Run ID: ERR161039
Sample name:
Date: 31-03-2023 14:43:54
Number of reads: 1603519
Percentage reads mapped: 45.0
Strain: lineage4.3.4
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 0.96 |
lineage4.3.4 | Euro-American (LAM) | LAM | RD174 | 1.0 |
lineage1.2.1.2 | Indo-Oceanic | NA | RD239 | 0.05 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6100 | c.861G>C | synonymous_variant | 0.31 |
gyrB | 6109 | c.870G>A | synonymous_variant | 0.39 |
gyrB | 6115 | c.876A>G | synonymous_variant | 0.42 |
gyrB | 6124 | c.885C>A | synonymous_variant | 0.42 |
gyrB | 6127 | c.888G>C | synonymous_variant | 0.45 |
gyrB | 6140 | p.Val301Leu | missense_variant | 0.48 |
gyrB | 6148 | c.909C>T | synonymous_variant | 0.53 |
gyrB | 6169 | c.930C>T | synonymous_variant | 0.55 |
gyrB | 6196 | c.957C>A | synonymous_variant | 0.62 |
gyrB | 6203 | p.Ser322Ala | missense_variant | 0.58 |
gyrB | 6214 | c.975G>A | synonymous_variant | 0.61 |
gyrB | 6223 | c.984G>C | synonymous_variant | 0.58 |
gyrB | 6250 | c.1011A>G | synonymous_variant | 0.63 |
gyrB | 6253 | c.1014G>C | synonymous_variant | 0.64 |
gyrB | 6286 | c.1047T>C | synonymous_variant | 0.62 |
gyrB | 6292 | c.1053G>C | synonymous_variant | 0.61 |
gyrB | 6295 | c.1056A>G | synonymous_variant | 0.62 |
gyrB | 6298 | c.1059C>T | synonymous_variant | 0.63 |
gyrA | 6307 | c.-995T>C | upstream_gene_variant | 0.63 |
gyrA | 6310 | c.-992G>C | upstream_gene_variant | 0.62 |
gyrA | 6331 | c.-971A>G | upstream_gene_variant | 0.64 |
gyrA | 6362 | c.-940T>C | upstream_gene_variant | 0.61 |
gyrA | 6376 | c.-926G>A | upstream_gene_variant | 0.54 |
gyrA | 6382 | c.-920A>G | upstream_gene_variant | 0.52 |
gyrA | 6388 | c.-914T>C | upstream_gene_variant | 0.51 |
gyrA | 6400 | c.-902C>G | upstream_gene_variant | 0.41 |
gyrA | 6403 | c.-899T>C | upstream_gene_variant | 0.38 |
gyrA | 6415 | c.-887G>C | upstream_gene_variant | 0.24 |
gyrA | 6421 | c.-881C>T | upstream_gene_variant | 0.24 |
gyrA | 6427 | c.-875T>C | upstream_gene_variant | 0.18 |
gyrA | 6490 | c.-812T>C | upstream_gene_variant | 0.21 |
gyrA | 6496 | c.-806G>C | upstream_gene_variant | 0.31 |
gyrA | 6499 | c.-803A>C | upstream_gene_variant | 0.33 |
gyrA | 6523 | c.-779G>T | upstream_gene_variant | 0.48 |
gyrA | 6526 | c.-776T>C | upstream_gene_variant | 0.47 |
gyrB | 6531 | p.Ser431Thr | missense_variant | 0.46 |
gyrA | 6547 | c.-755T>C | upstream_gene_variant | 0.44 |
gyrA | 6556 | c.-746C>G | upstream_gene_variant | 0.44 |
gyrA | 6571 | c.-731T>C | upstream_gene_variant | 0.43 |
gyrA | 6577 | c.-725T>C | upstream_gene_variant | 0.42 |
gyrA | 6583 | c.-719G>C | upstream_gene_variant | 0.41 |
gyrA | 6598 | c.-704C>G | upstream_gene_variant | 0.38 |
gyrA | 6610 | c.-692C>G | upstream_gene_variant | 0.19 |
gyrA | 6613 | c.-689A>G | upstream_gene_variant | 0.19 |
gyrA | 6619 | c.-683T>G | upstream_gene_variant | 0.19 |
gyrA | 6622 | c.-680C>T | upstream_gene_variant | 0.21 |
gyrA | 6625 | c.-677G>A | upstream_gene_variant | 0.19 |
gyrA | 6628 | c.-674C>T | upstream_gene_variant | 0.19 |
gyrA | 6634 | c.-668T>C | upstream_gene_variant | 0.21 |
gyrA | 6637 | c.-665T>C | upstream_gene_variant | 0.21 |
gyrA | 6640 | c.-662A>C | upstream_gene_variant | 0.27 |
gyrA | 6649 | c.-653T>G | upstream_gene_variant | 0.36 |
gyrA | 6652 | c.-650C>G | upstream_gene_variant | 0.39 |
gyrA | 6655 | c.-647T>C | upstream_gene_variant | 0.4 |
gyrA | 6670 | c.-632G>C | upstream_gene_variant | 0.54 |
gyrA | 6673 | c.-629A>C | upstream_gene_variant | 0.55 |
gyrA | 6700 | c.-602T>C | upstream_gene_variant | 0.6 |
gyrA | 6709 | c.-593A>G | upstream_gene_variant | 0.6 |
gyrA | 6712 | c.-590G>C | upstream_gene_variant | 0.63 |
gyrA | 6730 | c.-572A>G | upstream_gene_variant | 0.73 |
gyrA | 6733 | c.-569G>A | upstream_gene_variant | 0.75 |
gyrA | 6745 | c.-557T>C | upstream_gene_variant | 0.75 |
gyrA | 6760 | c.-542G>C | upstream_gene_variant | 0.77 |
gyrA | 6775 | c.-527G>C | upstream_gene_variant | 0.72 |
gyrB | 6797 | p.Gly520Ser | missense_variant | 0.68 |
gyrA | 6808 | c.-494C>A | upstream_gene_variant | 0.71 |
gyrA | 6841 | c.-461T>C | upstream_gene_variant | 0.51 |
gyrA | 6844 | c.-458T>C | upstream_gene_variant | 0.5 |
gyrA | 6853 | c.-449A>G | upstream_gene_variant | 0.35 |
gyrA | 6856 | c.-446T>C | upstream_gene_variant | 0.33 |
gyrA | 6859 | c.-443T>C | upstream_gene_variant | 0.31 |
gyrA | 6865 | c.-437G>C | upstream_gene_variant | 0.29 |
gyrA | 6869 | c.-433T>C | upstream_gene_variant | 0.3 |
gyrA | 6872 | c.-430_-428delTTGinsCTC | upstream_gene_variant | 0.31 |
gyrA | 6878 | c.-424T>C | upstream_gene_variant | 0.3 |
gyrA | 6881 | c.-421T>C | upstream_gene_variant | 0.3 |
gyrA | 6898 | c.-404G>C | upstream_gene_variant | 0.36 |
gyrA | 6904 | c.-398C>G | upstream_gene_variant | 0.32 |
gyrA | 6910 | c.-392G>A | upstream_gene_variant | 0.33 |
gyrA | 6925 | c.-377T>C | upstream_gene_variant | 0.38 |
gyrA | 6931 | c.-371A>G | upstream_gene_variant | 0.44 |
gyrA | 6934 | c.-368A>G | upstream_gene_variant | 0.51 |
gyrA | 6949 | c.-353A>G | upstream_gene_variant | 0.53 |
gyrA | 6967 | c.-335T>C | upstream_gene_variant | 0.61 |
gyrA | 6970 | c.-332C>T | upstream_gene_variant | 0.64 |
gyrA | 6976 | c.-326A>G | upstream_gene_variant | 0.67 |
gyrA | 7006 | c.-296T>C | upstream_gene_variant | 0.71 |
gyrA | 7018 | c.-284G>C | upstream_gene_variant | 0.7 |
gyrA | 7033 | c.-269G>C | upstream_gene_variant | 0.64 |
gyrB | 7051 | p.Glu604Asp | missense_variant | 0.63 |
gyrA | 7060 | c.-242T>C | upstream_gene_variant | 0.58 |
gyrA | 7066 | c.-236G>C | upstream_gene_variant | 0.54 |
gyrA | 7078 | c.-224A>G | upstream_gene_variant | 0.41 |
gyrA | 7093 | c.-209T>C | upstream_gene_variant | 0.35 |
gyrA | 7099 | c.-203G>A | upstream_gene_variant | 0.32 |
gyrA | 7108 | c.-194G>A | upstream_gene_variant | 0.31 |
gyrA | 7114 | c.-188C>G | upstream_gene_variant | 0.31 |
gyrA | 7123 | c.-179C>G | upstream_gene_variant | 0.26 |
gyrA | 7129 | c.-173T>C | upstream_gene_variant | 0.23 |
gyrA | 7132 | c.-170T>G | upstream_gene_variant | 0.23 |
gyrA | 7136 | c.-166T>C | upstream_gene_variant | 0.23 |
gyrA | 7141 | c.-161T>C | upstream_gene_variant | 0.23 |
gyrA | 7144 | c.-158A>G | upstream_gene_variant | 0.23 |
gyrA | 7147 | c.-155G>C | upstream_gene_variant | 0.23 |
gyrA | 7150 | c.-152G>C | upstream_gene_variant | 0.25 |
gyrA | 7153 | c.-149G>C | upstream_gene_variant | 0.24 |
gyrA | 7156 | c.-146C>T | upstream_gene_variant | 0.28 |
gyrA | 7178 | c.-124T>C | upstream_gene_variant | 0.42 |
gyrA | 7189 | c.-113C>T | upstream_gene_variant | 0.28 |
gyrA | 7213 | c.-89G>C | upstream_gene_variant | 0.23 |
gyrA | 7216 | c.-86G>T | upstream_gene_variant | 0.23 |
gyrA | 7225 | c.-77T>C | upstream_gene_variant | 0.22 |
gyrA | 7243 | c.-59G>A | upstream_gene_variant | 0.21 |
gyrA | 7246 | c.-56T>C | upstream_gene_variant | 0.21 |
gyrA | 7252 | c.-50G>C | upstream_gene_variant | 0.21 |
gyrA | 7349 | c.48A>G | synonymous_variant | 0.24 |
gyrA | 7355 | c.54T>C | synonymous_variant | 0.31 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7394 | c.93T>C | synonymous_variant | 0.55 |
gyrA | 7415 | c.114C>G | synonymous_variant | 0.53 |
gyrA | 7430 | c.129G>A | synonymous_variant | 0.57 |
gyrA | 7433 | c.132G>A | synonymous_variant | 0.57 |
gyrA | 7442 | c.141G>C | synonymous_variant | 0.59 |
gyrA | 7451 | c.150C>G | synonymous_variant | 0.64 |
gyrA | 7457 | c.156T>C | synonymous_variant | 0.61 |
gyrA | 7469 | c.168C>G | synonymous_variant | 0.65 |
gyrA | 7475 | c.174A>G | synonymous_variant | 0.64 |
gyrA | 7484 | c.183T>C | synonymous_variant | 0.67 |
gyrA | 7490 | c.189C>G | synonymous_variant | 0.68 |
gyrA | 7502 | c.201C>T | synonymous_variant | 0.65 |
gyrA | 7523 | c.222C>G | synonymous_variant | 0.67 |
gyrA | 7526 | c.225G>C | synonymous_variant | 0.66 |
gyrA | 7541 | c.240C>G | synonymous_variant | 0.66 |
gyrA | 7565 | c.264C>T | synonymous_variant | 0.58 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7595 | c.294C>G | synonymous_variant | 0.53 |
gyrA | 7607 | c.306C>G | synonymous_variant | 0.53 |
gyrA | 7622 | c.321C>T | synonymous_variant | 0.49 |
gyrA | 7625 | c.324G>C | synonymous_variant | 0.51 |
gyrA | 7631 | c.330G>C | synonymous_variant | 0.49 |
gyrA | 7655 | c.354G>A | synonymous_variant | 0.46 |
gyrA | 7658 | c.357A>G | synonymous_variant | 0.46 |
gyrA | 7664 | c.363T>C | synonymous_variant | 0.48 |
gyrA | 7670 | c.369A>G | synonymous_variant | 0.52 |
gyrA | 7676 | c.375G>C | synonymous_variant | 0.55 |
gyrA | 7685 | c.384G>A | synonymous_variant | 0.52 |
gyrA | 7688 | c.387C>T | synonymous_variant | 0.55 |
gyrA | 7691 | c.390C>G | synonymous_variant | 0.56 |
gyrA | 7697 | c.396C>G | synonymous_variant | 0.58 |
gyrA | 7706 | c.405C>T | synonymous_variant | 0.53 |
gyrA | 7710 | c.409T>C | synonymous_variant | 0.51 |
gyrA | 7728 | c.427_429delAGGinsCGC | synonymous_variant | 0.43 |
gyrA | 7759 | p.Ile153Thr | missense_variant | 0.49 |
gyrA | 7763 | c.462T>G | synonymous_variant | 0.49 |
gyrA | 7775 | c.474C>G | synonymous_variant | 0.48 |
gyrA | 7784 | c.483A>G | synonymous_variant | 0.52 |
gyrA | 7796 | c.495G>A | synonymous_variant | 0.55 |
gyrA | 7799 | c.498A>G | synonymous_variant | 0.57 |
gyrA | 7832 | c.531G>C | synonymous_variant | 0.56 |
gyrA | 7835 | c.534A>C | synonymous_variant | 0.57 |
gyrA | 7847 | c.546G>C | synonymous_variant | 0.59 |
gyrA | 7859 | c.558A>C | synonymous_variant | 0.51 |
gyrA | 7862 | c.561C>G | synonymous_variant | 0.51 |
gyrA | 7865 | c.564T>C | synonymous_variant | 0.5 |
gyrA | 7886 | c.585T>C | synonymous_variant | 0.39 |
gyrA | 7892 | c.591G>C | synonymous_variant | 0.33 |
gyrA | 8054 | c.753T>C | synonymous_variant | 0.23 |
gyrA | 8057 | c.756A>G | synonymous_variant | 0.26 |
gyrA | 8071 | p.Val257Ala | missense_variant | 0.29 |
gyrA | 8076 | p.Val259Ile | missense_variant | 0.3 |
gyrA | 8084 | c.783G>A | synonymous_variant | 0.39 |
gyrA | 8090 | c.789C>A | synonymous_variant | 0.41 |
gyrA | 8096 | c.795T>G | synonymous_variant | 0.41 |
gyrA | 8099 | c.798T>C | synonymous_variant | 0.42 |
gyrA | 8102 | c.801C>G | synonymous_variant | 0.43 |
gyrA | 8111 | c.810G>C | synonymous_variant | 0.43 |
gyrA | 8156 | c.855T>C | synonymous_variant | 0.37 |
gyrA | 8168 | c.867A>G | synonymous_variant | 0.29 |
gyrA | 8177 | c.876A>C | synonymous_variant | 0.19 |
gyrA | 8253 | p.Ile318Leu | missense_variant | 0.34 |
gyrA | 8264 | c.963T>C | synonymous_variant | 0.38 |
gyrA | 8283 | p.Ile328Leu | missense_variant | 0.51 |
gyrA | 8288 | c.987T>C | synonymous_variant | 0.55 |
gyrA | 8294 | c.993T>C | synonymous_variant | 0.6 |
gyrA | 8324 | c.1023T>C | synonymous_variant | 0.65 |
gyrA | 8339 | c.1038A>G | synonymous_variant | 0.65 |
gyrA | 8342 | c.1041G>C | synonymous_variant | 0.64 |
gyrA | 8372 | c.1071G>A | synonymous_variant | 0.52 |
gyrA | 8375 | c.1074G>C | synonymous_variant | 0.49 |
gyrA | 8378 | c.1077C>T | synonymous_variant | 0.49 |
gyrA | 8391 | p.Tyr364His | missense_variant | 0.51 |
gyrA | 8399 | c.1098T>C | synonymous_variant | 0.44 |
gyrA | 8408 | c.1107A>G | synonymous_variant | 0.41 |
gyrA | 8420 | c.1119T>C | synonymous_variant | 0.4 |
gyrA | 8453 | c.1152A>C | synonymous_variant | 0.33 |
gyrA | 8459 | c.1158G>A | synonymous_variant | 0.29 |
gyrA | 8471 | c.1170T>C | synonymous_variant | 0.24 |
gyrA | 8477 | c.1176C>T | synonymous_variant | 0.2 |
gyrA | 8480 | c.1179C>T | synonymous_variant | 0.19 |
gyrA | 8486 | c.1185T>C | synonymous_variant | 0.18 |
gyrA | 8580 | p.Ile427Val | missense_variant | 0.18 |
gyrA | 8597 | c.1296C>G | synonymous_variant | 0.29 |
gyrA | 8603 | c.1302A>C | synonymous_variant | 0.31 |
gyrA | 8619 | c.1318T>C | synonymous_variant | 0.39 |
gyrA | 8624 | c.1323G>C | synonymous_variant | 0.4 |
gyrA | 8627 | c.1326C>G | synonymous_variant | 0.4 |
gyrA | 8636 | c.1335A>T | synonymous_variant | 0.43 |
gyrA | 8637 | c.1336C>T | synonymous_variant | 0.43 |
gyrA | 8642 | c.1341A>G | synonymous_variant | 0.44 |
gyrA | 8648 | c.1347G>A | synonymous_variant | 0.5 |
gyrA | 8672 | c.1371A>G | synonymous_variant | 0.43 |
gyrA | 8678 | c.1377G>A | synonymous_variant | 0.41 |
gyrA | 8684 | c.1383G>A | synonymous_variant | 0.4 |
gyrA | 8690 | c.1389C>T | synonymous_variant | 0.39 |
gyrA | 8693 | c.1392T>C | synonymous_variant | 0.37 |
gyrA | 8705 | c.1404C>T | synonymous_variant | 0.23 |
gyrA | 8706 | c.1405C>T | synonymous_variant | 0.2 |
gyrA | 8718 | p.Glu473Lys | missense_variant | 0.17 |
gyrA | 8795 | c.1494C>T | synonymous_variant | 0.93 |
gyrA | 8829 | c.1528T>C | synonymous_variant | 0.33 |
gyrA | 8836 | p.Ala512Val | missense_variant | 0.37 |
gyrA | 8840 | c.1539C>G | synonymous_variant | 0.38 |
gyrA | 8852 | c.1551T>C | synonymous_variant | 0.37 |
gyrA | 8858 | c.1557T>C | synonymous_variant | 0.41 |
gyrA | 8870 | c.1569G>C | synonymous_variant | 0.44 |
gyrA | 8897 | c.1596T>C | synonymous_variant | 0.59 |
gyrA | 8903 | c.1602T>C | synonymous_variant | 0.6 |
gyrA | 8915 | c.1614A>G | synonymous_variant | 0.61 |
gyrA | 8918 | c.1617C>G | synonymous_variant | 0.59 |
gyrA | 8930 | c.1629C>G | synonymous_variant | 0.59 |
gyrA | 8933 | c.1632G>C | synonymous_variant | 0.58 |
gyrA | 8936 | c.1635G>A | synonymous_variant | 0.58 |
gyrA | 8939 | c.1638T>C | synonymous_variant | 0.58 |
gyrA | 8942 | c.1641G>C | synonymous_variant | 0.59 |
gyrA | 8978 | c.1677C>T | synonymous_variant | 0.62 |
gyrA | 8987 | c.1686C>G | synonymous_variant | 0.55 |
gyrA | 8990 | c.1689C>G | synonymous_variant | 0.53 |
gyrA | 8996 | c.1695T>C | synonymous_variant | 0.54 |
gyrA | 8998 | p.Leu566Trp | missense_variant | 0.55 |
gyrA | 9014 | c.1713C>G | synonymous_variant | 0.5 |
gyrA | 9023 | c.1722A>C | synonymous_variant | 0.48 |
gyrA | 9029 | c.1728T>G | synonymous_variant | 0.51 |
gyrA | 9056 | c.1755C>G | synonymous_variant | 0.46 |
gyrA | 9059 | c.1758G>A | synonymous_variant | 0.43 |
gyrA | 9062 | c.1761C>T | synonymous_variant | 0.43 |
gyrA | 9065 | c.1764C>G | synonymous_variant | 0.43 |
gyrA | 9074 | c.1773G>A | synonymous_variant | 0.43 |
gyrA | 9089 | c.1788G>C | synonymous_variant | 0.43 |
gyrA | 9101 | c.1800A>G | synonymous_variant | 0.36 |
gyrA | 9104 | c.1803C>G | synonymous_variant | 0.34 |
gyrA | 9110 | c.1809G>A | synonymous_variant | 0.34 |
gyrA | 9113 | c.1812C>T | synonymous_variant | 0.3 |
gyrA | 9119 | c.1818A>G | synonymous_variant | 0.28 |
gyrA | 9167 | c.1866C>T | synonymous_variant | 0.29 |
gyrA | 9182 | c.1881T>C | synonymous_variant | 0.3 |
gyrA | 9191 | c.1890G>T | synonymous_variant | 0.32 |
gyrA | 9204 | p.Ser635Thr | missense_variant | 0.37 |
gyrA | 9212 | c.1911G>C | synonymous_variant | 0.39 |
gyrA | 9227 | c.1926C>G | synonymous_variant | 0.51 |
gyrA | 9230 | c.1929T>C | synonymous_variant | 0.53 |
gyrA | 9236 | c.1935G>C | synonymous_variant | 0.53 |
gyrA | 9242 | c.1941A>G | synonymous_variant | 0.54 |
gyrA | 9252 | p.Val651Ile | missense_variant | 0.5 |
gyrA | 9267 | p.Asn656Gly | missense_variant | 0.38 |
gyrA | 9284 | c.1983T>G | synonymous_variant | 0.29 |
gyrA | 9291 | c.1990C>T | synonymous_variant | 0.29 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9323 | c.2022C>G | synonymous_variant | 0.24 |
gyrA | 9335 | c.2034G>C | synonymous_variant | 0.22 |
gyrA | 9345 | c.2044A>C | synonymous_variant | 0.2 |
gyrA | 9352 | p.Ser684Leu | missense_variant | 0.78 |
gyrA | 9374 | c.2073G>C | synonymous_variant | 0.2 |
gyrA | 9377 | c.2076A>G | synonymous_variant | 0.2 |
gyrA | 9383 | c.2082T>C | synonymous_variant | 0.29 |
gyrA | 9386 | c.2085T>C | synonymous_variant | 0.31 |
gyrA | 9419 | c.2118T>C | synonymous_variant | 0.33 |
gyrA | 9420 | p.Ile707Ala | missense_variant | 0.31 |
gyrA | 9429 | p.Arg710Tyr | missense_variant | 0.31 |
gyrA | 9441 | c.2140C>T | synonymous_variant | 0.36 |
gyrA | 9449 | c.2148C>G | synonymous_variant | 0.38 |
gyrA | 9452 | c.2151G>C | synonymous_variant | 0.38 |
gyrA | 9455 | c.2154T>G | synonymous_variant | 0.37 |
gyrA | 9464 | c.2163C>A | synonymous_variant | 0.35 |
gyrA | 9476 | c.2175G>C | synonymous_variant | 0.34 |
gyrA | 9485 | c.2184A>G | synonymous_variant | 0.18 |
gyrA | 9644 | c.2343T>C | synonymous_variant | 0.26 |
gyrA | 9653 | c.2352C>T | synonymous_variant | 0.33 |
gyrA | 9656 | c.2355C>G | synonymous_variant | 0.33 |
gyrA | 9665 | c.2364A>C | synonymous_variant | 0.36 |
gyrA | 9668 | c.2367C>G | synonymous_variant | 0.4 |
gyrA | 9674 | c.2373T>C | synonymous_variant | 0.42 |
gyrA | 9683 | c.2382G>C | synonymous_variant | 0.45 |
gyrA | 9695 | c.2394C>T | synonymous_variant | 0.41 |
gyrA | 9701 | c.2400T>C | synonymous_variant | 0.45 |
gyrA | 9716 | c.2415T>C | synonymous_variant | 0.35 |
gyrA | 9717 | c.2416C>T | synonymous_variant | 0.35 |
gyrA | 9740 | c.2439G>A | synonymous_variant | 0.27 |
fgd1 | 490869 | c.87C>T | synonymous_variant | 0.17 |
fgd1 | 490875 | c.93C>G | synonymous_variant | 0.2 |
fgd1 | 490890 | c.108C>T | synonymous_variant | 0.25 |
fgd1 | 490899 | c.117C>T | synonymous_variant | 0.27 |
fgd1 | 490905 | c.123T>C | synonymous_variant | 0.27 |
fgd1 | 490911 | c.129T>G | synonymous_variant | 0.27 |
fgd1 | 490917 | c.135C>G | synonymous_variant | 0.31 |
fgd1 | 490921 | p.Gln47Lys | missense_variant | 0.31 |
fgd1 | 490929 | c.147C>G | synonymous_variant | 0.34 |
fgd1 | 490932 | c.150T>C | synonymous_variant | 0.32 |
fgd1 | 490962 | c.180T>C | synonymous_variant | 0.32 |
fgd1 | 490971 | c.189A>G | synonymous_variant | 0.21 |
fgd1 | 490974 | c.192T>C | synonymous_variant | 0.23 |
fgd1 | 490978 | p.Asn66Glu | missense_variant | 0.23 |
fgd1 | 490984 | p.Leu68Ile | missense_variant | 0.26 |
fgd1 | 490987 | p.Leu69Val | missense_variant | 0.27 |
fgd1 | 490998 | c.216T>C | synonymous_variant | 0.28 |
fgd1 | 491007 | c.225G>C | synonymous_variant | 0.23 |
fgd1 | 491013 | c.231C>G | synonymous_variant | 0.2 |
fgd1 | 491016 | c.234C>G | synonymous_variant | 0.21 |
fgd1 | 491022 | c.240C>G | synonymous_variant | 0.21 |
fgd1 | 491106 | c.324T>G | synonymous_variant | 0.24 |
fgd1 | 491113 | c.331C>T | synonymous_variant | 0.29 |
fgd1 | 491121 | c.339A>G | synonymous_variant | 0.33 |
fgd1 | 491133 | c.351A>C | synonymous_variant | 0.39 |
fgd1 | 491142 | c.360C>T | synonymous_variant | 0.39 |
fgd1 | 491144 | p.Ala121Glu | missense_variant | 0.4 |
fgd1 | 491181 | c.399T>C | synonymous_variant | 0.47 |
fgd1 | 491191 | p.Gly137Arg | missense_variant | 0.51 |
fgd1 | 491196 | c.414A>G | synonymous_variant | 0.51 |
fgd1 | 491202 | c.420G>C | synonymous_variant | 0.48 |
fgd1 | 491203 | p.Gln141Glu | missense_variant | 0.48 |
fgd1 | 491212 | p.Ser144Arg | missense_variant | 0.48 |
fgd1 | 491217 | c.435T>C | synonymous_variant | 0.5 |
fgd1 | 491232 | c.450T>C | synonymous_variant | 0.49 |
fgd1 | 491241 | p.Asp153Glu | missense_variant | 0.54 |
fgd1 | 491244 | c.462T>C | synonymous_variant | 0.55 |
fgd1 | 491259 | c.477T>C | synonymous_variant | 0.61 |
fgd1 | 491283 | p.Asp167Glu | missense_variant | 0.59 |
fgd1 | 491286 | c.504G>C | synonymous_variant | 0.6 |
fgd1 | 491295 | c.513C>G | synonymous_variant | 0.6 |
fgd1 | 491310 | c.528C>G | synonymous_variant | 0.62 |
fgd1 | 491313 | c.531C>A | synonymous_variant | 0.63 |
fgd1 | 491331 | c.549G>A | synonymous_variant | 0.64 |
fgd1 | 491340 | c.558C>G | synonymous_variant | 0.61 |
fgd1 | 491343 | c.561C>G | synonymous_variant | 0.6 |
fgd1 | 491349 | c.567T>C | synonymous_variant | 0.6 |
fgd1 | 491364 | c.582T>C | synonymous_variant | 0.47 |
fgd1 | 491388 | c.606C>G | synonymous_variant | 0.38 |
fgd1 | 491409 | c.627G>C | synonymous_variant | 0.21 |
fgd1 | 491472 | c.690A>G | synonymous_variant | 0.29 |
fgd1 | 491484 | c.702C>T | synonymous_variant | 0.35 |
fgd1 | 491508 | c.726A>C | synonymous_variant | 0.39 |
fgd1 | 491509 | p.Leu243Arg | missense_variant | 0.39 |
fgd1 | 491512 | p.Asn244Glu | missense_variant | 0.41 |
fgd1 | 491526 | c.744T>C | synonymous_variant | 0.48 |
fgd1 | 491542 | c.760T>C | synonymous_variant | 0.54 |
fgd1 | 491547 | c.765A>C | synonymous_variant | 0.54 |
fgd1 | 491550 | c.768T>C | synonymous_variant | 0.55 |
fgd1 | 491556 | c.774G>A | synonymous_variant | 0.59 |
fgd1 | 491589 | c.807G>A | synonymous_variant | 0.56 |
fgd1 | 491595 | c.813C>G | synonymous_variant | 0.54 |
fgd1 | 491598 | c.816C>A | synonymous_variant | 0.57 |
fgd1 | 491601 | c.819T>C | synonymous_variant | 0.57 |
fgd1 | 491610 | c.828A>C | synonymous_variant | 0.57 |
fgd1 | 491640 | c.858G>C | synonymous_variant | 0.5 |
fgd1 | 491646 | c.864G>T | synonymous_variant | 0.48 |
fgd1 | 491658 | c.876A>G | synonymous_variant | 0.46 |
fgd1 | 491670 | c.888G>A | synonymous_variant | 0.28 |
fgd1 | 491673 | c.891A>C | synonymous_variant | 0.28 |
fgd1 | 491676 | c.894T>C | synonymous_variant | 0.25 |
fgd1 | 491679 | c.897A>G | synonymous_variant | 0.25 |
fgd1 | 491685 | c.903G>C | synonymous_variant | 0.25 |
fgd1 | 491688 | c.906A>G | synonymous_variant | 0.24 |
fgd1 | 491697 | c.915G>C | synonymous_variant | 0.24 |
fgd1 | 491703 | c.921C>T | synonymous_variant | 0.24 |
fgd1 | 491709 | c.927A>C | synonymous_variant | 0.22 |
mshA | 575629 | c.282A>G | synonymous_variant | 0.26 |
mshA | 575632 | c.285G>C | synonymous_variant | 0.24 |
mshA | 575633 | p.Ala96Thr | missense_variant | 0.25 |
mshA | 575641 | c.294A>G | synonymous_variant | 0.26 |
mshA | 575645 | p.Val100Ile | missense_variant | 0.26 |
mshA | 575659 | c.312A>G | synonymous_variant | 0.34 |
mshA | 575665 | c.318G>T | synonymous_variant | 0.36 |
mshA | 575689 | c.342G>C | synonymous_variant | 0.5 |
mshA | 575695 | c.348C>G | synonymous_variant | 0.44 |
mshA | 575701 | c.354G>A | synonymous_variant | 0.39 |
mshA | 575704 | c.357T>C | synonymous_variant | 0.37 |
mshA | 575705 | c.358T>C | synonymous_variant | 0.38 |
mshA | 575713 | c.366G>A | synonymous_variant | 0.51 |
mshA | 575734 | c.387T>G | synonymous_variant | 0.56 |
mshA | 575737 | c.390T>C | synonymous_variant | 0.54 |
mshA | 575740 | c.393G>C | synonymous_variant | 0.54 |
mshA | 575770 | c.423G>C | synonymous_variant | 0.46 |
mshA | 575771 | p.Val142Ser | missense_variant | 0.45 |
mshA | 575782 | c.435G>C | synonymous_variant | 0.48 |
mshA | 575785 | c.438T>C | synonymous_variant | 0.5 |
mshA | 575812 | c.465C>T | synonymous_variant | 0.53 |
mshA | 575821 | c.474G>C | synonymous_variant | 0.53 |
mshA | 575824 | c.477T>A | synonymous_variant | 0.54 |
mshA | 575842 | c.495G>C | synonymous_variant | 0.57 |
mshA | 575845 | c.498C>G | synonymous_variant | 0.56 |
mshA | 575864 | c.517T>C | synonymous_variant | 0.61 |
mshA | 575878 | c.531A>G | synonymous_variant | 0.65 |
mshA | 575893 | c.546C>G | synonymous_variant | 0.56 |
mshA | 575908 | c.561A>G | synonymous_variant | 0.6 |
mshA | 575920 | c.573C>T | synonymous_variant | 0.62 |
mshA | 575924 | p.Gly193Thr | missense_variant | 0.59 |
mshA | 575932 | c.585G>A | synonymous_variant | 0.47 |
mshA | 575944 | c.597T>C | synonymous_variant | 0.46 |
mshA | 575953 | c.606G>C | synonymous_variant | 0.42 |
mshA | 575965 | c.618C>G | synonymous_variant | 0.43 |
mshA | 575980 | c.633T>C | synonymous_variant | 0.25 |
ccsA | 620247 | p.Leu119Phe | missense_variant | 0.45 |
ccsA | 620249 | p.Ser120Cys | missense_variant | 0.45 |
ccsA | 620256 | c.366C>G | synonymous_variant | 0.44 |
ccsA | 620257 | p.Ile123Val | missense_variant | 0.44 |
ccsA | 620265 | c.375C>G | synonymous_variant | 0.45 |
ccsA | 620269 | p.Val127Ile | missense_variant | 0.45 |
ccsA | 620275 | c.385_387delCTGinsTTA | synonymous_variant | 0.47 |
ccsA | 620283 | c.393T>A | synonymous_variant | 0.51 |
ccsA | 620284 | p.Ala132Pro | missense_variant | 0.51 |
ccsA | 620288 | p.Arg133Gln | missense_variant | 0.51 |
ccsA | 620307 | c.417C>T | synonymous_variant | 0.56 |
ccsA | 620317 | p.Val143Leu | missense_variant | 0.35 |
ccsA | 620331 | c.441C>T | synonymous_variant | 0.21 |
ccsA | 620332 | c.442C>T | synonymous_variant | 0.21 |
ccsA | 620337 | c.447C>G | synonymous_variant | 0.21 |
ccsA | 620340 | c.450C>G | synonymous_variant | 0.21 |
ccsA | 620349 | c.459A>G | synonymous_variant | 0.24 |
ccsA | 620367 | c.477T>C | synonymous_variant | 0.35 |
ccsA | 620373 | c.483C>G | synonymous_variant | 0.43 |
ccsA | 620388 | c.498A>G | synonymous_variant | 0.45 |
ccsA | 620404 | c.514C>T | synonymous_variant | 0.48 |
ccsA | 620412 | c.522T>C | synonymous_variant | 0.44 |
ccsA | 620415 | c.525T>C | synonymous_variant | 0.47 |
ccsA | 620418 | c.528G>C | synonymous_variant | 0.5 |
ccsA | 620439 | c.549T>G | synonymous_variant | 0.57 |
ccsA | 620445 | c.555A>G | synonymous_variant | 0.53 |
ccsA | 620457 | c.567C>G | synonymous_variant | 0.51 |
ccsA | 620460 | c.570T>C | synonymous_variant | 0.49 |
ccsA | 620481 | c.591T>G | synonymous_variant | 0.29 |
ccsA | 620482 | p.Val198Leu | missense_variant | 0.25 |
ccsA | 620487 | c.597C>G | synonymous_variant | 0.24 |
ccsA | 620490 | c.600A>G | synonymous_variant | 0.25 |
ccsA | 620502 | c.612T>C | synonymous_variant | 0.2 |
ccsA | 620589 | c.699G>A | synonymous_variant | 0.3 |
ccsA | 620597 | p.Ala236Gly | missense_variant | 0.3 |
ccsA | 620604 | c.714C>G | synonymous_variant | 0.28 |
ccsA | 620607 | c.717T>C | synonymous_variant | 0.34 |
ccsA | 620613 | c.723C>T | synonymous_variant | 0.5 |
ccsA | 620634 | c.744C>G | synonymous_variant | 0.54 |
ccsA | 620647 | p.Glu253Gln | missense_variant | 0.53 |
ccsA | 620652 | c.762C>A | synonymous_variant | 0.51 |
ccsA | 620658 | c.768C>T | synonymous_variant | 0.5 |
ccsA | 620661 | c.771C>G | synonymous_variant | 0.5 |
ccsA | 620670 | c.780C>A | synonymous_variant | 0.49 |
ccsA | 620682 | c.792G>A | synonymous_variant | 0.44 |
ccsA | 620692 | p.Ser268Ala | missense_variant | 0.44 |
ccsA | 620698 | p.Val270Ile | missense_variant | 0.4 |
ccsA | 620707 | p.Val273Met | missense_variant | 0.25 |
ccsA | 620748 | c.858T>A | synonymous_variant | 0.36 |
ccsA | 620752 | p.Arg288Gly | missense_variant | 0.4 |
ccsA | 620758 | c.868_870delCGCinsAGA | synonymous_variant | 0.38 |
ccsA | 620778 | c.888T>C | synonymous_variant | 0.48 |
ccsA | 620780 | p.Val297Ala | missense_variant | 0.48 |
ccsA | 620787 | c.897C>A | synonymous_variant | 0.43 |
ccsA | 620796 | c.906C>A | synonymous_variant | 0.38 |
ccsA | 620808 | c.918T>C | synonymous_variant | 0.37 |
ccsA | 620832 | c.942C>T | synonymous_variant | 0.35 |
ccsA | 620835 | c.945C>G | synonymous_variant | 0.31 |
ccsA | 620847 | c.957G>A | synonymous_variant | 0.21 |
ccsA | 620856 | c.966C>T | synonymous_variant | 0.17 |
rpoB | 759616 | c.-191C>T | upstream_gene_variant | 0.36 |
rpoB | 759621 | c.-186C>T | upstream_gene_variant | 0.38 |
rpoB | 759643 | c.-164T>C | upstream_gene_variant | 0.34 |
rpoB | 759647 | c.-160T>C | upstream_gene_variant | 0.34 |
rpoB | 759671 | c.-136G>C | upstream_gene_variant | 0.29 |
rpoB | 759672 | c.-135G>A | upstream_gene_variant | 0.29 |
rpoB | 759674 | c.-133T>C | upstream_gene_variant | 0.29 |
rpoB | 759678 | c.-129T>C | upstream_gene_variant | 0.31 |
rpoB | 760070 | c.264T>G | synonymous_variant | 0.3 |
rpoB | 760091 | c.285G>C | synonymous_variant | 0.39 |
rpoB | 760101 | c.295T>C | synonymous_variant | 0.48 |
rpoB | 760106 | c.300G>C | synonymous_variant | 0.48 |
rpoB | 760112 | c.306T>C | synonymous_variant | 0.5 |
rpoB | 760118 | c.312T>A | synonymous_variant | 0.52 |
rpoB | 760121 | c.315T>G | synonymous_variant | 0.59 |
rpoB | 760130 | p.Asp108Glu | missense_variant | 0.61 |
rpoB | 760139 | c.333A>C | synonymous_variant | 0.61 |
rpoB | 760172 | c.366G>C | synonymous_variant | 0.61 |
rpoB | 760181 | c.375T>C | synonymous_variant | 0.62 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.62 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.63 |
rpoB | 760253 | c.447T>C | synonymous_variant | 0.61 |
rpoB | 760307 | c.501T>C | synonymous_variant | 0.62 |
rpoB | 760310 | c.504G>T | synonymous_variant | 0.6 |
rpoB | 760328 | c.522G>C | synonymous_variant | 0.59 |
rpoB | 760331 | c.525G>C | synonymous_variant | 0.57 |
rpoB | 760337 | c.531C>G | synonymous_variant | 0.51 |
rpoB | 760340 | c.534G>C | synonymous_variant | 0.54 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.58 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.6 |
rpoB | 760388 | c.582C>T | synonymous_variant | 0.52 |
rpoB | 760389 | c.583_584delAGinsTC | synonymous_variant | 0.49 |
rpoB | 760415 | c.609C>T | synonymous_variant | 0.6 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.58 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.6 |
rpoB | 760457 | c.651C>T | synonymous_variant | 0.56 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.49 |
rpoB | 760481 | c.675G>T | synonymous_variant | 0.51 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.52 |
rpoB | 760490 | c.684C>G | synonymous_variant | 0.52 |
rpoB | 760522 | p.Ser239Asn | missense_variant | 0.52 |
rpoB | 760532 | c.726T>C | synonymous_variant | 0.48 |
rpoB | 760533 | p.Val243Ser | missense_variant | 0.48 |
rpoB | 760547 | c.741G>C | synonymous_variant | 0.52 |
rpoB | 760563 | p.Arg253Met | missense_variant | 0.56 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.56 |
rpoB | 760611 | c.805T>C | synonymous_variant | 0.51 |
rpoB | 760634 | c.828T>C | synonymous_variant | 0.57 |
rpoB | 760643 | c.837G>A | synonymous_variant | 0.56 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.58 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.58 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.58 |
rpoB | 760670 | c.864G>C | synonymous_variant | 0.58 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.58 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.56 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.56 |
rpoB | 760710 | c.904C>T | synonymous_variant | 0.49 |
rpoB | 760715 | c.909C>T | synonymous_variant | 0.47 |
rpoB | 760724 | c.918T>C | synonymous_variant | 0.39 |
rpoB | 760730 | c.924T>C | synonymous_variant | 0.3 |
rpoB | 760745 | c.939G>A | synonymous_variant | 0.17 |
rpoB | 760796 | c.990A>G | synonymous_variant | 0.28 |
rpoB | 760802 | c.996C>G | synonymous_variant | 0.33 |
rpoB | 760805 | c.999G>C | synonymous_variant | 0.37 |
rpoB | 760817 | c.1011A>G | synonymous_variant | 0.45 |
rpoB | 760820 | c.1014T>C | synonymous_variant | 0.46 |
rpoB | 760826 | c.1020C>G | synonymous_variant | 0.5 |
rpoB | 760830 | c.1024T>C | synonymous_variant | 0.52 |
rpoB | 760841 | c.1035T>C | synonymous_variant | 0.61 |
rpoB | 760845 | p.Thr347Ala | missense_variant | 0.62 |
rpoB | 760859 | c.1053T>C | synonymous_variant | 0.63 |
rpoB | 760862 | c.1056G>C | synonymous_variant | 0.64 |
rpoB | 760886 | c.1080A>G | synonymous_variant | 0.63 |
rpoB | 760916 | c.1110C>T | synonymous_variant | 0.59 |
rpoB | 760919 | c.1113C>G | synonymous_variant | 0.59 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.58 |
rpoB | 760934 | c.1128C>T | synonymous_variant | 0.6 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.59 |
rpoB | 760970 | c.1164G>C | synonymous_variant | 0.6 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.6 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.59 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.56 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.56 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.56 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.54 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.6 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.59 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.59 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 0.42 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.42 |
rpoB | 761150 | c.1344A>G | synonymous_variant | 0.4 |
rpoB | 761153 | c.1347G>C | synonymous_variant | 0.38 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.41 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.41 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.35 |
rpoB | 761183 | c.1377T>C | synonymous_variant | 0.36 |
rpoB | 761189 | c.1383T>G | synonymous_variant | 0.37 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.47 |
rpoB | 761204 | c.1398C>G | synonymous_variant | 0.53 |
rpoB | 761217 | p.Pro471Ser | missense_variant | 0.59 |
rpoB | 761222 | c.1416G>C | synonymous_variant | 0.64 |
rpoB | 761240 | c.1434C>T | synonymous_variant | 0.66 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.63 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.6 |
rpoB | 761258 | c.1452G>A | synonymous_variant | 0.6 |
rpoB | 761261 | c.1455G>C | synonymous_variant | 0.58 |
rpoB | 761264 | c.1458C>G | synonymous_variant | 0.58 |
rpoB | 761273 | c.1467T>C | synonymous_variant | 0.6 |
rpoB | 761282 | c.1476C>G | synonymous_variant | 0.58 |
rpoB | 761345 | c.1539G>T | synonymous_variant | 0.53 |
rpoB | 761346 | p.Val514Arg | missense_variant | 0.54 |
rpoB | 761357 | c.1551G>C | synonymous_variant | 0.56 |
rpoB | 761362 | p.Ser519Thr | missense_variant | 0.56 |
rpoB | 761374 | p.Val523Glu | missense_variant | 0.54 |
rpoB | 761396 | c.1590G>A | synonymous_variant | 0.52 |
rpoB | 761408 | c.1602G>C | synonymous_variant | 0.4 |
rpoB | 761411 | c.1605G>C | synonymous_variant | 0.37 |
rpoB | 761414 | c.1608A>G | synonymous_variant | 0.36 |
rpoB | 761423 | c.1617T>C | synonymous_variant | 0.34 |
rpoB | 761447 | c.1641C>G | synonymous_variant | 0.21 |
rpoB | 761451 | p.Val549Thr | missense_variant | 0.21 |
rpoB | 761471 | c.1665C>G | synonymous_variant | 0.29 |
rpoB | 761483 | c.1677G>C | synonymous_variant | 0.26 |
rpoB | 761492 | c.1686G>C | synonymous_variant | 0.29 |
rpoB | 761501 | c.1695G>C | synonymous_variant | 0.29 |
rpoB | 761502 | p.Pro566Ser | missense_variant | 0.29 |
rpoB | 761510 | c.1704T>G | synonymous_variant | 0.38 |
rpoB | 761528 | c.1722C>T | synonymous_variant | 0.44 |
rpoB | 761531 | c.1725C>G | synonymous_variant | 0.43 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.43 |
rpoB | 761549 | c.1743G>T | synonymous_variant | 0.52 |
rpoB | 761564 | c.1758G>C | synonymous_variant | 0.49 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.47 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.46 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.5 |
rpoB | 761600 | c.1794T>C | synonymous_variant | 0.52 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.53 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.58 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.58 |
rpoB | 761645 | c.1839C>G | synonymous_variant | 0.47 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.49 |
rpoB | 761651 | c.1845C>T | synonymous_variant | 0.45 |
rpoB | 761655 | p.Ala617Arg | missense_variant | 0.47 |
rpoB | 761675 | c.1869G>C | synonymous_variant | 0.52 |
rpoB | 761687 | c.1881C>T | synonymous_variant | 0.5 |
rpoB | 761690 | c.1884G>C | synonymous_variant | 0.5 |
rpoB | 761693 | c.1887G>C | synonymous_variant | 0.51 |
rpoB | 761723 | p.Glu639Asp | missense_variant | 0.48 |
rpoB | 761724 | p.Glu640Gln | missense_variant | 0.48 |
rpoB | 761732 | c.1926C>T | synonymous_variant | 0.51 |
rpoB | 761750 | c.1944G>C | synonymous_variant | 0.6 |
rpoB | 761765 | c.1959T>C | synonymous_variant | 0.63 |
rpoB | 761778 | p.Asn658Asp | missense_variant | 0.64 |
rpoB | 761791 | p.Arg662His | missense_variant | 0.58 |
rpoB | 761813 | c.2007T>C | synonymous_variant | 0.56 |
rpoB | 761819 | c.2013G>C | synonymous_variant | 0.56 |
rpoB | 761834 | c.2028T>C | synonymous_variant | 0.54 |
rpoB | 761847 | p.Cys681Arg | missense_variant | 0.52 |
rpoB | 761852 | c.2046C>G | synonymous_variant | 0.5 |
rpoB | 761858 | c.2052G>C | synonymous_variant | 0.49 |
rpoB | 761864 | c.2058G>C | synonymous_variant | 0.44 |
rpoB | 761870 | p.Asp688Glu | missense_variant | 0.45 |
rpoB | 761873 | c.2067A>G | synonymous_variant | 0.45 |
rpoB | 761882 | c.2076C>G | synonymous_variant | 0.47 |
rpoB | 761885 | c.2079T>C | synonymous_variant | 0.53 |
rpoB | 761888 | c.2082G>A | synonymous_variant | 0.55 |
rpoB | 761909 | c.2103T>C | synonymous_variant | 0.59 |
rpoB | 761912 | c.2106T>G | synonymous_variant | 0.54 |
rpoB | 761916 | p.Asp704Gln | missense_variant | 0.51 |
rpoB | 761921 | c.2115C>T | synonymous_variant | 0.51 |
rpoB | 761948 | c.2142G>A | synonymous_variant | 0.51 |
rpoB | 761951 | c.2145G>C | synonymous_variant | 0.53 |
rpoB | 761954 | c.2148C>G | synonymous_variant | 0.57 |
rpoB | 762008 | c.2202C>G | synonymous_variant | 0.59 |
rpoB | 762017 | c.2211A>G | synonymous_variant | 0.65 |
rpoB | 762024 | p.Val740Ile | missense_variant | 0.61 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.67 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.59 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.58 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.56 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.59 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.61 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.65 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 0.61 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.59 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.59 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.66 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.61 |
rpoB | 762233 | c.2427G>T | synonymous_variant | 0.69 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.69 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.68 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.75 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.71 |
rpoB | 762296 | c.2490G>A | synonymous_variant | 0.71 |
rpoB | 762305 | c.2499G>T | synonymous_variant | 0.7 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.65 |
rpoB | 762329 | c.2523G>C | synonymous_variant | 0.63 |
rpoB | 762338 | c.2532T>C | synonymous_variant | 0.66 |
rpoB | 762347 | c.2541T>C | synonymous_variant | 0.6 |
rpoB | 762362 | p.Glu852Asp | missense_variant | 0.64 |
rpoB | 762369 | c.2563T>C | synonymous_variant | 0.59 |
rpoC | 762380 | c.-990T>C | upstream_gene_variant | 0.55 |
rpoC | 762389 | c.-981G>A | upstream_gene_variant | 0.58 |
rpoC | 762395 | c.-975G>C | upstream_gene_variant | 0.56 |
rpoC | 762398 | c.-972T>C | upstream_gene_variant | 0.56 |
rpoC | 762401 | c.-969G>C | upstream_gene_variant | 0.59 |
rpoC | 762410 | c.-960T>C | upstream_gene_variant | 0.56 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 0.52 |
rpoC | 762434 | c.-936T>C | upstream_gene_variant | 0.51 |
rpoC | 762449 | c.-921C>A | upstream_gene_variant | 0.51 |
rpoC | 762452 | c.-918G>A | upstream_gene_variant | 0.52 |
rpoC | 762467 | c.-903C>T | upstream_gene_variant | 0.54 |
rpoC | 762491 | c.-879T>C | upstream_gene_variant | 0.55 |
rpoC | 762509 | c.-861T>G | upstream_gene_variant | 0.54 |
rpoB | 762510 | p.Ala902Pro | missense_variant | 0.54 |
rpoC | 762521 | c.-849C>T | upstream_gene_variant | 0.6 |
rpoC | 762533 | c.-837T>C | upstream_gene_variant | 0.54 |
rpoC | 762536 | c.-834T>C | upstream_gene_variant | 0.53 |
rpoC | 762537 | c.-833T>C | upstream_gene_variant | 0.53 |
rpoC | 762545 | c.-825C>G | upstream_gene_variant | 0.52 |
rpoC | 762551 | c.-819C>T | upstream_gene_variant | 0.52 |
rpoC | 762581 | c.-789T>C | upstream_gene_variant | 0.41 |
rpoC | 762582 | c.-788T>C | upstream_gene_variant | 0.4 |
rpoC | 762587 | c.-783G>A | upstream_gene_variant | 0.4 |
rpoC | 762599 | c.-771T>C | upstream_gene_variant | 0.38 |
rpoC | 762605 | c.-765T>C | upstream_gene_variant | 0.33 |
rpoC | 762608 | c.-762C>G | upstream_gene_variant | 0.32 |
rpoC | 762734 | c.-636G>A | upstream_gene_variant | 0.3 |
rpoB | 762759 | p.Cys985Ala | missense_variant | 0.42 |
rpoC | 762782 | c.-588T>C | upstream_gene_variant | 0.47 |
rpoC | 762785 | c.-585C>T | upstream_gene_variant | 0.51 |
rpoB | 762799 | p.Ala998Gly | missense_variant | 0.55 |
rpoC | 762812 | c.-558C>G | upstream_gene_variant | 0.52 |
rpoB | 762815 | p.Met1003Ile | missense_variant | 0.49 |
rpoC | 762818 | c.-552C>G | upstream_gene_variant | 0.48 |
rpoB | 762820 | p.Phe1005Tyr | missense_variant | 0.48 |
rpoC | 762831 | c.-539_-538delAGinsTC | upstream_gene_variant | 0.47 |
rpoC | 762836 | c.-534C>T | upstream_gene_variant | 0.47 |
rpoB | 762856 | c.3050_3051insGAC | disruptive_inframe_insertion | 0.53 |
rpoB | 762860 | c.3056_3058delTTG | disruptive_inframe_deletion | 0.48 |
rpoC | 762890 | c.-480C>T | upstream_gene_variant | 0.57 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.56 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.62 |
rpoC | 762995 | c.-375G>C | upstream_gene_variant | 0.62 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.71 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 0.73 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.71 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.74 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.67 |
rpoC | 763115 | c.-255T>G | upstream_gene_variant | 0.55 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.54 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.59 |
rpoC | 763169 | c.-201A>G | upstream_gene_variant | 0.61 |
rpoC | 763193 | c.-177C>G | upstream_gene_variant | 0.67 |
rpoC | 763202 | c.-168A>C | upstream_gene_variant | 0.61 |
rpoC | 763205 | c.-165G>C | upstream_gene_variant | 0.64 |
rpoC | 763208 | c.-162T>C | upstream_gene_variant | 0.65 |
rpoC | 763214 | c.-156T>C | upstream_gene_variant | 0.64 |
rpoC | 763226 | c.-144A>G | upstream_gene_variant | 0.63 |
rpoB | 763227 | p.Leu1141Met | missense_variant | 0.62 |
rpoB | 763235 | p.Glu1143Asp | missense_variant | 0.61 |
rpoC | 763238 | c.-132T>C | upstream_gene_variant | 0.58 |
rpoB | 763241 | p.Glu1145Asp | missense_variant | 0.6 |
rpoC | 763259 | c.-111G>C | upstream_gene_variant | 0.38 |
rpoC | 763262 | c.-108C>T | upstream_gene_variant | 0.34 |
rpoC | 763268 | c.-102C>G | upstream_gene_variant | 0.31 |
rpoC | 763375 | c.6C>A | synonymous_variant | 0.19 |
rpoC | 763402 | c.33C>G | synonymous_variant | 0.29 |
rpoC | 763408 | c.39T>C | synonymous_variant | 0.3 |
rpoC | 763409 | c.40_42delCTTinsTTG | synonymous_variant | 0.3 |
rpoC | 763414 | c.45T>C | synonymous_variant | 0.33 |
rpoC | 763420 | c.51G>C | synonymous_variant | 0.38 |
rpoC | 763423 | p.Glu18Asp | missense_variant | 0.42 |
rpoC | 763430 | c.61A>C | synonymous_variant | 0.42 |
rpoC | 763435 | c.66A>G | synonymous_variant | 0.49 |
rpoC | 763441 | c.72C>G | synonymous_variant | 0.52 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.55 |
rpoC | 763453 | c.84C>G | synonymous_variant | 0.62 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.64 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.68 |
rpoC | 763483 | c.114G>A | synonymous_variant | 0.68 |
rpoC | 763484 | c.115_117delCTTinsTTG | synonymous_variant | 0.68 |
rpoC | 763492 | c.123G>C | synonymous_variant | 0.7 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.66 |
rpoC | 763531 | c.162G>C | synonymous_variant | 0.64 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.59 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.68 |
rpoC | 763621 | c.252C>T | synonymous_variant | 0.73 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.74 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.76 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.69 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.68 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.66 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.65 |
rpoC | 763702 | c.333C>T | synonymous_variant | 0.62 |
rpoC | 763708 | c.339G>T | synonymous_variant | 0.56 |
rpoC | 763709 | c.340C>T | synonymous_variant | 0.56 |
rpoC | 763714 | c.345G>A | synonymous_variant | 0.57 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.57 |
rpoC | 763720 | c.351G>C | synonymous_variant | 0.57 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.64 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.64 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.64 |
rpoC | 763765 | c.396T>G | synonymous_variant | 0.63 |
rpoC | 763768 | c.399C>G | synonymous_variant | 0.62 |
rpoC | 763771 | c.402C>T | synonymous_variant | 0.63 |
rpoC | 763780 | c.411C>G | synonymous_variant | 0.6 |
rpoC | 763783 | c.414G>C | synonymous_variant | 0.57 |
rpoC | 763801 | c.432C>G | synonymous_variant | 0.5 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.49 |
rpoC | 763813 | c.444C>G | synonymous_variant | 0.49 |
rpoC | 763831 | c.462A>G | synonymous_variant | 0.43 |
rpoC | 763835 | p.Ala156Thr | missense_variant | 0.38 |
rpoC | 763852 | c.483C>G | synonymous_variant | 0.29 |
rpoC | 763858 | c.489A>G | synonymous_variant | 0.29 |
rpoC | 763872 | p.Gly168Ala | missense_variant | 0.35 |
rpoC | 763876 | p.Glu169Asp | missense_variant | 0.37 |
rpoC | 763879 | c.510A>C | synonymous_variant | 0.37 |
rpoC | 763885 | c.516C>G | synonymous_variant | 0.38 |
rpoC | 763888 | c.519G>T | synonymous_variant | 0.4 |
rpoC | 763894 | c.525A>G | synonymous_variant | 0.43 |
rpoC | 763903 | c.534G>A | synonymous_variant | 0.49 |
rpoC | 763921 | c.552G>C | synonymous_variant | 0.59 |
rpoC | 763939 | c.570G>A | synonymous_variant | 0.62 |
rpoC | 763978 | c.609C>G | synonymous_variant | 0.61 |
rpoC | 763987 | c.618C>T | synonymous_variant | 0.62 |
rpoC | 763996 | c.627T>C | synonymous_variant | 0.6 |
rpoC | 764002 | c.633C>G | synonymous_variant | 0.6 |
rpoC | 764011 | c.642T>C | synonymous_variant | 0.59 |
rpoC | 764024 | c.655T>C | synonymous_variant | 0.52 |
rpoC | 764040 | p.Ser224Asn | missense_variant | 0.55 |
rpoC | 764044 | c.675T>C | synonymous_variant | 0.56 |
rpoC | 764059 | c.690G>C | synonymous_variant | 0.56 |
rpoC | 764077 | c.708C>T | synonymous_variant | 0.58 |
rpoC | 764083 | c.714A>G | synonymous_variant | 0.58 |
rpoC | 764098 | c.729A>G | synonymous_variant | 0.56 |
rpoC | 764101 | c.732C>G | synonymous_variant | 0.56 |
rpoC | 764167 | c.798G>A | synonymous_variant | 0.49 |
rpoC | 764169 | p.Asn267Ser | missense_variant | 0.51 |
rpoC | 764179 | c.810C>T | synonymous_variant | 0.58 |
rpoC | 764188 | c.819A>G | synonymous_variant | 0.54 |
rpoC | 764194 | p.Glu275Asp | missense_variant | 0.54 |
rpoC | 764195 | p.Ser276Ala | missense_variant | 0.57 |
rpoC | 764203 | c.834G>T | synonymous_variant | 0.59 |
rpoC | 764206 | p.Asp279Glu | missense_variant | 0.56 |
rpoC | 764217 | p.Asn283Ser | missense_variant | 0.54 |
rpoC | 764248 | c.879C>G | synonymous_variant | 0.59 |
rpoC | 764257 | c.888G>C | synonymous_variant | 0.6 |
rpoC | 764266 | c.897T>C | synonymous_variant | 0.63 |
rpoC | 764278 | c.909A>G | synonymous_variant | 0.58 |
rpoC | 764284 | c.915G>C | synonymous_variant | 0.59 |
rpoC | 764285 | p.Gly306Thr | missense_variant | 0.59 |
rpoC | 764311 | c.942C>T | synonymous_variant | 0.6 |
rpoC | 764317 | c.948C>G | synonymous_variant | 0.6 |
rpoC | 764320 | c.951C>G | synonymous_variant | 0.6 |
rpoC | 764344 | c.975C>T | synonymous_variant | 0.69 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.6 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 0.55 |
rpoC | 764392 | c.1023C>T | synonymous_variant | 0.58 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.6 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.48 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.51 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.52 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.51 |
rpoC | 764494 | c.1125G>A | synonymous_variant | 0.5 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.48 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.53 |
rpoC | 764510 | c.1141C>T | synonymous_variant | 0.56 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.63 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.61 |
rpoC | 764536 | c.1167G>T | synonymous_variant | 0.64 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.64 |
rpoC | 764551 | c.1182G>C | synonymous_variant | 0.76 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.7 |
rpoC | 764575 | c.1206T>C | synonymous_variant | 0.72 |
rpoC | 764578 | c.1209C>T | synonymous_variant | 0.71 |
rpoC | 764611 | c.1242G>C | synonymous_variant | 0.66 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.68 |
rpoC | 764635 | c.1266C>G | synonymous_variant | 0.67 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.66 |
rpoC | 764656 | c.1287C>G | synonymous_variant | 0.66 |
rpoC | 764716 | c.1347G>T | synonymous_variant | 0.66 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.61 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.64 |
rpoC | 764791 | c.1422C>G | synonymous_variant | 0.6 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.58 |
rpoC | 764812 | c.1443C>G | synonymous_variant | 0.6 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.58 |
rpoC | 764830 | c.1461C>G | synonymous_variant | 0.58 |
rpoC | 764851 | c.1482C>T | synonymous_variant | 0.56 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.48 |
rpoC | 764872 | c.1503A>G | synonymous_variant | 0.52 |
rpoC | 764875 | c.1506C>G | synonymous_variant | 0.53 |
rpoC | 764887 | c.1518G>C | synonymous_variant | 0.52 |
rpoC | 764888 | c.1519_1521delTTGinsCTC | synonymous_variant | 0.52 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.65 |
rpoC | 764923 | c.1554A>G | synonymous_variant | 0.65 |
rpoC | 764932 | c.1563C>G | synonymous_variant | 0.64 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.67 |
rpoC | 764995 | c.1626C>T | synonymous_variant | 1.0 |
rpoC | 765007 | c.1638T>G | synonymous_variant | 0.57 |
rpoC | 765016 | c.1647C>A | synonymous_variant | 0.62 |
rpoC | 765019 | c.1650A>G | synonymous_variant | 0.62 |
rpoC | 765034 | c.1665T>C | synonymous_variant | 0.54 |
rpoC | 765040 | c.1671T>C | synonymous_variant | 0.49 |
rpoC | 765041 | c.1672T>C | synonymous_variant | 0.47 |
rpoC | 765047 | c.1678T>C | synonymous_variant | 0.45 |
rpoC | 765052 | c.1683C>G | synonymous_variant | 0.46 |
rpoC | 765055 | c.1686C>G | synonymous_variant | 0.47 |
rpoC | 765076 | c.1707A>G | synonymous_variant | 0.5 |
rpoC | 765079 | c.1710T>G | synonymous_variant | 0.48 |
rpoC | 765082 | c.1713G>C | synonymous_variant | 0.45 |
rpoC | 765085 | c.1716T>C | synonymous_variant | 0.46 |
rpoC | 765142 | c.1773G>A | synonymous_variant | 0.35 |
rpoC | 765145 | c.1776C>T | synonymous_variant | 0.34 |
rpoC | 765151 | c.1782G>C | synonymous_variant | 0.23 |
rpoC | 765367 | c.1998C>A | synonymous_variant | 0.39 |
rpoC | 765404 | p.Leu679Val | missense_variant | 0.43 |
rpoC | 765409 | c.2040T>C | synonymous_variant | 0.44 |
rpoC | 765412 | c.2043T>C | synonymous_variant | 0.46 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.49 |
rpoC | 765452 | p.Ala695Ser | missense_variant | 0.58 |
rpoC | 765466 | c.2097C>T | synonymous_variant | 0.55 |
rpoC | 765478 | c.2109T>G | synonymous_variant | 0.52 |
rpoC | 765493 | c.2124G>C | synonymous_variant | 0.5 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.46 |
rpoC | 765547 | c.2178C>G | synonymous_variant | 0.33 |
rpoC | 765548 | c.2179_2181delAGCinsTCG | synonymous_variant | 0.33 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.33 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.33 |
rpoC | 765559 | c.2190G>C | synonymous_variant | 0.32 |
rpoC | 765578 | c.2209C>T | synonymous_variant | 0.45 |
rpoC | 765584 | p.Pro739Ala | missense_variant | 0.41 |
rpoC | 765590 | p.Arg741Gly | missense_variant | 0.39 |
rpoC | 765596 | p.Lys743Gln | missense_variant | 0.43 |
rpoC | 765611 | p.His748Ala | missense_variant | 0.37 |
rpoC | 765619 | c.2250G>A | synonymous_variant | 0.42 |
rpoC | 765625 | c.2256C>A | synonymous_variant | 0.4 |
rpoC | 765628 | c.2259G>C | synonymous_variant | 0.39 |
rpoC | 765658 | c.2289C>T | synonymous_variant | 0.44 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.5 |
rpoC | 765728 | p.Gln787Glu | missense_variant | 0.56 |
rpoC | 765734 | c.2365T>C | synonymous_variant | 0.57 |
rpoC | 765739 | c.2370G>C | synonymous_variant | 0.57 |
rpoC | 765740 | p.Glu791Lys | missense_variant | 0.57 |
rpoC | 765772 | c.2403C>G | synonymous_variant | 0.7 |
rpoC | 765787 | c.2418C>T | synonymous_variant | 0.68 |
rpoC | 765793 | c.2424C>G | synonymous_variant | 0.66 |
rpoC | 765796 | c.2427C>T | synonymous_variant | 0.64 |
rpoC | 765811 | c.2442T>C | synonymous_variant | 0.67 |
rpoC | 765814 | c.2445A>G | synonymous_variant | 0.67 |
rpoC | 765823 | c.2454C>G | synonymous_variant | 0.65 |
rpoC | 765826 | c.2457T>C | synonymous_variant | 0.65 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 0.59 |
rpoC | 765868 | c.2499G>A | synonymous_variant | 0.51 |
rpoC | 765871 | c.2502T>G | synonymous_variant | 0.51 |
rpoC | 765875 | p.Val836Ile | missense_variant | 0.51 |
rpoC | 765883 | c.2514C>G | synonymous_variant | 0.54 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.54 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.56 |
rpoC | 765904 | c.2535C>G | synonymous_variant | 0.54 |
rpoC | 765908 | c.2539C>T | synonymous_variant | 0.53 |
rpoC | 765937 | c.2568T>G | synonymous_variant | 0.49 |
rpoC | 765940 | c.2571A>G | synonymous_variant | 0.49 |
rpoC | 765952 | c.2583G>C | synonymous_variant | 0.43 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.45 |
rpoC | 765979 | c.2610C>G | synonymous_variant | 0.41 |
rpoC | 765982 | c.2613C>T | synonymous_variant | 0.39 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.34 |
rpoC | 766012 | c.2643C>G | synonymous_variant | 0.25 |
rpoC | 766243 | c.2874C>G | synonymous_variant | 0.18 |
rpoC | 766249 | c.2880C>G | synonymous_variant | 0.22 |
rpoC | 766270 | c.2901G>C | synonymous_variant | 0.47 |
rpoC | 766280 | p.Ser971Gly | missense_variant | 0.47 |
rpoC | 766288 | c.2919C>G | synonymous_variant | 0.5 |
rpoC | 766291 | c.2922G>C | synonymous_variant | 0.46 |
rpoC | 766298 | p.Thr977Val | missense_variant | 0.45 |
rpoC | 766315 | c.2946C>G | synonymous_variant | 0.51 |
rpoC | 766345 | c.2976T>C | synonymous_variant | 0.52 |
rpoC | 766348 | c.2979A>G | synonymous_variant | 0.52 |
rpoC | 766357 | c.2988C>T | synonymous_variant | 0.53 |
rpoC | 766363 | c.2994G>C | synonymous_variant | 0.47 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.42 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.42 |
rpoC | 766393 | c.3024C>G | synonymous_variant | 0.47 |
rpoC | 766411 | c.3042C>G | synonymous_variant | 0.48 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.52 |
rpoC | 766456 | c.3087C>G | synonymous_variant | 0.51 |
rpoC | 766471 | c.3102G>C | synonymous_variant | 0.52 |
rpoC | 766486 | c.3117A>G | synonymous_variant | 0.51 |
rpoC | 766492 | c.3123T>C | synonymous_variant | 0.49 |
rpoC | 766495 | c.3126C>T | synonymous_variant | 0.5 |
rpoC | 766510 | c.3141C>A | synonymous_variant | 0.52 |
rpoC | 766528 | c.3159T>G | synonymous_variant | 0.48 |
rpoC | 766540 | p.Asp1057Glu | missense_variant | 0.4 |
rpoC | 766546 | p.Glu1059Asp | missense_variant | 0.39 |
rpoC | 766549 | c.3180G>C | synonymous_variant | 0.42 |
rpoC | 766570 | c.3201T>C | synonymous_variant | 0.44 |
rpoC | 766585 | c.3216T>C | synonymous_variant | 0.43 |
rpoC | 766607 | p.Ile1080Leu | missense_variant | 0.49 |
rpoC | 766618 | c.3249G>C | synonymous_variant | 0.5 |
rpoC | 766624 | c.3255G>C | synonymous_variant | 0.47 |
rpoC | 766645 | c.3276A>G | synonymous_variant | 0.45 |
rpoC | 766651 | c.3282T>C | synonymous_variant | 0.36 |
rpoC | 766652 | p.Ser1095Thr | missense_variant | 0.34 |
rpoC | 766657 | c.3288A>G | synonymous_variant | 0.34 |
rpoC | 766661 | p.Val1098Leu | missense_variant | 0.33 |
rpoC | 766666 | c.3297C>T | synonymous_variant | 0.33 |
rpoC | 766667 | p.Ser1100Ala | missense_variant | 0.39 |
rpoC | 766672 | c.3303T>C | synonymous_variant | 0.39 |
rpoC | 766714 | c.3345G>C | synonymous_variant | 0.33 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.35 |
rpoC | 766738 | c.3369G>C | synonymous_variant | 0.41 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.51 |
rpoC | 766792 | c.3423C>T | synonymous_variant | 0.56 |
rpoC | 766798 | c.3429C>G | synonymous_variant | 0.64 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.67 |
rpoC | 766843 | c.3474T>C | synonymous_variant | 0.61 |
rpoC | 766846 | c.3477C>G | synonymous_variant | 0.59 |
rpoC | 766855 | c.3486G>T | synonymous_variant | 0.6 |
rpoC | 766861 | c.3492G>T | synonymous_variant | 0.65 |
rpoC | 766895 | c.3526T>C | synonymous_variant | 0.61 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.61 |
rpoC | 766903 | c.3534C>T | synonymous_variant | 0.59 |
rpoC | 766933 | c.3564A>C | synonymous_variant | 0.63 |
rpoC | 766942 | c.3573C>T | synonymous_variant | 0.61 |
rpoC | 766945 | c.3576A>G | synonymous_variant | 0.63 |
rpoC | 766960 | c.3591C>T | synonymous_variant | 0.64 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.63 |
rpoC | 766972 | c.3603G>C | synonymous_variant | 0.63 |
rpoC | 766978 | c.3609C>T | synonymous_variant | 0.58 |
rpoC | 766981 | c.3612T>C | synonymous_variant | 0.55 |
rpoC | 766984 | c.3615G>T | synonymous_variant | 0.56 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.57 |
rpoC | 767002 | c.3633G>C | synonymous_variant | 0.55 |
rpoC | 767020 | c.3651C>G | synonymous_variant | 0.51 |
rpoC | 767032 | c.3663G>C | synonymous_variant | 0.54 |
rpoC | 767035 | c.3666G>C | synonymous_variant | 0.55 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.5 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.5 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.62 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.59 |
rpoC | 767158 | c.3789T>G | synonymous_variant | 0.6 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.54 |
rpoC | 767191 | c.3822C>G | synonymous_variant | 0.5 |
rpoC | 767206 | c.3837C>G | synonymous_variant | 0.47 |
rpoC | 767209 | c.3840T>C | synonymous_variant | 0.48 |
rpoC | 767221 | c.3852C>G | synonymous_variant | 0.47 |
rpoC | 767233 | c.3864T>C | synonymous_variant | 0.46 |
rpoC | 767263 | c.3894T>C | synonymous_variant | 0.29 |
rpoC | 767264 | p.Ala1299Gln | missense_variant | 0.26 |
rpoC | 767269 | c.3900C>G | synonymous_variant | 0.26 |
rpoC | 767275 | c.3906T>C | synonymous_variant | 0.24 |
rpoC | 767278 | c.3909T>C | synonymous_variant | 0.24 |
rpoC | 767281 | c.3912C>G | synonymous_variant | 0.22 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpS5 | 779609 | c.-704C>T | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781571 | c.12C>T | synonymous_variant | 0.3 |
rpsL | 781592 | c.33T>G | synonymous_variant | 0.4 |
rpsL | 781595 | c.36T>C | synonymous_variant | 0.4 |
rpsL | 781598 | c.39G>C | synonymous_variant | 0.38 |
rpsL | 781608 | p.Ser17Gly | missense_variant | 0.48 |
rpsL | 781628 | c.69T>C | synonymous_variant | 0.61 |
rpsL | 781631 | c.72G>C | synonymous_variant | 0.61 |
rpsL | 781649 | c.90T>C | synonymous_variant | 0.65 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.66 |
rpsL | 781658 | c.99A>G | synonymous_variant | 0.65 |
rpsL | 781673 | c.114C>T | synonymous_variant | 0.66 |
rpsL | 781679 | c.120C>G | synonymous_variant | 0.67 |
rpsL | 781709 | c.150G>C | synonymous_variant | 0.62 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.59 |
rpsL | 781718 | c.159C>G | synonymous_variant | 0.58 |
rpsL | 781724 | c.165G>C | synonymous_variant | 0.58 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.58 |
rpsL | 781733 | c.174G>T | synonymous_variant | 0.61 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.6 |
rpsL | 781742 | c.183C>T | synonymous_variant | 0.61 |
rpsL | 781754 | c.195G>T | synonymous_variant | 0.62 |
rpsL | 781766 | c.207C>T | synonymous_variant | 0.64 |
rpsL | 781808 | c.249C>T | synonymous_variant | 0.67 |
rpsL | 781832 | c.273T>G | synonymous_variant | 0.63 |
rpsL | 781835 | c.276T>C | synonymous_variant | 0.65 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.65 |
rpsL | 781865 | c.306G>C | synonymous_variant | 0.63 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.64 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.63 |
rpsL | 781877 | c.318T>C | synonymous_variant | 0.66 |
rpsL | 781889 | c.330C>T | synonymous_variant | 0.68 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.67 |
rpsL | 781898 | c.339A>G | synonymous_variant | 0.7 |
rpsL | 781907 | c.348T>C | synonymous_variant | 0.66 |
rpsL | 781913 | c.354C>T | synonymous_variant | 0.67 |
rpsL | 781916 | c.357T>C | synonymous_variant | 0.69 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.62 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.6 |
rplC | 800633 | c.-176T>C | upstream_gene_variant | 0.63 |
rplC | 800642 | c.-167C>T | upstream_gene_variant | 0.64 |
rplC | 800648 | c.-161A>T | upstream_gene_variant | 0.59 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.62 |
rplC | 800666 | c.-143C>T | upstream_gene_variant | 0.64 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.62 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.63 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.59 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.52 |
rplC | 800726 | c.-83G>A | upstream_gene_variant | 0.48 |
rplC | 800738 | c.-71T>G | upstream_gene_variant | 0.44 |
rplC | 800747 | c.-62C>G | upstream_gene_variant | 0.44 |
rplC | 800753 | c.-56C>A | upstream_gene_variant | 0.41 |
rplC | 800759 | c.-50C>T | upstream_gene_variant | 0.4 |
rplC | 800762 | c.-47T>G | upstream_gene_variant | 0.4 |
rplC | 800765 | c.-44G>C | upstream_gene_variant | 0.42 |
rplC | 800814 | c.6A>G | synonymous_variant | 0.31 |
rplC | 800815 | c.7C>A | synonymous_variant | 0.31 |
rplC | 800829 | c.21C>G | synonymous_variant | 0.34 |
rplC | 800832 | c.24T>C | synonymous_variant | 0.34 |
rplC | 800841 | c.33G>T | synonymous_variant | 0.35 |
rplC | 800844 | c.36T>C | synonymous_variant | 0.32 |
rplC | 800856 | c.48A>G | synonymous_variant | 0.29 |
rplC | 800865 | c.57A>G | synonymous_variant | 0.2 |
rplC | 800889 | c.81C>G | synonymous_variant | 0.18 |
rplC | 800916 | c.108A>G | synonymous_variant | 0.2 |
rplC | 800922 | c.114C>A | synonymous_variant | 0.23 |
rplC | 800934 | c.126C>G | synonymous_variant | 0.26 |
rplC | 800937 | c.129A>G | synonymous_variant | 0.26 |
rplC | 800940 | c.132C>G | synonymous_variant | 0.29 |
rplC | 800946 | c.138T>C | synonymous_variant | 0.34 |
rplC | 800962 | c.154C>T | synonymous_variant | 0.37 |
rplC | 800967 | c.159C>T | synonymous_variant | 0.36 |
rplC | 800970 | c.162T>C | synonymous_variant | 0.38 |
rplC | 800982 | c.174C>T | synonymous_variant | 0.4 |
rplC | 800985 | c.177A>C | synonymous_variant | 0.38 |
rplC | 801008 | p.Thr67Asn | missense_variant | 0.35 |
rplC | 801027 | c.219C>G | synonymous_variant | 0.24 |
rplC | 801030 | c.222C>T | synonymous_variant | 0.22 |
rplC | 801171 | c.363A>G | synonymous_variant | 0.22 |
rplC | 801174 | c.366T>C | synonymous_variant | 0.25 |
rplC | 801183 | c.375C>G | synonymous_variant | 0.35 |
rplC | 801201 | c.393C>T | synonymous_variant | 0.39 |
rplC | 801210 | c.402T>G | synonymous_variant | 0.38 |
rplC | 801222 | c.414T>C | synonymous_variant | 0.38 |
rplC | 801228 | c.420T>C | synonymous_variant | 0.37 |
rplC | 801231 | c.423C>T | synonymous_variant | 0.38 |
rplC | 801240 | c.432G>A | synonymous_variant | 0.38 |
rplC | 801243 | c.435C>T | synonymous_variant | 0.38 |
rplC | 801246 | c.438C>T | synonymous_variant | 0.38 |
rplC | 801267 | c.459A>C | synonymous_variant | 0.33 |
rplC | 801273 | c.465C>G | synonymous_variant | 0.18 |
rplC | 801285 | c.477G>A | synonymous_variant | 0.22 |
rplC | 801300 | c.492C>G | synonymous_variant | 0.25 |
rplC | 801312 | c.504G>C | synonymous_variant | 0.27 |
rplC | 801321 | c.513C>T | synonymous_variant | 0.24 |
rplC | 801324 | c.516T>C | synonymous_variant | 0.26 |
rplC | 801330 | c.522G>C | synonymous_variant | 0.25 |
rplC | 801337 | p.Val177Thr | missense_variant | 0.24 |
rplC | 801341 | p.Leu178Gln | missense_variant | 0.25 |
rplC | 801357 | c.549T>C | synonymous_variant | 0.34 |
rplC | 801399 | c.591G>C | synonymous_variant | 0.31 |
rplC | 801400 | p.Val198Ile | missense_variant | 0.31 |
rplC | 801405 | c.597T>C | synonymous_variant | 0.33 |
rplC | 801413 | p.Thr202Asn | missense_variant | 0.31 |
rplC | 801417 | c.609T>C | synonymous_variant | 0.33 |
rplC | 801420 | c.612A>G | synonymous_variant | 0.33 |
rplC | 801438 | c.630T>C | synonymous_variant | 0.3 |
fbiC | 1303455 | c.525C>G | synonymous_variant | 0.21 |
fbiC | 1303464 | c.534A>G | synonymous_variant | 0.2 |
fbiC | 1303470 | c.540T>G | synonymous_variant | 0.2 |
fbiC | 1303480 | p.Gln184Glu | missense_variant | 0.2 |
fbiC | 1303488 | c.558G>A | synonymous_variant | 0.22 |
fbiC | 1303500 | c.570C>T | synonymous_variant | 0.26 |
fbiC | 1303501 | c.571C>T | synonymous_variant | 0.26 |
fbiC | 1303509 | c.579G>C | synonymous_variant | 0.33 |
fbiC | 1303512 | c.582T>C | synonymous_variant | 0.33 |
fbiC | 1303531 | p.Met201Leu | missense_variant | 0.35 |
fbiC | 1303537 | c.607C>A | synonymous_variant | 0.39 |
fbiC | 1303545 | c.615A>G | synonymous_variant | 0.41 |
fbiC | 1303557 | c.627G>C | synonymous_variant | 0.53 |
fbiC | 1303560 | c.630G>A | synonymous_variant | 0.55 |
fbiC | 1303584 | c.654C>G | synonymous_variant | 0.58 |
fbiC | 1303611 | c.681G>C | synonymous_variant | 0.62 |
fbiC | 1303632 | c.702T>C | synonymous_variant | 0.61 |
fbiC | 1303638 | c.708A>G | synonymous_variant | 0.6 |
fbiC | 1303641 | c.711C>T | synonymous_variant | 0.58 |
fbiC | 1303659 | c.729T>G | synonymous_variant | 0.44 |
fbiC | 1303660 | p.Val244Thr | missense_variant | 0.44 |
fbiC | 1303663 | c.733C>T | synonymous_variant | 0.48 |
fbiC | 1303695 | c.765T>C | synonymous_variant | 0.44 |
fbiC | 1303707 | c.777G>A | synonymous_variant | 0.4 |
fbiC | 1303708 | c.778T>C | synonymous_variant | 0.4 |
fbiC | 1303731 | c.801A>G | synonymous_variant | 0.4 |
fbiC | 1303732 | p.Ser268His | missense_variant | 0.4 |
fbiC | 1303740 | c.810C>T | synonymous_variant | 0.46 |
fbiC | 1303746 | p.Asp272Glu | missense_variant | 0.44 |
fbiC | 1303749 | c.819G>A | synonymous_variant | 0.42 |
fbiC | 1303752 | c.822A>G | synonymous_variant | 0.42 |
fbiC | 1303758 | c.828G>C | synonymous_variant | 0.44 |
fbiC | 1303764 | c.834C>T | synonymous_variant | 0.43 |
fbiC | 1303785 | c.855G>T | synonymous_variant | 0.34 |
fbiC | 1303788 | c.858T>C | synonymous_variant | 0.33 |
fbiC | 1303789 | p.Ile287Val | missense_variant | 0.33 |
fbiC | 1303827 | c.897A>G | synonymous_variant | 0.3 |
fbiC | 1303833 | c.903C>G | synonymous_variant | 0.27 |
fbiC | 1303866 | p.Glu312Asp | missense_variant | 0.24 |
fbiC | 1303872 | c.942C>T | synonymous_variant | 0.23 |
fbiC | 1303878 | c.948G>C | synonymous_variant | 0.25 |
fbiC | 1303881 | c.951G>C | synonymous_variant | 0.25 |
fbiC | 1303884 | c.954T>G | synonymous_variant | 0.24 |
fbiC | 1303887 | c.957G>A | synonymous_variant | 0.26 |
fbiC | 1304067 | c.1137G>C | synonymous_variant | 0.19 |
fbiC | 1304098 | p.Gln390Glu | missense_variant | 0.18 |
fbiC | 1304508 | p.Glu526Asp | missense_variant | 0.21 |
fbiC | 1304511 | c.1581C>T | synonymous_variant | 0.23 |
fbiC | 1304517 | c.1587C>T | synonymous_variant | 0.35 |
fbiC | 1304533 | c.1603T>C | synonymous_variant | 0.47 |
fbiC | 1304544 | p.Asp538Glu | missense_variant | 0.5 |
fbiC | 1304546 | p.Val539Ala | missense_variant | 0.54 |
fbiC | 1304553 | c.1623C>T | synonymous_variant | 0.5 |
fbiC | 1304556 | c.1626C>T | synonymous_variant | 0.52 |
fbiC | 1304559 | p.Glu543Asp | missense_variant | 0.51 |
fbiC | 1304568 | c.1638T>C | synonymous_variant | 0.55 |
fbiC | 1304574 | c.1644C>G | synonymous_variant | 0.57 |
fbiC | 1304580 | c.1650T>C | synonymous_variant | 0.56 |
fbiC | 1304604 | c.1674C>T | synonymous_variant | 0.48 |
fbiC | 1304610 | c.1680C>G | synonymous_variant | 0.45 |
fbiC | 1304613 | c.1683T>C | synonymous_variant | 0.4 |
fbiC | 1304622 | c.1692C>T | synonymous_variant | 0.36 |
fbiC | 1304628 | c.1698G>C | synonymous_variant | 0.31 |
fbiC | 1304634 | c.1704C>G | synonymous_variant | 0.27 |
fbiC | 1304640 | c.1710A>C | synonymous_variant | 0.26 |
fbiC | 1304646 | c.1716T>C | synonymous_variant | 0.26 |
fbiC | 1304661 | c.1731C>T | synonymous_variant | 0.24 |
fbiC | 1304742 | c.1812T>C | synonymous_variant | 0.18 |
fbiC | 1304748 | c.1818T>C | synonymous_variant | 0.21 |
fbiC | 1304757 | c.1827A>G | synonymous_variant | 0.27 |
fbiC | 1304774 | p.Ala615Val | missense_variant | 0.37 |
fbiC | 1304784 | c.1854T>G | synonymous_variant | 0.38 |
fbiC | 1304787 | c.1857T>C | synonymous_variant | 0.38 |
fbiC | 1304790 | c.1860C>G | synonymous_variant | 0.37 |
fbiC | 1304799 | c.1869G>A | synonymous_variant | 0.37 |
fbiC | 1304811 | c.1881C>G | synonymous_variant | 0.36 |
fbiC | 1304826 | c.1896G>C | synonymous_variant | 0.33 |
fbiC | 1304853 | c.1923C>T | synonymous_variant | 0.23 |
fbiC | 1304855 | p.Val642Ala | missense_variant | 0.21 |
fbiC | 1304946 | c.2016G>T | synonymous_variant | 0.21 |
fbiC | 1304955 | c.2025G>A | synonymous_variant | 0.33 |
fbiC | 1304958 | c.2028T>G | synonymous_variant | 0.34 |
fbiC | 1304961 | c.2031C>T | synonymous_variant | 0.33 |
fbiC | 1304967 | c.2037G>A | synonymous_variant | 0.38 |
fbiC | 1304970 | c.2040G>T | synonymous_variant | 0.4 |
fbiC | 1304988 | c.2058G>C | synonymous_variant | 0.49 |
fbiC | 1304994 | c.2064A>G | synonymous_variant | 0.46 |
fbiC | 1304995 | p.Leu689Met | missense_variant | 0.46 |
fbiC | 1305006 | p.Glu692Asp | missense_variant | 0.52 |
fbiC | 1305015 | c.2085G>C | synonymous_variant | 0.53 |
fbiC | 1305021 | c.2091C>G | synonymous_variant | 0.53 |
fbiC | 1305042 | c.2112A>G | synonymous_variant | 0.46 |
fbiC | 1305045 | c.2115A>G | synonymous_variant | 0.45 |
fbiC | 1305069 | c.2139G>C | synonymous_variant | 0.37 |
fbiC | 1305075 | c.2145T>C | synonymous_variant | 0.39 |
fbiC | 1305078 | c.2148A>G | synonymous_variant | 0.37 |
fbiC | 1305092 | p.Ala721Gly | missense_variant | 0.31 |
fbiC | 1305099 | c.2169T>C | synonymous_variant | 0.21 |
fbiC | 1305102 | p.Asn724Lys | missense_variant | 0.2 |
fbiC | 1305106 | c.2176C>T | synonymous_variant | 0.19 |
fbiC | 1305114 | c.2184T>C | synonymous_variant | 0.19 |
fbiC | 1305135 | c.2205C>A | synonymous_variant | 0.19 |
fbiC | 1305204 | c.2274C>G | synonymous_variant | 0.2 |
fbiC | 1305369 | c.2439G>A | synonymous_variant | 0.51 |
fbiC | 1305375 | c.2445C>G | synonymous_variant | 0.53 |
fbiC | 1305390 | c.2460C>G | synonymous_variant | 0.53 |
fbiC | 1305393 | c.2463T>C | synonymous_variant | 0.53 |
fbiC | 1305420 | c.2490C>A | synonymous_variant | 0.4 |
fbiC | 1305421 | p.Ala831Ser | missense_variant | 0.4 |
fbiC | 1305444 | c.2514A>G | synonymous_variant | 0.19 |
fbiC | 1305446 | p.Gly839Ala | missense_variant | 0.18 |
atpE | 1460849 | c.-196G>A | upstream_gene_variant | 0.19 |
atpE | 1461050 | c.6C>T | synonymous_variant | 0.19 |
atpE | 1461074 | c.30C>T | synonymous_variant | 0.37 |
atpE | 1461093 | p.Met17Leu | missense_variant | 0.41 |
atpE | 1461097 | p.Ala18Gly | missense_variant | 0.45 |
atpE | 1461107 | c.63C>A | synonymous_variant | 0.45 |
atpE | 1461108 | p.Ile22Val | missense_variant | 0.48 |
atpE | 1461118 | p.Gly25Ala | missense_variant | 0.61 |
atpE | 1461149 | c.105T>G | synonymous_variant | 0.61 |
atpE | 1461161 | c.117C>T | synonymous_variant | 0.57 |
atpE | 1461167 | c.123G>C | synonymous_variant | 0.56 |
atpE | 1461170 | c.126A>G | synonymous_variant | 0.55 |
atpE | 1461173 | c.129C>T | synonymous_variant | 0.57 |
atpE | 1461176 | c.132G>A | synonymous_variant | 0.53 |
atpE | 1461179 | c.135G>A | synonymous_variant | 0.52 |
atpE | 1461182 | c.138A>G | synonymous_variant | 0.5 |
atpE | 1461185 | c.141G>C | synonymous_variant | 0.54 |
atpE | 1461197 | c.153A>G | synonymous_variant | 0.56 |
atpE | 1461212 | c.168C>G | synonymous_variant | 0.51 |
atpE | 1461219 | c.175T>C | synonymous_variant | 0.48 |
atpE | 1461224 | c.180T>G | synonymous_variant | 0.4 |
atpE | 1461254 | c.210T>C | synonymous_variant | 0.33 |
atpE | 1461269 | c.225C>A | synonymous_variant | 0.33 |
atpE | 1461275 | c.231T>C | synonymous_variant | 0.3 |
atpE | 1461281 | c.237C>A | synonymous_variant | 0.26 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 0.77 |
rrs | 1471925 | n.80_81insG | non_coding_transcript_exon_variant | 0.77 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.79 |
rrs | 1471936 | n.91A>G | non_coding_transcript_exon_variant | 0.79 |
rrs | 1471996 | n.151C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472029 | n.184C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472298 | n.453G>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472309 | n.464C>G | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472311 | n.466C>T | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472314 | n.469A>G | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472447 | n.602C>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472450 | n.605A>C | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472451 | n.606C>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472462 | n.617T>G | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472489 | n.644A>G | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472857 | n.1012A>G | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472858 | n.1013G>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472860 | n.1015C>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472861 | n.1016G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473283 | n.1438T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473300 | n.1455C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1473668 | n.11C>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1473670 | n.13A>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1473698 | n.41G>A | non_coding_transcript_exon_variant | 0.65 |
rrl | 1473699 | n.42A>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1473701 | n.44A>G | non_coding_transcript_exon_variant | 0.66 |
rrl | 1473743 | n.86C>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1473782 | n.125A>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1473788 | n.131A>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473807 | n.150T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473812 | n.155G>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1473814 | n.157A>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1473815 | n.158T>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1473816 | n.159C>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1473822 | n.165A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1473836 | n.179A>G | non_coding_transcript_exon_variant | 0.37 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.48 |
rrl | 1473887 | n.230T>G | non_coding_transcript_exon_variant | 0.46 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1473899 | n.242A>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474201 | n.544T>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474202 | n.545T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474275 | n.618T>G | non_coding_transcript_exon_variant | 0.66 |
rrl | 1474282 | n.625G>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474286 | n.630delT | non_coding_transcript_exon_variant | 0.59 |
rrl | 1474308 | n.653_654delTG | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474374 | n.717T>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474446 | n.789C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474552 | n.895C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474715 | n.1058T>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474716 | n.1059A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474753 | n.1096A>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1475030 | n.1373_1374insT | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1475062 | n.1405A>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1475202 | n.1545G>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1475206 | n.1549C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475217 | n.1560T>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1475239 | n.1582A>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1475240 | n.1583C>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475241 | n.1584C>G | non_coding_transcript_exon_variant | 0.46 |
rrl | 1475242 | n.1585G>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1475252 | n.1595C>T | non_coding_transcript_exon_variant | 0.49 |
rrl | 1475253 | n.1596T>G | non_coding_transcript_exon_variant | 0.49 |
rrl | 1475257 | n.1600C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475273 | n.1616T>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475276 | n.1619T>G | non_coding_transcript_exon_variant | 0.59 |
rrl | 1475277 | n.1620G>C | non_coding_transcript_exon_variant | 0.61 |
rrl | 1475278 | n.1621G>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475291 | n.1634A>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1475378 | n.1721A>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1475379 | n.1722G>C | non_coding_transcript_exon_variant | 0.59 |
rrl | 1475380 | n.1723C>A | non_coding_transcript_exon_variant | 0.59 |
rrl | 1475405 | n.1748A>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1475413 | n.1756A>G | non_coding_transcript_exon_variant | 0.74 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1475430 | n.1773T>A | non_coding_transcript_exon_variant | 0.72 |
rrl | 1475436 | n.1779C>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475480 | n.1823A>C | non_coding_transcript_exon_variant | 0.72 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475484 | n.1827A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475499 | n.1842C>G | non_coding_transcript_exon_variant | 0.72 |
rrl | 1475532 | n.1875A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475539 | n.1882A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475544 | n.1887A>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475647 | n.1990G>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.66 |
rrl | 1475707 | n.2050T>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475762 | n.2105G>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475989 | n.2332T>C | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475995 | n.2338G>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475997 | n.2340A>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476033 | n.2376T>A | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476034 | n.2377C>A | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476035 | n.2378G>A | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476046 | n.2389G>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476246 | n.2589G>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476251 | n.2594T>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476252 | n.2595T>A | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476529 | n.2872A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476664 | n.3007T>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476665 | n.3008T>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476674 | n.3017T>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476679 | n.3022T>C | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476689 | n.3033delC | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476716 | n.3059A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476723 | n.3066T>A | non_coding_transcript_exon_variant | 0.32 |
inhA | 1673556 | c.-646C>T | upstream_gene_variant | 0.27 |
inhA | 1673565 | c.-637G>C | upstream_gene_variant | 0.3 |
inhA | 1673568 | c.-634C>G | upstream_gene_variant | 0.28 |
inhA | 1673574 | c.-628C>G | upstream_gene_variant | 0.3 |
inhA | 1673580 | c.-622T>C | upstream_gene_variant | 0.28 |
inhA | 1673589 | c.-613A>G | upstream_gene_variant | 0.26 |
inhA | 1673595 | c.-607A>C | upstream_gene_variant | 0.26 |
fabG1 | 1673596 | p.Lys53Asp | missense_variant | 0.26 |
inhA | 1673607 | c.-595T>C | upstream_gene_variant | 0.36 |
inhA | 1673616 | c.-586A>G | upstream_gene_variant | 0.37 |
fabG1 | 1673633 | p.Ser65Asn | missense_variant | 0.4 |
fabG1 | 1673657 | p.Thr73Lys | missense_variant | 0.41 |
inhA | 1673664 | c.-538A>C | upstream_gene_variant | 0.42 |
inhA | 1673667 | c.-535A>G | upstream_gene_variant | 0.44 |
fabG1 | 1673698 | p.Ser87Ala | missense_variant | 0.55 |
inhA | 1673712 | c.-490A>G | upstream_gene_variant | 0.53 |
fabG1 | 1673713 | p.Ser92Ala | missense_variant | 0.54 |
inhA | 1673724 | c.-478A>G | upstream_gene_variant | 0.55 |
inhA | 1673748 | c.-454A>G | upstream_gene_variant | 0.5 |
fabG1 | 1673756 | p.Glu106Val | missense_variant | 0.51 |
fabG1 | 1673767 | p.Asn110Asp | missense_variant | 0.48 |
inhA | 1673781 | c.-421C>T | upstream_gene_variant | 0.42 |
inhA | 1673790 | c.-412C>T | upstream_gene_variant | 0.41 |
inhA | 1673802 | c.-400A>G | upstream_gene_variant | 0.42 |
inhA | 1673826 | c.-376C>G | upstream_gene_variant | 0.24 |
fabG1 | 1673829 | p.Asn130Lys | missense_variant | 0.22 |
fabG1 | 1673830 | p.Lys131Arg | missense_variant | 0.24 |
inhA | 1673838 | c.-364T>C | upstream_gene_variant | 0.26 |
inhA | 1673841 | c.-361A>G | upstream_gene_variant | 0.29 |
inhA | 1673847 | c.-355A>C | upstream_gene_variant | 0.32 |
fabG1 | 1673853 | p.Ile138Met | missense_variant | 0.34 |
inhA | 1673862 | c.-340C>G | upstream_gene_variant | 0.38 |
fabG1 | 1673870 | p.Ser144Thr | missense_variant | 0.42 |
inhA | 1673898 | c.-304C>T | upstream_gene_variant | 0.38 |
inhA | 1673901 | c.-301A>G | upstream_gene_variant | 0.36 |
inhA | 1673904 | c.-298C>G | upstream_gene_variant | 0.35 |
inhA | 1673916 | c.-286A>T | upstream_gene_variant | 0.38 |
inhA | 1673917 | c.-285G>T | upstream_gene_variant | 0.38 |
inhA | 1673922 | c.-280T>C | upstream_gene_variant | 0.39 |
inhA | 1673955 | c.-247G>A | upstream_gene_variant | 0.44 |
inhA | 1673958 | c.-244G>A | upstream_gene_variant | 0.42 |
inhA | 1673961 | c.-241A>C | upstream_gene_variant | 0.43 |
inhA | 1673964 | c.-238C>T | upstream_gene_variant | 0.41 |
inhA | 1673976 | c.-226T>C | upstream_gene_variant | 0.4 |
inhA | 1673985 | c.-217C>A | upstream_gene_variant | 0.47 |
inhA | 1674006 | c.-196T>C | upstream_gene_variant | 0.36 |
inhA | 1674012 | c.-190C>G | upstream_gene_variant | 0.31 |
inhA | 1674465 | c.264C>T | synonymous_variant | 0.21 |
inhA | 1674471 | c.270G>C | synonymous_variant | 0.27 |
inhA | 1674486 | c.285T>C | synonymous_variant | 0.3 |
inhA | 1674489 | c.288G>C | synonymous_variant | 0.3 |
inhA | 1674500 | p.Gln100Pro | missense_variant | 0.33 |
inhA | 1674503 | p.Thr101Ser | missense_variant | 0.31 |
inhA | 1674531 | p.Asp110Glu | missense_variant | 0.44 |
inhA | 1674537 | c.336C>A | synonymous_variant | 0.39 |
inhA | 1674540 | c.339C>T | synonymous_variant | 0.38 |
inhA | 1674542 | p.Ala114Glu | missense_variant | 0.39 |
inhA | 1674576 | c.375T>C | synonymous_variant | 0.34 |
inhA | 1674579 | c.378G>A | synonymous_variant | 0.33 |
inhA | 1674582 | c.381T>C | synonymous_variant | 0.33 |
inhA | 1674585 | c.384T>A | synonymous_variant | 0.33 |
inhA | 1674589 | p.Met130Leu | missense_variant | 0.32 |
inhA | 1674601 | p.Leu134Val | missense_variant | 0.29 |
inhA | 1674609 | c.408G>C | synonymous_variant | 0.27 |
inhA | 1674669 | c.468G>C | synonymous_variant | 0.23 |
inhA | 1674690 | c.489C>G | synonymous_variant | 0.29 |
inhA | 1674702 | c.501G>A | synonymous_variant | 0.28 |
inhA | 1674703 | c.502T>C | synonymous_variant | 0.28 |
inhA | 1674714 | c.513C>G | synonymous_variant | 0.29 |
inhA | 1674718 | c.517_519delAGGinsCGC | synonymous_variant | 0.27 |
inhA | 1674726 | c.525G>C | synonymous_variant | 0.29 |
inhA | 1674729 | c.528G>C | synonymous_variant | 0.3 |
inhA | 1674741 | c.540C>T | synonymous_variant | 0.29 |
inhA | 1674742 | p.Lys181Pro | missense_variant | 0.29 |
inhA | 1674756 | c.555T>A | synonymous_variant | 0.19 |
inhA | 1674759 | c.558G>C | synonymous_variant | 0.19 |
inhA | 1674801 | c.600T>C | synonymous_variant | 0.23 |
inhA | 1674813 | c.612C>A | synonymous_variant | 0.25 |
inhA | 1674816 | c.615T>C | synonymous_variant | 0.26 |
inhA | 1674835 | p.Gly212Ser | missense_variant | 0.32 |
inhA | 1674839 | p.Ala213Gly | missense_variant | 0.32 |
inhA | 1674846 | p.Ile215Met | missense_variant | 0.33 |
inhA | 1674859 | p.Glu220Gln | missense_variant | 0.36 |
inhA | 1674870 | c.669T>C | synonymous_variant | 0.42 |
inhA | 1674876 | c.675C>G | synonymous_variant | 0.34 |
inhA | 1674879 | c.678T>G | synonymous_variant | 0.34 |
inhA | 1674892 | p.Asn231Asp | missense_variant | 0.28 |
inhA | 1674900 | c.699G>A | synonymous_variant | 0.29 |
inhA | 1674903 | c.702T>C | synonymous_variant | 0.26 |
inhA | 1674906 | c.705G>C | synonymous_variant | 0.24 |
inhA | 1674912 | c.711G>A | synonymous_variant | 0.23 |
inhA | 1674915 | c.714C>T | synonymous_variant | 0.23 |
inhA | 1674957 | c.756G>C | synonymous_variant | 0.24 |
inhA | 1674966 | c.765T>C | synonymous_variant | 0.33 |
inhA | 1674978 | c.777C>T | synonymous_variant | 0.32 |
inhA | 1674990 | c.789C>G | synonymous_variant | 0.32 |
inhA | 1674996 | c.795C>T | synonymous_variant | 0.31 |
inhA | 1674998 | p.Thr266Asn | missense_variant | 0.3 |
rpsA | 1833516 | c.-26A>C | upstream_gene_variant | 0.36 |
rpsA | 1833518 | c.-24C>A | upstream_gene_variant | 0.42 |
rpsA | 1833554 | p.Thr5Ala | missense_variant | 0.59 |
rpsA | 1833568 | c.27G>A | synonymous_variant | 0.62 |
rpsA | 1833589 | c.48A>C | synonymous_variant | 0.66 |
rpsA | 1833595 | c.54T>G | synonymous_variant | 0.68 |
rpsA | 1833616 | c.75A>C | synonymous_variant | 0.59 |
rpsA | 1833619 | c.78A>C | synonymous_variant | 0.6 |
rpsA | 1833625 | c.84A>G | synonymous_variant | 0.63 |
rpsA | 1833628 | c.87G>A | synonymous_variant | 0.64 |
rpsA | 1833634 | c.93G>A | synonymous_variant | 0.7 |
rpsA | 1833664 | c.123C>G | synonymous_variant | 0.68 |
rpsA | 1833670 | c.129C>A | synonymous_variant | 0.67 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.65 |
rpsA | 1833679 | c.138G>T | synonymous_variant | 0.66 |
rpsA | 1833688 | c.147C>T | synonymous_variant | 0.69 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.67 |
rpsA | 1833697 | c.156C>G | synonymous_variant | 0.68 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.57 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.61 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.59 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.59 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.58 |
rpsA | 1833778 | c.237C>G | synonymous_variant | 0.55 |
rpsA | 1833781 | c.240T>G | synonymous_variant | 0.54 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.49 |
rpsA | 1833794 | p.Glu85Lys | missense_variant | 0.47 |
rpsA | 1833797 | p.Val86Ile | missense_variant | 0.48 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.52 |
rpsA | 1833806 | c.265C>T | synonymous_variant | 0.55 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.57 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.58 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.53 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.6 |
rpsA | 1833892 | c.351G>A | synonymous_variant | 0.63 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.63 |
rpsA | 1833952 | c.411C>T | synonymous_variant | 0.62 |
rpsA | 1833971 | c.430C>T | synonymous_variant | 0.64 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.66 |
rpsA | 1833988 | c.447C>G | synonymous_variant | 0.63 |
rpsA | 1833991 | c.450C>G | synonymous_variant | 0.63 |
rpsA | 1833994 | c.453G>T | synonymous_variant | 0.66 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.68 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.63 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.62 |
rpsA | 1834024 | c.483G>T | synonymous_variant | 0.62 |
rpsA | 1834087 | c.546C>T | synonymous_variant | 0.48 |
rpsA | 1834097 | c.556_557delTCinsAG | synonymous_variant | 0.38 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.38 |
rpsA | 1834105 | c.564C>G | synonymous_variant | 0.37 |
rpsA | 1834135 | c.594G>C | synonymous_variant | 0.35 |
rpsA | 1834150 | c.609G>C | synonymous_variant | 0.31 |
rpsA | 1834153 | c.612T>C | synonymous_variant | 0.26 |
rpsA | 1834154 | p.Asn205Gln | missense_variant | 0.26 |
rpsA | 1834157 | c.616T>C | synonymous_variant | 0.26 |
rpsA | 1834162 | c.621A>G | synonymous_variant | 0.31 |
rpsA | 1834165 | c.624A>G | synonymous_variant | 0.32 |
rpsA | 1834169 | p.Thr210Ala | missense_variant | 0.33 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.34 |
rpsA | 1834186 | c.645C>G | synonymous_variant | 0.36 |
rpsA | 1834189 | c.648G>T | synonymous_variant | 0.37 |
rpsA | 1834192 | c.651C>T | synonymous_variant | 0.4 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.42 |
rpsA | 1834231 | c.690T>G | synonymous_variant | 0.42 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.4 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.38 |
rpsA | 1834258 | c.717G>A | synonymous_variant | 0.35 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.35 |
rpsA | 1834262 | c.721_723delTCGinsAGT | synonymous_variant | 0.35 |
rpsA | 1834297 | c.756C>G | synonymous_variant | 0.45 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.46 |
rpsA | 1834330 | c.789C>T | synonymous_variant | 0.54 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.59 |
rpsA | 1834354 | c.813G>A | synonymous_variant | 0.61 |
rpsA | 1834357 | c.816T>G | synonymous_variant | 0.6 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.58 |
rpsA | 1834369 | c.828C>G | synonymous_variant | 0.57 |
rpsA | 1834411 | c.870T>G | synonymous_variant | 0.51 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.54 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.53 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.53 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.52 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.54 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.53 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.54 |
rpsA | 1834498 | c.957C>T | synonymous_variant | 0.54 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.53 |
rpsA | 1834531 | c.990C>T | synonymous_variant | 0.55 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.57 |
rpsA | 1834552 | c.1011G>C | synonymous_variant | 0.58 |
rpsA | 1834555 | c.1014T>G | synonymous_variant | 0.57 |
rpsA | 1834557 | p.Ala339Gly | missense_variant | 0.58 |
rpsA | 1834582 | c.1041G>A | synonymous_variant | 0.64 |
rpsA | 1834598 | c.1057C>T | synonymous_variant | 0.64 |
rpsA | 1834606 | c.1065C>G | synonymous_variant | 0.65 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.66 |
rpsA | 1834615 | c.1074C>T | synonymous_variant | 0.65 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.6 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.6 |
rpsA | 1834669 | c.1128G>C | synonymous_variant | 0.56 |
rpsA | 1834690 | c.1149T>C | synonymous_variant | 0.53 |
rpsA | 1834720 | c.1179C>G | synonymous_variant | 0.61 |
rpsA | 1834732 | c.1191T>C | synonymous_variant | 0.59 |
rpsA | 1834733 | p.Ala398Pro | missense_variant | 0.6 |
rpsA | 1834753 | c.1212T>C | synonymous_variant | 0.56 |
rpsA | 1834759 | c.1218A>T | synonymous_variant | 0.53 |
rpsA | 1834765 | p.Glu408Asp | missense_variant | 0.44 |
rpsA | 1834766 | p.Lys409Ala | missense_variant | 0.44 |
rpsA | 1834780 | c.1239A>G | synonymous_variant | 0.46 |
rpsA | 1834786 | c.1245A>G | synonymous_variant | 0.47 |
rpsA | 1834789 | c.1248T>C | synonymous_variant | 0.45 |
rpsA | 1834792 | c.1251G>C | synonymous_variant | 0.45 |
rpsA | 1834828 | c.1287C>G | synonymous_variant | 0.24 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102203 | c.840T>C | synonymous_variant | 0.23 |
ndh | 2102218 | c.825C>G | synonymous_variant | 0.27 |
ndh | 2102233 | c.810G>A | synonymous_variant | 0.26 |
ndh | 2102239 | c.804C>A | synonymous_variant | 0.27 |
ndh | 2102246 | p.Val266Thr | missense_variant | 0.26 |
ndh | 2102248 | c.795C>T | synonymous_variant | 0.26 |
ndh | 2102251 | c.792C>G | synonymous_variant | 0.26 |
ndh | 2102257 | p.Ser262Pro | missense_variant | 0.29 |
ndh | 2102266 | c.777C>A | synonymous_variant | 0.28 |
ndh | 2102269 | c.774C>G | synonymous_variant | 0.28 |
ndh | 2102389 | c.654G>C | synonymous_variant | 0.22 |
ndh | 2102401 | c.642T>C | synonymous_variant | 0.3 |
ndh | 2102407 | c.636T>C | synonymous_variant | 0.31 |
ndh | 2102410 | c.633G>C | synonymous_variant | 0.31 |
ndh | 2102413 | c.630G>C | synonymous_variant | 0.31 |
ndh | 2102422 | c.621C>G | synonymous_variant | 0.41 |
ndh | 2102427 | p.Ser206Pro | missense_variant | 0.44 |
ndh | 2102440 | c.603C>T | synonymous_variant | 0.5 |
ndh | 2102460 | p.His195Tyr | missense_variant | 0.54 |
ndh | 2102469 | c.574C>T | synonymous_variant | 0.44 |
ndh | 2102470 | c.573G>A | synonymous_variant | 0.44 |
ndh | 2102482 | c.561A>G | synonymous_variant | 0.39 |
ndh | 2102494 | c.549T>C | synonymous_variant | 0.28 |
ndh | 2102497 | c.546T>C | synonymous_variant | 0.26 |
ndh | 2102506 | c.537C>T | synonymous_variant | 0.29 |
ndh | 2102509 | c.534T>C | synonymous_variant | 0.28 |
ndh | 2102512 | c.531G>C | synonymous_variant | 0.28 |
ndh | 2102518 | c.525T>C | synonymous_variant | 0.29 |
katG | 2155205 | p.Ser303Ala | missense_variant | 0.19 |
katG | 2155225 | p.Met296Gln | missense_variant | 0.3 |
katG | 2155233 | p.Leu293Ile | missense_variant | 0.29 |
katG | 2155242 | c.870T>C | synonymous_variant | 0.37 |
katG | 2155251 | c.861A>G | synonymous_variant | 0.24 |
katG | 2155257 | c.855C>A | synonymous_variant | 0.25 |
katG | 2155263 | c.849G>T | synonymous_variant | 0.21 |
katG | 2155266 | c.846T>C | synonymous_variant | 0.21 |
katG | 2155272 | c.840G>C | synonymous_variant | 0.23 |
katG | 2155284 | c.828T>C | synonymous_variant | 0.21 |
katG | 2155293 | c.819T>C | synonymous_variant | 0.24 |
katG | 2155298 | p.Phe272Val | missense_variant | 0.24 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289909 | c.-668G>A | upstream_gene_variant | 1.0 |
kasA | 2517917 | c.-198G>T | upstream_gene_variant | 0.69 |
kasA | 2517941 | c.-174C>G | upstream_gene_variant | 0.67 |
kasA | 2517989 | c.-126T>C | upstream_gene_variant | 0.49 |
kasA | 2517994 | c.-121_-120delCCinsAG | upstream_gene_variant | 0.42 |
kasA | 2518019 | c.-96A>G | upstream_gene_variant | 0.24 |
kasA | 2518132 | c.18C>T | synonymous_variant | 0.26 |
kasA | 2518138 | c.24T>C | synonymous_variant | 0.38 |
kasA | 2518162 | c.48G>A | synonymous_variant | 0.54 |
kasA | 2518174 | c.60A>G | synonymous_variant | 0.57 |
kasA | 2518190 | p.Ser26Ala | missense_variant | 0.6 |
kasA | 2518220 | c.106C>T | synonymous_variant | 0.67 |
kasA | 2518234 | c.120G>A | synonymous_variant | 0.58 |
kasA | 2518248 | p.Ala45Val | missense_variant | 0.49 |
kasA | 2518267 | c.153C>G | synonymous_variant | 0.46 |
kasA | 2518273 | c.159G>A | synonymous_variant | 0.43 |
kasA | 2518279 | c.165T>C | synonymous_variant | 0.4 |
kasA | 2518282 | c.168A>G | synonymous_variant | 0.32 |
kasA | 2518283 | p.Ala57Pro | missense_variant | 0.32 |
kasA | 2518313 | p.Pro67Ala | missense_variant | 0.19 |
kasA | 2518322 | p.Ser70Asp | missense_variant | 0.2 |
kasA | 2518333 | c.219C>T | synonymous_variant | 0.2 |
kasA | 2518336 | c.222A>G | synonymous_variant | 0.19 |
kasA | 2518343 | p.Met77Leu | missense_variant | 0.31 |
kasA | 2518348 | c.234A>G | synonymous_variant | 0.29 |
kasA | 2518417 | c.303G>C | synonymous_variant | 0.24 |
kasA | 2518429 | c.315A>C | synonymous_variant | 0.31 |
kasA | 2518435 | c.321G>C | synonymous_variant | 0.28 |
kasA | 2518444 | c.330T>C | synonymous_variant | 0.33 |
kasA | 2518447 | c.333T>C | synonymous_variant | 0.33 |
kasA | 2518448 | p.Val112Ile | missense_variant | 0.36 |
kasA | 2518462 | c.348A>G | synonymous_variant | 0.49 |
kasA | 2518468 | c.354A>C | synonymous_variant | 0.5 |
kasA | 2518475 | c.361A>C | synonymous_variant | 0.54 |
kasA | 2518486 | c.372G>A | synonymous_variant | 0.5 |
kasA | 2518506 | p.Ala131Glu | missense_variant | 0.51 |
kasA | 2518519 | c.405G>C | synonymous_variant | 0.53 |
kasA | 2518528 | c.414C>G | synonymous_variant | 0.54 |
kasA | 2518531 | c.417G>A | synonymous_variant | 0.51 |
kasA | 2518540 | c.426T>C | synonymous_variant | 0.52 |
kasA | 2518561 | c.447T>C | synonymous_variant | 0.41 |
kasA | 2518564 | c.450C>T | synonymous_variant | 0.4 |
kasA | 2518571 | p.Val153Thr | missense_variant | 0.37 |
kasA | 2518574 | p.Ile154Val | missense_variant | 0.39 |
kasA | 2518588 | c.474T>G | synonymous_variant | 0.48 |
kasA | 2518591 | c.477G>C | synonymous_variant | 0.49 |
kasA | 2518624 | c.510C>G | synonymous_variant | 0.43 |
kasA | 2518636 | c.522C>T | synonymous_variant | 0.35 |
kasA | 2518642 | c.528A>G | synonymous_variant | 0.33 |
kasA | 2518645 | c.531G>C | synonymous_variant | 0.32 |
kasA | 2518651 | c.537C>G | synonymous_variant | 0.32 |
kasA | 2518657 | c.543G>C | synonymous_variant | 0.34 |
kasA | 2518663 | c.549T>G | synonymous_variant | 0.35 |
kasA | 2518672 | c.558G>C | synonymous_variant | 0.43 |
kasA | 2518688 | p.Val192Ile | missense_variant | 0.39 |
kasA | 2518696 | c.582C>G | synonymous_variant | 0.37 |
kasA | 2518705 | c.591T>C | synonymous_variant | 0.3 |
kasA | 2518714 | c.600A>C | synonymous_variant | 0.28 |
kasA | 2518715 | p.Pro201Gly | missense_variant | 0.28 |
kasA | 2518723 | c.609G>A | synonymous_variant | 0.33 |
kasA | 2518727 | c.613C>T | synonymous_variant | 0.33 |
kasA | 2518732 | c.618C>G | synonymous_variant | 0.33 |
kasA | 2518735 | c.621C>T | synonymous_variant | 0.33 |
kasA | 2518747 | c.633C>G | synonymous_variant | 0.38 |
kasA | 2518780 | p.Glu222Asp | missense_variant | 0.34 |
kasA | 2518783 | c.669T>C | synonymous_variant | 0.33 |
kasA | 2518786 | c.672G>A | synonymous_variant | 0.33 |
kasA | 2518787 | p.Arg225Gly | missense_variant | 0.33 |
kasA | 2518792 | c.678C>G | synonymous_variant | 0.3 |
kasA | 2518795 | c.681C>G | synonymous_variant | 0.31 |
kasA | 2518798 | c.684G>T | synonymous_variant | 0.35 |
kasA | 2518810 | c.696G>A | synonymous_variant | 0.32 |
kasA | 2518822 | c.708C>T | synonymous_variant | 0.31 |
kasA | 2518825 | c.711T>C | synonymous_variant | 0.34 |
kasA | 2518834 | c.720C>T | synonymous_variant | 0.37 |
kasA | 2518840 | c.726C>G | synonymous_variant | 0.2 |
kasA | 2518843 | c.729T>C | synonymous_variant | 0.26 |
kasA | 2518849 | c.735G>C | synonymous_variant | 0.24 |
kasA | 2518853 | p.Leu247Val | missense_variant | 0.3 |
kasA | 2518864 | c.750G>C | synonymous_variant | 0.24 |
kasA | 2518879 | c.765A>G | synonymous_variant | 0.29 |
kasA | 2518885 | c.771T>C | synonymous_variant | 0.34 |
kasA | 2518898 | c.784T>C | synonymous_variant | 0.37 |
kasA | 2518906 | c.792A>T | synonymous_variant | 0.34 |
kasA | 2518907 | c.793T>C | synonymous_variant | 0.34 |
kasA | 2518927 | c.813C>T | synonymous_variant | 0.29 |
kasA | 2518930 | c.816G>C | synonymous_variant | 0.29 |
kasA | 2518939 | c.825T>C | synonymous_variant | 0.24 |
kasA | 2518942 | c.828T>C | synonymous_variant | 0.24 |
kasA | 2519062 | c.948T>G | synonymous_variant | 0.22 |
kasA | 2519072 | p.Ala320Thr | missense_variant | 0.18 |
kasA | 2519077 | c.963G>C | synonymous_variant | 0.19 |
kasA | 2519095 | c.981C>G | synonymous_variant | 0.18 |
kasA | 2519107 | c.993T>C | synonymous_variant | 0.19 |
kasA | 2519110 | p.Asp332Glu | missense_variant | 0.22 |
kasA | 2519122 | c.1008G>A | synonymous_variant | 0.25 |
kasA | 2519131 | c.1017G>A | synonymous_variant | 0.23 |
kasA | 2519135 | p.Ser341Gly | missense_variant | 0.23 |
kasA | 2519152 | c.1038G>C | synonymous_variant | 0.26 |
kasA | 2519158 | c.1044C>T | synonymous_variant | 0.26 |
kasA | 2519161 | c.1047G>C | synonymous_variant | 0.26 |
kasA | 2519167 | c.1053T>C | synonymous_variant | 0.26 |
kasA | 2519170 | c.1056G>T | synonymous_variant | 0.28 |
kasA | 2519171 | c.1057_1059delCTCinsTTG | synonymous_variant | 0.28 |
kasA | 2519185 | c.1071C>G | synonymous_variant | 0.28 |
kasA | 2519188 | c.1074G>C | synonymous_variant | 0.3 |
kasA | 2519215 | c.1101C>T | synonymous_variant | 0.35 |
kasA | 2519221 | c.1107G>C | synonymous_variant | 0.32 |
kasA | 2519224 | c.1110C>G | synonymous_variant | 0.32 |
kasA | 2519234 | p.Glu374His | missense_variant | 0.24 |
kasA | 2519239 | c.1125A>C | synonymous_variant | 0.22 |
kasA | 2519242 | c.1128C>T | synonymous_variant | 0.22 |
kasA | 2519245 | c.1131T>C | synonymous_variant | 0.26 |
kasA | 2519248 | c.1134C>G | synonymous_variant | 0.29 |
kasA | 2519257 | c.1143C>T | synonymous_variant | 0.33 |
kasA | 2519260 | c.1146T>C | synonymous_variant | 0.35 |
kasA | 2519266 | c.1152C>G | synonymous_variant | 0.38 |
kasA | 2519281 | c.1167G>C | synonymous_variant | 0.37 |
kasA | 2519284 | c.1170C>T | synonymous_variant | 0.37 |
kasA | 2519293 | p.Asp393Glu | missense_variant | 0.31 |
kasA | 2519297 | p.Arg395Lys | missense_variant | 0.31 |
kasA | 2519305 | c.1191A>C | synonymous_variant | 0.28 |
kasA | 2519306 | p.Val398Ile | missense_variant | 0.28 |
kasA | 2519332 | c.1218C>G | synonymous_variant | 0.32 |
kasA | 2519338 | c.1224T>C | synonymous_variant | 0.29 |
kasA | 2519341 | c.1227G>C | synonymous_variant | 0.26 |
ahpC | 2726279 | c.87G>A | synonymous_variant | 0.19 |
ahpC | 2726287 | p.Gly32Asp | missense_variant | 0.19 |
ahpC | 2726300 | c.108C>G | synonymous_variant | 0.24 |
ahpC | 2726303 | c.111T>C | synonymous_variant | 0.25 |
ahpC | 2726307 | p.Thr39Ser | missense_variant | 0.26 |
ahpC | 2726312 | c.120T>C | synonymous_variant | 0.21 |
ahpC | 2726318 | p.Glu42Asp | missense_variant | 0.25 |
ahpC | 2726324 | c.132A>C | synonymous_variant | 0.3 |
ahpC | 2726348 | c.156T>C | synonymous_variant | 0.32 |
ahpC | 2726354 | c.162G>C | synonymous_variant | 0.24 |
ahpC | 2726357 | c.165A>G | synonymous_variant | 0.25 |
ahpC | 2726579 | c.387T>C | synonymous_variant | 0.23 |
ahpC | 2726582 | c.390G>C | synonymous_variant | 0.28 |
ahpC | 2726591 | c.399C>G | synonymous_variant | 0.34 |
ahpC | 2726597 | c.405C>G | synonymous_variant | 0.35 |
ahpC | 2726600 | c.408T>C | synonymous_variant | 0.36 |
ahpC | 2726621 | c.429G>A | synonymous_variant | 0.38 |
ahpC | 2726627 | c.435G>A | synonymous_variant | 0.38 |
ahpC | 2726638 | p.Ala149Val | missense_variant | 0.37 |
ahpC | 2726645 | c.453C>G | synonymous_variant | 0.35 |
ahpC | 2726657 | c.465A>C | synonymous_variant | 0.4 |
ahpC | 2726669 | c.477T>C | synonymous_variant | 0.38 |
ahpC | 2726675 | c.483A>G | synonymous_variant | 0.33 |
ahpC | 2726681 | c.489A>G | synonymous_variant | 0.3 |
ahpC | 2726687 | c.495C>G | synonymous_variant | 0.23 |
folC | 2746561 | c.1038C>G | synonymous_variant | 0.31 |
folC | 2746564 | c.1035A>G | synonymous_variant | 0.31 |
folC | 2746584 | c.1015T>C | synonymous_variant | 0.35 |
folC | 2746609 | c.990T>C | synonymous_variant | 0.43 |
folC | 2746612 | c.987C>A | synonymous_variant | 0.41 |
folC | 2746615 | c.984C>G | synonymous_variant | 0.41 |
folC | 2746631 | p.Gly323Val | missense_variant | 0.4 |
folC | 2747302 | c.297A>G | synonymous_variant | 0.32 |
folC | 2747314 | c.285A>C | synonymous_variant | 0.33 |
folC | 2747317 | c.282C>A | synonymous_variant | 0.37 |
folC | 2747341 | p.Val86Leu | missense_variant | 0.38 |
folC | 2747359 | c.240C>G | synonymous_variant | 0.45 |
folC | 2747374 | c.225G>A | synonymous_variant | 0.51 |
folC | 2747395 | c.204T>C | synonymous_variant | 0.41 |
folC | 2747398 | c.201C>T | synonymous_variant | 0.38 |
folC | 2747404 | c.195G>C | synonymous_variant | 0.34 |
folC | 2747407 | c.192T>C | synonymous_variant | 0.32 |
folC | 2747410 | p.Ser63Gly | missense_variant | 0.35 |
folC | 2747419 | c.180C>G | synonymous_variant | 0.32 |
folC | 2747422 | c.177G>A | synonymous_variant | 0.32 |
folC | 2747430 | c.169C>T | synonymous_variant | 0.36 |
folC | 2747442 | c.157T>C | synonymous_variant | 0.22 |
pepQ | 2859704 | c.715T>C | synonymous_variant | 0.19 |
pepQ | 2859711 | c.708C>G | synonymous_variant | 0.21 |
pepQ | 2859714 | c.705C>G | synonymous_variant | 0.21 |
pepQ | 2859732 | c.687C>T | synonymous_variant | 0.24 |
pepQ | 2859735 | c.684G>C | synonymous_variant | 0.23 |
pepQ | 2859739 | p.Ala227Gly | missense_variant | 0.21 |
pepQ | 2859750 | c.669C>T | synonymous_variant | 0.19 |
ribD | 2987307 | p.Ala157Pro | missense_variant | 0.26 |
Rv2752c | 3064860 | c.1332G>C | synonymous_variant | 0.2 |
Rv2752c | 3064956 | c.1236T>C | synonymous_variant | 0.28 |
Rv2752c | 3064965 | c.1227G>C | synonymous_variant | 0.37 |
Rv2752c | 3064968 | c.1224G>A | synonymous_variant | 0.35 |
Rv2752c | 3064980 | c.1212C>G | synonymous_variant | 0.38 |
Rv2752c | 3064995 | c.1197C>G | synonymous_variant | 0.43 |
Rv2752c | 3064998 | c.1194A>G | synonymous_variant | 0.44 |
Rv2752c | 3065013 | c.1179G>C | synonymous_variant | 0.46 |
Rv2752c | 3065040 | c.1152C>G | synonymous_variant | 0.33 |
Rv2752c | 3065052 | c.1140G>A | synonymous_variant | 0.24 |
Rv2752c | 3065655 | c.537C>T | synonymous_variant | 0.18 |
Rv2752c | 3065673 | p.Phe173Leu | missense_variant | 0.19 |
Rv2752c | 3065676 | c.516G>A | synonymous_variant | 0.21 |
Rv2752c | 3065867 | c.325T>C | synonymous_variant | 0.23 |
Rv2752c | 3065877 | c.315G>C | synonymous_variant | 0.31 |
Rv2752c | 3065889 | c.303G>C | synonymous_variant | 0.32 |
Rv2752c | 3065892 | c.300C>T | synonymous_variant | 0.32 |
Rv2752c | 3065901 | c.291A>T | synonymous_variant | 0.45 |
Rv2752c | 3065916 | c.276T>C | synonymous_variant | 0.42 |
Rv2752c | 3065946 | p.Gly82Ala | missense_variant | 0.49 |
Rv2752c | 3065957 | c.235T>C | synonymous_variant | 0.49 |
Rv2752c | 3065972 | p.Ile74Val | missense_variant | 0.34 |
Rv2752c | 3065976 | c.216C>T | synonymous_variant | 0.33 |
Rv2752c | 3065979 | c.213T>C | synonymous_variant | 0.34 |
Rv2752c | 3065982 | c.210G>C | synonymous_variant | 0.34 |
Rv2752c | 3065993 | p.Val67Ile | missense_variant | 0.27 |
Rv2752c | 3065997 | c.195C>T | synonymous_variant | 0.24 |
Rv2752c | 3066002 | p.Met64Leu | missense_variant | 0.21 |
Rv2752c | 3066003 | c.189C>T | synonymous_variant | 0.21 |
Rv2752c | 3066075 | c.117A>G | synonymous_variant | 0.2 |
Rv2752c | 3066087 | c.105A>G | synonymous_variant | 0.29 |
Rv2752c | 3066096 | c.96G>C | synonymous_variant | 0.32 |
Rv2752c | 3066118 | p.Asn25Ser | missense_variant | 0.33 |
Rv2752c | 3066129 | c.63G>C | synonymous_variant | 0.35 |
Rv2752c | 3066146 | c.46T>C | synonymous_variant | 0.32 |
Rv2752c | 3066154 | p.Ser13Val | missense_variant | 0.22 |
Rv2752c | 3066168 | c.24A>T | synonymous_variant | 0.22 |
Rv2752c | 3066335 | c.-144T>C | upstream_gene_variant | 0.21 |
Rv2752c | 3066336 | c.-145C>G | upstream_gene_variant | 0.21 |
Rv2752c | 3066339 | c.-148G>C | upstream_gene_variant | 0.39 |
Rv2752c | 3066350 | c.-159T>A | upstream_gene_variant | 0.38 |
Rv2752c | 3066360 | c.-169T>C | upstream_gene_variant | 0.42 |
Rv2752c | 3066363 | c.-172G>C | upstream_gene_variant | 0.42 |
Rv2752c | 3066381 | c.-190C>T | upstream_gene_variant | 0.37 |
Rv2752c | 3066390 | c.-199C>A | upstream_gene_variant | 0.32 |
thyX | 3067304 | p.Glu214Ala | missense_variant | 0.29 |
thyX | 3067316 | c.630A>G | synonymous_variant | 0.4 |
thyX | 3067337 | p.His203Gln | missense_variant | 0.5 |
thyX | 3067347 | p.Ala200Gly | missense_variant | 0.49 |
thyX | 3067349 | c.597G>T | synonymous_variant | 0.49 |
thyX | 3067355 | c.591A>G | synonymous_variant | 0.49 |
thyX | 3067358 | c.588C>T | synonymous_variant | 0.54 |
thyX | 3067364 | c.582C>T | synonymous_variant | 0.54 |
thyX | 3067391 | c.555G>C | synonymous_variant | 0.55 |
thyX | 3067406 | c.540A>G | synonymous_variant | 0.49 |
thyX | 3067427 | c.519G>C | synonymous_variant | 0.51 |
thyX | 3067433 | c.513C>T | synonymous_variant | 0.46 |
thyX | 3067436 | c.510C>G | synonymous_variant | 0.45 |
thyX | 3067439 | c.507A>G | synonymous_variant | 0.42 |
thyX | 3067442 | c.504C>G | synonymous_variant | 0.41 |
thyX | 3067454 | c.492C>A | synonymous_variant | 0.42 |
thyX | 3067475 | p.Gln157Glu | missense_variant | 0.35 |
thyX | 3067500 | p.Lys149Arg | missense_variant | 0.24 |
thyX | 3067503 | p.Ala148Gly | missense_variant | 0.28 |
thyX | 3067515 | p.Ser144Thr | missense_variant | 0.22 |
thyX | 3067517 | c.429C>T | synonymous_variant | 0.19 |
thyX | 3067595 | c.351C>G | synonymous_variant | 0.26 |
thyX | 3067602 | p.Arg115Gln | missense_variant | 0.24 |
thyX | 3067607 | p.Asp113Gln | missense_variant | 0.24 |
thyX | 3067611 | p.Lys112Arg | missense_variant | 0.24 |
thyX | 3067616 | c.330C>G | synonymous_variant | 0.26 |
thyX | 3067619 | c.327A>G | synonymous_variant | 0.31 |
thyX | 3067631 | c.315C>G | synonymous_variant | 0.42 |
thyX | 3067640 | c.306G>A | synonymous_variant | 0.5 |
thyX | 3067643 | c.303C>T | synonymous_variant | 0.54 |
thyX | 3067658 | c.288C>T | synonymous_variant | 0.57 |
thyX | 3067661 | c.285C>G | synonymous_variant | 0.57 |
thyX | 3067676 | c.270C>T | synonymous_variant | 0.47 |
thyX | 3067682 | c.264G>T | synonymous_variant | 0.46 |
thyX | 3067685 | c.261A>G | synonymous_variant | 0.46 |
thyX | 3067691 | p.Ile85Val | missense_variant | 0.47 |
thyX | 3067694 | c.252G>C | synonymous_variant | 0.47 |
thyX | 3067718 | c.228C>G | synonymous_variant | 0.51 |
thyX | 3067721 | c.225T>C | synonymous_variant | 0.48 |
thyX | 3067727 | c.219A>C | synonymous_variant | 0.48 |
thyX | 3067738 | p.Phe70Leu | missense_variant | 0.49 |
thyX | 3067742 | c.204A>G | synonymous_variant | 0.45 |
thyX | 3067745 | c.201C>G | synonymous_variant | 0.46 |
thyX | 3067761 | p.Arg62Lys | missense_variant | 0.46 |
thyX | 3067766 | c.180C>T | synonymous_variant | 0.49 |
thyX | 3067769 | c.177C>A | synonymous_variant | 0.47 |
thyX | 3067781 | c.165C>G | synonymous_variant | 0.49 |
thyX | 3067792 | p.Pro52Ala | missense_variant | 0.5 |
thyX | 3067793 | c.153T>C | synonymous_variant | 0.49 |
thyX | 3067814 | c.132T>C | synonymous_variant | 0.39 |
thyX | 3067820 | c.126C>G | synonymous_variant | 0.4 |
thyX | 3067844 | c.102G>A | synonymous_variant | 0.2 |
thyX | 3067848 | p.Pro33His | missense_variant | 0.19 |
thyX | 3067859 | c.87C>T | synonymous_variant | 0.19 |
thyA | 3073794 | c.678A>G | synonymous_variant | 0.18 |
thyA | 3073800 | c.672G>A | synonymous_variant | 0.21 |
thyA | 3073803 | c.669G>A | synonymous_variant | 0.24 |
thyA | 3073806 | c.666C>G | synonymous_variant | 0.19 |
thyA | 3073821 | p.Arg217His | missense_variant | 0.41 |
thyA | 3073824 | c.648A>G | synonymous_variant | 0.39 |
thyA | 3073827 | c.645A>G | synonymous_variant | 0.38 |
thyA | 3073836 | c.636C>T | synonymous_variant | 0.44 |
thyA | 3073839 | c.633T>C | synonymous_variant | 0.45 |
thyA | 3073860 | c.612C>T | synonymous_variant | 0.59 |
thyA | 3073863 | c.609T>C | synonymous_variant | 0.59 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 0.4 |
thyA | 3073881 | c.591C>T | synonymous_variant | 0.58 |
thyA | 3073889 | p.Ser195Ala | missense_variant | 0.58 |
thyA | 3073892 | c.580T>C | synonymous_variant | 0.56 |
thyA | 3073893 | c.579C>T | synonymous_variant | 0.56 |
thyA | 3073902 | c.570C>G | synonymous_variant | 0.63 |
thyA | 3073920 | c.552C>G | synonymous_variant | 0.61 |
thyA | 3073926 | c.546G>A | synonymous_variant | 0.63 |
thyA | 3073929 | c.543T>C | synonymous_variant | 0.62 |
thyA | 3073953 | c.519T>A | synonymous_variant | 0.54 |
thyA | 3073956 | c.516G>C | synonymous_variant | 0.53 |
thyA | 3073959 | c.513T>C | synonymous_variant | 0.53 |
thyA | 3073977 | c.495A>G | synonymous_variant | 0.45 |
thyA | 3074004 | c.468T>C | synonymous_variant | 0.34 |
thyA | 3074010 | c.462C>G | synonymous_variant | 0.35 |
thyA | 3074013 | c.459C>T | synonymous_variant | 0.32 |
thyA | 3074022 | c.450C>T | synonymous_variant | 0.21 |
thyA | 3074029 | p.Ala148Val | missense_variant | 0.19 |
thyA | 3074037 | c.435C>G | synonymous_variant | 0.19 |
thyA | 3074076 | c.396C>G | synonymous_variant | 0.42 |
thyA | 3074097 | c.375C>A | synonymous_variant | 0.41 |
thyA | 3074103 | c.369C>G | synonymous_variant | 0.37 |
thyA | 3074106 | c.366T>C | synonymous_variant | 0.37 |
thyA | 3074117 | c.355C>T | synonymous_variant | 0.4 |
thyA | 3074120 | c.352T>C | synonymous_variant | 0.35 |
thyA | 3074121 | p.Asp117Lys | missense_variant | 0.35 |
thyA | 3074134 | c.337_338delAGinsTC | synonymous_variant | 0.35 |
thyA | 3074147 | p.Ile109Val | missense_variant | 0.42 |
thyA | 3074154 | c.318T>C | synonymous_variant | 0.41 |
thyA | 3074160 | c.312A>G | synonymous_variant | 0.4 |
thyA | 3074165 | p.Ala103Thr | missense_variant | 0.36 |
thyA | 3074334 | c.138T>C | synonymous_variant | 0.26 |
thyA | 3074339 | p.Leu45Ile | missense_variant | 0.26 |
thyA | 3074349 | c.123T>G | synonymous_variant | 0.29 |
thyA | 3074360 | c.112T>C | synonymous_variant | 0.3 |
thyA | 3074361 | c.111T>C | synonymous_variant | 0.3 |
thyA | 3074376 | p.Gln32His | missense_variant | 0.19 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087487 | p.Tyr223Phe | missense_variant | 0.19 |
ald | 3087499 | p.Gly227Asp | missense_variant | 0.22 |
ald | 3087527 | c.708T>C | synonymous_variant | 0.19 |
ald | 3087530 | c.711G>A | synonymous_variant | 0.2 |
fprA | 3473812 | c.-195G>A | upstream_gene_variant | 0.37 |
fprA | 3473815 | c.-192G>C | upstream_gene_variant | 0.36 |
fprA | 3473843 | c.-164C>G | upstream_gene_variant | 0.39 |
fprA | 3473848 | c.-159_-157delCAAinsGAG | upstream_gene_variant | 0.38 |
fprA | 3473866 | c.-141T>C | upstream_gene_variant | 0.27 |
fprA | 3473869 | c.-138A>G | upstream_gene_variant | 0.23 |
fprA | 3473872 | c.-135G>A | upstream_gene_variant | 0.23 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474130 | c.124T>C | synonymous_variant | 0.33 |
fprA | 3474135 | c.129G>C | synonymous_variant | 0.32 |
fprA | 3474138 | c.132T>G | synonymous_variant | 0.31 |
fprA | 3474141 | c.135C>G | synonymous_variant | 0.39 |
fprA | 3474153 | c.147G>C | synonymous_variant | 0.5 |
fprA | 3474162 | c.156G>C | synonymous_variant | 0.56 |
fprA | 3474168 | c.162G>A | synonymous_variant | 0.55 |
fprA | 3474171 | c.165G>C | synonymous_variant | 0.53 |
fprA | 3474174 | c.168T>C | synonymous_variant | 0.53 |
fprA | 3474204 | c.198A>G | synonymous_variant | 0.49 |
fprA | 3474213 | c.207G>A | synonymous_variant | 0.45 |
fprA | 3474216 | c.210G>C | synonymous_variant | 0.39 |
fprA | 3474217 | p.Ala71Ser | missense_variant | 0.4 |
fprA | 3474237 | c.231C>G | synonymous_variant | 0.32 |
fprA | 3474729 | c.723G>A | synonymous_variant | 0.31 |
fprA | 3474765 | c.759T>C | synonymous_variant | 0.43 |
fprA | 3474771 | c.765T>C | synonymous_variant | 0.42 |
fprA | 3474777 | p.Asp257Glu | missense_variant | 0.44 |
fprA | 3474783 | c.777A>G | synonymous_variant | 0.44 |
fprA | 3474790 | p.Pro262Ser | missense_variant | 0.41 |
fprA | 3474801 | c.795C>T | synonymous_variant | 0.42 |
fprA | 3474804 | c.798C>A | synonymous_variant | 0.4 |
fprA | 3474807 | p.Met267Ile | missense_variant | 0.41 |
fprA | 3474825 | c.819C>A | synonymous_variant | 0.44 |
fprA | 3474899 | p.Gly298Asp | missense_variant | 0.17 |
Rv3236c | 3612009 | p.Ala370Thr | missense_variant | 1.0 |
fbiB | 3640599 | c.-936C>G | upstream_gene_variant | 0.18 |
fbiA | 3640660 | p.Gln40Glu | missense_variant | 0.17 |
fbiA | 3640681 | p.Val47Ile | missense_variant | 0.23 |
fbiA | 3640701 | p.Ile53Met | missense_variant | 0.21 |
fbiB | 3640707 | c.-828G>C | upstream_gene_variant | 0.22 |
fbiB | 3640713 | c.-822T>C | upstream_gene_variant | 0.21 |
fbiB | 3640722 | c.-813G>C | upstream_gene_variant | 0.2 |
fbiB | 3640725 | c.-810T>C | upstream_gene_variant | 0.2 |
fbiB | 3640743 | c.-792T>C | upstream_gene_variant | 0.23 |
fbiB | 3640747 | c.-788C>T | upstream_gene_variant | 0.24 |
fbiB | 3640758 | c.-777G>C | upstream_gene_variant | 0.26 |
fbiB | 3640761 | c.-774G>C | upstream_gene_variant | 0.24 |
fbiB | 3640767 | c.-768C>G | upstream_gene_variant | 0.25 |
fbiA | 3640768 | p.Gln76Glu | missense_variant | 0.25 |
fbiB | 3640797 | c.-738T>C | upstream_gene_variant | 0.21 |
fbiA | 3640808 | p.Met89Lys | missense_variant | 0.25 |
fbiA | 3640810 | p.Gln90Glu | missense_variant | 0.25 |
fbiB | 3640821 | c.-714G>T | upstream_gene_variant | 0.21 |
fbiB | 3640824 | c.-711C>T | upstream_gene_variant | 0.21 |
fbiB | 3640827 | c.-708T>C | upstream_gene_variant | 0.21 |
fbiB | 3641016 | c.-519C>T | upstream_gene_variant | 0.2 |
fbiB | 3641019 | c.-516G>C | upstream_gene_variant | 0.21 |
fbiB | 3641046 | c.-489T>C | upstream_gene_variant | 0.21 |
fbiB | 3641049 | c.-486T>C | upstream_gene_variant | 0.21 |
fbiB | 3641052 | c.-483G>A | upstream_gene_variant | 0.21 |
fbiB | 3641073 | c.-462T>C | upstream_gene_variant | 0.19 |
fbiB | 3642542 | c.1008A>G | synonymous_variant | 0.2 |
fbiB | 3642571 | p.Glu346Gly | missense_variant | 0.33 |
fbiB | 3642578 | c.1044C>G | synonymous_variant | 0.32 |
fbiB | 3642581 | c.1047A>C | synonymous_variant | 0.33 |
fbiB | 3642587 | p.Met351Ile | missense_variant | 0.31 |
fbiB | 3642588 | p.Leu352Met | missense_variant | 0.31 |
fbiB | 3642602 | c.1068A>C | synonymous_variant | 0.33 |
fbiB | 3642605 | c.1071A>G | synonymous_variant | 0.33 |
fbiB | 3642611 | c.1077C>T | synonymous_variant | 0.33 |
fbiB | 3642614 | c.1080C>T | synonymous_variant | 0.33 |
fbiB | 3642620 | c.1086T>C | synonymous_variant | 0.33 |
fbiB | 3642626 | c.1092C>G | synonymous_variant | 0.33 |
fbiB | 3642719 | c.1185T>C | synonymous_variant | 0.22 |
fbiB | 3642743 | c.1209T>C | synonymous_variant | 0.33 |
fbiB | 3642749 | c.1215T>C | synonymous_variant | 0.39 |
fbiB | 3642772 | p.Asp413Gly | missense_variant | 0.33 |
fbiB | 3642779 | c.1245A>T | synonymous_variant | 0.28 |
fbiB | 3642781 | p.Val416Gly | missense_variant | 0.27 |
fbiB | 3642785 | c.1251C>T | synonymous_variant | 0.26 |
fbiB | 3642791 | c.1257G>A | synonymous_variant | 0.24 |
alr | 3840719 | c.702A>G | synonymous_variant | 1.0 |
alr | 3841068 | p.Ile118Thr | missense_variant | 0.31 |
alr | 3841077 | p.Pro115Arg | missense_variant | 0.33 |
alr | 3841079 | c.342T>C | synonymous_variant | 0.33 |
alr | 3841088 | c.333C>G | synonymous_variant | 0.32 |
alr | 3841106 | c.315T>C | synonymous_variant | 0.33 |
alr | 3841112 | c.309T>C | synonymous_variant | 0.34 |
alr | 3841115 | c.306T>C | synonymous_variant | 0.32 |
alr | 3841118 | c.303C>G | synonymous_variant | 0.32 |
alr | 3841123 | c.298C>T | synonymous_variant | 0.31 |
alr | 3841127 | c.294A>G | synonymous_variant | 0.29 |
alr | 3841151 | c.270C>T | synonymous_variant | 0.25 |
rpoA | 3877494 | p.Glu338Asp | missense_variant | 0.32 |
rpoA | 3877503 | p.Ala335Gly | missense_variant | 0.41 |
rpoA | 3877509 | p.Glu333Asp | missense_variant | 0.39 |
rpoA | 3877513 | p.Thr332Ser | missense_variant | 0.38 |
rpoA | 3877515 | c.993G>C | synonymous_variant | 0.39 |
rpoA | 3877521 | c.987C>A | synonymous_variant | 0.44 |
rpoA | 3877542 | c.966C>T | synonymous_variant | 0.56 |
rpoA | 3877557 | c.951C>G | synonymous_variant | 0.59 |
rpoA | 3877569 | p.Pro313Ala | missense_variant | 0.61 |
rpoA | 3877584 | c.924C>G | synonymous_variant | 0.62 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.65 |
rpoA | 3877593 | c.915C>T | synonymous_variant | 0.65 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.68 |
rpoA | 3877638 | c.870T>C | synonymous_variant | 0.63 |
rpoA | 3877656 | c.852T>C | synonymous_variant | 0.6 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.64 |
rpoA | 3877679 | p.Ala277Ser | missense_variant | 0.65 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.67 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.66 |
rpoA | 3877704 | c.804G>T | synonymous_variant | 0.68 |
rpoA | 3877728 | c.780C>G | synonymous_variant | 0.62 |
rpoA | 3877731 | c.777G>C | synonymous_variant | 0.6 |
rpoA | 3877737 | c.771G>C | synonymous_variant | 0.63 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.64 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.61 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.64 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.62 |
rpoA | 3877794 | c.714G>A | synonymous_variant | 0.6 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.59 |
rpoA | 3877827 | c.681C>G | synonymous_variant | 0.56 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.52 |
rpoA | 3877848 | c.660C>G | synonymous_variant | 0.6 |
rpoA | 3877857 | c.651G>A | synonymous_variant | 0.58 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.55 |
rpoA | 3877872 | c.636C>T | synonymous_variant | 0.48 |
rpoA | 3877875 | c.633T>G | synonymous_variant | 0.47 |
rpoA | 3877878 | c.630G>C | synonymous_variant | 0.48 |
rpoA | 3877881 | c.627G>T | synonymous_variant | 0.48 |
rpoA | 3877893 | c.615C>G | synonymous_variant | 0.47 |
rpoA | 3877899 | p.Ser203Thr | missense_variant | 0.45 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.43 |
rpoA | 3877908 | p.Asn200Ser | missense_variant | 0.44 |
rpoA | 3877920 | c.588G>C | synonymous_variant | 0.49 |
rpoA | 3877926 | c.582G>C | synonymous_variant | 0.56 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.47 |
rpoA | 3877986 | c.522G>C | synonymous_variant | 0.47 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.47 |
rpoA | 3877992 | c.516C>G | synonymous_variant | 0.47 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.54 |
rpoA | 3878016 | c.492C>G | synonymous_variant | 0.55 |
rpoA | 3878022 | c.486T>C | synonymous_variant | 0.54 |
rpoA | 3878025 | c.483C>T | synonymous_variant | 0.52 |
rpoA | 3878031 | c.477T>C | synonymous_variant | 0.52 |
rpoA | 3878040 | c.468T>C | synonymous_variant | 0.52 |
rpoA | 3878046 | c.462T>G | synonymous_variant | 0.49 |
rpoA | 3878050 | p.Arg153Lys | missense_variant | 0.48 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.52 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.49 |
rpoA | 3878067 | c.441C>G | synonymous_variant | 0.52 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.52 |
rpoA | 3878094 | c.414C>G | synonymous_variant | 0.59 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.54 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.55 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.6 |
rpoA | 3878130 | c.378C>G | synonymous_variant | 0.61 |
rpoA | 3878133 | c.375C>T | synonymous_variant | 0.62 |
rpoA | 3878143 | p.Gly122Asp | missense_variant | 0.64 |
rpoA | 3878145 | c.363C>T | synonymous_variant | 0.66 |
rpoA | 3878184 | c.324C>T | synonymous_variant | 0.61 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.64 |
rpoA | 3878199 | c.309T>C | synonymous_variant | 0.66 |
rpoA | 3878205 | c.303T>C | synonymous_variant | 0.68 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.68 |
rpoA | 3878241 | c.267G>A | synonymous_variant | 0.73 |
rpoA | 3878247 | c.261G>C | synonymous_variant | 0.76 |
rpoA | 3878268 | c.240C>G | synonymous_variant | 0.74 |
rpoA | 3878283 | p.Glu75Asp | missense_variant | 0.74 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.74 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.72 |
rpoA | 3878304 | c.204G>C | synonymous_variant | 0.68 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 0.65 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.67 |
rpoA | 3878331 | c.177A>G | synonymous_variant | 0.68 |
rpoA | 3878337 | c.171T>C | synonymous_variant | 0.71 |
rpoA | 3878358 | c.150C>G | synonymous_variant | 0.67 |
rpoA | 3878364 | c.144A>C | synonymous_variant | 0.65 |
rpoA | 3878385 | c.123C>G | synonymous_variant | 0.58 |
rpoA | 3878391 | c.117T>C | synonymous_variant | 0.58 |
rpoA | 3878403 | c.105C>T | synonymous_variant | 0.55 |
rpoA | 3878406 | c.102G>T | synonymous_variant | 0.54 |
rpoA | 3878409 | c.99C>G | synonymous_variant | 0.52 |
rpoA | 3878427 | c.81G>A | synonymous_variant | 0.55 |
rpoA | 3878442 | c.66G>C | synonymous_variant | 0.44 |
rpoA | 3878451 | c.57C>G | synonymous_variant | 0.42 |
rpoA | 3878454 | c.54A>G | synonymous_variant | 0.4 |
rpoA | 3878458 | p.Asn17Thr | missense_variant | 0.4 |
rpoA | 3878468 | p.Leu14Val | missense_variant | 0.3 |
rpoA | 3878470 | p.Val13Ala | missense_variant | 0.32 |
rpoA | 3878472 | p.Asp12Glu | missense_variant | 0.32 |
rpoA | 3878475 | c.33G>A | synonymous_variant | 0.33 |
rpoA | 3878484 | c.24C>A | synonymous_variant | 0.34 |
rpoA | 3878490 | c.18C>A | synonymous_variant | 0.35 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.25 |
ddn | 3986646 | c.-198_-196delCTCinsTTG | upstream_gene_variant | 0.37 |
ddn | 3986654 | c.-190C>T | upstream_gene_variant | 0.37 |
ddn | 3986655 | c.-189A>T | upstream_gene_variant | 0.36 |
ddn | 3986660 | c.-184C>T | upstream_gene_variant | 0.36 |
ddn | 3986667 | c.-177_-175delCTCinsACG | upstream_gene_variant | 0.35 |
ddn | 3986696 | c.-148G>C | upstream_gene_variant | 0.33 |
ddn | 3986699 | c.-145C>G | upstream_gene_variant | 0.23 |
clpC1 | 4038233 | c.2472C>T | synonymous_variant | 0.21 |
clpC1 | 4038239 | c.2466T>A | synonymous_variant | 0.35 |
clpC1 | 4038255 | p.Val817Lys | missense_variant | 0.37 |
clpC1 | 4038271 | p.Pro812Ala | missense_variant | 0.34 |
clpC1 | 4038272 | c.2433T>C | synonymous_variant | 0.33 |
clpC1 | 4038275 | c.2430A>G | synonymous_variant | 0.35 |
clpC1 | 4038278 | c.2427T>C | synonymous_variant | 0.37 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 0.6 |
clpC1 | 4038308 | p.Val799Ile | missense_variant | 0.48 |
clpC1 | 4038314 | c.2391T>C | synonymous_variant | 0.49 |
clpC1 | 4038347 | c.2358G>C | synonymous_variant | 0.44 |
clpC1 | 4038350 | c.2355C>T | synonymous_variant | 0.45 |
clpC1 | 4038356 | c.2349T>C | synonymous_variant | 0.4 |
clpC1 | 4038359 | c.2346A>G | synonymous_variant | 0.4 |
clpC1 | 4038368 | c.2337T>C | synonymous_variant | 0.44 |
clpC1 | 4038377 | c.2328C>G | synonymous_variant | 0.48 |
clpC1 | 4038398 | c.2307G>T | synonymous_variant | 0.42 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 0.41 |
clpC1 | 4038410 | c.2295C>T | synonymous_variant | 0.42 |
clpC1 | 4038419 | c.2286T>C | synonymous_variant | 0.41 |
clpC1 | 4038428 | c.2277G>T | synonymous_variant | 0.43 |
clpC1 | 4038436 | p.Ala757Ser | missense_variant | 0.4 |
clpC1 | 4038444 | p.Ala754Lys | missense_variant | 0.35 |
clpC1 | 4038446 | c.2259T>C | synonymous_variant | 0.35 |
clpC1 | 4038456 | p.Val750Glu | missense_variant | 0.46 |
clpC1 | 4038485 | p.Gly740Lys | missense_variant | 0.46 |
clpC1 | 4038488 | p.Ala739Glu | missense_variant | 0.45 |
clpC1 | 4038498 | p.Ser736Asn | missense_variant | 0.55 |
clpC1 | 4038509 | p.Asp732Glu | missense_variant | 0.55 |
clpC1 | 4038530 | c.2175G>A | synonymous_variant | 0.61 |
clpC1 | 4038536 | c.2169C>T | synonymous_variant | 0.62 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.59 |
clpC1 | 4038623 | c.2082A>G | synonymous_variant | 0.46 |
clpC1 | 4038644 | p.Glu687Ala | missense_variant | 0.28 |
clpC1 | 4038650 | c.2055C>G | synonymous_variant | 0.28 |
clpC1 | 4038653 | c.2052C>T | synonymous_variant | 0.28 |
clpC1 | 4038658 | p.Lys683Gln | missense_variant | 0.28 |
clpC1 | 4038661 | p.Ser682Thr | missense_variant | 0.27 |
clpC1 | 4038662 | c.2043T>C | synonymous_variant | 0.32 |
clpC1 | 4038679 | p.Pro676Ala | missense_variant | 0.42 |
clpC1 | 4038683 | c.2022T>C | synonymous_variant | 0.42 |
clpC1 | 4038692 | p.Ser671Ala | missense_variant | 0.32 |
clpC1 | 4038695 | c.2010C>G | synonymous_variant | 0.29 |
clpC1 | 4038701 | c.2004G>C | synonymous_variant | 0.32 |
clpC1 | 4038704 | c.2001T>C | synonymous_variant | 0.35 |
clpC1 | 4038713 | c.1992T>C | synonymous_variant | 0.4 |
clpC1 | 4038749 | c.1956C>T | synonymous_variant | 0.48 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.51 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 0.59 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.65 |
clpC1 | 4038815 | c.1890G>A | synonymous_variant | 0.66 |
clpC1 | 4038818 | c.1887G>A | synonymous_variant | 0.66 |
clpC1 | 4038845 | c.1860G>C | synonymous_variant | 0.66 |
clpC1 | 4038857 | c.1848C>A | synonymous_variant | 0.27 |
clpC1 | 4038869 | c.1836G>A | synonymous_variant | 0.7 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.74 |
clpC1 | 4038884 | c.1821C>T | synonymous_variant | 0.69 |
clpC1 | 4038887 | c.1818G>A | synonymous_variant | 0.67 |
clpC1 | 4038899 | c.1806C>G | synonymous_variant | 0.69 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.66 |
clpC1 | 4038914 | c.1791G>A | synonymous_variant | 0.64 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 0.67 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.62 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.63 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.67 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.59 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.58 |
clpC1 | 4038980 | c.1725C>T | synonymous_variant | 0.59 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.59 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.57 |
clpC1 | 4039001 | p.Asn568Glu | missense_variant | 0.57 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.58 |
clpC1 | 4039034 | c.1671C>G | synonymous_variant | 0.58 |
clpC1 | 4039037 | c.1668T>G | synonymous_variant | 0.57 |
clpC1 | 4039064 | c.1641C>T | synonymous_variant | 0.6 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.54 |
clpC1 | 4039103 | c.1602T>C | synonymous_variant | 0.5 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.51 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.51 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.51 |
clpC1 | 4039124 | c.1581C>A | synonymous_variant | 0.52 |
clpC1 | 4039133 | c.1572C>G | synonymous_variant | 0.5 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.52 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.51 |
clpC1 | 4039154 | c.1551G>C | synonymous_variant | 0.54 |
clpC1 | 4039163 | p.Leu514Ile | missense_variant | 0.47 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.51 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.53 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.55 |
clpC1 | 4039208 | c.1497C>G | synonymous_variant | 0.53 |
clpC1 | 4039271 | c.1434G>A | synonymous_variant | 0.49 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.45 |
clpC1 | 4039277 | c.1428C>T | synonymous_variant | 0.44 |
clpC1 | 4039286 | c.1419T>C | synonymous_variant | 0.41 |
clpC1 | 4039292 | c.1413C>T | synonymous_variant | 0.37 |
clpC1 | 4039295 | c.1410A>T | synonymous_variant | 0.34 |
clpC1 | 4039298 | c.1407T>C | synonymous_variant | 0.37 |
clpC1 | 4039304 | c.1401G>A | synonymous_variant | 0.36 |
clpC1 | 4039313 | c.1392C>T | synonymous_variant | 0.24 |
clpC1 | 4039364 | c.1341C>G | synonymous_variant | 0.23 |
clpC1 | 4039382 | c.1323C>G | synonymous_variant | 0.37 |
clpC1 | 4039391 | c.1314T>G | synonymous_variant | 0.32 |
clpC1 | 4039394 | c.1311G>C | synonymous_variant | 0.35 |
clpC1 | 4039397 | c.1308A>G | synonymous_variant | 0.35 |
clpC1 | 4039406 | c.1299G>C | synonymous_variant | 0.35 |
clpC1 | 4039409 | c.1296T>C | synonymous_variant | 0.37 |
clpC1 | 4039412 | c.1293T>G | synonymous_variant | 0.38 |
clpC1 | 4039415 | c.1290G>A | synonymous_variant | 0.42 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.53 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.59 |
clpC1 | 4039454 | c.1251A>T | synonymous_variant | 0.57 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 0.53 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.53 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.54 |
clpC1 | 4039481 | c.1224T>G | synonymous_variant | 0.52 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.46 |
clpC1 | 4039541 | c.1164C>G | synonymous_variant | 0.42 |
clpC1 | 4039554 | p.Thr384Ser | missense_variant | 0.39 |
clpC1 | 4039556 | c.1149G>C | synonymous_variant | 0.39 |
clpC1 | 4039559 | c.1146C>T | synonymous_variant | 0.38 |
clpC1 | 4039566 | p.Val380Thr | missense_variant | 0.38 |
clpC1 | 4039568 | p.Met379Ile | missense_variant | 0.38 |
clpC1 | 4039574 | p.Ala377Ser | missense_variant | 0.37 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.38 |
clpC1 | 4039586 | c.1119G>C | synonymous_variant | 0.48 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.65 |
clpC1 | 4039621 | c.1084C>T | synonymous_variant | 0.65 |
clpC1 | 4039622 | c.1083C>T | synonymous_variant | 0.65 |
clpC1 | 4039661 | c.1044T>C | synonymous_variant | 0.71 |
clpC1 | 4039664 | c.1041G>C | synonymous_variant | 0.71 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.6 |
clpC1 | 4039748 | c.957G>C | synonymous_variant | 0.53 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.53 |
clpC1 | 4039760 | c.945T>C | synonymous_variant | 0.5 |
clpC1 | 4039766 | c.939T>C | synonymous_variant | 0.43 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.42 |
clpC1 | 4039775 | c.930G>C | synonymous_variant | 0.4 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.37 |
clpC1 | 4039790 | c.915C>G | synonymous_variant | 0.35 |
clpC1 | 4039802 | c.903G>A | synonymous_variant | 0.35 |
clpC1 | 4039805 | c.900C>A | synonymous_variant | 0.33 |
clpC1 | 4039817 | c.888A>C | synonymous_variant | 0.41 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.45 |
clpC1 | 4039823 | c.882T>G | synonymous_variant | 0.46 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 0.49 |
clpC1 | 4039832 | c.873C>G | synonymous_variant | 0.49 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.5 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.44 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.44 |
clpC1 | 4039922 | c.783C>T | synonymous_variant | 0.43 |
clpC1 | 4039925 | c.780C>G | synonymous_variant | 0.4 |
clpC1 | 4039928 | c.775_777delAGCinsTCA | synonymous_variant | 0.39 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.42 |
clpC1 | 4039937 | c.768G>C | synonymous_variant | 0.44 |
clpC1 | 4039943 | c.762G>A | synonymous_variant | 0.46 |
clpC1 | 4039946 | c.759A>T | synonymous_variant | 0.47 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.51 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.55 |
clpC1 | 4039994 | p.Glu237Asp | missense_variant | 0.57 |
clpC1 | 4040010 | p.Ala232Asn | missense_variant | 0.51 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.5 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.56 |
clpC1 | 4040087 | c.618G>T | synonymous_variant | 0.49 |
clpC1 | 4040089 | c.611_615delTCTCT | frameshift_variant | 0.49 |
clpC1 | 4040096 | c.608_609insTTTGA | frameshift_variant | 0.5 |
clpC1 | 4040105 | c.600C>G | synonymous_variant | 0.56 |
clpC1 | 4040135 | c.570C>T | synonymous_variant | 0.39 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.31 |
clpC1 | 4040147 | c.558A>G | synonymous_variant | 0.33 |
clpC1 | 4040153 | c.552A>G | synonymous_variant | 0.28 |
clpC1 | 4040159 | c.546G>C | synonymous_variant | 0.28 |
clpC1 | 4040162 | c.543G>C | synonymous_variant | 0.28 |
clpC1 | 4040165 | c.540G>C | synonymous_variant | 0.26 |
clpC1 | 4040171 | c.534C>G | synonymous_variant | 0.29 |
clpC1 | 4040249 | c.456A>G | synonymous_variant | 0.23 |
clpC1 | 4040252 | c.453C>T | synonymous_variant | 0.24 |
clpC1 | 4040257 | p.Ala150Thr | missense_variant | 0.3 |
clpC1 | 4040267 | c.438A>G | synonymous_variant | 0.42 |
clpC1 | 4040273 | c.432T>C | synonymous_variant | 0.46 |
clpC1 | 4040279 | c.426C>G | synonymous_variant | 0.46 |
clpC1 | 4040291 | c.414G>C | synonymous_variant | 0.46 |
clpC1 | 4040300 | c.405C>T | synonymous_variant | 0.42 |
clpC1 | 4040324 | c.381G>C | synonymous_variant | 0.42 |
clpC1 | 4040335 | c.370C>T | synonymous_variant | 0.42 |
clpC1 | 4040348 | c.357G>T | synonymous_variant | 0.38 |
clpC1 | 4040354 | c.351A>G | synonymous_variant | 0.33 |
clpC1 | 4040357 | c.348T>C | synonymous_variant | 0.29 |
clpC1 | 4040363 | c.342A>T | synonymous_variant | 0.26 |
clpC1 | 4040411 | c.294T>C | synonymous_variant | 0.35 |
clpC1 | 4040423 | c.282A>G | synonymous_variant | 0.33 |
clpC1 | 4040426 | c.279T>C | synonymous_variant | 0.34 |
clpC1 | 4040444 | c.261C>G | synonymous_variant | 0.39 |
clpC1 | 4040450 | c.255A>G | synonymous_variant | 0.38 |
clpC1 | 4040453 | c.252C>G | synonymous_variant | 0.39 |
clpC1 | 4040459 | c.246C>A | synonymous_variant | 0.41 |
clpC1 | 4040465 | c.240T>C | synonymous_variant | 0.46 |
clpC1 | 4040468 | c.237G>A | synonymous_variant | 0.48 |
clpC1 | 4040480 | c.225T>C | synonymous_variant | 0.52 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 0.43 |
clpC1 | 4040531 | c.174T>C | synonymous_variant | 0.47 |
clpC1 | 4040546 | c.159G>A | synonymous_variant | 0.48 |
clpC1 | 4040567 | c.138C>A | synonymous_variant | 0.5 |
clpC1 | 4040570 | c.135C>G | synonymous_variant | 0.47 |
clpC1 | 4040573 | c.132T>A | synonymous_variant | 0.47 |
clpC1 | 4040582 | c.123G>C | synonymous_variant | 0.48 |
clpC1 | 4040588 | c.117T>C | synonymous_variant | 0.46 |
clpC1 | 4040594 | c.111G>C | synonymous_variant | 0.46 |
clpC1 | 4040600 | c.103_105delTTAinsCTG | synonymous_variant | 0.43 |
clpC1 | 4040603 | c.102T>G | synonymous_variant | 0.42 |
clpC1 | 4040606 | c.99T>C | synonymous_variant | 0.44 |
clpC1 | 4040615 | c.90C>T | synonymous_variant | 0.48 |
clpC1 | 4040644 | c.61A>C | synonymous_variant | 0.48 |
clpC1 | 4040654 | c.51G>A | synonymous_variant | 0.44 |
clpC1 | 4040657 | c.48T>G | synonymous_variant | 0.43 |
clpC1 | 4040687 | c.18C>G | synonymous_variant | 0.55 |
clpC1 | 4040696 | c.9A>G | synonymous_variant | 0.55 |
clpC1 | 4040699 | c.6C>T | synonymous_variant | 0.57 |
clpC1 | 4040705 | c.-1G>A | upstream_gene_variant | 0.55 |
clpC1 | 4040711 | c.-7G>A | upstream_gene_variant | 0.54 |
clpC1 | 4040734 | c.-31delT | upstream_gene_variant | 0.5 |
clpC1 | 4040745 | c.-41G>C | upstream_gene_variant | 0.45 |
clpC1 | 4040747 | c.-43T>C | upstream_gene_variant | 0.45 |
clpC1 | 4040750 | c.-46G>A | upstream_gene_variant | 0.45 |
clpC1 | 4040763 | c.-59C>T | upstream_gene_variant | 0.37 |
clpC1 | 4040777 | c.-73A>C | upstream_gene_variant | 0.19 |
panD | 4044138 | c.144T>C | synonymous_variant | 0.22 |
panD | 4044150 | c.132A>G | synonymous_variant | 0.21 |
embC | 4239674 | c.-189C>T | upstream_gene_variant | 0.4 |
embC | 4239680 | c.-183C>G | upstream_gene_variant | 0.36 |
embC | 4239688 | c.-175A>G | upstream_gene_variant | 0.33 |
embC | 4239696 | c.-167_-165delCATinsAAC | upstream_gene_variant | 0.34 |
embC | 4239699 | c.-164_-162delAACinsGAG | upstream_gene_variant | 0.32 |
embC | 4239703 | c.-160_-159delGCinsCA | upstream_gene_variant | 0.31 |
embC | 4239710 | c.-153C>G | upstream_gene_variant | 0.31 |
embC | 4239723 | c.-140C>G | upstream_gene_variant | 0.32 |
embC | 4240553 | p.Met231Leu | missense_variant | 0.21 |
embC | 4240561 | c.699C>G | synonymous_variant | 0.25 |
embC | 4240576 | c.714A>G | synonymous_variant | 0.2 |
embC | 4240579 | c.717G>T | synonymous_variant | 0.21 |
embC | 4240580 | c.718_720delCTCinsTTG | synonymous_variant | 0.21 |
embC | 4240587 | p.Gly242Val | missense_variant | 0.2 |
embC | 4240594 | c.732C>G | synonymous_variant | 0.21 |
embC | 4240600 | c.738G>C | synonymous_variant | 0.21 |
embC | 4240603 | c.741G>A | synonymous_variant | 0.21 |
embC | 4240632 | p.Met257Thr | missense_variant | 0.25 |
embC | 4240642 | c.780G>C | synonymous_variant | 0.23 |
embC | 4240717 | c.855T>C | synonymous_variant | 0.29 |
embC | 4240732 | c.870C>T | synonymous_variant | 0.34 |
embC | 4240736 | p.Ser292Ala | missense_variant | 0.44 |
embC | 4240783 | c.921G>C | synonymous_variant | 0.61 |
embC | 4240786 | c.924C>A | synonymous_variant | 0.61 |
embC | 4240789 | c.927T>C | synonymous_variant | 0.58 |
embC | 4240819 | c.957A>C | synonymous_variant | 0.59 |
embC | 4240822 | c.960C>G | synonymous_variant | 0.58 |
embC | 4240831 | c.969T>G | synonymous_variant | 0.62 |
embC | 4240859 | c.997C>T | synonymous_variant | 0.54 |
embC | 4240875 | p.Ser338Thr | missense_variant | 0.49 |
embC | 4240879 | c.1017G>C | synonymous_variant | 0.5 |
embC | 4240885 | c.1023T>C | synonymous_variant | 0.51 |
embC | 4240897 | c.1035C>G | synonymous_variant | 0.5 |
embC | 4240900 | c.1038A>G | synonymous_variant | 0.5 |
embC | 4240910 | p.Ala350Leu | missense_variant | 0.39 |
embC | 4240921 | c.1059C>G | synonymous_variant | 0.36 |
embC | 4240922 | p.Thr354Ala | missense_variant | 0.33 |
embC | 4240936 | c.1074A>G | synonymous_variant | 0.33 |
embC | 4240948 | c.1086G>A | synonymous_variant | 0.24 |
embC | 4240954 | c.1092T>C | synonymous_variant | 0.22 |
embC | 4240957 | c.1095C>G | synonymous_variant | 0.22 |
embC | 4240969 | c.1107C>T | synonymous_variant | 0.3 |
embC | 4240975 | c.1113C>G | synonymous_variant | 0.26 |
embC | 4240981 | c.1119G>C | synonymous_variant | 0.25 |
embC | 4240983 | p.Ser374Asn | missense_variant | 0.24 |
embC | 4240990 | c.1128A>G | synonymous_variant | 0.26 |
embC | 4240996 | c.1134G>C | synonymous_variant | 0.3 |
embC | 4241005 | c.1143G>C | synonymous_variant | 0.38 |
embC | 4241008 | c.1146G>C | synonymous_variant | 0.39 |
embC | 4241017 | c.1155T>C | synonymous_variant | 0.45 |
embC | 4241023 | c.1161T>G | synonymous_variant | 0.43 |
embC | 4241024 | p.Val388Phe | missense_variant | 0.44 |
embC | 4241039 | p.Asp393Asn | missense_variant | 0.55 |
embC | 4241047 | c.1185C>A | synonymous_variant | 0.6 |
embC | 4241050 | c.1188T>G | synonymous_variant | 0.63 |
embC | 4241089 | c.1227C>G | synonymous_variant | 0.69 |
embC | 4241095 | c.1233C>T | synonymous_variant | 0.69 |
embC | 4241107 | c.1245G>C | synonymous_variant | 0.66 |
embC | 4241123 | c.1261C>A | synonymous_variant | 0.62 |
embC | 4241140 | c.1278A>C | synonymous_variant | 0.58 |
embC | 4241141 | p.Ile427Val | missense_variant | 0.58 |
embC | 4241153 | p.Ile431Val | missense_variant | 0.61 |
embC | 4241158 | c.1296T>C | synonymous_variant | 0.6 |
embC | 4241161 | c.1299C>G | synonymous_variant | 0.59 |
embC | 4241162 | c.1300T>C | synonymous_variant | 0.57 |
embC | 4241188 | c.1326C>T | synonymous_variant | 0.5 |
embC | 4241203 | c.1341T>G | synonymous_variant | 0.44 |
embC | 4241207 | c.1345C>T | synonymous_variant | 0.45 |
embC | 4241215 | c.1353C>G | synonymous_variant | 0.41 |
embC | 4241230 | c.1368A>G | synonymous_variant | 0.22 |
embC | 4241233 | c.1371G>C | synonymous_variant | 0.17 |
embC | 4241407 | c.1545A>G | synonymous_variant | 0.23 |
embC | 4241416 | c.1554C>T | synonymous_variant | 0.32 |
embC | 4241425 | c.1563G>T | synonymous_variant | 0.43 |
embC | 4241449 | c.1587C>G | synonymous_variant | 0.53 |
embC | 4241453 | p.Ile531Val | missense_variant | 0.5 |
embC | 4241458 | c.1596C>G | synonymous_variant | 0.37 |
embC | 4241470 | c.1608C>G | synonymous_variant | 0.32 |
embC | 4241578 | c.1716G>C | synonymous_variant | 0.27 |
embC | 4241579 | p.Ile573Val | missense_variant | 0.27 |
embC | 4241584 | c.1722T>C | synonymous_variant | 0.26 |
embC | 4241587 | c.1725C>G | synonymous_variant | 0.26 |
embC | 4241591 | p.Leu577Ile | missense_variant | 0.26 |
embC | 4241614 | c.1752A>C | synonymous_variant | 0.29 |
embC | 4241644 | c.1782G>C | synonymous_variant | 0.34 |
embC | 4241648 | c.1786T>C | synonymous_variant | 0.31 |
embC | 4241656 | c.1794G>C | synonymous_variant | 0.27 |
embC | 4242311 | p.Gly817Ser | missense_variant | 0.23 |
embA | 4242319 | c.-914A>G | upstream_gene_variant | 0.19 |
embC | 4242320 | p.Pro820Ala | missense_variant | 0.19 |
embA | 4242331 | c.-902A>G | upstream_gene_variant | 0.32 |
embA | 4242334 | c.-899G>C | upstream_gene_variant | 0.36 |
embA | 4242343 | c.-890G>C | upstream_gene_variant | 0.4 |
embA | 4242367 | c.-866C>G | upstream_gene_variant | 0.51 |
embA | 4242391 | c.-842G>C | upstream_gene_variant | 0.42 |
embA | 4242394 | c.-839C>T | upstream_gene_variant | 0.41 |
embA | 4242397 | c.-836G>C | upstream_gene_variant | 0.38 |
embA | 4242400 | c.-833C>T | upstream_gene_variant | 0.39 |
embA | 4242403 | c.-830T>G | upstream_gene_variant | 0.41 |
embA | 4242406 | c.-827A>G | upstream_gene_variant | 0.44 |
embA | 4242421 | c.-812C>T | upstream_gene_variant | 0.33 |
embC | 4242428 | p.Ala856Ser | missense_variant | 0.21 |
embA | 4242433 | c.-800C>G | upstream_gene_variant | 0.19 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 0.97 |
embA | 4244154 | p.Thr308Pro | missense_variant | 0.34 |
embA | 4244157 | p.Ser309Ala | missense_variant | 0.33 |
embA | 4244165 | c.933T>G | synonymous_variant | 0.35 |
embA | 4244168 | c.936C>G | synonymous_variant | 0.35 |
embA | 4244171 | p.Gln313His | missense_variant | 0.36 |
embA | 4244178 | p.Ala316Ser | missense_variant | 0.36 |
embA | 4244198 | c.966C>G | synonymous_variant | 0.41 |
embA | 4244210 | c.978G>A | synonymous_variant | 0.38 |
embA | 4244216 | c.984C>G | synonymous_variant | 0.36 |
embA | 4244228 | c.996A>G | synonymous_variant | 0.32 |
embA | 4244233 | p.Ala334Gly | missense_variant | 0.21 |
embA | 4244324 | c.1092T>G | synonymous_variant | 0.23 |
embA | 4244327 | c.1095T>C | synonymous_variant | 0.22 |
embA | 4244339 | c.1107G>C | synonymous_variant | 0.22 |
embA | 4244340 | p.Ser370Ala | missense_variant | 0.23 |
embA | 4244360 | c.1128C>T | synonymous_variant | 0.27 |
embA | 4244366 | c.1134C>T | synonymous_variant | 0.23 |
embA | 4244372 | c.1140T>G | synonymous_variant | 0.21 |
embA | 4244390 | c.1158G>C | synonymous_variant | 0.2 |
embA | 4245047 | c.1815G>C | synonymous_variant | 0.38 |
embA | 4245051 | p.Val607Ile | missense_variant | 0.33 |
embA | 4245074 | c.1842G>T | synonymous_variant | 0.44 |
embA | 4245083 | c.1851A>C | synonymous_variant | 0.5 |
embA | 4245089 | c.1857G>C | synonymous_variant | 0.5 |
embA | 4245101 | c.1869G>C | synonymous_variant | 0.49 |
embA | 4245125 | c.1893G>A | synonymous_variant | 0.55 |
embA | 4245170 | c.1938G>A | synonymous_variant | 0.62 |
embA | 4245182 | c.1950T>C | synonymous_variant | 0.61 |
embA | 4245198 | p.Leu656Phe | missense_variant | 0.64 |
embA | 4245206 | c.1974A>C | synonymous_variant | 0.6 |
embA | 4245207 | c.1975T>C | synonymous_variant | 0.6 |
embA | 4245215 | c.1983A>C | synonymous_variant | 0.66 |
embA | 4245224 | c.1992T>C | synonymous_variant | 0.57 |
embA | 4245263 | c.2031A>G | synonymous_variant | 0.47 |
embA | 4245282 | p.Ile684Val | missense_variant | 0.36 |
embA | 4245285 | c.2053T>C | synonymous_variant | 0.36 |
embA | 4245293 | c.2061T>C | synonymous_variant | 0.37 |
embA | 4245299 | c.2067A>G | synonymous_variant | 0.39 |
embA | 4245311 | c.2079C>G | synonymous_variant | 0.38 |
embA | 4245317 | c.2085G>C | synonymous_variant | 0.35 |
embA | 4245327 | p.Ala699Leu | missense_variant | 0.33 |
embA | 4245340 | p.Gly703Ala | missense_variant | 0.29 |
embA | 4245355 | p.Ala708Gly | missense_variant | 0.25 |
embA | 4245458 | c.2226G>A | synonymous_variant | 0.22 |
embA | 4245464 | c.2232C>T | synonymous_variant | 0.37 |
embA | 4245476 | c.2244C>T | synonymous_variant | 0.46 |
embA | 4245501 | p.Ala757Lys | missense_variant | 0.43 |
embA | 4245514 | p.Asp761Ala | missense_variant | 0.37 |
embB | 4245518 | c.-996A>C | upstream_gene_variant | 0.35 |
embB | 4245524 | c.-990G>C | upstream_gene_variant | 0.33 |
embB | 4245530 | c.-984T>C | upstream_gene_variant | 0.33 |
embA | 4245531 | p.Ile767Val | missense_variant | 0.33 |
embA | 4245535 | p.Ser768Asn | missense_variant | 0.34 |
embB | 4245539 | c.-975C>G | upstream_gene_variant | 0.32 |
embB | 4245545 | c.-969C>G | upstream_gene_variant | 0.33 |
embB | 4245560 | c.-954C>T | upstream_gene_variant | 0.27 |
embB | 4245614 | c.-900C>T | upstream_gene_variant | 0.22 |
embB | 4245620 | c.-894T>C | upstream_gene_variant | 0.27 |
embB | 4245626 | c.-888G>A | upstream_gene_variant | 0.35 |
embB | 4245641 | c.-873C>T | upstream_gene_variant | 0.35 |
embB | 4245644 | c.-870C>G | upstream_gene_variant | 0.33 |
embA | 4245650 | p.Ile806Met | missense_variant | 0.33 |
embA | 4245652 | p.Thr807Ser | missense_variant | 0.33 |
embB | 4245674 | c.-840A>C | upstream_gene_variant | 0.42 |
embB | 4245677 | c.-837G>C | upstream_gene_variant | 0.43 |
embB | 4245683 | c.-831C>G | upstream_gene_variant | 0.47 |
embB | 4245689 | c.-825C>G | upstream_gene_variant | 0.43 |
embA | 4245693 | p.Ile821Val | missense_variant | 0.44 |
embB | 4245719 | c.-795G>C | upstream_gene_variant | 0.46 |
embB | 4245725 | c.-789A>G | upstream_gene_variant | 0.41 |
embB | 4245726 | c.-788T>C | upstream_gene_variant | 0.41 |
embB | 4245731 | c.-783C>T | upstream_gene_variant | 0.4 |
embB | 4245734 | c.-780G>C | upstream_gene_variant | 0.41 |
embB | 4245737 | c.-777A>G | upstream_gene_variant | 0.4 |
embB | 4245740 | c.-774T>C | upstream_gene_variant | 0.41 |
embB | 4245764 | c.-750G>C | upstream_gene_variant | 0.39 |
embB | 4245785 | c.-729G>A | upstream_gene_variant | 0.19 |
embB | 4245791 | c.-723C>G | upstream_gene_variant | 0.19 |
embB | 4247380 | c.867C>G | synonymous_variant | 0.29 |
embB | 4247395 | c.882C>G | synonymous_variant | 0.29 |
embB | 4247398 | c.885G>C | synonymous_variant | 0.29 |
embB | 4247401 | c.888T>C | synonymous_variant | 0.28 |
embB | 4247404 | c.891G>C | synonymous_variant | 0.28 |
embB | 4247407 | c.894G>C | synonymous_variant | 0.27 |
embB | 4247437 | c.924A>C | synonymous_variant | 0.39 |
embB | 4247470 | c.957T>C | synonymous_variant | 0.46 |
embB | 4247476 | c.963C>A | synonymous_variant | 0.4 |
embB | 4247491 | c.978G>C | synonymous_variant | 0.36 |
embB | 4247497 | c.984T>C | synonymous_variant | 0.36 |
embB | 4247500 | c.987C>G | synonymous_variant | 0.37 |
embB | 4247512 | c.999T>C | synonymous_variant | 0.32 |
embB | 4247716 | c.1203C>T | synonymous_variant | 0.29 |
embB | 4247717 | c.1204C>T | synonymous_variant | 0.28 |
embB | 4247725 | c.1212G>C | synonymous_variant | 0.29 |
embB | 4247729 | p.Gly406Pro | missense_variant | 0.32 |
embB | 4247741 | p.Leu410Val | missense_variant | 0.36 |
embB | 4247753 | p.Val414Ile | missense_variant | 0.47 |
embB | 4247773 | c.1260G>A | synonymous_variant | 0.5 |
embB | 4247785 | c.1272G>A | synonymous_variant | 0.51 |
embB | 4247797 | c.1284C>G | synonymous_variant | 0.49 |
embB | 4247800 | c.1287A>G | synonymous_variant | 0.5 |
embB | 4247806 | c.1293G>C | synonymous_variant | 0.49 |
embB | 4247821 | c.1308T>C | synonymous_variant | 0.44 |
embB | 4247827 | c.1314C>G | synonymous_variant | 0.43 |
embB | 4247830 | c.1317A>G | synonymous_variant | 0.41 |
embB | 4247839 | c.1326G>C | synonymous_variant | 0.37 |
embB | 4247842 | c.1329T>C | synonymous_variant | 0.34 |
embB | 4248109 | c.1596C>G | synonymous_variant | 0.26 |
embB | 4248112 | c.1599C>G | synonymous_variant | 0.26 |
embB | 4248118 | c.1605T>C | synonymous_variant | 0.37 |
embB | 4248130 | c.1617G>C | synonymous_variant | 0.43 |
embB | 4248133 | c.1620C>G | synonymous_variant | 0.42 |
embB | 4248142 | c.1629T>C | synonymous_variant | 0.45 |
embB | 4248143 | c.1630T>C | synonymous_variant | 0.45 |
embB | 4248157 | c.1644A>G | synonymous_variant | 0.5 |
embB | 4248161 | c.1648C>T | synonymous_variant | 0.53 |
embB | 4248178 | c.1665C>T | synonymous_variant | 0.55 |
embB | 4248185 | c.1672T>C | synonymous_variant | 0.6 |
embB | 4248199 | c.1686A>G | synonymous_variant | 0.63 |
embB | 4248206 | p.Ser565Gly | missense_variant | 0.63 |
embB | 4248214 | c.1701C>T | synonymous_variant | 0.6 |
embB | 4248220 | c.1707A>G | synonymous_variant | 0.62 |
embB | 4248232 | c.1719G>T | synonymous_variant | 0.62 |
embB | 4248277 | c.1764G>C | synonymous_variant | 0.58 |
embB | 4248286 | c.1773G>A | synonymous_variant | 0.57 |
embB | 4248313 | c.1800C>T | synonymous_variant | 0.53 |
embB | 4248316 | c.1803C>G | synonymous_variant | 0.53 |
embB | 4248319 | c.1806A>G | synonymous_variant | 0.53 |
embB | 4248323 | p.Ala604Ser | missense_variant | 0.51 |
embB | 4248343 | c.1830G>C | synonymous_variant | 0.47 |
embB | 4248350 | c.1837T>C | synonymous_variant | 0.41 |
embB | 4248355 | c.1842A>G | synonymous_variant | 0.39 |
embB | 4248358 | c.1845C>G | synonymous_variant | 0.4 |
embB | 4248361 | c.1848A>G | synonymous_variant | 0.39 |
embB | 4248362 | p.Ser617Ala | missense_variant | 0.39 |
embB | 4248389 | p.Met626Val | missense_variant | 0.26 |
embB | 4249276 | c.2763A>G | synonymous_variant | 0.19 |
embB | 4249282 | c.2769A>C | synonymous_variant | 0.32 |
embB | 4249291 | c.2778C>G | synonymous_variant | 0.4 |
embB | 4249306 | c.2793C>T | synonymous_variant | 0.37 |
embB | 4249316 | p.Ala935Pro | missense_variant | 0.33 |
embB | 4249321 | c.2808A>C | synonymous_variant | 0.33 |
embB | 4249324 | c.2811A>C | synonymous_variant | 0.36 |
embB | 4249330 | p.Met939Ile | missense_variant | 0.34 |
embB | 4249334 | p.Ala941Ser | missense_variant | 0.32 |
embB | 4249339 | c.2826T>C | synonymous_variant | 0.32 |
embB | 4249340 | c.2828_2829insGAC | disruptive_inframe_insertion | 0.32 |
embB | 4249345 | c.2834_2836delCGG | disruptive_inframe_deletion | 0.32 |
embB | 4249381 | c.2868A>G | synonymous_variant | 0.28 |
embB | 4249387 | c.2874G>A | synonymous_variant | 0.24 |
embB | 4249394 | p.Ile961Val | missense_variant | 0.21 |
embB | 4249405 | c.2892C>T | synonymous_variant | 0.23 |
embB | 4249417 | c.2904A>G | synonymous_variant | 0.34 |
embB | 4249423 | p.Asp970Glu | missense_variant | 0.35 |
embB | 4249424 | c.2911C>T | synonymous_variant | 0.34 |
embB | 4249432 | c.2919A>G | synonymous_variant | 0.42 |
embB | 4249441 | c.2928A>G | synonymous_variant | 0.35 |
embB | 4249444 | c.2931T>C | synonymous_variant | 0.34 |
embB | 4249447 | c.2934G>C | synonymous_variant | 0.34 |
embB | 4249454 | p.Thr981Ser | missense_variant | 0.31 |
embB | 4249469 | p.Leu986Met | missense_variant | 0.32 |
embB | 4249480 | c.2967G>T | synonymous_variant | 0.34 |
embB | 4249483 | c.2970C>G | synonymous_variant | 0.35 |
embB | 4249486 | c.2973T>G | synonymous_variant | 0.36 |
embB | 4249487 | c.2974T>C | synonymous_variant | 0.35 |
embB | 4249525 | c.3012T>C | synonymous_variant | 0.4 |
embB | 4249528 | c.3015C>T | synonymous_variant | 0.38 |
embB | 4249529 | p.Ile1006Val | missense_variant | 0.38 |
embB | 4249532 | p.Ala1007Thr | missense_variant | 0.39 |
embB | 4249537 | c.3024A>G | synonymous_variant | 0.39 |
embB | 4249540 | c.3027C>T | synonymous_variant | 0.41 |
embB | 4249558 | c.3045A>G | synonymous_variant | 0.42 |
embB | 4249564 | c.3051C>T | synonymous_variant | 0.38 |
embB | 4249568 | p.Ser1019Thr | missense_variant | 0.4 |
embB | 4249573 | c.3060T>C | synonymous_variant | 0.39 |
embB | 4249581 | p.Leu1023Gln | missense_variant | 0.38 |
embB | 4249594 | c.3081G>C | synonymous_variant | 0.43 |
embB | 4249600 | c.3087A>G | synonymous_variant | 0.42 |
embB | 4249607 | p.Thr1032Val | missense_variant | 0.31 |
embB | 4249618 | c.3105C>T | synonymous_variant | 0.37 |
embB | 4249627 | c.3114G>C | synonymous_variant | 0.34 |
embB | 4249637 | p.Leu1042Val | missense_variant | 0.28 |
embB | 4249640 | c.3127_3129delTTGinsCTC | synonymous_variant | 0.29 |
embB | 4249648 | c.3135G>C | synonymous_variant | 0.31 |
embB | 4249651 | c.3138C>G | synonymous_variant | 0.3 |
embB | 4249657 | c.3144C>G | synonymous_variant | 0.3 |
embB | 4249663 | c.3150C>G | synonymous_variant | 0.32 |
aftB | 4267544 | c.1293T>C | synonymous_variant | 0.17 |
aftB | 4267556 | c.1281G>C | synonymous_variant | 0.28 |
aftB | 4267571 | c.1266T>C | synonymous_variant | 0.29 |
aftB | 4267586 | c.1251C>G | synonymous_variant | 0.38 |
aftB | 4267601 | c.1236C>G | synonymous_variant | 0.45 |
aftB | 4267607 | c.1230G>A | synonymous_variant | 0.45 |
aftB | 4267628 | c.1209C>G | synonymous_variant | 0.45 |
aftB | 4267649 | c.1188T>C | synonymous_variant | 0.31 |
aftB | 4267655 | c.1182C>A | synonymous_variant | 0.3 |
aftB | 4267658 | c.1179G>C | synonymous_variant | 0.28 |
aftB | 4267667 | c.1170A>G | synonymous_variant | 0.29 |
aftB | 4268125 | p.Ser238Gly | missense_variant | 0.21 |
aftB | 4269057 | c.-221C>T | upstream_gene_variant | 0.24 |
ubiA | 4269075 | p.Ile253Val | missense_variant | 0.28 |
aftB | 4269096 | c.-260C>G | upstream_gene_variant | 0.37 |
aftB | 4269099 | c.-263G>C | upstream_gene_variant | 0.38 |
aftB | 4269102 | c.-268_-266delAGCinsTCG | upstream_gene_variant | 0.4 |
ubiA | 4269110 | p.Gly242Arg | missense_variant | 0.41 |
aftB | 4269114 | c.-278C>T | upstream_gene_variant | 0.4 |
ubiA | 4269143 | p.Leu231Val | missense_variant | 0.48 |
aftB | 4269144 | c.-308C>G | upstream_gene_variant | 0.48 |
ubiA | 4269149 | p.Val229Leu | missense_variant | 0.54 |
ubiA | 4269164 | p.Leu224Met | missense_variant | 0.58 |
aftB | 4269165 | c.-329G>C | upstream_gene_variant | 0.58 |
aftB | 4269186 | c.-350C>G | upstream_gene_variant | 0.66 |
aftB | 4269198 | c.-362C>T | upstream_gene_variant | 0.74 |
aftB | 4269201 | c.-365A>G | upstream_gene_variant | 0.73 |
aftB | 4269206 | c.-370C>T | upstream_gene_variant | 0.73 |
aftB | 4269210 | c.-374G>A | upstream_gene_variant | 0.73 |
ubiA | 4269220 | p.Ala205Lys | missense_variant | 0.75 |
aftB | 4269222 | c.-386T>C | upstream_gene_variant | 0.73 |
aftB | 4269242 | c.-406C>T | upstream_gene_variant | 0.63 |
aftB | 4269249 | c.-413G>A | upstream_gene_variant | 0.57 |
aftB | 4269258 | c.-422C>T | upstream_gene_variant | 0.48 |
aftB | 4269264 | c.-428C>G | upstream_gene_variant | 0.4 |
ubiA | 4269514 | p.Val107Ala | missense_variant | 0.18 |
ubiA | 4269523 | p.Thr104Ser | missense_variant | 0.19 |
aftB | 4269582 | c.-746C>T | upstream_gene_variant | 0.21 |
ubiA | 4269718 | p.Ala39Glu | missense_variant | 0.32 |
ethA | 4328455 | c.-982G>C | upstream_gene_variant | 0.19 |
ethA | 4328471 | c.-998A>G | upstream_gene_variant | 0.25 |
ethA | 4328473 | c.-1000G>C | upstream_gene_variant | 0.25 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |