Run ID: ERR2509673
Sample name:
Date: 31-03-2023 18:32:09
Number of reads: 5681854
Percentage reads mapped: 82.65
Strain: lineage2.2.1
Drug-resistance: Other
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 | 1.0 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
embB | 4247448 | p.His312Arg | missense_variant | 0.22 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6209 | c.970C>T | synonymous_variant | 0.15 |
gyrA | 6824 | c.-478C>T | upstream_gene_variant | 0.17 |
gyrA | 6841 | c.-461T>C | upstream_gene_variant | 0.17 |
gyrA | 6844 | c.-458T>G | upstream_gene_variant | 0.19 |
gyrA | 6853 | c.-449A>G | upstream_gene_variant | 0.19 |
gyrA | 6856 | c.-446T>C | upstream_gene_variant | 0.18 |
gyrA | 6859 | c.-443T>C | upstream_gene_variant | 0.19 |
gyrA | 6862 | c.-440C>G | upstream_gene_variant | 0.18 |
gyrA | 6878 | c.-424T>C | upstream_gene_variant | 0.15 |
gyrA | 6881 | c.-421T>C | upstream_gene_variant | 0.15 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7451 | c.150C>G | synonymous_variant | 0.16 |
gyrA | 7457 | c.156T>C | synonymous_variant | 0.17 |
gyrA | 7472 | c.171T>C | synonymous_variant | 0.19 |
gyrA | 7475 | c.174A>C | synonymous_variant | 0.19 |
gyrA | 7480 | p.Phe60Tyr | missense_variant | 0.19 |
gyrA | 7484 | c.183T>C | synonymous_variant | 0.19 |
gyrA | 7487 | c.186C>G | synonymous_variant | 0.19 |
gyrA | 7490 | c.189C>T | synonymous_variant | 0.21 |
gyrA | 7523 | c.222C>G | synonymous_variant | 0.25 |
gyrA | 7532 | c.231T>C | synonymous_variant | 0.24 |
gyrA | 7541 | c.240C>G | synonymous_variant | 0.23 |
gyrA | 7571 | c.270G>C | synonymous_variant | 0.18 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7595 | c.294C>G | synonymous_variant | 0.16 |
gyrA | 7607 | c.306C>G | synonymous_variant | 0.15 |
gyrA | 7626 | c.325C>T | synonymous_variant | 0.17 |
gyrA | 7631 | c.330G>C | synonymous_variant | 0.15 |
gyrA | 7728 | c.427_429delAGGinsCGC | synonymous_variant | 0.14 |
gyrA | 7760 | c.459C>T | synonymous_variant | 0.21 |
gyrA | 7763 | c.462T>C | synonymous_variant | 0.2 |
gyrA | 7799 | c.498A>G | synonymous_variant | 0.19 |
gyrA | 7835 | c.534A>G | synonymous_variant | 0.17 |
gyrA | 7838 | c.537C>G | synonymous_variant | 0.16 |
gyrA | 7892 | c.591G>C | synonymous_variant | 0.15 |
gyrA | 7898 | p.Asp199Glu | missense_variant | 0.17 |
gyrA | 7919 | p.Glu206Asp | missense_variant | 0.15 |
gyrA | 7923 | p.His208Tyr | missense_variant | 0.13 |
gyrA | 8111 | c.810G>C | synonymous_variant | 0.15 |
gyrA | 8168 | c.867A>G | synonymous_variant | 0.15 |
gyrA | 8177 | c.876A>C | synonymous_variant | 0.15 |
gyrA | 8198 | c.897T>C | synonymous_variant | 0.17 |
gyrA | 8207 | c.906T>C | synonymous_variant | 0.15 |
gyrA | 8219 | c.918T>C | synonymous_variant | 0.15 |
gyrA | 8225 | c.924T>C | synonymous_variant | 0.15 |
gyrA | 8462 | c.1161A>G | synonymous_variant | 0.14 |
gyrA | 8471 | c.1170T>C | synonymous_variant | 0.15 |
gyrA | 8480 | c.1179C>T | synonymous_variant | 0.14 |
gyrA | 8852 | c.1551T>C | synonymous_variant | 0.17 |
gyrA | 8858 | c.1557T>C | synonymous_variant | 0.15 |
gyrA | 9242 | c.1941A>C | synonymous_variant | 0.18 |
gyrA | 9252 | p.Val651Ile | missense_variant | 0.2 |
gyrA | 9275 | c.1974G>A | synonymous_variant | 0.18 |
gyrA | 9278 | c.1977G>C | synonymous_variant | 0.16 |
gyrA | 9281 | c.1980C>G | synonymous_variant | 0.17 |
gyrA | 9284 | c.1983T>C | synonymous_variant | 0.18 |
gyrA | 9291 | c.1990C>T | synonymous_variant | 0.19 |
gyrA | 9296 | c.1995T>C | synonymous_variant | 0.19 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9311 | c.2010C>T | synonymous_variant | 0.17 |
gyrA | 9323 | c.2022C>G | synonymous_variant | 0.15 |
gyrA | 9335 | c.2034G>C | synonymous_variant | 0.14 |
gyrA | 9665 | c.2364A>G | synonymous_variant | 0.16 |
gyrA | 9666 | p.Arg789Gly | missense_variant | 0.16 |
gyrA | 9674 | c.2373T>C | synonymous_variant | 0.15 |
gyrA | 9677 | c.2376C>T | synonymous_variant | 0.15 |
gyrA | 9701 | c.2400T>C | synonymous_variant | 0.15 |
fgd1 | 490827 | c.45C>T | synonymous_variant | 0.19 |
fgd1 | 490833 | c.51G>C | synonymous_variant | 0.23 |
fgd1 | 490842 | c.60C>G | synonymous_variant | 0.23 |
fgd1 | 490851 | c.69A>C | synonymous_variant | 0.23 |
fgd1 | 490887 | c.105G>C | synonymous_variant | 0.24 |
fgd1 | 490902 | c.120T>C | synonymous_variant | 0.18 |
fgd1 | 490905 | c.123T>C | synonymous_variant | 0.17 |
fgd1 | 490911 | c.129T>G | synonymous_variant | 0.16 |
fgd1 | 490917 | c.135C>A | synonymous_variant | 0.14 |
fgd1 | 491106 | c.324T>C | synonymous_variant | 0.16 |
fgd1 | 491121 | c.339A>G | synonymous_variant | 0.21 |
fgd1 | 491137 | p.Glu119Gln | missense_variant | 0.25 |
fgd1 | 491144 | p.Ala121Glu | missense_variant | 0.25 |
fgd1 | 491166 | c.384G>C | synonymous_variant | 0.31 |
fgd1 | 491181 | c.399T>C | synonymous_variant | 0.34 |
fgd1 | 491191 | p.Gly137Arg | missense_variant | 0.34 |
fgd1 | 491196 | c.414A>G | synonymous_variant | 0.33 |
fgd1 | 491202 | c.420G>C | synonymous_variant | 0.31 |
fgd1 | 491203 | p.Gln141Glu | missense_variant | 0.31 |
fgd1 | 491212 | p.Ser144Arg | missense_variant | 0.34 |
fgd1 | 491217 | c.435T>C | synonymous_variant | 0.33 |
fgd1 | 491232 | c.450T>C | synonymous_variant | 0.29 |
fgd1 | 491241 | p.Asp153Glu | missense_variant | 0.34 |
fgd1 | 491244 | c.462T>C | synonymous_variant | 0.33 |
fgd1 | 491259 | c.477T>C | synonymous_variant | 0.37 |
fgd1 | 491286 | c.504G>C | synonymous_variant | 0.41 |
fgd1 | 491292 | c.510G>C | synonymous_variant | 0.38 |
fgd1 | 491295 | c.513C>G | synonymous_variant | 0.35 |
fgd1 | 491296 | p.Val172Ile | missense_variant | 0.38 |
fgd1 | 491319 | c.537G>C | synonymous_variant | 0.29 |
fgd1 | 491331 | c.549G>A | synonymous_variant | 0.25 |
fgd1 | 491349 | c.567T>C | synonymous_variant | 0.18 |
fgd1 | 491502 | c.720G>A | synonymous_variant | 0.21 |
fgd1 | 491508 | c.726A>G | synonymous_variant | 0.19 |
fgd1 | 491509 | c.727T>C | synonymous_variant | 0.19 |
fgd1 | 491512 | p.Asn244Glu | missense_variant | 0.19 |
fgd1 | 491526 | c.744T>C | synonymous_variant | 0.21 |
fgd1 | 491532 | c.750G>T | synonymous_variant | 0.22 |
fgd1 | 491542 | c.760T>C | synonymous_variant | 0.21 |
fgd1 | 491547 | c.765A>C | synonymous_variant | 0.21 |
fgd1 | 491550 | c.768T>C | synonymous_variant | 0.21 |
fgd1 | 491583 | c.801G>A | synonymous_variant | 0.18 |
