Run ID: ERR1035162
Sample name:
Date: 18-08-2022 11:54:09
Number of reads: 732427
Percentage reads mapped: 17.24
Strain:
Drug-resistance: Other
| Drug | Resistance | Supporting mutations |
|---|
| Lineage | Family | Main Spoligotype | RDs | Frequency |
|---|---|---|---|---|
| lineage4.2.2 | Euro-American (Ural) | T;LAM7-TUR | None | 0.06 |
| 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 | 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 | 5542 | c.303A>C | synonymous_variant | 1.0 |
| gyrB | 5545 | c.306A>G | synonymous_variant | 1.0 |
| gyrB | 5548 | c.309A>G | synonymous_variant | 1.0 |
| gyrB | 5551 | c.312T>C | synonymous_variant | 1.0 |
| gyrB | 5560 | c.321C>G | synonymous_variant | 1.0 |
| gyrB | 5746 | c.507A>G | synonymous_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 | 1.0 |
| gyrB | 5869 | c.630C>T | synonymous_variant | 1.0 |
| gyrB | 5870 | p.Glu211Gln | missense_variant | 1.0 |
| gyrB | 5873 | c.634A>C | synonymous_variant | 1.0 |
| gyrB | 5884 | c.645A>G | synonymous_variant | 1.0 |
| gyrB | 5902 | c.663A>G | synonymous_variant | 1.0 |
| gyrB | 6097 | c.858G>A | synonymous_variant | 1.0 |
| gyrB | 6115 | c.876A>G | synonymous_variant | 1.0 |
| gyrB | 6121 | c.882C>T | synonymous_variant | 1.0 |
| gyrB | 6127 | c.888G>C | synonymous_variant | 1.0 |
| gyrB | 6145 | c.906C>T | synonymous_variant | 1.0 |
| 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 | 0.98 |
| 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 | 6400 | c.-902C>G | upstream_gene_variant | 1.0 |
| gyrA | 6403 | c.-899T>C | upstream_gene_variant | 1.0 |
| gyrA | 6415 | c.-887G>C | 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 | 6898 | c.-404G>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 | 7210 | c.-92C>T | upstream_gene_variant | 1.0 |
| gyrA | 7213 | c.-89G>A | upstream_gene_variant | 1.0 |
| gyrA | 7216 | c.-86G>C | upstream_gene_variant | 1.0 |
| gyrA | 7219 | c.-83C>A | upstream_gene_variant | 1.0 |
| gyrA | 7231 | c.-71C>G | upstream_gene_variant | 1.0 |
| gyrA | 7349 | c.48A>G | synonymous_variant | 1.0 |
| gyrA | 7355 | c.54T>C | synonymous_variant | 1.0 |
| gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
| gyrA | 7391 | c.90C>T | synonymous_variant | 1.0 |
| gyrA | 7394 | c.93T>C | synonymous_variant | 1.0 |
| gyrA | 7406 | c.105G>C | synonymous_variant | 1.0 |
| gyrA | 7523 | c.222C>A | synonymous_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 | 7703 | c.402G>A | synonymous_variant | 1.0 |
| gyrA | 7715 | c.414G>C | synonymous_variant | 1.0 |
| gyrA | 7728 | c.427_429delAGGinsCGC | 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 | 0.97 |
| 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 | 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 | 1.0 |
| 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 | 8627 | c.1326C>T | synonymous_variant | 1.0 |
| gyrA | 8633 | c.1332C>G | synonymous_variant | 1.0 |
| gyrA | 8645 | c.1344C>T | synonymous_variant | 1.0 |
| gyrA | 8655 | p.Ile452Val | missense_variant | 1.0 |
| gyrA | 8666 | c.1365G>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 | 8723 | c.1422G>A | synonymous_variant | 1.0 |
| gyrA | 8729 | c.1428T>C | synonymous_variant | 1.0 |
| gyrA | 8732 | c.1431G>C | synonymous_variant | 1.0 |
| gyrA | 8752 | p.Ala484Gly | missense_variant | 1.0 |
| gyrA | 8756 | c.1455A>G | synonymous_variant | 1.0 |
| gyrA | 8762 | c.1461G>C | synonymous_variant | 1.0 |
| gyrA | 8767 | p.Arg489Lys | missense_variant | 1.0 |
| gyrA | 8783 | c.1482G>T | synonymous_variant | 1.0 |
| gyrA | 8786 | c.1485T>C | synonymous_variant | 1.0 |
| gyrA | 8795 | c.1494C>T | synonymous_variant | 1.0 |
| gyrA | 8796 | p.Ile499Val | missense_variant | 1.0 |
| gyrA | 8801 | c.1500G>C | synonymous_variant | 1.0 |
| gyrA | 8810 | c.1509A>C | synonymous_variant | 1.0 |
| gyrA | 8813 | c.1512C>T | synonymous_variant | 1.0 |
| gyrA | 8825 | c.1524G>A | synonymous_variant | 1.0 |
| gyrA | 8828 | c.1527T>C | synonymous_variant | 1.0 |
| gyrA | 8829 | c.1528T>C | synonymous_variant | 1.0 |
| gyrA | 8852 | c.1551T>G | synonymous_variant | 1.0 |
| gyrA | 8858 | c.1557T>C | synonymous_variant | 1.0 |
| gyrA | 8870 | c.1569G>C | synonymous_variant | 1.0 |
| gyrA | 8873 | c.1572A>C | synonymous_variant | 1.0 |
| gyrA | 8876 | c.1575C>T | 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 | 9050 | p.Asp583Glu | missense_variant | 1.0 |
| gyrA | 9065 | c.1764C>G | synonymous_variant | 1.0 |
| gyrA | 9068 | c.1767G>C | synonymous_variant | 1.0 |
| gyrA | 9071 | c.1770G>C | synonymous_variant | 1.0 |
| gyrA | 9080 | c.1779G>C | synonymous_variant | 1.0 |
| gyrA | 9089 | c.1788G>C | synonymous_variant | 1.0 |
| gyrA | 9101 | c.1800A>G | synonymous_variant | 1.0 |
| gyrA | 9119 | c.1818A>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 | 9413 | c.2112G>A | synonymous_variant | 1.0 |
| gyrA | 9419 | c.2118T>C | synonymous_variant | 1.0 |
| gyrA | 9420 | p.Ile707Ala | missense_variant | 1.0 |
| gyrA | 9449 | c.2148C>G | synonymous_variant | 1.0 |
| gyrA | 9452 | c.2151G>C | synonymous_variant | 1.0 |
| gyrA | 9476 | c.2175G>C | synonymous_variant | 1.0 |
| gyrA | 9479 | c.2178G>T | synonymous_variant | 1.0 |
