Run ID: SRR3675502
Sample name:
Date: 04-04-2023 05:30:57
Number of reads: 154475
Percentage reads mapped: 19.24
Strain:
Drug-resistance: Other
| Drug | Resistance | Supporting mutations |
|---|
| Lineage | Family | Main Spoligotype | RDs | Frequency |
|---|
| Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
|---|---|---|---|---|---|
| embB | 4247448 | p.His312Arg | missense_variant | 1.0 | ethambutol |
| embB | 4247663 | p.Tyr384Asn | missense_variant | 1.0 | ethambutol |
| embB | 4247822 | p.Thr437Ala | missense_variant | 1.0 | ethambutol |
| Gene | Chromosome position | Mutation | Type | Estimated fraction |
|---|---|---|---|---|
| gyrB | 5229 | c.-11G>A | upstream_gene_variant | 1.0 |
| gyrB | 5230 | c.-10T>C | upstream_gene_variant | 1.0 |
| gyrB | 5238 | c.-2T>C | upstream_gene_variant | 1.0 |
| gyrB | 5254 | c.15A>G | synonymous_variant | 1.0 |
| gyrB | 5284 | c.45G>A | synonymous_variant | 1.0 |
| gyrB | 5287 | c.48T>C | synonymous_variant | 1.0 |
| gyrB | 5293 | c.54C>G | synonymous_variant | 1.0 |
| gyrB | 5302 | c.63A>G | synonymous_variant | 1.0 |
| gyrB | 5305 | c.66G>A | synonymous_variant | 1.0 |
| gyrB | 5308 | c.69G>A | synonymous_variant | 1.0 |
| gyrB | 5341 | c.102T>C | synonymous_variant | 1.0 |
| gyrB | 5359 | c.120C>T | synonymous_variant | 1.0 |
| gyrB | 5363 | c.124_126delTTAinsCTG | synonymous_variant | 1.0 |
| gyrB | 5377 | c.138T>C | synonymous_variant | 1.0 |
| gyrB | 5422 | c.183T>C | synonymous_variant | 1.0 |
| gyrB | 5425 | c.186A>G | synonymous_variant | 1.0 |
| gyrB | 5426 | p.Thr63Ala | missense_variant | 1.0 |
| gyrB | 5431 | c.192A>C | synonymous_variant | 1.0 |
| gyrB | 5434 | c.195G>A | synonymous_variant | 1.0 |
| gyrB | 5436 | p.Asn66Ser | missense_variant | 1.0 |
| gyrB | 5440 | c.201A>G | synonymous_variant | 1.0 |
| gyrB | 5449 | c.210T>C | synonymous_variant | 1.0 |
| gyrB | 5455 | c.216T>C | synonymous_variant | 1.0 |
| gyrB | 5470 | c.231C>G | synonymous_variant | 1.0 |
| gyrB | 5485 | c.246C>T | synonymous_variant | 1.0 |
| gyrB | 5488 | c.249C>A | synonymous_variant | 1.0 |
| gyrB | 5491 | c.252T>C | synonymous_variant | 1.0 |
| gyrB | 5500 | c.261C>A | synonymous_variant | 1.0 |
| gyrB | 5502 | p.Thr88Met | missense_variant | 1.0 |
| gyrB | 5527 | c.288C>G | synonymous_variant | 1.0 |
| gyrB | 5644 | c.405C>G | synonymous_variant | 1.0 |
| gyrB | 5647 | c.408A>G | synonymous_variant | 1.0 |
| gyrB | 5650 | c.411C>G | synonymous_variant | 1.0 |
| gyrB | 5668 | c.429G>C | synonymous_variant | 1.0 |
| gyrB | 5669 | p.Tyr144His | missense_variant | 1.0 |
| gyrB | 5680 | c.441T>G | synonymous_variant | 1.0 |
| gyrB | 5689 | c.450T>C | synonymous_variant | 1.0 |
| gyrB | 5695 | c.456G>A | synonymous_variant | 1.0 |
| gyrB | 5698 | c.459G>C | synonymous_variant | 1.0 |
| gyrB | 5701 | c.462A>G | synonymous_variant | 1.0 |
| gyrB | 5704 | c.465C>G | synonymous_variant | 1.0 |
| gyrB | 5705 | p.Leu156Met | missense_variant | 1.0 |
| gyrB | 5710 | c.471C>A | synonymous_variant | 1.0 |
| gyrB | 5722 | c.483G>C | synonymous_variant | 1.0 |
| gyrB | 5731 | c.492C>T | synonymous_variant | 1.0 |
| gyrB | 5740 | c.501G>C | synonymous_variant | 1.0 |
| gyrB | 5743 | c.504G>C | synonymous_variant | 1.0 |
| gyrB | 5744 | p.Ser169Thr | missense_variant | 1.0 |
| gyrB | 5767 | c.528C>T | synonymous_variant | 1.0 |
| gyrB | 5771 | p.Ala178Asn | missense_variant | 1.0 |
| gyrB | 5779 | c.540C>T | synonymous_variant | 1.0 |
| gyrB | 5782 | c.543A>G | synonymous_variant | 1.0 |
| gyrB | 5788 | c.549G>C | synonymous_variant | 1.0 |
| gyrB | 5791 | c.552A>G | synonymous_variant | 1.0 |
| gyrB | 5812 | c.573C>A | synonymous_variant | 1.0 |
| gyrB | 5815 | c.576C>A | synonymous_variant | 1.0 |
| gyrB | 5819 | c.580C>T | synonymous_variant | 1.0 |
| gyrB | 5824 | c.585A>G | synonymous_variant | 1.0 |
| gyrB | 5836 | c.597C>T | synonymous_variant | 1.0 |
| gyrB | 5851 | c.612G>C | synonymous_variant | 1.0 |
| gyrB | 5860 | c.621C>T | synonymous_variant | 0.67 |
| gyrB | 6067 | c.828G>C | synonymous_variant | 1.0 |
| gyrB | 6073 | c.834T>C | synonymous_variant | 1.0 |
| gyrB | 6079 | c.840C>T | synonymous_variant | 1.0 |
| gyrB | 6085 | c.846C>A | synonymous_variant | 1.0 |
| gyrB | 6086 | p.Thr283Pro | missense_variant | 1.0 |
| gyrB | 6091 | c.852G>C | synonymous_variant | 0.75 |
| gyrB | 6097 | c.858G>A | synonymous_variant | 0.75 |
| gyrB | 6115 | c.876A>G | synonymous_variant | 0.83 |
| gyrB | 6121 | c.882C>T | synonymous_variant | 0.83 |
| gyrB | 6127 | c.888G>C | synonymous_variant | 0.83 |
| gyrB | 6145 | c.906C>T | synonymous_variant | 0.83 |
| gyrB | 6178 | c.939C>T | synonymous_variant | 1.0 |
| gyrB | 6181 | c.942C>G | synonymous_variant | 1.0 |
| gyrB | 6196 | c.957C>G | synonymous_variant | 1.0 |
| gyrB | 6214 | c.975G>C | synonymous_variant | 1.0 |
| gyrB | 6247 | c.1008G>A | synonymous_variant | 1.0 |
| gyrB | 6250 | c.1011A>G | synonymous_variant | 1.0 |
| gyrB | 6253 | c.1014G>C | synonymous_variant | 1.0 |
| gyrB | 6259 | p.Asp340Glu | missense_variant | 1.0 |
| gyrB | 6280 | c.1041T>C | synonymous_variant | 1.0 |
| gyrB | 6286 | c.1047T>C | synonymous_variant | 1.0 |
| gyrB | 6298 | c.1059C>G | synonymous_variant | 1.0 |
| gyrB | 6299 | c.1060C>T | synonymous_variant | 1.0 |
| gyrA | 6307 | c.-995T>G | upstream_gene_variant | 1.0 |
| gyrA | 6313 | c.-989C>T | upstream_gene_variant | 1.0 |
| gyrA | 6319 | c.-983G>C | upstream_gene_variant | 1.0 |
| gyrA | 6331 | c.-971A>G | upstream_gene_variant | 1.0 |
| gyrA | 6358 | c.-944C>G | upstream_gene_variant | 1.0 |
| gyrA | 6361 | c.-941G>A | upstream_gene_variant | 1.0 |
| gyrA | 6362 | c.-940T>C | upstream_gene_variant | 1.0 |
| gyrA | 6379 | c.-923C>G | upstream_gene_variant | 1.0 |
| gyrA | 6382 | c.-920A>G | upstream_gene_variant | 1.0 |
| gyrA | 6388 | c.-914T>C | upstream_gene_variant | 1.0 |
| gyrA | 6610 | c.-692C>G | upstream_gene_variant | 1.0 |
| gyrA | 6613 | c.-689A>G | upstream_gene_variant | 1.0 |
| gyrA | 6616 | c.-686A>G | upstream_gene_variant | 1.0 |
| gyrA | 6622 | c.-680C>T | upstream_gene_variant | 1.0 |
| gyrA | 6625 | c.-677G>A | upstream_gene_variant | 1.0 |
| gyrA | 6634 | c.-668T>C | upstream_gene_variant | 1.0 |
| gyrA | 6637 | c.-665T>G | upstream_gene_variant | 1.0 |
| gyrA | 6640 | c.-662A>G | upstream_gene_variant | 1.0 |
| gyrA | 6643 | c.-659A>G | upstream_gene_variant | 1.0 |
| gyrA | 6655 | c.-647T>C | upstream_gene_variant | 1.0 |
| gyrA | 6670 | c.-632G>C | upstream_gene_variant | 1.0 |
| gyrA | 6673 | c.-629A>C | upstream_gene_variant | 1.0 |
| gyrA | 6674 | c.-628_-626delCTTinsTTG | upstream_gene_variant | 1.0 |
| gyrA | 6680 | c.-622C>T | upstream_gene_variant | 1.0 |
| gyrA | 6700 | c.-602T>C | upstream_gene_variant | 1.0 |
| gyrA | 6703 | c.-599G>C | upstream_gene_variant | 1.0 |
| gyrA | 6709 | c.-593A>G | upstream_gene_variant | 1.0 |
| gyrA | 6712 | c.-590G>C | upstream_gene_variant | 1.0 |
| gyrA | 6730 | c.-572A>G | upstream_gene_variant | 1.0 |
| gyrA | 6745 | c.-557T>C | upstream_gene_variant | 1.0 |
| gyrA | 6760 | c.-542G>C | upstream_gene_variant | 1.0 |
| gyrA | 6764 | c.-538C>T | upstream_gene_variant | 1.0 |
| gyrA | 6769 | c.-533C>T | upstream_gene_variant | 1.0 |
| gyrA | 6775 | c.-527G>C | upstream_gene_variant | 1.0 |
| gyrA | 6787 | c.-515G>A | upstream_gene_variant | 1.0 |
| gyrA | 6793 | c.-509T>C | upstream_gene_variant | 1.0 |
| gyrB | 6798 | p.Gly520Ala | missense_variant | 1.0 |
| gyrB | 6801 | p.Lys521Arg | missense_variant | 1.0 |
| gyrA | 6808 | c.-494C>T | upstream_gene_variant | 1.0 |
| gyrA | 6826 | c.-476G>C | upstream_gene_variant | 1.0 |
| gyrA | 6925 | c.-377T>C | upstream_gene_variant | 1.0 |
| gyrA | 6926 | c.-376T>C | upstream_gene_variant | 1.0 |
| gyrA | 6931 | c.-371A>C | upstream_gene_variant | 1.0 |
| gyrA | 6934 | c.-368A>G | upstream_gene_variant | 1.0 |
| gyrA | 6950 | c.-352_-350delCTCinsTTG | upstream_gene_variant | 1.0 |
| gyrA | 6955 | c.-347G>A | upstream_gene_variant | 1.0 |
| gyrA | 6961 | c.-341G>A | upstream_gene_variant | 1.0 |
| gyrA | 6964 | c.-338C>T | upstream_gene_variant | 1.0 |
| gyrA | 6965 | c.-337_-335delAGTinsTCC | upstream_gene_variant | 1.0 |
| gyrA | 6973 | c.-329G>C | upstream_gene_variant | 1.0 |
| gyrA | 6982 | c.-320A>C | upstream_gene_variant | 1.0 |
| gyrA | 6991 | c.-311C>T | upstream_gene_variant | 1.0 |
| gyrA | 6994 | c.-308C>T | upstream_gene_variant | 1.0 |
| gyrA | 6997 | c.-305G>A | upstream_gene_variant | 1.0 |
| gyrA | 7000 | c.-302C>T | upstream_gene_variant | 1.0 |
| gyrA | 7006 | c.-296T>G | upstream_gene_variant | 1.0 |
| gyrA | 7007 | c.-295C>T | upstream_gene_variant | 1.0 |
| gyrA | 7012 | c.-290G>C | upstream_gene_variant | 1.0 |
| gyrA | 7018 | c.-284G>A | upstream_gene_variant | 1.0 |
| gyrA | 7024 | c.-278G>C | upstream_gene_variant | 1.0 |
| gyrA | 7030 | c.-272C>A | upstream_gene_variant | 1.0 |
| gyrA | 7033 | c.-269G>C | upstream_gene_variant | 1.0 |
| gyrA | 7060 | c.-242T>C | upstream_gene_variant | 1.0 |
| gyrA | 7066 | c.-236G>C | upstream_gene_variant | 1.0 |
| gyrA | 7081 | c.-221T>C | upstream_gene_variant | 1.0 |
| gyrA | 7090 | c.-212C>T | upstream_gene_variant | 1.0 |
| gyrA | 7093 | c.-209T>C | upstream_gene_variant | 1.0 |
| gyrA | 7099 | c.-203G>A | upstream_gene_variant | 1.0 |
| gyrA | 7108 | c.-194G>A | upstream_gene_variant | 1.0 |
| gyrA | 7120 | c.-182T>C | upstream_gene_variant | 1.0 |
| gyrA | 7123 | c.-179C>G | upstream_gene_variant | 1.0 |
| gyrA | 7129 | c.-173T>G | upstream_gene_variant | 1.0 |
| gyrA | 7132 | c.-170T>G | upstream_gene_variant | 1.0 |
| gyrA | 7141 | c.-161T>C | upstream_gene_variant | 1.0 |
| gyrA | 7147 | c.-155G>C | upstream_gene_variant | 1.0 |
| gyrA | 7151 | c.-151C>T | upstream_gene_variant | 1.0 |
| gyrA | 7165 | c.-137C>A | upstream_gene_variant | 1.0 |
| gyrA | 7178 | c.-124T>C | upstream_gene_variant | 1.0 |
| gyrA | 7207 | c.-95C>G | upstream_gene_variant | 1.0 |
| gyrA | 7532 | c.231T>C | synonymous_variant | 1.0 |
| gyrA | 7541 | c.240C>G | synonymous_variant | 1.0 |
| gyrA | 7547 | c.246C>T | synonymous_variant | 1.0 |
| gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
| gyrA | 7595 | c.294C>G | synonymous_variant | 1.0 |
| gyrA | 7601 | c.300C>G | synonymous_variant | 1.0 |
| gyrA | 7619 | c.318C>T | synonymous_variant | 1.0 |
| gyrA | 7622 | c.321C>T | synonymous_variant | 1.0 |
| gyrA | 7631 | c.330G>C | synonymous_variant | 1.0 |
| gyrA | 7652 | c.351C>G | synonymous_variant | 1.0 |
| gyrA | 7664 | c.363T>C | synonymous_variant | 1.0 |
| gyrA | 7667 | c.366C>T | synonymous_variant | 1.0 |
| gyrA | 7766 | c.465C>T | synonymous_variant | 1.0 |
| gyrA | 7769 | c.468C>T | synonymous_variant | 1.0 |
| gyrA | 7784 | c.483A>G | synonymous_variant | 1.0 |
| gyrA | 7787 | c.486G>A | synonymous_variant | 1.0 |
| gyrA | 7799 | c.498A>G | synonymous_variant | 1.0 |
| gyrA | 7832 | c.531G>T | synonymous_variant | 1.0 |
| gyrA | 7835 | c.534A>C | synonymous_variant | 1.0 |
| gyrA | 7838 | c.537C>T | synonymous_variant | 1.0 |
| gyrA | 7850 | c.549C>G | synonymous_variant | 1.0 |
| gyrA | 7859 | c.558A>C | synonymous_variant | 1.0 |
| gyrA | 7886 | c.585T>C | synonymous_variant | 1.0 |
| gyrA | 7889 | c.588G>A | synonymous_variant | 1.0 |
| gyrA | 7892 | c.591G>C | synonymous_variant | 1.0 |
| gyrA | 7919 | p.Glu206Asp | missense_variant | 1.0 |
| gyrA | 7923 | p.His208Tyr | missense_variant | 1.0 |
| gyrA | 7940 | c.639G>A | synonymous_variant | 1.0 |
| gyrA | 7941 | p.Glu214Thr | missense_variant | 1.0 |
| gyrA | 7946 | c.645C>G | synonymous_variant | 1.0 |
| gyrA | 7958 | c.657C>G | synonymous_variant | 1.0 |
| gyrA | 7963 | p.Gly221Glu | missense_variant | 1.0 |
| gyrA | 7970 | c.669T>C | synonymous_variant | 1.0 |
| gyrA | 7973 | c.672A>G | synonymous_variant | 1.0 |
| gyrA | 7979 | c.678G>C | synonymous_variant | 1.0 |
| gyrA | 7988 | c.687G>C | synonymous_variant | 1.0 |
| gyrA | 7997 | c.696A>G | synonymous_variant | 1.0 |
| gyrA | 8000 | c.699G>C | synonymous_variant | 1.0 |
| gyrA | 8020 | p.Thr240Ile | missense_variant | 1.0 |
| gyrA | 8024 | c.723T>C | synonymous_variant | 1.0 |
| gyrA | 8027 | c.726T>C | synonymous_variant | 0.8 |
| gyrA | 8030 | c.729C>A | synonymous_variant | 1.0 |
| gyrA | 8036 | c.735A>G | synonymous_variant | 1.0 |
| gyrA | 8039 | c.738T>C | synonymous_variant | 1.0 |
| gyrA | 8042 | c.741C>T | synonymous_variant | 1.0 |
| gyrA | 8048 | c.747C>T | synonymous_variant | 1.0 |
| gyrA | 8054 | c.753T>C | synonymous_variant | 1.0 |
| gyrA | 8057 | c.756A>G | synonymous_variant | 1.0 |
| gyrA | 8069 | c.768T>C | synonymous_variant | 1.0 |
| gyrA | 8078 | c.777A>G | synonymous_variant | 1.0 |
| gyrA | 8084 | c.783G>A | synonymous_variant | 1.0 |
| gyrA | 8090 | c.789C>G | synonymous_variant | 1.0 |
| gyrA | 8096 | c.795T>C | synonymous_variant | 1.0 |
| gyrA | 8099 | c.798T>C | synonymous_variant | 1.0 |
| gyrA | 8105 | c.804G>T | synonymous_variant | 1.0 |
| gyrA | 8111 | c.810G>C | synonymous_variant | 1.0 |
| gyrA | 8121 | c.820T>C | synonymous_variant | 1.0 |
| gyrA | 8156 | c.855T>C | synonymous_variant | 1.0 |
| gyrA | 8168 | c.867A>G | synonymous_variant | 1.0 |
| gyrA | 8174 | c.873C>G | synonymous_variant | 1.0 |
| gyrA | 8177 | c.876A>C | synonymous_variant | 1.0 |
| gyrA | 8189 | c.888G>T | synonymous_variant | 1.0 |
| gyrA | 8195 | c.894C>T | synonymous_variant | 1.0 |
| gyrA | 8198 | c.897T>C | synonymous_variant | 1.0 |
| gyrA | 8199 | p.Ser300Ala | missense_variant | 1.0 |
| gyrA | 8207 | c.906T>C | synonymous_variant | 1.0 |
| gyrA | 8217 | p.Ser306Gly | missense_variant | 1.0 |
| gyrA | 8225 | p.Asp308Glu | missense_variant | 1.0 |
| gyrA | 8235 | p.Leu312Val | missense_variant | 1.0 |
| gyrA | 8247 | p.Ile316Val | missense_variant | 1.0 |
| gyrA | 8253 | p.Ile318Leu | missense_variant | 1.0 |
| gyrA | 8258 | c.957G>A | synonymous_variant | 1.0 |
| gyrA | 8264 | c.963T>C | synonymous_variant | 1.0 |
| gyrA | 8267 | c.966G>C | synonymous_variant | 1.0 |
| gyrA | 8282 | c.981G>A | synonymous_variant | 1.0 |
| gyrA | 8283 | p.Ile328Leu | missense_variant | 1.0 |
| gyrA | 8288 | c.987T>C | synonymous_variant | 1.0 |
| gyrA | 8294 | c.993T>C | synonymous_variant | 1.0 |
| gyrA | 8315 | c.1014G>A | synonymous_variant | 1.0 |
| gyrA | 8318 | c.1017C>G | synonymous_variant | 1.0 |
| gyrA | 8324 | c.1023T>C | synonymous_variant | 1.0 |
| gyrA | 8339 | c.1038A>G | synonymous_variant | 1.0 |
| gyrA | 8340 | p.Ala347Ser | missense_variant | 1.0 |
| gyrA | 8375 | c.1074G>C | synonymous_variant | 1.0 |
| gyrA | 8382 | p.Leu361Met | missense_variant | 1.0 |
| gyrA | 8393 | c.1092T>C | synonymous_variant | 1.0 |
| gyrA | 8399 | c.1098T>C | synonymous_variant | 1.0 |
| gyrA | 8402 | p.Asp367Glu | missense_variant | 1.0 |
| gyrA | 8420 | c.1119T>C | synonymous_variant | 1.0 |
| gyrA | 8421 | p.Val374Ile | missense_variant | 1.0 |
| gyrA | 8433 | p.Thr378Arg | missense_variant | 1.0 |
| gyrA | 8447 | c.1146C>A | synonymous_variant | 1.0 |
| gyrA | 8450 | c.1149G>A | synonymous_variant | 1.0 |
| gyrA | 8453 | c.1152A>C | synonymous_variant | 1.0 |
| gyrA | 8462 | c.1161A>G | synonymous_variant | 1.0 |
| gyrA | 8471 | c.1170T>C | synonymous_variant | 1.0 |
| gyrA | 8486 | c.1185T>C | synonymous_variant | 1.0 |
| gyrA | 8510 | c.1209G>A | synonymous_variant | 1.0 |
| gyrA | 8513 | c.1212C>G | synonymous_variant | 1.0 |
| gyrA | 8516 | c.1215T>C | synonymous_variant | 1.0 |
| gyrA | 8519 | c.1218A>C | synonymous_variant | 1.0 |
| gyrA | 8531 | c.1230G>A | synonymous_variant | 1.0 |
| gyrA | 8546 | c.1245T>C | synonymous_variant | 1.0 |
| gyrA | 8561 | c.1260A>G | synonymous_variant | 1.0 |
| gyrA | 8562 | c.1261C>T | synonymous_variant | 1.0 |
| gyrA | 8571 | c.1270C>T | synonymous_variant | 1.0 |
| gyrA | 8603 | c.1302A>G | synonymous_variant | 1.0 |
| gyrA | 8609 | c.1308G>C | synonymous_variant | 1.0 |
| gyrA | 8619 | c.1318T>C | synonymous_variant | 1.0 |
| gyrA | 8693 | c.1392T>C | synonymous_variant | 1.0 |
| gyrA | 8694 | c.1393C>T | synonymous_variant | 1.0 |
| gyrA | 8711 | c.1410A>C | synonymous_variant | 1.0 |
| gyrA | 8897 | c.1596T>C | synonymous_variant | 1.0 |
| gyrA | 8903 | c.1602T>C | synonymous_variant | 1.0 |
| gyrA | 8915 | c.1614A>G | synonymous_variant | 1.0 |
| gyrA | 8924 | c.1623C>G | synonymous_variant | 1.0 |
| gyrA | 8933 | c.1632G>A | synonymous_variant | 1.0 |
| gyrA | 8939 | c.1638T>C | synonymous_variant | 1.0 |
| gyrA | 8942 | c.1641G>C | synonymous_variant | 1.0 |
| gyrA | 8945 | c.1644G>T | synonymous_variant | 1.0 |
| gyrA | 8946 | c.1645_1647delTTGinsCTC | synonymous_variant | 1.0 |
| gyrA | 8981 | c.1680G>C | synonymous_variant | 1.0 |
| gyrA | 8987 | c.1686C>G | synonymous_variant | 1.0 |
| gyrA | 8998 | p.Leu566Trp | missense_variant | 1.0 |
| gyrA | 9003 | c.1702C>T | synonymous_variant | 1.0 |
| gyrA | 9017 | c.1716C>T | synonymous_variant | 1.0 |
| gyrA | 9023 | c.1722A>C | synonymous_variant | 1.0 |
| gyrA | 9029 | c.1728T>G | synonymous_variant | 1.0 |
| gyrA | 9101 | c.1800A>G | synonymous_variant | 1.0 |
| gyrA | 9119 | c.1818A>G | synonymous_variant | 1.0 |
| gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
| gyrA | 9146 | c.1845C>G | synonymous_variant | 1.0 |
| gyrA | 9149 | c.1848C>T | synonymous_variant | 1.0 |
| gyrA | 9153 | p.Thr618Glu | missense_variant | 1.0 |
| gyrA | 9158 | c.1857C>T | synonymous_variant | 1.0 |
| gyrA | 9161 | c.1860C>T | synonymous_variant | 1.0 |
| gyrA | 9167 | c.1866C>T | synonymous_variant | 1.0 |
| gyrA | 9174 | c.1873C>T | synonymous_variant | 1.0 |
| gyrA | 9182 | c.1881T>C | synonymous_variant | 1.0 |
| gyrA | 9183 | p.Arg628Lys | missense_variant | 1.0 |
| gyrA | 9197 | c.1896G>C | synonymous_variant | 1.0 |
| gyrA | 9200 | c.1899A>G | synonymous_variant | 1.0 |
| gyrA | 9218 | c.1917C>T | synonymous_variant | 1.0 |
| gyrA | 9230 | c.1929T>C | synonymous_variant | 1.0 |
| gyrA | 9236 | c.1935G>C | synonymous_variant | 1.0 |
| gyrA | 9242 | c.1941A>C | synonymous_variant | 1.0 |
| gyrA | 9252 | p.Val651Ile | missense_variant | 1.0 |
| gyrA | 9257 | c.1956C>T | synonymous_variant | 1.0 |
| gyrA | 9284 | c.1983T>G | synonymous_variant | 1.0 |
| gyrA | 9296 | c.1995T>C | synonymous_variant | 1.0 |
| gyrA | 9304 | p.Gly668Glu | missense_variant | 1.0 |
| gyrA | 9315 | c.2014C>T | synonymous_variant | 1.0 |
| gyrA | 9323 | c.2022C>T | synonymous_variant | 1.0 |
| gyrA | 9341 | c.2040C>G | synonymous_variant | 1.0 |
| gyrA | 9345 | c.2044A>C | synonymous_variant | 1.0 |
| gyrA | 9371 | c.2070G>A | synonymous_variant | 1.0 |
| gyrA | 9374 | c.2073G>C | synonymous_variant | 1.0 |
| gyrA | 9377 | c.2076A>G | synonymous_variant | 1.0 |
| gyrA | 9383 | c.2082T>C | synonymous_variant | 1.0 |
| gyrA | 9386 | c.2085T>G | synonymous_variant | 1.0 |
| gyrA | 9395 | c.2094G>C | synonymous_variant | 1.0 |
| gyrA | 9398 | c.2097T>G | synonymous_variant | 1.0 |
| gyrA | 9401 | c.2100G>A | synonymous_variant | 1.0 |
| gyrA | 9449 | c.2148C>G | synonymous_variant | 1.0 |
| gyrA | 9452 | c.2151G>C | synonymous_variant | 1.0 |
| gyrA | 9585 | c.2284T>C | synonymous_variant | 1.0 |
| gyrA | 9590 | c.2289T>G | synonymous_variant | 1.0 |
| gyrA | 9593 | c.2292G>A | synonymous_variant | 1.0 |
| gyrA | 9602 | c.2301T>C | synonymous_variant | 1.0 |
| gyrA | 9604 | p.Val768Ala | missense_variant | 1.0 |
| gyrA | 9626 | c.2325T>C | synonymous_variant | 1.0 |
| gyrA | 9629 | c.2328C>A | synonymous_variant | 1.0 |
| gyrA | 9630 | p.Val777Ile | missense_variant | 1.0 |
| gyrA | 9635 | c.2334T>C | synonymous_variant | 1.0 |
| gyrA | 9644 | c.2343T>C | synonymous_variant | 1.0 |
| gyrA | 9650 | c.2349G>C | synonymous_variant | 1.0 |
| gyrA | 9656 | c.2355C>G | synonymous_variant | 1.0 |
| gyrA | 9659 | c.2358C>G | synonymous_variant | 1.0 |
| gyrA | 9668 | c.2367C>A | synonymous_variant | 1.0 |
| gyrA | 9689 | c.2388G>C | synonymous_variant | 1.0 |
| gyrA | 9704 | c.2403T>C | synonymous_variant | 1.0 |
| gyrA | 9707 | c.2406G>C | synonymous_variant | 1.0 |
| gyrA | 9716 | c.2415T>C | synonymous_variant | 1.0 |
| gyrA | 9722 | c.2421C>T | synonymous_variant | 1.0 |
| fgd1 | 490851 | c.69A>T | synonymous_variant | 1.0 |
| fgd1 | 490853 | p.Ala24Gly | missense_variant | 1.0 |
| fgd1 | 490863 | c.81C>A | synonymous_variant | 1.0 |
| fgd1 | 490869 | c.87C>T | synonymous_variant | 1.0 |
| fgd1 | 490890 | c.108C>G | synonymous_variant | 1.0 |
| fgd1 | 490896 | c.114C>T | synonymous_variant | 1.0 |
| fgd1 | 490905 | c.123T>C | synonymous_variant | 1.0 |
| fgd1 | 490911 | c.129T>C | synonymous_variant | 1.0 |
| fgd1 | 490921 | p.Gln47Lys | missense_variant | 1.0 |
| fgd1 | 490929 | c.147C>G | synonymous_variant | 1.0 |
| fgd1 | 490932 | c.150T>C | synonymous_variant | 1.0 |
| fgd1 | 490935 | c.153C>G | synonymous_variant | 1.0 |
| fgd1 | 490945 | c.163C>T | synonymous_variant | 1.0 |
| fgd1 | 490962 | c.180T>C | synonymous_variant | 1.0 |
| fgd1 | 490971 | c.189A>G | synonymous_variant | 1.0 |
| fgd1 | 490974 | c.192T>C | synonymous_variant | 1.0 |
| fgd1 | 490980 | p.Asn66Lys | missense_variant | 1.0 |
| fgd1 | 490984 | p.Leu68Val | missense_variant | 1.0 |
| fgd1 | 490995 | c.213C>T | synonymous_variant | 1.0 |
| fgd1 | 490998 | c.216T>C | synonymous_variant | 1.0 |
| fgd1 | 491007 | c.225G>C | synonymous_variant | 1.0 |
| fgd1 | 491013 | c.231C>G | synonymous_variant | 1.0 |
| fgd1 | 491043 | c.261T>G | synonymous_variant | 1.0 |
| fgd1 | 491049 | c.267T>G | synonymous_variant | 1.0 |
| fgd1 | 491063 | p.Gly94Ala | missense_variant | 1.0 |
| fgd1 | 491067 | c.285C>T | synonymous_variant | 1.0 |
| fgd1 | 491077 | p.Asn99Asp | missense_variant | 1.0 |
| fgd1 | 491085 | c.303T>G | synonymous_variant | 1.0 |
| fgd1 | 491091 | c.309T>G | synonymous_variant | 1.0 |
| fgd1 | 491094 | c.312C>T | synonymous_variant | 1.0 |
| fgd1 | 491106 | c.324T>C | synonymous_variant | 1.0 |
| fgd1 | 491121 | c.339A>G | synonymous_variant | 1.0 |
| fgd1 | 491142 | c.360C>G | synonymous_variant | 1.0 |
| fgd1 | 491151 | c.369G>A | synonymous_variant | 1.0 |
| fgd1 | 491154 | p.Glu124Asp | missense_variant | 1.0 |
| fgd1 | 491163 | c.381G>A | synonymous_variant | 1.0 |
| fgd1 | 491166 | c.384G>C | synonymous_variant | 1.0 |
| fgd1 | 491181 | c.399T>C | synonymous_variant | 1.0 |
| fgd1 | 491191 | p.Gly137Arg | missense_variant | 1.0 |
| fgd1 | 491196 | c.414A>G | synonymous_variant | 1.0 |
| fgd1 | 491478 | c.696G>A | synonymous_variant | 1.0 |
| fgd1 | 491487 | c.705C>T | synonymous_variant | 1.0 |
| fgd1 | 491496 | c.714C>T | synonymous_variant | 1.0 |
| fgd1 | 491499 | c.717G>C | synonymous_variant | 1.0 |
| fgd1 | 491508 | c.726A>T | synonymous_variant | 1.0 |
| fgd1 | 491512 | p.Asn244Gln | missense_variant | 1.0 |
| fgd1 | 491523 | c.741G>A | synonymous_variant | 1.0 |
| fgd1 | 491526 | c.744T>C | synonymous_variant | 1.0 |
| fgd1 | 491542 | c.760T>C | synonymous_variant | 1.0 |
| fgd1 | 491547 | c.765A>C | synonymous_variant | 1.0 |
| fgd1 | 491550 | c.768T>C | synonymous_variant | 1.0 |
| fgd1 | 491553 | c.771G>A | synonymous_variant | 1.0 |
| fgd1 | 491601 | c.819T>C | synonymous_variant | 1.0 |
| fgd1 | 491604 | c.822G>C | synonymous_variant | 1.0 |
| fgd1 | 491610 | c.828A>G | synonymous_variant | 1.0 |
| fgd1 | 491616 | c.834A>G | synonymous_variant | 1.0 |
| fgd1 | 491628 | c.846G>A | synonymous_variant | 1.0 |
| mshA | 575586 | p.Ala80Gly | missense_variant | 1.0 |
| mshA | 575590 | c.243T>G | synonymous_variant | 1.0 |
| mshA | 575593 | c.246G>A | synonymous_variant | 1.0 |
| mshA | 575596 | c.249C>T | synonymous_variant | 1.0 |
| mshA | 575629 | c.282A>T | synonymous_variant | 1.0 |
| mshA | 575633 | p.Ala96Thr | missense_variant | 1.0 |
| mshA | 575652 | p.Arg102Gln | missense_variant | 1.0 |
| mshA | 575659 | c.312A>G | synonymous_variant | 1.0 |
| mshA | 575662 | c.315C>A | synonymous_variant | 1.0 |
| mshA | 575665 | c.318G>C | synonymous_variant | 1.0 |
| mshA | 575686 | c.339G>A | synonymous_variant | 1.0 |
| mshA | 575689 | c.342G>C | synonymous_variant | 1.0 |
| mshA | 575692 | c.345G>A | synonymous_variant | 1.0 |
| mshA | 575705 | c.358T>C | synonymous_variant | 1.0 |
| mshA | 575713 | c.366G>A | synonymous_variant | 1.0 |
| mshA | 575732 | c.385_387delCTTinsTTG | synonymous_variant | 1.0 |
| mshA | 575737 | c.390T>C | synonymous_variant | 1.0 |
| mshA | 575746 | c.399C>G | synonymous_variant | 1.0 |
| mshA | 575767 | c.420G>A | synonymous_variant | 1.0 |
| mshA | 575770 | c.423G>C | synonymous_variant | 1.0 |
| mshA | 575772 | p.Val142Ala | missense_variant | 1.0 |
| mshA | 575785 | c.438T>C | synonymous_variant | 1.0 |
| mshA | 575821 | c.474G>C | synonymous_variant | 1.0 |
| mshA | 575824 | c.477T>C | synonymous_variant | 1.0 |
| mshA | 575842 | c.495G>C | synonymous_variant | 1.0 |
| mshA | 575848 | c.501C>T | synonymous_variant | 1.0 |
| mshA | 575872 | c.525C>T | synonymous_variant | 1.0 |
| mshA | 575878 | c.531A>T | synonymous_variant | 1.0 |
| mshA | 575884 | c.537G>C | synonymous_variant | 1.0 |
| mshA | 575893 | c.546C>G | synonymous_variant | 1.0 |
| ccsA | 619697 | c.-194A>C | upstream_gene_variant | 1.0 |
| ccsA | 619708 | c.-183G>C | upstream_gene_variant | 1.0 |
| ccsA | 619713 | c.-178_-177delCGinsTC | upstream_gene_variant | 1.0 |
| ccsA | 619720 | c.-171C>T | upstream_gene_variant | 1.0 |
| ccsA | 619727 | c.-164_-162delACGinsGCC | upstream_gene_variant | 1.0 |
| ccsA | 619744 | c.-147A>G | upstream_gene_variant | 1.0 |
| ccsA | 619766 | c.-125A>G | upstream_gene_variant | 1.0 |
| ccsA | 619771 | c.-120C>G | upstream_gene_variant | 1.0 |
| ccsA | 619786 | c.-105G>C | upstream_gene_variant | 1.0 |
| ccsA | 619792 | c.-99C>T | upstream_gene_variant | 1.0 |
| ccsA | 619794 | c.-97C>A | upstream_gene_variant | 1.0 |
| ccsA | 620214 | c.324C>A | synonymous_variant | 1.0 |
| ccsA | 620245 | p.Leu119Met | missense_variant | 1.0 |
| ccsA | 620256 | c.366C>G | synonymous_variant | 1.0 |
| ccsA | 620257 | p.Ile123Val | missense_variant | 1.0 |
| ccsA | 620271 | c.381C>G | synonymous_variant | 1.0 |
| ccsA | 620283 | c.393T>C | synonymous_variant | 1.0 |
| ccsA | 620284 | p.Ala132Pro | missense_variant | 1.0 |
| ccsA | 620288 | p.Arg133Gln | missense_variant | 1.0 |
| ccsA | 620290 | p.Tyr134Asn | missense_variant | 1.0 |
| ccsA | 620295 | c.405G>T | synonymous_variant | 1.0 |
| ccsA | 620314 | c.424C>T | synonymous_variant | 1.0 |
| ccsA | 620325 | c.435G>T | synonymous_variant | 1.0 |
| ccsA | 620571 | c.681A>G | synonymous_variant | 1.0 |
| ccsA | 620604 | c.714C>G | synonymous_variant | 1.0 |
| ccsA | 620607 | c.717T>G | synonymous_variant | 1.0 |
| ccsA | 620613 | c.723C>T | synonymous_variant | 1.0 |
| ccsA | 620619 | c.729G>A | synonymous_variant | 1.0 |
| ccsA | 620622 | c.732G>C | synonymous_variant | 1.0 |
| ccsA | 620625 | c.735A>C | synonymous_variant | 1.0 |
| ccsA | 620631 | c.741T>G | synonymous_variant | 1.0 |
| ccsA | 620661 | c.771C>T | synonymous_variant | 1.0 |
| ccsA | 620685 | c.795G>A | synonymous_variant | 1.0 |
| ccsA | 620710 | p.Val274Ile | missense_variant | 1.0 |
| ccsA | 620721 | c.831G>C | synonymous_variant | 1.0 |
| ccsA | 620727 | c.837G>T | synonymous_variant | 1.0 |
| ccsA | 620730 | c.840C>T | synonymous_variant | 1.0 |
| ccsA | 620733 | c.843G>C | synonymous_variant | 1.0 |
| ccsA | 620734 | c.844C>A | synonymous_variant | 1.0 |
| ccsA | 620742 | c.852G>C | synonymous_variant | 1.0 |
| ccsA | 620748 | c.858T>C | synonymous_variant | 1.0 |
| ccsA | 620760 | c.870C>G | synonymous_variant | 1.0 |
| ccsA | 620766 | c.876C>G | synonymous_variant | 1.0 |
| ccsA | 620773 | p.Ile295Val | missense_variant | 1.0 |
| ccsA | 620783 | p.Ala298Val | missense_variant | 1.0 |
| ccsA | 620787 | c.897C>G | synonymous_variant | 1.0 |
| ccsA | 620808 | c.918T>C | synonymous_variant | 1.0 |
| ccsA | 620829 | c.939G>T | synonymous_variant | 1.0 |
| ccsA | 620838 | c.948C>T | synonymous_variant | 1.0 |
| ccsA | 620839 | c.949C>T | synonymous_variant | 1.0 |
| ccsA | 620847 | c.957G>C | synonymous_variant | 1.0 |
| rpoB | 759635 | c.-172C>T | upstream_gene_variant | 1.0 |
| rpoB | 759644 | c.-163T>A | upstream_gene_variant | 1.0 |
| rpoB | 759647 | c.-160T>C | upstream_gene_variant | 1.0 |
| rpoB | 759661 | c.-146G>C | upstream_gene_variant | 1.0 |
| rpoB | 759670 | c.-137C>T | upstream_gene_variant | 1.0 |
| rpoB | 759671 | c.-136G>T | upstream_gene_variant | 1.0 |
| rpoB | 759675 | c.-132T>C | upstream_gene_variant | 1.0 |
| rpoB | 759676 | c.-131A>G | upstream_gene_variant | 1.0 |
| rpoB | 759701 | c.-106A>T | upstream_gene_variant | 1.0 |
| rpoB | 759725 | c.-82A>C | upstream_gene_variant | 1.0 |
| rpoB | 759850 | p.Pro15Gln | missense_variant | 1.0 |
| rpoB | 759869 | c.63C>T | synonymous_variant | 1.0 |
| rpoB | 759872 | c.66G>A | synonymous_variant | 1.0 |
| rpoB | 759875 | c.69T>C | synonymous_variant | 1.0 |
| rpoB | 759877 | p.Asn24Ser | missense_variant | 1.0 |
| rpoB | 759884 | c.78A>G | synonymous_variant | 1.0 |
| rpoB | 759896 | c.90A>T | synonymous_variant | 1.0 |
| rpoB | 759899 | c.93C>T | synonymous_variant | 1.0 |
| rpoB | 759905 | c.99C>T | synonymous_variant | 1.0 |
| rpoB | 759914 | c.108T>C | synonymous_variant | 1.0 |
| rpoB | 759920 | c.114G>C | synonymous_variant | 1.0 |
| rpoB | 759929 | c.123A>G | synonymous_variant | 1.0 |
| rpoB | 759932 | c.126T>G | synonymous_variant | 1.0 |
| rpoB | 759944 | c.138A>G | synonymous_variant | 1.0 |
| rpoB | 759945 | c.139_141delCTCinsTTG | synonymous_variant | 1.0 |
| rpoB | 759956 | c.150C>G | synonymous_variant | 1.0 |
| rpoB | 759965 | c.159T>C | synonymous_variant | 1.0 |
| rpoB | 759989 | c.183G>C | synonymous_variant | 1.0 |
| rpoB | 759991 | p.Pro62Gln | missense_variant | 1.0 |
| rpoB | 760059 | p.Tyr85Asp | missense_variant | 1.0 |
| rpoB | 760067 | c.261G>C | synonymous_variant | 1.0 |
| rpoB | 760070 | c.264T>A | synonymous_variant | 1.0 |
| rpoB | 760101 | c.295T>C | synonymous_variant | 1.0 |
| rpoB | 760106 | c.300G>C | synonymous_variant | 1.0 |
| rpoB | 760112 | c.306T>C | synonymous_variant | 1.0 |
| rpoB | 760118 | c.312T>C | synonymous_variant | 1.0 |
| rpoB | 760121 | c.315T>C | synonymous_variant | 1.0 |
| rpoB | 760130 | p.Asp108Glu | missense_variant | 1.0 |
| rpoB | 760142 | c.336C>G | synonymous_variant | 1.0 |
| rpoB | 760172 | c.366G>C | synonymous_variant | 1.0 |
| rpoB | 760181 | c.375T>C | synonymous_variant | 1.0 |
| rpoB | 760184 | c.378A>G | synonymous_variant | 1.0 |
| rpoB | 760193 | c.387C>G | synonymous_variant | 1.0 |
| rpoB | 760196 | c.390C>G | synonymous_variant | 1.0 |
| rpoB | 760202 | c.396G>A | synonymous_variant | 1.0 |
| rpoB | 760223 | c.417T>C | synonymous_variant | 1.0 |
| rpoB | 760235 | c.429T>C | synonymous_variant | 1.0 |
| rpoB | 760256 | c.450C>T | synonymous_variant | 1.0 |
| rpoB | 760298 | c.492G>C | synonymous_variant | 1.0 |
| rpoB | 760307 | c.501T>C | synonymous_variant | 1.0 |
| rpoB | 760328 | c.522G>C | synonymous_variant | 1.0 |
| rpoB | 760340 | c.534G>T | synonymous_variant | 1.0 |
| rpoB | 760343 | c.537G>C | synonymous_variant | 1.0 |
| rpoB | 760361 | c.555T>C | synonymous_variant | 1.0 |
| rpoB | 760406 | c.600G>C | synonymous_variant | 1.0 |
| rpoB | 760409 | c.603C>T | synonymous_variant | 1.0 |
| rpoB | 760412 | c.606C>G | synonymous_variant | 1.0 |
| rpoB | 760415 | c.609C>G | synonymous_variant | 1.0 |
| rpoB | 760418 | c.612G>C | synonymous_variant | 1.0 |
| rpoB | 760424 | c.618C>G | synonymous_variant | 1.0 |
| rpoB | 760430 | c.624T>C | synonymous_variant | 1.0 |
| rpoB | 760445 | c.639C>T | synonymous_variant | 1.0 |
| rpoB | 760475 | c.669A>G | synonymous_variant | 1.0 |
| rpoB | 760484 | c.678A>G | synonymous_variant | 1.0 |
| rpoB | 760508 | c.702G>C | synonymous_variant | 1.0 |
| rpoB | 760511 | c.705G>C | synonymous_variant | 1.0 |
| rpoB | 760528 | p.Gln241Arg | missense_variant | 1.0 |
| rpoB | 760532 | c.726T>C | synonymous_variant | 1.0 |
| rpoB | 760533 | p.Val243Thr | missense_variant | 1.0 |
| rpoB | 760563 | p.Arg253Met | missense_variant | 1.0 |
| rpoB | 760577 | c.771G>A | synonymous_variant | 1.0 |
| rpoB | 760591 | p.Val262Ala | missense_variant | 1.0 |
| rpoB | 760604 | c.798G>A | synonymous_variant | 1.0 |
| rpoB | 760607 | c.801G>C | synonymous_variant | 1.0 |
| rpoB | 760611 | c.805T>C | synonymous_variant | 1.0 |
| rpoB | 760625 | c.819C>A | synonymous_variant | 1.0 |
| rpoB | 760646 | c.840C>G | synonymous_variant | 1.0 |
| rpoB | 760655 | c.849A>G | synonymous_variant | 1.0 |
| rpoB | 760661 | c.855A>C | synonymous_variant | 1.0 |
| rpoB | 760664 | c.858G>C | synonymous_variant | 1.0 |
| rpoB | 760670 | c.864G>C | synonymous_variant | 1.0 |
| rpoB | 760673 | c.867G>A | synonymous_variant | 1.0 |
| rpoB | 760674 | c.868T>C | synonymous_variant | 1.0 |
| rpoB | 760679 | c.873A>G | synonymous_variant | 1.0 |
| rpoB | 760683 | c.877T>C | synonymous_variant | 1.0 |
| rpoB | 760718 | c.912C>T | synonymous_variant | 1.0 |
| rpoB | 760724 | c.918T>C | synonymous_variant | 1.0 |
| rpoB | 760779 | p.Ser325Thr | missense_variant | 1.0 |
| rpoB | 760805 | c.999G>C | synonymous_variant | 1.0 |
| rpoB | 760817 | c.1011A>G | synonymous_variant | 1.0 |
| rpoB | 760830 | c.1024T>C | synonymous_variant | 1.0 |
| rpoB | 760841 | c.1035T>C | synonymous_variant | 1.0 |
| rpoB | 760845 | p.Thr347Ala | missense_variant | 1.0 |
| rpoB | 760859 | c.1053T>G | synonymous_variant | 1.0 |
| rpoB | 760868 | c.1062C>G | synonymous_variant | 1.0 |
| rpoB | 760919 | c.1113C>G | synonymous_variant | 1.0 |
| rpoB | 760920 | c.1114C>T | synonymous_variant | 1.0 |
| rpoB | 760928 | c.1122G>C | synonymous_variant | 1.0 |
| rpoB | 760946 | c.1140A>G | synonymous_variant | 1.0 |
| rpoB | 760971 | c.1165C>A | synonymous_variant | 1.0 |
| rpoB | 760994 | c.1188G>A | synonymous_variant | 1.0 |
| rpoB | 761006 | c.1200C>T | synonymous_variant | 1.0 |
| rpoB | 761015 | c.1209G>C | synonymous_variant | 1.0 |
| rpoB | 761027 | c.1221A>G | synonymous_variant | 1.0 |
| rpoB | 761036 | c.1230G>A | synonymous_variant | 1.0 |
| rpoB | 761037 | c.1231T>C | synonymous_variant | 1.0 |
| rpoB | 761051 | c.1245G>C | synonymous_variant | 1.0 |
| rpoB | 761066 | c.1260G>C | synonymous_variant | 1.0 |
| rpoB | 761096 | c.1290G>C | synonymous_variant | 1.0 |
| rpoB | 761097 | c.1291_1292delAGinsTC | synonymous_variant | 1.0 |
| rpoB | 761102 | c.1296A>G | synonymous_variant | 1.0 |
| rpoB | 761132 | c.1326G>C | synonymous_variant | 1.0 |
| rpoB | 761133 | c.1327_1329delTTGinsCTC | synonymous_variant | 1.0 |
| rpoB | 761150 | c.1344A>G | synonymous_variant | 1.0 |
| rpoB | 761153 | c.1347G>T | synonymous_variant | 1.0 |
| rpoB | 761168 | c.1362C>G | synonymous_variant | 1.0 |
| rpoB | 761180 | c.1374A>C | synonymous_variant | 1.0 |
| rpoB | 761183 | c.1377T>G | synonymous_variant | 1.0 |
| rpoB | 761201 | c.1395G>A | synonymous_variant | 1.0 |
| rpoB | 761204 | c.1398C>G | synonymous_variant | 1.0 |
| rpoB | 761207 | c.1401C>T | synonymous_variant | 1.0 |
| rpoB | 761234 | c.1428G>C | synonymous_variant | 1.0 |
| rpoB | 761249 | c.1443A>G | synonymous_variant | 1.0 |
| rpoB | 761255 | c.1449T>G | synonymous_variant | 1.0 |
| rpoB | 761261 | c.1455G>T | synonymous_variant | 1.0 |
| rpoB | 761273 | c.1467T>C | synonymous_variant | 1.0 |
| rpoB | 761300 | c.1494G>A | synonymous_variant | 1.0 |
| rpoB | 761318 | c.1512G>C | synonymous_variant | 1.0 |
| rpoB | 761327 | c.1521A>G | synonymous_variant | 1.0 |
| rpoB | 761346 | p.Val514Ile | missense_variant | 1.0 |
| rpoB | 761379 | c.1573C>T | synonymous_variant | 1.0 |
| rpoB | 761384 | c.1578C>G | synonymous_variant | 1.0 |
| rpoB | 761408 | c.1602G>C | synonymous_variant | 1.0 |
| rpoB | 761423 | c.1617T>C | synonymous_variant | 1.0 |
| rpoB | 761435 | c.1629T>C | synonymous_variant | 1.0 |
| rpoB | 761438 | c.1632G>T | synonymous_variant | 1.0 |
| rpoB | 761441 | p.Asp545Glu | missense_variant | 1.0 |
| rpoB | 761444 | c.1638T>C | synonymous_variant | 1.0 |
| rpoB | 761447 | c.1641C>G | synonymous_variant | 1.0 |
| rpoB | 761471 | c.1665C>G | synonymous_variant | 1.0 |
| rpoB | 761483 | c.1677G>C | synonymous_variant | 1.0 |
| rpoB | 761492 | c.1686G>C | synonymous_variant | 1.0 |
| rpoB | 761502 | p.Pro566Ala | missense_variant | 1.0 |
| rpoB | 761510 | c.1704T>G | synonymous_variant | 1.0 |
| rpoB | 761537 | c.1731C>G | synonymous_variant | 1.0 |
| rpoB | 761561 | c.1755C>G | synonymous_variant | 1.0 |
| rpoB | 761564 | c.1758G>C | synonymous_variant | 1.0 |
| rpoB | 761573 | c.1767C>G | synonymous_variant | 1.0 |
| rpoB | 761579 | c.1773G>C | synonymous_variant | 1.0 |
| rpoB | 761600 | c.1794T>G | synonymous_variant | 1.0 |
| rpoB | 761603 | c.1797C>T | synonymous_variant | 1.0 |
| rpoB | 761606 | c.1800C>G | synonymous_variant | 1.0 |
| rpoB | 761612 | c.1806G>T | synonymous_variant | 1.0 |
| rpoB | 761615 | c.1809A>C | synonymous_variant | 1.0 |
| rpoB | 761636 | c.1830G>T | synonymous_variant | 1.0 |
| rpoB | 761645 | c.1839C>G | synonymous_variant | 1.0 |
| rpoB | 761648 | c.1842T>C | synonymous_variant | 1.0 |
| rpoB | 761657 | c.1851C>G | synonymous_variant | 1.0 |
| rpoB | 761675 | c.1869G>C | synonymous_variant | 1.0 |
| rpoB | 761682 | c.1876C>T | synonymous_variant | 1.0 |
| rpoB | 761687 | c.1881C>T | synonymous_variant | 1.0 |
| rpoB | 761693 | c.1887G>C | synonymous_variant | 1.0 |
| rpoB | 761708 | c.1902C>T | synonymous_variant | 1.0 |
| rpoB | 761735 | c.1929C>G | synonymous_variant | 1.0 |
| rpoB | 761750 | c.1944G>C | synonymous_variant | 1.0 |
| rpoB | 761765 | c.1959T>C | synonymous_variant | 1.0 |
| rpoB | 761772 | p.His656Ala | missense_variant | 1.0 |
| rpoB | 761778 | p.Asn658Asp | missense_variant | 1.0 |
| rpoB | 761791 | p.Arg662His | missense_variant | 1.0 |
| rpoB | 761813 | c.2007T>C | synonymous_variant | 1.0 |
| rpoB | 761819 | c.2013G>C | synonymous_variant | 1.0 |
| rpoB | 761822 | c.2016C>G | synonymous_variant | 1.0 |
| rpoB | 761834 | c.2028T>C | synonymous_variant | 1.0 |
| rpoB | 761848 | p.Cys681Ser | missense_variant | 1.0 |
| rpoB | 761852 | c.2046C>G | synonymous_variant | 1.0 |
| rpoB | 761864 | c.2058G>C | synonymous_variant | 1.0 |
| rpoB | 761867 | c.2061C>A | synonymous_variant | 1.0 |
| rpoB | 761870 | p.Asp688Glu | missense_variant | 1.0 |
| rpoB | 761873 | c.2067A>G | synonymous_variant | 1.0 |
| rpoB | 761876 | c.2070C>A | synonymous_variant | 1.0 |
| rpoB | 761885 | c.2079T>C | synonymous_variant | 1.0 |
| rpoB | 761891 | c.2085G>C | synonymous_variant | 1.0 |
| rpoB | 761906 | c.2100C>G | synonymous_variant | 1.0 |
| rpoB | 761912 | c.2106T>C | synonymous_variant | 1.0 |
| rpoB | 761913 | p.Asp703Gln | missense_variant | 1.0 |
| rpoB | 761916 | p.Asp704Asn | missense_variant | 1.0 |
| rpoB | 761954 | c.2148C>G | synonymous_variant | 1.0 |
| rpoB | 761990 | c.2184G>C | synonymous_variant | 1.0 |
| rpoB | 762008 | c.2202C>G | synonymous_variant | 1.0 |
| rpoB | 762011 | c.2205G>C | synonymous_variant | 1.0 |
| rpoB | 762017 | c.2211A>G | synonymous_variant | 1.0 |
| rpoB | 762020 | c.2214G>A | synonymous_variant | 1.0 |
| rpoB | 762024 | p.Val740Ile | missense_variant | 1.0 |
| rpoB | 762053 | c.2247T>C | synonymous_variant | 1.0 |
| rpoB | 762062 | c.2256T>C | synonymous_variant | 1.0 |
| rpoB | 762065 | c.2259T>C | synonymous_variant | 1.0 |
| rpoB | 762071 | c.2265C>T | synonymous_variant | 1.0 |
| rpoB | 762083 | c.2277T>C | synonymous_variant | 1.0 |
| rpoB | 762086 | c.2280G>C | synonymous_variant | 1.0 |
| rpoB | 762114 | p.Ile770Val | missense_variant | 1.0 |
| rpoB | 762119 | c.2313C>T | synonymous_variant | 1.0 |
| rpoB | 762131 | c.2325C>G | synonymous_variant | 1.0 |
| rpoB | 762134 | c.2328C>G | synonymous_variant | 1.0 |
| rpoB | 762167 | c.2361T>C | synonymous_variant | 1.0 |
| rpoB | 762185 | c.2379G>C | synonymous_variant | 1.0 |
| rpoB | 762218 | c.2412T>G | synonymous_variant | 1.0 |
| rpoB | 762224 | c.2418C>G | synonymous_variant | 1.0 |
| rpoB | 762236 | c.2430G>A | synonymous_variant | 0.9 |
| rpoB | 762254 | c.2448T>G | synonymous_variant | 0.91 |
| rpoB | 762257 | c.2451C>G | synonymous_variant | 0.91 |
| rpoB | 762266 | c.2460T>C | synonymous_variant | 0.9 |
| rpoB | 762269 | c.2463G>A | synonymous_variant | 0.9 |
| rpoB | 762278 | c.2472C>G | synonymous_variant | 0.9 |
| rpoB | 762284 | c.2478G>C | synonymous_variant | 0.91 |
| rpoB | 762293 | c.2487T>C | synonymous_variant | 0.89 |
| rpoB | 762317 | c.2511A>G | synonymous_variant | 0.75 |
| rpoC | 762395 | c.-975G>C | upstream_gene_variant | 1.0 |
| rpoC | 762398 | c.-972T>C | upstream_gene_variant | 1.0 |
| rpoC | 762401 | c.-969G>C | upstream_gene_variant | 1.0 |
| rpoC | 762404 | c.-966T>C | upstream_gene_variant | 1.0 |
| rpoC | 762410 | c.-960T>C | upstream_gene_variant | 1.0 |
| rpoC | 762416 | c.-954A>G | upstream_gene_variant | 1.0 |
| rpoC | 762434 | c.-936T>C | upstream_gene_variant | 1.0 |
| rpoC | 762470 | c.-900G>C | upstream_gene_variant | 1.0 |
| rpoB | 762486 | p.Pro894Ala | missense_variant | 1.0 |
| rpoB | 762489 | p.Val895Gln | missense_variant | 1.0 |
| rpoB | 762510 | p.Ala902Pro | missense_variant | 1.0 |
| rpoC | 762518 | c.-852C>G | upstream_gene_variant | 1.0 |
| rpoC | 762533 | c.-837T>C | upstream_gene_variant | 1.0 |
| rpoC | 762536 | c.-834T>C | upstream_gene_variant | 1.0 |
| rpoC | 762537 | c.-833T>C | upstream_gene_variant | 1.0 |
| rpoC | 762551 | c.-819C>T | upstream_gene_variant | 1.0 |
| rpoC | 762557 | c.-813G>C | upstream_gene_variant | 1.0 |
| rpoC | 762581 | c.-789T>C | upstream_gene_variant | 1.0 |
| rpoC | 762582 | c.-788T>C | upstream_gene_variant | 1.0 |
| rpoC | 762587 | c.-783G>A | upstream_gene_variant | 1.0 |
| rpoC | 762599 | c.-771T>A | upstream_gene_variant | 1.0 |
| rpoC | 762605 | c.-765T>C | upstream_gene_variant | 1.0 |
| rpoC | 762608 | c.-762C>G | upstream_gene_variant | 1.0 |
| rpoC | 762776 | c.-594C>T | upstream_gene_variant | 1.0 |
| rpoC | 762782 | c.-588T>C | upstream_gene_variant | 1.0 |
| rpoB | 762799 | p.Ala998Gly | missense_variant | 1.0 |
| rpoC | 762812 | c.-558C>G | upstream_gene_variant | 1.0 |
| rpoB | 762813 | p.Met1003Val | missense_variant | 1.0 |
| rpoC | 762827 | c.-543G>C | upstream_gene_variant | 1.0 |
| rpoC | 762830 | c.-540C>T | upstream_gene_variant | 1.0 |
| rpoC | 762857 | c.-513C>G | upstream_gene_variant | 1.0 |
| rpoC | 762860 | c.-510G>T | upstream_gene_variant | 1.0 |
| rpoC | 762899 | c.-471G>C | upstream_gene_variant | 1.0 |
| rpoC | 762929 | c.-441G>C | upstream_gene_variant | 1.0 |
| rpoC | 762995 | c.-375G>C | upstream_gene_variant | 1.0 |
| rpoC | 763028 | c.-342T>C | upstream_gene_variant | 1.0 |
| rpoC | 763031 | c.-339T>G | upstream_gene_variant | 1.0 |
| rpoC | 763034 | c.-336C>G | upstream_gene_variant | 1.0 |
| rpoC | 763040 | c.-330C>G | upstream_gene_variant | 1.0 |
| rpoC | 763050 | c.-320C>T | upstream_gene_variant | 1.0 |
| rpoC | 763070 | c.-300T>C | upstream_gene_variant | 1.0 |
| rpoC | 763076 | c.-294C>T | upstream_gene_variant | 1.0 |
| rpoC | 763085 | c.-285C>G | upstream_gene_variant | 1.0 |
| rpoC | 763094 | c.-276G>C | upstream_gene_variant | 1.0 |
| rpoC | 763115 | c.-255T>C | upstream_gene_variant | 1.0 |
| rpoC | 763124 | c.-246C>T | upstream_gene_variant | 1.0 |
| rpoC | 763127 | c.-243G>C | upstream_gene_variant | 1.0 |
| rpoC | 763169 | c.-201A>G | upstream_gene_variant | 1.0 |
| rpoC | 763193 | c.-177C>G | upstream_gene_variant | 1.0 |
| rpoC | 763202 | c.-168A>G | upstream_gene_variant | 1.0 |
| rpoC | 763206 | c.-164_-162delAGTinsTCC | upstream_gene_variant | 1.0 |
| rpoC | 763214 | c.-156T>C | upstream_gene_variant | 1.0 |
| rpoC | 763226 | c.-144A>G | upstream_gene_variant | 1.0 |
| rpoC | 763238 | c.-132T>C | upstream_gene_variant | 1.0 |
| rpoC | 763375 | c.6C>A | synonymous_variant | 1.0 |
| rpoC | 763408 | c.39T>C | synonymous_variant | 1.0 |
| rpoC | 763411 | c.42T>G | synonymous_variant | 1.0 |
| rpoC | 763414 | c.45T>C | synonymous_variant | 1.0 |
| rpoC | 763430 | c.61A>C | synonymous_variant | 1.0 |
| rpoC | 763435 | c.66A>G | synonymous_variant | 1.0 |
| rpoC | 763444 | c.75T>C | synonymous_variant | 1.0 |
| rpoC | 763456 | c.87A>G | synonymous_variant | 1.0 |
| rpoC | 763468 | c.99G>C | synonymous_variant | 1.0 |
| rpoC | 763486 | c.117T>C | synonymous_variant | 1.0 |
| rpoC | 763505 | c.136C>T | synonymous_variant | 1.0 |
| rpoC | 763561 | c.192G>A | synonymous_variant | 1.0 |
| rpoC | 763600 | c.231C>T | synonymous_variant | 1.0 |
| rpoC | 763606 | c.237C>T | synonymous_variant | 1.0 |
| rpoC | 763618 | c.249C>A | synonymous_variant | 1.0 |
| rpoC | 763633 | c.264T>C | synonymous_variant | 1.0 |
| rpoC | 763636 | c.267T>G | synonymous_variant | 1.0 |
| rpoC | 763639 | c.270G>A | synonymous_variant | 1.0 |
| rpoC | 763658 | c.289_291delCTTinsTTG | synonymous_variant | 1.0 |
| rpoC | 763666 | c.297G>A | synonymous_variant | 1.0 |
| rpoC | 763696 | c.327T>C | synonymous_variant | 1.0 |
| rpoC | 763699 | c.330G>C | synonymous_variant | 1.0 |
| rpoC | 763702 | c.333C>G | synonymous_variant | 1.0 |
| rpoC | 763708 | c.339G>C | synonymous_variant | 1.0 |
| rpoC | 763714 | c.345G>C | synonymous_variant | 1.0 |
| rpoC | 763717 | c.348T>C | synonymous_variant | 1.0 |
| rpoC | 763732 | c.363C>G | synonymous_variant | 1.0 |
| rpoC | 763735 | c.366G>C | synonymous_variant | 1.0 |
| rpoC | 763744 | c.375G>C | synonymous_variant | 1.0 |
| rpoC | 763765 | c.396T>C | synonymous_variant | 1.0 |
| rpoC | 763771 | c.402C>T | synonymous_variant | 1.0 |
| rpoC | 763781 | p.Ser138Ala | missense_variant | 1.0 |
| rpoC | 763801 | c.432C>G | synonymous_variant | 1.0 |
| rpoC | 763807 | c.438T>C | synonymous_variant | 1.0 |
| rpoC | 763813 | c.444C>G | synonymous_variant | 1.0 |
| rpoC | 763819 | c.450G>C | synonymous_variant | 1.0 |
| rpoC | 763835 | p.Ala156Met | missense_variant | 1.0 |
| rpoC | 763855 | c.486C>T | synonymous_variant | 1.0 |
| rpoC | 763858 | c.489A>G | synonymous_variant | 1.0 |
| rpoC | 763867 | c.498C>G | synonymous_variant | 1.0 |
| rpoC | 763872 | p.Gly168Ala | missense_variant | 1.0 |
| rpoC | 763876 | p.Glu169Asp | missense_variant | 1.0 |
| rpoC | 763877 | c.508_510delCTAinsTTG | synonymous_variant | 1.0 |
| rpoC | 763882 | c.513G>A | synonymous_variant | 1.0 |
| rpoC | 763885 | c.516C>G | synonymous_variant | 1.0 |
| rpoC | 763888 | c.519G>C | synonymous_variant | 1.0 |
| rpoC | 763891 | c.522G>C | synonymous_variant | 1.0 |
| rpoC | 763916 | p.Glu183Gln | missense_variant | 1.0 |
| rpoC | 763945 | c.576T>C | synonymous_variant | 1.0 |
| rpoC | 763948 | c.579G>C | synonymous_variant | 1.0 |
| rpoC | 763951 | c.582G>A | synonymous_variant | 1.0 |
| rpoC | 763987 | c.618C>T | synonymous_variant | 1.0 |
| rpoC | 763991 | p.Ile208Leu | missense_variant | 1.0 |
| rpoC | 763996 | c.627T>C | synonymous_variant | 1.0 |
| rpoC | 764005 | c.636G>C | synonymous_variant | 1.0 |
| rpoC | 764011 | c.642T>C | synonymous_variant | 1.0 |
| rpoC | 764024 | c.655T>C | synonymous_variant | 1.0 |
| rpoC | 764040 | p.Ser224Asn | missense_variant | 1.0 |
| rpoC | 764044 | c.675T>C | synonymous_variant | 1.0 |
| rpoC | 764059 | c.690G>C | synonymous_variant | 1.0 |
| rpoC | 764083 | c.714A>G | synonymous_variant | 1.0 |
| rpoC | 764101 | c.732C>G | synonymous_variant | 1.0 |
| rpoC | 764102 | p.Val245Gln | missense_variant | 1.0 |
| rpoC | 764119 | c.750G>A | synonymous_variant | 1.0 |
| rpoC | 764131 | c.762T>C | synonymous_variant | 1.0 |
| rpoC | 764140 | c.771C>T | synonymous_variant | 1.0 |
| rpoC | 764161 | c.792G>C | synonymous_variant | 1.0 |
| rpoC | 764203 | c.834G>C | synonymous_variant | 1.0 |
| rpoC | 764206 | p.Asp279Glu | missense_variant | 1.0 |
| rpoC | 764217 | p.Asn283Ser | missense_variant | 1.0 |
| rpoC | 764254 | c.885G>C | synonymous_variant | 1.0 |
| rpoC | 764266 | c.897T>C | synonymous_variant | 1.0 |
| rpoC | 764269 | c.900G>C | synonymous_variant | 1.0 |
| rpoC | 764272 | c.903G>T | synonymous_variant | 1.0 |
| rpoC | 764278 | c.909A>G | synonymous_variant | 1.0 |
| rpoC | 764284 | c.915G>C | synonymous_variant | 1.0 |
| rpoC | 764317 | c.948C>T | synonymous_variant | 1.0 |
| rpoC | 764344 | c.975C>T | synonymous_variant | 1.0 |
| rpoC | 764347 | c.978G>C | synonymous_variant | 1.0 |
| rpoC | 764365 | c.996C>T | synonymous_variant | 1.0 |
| rpoC | 764380 | c.1011G>C | synonymous_variant | 1.0 |
| rpoC | 764381 | c.1012_1013delTCinsAG | synonymous_variant | 1.0 |
| rpoC | 764387 | c.1018T>C | synonymous_variant | 1.0 |
| rpoC | 764404 | c.1035C>A | synonymous_variant | 1.0 |
| rpoC | 764405 | c.1036A>C | synonymous_variant | 1.0 |
| rpoC | 764419 | c.1050C>G | synonymous_variant | 1.0 |
| rpoC | 764431 | c.1062G>C | synonymous_variant | 1.0 |
| rpoC | 764434 | c.1065A>G | synonymous_variant | 1.0 |
| rpoC | 764435 | c.1066_1068delAGGinsCGA | synonymous_variant | 1.0 |
| rpoC | 764446 | c.1077T>C | synonymous_variant | 1.0 |
| rpoC | 764449 | c.1080G>C | synonymous_variant | 1.0 |
| rpoC | 764452 | c.1083T>C | synonymous_variant | 1.0 |
| rpoC | 764458 | c.1089G>C | synonymous_variant | 1.0 |
| rpoC | 764461 | c.1092A>G | synonymous_variant | 1.0 |
| rpoC | 764497 | c.1128A>G | synonymous_variant | 1.0 |
| rpoC | 764500 | c.1131C>G | synonymous_variant | 1.0 |
| rpoC | 764503 | c.1134G>C | synonymous_variant | 1.0 |
| rpoC | 764521 | c.1152T>C | synonymous_variant | 1.0 |
| rpoC | 764524 | c.1155C>A | synonymous_variant | 1.0 |
| rpoC | 764527 | c.1158C>T | synonymous_variant | 1.0 |
| rpoC | 764533 | c.1164C>T | synonymous_variant | 1.0 |
| rpoC | 764536 | c.1167G>A | synonymous_variant | 1.0 |
| rpoC | 764539 | c.1170C>G | synonymous_variant | 1.0 |
| rpoC | 764575 | c.1206T>G | synonymous_variant | 1.0 |
| rpoC | 764576 | c.1207_1208delTCinsAG | synonymous_variant | 1.0 |
| rpoC | 764587 | c.1218C>G | synonymous_variant | 1.0 |
| rpoC | 764648 | c.1279C>A | synonymous_variant | 1.0 |
| rpoC | 764653 | c.1284G>C | synonymous_variant | 1.0 |
| rpoC | 764656 | c.1287C>T | synonymous_variant | 1.0 |
| rpoC | 764668 | c.1299C>T | synonymous_variant | 1.0 |
| rpoC | 764674 | c.1305G>A | synonymous_variant | 1.0 |
| rpoC | 764681 | c.1312C>T | synonymous_variant | 1.0 |
| rpoC | 764746 | c.1377G>T | synonymous_variant | 1.0 |
| rpoC | 764752 | c.1383G>C | synonymous_variant | 1.0 |
| rpoC | 764755 | c.1386C>T | synonymous_variant | 1.0 |
| rpoC | 764764 | c.1395T>C | synonymous_variant | 1.0 |
| rpoC | 764767 | c.1398G>C | synonymous_variant | 1.0 |
| rpoC | 764791 | c.1422C>G | synonymous_variant | 1.0 |
| rpoC | 764800 | c.1431G>A | synonymous_variant | 1.0 |
| rpoC | 764803 | c.1434C>T | synonymous_variant | 1.0 |
| rpoC | 764809 | c.1440C>T | synonymous_variant | 1.0 |
| rpoC | 764815 | c.1446A>G | synonymous_variant | 1.0 |
| rpoC | 764830 | c.1461C>G | synonymous_variant | 1.0 |
| rpoC | 764833 | c.1464A>G | synonymous_variant | 1.0 |
| rpoC | 764872 | c.1503A>G | synonymous_variant | 1.0 |
| rpoC | 764875 | c.1506C>A | synonymous_variant | 1.0 |
| rpoC | 764888 | c.1519_1521delTTGinsCTC | synonymous_variant | 1.0 |
| rpoC | 764902 | c.1533C>G | synonymous_variant | 1.0 |
| rpoC | 764911 | c.1542A>G | synonymous_variant | 1.0 |
| rpoC | 764918 | p.Val517Ile | missense_variant | 1.0 |
| rpoC | 764923 | c.1554A>G | synonymous_variant | 1.0 |
| rpoC | 764932 | c.1563C>G | synonymous_variant | 1.0 |
| rpoC | 765007 | c.1638T>G | synonymous_variant | 1.0 |
| rpoC | 765100 | c.1731G>C | synonymous_variant | 1.0 |
| rpoC | 765103 | c.1734G>A | synonymous_variant | 1.0 |
| rpoC | 765115 | c.1746G>A | synonymous_variant | 1.0 |
| rpoC | 765122 | c.1753C>T | synonymous_variant | 1.0 |
| rpoC | 765376 | c.2007C>G | synonymous_variant | 1.0 |
| rpoC | 765383 | p.Met672Leu | missense_variant | 1.0 |
| rpoC | 765395 | c.2026C>T | synonymous_variant | 1.0 |
| rpoC | 765405 | p.Leu679Pro | missense_variant | 1.0 |
| rpoC | 765409 | c.2040T>C | synonymous_variant | 1.0 |
| rpoC | 765430 | c.2061G>A | synonymous_variant | 1.0 |
| rpoC | 765445 | c.2076G>T | synonymous_variant | 1.0 |
| rpoC | 765451 | c.2082C>G | synonymous_variant | 1.0 |
| rpoC | 765452 | p.Ala695Ser | missense_variant | 1.0 |
| rpoC | 765478 | c.2109T>C | synonymous_variant | 1.0 |
| rpoC | 765496 | c.2127C>G | synonymous_variant | 1.0 |
| rpoC | 765499 | c.2130C>G | synonymous_variant | 1.0 |
| rpoC | 765526 | c.2157C>G | synonymous_variant | 1.0 |
| rpoC | 765541 | c.2172C>A | synonymous_variant | 1.0 |
| rpoC | 765547 | c.2178C>A | synonymous_variant | 1.0 |
| rpoC | 765553 | c.2184C>T | synonymous_variant | 1.0 |
| rpoC | 765556 | c.2187G>C | synonymous_variant | 1.0 |
| rpoC | 765562 | c.2193G>C | synonymous_variant | 1.0 |
| rpoC | 765583 | c.2214G>T | synonymous_variant | 1.0 |
| rpoC | 765586 | c.2217G>A | synonymous_variant | 1.0 |
| rpoC | 765589 | c.2220G>C | synonymous_variant | 1.0 |
| rpoC | 765610 | c.2241C>T | synonymous_variant | 1.0 |
| rpoC | 765612 | p.His748Arg | missense_variant | 1.0 |
| rpoC | 765622 | p.Glu751Asp | missense_variant | 0.95 |
| rpoC | 765628 | c.2259G>C | synonymous_variant | 1.0 |
| rpoC | 765676 | c.2307G>A | synonymous_variant | 1.0 |
| rpoC | 765688 | c.2319G>C | synonymous_variant | 1.0 |
| rpoC | 765689 | c.2320C>T | synonymous_variant | 1.0 |
| rpoC | 765694 | c.2325G>C | synonymous_variant | 1.0 |
| rpoC | 765700 | c.2331T>C | synonymous_variant | 1.0 |
| rpoC | 765724 | c.2355C>G | synonymous_variant | 1.0 |
| rpoC | 765727 | c.2358T>C | synonymous_variant | 1.0 |
| rpoC | 765734 | c.2365T>C | synonymous_variant | 1.0 |
| rpoC | 765748 | c.2379C>T | synonymous_variant | 1.0 |
| rpoC | 765752 | p.Asp795Ser | missense_variant | 1.0 |
| rpoC | 765757 | c.2388C>T | synonymous_variant | 1.0 |
| rpoC | 765784 | c.2415C>G | synonymous_variant | 1.0 |
| rpoC | 765787 | c.2418C>T | synonymous_variant | 1.0 |
| rpoC | 765790 | c.2421C>T | synonymous_variant | 1.0 |
| rpoC | 765793 | c.2424C>G | synonymous_variant | 1.0 |
| rpoC | 765796 | c.2427C>T | synonymous_variant | 1.0 |
| rpoC | 765811 | c.2442T>C | synonymous_variant | 1.0 |
| rpoC | 765814 | c.2445A>G | synonymous_variant | 1.0 |
| rpoC | 765826 | c.2457T>A | synonymous_variant | 1.0 |
| rpoC | 765835 | c.2466C>T | synonymous_variant | 1.0 |
| rpoC | 765850 | c.2481G>C | synonymous_variant | 1.0 |
| rpoC | 765883 | c.2514C>G | synonymous_variant | 1.0 |
| rpoC | 765886 | c.2517C>G | synonymous_variant | 1.0 |
| rpoC | 765892 | c.2523T>C | synonymous_variant | 1.0 |
| rpoC | 765910 | c.2541G>C | synonymous_variant | 1.0 |
| rpoC | 765934 | c.2565C>T | synonymous_variant | 1.0 |
| rpoC | 765952 | c.2583G>C | synonymous_variant | 1.0 |
| rpoC | 765967 | c.2598C>T | synonymous_variant | 1.0 |
| rpoC | 765979 | c.2610C>G | synonymous_variant | 1.0 |
| rpoC | 765994 | c.2625A>T | synonymous_variant | 1.0 |
| rpoC | 765997 | c.2628T>C | synonymous_variant | 1.0 |
| rpoC | 766021 | c.2652G>C | synonymous_variant | 1.0 |
| rpoC | 766270 | c.2901G>C | synonymous_variant | 1.0 |
| rpoC | 766274 | p.Ala969Thr | missense_variant | 1.0 |
| rpoC | 766280 | p.Ser971Gly | missense_variant | 1.0 |
| rpoC | 766300 | c.2931C>G | synonymous_variant | 1.0 |
| rpoC | 766303 | c.2934C>T | synonymous_variant | 1.0 |
| rpoC | 766306 | c.2937C>T | synonymous_variant | 1.0 |
| rpoC | 766312 | c.2943T>C | synonymous_variant | 1.0 |
| rpoC | 766315 | c.2946C>G | synonymous_variant | 1.0 |
| rpoC | 766324 | c.2955C>T | synonymous_variant | 1.0 |
| rpoC | 766351 | c.2982C>G | synonymous_variant | 1.0 |
| rpoC | 766360 | c.2991C>T | synonymous_variant | 1.0 |
| rpoC | 766381 | c.3012C>T | synonymous_variant | 1.0 |
| rpoC | 766384 | c.3015A>G | synonymous_variant | 1.0 |
| rpoC | 766387 | c.3018C>G | synonymous_variant | 1.0 |
| rpoC | 766393 | c.3024C>G | synonymous_variant | 1.0 |
| rpoC | 766397 | c.3028C>T | synonymous_variant | 1.0 |
| rpoC | 766408 | c.3039C>T | synonymous_variant | 1.0 |
| rpoC | 766417 | c.3048C>T | synonymous_variant | 1.0 |
| rpoC | 766426 | c.3057C>T | synonymous_variant | 1.0 |
| rpoC | 766483 | c.3114G>C | synonymous_variant | 1.0 |
| rpoC | 766486 | c.3117A>G | synonymous_variant | 1.0 |
| rpoC | 766492 | c.3123T>C | synonymous_variant | 1.0 |
| rpoC | 766495 | c.3126C>T | synonymous_variant | 1.0 |
| rpoC | 766519 | c.3150C>A | synonymous_variant | 1.0 |
| rpoC | 766528 | c.3159T>C | synonymous_variant | 1.0 |
| rpoC | 766534 | c.3165C>G | synonymous_variant | 1.0 |
| rpoC | 766537 | c.3168G>A | synonymous_variant | 1.0 |
| rpoC | 766543 | c.3174C>T | synonymous_variant | 1.0 |
| rpoC | 766549 | c.3180G>T | synonymous_variant | 1.0 |
| rpoC | 766570 | c.3201T>G | synonymous_variant | 1.0 |
| rpoC | 766573 | c.3204T>C | synonymous_variant | 1.0 |
| rpoC | 766583 | p.Gly1072Ser | missense_variant | 1.0 |
| rpoC | 766591 | c.3222A>G | synonymous_variant | 1.0 |
| rpoC | 766594 | c.3225G>C | synonymous_variant | 1.0 |
| rpoC | 766597 | c.3228C>G | synonymous_variant | 1.0 |
| rpoC | 766607 | p.Ile1080Leu | missense_variant | 1.0 |
| rpoC | 766621 | c.3252G>A | synonymous_variant | 1.0 |
| rpoC | 766645 | c.3276A>G | synonymous_variant | 1.0 |
| rpoC | 766651 | c.3282T>C | synonymous_variant | 1.0 |
| rpoC | 766654 | c.3285C>G | synonymous_variant | 1.0 |
| rpoC | 766657 | c.3288A>G | synonymous_variant | 1.0 |
| rpoC | 766672 | c.3303T>C | synonymous_variant | 1.0 |
| rpoC | 766681 | c.3312C>T | synonymous_variant | 1.0 |
| rpoC | 766684 | c.3315C>G | synonymous_variant | 1.0 |
| rpoC | 766700 | c.3331C>T | synonymous_variant | 1.0 |
| rpoC | 766714 | c.3345G>C | synonymous_variant | 1.0 |
| rpoC | 766726 | c.3357T>C | synonymous_variant | 1.0 |
| rpoC | 766747 | c.3378C>T | synonymous_variant | 1.0 |
| rpoC | 766765 | c.3396A>C | synonymous_variant | 1.0 |
| rpoC | 766774 | c.3405T>C | synonymous_variant | 1.0 |
| rpoC | 766792 | c.3423C>G | synonymous_variant | 1.0 |
| rpoC | 766795 | c.3426C>T | synonymous_variant | 1.0 |
| rpoC | 766801 | c.3432C>T | synonymous_variant | 1.0 |
| rpoC | 766804 | c.3435A>G | synonymous_variant | 1.0 |
| rpoC | 766843 | c.3474T>G | synonymous_variant | 1.0 |
| rpoC | 766864 | c.3495G>C | synonymous_variant | 1.0 |
| rpoC | 766894 | c.3525T>C | synonymous_variant | 1.0 |
| rpoC | 766895 | c.3526T>C | synonymous_variant | 1.0 |
| rpoC | 766900 | c.3531T>C | synonymous_variant | 1.0 |
| rpoC | 766903 | c.3534C>T | synonymous_variant | 1.0 |
| rpoC | 766907 | c.3538C>T | synonymous_variant | 1.0 |
| rpoC | 766918 | c.3549C>T | synonymous_variant | 1.0 |
| rpoC | 766921 | c.3552G>C | synonymous_variant | 1.0 |
| rpoC | 766933 | c.3564A>G | synonymous_variant | 1.0 |
| rpoC | 766945 | c.3576A>G | synonymous_variant | 1.0 |
| rpoC | 766963 | c.3594T>C | synonymous_variant | 1.0 |
| rpoC | 766972 | c.3603G>C | synonymous_variant | 1.0 |
| rpoC | 766975 | c.3606C>T | synonymous_variant | 1.0 |
| rpoC | 766996 | c.3627C>T | synonymous_variant | 1.0 |
| rpoC | 767002 | c.3633G>C | synonymous_variant | 1.0 |
| rpoC | 767033 | c.3664_3666delTCGinsAGT | synonymous_variant | 1.0 |
| rpoC | 767059 | c.3690T>G | synonymous_variant | 1.0 |
| rpoC | 767062 | c.3693C>A | synonymous_variant | 1.0 |
| rpoC | 767098 | c.3729T>C | synonymous_variant | 1.0 |
| rpoC | 767119 | c.3750A>G | synonymous_variant | 1.0 |
| rpoC | 767167 | c.3798C>T | synonymous_variant | 1.0 |
| rpoC | 767180 | p.Ala1271Gln | missense_variant | 1.0 |
| rpoC | 767185 | c.3816G>T | synonymous_variant | 1.0 |
| rpoC | 767191 | c.3822C>G | synonymous_variant | 1.0 |
| rpoC | 767200 | c.3831G>A | synonymous_variant | 1.0 |
| rpoC | 767206 | c.3837C>A | synonymous_variant | 1.0 |
| rpoC | 767209 | c.3840T>G | synonymous_variant | 1.0 |
| rpoC | 767212 | c.3843G>C | synonymous_variant | 1.0 |
| rpoC | 767221 | c.3852C>G | synonymous_variant | 1.0 |
| rpoC | 767233 | c.3864T>C | synonymous_variant | 1.0 |
| rpoC | 767263 | c.3894T>C | synonymous_variant | 1.0 |
| rpoC | 767264 | p.Ala1299Gln | missense_variant | 1.0 |
| rpoC | 767275 | c.3906T>A | synonymous_variant | 1.0 |
| rpoC | 767278 | c.3909T>C | synonymous_variant | 1.0 |
| rpoC | 767281 | c.3912C>G | synonymous_variant | 1.0 |
| rpoC | 767284 | c.3915C>T | synonymous_variant | 1.0 |
| rpoC | 767287 | c.3918G>A | synonymous_variant | 1.0 |
| rpsL | 781571 | c.12C>T | synonymous_variant | 1.0 |
| rpsL | 781586 | c.27C>A | synonymous_variant | 1.0 |
| rpsL | 781608 | p.Ser17Ala | missense_variant | 1.0 |
| rpsL | 781628 | c.69T>C | synonymous_variant | 1.0 |
| rpsL | 781631 | c.72G>C | synonymous_variant | 1.0 |
| rpsL | 781649 | c.90T>C | synonymous_variant | 1.0 |
| rpsL | 781655 | c.96T>C | synonymous_variant | 1.0 |
| rpsL | 781658 | c.99A>G | synonymous_variant | 1.0 |
| rpsL | 781664 | c.105C>T | synonymous_variant | 1.0 |
| rpsL | 781667 | c.108C>G | synonymous_variant | 1.0 |
| rpsL | 781709 | c.150G>C | synonymous_variant | 1.0 |
| rpsL | 781715 | c.156T>C | synonymous_variant | 1.0 |
| rpsL | 781718 | c.159C>G | synonymous_variant | 1.0 |
| rpsL | 781721 | c.162C>G | synonymous_variant | 1.0 |
| rpsL | 781728 | c.169T>C | synonymous_variant | 1.0 |
| rpsL | 781742 | c.183C>T | synonymous_variant | 1.0 |
| rpsL | 781760 | c.201T>C | synonymous_variant | 1.0 |
| rpsL | 781808 | c.249C>T | synonymous_variant | 1.0 |
| rpsL | 781832 | c.273T>C | synonymous_variant | 1.0 |
| rpsL | 781841 | c.282C>G | synonymous_variant | 1.0 |
| rpsL | 781847 | c.288G>A | synonymous_variant | 1.0 |
| rpsL | 781865 | c.306G>C | synonymous_variant | 1.0 |
| rpsL | 781868 | c.309T>C | synonymous_variant | 1.0 |
| rpsL | 781871 | c.312G>C | synonymous_variant | 1.0 |
| rpsL | 781877 | c.318T>A | synonymous_variant | 1.0 |
| rpsL | 781880 | c.321C>G | synonymous_variant | 1.0 |
| rpsL | 781892 | c.333A>G | synonymous_variant | 1.0 |
| rpsL | 781898 | c.339A>T | synonymous_variant | 1.0 |
| rpsL | 781916 | c.357T>C | synonymous_variant | 1.0 |
| rpsL | 781929 | p.Gly124Ser | missense_variant | 1.0 |
| rplC | 800612 | c.-197A>G | upstream_gene_variant | 1.0 |
| rplC | 800618 | c.-191T>C | upstream_gene_variant | 1.0 |
| rplC | 800648 | c.-161A>C | upstream_gene_variant | 1.0 |
| rplC | 800693 | c.-116A>C | upstream_gene_variant | 1.0 |
| rplC | 800714 | c.-95C>T | upstream_gene_variant | 1.0 |
| rplC | 800715 | c.-94A>C | upstream_gene_variant | 1.0 |
| rplC | 800720 | c.-89T>C | upstream_gene_variant | 1.0 |
| rplC | 800723 | c.-86C>G | upstream_gene_variant | 1.0 |
| rplC | 800735 | c.-74C>G | upstream_gene_variant | 1.0 |
| rplC | 800738 | c.-71T>C | upstream_gene_variant | 1.0 |
| rplC | 800744 | c.-65G>C | upstream_gene_variant | 1.0 |
| rplC | 800759 | c.-50C>T | upstream_gene_variant | 1.0 |
| rplC | 800771 | c.-38C>T | upstream_gene_variant | 1.0 |
| rplC | 800783 | c.-26C>T | upstream_gene_variant | 1.0 |
| rplC | 800797 | c.-12T>G | upstream_gene_variant | 1.0 |
| rplC | 800799 | c.-10G>C | upstream_gene_variant | 1.0 |
| rplC | 800800 | c.-9G>T | upstream_gene_variant | 1.0 |
| rplC | 800801 | c.-8A>G | upstream_gene_variant | 1.0 |
| rplC | 800817 | c.9A>C | synonymous_variant | 1.0 |
| rplC | 800844 | c.36T>C | synonymous_variant | 1.0 |
| rplC | 800865 | c.57A>G | synonymous_variant | 1.0 |
| rplC | 800867 | p.Ser20Asn | missense_variant | 1.0 |
| rplC | 800877 | c.69A>C | synonymous_variant | 1.0 |
| rplC | 800907 | c.99C>G | synonymous_variant | 1.0 |
| rplC | 800913 | c.105G>C | synonymous_variant | 1.0 |
| rplC | 800916 | c.108A>T | synonymous_variant | 1.0 |
| rplC | 800922 | c.114C>G | synonymous_variant | 1.0 |
| rplC | 800934 | c.126C>G | synonymous_variant | 1.0 |
| rplC | 800937 | c.129A>G | synonymous_variant | 1.0 |
| rplC | 800946 | c.138T>G | synonymous_variant | 1.0 |
| rplC | 800949 | c.141T>C | synonymous_variant | 1.0 |
| rplC | 800955 | c.147C>G | synonymous_variant | 1.0 |
| rplC | 800958 | c.150G>A | synonymous_variant | 1.0 |
| rplC | 800970 | c.162T>C | synonymous_variant | 1.0 |
| rplC | 800976 | c.168G>A | synonymous_variant | 1.0 |
| rplC | 800982 | c.174C>T | synonymous_variant | 1.0 |
| rplC | 801147 | c.339T>C | synonymous_variant | 1.0 |
| rplC | 801153 | c.345G>C | synonymous_variant | 1.0 |
| rplC | 801174 | c.366T>C | synonymous_variant | 1.0 |
| rplC | 801177 | c.369C>T | synonymous_variant | 0.4 |
| rplC | 801201 | c.393C>T | synonymous_variant | 1.0 |
| rplC | 801210 | c.402T>C | synonymous_variant | 1.0 |
| rplC | 801216 | c.408C>A | synonymous_variant | 1.0 |
| rplC | 801219 | c.411C>T | synonymous_variant | 1.0 |
| rplC | 801220 | p.Ser138Ala | missense_variant | 1.0 |
| rplC | 801246 | c.438C>G | synonymous_variant | 1.0 |
| rplC | 801252 | c.444G>C | synonymous_variant | 1.0 |
| rplC | 801267 | c.459A>T | synonymous_variant | 1.0 |
| rplC | 801276 | c.468G>C | synonymous_variant | 1.0 |
| rplC | 801297 | c.489C>T | synonymous_variant | 1.0 |
| rplC | 801312 | c.504G>C | synonymous_variant | 1.0 |
| rplC | 801339 | c.531T>G | synonymous_variant | 1.0 |
| rplC | 801341 | p.Leu178Gln | missense_variant | 1.0 |
| rplC | 801348 | c.540T>G | synonymous_variant | 1.0 |
| rplC | 801357 | c.549T>C | synonymous_variant | 1.0 |
| rplC | 801372 | c.564G>A | synonymous_variant | 1.0 |
| rplC | 801396 | c.588T>C | synonymous_variant | 1.0 |
| rplC | 801405 | c.597T>C | synonymous_variant | 1.0 |
| rplC | 801417 | c.609T>C | synonymous_variant | 1.0 |
| rplC | 801423 | c.615G>C | synonymous_variant | 1.0 |
| rplC | 801426 | c.618C>G | synonymous_variant | 1.0 |
| rplC | 801438 | c.630T>C | synonymous_variant | 1.0 |
| rplC | 801447 | c.639A>G | synonymous_variant | 1.0 |
| rplC | 801456 | c.648G>A | synonymous_variant | 1.0 |
| rplC | 801461 | c.653G>A | splice_region_variant&stop_retained_variant | 1.0 |
| fbiC | 1303737 | c.807G>A | synonymous_variant | 1.0 |
| fbiC | 1303749 | c.819G>C | synonymous_variant | 1.0 |
| fbiC | 1303752 | c.822A>G | synonymous_variant | 1.0 |
| fbiC | 1303768 | p.Ser280Ala | missense_variant | 1.0 |
| fbiC | 1303785 | c.855G>C | synonymous_variant | 1.0 |
| fbiC | 1303789 | p.Ile287Val | missense_variant | 1.0 |
| fbiC | 1303794 | c.864A>G | synonymous_variant | 1.0 |
| fbiC | 1303818 | c.888C>G | synonymous_variant | 1.0 |
| fbiC | 1303825 | p.Glu299Lys | missense_variant | 1.0 |
| fbiC | 1304499 | c.1569T>A | synonymous_variant | 1.0 |
| fbiC | 1304502 | c.1572G>A | synonymous_variant | 1.0 |
| fbiC | 1304511 | c.1581C>T | synonymous_variant | 1.0 |
| fbiC | 1304520 | c.1590A>G | synonymous_variant | 1.0 |
| fbiC | 1304521 | p.Leu531Val | missense_variant | 1.0 |
| fbiC | 1304526 | c.1596T>G | synonymous_variant | 1.0 |
| fbiC | 1304546 | p.Val539Ala | missense_variant | 1.0 |
| fbiC | 1304556 | c.1626C>T | synonymous_variant | 1.0 |
| fbiC | 1304559 | p.Glu543Asp | missense_variant | 1.0 |
| fbiC | 1304565 | c.1635C>G | synonymous_variant | 1.0 |
| fbiC | 1304580 | c.1650T>C | synonymous_variant | 1.0 |
| fbiC | 1304598 | c.1668C>T | synonymous_variant | 1.0 |
| fbiC | 1304613 | c.1683T>C | synonymous_variant | 1.0 |
| fbiC | 1304625 | c.1695C>T | synonymous_variant | 1.0 |
| fbiC | 1304628 | c.1698G>C | synonymous_variant | 1.0 |
| fbiC | 1304649 | c.1719C>T | synonymous_variant | 1.0 |
| fbiC | 1304658 | c.1728C>G | synonymous_variant | 1.0 |
| fbiC | 1304661 | c.1731C>T | synonymous_variant | 1.0 |
| fbiC | 1304675 | p.Gly582Asp | missense_variant | 1.0 |
| fbiC | 1304679 | c.1749G>A | synonymous_variant | 1.0 |
| fbiC | 1304691 | c.1761G>C | synonymous_variant | 1.0 |
| fbiC | 1304694 | c.1764A>C | synonymous_variant | 1.0 |
| fbiC | 1304703 | c.1773C>T | synonymous_variant | 1.0 |
| fbiC | 1304715 | c.1785G>T | synonymous_variant | 1.0 |
| fbiC | 1304724 | c.1794A>G | synonymous_variant | 1.0 |
| fbiC | 1304727 | c.1797A>G | synonymous_variant | 1.0 |
| fbiC | 1304742 | c.1812T>C | synonymous_variant | 1.0 |
| fbiC | 1304751 | c.1821C>G | synonymous_variant | 1.0 |
| fbiC | 1304757 | c.1827A>G | synonymous_variant | 1.0 |
| fbiC | 1304784 | c.1854T>G | synonymous_variant | 1.0 |
| fbiC | 1304787 | c.1857T>C | synonymous_variant | 1.0 |
| fbiC | 1304790 | c.1860C>A | synonymous_variant | 1.0 |
| fbiC | 1304799 | c.1869G>C | synonymous_variant | 1.0 |
| fbiC | 1304808 | c.1878C>G | synonymous_variant | 1.0 |
| fbiC | 1304809 | p.Ser627Glu | missense_variant | 1.0 |
| fbiC | 1304832 | c.1902C>T | synonymous_variant | 1.0 |
| fbiC | 1304856 | c.1926C>G | synonymous_variant | 1.0 |
| fbiC | 1304893 | p.Gly655Ser | missense_variant | 1.0 |
| fbiC | 1304901 | c.1971C>T | synonymous_variant | 1.0 |
| fbiC | 1304915 | p.Asp662Gly | missense_variant | 1.0 |
| fbiC | 1304922 | c.1992C>T | synonymous_variant | 1.0 |
| fbiC | 1304925 | c.1995G>C | synonymous_variant | 1.0 |
| fbiC | 1304928 | c.1998T>C | synonymous_variant | 1.0 |
| fbiC | 1304934 | c.2004C>G | synonymous_variant | 1.0 |
| fbiC | 1304937 | c.2007G>C | synonymous_variant | 1.0 |
| fbiC | 1304940 | c.2010A>G | synonymous_variant | 1.0 |
| fbiC | 1304943 | c.2013C>T | synonymous_variant | 1.0 |
| fbiC | 1304946 | c.2016G>C | synonymous_variant | 1.0 |
| fbiC | 1304958 | c.2028T>G | synonymous_variant | 1.0 |
| fbiC | 1304983 | c.2053C>T | synonymous_variant | 1.0 |
| fbiC | 1304994 | c.2064A>G | synonymous_variant | 1.0 |
| fbiC | 1304995 | c.2065T>C | synonymous_variant | 1.0 |
| fbiC | 1305001 | p.Ile691Val | missense_variant | 1.0 |
| fbiC | 1305006 | c.2076A>G | synonymous_variant | 1.0 |
| fbiC | 1305015 | c.2085G>C | synonymous_variant | 1.0 |
| fbiC | 1305066 | c.2136T>C | synonymous_variant | 1.0 |
| fbiC | 1305069 | c.2139G>C | synonymous_variant | 1.0 |
| fbiC | 1305074 | p.Ser715Thr | missense_variant | 1.0 |
| fbiC | 1305078 | c.2148A>C | synonymous_variant | 1.0 |
| fbiC | 1305088 | p.Val720Ile | missense_variant | 1.0 |
| fbiC | 1305096 | c.2166T>C | synonymous_variant | 1.0 |
| fbiC | 1305099 | c.2169T>C | synonymous_variant | 1.0 |
| fbiC | 1305111 | c.2181C>T | synonymous_variant | 1.0 |
| fbiC | 1305117 | c.2187T>C | synonymous_variant | 1.0 |
| fbiC | 1305120 | c.2190G>A | synonymous_variant | 1.0 |
| fbiC | 1305126 | c.2196T>C | synonymous_variant | 1.0 |
| fbiC | 1305150 | c.2220C>G | synonymous_variant | 1.0 |
| fbiC | 1305154 | c.2224T>C | synonymous_variant | 1.0 |
| fbiC | 1305159 | c.2229G>C | synonymous_variant | 1.0 |
| fbiC | 1305162 | c.2232C>T | synonymous_variant | 1.0 |
| fbiC | 1305165 | c.2235G>C | synonymous_variant | 1.0 |
| fbiC | 1305186 | c.2256C>T | synonymous_variant | 1.0 |
| fbiC | 1305192 | c.2262C>G | synonymous_variant | 1.0 |
| fbiC | 1305195 | c.2265T>G | synonymous_variant | 1.0 |
| fbiC | 1305204 | c.2274C>A | synonymous_variant | 1.0 |
| Rv1258c | 1406225 | c.1116C>T | synonymous_variant | 1.0 |
| Rv1258c | 1406234 | c.1107A>G | synonymous_variant | 1.0 |
| Rv1258c | 1406237 | c.1104T>C | synonymous_variant | 1.0 |
| Rv1258c | 1406248 | c.1093T>C | synonymous_variant | 1.0 |
| Rv1258c | 1406249 | c.1090_1092delCTGinsTTA | synonymous_variant | 1.0 |
| Rv1258c | 1406252 | c.1089T>A | synonymous_variant | 1.0 |
| Rv1258c | 1406270 | c.1071C>T | synonymous_variant | 1.0 |
| Rv1258c | 1406291 | c.1050G>A | synonymous_variant | 1.0 |
| Rv1258c | 1406297 | c.1044A>G | synonymous_variant | 1.0 |
| Rv1258c | 1406314 | p.His343Tyr | missense_variant | 1.0 |
| Rv1258c | 1406315 | p.Gln342His | missense_variant | 1.0 |
| Rv1258c | 1406318 | p.Ala341Pro | missense_variant | 1.0 |
| Rv1258c | 1406327 | c.1014G>C | synonymous_variant | 1.0 |
| Rv1258c | 1406330 | c.1011G>A | synonymous_variant | 1.0 |
| Rv1258c | 1406333 | p.Ile336Met | missense_variant | 1.0 |
| Rv1258c | 1406345 | c.996T>C | synonymous_variant | 1.0 |
| Rv1258c | 1406351 | c.990G>C | synonymous_variant | 1.0 |
| Rv1258c | 1406360 | c.981C>G | synonymous_variant | 1.0 |
| Rv1258c | 1406363 | c.978A>G | synonymous_variant | 1.0 |
| Rv1258c | 1406369 | c.972G>C | synonymous_variant | 1.0 |
| atpE | 1461014 | c.-31G>C | upstream_gene_variant | 1.0 |
| atpE | 1461017 | c.-28T>A | upstream_gene_variant | 1.0 |
| atpE | 1461025 | c.-20C>T | upstream_gene_variant | 1.0 |
| atpE | 1461101 | c.57T>C | synonymous_variant | 1.0 |
| atpE | 1461107 | c.63C>G | synonymous_variant | 1.0 |
| atpE | 1461131 | c.87T>C | synonymous_variant | 1.0 |
| atpE | 1461161 | c.117C>T | synonymous_variant | 1.0 |
| atpE | 1461167 | c.123G>T | synonymous_variant | 1.0 |
| atpE | 1461170 | c.126A>G | synonymous_variant | 1.0 |
| atpE | 1461185 | c.141G>A | synonymous_variant | 1.0 |
| atpE | 1461197 | c.153A>C | synonymous_variant | 1.0 |
| atpE | 1461219 | c.175T>C | synonymous_variant | 1.0 |
| atpE | 1461224 | c.180T>C | synonymous_variant | 1.0 |
| atpE | 1461230 | c.186G>T | synonymous_variant | 1.0 |
| atpE | 1461233 | c.189A>C | synonymous_variant | 1.0 |
| atpE | 1461254 | c.210T>C | synonymous_variant | 1.0 |
| rrs | 1471935 | n.90T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471969 | n.124T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471984 | n.139T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471985 | n.140T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472030 | n.185G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472031 | n.186G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472033 | n.188A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472034 | n.189T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472040 | n.195T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473399 | n.-258delC | upstream_gene_variant | 1.0 |
| rrl | 1473410 | n.-248G>A | upstream_gene_variant | 1.0 |
| rrl | 1473417 | n.-241C>T | upstream_gene_variant | 1.0 |
| rrl | 1473419 | n.-239T>C | upstream_gene_variant | 1.0 |
| rrl | 1473421 | n.-237G>A | upstream_gene_variant | 1.0 |
| rrl | 1473437 | n.-221T>C | upstream_gene_variant | 1.0 |
| rrl | 1473449 | n.-209G>A | upstream_gene_variant | 1.0 |
| rrl | 1473453 | n.-205G>A | upstream_gene_variant | 1.0 |
| rrl | 1473465 | n.-193T>C | upstream_gene_variant | 1.0 |
| rrl | 1473473 | n.-184_-180delAGTTG | upstream_gene_variant | 1.0 |
| rrl | 1473481 | n.-177C>A | upstream_gene_variant | 1.0 |
| rrl | 1473493 | n.-165G>A | upstream_gene_variant | 1.0 |
| rrl | 1473517 | n.-141A>G | upstream_gene_variant | 1.0 |
| rrl | 1473519 | n.-139_-138insC | upstream_gene_variant | 1.0 |
| rrl | 1473525 | n.-133C>G | upstream_gene_variant | 1.0 |
| rrl | 1473541 | n.-117G>A | upstream_gene_variant | 1.0 |
| rrl | 1473542 | n.-116C>T | upstream_gene_variant | 1.0 |
| rrl | 1473571 | n.-87C>T | upstream_gene_variant | 1.0 |
| rrl | 1473592 | n.-66_-65insA | upstream_gene_variant | 1.0 |
| rrl | 1473600 | n.-58A>G | upstream_gene_variant | 1.0 |
| rrl | 1473603 | n.-55C>T | upstream_gene_variant | 1.0 |
| rrl | 1473607 | n.-50_-49delGG | upstream_gene_variant | 1.0 |
| rrl | 1473613 | n.-45G>C | upstream_gene_variant | 1.0 |
| rrl | 1473614 | n.-44C>G | upstream_gene_variant | 1.0 |
| rrl | 1473618 | n.-40G>A | upstream_gene_variant | 1.0 |
| rrl | 1473626 | n.-32_-31insT | upstream_gene_variant | 1.0 |
| rrl | 1473635 | n.-23_-22insTTT | upstream_gene_variant | 1.0 |
| rrl | 1473648 | n.-9_-7delTTG | upstream_gene_variant | 1.0 |
| rrl | 1473731 | n.74T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473887 | n.230T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473888 | n.231T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473924 | n.267_268insT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473986 | n.329T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474009 | n.352A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474034 | n.377G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474083 | n.426C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474201 | n.544T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474285 | n.630_631delTC | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474376 | n.719T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474419 | n.762A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474430 | n.773C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474437 | n.781_782delAA | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474717 | n.1060A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474794 | n.1137C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474950 | n.1293G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474952 | n.1296_1300delCATCC | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474961 | n.1304T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474962 | n.1305T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474963 | n.1306G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474964 | n.1307T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474967 | n.1311_1315delGGGTG | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475005 | n.1348C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475006 | n.1349A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475028 | n.1371G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475266 | n.1609T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475273 | n.1616T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475289 | n.1632G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475290 | n.1633A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475291 | n.1634A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475333 | n.1676T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475369 | n.1712G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475403 | n.1746T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475638 | n.1981C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476035 | n.2378G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476089 | n.2432T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476095 | n.2438C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476117 | n.2460G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476529 | n.2872A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476580 | n.2923G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476679 | n.3022T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476726 | n.3069A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476732 | n.3075T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476755 | n.3098G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476759 | n.3102T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476770 | n.3113T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476771 | n.3114G>A | non_coding_transcript_exon_variant | 1.0 |
| fabG1 | 1673465 | p.Ala9Gly | missense_variant | 1.0 |
| inhA | 1673475 | c.-727A>C | upstream_gene_variant | 1.0 |
| inhA | 1673493 | c.-709C>T | upstream_gene_variant | 1.0 |
| inhA | 1673499 | c.-703T>C | upstream_gene_variant | 1.0 |
| inhA | 1673505 | c.-697A>T | upstream_gene_variant | 1.0 |
| inhA | 1673517 | c.-685G>A | upstream_gene_variant | 1.0 |
| inhA | 1673535 | c.-667A>G | upstream_gene_variant | 1.0 |
| inhA | 1673547 | c.-655T>C | upstream_gene_variant | 1.0 |
| inhA | 1673568 | c.-634C>G | upstream_gene_variant | 1.0 |
| inhA | 1673574 | c.-628C>G | upstream_gene_variant | 1.0 |
| inhA | 1673589 | c.-613A>C | upstream_gene_variant | 1.0 |
| inhA | 1673595 | c.-607A>C | upstream_gene_variant | 1.0 |
| fabG1 | 1673596 | p.Lys53Glu | missense_variant | 1.0 |
| inhA | 1673607 | c.-595T>C | upstream_gene_variant | 1.0 |
| fabG1 | 1673609 | p.Gly57Ala | missense_variant | 1.0 |
| inhA | 1673616 | c.-586A>G | upstream_gene_variant | 1.0 |
| inhA | 1673619 | c.-583T>C | upstream_gene_variant | 1.0 |
| fabG1 | 1673657 | p.Thr73Lys | missense_variant | 1.0 |
| inhA | 1673660 | c.-542C>A | upstream_gene_variant | 1.0 |
| inhA | 1673664 | c.-538A>C | upstream_gene_variant | 1.0 |
| inhA | 1673667 | c.-535A>G | upstream_gene_variant | 1.0 |
| inhA | 1673679 | c.-523T>G | upstream_gene_variant | 1.0 |
| inhA | 1673682 | c.-520G>C | upstream_gene_variant | 1.0 |
| inhA | 1673685 | c.-517C>T | upstream_gene_variant | 1.0 |
| fabG1 | 1673710 | p.Leu91Val | missense_variant | 1.0 |
| inhA | 1673715 | c.-487C>T | upstream_gene_variant | 1.0 |
| inhA | 1673724 | c.-478A>G | upstream_gene_variant | 1.0 |
| inhA | 1673730 | c.-472C>G | upstream_gene_variant | 1.0 |
| fabG1 | 1673733 | p.Met98Ile | missense_variant | 1.0 |
| inhA | 1673736 | c.-466G>A | upstream_gene_variant | 1.0 |
| inhA | 1673745 | c.-457G>A | upstream_gene_variant | 1.0 |
| inhA | 1673748 | c.-454A>G | upstream_gene_variant | 1.0 |
| fabG1 | 1673749 | p.Lys104Arg | missense_variant | 1.0 |
| fabG1 | 1673767 | p.Asn110Asp | missense_variant | 1.0 |
| inhA | 1673784 | c.-418G>A | upstream_gene_variant | 1.0 |
| fabG1 | 1673797 | p.Ala120Thr | missense_variant | 1.0 |
| inhA | 1673802 | c.-400A>G | upstream_gene_variant | 1.0 |
| fabG1 | 1673809 | p.Ser124Ala | missense_variant | 1.0 |
| inhA | 1673871 | c.-331C>T | upstream_gene_variant | 1.0 |
| inhA | 1673946 | c.-256C>A | upstream_gene_variant | 1.0 |
| inhA | 1673955 | c.-247G>C | upstream_gene_variant | 1.0 |
| fabG1 | 1673960 | p.Ala174Val | missense_variant | 1.0 |
| inhA | 1673970 | c.-232C>G | upstream_gene_variant | 1.0 |
| inhA | 1673976 | c.-226T>C | upstream_gene_variant | 1.0 |
| inhA | 1673982 | c.-220G>C | upstream_gene_variant | 1.0 |
| inhA | 1673988 | c.-214G>C | upstream_gene_variant | 1.0 |
| inhA | 1673991 | c.-211C>G | upstream_gene_variant | 1.0 |
| inhA | 1674015 | c.-187C>A | upstream_gene_variant | 1.0 |
| inhA | 1674018 | c.-184G>C | upstream_gene_variant | 1.0 |
| inhA | 1674024 | c.-178T>C | upstream_gene_variant | 1.0 |
| inhA | 1674542 | p.Ala114Glu | missense_variant | 1.0 |
| inhA | 1674546 | c.345T>C | synonymous_variant | 1.0 |
| inhA | 1674561 | c.360C>T | synonymous_variant | 1.0 |
| inhA | 1674570 | c.369G>C | synonymous_variant | 1.0 |
| inhA | 1674573 | c.372G>C | synonymous_variant | 1.0 |
| inhA | 1674576 | c.375T>C | synonymous_variant | 1.0 |
| inhA | 1674579 | c.378G>C | synonymous_variant | 1.0 |
| inhA | 1674582 | c.381T>C | synonymous_variant | 1.0 |
| inhA | 1674585 | c.384T>A | synonymous_variant | 1.0 |
| inhA | 1674588 | c.387G>C | synonymous_variant | 1.0 |
| inhA | 1674594 | c.393C>A | synonymous_variant | 1.0 |
| inhA | 1674601 | c.400C>T | synonymous_variant | 1.0 |
| inhA | 1674609 | c.408G>C | synonymous_variant | 1.0 |
| inhA | 1674618 | c.417C>T | synonymous_variant | 1.0 |
| inhA | 1674620 | p.Pro140Arg | missense_variant | 1.0 |
| inhA | 1674624 | c.423A>T | synonymous_variant | 1.0 |
| inhA | 1674627 | c.426T>C | synonymous_variant | 1.0 |
| inhA | 1674675 | c.474C>T | synonymous_variant | 1.0 |
| inhA | 1674703 | c.502T>C | synonymous_variant | 1.0 |
| inhA | 1674718 | c.517A>C | synonymous_variant | 1.0 |
| inhA | 1674729 | c.528G>C | synonymous_variant | 1.0 |
| inhA | 1674756 | c.555T>C | synonymous_variant | 1.0 |
| inhA | 1674762 | c.561T>C | synonymous_variant | 1.0 |
| inhA | 1674774 | c.573A>C | synonymous_variant | 1.0 |
| inhA | 1674777 | c.576C>G | synonymous_variant | 1.0 |
| inhA | 1674780 | c.579T>G | synonymous_variant | 1.0 |
| inhA | 1674799 | p.Ser200Ala | missense_variant | 1.0 |
| inhA | 1674804 | c.603G>A | synonymous_variant | 1.0 |
| inhA | 1674822 | c.621C>G | synonymous_variant | 1.0 |
| inhA | 1674852 | c.651G>A | synonymous_variant | 1.0 |
| inhA | 1674858 | c.657G>A | synonymous_variant | 1.0 |
| inhA | 1674870 | c.669T>C | synonymous_variant | 1.0 |
| inhA | 1674879 | c.678T>G | synonymous_variant | 1.0 |
| inhA | 1674882 | c.681G>C | synonymous_variant | 1.0 |
| inhA | 1674885 | c.684C>T | synonymous_variant | 1.0 |
| inhA | 1674903 | c.702T>C | synonymous_variant | 1.0 |
| inhA | 1674904 | p.Ala235Pro | missense_variant | 1.0 |
| inhA | 1674912 | c.711G>C | synonymous_variant | 1.0 |
| inhA | 1674924 | c.723G>C | synonymous_variant | 1.0 |
| inhA | 1674927 | c.726G>C | synonymous_variant | 1.0 |
| inhA | 1674942 | c.741T>G | synonymous_variant | 1.0 |
| inhA | 1674945 | p.Asp248Glu | missense_variant | 1.0 |
| inhA | 1674957 | c.756G>C | synonymous_variant | 1.0 |
| inhA | 1674966 | c.765T>G | synonymous_variant | 1.0 |
| inhA | 1674977 | p.Tyr259Phe | missense_variant | 1.0 |
| inhA | 1674993 | c.792G>C | synonymous_variant | 1.0 |
| inhA | 1674999 | c.798C>T | synonymous_variant | 1.0 |
| inhA | 1675002 | c.801A>G | synonymous_variant | 1.0 |
| rpsA | 1833554 | p.Thr5Ala | missense_variant | 1.0 |
| rpsA | 1833589 | c.48A>T | synonymous_variant | 1.0 |
| rpsA | 1833593 | p.Ser18Thr | missense_variant | 1.0 |
| rpsA | 1833604 | c.63C>T | synonymous_variant | 1.0 |
| rpsA | 1833610 | c.69C>A | synonymous_variant | 1.0 |
| rpsA | 1833661 | c.120A>G | synonymous_variant | 1.0 |
| rpsA | 1833664 | c.123C>A | synonymous_variant | 1.0 |
| rpsA | 1833718 | c.177C>T | synonymous_variant | 1.0 |
| rpsA | 1833724 | c.183C>G | synonymous_variant | 1.0 |
| rpsA | 1833727 | c.186G>C | synonymous_variant | 1.0 |
| rpsA | 1833742 | c.201A>G | synonymous_variant | 1.0 |
| rpsA | 1833745 | c.204G>C | synonymous_variant | 1.0 |
| rpsA | 1833754 | c.213G>A | synonymous_variant | 1.0 |
| rpsA | 1833802 | c.261A>G | synonymous_variant | 1.0 |
| rpsA | 1833841 | c.300C>G | synonymous_variant | 1.0 |
| rpsA | 1833847 | c.306C>G | synonymous_variant | 1.0 |
| rpsA | 1833850 | c.309C>G | synonymous_variant | 1.0 |
| rpsA | 1833856 | c.315A>G | synonymous_variant | 1.0 |
| rpsA | 1833874 | c.333T>C | synonymous_variant | 1.0 |
| rpsA | 1833928 | c.387G>C | synonymous_variant | 1.0 |
| rpsA | 1833949 | c.408T>C | synonymous_variant | 1.0 |
| rpsA | 1833979 | c.438T>C | synonymous_variant | 1.0 |
| rpsA | 1834000 | c.459G>C | synonymous_variant | 1.0 |
| rpsA | 1834015 | c.474G>C | synonymous_variant | 1.0 |
| rpsA | 1834024 | c.483G>A | synonymous_variant | 1.0 |
| rpsA | 1834030 | c.489C>G | synonymous_variant | 1.0 |
| rpsA | 1834051 | c.510G>A | synonymous_variant | 1.0 |
| rpsA | 1834102 | c.561T>G | synonymous_variant | 1.0 |
| rpsA | 1834105 | c.564C>G | synonymous_variant | 1.0 |
| rpsA | 1834135 | c.594G>C | synonymous_variant | 1.0 |
| rpsA | 1834148 | c.607C>T | synonymous_variant | 1.0 |
| rpsA | 1834153 | c.612T>C | synonymous_variant | 1.0 |
| rpsA | 1834154 | p.Asn205Gln | missense_variant | 1.0 |
| rpsA | 1834157 | c.616T>C | synonymous_variant | 1.0 |
| rpsA | 1834162 | c.621A>G | synonymous_variant | 1.0 |
| rpsA | 1834165 | c.624A>G | synonymous_variant | 1.0 |
| rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
| rpsA | 1834186 | c.645C>G | synonymous_variant | 1.0 |
| rpsA | 1834189 | c.648G>C | synonymous_variant | 1.0 |
| rpsA | 1834195 | c.654G>C | synonymous_variant | 1.0 |
| rpsA | 1834213 | c.672G>C | synonymous_variant | 1.0 |
| rpsA | 1834222 | c.681T>C | synonymous_variant | 1.0 |
| rpsA | 1834225 | c.684C>G | synonymous_variant | 1.0 |
| rpsA | 1834249 | c.708T>C | synonymous_variant | 1.0 |
| rpsA | 1834261 | c.720A>G | synonymous_variant | 1.0 |
| rpsA | 1834264 | c.723G>A | synonymous_variant | 1.0 |
| rpsA | 1834294 | c.753G>A | synonymous_variant | 1.0 |
| rpsA | 1834297 | c.756C>T | synonymous_variant | 1.0 |
| rpsA | 1834303 | c.762T>G | synonymous_variant | 1.0 |
| rpsA | 1834306 | c.765T>C | synonymous_variant | 1.0 |
| rpsA | 1834318 | c.777C>G | synonymous_variant | 1.0 |
| rpsA | 1834336 | c.795C>G | synonymous_variant | 1.0 |
| rpsA | 1834339 | c.798C>T | synonymous_variant | 1.0 |
| rpsA | 1834348 | c.807T>C | synonymous_variant | 1.0 |
| rpsA | 1834366 | c.825A>G | synonymous_variant | 1.0 |
| rpsA | 1834369 | c.828C>G | synonymous_variant | 1.0 |
| rpsA | 1834375 | c.834G>A | synonymous_variant | 1.0 |
| rpsA | 1834396 | c.855G>C | synonymous_variant | 1.0 |
| rpsA | 1834411 | c.870T>C | synonymous_variant | 1.0 |
| rpsA | 1834417 | c.876G>C | synonymous_variant | 1.0 |
| rpsA | 1834423 | c.882G>C | synonymous_variant | 1.0 |
| rpsA | 1834451 | c.910T>C | synonymous_variant | 1.0 |
| rpsA | 1834456 | c.915T>G | synonymous_variant | 1.0 |
| rpsA | 1834468 | c.927A>G | synonymous_variant | 1.0 |
| rpsA | 1834489 | c.948T>C | synonymous_variant | 1.0 |
| rpsA | 1834495 | c.954G>A | synonymous_variant | 1.0 |
| rpsA | 1834528 | c.987T>C | synonymous_variant | 1.0 |
| rpsA | 1834546 | c.1005T>C | synonymous_variant | 1.0 |
| rpsA | 1834609 | c.1068T>C | synonymous_variant | 1.0 |
| rpsA | 1834615 | c.1074C>T | synonymous_variant | 1.0 |
| rpsA | 1834618 | c.1077G>C | synonymous_variant | 1.0 |
| rpsA | 1834624 | c.1083G>A | synonymous_variant | 1.0 |
| rpsA | 1834633 | c.1092A>G | synonymous_variant | 1.0 |
| rpsA | 1834639 | c.1098T>C | synonymous_variant | 1.0 |
| rpsA | 1834690 | c.1149T>C | synonymous_variant | 1.0 |
| rpsA | 1834732 | c.1191T>C | synonymous_variant | 1.0 |
| rpsA | 1834747 | c.1206A>G | synonymous_variant | 1.0 |
| rpsA | 1834751 | p.Leu404Met | missense_variant | 1.0 |
| rpsA | 1834756 | c.1215G>A | synonymous_variant | 1.0 |
| rpsA | 1834759 | c.1218A>T | synonymous_variant | 1.0 |
| rpsA | 1834765 | p.Glu408Asp | missense_variant | 1.0 |
| rpsA | 1834766 | p.Lys409Ala | missense_variant | 1.0 |
| rpsA | 1834774 | c.1233C>T | synonymous_variant | 1.0 |
| rpsA | 1834775 | p.Ala412Asn | missense_variant | 1.0 |
| rpsA | 1834780 | c.1239A>G | synonymous_variant | 1.0 |
| rpsA | 1834789 | c.1248T>C | synonymous_variant | 1.0 |
| rpsA | 1834792 | c.1251G>C | synonymous_variant | 1.0 |
| rpsA | 1834810 | c.1269C>G | synonymous_variant | 1.0 |
| ndh | 2102572 | c.471A>G | synonymous_variant | 1.0 |
| ndh | 2102575 | c.468G>A | synonymous_variant | 1.0 |
| ndh | 2102581 | c.462T>G | synonymous_variant | 1.0 |
| ndh | 2102590 | c.453A>T | synonymous_variant | 1.0 |
| ndh | 2102593 | c.450C>G | synonymous_variant | 1.0 |
| ndh | 2102596 | c.447C>A | synonymous_variant | 1.0 |
| ndh | 2102599 | c.444T>G | synonymous_variant | 1.0 |
| ndh | 2102604 | p.Leu147Val | missense_variant | 1.0 |
| ndh | 2102608 | c.433_435delTTGinsCTC | synonymous_variant | 0.67 |
| ndh | 2102614 | c.429C>T | synonymous_variant | 1.0 |
| ndh | 2102617 | c.426C>T | synonymous_variant | 0.67 |
| ndh | 2102626 | c.417G>A | synonymous_variant | 0.67 |
| ndh | 2102635 | c.408C>G | synonymous_variant | 0.67 |
| ndh | 2102638 | c.405A>G | synonymous_variant | 1.0 |
| ndh | 2102644 | c.399A>G | synonymous_variant | 1.0 |
| ndh | 2102653 | c.390T>C | synonymous_variant | 0.67 |
| ndh | 2102671 | c.372T>C | synonymous_variant | 1.0 |
| kasA | 2517941 | c.-174C>G | upstream_gene_variant | 1.0 |
| kasA | 2517956 | c.-159G>A | upstream_gene_variant | 1.0 |
| kasA | 2517989 | c.-126T>C | upstream_gene_variant | 1.0 |
| kasA | 2518019 | c.-96A>G | upstream_gene_variant | 1.0 |
| kasA | 2518025 | c.-90G>C | upstream_gene_variant | 1.0 |
| kasA | 2518031 | c.-84G>T | upstream_gene_variant | 1.0 |
| kasA | 2518034 | c.-81T>C | upstream_gene_variant | 1.0 |
| kasA | 2518035 | c.-80C>G | upstream_gene_variant | 1.0 |
| kasA | 2518041 | c.-74T>C | upstream_gene_variant | 1.0 |
| kasA | 2518046 | c.-69C>G | upstream_gene_variant | 1.0 |
| kasA | 2518049 | c.-66G>C | upstream_gene_variant | 1.0 |
| kasA | 2518053 | c.-62_-60delATTinsCTC | upstream_gene_variant | 1.0 |
| kasA | 2518073 | c.-42T>G | upstream_gene_variant | 1.0 |
| kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
| kasA | 2518088 | c.-27T>C | upstream_gene_variant | 1.0 |
| kasA | 2518089 | c.-26C>A | upstream_gene_variant | 1.0 |
| kasA | 2518187 | p.Ile25Val | missense_variant | 1.0 |
| kasA | 2518248 | p.Ala45Val | missense_variant | 1.0 |
| kasA | 2518252 | c.138C>T | synonymous_variant | 1.0 |
| kasA | 2518279 | c.165T>C | synonymous_variant | 1.0 |
| kasA | 2518283 | p.Ala57Pro | missense_variant | 1.0 |
| kasA | 2518297 | c.183C>T | synonymous_variant | 1.0 |
| kasA | 2518300 | c.186T>C | synonymous_variant | 1.0 |
| kasA | 2518312 | c.198T>C | synonymous_variant | 1.0 |
| kasA | 2518318 | c.204C>G | synonymous_variant | 1.0 |
| kasA | 2518323 | p.Ser70Asn | missense_variant | 1.0 |
| kasA | 2518334 | c.220_222delCGAinsAGG | synonymous_variant | 1.0 |
| kasA | 2518339 | c.225C>G | synonymous_variant | 1.0 |
| kasA | 2518348 | c.234A>G | synonymous_variant | 1.0 |
| kasA | 2518504 | c.390T>C | synonymous_variant | 1.0 |
| kasA | 2518506 | p.Ala131Glu | missense_variant | 1.0 |
| kasA | 2518513 | c.399C>G | synonymous_variant | 1.0 |
| kasA | 2518519 | c.405G>C | synonymous_variant | 1.0 |
| kasA | 2518534 | c.420G>C | synonymous_variant | 1.0 |
| kasA | 2518537 | c.423C>G | synonymous_variant | 1.0 |
| kasA | 2518561 | c.447T>C | synonymous_variant | 1.0 |
| kasA | 2518567 | c.453G>T | synonymous_variant | 1.0 |
| kasA | 2518573 | c.459G>C | synonymous_variant | 1.0 |
| kasA | 2518574 | p.Ile154Val | missense_variant | 1.0 |
| kasA | 2518588 | c.474T>C | synonymous_variant | 1.0 |
| kasA | 2518591 | c.477G>C | synonymous_variant | 1.0 |
| kasA | 2518618 | c.504G>C | synonymous_variant | 1.0 |
| kasA | 2518633 | c.519G>C | synonymous_variant | 1.0 |
| kasA | 2518642 | c.528A>G | synonymous_variant | 1.0 |
| kasA | 2518672 | c.558G>C | synonymous_variant | 1.0 |
| kasA | 2518681 | c.567C>T | synonymous_variant | 1.0 |
| kasA | 2518684 | c.570C>A | synonymous_variant | 1.0 |
| kasA | 2518711 | c.597A>G | synonymous_variant | 1.0 |
| kasA | 2518714 | c.600A>T | synonymous_variant | 1.0 |
| kasA | 2518735 | c.621C>A | synonymous_variant | 1.0 |
| kasA | 2518744 | c.630C>T | synonymous_variant | 1.0 |
| kasA | 2518747 | c.633C>G | synonymous_variant | 1.0 |
| kasA | 2518756 | c.642G>C | synonymous_variant | 1.0 |
| kasA | 2518783 | c.669T>C | synonymous_variant | 1.0 |
| kasA | 2518789 | c.675G>T | synonymous_variant | 1.0 |
| kasA | 2518795 | c.681C>G | synonymous_variant | 1.0 |
| kasA | 2518798 | c.684G>C | synonymous_variant | 1.0 |
| kasA | 2518816 | c.702C>T | synonymous_variant | 1.0 |
| kasA | 2518822 | c.708C>T | synonymous_variant | 1.0 |
| kasA | 2518825 | c.711T>C | synonymous_variant | 1.0 |
| kasA | 2518855 | c.741C>G | synonymous_variant | 1.0 |
| kasA | 2518856 | p.Ile248Leu | missense_variant | 1.0 |
| kasA | 2518864 | c.750G>C | synonymous_variant | 1.0 |
| kasA | 2518885 | c.771T>C | synonymous_variant | 1.0 |
| kasA | 2518894 | c.780G>A | synonymous_variant | 1.0 |
| kasA | 2518903 | c.789C>T | synonymous_variant | 1.0 |
| kasA | 2518906 | c.792A>G | synonymous_variant | 1.0 |
| kasA | 2518910 | c.796C>T | synonymous_variant | 1.0 |
| kasA | 2518939 | c.825T>C | synonymous_variant | 1.0 |
| kasA | 2518942 | c.828T>C | synonymous_variant | 1.0 |
| kasA | 2518951 | c.837G>A | synonymous_variant | 1.0 |
| kasA | 2518960 | c.846C>G | synonymous_variant | 1.0 |
| kasA | 2518963 | c.849T>C | synonymous_variant | 1.0 |
| kasA | 2518969 | c.855T>G | synonymous_variant | 1.0 |
| kasA | 2518978 | c.864T>C | synonymous_variant | 1.0 |
| kasA | 2518979 | c.865A>C | synonymous_variant | 1.0 |
| kasA | 2518990 | c.876T>G | synonymous_variant | 1.0 |
| kasA | 2518993 | c.879C>G | synonymous_variant | 1.0 |
| kasA | 2519008 | c.894C>G | synonymous_variant | 1.0 |
| kasA | 2519011 | c.897G>C | synonymous_variant | 1.0 |
| kasA | 2519017 | c.903G>C | synonymous_variant | 1.0 |
| kasA | 2519020 | c.906G>C | synonymous_variant | 1.0 |
| kasA | 2519021 | p.Ala303Lys | missense_variant | 1.0 |
| kasA | 2519029 | c.915C>T | synonymous_variant | 1.0 |
| kasA | 2519041 | c.927C>T | synonymous_variant | 1.0 |
| ahpC | 2726243 | c.51T>G | synonymous_variant | 1.0 |
| ahpC | 2726244 | c.52_54delCTCinsTTG | synonymous_variant | 1.0 |
| ahpC | 2726249 | c.57C>T | synonymous_variant | 1.0 |
| ahpC | 2726255 | c.63T>C | synonymous_variant | 1.0 |
| ahpC | 2726258 | c.66C>T | synonymous_variant | 1.0 |
| ahpC | 2726264 | c.72C>G | synonymous_variant | 1.0 |
| ahpC | 2726303 | c.111T>C | synonymous_variant | 1.0 |
| ahpC | 2726304 | p.Ile38Val | missense_variant | 1.0 |
| ahpC | 2726311 | p.Ser40Asn | missense_variant | 1.0 |
| ahpC | 2726315 | p.Asp41Glu | missense_variant | 1.0 |
| ahpC | 2726318 | p.Glu42Asp | missense_variant | 1.0 |
| ahpC | 2726324 | c.132A>G | synonymous_variant | 1.0 |
| ahpC | 2726336 | c.144G>C | synonymous_variant | 1.0 |
| ahpC | 2726348 | c.156T>C | synonymous_variant | 1.0 |
| ahpC | 2726354 | c.162G>C | synonymous_variant | 1.0 |
| ahpC | 2726357 | c.165A>G | synonymous_variant | 1.0 |
| ahpC | 2726366 | c.174G>C | synonymous_variant | 1.0 |
| ahpC | 2726378 | c.186T>G | synonymous_variant | 1.0 |
| ahpC | 2726393 | c.201G>C | synonymous_variant | 1.0 |
| ahpC | 2726397 | p.Ser69Gly | missense_variant | 1.0 |
| ahpC | 2726408 | c.216T>C | synonymous_variant | 1.0 |
| ahpC | 2726430 | p.Ala80Thr | missense_variant | 1.0 |
| ahpC | 2726441 | c.249G>C | synonymous_variant | 1.0 |
| ahpC | 2726444 | c.252G>A | synonymous_variant | 1.0 |
| ahpC | 2726447 | c.255T>C | synonymous_variant | 1.0 |
| ahpC | 2726450 | c.258G>C | synonymous_variant | 1.0 |
| ahpC | 2726453 | c.261T>C | synonymous_variant | 1.0 |
| ahpC | 2726467 | p.Ala92Val | missense_variant | 1.0 |
| ahpC | 2726471 | c.279T>C | synonymous_variant | 1.0 |
| ahpC | 2726483 | c.291T>C | synonymous_variant | 1.0 |
| ahpC | 2726486 | c.294A>C | synonymous_variant | 1.0 |
| ahpC | 2726493 | p.Asn101Glu | missense_variant | 1.0 |
| folC | 2747239 | c.360T>C | synonymous_variant | 1.0 |
| folC | 2747263 | c.336C>A | synonymous_variant | 1.0 |
| folC | 2747275 | c.324T>C | synonymous_variant | 1.0 |
| folC | 2747278 | c.321C>G | synonymous_variant | 1.0 |
| folC | 2747288 | p.Pro104Val | missense_variant | 1.0 |
| folC | 2747290 | c.309A>G | synonymous_variant | 1.0 |
| folC | 2747302 | c.297A>G | synonymous_variant | 1.0 |
| folC | 2747314 | c.285A>C | synonymous_variant | 1.0 |
| folC | 2747323 | c.276C>G | synonymous_variant | 1.0 |
| folC | 2747326 | p.Arg91Gln | missense_variant | 1.0 |
| folC | 2747329 | c.270C>T | synonymous_variant | 1.0 |
| folC | 2747334 | c.265C>T | synonymous_variant | 1.0 |
| folC | 2747341 | c.258C>G | synonymous_variant | 1.0 |
| folC | 2747346 | c.253C>T | synonymous_variant | 1.0 |
| folC | 2747347 | c.252G>A | synonymous_variant | 1.0 |
| folC | 2747359 | c.240C>G | synonymous_variant | 1.0 |
| folC | 2747371 | c.228C>G | synonymous_variant | 1.0 |
| folC | 2747386 | c.213C>G | synonymous_variant | 1.0 |
| folC | 2747389 | c.210G>C | synonymous_variant | 1.0 |
| folC | 2747395 | c.204T>C | synonymous_variant | 1.0 |
| folC | 2747398 | c.201C>T | synonymous_variant | 1.0 |
| folC | 2747404 | c.195G>C | synonymous_variant | 1.0 |
| folC | 2747414 | p.Arg62Leu | missense_variant | 1.0 |
| folC | 2747419 | c.180C>G | synonymous_variant | 1.0 |
| folC | 2747422 | c.177G>A | synonymous_variant | 1.0 |
| folC | 2747425 | c.174C>T | synonymous_variant | 1.0 |
| folC | 2747439 | p.Met54Leu | missense_variant | 1.0 |
| folC | 2747442 | c.157T>C | synonymous_variant | 1.0 |
| folC | 2747454 | c.145C>A | synonymous_variant | 1.0 |
| folC | 2747467 | p.Asp44Glu | missense_variant | 1.0 |
| folC | 2747491 | c.108A>G | synonymous_variant | 1.0 |
| folC | 2747497 | c.102C>G | synonymous_variant | 1.0 |
| folC | 2747500 | c.99A>G | synonymous_variant | 1.0 |
| folC | 2747503 | c.96T>C | synonymous_variant | 1.0 |
| folC | 2747509 | c.90T>C | synonymous_variant | 1.0 |
| pepQ | 2859431 | c.988T>C | synonymous_variant | 1.0 |
| pepQ | 2859438 | c.981T>C | synonymous_variant | 1.0 |
| pepQ | 2859468 | c.951G>T | synonymous_variant | 1.0 |
| pepQ | 2859489 | p.Val310Ala | missense_variant | 1.0 |
| pepQ | 2859510 | c.909T>C | synonymous_variant | 1.0 |
| pepQ | 2859528 | c.891T>C | synonymous_variant | 1.0 |
| pepQ | 2859540 | c.879A>T | synonymous_variant | 1.0 |
| pepQ | 2859546 | c.873T>C | synonymous_variant | 1.0 |
| pepQ | 2859552 | p.His289Asn | missense_variant | 1.0 |
| pepQ | 2859555 | p.Glu288Asp | missense_variant | 1.0 |
| pepQ | 2859567 | c.852C>G | synonymous_variant | 1.0 |
| pepQ | 2859575 | p.Ala282Thr | missense_variant | 1.0 |
| pepQ | 2859581 | c.838C>T | synonymous_variant | 1.0 |
| pepQ | 2860314 | c.105C>T | synonymous_variant | 1.0 |
| pepQ | 2860317 | c.102A>C | synonymous_variant | 1.0 |
| pepQ | 2860329 | c.90G>C | synonymous_variant | 1.0 |
| pepQ | 2860332 | c.87C>T | synonymous_variant | 1.0 |
| pepQ | 2860345 | p.Ser25Thr | missense_variant | 1.0 |
| pepQ | 2860349 | p.Ile24Val | missense_variant | 1.0 |
| pepQ | 2860364 | c.55T>C | synonymous_variant | 1.0 |
| pepQ | 2860365 | c.54G>A | synonymous_variant | 1.0 |
| pepQ | 2860370 | p.Ser17Ala | missense_variant | 1.0 |
| pepQ | 2860375 | p.Ala15Gly | missense_variant | 1.0 |
| pepQ | 2860377 | c.42C>T | synonymous_variant | 1.0 |
| pepQ | 2860382 | p.Gln13Lys | missense_variant | 1.0 |
| pepQ | 2860383 | c.36A>C | synonymous_variant | 1.0 |
| pepQ | 2860389 | c.30G>C | synonymous_variant | 1.0 |
| pepQ | 2860392 | p.Lys9Asn | missense_variant | 1.0 |
| pepQ | 2860397 | p.Asp8His | missense_variant | 1.0 |
| pepQ | 2860423 | c.-5G>C | upstream_gene_variant | 1.0 |
| pepQ | 2860447 | c.-29A>G | upstream_gene_variant | 1.0 |
| pepQ | 2860448 | c.-30C>A | upstream_gene_variant | 1.0 |
| pepQ | 2860499 | c.-81C>G | upstream_gene_variant | 1.0 |
| pepQ | 2860503 | c.-87_-85delGAGinsCAC | upstream_gene_variant | 1.0 |
| pepQ | 2860511 | c.-93C>T | upstream_gene_variant | 1.0 |
| pepQ | 2860514 | c.-96G>A | upstream_gene_variant | 1.0 |
| pepQ | 2860523 | c.-105T>C | upstream_gene_variant | 1.0 |
| pepQ | 2860524 | c.-106A>G | upstream_gene_variant | 1.0 |
| Rv2752c | 3064590 | c.1602C>T | synonymous_variant | 1.0 |
| Rv2752c | 3064596 | c.1596G>C | synonymous_variant | 1.0 |
| Rv2752c | 3064599 | c.1593A>G | synonymous_variant | 1.0 |
| Rv2752c | 3064602 | c.1590T>G | synonymous_variant | 1.0 |
| Rv2752c | 3064612 | p.Ile527Thr | missense_variant | 1.0 |
| Rv2752c | 3064614 | c.1578G>C | synonymous_variant | 1.0 |
| Rv2752c | 3064635 | c.1557G>C | synonymous_variant | 1.0 |
| Rv2752c | 3064640 | c.1552T>C | synonymous_variant | 1.0 |
| Rv2752c | 3064653 | c.1539A>G | synonymous_variant | 1.0 |
| Rv2752c | 3064656 | c.1536G>A | synonymous_variant | 1.0 |
| Rv2752c | 3064659 | c.1533G>C | synonymous_variant | 1.0 |
| Rv2752c | 3064680 | c.1512C>G | synonymous_variant | 1.0 |
| Rv2752c | 3064752 | p.Arg480Lys | missense_variant | 1.0 |
| Rv2752c | 3064761 | c.1431C>G | synonymous_variant | 1.0 |
| Rv2752c | 3065146 | p.Phe349Tyr | missense_variant | 1.0 |
| Rv2752c | 3065163 | c.1029C>A | synonymous_variant | 1.0 |
| Rv2752c | 3065202 | p.Ala330Ser | missense_variant | 1.0 |
| Rv2752c | 3065210 | c.982T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065211 | c.981G>T | synonymous_variant | 1.0 |
| Rv2752c | 3065217 | c.975C>T | synonymous_variant | 1.0 |
| Rv2752c | 3065226 | c.966G>A | synonymous_variant | 1.0 |
| Rv2752c | 3065229 | c.963G>C | synonymous_variant | 1.0 |
| Rv2752c | 3065232 | c.960T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065241 | c.951A>G | synonymous_variant | 1.0 |
| Rv2752c | 3065244 | c.948G>T | synonymous_variant | 1.0 |
| Rv2752c | 3065262 | c.930G>A | synonymous_variant | 1.0 |
| Rv2752c | 3065268 | c.924A>G | synonymous_variant | 1.0 |
| Rv2752c | 3065271 | c.921C>G | synonymous_variant | 1.0 |
| Rv2752c | 3065406 | c.786C>G | synonymous_variant | 1.0 |
| Rv2752c | 3065412 | c.780G>A | synonymous_variant | 1.0 |
| Rv2752c | 3065430 | c.762A>T | synonymous_variant | 1.0 |
| Rv2752c | 3065442 | c.750T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065451 | c.741G>A | synonymous_variant | 1.0 |
| Rv2752c | 3065457 | c.735A>T | synonymous_variant | 1.0 |
| Rv2752c | 3065463 | c.729T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065469 | c.723C>T | synonymous_variant | 1.0 |
| Rv2752c | 3065478 | c.714C>T | synonymous_variant | 1.0 |
| Rv2752c | 3065481 | c.711T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065484 | c.708G>A | synonymous_variant | 1.0 |
| Rv2752c | 3065487 | c.705T>G | synonymous_variant | 1.0 |
| Rv2752c | 3065490 | c.702A>C | synonymous_variant | 1.0 |
| Rv2752c | 3065493 | c.699G>C | synonymous_variant | 1.0 |
| Rv2752c | 3065499 | c.693A>C | synonymous_variant | 1.0 |
| Rv2752c | 3065502 | p.Asp230Glu | missense_variant | 1.0 |
| Rv2752c | 3065508 | c.684T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065517 | c.673_675delCTCinsTTG | synonymous_variant | 1.0 |
| Rv2752c | 3065532 | c.660A>C | synonymous_variant | 1.0 |
| Rv2752c | 3065556 | c.636G>A | synonymous_variant | 1.0 |
| Rv2752c | 3065580 | c.612G>C | synonymous_variant | 1.0 |
| Rv2752c | 3065583 | c.609G>C | synonymous_variant | 1.0 |
| Rv2752c | 3065594 | c.598C>T | synonymous_variant | 1.0 |
| Rv2752c | 3065595 | p.Leu199Phe | missense_variant | 1.0 |
| Rv2752c | 3065612 | p.Thr194Ala | missense_variant | 1.0 |
| Rv2752c | 3065625 | c.567G>C | synonymous_variant | 1.0 |
| Rv2752c | 3065634 | c.558G>C | synonymous_variant | 1.0 |
| Rv2752c | 3065637 | c.555A>G | synonymous_variant | 1.0 |
| Rv2752c | 3065640 | c.552T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065652 | c.540C>A | synonymous_variant | 1.0 |
| Rv2752c | 3065658 | p.Pro178Leu | missense_variant | 1.0 |
| Rv2752c | 3065661 | c.531A>G | synonymous_variant | 1.0 |
| Rv2752c | 3065666 | c.526T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065675 | p.Phe173Leu | missense_variant | 1.0 |
| Rv2752c | 3065699 | p.Ile165Val | missense_variant | 1.0 |
| Rv2752c | 3065703 | c.489A>C | synonymous_variant | 1.0 |
| Rv2752c | 3065925 | c.267G>C | synonymous_variant | 1.0 |
| Rv2752c | 3065947 | p.Gly82Ala | missense_variant | 1.0 |
| Rv2752c | 3065952 | c.240C>G | synonymous_variant | 1.0 |
| Rv2752c | 3066071 | c.121T>C | synonymous_variant | 1.0 |
| Rv2752c | 3066075 | c.117A>G | synonymous_variant | 1.0 |
| Rv2752c | 3066084 | c.108C>T | synonymous_variant | 1.0 |
| Rv2752c | 3066087 | c.105A>G | synonymous_variant | 1.0 |
| Rv2752c | 3066118 | p.Asn25Gly | missense_variant | 1.0 |
| Rv2752c | 3066122 | p.Ile24Val | missense_variant | 1.0 |
| Rv2752c | 3066129 | c.63G>C | synonymous_variant | 1.0 |
| thyX | 3067781 | c.165C>G | synonymous_variant | 1.0 |
| thyX | 3067784 | c.162C>T | synonymous_variant | 1.0 |
| thyX | 3067787 | p.Lys53Arg | missense_variant | 1.0 |
| thyX | 3067793 | c.153T>C | synonymous_variant | 1.0 |
| thyX | 3067814 | c.132T>C | synonymous_variant | 1.0 |
| thyX | 3067817 | c.129C>T | synonymous_variant | 1.0 |
| thyX | 3067820 | c.126C>G | synonymous_variant | 1.0 |
| thyX | 3067832 | c.114C>T | synonymous_variant | 1.0 |
| thyX | 3067838 | c.108C>G | synonymous_variant | 1.0 |
| thyX | 3067847 | p.Pro33Ser | missense_variant | 1.0 |
| thyX | 3067850 | c.96A>C | synonymous_variant | 1.0 |
| thyA | 3073848 | c.624C>T | synonymous_variant | 1.0 |
| thyA | 3073857 | c.615C>T | synonymous_variant | 1.0 |
| thyA | 3073860 | c.612C>T | synonymous_variant | 1.0 |
| thyA | 3073863 | c.609T>C | synonymous_variant | 1.0 |
| thyA | 3073878 | c.594G>A | synonymous_variant | 1.0 |
| thyA | 3073887 | p.Ser195Asp | missense_variant | 1.0 |
| thyA | 3073892 | c.580T>C | synonymous_variant | 1.0 |
| thyA | 3073894 | p.Gly193Asp | missense_variant | 1.0 |
| thyA | 3073898 | p.Ala192Ser | missense_variant | 1.0 |
| thyA | 3073902 | c.570C>A | synonymous_variant | 1.0 |
| thyA | 3073929 | c.543T>C | synonymous_variant | 1.0 |
| thyA | 3073932 | c.540C>T | synonymous_variant | 1.0 |
| thyA | 3073947 | c.525G>C | synonymous_variant | 1.0 |
| thyA | 3073953 | c.519T>C | synonymous_variant | 1.0 |
| thyA | 3073956 | c.516G>C | synonymous_variant | 1.0 |
| thyA | 3073962 | c.510G>C | synonymous_variant | 1.0 |
| thyA | 3073977 | c.495A>G | synonymous_variant | 1.0 |
| thyA | 3073989 | c.483T>C | synonymous_variant | 1.0 |
| thyA | 3073997 | c.475C>T | synonymous_variant | 1.0 |
| thyA | 3074031 | c.441T>C | synonymous_variant | 1.0 |
| thyA | 3074037 | c.435C>G | synonymous_variant | 1.0 |
| thyA | 3074045 | c.427C>T | synonymous_variant | 1.0 |
| thyA | 3074053 | p.Arg140Gln | missense_variant | 1.0 |
| thyA | 3074056 | p.Glu139Pro | missense_variant | 1.0 |
| thyA | 3074061 | p.Glu137Asp | missense_variant | 1.0 |
| thyA | 3074091 | c.381C>G | synonymous_variant | 1.0 |
| thyA | 3074123 | p.Asp117Asn | missense_variant | 1.0 |
| thyA | 3074127 | c.345G>T | synonymous_variant | 1.0 |
| thyA | 3074130 | c.342G>C | synonymous_variant | 1.0 |
| thyA | 3074133 | c.339C>T | synonymous_variant | 1.0 |
| thyA | 3074151 | c.321G>A | synonymous_variant | 1.0 |
| thyA | 3074157 | c.315C>G | synonymous_variant | 1.0 |
| thyA | 3074160 | c.312A>T | synonymous_variant | 1.0 |
| thyA | 3074163 | c.309T>C | synonymous_variant | 1.0 |
| thyA | 3074172 | c.300G>C | synonymous_variant | 1.0 |
| thyA | 3074175 | c.297A>G | synonymous_variant | 1.0 |
| thyA | 3074184 | c.288A>G | synonymous_variant | 1.0 |
| thyA | 3074187 | c.285T>C | synonymous_variant | 1.0 |
| thyA | 3074190 | c.282C>T | synonymous_variant | 1.0 |
| thyA | 3074196 | c.276G>T | synonymous_variant | 1.0 |
| thyA | 3074199 | c.273G>A | synonymous_variant | 1.0 |
| thyA | 3074205 | p.Glu89Asp | missense_variant | 1.0 |
| thyA | 3074208 | c.264C>T | synonymous_variant | 1.0 |
| thyA | 3074214 | p.Asp86Glu | missense_variant | 1.0 |
| thyA | 3074217 | c.255T>C | synonymous_variant | 1.0 |
| thyA | 3074247 | c.225C>T | synonymous_variant | 1.0 |
| thyA | 3074252 | p.Glu74Gln | missense_variant | 1.0 |
| thyA | 3074256 | c.216G>A | synonymous_variant | 1.0 |
| thyA | 3074262 | c.210T>C | synonymous_variant | 1.0 |
| thyA | 3074268 | c.204T>C | synonymous_variant | 1.0 |
| thyA | 3074274 | c.198T>C | synonymous_variant | 1.0 |
| thyA | 3074283 | c.189G>A | synonymous_variant | 1.0 |
| thyA | 3074286 | c.186T>C | synonymous_variant | 1.0 |
| thyA | 3074297 | c.175C>T | synonymous_variant | 1.0 |
| thyA | 3074307 | c.165A>G | synonymous_variant | 1.0 |
| thyA | 3074313 | c.159A>G | synonymous_variant | 1.0 |
| thyA | 3074334 | c.138T>C | synonymous_variant | 1.0 |
| thyA | 3074349 | c.123T>C | synonymous_variant | 1.0 |
| thyA | 3074355 | c.117G>C | synonymous_variant | 1.0 |
| thyA | 3074360 | c.112T>C | synonymous_variant | 1.0 |
| thyA | 3074361 | c.111T>C | synonymous_variant | 1.0 |
| thyA | 3074367 | c.103_105delCGCinsAGG | synonymous_variant | 1.0 |
| thyA | 3074370 | p.Met34Ile | missense_variant | 1.0 |
| thyA | 3074391 | c.81C>G | synonymous_variant | 1.0 |
| thyA | 3074397 | c.75A>C | synonymous_variant | 1.0 |
| thyA | 3074409 | c.63C>T | synonymous_variant | 1.0 |
| thyA | 3074423 | p.Pro17Ala | missense_variant | 1.0 |
| thyA | 3074426 | p.Thr16Ser | missense_variant | 1.0 |
| fprA | 3474180 | c.174C>G | synonymous_variant | 1.0 |
| fbiA | 3640365 | c.-178C>G | upstream_gene_variant | 1.0 |
| fbiB | 3641208 | c.-327C>T | upstream_gene_variant | 1.0 |
| fbiB | 3641217 | c.-318C>G | upstream_gene_variant | 1.0 |
| fbiB | 3641226 | c.-309G>C | upstream_gene_variant | 1.0 |
| fbiB | 3641229 | c.-306T>C | upstream_gene_variant | 1.0 |
| fbiB | 3641232 | c.-303C>T | upstream_gene_variant | 1.0 |
| fbiB | 3641235 | c.-300G>C | upstream_gene_variant | 1.0 |
| fbiB | 3641239 | c.-296T>C | upstream_gene_variant | 1.0 |
| fbiA | 3641246 | p.Glu235Ala | missense_variant | 1.0 |
| fbiA | 3641248 | p.Ala236Thr | missense_variant | 1.0 |
| fbiA | 3641251 | p.Thr237Pro | missense_variant | 1.0 |
| fbiB | 3641256 | c.-279A>G | upstream_gene_variant | 1.0 |
| fbiB | 3641286 | c.-249C>A | upstream_gene_variant | 1.0 |
| fbiA | 3641288 | p.Glu249Gly | missense_variant | 1.0 |
| fbiB | 3641292 | c.-243G>A | upstream_gene_variant | 1.0 |
| fbiA | 3641314 | p.Thr258Ala | missense_variant | 1.0 |
| fbiB | 3641319 | c.-216C>T | upstream_gene_variant | 1.0 |
| fbiB | 3641322 | c.-213T>C | upstream_gene_variant | 1.0 |
| fbiB | 3641328 | c.-207T>A | upstream_gene_variant | 1.0 |
| fbiB | 3641352 | c.-183C>G | upstream_gene_variant | 1.0 |
| fbiB | 3641355 | c.-180T>G | upstream_gene_variant | 1.0 |
| fbiA | 3641374 | p.Ala278Ser | missense_variant | 1.0 |
| fbiB | 3641948 | c.414G>A | synonymous_variant | 1.0 |
| fbiB | 3641951 | c.417G>C | synonymous_variant | 1.0 |
| fbiB | 3641957 | c.423C>T | synonymous_variant | 1.0 |
| fbiB | 3641966 | c.432C>G | synonymous_variant | 1.0 |
| fbiB | 3641969 | c.435C>G | synonymous_variant | 1.0 |
| fbiB | 3641975 | c.441C>G | synonymous_variant | 1.0 |
| fbiB | 3641976 | p.Ile148Val | missense_variant | 1.0 |
| alr | 3840248 | c.1173C>A | synonymous_variant | 1.0 |
| alr | 3840272 | c.1149C>G | synonymous_variant | 1.0 |
| alr | 3840275 | c.1146T>G | synonymous_variant | 1.0 |
| alr | 3840293 | c.1128T>G | synonymous_variant | 1.0 |
| alr | 3840296 | c.1125G>C | synonymous_variant | 1.0 |
| alr | 3840305 | c.1116T>C | synonymous_variant | 1.0 |
| alr | 3840312 | p.Ile370Ala | missense_variant | 1.0 |
| alr | 3840317 | c.1104G>C | synonymous_variant | 1.0 |
| alr | 3840328 | c.1093T>C | synonymous_variant | 1.0 |
| alr | 3840332 | c.1089G>C | synonymous_variant | 1.0 |
| alr | 3840341 | c.1080C>T | synonymous_variant | 1.0 |
| alr | 3840353 | c.1068T>C | synonymous_variant | 1.0 |
| alr | 3840356 | p.Leu355Val | missense_variant | 1.0 |
| alr | 3840362 | c.1059G>C | synonymous_variant | 1.0 |
| alr | 3840371 | c.1050G>C | synonymous_variant | 1.0 |
| alr | 3840380 | p.Met347Val | missense_variant | 1.0 |
| alr | 3840403 | c.1018C>A | synonymous_variant | 1.0 |
| alr | 3840404 | c.1017G>C | synonymous_variant | 1.0 |
| alr | 3840407 | c.1014G>C | synonymous_variant | 1.0 |
| alr | 3840410 | c.1011T>C | synonymous_variant | 1.0 |
| alr | 3840413 | c.1008C>G | synonymous_variant | 1.0 |
| alr | 3840416 | p.Cys335Arg | missense_variant | 1.0 |
| alr | 3840422 | c.997_999delAGAinsCGG | synonymous_variant | 1.0 |
| alr | 3840443 | c.978G>C | synonymous_variant | 1.0 |
| alr | 3840446 | c.975G>T | synonymous_variant | 1.0 |
| alr | 3840473 | c.948C>T | synonymous_variant | 1.0 |
| alr | 3840476 | c.945A>C | synonymous_variant | 1.0 |
| alr | 3840502 | p.Leu307Val | missense_variant | 1.0 |
| alr | 3840503 | p.Asn306Thr | missense_variant | 1.0 |
| alr | 3840513 | p.Arg303His | missense_variant | 1.0 |
| alr | 3840515 | c.906A>G | synonymous_variant | 1.0 |
| alr | 3840527 | c.894A>C | synonymous_variant | 1.0 |
| alr | 3840536 | c.885T>C | synonymous_variant | 1.0 |
| alr | 3840551 | c.870G>A | synonymous_variant | 1.0 |
| alr | 3840554 | c.867G>A | synonymous_variant | 1.0 |
| alr | 3840557 | p.Arg288Pro | missense_variant | 1.0 |
| alr | 3840562 | p.Ile287Val | missense_variant | 1.0 |
| alr | 3840566 | c.855A>G | synonymous_variant | 1.0 |
| alr | 3840569 | p.Val284Ile | missense_variant | 1.0 |
| alr | 3840578 | c.843T>G | synonymous_variant | 1.0 |
| alr | 3840584 | c.837T>C | synonymous_variant | 1.0 |
| alr | 3840599 | c.822G>C | synonymous_variant | 1.0 |
| rpoA | 3877533 | c.975C>G | synonymous_variant | 1.0 |
| rpoA | 3877557 | c.951C>G | synonymous_variant | 1.0 |
| rpoA | 3877567 | p.Ser314Thr | missense_variant | 1.0 |
| rpoA | 3877569 | c.939G>C | synonymous_variant | 1.0 |
| rpoA | 3877575 | c.933C>T | synonymous_variant | 1.0 |
| rpoA | 3877587 | c.921A>G | synonymous_variant | 1.0 |
| rpoA | 3877593 | c.915C>T | synonymous_variant | 1.0 |
| rpoA | 3877602 | c.906C>T | synonymous_variant | 1.0 |
| rpoA | 3877613 | p.Ile299Val | missense_variant | 1.0 |
| rpoA | 3877620 | c.888G>A | synonymous_variant | 1.0 |
| rpoA | 3877647 | c.861C>A | synonymous_variant | 1.0 |
| rpoA | 3877656 | c.852T>C | synonymous_variant | 1.0 |
| rpoA | 3877659 | c.849G>A | synonymous_variant | 1.0 |
| rpoA | 3877668 | c.840A>G | synonymous_variant | 1.0 |
| rpoA | 3877674 | c.834C>T | synonymous_variant | 1.0 |
| rpoA | 3877679 | p.Ala277Ser | missense_variant | 1.0 |
| rpoA | 3877680 | c.828G>C | synonymous_variant | 1.0 |
| rpoA | 3877685 | c.823C>T | synonymous_variant | 1.0 |
| rpoA | 3877689 | c.819C>T | synonymous_variant | 1.0 |
| rpoA | 3877692 | c.816G>C | synonymous_variant | 1.0 |
| rpoA | 3877704 | c.804G>C | synonymous_variant | 1.0 |
| rpoA | 3877731 | c.777G>T | synonymous_variant | 1.0 |
| rpoA | 3877734 | c.774G>C | synonymous_variant | 1.0 |
| rpoA | 3877737 | c.771G>T | synonymous_variant | 1.0 |
| rpoA | 3877743 | c.765T>C | synonymous_variant | 1.0 |
| rpoA | 3877746 | c.762G>C | synonymous_variant | 1.0 |
| rpoA | 3877752 | c.756C>T | synonymous_variant | 1.0 |
| rpoA | 3877755 | c.753C>A | synonymous_variant | 1.0 |
| rpoA | 3877764 | c.744C>G | synonymous_variant | 1.0 |
| rpoA | 3877770 | c.738A>G | synonymous_variant | 1.0 |
| rpoA | 3877776 | c.732T>C | synonymous_variant | 1.0 |
| rpoA | 3877782 | c.726T>C | synonymous_variant | 1.0 |
| rpoA | 3877830 | c.678C>T | synonymous_variant | 1.0 |
| rpoA | 3877836 | c.672A>G | synonymous_variant | 1.0 |
| rpoA | 3877839 | c.669G>C | synonymous_variant | 1.0 |
| rpoA | 3877848 | c.660C>T | synonymous_variant | 1.0 |
| rpoA | 3877875 | c.633T>G | synonymous_variant | 1.0 |
| rpoA | 3877886 | c.622C>T | synonymous_variant | 1.0 |
| rpoA | 3877896 | c.612G>C | synonymous_variant | 1.0 |
| rpoA | 3877899 | p.Ser203Thr | missense_variant | 1.0 |
| rpoA | 3877905 | c.603A>G | synonymous_variant | 1.0 |
| rpoA | 3877909 | p.Asn200Ser | missense_variant | 1.0 |
| rpoA | 3877926 | c.582G>C | synonymous_variant | 1.0 |
| rpoA | 3877929 | c.579C>T | synonymous_variant | 1.0 |
| rpoA | 3877950 | c.558C>T | synonymous_variant | 1.0 |
| rpoA | 3877971 | p.Asp179Glu | missense_variant | 1.0 |
| rpoA | 3877986 | c.522G>C | synonymous_variant | 1.0 |
| rpoA | 3877989 | c.519A>G | synonymous_variant | 1.0 |
| rpoA | 3878001 | c.507A>G | synonymous_variant | 1.0 |
| rpoA | 3878022 | c.486T>C | synonymous_variant | 1.0 |
| rpoA | 3878025 | c.483C>T | synonymous_variant | 1.0 |
| rpoA | 3878028 | c.480G>C | synonymous_variant | 1.0 |
| rpoA | 3878031 | c.477T>C | synonymous_variant | 1.0 |
| rpoA | 3878043 | c.465G>T | synonymous_variant | 1.0 |
| rpoA | 3878058 | c.450G>C | synonymous_variant | 1.0 |
| rpoA | 3878061 | c.447G>C | synonymous_variant | 1.0 |
| rpoA | 3878070 | c.438T>C | synonymous_variant | 1.0 |
| rpoA | 3878085 | c.423G>A | synonymous_variant | 1.0 |
| rpoA | 3878097 | c.411G>A | synonymous_variant | 1.0 |
| rpoA | 3878100 | c.408C>G | synonymous_variant | 1.0 |
| rpoA | 3878106 | c.402G>C | synonymous_variant | 1.0 |
| rpoA | 3878118 | c.390T>C | synonymous_variant | 1.0 |
| rpoA | 3878126 | c.382C>T | synonymous_variant | 1.0 |
| rpoA | 3878127 | c.381G>C | synonymous_variant | 1.0 |
| rpoA | 3878157 | c.351C>G | synonymous_variant | 1.0 |
| rpoA | 3878163 | c.345C>T | synonymous_variant | 1.0 |
| rpoA | 3878172 | c.336G>C | synonymous_variant | 1.0 |
| rpoA | 3878193 | c.315T>C | synonymous_variant | 1.0 |
| rpoA | 3878202 | c.306G>C | synonymous_variant | 1.0 |
| rpoA | 3878211 | c.297G>A | synonymous_variant | 1.0 |
| rpoA | 3878217 | c.291A>G | synonymous_variant | 1.0 |
| rpoA | 3878247 | c.261G>C | synonymous_variant | 1.0 |
| rpoA | 3878256 | c.252G>C | synonymous_variant | 1.0 |
| rpoA | 3878262 | c.246C>T | synonymous_variant | 1.0 |
| rpoA | 3878271 | c.237T>C | synonymous_variant | 1.0 |
| rpoA | 3878283 | p.Glu75Asp | missense_variant | 1.0 |
| rpoA | 3878292 | c.216T>C | synonymous_variant | 1.0 |
| rpoA | 3878295 | c.213A>G | synonymous_variant | 1.0 |
| rpoA | 3878298 | c.210A>G | synonymous_variant | 1.0 |
| rpoA | 3878322 | c.186A>G | synonymous_variant | 1.0 |
| rpoA | 3878331 | c.177A>G | synonymous_variant | 1.0 |
| rpoA | 3878334 | c.174T>C | synonymous_variant | 1.0 |
| rpoA | 3878337 | c.171T>C | synonymous_variant | 1.0 |
| rpoA | 3878364 | c.144A>T | synonymous_variant | 1.0 |
| rpoA | 3878367 | c.141C>G | synonymous_variant | 1.0 |
| rpoA | 3878370 | c.138T>C | synonymous_variant | 1.0 |
| rpoA | 3878376 | c.132G>A | synonymous_variant | 1.0 |
| rpoA | 3878381 | c.127C>T | synonymous_variant | 1.0 |
| rpoA | 3878391 | c.117T>A | synonymous_variant | 1.0 |
| rpoA | 3878403 | c.105C>T | synonymous_variant | 1.0 |
| rpoA | 3878406 | c.102G>T | synonymous_variant | 1.0 |
| rpoA | 3878412 | c.96C>T | synonymous_variant | 1.0 |
| rpoA | 3878424 | c.84G>C | synonymous_variant | 1.0 |
| rpoA | 3878442 | p.Val22Thr | missense_variant | 1.0 |
| rpoA | 3878454 | c.54A>G | synonymous_variant | 1.0 |
| rpoA | 3878472 | p.Asp12Glu | missense_variant | 1.0 |
| rpoA | 3878478 | c.30C>G | synonymous_variant | 1.0 |
| rpoA | 3878483 | c.25C>T | synonymous_variant | 1.0 |
| rpoA | 3878490 | c.18C>T | synonymous_variant | 1.0 |
| rpoA | 3878698 | c.-191A>C | upstream_gene_variant | 1.0 |
| ddn | 3986648 | c.-196C>G | upstream_gene_variant | 1.0 |
| ddn | 3986657 | c.-187C>G | upstream_gene_variant | 1.0 |
| ddn | 3986663 | c.-181G>A | upstream_gene_variant | 1.0 |
| ddn | 3986667 | c.-177_-176delCTinsAC | upstream_gene_variant | 1.0 |
| ddn | 3986696 | c.-148G>T | upstream_gene_variant | 1.0 |
| ddn | 3986711 | c.-133C>G | upstream_gene_variant | 1.0 |
| ddn | 3986975 | c.132T>C | synonymous_variant | 1.0 |
| ddn | 3986984 | c.141G>T | synonymous_variant | 1.0 |
| ddn | 3987028 | p.Asn62Ser | missense_variant | 1.0 |
| ddn | 3987035 | c.192C>G | synonymous_variant | 1.0 |
| ddn | 3987053 | c.210T>C | synonymous_variant | 1.0 |
| ddn | 3987055 | p.Gly71Asp | missense_variant | 1.0 |
| ddn | 3987062 | c.219C>G | synonymous_variant | 1.0 |
| ddn | 3987065 | c.222T>C | synonymous_variant | 1.0 |
| ddn | 3987071 | c.228G>C | synonymous_variant | 1.0 |
| ddn | 3987089 | c.246G>C | synonymous_variant | 1.0 |
| ddn | 3987092 | p.Glu83Asp | missense_variant | 1.0 |
| ddn | 3987095 | p.Lys84Asn | missense_variant | 0.5 |
| ddn | 3987098 | c.255C>T | synonymous_variant | 1.0 |
| clpC1 | 4038238 | p.Thr823Ala | missense_variant | 1.0 |
| clpC1 | 4038239 | c.2466T>C | synonymous_variant | 1.0 |
| clpC1 | 4038271 | p.Pro812Ala | missense_variant | 1.0 |
| clpC1 | 4038272 | c.2433T>C | synonymous_variant | 1.0 |
| clpC1 | 4038278 | c.2427T>C | synonymous_variant | 1.0 |
| clpC1 | 4038302 | c.2403C>G | synonymous_variant | 1.0 |
| clpC1 | 4038308 | c.2397G>C | synonymous_variant | 1.0 |
| clpC1 | 4038314 | c.2391T>G | synonymous_variant | 1.0 |
| clpC1 | 4038335 | c.2370C>T | synonymous_variant | 1.0 |
| clpC1 | 4038344 | c.2361G>A | synonymous_variant | 1.0 |
| clpC1 | 4038350 | c.2355C>G | synonymous_variant | 1.0 |
| clpC1 | 4038356 | c.2349T>C | synonymous_variant | 1.0 |
| clpC1 | 4038359 | c.2346A>G | synonymous_variant | 1.0 |
| clpC1 | 4038368 | c.2337T>C | synonymous_variant | 1.0 |
| clpC1 | 4038383 | c.2322G>A | synonymous_variant | 1.0 |
| clpC1 | 4038388 | c.2317T>C | synonymous_variant | 1.0 |
| clpC1 | 4038392 | c.2313C>T | synonymous_variant | 1.0 |
| clpC1 | 4038398 | c.2307G>T | synonymous_variant | 1.0 |
| clpC1 | 4038403 | c.2302T>C | synonymous_variant | 1.0 |
| clpC1 | 4038407 | c.2298G>C | synonymous_variant | 1.0 |
| clpC1 | 4038419 | c.2286T>C | synonymous_variant | 1.0 |
| clpC1 | 4038436 | p.Ala757Ser | missense_variant | 1.0 |
| clpC1 | 4038444 | p.Ala754Lys | missense_variant | 1.0 |
| clpC1 | 4038446 | c.2259T>C | synonymous_variant | 1.0 |
| clpC1 | 4038456 | p.Val750Glu | missense_variant | 1.0 |
| clpC1 | 4038508 | c.2197C>T | synonymous_variant | 1.0 |
| clpC1 | 4038519 | p.Arg729Gln | missense_variant | 1.0 |
| clpC1 | 4038530 | p.Glu725Asp | missense_variant | 1.0 |
| clpC1 | 4038533 | c.2172C>T | synonymous_variant | 1.0 |
| clpC1 | 4038536 | c.2169C>T | synonymous_variant | 1.0 |
| clpC1 | 4038587 | c.2118C>T | synonymous_variant | 1.0 |
| clpC1 | 4038596 | c.2109A>G | synonymous_variant | 1.0 |
| clpC1 | 4038602 | c.2103G>C | synonymous_variant | 1.0 |
| clpC1 | 4038623 | c.2082A>G | synonymous_variant | 1.0 |
| clpC1 | 4038653 | c.2052C>T | synonymous_variant | 1.0 |
| clpC1 | 4038661 | p.Ser682Thr | missense_variant | 1.0 |
| clpC1 | 4038662 | c.2043T>C | synonymous_variant | 1.0 |
| clpC1 | 4038665 | c.2040C>G | synonymous_variant | 1.0 |
| clpC1 | 4038668 | c.2037G>C | synonymous_variant | 1.0 |
| clpC1 | 4038671 | c.2034T>C | synonymous_variant | 1.0 |
| clpC1 | 4038677 | c.2028G>A | synonymous_variant | 1.0 |
| clpC1 | 4038686 | c.2019C>T | synonymous_variant | 1.0 |
| clpC1 | 4038695 | c.2010C>A | synonymous_variant | 1.0 |
| clpC1 | 4038698 | c.2007C>G | synonymous_variant | 1.0 |
| clpC1 | 4038703 | c.2002C>T | synonymous_variant | 1.0 |
| clpC1 | 4038704 | c.2001T>C | synonymous_variant | 1.0 |
| clpC1 | 4038707 | c.1998C>G | synonymous_variant | 1.0 |
| clpC1 | 4038713 | c.1992T>C | synonymous_variant | 1.0 |
| clpC1 | 4038755 | c.1950G>T | synonymous_variant | 1.0 |
| clpC1 | 4038773 | c.1932T>C | synonymous_variant | 1.0 |
| clpC1 | 4038790 | c.1915C>T | synonymous_variant | 1.0 |
| clpC1 | 4038800 | c.1905C>T | synonymous_variant | 1.0 |
| clpC1 | 4038812 | c.1893T>C | synonymous_variant | 1.0 |
| clpC1 | 4038838 | c.1867C>T | synonymous_variant | 1.0 |
| clpC1 | 4038839 | c.1866G>C | synonymous_variant | 1.0 |
| clpC1 | 4038878 | c.1827A>G | synonymous_variant | 1.0 |
| clpC1 | 4038902 | c.1803C>T | synonymous_variant | 1.0 |
| clpC1 | 4038908 | c.1797C>G | synonymous_variant | 1.0 |
| clpC1 | 4038914 | c.1791G>C | synonymous_variant | 1.0 |
| clpC1 | 4038923 | c.1782A>G | synonymous_variant | 1.0 |
| clpC1 | 4038953 | c.1752A>G | synonymous_variant | 1.0 |
| clpC1 | 4038956 | c.1749T>C | synonymous_variant | 1.0 |
| clpC1 | 4038965 | c.1740T>C | synonymous_variant | 1.0 |
| clpC1 | 4038971 | c.1734T>C | synonymous_variant | 1.0 |
| clpC1 | 4038974 | c.1731T>C | synonymous_variant | 1.0 |
| clpC1 | 4038980 | c.1725C>T | synonymous_variant | 1.0 |
| clpC1 | 4038989 | c.1716T>C | synonymous_variant | 1.0 |
| clpC1 | 4038995 | c.1710G>A | synonymous_variant | 1.0 |
| clpC1 | 4039009 | c.1696C>T | synonymous_variant | 1.0 |
| clpC1 | 4039022 | c.1683A>G | synonymous_variant | 1.0 |
| clpC1 | 4039037 | c.1668T>C | synonymous_variant | 1.0 |
| clpC1 | 4039085 | c.1620A>G | synonymous_variant | 1.0 |
| clpC1 | 4039090 | c.1615C>T | synonymous_variant | 1.0 |
| clpC1 | 4039097 | c.1608G>C | synonymous_variant | 1.0 |
| clpC1 | 4039103 | c.1602T>C | synonymous_variant | 1.0 |
| clpC1 | 4039106 | c.1599G>C | synonymous_variant | 1.0 |
| clpC1 | 4039112 | c.1593C>G | synonymous_variant | 1.0 |
| clpC1 | 4039121 | c.1584T>C | synonymous_variant | 1.0 |
| clpC1 | 4039133 | c.1572C>G | synonymous_variant | 1.0 |
| clpC1 | 4039142 | c.1563A>G | synonymous_variant | 1.0 |
| clpC1 | 4039145 | c.1560G>C | synonymous_variant | 1.0 |
| clpC1 | 4039169 | p.Glu512Asp | missense_variant | 1.0 |
| clpC1 | 4039172 | c.1533A>G | synonymous_variant | 1.0 |
| clpC1 | 4039183 | c.1522T>C | synonymous_variant | 1.0 |
| clpC1 | 4039187 | c.1518G>C | synonymous_variant | 1.0 |
| clpC1 | 4039226 | c.1479T>C | synonymous_variant | 1.0 |
| clpC1 | 4039274 | c.1431G>C | synonymous_variant | 1.0 |
| clpC1 | 4039286 | c.1419T>C | synonymous_variant | 1.0 |
| clpC1 | 4039292 | c.1413C>T | synonymous_variant | 1.0 |
| clpC1 | 4039295 | c.1410A>G | synonymous_variant | 1.0 |
| clpC1 | 4039319 | c.1386T>C | synonymous_variant | 1.0 |
| clpC1 | 4039322 | c.1383T>C | synonymous_variant | 1.0 |
| clpC1 | 4039337 | c.1368A>C | synonymous_variant | 1.0 |
| clpC1 | 4039352 | c.1353C>T | synonymous_variant | 1.0 |
| clpC1 | 4039391 | c.1314T>G | synonymous_variant | 1.0 |
| clpC1 | 4039409 | c.1296T>C | synonymous_variant | 1.0 |
| clpC1 | 4039412 | c.1293T>G | synonymous_variant | 1.0 |
| clpC1 | 4039430 | c.1275T>C | synonymous_variant | 1.0 |
| clpC1 | 4039442 | c.1261_1263delCTAinsTTG | synonymous_variant | 1.0 |
| clpC1 | 4039448 | c.1257A>G | synonymous_variant | 1.0 |
| clpC1 | 4039454 | c.1251A>G | synonymous_variant | 1.0 |
| clpC1 | 4039484 | c.1221T>G | synonymous_variant | 1.0 |
| clpC1 | 4039493 | c.1212C>T | synonymous_variant | 1.0 |
| clpC1 | 4039514 | c.1191C>T | synonymous_variant | 1.0 |
| clpC1 | 4039517 | c.1188C>G | synonymous_variant | 1.0 |
| clpC1 | 4039541 | c.1164C>A | synonymous_variant | 1.0 |
| clpC1 | 4039552 | c.1153C>T | synonymous_variant | 1.0 |
| clpC1 | 4039553 | c.1152C>G | synonymous_variant | 1.0 |
| clpC1 | 4039559 | c.1146C>G | synonymous_variant | 1.0 |
| clpC1 | 4039562 | c.1143C>G | synonymous_variant | 1.0 |
| clpC1 | 4039574 | p.Ala377Ser | missense_variant | 1.0 |
| clpC1 | 4039577 | c.1128T>C | synonymous_variant | 1.0 |
| clpC1 | 4039586 | c.1119G>C | synonymous_variant | 1.0 |
| clpC1 | 4039601 | c.1104G>C | synonymous_variant | 1.0 |
| clpC1 | 4039610 | c.1095G>C | synonymous_variant | 1.0 |
| clpC1 | 4039616 | c.1089G>C | synonymous_variant | 1.0 |
| clpC1 | 4039622 | c.1083C>T | synonymous_variant | 1.0 |
| clpC1 | 4039661 | c.1044T>C | synonymous_variant | 1.0 |
| clpC1 | 4039664 | c.1041G>C | synonymous_variant | 1.0 |
| clpC1 | 4039693 | c.1012C>T | synonymous_variant | 1.0 |
| clpC1 | 4039694 | c.1011G>C | synonymous_variant | 1.0 |
| clpC1 | 4039724 | c.981A>G | synonymous_variant | 1.0 |
| clpC1 | 4039733 | c.972G>A | synonymous_variant | 1.0 |
| clpC1 | 4039751 | c.954A>G | synonymous_variant | 1.0 |
| clpC1 | 4039754 | c.951G>T | synonymous_variant | 1.0 |
| clpC1 | 4039763 | c.942C>T | synonymous_variant | 1.0 |
| clpC1 | 4039766 | c.939T>G | synonymous_variant | 1.0 |
| clpC1 | 4039778 | c.927A>G | synonymous_variant | 1.0 |
| clpC1 | 4039784 | c.921C>T | synonymous_variant | 1.0 |
| clpC1 | 4039787 | c.916_918delTCGinsAGC | synonymous_variant | 1.0 |
| clpC1 | 4039793 | c.912C>G | synonymous_variant | 1.0 |
| clpC1 | 4039802 | c.903G>C | synonymous_variant | 1.0 |
| clpC1 | 4039817 | c.888A>C | synonymous_variant | 1.0 |
| clpC1 | 4039826 | c.879C>G | synonymous_variant | 1.0 |
| clpC1 | 4039831 | c.874T>C | synonymous_variant | 1.0 |
| clpC1 | 4039850 | c.855T>C | synonymous_variant | 1.0 |
| clpC1 | 4039865 | c.840T>C | synonymous_variant | 1.0 |
| clpC1 | 4039868 | c.837C>T | synonymous_variant | 1.0 |
| clpC1 | 4039904 | c.801A>G | synonymous_variant | 1.0 |
| clpC1 | 4039928 | c.775_777delAGCinsTCG | synonymous_variant | 1.0 |
| clpC1 | 4039931 | c.774T>C | synonymous_variant | 1.0 |
| clpC1 | 4039942 | c.763C>T | synonymous_variant | 1.0 |
| clpC1 | 4039946 | c.759A>G | synonymous_variant | 1.0 |
| clpC1 | 4039952 | c.753T>C | synonymous_variant | 1.0 |
| clpC1 | 4039958 | c.747G>C | synonymous_variant | 1.0 |
| clpC1 | 4039991 | c.714G>C | synonymous_variant | 1.0 |
| clpC1 | 4039996 | p.Glu237Gln | missense_variant | 1.0 |
| clpC1 | 4040015 | c.690G>C | synonymous_variant | 1.0 |
| clpC1 | 4040018 | c.687G>C | synonymous_variant | 1.0 |
| clpC1 | 4040021 | c.684A>C | synonymous_variant | 1.0 |
| clpC1 | 4040033 | c.672G>C | synonymous_variant | 1.0 |
| clpC1 | 4040036 | c.669C>G | synonymous_variant | 1.0 |
| clpC1 | 4040048 | c.657C>T | synonymous_variant | 1.0 |
| clpC1 | 4040091 | c.613_614delTCinsAG | synonymous_variant | 1.0 |
| clpC1 | 4040093 | c.612C>G | synonymous_variant | 1.0 |
| clpC1 | 4040105 | c.600C>G | synonymous_variant | 1.0 |
| clpC1 | 4040147 | c.558A>G | synonymous_variant | 1.0 |
| clpC1 | 4040153 | c.552A>G | synonymous_variant | 1.0 |
| clpC1 | 4040159 | c.546G>C | synonymous_variant | 1.0 |
| clpC1 | 4040162 | c.543G>C | synonymous_variant | 1.0 |
| clpC1 | 4040171 | c.534C>G | synonymous_variant | 1.0 |
| clpC1 | 4040314 | c.391C>T | synonymous_variant | 1.0 |
| clpC1 | 4040411 | c.294T>G | synonymous_variant | 1.0 |
| clpC1 | 4040414 | c.291G>A | synonymous_variant | 1.0 |
| clpC1 | 4040423 | c.282A>G | synonymous_variant | 1.0 |
| clpC1 | 4040426 | c.279T>C | synonymous_variant | 1.0 |
| clpC1 | 4040444 | c.261C>T | synonymous_variant | 1.0 |
| clpC1 | 4040450 | c.255A>G | synonymous_variant | 1.0 |
| clpC1 | 4040456 | c.249C>G | synonymous_variant | 1.0 |
| clpC1 | 4040459 | c.246C>G | synonymous_variant | 1.0 |
| clpC1 | 4040462 | c.243C>T | synonymous_variant | 1.0 |
| clpC1 | 4040471 | c.234T>C | synonymous_variant | 1.0 |
| clpC1 | 4040480 | c.225T>C | synonymous_variant | 1.0 |
| clpC1 | 4040495 | c.210C>G | synonymous_variant | 1.0 |
| clpC1 | 4040510 | c.195G>A | synonymous_variant | 1.0 |
| clpC1 | 4040513 | c.192G>A | synonymous_variant | 1.0 |
| clpC1 | 4040522 | c.183T>C | synonymous_variant | 1.0 |
| clpC1 | 4040528 | c.177G>C | synonymous_variant | 1.0 |
| clpC1 | 4040531 | c.174T>G | synonymous_variant | 1.0 |
| clpC1 | 4040546 | c.159G>T | synonymous_variant | 1.0 |
| clpC1 | 4040551 | c.154T>C | synonymous_variant | 1.0 |
| clpC1 | 4040561 | c.144A>G | synonymous_variant | 1.0 |
| clpC1 | 4040573 | c.132T>A | synonymous_variant | 1.0 |
| clpC1 | 4040579 | c.126A>G | synonymous_variant | 1.0 |
| clpC1 | 4040582 | c.123G>C | synonymous_variant | 1.0 |
| clpC1 | 4040594 | c.111G>T | synonymous_variant | 1.0 |
| clpC1 | 4040597 | c.108C>T | synonymous_variant | 1.0 |
| clpC1 | 4040600 | c.105A>G | synonymous_variant | 1.0 |
| clpC1 | 4040603 | c.102T>G | synonymous_variant | 1.0 |
| clpC1 | 4040636 | c.69C>G | synonymous_variant | 1.0 |
| clpC1 | 4040644 | c.61A>C | synonymous_variant | 1.0 |
| clpC1 | 4040654 | c.51G>A | synonymous_variant | 1.0 |
| clpC1 | 4040657 | c.48T>G | synonymous_variant | 1.0 |
| clpC1 | 4040662 | c.43C>T | synonymous_variant | 1.0 |
| clpC1 | 4040674 | c.31A>C | synonymous_variant | 1.0 |
| embC | 4240093 | c.231C>T | synonymous_variant | 1.0 |
| embC | 4240105 | p.Asp81Glu | missense_variant | 1.0 |
| embC | 4240106 | c.244_246delTTGinsCTC | synonymous_variant | 1.0 |
| embC | 4240123 | c.261C>G | synonymous_variant | 1.0 |
| embC | 4240128 | p.Gln89Arg | missense_variant | 1.0 |
| embC | 4240150 | c.288A>G | synonymous_variant | 1.0 |
| embC | 4240151 | p.Ser97Pro | missense_variant | 1.0 |
| embC | 4240171 | c.309G>C | synonymous_variant | 1.0 |
| embC | 4240175 | c.313T>C | synonymous_variant | 1.0 |
| embC | 4240183 | c.321A>G | synonymous_variant | 1.0 |
| embC | 4240201 | c.339G>C | synonymous_variant | 1.0 |
| embC | 4240204 | c.342T>C | synonymous_variant | 1.0 |
| embC | 4240207 | p.Lys115Asn | missense_variant | 1.0 |
| embC | 4240216 | c.354T>C | synonymous_variant | 1.0 |
| embC | 4240228 | c.366G>C | synonymous_variant | 1.0 |
| embC | 4240229 | p.Leu123Ile | missense_variant | 1.0 |
| embC | 4240234 | c.372A>G | synonymous_variant | 1.0 |
| embC | 4240237 | c.375G>C | synonymous_variant | 1.0 |
| embC | 4240255 | c.393G>A | synonymous_variant | 0.86 |
| embC | 4240258 | c.396T>G | synonymous_variant | 1.0 |
| embC | 4240267 | c.405T>C | synonymous_variant | 1.0 |
| embC | 4240277 | p.Leu139Val | missense_variant | 1.0 |
| embC | 4240284 | p.Thr141Ser | missense_variant | 1.0 |
| embC | 4240288 | c.426C>T | synonymous_variant | 1.0 |
| embC | 4240297 | c.435T>C | synonymous_variant | 1.0 |
| embC | 4240420 | c.558T>C | synonymous_variant | 1.0 |
| embC | 4240427 | p.Ser189Gly | missense_variant | 1.0 |
| embC | 4240441 | c.579C>T | synonymous_variant | 1.0 |
| embC | 4240444 | c.582C>G | synonymous_variant | 1.0 |
| embC | 4240471 | c.609C>T | synonymous_variant | 1.0 |
| embC | 4240475 | p.Ala205Ser | missense_variant | 1.0 |
| embC | 4240484 | p.Ala208Thr | missense_variant | 1.0 |
| embC | 4240489 | c.627A>G | synonymous_variant | 1.0 |
| embC | 4240495 | c.633T>C | synonymous_variant | 1.0 |
| embC | 4240512 | p.Ser217Thr | missense_variant | 1.0 |
| embC | 4240516 | c.654G>C | synonymous_variant | 1.0 |
| embC | 4240519 | c.657T>C | synonymous_variant | 1.0 |
| embC | 4240543 | c.681G>C | synonymous_variant | 1.0 |
| embC | 4240561 | c.699C>G | synonymous_variant | 1.0 |
| embC | 4240693 | c.831T>C | synonymous_variant | 1.0 |
| embC | 4240699 | c.837C>A | synonymous_variant | 1.0 |
| embC | 4240717 | c.855T>C | synonymous_variant | 1.0 |
| embC | 4240726 | c.864G>C | synonymous_variant | 1.0 |
| embC | 4240741 | c.879C>T | synonymous_variant | 1.0 |
| embC | 4240777 | c.915G>A | synonymous_variant | 1.0 |
| embC | 4240780 | c.918T>C | synonymous_variant | 1.0 |
| embC | 4240783 | c.921G>C | synonymous_variant | 1.0 |
| embC | 4240795 | c.933C>G | synonymous_variant | 1.0 |
| embC | 4240801 | c.939C>T | synonymous_variant | 1.0 |
| embC | 4240831 | c.969T>C | synonymous_variant | 1.0 |
| embC | 4240945 | c.1083T>C | synonymous_variant | 1.0 |
| embC | 4240954 | c.1092T>C | synonymous_variant | 1.0 |
| embC | 4240960 | c.1098G>T | synonymous_variant | 1.0 |
| embC | 4240963 | c.1101G>C | synonymous_variant | 1.0 |
| embC | 4240966 | c.1104G>C | synonymous_variant | 1.0 |
| embC | 4240978 | c.1116G>A | synonymous_variant | 1.0 |
| embC | 4240979 | p.Thr373His | missense_variant | 1.0 |
| embC | 4240987 | c.1125G>C | synonymous_variant | 1.0 |
| embC | 4240990 | c.1128A>T | synonymous_variant | 1.0 |
| embC | 4241002 | c.1140G>A | synonymous_variant | 1.0 |
| embC | 4241011 | c.1149C>T | synonymous_variant | 1.0 |
| embC | 4241017 | c.1155T>C | synonymous_variant | 1.0 |
| embC | 4241023 | c.1161T>G | synonymous_variant | 1.0 |
| embC | 4241026 | c.1164C>G | synonymous_variant | 1.0 |
| embC | 4241039 | p.Asp393Asn | missense_variant | 1.0 |
| embC | 4241050 | c.1188T>G | synonymous_variant | 1.0 |
| embC | 4241056 | c.1194C>G | synonymous_variant | 1.0 |
| embC | 4241095 | c.1233C>T | synonymous_variant | 1.0 |
| embC | 4241107 | c.1245G>C | synonymous_variant | 1.0 |
| embC | 4241140 | c.1278A>G | synonymous_variant | 1.0 |
| embC | 4241153 | p.Ile431Leu | missense_variant | 1.0 |
| embC | 4241401 | c.1539C>T | synonymous_variant | 1.0 |
| embC | 4241416 | c.1554C>A | synonymous_variant | 1.0 |
| embC | 4241719 | c.1857G>C | synonymous_variant | 1.0 |
| embC | 4241728 | c.1866C>T | synonymous_variant | 1.0 |
| embC | 4241741 | p.Val627Ile | missense_variant | 1.0 |
| embC | 4241750 | p.Leu630Met | missense_variant | 1.0 |
| embC | 4241755 | c.1893C>G | synonymous_variant | 1.0 |
| embC | 4241761 | c.1899G>C | synonymous_variant | 1.0 |
| embC | 4241788 | c.1926C>T | synonymous_variant | 1.0 |
| embC | 4241791 | c.1929G>C | synonymous_variant | 1.0 |
| embC | 4241797 | c.1935C>T | synonymous_variant | 1.0 |
| embC | 4241809 | c.1947A>G | synonymous_variant | 1.0 |
| embC | 4241818 | c.1956C>T | synonymous_variant | 1.0 |
| embC | 4241821 | c.1959G>A | synonymous_variant | 1.0 |
| embC | 4241824 | c.1962T>C | synonymous_variant | 1.0 |
| embC | 4241836 | c.1974A>C | synonymous_variant | 1.0 |
| embC | 4241845 | c.1983T>C | synonymous_variant | 1.0 |
| embC | 4242139 | c.2277G>C | synonymous_variant | 1.0 |
| embC | 4242146 | p.Asn762Glu | missense_variant | 1.0 |
| embC | 4242151 | c.2289A>C | synonymous_variant | 1.0 |
| embC | 4242161 | p.Ala767Pro | missense_variant | 1.0 |
| embC | 4242166 | c.2304G>A | synonymous_variant | 1.0 |
| embC | 4242171 | p.Thr770Ser | missense_variant | 1.0 |
| embC | 4242175 | c.2313G>T | synonymous_variant | 1.0 |
| embC | 4242179 | p.Leu773Val | missense_variant | 1.0 |
| embC | 4242190 | c.2328C>T | synonymous_variant | 1.0 |
| embC | 4242196 | c.2334A>G | synonymous_variant | 1.0 |
| embC | 4242202 | c.2340C>A | synonymous_variant | 1.0 |
| embC | 4242208 | c.2346T>A | synonymous_variant | 1.0 |
| embC | 4242214 | c.2352C>G | synonymous_variant | 1.0 |
| embC | 4242217 | c.2355C>T | synonymous_variant | 1.0 |
| embC | 4242220 | c.2358A>G | synonymous_variant | 1.0 |
| embC | 4242229 | c.2367C>A | synonymous_variant | 1.0 |
| embA | 4242238 | c.-995C>T | upstream_gene_variant | 1.0 |
| embA | 4242241 | c.-992C>T | upstream_gene_variant | 1.0 |
| embC | 4242245 | p.Thr795Ser | missense_variant | 1.0 |
| embA | 4242847 | c.-386C>A | upstream_gene_variant | 1.0 |
| embA | 4242859 | c.-374C>T | upstream_gene_variant | 1.0 |
| embC | 4242863 | p.Tyr1001Asn | missense_variant | 1.0 |
| embA | 4242871 | c.-362C>T | upstream_gene_variant | 1.0 |
| embC | 4242873 | p.Asp1004Val | missense_variant | 1.0 |
| embA | 4242883 | c.-350C>G | upstream_gene_variant | 1.0 |
| embC | 4242885 | p.Lys1008Thr | missense_variant | 1.0 |
| embA | 4242919 | c.-314A>G | upstream_gene_variant | 1.0 |
| embA | 4242925 | c.-308C>T | upstream_gene_variant | 1.0 |
| embA | 4242928 | c.-305A>T | upstream_gene_variant | 1.0 |
| embA | 4242931 | c.-302G>C | upstream_gene_variant | 1.0 |
| embA | 4242934 | c.-299G>C | upstream_gene_variant | 1.0 |
| embA | 4242940 | c.-293T>C | upstream_gene_variant | 1.0 |
| embC | 4242941 | p.His1027Lys | missense_variant | 1.0 |
| embA | 4242946 | c.-287T>C | upstream_gene_variant | 1.0 |
| embA | 4242952 | c.-281T>C | upstream_gene_variant | 1.0 |
| embA | 4242958 | c.-275G>C | upstream_gene_variant | 1.0 |
| embA | 4242974 | c.-259C>T | upstream_gene_variant | 1.0 |
| embC | 4242980 | p.Met1040Leu | missense_variant | 1.0 |
| embA | 4243222 | c.-11C>G | upstream_gene_variant | 1.0 |
| embA | 4243228 | c.-5G>C | upstream_gene_variant | 1.0 |
| embA | 4243240 | p.His3Leu | missense_variant | 1.0 |
| embA | 4243271 | c.39A>C | synonymous_variant | 1.0 |
| embA | 4243279 | p.Ala16Val | missense_variant | 1.0 |
| embA | 4243301 | c.69G>C | synonymous_variant | 1.0 |
| embA | 4243304 | c.72T>A | synonymous_variant | 1.0 |
| embA | 4243311 | c.79C>T | synonymous_variant | 1.0 |
| embA | 4243318 | p.Gly29Ala | missense_variant | 1.0 |
| embA | 4243320 | p.Ile30Leu | missense_variant | 1.0 |
| embA | 4243343 | p.Asn37Lys | missense_variant | 1.0 |
| embA | 4243346 | c.114A>G | synonymous_variant | 1.0 |
| embA | 4243349 | c.117C>G | synonymous_variant | 1.0 |
| embA | 4243352 | c.120C>G | synonymous_variant | 1.0 |
| embA | 4243362 | p.Phe44Leu | missense_variant | 1.0 |
| embA | 4244567 | c.1335C>G | synonymous_variant | 1.0 |
| embA | 4244576 | c.1344G>C | synonymous_variant | 1.0 |
| embA | 4244582 | c.1350T>C | synonymous_variant | 1.0 |
| embA | 4244585 | c.1353A>C | synonymous_variant | 1.0 |
| embA | 4244588 | c.1356G>C | synonymous_variant | 1.0 |
| embA | 4244603 | c.1371G>A | synonymous_variant | 1.0 |
| embA | 4244612 | c.1380C>G | synonymous_variant | 1.0 |
| embA | 4244615 | c.1383G>A | synonymous_variant | 1.0 |
| embA | 4244616 | p.Ala462Ser | missense_variant | 1.0 |
| embA | 4244619 | c.1387T>C | synonymous_variant | 1.0 |
| embA | 4244645 | c.1413T>C | synonymous_variant | 1.0 |
| embA | 4244648 | c.1416G>C | synonymous_variant | 1.0 |
| embA | 4244649 | p.Asp473Ser | missense_variant | 1.0 |
| embA | 4244663 | c.1431C>G | synonymous_variant | 1.0 |
| embA | 4244669 | c.1437G>C | synonymous_variant | 1.0 |
| embA | 4244675 | c.1443A>G | synonymous_variant | 1.0 |
| embA | 4244681 | c.1449A>G | synonymous_variant | 1.0 |
| embA | 4244684 | c.1452C>G | synonymous_variant | 1.0 |
| embA | 4244702 | c.1470C>G | synonymous_variant | 1.0 |
| embA | 4244705 | c.1473G>C | synonymous_variant | 1.0 |
| embA | 4244708 | c.1476C>G | synonymous_variant | 1.0 |
| embA | 4244714 | c.1482C>G | synonymous_variant | 1.0 |
| embA | 4245083 | c.1851A>C | synonymous_variant | 1.0 |
| embA | 4245101 | c.1869G>C | synonymous_variant | 1.0 |
| embA | 4245110 | c.1878C>T | synonymous_variant | 1.0 |
| embA | 4245137 | c.1905T>C | synonymous_variant | 1.0 |
| embA | 4245149 | c.1917C>G | synonymous_variant | 1.0 |
| embA | 4245215 | c.1983A>C | synonymous_variant | 1.0 |
| embA | 4245224 | c.1992T>C | synonymous_variant | 1.0 |
| embA | 4245248 | c.2016G>A | synonymous_variant | 1.0 |
| embA | 4245257 | c.2025A>G | synonymous_variant | 1.0 |
| embA | 4245263 | c.2031A>G | synonymous_variant | 1.0 |
| embA | 4245281 | c.2049C>G | synonymous_variant | 1.0 |
| embA | 4245282 | p.Ile684Val | missense_variant | 1.0 |
| embA | 4245285 | c.2053T>C | synonymous_variant | 1.0 |
| embA | 4245293 | c.2061T>A | synonymous_variant | 1.0 |
| embA | 4245296 | c.2064G>C | synonymous_variant | 1.0 |
| embA | 4245299 | c.2067A>G | synonymous_variant | 1.0 |
| embA | 4245300 | c.2068C>T | synonymous_variant | 1.0 |
| embA | 4245311 | c.2079C>T | synonymous_variant | 1.0 |
| embA | 4245326 | c.2094C>G | synonymous_variant | 1.0 |
| embA | 4245327 | p.Ala699Leu | missense_variant | 1.0 |
| embA | 4245345 | p.Met705Leu | missense_variant | 1.0 |
| embA | 4245355 | p.Ala708Gly | missense_variant | 1.0 |
| embA | 4245402 | p.Thr724Ala | missense_variant | 1.0 |
| embA | 4245409 | c.2178_2179delCA | frameshift_variant | 1.0 |
| embA | 4245413 | p.Ser727Arg | missense_variant | 1.0 |
| embA | 4245414 | c.2182_2183insAT | frameshift_variant | 1.0 |
| embA | 4245424 | c.2192_2193insGCCCAG | disruptive_inframe_insertion | 1.0 |
| embA | 4245431 | c.2199T>C | synonymous_variant | 1.0 |
| embA | 4245434 | c.2202G>C | synonymous_variant | 1.0 |
| embA | 4245458 | c.2226G>A | synonymous_variant | 1.0 |
| embA | 4245464 | c.2232C>T | synonymous_variant | 1.0 |
| embA | 4245473 | c.2241C>T | synonymous_variant | 1.0 |
| embA | 4245488 | c.2256G>C | synonymous_variant | 1.0 |
| embA | 4245497 | c.2265C>T | synonymous_variant | 1.0 |
| embA | 4245501 | p.Ala757Thr | missense_variant | 1.0 |
| embA | 4245510 | p.Pro760Ser | missense_variant | 1.0 |
| embB | 4245524 | c.-990G>C | upstream_gene_variant | 1.0 |
| embB | 4245575 | c.-939C>G | upstream_gene_variant | 1.0 |
| embB | 4245662 | c.-852G>C | upstream_gene_variant | 1.0 |
| embB | 4245674 | c.-840A>T | upstream_gene_variant | 1.0 |
| embB | 4245677 | c.-837G>C | upstream_gene_variant | 1.0 |
| embB | 4245683 | c.-831C>T | upstream_gene_variant | 1.0 |
| embA | 4245693 | p.Ile821Val | missense_variant | 1.0 |
| embB | 4245714 | c.-800C>T | upstream_gene_variant | 1.0 |
| embB | 4245764 | c.-750G>C | upstream_gene_variant | 1.0 |
| embA | 4245772 | p.Asn847Thr | missense_variant | 1.0 |
| embB | 4245803 | c.-711C>T | upstream_gene_variant | 1.0 |
| embB | 4245806 | c.-708G>A | upstream_gene_variant | 1.0 |
| embB | 4245807 | c.-707_-705delTTAinsCTG | upstream_gene_variant | 1.0 |
| embB | 4245812 | c.-702G>T | upstream_gene_variant | 1.0 |
| embA | 4245813 | p.Pro861Ala | missense_variant | 1.0 |
| embA | 4245822 | p.Pro864Ala | missense_variant | 1.0 |
| embB | 4245839 | c.-675G>C | upstream_gene_variant | 1.0 |
| embA | 4245843 | p.Val871Ile | missense_variant | 1.0 |
| embB | 4245848 | c.-666C>G | upstream_gene_variant | 1.0 |
| embB | 4245851 | c.-663G>C | upstream_gene_variant | 1.0 |
| embB | 4245857 | c.-657C>G | upstream_gene_variant | 1.0 |
| embB | 4245869 | c.-645C>T | upstream_gene_variant | 1.0 |
| embB | 4245875 | c.-639G>A | upstream_gene_variant | 1.0 |
| embB | 4245887 | c.-627T>C | upstream_gene_variant | 1.0 |
| embA | 4245891 | p.Ile887Val | missense_variant | 1.0 |
| embB | 4245905 | c.-609C>T | upstream_gene_variant | 1.0 |
| embB | 4245906 | c.-608C>T | upstream_gene_variant | 1.0 |
| embB | 4245923 | c.-591C>A | upstream_gene_variant | 1.0 |
| embA | 4245930 | p.Gly900Arg | missense_variant | 0.75 |
| embB | 4245935 | c.-579G>C | upstream_gene_variant | 1.0 |
| embA | 4245942 | p.Arg904Gly | missense_variant | 1.0 |
| embB | 4245953 | c.-561A>G | upstream_gene_variant | 1.0 |
| embB | 4245956 | c.-558G>C | upstream_gene_variant | 1.0 |
| embB | 4245965 | c.-549A>G | upstream_gene_variant | 1.0 |
| embB | 4245968 | c.-546T>C | upstream_gene_variant | 1.0 |
| embA | 4245978 | p.Ile916Leu | missense_variant | 1.0 |
| embB | 4245983 | c.-531A>G | upstream_gene_variant | 1.0 |
| embB | 4245992 | c.-522C>G | upstream_gene_variant | 1.0 |
| embB | 4246004 | c.-510T>C | upstream_gene_variant | 1.0 |
| embB | 4246005 | c.-509C>T | upstream_gene_variant | 1.0 |
| embB | 4246013 | c.-501T>C | upstream_gene_variant | 1.0 |
| embA | 4246020 | p.Ala930Thr | missense_variant | 1.0 |
| embB | 4246028 | c.-486G>C | upstream_gene_variant | 1.0 |
| embB | 4246070 | c.-444G>C | upstream_gene_variant | 1.0 |
| embB | 4246082 | c.-432T>C | upstream_gene_variant | 1.0 |
| embB | 4246109 | c.-405C>G | upstream_gene_variant | 1.0 |
| embB | 4246115 | c.-399T>C | upstream_gene_variant | 1.0 |
| embA | 4246128 | p.Ser966Thr | missense_variant | 1.0 |
| embA | 4246138 | p.Arg969Gln | missense_variant | 1.0 |
| embB | 4246140 | c.-374T>C | upstream_gene_variant | 1.0 |
| embB | 4246148 | c.-366G>C | upstream_gene_variant | 1.0 |
| embB | 4246151 | c.-363A>C | upstream_gene_variant | 1.0 |
| embA | 4246152 | p.Ala974Arg | missense_variant | 1.0 |
| embB | 4246205 | c.-309A>G | upstream_gene_variant | 1.0 |
| embA | 4246254 | p.Leu1008Met | missense_variant | 1.0 |
| embB | 4246259 | c.-255G>C | upstream_gene_variant | 1.0 |
| embB | 4246265 | c.-249C>T | upstream_gene_variant | 1.0 |
| embB | 4246268 | c.-246G>A | upstream_gene_variant | 1.0 |
| embA | 4246279 | p.Ala1016Val | missense_variant | 1.0 |
| embB | 4246292 | c.-222A>G | upstream_gene_variant | 1.0 |
| embB | 4246307 | c.-207G>C | upstream_gene_variant | 1.0 |
| embB | 4246316 | c.-198T>C | upstream_gene_variant | 1.0 |
| embB | 4246346 | c.-168C>G | upstream_gene_variant | 1.0 |
| embA | 4246359 | p.Ala1043Ser | missense_variant | 1.0 |
| embB | 4246373 | c.-141T>C | upstream_gene_variant | 1.0 |
| embB | 4246376 | c.-138G>C | upstream_gene_variant | 1.0 |
| embA | 4246398 | p.Ser1056Thr | missense_variant | 1.0 |
| embA | 4246413 | p.His1061Tyr | missense_variant | 1.0 |
| embB | 4247089 | c.576G>C | synonymous_variant | 1.0 |
| embB | 4247095 | c.582G>A | synonymous_variant | 1.0 |
| embB | 4247104 | c.591G>A | synonymous_variant | 1.0 |
| embB | 4247113 | c.600G>A | synonymous_variant | 1.0 |
| embB | 4247114 | p.Ala201Lys | missense_variant | 1.0 |
| embB | 4247117 | p.Val202Leu | missense_variant | 1.0 |
| embB | 4247137 | c.624C>G | synonymous_variant | 1.0 |
| embB | 4247140 | c.627G>C | synonymous_variant | 1.0 |
| embB | 4247150 | p.Arg213Thr | missense_variant | 1.0 |
| embB | 4247155 | c.642G>A | synonymous_variant | 1.0 |
| embB | 4247179 | p.Ile222Met | missense_variant | 1.0 |
| embB | 4247180 | p.Ile223Val | missense_variant | 1.0 |
| embB | 4247185 | c.672G>C | synonymous_variant | 1.0 |
| embB | 4247212 | c.699G>C | synonymous_variant | 1.0 |
| embB | 4247213 | p.Ile234Val | missense_variant | 1.0 |
| embB | 4247219 | c.706T>C | synonymous_variant | 1.0 |
| embB | 4247365 | c.852A>C | synonymous_variant | 1.0 |
| embB | 4247370 | p.Gly286Ala | missense_variant | 1.0 |
| embB | 4247386 | c.873T>C | synonymous_variant | 1.0 |
| embB | 4247398 | c.885G>C | synonymous_variant | 1.0 |
| embB | 4247401 | c.888T>C | synonymous_variant | 1.0 |
| embB | 4247404 | c.891G>C | synonymous_variant | 1.0 |
| embB | 4247407 | c.894G>C | synonymous_variant | 1.0 |
| embB | 4247440 | c.927C>G | synonymous_variant | 1.0 |
| embB | 4247470 | c.957T>C | synonymous_variant | 1.0 |
| embB | 4247497 | c.984T>C | synonymous_variant | 1.0 |
| embB | 4247500 | c.987C>G | synonymous_variant | 1.0 |
| embB | 4247512 | c.999T>C | synonymous_variant | 1.0 |
| embB | 4247554 | c.1041T>C | synonymous_variant | 1.0 |
| embB | 4247555 | p.Leu348Ile | missense_variant | 1.0 |
| embB | 4247566 | c.1053C>G | synonymous_variant | 1.0 |
| embB | 4247579 | p.Ala356Phe | missense_variant | 1.0 |
| embB | 4247590 | c.1077A>G | synonymous_variant | 1.0 |
| embB | 4247608 | c.1095G>C | synonymous_variant | 1.0 |
| embB | 4247611 | c.1098G>C | synonymous_variant | 1.0 |
| embB | 4247632 | c.1119C>G | synonymous_variant | 1.0 |
| embB | 4247645 | p.Glu378Thr | missense_variant | 1.0 |
| embB | 4247648 | p.Ala379Ser | missense_variant | 1.0 |
| embB | 4247657 | p.Pro382Ala | missense_variant | 1.0 |
| embB | 4247671 | c.1158G>A | synonymous_variant | 1.0 |
| embB | 4247679 | p.Met389Thr | missense_variant | 1.0 |
| embB | 4247684 | c.1171T>C | synonymous_variant | 1.0 |
| embB | 4247722 | c.1209G>C | synonymous_variant | 1.0 |
| embB | 4247725 | c.1212G>C | synonymous_variant | 1.0 |
| embB | 4247728 | c.1215G>A | synonymous_variant | 1.0 |
| embB | 4247743 | c.1230C>G | synonymous_variant | 1.0 |
| embB | 4247761 | c.1248T>C | synonymous_variant | 1.0 |
| embB | 4247779 | c.1266C>G | synonymous_variant | 1.0 |
| embB | 4247785 | c.1272G>C | synonymous_variant | 1.0 |
| embB | 4247800 | c.1287A>C | synonymous_variant | 1.0 |
| embB | 4247815 | c.1302C>G | synonymous_variant | 1.0 |
| embB | 4247816 | p.Val435Ile | missense_variant | 1.0 |
| embB | 4247819 | p.Val436Ile | missense_variant | 1.0 |
| embB | 4247830 | c.1317A>G | synonymous_variant | 1.0 |
| embB | 4247836 | c.1323A>G | synonymous_variant | 1.0 |
| embB | 4247839 | c.1326G>C | synonymous_variant | 1.0 |
| embB | 4247858 | c.1345C>T | synonymous_variant | 1.0 |
| embB | 4247899 | p.Met462Ile | missense_variant | 1.0 |
| embB | 4247911 | p.Leu466Phe | missense_variant | 1.0 |
| embB | 4247915 | p.Arg468Lys | missense_variant | 1.0 |
| embB | 4247920 | c.1407T>C | synonymous_variant | 1.0 |
| embB | 4247923 | c.1410T>C | synonymous_variant | 1.0 |
| embB | 4247932 | c.1419C>G | synonymous_variant | 1.0 |
| embB | 4247948 | p.Val479Leu | missense_variant | 1.0 |
| embB | 4247975 | p.Val488Ile | missense_variant | 1.0 |
| embB | 4247989 | c.1476G>C | synonymous_variant | 1.0 |
| embB | 4248007 | c.1494C>G | synonymous_variant | 1.0 |
| embB | 4248042 | p.Ala510Gly | missense_variant | 1.0 |
| embB | 4248052 | c.1539G>T | synonymous_variant | 1.0 |
| embB | 4248055 | c.1542G>C | synonymous_variant | 1.0 |
| embB | 4248058 | c.1545C>T | synonymous_variant | 1.0 |
| embB | 4248061 | c.1548G>A | synonymous_variant | 1.0 |
| embB | 4248064 | c.1551G>C | synonymous_variant | 1.0 |
| embB | 4248070 | c.1557T>C | synonymous_variant | 1.0 |
| embB | 4248094 | c.1581C>T | synonymous_variant | 1.0 |
| embB | 4248130 | c.1617G>C | synonymous_variant | 1.0 |
| embB | 4248142 | c.1629T>C | synonymous_variant | 1.0 |
| embB | 4248143 | c.1630T>C | synonymous_variant | 1.0 |
| embB | 4248154 | c.1641G>T | synonymous_variant | 1.0 |
| embB | 4248157 | c.1644A>T | synonymous_variant | 1.0 |
| embB | 4248163 | c.1650G>A | synonymous_variant | 1.0 |
| embB | 4248169 | c.1656C>T | synonymous_variant | 1.0 |
| embB | 4248175 | c.1662G>A | synonymous_variant | 1.0 |
| embB | 4248178 | c.1665C>T | synonymous_variant | 1.0 |
| embB | 4248206 | p.Ser565Gly | missense_variant | 1.0 |
| embB | 4248214 | c.1701C>G | synonymous_variant | 1.0 |
| embB | 4248217 | c.1704C>G | synonymous_variant | 1.0 |
| embB | 4248220 | c.1707A>G | synonymous_variant | 1.0 |
| embB | 4248233 | c.1720C>T | synonymous_variant | 1.0 |
| embB | 4248252 | p.Gly580Ala | missense_variant | 1.0 |
| embB | 4248266 | c.1753C>T | synonymous_variant | 1.0 |
| embB | 4248277 | c.1764G>C | synonymous_variant | 1.0 |
| embB | 4248280 | c.1767C>G | synonymous_variant | 1.0 |
| embB | 4248316 | c.1803C>G | synonymous_variant | 1.0 |
| embB | 4248319 | c.1806A>G | synonymous_variant | 1.0 |
| embB | 4248334 | c.1821C>G | synonymous_variant | 1.0 |
| embB | 4248358 | c.1845C>G | synonymous_variant | 1.0 |
| embB | 4248361 | c.1848A>G | synonymous_variant | 1.0 |
| embB | 4248379 | c.1866G>A | synonymous_variant | 1.0 |
| embB | 4248407 | p.Leu632Val | missense_variant | 1.0 |
| embB | 4248412 | p.Phe633Leu | missense_variant | 1.0 |
| embB | 4248416 | p.Leu635Met | missense_variant | 1.0 |
| embB | 4248424 | c.1911G>A | synonymous_variant | 1.0 |
| embB | 4248430 | c.1917T>C | synonymous_variant | 1.0 |
| embB | 4248448 | c.1935C>T | synonymous_variant | 1.0 |
| embB | 4248457 | c.1944T>C | synonymous_variant | 1.0 |
| embB | 4248472 | c.1959T>C | synonymous_variant | 1.0 |
| embB | 4248496 | c.1983G>C | synonymous_variant | 1.0 |
| embB | 4248504 | p.Asp664Ala | missense_variant | 1.0 |
| embB | 4248508 | c.1995G>A | synonymous_variant | 1.0 |
| embB | 4248514 | c.2001A>G | synonymous_variant | 1.0 |
| embB | 4248535 | c.2022C>G | synonymous_variant | 1.0 |
| embB | 4248541 | c.2028T>C | synonymous_variant | 1.0 |
| embB | 4248544 | c.2031G>C | synonymous_variant | 1.0 |
| embB | 4248547 | c.2034C>T | synonymous_variant | 0.67 |
| embB | 4248553 | c.2040C>G | synonymous_variant | 1.0 |
| embB | 4248555 | p.Gly681Val | missense_variant | 1.0 |
| embB | 4248559 | c.2046T>C | synonymous_variant | 1.0 |
| embB | 4248574 | c.2061C>T | synonymous_variant | 1.0 |
| embB | 4248580 | c.2067G>A | synonymous_variant | 1.0 |
| embB | 4248586 | c.2073C>G | synonymous_variant | 1.0 |
| embB | 4248880 | c.2367G>C | synonymous_variant | 1.0 |
| embB | 4248892 | c.2379A>G | synonymous_variant | 1.0 |
| embB | 4248898 | c.2385A>G | synonymous_variant | 1.0 |
| embB | 4248904 | c.2391G>C | synonymous_variant | 1.0 |
| embB | 4248907 | c.2394G>C | synonymous_variant | 1.0 |
| embB | 4248964 | c.2451G>C | synonymous_variant | 1.0 |
| embB | 4248967 | c.2454G>C | synonymous_variant | 1.0 |
| embB | 4248973 | c.2460G>A | synonymous_variant | 1.0 |
| embB | 4248976 | c.2463G>C | synonymous_variant | 1.0 |
| embB | 4248978 | p.Thr822Lys | missense_variant | 1.0 |
| embB | 4248981 | p.Ser823Thr | missense_variant | 1.0 |
| embB | 4248983 | p.Pro824Ala | missense_variant | 1.0 |
| embB | 4248997 | c.2484T>A | synonymous_variant | 1.0 |
| embB | 4249000 | c.2487T>G | synonymous_variant | 1.0 |
| embB | 4249018 | c.2505T>C | synonymous_variant | 1.0 |
| embB | 4249019 | p.Gly836Gln | missense_variant | 1.0 |
| embB | 4249030 | c.2517C>G | synonymous_variant | 1.0 |
| embB | 4249033 | c.2520C>G | synonymous_variant | 1.0 |
| embB | 4249039 | c.2526A>T | synonymous_variant | 1.0 |
| embB | 4249043 | c.2530T>C | synonymous_variant | 1.0 |
| embB | 4249048 | c.2535A>C | synonymous_variant | 1.0 |
| embB | 4249066 | c.2553C>G | synonymous_variant | 1.0 |
| embB | 4249276 | c.2763A>C | synonymous_variant | 1.0 |
| embB | 4249282 | c.2769A>G | synonymous_variant | 1.0 |
| embB | 4249285 | c.2772G>A | synonymous_variant | 1.0 |
| embB | 4249288 | c.2775G>A | synonymous_variant | 1.0 |
| embB | 4249294 | c.2781G>A | synonymous_variant | 1.0 |
| embB | 4249297 | c.2784G>C | synonymous_variant | 1.0 |
| embB | 4249303 | c.2790C>A | synonymous_variant | 1.0 |
| embB | 4249306 | c.2793C>T | synonymous_variant | 1.0 |
| embB | 4249312 | c.2799C>G | synonymous_variant | 1.0 |
| embB | 4249321 | c.2808A>C | synonymous_variant | 1.0 |
| embB | 4249323 | p.Ala937Asp | missense_variant | 1.0 |
| embB | 4249339 | c.2826T>C | synonymous_variant | 1.0 |
| embB | 4249348 | c.2835G>C | synonymous_variant | 1.0 |
| embB | 4249360 | c.2847G>C | synonymous_variant | 1.0 |
| embB | 4249369 | c.2856T>C | synonymous_variant | 1.0 |
| embB | 4249375 | c.2862G>C | synonymous_variant | 1.0 |
| embB | 4249381 | c.2868A>C | synonymous_variant | 1.0 |
| embB | 4249417 | c.2904A>G | synonymous_variant | 1.0 |
| embB | 4249429 | c.2916C>G | synonymous_variant | 1.0 |
| embB | 4249432 | c.2919A>G | synonymous_variant | 1.0 |
| embB | 4249433 | c.2920C>T | synonymous_variant | 1.0 |
| embB | 4249444 | c.2931T>C | synonymous_variant | 1.0 |
| embB | 4249447 | c.2934G>C | synonymous_variant | 1.0 |
| embB | 4249453 | c.2940G>C | synonymous_variant | 1.0 |
| embB | 4249456 | c.2943G>C | synonymous_variant | 1.0 |
| embB | 4249459 | c.2946G>A | synonymous_variant | 1.0 |
| embB | 4249474 | c.2961C>T | synonymous_variant | 1.0 |
| embB | 4249486 | c.2973T>G | synonymous_variant | 1.0 |
| embB | 4249487 | c.2974_2976delTTGinsCTC | synonymous_variant | 1.0 |
| embB | 4249492 | c.2979C>G | synonymous_variant | 1.0 |
| embB | 4249501 | c.2988C>T | synonymous_variant | 1.0 |
| embB | 4249521 | p.Ala1003Val | missense_variant | 1.0 |
| embB | 4249525 | c.3012T>C | synonymous_variant | 1.0 |
| embB | 4249529 | p.Ile1006Val | missense_variant | 1.0 |
| embB | 4249532 | p.Ala1007Thr | missense_variant | 1.0 |
| embB | 4249540 | c.3027C>T | synonymous_variant | 1.0 |
| embB | 4249546 | c.3033G>A | synonymous_variant | 1.0 |
| embB | 4249568 | p.Ser1019Asn | missense_variant | 1.0 |
| embB | 4249573 | c.3060T>C | synonymous_variant | 1.0 |
| embB | 4249594 | c.3081G>C | synonymous_variant | 1.0 |
| embB | 4249607 | p.Thr1032Val | missense_variant | 1.0 |
| embB | 4249618 | c.3105C>G | synonymous_variant | 1.0 |
| embB | 4249624 | c.3111C>T | synonymous_variant | 1.0 |
| embB | 4249627 | c.3114G>C | synonymous_variant | 1.0 |
| embB | 4249640 | c.3127T>C | synonymous_variant | 1.0 |
| embB | 4249648 | c.3135G>C | synonymous_variant | 1.0 |
| embB | 4249654 | c.3141C>T | synonymous_variant | 1.0 |
| embB | 4249657 | c.3144C>G | synonymous_variant | 1.0 |
| embB | 4249663 | c.3150C>G | synonymous_variant | 1.0 |
| embB | 4249666 | c.3153C>T | synonymous_variant | 1.0 |
| embB | 4249669 | c.3156C>T | synonymous_variant | 1.0 |
| embB | 4249675 | c.3162C>G | synonymous_variant | 1.0 |
| embB | 4249693 | c.3180T>C | synonymous_variant | 1.0 |
| aftB | 4267196 | c.1641C>T | synonymous_variant | 1.0 |
| aftB | 4267211 | c.1626C>G | synonymous_variant | 1.0 |
| aftB | 4267214 | c.1623A>C | synonymous_variant | 1.0 |
| aftB | 4267235 | c.1602G>C | synonymous_variant | 1.0 |
| aftB | 4267244 | c.1593T>C | synonymous_variant | 1.0 |
| aftB | 4267253 | c.1584T>C | synonymous_variant | 1.0 |
| aftB | 4267262 | c.1575T>G | synonymous_variant | 1.0 |
| aftB | 4267266 | p.Ala524Gly | missense_variant | 1.0 |
| aftB | 4267268 | c.1569T>C | synonymous_variant | 1.0 |
| aftB | 4267276 | c.1561C>T | synonymous_variant | 1.0 |
| aftB | 4267289 | p.Ala516Gln | missense_variant | 1.0 |
| aftB | 4267297 | c.1540T>C | synonymous_variant | 1.0 |
| aftB | 4267298 | c.1539A>G | synonymous_variant | 1.0 |
| aftB | 4267305 | p.Val511Ala | missense_variant | 1.0 |
| aftB | 4267316 | c.1521A>G | synonymous_variant | 1.0 |
| aftB | 4267328 | c.1507_1509delCGGinsAGA | synonymous_variant | 1.0 |
| aftB | 4267340 | c.1497G>A | synonymous_variant | 1.0 |
| aftB | 4267343 | c.1494C>G | synonymous_variant | 1.0 |
| aftB | 4267483 | c.1354T>C | synonymous_variant | 1.0 |
| aftB | 4267484 | c.1353A>G | synonymous_variant | 1.0 |
| aftB | 4267489 | c.1348T>C | synonymous_variant | 1.0 |
| aftB | 4267490 | c.1347G>T | synonymous_variant | 1.0 |
| aftB | 4267493 | c.1344G>C | synonymous_variant | 1.0 |
| aftB | 4267499 | c.1338G>C | synonymous_variant | 1.0 |
| aftB | 4267510 | p.Asn443Asp | missense_variant | 1.0 |
| aftB | 4267511 | c.1326C>T | synonymous_variant | 1.0 |
| aftB | 4267517 | c.1320A>C | synonymous_variant | 1.0 |
| aftB | 4267520 | c.1317T>G | synonymous_variant | 1.0 |
| aftB | 4267529 | c.1308T>C | synonymous_variant | 1.0 |
| aftB | 4267535 | c.1302A>G | synonymous_variant | 1.0 |
| aftB | 4267556 | c.1281G>C | synonymous_variant | 1.0 |
| aftB | 4267574 | c.1263G>C | synonymous_variant | 1.0 |
| aftB | 4267580 | c.1257G>A | synonymous_variant | 1.0 |
| aftB | 4267592 | c.1245C>G | synonymous_variant | 1.0 |
| aftB | 4267793 | c.1044C>T | synonymous_variant | 1.0 |
| aftB | 4267802 | c.1035T>C | synonymous_variant | 1.0 |
| aftB | 4267805 | c.1032T>C | synonymous_variant | 1.0 |
| aftB | 4267808 | c.1029G>C | synonymous_variant | 1.0 |
| aftB | 4267826 | c.1011G>C | synonymous_variant | 1.0 |
| aftB | 4267838 | c.999T>C | synonymous_variant | 1.0 |
| aftB | 4267841 | c.996C>T | synonymous_variant | 1.0 |
| aftB | 4267856 | c.981T>C | synonymous_variant | 1.0 |
| aftB | 4267879 | p.Val320Leu | missense_variant | 1.0 |
| aftB | 4267891 | p.Val316Ile | missense_variant | 1.0 |
| aftB | 4267892 | p.Ile315Met | missense_variant | 1.0 |
| aftB | 4267898 | c.939T>C | synonymous_variant | 1.0 |
| aftB | 4267907 | c.930C>G | synonymous_variant | 1.0 |
| aftB | 4267912 | p.Pro309Ala | missense_variant | 1.0 |
| aftB | 4267916 | c.921T>C | synonymous_variant | 1.0 |
| aftB | 4267919 | c.918A>G | synonymous_variant | 1.0 |
| aftB | 4267922 | c.915G>A | synonymous_variant | 1.0 |
| aftB | 4267940 | c.897T>G | synonymous_variant | 1.0 |
| aftB | 4268048 | c.789G>C | synonymous_variant | 1.0 |
| aftB | 4268060 | c.777C>T | synonymous_variant | 1.0 |
| aftB | 4268066 | p.Val257Leu | missense_variant | 1.0 |
| aftB | 4268069 | c.768C>T | synonymous_variant | 1.0 |
| aftB | 4268081 | c.756A>G | synonymous_variant | 1.0 |
| aftB | 4268099 | c.738G>C | synonymous_variant | 1.0 |
| aftB | 4268105 | c.732T>C | synonymous_variant | 1.0 |
| aftB | 4268125 | p.Ser238Gly | missense_variant | 1.0 |
| aftB | 4268126 | c.711G>C | synonymous_variant | 1.0 |
| aftB | 4268129 | c.708T>G | synonymous_variant | 1.0 |
| aftB | 4268134 | c.703C>T | synonymous_variant | 1.0 |
| aftB | 4268135 | c.700_702delCTGinsTTA | synonymous_variant | 1.0 |
| aftB | 4268138 | p.Gly233Ala | missense_variant | 1.0 |
| aftB | 4268144 | c.693T>C | synonymous_variant | 1.0 |
| aftB | 4268171 | c.666G>C | synonymous_variant | 1.0 |
| aftB | 4268179 | c.658T>C | synonymous_variant | 1.0 |
| aftB | 4268183 | c.654A>C | synonymous_variant | 1.0 |
| aftB | 4268194 | p.Leu215Val | missense_variant | 1.0 |
| aftB | 4268207 | c.630C>G | synonymous_variant | 1.0 |
| aftB | 4268213 | c.624T>C | synonymous_variant | 1.0 |
| aftB | 4268228 | c.609C>G | synonymous_variant | 1.0 |
| aftB | 4268233 | p.Ile202Val | missense_variant | 1.0 |
| aftB | 4268236 | c.601T>C | synonymous_variant | 1.0 |
| aftB | 4268248 | c.589C>T | synonymous_variant | 1.0 |
| aftB | 4268249 | c.588G>C | synonymous_variant | 1.0 |
| aftB | 4268255 | c.582G>C | synonymous_variant | 1.0 |
| aftB | 4268261 | p.Ile192Met | missense_variant | 1.0 |
| aftB | 4268270 | p.Phe189Leu | missense_variant | 1.0 |
| aftB | 4268273 | c.564A>G | synonymous_variant | 1.0 |
| aftB | 4268282 | c.555G>C | synonymous_variant | 1.0 |
| aftB | 4268285 | c.552A>G | synonymous_variant | 1.0 |
| aftB | 4268288 | c.549G>C | synonymous_variant | 1.0 |
| ubiA | 4269629 | p.Val69Met | missense_variant | 1.0 |
| aftB | 4269660 | c.-824C>A | upstream_gene_variant | 1.0 |
| ubiA | 4269663 | p.Met57Val | missense_variant | 1.0 |
| aftB | 4269669 | c.-833G>T | upstream_gene_variant | 1.0 |
| ubiA | 4269676 | p.Ser53Thr | missense_variant | 1.0 |
| aftB | 4269678 | c.-842C>G | upstream_gene_variant | 1.0 |
| ubiA | 4269688 | p.Val49Ala | missense_variant | 1.0 |
| aftB | 4269690 | c.-854C>T | upstream_gene_variant | 1.0 |
| aftB | 4269699 | c.-863C>A | upstream_gene_variant | 1.0 |
| aftB | 4269705 | c.-869T>C | upstream_gene_variant | 1.0 |
| ubiA | 4269710 | p.Gly42Arg | missense_variant | 1.0 |
| ubiA | 4269715 | p.Leu40Ala | missense_variant | 1.0 |
| aftB | 4269723 | c.-887G>C | upstream_gene_variant | 1.0 |
| aftB | 4269744 | c.-908G>C | upstream_gene_variant | 1.0 |
| aftB | 4269762 | c.-926C>G | upstream_gene_variant | 1.0 |
| ubiA | 4269771 | p.Ile21Met | missense_variant | 1.0 |
| ethA | 4326331 | c.1143C>G | synonymous_variant | 1.0 |
| ethA | 4326337 | c.1137C>T | synonymous_variant | 1.0 |
| ethA | 4326343 | c.1131C>T | synonymous_variant | 1.0 |
| ethA | 4326430 | c.1044T>C | synonymous_variant | 1.0 |
| ethA | 4326457 | p.Ile339Val | missense_variant | 1.0 |
| ethA | 4326469 | c.1005T>C | synonymous_variant | 1.0 |
| ethA | 4326475 | c.999G>T | synonymous_variant | 1.0 |
| ethA | 4326481 | c.993C>T | synonymous_variant | 1.0 |
| ethA | 4326484 | c.990T>A | synonymous_variant | 1.0 |
| ethA | 4326487 | c.987A>C | synonymous_variant | 1.0 |
| ethA | 4326490 | c.984C>T | synonymous_variant | 1.0 |
| ethA | 4326507 | p.Thr323Ser | missense_variant | 1.0 |
| ethA | 4326510 | p.Ala322Pro | missense_variant | 1.0 |
| ethA | 4326520 | p.Glu318Asp | missense_variant | 1.0 |
| ethA | 4326523 | c.951T>C | synonymous_variant | 1.0 |
| ethA | 4326535 | c.939G>C | synonymous_variant | 1.0 |
| ethR | 4326556 | c.-993A>G | upstream_gene_variant | 1.0 |
| ethA | 4326563 | p.Ala304Gly | missense_variant | 1.0 |
| ethR | 4326565 | c.-984C>A | upstream_gene_variant | 1.0 |
| ethR | 4326591 | c.-958A>G | upstream_gene_variant | 1.0 |
| ethR | 4326598 | c.-951T>C | upstream_gene_variant | 1.0 |
| ethR | 4326610 | c.-939G>C | upstream_gene_variant | 1.0 |
| ethR | 4326613 | c.-936G>A | upstream_gene_variant | 1.0 |
| ethR | 4326628 | c.-921G>A | upstream_gene_variant | 1.0 |
| ethR | 4326637 | c.-912T>G | upstream_gene_variant | 1.0 |
| ethR | 4326640 | c.-909C>T | upstream_gene_variant | 1.0 |
| ethR | 4326646 | c.-903G>A | upstream_gene_variant | 1.0 |
| ethR | 4326649 | c.-900C>A | upstream_gene_variant | 1.0 |
| ethR | 4326652 | c.-897C>T | upstream_gene_variant | 1.0 |
| ethR | 4326658 | c.-891T>C | upstream_gene_variant | 1.0 |
| ethR | 4326661 | c.-888C>T | upstream_gene_variant | 1.0 |
| ethA | 4326678 | p.Ser266Gly | missense_variant | 1.0 |
| ethA | 4326681 | p.Leu265Met | missense_variant | 1.0 |
| ethR | 4326697 | c.-852G>C | upstream_gene_variant | 1.0 |
| ethR | 4326703 | c.-846T>C | upstream_gene_variant | 1.0 |
| ethR | 4326847 | c.-702G>C | upstream_gene_variant | 1.0 |
| ethR | 4326850 | c.-699T>C | upstream_gene_variant | 1.0 |
| ethR | 4326853 | c.-696G>A | upstream_gene_variant | 1.0 |
| ethR | 4326856 | c.-693C>T | upstream_gene_variant | 1.0 |
| ethA | 4326874 | p.Lys200Asn | missense_variant | 1.0 |
| ethR | 4326880 | c.-669G>A | upstream_gene_variant | 1.0 |
| ethR | 4326886 | c.-663G>A | upstream_gene_variant | 1.0 |
| ethR | 4326895 | c.-654C>T | upstream_gene_variant | 1.0 |
| ethR | 4326901 | c.-648C>A | upstream_gene_variant | 1.0 |
| ethR | 4326907 | c.-642C>A | upstream_gene_variant | 1.0 |
| ethR | 4326913 | c.-636C>G | upstream_gene_variant | 1.0 |
| ethR | 4326919 | c.-630T>G | upstream_gene_variant | 1.0 |
| ethR | 4326928 | c.-621G>T | upstream_gene_variant | 1.0 |
| ethA | 4326949 | p.Ala175Gly | missense_variant | 1.0 |
| ethA | 4326952 | p.Asp174Glu | missense_variant | 1.0 |
| ethA | 4326994 | p.Pro160Ala | missense_variant | 1.0 |
| ethR | 4326997 | c.-552C>A | upstream_gene_variant | 1.0 |
| ethA | 4327001 | p.Val158Ala | missense_variant | 1.0 |
| ethR | 4327006 | c.-543A>G | upstream_gene_variant | 1.0 |
| ethA | 4327010 | p.Glu155Ala | missense_variant | 1.0 |
| ethA | 4327014 | p.Ser154Ala | missense_variant | 1.0 |
| ethA | 4327020 | p.Ala152Pro | missense_variant | 1.0 |
| ethR | 4327021 | c.-528G>A | upstream_gene_variant | 1.0 |
| ethA | 4327025 | p.Arg150Lys | missense_variant | 1.0 |
| ethR | 4327033 | c.-516G>A | upstream_gene_variant | 1.0 |
| ethA | 4327039 | p.Glu145Gln | missense_variant | 1.0 |
| ethA | 4327042 | p.Asp144Glu | missense_variant | 1.0 |
| ethR | 4327054 | c.-495G>A | upstream_gene_variant | 1.0 |
| ethR | 4327072 | c.-477G>C | upstream_gene_variant | 1.0 |
| ethR | 4327249 | c.-300G>A | upstream_gene_variant | 1.0 |
| ethR | 4327252 | c.-297C>G | upstream_gene_variant | 1.0 |
| ethR | 4327258 | c.-291C>A | upstream_gene_variant | 1.0 |
| ethA | 4327261 | p.Gly71Glu | missense_variant | 1.0 |
| ethR | 4327273 | c.-276A>G | upstream_gene_variant | 1.0 |
| ethR | 4327279 | c.-270_-268delTCGinsCCT | upstream_gene_variant | 1.0 |
| ethR | 4327285 | c.-264A>G | upstream_gene_variant | 1.0 |
| ethR | 4327288 | c.-261T>C | upstream_gene_variant | 1.0 |
| ethR | 4327291 | c.-258C>G | upstream_gene_variant | 1.0 |
| ethA | 4327296 | p.Tyr60His | missense_variant | 1.0 |
| ethR | 4327300 | c.-249G>A | upstream_gene_variant | 1.0 |
| ethR | 4327306 | c.-243G>A | upstream_gene_variant | 1.0 |
| ethR | 4327318 | c.-231T>G | upstream_gene_variant | 1.0 |
| ethR | 4327327 | c.-222A>G | upstream_gene_variant | 1.0 |
| ethR | 4327330 | c.-219G>A | upstream_gene_variant | 1.0 |
| ethR | 4327335 | c.-214A>G | upstream_gene_variant | 1.0 |
| ethR | 4327336 | c.-213A>G | upstream_gene_variant | 1.0 |
| ethA | 4327356 | p.Ser40Ala | missense_variant | 1.0 |
| ethA | 4327357 | p.Glu39Ser | missense_variant | 1.0 |
| ethA | 4327971 | c.-498A>G | upstream_gene_variant | 1.0 |
| ethR | 4327987 | p.Ala147Ser | missense_variant | 1.0 |
| ethA | 4327995 | c.-522C>G | upstream_gene_variant | 1.0 |
| ethR | 4328000 | p.Ala151Glu | missense_variant | 1.0 |
| ethR | 4328010 | p.Asp154Glu | missense_variant | 1.0 |
| ethR | 4328011 | p.Ala155Thr | missense_variant | 1.0 |
| ethA | 4328025 | c.-552T>G | upstream_gene_variant | 1.0 |
| ethA | 4328031 | c.-558C>G | upstream_gene_variant | 1.0 |
| ethA | 4328034 | c.-561C>G | upstream_gene_variant | 1.0 |
| ethR | 4328038 | p.Arg164Val | missense_variant | 1.0 |
| ethR | 4328044 | p.Leu166Val | missense_variant | 1.0 |
| ethA | 4328049 | c.-576C>G | upstream_gene_variant | 1.0 |
| ethR | 4328054 | p.His169Leu | missense_variant | 1.0 |
| ethA | 4328067 | c.-594T>G | upstream_gene_variant | 1.0 |
| ethA | 4328076 | c.-603G>A | upstream_gene_variant | 1.0 |
| ethA | 4328088 | c.-615C>T | upstream_gene_variant | 1.0 |