fgd1 | 491595 | c.813C>G | synonymous_variant | 0.16 |
fgd1 | 491601 | c.819T>C | synonymous_variant | 0.16 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 0.99 |
ccsA | 620349 | c.459A>G | synonymous_variant | 0.14 |
ccsA | 620362 | p.Ala158Thr | missense_variant | 0.18 |
ccsA | 620367 | c.477T>C | synonymous_variant | 0.18 |
ccsA | 620373 | c.483C>G | synonymous_variant | 0.21 |
ccsA | 620385 | c.495G>C | synonymous_variant | 0.22 |
ccsA | 620388 | c.498A>G | synonymous_variant | 0.22 |
ccsA | 620412 | c.522T>C | synonymous_variant | 0.23 |
ccsA | 620415 | c.525T>C | synonymous_variant | 0.22 |
ccsA | 620433 | c.543C>G | synonymous_variant | 0.2 |
ccsA | 620436 | c.546T>C | synonymous_variant | 0.19 |
ccsA | 620439 | c.549T>C | synonymous_variant | 0.19 |
ccsA | 620445 | c.555A>G | synonymous_variant | 0.18 |
ccsA | 620461 | p.Val191Ile | missense_variant | 0.15 |
ccsA | 620604 | c.714C>T | synonymous_variant | 0.13 |
ccsA | 620619 | c.729G>C | synonymous_variant | 0.15 |
ccsA | 620622 | c.732G>C | synonymous_variant | 0.17 |
ccsA | 620625 | p.Ile245Met | missense_variant | 0.99 |
ccsA | 620631 | c.741T>C | synonymous_variant | 0.18 |
ccsA | 620646 | c.756G>A | synonymous_variant | 0.2 |
ccsA | 620661 | c.771C>G | synonymous_variant | 0.2 |
ccsA | 620778 | c.888T>C | synonymous_variant | 0.17 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.15 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.14 |
rpoB | 760253 | c.447T>C | synonymous_variant | 0.16 |
rpoB | 760283 | c.477G>C | synonymous_variant | 0.16 |
rpoB | 760307 | c.501T>C | synonymous_variant | 0.16 |
rpoB | 760328 | c.522G>C | synonymous_variant | 0.19 |
rpoB | 760331 | c.525G>C | synonymous_variant | 0.19 |
rpoB | 760337 | c.531C>G | synonymous_variant | 0.17 |
rpoB | 760340 | c.534G>C | synonymous_variant | 0.17 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.21 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.23 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.2 |
rpoB | 760418 | c.612G>C | synonymous_variant | 0.18 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.19 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.2 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.15 |
rpoB | 760522 | p.Ser239Asn | missense_variant | 0.17 |
rpoB | 760564 | p.Arg253Leu | missense_variant | 0.14 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.14 |
rpoB | 760611 | c.805T>C | synonymous_variant | 0.18 |
rpoB | 760634 | c.828T>C | synonymous_variant | 0.21 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.18 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.18 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.17 |
rpoB | 760670 | c.864G>C | synonymous_variant | 0.17 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.18 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.16 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.16 |
rpoB | 760859 | c.1053T>C | synonymous_variant | 0.14 |
rpoB | 760862 | c.1056G>C | synonymous_variant | 0.14 |
rpoB | 760869 | p.Val355Ile | missense_variant | 0.16 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 0.16 |
rpoB | 760934 | c.1128C>T | synonymous_variant | 0.17 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.16 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.15 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.15 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 0.15 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.14 |
rpoB | 761051 | c.1245G>T | synonymous_variant | 0.14 |
rpoB | 761054 | c.1248G>A | synonymous_variant | 0.14 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.15 |
rpoB | 761063 | c.1257C>G | synonymous_variant | 0.15 |
rpoB | 761097 | c.1291_1292delAGinsTC | synonymous_variant | 0.15 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.17 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.16 |
rpoB | 761183 | c.1377T>G | synonymous_variant | 0.15 |
rpoB | 761189 | c.1383T>G | synonymous_variant | 0.17 |
rpoB | 761222 | c.1416G>C | synonymous_variant | 0.24 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.22 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.21 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.2 |
rpoB | 761297 | c.1491C>T | synonymous_variant | 0.16 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.17 |
rpoB | 761510 | c.1704T>C | synonymous_variant | 0.16 |
rpoB | 761531 | c.1725C>G | synonymous_variant | 0.21 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.23 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.2 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.2 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.22 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.25 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.24 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.23 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.24 |
rpoB | 761645 | c.1839C>G | synonymous_variant | 0.23 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.23 |
rpoB | 761657 | c.1851C>G | synonymous_variant | 0.22 |
rpoB | 761675 | c.1869G>C | synonymous_variant | 0.17 |
rpoB | 761815 | p.Ala670Asp | missense_variant | 0.13 |
rpoB | 761847 | p.Cys681Ser | missense_variant | 0.14 |
rpoB | 761873 | c.2067A>G | synonymous_variant | 0.16 |
rpoB | 761882 | c.2076C>G | synonymous_variant | 0.17 |
rpoB | 761885 | c.2079T>C | synonymous_variant | 0.15 |
rpoB | 761891 | c.2085G>C | synonymous_variant | 0.16 |
rpoB | 761906 | c.2100C>G | synonymous_variant | 0.17 |
rpoB | 761909 | c.2103T>C | synonymous_variant | 0.17 |
rpoB | 761912 | c.2106T>C | synonymous_variant | 0.17 |
rpoB | 761915 | p.Asp703Glu | missense_variant | 0.17 |
rpoB | 761916 | p.Asp704Asn | missense_variant | 0.17 |
rpoB | 761924 | c.2118G>A | synonymous_variant | 0.22 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.24 |
rpoB | 761954 | c.2148C>G | synonymous_variant | 0.24 |
rpoB | 761969 | c.2163G>A | synonymous_variant | 0.26 |
rpoB | 761999 | c.2193G>C | synonymous_variant | 0.25 |
rpoB | 762008 | c.2202C>G | synonymous_variant | 0.26 |
rpoB | 762014 | c.2208C>T | synonymous_variant | 0.22 |
rpoB | 762017 | c.2211A>G | synonymous_variant | 0.22 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.22 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.21 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.21 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.18 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.19 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.17 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.16 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 0.2 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.17 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.18 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.2 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.21 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.22 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.24 |
rpoB | 762218 | c.2412T>G | synonymous_variant | 0.26 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.23 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.23 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.24 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.23 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.16 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.16 |
rpoC | 763076 | c.-294C>G | upstream_gene_variant | 0.15 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.14 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.17 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.17 |
rpoC | 763158 | c.-212C>T | upstream_gene_variant | 0.16 |
rpoC | 763441 | c.72C>G | synonymous_variant | 0.19 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.18 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.18 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.16 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.15 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.16 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.2 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.17 |
rpoC | 763919 | c.550C>T | synonymous_variant | 0.14 |
rpoC | 764257 | c.888G>C | synonymous_variant | 0.14 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.14 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.14 |
rpoC | 764714 | c.1345C>T | synonymous_variant | 0.18 |
rpoC | 764720 | c.1351C>T | synonymous_variant | 0.17 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.16 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.2 |
rpoC | 764791 | c.1422C>G | synonymous_variant | 0.16 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.15 |
rpoC | 764812 | c.1443C>G | synonymous_variant | 0.15 |
rpoC | 764830 | c.1461C>G | synonymous_variant | 0.17 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.16 |
rpoC | 764872 | c.1503A>G | synonymous_variant | 0.16 |
rpoC | 764893 | c.1524T>C | synonymous_variant | 0.17 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.19 |
rpoC | 764923 | c.1554A>G | synonymous_variant | 0.19 |
rpoC | 764932 | c.1563C>A | synonymous_variant | 0.15 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.15 |
rpoC | 765383 | p.Met672Leu | missense_variant | 0.21 |
rpoC | 765404 | p.Leu679Val | missense_variant | 0.22 |
rpoC | 765409 | c.2040T>C | synonymous_variant | 0.23 |
rpoC | 765412 | c.2043T>C | synonymous_variant | 0.23 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.24 |
rpoC | 765451 | c.2082C>G | synonymous_variant | 0.16 |
rpoC | 765452 | p.Ala695Ser | missense_variant | 0.17 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.15 |
rpoC | 765493 | c.2124G>C | synonymous_variant | 0.16 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.15 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.2 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.18 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.17 |
rpoC | 765559 | c.2190G>C | synonymous_variant | 0.17 |
rpoC | 765578 | c.2209C>T | synonymous_variant | 0.15 |
rpoC | 765583 | c.2214G>T | synonymous_variant | 0.14 |
rpoC | 765613 | p.His748Gln | missense_variant | 0.15 |
rpoC | 765625 | c.2256C>G | synonymous_variant | 0.15 |
rpoC | 765658 | c.2289C>T | synonymous_variant | 0.15 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.15 |
rpoC | 765826 | c.2457T>C | synonymous_variant | 0.15 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 0.16 |
rpoC | 765883 | c.2514C>G | synonymous_variant | 0.23 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.21 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.19 |
rpoC | 765928 | c.2559C>G | synonymous_variant | 0.16 |
rpoC | 766069 | c.2700G>A | synonymous_variant | 0.14 |
rpoC | 766082 | p.Ala905Gln | missense_variant | 0.15 |
rpoC | 766096 | c.2727G>C | synonymous_variant | 0.17 |
rpoC | 766105 | c.2736C>T | synonymous_variant | 0.18 |
rpoC | 766129 | c.2760C>G | synonymous_variant | 0.17 |
rpoC | 766135 | c.2766G>A | synonymous_variant | 0.18 |
rpoC | 766142 | c.2773C>T | synonymous_variant | 0.14 |
rpoC | 766345 | c.2976T>C | synonymous_variant | 0.15 |
rpoC | 766363 | c.2994G>C | synonymous_variant | 0.17 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.21 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.21 |
rpoC | 766390 | c.3021C>T | synonymous_variant | 0.2 |
rpoC | 766408 | c.3039C>T | synonymous_variant | 0.19 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.17 |
rpoC | 766444 | c.3075C>G | synonymous_variant | 0.19 |
rpoC | 766447 | c.3078T>C | synonymous_variant | 0.2 |
rpoC | 766483 | c.3114G>C | synonymous_variant | 0.2 |
rpoC | 766484 | p.Val1039Ile | missense_variant | 0.2 |
rpoC | 766492 | c.3123T>C | synonymous_variant | 0.22 |
rpoC | 766495 | c.3126C>T | synonymous_variant | 0.22 |
rpoC | 766528 | c.3159T>G | synonymous_variant | 0.21 |
rpoC | 766543 | c.3174C>T | synonymous_variant | 0.16 |
rpoC | 766573 | c.3204T>C | synonymous_variant | 0.15 |
rpoC | 766583 | p.Gly1072Ser | missense_variant | 0.15 |
rpoC | 766597 | c.3228C>G | synonymous_variant | 0.15 |
rpoC | 766609 | p.Ile1080Met | missense_variant | 0.15 |
rpoC | 766630 | c.3261G>C | synonymous_variant | 0.18 |
rpoC | 766645 | c.3276A>G | synonymous_variant | 0.22 |
rpoC | 766651 | c.3282T>C | synonymous_variant | 0.25 |
rpoC | 766657 | c.3288A>G | synonymous_variant | 0.25 |
rpoC | 766672 | c.3303T>C | synonymous_variant | 0.27 |
rpoC | 766738 | c.3369G>T | synonymous_variant | 0.31 |
rpoC | 766750 | c.3381C>G | synonymous_variant | 0.3 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.29 |
