Run ID: SRR6046611
Sample name:
Date: 04-04-2023 12:20:10
Number of reads: 103839
Percentage reads mapped: 8.06
Strain: lineage4.9
Drug-resistance: HR-TB
| Drug | Resistance | Supporting mutations |
|---|
| Lineage | Family | Main Spoligotype | RDs | Frequency |
|---|---|---|---|---|
| lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
| lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 0.99 |
| Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
|---|---|---|---|---|---|
| katG | 2155690 | c.421_422insGT | frameshift_variant | 1.0 | isoniazid |
| Gene | Chromosome position | Mutation | Type | Estimated fraction |
|---|---|---|---|---|
| gyrB | 6086 | p.Thr283Glu | missense_variant | 1.0 |
| gyrB | 6091 | c.852G>C | 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 | 6130 | c.891T>C | synonymous_variant | 1.0 |
| gyrB | 6169 | c.930C>G | synonymous_variant | 1.0 |
| gyrB | 6181 | c.942C>T | synonymous_variant | 1.0 |
| gyrB | 6184 | c.945C>G | synonymous_variant | 1.0 |
| gyrB | 6193 | c.954G>A | synonymous_variant | 1.0 |
| gyrB | 6196 | c.957C>A | synonymous_variant | 1.0 |
| gyrB | 6202 | c.963C>T | synonymous_variant | 1.0 |
| gyrB | 6203 | p.Ser322Ala | missense_variant | 1.0 |
| gyrB | 6211 | c.972G>C | synonymous_variant | 1.0 |
| gyrB | 6215 | p.Ser326Thr | missense_variant | 1.0 |
| gyrB | 6223 | c.984G>C | synonymous_variant | 1.0 |
| gyrB | 6241 | p.Asp334Glu | missense_variant | 1.0 |
| gyrB | 6242 | p.Arg335Lys | missense_variant | 1.0 |
| gyrB | 6250 | c.1011A>T | synonymous_variant | 1.0 |
| gyrB | 6253 | c.1014G>C | synonymous_variant | 1.0 |
| gyrB | 6259 | p.Asp340Glu | missense_variant | 1.0 |
| gyrB | 6266 | p.Pro343Thr | missense_variant | 1.0 |
| gyrB | 6274 | c.1035C>T | synonymous_variant | 1.0 |
| gyrB | 6277 | c.1038C>G | synonymous_variant | 1.0 |
| gyrB | 6286 | c.1047T>C | synonymous_variant | 1.0 |
| gyrB | 6289 | c.1050C>T | synonymous_variant | 1.0 |
| gyrB | 6292 | c.1053G>T | synonymous_variant | 1.0 |
| gyrB | 6295 | c.1056A>G | synonymous_variant | 1.0 |
| gyrB | 6299 | c.1060C>T | synonymous_variant | 1.0 |
| gyrA | 6307 | c.-995T>G | upstream_gene_variant | 1.0 |
| gyrB | 6326 | p.Ser363Gly | missense_variant | 1.0 |
| gyrA | 6331 | c.-971A>G | upstream_gene_variant | 1.0 |
| gyrA | 6352 | c.-950C>G | upstream_gene_variant | 1.0 |
| gyrA | 6362 | c.-940T>C | upstream_gene_variant | 1.0 |
| gyrA | 6382 | c.-920A>G | upstream_gene_variant | 1.0 |
| gyrA | 6400 | c.-902C>G | upstream_gene_variant | 1.0 |
| gyrA | 6409 | c.-893A>G | upstream_gene_variant | 1.0 |
| gyrA | 6541 | c.-761C>T | upstream_gene_variant | 1.0 |
| gyrA | 6550 | c.-752A>G | upstream_gene_variant | 1.0 |
| gyrA | 6551 | c.-751T>C | upstream_gene_variant | 1.0 |
| gyrA | 6571 | c.-731T>C | upstream_gene_variant | 1.0 |
| gyrA | 6577 | c.-725T>C | upstream_gene_variant | 1.0 |
| gyrA | 6580 | c.-722C>G | upstream_gene_variant | 1.0 |
| gyrA | 6583 | c.-719G>C | upstream_gene_variant | 1.0 |
| gyrB | 6590 | p.Arg451Ser | missense_variant | 1.0 |
| gyrA | 6610 | c.-692C>G | upstream_gene_variant | 1.0 |
| gyrA | 6613 | c.-689A>G | upstream_gene_variant | 1.0 |
| gyrA | 6616 | c.-686A>G | upstream_gene_variant | 1.0 |
| gyrA | 6628 | c.-674C>T | upstream_gene_variant | 1.0 |
| gyrA | 6631 | c.-671C>T | upstream_gene_variant | 1.0 |
| gyrA | 6637 | c.-665T>G | upstream_gene_variant | 1.0 |
| gyrA | 6640 | c.-662A>C | upstream_gene_variant | 1.0 |
| gyrA | 6643 | c.-659A>G | upstream_gene_variant | 1.0 |
| gyrA | 6646 | c.-656C>T | upstream_gene_variant | 1.0 |
| gyrA | 6649 | c.-653T>C | upstream_gene_variant | 1.0 |
| gyrA | 6655 | c.-647T>C | upstream_gene_variant | 1.0 |
| gyrA | 6670 | c.-632G>A | upstream_gene_variant | 1.0 |
| gyrA | 6673 | c.-629A>C | upstream_gene_variant | 1.0 |
| gyrA | 6676 | c.-626T>G | upstream_gene_variant | 1.0 |
| gyrA | 6685 | c.-617C>A | 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 | 6706 | c.-596G>A | upstream_gene_variant | 1.0 |
| gyrA | 6709 | c.-593A>G | upstream_gene_variant | 1.0 |
| gyrA | 6715 | c.-587C>T | upstream_gene_variant | 1.0 |
| gyrA | 6727 | c.-575G>T | upstream_gene_variant | 1.0 |
| gyrA | 6728 | c.-574_-572delCTAinsTTG | upstream_gene_variant | 1.0 |
| gyrA | 6739 | c.-563C>G | upstream_gene_variant | 1.0 |
| gyrA | 6745 | c.-557T>C | upstream_gene_variant | 1.0 |
| gyrA | 6751 | c.-551G>C | upstream_gene_variant | 1.0 |
| gyrA | 6775 | c.-527G>A | upstream_gene_variant | 1.0 |
| gyrA | 6778 | c.-524C>T | upstream_gene_variant | 1.0 |
| gyrA | 6793 | c.-509T>C | upstream_gene_variant | 1.0 |
| gyrB | 6794 | p.Ile519Leu | missense_variant | 1.0 |
| gyrB | 6798 | p.Gly520Ala | missense_variant | 1.0 |
| gyrA | 6811 | c.-491C>T | upstream_gene_variant | 1.0 |
| gyrA | 6841 | c.-461T>C | upstream_gene_variant | 1.0 |
| gyrA | 6853 | c.-449A>G | upstream_gene_variant | 1.0 |
| gyrA | 6856 | c.-446T>C | upstream_gene_variant | 1.0 |
| gyrA | 6859 | c.-443T>C | upstream_gene_variant | 1.0 |
| gyrA | 6862 | c.-440C>G | upstream_gene_variant | 1.0 |
| gyrA | 6866 | c.-436C>T | upstream_gene_variant | 1.0 |
| gyrA | 6878 | c.-424T>C | upstream_gene_variant | 1.0 |
| gyrA | 6881 | c.-421T>C | upstream_gene_variant | 1.0 |
| gyrA | 6898 | c.-404G>C | upstream_gene_variant | 1.0 |
| gyrB | 6905 | p.Ile556Val | missense_variant | 1.0 |
| gyrB | 6911 | p.Asn558His | missense_variant | 1.0 |
| gyrA | 6916 | c.-386G>C | upstream_gene_variant | 1.0 |
| gyrA | 6919 | c.-383T>C | upstream_gene_variant | 1.0 |
| gyrB | 6920 | p.Val561Ile | missense_variant | 1.0 |
| gyrA | 6925 | c.-377T>C | upstream_gene_variant | 1.0 |
| gyrA | 6931 | c.-371A>G | upstream_gene_variant | 1.0 |
| gyrA | 6934 | c.-368A>G | upstream_gene_variant | 1.0 |
| gyrA | 6949 | c.-353A>G | upstream_gene_variant | 1.0 |
| gyrA | 6964 | c.-338C>T | upstream_gene_variant | 1.0 |
| gyrB | 6968 | p.Asp577Gln | missense_variant | 1.0 |
| gyrA | 6976 | c.-326A>G | upstream_gene_variant | 1.0 |
| gyrA | 6982 | c.-320A>C | upstream_gene_variant | 1.0 |
| gyrA | 6988 | c.-314C>G | upstream_gene_variant | 1.0 |
| gyrA | 6994 | c.-308C>T | upstream_gene_variant | 1.0 |
| gyrA | 7003 | c.-299C>T | upstream_gene_variant | 1.0 |
| gyrA | 7006 | c.-296T>G | upstream_gene_variant | 1.0 |
| gyrA | 7007 | c.-295C>T | upstream_gene_variant | 1.0 |
| gyrB | 7010 | p.Leu591Met | missense_variant | 1.0 |
| gyrA | 7015 | c.-287G>A | upstream_gene_variant | 1.0 |
| gyrA | 7018 | c.-284G>C | upstream_gene_variant | 1.0 |
| gyrA | 7024 | c.-278G>C | upstream_gene_variant | 1.0 |
| gyrA | 7033 | c.-269G>T | upstream_gene_variant | 1.0 |
| gyrB | 7051 | p.Glu604Asp | missense_variant | 1.0 |
| gyrA | 7060 | c.-242T>C | upstream_gene_variant | 1.0 |
| gyrA | 7066 | c.-236G>C | upstream_gene_variant | 1.0 |
| gyrA | 7078 | c.-224A>G | upstream_gene_variant | 1.0 |
| gyrA | 7081 | c.-221T>C | upstream_gene_variant | 1.0 |
| gyrA | 7084 | c.-218A>G | upstream_gene_variant | 1.0 |
| gyrA | 7093 | c.-209T>G | upstream_gene_variant | 1.0 |
| gyrA | 7099 | c.-203G>A | upstream_gene_variant | 1.0 |
| gyrA | 7100 | c.-202T>C | upstream_gene_variant | 1.0 |
| gyrA | 7123 | c.-179C>G | upstream_gene_variant | 1.0 |
| gyrA | 7129 | c.-173T>C | upstream_gene_variant | 1.0 |
| gyrA | 7141 | c.-161T>C | upstream_gene_variant | 1.0 |
| gyrA | 7144 | c.-158A>G | upstream_gene_variant | 1.0 |
| gyrA | 7150 | c.-152G>T | upstream_gene_variant | 1.0 |
| gyrA | 7153 | c.-149G>C | upstream_gene_variant | 1.0 |
| gyrA | 7159 | c.-143C>T | upstream_gene_variant | 1.0 |
| gyrA | 7168 | c.-134C>G | upstream_gene_variant | 1.0 |
| gyrA | 7174 | c.-128C>T | upstream_gene_variant | 1.0 |
| gyrA | 7186 | c.-116C>G | upstream_gene_variant | 1.0 |
| gyrA | 7189 | c.-113C>T | upstream_gene_variant | 1.0 |
| gyrA | 7207 | c.-95C>G | upstream_gene_variant | 1.0 |
| gyrB | 7210 | p.Asp657Glu | missense_variant | 1.0 |
| gyrA | 7216 | c.-86G>T | upstream_gene_variant | 1.0 |
| gyrA | 7225 | c.-77T>C | upstream_gene_variant | 1.0 |
| gyrA | 7234 | c.-68C>A | upstream_gene_variant | 1.0 |
| gyrA | 7391 | c.90C>T | synonymous_variant | 1.0 |
| gyrA | 7394 | c.93T>C | synonymous_variant | 1.0 |
| gyrA | 7397 | c.96G>C | synonymous_variant | 1.0 |
| gyrA | 7412 | c.111C>G | synonymous_variant | 1.0 |
| gyrA | 7421 | c.120G>C | synonymous_variant | 1.0 |
| gyrA | 7424 | c.123G>C | synonymous_variant | 1.0 |
| gyrA | 7427 | c.126G>C | synonymous_variant | 1.0 |
| gyrA | 7430 | c.129G>A | synonymous_variant | 1.0 |
| gyrA | 7433 | c.132G>T | synonymous_variant | 1.0 |
| gyrA | 7442 | c.141G>C | synonymous_variant | 1.0 |
| gyrA | 7451 | c.150C>G | synonymous_variant | 1.0 |
| gyrA | 7457 | c.156T>C | synonymous_variant | 1.0 |
| gyrA | 7463 | c.162G>C | synonymous_variant | 1.0 |
| gyrA | 7466 | c.165G>C | synonymous_variant | 1.0 |
| gyrA | 7469 | c.168C>A | synonymous_variant | 1.0 |
| gyrA | 7472 | c.171T>C | synonymous_variant | 1.0 |
| gyrA | 7475 | c.174A>G | synonymous_variant | 1.0 |
| gyrA | 7480 | p.Phe60Tyr | missense_variant | 1.0 |
| gyrA | 7484 | c.183T>C | synonymous_variant | 1.0 |
| gyrA | 7499 | c.198G>C | synonymous_variant | 1.0 |
| gyrA | 7502 | c.201C>T | synonymous_variant | 1.0 |
| gyrA | 7523 | c.222C>G | synonymous_variant | 1.0 |
| gyrA | 7526 | c.225G>T | synonymous_variant | 1.0 |
| gyrA | 7532 | c.231T>C | synonymous_variant | 1.0 |
| gyrA | 7547 | c.246C>T | synonymous_variant | 1.0 |
| gyrA | 7553 | c.252C>T | synonymous_variant | 1.0 |
| gyrA | 7559 | c.258G>A | synonymous_variant | 1.0 |
| gyrA | 7569 | p.Ala90Ser | missense_variant | 1.0 |
| gyrA | 7574 | c.273G>T | synonymous_variant | 1.0 |
| gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
| gyrA | 7592 | c.291G>C | synonymous_variant | 1.0 |
| gyrA | 7601 | c.300C>A | synonymous_variant | 1.0 |
| gyrA | 7622 | c.321C>T | synonymous_variant | 1.0 |
| gyrA | 7637 | c.336C>G | synonymous_variant | 1.0 |
| gyrA | 7649 | c.348C>T | synonymous_variant | 1.0 |
| gyrA | 7652 | c.351C>T | synonymous_variant | 1.0 |
| gyrA | 7658 | c.357A>G | synonymous_variant | 1.0 |
| gyrA | 7661 | c.360C>T | synonymous_variant | 1.0 |
| gyrA | 7664 | c.363T>C | synonymous_variant | 1.0 |
| gyrA | 7670 | c.369A>C | synonymous_variant | 1.0 |
| gyrA | 7671 | p.Pro124Ala | missense_variant | 1.0 |
| gyrA | 7676 | c.375G>C | synonymous_variant | 1.0 |
| gyrA | 7679 | c.378G>C | synonymous_variant | 1.0 |
| gyrA | 7683 | c.382_384delAGGinsCGT | synonymous_variant | 1.0 |
| gyrA | 7694 | c.393A>G | synonymous_variant | 1.0 |
| gyrA | 7703 | c.402G>T | synonymous_variant | 1.0 |
| gyrA | 7709 | c.408G>C | synonymous_variant | 1.0 |
| gyrA | 7710 | c.409T>C | synonymous_variant | 1.0 |
| gyrA | 7715 | c.414G>C | synonymous_variant | 1.0 |
| gyrA | 7728 | c.427_429delAGGinsCGT | synonymous_variant | 1.0 |
| gyrA | 7759 | p.Ile153Ser | missense_variant | 1.0 |
| gyrA | 7763 | c.462T>C | synonymous_variant | 1.0 |
| gyrA | 7778 | c.477G>T | synonymous_variant | 1.0 |
| gyrA | 7781 | c.480G>C | synonymous_variant | 1.0 |
| gyrA | 7782 | p.Gln161Met | missense_variant | 1.0 |
| gyrA | 7793 | c.492G>C | synonymous_variant | 1.0 |
| gyrA | 7799 | c.498A>G | synonymous_variant | 1.0 |
| gyrA | 7814 | c.513C>G | synonymous_variant | 1.0 |
| gyrA | 7817 | c.516C>T | synonymous_variant | 1.0 |
| gyrA | 7832 | c.531G>C | synonymous_variant | 1.0 |
| gyrA | 7835 | c.534A>G | synonymous_variant | 1.0 |
| gyrA | 7841 | c.540C>T | synonymous_variant | 1.0 |
| gyrA | 7847 | c.546G>C | synonymous_variant | 1.0 |
| gyrA | 7853 | c.552C>T | synonymous_variant | 1.0 |
| gyrA | 8837 | c.1536C>A | synonymous_variant | 1.0 |
| gyrA | 8852 | c.1551T>C | synonymous_variant | 1.0 |
| gyrA | 8858 | c.1557T>G | synonymous_variant | 1.0 |
| gyrA | 8867 | c.1566A>G | synonymous_variant | 1.0 |
| gyrA | 8870 | c.1569G>C | synonymous_variant | 1.0 |
| gyrA | 8873 | c.1572A>G | synonymous_variant | 1.0 |
| gyrA | 8888 | c.1587C>T | synonymous_variant | 1.0 |
| gyrA | 8903 | c.1602T>C | synonymous_variant | 1.0 |
| gyrA | 8909 | c.1608C>T | synonymous_variant | 1.0 |
| gyrA | 8915 | c.1614A>G | synonymous_variant | 1.0 |
| gyrA | 8933 | c.1632G>A | synonymous_variant | 1.0 |
| gyrA | 8942 | c.1641G>C | synonymous_variant | 1.0 |
| gyrA | 8945 | c.1644G>C | synonymous_variant | 1.0 |
| gyrA | 8946 | c.1645T>C | synonymous_variant | 1.0 |
| gyrA | 8967 | p.Ala556Lys | missense_variant | 1.0 |
| gyrA | 8987 | c.1686C>G | synonymous_variant | 1.0 |
| gyrA | 8990 | c.1689C>G | synonymous_variant | 1.0 |
| gyrA | 8993 | c.1692C>T | synonymous_variant | 1.0 |
| gyrA | 8996 | c.1695T>C | synonymous_variant | 1.0 |
| gyrA | 8998 | p.Leu566Trp | missense_variant | 1.0 |
| gyrA | 9018 | p.Gln573Lys | missense_variant | 1.0 |
| gyrA | 9023 | c.1722A>C | synonymous_variant | 1.0 |
| gyrA | 9026 | c.1725G>C | synonymous_variant | 1.0 |
| gyrA | 9029 | c.1728T>C | synonymous_variant | 1.0 |
| gyrA | 9032 | c.1731T>C | synonymous_variant | 1.0 |
| gyrA | 9035 | c.1734G>C | synonymous_variant | 1.0 |
| gyrA | 9038 | c.1737C>G | synonymous_variant | 1.0 |
| gyrA | 9044 | c.1743C>A | synonymous_variant | 1.0 |
| gyrA | 9051 | c.1750T>C | synonymous_variant | 1.0 |
| gyrA | 9062 | c.1761C>G | synonymous_variant | 1.0 |
| gyrA | 9063 | p.Ser588Ala | missense_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>T | synonymous_variant | 1.0 |
| gyrA | 9089 | c.1788G>C | synonymous_variant | 1.0 |
| gyrA | 9099 | c.1798_1800delTTAinsCTG | synonymous_variant | 1.0 |
| gyrA | 9113 | c.1812C>G | synonymous_variant | 1.0 |
| fgd1 | 491523 | c.741G>C | 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 | 491548 | p.Ala256Pro | missense_variant | 1.0 |
| fgd1 | 491569 | p.Asp263His | missense_variant | 1.0 |
| fgd1 | 491577 | c.795G>C | synonymous_variant | 1.0 |
| fgd1 | 491590 | p.Lys270Arg | missense_variant | 1.0 |
| fgd1 | 491601 | c.819T>C | synonymous_variant | 1.0 |
| fgd1 | 491603 | p.Ala274Glu | missense_variant | 1.0 |
| fgd1 | 491610 | c.828A>C | synonymous_variant | 1.0 |
| fgd1 | 491620 | p.Ile280Val | missense_variant | 1.0 |
| fgd1 | 491640 | c.858G>C | synonymous_variant | 1.0 |
| fgd1 | 491643 | c.861G>C | synonymous_variant | 1.0 |
| fgd1 | 491646 | c.864G>C | synonymous_variant | 1.0 |
| fgd1 | 491652 | c.870C>G | synonymous_variant | 1.0 |
| fgd1 | 491658 | c.876A>G | synonymous_variant | 1.0 |
| fgd1 | 491664 | c.882C>G | synonymous_variant | 1.0 |
| fgd1 | 491667 | c.885A>G | synonymous_variant | 1.0 |
| mshA | 575704 | c.357T>C | synonymous_variant | 1.0 |
| mshA | 575734 | c.387T>G | synonymous_variant | 1.0 |
| mshA | 575737 | c.390T>C | synonymous_variant | 1.0 |
| mshA | 575740 | c.393G>A | synonymous_variant | 1.0 |
| mshA | 575744 | p.Ala133Thr | missense_variant | 1.0 |
| mshA | 575761 | c.414C>G | synonymous_variant | 0.83 |
| mshA | 575771 | p.Val142Ile | missense_variant | 0.83 |
| mshA | 575779 | c.432A>G | synonymous_variant | 1.0 |
| mshA | 575782 | c.435G>C | synonymous_variant | 0.83 |
| mshA | 575785 | c.438T>C | synonymous_variant | 1.0 |
| mshA | 575792 | p.Asp149Asn | missense_variant | 1.0 |
| mshA | 575795 | p.Ile150Leu | missense_variant | 1.0 |
| mshA | 575800 | c.453G>T | synonymous_variant | 1.0 |
| mshA | 575818 | c.471G>C | synonymous_variant | 1.0 |
| mshA | 575821 | c.474G>C | synonymous_variant | 1.0 |
| mshA | 575824 | c.477T>C | synonymous_variant | 1.0 |
| mshA | 575829 | p.Val161Ala | missense_variant | 1.0 |
| mshA | 575842 | c.495G>C | synonymous_variant | 1.0 |
| ccsA | 620311 | p.Leu141Val | missense_variant | 1.0 |
| ccsA | 620317 | p.Val143Ile | missense_variant | 1.0 |
| ccsA | 620328 | c.438G>C | synonymous_variant | 1.0 |
| ccsA | 620340 | c.450C>G | synonymous_variant | 1.0 |
| ccsA | 620349 | c.459A>G | synonymous_variant | 1.0 |
| ccsA | 620352 | c.462C>G | synonymous_variant | 1.0 |
| ccsA | 620354 | p.Trp155Tyr | missense_variant | 1.0 |
| ccsA | 620362 | p.Ala158Thr | missense_variant | 1.0 |
| ccsA | 620365 | p.Asn159Tyr | missense_variant | 1.0 |
| ccsA | 620388 | c.498A>G | synonymous_variant | 1.0 |
| ccsA | 620397 | c.507C>G | synonymous_variant | 1.0 |
| ccsA | 620415 | c.525T>C | synonymous_variant | 1.0 |
| ccsA | 620418 | c.528G>C | synonymous_variant | 1.0 |
| ccsA | 620421 | c.531G>C | synonymous_variant | 1.0 |
| ccsA | 620427 | c.537C>G | synonymous_variant | 1.0 |
| ccsA | 620436 | c.546T>A | synonymous_variant | 1.0 |
| ccsA | 620439 | c.549T>G | synonymous_variant | 1.0 |
| ccsA | 620442 | c.552G>C | synonymous_variant | 1.0 |
| ccsA | 620445 | c.555A>C | synonymous_variant | 1.0 |
| ccsA | 620460 | c.570T>G | synonymous_variant | 1.0 |
| ccsA | 620463 | c.573C>G | synonymous_variant | 1.0 |
| ccsA | 620466 | c.576C>G | synonymous_variant | 1.0 |
| ccsA | 620473 | c.583C>T | synonymous_variant | 1.0 |
| rpoB | 760061 | c.255C>T | synonymous_variant | 1.0 |
| rpoB | 760070 | c.264T>G | synonymous_variant | 1.0 |
| rpoB | 760079 | c.273G>A | synonymous_variant | 1.0 |
| rpoB | 760091 | c.285G>C | synonymous_variant | 1.0 |
| rpoB | 760101 | c.295T>C | synonymous_variant | 1.0 |
| rpoB | 760106 | c.300G>C | synonymous_variant | 1.0 |
| rpoB | 760110 | c.304_306delTCTinsAGC | synonymous_variant | 1.0 |
| rpoB | 760118 | c.312T>G | synonymous_variant | 1.0 |
| rpoB | 760121 | c.315T>C | synonymous_variant | 1.0 |
| rpoB | 760130 | p.Asp108Glu | missense_variant | 1.0 |
| rpoB | 760178 | c.372G>A | synonymous_variant | 1.0 |
| rpoB | 760181 | c.375T>C | synonymous_variant | 1.0 |
| rpoB | 760184 | c.378A>G | synonymous_variant | 1.0 |
| rpoB | 760196 | c.390C>G | synonymous_variant | 1.0 |
| rpoB | 760235 | c.429T>C | synonymous_variant | 1.0 |
| rpoB | 760244 | c.438G>C | synonymous_variant | 1.0 |
| rpoB | 760256 | c.450C>T | synonymous_variant | 1.0 |
| rpoB | 760274 | p.Glu156Asp | missense_variant | 1.0 |
| rpoB | 760276 | p.Lys157Met | missense_variant | 1.0 |
| rpoB | 760283 | c.477G>C | synonymous_variant | 1.0 |
| rpoB | 760298 | c.492G>C | synonymous_variant | 1.0 |
| rpoB | 760307 | c.501T>C | synonymous_variant | 1.0 |
| rpoB | 760313 | c.507G>C | synonymous_variant | 1.0 |
| rpoB | 760317 | c.511_513delAGCinsTCG | synonymous_variant | 1.0 |
| rpoB | 760325 | c.519G>C | synonymous_variant | 1.0 |
| rpoB | 760328 | c.522G>C | synonymous_variant | 1.0 |
| rpoB | 760331 | c.525G>T | synonymous_variant | 1.0 |
| rpoB | 760337 | c.531C>G | synonymous_variant | 1.0 |
| rpoB | 760340 | c.534G>T | synonymous_variant | 1.0 |
| rpoB | 760343 | c.537G>C | synonymous_variant | 1.0 |
| rpoB | 760357 | p.Thr184Asn | missense_variant | 1.0 |
| rpoB | 760361 | c.555T>C | synonymous_variant | 1.0 |
| rpoB | 760370 | c.564C>G | synonymous_variant | 1.0 |
| rpoB | 760376 | p.Asp190Glu | missense_variant | 1.0 |
| rpoB | 760382 | c.576G>C | synonymous_variant | 1.0 |
| rpoB | 760400 | c.594G>C | synonymous_variant | 1.0 |
| rpoB | 760403 | c.597C>T | synonymous_variant | 1.0 |
| rpoB | 760406 | c.600G>C | synonymous_variant | 1.0 |
| rpoB | 760407 | p.Ser201Gly | missense_variant | 1.0 |
| rpoB | 760415 | c.609C>T | synonymous_variant | 1.0 |
| rpoB | 760418 | c.612G>A | synonymous_variant | 1.0 |
| rpoB | 760430 | c.624T>C | synonymous_variant | 1.0 |
| rpoB | 760436 | c.630C>G | synonymous_variant | 1.0 |
| rpoB | 760457 | c.651C>T | synonymous_variant | 1.0 |
| rpoB | 760475 | c.669A>G | synonymous_variant | 1.0 |
| rpoB | 760481 | c.675G>C | synonymous_variant | 1.0 |
| rpoB | 760484 | c.678A>G | synonymous_variant | 1.0 |
| rpoB | 760487 | c.681G>C | synonymous_variant | 1.0 |
| rpoB | 760502 | c.696C>G | synonymous_variant | 1.0 |
| rpoB | 760511 | c.705G>C | synonymous_variant | 1.0 |
| rpoB | 760522 | p.Ser239Asn | missense_variant | 1.0 |
| rpoB | 760528 | p.Gln241Arg | missense_variant | 1.0 |
| rpoB | 760532 | c.726T>C | synonymous_variant | 1.0 |
| rpoB | 760541 | c.735G>C | synonymous_variant | 1.0 |
| rpoB | 760561 | c.757_758delCG | frameshift_variant | 1.0 |
| rpoB | 760571 | c.765G>C | synonymous_variant | 1.0 |
| rpoB | 760588 | p.Thr261Ile | missense_variant | 1.0 |
| rpoB | 760591 | p.Val262Ala | missense_variant | 1.0 |
| rpoB | 760596 | p.Thr264Pro | missense_variant | 1.0 |
| rpoB | 760601 | c.795C>T | synonymous_variant | 1.0 |
| rpoB | 760611 | c.805T>C | synonymous_variant | 1.0 |
| rpoB | 760616 | c.810C>T | 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>G | synonymous_variant | 1.0 |
| rpoB | 760668 | p.Thr288Ala | missense_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 | 760721 | c.915C>T | synonymous_variant | 1.0 |
| rpoB | 760727 | c.921C>G | synonymous_variant | 1.0 |
| rpoB | 760730 | c.924T>C | synonymous_variant | 1.0 |
| rpoB | 760736 | c.930C>G | synonymous_variant | 1.0 |
| rpoB | 760805 | c.999G>C | synonymous_variant | 1.0 |
| rpoB | 760817 | c.1011A>G | synonymous_variant | 1.0 |
| rpoB | 760820 | c.1014T>C | synonymous_variant | 1.0 |
| rpoB | 760823 | c.1017G>C | synonymous_variant | 1.0 |
| rpoB | 760826 | c.1020C>G | synonymous_variant | 1.0 |
| rpoB | 760830 | c.1024T>C | synonymous_variant | 1.0 |
| rpoB | 760841 | c.1035T>C | synonymous_variant | 1.0 |
| rpoB | 760858 | p.Val351Ala | missense_variant | 1.0 |
| rpoB | 760862 | c.1056G>C | synonymous_variant | 1.0 |
| rpoB | 760868 | c.1062C>T | synonymous_variant | 1.0 |
| rpoB | 760886 | p.Glu360Asp | missense_variant | 1.0 |
| rpoB | 760887 | p.Thr361Val | missense_variant | 1.0 |
| rpoB | 760895 | c.1089C>T | synonymous_variant | 1.0 |
| rpoB | 760910 | c.1104C>T | synonymous_variant | 1.0 |
| rpoB | 760916 | c.1110C>T | synonymous_variant | 1.0 |
| rpoB | 760919 | c.1113C>T | synonymous_variant | 1.0 |
| rpoB | 760928 | c.1122G>C | synonymous_variant | 1.0 |
| rpoB | 760946 | c.1140A>G | synonymous_variant | 1.0 |
| rpoB | 760955 | c.1149C>T | synonymous_variant | 1.0 |
| rpoB | 760965 | p.Met387Leu | missense_variant | 1.0 |
| rpoB | 760970 | c.1164G>C | synonymous_variant | 1.0 |
| rpoB | 760973 | c.1167G>C | synonymous_variant | 1.0 |
| rpoB | 760982 | c.1176G>C | synonymous_variant | 1.0 |
| rpoB | 760985 | c.1179G>T | synonymous_variant | 1.0 |
| rpoB | 760988 | c.1182C>G | synonymous_variant | 1.0 |
| rpoB | 760991 | c.1185G>C | synonymous_variant | 1.0 |
| rpoB | 760997 | c.1191G>C | 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>C | synonymous_variant | 1.0 |
| rpoB | 761036 | c.1230G>C | synonymous_variant | 1.0 |
| rpoB | 761037 | c.1231T>C | synonymous_variant | 1.0 |
| rpoB | 761051 | c.1245G>T | synonymous_variant | 1.0 |
| rpoB | 761054 | c.1248G>C | synonymous_variant | 1.0 |
| rpoB | 761057 | c.1251G>C | synonymous_variant | 1.0 |
| rpoB | 761060 | c.1254C>G | synonymous_variant | 1.0 |
| rpoB | 761063 | c.1257C>G | synonymous_variant | 1.0 |
| rpoB | 761084 | c.1278C>A | synonymous_variant | 1.0 |
| rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 1.0 |
| rpoB | 761102 | c.1296A>G | synonymous_variant | 1.0 |
| rpoB | 761132 | c.1326G>T | synonymous_variant | 0.94 |
| rpoB | 761133 | c.1327T>C | synonymous_variant | 1.0 |
| rpoB | 761147 | c.1341C>T | synonymous_variant | 1.0 |
| rpoB | 761150 | c.1344A>T | synonymous_variant | 1.0 |
| rpoB | 761165 | c.1359G>C | synonymous_variant | 0.93 |
| rpoB | 761178 | p.Ser458Thr | missense_variant | 1.0 |
| rpoB | 761186 | p.Glu460Asp | missense_variant | 1.0 |
| rpoB | 761195 | c.1389G>C | synonymous_variant | 1.0 |
| rpoB | 761198 | c.1392G>T | synonymous_variant | 1.0 |
| rpoB | 761219 | c.1413G>C | 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 | 761258 | c.1452G>A | synonymous_variant | 1.0 |
| rpoB | 761261 | c.1455G>C | synonymous_variant | 0.95 |
| rpoB | 761264 | c.1458C>G | synonymous_variant | 1.0 |
| rpoB | 761273 | c.1467T>C | synonymous_variant | 1.0 |
| rpoB | 761318 | c.1512G>C | synonymous_variant | 1.0 |
| rpoB | 761327 | c.1521A>G | synonymous_variant | 1.0 |
| rpoB | 761348 | c.1542C>T | synonymous_variant | 1.0 |
| rpoB | 761351 | p.Asp515Glu | missense_variant | 1.0 |
| rpoB | 761354 | c.1548C>T | synonymous_variant | 1.0 |
| rpoB | 761357 | c.1551G>C | synonymous_variant | 1.0 |
| rpoB | 761360 | c.1554T>C | synonymous_variant | 1.0 |
| rpoB | 761362 | p.Ser519Thr | missense_variant | 1.0 |
| rpoB | 761373 | p.Val523His | missense_variant | 1.0 |
| rpoB | 761393 | c.1587G>A | synonymous_variant | 1.0 |
| rpoB | 761408 | c.1602G>T | synonymous_variant | 1.0 |
| rpoB | 761516 | c.1710G>C | synonymous_variant | 1.0 |
| rpoB | 761519 | c.1713C>T | synonymous_variant | 1.0 |
| rpoB | 761537 | c.1731C>G | synonymous_variant | 1.0 |
| rpoB | 761555 | c.1749G>C | synonymous_variant | 1.0 |
| rpoB | 761558 | c.1752C>G | synonymous_variant | 1.0 |
| rpoB | 761564 | c.1758G>C | synonymous_variant | 1.0 |
| rpoB | 761570 | c.1764T>C | synonymous_variant | 1.0 |
| rpoB | 761573 | c.1767C>G | synonymous_variant | 1.0 |
| rpoB | 761579 | c.1773G>C | 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>A | synonymous_variant | 1.0 |
| rpoB | 761661 | c.1855C>T | synonymous_variant | 1.0 |
| rpoB | 761669 | c.1863C>T | synonymous_variant | 1.0 |
| rpoB | 761675 | c.1869G>T | synonymous_variant | 1.0 |
| rpoB | 761684 | c.1878G>T | synonymous_variant | 1.0 |
| rpoB | 761687 | c.1881C>T | synonymous_variant | 1.0 |
| rpoB | 761690 | c.1884G>C | synonymous_variant | 1.0 |
| rpoB | 761714 | c.1908C>T | synonymous_variant | 1.0 |
| rpoB | 761720 | c.1914C>G | synonymous_variant | 1.0 |
| rpoB | 761723 | c.1917A>G | synonymous_variant | 1.0 |
| rpoB | 761724 | p.Glu640Lys | missense_variant | 1.0 |
| rpoB | 761728 | p.Ser641Thr | missense_variant | 1.0 |
| rpoB | 761732 | c.1926C>T | synonymous_variant | 1.0 |
| rpoB | 761741 | c.1935G>A | synonymous_variant | 1.0 |
| rpoB | 761750 | c.1944G>C | synonymous_variant | 1.0 |
| rpoB | 761760 | p.Ile652Val | missense_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.Arg662Gln | missense_variant | 1.0 |
| rpoB | 761794 | p.Thr663Ser | missense_variant | 1.0 |
| rpoB | 761802 | p.Met666Leu | missense_variant | 1.0 |
| rpoB | 761807 | c.2001C>T | synonymous_variant | 1.0 |
| rpoB | 761813 | c.2007T>C | synonymous_variant | 1.0 |
| rpoB | 761816 | c.2010C>G | synonymous_variant | 1.0 |
| rpoB | 761822 | c.2016C>G | synonymous_variant | 1.0 |
| rpoB | 761834 | c.2028T>C | synonymous_variant | 1.0 |
| rpoB | 761847 | p.Cys681Arg | missense_variant | 1.0 |
| rpoB | 761855 | c.2049C>T | synonymous_variant | 1.0 |
| rpoB | 761863 | p.Ala686Glu | missense_variant | 1.0 |
| rpoB | 761867 | c.2061C>T | synonymous_variant | 1.0 |
| rpoB | 761868 | p.Asp688Gln | missense_variant | 1.0 |
| rpoB | 761873 | c.2067A>G | synonymous_variant | 1.0 |
| rpoB | 761881 | p.Ala692Val | missense_variant | 1.0 |
| rpoB | 761891 | c.2085G>T | synonymous_variant | 1.0 |
| rpoB | 761897 | c.2091C>G | synonymous_variant | 1.0 |
| rpoB | 761906 | c.2100C>T | synonymous_variant | 1.0 |
| rpoB | 761909 | c.2103T>C | synonymous_variant | 1.0 |
| rpoB | 761912 | c.2106T>C | synonymous_variant | 1.0 |
| rpoB | 761915 | p.Asp703Glu | missense_variant | 1.0 |
| rpoB | 761916 | p.Asp704Asn | missense_variant | 1.0 |
| rpoB | 761924 | c.2118G>A | synonymous_variant | 1.0 |
| rpoB | 761930 | c.2124G>T | synonymous_variant | 1.0 |
| rpoB | 761933 | c.2127G>C | synonymous_variant | 1.0 |
| rpoB | 761936 | c.2130C>T | synonymous_variant | 1.0 |
| rpoB | 761948 | c.2142G>C | synonymous_variant | 1.0 |
| rpoB | 761954 | c.2148C>G | synonymous_variant | 1.0 |
| rpoB | 761969 | c.2163G>A | synonymous_variant | 1.0 |
| rpoB | 761990 | c.2184G>C | synonymous_variant | 1.0 |
| rpoB | 762004 | p.Asn733Ser | missense_variant | 1.0 |
| rpoB | 762014 | c.2208C>G | synonymous_variant | 1.0 |
| rpoB | 762038 | c.2232C>T | synonymous_variant | 1.0 |
| rpoB | 762047 | c.2241G>A | synonymous_variant | 1.0 |
| rpoB | 762053 | c.2247T>C | synonymous_variant | 1.0 |
| rpoB | 762056 | c.2250G>A | synonymous_variant | 1.0 |
| rpoB | 762065 | c.2259T>G | 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 | 762101 | c.2295C>G | synonymous_variant | 1.0 |
| rpoB | 762114 | p.Ile770Val | missense_variant | 1.0 |
| rpoB | 762122 | c.2316C>T | synonymous_variant | 1.0 |
| rpoB | 762131 | c.2325C>G | synonymous_variant | 1.0 |
| rpoB | 762134 | c.2328C>A | synonymous_variant | 1.0 |
| rpoB | 762137 | c.2331C>T | synonymous_variant | 1.0 |
| rpoB | 762140 | c.2334G>C | synonymous_variant | 1.0 |
| rpoB | 762143 | c.2337T>C | synonymous_variant | 1.0 |
| rpoB | 762149 | c.2343G>C | synonymous_variant | 1.0 |
| rpoB | 762158 | c.2352G>C | synonymous_variant | 1.0 |
| rpoB | 762176 | c.2370T>C | synonymous_variant | 1.0 |
| rpoB | 762185 | c.2379G>C | synonymous_variant | 1.0 |
| rpoB | 762194 | c.2388G>C | synonymous_variant | 1.0 |
| rpoB | 762236 | c.2430G>C | synonymous_variant | 1.0 |
| rpoB | 762245 | c.2439G>C | synonymous_variant | 1.0 |
| rpoB | 762284 | c.2478G>T | synonymous_variant | 1.0 |
| rpoB | 762293 | c.2487T>C | synonymous_variant | 1.0 |
| rpoB | 762296 | c.2490G>T | synonymous_variant | 1.0 |
| rpoB | 762314 | c.2508C>T | synonymous_variant | 1.0 |
| rpoB | 762317 | c.2511A>G | synonymous_variant | 1.0 |
| rpoB | 762329 | c.2523G>C | synonymous_variant | 1.0 |
| rpoB | 762338 | c.2532T>C | synonymous_variant | 1.0 |
| rpoB | 762341 | c.2535G>C | synonymous_variant | 1.0 |
| rpoB | 762344 | c.2538G>C | synonymous_variant | 1.0 |
| rpoB | 762347 | c.2541T>C | synonymous_variant | 1.0 |
| rpoB | 762350 | c.2544C>G | synonymous_variant | 1.0 |
| rpoB | 762356 | p.Glu850Asp | missense_variant | 1.0 |
| rpoB | 762362 | p.Glu852Asp | missense_variant | 1.0 |
| rpoB | 762368 | p.Glu854Asp | missense_variant | 1.0 |
| rpoB | 762369 | c.2563T>C | synonymous_variant | 1.0 |
| rpoC | 762374 | c.-996G>T | upstream_gene_variant | 1.0 |
| rpoC | 762380 | c.-990T>C | upstream_gene_variant | 1.0 |
| rpoC | 762383 | c.-987C>G | upstream_gene_variant | 1.0 |
| rpoC | 762392 | c.-978G>C | upstream_gene_variant | 1.0 |
| rpoC | 762395 | c.-975G>T | upstream_gene_variant | 1.0 |
| rpoC | 762398 | c.-972T>C | upstream_gene_variant | 1.0 |
| rpoC | 762404 | c.-966T>C | upstream_gene_variant | 1.0 |
| rpoC | 762407 | c.-963G>C | upstream_gene_variant | 1.0 |
| rpoC | 762410 | c.-960T>G | upstream_gene_variant | 1.0 |
| rpoC | 762416 | c.-954A>G | upstream_gene_variant | 1.0 |
| rpoC | 762449 | c.-921C>A | upstream_gene_variant | 1.0 |
| rpoC | 762452 | c.-918G>C | upstream_gene_variant | 1.0 |
| rpoC | 762470 | c.-900G>C | upstream_gene_variant | 1.0 |
| rpoC | 762488 | c.-882G>C | upstream_gene_variant | 1.0 |
| rpoC | 762491 | c.-879T>C | upstream_gene_variant | 1.0 |
| rpoC | 762509 | c.-861T>G | upstream_gene_variant | 1.0 |
| rpoB | 762510 | p.Ala902Pro | missense_variant | 1.0 |
| rpoC | 762515 | c.-855C>T | upstream_gene_variant | 1.0 |
| rpoB | 762531 | p.Ile909Val | missense_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 | 762560 | c.-810A>T | upstream_gene_variant | 1.0 |
| rpoC | 762563 | c.-807G>T | upstream_gene_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>C | upstream_gene_variant | 1.0 |
| rpoC | 762863 | c.-507T>C | upstream_gene_variant | 1.0 |
| rpoC | 762866 | c.-504C>T | upstream_gene_variant | 1.0 |
| rpoB | 762879 | p.Met1025Leu | missense_variant | 1.0 |
| rpoC | 762894 | c.-476C>T | upstream_gene_variant | 1.0 |
| rpoC | 762899 | c.-471G>C | upstream_gene_variant | 1.0 |
| rpoC | 762917 | c.-453C>G | upstream_gene_variant | 1.0 |
| rpoC | 762920 | c.-450C>T | upstream_gene_variant | 1.0 |
| rpoC | 762923 | c.-447C>G | upstream_gene_variant | 1.0 |
| rpoC | 762929 | c.-441G>C | upstream_gene_variant | 1.0 |
| rpoC | 762959 | c.-411G>C | upstream_gene_variant | 1.0 |
| rpoC | 762962 | c.-408C>T | upstream_gene_variant | 1.0 |
| rpoC | 762995 | c.-375G>T | 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 | 763070 | c.-300T>C | upstream_gene_variant | 1.0 |
| rpoC | 763082 | c.-288C>T | upstream_gene_variant | 1.0 |
| rpoC | 763088 | c.-282C>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 | 763127 | c.-243G>C | upstream_gene_variant | 1.0 |
| rpoC | 763136 | c.-234C>T | upstream_gene_variant | 1.0 |
| rpoC | 763139 | c.-231C>T | upstream_gene_variant | 1.0 |
| rpoC | 763157 | c.-213G>T | upstream_gene_variant | 1.0 |
| rpoC | 763160 | c.-210G>A | upstream_gene_variant | 1.0 |
| rpoC | 763166 | c.-204A>G | upstream_gene_variant | 1.0 |
| rpoC | 763172 | c.-198G>C | 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 | 763205 | c.-165G>C | upstream_gene_variant | 1.0 |
| rpoB | 763207 | p.Ser1134Lys | missense_variant | 1.0 |
| rpoC | 763214 | c.-156T>C | upstream_gene_variant | 1.0 |
| rpoC | 763217 | c.-153G>C | upstream_gene_variant | 1.0 |
| rpoC | 763220 | c.-150G>C | upstream_gene_variant | 1.0 |
| rpoC | 763226 | c.-144A>G | upstream_gene_variant | 1.0 |
| rpoB | 763227 | p.Leu1141Met | missense_variant | 1.0 |
| rpoB | 763235 | p.Glu1143Asp | missense_variant | 1.0 |
| rpoC | 763238 | c.-132T>C | upstream_gene_variant | 1.0 |
| rpoB | 763241 | p.Glu1145Asp | missense_variant | 1.0 |
| rpoC | 763259 | c.-111G>C | upstream_gene_variant | 1.0 |
| rpoC | 763262 | c.-108C>T | upstream_gene_variant | 1.0 |
| rpoC | 763265 | c.-105G>C | upstream_gene_variant | 1.0 |
| rpoC | 763268 | c.-102C>G | upstream_gene_variant | 1.0 |
| rpoC | 763283 | c.-87T>C | upstream_gene_variant | 1.0 |
| rpoC | 763365 | c.-5G>T | upstream_gene_variant | 1.0 |
| rpoC | 763402 | c.33C>T | synonymous_variant | 1.0 |
| rpoC | 763408 | c.39T>C | synonymous_variant | 1.0 |
| rpoC | 763411 | c.42T>C | synonymous_variant | 1.0 |
| rpoC | 763414 | c.45T>G | synonymous_variant | 1.0 |
| rpoC | 763415 | p.Thr16Ser | missense_variant | 1.0 |
| rpoC | 763423 | p.Glu18Asp | missense_variant | 1.0 |
| rpoC | 763430 | c.61_63delAGGinsCGT | synonymous_variant | 1.0 |
| rpoC | 763433 | p.Gln22Asn | missense_variant | 1.0 |
| rpoC | 763443 | p.Tyr25Phe | missense_variant | 1.0 |
| rpoC | 763450 | c.81G>A | synonymous_variant | 1.0 |
| rpoC | 763456 | c.87A>G | synonymous_variant | 1.0 |
| rpoC | 763468 | c.99G>C | synonymous_variant | 1.0 |
| rpoC | 763480 | c.111C>A | synonymous_variant | 1.0 |
| rpoC | 763486 | c.117T>G | synonymous_variant | 1.0 |
| rpoC | 763492 | c.123G>C | synonymous_variant | 1.0 |
| rpoC | 763528 | c.159G>A | synonymous_variant | 1.0 |
| rpoC | 763531 | c.162G>T | synonymous_variant | 1.0 |
| rpoC | 763546 | c.177A>G | synonymous_variant | 1.0 |
| rpoC | 763570 | c.201G>C | synonymous_variant | 1.0 |
| rpoC | 763594 | c.225C>T | synonymous_variant | 1.0 |
| rpoC | 763606 | c.237C>T | synonymous_variant | 1.0 |
| rpoC | 763615 | c.246G>A | synonymous_variant | 1.0 |
| rpoC | 763618 | c.249C>T | synonymous_variant | 1.0 |
| rpoC | 763657 | c.288G>A | synonymous_variant | 1.0 |
| rpoC | 763660 | c.291T>G | synonymous_variant | 1.0 |
| rpoC | 763666 | c.297G>C | synonymous_variant | 1.0 |
| rpoC | 763669 | c.300C>G | synonymous_variant | 1.0 |
| rpoC | 763675 | c.306C>G | synonymous_variant | 1.0 |
| rpoC | 763699 | c.330G>T | synonymous_variant | 1.0 |
| rpoC | 763702 | c.333C>G | synonymous_variant | 1.0 |
| rpoC | 763708 | c.339G>C | synonymous_variant | 1.0 |
| rpoC | 763711 | c.342G>T | synonymous_variant | 1.0 |
| rpoC | 763714 | c.345G>C | synonymous_variant | 1.0 |
| rpoC | 763717 | c.348T>C | synonymous_variant | 1.0 |
| rpoC | 763723 | c.354G>C | synonymous_variant | 1.0 |
| rpoC | 763732 | c.363C>G | synonymous_variant | 1.0 |
| rpoC | 763735 | c.366G>C | synonymous_variant | 1.0 |
| rpoC | 763741 | c.372C>T | synonymous_variant | 1.0 |
| rpoC | 763744 | c.375G>C | synonymous_variant | 1.0 |
| rpoC | 763765 | c.396T>C | synonymous_variant | 1.0 |
| rpoC | 763774 | c.405G>C | synonymous_variant | 1.0 |
| rpoC | 763781 | p.Ser138Ala | missense_variant | 1.0 |
| rpoC | 763792 | p.Glu141Asp | missense_variant | 1.0 |
| rpoC | 763796 | p.Met143Leu | missense_variant | 1.0 |
| rpoC | 763807 | c.438T>C | synonymous_variant | 1.0 |
| rpoC | 763810 | c.441G>A | synonymous_variant | 1.0 |
| rpoC | 763816 | c.447C>G | synonymous_variant | 1.0 |
| rpoC | 763831 | c.462A>G | synonymous_variant | 1.0 |
| rpoC | 763836 | p.Ala156Glu | missense_variant | 1.0 |
| rpoC | 763891 | c.522G>T | synonymous_variant | 1.0 |
| rpoC | 763894 | c.525A>G | synonymous_variant | 1.0 |
| rpoC | 763900 | c.531G>C | synonymous_variant | 1.0 |
| rpoC | 763933 | c.564C>T | synonymous_variant | 1.0 |
| rpoC | 763940 | p.Ala191Ser | missense_variant | 1.0 |
| rpoC | 763945 | c.576T>C | synonymous_variant | 1.0 |
| rpoC | 763947 | p.Ala193Val | missense_variant | 1.0 |
| rpoC | 763951 | c.582G>C | synonymous_variant | 1.0 |
| rpoC | 763960 | c.591T>G | 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 | 763999 | c.630C>T | synonymous_variant | 1.0 |
| rpoC | 764002 | c.633C>G | synonymous_variant | 1.0 |
| rpoC | 764003 | p.Ala212Ser | missense_variant | 1.0 |
| rpoC | 764024 | c.655_657delTTGinsCTC | synonymous_variant | 1.0 |
| rpoC | 764029 | p.Glu220Asp | missense_variant | 1.0 |
| rpoC | 764032 | p.Asp221Glu | missense_variant | 1.0 |
| rpoC | 764040 | p.Ser224Thr | missense_variant | 1.0 |
| rpoC | 764044 | c.675T>C | synonymous_variant | 1.0 |
| rpoC | 764059 | c.690G>T | synonymous_variant | 1.0 |
| rpoC | 764080 | c.711C>T | synonymous_variant | 1.0 |
| rpoC | 764083 | c.714A>G | synonymous_variant | 1.0 |
| rpoC | 764084 | p.Asn239Val | missense_variant | 1.0 |
| rpoC | 764098 | c.729A>G | synonymous_variant | 1.0 |
| rpoC | 764099 | p.Leu244Ile | missense_variant | 1.0 |
| rpoC | 764242 | c.873C>T | synonymous_variant | 1.0 |
| rpoC | 764245 | c.876C>G | synonymous_variant | 1.0 |
| rpoC | 764254 | c.885G>C | synonymous_variant | 1.0 |
| rpoC | 764266 | c.897T>G | synonymous_variant | 1.0 |
| rpoC | 764278 | c.909A>G | synonymous_variant | 1.0 |
| rpoC | 764279 | p.Gln304Asn | missense_variant | 1.0 |
| rpoC | 764284 | c.915G>C | synonymous_variant | 1.0 |
| rpoC | 764285 | p.Gly306Thr | missense_variant | 1.0 |
| rpoC | 764296 | c.927G>C | synonymous_variant | 1.0 |
| rpoC | 764297 | p.Met310Gly | missense_variant | 1.0 |
| rpoC | 764317 | c.948C>G | synonymous_variant | 1.0 |
| rpoC | 764320 | c.951C>A | synonymous_variant | 1.0 |
| rpoC | 764353 | c.984G>T | synonymous_variant | 1.0 |
| rpoC | 764362 | c.993C>T | synonymous_variant | 1.0 |
| rpoC | 764365 | c.996C>T | synonymous_variant | 1.0 |
| rpoC | 764371 | c.1002G>C | synonymous_variant | 1.0 |
| rpoC | 764377 | c.1008C>G | synonymous_variant | 1.0 |
| rpoC | 764380 | c.1011G>C | synonymous_variant | 1.0 |
| rpoC | 764386 | c.1017C>T | synonymous_variant | 1.0 |
| rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 1.0 |
| rpoC | 764405 | c.1036_1038delAGGinsCGT | synonymous_variant | 1.0 |
| rpoC | 764428 | c.1059G>C | 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 | 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 | 764510 | c.1141C>T | synonymous_variant | 1.0 |
| rpoC | 764521 | c.1152T>C | synonymous_variant | 1.0 |
| rpoC | 764527 | c.1158C>T | synonymous_variant | 1.0 |
| rpoC | 764530 | c.1161C>T | synonymous_variant | 1.0 |
| rpoC | 764533 | c.1164C>A | synonymous_variant | 1.0 |
| rpoC | 764536 | c.1167G>T | synonymous_variant | 1.0 |
| rpoC | 764539 | c.1170C>G | synonymous_variant | 1.0 |
| rpoC | 764548 | c.1179G>A | synonymous_variant | 1.0 |
| rpoC | 764554 | c.1185C>T | synonymous_variant | 1.0 |
| rpoC | 764566 | c.1197C>G | synonymous_variant | 1.0 |
| rpoC | 764575 | c.1206T>G | synonymous_variant | 1.0 |
| rpoC | 764602 | c.1233C>T | synonymous_variant | 1.0 |
| rpoC | 764605 | c.1236G>T | synonymous_variant | 1.0 |
| rpoC | 764611 | c.1242G>T | synonymous_variant | 1.0 |
| rpoC | 764626 | c.1257C>T | synonymous_variant | 1.0 |
| rpoC | 764632 | c.1263T>C | synonymous_variant | 1.0 |
| rpoC | 764650 | c.1281G>T | synonymous_variant | 1.0 |
| rpoC | 764692 | c.1323C>T | synonymous_variant | 1.0 |
| rpoC | 764713 | c.1344G>C | synonymous_variant | 1.0 |
| rpoC | 764746 | c.1377G>T | synonymous_variant | 0.98 |
| rpoC | 764752 | c.1383G>C | synonymous_variant | 1.0 |
| rpoC | 764755 | c.1386C>T | synonymous_variant | 1.0 |
| rpoC | 764758 | c.1389C>G | synonymous_variant | 1.0 |
| rpoC | 764764 | c.1395T>C | synonymous_variant | 1.0 |
| rpoC | 764797 | c.1428G>C | synonymous_variant | 1.0 |
| rpoC | 764803 | c.1434C>T | synonymous_variant | 1.0 |
| rpoC | 764809 | c.1440C>T | synonymous_variant | 1.0 |
| rpoC | 764810 | p.Pro481Ala | missense_variant | 1.0 |
| rpoC | 764815 | c.1446A>G | synonymous_variant | 1.0 |
| rpoC | 764827 | c.1458G>C | synonymous_variant | 1.0 |
| rpoC | 764858 | c.1489T>C | synonymous_variant | 1.0 |
| rpoC | 764869 | c.1500C>T | synonymous_variant | 1.0 |
| rpoC | 764875 | c.1506C>A | synonymous_variant | 1.0 |
| rpoC | 764887 | c.1518G>C | synonymous_variant | 1.0 |
| rpoC | 764888 | c.1519T>C | synonymous_variant | 1.0 |
| rpoC | 764911 | c.1542A>G | synonymous_variant | 1.0 |
| rpoC | 764912 | p.Met515Gln | missense_variant | 1.0 |
| rpoC | 764932 | c.1563C>A | synonymous_variant | 1.0 |
| rpoC | 764962 | c.1593G>C | synonymous_variant | 1.0 |
| rpoC | 764968 | c.1599T>C | synonymous_variant | 1.0 |
| rpoC | 764995 | c.1626C>T | synonymous_variant | 1.0 |
| rpoC | 765004 | c.1635G>C | synonymous_variant | 1.0 |
| rpoC | 765007 | c.1638T>G | synonymous_variant | 1.0 |
| rpoC | 765008 | c.1639T>C | synonymous_variant | 1.0 |
| rpoC | 765011 | c.1642_1644delAGCinsTCG | synonymous_variant | 1.0 |
| rpoC | 765016 | c.1647C>G | synonymous_variant | 1.0 |
| rpoC | 765019 | c.1650A>G | synonymous_variant | 1.0 |
| rpoC | 765040 | c.1671T>C | synonymous_variant | 1.0 |
| rpoC | 765041 | c.1672T>C | synonymous_variant | 1.0 |
| rpoC | 765047 | c.1678T>C | synonymous_variant | 1.0 |
| rpoC | 765055 | c.1686C>G | synonymous_variant | 1.0 |
| rpoC | 765073 | c.1704G>C | synonymous_variant | 1.0 |
| rpoC | 765076 | c.1707A>G | synonymous_variant | 1.0 |
| rpoC | 765079 | c.1710T>G | synonymous_variant | 1.0 |
| rpoC | 765082 | c.1713G>T | synonymous_variant | 1.0 |
| rpoC | 765085 | c.1716T>C | synonymous_variant | 1.0 |
| rpoC | 765103 | c.1734G>T | synonymous_variant | 1.0 |
| rpoC | 765121 | c.1752G>T | synonymous_variant | 1.0 |
| rpoC | 765278 | c.1909C>T | synonymous_variant | 1.0 |
| rpoC | 765288 | p.Leu640Gln | missense_variant | 1.0 |
| rpoC | 765292 | c.1923G>T | synonymous_variant | 1.0 |
| rpoC | 765305 | p.Ile646Val | missense_variant | 1.0 |
| rpoC | 765319 | c.1950A>G | synonymous_variant | 1.0 |
| rpoC | 765323 | c.1955_1957delGCC | disruptive_inframe_deletion | 1.0 |
| rpoC | 765328 | p.His653Gln | missense_variant | 1.0 |
| rpoC | 765330 | p.Ser654Asn | missense_variant | 1.0 |
| rpoC | 765334 | c.1965C>T | synonymous_variant | 1.0 |
| rpoC | 765343 | c.1974G>A | synonymous_variant | 1.0 |
| rpoC | 765352 | c.1983G>C | synonymous_variant | 1.0 |
| rpoC | 765358 | p.Met663Ile | missense_variant | 1.0 |
| rpoC | 765370 | c.2001G>C | synonymous_variant | 1.0 |
| rpoC | 765376 | c.2007C>T | synonymous_variant | 1.0 |
| rpoC | 765379 | c.2010G>C | synonymous_variant | 1.0 |
| rpoC | 765383 | p.Met672Leu | missense_variant | 1.0 |
| rpoC | 765403 | c.2034G>C | synonymous_variant | 1.0 |
| rpoC | 765405 | p.Leu679His | missense_variant | 1.0 |
| rpoC | 765409 | c.2040T>G | synonymous_variant | 1.0 |
| rpoC | 765421 | c.2052C>G | synonymous_variant | 1.0 |
| rpoC | 765449 | p.Ala694Ser | missense_variant | 1.0 |
| rpoC | 765454 | c.2085C>G | synonymous_variant | 1.0 |
| rpoC | 765469 | c.2100G>C | synonymous_variant | 1.0 |
| rpoC | 765478 | c.2109T>G | synonymous_variant | 1.0 |
| rpoC | 765480 | p.Tyr704Phe | missense_variant | 1.0 |
| rpoC | 765499 | c.2130C>G | synonymous_variant | 1.0 |
| rpoC | 765529 | c.2160C>T | synonymous_variant | 1.0 |
| rpoC | 765533 | p.Tyr722His | missense_variant | 1.0 |
| rpoC | 765544 | c.2175C>G | synonymous_variant | 1.0 |
| rpoC | 765548 | c.2179_2180delAGinsTC | synonymous_variant | 1.0 |
| rpoC | 765553 | c.2184C>T | synonymous_variant | 1.0 |
| rpoC | 765591 | p.Arg741Gln | missense_variant | 1.0 |
| rpoC | 765596 | p.Lys743Ala | missense_variant | 1.0 |
| rpoC | 765607 | c.2238C>G | synonymous_variant | 1.0 |
| rpoC | 765612 | p.His748Arg | missense_variant | 1.0 |
| rpoC | 765620 | p.Glu751Lys | missense_variant | 1.0 |
| rpoC | 765623 | p.Arg752Glu | missense_variant | 1.0 |
| rpoC | 765631 | p.Asp754Glu | missense_variant | 1.0 |
| rpoC | 765632 | p.Lys755Arg | missense_variant | 1.0 |
| rpoC | 765635 | p.Val756Ile | missense_variant | 1.0 |
| rpoC | 765648 | p.Phe760Tyr | missense_variant | 1.0 |
| rpoC | 765658 | c.2289C>T | synonymous_variant | 1.0 |
| rpoC | 765861 | p.Phe831Tyr | missense_variant | 1.0 |
| rpoC | 765871 | c.2502T>G | synonymous_variant | 1.0 |
| rpoC | 765875 | p.Val836Ile | missense_variant | 1.0 |
| rpoC | 765907 | c.2538G>T | synonymous_variant | 1.0 |
| rpoC | 765928 | c.2559C>G | synonymous_variant | 1.0 |
| rpoC | 765937 | c.2568T>C | synonymous_variant | 1.0 |
| rpoC | 765940 | c.2571A>T | synonymous_variant | 1.0 |
| rpoC | 765946 | c.2577C>T | synonymous_variant | 1.0 |
| rpoC | 765947 | c.2578T>C | synonymous_variant | 1.0 |
| rpoC | 765962 | c.2593_2595delTTGinsCTT | synonymous_variant | 1.0 |
| rpoC | 765967 | c.2598C>T | synonymous_variant | 1.0 |
| rpoC | 765973 | c.2604C>G | synonymous_variant | 1.0 |
| rpoC | 765979 | c.2610C>G | synonymous_variant | 1.0 |
| rpoC | 765994 | c.2625A>T | synonymous_variant | 1.0 |
| rpoC | 766012 | c.2643C>G | synonymous_variant | 1.0 |
| rpoC | 766021 | c.2652G>C | synonymous_variant | 1.0 |
| rpoC | 766043 | p.Gln892Gly | missense_variant | 1.0 |
| rpoC | 766300 | c.2931C>G | synonymous_variant | 1.0 |
| rpoC | 766309 | c.2940G>C | synonymous_variant | 1.0 |
| rpoC | 766312 | c.2943T>C | synonymous_variant | 1.0 |
| rpoC | 766315 | c.2946C>G | synonymous_variant | 1.0 |
| rpoC | 766321 | c.2952C>G | synonymous_variant | 1.0 |
| rpoC | 766333 | c.2964G>T | synonymous_variant | 1.0 |
| rpoC | 766345 | c.2976T>C | synonymous_variant | 1.0 |
| rpoC | 766348 | c.2979A>G | synonymous_variant | 1.0 |
| rpoC | 766351 | c.2982C>G | synonymous_variant | 1.0 |
| rpoC | 766353 | p.Val995Ala | missense_variant | 1.0 |
| rpoC | 766369 | c.3000C>G | synonymous_variant | 1.0 |
| rpoC | 766375 | c.3006C>G | synonymous_variant | 1.0 |
| rpoC | 766381 | c.3012C>T | synonymous_variant | 1.0 |
| rpoC | 766384 | c.3015A>G | synonymous_variant | 1.0 |
| rpoC | 766390 | c.3021C>T | synonymous_variant | 1.0 |
| rpoC | 766408 | c.3039C>T | synonymous_variant | 1.0 |
| rpoC | 766435 | p.Glu1022Asp | missense_variant | 1.0 |
| rpoC | 766568 | p.Val1067Ile | missense_variant | 1.0 |
| rpoC | 766573 | c.3204T>G | synonymous_variant | 1.0 |
| rpoC | 766576 | c.3207C>T | synonymous_variant | 1.0 |
| rpoC | 766582 | c.3213C>T | synonymous_variant | 1.0 |
| rpoC | 766585 | c.3216T>C | synonymous_variant | 1.0 |
| rpoC | 766594 | c.3225G>T | synonymous_variant | 1.0 |
| rpoC | 766607 | p.Ile1080Leu | missense_variant | 1.0 |
| rpoC | 766618 | c.3249G>T | synonymous_variant | 1.0 |
| rpoC | 766931 | p.Ala1188Thr | missense_variant | 1.0 |
| rpoC | 766935 | p.Glu1189Ala | missense_variant | 1.0 |
| rpoC | 766942 | c.3573C>T | synonymous_variant | 1.0 |
| rpoC | 766945 | c.3576A>C | synonymous_variant | 1.0 |
| rpoC | 766951 | c.3582G>C | synonymous_variant | 1.0 |
| rpoC | 766961 | p.Gly1198Asn | missense_variant | 1.0 |
| rpoC | 766981 | c.3612T>C | synonymous_variant | 1.0 |
| rpoC | 766996 | c.3627C>T | synonymous_variant | 1.0 |
| rpoC | 767002 | c.3633G>C | synonymous_variant | 1.0 |
| rpoC | 767008 | c.3639G>A | synonymous_variant | 1.0 |
| rpoC | 767044 | c.3675G>C | synonymous_variant | 1.0 |
| rpoC | 767071 | c.3702C>G | synonymous_variant | 1.0 |
| rpoC | 767080 | c.3711G>T | synonymous_variant | 1.0 |
| rpoC | 767098 | c.3729T>C | synonymous_variant | 1.0 |
| rpoC | 767100 | p.Lys1244Arg | missense_variant | 1.0 |
| rpoC | 767104 | c.3735C>G | synonymous_variant | 1.0 |
| rpoC | 767107 | c.3738C>T | synonymous_variant | 1.0 |
| rpoC | 767119 | c.3750A>G | synonymous_variant | 1.0 |
| rpoC | 767125 | c.3756G>C | synonymous_variant | 1.0 |
| rpoC | 767134 | c.3765C>T | synonymous_variant | 1.0 |
| rpoC | 767138 | c.3769C>T | synonymous_variant | 1.0 |
| rpoC | 767180 | p.Ala1271Ser | missense_variant | 1.0 |
| rpoC | 767188 | c.3819G>A | synonymous_variant | 1.0 |
| rpoC | 767191 | c.3822C>G | synonymous_variant | 1.0 |
| rpoC | 767197 | c.3828G>A | synonymous_variant | 1.0 |
| rpoC | 767203 | c.3834C>G | synonymous_variant | 1.0 |
| rpoC | 767206 | c.3837C>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 | 767254 | c.3885G>C | synonymous_variant | 1.0 |
| rpoC | 767264 | p.Ala1299Ser | missense_variant | 1.0 |
| rpoC | 767267 | p.Ala1300Asn | missense_variant | 1.0 |
| rpoC | 767281 | c.3912C>G | synonymous_variant | 1.0 |
| rpoC | 767284 | c.3915C>G | synonymous_variant | 1.0 |
| rpoC | 767296 | c.3927C>T | synonymous_variant | 1.0 |
| rpsL | 781546 | c.-14T>C | upstream_gene_variant | 1.0 |
| rpsL | 781559 | c.-1G>C | upstream_gene_variant | 1.0 |
| rpsL | 781572 | p.Gln5Asn | missense_variant | 1.0 |
| rpsL | 781586 | c.27C>T | synonymous_variant | 1.0 |
| rpsL | 781595 | c.36T>C | synonymous_variant | 1.0 |
| rpsL | 781608 | p.Ser17Ala | missense_variant | 1.0 |
| rpsL | 781616 | c.57C>G | synonymous_variant | 1.0 |
| rpsL | 781622 | c.63C>T | synonymous_variant | 1.0 |
| rpsL | 781628 | c.69T>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 | 781670 | c.111G>C | synonymous_variant | 1.0 |
| rpsL | 781682 | c.123T>C | synonymous_variant | 1.0 |
| rpsL | 781706 | c.147T>G | synonymous_variant | 1.0 |
| rpsL | 781715 | c.156T>G | synonymous_variant | 1.0 |
| rpsL | 781721 | c.162C>T | synonymous_variant | 1.0 |
| rpsL | 781725 | p.Lys56Arg | missense_variant | 1.0 |
| rpsL | 781728 | c.169T>C | synonymous_variant | 1.0 |
| rpsL | 781733 | c.174G>C | synonymous_variant | 1.0 |
| rpsL | 781736 | c.177T>C | synonymous_variant | 1.0 |
| rpsL | 781737 | p.Gln60Ala | missense_variant | 1.0 |
| rpsL | 781742 | c.183C>G | synonymous_variant | 1.0 |
| rpsL | 781751 | c.192G>C | synonymous_variant | 1.0 |
| rpsL | 781754 | c.195G>T | synonymous_variant | 1.0 |
| rpsL | 781760 | c.201T>C | synonymous_variant | 1.0 |
| rpsL | 781763 | c.204C>G | synonymous_variant | 1.0 |
| rpsL | 781766 | c.207C>T | synonymous_variant | 1.0 |
| rpsL | 781772 | c.213C>T | synonymous_variant | 1.0 |
| rpsL | 781802 | c.243G>C | synonymous_variant | 1.0 |
| rpsL | 781811 | c.252C>T | synonymous_variant | 1.0 |
| rpsL | 781814 | c.255C>T | synonymous_variant | 1.0 |
| rpsL | 781817 | c.258G>T | synonymous_variant | 1.0 |
| rpsL | 781829 | c.270G>C | synonymous_variant | 1.0 |
| rpsL | 781832 | c.273T>C | synonymous_variant | 1.0 |
| rpsL | 781859 | c.300T>C | synonymous_variant | 1.0 |
| rpsL | 781862 | c.303G>A | synonymous_variant | 1.0 |
| rpsL | 781871 | c.312G>C | synonymous_variant | 1.0 |
| rpsL | 781877 | c.318T>A | synonymous_variant | 1.0 |
| rpsL | 781892 | c.333A>G | synonymous_variant | 1.0 |
| rpsL | 781898 | c.339A>T | synonymous_variant | 1.0 |
| rpsL | 781907 | c.348T>C | synonymous_variant | 1.0 |
| rpsL | 781910 | c.351C>T | synonymous_variant | 1.0 |
| rpsL | 781916 | c.357T>C | synonymous_variant | 1.0 |
| rpsL | 781929 | p.Gly124Ser | missense_variant | 1.0 |
| rpsL | 781933 | c.374G>A | splice_region_variant&stop_retained_variant | 1.0 |
| rplC | 800612 | c.-197A>G | upstream_gene_variant | 1.0 |
| rplC | 800639 | c.-170C>T | upstream_gene_variant | 1.0 |
| rplC | 800645 | c.-164C>G | upstream_gene_variant | 1.0 |
| rplC | 800648 | c.-161A>G | upstream_gene_variant | 1.0 |
| rplC | 800654 | c.-155T>C | upstream_gene_variant | 1.0 |
| rplC | 800666 | c.-143C>T | upstream_gene_variant | 1.0 |
| rplC | 800672 | c.-137G>C | upstream_gene_variant | 1.0 |
| rplC | 800678 | c.-131C>T | upstream_gene_variant | 1.0 |
| rplC | 800693 | c.-116A>C | upstream_gene_variant | 1.0 |
| rplC | 800703 | c.-106_-104delTTGinsCTC | 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 | 800760 | c.-49_-47delCTTinsTTG | upstream_gene_variant | 1.0 |
| rplC | 800780 | c.-29C>G | upstream_gene_variant | 1.0 |
| rplC | 800796 | c.-12_-9delTTGG | upstream_gene_variant | 1.0 |
| rplC | 800808 | c.-1A>C | upstream_gene_variant | 1.0 |
| rplC | 800815 | c.7C>A | synonymous_variant | 1.0 |
| rplC | 800820 | c.12G>A | synonymous_variant | 1.0 |
| rplC | 800823 | c.15C>A | synonymous_variant | 1.0 |
| rplC | 800829 | c.21C>G | synonymous_variant | 1.0 |
| rplC | 800832 | c.24T>C | synonymous_variant | 1.0 |
| rplC | 800850 | c.42G>A | synonymous_variant | 1.0 |
| rplC | 800856 | c.48A>G | synonymous_variant | 1.0 |
| rplC | 800865 | p.Glu19Asp | missense_variant | 1.0 |
| rplC | 800867 | p.Ser20Asn | missense_variant | 1.0 |
| rplC | 800872 | c.64_66delAGAinsCGG | synonymous_variant | 1.0 |
| rplC | 800877 | c.69A>T | synonymous_variant | 1.0 |
| rplC | 800880 | c.72A>C | synonymous_variant | 1.0 |
| rplC | 800892 | c.84G>C | synonymous_variant | 1.0 |
| rplC | 800904 | c.96G>A | synonymous_variant | 1.0 |
| fbiC | 1303435 | p.Ser169Thr | missense_variant | 1.0 |
| fbiC | 1303441 | c.511T>C | synonymous_variant | 1.0 |
| fbiC | 1303444 | p.Ser172Asp | missense_variant | 1.0 |
| fbiC | 1303449 | c.519C>T | synonymous_variant | 1.0 |
| fbiC | 1303464 | c.534A>G | synonymous_variant | 1.0 |
| fbiC | 1303470 | c.540T>G | synonymous_variant | 1.0 |
| fbiC | 1303473 | c.543G>C | synonymous_variant | 1.0 |
| fbiC | 1303480 | p.Gln184Glu | missense_variant | 1.0 |
| fbiC | 1303485 | c.555C>G | synonymous_variant | 1.0 |
| fbiC | 1303488 | c.558G>T | synonymous_variant | 1.0 |
| fbiC | 1303492 | c.562_564delTTGinsCTT | synonymous_variant | 1.0 |
| fbiC | 1303500 | c.570C>T | synonymous_variant | 1.0 |
| fbiC | 1303506 | c.576C>T | synonymous_variant | 1.0 |
| fbiC | 1303512 | c.582T>C | synonymous_variant | 1.0 |
| fbiC | 1303527 | c.597G>C | synonymous_variant | 1.0 |
| fbiC | 1303531 | p.Met201Leu | missense_variant | 1.0 |
| fbiC | 1303534 | p.Ser202Ala | missense_variant | 1.0 |
| fbiC | 1303545 | c.615A>G | synonymous_variant | 1.0 |
| fbiC | 1303551 | c.621G>C | synonymous_variant | 1.0 |
| fbiC | 1303554 | c.624G>C | synonymous_variant | 1.0 |
| fbiC | 1303575 | c.645G>C | synonymous_variant | 1.0 |
| fbiC | 1303581 | c.651G>C | synonymous_variant | 1.0 |
| fbiC | 1303584 | c.654C>G | synonymous_variant | 1.0 |
| fbiC | 1303590 | c.660A>G | synonymous_variant | 1.0 |
| fbiC | 1303594 | c.664C>T | synonymous_variant | 1.0 |
| fbiC | 1303680 | c.750G>A | synonymous_variant | 1.0 |
| fbiC | 1303686 | c.756C>G | synonymous_variant | 1.0 |
| fbiC | 1303689 | c.759T>C | synonymous_variant | 1.0 |
| fbiC | 1303695 | c.765T>C | synonymous_variant | 1.0 |
| fbiC | 1303698 | c.768C>G | synonymous_variant | 1.0 |
| fbiC | 1303701 | c.771C>G | synonymous_variant | 1.0 |
| fbiC | 1303726 | p.Thr266Asp | missense_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 | 1303740 | c.810C>T | synonymous_variant | 1.0 |
| fbiC | 1303746 | p.Asp272Glu | missense_variant | 1.0 |
| fbiC | 1303750 | p.Leu274Ile | missense_variant | 1.0 |
| fbiC | 1303761 | c.831T>C | synonymous_variant | 1.0 |
| fbiC | 1303768 | p.Ser280Val | missense_variant | 1.0 |
| fbiC | 1303779 | c.849G>A | synonymous_variant | 1.0 |
| fbiC | 1303789 | p.Ile287Val | missense_variant | 1.0 |
| fbiC | 1303794 | c.864A>G | synonymous_variant | 1.0 |
| fbiC | 1303812 | c.882C>T | synonymous_variant | 1.0 |
| fbiC | 1304465 | p.Gly512Asp | missense_variant | 1.0 |
| fbiC | 1304484 | c.1554C>G | synonymous_variant | 1.0 |
| fbiC | 1304493 | p.Asp521Glu | missense_variant | 1.0 |
| fbiC | 1304499 | c.1569T>G | synonymous_variant | 1.0 |
| fbiC | 1304503 | p.Leu525Met | missense_variant | 1.0 |
| fbiC | 1304512 | p.Val528Leu | missense_variant | 1.0 |
| fbiC | 1304517 | c.1587C>T | synonymous_variant | 1.0 |
| fbiC | 1304520 | c.1590A>G | synonymous_variant | 1.0 |
| fbiC | 1304533 | p.Leu535Ile | missense_variant | 1.0 |
| fbiC | 1304538 | c.1608C>T | synonymous_variant | 1.0 |
| fbiC | 1304539 | p.Arg537Ala | missense_variant | 1.0 |
| fbiC | 1304547 | c.1617C>G | synonymous_variant | 1.0 |
| fbiC | 1304550 | c.1620C>G | synonymous_variant | 1.0 |
| fbiC | 1304556 | c.1626C>T | synonymous_variant | 1.0 |
| fbiC | 1304559 | p.Glu543Asp | missense_variant | 1.0 |
| fbiC | 1304562 | c.1632G>C | synonymous_variant | 1.0 |
| fbiC | 1304565 | c.1635C>G | synonymous_variant | 1.0 |
| fbiC | 1304567 | p.Phe546Tyr | missense_variant | 1.0 |
| fbiC | 1304574 | c.1644C>G | synonymous_variant | 1.0 |
| fbiC | 1304580 | c.1650T>G | synonymous_variant | 1.0 |
| fbiC | 1304613 | c.1683T>C | synonymous_variant | 1.0 |
| atpE | 1461083 | c.39T>C | synonymous_variant | 1.0 |
| atpE | 1461086 | c.42A>T | synonymous_variant | 1.0 |
| atpE | 1461087 | c.43C>T | synonymous_variant | 1.0 |
| atpE | 1461132 | p.Val30Ile | missense_variant | 1.0 |
| atpE | 1461146 | c.102G>T | synonymous_variant | 1.0 |
| atpE | 1461149 | c.105T>G | synonymous_variant | 1.0 |
| atpE | 1461161 | c.117C>G | synonymous_variant | 1.0 |
| atpE | 1461164 | c.120C>T | synonymous_variant | 1.0 |
| atpE | 1461167 | c.123G>T | synonymous_variant | 1.0 |
| atpE | 1461170 | c.126A>G | synonymous_variant | 1.0 |
| atpE | 1461179 | c.135G>T | synonymous_variant | 1.0 |
| atpE | 1461182 | c.138A>G | synonymous_variant | 1.0 |
| atpE | 1461185 | c.141G>C | synonymous_variant | 1.0 |
| atpE | 1461197 | c.153A>G | synonymous_variant | 1.0 |
| atpE | 1461219 | c.175T>C | synonymous_variant | 1.0 |
| atpE | 1461230 | c.186G>T | synonymous_variant | 1.0 |
| atpE | 1461233 | c.189A>C | synonymous_variant | 1.0 |
| atpE | 1461251 | c.207G>C | synonymous_variant | 1.0 |
| atpE | 1461254 | c.210T>C | synonymous_variant | 1.0 |
| rrs | 1471922 | n.78delT | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471931 | n.87delA | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471985 | n.140T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472030 | n.185G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472031 | n.186G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472032 | n.187G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472033 | n.188A>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472035 | n.190G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472040 | n.195T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472041 | n.196C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472042 | n.197T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472043 | n.198T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472050 | n.205G>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 | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472287 | n.442C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472297 | n.453_465delGTCCGGGTTCTCT | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472327 | n.482G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472337 | n.492C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472380 | n.535G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472838 | n.993A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472846 | n.1001C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472847 | n.1002G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472860 | n.1015C>T | non_coding_transcript_exon_variant | 0.96 |
| rrs | 1472861 | n.1016G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472877 | n.1032T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472957 | n.1112C>T | 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 |
| rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473082 | n.1237G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473099 | n.1254T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473129 | n.1284C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473288 | n.1443C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473291 | n.1446G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473676 | n.19G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473684 | n.27G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473699 | n.43delG | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473707 | n.50T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473717 | n.60G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473731 | n.74T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473746 | n.89T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473756 | n.99G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473812 | n.155G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473814 | n.157A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473815 | n.158T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473829 | n.172G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473831 | n.174G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473832 | n.175C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473839 | n.182G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473887 | n.230T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473888 | n.231T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473923 | n.266C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473924 | n.267_268insT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473937 | n.280C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473943 | n.286G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473945 | n.288T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473946 | n.289A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473950 | n.293G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474030 | n.373G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474044 | n.387C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474051 | n.394T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474054 | n.397T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474056 | n.399T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474061 | n.404T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474074 | n.417C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474089 | n.432C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474093 | n.436G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474100 | n.443C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474103 | n.446A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474106 | n.449_450insCT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474109 | n.453_454delAT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474130 | n.473C>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 | 1474181 | n.524_525insT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474184 | n.527C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474185 | n.529delA | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474263 | n.606G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474282 | n.625G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474291 | n.635_649delTTCCTCTCCGGAGGA | 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 | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474376 | n.719T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474413 | n.756A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474415 | n.759_781delCACACGCGCATACGCGCGTGTGA | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474507 | n.850G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474639 | n.982G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474640 | n.983C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474717 | n.1060A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474722 | n.1065T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474743 | n.1086T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474803 | n.1146G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475031 | n.1374G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475061 | n.1406delA | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475076 | n.1419C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475120 | n.1463G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475129 | n.1472G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475202 | n.1545G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475209 | n.1552G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475220 | n.1563G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475297 | n.1640C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475337 | n.1680C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475343 | n.1686A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475346 | n.1689C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475353 | n.1696A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475358 | n.1701T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475361 | n.1704G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475369 | n.1712G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475374 | n.1719_1722delAGAG | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475382 | n.1725_1726insCATC | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475395 | n.1738T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475396 | n.1739C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475397 | n.1740G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475398 | n.1741C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475401 | n.1745delC | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475406 | n.1749T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475443 | n.1786G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475475 | n.1818C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475479 | n.1822C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475573 | n.1916G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475649 | n.1992A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475760 | n.2105_2106delGC | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475764 | n.2107A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475765 | n.2108A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475989 | n.2332T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475993 | n.2336C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476033 | n.2376T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476046 | n.2389G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476056 | n.2399G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476058 | n.2401T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476085 | n.2428G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476088 | n.2431A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476103 | n.2446C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476105 | n.2448G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476106 | n.2449A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476114 | n.2457T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476221 | n.2564T>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 | 1476260 | n.2603A>G | 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 | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476608 | n.2951C>G | 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 | 1476665 | n.3008T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476666 | n.3009C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476674 | n.3017T>C | non_coding_transcript_exon_variant | 0.8 |
| rrl | 1476684 | n.3027C>T | non_coding_transcript_exon_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>C | upstream_gene_variant | 1.0 |
| fabG1 | 1673680 | p.Pro81Ala | missense_variant | 1.0 |
| inhA | 1673692 | c.-510C>T | upstream_gene_variant | 1.0 |
| inhA | 1673703 | c.-499C>T | upstream_gene_variant | 1.0 |
| fabG1 | 1673709 | c.271_272delCT | frameshift_variant | 1.0 |
| fabG1 | 1673714 | c.275_276insG | frameshift_variant | 1.0 |
| fabG1 | 1673717 | c.278_279insA | frameshift_variant | 1.0 |
| inhA | 1673724 | c.-478A>G | upstream_gene_variant | 1.0 |
| inhA | 1673730 | c.-472C>G | upstream_gene_variant | 1.0 |
| inhA | 1673736 | c.-466G>C | upstream_gene_variant | 1.0 |
| inhA | 1673742 | c.-460C>G | upstream_gene_variant | 1.0 |
| inhA | 1673748 | c.-454A>G | upstream_gene_variant | 1.0 |
| fabG1 | 1673758 | p.Lys107Gln | missense_variant | 1.0 |
| inhA | 1673772 | c.-430C>G | upstream_gene_variant | 1.0 |
| inhA | 1673778 | c.-424C>G | upstream_gene_variant | 1.0 |
| inhA | 1673802 | c.-400A>G | upstream_gene_variant | 1.0 |
| inhA | 1673808 | c.-394A>C | upstream_gene_variant | 1.0 |
| fabG1 | 1673829 | p.Asn130Lys | missense_variant | 1.0 |
| fabG1 | 1673830 | p.Lys131Arg | missense_variant | 1.0 |
| inhA | 1673838 | c.-364T>C | upstream_gene_variant | 1.0 |
| inhA | 1673841 | c.-361A>G | upstream_gene_variant | 1.0 |
| inhA | 1673847 | c.-355A>C | upstream_gene_variant | 1.0 |
| inhA | 1673853 | c.-349A>C | upstream_gene_variant | 1.0 |
| inhA | 1673868 | c.-334C>T | upstream_gene_variant | 1.0 |
| fabG1 | 1673870 | p.Ser144Thr | missense_variant | 1.0 |
| inhA | 1673877 | c.-325C>A | upstream_gene_variant | 1.0 |
| inhA | 1673901 | c.-301A>G | upstream_gene_variant | 1.0 |
| inhA | 1673916 | c.-286A>G | 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 |
| fabG1 | 1673926 | p.Met163Leu | missense_variant | 1.0 |
| inhA | 1673931 | c.-271C>G | upstream_gene_variant | 1.0 |
| inhA | 1673940 | c.-262C>T | upstream_gene_variant | 1.0 |
| inhA | 1673946 | c.-256C>T | upstream_gene_variant | 1.0 |
| inhA | 1673952 | c.-250G>C | upstream_gene_variant | 1.0 |
| inhA | 1673955 | c.-247G>C | upstream_gene_variant | 1.0 |
| fabG1 | 1674006 | p.Asp189Glu | missense_variant | 1.0 |
| inhA | 1674012 | c.-190C>T | upstream_gene_variant | 1.0 |
| inhA | 1674021 | c.-181G>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 | 1674042 | c.-160G>T | upstream_gene_variant | 1.0 |
| fabG1 | 1674049 | p.Gln204Glu | missense_variant | 1.0 |
| inhA | 1674054 | c.-148T>C | upstream_gene_variant | 1.0 |
| inhA | 1674060 | c.-142A>G | upstream_gene_variant | 1.0 |
| inhA | 1674072 | c.-130C>G | upstream_gene_variant | 1.0 |
| inhA | 1674078 | c.-124C>G | upstream_gene_variant | 1.0 |
| fabG1 | 1674079 | p.Pro214Ala | missense_variant | 1.0 |
| inhA | 1674120 | c.-82G>A | upstream_gene_variant | 1.0 |
| inhA | 1674126 | c.-76G>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 | 1674144 | c.-58G>A | upstream_gene_variant | 1.0 |
| inhA | 1674147 | c.-55C>G | upstream_gene_variant | 1.0 |
| inhA | 1674156 | c.-46C>T | upstream_gene_variant | 1.0 |
| inhA | 1674159 | c.-43C>T | upstream_gene_variant | 1.0 |
| inhA | 1674171 | c.-31T>C | upstream_gene_variant | 1.0 |
| inhA | 1674531 | p.Asp110Glu | missense_variant | 1.0 |
| inhA | 1674534 | c.333G>C | synonymous_variant | 1.0 |
| inhA | 1674539 | p.Tyr113Phe | missense_variant | 1.0 |
| inhA | 1674542 | p.Ala114Glu | missense_variant | 1.0 |
| inhA | 1674550 | p.Ser117Ala | missense_variant | 1.0 |
| inhA | 1674559 | p.Ile120Phe | missense_variant | 1.0 |
| inhA | 1674575 | p.Tyr125Phe | missense_variant | 1.0 |
| inhA | 1674585 | c.384T>G | synonymous_variant | 1.0 |
| inhA | 1674589 | p.Met130Leu | missense_variant | 1.0 |
| inhA | 1674600 | c.399G>A | synonymous_variant | 1.0 |
| inhA | 1674601 | c.400C>T | synonymous_variant | 1.0 |
| inhA | 1674609 | c.408G>C | synonymous_variant | 1.0 |
| inhA | 1674618 | c.417C>T | synonymous_variant | 1.0 |
| inhA | 1674621 | c.420C>G | synonymous_variant | 1.0 |
| inhA | 1674624 | c.423A>C | synonymous_variant | 1.0 |
| inhA | 1674627 | c.426T>C | synonymous_variant | 1.0 |
| inhA | 1674628 | c.427_428delTCinsAG | synonymous_variant | 1.0 |
| inhA | 1674636 | c.435C>G | synonymous_variant | 1.0 |
| inhA | 1674656 | p.Ser152Thr | missense_variant | 1.0 |
| inhA | 1674663 | c.462G>C | synonymous_variant | 1.0 |
| inhA | 1674670 | p.Ala157Phe | missense_variant | 1.0 |
| inhA | 1674690 | c.489C>G | synonymous_variant | 1.0 |
| inhA | 1674771 | c.570C>G | synonymous_variant | 1.0 |
| inhA | 1674774 | c.573A>C | synonymous_variant | 1.0 |
| inhA | 1674777 | c.576C>T | synonymous_variant | 1.0 |
| inhA | 1674795 | c.594G>A | synonymous_variant | 1.0 |
| inhA | 1674801 | c.600T>C | synonymous_variant | 1.0 |
| inhA | 1674804 | c.603G>C | synonymous_variant | 1.0 |
| inhA | 1674813 | c.612C>T | synonymous_variant | 1.0 |
| inhA | 1674855 | c.654C>G | synonymous_variant | 1.0 |
| inhA | 1674861 | p.Glu220Asp | missense_variant | 1.0 |
| inhA | 1674876 | c.675C>T | synonymous_variant | 1.0 |
| inhA | 1674879 | c.678T>C | synonymous_variant | 1.0 |
| inhA | 1674892 | p.Asn231Asp | missense_variant | 1.0 |
| inhA | 1674903 | c.702T>C | synonymous_variant | 1.0 |
| inhA | 1674904 | p.Ala235Pro | missense_variant | 1.0 |
| inhA | 1674909 | c.708G>T | synonymous_variant | 1.0 |
| inhA | 1674939 | c.738G>C | synonymous_variant | 1.0 |
| inhA | 1674942 | c.741T>C | synonymous_variant | 1.0 |
| inhA | 1674945 | c.744C>T | synonymous_variant | 1.0 |
| inhA | 1674954 | c.753G>C | synonymous_variant | 1.0 |
| inhA | 1674957 | c.756G>C | synonymous_variant | 1.0 |
| inhA | 1674963 | c.762G>C | synonymous_variant | 1.0 |
| inhA | 1674966 | c.765T>C | synonymous_variant | 1.0 |
| inhA | 1674977 | p.Tyr259Phe | missense_variant | 1.0 |
| rpsA | 1833511 | c.-31G>T | upstream_gene_variant | 1.0 |
| rpsA | 1833514 | c.-28C>A | upstream_gene_variant | 1.0 |
| rpsA | 1833517 | c.-24delC | upstream_gene_variant | 1.0 |
| rpsA | 1833536 | c.-6A>C | upstream_gene_variant | 1.0 |
| rpsA | 1833547 | c.6G>A | synonymous_variant | 1.0 |
| rpsA | 1833559 | c.18C>G | synonymous_variant | 1.0 |
| rpsA | 1833578 | p.Val13Ile | missense_variant | 1.0 |
| rpsA | 1833589 | c.48A>T | synonymous_variant | 1.0 |
| rpsA | 1833595 | c.54T>G | synonymous_variant | 1.0 |
| rpsA | 1833596 | p.Ser19Ala | missense_variant | 1.0 |
| rpsA | 1833604 | c.63C>T | synonymous_variant | 1.0 |
| rpsA | 1833616 | c.75A>T | synonymous_variant | 1.0 |
| rpsA | 1833619 | c.78A>C | synonymous_variant | 1.0 |
| rpsA | 1833622 | c.81C>T | synonymous_variant | 1.0 |
| rpsA | 1833625 | c.84A>G | synonymous_variant | 1.0 |
| rpsA | 1833664 | c.123C>G | synonymous_variant | 1.0 |
| rpsA | 1833676 | c.135A>G | synonymous_variant | 1.0 |
| rpsA | 1833679 | c.138G>T | synonymous_variant | 1.0 |
| rpsA | 1833685 | c.144G>C | synonymous_variant | 1.0 |
| rpsA | 1833691 | c.150G>A | synonymous_variant | 1.0 |
| rpsA | 1833694 | c.153G>T | synonymous_variant | 1.0 |
| rpsA | 1833697 | c.156C>T | synonymous_variant | 1.0 |
| rpsA | 1833700 | c.159C>T | synonymous_variant | 1.0 |
| rpsA | 1833709 | c.168C>T | synonymous_variant | 1.0 |
| rpsA | 1833724 | c.183C>T | synonymous_variant | 1.0 |
| rpsA | 1833727 | c.186G>C | synonymous_variant | 1.0 |
| rpsA | 1833733 | c.192C>G | synonymous_variant | 1.0 |
| rpsA | 1833734 | p.Ala65Ser | missense_variant | 1.0 |
| rpsA | 1833745 | c.204G>C | synonymous_variant | 1.0 |
| rpsA | 1833748 | c.207C>G | synonymous_variant | 1.0 |
| rpsA | 1833760 | c.219C>T | synonymous_variant | 1.0 |
| rpsA | 1833772 | c.231C>T | synonymous_variant | 1.0 |
| rpsA | 1833787 | c.246C>G | synonymous_variant | 1.0 |
| rpsA | 1833790 | c.249T>C | synonymous_variant | 1.0 |
| rpsA | 1833802 | c.261A>G | synonymous_variant | 1.0 |
| rpsA | 1833811 | c.270G>T | synonymous_variant | 1.0 |
| rpsA | 1833823 | c.282G>A | synonymous_variant | 1.0 |
| rpsA | 1833832 | c.291G>A | synonymous_variant | 1.0 |
| rpsA | 1833838 | c.297G>T | synonymous_variant | 1.0 |
| rpsA | 1833841 | c.300C>G | synonymous_variant | 1.0 |
| rpsA | 1833847 | c.306C>G | synonymous_variant | 1.0 |
| rpsA | 1833856 | c.315A>G | synonymous_variant | 1.0 |
| rpsA | 1833862 | c.321G>T | synonymous_variant | 1.0 |
| rpsA | 1833874 | c.333T>G | synonymous_variant | 1.0 |
| rpsA | 1833877 | c.336C>G | synonymous_variant | 1.0 |
| rpsA | 1833886 | c.345C>G | synonymous_variant | 1.0 |
| rpsA | 1833892 | c.351G>A | synonymous_variant | 1.0 |
| rpsA | 1833894 | p.Ala118Glu | missense_variant | 1.0 |
| rpsA | 1833898 | c.357C>G | synonymous_variant | 1.0 |
| rpsA | 1833928 | c.387G>C | synonymous_variant | 1.0 |
| rpsA | 1833949 | c.408T>C | synonymous_variant | 1.0 |
| rpsA | 1833961 | c.420C>G | synonymous_variant | 1.0 |
| rpsA | 1833970 | c.429G>C | synonymous_variant | 1.0 |
| rpsA | 1833979 | c.438T>C | synonymous_variant | 1.0 |
| rpsA | 1833991 | c.450C>A | synonymous_variant | 1.0 |
| rpsA | 1834000 | c.459G>C | synonymous_variant | 1.0 |
| rpsA | 1834009 | c.468C>T | synonymous_variant | 1.0 |
| rpsA | 1834012 | c.471G>T | synonymous_variant | 1.0 |
| rpsA | 1834015 | c.474G>C | synonymous_variant | 1.0 |
| rpsA | 1834021 | c.480C>T | synonymous_variant | 1.0 |
| rpsA | 1834030 | c.489C>G | synonymous_variant | 1.0 |
| rpsA | 1834069 | c.528G>C | synonymous_variant | 1.0 |
| rpsA | 1834073 | p.Lys178Arg | missense_variant | 1.0 |
| rpsA | 1834099 | c.558C>G | synonymous_variant | 1.0 |
| rpsA | 1834102 | c.561T>C | synonymous_variant | 1.0 |
| rpsA | 1834105 | c.564C>G | synonymous_variant | 1.0 |
| rpsA | 1834112 | c.571C>T | synonymous_variant | 1.0 |
| rpsA | 1834129 | c.588C>G | synonymous_variant | 1.0 |
| rpsA | 1834135 | c.594G>C | synonymous_variant | 1.0 |
| rpsA | 1834148 | c.607C>T | synonymous_variant | 1.0 |
| rpsA | 1834165 | c.624A>G | synonymous_variant | 1.0 |
| rpsA | 1834169 | p.Thr210Ala | missense_variant | 1.0 |
| rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
| rpsA | 1834213 | c.672G>C | synonymous_variant | 1.0 |
| rpsA | 1834228 | c.687C>T | synonymous_variant | 1.0 |
| rpsA | 1834231 | c.690T>G | synonymous_variant | 1.0 |
| rpsA | 1834234 | c.693G>T | synonymous_variant | 1.0 |
| rpsA | 1834240 | c.699T>C | synonymous_variant | 1.0 |
| rpsA | 1834249 | c.708T>C | synonymous_variant | 1.0 |
| rpsA | 1834252 | c.711C>G | synonymous_variant | 1.0 |
| rpsA | 1834261 | c.720A>G | synonymous_variant | 1.0 |
| rpsA | 1834264 | c.723G>C | synonymous_variant | 1.0 |
| rpsA | 1834279 | c.738C>T | 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 | 1834327 | c.786G>T | synonymous_variant | 1.0 |
| rpsA | 1834348 | c.807T>C | synonymous_variant | 1.0 |
| rpsA | 1834366 | c.825A>G | synonymous_variant | 1.0 |
| rpsA | 1834375 | c.834G>A | synonymous_variant | 1.0 |
| rpsA | 1834378 | c.837T>C | synonymous_variant | 1.0 |
| rpsA | 1834396 | c.855G>T | 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 | 1834435 | c.894G>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 | 1834483 | c.942G>A | synonymous_variant | 1.0 |
| rpsA | 1834489 | c.948T>C | synonymous_variant | 1.0 |
| rpsA | 1834519 | c.978G>C | synonymous_variant | 1.0 |
| rpsA | 1834520 | p.Ala327Ser | missense_variant | 1.0 |
| rpsA | 1834528 | c.987T>C | synonymous_variant | 1.0 |
| rpsA | 1834543 | c.1002C>G | synonymous_variant | 1.0 |
| rpsA | 1834546 | c.1005T>C | synonymous_variant | 1.0 |
| rpsA | 1834552 | c.1011G>T | synonymous_variant | 1.0 |
| rpsA | 1834555 | c.1014T>G | synonymous_variant | 1.0 |
| rpsA | 1834557 | p.Ala339Gly | missense_variant | 1.0 |
| rpsA | 1834606 | c.1065C>T | synonymous_variant | 1.0 |
| rpsA | 1834609 | c.1068T>C | synonymous_variant | 1.0 |
| rpsA | 1834619 | c.1078T>C | synonymous_variant | 1.0 |
| rpsA | 1834622 | c.1081_1083delTCGinsAGC | synonymous_variant | 1.0 |
| rpsA | 1834633 | c.1092A>G | synonymous_variant | 1.0 |
| rpsA | 1834639 | c.1098T>C | synonymous_variant | 1.0 |
| rpsA | 1834666 | c.1125G>C | synonymous_variant | 1.0 |
| rpsA | 1834667 | p.Ala376Ser | missense_variant | 1.0 |
| rpsA | 1834690 | c.1149T>C | synonymous_variant | 1.0 |
| rpsA | 1834700 | p.Gln387Ala | missense_variant | 0.95 |
| rpsA | 1834705 | c.1164C>G | synonymous_variant | 1.0 |
| rpsA | 1834720 | c.1179C>G | synonymous_variant | 1.0 |
| rpsA | 1834732 | c.1191T>C | synonymous_variant | 1.0 |
| rpsA | 1834738 | c.1197A>G | synonymous_variant | 1.0 |
| rpsA | 1834747 | c.1206A>G | synonymous_variant | 1.0 |
| rpsA | 1834759 | c.1218A>C | synonymous_variant | 1.0 |
| rpsA | 1834765 | p.Glu408Asp | missense_variant | 1.0 |
| rpsA | 1834774 | c.1233C>T | synonymous_variant | 1.0 |
| rpsA | 1834776 | p.Ala412Glu | missense_variant | 1.0 |
| rpsA | 1834780 | c.1239A>G | synonymous_variant | 1.0 |
| rpsA | 1834786 | c.1245A>G | synonymous_variant | 1.0 |
| rpsA | 1834789 | c.1248T>C | synonymous_variant | 1.0 |
| rpsA | 1834810 | c.1269C>T | synonymous_variant | 1.0 |
| rpsA | 1834813 | c.1272G>T | synonymous_variant | 1.0 |
| ndh | 2102857 | c.186T>C | synonymous_variant | 1.0 |
| ndh | 2102899 | c.144T>C | synonymous_variant | 1.0 |
| ndh | 2102908 | c.135C>T | synonymous_variant | 1.0 |
| ndh | 2102916 | p.Ile43Val | missense_variant | 1.0 |
| ndh | 2102921 | p.Lys41Thr | missense_variant | 1.0 |
| ndh | 2102925 | p.Ile40Val | missense_variant | 1.0 |
| ndh | 2102929 | c.114T>C | synonymous_variant | 1.0 |
| ndh | 2102934 | p.Asp37Asn | missense_variant | 1.0 |
| ndh | 2102938 | c.105G>T | synonymous_variant | 1.0 |
| ndh | 2102947 | p.Lys32Thr | missense_variant | 1.0 |
| ndh | 2102953 | c.90A>C | synonymous_variant | 1.0 |
| ndh | 2102960 | p.Asn28Thr | missense_variant | 1.0 |
| ndh | 2102962 | c.81A>G | synonymous_variant | 1.0 |
| katG | 2155662 | c.450G>C | synonymous_variant | 1.0 |
| katG | 2155674 | c.438G>C | synonymous_variant | 1.0 |
| katG | 2155683 | p.Lys143Arg | missense_variant | 1.0 |
| katG | 2155716 | c.396T>G | synonymous_variant | 1.0 |
| katG | 2155722 | c.390G>A | synonymous_variant | 1.0 |
| katG | 2155741 | p.Gly124Ala | missense_variant | 1.0 |
| katG | 2155743 | c.369G>C | synonymous_variant | 1.0 |
| katG | 2155746 | c.366C>G | synonymous_variant | 1.0 |
| katG | 2155761 | c.351C>T | synonymous_variant | 1.0 |
| katG | 2155765 | p.His116Gly | missense_variant | 1.0 |
| katG | 2155769 | p.Ile115Val | missense_variant | 1.0 |
| katG | 2155785 | c.327T>C | synonymous_variant | 1.0 |
| katG | 2155794 | c.318G>C | synonymous_variant | 1.0 |
| kasA | 2517917 | c.-198G>C | upstream_gene_variant | 1.0 |
| kasA | 2517941 | c.-174C>G | upstream_gene_variant | 1.0 |
| kasA | 2517953 | c.-162C>T | upstream_gene_variant | 1.0 |
| kasA | 2517959 | c.-156C>T | upstream_gene_variant | 1.0 |
| kasA | 2517962 | c.-153C>G | upstream_gene_variant | 1.0 |
| kasA | 2517965 | c.-150C>G | upstream_gene_variant | 1.0 |
| kasA | 2517968 | c.-147T>C | upstream_gene_variant | 1.0 |
| kasA | 2517974 | c.-141T>C | upstream_gene_variant | 1.0 |
| kasA | 2518756 | c.642G>C | synonymous_variant | 1.0 |
| kasA | 2518768 | c.654C>G | synonymous_variant | 1.0 |
| kasA | 2518771 | c.657C>A | synonymous_variant | 1.0 |
| kasA | 2518774 | c.660C>T | synonymous_variant | 1.0 |
| kasA | 2518783 | c.669T>C | synonymous_variant | 1.0 |
| kasA | 2518787 | p.Arg225Lys | missense_variant | 1.0 |
| kasA | 2518792 | c.678C>T | synonymous_variant | 1.0 |
| kasA | 2518795 | c.681C>T | synonymous_variant | 1.0 |
| kasA | 2518798 | c.684G>T | synonymous_variant | 1.0 |
| kasA | 2518809 | p.Lys232Arg | missense_variant | 1.0 |
| kasA | 2518822 | c.708C>A | synonymous_variant | 1.0 |
| kasA | 2518825 | c.711T>C | synonymous_variant | 1.0 |
| kasA | 2518846 | c.732G>C | synonymous_variant | 1.0 |
| kasA | 2518849 | c.735G>C | synonymous_variant | 1.0 |
| kasA | 2518853 | p.Leu247Val | missense_variant | 1.0 |
| kasA | 2518864 | c.750G>C | synonymous_variant | 1.0 |
| kasA | 2518867 | c.753G>A | synonymous_variant | 1.0 |
| ahpC | 2726571 | p.Ala127Ser | missense_variant | 1.0 |
| ahpC | 2726576 | c.384C>T | synonymous_variant | 1.0 |
| ahpC | 2726582 | c.390G>C | synonymous_variant | 1.0 |
| ahpC | 2726593 | p.Val134Ala | missense_variant | 1.0 |
| ahpC | 2726600 | c.408T>C | synonymous_variant | 1.0 |
| ahpC | 2726613 | p.Asn141Asp | missense_variant | 1.0 |
| ahpC | 2726619 | p.Glu143Ile | missense_variant | 1.0 |
| ahpC | 2726636 | c.444G>T | synonymous_variant | 1.0 |
| ahpC | 2726638 | p.Ala149Val | missense_variant | 1.0 |
| ahpC | 2726642 | c.450C>A | synonymous_variant | 1.0 |
| ahpC | 2726651 | c.459G>C | synonymous_variant | 1.0 |
| ahpC | 2726657 | c.465A>C | synonymous_variant | 1.0 |
| ahpC | 2726663 | c.471C>T | synonymous_variant | 1.0 |
| ahpC | 2726669 | p.Asp159Glu | missense_variant | 1.0 |
| ahpC | 2726675 | c.483A>G | synonymous_variant | 1.0 |
| ahpC | 2726678 | c.486G>C | synonymous_variant | 1.0 |
| ahpC | 2726681 | c.489A>T | synonymous_variant | 1.0 |
| ahpC | 2726687 | c.495C>G | synonymous_variant | 1.0 |
| ahpC | 2726693 | c.501C>A | synonymous_variant | 1.0 |
| ahpC | 2726696 | c.504C>G | synonymous_variant | 1.0 |
| ahpC | 2726717 | c.525A>C | synonymous_variant | 1.0 |
| ahpC | 2726735 | c.543C>T | synonymous_variant | 1.0 |
| Rv2752c | 3065982 | c.210G>C | synonymous_variant | 1.0 |
| Rv2752c | 3065985 | c.207C>T | synonymous_variant | 1.0 |
| Rv2752c | 3065993 | p.Val67Ile | missense_variant | 1.0 |
| Rv2752c | 3066000 | p.Met64Ile | missense_variant | 1.0 |
| Rv2752c | 3066018 | c.174T>C | synonymous_variant | 1.0 |
| Rv2752c | 3066021 | c.171C>G | synonymous_variant | 1.0 |
| Rv2752c | 3066024 | c.168T>C | synonymous_variant | 1.0 |
| Rv2752c | 3066027 | c.165C>G | synonymous_variant | 1.0 |
| Rv2752c | 3066033 | p.Asp53Glu | missense_variant | 1.0 |
| Rv2752c | 3066036 | c.156C>T | synonymous_variant | 1.0 |
| Rv2752c | 3066042 | c.150T>G | synonymous_variant | 1.0 |
| Rv2752c | 3066045 | c.147T>C | synonymous_variant | 1.0 |
| Rv2752c | 3066048 | c.142_144delTTGinsCTC | synonymous_variant | 1.0 |
| Rv2752c | 3066054 | c.138T>A | synonymous_variant | 1.0 |
| Rv2752c | 3066066 | c.126T>C | synonymous_variant | 1.0 |
| Rv2752c | 3066071 | c.121T>C | synonymous_variant | 1.0 |
| Rv2752c | 3066075 | c.117A>T | synonymous_variant | 1.0 |
| Rv2752c | 3066081 | p.Leu37Arg | missense_variant | 1.0 |
| Rv2752c | 3066084 | p.His36Leu | missense_variant | 1.0 |
| Rv2752c | 3066087 | c.105A>G | synonymous_variant | 1.0 |
| Rv2752c | 3066118 | p.Asn25Ser | missense_variant | 1.0 |
| thyX | 3067316 | c.630A>C | synonymous_variant | 1.0 |
| thyX | 3067322 | c.624C>T | synonymous_variant | 1.0 |
| thyX | 3067325 | c.621A>G | synonymous_variant | 1.0 |
| thyX | 3067340 | c.606G>A | synonymous_variant | 1.0 |
| thyX | 3067349 | c.597G>C | synonymous_variant | 1.0 |
| thyX | 3067355 | c.591A>G | synonymous_variant | 1.0 |
| thyX | 3067367 | c.579G>C | synonymous_variant | 1.0 |
| thyX | 3067379 | c.567C>T | synonymous_variant | 1.0 |
| thyX | 3067385 | c.561C>G | synonymous_variant | 1.0 |
| thyX | 3067391 | c.555G>C | synonymous_variant | 1.0 |
| thyX | 3067394 | c.552G>C | synonymous_variant | 1.0 |
| thyX | 3067400 | c.544_546delCGCinsAGG | synonymous_variant | 1.0 |
| thyX | 3067406 | c.540A>G | synonymous_variant | 1.0 |
| thyX | 3067415 | c.531C>T | synonymous_variant | 1.0 |
| thyX | 3067418 | c.528C>G | synonymous_variant | 1.0 |
| thyX | 3067429 | p.Ala173Ser | missense_variant | 1.0 |
| thyX | 3067430 | c.516C>G | synonymous_variant | 1.0 |
| thyX | 3067439 | c.507A>G | synonymous_variant | 1.0 |
| thyA | 3073851 | c.621C>T | synonymous_variant | 1.0 |
| thyA | 3073854 | c.618C>T | synonymous_variant | 1.0 |
| thyA | 3073874 | p.Ile200Val | missense_variant | 1.0 |
| thyA | 3073878 | p.Glu198Asp | missense_variant | 1.0 |
| thyA | 3073881 | c.591C>G | synonymous_variant | 1.0 |
| thyA | 3073888 | p.Ser195Gly | missense_variant | 1.0 |
| thyA | 3073890 | c.580_582delTTGinsCTC | synonymous_variant | 1.0 |
| thyA | 3073893 | c.579C>A | synonymous_variant | 1.0 |
| thyA | 3073902 | c.570C>G | synonymous_variant | 1.0 |
| thyA | 3073905 | c.567C>G | synonymous_variant | 1.0 |
| thyA | 3073925 | c.547T>C | synonymous_variant | 1.0 |
| thyA | 3073929 | c.543T>C | synonymous_variant | 1.0 |
| thyA | 3073950 | c.522G>C | synonymous_variant | 1.0 |
| thyA | 3073953 | c.519T>G | synonymous_variant | 1.0 |
| thyA | 3073956 | c.516G>C | synonymous_variant | 1.0 |
| thyA | 3073980 | c.492C>T | synonymous_variant | 1.0 |
| thyA | 3073983 | c.489C>G | synonymous_variant | 1.0 |
| thyA | 3073989 | c.483T>C | synonymous_variant | 1.0 |
| thyA | 3073999 | p.Arg158Lys | missense_variant | 1.0 |
| thyA | 3074004 | c.468T>C | synonymous_variant | 1.0 |
| thyA | 3074010 | c.462C>T | synonymous_variant | 1.0 |
| thyA | 3074028 | c.444G>C | synonymous_variant | 1.0 |
| thyA | 3074031 | c.441T>C | synonymous_variant | 1.0 |
| thyA | 3074040 | c.432G>A | 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 | c.411A>G | synonymous_variant | 1.0 |
| thyA | 3074076 | c.396C>G | synonymous_variant | 1.0 |
| thyA | 3074082 | c.390G>C | synonymous_variant | 1.0 |
| thyA | 3074089 | p.Ile128Asn | missense_variant | 1.0 |
| thyA | 3074097 | c.375C>G | synonymous_variant | 1.0 |
| thyA | 3074106 | p.Asp122Asn | missense_variant | 1.0 |
| thyA | 3074120 | p.Leu118Met | missense_variant | 1.0 |
| thyA | 3074121 | p.Asp117Glu | missense_variant | 1.0 |
| thyA | 3074130 | c.342G>C | synonymous_variant | 1.0 |
| thyA | 3074133 | c.339C>T | synonymous_variant | 1.0 |
| thyA | 3074154 | c.318T>G | synonymous_variant | 1.0 |
| rpoA | 3877527 | c.981C>G | synonymous_variant | 1.0 |
| rpoA | 3877542 | c.966C>A | synonymous_variant | 1.0 |
| rpoA | 3877545 | c.963G>C | synonymous_variant | 1.0 |
| rpoA | 3877557 | c.951C>G | synonymous_variant | 1.0 |
| rpoA | 3877560 | c.948C>T | synonymous_variant | 1.0 |
| rpoA | 3877569 | p.Pro313Thr | missense_variant | 1.0 |
| rpoA | 3877587 | c.921A>G | synonymous_variant | 1.0 |
| rpoA | 3877593 | c.915C>T | synonymous_variant | 1.0 |
| rpoA | 3877617 | c.891G>C | synonymous_variant | 1.0 |
| rpoA | 3877638 | c.870T>C | synonymous_variant | 1.0 |
| rpoA | 3877647 | c.861C>T | synonymous_variant | 1.0 |
| rpoA | 3877656 | c.852T>G | synonymous_variant | 1.0 |
| rpoA | 3877665 | c.843C>G | synonymous_variant | 1.0 |
| rpoA | 3877668 | c.840A>G | synonymous_variant | 1.0 |
| rpoA | 3877677 | c.831G>C | synonymous_variant | 1.0 |
| rpoA | 3877680 | c.828G>T | synonymous_variant | 1.0 |
| rpoA | 3877686 | c.822A>G | synonymous_variant | 1.0 |
| rpoA | 3877692 | c.816G>C | synonymous_variant | 1.0 |
| rpoA | 3877704 | c.804G>T | synonymous_variant | 1.0 |
| rpoA | 3877728 | c.780C>G | synonymous_variant | 1.0 |
| rpoA | 3877731 | c.777G>T | synonymous_variant | 1.0 |
| rpoA | 3877734 | c.774G>C | synonymous_variant | 1.0 |
| rpoA | 3877737 | c.771G>C | synonymous_variant | 1.0 |
| rpoA | 3877743 | c.765T>C | synonymous_variant | 1.0 |
| rpoA | 3877752 | p.Asp252Glu | missense_variant | 1.0 |
| rpoA | 3877758 | c.750G>C | synonymous_variant | 1.0 |
| rpoA | 3877764 | c.744C>G | synonymous_variant | 1.0 |
| rpoA | 3877770 | c.738A>G | synonymous_variant | 1.0 |
| rpoA | 3877773 | c.735G>C | synonymous_variant | 1.0 |
| rpoA | 3877782 | c.726T>C | synonymous_variant | 1.0 |
| rpoA | 3877785 | c.723C>A | synonymous_variant | 1.0 |
| rpoA | 3877815 | c.693C>T | synonymous_variant | 1.0 |
| rpoA | 3877827 | c.681C>T | synonymous_variant | 1.0 |
| rpoA | 3877836 | c.672A>G | synonymous_variant | 1.0 |
| rpoA | 3877839 | c.669G>C | synonymous_variant | 1.0 |
| rpoA | 3877848 | c.660C>G | synonymous_variant | 1.0 |
| rpoA | 3877856 | c.652T>C | synonymous_variant | 1.0 |
| rpoA | 3877866 | c.642G>A | synonymous_variant | 1.0 |
| rpoA | 3877875 | c.633T>C | synonymous_variant | 1.0 |
| rpoA | 3877881 | c.627G>T | synonymous_variant | 1.0 |
| rpoA | 3877893 | c.615C>T | synonymous_variant | 1.0 |
| rpoA | 3877901 | p.Ser203Gly | missense_variant | 1.0 |
| rpoA | 3877905 | c.603A>G | synonymous_variant | 1.0 |
| rpoA | 3877908 | c.600T>C | synonymous_variant | 1.0 |
| rpoA | 3877920 | c.588G>C | synonymous_variant | 1.0 |
| rpoA | 3877929 | p.Ile193Val | missense_variant | 1.0 |
| rpoA | 3877962 | c.546G>C | synonymous_variant | 1.0 |
| rpoA | 3877971 | p.Asp179Glu | missense_variant | 1.0 |
| rpoA | 3877974 | c.534G>C | synonymous_variant | 1.0 |
| rpoA | 3877977 | p.Lys177Asn | missense_variant | 1.0 |
| rpoA | 3877989 | c.519A>G | synonymous_variant | 1.0 |
| rpoA | 3878001 | c.507A>G | synonymous_variant | 1.0 |
| rpoA | 3878019 | c.489A>C | synonymous_variant | 1.0 |
| rpoA | 3878031 | c.477T>C | synonymous_variant | 1.0 |
| rpoA | 3878034 | c.474A>G | synonymous_variant | 1.0 |
| rpoA | 3878046 | c.462T>C | synonymous_variant | 1.0 |
| rpoA | 3878050 | p.Arg153Lys | missense_variant | 1.0 |
| rpoA | 3878055 | c.453A>G | synonymous_variant | 1.0 |
| rpoA | 3878061 | c.447G>C | synonymous_variant | 1.0 |
| rpoA | 3878070 | c.438T>C | synonymous_variant | 1.0 |
| rpoA | 3878073 | c.435C>T | synonymous_variant | 1.0 |
| rpoA | 3878079 | c.429C>T | synonymous_variant | 1.0 |
| rpoA | 3878082 | c.426T>C | synonymous_variant | 1.0 |
| rpoA | 3878097 | c.411G>A | synonymous_variant | 1.0 |
| rpoA | 3878102 | p.Val136Ile | missense_variant | 1.0 |
| rpoA | 3878103 | c.405A>G | synonymous_variant | 1.0 |
| rpoA | 3878118 | c.390T>C | synonymous_variant | 1.0 |
| rpoA | 3878130 | c.378C>G | synonymous_variant | 1.0 |
| rpoA | 3878143 | p.Gly122Asp | missense_variant | 1.0 |
| rpoA | 3878157 | c.351C>T | synonymous_variant | 1.0 |
| rpoA | 3878160 | c.348C>G | synonymous_variant | 1.0 |
| rpoA | 3878163 | c.345C>T | synonymous_variant | 1.0 |
| rpoA | 3878169 | c.339G>C | synonymous_variant | 1.0 |
| rpoA | 3878184 | c.324C>T | synonymous_variant | 1.0 |
| rpoA | 3878187 | c.321C>T | synonymous_variant | 1.0 |
| rpoA | 3878193 | c.315T>C | synonymous_variant | 1.0 |
| rpoA | 3878196 | p.Glu104Ala | missense_variant | 1.0 |
| rpoA | 3878199 | c.309T>C | synonymous_variant | 1.0 |
| rpoA | 3878205 | c.303T>A | synonymous_variant | 1.0 |
| rpoA | 3878217 | c.291A>G | synonymous_variant | 1.0 |
| rpoA | 3878259 | c.249G>C | synonymous_variant | 1.0 |
| rpoA | 3878271 | c.237T>C | synonymous_variant | 1.0 |
| rpoA | 3878283 | p.Glu75Asp | missense_variant | 1.0 |
| rpoA | 3878292 | c.216T>C | synonymous_variant | 1.0 |
| rpoA | 3878298 | c.210A>G | synonymous_variant | 1.0 |
| rpoA | 3878301 | c.207C>G | synonymous_variant | 1.0 |
| rpoA | 3878304 | c.204G>A | synonymous_variant | 1.0 |
| rpoA | 3878310 | c.198G>T | synonymous_variant | 1.0 |
| rpoA | 3878313 | c.195G>C | synonymous_variant | 1.0 |
| rpoA | 3878322 | c.186A>G | synonymous_variant | 1.0 |
| rpoA | 3878331 | c.177A>C | synonymous_variant | 1.0 |
| rpoA | 3878337 | c.171T>C | synonymous_variant | 1.0 |
| rpoA | 3878343 | c.165C>G | synonymous_variant | 1.0 |
| rpoA | 3878346 | c.162T>C | synonymous_variant | 1.0 |
| rpoA | 3878364 | c.144A>C | synonymous_variant | 1.0 |
| rpoA | 3878367 | c.141C>G | synonymous_variant | 1.0 |
| rpoA | 3878370 | c.138T>C | synonymous_variant | 1.0 |
| rpoA | 3878373 | c.135G>C | synonymous_variant | 1.0 |
| rpoA | 3878379 | c.129G>C | synonymous_variant | 1.0 |
| rpoA | 3878391 | c.117T>G | synonymous_variant | 1.0 |
| rpoA | 3878400 | c.108T>C | synonymous_variant | 1.0 |
| rpoA | 3878403 | c.105C>T | synonymous_variant | 1.0 |
| ddn | 3986651 | c.-193G>A | upstream_gene_variant | 1.0 |
| ddn | 3986661 | c.-183C>A | upstream_gene_variant | 1.0 |
| ddn | 3986663 | c.-180_-177delAGCC | upstream_gene_variant | 1.0 |
| ddn | 3986669 | c.-175_-174insAACG | upstream_gene_variant | 1.0 |
| ddn | 3986672 | c.-172G>T | upstream_gene_variant | 1.0 |
| ddn | 3986673 | c.-171C>T | upstream_gene_variant | 1.0 |
| ddn | 3986690 | c.-154C>T | upstream_gene_variant | 1.0 |
| ddn | 3986693 | c.-151C>T | upstream_gene_variant | 1.0 |
| ddn | 3986696 | c.-148G>C | upstream_gene_variant | 1.0 |
| ddn | 3986699 | c.-145C>G | upstream_gene_variant | 1.0 |
| clpC1 | 4038587 | c.2118C>T | synonymous_variant | 1.0 |
| clpC1 | 4038596 | c.2109A>G | synonymous_variant | 1.0 |
| clpC1 | 4038602 | c.2103G>C | synonymous_variant | 1.0 |
| clpC1 | 4038623 | c.2082A>G | synonymous_variant | 1.0 |
| clpC1 | 4038713 | c.1992T>C | synonymous_variant | 1.0 |
| clpC1 | 4038737 | c.1968C>T | synonymous_variant | 1.0 |
| clpC1 | 4038740 | c.1965G>C | synonymous_variant | 1.0 |
| clpC1 | 4038743 | c.1962G>A | synonymous_variant | 1.0 |
| clpC1 | 4038755 | c.1950G>C | synonymous_variant | 1.0 |
| clpC1 | 4038767 | c.1938G>T | synonymous_variant | 1.0 |
| clpC1 | 4038770 | c.1935C>A | synonymous_variant | 1.0 |
| clpC1 | 4038782 | c.1923G>T | synonymous_variant | 1.0 |
| clpC1 | 4038790 | c.1915C>T | synonymous_variant | 1.0 |
| clpC1 | 4038795 | p.Ser637Thr | missense_variant | 1.0 |
| clpC1 | 4038812 | c.1893T>C | synonymous_variant | 1.0 |
| clpC1 | 4038815 | c.1890G>T | synonymous_variant | 1.0 |
| clpC1 | 4038821 | c.1884G>A | synonymous_variant | 1.0 |
| clpC1 | 4038830 | c.1875C>T | synonymous_variant | 1.0 |
| clpC1 | 4038839 | c.1866G>C | synonymous_variant | 1.0 |
| clpC1 | 4038842 | c.1863G>T | synonymous_variant | 1.0 |
| clpC1 | 4038857 | c.1846_1848delCGCinsAGG | synonymous_variant | 1.0 |
| clpC1 | 4038860 | c.1843_1845delCGGinsAGA | synonymous_variant | 1.0 |
| clpC1 | 4038863 | c.1842G>C | synonymous_variant | 1.0 |
| clpC1 | 4038878 | c.1827A>G | synonymous_variant | 1.0 |
| clpC1 | 4038881 | c.1824C>T | synonymous_variant | 1.0 |
| clpC1 | 4038908 | c.1797C>G | synonymous_variant | 1.0 |
| clpC1 | 4038911 | c.1794G>A | synonymous_variant | 1.0 |
| clpC1 | 4038914 | c.1791G>A | synonymous_variant | 1.0 |
| clpC1 | 4038923 | c.1782A>T | synonymous_variant | 1.0 |
| clpC1 | 4038926 | c.1777_1779delCGGinsAGA | synonymous_variant | 1.0 |
| clpC1 | 4038929 | c.1776G>A | synonymous_variant | 1.0 |
| clpC1 | 4038932 | c.1773G>C | synonymous_variant | 1.0 |
| clpC1 | 4038935 | c.1770C>G | synonymous_variant | 1.0 |
| clpC1 | 4038941 | c.1764G>C | synonymous_variant | 1.0 |
| clpC1 | 4038953 | c.1752A>G | synonymous_variant | 1.0 |
| clpC1 | 4038965 | c.1740T>C | synonymous_variant | 1.0 |
| clpC1 | 4038974 | c.1731T>C | synonymous_variant | 1.0 |
| clpC1 | 4038989 | c.1716T>C | synonymous_variant | 1.0 |
| clpC1 | 4038997 | c.1708T>C | synonymous_variant | 1.0 |
| clpC1 | 4039022 | c.1683A>G | synonymous_variant | 1.0 |
| clpC1 | 4039040 | c.1665C>G | synonymous_variant | 1.0 |
| clpC1 | 4039064 | c.1641C>T | synonymous_variant | 1.0 |
| clpC1 | 4039070 | c.1635G>C | synonymous_variant | 1.0 |
| clpC1 | 4039077 | p.Lys543Arg | missense_variant | 1.0 |
| clpC1 | 4039079 | c.1626C>G | synonymous_variant | 1.0 |
| clpC1 | 4039085 | c.1620A>G | synonymous_variant | 1.0 |
| clpC1 | 4039091 | c.1614G>T | synonymous_variant | 1.0 |
| clpC1 | 4039097 | c.1608G>T | synonymous_variant | 1.0 |
| clpC1 | 4039103 | c.1602T>C | synonymous_variant | 1.0 |
| clpC1 | 4039106 | c.1599G>C | synonymous_variant | 1.0 |
| clpC1 | 4039121 | c.1584T>C | synonymous_variant | 1.0 |
| clpC1 | 4039124 | c.1581C>G | synonymous_variant | 1.0 |
| clpC1 | 4039142 | c.1563A>G | synonymous_variant | 1.0 |
| clpC1 | 4039163 | c.1542G>A | synonymous_variant | 1.0 |
| clpC1 | 4039169 | p.Glu512Asp | missense_variant | 1.0 |
| clpC1 | 4039172 | c.1533A>G | synonymous_variant | 1.0 |
| clpC1 | 4039178 | c.1527G>C | synonymous_variant | 1.0 |
| clpC1 | 4039183 | c.1522T>C | synonymous_variant | 1.0 |
| clpC1 | 4039190 | c.1515C>G | synonymous_variant | 1.0 |
| clpC1 | 4039199 | p.Ala502Glu | missense_variant | 1.0 |
| clpC1 | 4039208 | c.1497C>G | synonymous_variant | 1.0 |
| clpC1 | 4039220 | c.1485G>C | synonymous_variant | 1.0 |
| clpC1 | 4039262 | c.1443C>T | synonymous_variant | 1.0 |
| clpC1 | 4039268 | c.1437C>T | synonymous_variant | 1.0 |
| clpC1 | 4039271 | c.1434G>A | synonymous_variant | 1.0 |
| clpC1 | 4039274 | c.1431G>C | synonymous_variant | 1.0 |
| clpC1 | 4039277 | c.1428C>T | synonymous_variant | 1.0 |
| clpC1 | 4039283 | c.1422C>T | synonymous_variant | 1.0 |
| clpC1 | 4039286 | c.1419T>G | synonymous_variant | 1.0 |
| clpC1 | 4039316 | p.Glu463Asp | missense_variant | 1.0 |
| clpC1 | 4039319 | c.1386T>A | synonymous_variant | 1.0 |
| clpC1 | 4039328 | c.1377A>G | synonymous_variant | 1.0 |
| clpC1 | 4039337 | p.Thr456Gln | missense_variant | 1.0 |
| clpC1 | 4039346 | p.Arg453Ser | missense_variant | 1.0 |
| clpC1 | 4039352 | c.1353C>T | synonymous_variant | 1.0 |
| clpC1 | 4039357 | c.1348C>T | synonymous_variant | 1.0 |
| clpC1 | 4039358 | p.Ser449Arg | missense_variant | 1.0 |
| clpC1 | 4039361 | c.1344C>G | synonymous_variant | 1.0 |
| clpC1 | 4039391 | c.1314T>C | synonymous_variant | 1.0 |
| clpC1 | 4039409 | c.1296T>C | synonymous_variant | 1.0 |
| clpC1 | 4039412 | c.1293T>G | synonymous_variant | 1.0 |
| clpC1 | 4039415 | p.Glu430Asp | missense_variant | 1.0 |
| clpC1 | 4039430 | c.1275T>C | synonymous_variant | 1.0 |
| clpC1 | 4039442 | c.1263A>G | synonymous_variant | 1.0 |
| clpC1 | 4039454 | c.1251A>T | synonymous_variant | 1.0 |
| clpC1 | 4039463 | c.1242C>G | synonymous_variant | 1.0 |
| clpC1 | 4039466 | c.1239T>C | synonymous_variant | 1.0 |
| clpC1 | 4039469 | c.1236T>C | synonymous_variant | 1.0 |
| clpC1 | 4039472 | c.1233G>C | synonymous_variant | 1.0 |
| clpC1 | 4039478 | c.1227G>C | synonymous_variant | 1.0 |
| clpC1 | 4039481 | c.1224T>C | synonymous_variant | 1.0 |
| clpC1 | 4039487 | c.1218G>C | synonymous_variant | 1.0 |
| clpC1 | 4039522 | c.1183C>T | synonymous_variant | 1.0 |
| clpC1 | 4039528 | c.1177C>A | synonymous_variant | 1.0 |
| clpC1 | 4039541 | c.1164C>G | synonymous_variant | 1.0 |
| clpC1 | 4039544 | c.1161C>T | synonymous_variant | 1.0 |
| clpC1 | 4039556 | c.1149G>C | synonymous_variant | 1.0 |
| clpC1 | 4039559 | c.1146C>G | synonymous_variant | 1.0 |
| clpC1 | 4039562 | c.1143C>G | synonymous_variant | 1.0 |
| clpC1 | 4039570 | p.Met379Leu | missense_variant | 1.0 |
| clpC1 | 4039574 | p.Ala377Gly | missense_variant | 1.0 |
| clpC1 | 4039577 | c.1128T>C | synonymous_variant | 1.0 |
| clpC1 | 4039586 | c.1119G>C | synonymous_variant | 1.0 |
| clpC1 | 4039610 | c.1095G>C | synonymous_variant | 1.0 |
| clpC1 | 4039616 | c.1089G>C | synonymous_variant | 1.0 |
| clpC1 | 4039622 | c.1083C>T | synonymous_variant | 1.0 |
| clpC1 | 4039628 | c.1077C>G | synonymous_variant | 1.0 |
| clpC1 | 4039640 | c.1065C>G | synonymous_variant | 1.0 |
| clpC1 | 4039646 | c.1059G>A | synonymous_variant | 1.0 |
| clpC1 | 4039649 | c.1056G>T | synonymous_variant | 1.0 |
| clpC1 | 4039652 | c.1053G>C | synonymous_variant | 1.0 |
| clpC1 | 4039682 | c.1023C>G | synonymous_variant | 1.0 |
| clpC1 | 4039694 | c.1011G>C | synonymous_variant | 1.0 |
| clpC1 | 4039724 | c.981A>G | synonymous_variant | 1.0 |
| clpC1 | 4039727 | c.978C>T | synonymous_variant | 1.0 |
| clpC1 | 4039733 | c.972G>C | synonymous_variant | 1.0 |
| clpC1 | 4039739 | c.966C>G | synonymous_variant | 1.0 |
| clpC1 | 4039751 | c.954A>G | synonymous_variant | 1.0 |
| clpC1 | 4039757 | c.948A>G | synonymous_variant | 1.0 |
| clpC1 | 4039769 | c.936C>G | synonymous_variant | 1.0 |
| clpC1 | 4039775 | c.930G>C | synonymous_variant | 1.0 |
| clpC1 | 4039778 | c.927A>G | synonymous_variant | 1.0 |
| clpC1 | 4039781 | c.924G>C | synonymous_variant | 1.0 |
| clpC1 | 4039793 | c.912C>G | synonymous_variant | 1.0 |
| clpC1 | 4039814 | c.891C>G | synonymous_variant | 1.0 |
| clpC1 | 4039817 | c.888A>C | synonymous_variant | 1.0 |
| clpC1 | 4039820 | c.885T>G | synonymous_variant | 1.0 |
| clpC1 | 4039831 | c.874T>C | synonymous_variant | 1.0 |
| clpC1 | 4039844 | c.861C>T | synonymous_variant | 1.0 |
| clpC1 | 4039850 | c.855T>C | synonymous_variant | 1.0 |
| clpC1 | 4039865 | c.840T>C | synonymous_variant | 1.0 |
| clpC1 | 4039904 | c.801A>G | synonymous_variant | 1.0 |
| clpC1 | 4039907 | c.798G>A | synonymous_variant | 1.0 |
| clpC1 | 4039931 | c.774T>C | synonymous_variant | 1.0 |
| clpC1 | 4039934 | c.771G>C | synonymous_variant | 1.0 |
| clpC1 | 4039943 | c.762G>C | synonymous_variant | 1.0 |
| clpC1 | 4039946 | c.759A>G | synonymous_variant | 1.0 |
| clpC1 | 4039949 | c.756G>C | synonymous_variant | 1.0 |
| clpC1 | 4039952 | c.753T>C | synonymous_variant | 1.0 |
| clpC1 | 4039958 | c.747G>C | synonymous_variant | 1.0 |
| clpC1 | 4039964 | c.741C>G | synonymous_variant | 1.0 |
| clpC1 | 4039975 | p.Asp244Asn | missense_variant | 1.0 |
| clpC1 | 4039979 | c.726C>G | synonymous_variant | 1.0 |
| clpC1 | 4039982 | c.723G>A | synonymous_variant | 1.0 |
| clpC1 | 4040000 | c.705C>T | synonymous_variant | 1.0 |
| clpC1 | 4040003 | c.702G>C | synonymous_variant | 1.0 |
| clpC1 | 4040021 | c.684A>C | synonymous_variant | 1.0 |
| clpC1 | 4040024 | c.681A>G | synonymous_variant | 1.0 |
| clpC1 | 4040033 | c.672G>C | synonymous_variant | 1.0 |
| clpC1 | 4040042 | c.663C>T | synonymous_variant | 1.0 |
| clpC1 | 4040048 | c.657C>T | synonymous_variant | 1.0 |
| clpC1 | 4040057 | c.648C>T | synonymous_variant | 1.0 |
| clpC1 | 4040087 | c.618G>T | synonymous_variant | 1.0 |
| clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 1.0 |
| clpC1 | 4040093 | c.612C>G | synonymous_variant | 1.0 |
| clpC1 | 4040126 | c.579C>T | synonymous_variant | 1.0 |
| clpC1 | 4040141 | c.564C>T | synonymous_variant | 1.0 |
| clpC1 | 4040144 | c.561G>C | synonymous_variant | 1.0 |
| clpC1 | 4040147 | c.558A>G | synonymous_variant | 1.0 |
| clpC1 | 4040153 | c.552A>G | synonymous_variant | 1.0 |
| clpC1 | 4040159 | c.546G>C | synonymous_variant | 1.0 |
| clpC1 | 4040162 | c.543G>C | synonymous_variant | 1.0 |
| clpC1 | 4040165 | c.540G>C | synonymous_variant | 1.0 |
| clpC1 | 4040168 | c.537G>T | synonymous_variant | 1.0 |
| clpC1 | 4040171 | c.534C>G | synonymous_variant | 1.0 |
| clpC1 | 4040239 | p.Gly156Ser | missense_variant | 1.0 |
| clpC1 | 4040243 | c.462C>T | synonymous_variant | 1.0 |
| clpC1 | 4040248 | p.Ala153Ser | missense_variant | 1.0 |
| clpC1 | 4040249 | c.456A>G | synonymous_variant | 1.0 |
| clpC1 | 4040257 | p.Ala150Thr | missense_variant | 1.0 |
| clpC1 | 4040267 | c.438A>G | synonymous_variant | 1.0 |
| clpC1 | 4040273 | c.432T>C | synonymous_variant | 1.0 |
| clpC1 | 4040277 | c.427_428delTCinsAG | synonymous_variant | 1.0 |
| clpC1 | 4040279 | c.426C>G | synonymous_variant | 1.0 |
| clpC1 | 4040291 | c.414G>C | synonymous_variant | 1.0 |
| clpC1 | 4040300 | c.405C>T | synonymous_variant | 1.0 |
| clpC1 | 4040318 | c.387C>T | synonymous_variant | 1.0 |
| clpC1 | 4040330 | c.375C>G | synonymous_variant | 1.0 |
| clpC1 | 4040333 | c.372G>C | synonymous_variant | 1.0 |
| clpC1 | 4040342 | c.363C>T | synonymous_variant | 1.0 |
| clpC1 | 4040345 | c.360C>G | synonymous_variant | 1.0 |
| clpC1 | 4040348 | c.357G>C | synonymous_variant | 1.0 |
| clpC1 | 4040363 | c.342A>T | synonymous_variant | 1.0 |
| clpC1 | 4040380 | c.325T>C | synonymous_variant | 1.0 |
| clpC1 | 4040381 | c.324T>C | synonymous_variant | 1.0 |
| clpC1 | 4040387 | c.318A>G | synonymous_variant | 1.0 |
| clpC1 | 4040393 | c.312G>T | synonymous_variant | 1.0 |
| clpC1 | 4040411 | c.294T>C | synonymous_variant | 1.0 |
| clpC1 | 4040423 | c.282A>G | synonymous_variant | 1.0 |
| clpC1 | 4040426 | c.279T>C | synonymous_variant | 1.0 |
| clpC1 | 4040431 | c.274T>C | synonymous_variant | 1.0 |
| clpC1 | 4040441 | c.264C>G | synonymous_variant | 1.0 |
| clpC1 | 4040444 | c.261C>G | synonymous_variant | 1.0 |
| clpC1 | 4040450 | c.255A>G | synonymous_variant | 1.0 |
| clpC1 | 4040456 | c.249C>T | synonymous_variant | 1.0 |
| clpC1 | 4040459 | c.246C>G | synonymous_variant | 1.0 |
| clpC1 | 4040462 | c.243C>T | synonymous_variant | 1.0 |
| clpC1 | 4040465 | c.240T>C | synonymous_variant | 1.0 |
| clpC1 | 4040468 | c.237G>C | synonymous_variant | 1.0 |
| clpC1 | 4040480 | c.225T>C | synonymous_variant | 1.0 |
| clpC1 | 4040522 | c.183T>C | synonymous_variant | 1.0 |
| clpC1 | 4040531 | c.174T>G | synonymous_variant | 1.0 |
| clpC1 | 4040534 | c.171A>G | synonymous_variant | 1.0 |
| clpC1 | 4040540 | c.165G>C | synonymous_variant | 1.0 |
| clpC1 | 4040546 | c.159G>C | synonymous_variant | 1.0 |
| clpC1 | 4040558 | c.147G>T | synonymous_variant | 1.0 |
| clpC1 | 4040561 | c.144A>G | synonymous_variant | 1.0 |
| clpC1 | 4040579 | c.126A>G | synonymous_variant | 1.0 |
| clpC1 | 4040582 | c.123G>C | synonymous_variant | 1.0 |
| clpC1 | 4040585 | c.120A>G | synonymous_variant | 1.0 |
| clpC1 | 4040588 | c.117T>C | synonymous_variant | 1.0 |
| clpC1 | 4040591 | c.114C>T | synonymous_variant | 1.0 |
| clpC1 | 4040597 | c.108C>T | synonymous_variant | 1.0 |
| clpC1 | 4040600 | c.103_105delTTAinsCTG | synonymous_variant | 1.0 |
| clpC1 | 4040603 | c.102T>G | synonymous_variant | 1.0 |
| clpC1 | 4040606 | c.99T>C | synonymous_variant | 1.0 |
| clpC1 | 4040618 | c.87C>T | synonymous_variant | 1.0 |
| clpC1 | 4040642 | c.61_63delAGGinsCGC | synonymous_variant | 1.0 |
| clpC1 | 4040654 | c.51G>A | synonymous_variant | 1.0 |
| clpC1 | 4040657 | c.48T>C | synonymous_variant | 1.0 |
| embC | 4240726 | c.864G>C | synonymous_variant | 1.0 |
| embC | 4240732 | c.870C>T | synonymous_variant | 1.0 |
| embC | 4240741 | c.879C>T | synonymous_variant | 0.88 |
| embC | 4240756 | c.894G>C | synonymous_variant | 1.0 |
| embC | 4240768 | c.906G>C | synonymous_variant | 1.0 |
| embC | 4240771 | c.909G>C | synonymous_variant | 1.0 |
| embC | 4240772 | p.Ser304Ala | missense_variant | 1.0 |
| embC | 4240780 | c.918T>C | synonymous_variant | 1.0 |
| embC | 4240781 | p.Ala307Ser | missense_variant | 1.0 |
| embC | 4240789 | c.927T>C | synonymous_variant | 1.0 |
| embC | 4240798 | c.936C>T | synonymous_variant | 1.0 |
| embC | 4240819 | c.957A>C | synonymous_variant | 1.0 |
| embC | 4240826 | p.Ala322Ser | missense_variant | 1.0 |
| embC | 4240831 | c.969T>G | synonymous_variant | 1.0 |
| embC | 4240856 | p.Ala332Thr | missense_variant | 1.0 |
| embC | 4240859 | p.Leu333Ile | missense_variant | 1.0 |
| embC | 4240879 | c.1017G>C | synonymous_variant | 1.0 |
| embC | 4240886 | p.Ile342Val | missense_variant | 1.0 |
| embC | 4241098 | c.1236G>C | synonymous_variant | 1.0 |
| embC | 4241101 | c.1239G>C | synonymous_variant | 1.0 |
| embC | 4241104 | c.1242G>A | synonymous_variant | 1.0 |
| embC | 4241108 | p.Ala416Ser | missense_variant | 1.0 |
| embC | 4241111 | p.Val417Ile | missense_variant | 1.0 |
| embC | 4241121 | p.Ser420Asn | missense_variant | 1.0 |
| embC | 4241136 | p.Val425Ala | missense_variant | 1.0 |
| embC | 4241140 | c.1278A>C | synonymous_variant | 1.0 |
| embC | 4241141 | p.Ile427Val | missense_variant | 1.0 |
| embC | 4241152 | c.1290C>T | synonymous_variant | 1.0 |
| embC | 4241153 | p.Ile431Val | missense_variant | 1.0 |
| embC | 4241158 | c.1296T>C | synonymous_variant | 1.0 |
| embC | 4241161 | c.1299C>G | synonymous_variant | 1.0 |
| embC | 4241162 | c.1300_1302delTTGinsCTC | synonymous_variant | 1.0 |
| embC | 4241168 | c.1306C>T | synonymous_variant | 1.0 |
| embC | 4241179 | c.1317G>A | synonymous_variant | 1.0 |
| embC | 4241188 | c.1326C>T | synonymous_variant | 1.0 |
| embC | 4241194 | c.1332C>G | synonymous_variant | 1.0 |
| embC | 4241203 | c.1341T>C | synonymous_variant | 1.0 |