| gyrA | 9485 | c.2184A>C | synonymous_variant | 1.0 |
| gyrA | 9488 | c.2187G>C | synonymous_variant | 1.0 |
| gyrA | 9491 | c.2190C>T | synonymous_variant | 1.0 |
| gyrA | 9494 | c.2193T>C | synonymous_variant | 1.0 |
| gyrA | 9497 | c.2196G>C | synonymous_variant | 1.0 |
| gyrA | 9503 | c.2202T>C | synonymous_variant | 1.0 |
| gyrA | 9518 | c.2217A>G | synonymous_variant | 1.0 |
| gyrA | 9527 | c.2226A>G | synonymous_variant | 1.0 |
| gyrA | 9542 | c.2241T>C | synonymous_variant | 1.0 |
| gyrA | 9545 | c.2244A>G | synonymous_variant | 1.0 |
| gyrA | 9551 | c.2250G>A | synonymous_variant | 1.0 |
| gyrA | 9557 | c.2256G>C | synonymous_variant | 1.0 |
| gyrA | 9560 | c.2259C>G | synonymous_variant | 1.0 |
| gyrA | 9566 | c.2265C>T | 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 |
| gyrA | 9734 | c.2433A>T | synonymous_variant | 1.0 |
| fgd1 | 490809 | c.27A>G | synonymous_variant | 1.0 |
| fgd1 | 490818 | c.36C>T | synonymous_variant | 1.0 |
| fgd1 | 490830 | c.48A>C | 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 | 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 | 491203 | p.Gln141Glu | missense_variant | 1.0 |
| fgd1 | 491212 | p.Ser144Arg | missense_variant | 1.0 |
| fgd1 | 491232 | c.450T>C | synonymous_variant | 1.0 |
| fgd1 | 491241 | p.Asp153Glu | missense_variant | 1.0 |
| fgd1 | 491259 | c.477T>C | synonymous_variant | 1.0 |
| fgd1 | 491265 | c.483G>C | synonymous_variant | 1.0 |
| fgd1 | 491283 | p.Asp167Glu | missense_variant | 1.0 |
| fgd1 | 491286 | c.504G>C | synonymous_variant | 1.0 |
| fgd1 | 491295 | c.513C>G | synonymous_variant | 1.0 |
| fgd1 | 491298 | c.516C>G | synonymous_variant | 1.0 |
| fgd1 | 491316 | c.534C>T | synonymous_variant | 1.0 |
| fgd1 | 491331 | c.549G>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 | 575512 | c.165A>G | synonymous_variant | 1.0 |
| mshA | 575521 | c.174A>C | synonymous_variant | 1.0 |
| mshA | 575530 | c.183C>G | synonymous_variant | 1.0 |
| mshA | 575536 | c.189T>C | synonymous_variant | 1.0 |
| mshA | 575539 | c.192C>T | synonymous_variant | 1.0 |
| mshA | 575548 | c.201C>A | synonymous_variant | 1.0 |
| mshA | 575561 | p.Met72Val | missense_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 | 0.97 |
| 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 |
| mshA | 575902 | c.555C>T | synonymous_variant | 1.0 |
| mshA | 575908 | c.561A>G | synonymous_variant | 1.0 |
| mshA | 575920 | c.573C>T | synonymous_variant | 1.0 |
| mshA | 576469 | c.1122G>C | synonymous_variant | 1.0 |
| mshA | 576481 | c.1134C>G | synonymous_variant | 1.0 |
| mshA | 576490 | c.1143G>T | synonymous_variant | 1.0 |
| mshA | 576511 | c.1164C>G | synonymous_variant | 1.0 |
| mshA | 576517 | c.1170G>A | 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 | 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 | 0.93 |
| rpoB | 760059 | p.Tyr85Asp | missense_variant | 0.95 |
| 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 | 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 | 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 | 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 | 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 | 1.0 |
| rpoB | 762254 | c.2448T>G | synonymous_variant | 1.0 |
| rpoB | 762257 | c.2451C>G | synonymous_variant | 1.0 |
| rpoB | 762266 | c.2460T>C | synonymous_variant | 1.0 |
| rpoB | 762269 | c.2463G>A | synonymous_variant | 1.0 |
| rpoB | 762278 | c.2472C>G | synonymous_variant | 1.0 |
| rpoB | 762284 | c.2478G>C | synonymous_variant | 1.0 |
| rpoB | 762293 | c.2487T>C | synonymous_variant | 1.0 |
| rpoB | 762317 | c.2511A>G | synonymous_variant | 1.0 |
| rpoB | 762338 | c.2532T>C | synonymous_variant | 1.0 |
| rpoB | 762347 | c.2541T>C | synonymous_variant | 1.0 |
| rpoB | 762362 | p.Glu852Asp | missense_variant | 1.0 |
| rpoB | 762369 | c.2563_2565delTTGinsCTT | synonymous_variant | 0.93 |
| rpoC | 762374 | c.-996G>C | upstream_gene_variant | 0.94 |
| rpoC | 762380 | c.-990T>C | upstream_gene_variant | 1.0 |
| 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 | 0.96 |
| 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 | 763352 | c.-18T>A | 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 | 0.98 |
| 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 | 0.98 |
| 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 | 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 | 764948 | c.1579T>C | synonymous_variant | 1.0 |
| rpoC | 764968 | c.1599T>C | 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 | 765146 | p.Pro593Asp | missense_variant | 1.0 |
| rpoC | 765151 | c.1782G>C | synonymous_variant | 1.0 |
| rpoC | 765217 | c.1848C>G | synonymous_variant | 1.0 |
| rpoC | 765223 | c.1854G>C | synonymous_variant | 1.0 |
| rpoC | 765232 | c.1863G>C | synonymous_variant | 1.0 |
| rpoC | 765245 | c.1877_1878insGCT | disruptive_inframe_insertion | 1.0 |
| rpoC | 765249 | p.Leu627Ser | missense_variant | 1.0 |
| rpoC | 765250 | c.1882_1884delAGC | conservative_inframe_deletion | 1.0 |
| rpoC | 765287 | c.1918C>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 | 0.98 |
| 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 | 1.0 |
| 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 | 766043 | p.Gln892Gly | missense_variant | 1.0 |
| rpoC | 766255 | c.2886G>T | 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 | 0.98 |
| 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 | 801132 | c.324T>C | synonymous_variant | 1.0 |
| rplC | 801144 | c.336C>G | 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 | 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 | 801385 | c.577C>T | synonymous_variant | 1.0 |
| rplC | 801396 | c.588T>C | synonymous_variant | 1.0 |
| rplC | 801405 | c.597T>C | synonymous_variant | 1.0 |
| fbiC | 1303503 | c.573G>C | synonymous_variant | 1.0 |
| fbiC | 1303509 | c.579G>C | synonymous_variant | 0.94 |
| fbiC | 1303512 | c.582T>G | synonymous_variant | 1.0 |
| fbiC | 1303545 | c.615A>G | synonymous_variant | 1.0 |
| fbiC | 1303551 | c.621G>C | synonymous_variant | 1.0 |
| fbiC | 1303578 | c.648G>A | synonymous_variant | 1.0 |
| fbiC | 1303584 | c.654C>A | synonymous_variant | 1.0 |
| fbiC | 1303590 | c.660A>G | synonymous_variant | 1.0 |
| fbiC | 1303591 | c.661C>A | synonymous_variant | 1.0 |
| fbiC | 1303594 | c.664C>T | synonymous_variant | 1.0 |
| fbiC | 1303605 | c.675C>G | synonymous_variant | 1.0 |
| fbiC | 1303611 | c.681G>C | synonymous_variant | 1.0 |
| fbiC | 1303614 | c.684C>G | synonymous_variant | 1.0 |
| fbiC | 1303620 | c.690C>T | synonymous_variant | 1.0 |
| fbiC | 1303689 | c.759T>C | synonymous_variant | 1.0 |
| fbiC | 1303695 | c.765T>C | synonymous_variant | 1.0 |
| fbiC | 1303704 | c.774T>C | synonymous_variant | 1.0 |
| fbiC | 1303708 | c.778T>C | synonymous_variant | 1.0 |
| fbiC | 1303731 | c.801A>G | synonymous_variant | 1.0 |
| fbiC | 1303732 | p.Ser268Thr | missense_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 | 1304142 | c.1212G>C | synonymous_variant | 1.0 |
| fbiC | 1304163 | c.1233G>C | synonymous_variant | 1.0 |
| fbiC | 1304164 | p.Gly412Arg | missense_variant | 1.0 |
| fbiC | 1304172 | c.1242G>T | synonymous_variant | 1.0 |
| fbiC | 1304174 | p.Val415Ala | missense_variant | 1.0 |
| fbiC | 1304178 | c.1248G>C | synonymous_variant | 1.0 |
| fbiC | 1304181 | c.1251G>T | synonymous_variant | 1.0 |
| fbiC | 1304184 | c.1254G>C | synonymous_variant | 1.0 |
| fbiC | 1304200 | p.Leu424Phe | missense_variant | 1.0 |
| fbiC | 1304205 | c.1275C>G | synonymous_variant | 1.0 |
| fbiC | 1304208 | c.1278C>T | synonymous_variant | 1.0 |
| fbiC | 1304217 | p.Asn429Lys | missense_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 | 0.95 |
| 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 | 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 | 1305021 | c.2091C>G | synonymous_variant | 1.0 |
| fbiC | 1305027 | c.2097G>A | 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 |
| fbiC | 1305215 | p.Ser762Thr | missense_variant | 1.0 |
| fbiC | 1305219 | p.His763Gln | missense_variant | 1.0 |
| fbiC | 1305375 | c.2445C>G | synonymous_variant | 1.0 |
| fbiC | 1305393 | c.2463T>C | synonymous_variant | 1.0 |
| fbiC | 1305405 | c.2475A>T | synonymous_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 |
| atpE | 1461275 | c.231T>C | synonymous_variant | 1.0 |
| atpE | 1461278 | c.234A>G | 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 | 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 | 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 | 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 |
| 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 | 0.96 |
| 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 |
| fabG1 | 1673660 | p.Ala74Glu | missense_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 | 1673916 | c.-286A>T | upstream_gene_variant | 1.0 |
| inhA | 1673919 | c.-283G>C | upstream_gene_variant | 1.0 |
| inhA | 1673922 | c.-280T>C | upstream_gene_variant | 1.0 |
| inhA | 1673925 | c.-277C>G | 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 | 0.95 |
| 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 | 0.9 |
| 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 | 1674033 | c.-169T>C | upstream_gene_variant | 1.0 |
| fabG1 | 1674037 | p.Gln200Glu | missense_variant | 1.0 |
| inhA | 1674045 | c.-157G>A | upstream_gene_variant | 1.0 |
| inhA | 1674054 | c.-148T>C | upstream_gene_variant | 1.0 |
| inhA | 1674060 | c.-142A>G | upstream_gene_variant | 1.0 |
| fabG1 | 1674079 | p.Pro214Ala | missense_variant | 1.0 |
| inhA | 1674105 | c.-97C>T | upstream_gene_variant | 1.0 |
| inhA | 1674108 | c.-94C>T | upstream_gene_variant | 1.0 |
| inhA | 1674111 | c.-91G>A | upstream_gene_variant | 1.0 |
| inhA | 1674114 | c.-88T>G | upstream_gene_variant | 1.0 |
| inhA | 1674117 | c.-85C>G | upstream_gene_variant | 1.0 |
| inhA | 1674123 | c.-79T>C | upstream_gene_variant | 1.0 |
| inhA | 1674129 | c.-73C>T | upstream_gene_variant | 1.0 |
| inhA | 1674132 | c.-70T>C | upstream_gene_variant | 1.0 |
| inhA | 1674156 | c.-46C>T | upstream_gene_variant | 1.0 |
| inhA | 1674258 | c.57G>C | synonymous_variant | 1.0 |
| inhA | 1674273 | c.72C>T | synonymous_variant | 1.0 |
| inhA | 1674279 | c.78A>C | synonymous_variant | 1.0 |
| inhA | 1674285 | c.84A>G | synonymous_variant | 1.0 |
| inhA | 1674303 | c.102C>A | synonymous_variant | 1.0 |
| inhA | 1674315 | c.114C>G | synonymous_variant | 1.0 |
| inhA | 1674321 | c.120G>T | synonymous_variant | 1.0 |
| inhA | 1674331 | c.130C>T | synonymous_variant | 1.0 |
| inhA | 1674342 | c.141T>C | synonymous_variant | 1.0 |
| inhA | 1674348 | c.147C>G | synonymous_variant | 1.0 |
| inhA | 1674477 | c.276G>C | synonymous_variant | 1.0 |
| inhA | 1674480 | c.279T>C | synonymous_variant | 1.0 |
| inhA | 1674486 | c.285T>C | synonymous_variant | 1.0 |
| inhA | 1674489 | c.288G>C | synonymous_variant | 1.0 |
| inhA | 1674501 | c.300G>A | synonymous_variant | 1.0 |
| inhA | 1674503 | p.Thr101Ser | missense_variant | 1.0 |
| inhA | 1674513 | c.312C>G | synonymous_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 | 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 | 1674933 | c.732G>A | 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 | 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 | 1833694 | c.153G>T | 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 | 0.96 |
| rpsA | 1834148 | c.607C>T | synonymous_variant | 1.0 |
| rpsA | 1834174 | c.633C>T | 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>C | 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 | 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 | 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 | 1834810 | c.1269C>G | synonymous_variant | 1.0 |
| rpsA | 1834843 | c.1302G>A | synonymous_variant | 1.0 |
| rpsA | 1834846 | c.1305C>T | synonymous_variant | 1.0 |
| rpsA | 1834852 | c.1311C>G | synonymous_variant | 1.0 |
| tlyA | 1917929 | c.-11T>C | upstream_gene_variant | 1.0 |
| katG | 2155601 | p.Cys171Gly | missense_variant | 1.0 |
| katG | 2155614 | p.Val166Ile | missense_variant | 1.0 |
| katG | 2155617 | c.495T>C | synonymous_variant | 1.0 |
| katG | 2155632 | c.480A>C | synonymous_variant | 1.0 |
| katG | 2155637 | p.Leu159Ile | missense_variant | 0.95 |
| katG | 2155641 | p.Lys157Asn | missense_variant | 1.0 |
| katG | 2155649 | p.Tyr155His | missense_variant | 1.0 |
| katG | 2155680 | c.432G>C | synonymous_variant | 1.0 |
| katG | 2155691 | c.421T>C | synonymous_variant | 1.0 |
| katG | 2155704 | c.408C>G | 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 | 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 | 2518360 | c.246C>T | synonymous_variant | 1.0 |
| kasA | 2518393 | p.Gln93His | missense_variant | 1.0 |
| kasA | 2518396 | c.282A>C | synonymous_variant | 1.0 |
| kasA | 2518408 | c.294C>G | synonymous_variant | 1.0 |
| kasA | 2518417 | c.303G>C | synonymous_variant | 1.0 |
| kasA | 2518475 | c.361A>C | synonymous_variant | 1.0 |
| kasA | 2518480 | c.366T>C | synonymous_variant | 1.0 |
| kasA | 2518492 | c.378C>T | 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 | 2518645 | c.531G>C | synonymous_variant | 1.0 |
| kasA | 2518648 | c.534C>T | 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 | 2519251 | c.1137G>A | synonymous_variant | 1.0 |
| kasA | 2519260 | c.1146T>C | synonymous_variant | 1.0 |
| kasA | 2519266 | c.1152C>T | synonymous_variant | 1.0 |
| kasA | 2519272 | c.1158C>G | synonymous_variant | 1.0 |
| kasA | 2519281 | c.1167G>T | synonymous_variant | 1.0 |
| kasA | 2519347 | c.1233T>C | synonymous_variant | 1.0 |
| kasA | 2519359 | c.1245T>C | synonymous_variant | 1.0 |
| kasA | 2519364 | c.1250G>A | splice_region_variant&stop_retained_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 |
| folC | 2746728 | c.871T>C | synonymous_variant | 1.0 |
| folC | 2746744 | c.855T>G | synonymous_variant | 1.0 |
| folC | 2746747 | c.852G>C | synonymous_variant | 1.0 |
| folC | 2746753 | c.846C>G | synonymous_variant | 1.0 |
| folC | 2747086 | c.513A>C | synonymous_variant | 1.0 |
| folC | 2747089 | c.510G>C | synonymous_variant | 1.0 |
| folC | 2747107 | c.492G>C | synonymous_variant | 1.0 |
| folC | 2747110 | c.489T>C | synonymous_variant | 1.0 |
| folC | 2747113 | c.486C>G | synonymous_variant | 1.0 |
| folC | 2747116 | c.483G>C | synonymous_variant | 1.0 |
| folC | 2747221 | c.378G>A | synonymous_variant | 1.0 |
| folC | 2747230 | c.369C>G | synonymous_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 | 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 |
| 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 | 2860236 | c.183C>T | synonymous_variant | 1.0 |
| pepQ | 2860259 | c.160T>C | synonymous_variant | 1.0 |
| pepQ | 2860263 | c.156C>G | synonymous_variant | 1.0 |
| pepQ | 2860266 | p.Asp51Glu | missense_variant | 1.0 |
| pepQ | 2860272 | c.147G>A | synonymous_variant | 1.0 |
| pepQ | 2860275 | c.144T>C | synonymous_variant | 1.0 |
| pepQ | 2860293 | c.126A>G | 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 | 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 | 2860475 | c.-57C>T | upstream_gene_variant | 1.0 |
| pepQ | 2860476 | c.-58A>G | upstream_gene_variant | 1.0 |
| pepQ | 2860480 | c.-62G>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 |
| thyX | 3067247 | c.699C>A | synonymous_variant | 1.0 |
| thyX | 3067250 | c.696G>C | synonymous_variant | 1.0 |
| thyX | 3067277 | c.669C>A | synonymous_variant | 1.0 |
| thyX | 3067280 | p.Val222Ser | missense_variant | 1.0 |
| thyX | 3067284 | p.Ala221Asp | missense_variant | 1.0 |
| thyX | 3067292 | c.654G>A | synonymous_variant | 1.0 |
| thyX | 3067295 | c.651C>T | synonymous_variant | 1.0 |
| thyX | 3067304 | c.642A>G | synonymous_variant | 1.0 |
| thyX | 3067316 | c.630A>G | synonymous_variant | 1.0 |
| thyX | 3067325 | c.621A>G | synonymous_variant | 1.0 |
| thyX | 3067331 | c.615C>T | synonymous_variant | 1.0 |
| thyX | 3067355 | c.591A>C | synonymous_variant | 1.0 |
| thyX | 3067373 | c.573C>G | synonymous_variant | 1.0 |
| thyX | 3067391 | c.555G>C | synonymous_variant | 1.0 |
| thyX | 3067394 | c.552G>T | synonymous_variant | 1.0 |
| thyX | 3067406 | c.540A>G | synonymous_variant | 1.0 |
| thyX | 3067427 | c.519G>C | synonymous_variant | 1.0 |
| thyX | 3067430 | c.516C>T | synonymous_variant | 1.0 |
| thyX | 3067439 | c.507A>G | synonymous_variant | 1.0 |
| thyX | 3067445 | c.501C>A | synonymous_variant | 1.0 |
| thyX | 3067451 | c.495G>A | synonymous_variant | 1.0 |
| thyX | 3067457 | c.489C>G | synonymous_variant | 1.0 |
| thyX | 3067463 | p.Ile161Val | missense_variant | 1.0 |
| thyX | 3067466 | c.480G>C | synonymous_variant | 1.0 |
| thyX | 3067475 | c.471A>G | synonymous_variant | 1.0 |
| thyX | 3067493 | c.453A>G | synonymous_variant | 1.0 |
| thyX | 3067504 | p.Ala148Thr | missense_variant | 1.0 |
| thyX | 3067673 | c.273C>T | synonymous_variant | 1.0 |
| thyX | 3067721 | c.225T>C | synonymous_variant | 1.0 |
| thyX | 3067727 | c.219A>C | synonymous_variant | 1.0 |
| thyX | 3067742 | c.204A>T | synonymous_variant | 1.0 |
| thyX | 3067761 | p.Arg62Lys | missense_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 |
| thyX | 3067874 | c.72C>G | synonymous_variant | 1.0 |
| thyX | 3067886 | c.60A>G | 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 | 3074004 | c.468T>C | 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 | 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 |
| fbiD | 3339171 | c.54C>G | synonymous_variant | 1.0 |
| fbiD | 3339177 | c.60C>G | synonymous_variant | 1.0 |
| fbiD | 3339180 | c.63G>C | synonymous_variant | 1.0 |
| fbiD | 3339186 | c.69A>G | synonymous_variant | 1.0 |
| fbiD | 3339190 | c.73A>C | synonymous_variant | 1.0 |
| fbiD | 3339639 | c.522C>T | synonymous_variant | 1.0 |
| fbiD | 3339642 | c.525T>G | synonymous_variant | 1.0 |
| fbiA | 3640365 | c.-178C>G | upstream_gene_variant | 1.0 |
| fbiA | 3640392 | c.-151A>G | upstream_gene_variant | 1.0 |
| fbiA | 3640393 | c.-150A>C | upstream_gene_variant | 1.0 |
| fbiA | 3640394 | c.-149G>A | upstream_gene_variant | 1.0 |
| fbiA | 3640400 | c.-143G>C | upstream_gene_variant | 1.0 |
| fbiA | 3640402 | c.-141C>G | upstream_gene_variant | 1.0 |
| fbiA | 3640403 | c.-140G>C | upstream_gene_variant | 1.0 |
| fbiA | 3640413 | c.-130T>C | upstream_gene_variant | 1.0 |
| fbiA | 3640414 | c.-129G>A | upstream_gene_variant | 1.0 |
| fbiA | 3640416 | c.-127G>T | upstream_gene_variant | 1.0 |
| fbiA | 3640433 | c.-110T>C | upstream_gene_variant | 1.0 |
| fbiA | 3640442 | c.-101A>G | upstream_gene_variant | 1.0 |
| fbiA | 3640541 | c.-2A>G | upstream_gene_variant | 1.0 |
| fbiB | 3640560 | c.-975G>C | upstream_gene_variant | 1.0 |
| fbiA | 3640562 | p.Ala7Val | missense_variant | 1.0 |
| fbiB | 3640566 | c.-969T>G | upstream_gene_variant | 1.0 |
| fbiB | 3640587 | c.-948C>T | upstream_gene_variant | 1.0 |
| fbiB | 3640591 | c.-944_-942delCTCinsTTG | upstream_gene_variant | 1.0 |
| fbiB | 3640606 | c.-929C>T | 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 |
| fbiB | 3641900 | c.366G>C | synonymous_variant | 1.0 |
| fbiB | 3641909 | c.375T>C | synonymous_variant | 1.0 |
| fbiB | 3641924 | c.390A>G | synonymous_variant | 1.0 |
| fbiB | 3641925 | p.Thr131Ala | missense_variant | 1.0 |
| fbiB | 3641928 | c.394T>C | synonymous_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 |
| fbiB | 3641993 | c.459A>C | synonymous_variant | 1.0 |
| fbiB | 3642695 | c.1161G>C | synonymous_variant | 1.0 |
| fbiB | 3642701 | c.1167C>G | synonymous_variant | 1.0 |
| fbiB | 3642707 | c.1173C>T | synonymous_variant | 1.0 |
| alr | 3840213 | p.Arg403Leu | missense_variant | 1.0 |
| alr | 3840225 | p.Thr399Ser | missense_variant | 1.0 |
| alr | 3840230 | c.1191T>G | synonymous_variant | 1.0 |
| alr | 3840236 | c.1185A>G | synonymous_variant | 1.0 |
| alr | 3840242 | c.1179C>T | synonymous_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 | 3840317 | c.1104G>C | 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 |
| 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 | 3986933 | c.90C>A | synonymous_variant | 1.0 |
| ddn | 3986941 | p.Asp33Gly | missense_variant | 1.0 |
| ddn | 3986945 | c.102G>C | synonymous_variant | 1.0 |
| ddn | 3986951 | c.108T>C | synonymous_variant | 1.0 |
| ddn | 3986954 | c.111G>C | synonymous_variant | 1.0 |
| ddn | 3986957 | c.114C>T | synonymous_variant | 1.0 |
| ddn | 3986975 | c.132T>C | synonymous_variant | 1.0 |
| ddn | 3986984 | c.141G>T | synonymous_variant | 1.0 |
| ddn | 3987020 | c.177G>A | 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 | 3987065 | c.222T>C | synonymous_variant | 1.0 |
| ddn | 3987071 | c.228G>C | synonymous_variant | 1.0 |
| ddn | 3987089 | c.246G>C | synonymous_variant | 0.9 |
| ddn | 3987092 | p.Glu83Asp | missense_variant | 0.92 |
| ddn | 3987098 | c.255C>T | synonymous_variant | 0.92 |
| ddn | 3987138 | p.Gln99Ser | missense_variant | 0.91 |
| ddn | 3987143 | c.300A>G | synonymous_variant | 1.0 |
| panD | 4044189 | c.93C>T | synonymous_variant | 1.0 |
| panD | 4044195 | c.87T>C | synonymous_variant | 1.0 |
| panD | 4044210 | c.72C>G | synonymous_variant | 1.0 |
| panD | 4044219 | c.63C>T | synonymous_variant | 1.0 |
| panD | 4044224 | c.58C>T | synonymous_variant | 1.0 |
| panD | 4044228 | c.54C>G | synonymous_variant | 1.0 |
| panD | 4044243 | c.39C>G | synonymous_variant | 1.0 |
| panD | 4044246 | c.36C>T | synonymous_variant | 1.0 |
| embC | 4239671 | c.-192C>G | upstream_gene_variant | 1.0 |
| embC | 4239674 | c.-189C>G | upstream_gene_variant | 1.0 |
| embC | 4239680 | c.-183C>G | upstream_gene_variant | 1.0 |
| embC | 4240078 | c.216A>G | synonymous_variant | 1.0 |
| embC | 4240087 | c.225T>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 | 4240420 | c.558T>C | synonymous_variant | 1.0 |
| embC | 4240427 | p.Ser189Gly | missense_variant | 1.0 |
| embC | 4240441 | c.579C>T | synonymous_variant | 0.95 |
| embC | 4240444 | c.582C>G | synonymous_variant | 0.95 |
| embC | 4240471 | c.609C>T | synonymous_variant | 0.97 |
| embC | 4240475 | p.Ala205Ser | missense_variant | 0.97 |
| embC | 4240484 | p.Ala208Thr | missense_variant | 0.96 |
| embC | 4240489 | c.627A>G | synonymous_variant | 0.93 |
| embC | 4240495 | c.633T>C | synonymous_variant | 0.97 |
| 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 | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
| embC | 4240678 | c.816T>G | synonymous_variant | 0.93 |
| embC | 4240685 | p.Thr275Ala | missense_variant | 0.92 |
| embC | 4240693 | c.831T>C | synonymous_variant | 0.93 |
| embC | 4240699 | c.837C>A | synonymous_variant | 0.94 |
| embC | 4240717 | c.855T>C | synonymous_variant | 0.97 |
| embC | 4240726 | c.864G>C | synonymous_variant | 0.98 |
| embC | 4240741 | c.879C>T | synonymous_variant | 0.98 |
| 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 | 4240858 | c.996G>A | synonymous_variant | 1.0 |
| embC | 4240859 | p.Leu333Met | missense_variant | 1.0 |
| embC | 4240867 | c.1005T>G | synonymous_variant | 1.0 |
| embC | 4240870 | c.1008T>C | synonymous_variant | 1.0 |
| embC | 4240876 | c.1014C>T | synonymous_variant | 1.0 |
| embC | 4240879 | c.1017G>C | synonymous_variant | 0.96 |
| embC | 4240885 | c.1023T>C | synonymous_variant | 1.0 |
| embC | 4240886 | p.Ile342Val | missense_variant | 1.0 |
| embC | 4240897 | c.1035C>G | synonymous_variant | 1.0 |
| embC | 4240900 | c.1038A>G | synonymous_variant | 1.0 |
| embC | 4240987 | c.1125G>C | synonymous_variant | 1.0 |
| embC | 4240990 | c.1128A>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 | 4241161 | c.1299C>G | synonymous_variant | 1.0 |
| embC | 4241162 | c.1300T>C | synonymous_variant | 1.0 |
| embC | 4241167 | c.1305C>G | synonymous_variant | 1.0 |
| embC | 4241185 | c.1323G>C | synonymous_variant | 1.0 |
| embC | 4241197 | c.1335G>C | synonymous_variant | 1.0 |
| embC | 4241230 | c.1368A>G | synonymous_variant | 1.0 |
| embC | 4241380 | c.1518A>C | synonymous_variant | 1.0 |
| embC | 4241383 | c.1521G>C | synonymous_variant | 0.76 |
| embC | 4241386 | c.1524C>G | synonymous_variant | 1.0 |
| embC | 4241392 | c.1530G>C | synonymous_variant | 1.0 |
| embC | 4241401 | c.1539C>T | synonymous_variant | 1.0 |
| embC | 4241416 | c.1554C>A | synonymous_variant | 1.0 |
| embC | 4241449 | c.1587C>G | synonymous_variant | 1.0 |
| embC | 4241453 | p.Ile531Val | missense_variant | 1.0 |
| embC | 4241614 | c.1752A>G | synonymous_variant | 1.0 |
| embC | 4241617 | c.1755G>A | 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 | 4242067 | c.2205G>C | synonymous_variant | 1.0 |
| embC | 4242070 | c.2208T>C | synonymous_variant | 1.0 |
| embC | 4242079 | c.2217T>C | synonymous_variant | 1.0 |
| embC | 4242085 | c.2223A>G | synonymous_variant | 1.0 |
| embC | 4242088 | c.2226G>A | synonymous_variant | 1.0 |
| embC | 4242092 | p.Leu744Val | missense_variant | 1.0 |
| embC | 4242095 | p.Ala745Thr | missense_variant | 1.0 |
| embC | 4242106 | c.2244C>G | synonymous_variant | 1.0 |
| embC | 4242127 | c.2265G>A | synonymous_variant | 1.0 |
| embC | 4242128 | c.2266C>T | synonymous_variant | 1.0 |
| embC | 4242139 | c.2277G>C | synonymous_variant | 1.0 |
| embA | 4242748 | c.-485A>G | upstream_gene_variant | 1.0 |
| embC | 4242764 | p.Val968Leu | missense_variant | 1.0 |
| embA | 4242773 | c.-460_-458delCTGinsTTA | upstream_gene_variant | 1.0 |
| embC | 4242779 | p.Asn973Asp | missense_variant | 1.0 |
| embC | 4242791 | p.Ala977Ser | missense_variant | 1.0 |
| embC | 4242794 | p.Ala978Lys | missense_variant | 1.0 |
| embA | 4242823 | c.-410G>C | upstream_gene_variant | 1.0 |
| embA | 4242838 | c.-395C>G | upstream_gene_variant | 1.0 |
| embA | 4242844 | c.-389A>G | upstream_gene_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 | 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 | 4243334 | c.102T>G | synonymous_variant | 1.0 |
| embA | 4244132 | c.900G>C | synonymous_variant | 1.0 |
| embA | 4244165 | c.933T>G | synonymous_variant | 1.0 |
| embA | 4244170 | p.Gln313Arg | missense_variant | 1.0 |
| embA | 4244178 | p.Ala316Ser | missense_variant | 1.0 |
| embA | 4244198 | c.966C>A | synonymous_variant | 1.0 |
| embA | 4244207 | c.975C>G | synonymous_variant | 1.0 |
| embA | 4244213 | c.981C>G | synonymous_variant | 1.0 |
| embA | 4244219 | c.987C>G | synonymous_variant | 1.0 |
| embA | 4244327 | c.1095T>C | synonymous_variant | 1.0 |
| embA | 4244340 | p.Ser370Ala | missense_variant | 1.0 |
| embA | 4244345 | c.1113C>G | synonymous_variant | 1.0 |
| embA | 4244372 | c.1140T>A | synonymous_variant | 1.0 |
| embA | 4244390 | c.1158G>A | synonymous_variant | 1.0 |
| embA | 4244396 | c.1164T>C | synonymous_variant | 1.0 |
| embA | 4244408 | c.1176G>C | 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 | 4244802 | p.Leu524Met | missense_variant | 0.73 |
| embA | 4244805 | c.1573C>T | synonymous_variant | 0.62 |
| embA | 4244822 | c.1590G>A | synonymous_variant | 1.0 |
| embA | 4244823 | p.Val531Met | missense_variant | 1.0 |
| embA | 4244856 | p.Ala542Pro | missense_variant | 1.0 |
| embA | 4244885 | c.1653A>G | synonymous_variant | 1.0 |
| embA | 4244897 | c.1665T>G | synonymous_variant | 1.0 |
| embA | 4244903 | c.1671G>C | synonymous_variant | 1.0 |
| embA | 4244919 | c.1687_1689delCTCinsTTG | synonymous_variant | 1.0 |
| embA | 4245047 | c.1815G>C | synonymous_variant | 1.0 |
| embA | 4245051 | p.Val607Ile | missense_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 | 4245182 | c.1950T>C | synonymous_variant | 1.0 |
| embA | 4245186 | p.Thr652Ala | missense_variant | 1.0 |
| embA | 4245194 | c.1962G>A | synonymous_variant | 1.0 |
| embA | 4245195 | p.Ile655Val | missense_variant | 1.0 |
| embA | 4245200 | c.1968C>G | synonymous_variant | 1.0 |
| embA | 4245206 | c.1974A>C | synonymous_variant | 1.0 |
| embA | 4245207 | c.1975T>C | 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 | 4245285 | c.2053T>C | synonymous_variant | 1.0 |
| embA | 4245311 | c.2079C>T | synonymous_variant | 1.0 |
| embA | 4245345 | p.Met705Leu | missense_variant | 1.0 |
| embA | 4245355 | p.Ala708Gly | missense_variant | 1.0 |
| embA | 4245368 | c.2136T>C | synonymous_variant | 1.0 |
| embA | 4245375 | p.Leu715Met | missense_variant | 1.0 |
| embA | 4245402 | p.Thr724Ala | missense_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 | 4245566 | c.-948C>T | upstream_gene_variant | 1.0 |
| embB | 4245575 | c.-939C>G | upstream_gene_variant | 1.0 |
| embB | 4245594 | c.-920_-919delTCinsAG | upstream_gene_variant | 1.0 |
| embB | 4245602 | c.-912C>A | upstream_gene_variant | 1.0 |
| embB | 4245605 | c.-909G>A | upstream_gene_variant | 1.0 |
| embA | 4245606 | p.Leu792Val | missense_variant | 1.0 |
| embB | 4245620 | c.-894T>C | upstream_gene_variant | 1.0 |
| embB | 4245623 | c.-891G>A | 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 | 4245725 | c.-789A>G | upstream_gene_variant | 1.0 |
| embB | 4245726 | c.-788T>C | upstream_gene_variant | 1.0 |
| embB | 4245734 | c.-780G>C | upstream_gene_variant | 1.0 |
| embB | 4245737 | c.-777A>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 |
| 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 | 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 | 0.95 |
| 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 | 4246172 | c.-342C>T | upstream_gene_variant | 1.0 |
| embB | 4246184 | c.-330A>C | upstream_gene_variant | 1.0 |
| embB | 4246205 | c.-309A>G | upstream_gene_variant | 1.0 |
| embB | 4246211 | c.-303T>C | upstream_gene_variant | 1.0 |
| embB | 4246217 | c.-297G>A | upstream_gene_variant | 1.0 |
| embB | 4246220 | c.-294T>C | upstream_gene_variant | 1.0 |
| embB | 4246223 | c.-291C>T | upstream_gene_variant | 1.0 |
| embA | 4246227 | p.Ile999Val | missense_variant | 1.0 |
| embB | 4246235 | c.-279G>A | upstream_gene_variant | 1.0 |
| embB | 4246244 | c.-270G>A | 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 | 4246748 | p.Phe79Leu | missense_variant | 1.0 |
| embB | 4246762 | c.249G>T | synonymous_variant | 1.0 |
| embB | 4246768 | c.255C>T | synonymous_variant | 1.0 |
| embB | 4246771 | p.Asp86Glu | missense_variant | 1.0 |
| embB | 4246782 | p.Ala90Gly | missense_variant | 1.0 |
| embB | 4246784 | p.Met91Leu | missense_variant | 1.0 |
| embB | 4246789 | c.276A>G | synonymous_variant | 1.0 |
| embB | 4246792 | c.279C>G | synonymous_variant | 1.0 |
| embB | 4246793 | p.Ala94Gln | missense_variant | 1.0 |
| embB | 4246828 | c.315A>G | synonymous_variant | 1.0 |
| embB | 4246843 | c.330T>C | synonymous_variant | 1.0 |
| embB | 4246844 | c.331T>C | synonymous_variant | 1.0 |
| embB | 4246853 | p.Leu114Met | missense_variant | 1.0 |
| embB | 4246871 | p.Ala120Ser | missense_variant | 1.0 |
| embB | 4246879 | c.366C>G | synonymous_variant | 1.0 |
| embB | 4246882 | c.369G>C | synonymous_variant | 1.0 |
| embB | 4246894 | c.381C>T | synonymous_variant | 1.0 |
| embB | 4247062 | c.549G>C | synonymous_variant | 1.0 |
| embB | 4247089 | c.576G>C | synonymous_variant | 1.0 |
| embB | 4247095 | c.582G>A | synonymous_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 | 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 | 0.97 |
| embB | 4247555 | p.Leu348Ile | missense_variant | 0.97 |
| 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 | 4248001 | c.1488C>T | 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 | 0.97 |
| 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 | 0.98 |
| 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 | 4248349 | c.1836G>A | synonymous_variant | 1.0 |
| embB | 4248358 | c.1845C>G | synonymous_variant | 0.97 |
| 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 | 1.0 |
| 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 | 4248660 | p.Ala716Val | missense_variant | 1.0 |
| embB | 4248670 | c.2157C>T | synonymous_variant | 1.0 |
| embB | 4248676 | c.2163C>G | synonymous_variant | 1.0 |
| embB | 4248682 | c.2169G>C | synonymous_variant | 1.0 |
| embB | 4248697 | c.2184A>C | synonymous_variant | 1.0 |
| embB | 4248706 | c.2193G>C | synonymous_variant | 1.0 |
| embB | 4248731 | p.Val740Leu | missense_variant | 1.0 |
| embB | 4248742 | c.2229T>C | synonymous_variant | 1.0 |
| embB | 4248757 | c.2244A>C | synonymous_variant | 1.0 |
| embB | 4248907 | c.2394G>C | synonymous_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 | 4249693 | c.3180T>C | synonymous_variant | 1.0 |
| embB | 4249699 | c.3186T>A | synonymous_variant | 1.0 |
| embB | 4249702 | c.3189C>A | synonymous_variant | 1.0 |
| embB | 4249703 | c.3190C>T | synonymous_variant | 1.0 |
| embB | 4249711 | c.3198G>A | synonymous_variant | 1.0 |
| embB | 4249735 | c.3222T>G | synonymous_variant | 1.0 |
| embB | 4249741 | c.3228C>A | synonymous_variant | 1.0 |
| embB | 4249744 | c.3231G>A | synonymous_variant | 1.0 |
| embB | 4249750 | p.Glu1079Asp | missense_variant | 1.0 |
| embB | 4249751 | c.3238T>C | synonymous_variant | 1.0 |
| embB | 4249774 | c.3261C>A | synonymous_variant | 1.0 |
| embB | 4249775 | c.3262C>T | synonymous_variant | 1.0 |
| ubiA | 4268952 | c.882G>A | synonymous_variant | 1.0 |
| ubiA | 4268956 | p.Ala293Gly | missense_variant | 1.0 |
| ubiA | 4268978 | c.856C>T | synonymous_variant | 1.0 |
| ubiA | 4268994 | c.840T>C | synonymous_variant | 1.0 |
| ubiA | 4269000 | c.834G>A | synonymous_variant | 1.0 |
| ubiA | 4269006 | c.828T>C | synonymous_variant | 1.0 |
| ubiA | 4269012 | c.822G>C | synonymous_variant | 1.0 |
| ubiA | 4269027 | c.807C>G | synonymous_variant | 1.0 |
| ubiA | 4269030 | c.804C>G | synonymous_variant | 1.0 |
| ubiA | 4269033 | c.801T>C | synonymous_variant | 1.0 |
| ubiA | 4269045 | c.789G>C | synonymous_variant | 1.0 |
| ubiA | 4269162 | c.670_672delTTGinsCTC | synonymous_variant | 1.0 |
| ubiA | 4269177 | c.657G>A | synonymous_variant | 1.0 |
| ubiA | 4269180 | c.654G>T | synonymous_variant | 1.0 |
| ubiA | 4269195 | c.639C>T | synonymous_variant | 1.0 |
| ubiA | 4269216 | c.618C>T | synonymous_variant | 1.0 |
| ubiA | 4269222 | c.612T>G | synonymous_variant | 1.0 |
| ubiA | 4269225 | c.609C>T | synonymous_variant | 0.96 |
| ubiA | 4269231 | c.603C>T | synonymous_variant | 1.0 |
| ubiA | 4269234 | c.600A>G | synonymous_variant | 1.0 |
| ubiA | 4269243 | p.His197Gln | missense_variant | 1.0 |
| ubiA | 4269248 | c.586C>T | synonymous_variant | 1.0 |
| ubiA | 4269261 | c.573G>A | synonymous_variant | 1.0 |
| ubiA | 4269285 | c.549T>G | synonymous_variant | 1.0 |
| ubiA | 4269337 | p.Val166Ala | missense_variant | 1.0 |
| ubiA | 4269342 | c.492G>C | synonymous_variant | 1.0 |
| ubiA | 4269620 | p.Val72Ile | missense_variant | 1.0 |
| ubiA | 4269621 | c.213C>G | synonymous_variant | 1.0 |
| ubiA | 4269627 | p.Val69Ile | missense_variant | 1.0 |
| ubiA | 4269723 | c.111G>C | synonymous_variant | 1.0 |
| ubiA | 4269744 | c.90G>C | synonymous_variant | 1.0 |
| ubiA | 4269762 | c.72C>G | synonymous_variant | 1.0 |
| ubiA | 4269771 | p.Ile21Met | missense_variant | 1.0 |
| ethA | 4326298 | c.1176G>A | synonymous_variant | 1.0 |
| ethA | 4326304 | c.1170C>G | synonymous_variant | 1.0 |
| ethA | 4326322 | c.1152T>C | synonymous_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 | 4326346 | c.1128C>G | synonymous_variant | 1.0 |
| ethA | 4326352 | c.1122T>G | synonymous_variant | 1.0 |
| ethA | 4326380 | p.Thr365Lys | missense_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 | 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 |
| 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 | 0.93 |
| ethA | 4327356 | p.Ser40Ala | missense_variant | 1.0 |
| ethA | 4327357 | p.Glu39Ser | missense_variant | 1.0 |
| ethR | 4327390 | c.-159C>G | upstream_gene_variant | 1.0 |
| ethR | 4327396 | c.-153A>G | upstream_gene_variant | 1.0 |
| ethR | 4327408 | c.-141G>A | upstream_gene_variant | 1.0 |
| ethA | 4327695 | c.-222A>G | upstream_gene_variant | 1.0 |
| ethA | 4327707 | c.-234G>C | upstream_gene_variant | 1.0 |
| ethA | 4327710 | c.-237G>T | upstream_gene_variant | 1.0 |
| ethA | 4327713 | c.-240A>T | upstream_gene_variant | 1.0 |
| ethA | 4327716 | c.-243G>T | upstream_gene_variant | 1.0 |
| ethA | 4327720 | c.-247T>G | upstream_gene_variant | 1.0 |
| ethA | 4327765 | c.-292G>A | upstream_gene_variant | 1.0 |
| ethA | 4327770 | c.-297G>C | upstream_gene_variant | 1.0 |
| fgd1 | 473863 | c.-16919_*15366del | transcript_ablation | 1.0 |