rpoC | 766769 | c.3400C>T | synonymous_variant | 0.29 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.28 |
rpoC | 766801 | c.3432C>G | synonymous_variant | 0.24 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.23 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 0.24 |
rpoC | 766864 | c.3495G>C | synonymous_variant | 0.24 |
rpoC | 766894 | c.3525T>C | synonymous_variant | 0.23 |
rpoC | 766895 | c.3526T>C | synonymous_variant | 0.23 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.24 |
rpoC | 766933 | c.3564A>G | synonymous_variant | 0.18 |
rpoC | 766972 | c.3603G>C | synonymous_variant | 0.15 |
rpoC | 766978 | c.3609C>G | synonymous_variant | 0.17 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.17 |
rpoC | 767009 | p.Ser1214Thr | missense_variant | 0.14 |
rpoC | 767014 | c.3645G>C | synonymous_variant | 0.14 |
rpoC | 767033 | c.3664_3666delTCGinsAGC | synonymous_variant | 0.19 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.23 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.24 |
rpoC | 767074 | c.3705T>C | synonymous_variant | 0.24 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.23 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.24 |
rpoC | 767134 | c.3765C>G | synonymous_variant | 0.28 |
rpoC | 767158 | c.3789T>G | synonymous_variant | 0.29 |
rpoC | 767167 | c.3798C>G | synonymous_variant | 0.27 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.26 |
rpoC | 767191 | c.3822C>G | synonymous_variant | 0.28 |
rpoC | 767206 | c.3837C>G | synonymous_variant | 0.21 |
rpoC | 767209 | c.3840T>C | synonymous_variant | 0.2 |
rpoC | 767212 | c.3843G>C | synonymous_variant | 0.21 |
rpoC | 767221 | c.3852C>G | synonymous_variant | 0.24 |
rpoC | 767230 | c.3861G>C | synonymous_variant | 0.22 |
rpoC | 767233 | c.3864T>C | synonymous_variant | 0.2 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 0.98 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781751 | c.192G>C | synonymous_variant | 0.15 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.17 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.17 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.25 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.22 |
rplC | 800648 | c.-161A>C | upstream_gene_variant | 0.21 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.2 |
rplC | 800690 | c.-119C>T | upstream_gene_variant | 0.24 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.25 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.22 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.18 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.18 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.18 |
rplC | 800738 | c.-71T>C | upstream_gene_variant | 0.17 |
rplC | 800747 | c.-62C>G | upstream_gene_variant | 0.19 |
rplC | 800771 | c.-38C>T | upstream_gene_variant | 0.18 |
rplC | 800844 | c.36T>C | synonymous_variant | 0.18 |
rplC | 800877 | c.69A>C | synonymous_variant | 0.15 |
rplC | 800880 | c.72A>G | synonymous_variant | 0.15 |
rplC | 800889 | c.81C>G | synonymous_variant | 0.18 |
rplC | 800907 | c.99C>G | synonymous_variant | 0.22 |
rplC | 800916 | c.108A>G | synonymous_variant | 0.23 |
rplC | 800937 | c.129A>G | synonymous_variant | 0.17 |
rplC | 800939 | p.Arg44Gln | missense_variant | 0.15 |
rplC | 800955 | c.147C>G | synonymous_variant | 0.15 |
rplC | 800967 | c.159C>G | synonymous_variant | 0.16 |
rplC | 800970 | c.162T>C | synonymous_variant | 0.15 |
rplC | 801174 | c.366T>C | synonymous_variant | 0.16 |
rplC | 801222 | c.414T>C | synonymous_variant | 0.16 |
rplC | 801367 | p.Ala187Thr | missense_variant | 0.14 |
fbiC | 1303509 | c.579G>C | synonymous_variant | 0.17 |
fbiC | 1303512 | c.582T>C | synonymous_variant | 0.17 |
fbiC | 1303534 | p.Ser202Ala | missense_variant | 0.17 |
fbiC | 1303755 | c.825T>C | synonymous_variant | 0.14 |
fbiC | 1303785 | c.855G>C | synonymous_variant | 0.19 |
fbiC | 1303789 | p.Ile287Val | missense_variant | 0.18 |
fbiC | 1303818 | c.888C>G | synonymous_variant | 0.17 |
fbiC | 1303836 | c.906G>C | synonymous_variant | 0.18 |
fbiC | 1303845 | c.915C>G | synonymous_variant | 0.18 |
fbiC | 1303846 | p.Phe306Val | missense_variant | 0.18 |
fbiC | 1303854 | c.924T>C | synonymous_variant | 0.18 |
fbiC | 1303860 | c.930A>C | synonymous_variant | 0.2 |
fbiC | 1303881 | c.951G>C | synonymous_variant | 0.16 |
fbiC | 1303884 | c.954T>G | synonymous_variant | 0.17 |
fbiC | 1303911 | c.981G>C | synonymous_variant | 0.21 |
fbiC | 1303914 | c.984C>G | synonymous_variant | 0.22 |
fbiC | 1303920 | c.990C>G | synonymous_variant | 0.23 |
fbiC | 1303923 | c.993C>T | synonymous_variant | 0.22 |
fbiC | 1303929 | c.999G>C | synonymous_variant | 0.25 |
fbiC | 1303947 | c.1017T>C | synonymous_variant | 0.16 |
fbiC | 1303948 | p.Gly340Arg | missense_variant | 0.16 |
fbiC | 1303969 | p.Val347Ile | missense_variant | 0.17 |
fbiC | 1303973 | p.Gly348Ala | missense_variant | 0.18 |
fbiC | 1303981 | p.Val351Ile | missense_variant | 0.16 |
fbiC | 1303995 | c.1065C>T | synonymous_variant | 0.17 |
fbiC | 1304001 | c.1071C>G | synonymous_variant | 0.17 |
fbiC | 1304008 | c.1078T>C | synonymous_variant | 0.18 |
fbiC | 1304703 | c.1773C>G | synonymous_variant | 0.17 |
fbiC | 1304742 | c.1812T>C | synonymous_variant | 0.17 |
fbiC | 1304748 | c.1818T>C | synonymous_variant | 0.18 |
fbiC | 1304754 | c.1824G>A | synonymous_variant | 0.19 |
fbiC | 1304757 | c.1827A>G | synonymous_variant | 0.19 |
fbiC | 1304784 | c.1854T>C | synonymous_variant | 0.19 |
fbiC | 1304787 | c.1857T>C | synonymous_variant | 0.18 |
fbiC | 1304790 | c.1860C>G | synonymous_variant | 0.19 |
fbiC | 1304808 | c.1878C>G | synonymous_variant | 0.16 |
fbiC | 1304811 | c.1881C>G | synonymous_variant | 0.18 |
fbiC | 1304817 | c.1887T>C | synonymous_variant | 0.2 |
fbiC | 1304829 | c.1899T>C | synonymous_variant | 0.21 |
fbiC | 1304832 | c.1902C>G | synonymous_variant | 0.21 |
fbiC | 1304853 | c.1923C>G | synonymous_variant | 0.19 |
fbiC | 1304856 | c.1926C>G | synonymous_variant | 0.19 |
fbiC | 1304893 | p.Gly655Ser | missense_variant | 0.15 |
fbiC | 1304916 | c.1986T>C | synonymous_variant | 0.14 |
fbiC | 1304925 | c.1995G>C | synonymous_variant | 0.16 |
fbiC | 1304940 | c.2010A>G | synonymous_variant | 0.17 |
fbiC | 1304946 | c.2016G>C | synonymous_variant | 0.2 |
fbiC | 1304958 | c.2028T>G | synonymous_variant | 0.21 |
fbiC | 1304961 | c.2031C>T | synonymous_variant | 0.2 |
fbiC | 1304991 | c.2061G>C | synonymous_variant | 0.19 |
fbiC | 1304994 | c.2064A>G | synonymous_variant | 0.19 |
fbiC | 1304995 | c.2065T>C | synonymous_variant | 0.19 |
fbiC | 1305006 | c.2076A>G | synonymous_variant | 0.18 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472044 | n.199G>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473937 | n.280C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474823 | n.1166C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475638 | n.1981C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475659 | n.2002G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.17 |
inhA | 1674480 | c.279T>C | synonymous_variant | 0.15 |
inhA | 1674507 | c.306G>C | synonymous_variant | 0.16 |
inhA | 1674537 | c.336C>G | synonymous_variant | 0.15 |
inhA | 1674542 | p.Ala114Glu | missense_variant | 0.16 |
inhA | 1674549 | c.348G>C | synonymous_variant | 0.16 |
inhA | 1674555 | c.354G>A | synonymous_variant | 0.17 |
inhA | 1674561 | c.360C>T | synonymous_variant | 0.16 |
rpsA | 1833589 | c.48A>T | synonymous_variant | 0.14 |
rpsA | 1833619 | c.78A>C | synonymous_variant | 0.15 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.16 |
rpsA | 1833667 | c.126C>G | synonymous_variant | 0.17 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.21 |
rpsA | 1833790 | c.249T>A | synonymous_variant | 0.22 |
rpsA | 1833799 | c.258C>G | synonymous_variant | 0.21 |
rpsA | 1833811 | c.270G>C | synonymous_variant | 0.21 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.19 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.18 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.19 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.2 |
rpsA | 1833862 | c.321G>T | synonymous_variant | 0.2 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.19 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.21 |
rpsA | 1833940 | c.399C>G | synonymous_variant | 0.2 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.22 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.18 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.2 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.17 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.17 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834201 | c.660C>T | synonymous_variant | 0.17 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.19 |
rpsA | 1834225 | c.684C>G | synonymous_variant | 0.18 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.2 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.21 |
rpsA | 1834261 | c.720A>C | synonymous_variant | 0.2 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.19 |
rpsA | 1834297 | c.756C>G | synonymous_variant | 0.21 |
rpsA | 1834303 | c.762T>G | synonymous_variant | 0.18 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.17 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.23 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.23 |
rpsA | 1834375 | c.834G>A | synonymous_variant | 0.22 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.21 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.2 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.17 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.17 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.17 |
rpsA | 1834474 | c.933C>G | synonymous_variant | 0.14 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.17 |
rpsA | 1834498 | c.957C>T | synonymous_variant | 0.18 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.22 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.21 |
rpsA | 1834555 | c.1014T>C | synonymous_variant | 0.23 |
rpsA | 1834558 | c.1017C>G | synonymous_variant | 0.23 |
rpsA | 1834594 | c.1053C>T | synonymous_variant | 0.24 |
rpsA | 1834606 | c.1065C>G | synonymous_variant | 0.2 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102065 | c.978G>C | synonymous_variant | 0.15 |
ndh | 2102242 | c.801G>A | synonymous_variant | 0.14 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169866 | c.747G>C | synonymous_variant | 0.31 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2517947 | c.-168C>T | upstream_gene_variant | 0.21 |
kasA | 2517974 | c.-141T>C | upstream_gene_variant | 0.18 |
kasA | 2517989 | c.-126T>C | upstream_gene_variant | 0.15 |
kasA | 2517992 | c.-123C>G | upstream_gene_variant | 0.15 |
kasA | 2518540 | c.426T>G | synonymous_variant | 0.15 |
kasA | 2518561 | c.447T>C | synonymous_variant | 0.15 |
kasA | 2518609 | p.Met165Ile | missense_variant | 0.19 |
kasA | 2518621 | c.507G>A | synonymous_variant | 0.19 |
kasA | 2518642 | c.528A>G | synonymous_variant | 0.23 |
kasA | 2518663 | c.549T>C | synonymous_variant | 0.23 |
kasA | 2518672 | c.558G>C | synonymous_variant | 0.24 |
kasA | 2518687 | c.573C>T | synonymous_variant | 0.21 |
kasA | 2518696 | c.582C>G | synonymous_variant | 0.2 |
kasA | 2518702 | c.588C>T | synonymous_variant | 0.17 |
kasA | 2518711 | c.597A>G | synonymous_variant | 0.17 |
kasA | 2518714 | c.600A>C | synonymous_variant | 0.17 |
kasA | 2518732 | c.618C>G | synonymous_variant | 0.15 |
kasA | 2518768 | c.654C>G | synonymous_variant | 0.16 |
kasA | 2518783 | c.669T>C | synonymous_variant | 0.15 |
kasA | 2518792 | c.678C>G | synonymous_variant | 0.16 |
kasA | 2518795 | c.681C>G | synonymous_variant | 0.17 |
kasA | 2518816 | c.702C>A | synonymous_variant | 0.19 |
kasA | 2518822 | c.708C>G | synonymous_variant | 0.19 |
kasA | 2518825 | c.711T>C | synonymous_variant | 0.19 |
kasA | 2518855 | c.741C>G | synonymous_variant | 0.2 |
kasA | 2518864 | c.750G>C | synonymous_variant | 0.18 |
kasA | 2518879 | c.765A>G | synonymous_variant | 0.18 |
kasA | 2518885 | c.771T>C | synonymous_variant | 0.15 |
kasA | 2518888 | c.774C>T | synonymous_variant | 0.15 |
folC | 2747065 | c.534C>G | synonymous_variant | 0.17 |
folC | 2747086 | c.513A>C | synonymous_variant | 0.17 |
folC | 2747089 | c.510G>C | synonymous_variant | 0.18 |
folC | 2747098 | c.501C>G | synonymous_variant | 0.17 |
folC | 2747101 | c.498G>C | synonymous_variant | 0.17 |
folC | 2747107 | c.492G>C | synonymous_variant | 0.17 |
folC | 2747110 | c.489T>C | synonymous_variant | 0.17 |
folC | 2747113 | c.486C>G | synonymous_variant | 0.16 |
folC | 2747116 | c.483G>C | synonymous_variant | 0.17 |
