Run ID: ERR6198317
Sample name:
Date: 02-04-2023 01:50:50
Number of reads: 1385489
Percentage reads mapped: 84.96
Strain: La1.2
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
La1 | M.bovis | None | None | 0.99 |
La1.2 | M.bovis | None | None | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
pncA | 2289073 | p.His57Asp | missense_variant | 1.0 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5752 | c.513G>A | synonymous_variant | 1.0 |
gyrB | 6214 | c.975G>C | synonymous_variant | 0.14 |
gyrB | 6238 | c.999G>A | synonymous_variant | 0.16 |
gyrB | 6242 | c.1003_1005delCGCinsAGG | synonymous_variant | 0.16 |
gyrB | 6259 | p.Asp340Glu | missense_variant | 0.14 |
gyrA | 6406 | c.-896C>T | upstream_gene_variant | 1.0 |
gyrB | 6446 | p.Ala403Ser | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 0.98 |
gyrA | 7601 | c.300C>G | synonymous_variant | 0.15 |
gyrA | 7619 | c.318C>G | synonymous_variant | 0.15 |
gyrA | 7622 | c.321C>T | synonymous_variant | 0.15 |
gyrA | 7628 | c.327G>C | synonymous_variant | 0.14 |
gyrA | 7631 | c.330G>C | synonymous_variant | 0.14 |
gyrA | 7652 | c.351C>T | synonymous_variant | 0.14 |
gyrA | 7658 | c.357A>C | synonymous_variant | 0.15 |
gyrA | 7763 | c.462T>G | synonymous_variant | 0.18 |
gyrA | 7770 | p.Asp157His | missense_variant | 0.19 |
gyrA | 7821 | c.520C>T | synonymous_variant | 0.95 |
gyrA | 8285 | c.984C>T | synonymous_variant | 1.0 |
gyrA | 8516 | c.1215T>C | synonymous_variant | 0.15 |
gyrA | 8519 | c.1218A>G | synonymous_variant | 0.16 |
gyrA | 8537 | c.1236G>A | synonymous_variant | 0.14 |
gyrA | 8540 | c.1239C>G | synonymous_variant | 0.15 |
gyrA | 8561 | c.1260A>G | synonymous_variant | 0.19 |
gyrA | 8571 | c.1270C>T | synonymous_variant | 0.21 |
gyrA | 8603 | c.1302A>G | synonymous_variant | 0.24 |
gyrA | 8619 | c.1318T>C | synonymous_variant | 0.28 |
gyrA | 8624 | c.1323G>C | synonymous_variant | 0.27 |
gyrA | 8636 | c.1335A>C | synonymous_variant | 0.32 |
gyrA | 8642 | c.1341A>G | synonymous_variant | 0.3 |
gyrA | 8672 | c.1371A>G | synonymous_variant | 0.3 |
gyrA | 8693 | c.1392T>C | synonymous_variant | 0.32 |
gyrA | 8705 | c.1404C>T | synonymous_variant | 0.26 |
gyrA | 8706 | c.1405C>T | synonymous_variant | 0.18 |
gyrA | 8711 | c.1410A>C | synonymous_variant | 0.18 |
gyrA | 8714 | c.1413A>G | synonymous_variant | 0.18 |
gyrA | 8723 | c.1422G>C | synonymous_variant | 0.18 |
gyrA | 8741 | c.1440C>T | synonymous_variant | 0.95 |
gyrA | 9119 | c.1818A>G | synonymous_variant | 0.15 |
gyrA | 9137 | c.1836C>T | synonymous_variant | 0.16 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9146 | c.1845C>T | synonymous_variant | 0.16 |
gyrA | 9153 | p.Thr618Glu | missense_variant | 0.15 |
gyrA | 9164 | c.1863G>A | synonymous_variant | 0.15 |
gyrA | 9182 | c.1881T>C | synonymous_variant | 0.14 |
gyrA | 9191 | c.1890G>C | synonymous_variant | 0.14 |
gyrA | 9197 | c.1896G>C | synonymous_variant | 0.16 |
gyrA | 9200 | c.1899A>G | synonymous_variant | 0.16 |
gyrA | 9204 | p.Ser635Thr | missense_variant | 0.17 |
gyrA | 9276 | c.1975C>T | synonymous_variant | 0.14 |
gyrA | 9284 | c.1983T>C | synonymous_variant | 0.17 |
gyrA | 9296 | c.1995T>C | synonymous_variant | 0.15 |
gyrA | 9300 | p.Ala667Ser | missense_variant | 0.17 |
gyrA | 9304 | p.Gly668Glu | missense_variant | 1.0 |
gyrA | 9323 | c.2022C>G | synonymous_variant | 0.17 |
gyrA | 9335 | c.2034G>C | synonymous_variant | 0.16 |
gyrA | 9345 | c.2044A>C | synonymous_variant | 0.16 |
gyrA | 9377 | c.2076A>G | synonymous_variant | 0.19 |
gyrA | 9383 | c.2082T>A | synonymous_variant | 0.18 |
gyrA | 9386 | c.2085T>C | synonymous_variant | 0.18 |
gyrA | 9395 | c.2094G>C | synonymous_variant | 0.19 |
gyrA | 9398 | c.2097T>C | synonymous_variant | 0.18 |
gyrA | 9666 | p.Arg789Cys | missense_variant | 0.14 |
fgd1 | 491091 | c.309T>G | synonymous_variant | 0.15 |
fgd1 | 491097 | c.315G>C | synonymous_variant | 0.14 |
fgd1 | 491106 | c.324T>A | synonymous_variant | 0.17 |
fgd1 | 491113 | c.331C>T | synonymous_variant | 0.22 |
fgd1 | 491121 | c.339A>G | synonymous_variant | 0.22 |
fgd1 | 491133 | c.351A>C | synonymous_variant | 0.27 |
fgd1 | 491144 | p.Ala121Asp | missense_variant | 0.29 |
fgd1 | 491166 | c.384G>C | synonymous_variant | 0.26 |
fgd1 | 491178 | c.396G>A | synonymous_variant | 0.22 |
fgd1 | 491181 | c.399T>C | synonymous_variant | 0.22 |
fgd1 | 491191 | p.Gly137Arg | missense_variant | 0.21 |
fgd1 | 491194 | c.412_414delCTAinsTTG | synonymous_variant | 0.2 |
fgd1 | 491203 | p.Gln141Glu | missense_variant | 0.19 |
fgd1 | 491206 | c.424C>T | synonymous_variant | 0.19 |
fgd1 | 491212 | p.Ser144Arg | missense_variant | 0.18 |
fgd1 | 491232 | c.450T>C | synonymous_variant | 0.26 |
fgd1 | 491241 | p.Asp153Glu | missense_variant | 0.26 |
fgd1 | 491244 | c.462T>C | synonymous_variant | 0.26 |
fgd1 | 491250 | c.468G>C | synonymous_variant | 0.26 |
fgd1 | 491259 | c.477T>C | synonymous_variant | 0.27 |
fgd1 | 491313 | c.531C>G | synonymous_variant | 0.22 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576616 | c.1269G>C | synonymous_variant | 0.22 |
ccsA | 619709 | c.-182T>G | upstream_gene_variant | 0.19 |
ccsA | 620412 | c.522T>C | synonymous_variant | 0.15 |
ccsA | 620415 | c.525T>C | synonymous_variant | 0.15 |
ccsA | 620433 | c.543C>G | synonymous_variant | 0.18 |
ccsA | 620436 | c.546T>C | synonymous_variant | 0.19 |
ccsA | 620439 | c.549T>C | synonymous_variant | 0.18 |
ccsA | 620748 | c.858T>C | synonymous_variant | 0.15 |
ccsA | 620760 | c.870C>G | synonymous_variant | 0.14 |
ccsA | 620766 | c.876C>G | synonymous_variant | 0.14 |
rpoB | 760118 | c.312T>C | synonymous_variant | 0.14 |
rpoB | 760130 | p.Asp108Glu | missense_variant | 0.15 |
rpoB | 760139 | c.333A>G | synonymous_variant | 0.14 |
rpoB | 760142 | c.336C>G | synonymous_variant | 0.15 |
rpoB | 760751 | c.945G>C | synonymous_variant | 0.14 |
rpoB | 760763 | c.957C>T | synonymous_variant | 0.16 |
rpoB | 760769 | c.963C>G | synonymous_variant | 0.16 |
rpoB | 760793 | c.987A>G | synonymous_variant | 0.21 |
rpoB | 760805 | c.999G>C | synonymous_variant | 0.28 |
rpoB | 760817 | c.1011A>G | synonymous_variant | 0.17 |
rpoB | 760820 | c.1014T>C | synonymous_variant | 0.17 |
rpoB | 760826 | c.1020C>T | synonymous_variant | 0.21 |
rpoB | 760830 | c.1024T>C | synonymous_variant | 0.32 |
rpoB | 760841 | c.1035T>C | synonymous_variant | 0.32 |
rpoB | 760845 | p.Thr347Ala | missense_variant | 0.33 |
rpoB | 760859 | c.1053T>C | synonymous_variant | 0.26 |
rpoB | 760865 | c.1059C>T | synonymous_variant | 0.26 |
rpoB | 760869 | p.Val355Ile | missense_variant | 0.21 |
rpoB | 760913 | c.1107C>T | synonymous_variant | 0.25 |
rpoB | 760917 | c.1111_1113delCGCinsAGG | synonymous_variant | 0.27 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 0.3 |
rpoB | 760938 | c.1132C>T | synonymous_variant | 0.29 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.24 |
rpoB | 760970 | c.1164G>C | synonymous_variant | 0.21 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.16 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.15 |
rpoB | 761006 | c.1200C>G | synonymous_variant | 0.16 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.19 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.18 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.2 |
rpoB | 761150 | c.1344A>G | synonymous_variant | 0.17 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.14 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.16 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.17 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.14 |
rpoB | 762254 | c.2448T>G | synonymous_variant | 0.17 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.16 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.17 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.17 |
rpoB | 762329 | c.2523G>C | synonymous_variant | 0.15 |
rpoB | 762362 | p.Glu852Asp | missense_variant | 0.15 |
rpoB | 762369 | c.2563T>C | synonymous_variant | 0.16 |
rpoC | 762803 | c.-567C>T | upstream_gene_variant | 0.92 |
rpoC | 762827 | c.-543G>C | upstream_gene_variant | 0.15 |
rpoC | 762836 | c.-534C>T | upstream_gene_variant | 0.25 |
rpoC | 762857 | c.-513C>G | upstream_gene_variant | 0.26 |
rpoC | 762863 | c.-507T>G | upstream_gene_variant | 0.3 |
rpoB | 762868 | p.Tyr1021Phe | missense_variant | 0.26 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.14 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.15 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.15 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.16 |
rpoC | 763900 | c.531G>C | synonymous_variant | 0.17 |
rpoC | 763945 | c.576T>C | synonymous_variant | 0.29 |
rpoC | 763948 | c.579G>C | synonymous_variant | 0.3 |
rpoC | 763951 | c.582G>C | synonymous_variant | 0.3 |
rpoC | 763960 | c.591T>G | synonymous_variant | 0.29 |
rpoC | 763969 | c.600C>T | synonymous_variant | 0.3 |
rpoC | 763978 | c.609C>G | synonymous_variant | 0.28 |
rpoC | 763991 | p.Ile208Leu | missense_variant | 0.24 |
rpoC | 764002 | c.633C>G | synonymous_variant | 0.31 |
rpoC | 764005 | c.636G>C | synonymous_variant | 0.3 |
rpoC | 764024 | c.655T>C | synonymous_variant | 0.3 |
rpoC | 764044 | c.675T>C | synonymous_variant | 0.26 |
rpoC | 764059 | c.690G>C | synonymous_variant | 0.24 |
rpoC | 764116 | c.747C>T | synonymous_variant | 0.19 |
rpoC | 764119 | c.750G>A | synonymous_variant | 0.19 |
rpoC | 764161 | c.792G>C | synonymous_variant | 0.15 |
rpoC | 764278 | c.909A>G | synonymous_variant | 0.14 |
rpoC | 764317 | c.948C>G | synonymous_variant | 0.29 |
rpoC | 764320 | c.951C>G | synonymous_variant | 0.29 |
rpoC | 764326 | c.957G>C | synonymous_variant | 0.31 |
rpoC | 764344 | c.975C>T | synonymous_variant | 0.33 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.31 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 0.19 |
rpoC | 764392 | c.1023C>T | synonymous_variant | 0.14 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.21 |
rpoC | 764410 | c.1041G>C | synonymous_variant | 0.16 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.19 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.16 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.16 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.15 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.14 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.14 |
rpoC | 764500 | c.1131C>G | synonymous_variant | 0.16 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.17 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.27 |
rpoC | 764524 | c.1155C>A | synonymous_variant | 0.27 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.22 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.29 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.28 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.21 |
rpoC | 764576 | c.1207_1208delTCinsAG | synonymous_variant | 0.21 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.24 |
rpoC | 764611 | c.1242G>C | synonymous_variant | 0.23 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.23 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.18 |
rpoC | 764932 | c.1563C>G | synonymous_variant | 0.2 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.17 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.17 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.19 |
rpoC | 765007 | c.1638T>G | synonymous_variant | 0.16 |
rpoC | 765008 | c.1639T>C | synonymous_variant | 0.17 |
rpoC | 765016 | c.1647C>G | synonymous_variant | 0.15 |
rpoC | 765019 | c.1650A>G | synonymous_variant | 0.15 |
rpoC | 765352 | c.1983G>C | synonymous_variant | 0.14 |
rpoC | 765383 | p.Met672Leu | missense_variant | 0.21 |
rpoC | 765398 | c.2029C>T | synonymous_variant | 0.23 |
rpoC | 765404 | p.Leu679Val | missense_variant | 0.21 |
rpoC | 765409 | c.2040T>C | synonymous_variant | 0.2 |
rpoC | 765412 | c.2043T>C | synonymous_variant | 0.23 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.24 |
rpoC | 765451 | c.2082C>T | synonymous_variant | 0.29 |
rpoC | 765469 | c.2100G>C | synonymous_variant | 0.25 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.28 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.24 |
rpoC | 765508 | c.2139C>G | synonymous_variant | 0.25 |
rpoC | 765517 | c.2148C>G | synonymous_variant | 0.24 |
rpoC | 765529 | c.2160C>T | synonymous_variant | 0.24 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.17 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.22 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.24 |
rpoC | 765562 | c.2193G>C | synonymous_variant | 0.24 |
rpoC | 765578 | c.2209C>T | synonymous_variant | 0.24 |
rpoC | 765589 | c.2220G>C | synonymous_variant | 0.23 |
rpoC | 765613 | p.His748Gln | missense_variant | 0.18 |
rpoC | 765625 | c.2256C>G | synonymous_variant | 0.16 |
rpoC | 765628 | c.2259G>C | synonymous_variant | 0.17 |
rpoC | 765631 | p.Asp754Glu | missense_variant | 0.19 |
rpoC | 765688 | c.2319G>A | synonymous_variant | 0.14 |
rpoC | 766363 | c.2994G>C | synonymous_variant | 0.14 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.15 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.21 |
rpoC | 766795 | c.3426C>T | synonymous_variant | 0.23 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.27 |
rpoC | 766843 | c.3474T>C | synonymous_variant | 0.35 |
rpoC | 766861 | c.3492G>T | synonymous_variant | 0.37 |
rpoC | 766864 | c.3495G>C | synonymous_variant | 0.33 |
rpoC | 766883 | p.Ser1172Ala | missense_variant | 0.39 |
rpoC | 766894 | c.3525T>C | synonymous_variant | 0.38 |
rpoC | 766895 | c.3526T>C | synonymous_variant | 0.38 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.36 |
rpoC | 766903 | c.3534C>T | synonymous_variant | 0.38 |
rpoC | 766918 | c.3549C>T | synonymous_variant | 0.43 |
rpoC | 766933 | c.3564A>G | synonymous_variant | 0.38 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.35 |
rpoC | 766972 | c.3603G>C | synonymous_variant | 0.25 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.18 |
rpoC | 767023 | c.3654C>T | synonymous_variant | 0.26 |
rpoC | 767032 | c.3663G>C | synonymous_variant | 0.29 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.18 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.17 |
rpoC | 767065 | c.3696G>C | synonymous_variant | 0.17 |
rpoC | 767095 | c.3726C>T | synonymous_variant | 0.17 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.16 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.16 |
rpoC | 767134 | c.3765C>A | synonymous_variant | 0.15 |
rpoC | 767191 | c.3822C>G | synonymous_variant | 0.15 |
rpoC | 767206 | c.3837C>G | synonymous_variant | 0.18 |
rpoC | 767209 | c.3840T>C | synonymous_variant | 0.15 |
rpoC | 767212 | c.3843G>C | synonymous_variant | 0.18 |
rpoC | 767221 | c.3852C>G | synonymous_variant | 0.16 |
rpoC | 767230 | c.3861G>C | synonymous_variant | 0.17 |
rpoC | 767233 | c.3864T>C | synonymous_variant | 0.18 |
rpoC | 767263 | c.3894T>C | synonymous_variant | 0.14 |
rpoC | 767264 | p.Ala1299Gln | missense_variant | 0.14 |
rpoC | 767302 | c.3933C>G | synonymous_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781595 | c.36T>C | synonymous_variant | 0.14 |
rpsL | 781664 | c.105C>T | synonymous_variant | 0.18 |
rpsL | 781682 | c.123T>C | synonymous_variant | 0.15 |
rpsL | 781718 | c.159C>G | synonymous_variant | 0.19 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.15 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.15 |
rpsL | 781808 | c.249C>T | synonymous_variant | 0.16 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 1.0 |
fbiC | 1303671 | c.741C>T | synonymous_variant | 0.14 |
fbiC | 1303674 | c.744C>G | synonymous_variant | 0.22 |
fbiC | 1303681 | c.751T>C | synonymous_variant | 0.21 |
fbiC | 1303689 | c.759T>C | synonymous_variant | 0.22 |
fbiC | 1303695 | c.765T>C | synonymous_variant | 0.2 |
fbiC | 1303704 | c.774T>C | synonymous_variant | 0.25 |
fbiC | 1303705 | p.Leu259Met | missense_variant | 0.25 |
fbiC | 1303708 | c.778T>C | synonymous_variant | 0.25 |
fbiC | 1303731 | c.801A>G | synonymous_variant | 0.23 |
fbiC | 1303732 | p.Ser268Thr | missense_variant | 0.23 |
fbiC | 1303737 | c.807G>A | synonymous_variant | 0.21 |
fbiC | 1303740 | c.810C>T | synonymous_variant | 0.22 |
fbiC | 1303746 | p.Asp272Glu | missense_variant | 0.18 |
fbiC | 1303749 | c.819G>C | synonymous_variant | 0.17 |
fbiC | 1303752 | c.822A>G | synonymous_variant | 0.19 |
fbiC | 1303755 | c.825T>C | synonymous_variant | 0.19 |
fbiC | 1303788 | c.858T>C | synonymous_variant | 0.17 |
fbiC | 1303789 | p.Ile287Val | missense_variant | 0.16 |
fbiC | 1303846 | p.Phe306Val | missense_variant | 0.27 |
fbiC | 1303854 | c.924T>C | synonymous_variant | 0.28 |
fbiC | 1303857 | c.927C>G | synonymous_variant | 0.28 |
fbiC | 1303860 | c.930A>G | synonymous_variant | 0.27 |
fbiC | 1303866 | p.Glu312Asp | missense_variant | 0.26 |
fbiC | 1303869 | c.939T>C | synonymous_variant | 0.26 |
fbiC | 1303875 | c.945G>C | synonymous_variant | 0.25 |
fbiC | 1303878 | c.948G>A | synonymous_variant | 0.25 |
fbiC | 1303884 | c.954T>G | synonymous_variant | 0.25 |
fbiC | 1303890 | c.960G>C | synonymous_variant | 0.25 |
fbiC | 1303893 | c.963G>C | synonymous_variant | 0.27 |
fbiC | 1303905 | c.975G>C | synonymous_variant | 0.26 |
fbiC | 1303911 | c.981G>C | synonymous_variant | 0.27 |
fbiC | 1303935 | c.1005G>C | synonymous_variant | 0.28 |
fbiC | 1303947 | c.1017T>C | synonymous_variant | 0.25 |
fbiC | 1303948 | p.Gly340Arg | missense_variant | 0.24 |
fbiC | 1303956 | c.1026A>G | synonymous_variant | 0.23 |
fbiC | 1303961 | p.Arg344Leu | missense_variant | 0.25 |
fbiC | 1303971 | c.1041T>C | synonymous_variant | 0.23 |
fbiC | 1303998 | c.1068T>C | synonymous_variant | 0.15 |
fbiC | 1304007 | c.1077G>T | synonymous_variant | 0.14 |
fbiC | 1304019 | c.1089C>T | synonymous_variant | 0.19 |
fbiC | 1304022 | c.1092T>C | synonymous_variant | 0.17 |
fbiC | 1304040 | c.1110C>G | synonymous_variant | 0.19 |
fbiC | 1304856 | c.1926C>G | synonymous_variant | 0.15 |
fbiC | 1304893 | p.Gly655Ser | missense_variant | 0.19 |
fbiC | 1304916 | c.1986T>C | synonymous_variant | 0.15 |
fbiC | 1304919 | c.1989C>G | synonymous_variant | 0.22 |
fbiC | 1304928 | c.1998T>C | synonymous_variant | 0.17 |
fbiC | 1304931 | c.2001C>G | synonymous_variant | 0.22 |
fbiC | 1304934 | c.2004C>A | synonymous_variant | 0.17 |
fbiC | 1304937 | c.2007G>C | synonymous_variant | 0.17 |
fbiC | 1304940 | c.2010A>G | synonymous_variant | 0.16 |
fbiC | 1304952 | c.2022C>T | synonymous_variant | 0.15 |
fbiC | 1304955 | c.2025G>A | synonymous_variant | 0.17 |
fbiC | 1304958 | c.2028T>G | synonymous_variant | 0.15 |
fbiC | 1304991 | c.2061G>C | synonymous_variant | 0.21 |
fbiC | 1304994 | c.2064A>G | synonymous_variant | 0.17 |
fbiC | 1304995 | p.Leu689Glu | missense_variant | 0.17 |
fbiC | 1305006 | p.Glu692Asp | missense_variant | 0.19 |
fbiC | 1305015 | c.2085G>C | synonymous_variant | 0.17 |
fbiC | 1305021 | c.2091C>G | synonymous_variant | 0.15 |
fbiC | 1305033 | c.2103T>C | synonymous_variant | 0.14 |
Rv1258c | 1406663 | c.678C>T | synonymous_variant | 1.0 |
atpE | 1460855 | c.-190T>C | upstream_gene_variant | 0.13 |
atpE | 1461185 | c.141G>C | synonymous_variant | 0.16 |
atpE | 1461197 | c.153A>G | synonymous_variant | 0.16 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1471932 | n.87A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1471969 | n.124T>C | non_coding_transcript_exon_variant | 0.24 |
rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472030 | n.185G>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472031 | n.186G>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472033 | n.188A>G | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472034 | n.189T>C | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472040 | n.195T>C | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473752 | n.95G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473756 | n.99G>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1473813 | n.156C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1473839 | n.182G>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.32 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1473899 | n.242A>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1473943 | n.286G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473974 | n.317T>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474009 | n.352A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474012 | n.355C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474627 | n.970G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474717 | n.1060A>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.18 |
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 | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474952 | n.1296_1300delCATCC | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474961 | n.1304T>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474962 | n.1305T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474963 | n.1306G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474964 | n.1307T>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474967 | n.1311_1315delGGGTG | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474991 | n.1334T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474995 | n.1338T>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475005 | n.1348C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475013 | n.1356G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475027 | n.1370G>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475028 | n.1371G>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475088 | n.1431A>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475369 | n.1712G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475402 | n.1745C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475436 | n.1779C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475619 | n.1962C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475638 | n.1981C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475659 | n.2002G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476089 | n.2432T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476095 | n.2438C>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476117 | n.2460G>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476689 | n.3032A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476690 | n.3033C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476693 | n.3036G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476695 | n.3038T>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476716 | n.3059A>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476723 | n.3066T>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476726 | n.3069A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476732 | n.3075T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476746 | n.3089T>C | non_coding_transcript_exon_variant | 0.17 |
fabG1 | 1673553 | p.Asp38Glu | missense_variant | 0.21 |
inhA | 1674486 | c.285T>C | synonymous_variant | 0.18 |
inhA | 1674489 | c.288G>C | synonymous_variant | 0.16 |
inhA | 1674542 | p.Ala114Glu | missense_variant | 0.19 |
inhA | 1674549 | c.348G>C | synonymous_variant | 0.2 |
inhA | 1674624 | c.423A>T | synonymous_variant | 0.25 |
inhA | 1674627 | c.426T>G | synonymous_variant | 0.25 |
inhA | 1674654 | c.453G>C | synonymous_variant | 0.15 |
rpsA | 1833422 | c.-120G>T | upstream_gene_variant | 1.0 |
rpsA | 1833610 | c.69C>T | synonymous_variant | 0.17 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.21 |
rpsA | 1833664 | c.123C>G | synonymous_variant | 0.21 |
rpsA | 1833667 | c.126C>G | synonymous_variant | 0.2 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.17 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.17 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.24 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.22 |
rpsA | 1833760 | c.219C>T | synonymous_variant | 0.2 |
rpsA | 1833771 | p.Asn77Ser | missense_variant | 0.18 |
rpsA | 1833793 | c.252C>T | synonymous_variant | 0.18 |
rpsA | 1833808 | c.267G>T | synonymous_variant | 0.17 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 0.17 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.17 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.17 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.21 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.26 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.2 |
rpsA | 1833940 | c.399C>G | synonymous_variant | 0.15 |
rpsA | 1834859 | p.Ala440Thr | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102106 | p.Gly313Arg | missense_variant | 1.0 |
ndh | 2103173 | c.-132delG | upstream_gene_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155503 | c.609C>T | synonymous_variant | 1.0 |
katG | 2156025 | c.87C>A | synonymous_variant | 1.0 |
katG | 2156465 | c.-354C>T | upstream_gene_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168011 | p.Ser868Arg | missense_variant | 1.0 |
PPE35 | 2168814 | c.1798dupA | frameshift_variant | 1.0 |
PPE35 | 2170047 | p.Leu189Pro | missense_variant | 0.2 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2518174 | c.60A>G | synonymous_variant | 0.13 |
kasA | 2518183 | c.69G>A | synonymous_variant | 0.13 |
kasA | 2518190 | p.Ser26Ala | missense_variant | 0.16 |
kasA | 2518220 | c.106C>T | synonymous_variant | 0.18 |
kasA | 2518248 | p.Ala45Val | missense_variant | 0.17 |
pepQ | 2860159 | p.Ala87Gly | missense_variant | 0.4 |
Rv2752c | 3064831 | p.Ala454Ser | missense_variant | 0.15 |
Rv2752c | 3064838 | c.1354T>C | synonymous_variant | 0.19 |
Rv2752c | 3064839 | c.1353C>G | synonymous_variant | 0.19 |
Rv2752c | 3064860 | c.1332G>C | synonymous_variant | 0.16 |
Rv2752c | 3065048 | c.1144C>T | synonymous_variant | 0.19 |
Rv2752c | 3065055 | c.1137T>C | synonymous_variant | 0.23 |
Rv2752c | 3065085 | c.1105_1107delAGGinsCGC | synonymous_variant | 0.19 |
Rv2752c | 3065088 | c.1104A>C | synonymous_variant | 0.19 |
Rv2752c | 3065097 | c.1095C>T | synonymous_variant | 0.18 |
Rv2752c | 3065100 | c.1092C>G | synonymous_variant | 0.18 |
Rv2752c | 3065109 | c.1081_1083delAGAinsCGC | synonymous_variant | 0.15 |
Rv2752c | 3065142 | c.1050A>C | synonymous_variant | 0.14 |
Rv2752c | 3065146 | p.Phe349Tyr | missense_variant | 0.15 |
Rv2752c | 3065183 | p.Ser337Ala | missense_variant | 0.14 |
Rv2752c | 3065268 | c.924A>G | synonymous_variant | 0.18 |
Rv2752c | 3065288 | c.904T>C | synonymous_variant | 0.14 |
Rv2752c | 3065295 | p.Gln299Arg | missense_variant | 0.14 |
Rv2752c | 3065298 | p.Asp298Glu | missense_variant | 0.14 |
Rv2752c | 3065306 | p.Ala296Pro | missense_variant | 0.14 |
Rv2752c | 3065311 | p.Thr294Met | missense_variant | 0.14 |
Rv2752c | 3065313 | c.879A>G | synonymous_variant | 0.14 |
Rv2752c | 3065323 | p.Ala290Gly | missense_variant | 0.14 |
Rv2752c | 3065334 | p.Leu286Val | missense_variant | 0.13 |
Rv2752c | 3065355 | c.837A>G | synonymous_variant | 0.13 |
thyX | 3067430 | c.516C>G | synonymous_variant | 0.14 |
thyX | 3067433 | c.513C>G | synonymous_variant | 0.14 |
thyX | 3067676 | c.270C>G | synonymous_variant | 0.13 |
thyX | 3067681 | p.Cys89Arg | missense_variant | 0.17 |
thyX | 3067691 | c.255C>T | synonymous_variant | 0.17 |
thyX | 3067694 | c.252G>C | synonymous_variant | 0.15 |
thyX | 3067721 | c.225T>C | synonymous_variant | 0.15 |
thyX | 3067781 | c.165C>G | synonymous_variant | 0.2 |
thyX | 3067786 | p.Thr54Ala | missense_variant | 0.79 |
thyX | 3067799 | c.147G>A | synonymous_variant | 0.2 |
thyX | 3067802 | c.144C>G | synonymous_variant | 0.19 |
ald | 3086728 | c.-92C>T | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087084 | c.266delA | frameshift_variant | 1.0 |
fbiD | 3339154 | p.Ile13Leu | missense_variant | 1.0 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.8 |
Rv3083 | 3448745 | p.Ile81Ser | missense_variant | 1.0 |
Rv3083 | 3448783 | p.Val94Ile | missense_variant | 1.0 |
fprA | 3473809 | c.-198G>C | upstream_gene_variant | 0.19 |
fprA | 3473812 | c.-195G>A | upstream_gene_variant | 0.19 |
fprA | 3473843 | c.-164C>G | upstream_gene_variant | 0.17 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474427 | p.Val141Ile | missense_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
whiB7 | 3568425 | c.255T>G | synonymous_variant | 0.2 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.19 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.21 |
rpoA | 3878058 | c.450G>C | synonymous_variant | 0.15 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.14 |
rpoA | 3878073 | c.435C>T | synonymous_variant | 0.15 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.16 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.17 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.14 |
rpoA | 3878143 | p.Gly122Asp | missense_variant | 0.16 |
rpoA | 3878157 | c.351C>G | synonymous_variant | 0.19 |
rpoA | 3878163 | c.345C>T | synonymous_variant | 0.16 |
rpoA | 3878169 | c.339G>C | synonymous_variant | 0.19 |
rpoA | 3878175 | c.333G>C | synonymous_variant | 0.15 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.19 |
rpoA | 3878364 | c.144A>C | synonymous_variant | 0.17 |
rpoA | 3878385 | c.123C>G | synonymous_variant | 0.17 |
rpoA | 3878388 | c.120C>G | synonymous_variant | 0.17 |
rpoA | 3878391 | c.117T>C | synonymous_variant | 0.17 |
rpoA | 3878394 | c.114G>C | synonymous_variant | 0.17 |
rpoA | 3878415 | c.93C>T | synonymous_variant | 0.21 |
rpoA | 3878424 | c.84G>T | synonymous_variant | 0.2 |
rpoA | 3878433 | c.75G>C | synonymous_variant | 0.23 |
rpoA | 3878436 | c.72A>G | synonymous_variant | 0.24 |
rpoA | 3878442 | c.66G>C | synonymous_variant | 0.22 |
rpoA | 3878451 | c.57C>G | synonymous_variant | 0.17 |
rpoA | 3878454 | c.54A>C | synonymous_variant | 0.17 |
rpoA | 3878458 | p.Asn17Ser | missense_variant | 0.17 |
rpoA | 3878472 | p.Asp12Glu | missense_variant | 0.17 |
rpoA | 3878478 | c.30C>G | synonymous_variant | 0.18 |
rpoA | 3878484 | c.24C>A | synonymous_variant | 0.2 |
rpoA | 3878630 | c.-124delC | upstream_gene_variant | 1.0 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 1.0 |
clpC1 | 4038499 | p.Ser736Gly | missense_variant | 0.15 |
clpC1 | 4038519 | p.Arg729Gln | missense_variant | 0.15 |
clpC1 | 4038521 | c.2184C>T | synonymous_variant | 0.15 |
clpC1 | 4038530 | p.Glu725Asp | missense_variant | 0.16 |
clpC1 | 4038533 | p.Arg724Lys | missense_variant | 0.16 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.19 |
clpC1 | 4038683 | c.2022T>G | synonymous_variant | 0.15 |
clpC1 | 4038749 | c.1956C>A | synonymous_variant | 0.17 |
clpC1 | 4038755 | c.1950G>C | synonymous_variant | 0.17 |
clpC1 | 4038764 | c.1941C>G | synonymous_variant | 0.18 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.16 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.14 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 0.17 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.15 |
clpC1 | 4038815 | c.1890G>C | synonymous_variant | 0.16 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.21 |
clpC1 | 4038890 | c.1815G>A | synonymous_variant | 0.21 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.18 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.18 |
clpC1 | 4038917 | c.1788C>T | synonymous_variant | 0.18 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 0.24 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.25 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.29 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.22 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.18 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.18 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.2 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.19 |
clpC1 | 4039280 | c.1425G>A | synonymous_variant | 0.16 |
clpC1 | 4039286 | c.1419T>C | synonymous_variant | 0.21 |
clpC1 | 4039292 | c.1413C>T | synonymous_variant | 0.21 |
clpC1 | 4039298 | c.1407T>C | synonymous_variant | 0.21 |
clpC1 | 4039319 | c.1386T>C | synonymous_variant | 0.17 |
clpC1 | 4039322 | c.1383T>A | synonymous_variant | 0.19 |
clpC1 | 4039337 | c.1368A>T | synonymous_variant | 0.15 |
clpC1 | 4039346 | c.1359G>C | synonymous_variant | 0.16 |
clpC1 | 4039355 | c.1350G>C | synonymous_variant | 0.17 |
clpC1 | 4039364 | c.1341C>G | synonymous_variant | 0.15 |
clpC1 | 4039391 | c.1314T>C | synonymous_variant | 0.15 |
clpC1 | 4039439 | c.1266C>T | synonymous_variant | 0.17 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.17 |
clpC1 | 4039454 | c.1251A>G | synonymous_variant | 0.22 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.21 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.22 |
clpC1 | 4039481 | c.1224T>C | synonymous_variant | 0.22 |
clpC1 | 4039484 | c.1221T>C | synonymous_variant | 0.21 |
clpC1 | 4039487 | c.1218G>C | synonymous_variant | 0.21 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.15 |
clpC1 | 4039586 | c.1119G>C | synonymous_variant | 0.19 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.2 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.21 |
clpC1 | 4039622 | c.1083C>T | synonymous_variant | 0.2 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.2 |
clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 0.18 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.17 |
clpC1 | 4040105 | c.600C>G | synonymous_variant | 0.18 |
clpC1 | 4040108 | c.597G>C | synonymous_variant | 0.18 |
clpC1 | 4040126 | c.579C>T | synonymous_variant | 0.15 |
clpC1 | 4040387 | c.318A>G | synonymous_variant | 0.15 |
clpC1 | 4040393 | c.312G>C | synonymous_variant | 0.16 |
clpC1 | 4040411 | c.294T>C | synonymous_variant | 0.18 |
clpC1 | 4040423 | c.282A>G | synonymous_variant | 0.18 |
clpC1 | 4040426 | c.279T>C | synonymous_variant | 0.17 |
clpC1 | 4040431 | c.274T>C | synonymous_variant | 0.15 |
clpC1 | 4040444 | c.261C>T | synonymous_variant | 0.16 |
clpC1 | 4040450 | c.255A>G | synonymous_variant | 0.16 |
clpC1 | 4040459 | c.246C>G | synonymous_variant | 0.18 |
clpC1 | 4040462 | c.243C>G | synonymous_variant | 0.16 |
clpC1 | 4040465 | c.240T>C | synonymous_variant | 0.16 |
clpC1 | 4040471 | c.234T>C | synonymous_variant | 0.16 |
clpC1 | 4040477 | c.228G>A | synonymous_variant | 0.19 |
clpC1 | 4040480 | c.225T>G | synonymous_variant | 0.19 |
embC | 4240409 | p.Pro183Ala | missense_variant | 0.31 |
embC | 4240412 | p.Leu184Val | missense_variant | 0.22 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242970 | c.-263C>T | upstream_gene_variant | 1.0 |
embA | 4244220 | c.988C>T | synonymous_variant | 1.0 |
embA | 4245222 | p.Tyr664Gln | missense_variant | 0.14 |
embB | 4246551 | p.Asn13Ser | missense_variant | 1.0 |
embB | 4246864 | c.351C>T | synonymous_variant | 1.0 |
embB | 4247016 | p.Ser168Trp | missense_variant | 0.28 |
embB | 4247173 | c.660G>A | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4248328 | c.1815G>C | synonymous_variant | 0.19 |
embB | 4249487 | c.2974T>C | synonymous_variant | 0.17 |
embB | 4249498 | c.2985G>C | synonymous_variant | 0.16 |
aftB | 4267858 | p.Ile327Val | missense_variant | 1.0 |
ubiA | 4269209 | p.Ser209Ala | missense_variant | 0.13 |
ubiA | 4269243 | p.His197Gln | missense_variant | 0.14 |
aftB | 4269351 | c.-515C>T | upstream_gene_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |