | 0.31 |
ald | 3087685 | p.Ala289Val | missense_variant | 0.33 |
ald | 3087699 | p.Leu294Val | missense_variant | 0.2 |
ald | 3087704 | c.885T>C | synonymous_variant | 0.18 |
ald | 3087716 | c.897G>C | synonymous_variant | 0.18 |
ald | 3087761 | c.942C>G | synonymous_variant | 0.14 |
ald | 3087776 | c.957G>C | synonymous_variant | 0.17 |
ald | 3087787 | p.Glu323Ala | missense_variant | 0.19 |
ald | 3087791 | c.972T>C | synonymous_variant | 0.19 |
ald | 3087799 | p.His327Arg | missense_variant | 0.21 |
ald | 3087821 | c.1002G>C | synonymous_variant | 0.23 |
ald | 3087825 | p.Asn336Asp | missense_variant | 0.24 |
ald | 3087829 | p.Pro337Gln | missense_variant | 0.16 |
ald | 3087833 | c.1014A>T | synonymous_variant | 0.17 |
ald | 3087836 | c.1017A>G | synonymous_variant | 0.17 |
ald | 3087838 | p.Ala340Gly | missense_variant | 0.16 |
fbiD | 3339284 | p.Leu56Pro | missense_variant | 0.25 |
fprA | 3473812 | c.-195G>A | upstream_gene_variant | 0.15 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568521 | p.Leu53Phe | missense_variant | 0.15 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiB | 3641689 | p.Val52Ala | missense_variant | 0.16 |
fbiB | 3641717 | c.183T>G | synonymous_variant | 0.17 |
alr | 3840980 | c.441G>C | synonymous_variant | 0.15 |
alr | 3840994 | p.His143Asp | missense_variant | 0.17 |
alr | 3840997 | c.424T>C | synonymous_variant | 0.17 |
alr | 3841001 | c.420A>G | synonymous_variant | 0.18 |
alr | 3841010 | c.411A>G | synonymous_variant | 0.18 |
alr | 3841017 | p.Leu135Glu | missense_variant | 0.18 |
alr | 3841022 | c.399C>G | synonymous_variant | 0.22 |
alr | 3841028 | c.393G>C | synonymous_variant | 0.2 |
alr | 3841033 | p.Val130Ile | missense_variant | 0.2 |
alr | 3841037 | p.Val128Ile | missense_variant | 0.2 |
rpoA | 3877527 | c.981C>G | synonymous_variant | 0.17 |
rpoA | 3877553 | p.Glu319Gln | missense_variant | 0.17 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.17 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.22 |
rpoA | 3877656 | c.852T>G | synonymous_variant | 0.24 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.17 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.18 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.18 |
rpoA | 3877848 | c.660C>T | synonymous_variant | 0.19 |
rpoA | 3877857 | c.651G>A | synonymous_variant | 0.19 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.19 |
rpoA | 3877875 | c.633T>G | synonymous_variant | 0.19 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.25 |
rpoA | 3877986 | c.522G>C | synonymous_variant | 0.19 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.23 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.24 |
rpoA | 3878022 | c.486T>C | synonymous_variant | 0.29 |
rpoA | 3878028 | c.480G>C | synonymous_variant | 0.21 |
rpoA | 3878031 | c.477T>C | synonymous_variant | 0.22 |
rpoA | 3878040 | c.468T>C | synonymous_variant | 0.26 |
rpoA | 3878046 | c.462T>A | synonymous_variant | 0.26 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.26 |
rpoA | 3878058 | c.450G>T | synonymous_variant | 0.26 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.26 |
rpoA | 3878067 | c.441C>G | synonymous_variant | 0.24 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.22 |
rpoA | 3878076 | c.432C>T | synonymous_variant | 0.24 |
rpoA | 3878094 | c.414C>G | synonymous_variant | 0.19 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.16 |
rpoA | 3878130 | c.378C>G | synonymous_variant | 0.17 |
rpoA | 3878205 | c.303T>C | synonymous_variant | 0.19 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.19 |
rpoA | 3878226 | c.282C>G | synonymous_variant | 0.31 |
rpoA | 3878232 | c.276G>C | synonymous_variant | 0.39 |
rpoA | 3878247 | c.261G>C | synonymous_variant | 0.42 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.39 |
rpoA | 3878276 | c.232C>T | synonymous_variant | 0.39 |
rpoA | 3878283 | p.Glu75Ala | missense_variant | 0.39 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.34 |
rpoA | 3878304 | c.204G>C | synonymous_variant | 0.27 |
rpoA | 3878313 | c.195G>T | synonymous_variant | 0.28 |
rpoA | 3878346 | c.162T>C | synonymous_variant | 0.17 |
rpoA | 3878415 | c.93C>T | synonymous_variant | 0.27 |
rpoA | 3878436 | c.72A>G | synonymous_variant | 0.23 |
rpoA | 3878442 | c.66G>C | synonymous_variant | 0.23 |
rpoA | 3878454 | c.54A>C | synonymous_variant | 0.23 |
rpoA | 3878472 | p.Asp12Glu | missense_variant | 0.21 |
rpoA | 3878478 | c.30C>G | synonymous_variant | 0.21 |
rpoA | 3878484 | c.24C>A | synonymous_variant | 0.25 |
rpoA | 3878490 | c.18C>A | synonymous_variant | 0.29 |
rpoA | 3878496 | c.12A>T | synonymous_variant | 0.29 |
ddn | 3986648 | c.-196C>G | upstream_gene_variant | 0.22 |
clpC1 | 4038433 | c.2272C>T | synonymous_variant | 0.21 |
clpC1 | 4038434 | c.2271G>A | synonymous_variant | 0.2 |
clpC1 | 4038444 | p.Ala754Lys | missense_variant | 0.22 |
clpC1 | 4038446 | c.2259T>C | synonymous_variant | 0.22 |
clpC1 | 4038456 | p.Val750Glu | missense_variant | 0.25 |
clpC1 | 4038460 | p.Leu749Met | missense_variant | 0.28 |
clpC1 | 4038486 | p.Gly740Asn | missense_variant | 0.53 |
clpC1 | 4038489 | p.Ala739Gly | missense_variant | 0.53 |
clpC1 | 4038494 | c.2211G>C | synonymous_variant | 0.57 |
clpC1 | 4038497 | p.Ser736Gln | missense_variant | 0.53 |
clpC1 | 4038530 | p.Glu725Asp | missense_variant | 0.52 |
clpC1 | 4038551 | c.2154C>G | synonymous_variant | 0.47 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.39 |
clpC1 | 4038623 | c.2082A>G | synonymous_variant | 0.36 |
clpC1 | 4038640 | p.Asp689Asn | missense_variant | 0.26 |
clpC1 | 4038653 | c.2052C>T | synonymous_variant | 0.25 |
clpC1 | 4038658 | p.Lys683Gln | missense_variant | 0.21 |
clpC1 | 4038661 | p.Ser682Thr | missense_variant | 0.21 |
clpC1 | 4038662 | c.2043T>C | synonymous_variant | 0.21 |
clpC1 | 4038671 | c.2034T>C | synonymous_variant | 0.3 |
clpC1 | 4038683 | c.2022T>C | synonymous_variant | 0.23 |
clpC1 | 4038695 | c.2010C>G | synonymous_variant | 0.24 |
clpC1 | 4038701 | c.2004G>C | synonymous_variant | 0.24 |
clpC1 | 4038704 | c.2001T>C | synonymous_variant | 0.25 |
clpC1 | 4038707 | c.1998C>G | synonymous_variant | 0.24 |
clpC1 | 4038710 | c.1995G>C | synonymous_variant | 0.24 |
clpC1 | 4038713 | c.1992T>C | synonymous_variant | 0.25 |
clpC1 | 4038755 | c.1950G>T | synonymous_variant | 0.32 |
clpC1 | 4038770 | c.1935C>T | synonymous_variant | 0.32 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.32 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.32 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 0.31 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.16 |
clpC1 | 4038845 | c.1860G>C | synonymous_variant | 0.24 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 0.22 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.29 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.32 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.35 |
clpC1 | 4038923 | c.1780_1782delCTAinsTTG | synonymous_variant | 0.37 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.44 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.41 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.4 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.28 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.28 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.22 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.22 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.18 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.18 |
clpC1 | 4039226 | c.1479T>C | synonymous_variant | 0.3 |
clpC1 | 4039319 | c.1386T>C | synonymous_variant | 0.16 |
clpC1 | 4039328 | c.1377A>C | synonymous_variant | 0.16 |
clpC1 | 4039331 | c.1374C>G | synonymous_variant | 0.16 |
clpC1 | 4039337 | p.Thr456Lys | missense_variant | 0.17 |
clpC1 | 4039349 | c.1356C>T | synonymous_variant | 0.2 |
clpC1 | 4039352 | c.1353C>G | synonymous_variant | 0.21 |
clpC1 | 4039364 | c.1341C>G | synonymous_variant | 0.2 |
clpC1 | 4039391 | c.1314T>G | synonymous_variant | 0.27 |
clpC1 | 4039409 | c.1296T>C | synonymous_variant | 0.25 |
clpC1 | 4039412 | c.1293T>G | synonymous_variant | 0.25 |
clpC1 | 4039415 | p.Glu430Asp | missense_variant | 0.25 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.25 |
clpC1 | 4039664 | c.1041G>C | synonymous_variant | 0.23 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.26 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.3 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.23 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.25 |
clpC1 | 4039760 | c.945T>C | synonymous_variant | 0.21 |
clpC1 | 4039766 | c.939T>C | synonymous_variant | 0.19 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.19 |
clpC1 | 4039775 | c.930G>C | synonymous_variant | 0.19 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.19 |
clpC1 | 4039781 | c.924G>T | synonymous_variant | 0.18 |
clpC1 | 4039790 | c.915C>G | synonymous_variant | 0.18 |
clpC1 | 4039805 | c.900C>A | synonymous_variant | 0.18 |
clpC1 | 4039817 | c.888A>T | synonymous_variant | 0.16 |
clpC1 | 4039820 | c.885T>C | synonymous_variant | 0.17 |
clpC1 | 4039826 | c.879C>G | synonymous_variant | 0.24 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 0.24 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.25 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.28 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.28 |
clpC1 | 4039928 | c.775_777delAGCinsTCG | synonymous_variant | 0.21 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.25 |
clpC1 | 4039937 | c.768G>C | synonymous_variant | 0.23 |
clpC1 | 4039946 | c.759A>C | synonymous_variant | 0.25 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.24 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.3 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.32 |
clpC1 | 4039988 | c.717C>G | synonymous_variant | 0.35 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 0.35 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.38 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.38 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.35 |
clpC1 | 4040105 | c.600C>G | synonymous_variant | 0.16 |
clpC1 | 4040644 | c.61A>C | synonymous_variant | 0.2 |
clpC1 | 4040654 | c.51G>A | synonymous_variant | 0.2 |
clpC1 | 4040657 | c.48T>G | synonymous_variant | 0.2 |
panD | 4044105 | c.177G>C | synonymous_variant | 0.18 |
panD | 4044117 | c.165G>C | synonymous_variant | 0.2 |
panD | 4044120 | c.162A>G | synonymous_variant | 0.2 |
panD | 4044123 | c.159T>C | synonymous_variant | 0.2 |
panD | 4044138 | c.144T>C | synonymous_variant | 0.18 |
panD | 4044150 | c.132A>G | synonymous_variant | 0.2 |
embC | 4239973 | c.111T>G | synonymous_variant | 0.4 |
embC | 4240670 | p.Thr270Leu | missense_variant | 0.18 |
embC | 4240678 | c.816T>G | synonymous_variant | 0.22 |
embC | 4240685 | p.Thr275Ala | missense_variant | 0.24 |
embC | 4240693 | c.831T>C | synonymous_variant | 0.25 |
embC | 4240699 | c.837C>G | synonymous_variant | 0.26 |
embC | 4240726 | c.864G>C | synonymous_variant | 0.22 |
embC | 4240780 | c.918T>C | synonymous_variant | 0.26 |
embC | 4240783 | c.921G>C | synonymous_variant | 0.26 |
embC | 4240789 | c.927T>C | synonymous_variant | 0.29 |
embC | 4240819 | c.957A>G | synonymous_variant | 0.32 |
embC | 4240828 | c.966G>C | synonymous_variant | 0.33 |
embC | 4240831 | c.969T>C | synonymous_variant | 0.31 |
embC | 4241506 | c.1644G>C | synonymous_variant | 0.16 |
embC | 4241518 | c.1656A>G | synonymous_variant | 0.17 |
embC | 4241521 | c.1659T>C | synonymous_variant | 0.19 |
embC | 4241527 | c.1665C>G | synonymous_variant | 0.19 |
embC | 4241530 | c.1668C>A | synonymous_variant | 0.19 |
embC | 4241536 | c.1674A>G | synonymous_variant | 0.19 |
embC | 4241539 | c.1677T>C | synonymous_variant | 0.22 |
embC | 4241545 | c.1683T>C | synonymous_variant | 0.21 |
embC | 4241548 | c.1686T>C | synonymous_variant | 0.22 |
embC | 4241551 | c.1689A>G | synonymous_variant | 0.22 |
embC | 4241567 | p.Ile569Val | missense_variant | 0.33 |
embC | 4241572 | c.1710C>G | synonymous_variant | 0.33 |
embC | 4241578 | c.1716G>C | synonymous_variant | 0.33 |
embC | 4241584 | c.1722T>C | synonymous_variant | 0.36 |
embC | 4241591 | p.Leu577Val | missense_variant | 0.4 |
embC | 4241611 | c.1749G>C | synonymous_variant | 0.3 |
embC | 4241614 | c.1752A>C | synonymous_variant | 0.3 |
embC | 4241626 | c.1764T>C | synonymous_variant | 0.43 |
embC | 4241635 | c.1773G>C | synonymous_variant | 0.4 |
embC | 4241644 | c.1782G>C | synonymous_variant | 0.22 |
embC | 4241647 | c.1785G>A | synonymous_variant | 0.22 |
embC | 4241648 | c.1786T>C | synonymous_variant | 0.22 |
embC | 4241665 | c.1803G>C | synonymous_variant | 0.2 |
embC | 4241671 | c.1809T>G | synonymous_variant | 0.27 |
embC | 4241691 | p.Gly610Ala | missense_variant | 0.2 |
embC | 4241694 | p.Ala611Val | missense_variant | 0.21 |
embC | 4241698 | c.1836G>C | synonymous_variant | 0.21 |
embC | 4241704 | c.1842C>G | synonymous_variant | 0.2 |
embC | 4241995 | c.2133C>G | synonymous_variant | 0.18 |
embC | 4242002 | p.Leu714Val | missense_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4244572 | p.Arg447Leu | missense_variant | 0.15 |
embA | 4244831 | p.Phe533Leu | missense_variant | 0.14 |
embA | 4245056 | c.1824C>G | synonymous_variant | 0.22 |
embA | 4245060 | c.1828T>C | synonymous_variant | 0.2 |
embA | 4245077 | c.1845G>C | synonymous_variant | 0.38 |
embA | 4245083 | c.1851A>C | synonymous_variant | 0.38 |
embA | 4245101 | c.1869G>C | synonymous_variant | 0.33 |
embA | 4245137 | c.1905T>C | synonymous_variant | 0.3 |
embA | 4245146 | c.1914G>A | synonymous_variant | 0.25 |
embA | 4245149 | c.1917C>G | synonymous_variant | 0.25 |
embA | 4245167 | c.1935G>A | synonymous_variant | 0.24 |
embA | 4245173 | c.1941G>C | synonymous_variant | 0.24 |
embA | 4245198 | p.Leu656Ile | missense_variant | 0.17 |
embA | 4245811 | p.Pro860Leu | missense_variant | 0.14 |
embA | 4245815 | c.2584_2587delCGCA | frameshift_variant | 0.17 |
embB | 4245834 | c.-680C>T | upstream_gene_variant | 0.15 |
embB | 4245860 | c.-654C>G | upstream_gene_variant | 0.15 |
embB | 4245917 | c.-597G>A | upstream_gene_variant | 0.14 |
embA | 4246020 | p.Ala930Thr | missense_variant | 0.14 |
embB | 4246115 | c.-399T>G | upstream_gene_variant | 0.23 |
embA | 4246128 | p.Ser966Thr | missense_variant | 0.23 |
embB | 4247371 | c.858C>G | synonymous_variant | 0.16 |
embB | 4247375 | p.Leu288Val | missense_variant | 0.17 |
embB | 4247386 | c.873T>C | synonymous_variant | 0.16 |
embB | 4247389 | c.876C>G | synonymous_variant | 0.16 |
embB | 4247425 | c.912G>C | synonymous_variant | 0.17 |
embB | 4247437 | c.924A>G | synonymous_variant | 0.17 |
embB | 4247440 | c.927C>G | synonymous_variant | 0.17 |
embB | 4248094 | c.1581C>T | synonymous_variant | 0.17 |
embB | 4248097 | c.1584C>G | synonymous_variant | 0.19 |
embB | 4248130 | c.1617G>C | synonymous_variant | 0.22 |
embB | 4248133 | c.1620C>G | synonymous_variant | 0.22 |
embB | 4248145 | p.Leu544Phe | missense_variant | 0.21 |
embB | 4248157 | c.1644A>G | synonymous_variant | 0.19 |
embB | 4249432 | c.2919A>G | synonymous_variant | 0.18 |
embB | 4249441 | c.2928A>G | synonymous_variant | 0.18 |
embB | 4249444 | c.2931T>C | synonymous_variant | 0.2 |
embB | 4249447 | c.2934G>C | synonymous_variant | 0.2 |
embB | 4249469 | p.Leu986Met | missense_variant | 0.25 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
ubiA | 4269075 | p.Ile253Val | missense_variant | 0.24 |
aftB | 4269081 | c.-245G>C | upstream_gene_variant | 0.21 |
aftB | 4269084 | c.-248G>C | upstream_gene_variant | 0.2 |
aftB | 4269189 | c.-353C>T | upstream_gene_variant | 0.14 |
ethR | 4327928 | p.Ala127Asp | missense_variant | 0.2 |
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 |
gid | 4408421 | c.-219C>A | upstream_gene_variant | 0.29 |