folC | 2747293 | c.306G>A | synonymous_variant | 0.14 |
folC | 2747314 | c.285A>C | synonymous_variant | 0.16 |
folC | 2747317 | c.282C>G | synonymous_variant | 0.16 |
folC | 2747355 | p.Val82Ile | missense_variant | 0.16 |
folC | 2747362 | c.237G>C | synonymous_variant | 0.15 |
Rv2752c | 3064980 | c.1212C>G | synonymous_variant | 0.15 |
Rv2752c | 3064998 | c.1194A>G | synonymous_variant | 0.15 |
Rv2752c | 3065018 | p.Asn392His | missense_variant | 0.16 |
Rv2752c | 3065028 | c.1164G>C | synonymous_variant | 0.16 |
Rv2752c | 3065031 | c.1161G>C | synonymous_variant | 0.15 |
Rv2752c | 3065947 | p.Gly82Ala | missense_variant | 0.2 |
Rv2752c | 3065955 | c.235_237delTTGinsCTC | synonymous_variant | 0.21 |
Rv2752c | 3065979 | c.213T>C | synonymous_variant | 0.19 |
Rv2752c | 3065993 | p.Val67Ile | missense_variant | 0.16 |
Rv2752c | 3065994 | c.198T>C | synonymous_variant | 0.15 |
Rv2752c | 3065997 | c.195C>G | synonymous_variant | 0.15 |
Rv2752c | 3066024 | c.168T>C | synonymous_variant | 0.15 |
Rv2752c | 3066050 | p.Leu48Met | missense_variant | 0.15 |
Rv2752c | 3066054 | c.138T>G | synonymous_variant | 0.16 |
Rv2752c | 3066066 | c.126T>C | synonymous_variant | 0.16 |
thyX | 3067850 | c.96A>C | synonymous_variant | 0.15 |
thyA | 3073806 | c.666C>G | synonymous_variant | 0.21 |
thyA | 3073812 | c.660C>G | synonymous_variant | 0.14 |
thyA | 3073824 | c.648A>C | synonymous_variant | 0.21 |
thyA | 3073827 | c.645A>G | synonymous_variant | 0.22 |
thyA | 3073839 | c.633T>C | synonymous_variant | 0.25 |
thyA | 3073872 | p.Ile200Val | missense_variant | 0.31 |
thyA | 3073878 | c.594G>A | synonymous_variant | 0.3 |
thyA | 3073892 | c.580T>C | synonymous_variant | 0.26 |
thyA | 3073893 | c.579C>G | synonymous_variant | 0.26 |
thyA | 3073925 | c.547T>C | synonymous_variant | 0.2 |
thyA | 3073926 | c.546G>C | synonymous_variant | 0.2 |
thyA | 3073929 | c.543T>C | synonymous_variant | 0.2 |
thyA | 3073953 | c.519T>C | synonymous_variant | 0.2 |
thyA | 3073977 | c.495A>G | synonymous_variant | 0.2 |
thyA | 3073989 | c.483T>C | synonymous_variant | 0.2 |
thyA | 3074001 | c.471C>G | synonymous_variant | 0.19 |
thyA | 3074004 | c.468T>C | synonymous_variant | 0.18 |
thyA | 3074010 | c.462C>A | synonymous_variant | 0.22 |
thyA | 3074031 | c.441T>C | synonymous_variant | 0.2 |
thyA | 3074037 | c.435C>G | synonymous_variant | 0.19 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 0.99 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiA | 3641332 | p.Gly264Arg | missense_variant | 0.97 |
rpoA | 3877553 | p.Glu319Gln | missense_variant | 0.16 |
rpoA | 3877557 | c.951C>G | synonymous_variant | 0.17 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.24 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.23 |
rpoA | 3877638 | c.870T>C | synonymous_variant | 0.18 |
rpoA | 3877656 | c.852T>C | synonymous_variant | 0.2 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.15 |
rpoA | 3877704 | c.804G>T | synonymous_variant | 0.17 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.2 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.21 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.21 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.23 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.23 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.22 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.16 |
rpoA | 3877857 | c.651G>A | synonymous_variant | 0.2 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.2 |
rpoA | 3877872 | c.636C>T | synonymous_variant | 0.2 |
rpoA | 3877875 | c.633T>G | synonymous_variant | 0.18 |
rpoA | 3877899 | p.Ser203Thr | missense_variant | 0.15 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.14 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.15 |
rpoA | 3878094 | c.414C>G | synonymous_variant | 0.16 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.16 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.18 |
rpoA | 3878141 | p.Met123Leu | missense_variant | 0.19 |
rpoA | 3878142 | p.Gly122Glu | missense_variant | 0.19 |
rpoA | 3878169 | c.339G>C | synonymous_variant | 0.19 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.15 |
rpoA | 3878220 | c.288C>T | synonymous_variant | 0.14 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.15 |
rpoA | 3878284 | p.Glu75Ala | missense_variant | 0.16 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.16 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.17 |
rpoA | 3878304 | c.204G>C | synonymous_variant | 0.15 |
rpoA | 3878331 | c.177A>G | synonymous_variant | 0.15 |
rpoA | 3878334 | c.174T>C | synonymous_variant | 0.15 |
rpoA | 3878337 | c.171T>C | synonymous_variant | 0.15 |
rpoA | 3878346 | c.162T>C | synonymous_variant | 0.17 |
rpoA | 3878385 | c.123C>G | synonymous_variant | 0.14 |
rpoA | 3878391 | c.117T>C | synonymous_variant | 0.15 |
rpoA | 3878396 | c.112C>T | synonymous_variant | 0.15 |
rpoA | 3878436 | c.72A>G | synonymous_variant | 0.17 |
rpoA | 3878442 | c.66G>C | synonymous_variant | 0.16 |
rpoA | 3878698 | c.-191A>G | upstream_gene_variant | 0.16 |
rpoA | 3878701 | c.-194C>G | upstream_gene_variant | 0.16 |
ddn | 3986648 | c.-196C>G | upstream_gene_variant | 0.16 |
ddn | 3986655 | c.-189A>T | upstream_gene_variant | 0.15 |
clpC1 | 4038244 | p.Thr821Ala | missense_variant | 0.15 |
clpC1 | 4038310 | p.Val799Met | missense_variant | 0.14 |
clpC1 | 4038347 | c.2358G>C | synonymous_variant | 0.16 |
clpC1 | 4038356 | c.2349T>C | synonymous_variant | 0.15 |
clpC1 | 4038359 | c.2346A>G | synonymous_variant | 0.15 |
clpC1 | 4038368 | c.2337T>C | synonymous_variant | 0.15 |
clpC1 | 4038398 | c.2307G>T | synonymous_variant | 0.16 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 0.16 |
clpC1 | 4038434 | c.2271G>C | synonymous_variant | 0.15 |
clpC1 | 4038445 | p.Ala754Thr | missense_variant | 0.13 |
clpC1 | 4038452 | c.2253G>C | synonymous_variant | 0.15 |
clpC1 | 4038461 | p.Ala748Asp | missense_variant | 0.15 |
clpC1 | 4038498 | p.Ser736Thr | missense_variant | 0.17 |
clpC1 | 4038530 | p.Glu725Asp | missense_variant | 0.18 |
clpC1 | 4038536 | c.2169C>T | synonymous_variant | 0.19 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.17 |
clpC1 | 4038623 | c.2082A>G | synonymous_variant | 0.16 |
clpC1 | 4038640 | p.Asp689Asn | missense_variant | 0.15 |
clpC1 | 4038671 | c.2034T>C | synonymous_variant | 0.14 |
clpC1 | 4038695 | c.2010C>G | synonymous_variant | 0.14 |
clpC1 | 4038740 | c.1965G>C | synonymous_variant | 0.16 |
clpC1 | 4038755 | c.1950G>C | synonymous_variant | 0.21 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.2 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.21 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 0.18 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.17 |
clpC1 | 4038815 | c.1890G>T | synonymous_variant | 0.18 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.17 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.17 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.2 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.2 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.2 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.22 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.21 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.22 |
clpC1 | 4039073 | c.1632C>G | synonymous_variant | 0.22 |
clpC1 | 4039085 | c.1620A>G | synonymous_variant | 0.2 |
clpC1 | 4039090 | c.1615C>T | synonymous_variant | 0.18 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.17 |
clpC1 | 4039103 | c.1602T>C | synonymous_variant | 0.17 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.17 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.18 |
clpC1 | 4039127 | c.1578G>A | synonymous_variant | 0.14 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.15 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.16 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.17 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.17 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.17 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.17 |
clpC1 | 4039187 | c.1518G>C | synonymous_variant | 0.17 |
clpC1 | 4039190 | c.1515C>G | synonymous_variant | 0.17 |
clpC1 | 4039208 | c.1497C>G | synonymous_variant | 0.19 |
clpC1 | 4039226 | c.1479T>C | synonymous_variant | 0.2 |
clpC1 | 4039268 | c.1437C>G | synonymous_variant | 0.16 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.18 |
clpC1 | 4039286 | c.1419T>C | synonymous_variant | 0.18 |
clpC1 | 4039289 | c.1416T>C | synonymous_variant | 0.18 |
clpC1 | 4039295 | c.1410A>C | synonymous_variant | 0.18 |
clpC1 | 4039298 | c.1407T>C | synonymous_variant | 0.18 |
clpC1 | 4039319 | c.1386T>C | synonymous_variant | 0.21 |
clpC1 | 4039322 | c.1383T>C | synonymous_variant | 0.2 |
clpC1 | 4039328 | c.1377A>G | synonymous_variant | 0.19 |
clpC1 | 4039334 | c.1371G>C | synonymous_variant | 0.2 |
clpC1 | 4039337 | p.Thr456Gln | missense_variant | 0.21 |
clpC1 | 4039364 | c.1341C>G | synonymous_variant | 0.25 |
clpC1 | 4039388 | c.1317C>A | synonymous_variant | 0.23 |
clpC1 | 4039391 | c.1314T>G | synonymous_variant | 0.23 |
clpC1 | 4039409 | c.1296T>C | synonymous_variant | 0.17 |
clpC1 | 4039412 | c.1293T>G | synonymous_variant | 0.17 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.24 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.23 |
clpC1 | 4039448 | c.1257A>G | synonymous_variant | 0.25 |
clpC1 | 4039454 | c.1251A>G | synonymous_variant | 0.25 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 0.2 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.19 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.19 |
clpC1 | 4039481 | c.1224T>G | synonymous_variant | 0.2 |
clpC1 | 4039484 | c.1221T>G | synonymous_variant | 0.29 |
clpC1 | 4039493 | c.1212C>T | synonymous_variant | 0.26 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.24 |
clpC1 | 4039524 | p.Phe394Tyr | missense_variant | 0.2 |
clpC1 | 4039526 | c.1179G>C | synonymous_variant | 0.18 |
clpC1 | 4039532 | c.1173C>T | synonymous_variant | 0.2 |
clpC1 | 4039547 | c.1158C>G | synonymous_variant | 0.22 |
clpC1 | 4039553 | c.1152C>G | synonymous_variant | 0.23 |
clpC1 | 4039562 | c.1143C>G | synonymous_variant | 0.26 |
clpC1 | 4039576 | p.Ala377Ser | missense_variant | 0.27 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.27 |
clpC1 | 4039586 | c.1119G>C | synonymous_variant | 0.26 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.27 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.26 |
clpC1 | 4039622 | c.1083C>G | synonymous_variant | 0.26 |
clpC1 | 4039682 | c.1023C>G | synonymous_variant | 0.21 |
clpC1 | 4039685 | c.1020C>T | synonymous_variant | 0.23 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.22 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.16 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.16 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.16 |
clpC1 | 4039946 | c.759A>T | synonymous_variant | 0.17 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.17 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.18 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.19 |
clpC1 | 4039996 | p.Glu237Gln | missense_variant | 0.23 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.2 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.2 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.19 |
clpC1 | 4040036 | c.669C>G | synonymous_variant | 0.2 |
clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 0.17 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.16 |
clpC1 | 4040105 | c.600C>G | synonymous_variant | 0.21 |
clpC1 | 4040147 | c.558A>G | synonymous_variant | 0.16 |
clpC1 | 4040153 | c.552A>G | synonymous_variant | 0.16 |
clpC1 | 4040237 | c.468C>T | synonymous_variant | 0.14 |
clpC1 | 4040249 | c.456A>G | synonymous_variant | 0.22 |
clpC1 | 4040264 | c.441C>T | synonymous_variant | 0.24 |
clpC1 | 4040267 | c.438A>G | synonymous_variant | 0.23 |
clpC1 | 4040273 | c.432T>C | synonymous_variant | 0.25 |
clpC1 | 4040354 | c.351A>G | synonymous_variant | 0.23 |
clpC1 | 4040363 | c.342A>C | synonymous_variant | 0.22 |
clpC1 | 4040369 | c.336C>G | synonymous_variant | 0.2 |
clpC1 | 4040380 | c.325T>C | synonymous_variant | 0.16 |
clpC1 | 4040411 | c.294T>C | synonymous_variant | 0.18 |
clpC1 | 4040423 | c.282A>G | synonymous_variant | 0.16 |
clpC1 | 4040426 | c.279T>C | synonymous_variant | 0.16 |
clpC1 | 4040444 | c.261C>G | synonymous_variant | 0.16 |
clpC1 | 4040459 | c.246C>G | synonymous_variant | 0.16 |
clpC1 | 4040465 | c.240T>C | synonymous_variant | 0.17 |
clpC1 | 4040471 | c.234T>C | synonymous_variant | 0.19 |
clpC1 | 4040477 | c.228G>A | synonymous_variant | 0.18 |
clpC1 | 4040480 | c.225T>C | synonymous_variant | 0.18 |
embC | 4240183 | c.321A>G | synonymous_variant | 0.15 |
embC | 4240210 | c.348C>G | synonymous_variant | 0.15 |
embC | 4240514 | p.Val218Met | missense_variant | 0.14 |
embC | 4240543 | c.681G>C | synonymous_variant | 0.18 |
embC | 4240561 | c.699C>G | synonymous_variant | 0.15 |
embC | 4240600 | c.738G>C | synonymous_variant | 0.18 |
embC | 4240654 | c.792C>T | synonymous_variant | 0.13 |
embC | 4240671 | p.Thr270Ile | missense_variant | 0.18 |
embC | 4240678 | c.816T>G | synonymous_variant | 0.19 |
embC | 4240685 | p.Thr275Ala | missense_variant | 0.19 |
embC | 4240693 | c.831T>C | synonymous_variant | 0.2 |
embC | 4240706 | p.Val282Thr | missense_variant | 0.21 |
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 | 0.25 |
embC | 4240789 | c.927T>C | synonymous_variant | 0.27 |
embC | 4240819 | c.957A>G | synonymous_variant | 0.24 |
embC | 4240831 | c.969T>G | synonymous_variant | 0.26 |
embC | 4240867 | c.1005T>G | synonymous_variant | 0.24 |
embC | 4240870 | c.1008T>C | synonymous_variant | 0.23 |
embC | 4240879 | c.1017G>C | synonymous_variant | 0.21 |
embC | 4240880 | p.Ala340Thr | missense_variant | 0.22 |
embC | 4240885 | c.1023T>C | synonymous_variant | 0.22 |
embC | 4240897 | c.1035C>G | synonymous_variant | 0.21 |
embC | 4240900 | c.1038A>G | synonymous_variant | 0.21 |
embC | 4240919 | c.1057_1059delCTCinsTTG | synonymous_variant | 0.16 |
embC | 4241017 | c.1155T>C | synonymous_variant | 0.17 |
embC | 4241023 | c.1161T>G | synonymous_variant | 0.16 |
embC | 4241026 | c.1164C>G | synonymous_variant | 0.17 |
embC | 4241035 | c.1173G>A | synonymous_variant | 0.18 |
embC | 4241104 | c.1242G>A | synonymous_variant | 0.17 |
embC | 4241107 | c.1245G>C | synonymous_variant | 0.16 |
embC | 4241137 | c.1275G>C | synonymous_variant | 0.17 |
embC | 4241140 | c.1278A>G | synonymous_variant | 0.16 |
embC | 4241141 | p.Ile427Val | missense_variant | 0.17 |
embC | 4241158 | c.1296T>C | synonymous_variant | 0.17 |
embC | 4241161 | c.1299C>G | synonymous_variant | 0.15 |
embC | 4241162 | c.1300T>C | synonymous_variant | 0.15 |
embC | 4241443 | c.1581C>G | synonymous_variant | 0.15 |
embC | 4242425 | p.Arg855Gly | missense_variant | 0.36 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 0.99 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4245089 | c.1857G>C | synonymous_variant | 0.14 |
embA | 4245092 | c.1860C>G | synonymous_variant | 0.15 |
embA | 4245101 | c.1869G>C | synonymous_variant | 0.18 |
embA | 4245137 | c.1905T>C | synonymous_variant | 0.22 |
embA | 4245149 | c.1917C>G | synonymous_variant | 0.23 |
embA | 4245182 | c.1950T>C | synonymous_variant | 0.18 |
embA | 4245194 | c.1962G>C | synonymous_variant | 0.16 |
embA | 4245198 | p.Leu656Ile | missense_variant | 0.13 |
embA | 4246329 | p.Thr1033Leu | missense_variant | 0.18 |
embB | 4246355 | c.-159G>C | upstream_gene_variant | 0.24 |
embA | 4246359 | p.Ala1043Pro | missense_variant | 0.22 |
embB | 4246364 | c.-150G>C | upstream_gene_variant | 0.21 |
embB | 4246367 | c.-147C>T | upstream_gene_variant | 0.2 |
embB | 4246373 | c.-141T>C | upstream_gene_variant | 0.2 |
embB | 4246376 | c.-138G>C | upstream_gene_variant | 0.21 |
embB | 4247348 | p.Thr279Ala | missense_variant | 0.14 |
embB | 4247355 | p.Ala281Val | missense_variant | 0.15 |
embB | 4247358 | p.Val282Ala | missense_variant | 0.16 |
embB | 4247365 | c.852A>C | synonymous_variant | 0.18 |
embB | 4247371 | c.858C>G | synonymous_variant | 0.19 |
embB | 4247375 | p.Leu288Val | missense_variant | 0.2 |
embB | 4247386 | c.873T>C | synonymous_variant | 0.21 |
embB | 4247389 | c.876C>G | synonymous_variant | 0.22 |
embB | 4247395 | c.882C>G | synonymous_variant | 0.25 |
embB | 4247401 | c.888T>C | synonymous_variant | 0.27 |
embB | 4247437 | c.924A>G | synonymous_variant | 0.24 |
embB | 4247440 | c.927C>G | synonymous_variant | 0.24 |
embB | 4247464 | c.951C>G | synonymous_variant | 0.21 |
embB | 4247470 | c.957T>C | synonymous_variant | 0.21 |
embB | 4247491 | c.978G>C | synonymous_variant | 0.18 |
embB | 4247500 | c.987C>G | synonymous_variant | 0.16 |
embB | 4247512 | c.999T>C | synonymous_variant | 0.16 |
embB | 4247536 | c.1023C>G | synonymous_variant | 0.17 |
embB | 4247830 | c.1317A>C | synonymous_variant | 0.16 |
embB | 4247836 | c.1323A>G | synonymous_variant | 0.16 |
embB | 4247842 | c.1329T>C | synonymous_variant | 0.16 |
embB | 4248118 | c.1605T>C | synonymous_variant | 0.16 |
embB | 4248127 | c.1614G>C | synonymous_variant | 0.16 |
embB | 4248133 | c.1620C>G | synonymous_variant | 0.18 |
embB | 4248142 | c.1629T>C | synonymous_variant | 0.17 |
embB | 4248143 | c.1630T>C | synonymous_variant | 0.16 |
embB | 4248157 | c.1644A>G | synonymous_variant | 0.18 |
embB | 4248206 | p.Ser565Gly | missense_variant | 0.23 |
embB | 4248220 | c.1707A>G | synonymous_variant | 0.28 |
embB | 4248241 | c.1728C>T | synonymous_variant | 0.32 |
embB | 4248265 | c.1752C>T | synonymous_variant | 0.24 |
embB | 4248266 | c.1753C>T | synonymous_variant | 0.24 |
embB | 4248277 | c.1764G>C | synonymous_variant | 0.23 |
embB | 4248298 | c.1785C>T | synonymous_variant | 0.15 |
embB | 4248304 | c.1791G>C | synonymous_variant | 0.15 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 0.89 |
ubiA | 4269001 | p.Ala278Val | missense_variant | 0.17 |
aftB | 4269006 | c.-170T>C | upstream_gene_variant | 0.16 |
aftB | 4269009 | c.-173A>G | upstream_gene_variant | 0.16 |
aftB | 4269012 | c.-176G>C | upstream_gene_variant | 0.16 |
aftB | 4269033 | c.-197T>C | upstream_gene_variant | 0.18 |
aftB | 4269036 | c.-200C>G | upstream_gene_variant | 0.18 |
aftB | 4269042 | c.-206G>C | upstream_gene_variant | 0.18 |
aftB | 4269183 | c.-347T>C | upstream_gene_variant | 0.22 |
aftB | 4269201 | c.-365A>G | upstream_gene_variant | 0.22 |
ubiA | 4269209 | p.Ser209Ala | missense_variant | 0.22 |
ubiA | 4269220 | p.Ala205Lys | missense_variant | 0.2 |
aftB | 4269222 | c.-386T>G | upstream_gene_variant | 0.19 |
aftB | 4269225 | c.-389C>G | upstream_gene_variant | 0.19 |
aftB | 4269231 | c.-395C>G | upstream_gene_variant | 0.19 |
aftB | 4269234 | c.-398A>G | upstream_gene_variant | 0.19 |
ubiA | 4269243 | p.His197Gln | missense_variant | 0.18 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |