Run ID: SRR6046385
Sample name:
Date: 04-04-2023 12:15:42
Number of reads: 74497
Percentage reads mapped: 5.04
Strain: lineage4.9
Drug-resistance: Other
| 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 |
|---|---|---|---|---|---|
| gyrB | 6738 | p.Thr500Asn | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
| gyrA | 7572 | p.Ser91Ala | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
| Gene | Chromosome position | Mutation | Type | Estimated fraction |
|---|---|---|---|---|
| gyrB | 5341 | c.102T>C | synonymous_variant | 1.0 |
| gyrB | 5344 | c.105C>T | synonymous_variant | 1.0 |
| gyrB | 5356 | c.117G>A | synonymous_variant | 1.0 |
| gyrB | 5363 | c.124_126delTTAinsCTG | synonymous_variant | 1.0 |
| gyrB | 5371 | c.132T>C | synonymous_variant | 1.0 |
| gyrB | 5374 | c.135C>G | synonymous_variant | 1.0 |
| gyrB | 5377 | c.138T>C | synonymous_variant | 1.0 |
| gyrB | 5386 | c.147G>T | synonymous_variant | 1.0 |
| gyrB | 5389 | c.150C>G | synonymous_variant | 1.0 |
| gyrB | 5396 | p.Ala53Ser | missense_variant | 1.0 |
| gyrB | 5422 | c.183T>C | synonymous_variant | 1.0 |
| gyrB | 6115 | c.876A>G | synonymous_variant | 1.0 |
| gyrB | 6122 | p.Ala295Ser | missense_variant | 1.0 |
| gyrB | 6127 | c.888G>T | synonymous_variant | 1.0 |
| gyrB | 6130 | c.891T>C | synonymous_variant | 1.0 |
| gyrB | 6133 | c.894G>C | synonymous_variant | 1.0 |
| gyrB | 6172 | c.933C>T | synonymous_variant | 1.0 |
| gyrB | 6178 | c.939C>T | synonymous_variant | 1.0 |
| gyrB | 6187 | c.948C>T | synonymous_variant | 1.0 |
| gyrB | 6190 | c.951A>G | synonymous_variant | 1.0 |
| gyrB | 6193 | c.954G>A | synonymous_variant | 1.0 |
| gyrB | 6196 | c.957C>G | synonymous_variant | 1.0 |
| gyrB | 6203 | p.Ser322Ala | missense_variant | 1.0 |
| gyrB | 6214 | c.975G>C | synonymous_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 | 6247 | c.1008G>A | synonymous_variant | 1.0 |
| gyrB | 6250 | c.1011A>C | synonymous_variant | 1.0 |
| gyrB | 6253 | c.1014G>C | synonymous_variant | 1.0 |
| gyrB | 6259 | p.Asp340Glu | missense_variant | 1.0 |
| gyrB | 6266 | p.Pro343Gly | missense_variant | 1.0 |
| gyrB | 6280 | c.1041T>C | synonymous_variant | 1.0 |
| gyrB | 6298 | c.1059C>T | synonymous_variant | 1.0 |
| gyrA | 6307 | c.-995T>C | upstream_gene_variant | 1.0 |
| gyrB | 6308 | p.Val357Ile | missense_variant | 1.0 |
| gyrB | 6311 | p.Ile358Val | missense_variant | 1.0 |
| gyrA | 6314 | c.-988_-986delTCGinsAGC | upstream_gene_variant | 1.0 |
| gyrA | 6319 | c.-983G>A | upstream_gene_variant | 1.0 |
| gyrA | 6325 | c.-977C>G | upstream_gene_variant | 1.0 |
| gyrA | 6343 | c.-959G>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 | 6680 | c.-622C>T | upstream_gene_variant | 1.0 |
| gyrA | 6703 | c.-599G>C | upstream_gene_variant | 1.0 |
| gyrA | 6709 | c.-593A>G | upstream_gene_variant | 1.0 |
| gyrA | 6712 | c.-590G>C | upstream_gene_variant | 1.0 |
| gyrB | 6722 | p.Arg495Lys | missense_variant | 1.0 |
| gyrA | 6727 | c.-575G>C | upstream_gene_variant | 1.0 |
| gyrA | 6730 | c.-572A>C | upstream_gene_variant | 1.0 |
| gyrA | 6742 | c.-560A>G | upstream_gene_variant | 1.0 |
| gyrA | 6745 | c.-557T>C | upstream_gene_variant | 1.0 |
| gyrA | 6760 | c.-542G>C | upstream_gene_variant | 1.0 |
| gyrA | 6763 | c.-539G>C | upstream_gene_variant | 1.0 |
| gyrB | 6764 | p.Leu509Phe | missense_variant | 1.0 |
| gyrA | 6772 | c.-530C>G | upstream_gene_variant | 1.0 |
| gyrA | 6775 | c.-527G>T | upstream_gene_variant | 1.0 |
| gyrA | 6793 | c.-509T>C | upstream_gene_variant | 1.0 |
| gyrB | 6797 | p.Gly520Ser | missense_variant | 1.0 |
| gyrA | 6802 | c.-500G>A | upstream_gene_variant | 1.0 |
| gyrA | 6808 | c.-494C>G | upstream_gene_variant | 1.0 |
| gyrA | 6824 | c.-478C>T | upstream_gene_variant | 1.0 |
| gyrA | 6844 | c.-458T>C | upstream_gene_variant | 1.0 |
| gyrA | 6850 | c.-452C>A | 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 | 6865 | c.-437G>C | upstream_gene_variant | 1.0 |
| gyrA | 6872 | c.-430T>C | upstream_gene_variant | 1.0 |
| gyrA | 6877 | c.-425G>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 |
| gyrA | 6916 | c.-386G>C | upstream_gene_variant | 1.0 |
| gyrA | 6922 | c.-380G>C | upstream_gene_variant | 1.0 |
| gyrA | 6925 | c.-377T>C | upstream_gene_variant | 1.0 |
| gyrA | 6926 | c.-376T>C | upstream_gene_variant | 1.0 |
| gyrA | 6931 | c.-371A>G | upstream_gene_variant | 1.0 |
| gyrA | 6934 | c.-368A>G | upstream_gene_variant | 1.0 |
| gyrA | 6937 | c.-365G>C | upstream_gene_variant | 1.0 |
| gyrA | 6967 | c.-335T>C | upstream_gene_variant | 1.0 |
| gyrB | 6970 | p.Asp577Glu | 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 | 6985 | c.-317C>T | upstream_gene_variant | 1.0 |
| gyrA | 6994 | c.-308C>A | upstream_gene_variant | 0.92 |
| gyrA | 7006 | c.-296T>C | upstream_gene_variant | 1.0 |
| gyrB | 7014 | p.Glu592Ala | missense_variant | 1.0 |
| gyrA | 7018 | c.-284G>C | upstream_gene_variant | 1.0 |
| gyrA | 7021 | c.-281G>T | upstream_gene_variant | 1.0 |
| gyrB | 7025 | p.Lys596Ala | missense_variant | 1.0 |
| gyrB | 7051 | p.Glu604Asp | missense_variant | 0.91 |
| gyrA | 7060 | c.-242T>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 |
| gyrB | 7088 | p.Asp617Asn | missense_variant | 1.0 |
| gyrB | 7091 | p.Ala618Pro | missense_variant | 1.0 |
| gyrA | 7100 | c.-202T>C | upstream_gene_variant | 1.0 |
| gyrA | 7108 | c.-194G>A | upstream_gene_variant | 1.0 |
| gyrA | 7132 | c.-170T>G | upstream_gene_variant | 1.0 |
| gyrA | 7136 | c.-166_-164delTTGinsCTT | upstream_gene_variant | 1.0 |
| gyrA | 7151 | c.-151C>T | upstream_gene_variant | 1.0 |
| gyrA | 7165 | c.-137C>G | upstream_gene_variant | 1.0 |
| gyrA | 7171 | c.-131C>G | upstream_gene_variant | 1.0 |
| gyrA | 7177 | c.-125G>A | upstream_gene_variant | 1.0 |
| gyrA | 7178 | c.-124T>C | upstream_gene_variant | 1.0 |
| gyrA | 7184 | c.-118_-117delTCinsAG | upstream_gene_variant | 1.0 |
| gyrB | 7187 | p.Ile650Val | missense_variant | 1.0 |
| gyrA | 7198 | c.-104C>G | upstream_gene_variant | 1.0 |
| gyrA | 7207 | c.-95C>G | upstream_gene_variant | 1.0 |
| gyrB | 7210 | p.Asp657Glu | missense_variant | 1.0 |
| gyrA | 7213 | c.-89G>A | upstream_gene_variant | 1.0 |
| gyrA | 7216 | c.-86G>T | upstream_gene_variant | 1.0 |
| gyrA | 7225 | c.-77T>C | upstream_gene_variant | 1.0 |
| gyrA | 7237 | c.-65C>T | upstream_gene_variant | 1.0 |
| gyrA | 7517 | c.216G>A | synonymous_variant | 1.0 |
| gyrA | 7527 | p.Ser76Pro | missense_variant | 1.0 |
| gyrA | 7532 | c.231T>C | synonymous_variant | 1.0 |
| gyrA | 7533 | p.Ala78Ser | missense_variant | 1.0 |
| gyrA | 7538 | p.Glu79Asp | missense_variant | 1.0 |
| gyrA | 7547 | c.246C>T | synonymous_variant | 1.0 |
| gyrA | 7568 | c.267C>T | synonymous_variant | 1.0 |
| gyrA | 7569 | p.Ala90Ser | missense_variant | 1.0 |
| gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
| gyrA | 7589 | c.288G>C | synonymous_variant | 1.0 |
| gyrA | 7592 | c.291G>C | synonymous_variant | 1.0 |
| gyrA | 7595 | c.294C>G | synonymous_variant | 1.0 |
| gyrA | 7607 | c.306C>G | synonymous_variant | 1.0 |
| gyrA | 7613 | c.312G>C | synonymous_variant | 1.0 |
| gyrA | 7614 | p.Leu105Met | missense_variant | 1.0 |
| gyrA | 7619 | c.318C>T | synonymous_variant | 1.0 |
| gyrA | 7631 | c.330G>C | synonymous_variant | 1.0 |
| gyrA | 7688 | c.387C>T | synonymous_variant | 1.0 |
| gyrA | 7697 | c.396C>G | synonymous_variant | 1.0 |
| gyrA | 7700 | c.399G>C | synonymous_variant | 1.0 |
| gyrA | 7706 | c.405C>G | 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 | 7763 | c.462T>C | synonymous_variant | 1.0 |
| gyrA | 7775 | c.474C>T | synonymous_variant | 1.0 |
| gyrA | 8253 | p.Ile318Val | missense_variant | 1.0 |
| gyrA | 8258 | c.957G>A | synonymous_variant | 1.0 |
| gyrA | 8267 | c.966G>C | synonymous_variant | 1.0 |
| gyrA | 8279 | c.978G>C | synonymous_variant | 1.0 |
| gyrA | 8283 | p.Ile328Leu | missense_variant | 1.0 |
| gyrA | 8288 | c.987T>C | synonymous_variant | 1.0 |
| gyrA | 8294 | c.993T>G | synonymous_variant | 1.0 |
| gyrA | 8321 | c.1020C>T | synonymous_variant | 1.0 |
| gyrA | 8324 | c.1023T>C | synonymous_variant | 1.0 |
| gyrA | 8330 | c.1029C>G | synonymous_variant | 1.0 |
| gyrA | 8339 | c.1038A>G | synonymous_variant | 1.0 |
| gyrA | 8340 | p.Ala347Ser | missense_variant | 1.0 |
| gyrA | 8354 | c.1053G>C | synonymous_variant | 1.0 |
| gyrA | 8840 | c.1539C>T | synonymous_variant | 1.0 |
| gyrA | 8849 | c.1548C>G | synonymous_variant | 1.0 |
| gyrA | 8852 | c.1551T>C | synonymous_variant | 1.0 |
| gyrA | 8858 | c.1557T>C | synonymous_variant | 1.0 |
| gyrA | 8861 | c.1560C>T | 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>C | synonymous_variant | 1.0 |
| gyrA | 8882 | c.1581G>A | synonymous_variant | 1.0 |
| gyrA | 8903 | c.1602T>C | synonymous_variant | 1.0 |
| gyrA | 8915 | c.1614A>G | synonymous_variant | 1.0 |
| gyrA | 8918 | c.1617C>T | synonymous_variant | 1.0 |
| gyrA | 8924 | c.1623C>T | synonymous_variant | 1.0 |
| gyrA | 9242 | c.1941A>T | synonymous_variant | 1.0 |
| gyrA | 9248 | c.1947G>C | synonymous_variant | 1.0 |
| gyrA | 9254 | c.1953C>G | synonymous_variant | 1.0 |
| gyrA | 9260 | c.1959G>C | synonymous_variant | 1.0 |
| gyrA | 9263 | c.1962C>G | synonymous_variant | 1.0 |
| gyrA | 9284 | c.1983T>C | synonymous_variant | 1.0 |
| gyrA | 9287 | c.1986G>C | synonymous_variant | 1.0 |
| gyrA | 9290 | c.1989G>C | synonymous_variant | 1.0 |
| gyrA | 9296 | c.1995T>C | synonymous_variant | 1.0 |
| gyrA | 9299 | c.1998G>T | synonymous_variant | 1.0 |
| gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
| gyrA | 9311 | c.2010C>T | synonymous_variant | 1.0 |
| gyrA | 9315 | c.2014C>T | synonymous_variant | 1.0 |
| gyrA | 9323 | c.2022C>A | synonymous_variant | 1.0 |
| gyrA | 9330 | p.Asn677Gln | missense_variant | 1.0 |
| gyrA | 9335 | c.2034G>A | synonymous_variant | 1.0 |
| gyrA | 9341 | c.2040C>G | synonymous_variant | 1.0 |
| gyrA | 9345 | c.2044_2046delAGGinsCGC | synonymous_variant | 1.0 |
| gyrA | 9356 | c.2055G>C | synonymous_variant | 1.0 |
| gyrA | 9374 | c.2073G>C | synonymous_variant | 1.0 |
| gyrA | 9377 | c.2076A>G | synonymous_variant | 1.0 |
| gyrA | 9383 | c.2082T>G | synonymous_variant | 1.0 |
| gyrA | 9386 | c.2085T>C | synonymous_variant | 1.0 |
| gyrA | 9398 | c.2097T>C | synonymous_variant | 1.0 |
| gyrA | 9407 | c.2106C>T | synonymous_variant | 1.0 |
| rpoB | 760127 | p.Asp107Glu | missense_variant | 1.0 |
| rpoB | 760130 | p.Asp108Glu | missense_variant | 1.0 |
| rpoB | 760139 | c.333A>C | synonymous_variant | 1.0 |
| rpoB | 760140 | p.Pro112Ser | missense_variant | 1.0 |
| rpoB | 760143 | p.Val113Ile | missense_variant | 1.0 |
| rpoB | 760148 | p.Asp114Glu | missense_variant | 1.0 |
| rpoB | 760157 | c.351A>G | synonymous_variant | 1.0 |
| rpoB | 760172 | c.366G>C | synonymous_variant | 1.0 |
| rpoB | 760181 | c.375T>G | synonymous_variant | 1.0 |
| rpoB | 760184 | c.378A>G | synonymous_variant | 1.0 |
| rpoB | 760185 | c.379C>T | synonymous_variant | 1.0 |
| rpoB | 760199 | c.393C>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 | 760283 | c.477G>C | synonymous_variant | 1.0 |
| rpoB | 760298 | c.492G>C | synonymous_variant | 1.0 |
| rpoB | 760304 | c.498G>A | synonymous_variant | 1.0 |
| rpoB | 760307 | c.501T>C | synonymous_variant | 1.0 |
| rpoB | 760317 | c.511_512delAGinsTC | 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 | 760445 | c.639C>T | synonymous_variant | 1.0 |
| rpoB | 760463 | c.657C>T | synonymous_variant | 1.0 |
| rpoB | 760475 | c.669A>G | synonymous_variant | 1.0 |
| rpoB | 760481 | c.675G>T | synonymous_variant | 1.0 |
| rpoB | 760484 | c.678A>G | synonymous_variant | 1.0 |
| rpoB | 760487 | c.681G>C | synonymous_variant | 1.0 |
| rpoB | 760508 | c.702G>C | synonymous_variant | 1.0 |
| rpoB | 760522 | p.Ser239Asn | missense_variant | 1.0 |
| rpoB | 760532 | c.726T>C | synonymous_variant | 1.0 |
| rpoB | 760547 | c.741G>C | synonymous_variant | 1.0 |
| rpoB | 760563 | p.Arg253Met | missense_variant | 1.0 |
| rpoB | 760568 | c.762G>C | synonymous_variant | 1.0 |
| rpoB | 760571 | c.765G>C | synonymous_variant | 1.0 |
| rpoB | 760590 | c.785delT | frameshift_variant | 1.0 |
| rpoB | 760610 | c.804G>A | synonymous_variant | 1.0 |
| rpoB | 760611 | c.805_807delTTGinsCTC | 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 | 760670 | c.864G>C | synonymous_variant | 1.0 |
| rpoB | 760679 | c.873A>G | synonymous_variant | 1.0 |
| rpoB | 760682 | c.876C>T | synonymous_variant | 1.0 |
| rpoB | 760683 | c.877T>C | synonymous_variant | 1.0 |
| rpoB | 760715 | c.909C>G | synonymous_variant | 1.0 |
| rpoB | 760718 | c.912C>G | synonymous_variant | 1.0 |
| rpoB | 760724 | c.918T>C | synonymous_variant | 1.0 |
| rpoB | 760730 | c.924T>C | synonymous_variant | 1.0 |
| rpoB | 760751 | c.945G>C | synonymous_variant | 1.0 |
| rpoB | 760858 | p.Val351Ala | missense_variant | 1.0 |
| rpoB | 760868 | c.1062C>T | synonymous_variant | 1.0 |
| rpoB | 760883 | c.1077G>C | synonymous_variant | 1.0 |
| rpoB | 760886 | c.1080A>G | synonymous_variant | 1.0 |
| rpoB | 760887 | p.Thr361Val | missense_variant | 1.0 |
| rpoB | 760895 | c.1089C>T | synonymous_variant | 1.0 |
| rpoB | 760916 | c.1110C>T | synonymous_variant | 1.0 |
| rpoB | 760919 | c.1113C>T | synonymous_variant | 1.0 |
| rpoB | 760925 | c.1119T>C | synonymous_variant | 1.0 |
| rpoB | 760928 | c.1122G>C | synonymous_variant | 1.0 |
| rpoB | 760946 | c.1140A>G | synonymous_variant | 1.0 |
| rpoB | 760961 | c.1155C>G | synonymous_variant | 1.0 |
| rpoB | 760964 | c.1158C>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 | 760991 | c.1185G>C | synonymous_variant | 1.0 |
| rpoB | 761021 | c.1215G>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 | 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>G | synonymous_variant | 1.0 |
| rpoB | 761087 | c.1281C>T | synonymous_variant | 1.0 |
| rpoB | 761088 | c.1282_1284delAGCinsTCG | synonymous_variant | 1.0 |
| rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 1.0 |
| rpoB | 761102 | c.1296A>G | synonymous_variant | 1.0 |
| rpoB | 761123 | c.1317G>C | synonymous_variant | 1.0 |
| rpoB | 761132 | c.1326G>C | synonymous_variant | 1.0 |
| 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>T | synonymous_variant | 1.0 |
| rpoB | 761168 | c.1362C>G | synonymous_variant | 1.0 |
| rpoB | 761171 | c.1365C>T | synonymous_variant | 1.0 |
| rpoB | 761180 | c.1374A>C | synonymous_variant | 1.0 |
| rpoB | 761189 | c.1383T>C | synonymous_variant | 1.0 |
| rpoB | 761195 | c.1389G>C | synonymous_variant | 1.0 |
| rpoB | 761198 | c.1392G>C | synonymous_variant | 1.0 |
| rpoB | 761204 | c.1398C>G | synonymous_variant | 1.0 |
| rpoB | 761207 | c.1401C>T | synonymous_variant | 1.0 |
| rpoB | 761219 | c.1413G>C | synonymous_variant | 1.0 |
| rpoB | 761234 | c.1428G>T | 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 | 1.0 |
| rpoB | 761264 | c.1458C>G | synonymous_variant | 1.0 |
| rpoB | 761273 | c.1467T>C | synonymous_variant | 1.0 |
| rpoB | 761282 | c.1476C>T | synonymous_variant | 1.0 |
| rpoB | 761306 | c.1500C>G | synonymous_variant | 1.0 |
| rpoB | 761312 | c.1506G>C | synonymous_variant | 1.0 |
| rpoB | 761318 | c.1512G>T | synonymous_variant | 1.0 |
| rpoB | 761327 | c.1521A>G | synonymous_variant | 1.0 |
| rpoB | 761330 | c.1524G>C | synonymous_variant | 1.0 |
| rpoB | 761336 | c.1530C>T | synonymous_variant | 1.0 |
| rpoB | 761349 | p.Asp515Asn | missense_variant | 1.0 |
| rpoB | 761354 | c.1548C>T | synonymous_variant | 1.0 |
| rpoB | 761355 | p.Val517Arg | missense_variant | 1.0 |
| rpoB | 761360 | c.1554T>C | synonymous_variant | 1.0 |
| rpoB | 761362 | p.Ser519Thr | missense_variant | 1.0 |
| rpoB | 761370 | p.Ile522Val | missense_variant | 1.0 |
| rpoB | 761558 | c.1752C>G | synonymous_variant | 1.0 |
| rpoB | 761564 | c.1758G>C | synonymous_variant | 1.0 |
| rpoB | 761573 | c.1767C>G | synonymous_variant | 1.0 |
| rpoB | 761579 | c.1773G>C | synonymous_variant | 1.0 |
| rpoB | 761603 | c.1797C>G | synonymous_variant | 1.0 |
| rpoB | 761606 | c.1800C>G | synonymous_variant | 1.0 |
| rpoB | 761612 | c.1806G>C | synonymous_variant | 1.0 |
| rpoB | 761615 | c.1809A>G | synonymous_variant | 1.0 |
| rpoB | 761618 | c.1812C>T | synonymous_variant | 1.0 |
| rpoB | 761627 | c.1821C>T | synonymous_variant | 1.0 |
| rpoB | 761640 | c.1834C>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 | 761828 | p.His674Gln | missense_variant | 1.0 |
| rpoB | 761834 | c.2028T>A | synonymous_variant | 1.0 |
| rpoB | 761837 | c.2031C>T | synonymous_variant | 1.0 |
| rpoB | 761847 | p.Cys681Arg | missense_variant | 1.0 |
| rpoB | 761852 | c.2046C>G | 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 | 761892 | p.Ile696Leu | missense_variant | 1.0 |
| rpoB | 761900 | c.2094C>T | synonymous_variant | 1.0 |
| rpoB | 761903 | c.2097T>G | 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 | 761972 | c.2166C>A | synonymous_variant | 1.0 |
| rpoB | 761990 | c.2184G>C | synonymous_variant | 1.0 |
| rpoB | 762002 | c.2196C>G | synonymous_variant | 1.0 |
| rpoB | 762003 | p.Asn733Gln | missense_variant | 1.0 |
| rpoB | 762008 | c.2202C>G | synonymous_variant | 1.0 |
| rpoB | 762009 | c.2203C>T | synonymous_variant | 1.0 |
| rpoB | 762014 | c.2208C>G | synonymous_variant | 1.0 |
| rpoB | 762023 | c.2217C>T | synonymous_variant | 1.0 |
| rpoB | 762027 | c.2221_2223delCTCinsTTG | synonymous_variant | 1.0 |
| rpoB | 762038 | c.2232C>T | synonymous_variant | 1.0 |
| rpoB | 762053 | c.2247T>C | synonymous_variant | 1.0 |
| rpoB | 762083 | c.2277T>C | synonymous_variant | 1.0 |
| rpoB | 762086 | c.2280G>C | synonymous_variant | 1.0 |
| rpoB | 762104 | c.2298C>T | synonymous_variant | 1.0 |
| rpoB | 762114 | p.Ile770Val | missense_variant | 1.0 |
| rpoB | 762137 | c.2331C>T | synonymous_variant | 1.0 |
| rpoB | 762143 | c.2337T>C | synonymous_variant | 1.0 |
| rpoB | 762176 | c.2370T>G | synonymous_variant | 1.0 |
| rpoB | 762179 | c.2373C>T | synonymous_variant | 1.0 |
| rpoB | 762185 | c.2379G>C | synonymous_variant | 1.0 |
| rpoB | 762224 | c.2418C>G | synonymous_variant | 0.96 |
| rpoB | 762254 | c.2448T>G | synonymous_variant | 1.0 |
| rpoB | 762257 | c.2451C>G | synonymous_variant | 0.96 |
| rpoB | 762266 | c.2460T>C | synonymous_variant | 1.0 |
| rpoB | 762269 | c.2463G>A | synonymous_variant | 0.95 |
| rpoB | 762290 | c.2484C>T | synonymous_variant | 1.0 |
| rpoB | 762293 | c.2487T>C | synonymous_variant | 1.0 |
| rpoB | 762297 | c.2491C>T | synonymous_variant | 1.0 |
| rpoB | 762308 | c.2502G>C | synonymous_variant | 1.0 |
| rpoB | 762311 | c.2505C>T | synonymous_variant | 1.0 |
| rpoB | 762314 | c.2508C>T | synonymous_variant | 1.0 |
| rpoB | 762317 | c.2511A>G | synonymous_variant | 1.0 |
| rpoB | 762335 | c.2529C>G | synonymous_variant | 1.0 |
| rpoB | 762338 | c.2532T>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 | 762353 | c.2547C>G | synonymous_variant | 1.0 |
| rpoB | 762368 | p.Glu854Asp | missense_variant | 1.0 |
| rpoB | 762369 | c.2563T>C | synonymous_variant | 1.0 |
| rpoC | 762374 | c.-996G>C | upstream_gene_variant | 1.0 |
| rpoB | 762375 | p.Ala857Pro | missense_variant | 1.0 |
| rpoC | 762395 | c.-975G>C | upstream_gene_variant | 1.0 |
| rpoC | 762398 | c.-972T>G | upstream_gene_variant | 1.0 |
| rpoC | 762404 | c.-966T>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 |
| rpoB | 762426 | p.Ser874Gln | missense_variant | 1.0 |
| rpoC | 762434 | c.-936T>C | upstream_gene_variant | 1.0 |
| rpoC | 762449 | c.-921C>T | upstream_gene_variant | 1.0 |
| rpoC | 762452 | c.-918G>C | upstream_gene_variant | 1.0 |
| rpoC | 762467 | c.-903C>T | upstream_gene_variant | 1.0 |
| rpoC | 762470 | c.-900G>T | upstream_gene_variant | 1.0 |
| rpoB | 762489 | p.Val895Thr | missense_variant | 1.0 |
| rpoC | 762509 | c.-861T>G | upstream_gene_variant | 1.0 |
| rpoB | 762510 | p.Ala902Pro | missense_variant | 1.0 |
| rpoC | 762521 | c.-849C>T | upstream_gene_variant | 1.0 |
| rpoC | 762527 | c.-843G>C | upstream_gene_variant | 1.0 |
| rpoC | 762533 | c.-837T>C | upstream_gene_variant | 1.0 |
| rpoC | 762536 | c.-834T>C | upstream_gene_variant | 1.0 |
| rpoC | 762551 | c.-819C>T | upstream_gene_variant | 1.0 |
| rpoC | 762560 | c.-810A>G | upstream_gene_variant | 1.0 |
| rpoC | 762563 | c.-807G>T | upstream_gene_variant | 1.0 |
| rpoC | 762575 | c.-795C>T | upstream_gene_variant | 1.0 |
| rpoC | 762581 | c.-789T>C | upstream_gene_variant | 1.0 |
| rpoC | 762582 | c.-788T>C | upstream_gene_variant | 1.0 |
| rpoC | 762593 | c.-777C>T | upstream_gene_variant | 1.0 |
| rpoB | 762784 | c.2979delC | frameshift_variant | 1.0 |
| rpoB | 762787 | p.Val994Ala | missense_variant | 1.0 |
| rpoB | 762789 | c.2983_2984insA | frameshift_variant | 1.0 |
| rpoC | 762806 | c.-564C>T | upstream_gene_variant | 1.0 |
| rpoB | 762813 | p.Met1003Val | missense_variant | 1.0 |
| rpoC | 762816 | c.-554_-552delCTCinsTTG | upstream_gene_variant | 1.0 |
| rpoC | 762824 | c.-546C>T | upstream_gene_variant | 1.0 |
| rpoC | 762830 | c.-540C>T | upstream_gene_variant | 1.0 |
| rpoC | 762831 | c.-539_-538delAGinsTC | upstream_gene_variant | 1.0 |
| rpoC | 762836 | c.-534C>T | upstream_gene_variant | 1.0 |
| rpoC | 762857 | c.-513C>G | upstream_gene_variant | 1.0 |
| rpoB | 762858 | p.Thr1018Ala | missense_variant | 1.0 |
| rpoC | 762863 | c.-507T>C | upstream_gene_variant | 1.0 |
| rpoB | 762879 | p.Met1025Leu | missense_variant | 1.0 |
| rpoC | 762923 | c.-447C>G | upstream_gene_variant | 1.0 |
| rpoC | 762929 | c.-441G>C | upstream_gene_variant | 1.0 |
| rpoC | 762962 | c.-408C>T | upstream_gene_variant | 1.0 |
| rpoC | 762971 | c.-399G>C | upstream_gene_variant | 1.0 |
| rpoC | 762983 | c.-387C>T | upstream_gene_variant | 1.0 |
| rpoC | 762989 | c.-381G>T | upstream_gene_variant | 1.0 |
| rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.97 |
| rpoC | 763004 | c.-366G>A | upstream_gene_variant | 1.0 |
| rpoC | 763007 | c.-363C>T | upstream_gene_variant | 1.0 |
| rpoC | 763028 | c.-342T>C | upstream_gene_variant | 1.0 |
| rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
| rpoC | 763053 | c.-317_-315delTTGinsCTC | upstream_gene_variant | 0.97 |
| rpoC | 763070 | c.-300T>C | upstream_gene_variant | 1.0 |
| rpoB | 763074 | p.Thr1090Val | missense_variant | 1.0 |
| rpoC | 763085 | c.-285C>A | upstream_gene_variant | 1.0 |
| rpoC | 763094 | c.-276G>C | upstream_gene_variant | 1.0 |
| rpoC | 763103 | c.-267G>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 | 763130 | c.-240G>A | upstream_gene_variant | 1.0 |
| rpoC | 763133 | c.-237G>C | upstream_gene_variant | 1.0 |
| rpoC | 763136 | c.-234C>T | upstream_gene_variant | 1.0 |
| rpoC | 763145 | c.-225G>A | upstream_gene_variant | 1.0 |
| rpoC | 763158 | c.-212C>T | upstream_gene_variant | 1.0 |
| rpoC | 763166 | c.-204A>G | upstream_gene_variant | 1.0 |
| rpoC | 763169 | c.-201A>G | upstream_gene_variant | 1.0 |
| rpoC | 763178 | c.-192G>C | upstream_gene_variant | 1.0 |
| rpoC | 763363 | c.-7G>A | upstream_gene_variant | 1.0 |
| rpoC | 763375 | c.6C>A | synonymous_variant | 1.0 |
| rpoC | 763402 | c.33C>G | synonymous_variant | 1.0 |
| rpoC | 763411 | c.42T>G | synonymous_variant | 1.0 |
| rpoC | 763414 | c.45T>C | synonymous_variant | 1.0 |
| rpoC | 763420 | c.51G>C | synonymous_variant | 1.0 |
| rpoC | 763423 | p.Glu18Asp | missense_variant | 1.0 |
| rpoC | 763429 | c.60C>T | synonymous_variant | 1.0 |
| rpoC | 763430 | c.61_63delAGGinsCGC | synonymous_variant | 1.0 |
| rpoC | 763435 | c.66A>G | synonymous_variant | 1.0 |
| rpoC | 763444 | c.75T>C | synonymous_variant | 1.0 |
| rpoC | 763453 | c.84C>G | synonymous_variant | 1.0 |
| rpoC | 763456 | c.87A>G | synonymous_variant | 1.0 |
| rpoC | 763459 | c.90G>A | synonymous_variant | 1.0 |
| rpoC | 763468 | c.99G>C | synonymous_variant | 1.0 |
| rpoC | 763486 | c.117T>C | synonymous_variant | 1.0 |
| rpoC | 763528 | c.159G>T | synonymous_variant | 1.0 |
| rpoC | 763531 | c.162G>C | synonymous_variant | 1.0 |
| rpoC | 763534 | c.165T>C | synonymous_variant | 1.0 |
| rpoC | 763537 | c.168C>G | synonymous_variant | 1.0 |
| rpoC | 763546 | c.177A>G | synonymous_variant | 1.0 |
| rpoC | 763558 | c.189C>T | synonymous_variant | 1.0 |
| rpoC | 763570 | c.201G>T | synonymous_variant | 1.0 |
| rpoC | 763573 | c.204G>C | synonymous_variant | 1.0 |
| rpoC | 763594 | c.225C>T | synonymous_variant | 1.0 |
| rpoC | 763600 | c.231C>G | synonymous_variant | 1.0 |
| rpoC | 763603 | c.234C>T | synonymous_variant | 1.0 |
| rpoC | 763606 | c.237C>T | synonymous_variant | 1.0 |
| rpoC | 763633 | c.264T>G | synonymous_variant | 1.0 |
| rpoC | 763648 | c.279C>G | synonymous_variant | 1.0 |
| rpoC | 763651 | c.282C>T | synonymous_variant | 1.0 |
| rpoC | 763657 | c.288G>A | synonymous_variant | 1.0 |
| rpoC | 763666 | c.297G>C | synonymous_variant | 1.0 |
| rpoC | 763669 | c.300C>G | synonymous_variant | 1.0 |
| rpoC | 763696 | c.327T>C | synonymous_variant | 1.0 |
| rpoC | 763702 | c.333C>G | synonymous_variant | 1.0 |
| rpoC | 763703 | c.334_336delTCGinsAGC | synonymous_variant | 1.0 |
| rpoC | 763711 | c.342G>C | 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 | 763741 | c.372C>T | synonymous_variant | 1.0 |
| rpoC | 763765 | c.396T>C | synonymous_variant | 1.0 |
| rpoC | 763774 | c.405G>C | synonymous_variant | 1.0 |
| rpoC | 763781 | c.412_414delTCGinsAGC | synonymous_variant | 1.0 |
| rpoC | 763801 | c.432C>G | synonymous_variant | 1.0 |
| rpoC | 763807 | c.438T>C | synonymous_variant | 1.0 |
| rpoC | 763813 | c.444C>G | synonymous_variant | 1.0 |
| rpoC | 763819 | c.450G>C | synonymous_variant | 1.0 |
| rpoC | 763828 | c.459C>G | synonymous_variant | 1.0 |
| rpoC | 763831 | c.462A>G | synonymous_variant | 1.0 |
| rpoC | 763836 | p.Ala156Glu | missense_variant | 1.0 |
| rpoC | 763940 | p.Ala191Ser | missense_variant | 1.0 |
| rpoC | 763985 | p.Arg206Lys | missense_variant | 1.0 |
| rpoC | 763996 | c.627T>C | synonymous_variant | 1.0 |
| rpoC | 764005 | c.636G>C | synonymous_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.Ser224Asn | missense_variant | 1.0 |
| rpoC | 764044 | c.675T>C | synonymous_variant | 1.0 |
| rpoC | 764048 | p.Thr227Val | missense_variant | 1.0 |
| rpoC | 764056 | c.687G>C | synonymous_variant | 1.0 |
| rpoC | 764077 | c.708C>G | 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 | 764101 | c.732C>G | synonymous_variant | 1.0 |
| rpoC | 764102 | p.Val245Gln | missense_variant | 1.0 |
| rpoC | 764110 | c.741C>T | synonymous_variant | 1.0 |
| rpoC | 764131 | c.762T>C | synonymous_variant | 1.0 |
| rpoC | 764134 | c.765C>G | synonymous_variant | 1.0 |
| rpoC | 764149 | c.780G>C | synonymous_variant | 1.0 |
| rpoC | 764164 | p.Ile265Met | missense_variant | 1.0 |
| rpoC | 764188 | c.819A>G | synonymous_variant | 1.0 |
| rpoC | 764195 | p.Ser276Ala | missense_variant | 1.0 |
| rpoC | 764206 | p.Asp279Glu | missense_variant | 1.0 |
| rpoC | 764207 | p.Val280Thr | missense_variant | 1.0 |
| rpoC | 764215 | c.846A>C | synonymous_variant | 1.0 |
| rpoC | 764217 | p.Asn283Thr | missense_variant | 1.0 |
| rpoC | 764221 | c.852C>T | synonymous_variant | 1.0 |
| rpoC | 764227 | c.858G>C | synonymous_variant | 1.0 |
| rpoC | 764239 | c.870T>G | synonymous_variant | 1.0 |
| rpoC | 764245 | c.876C>G | synonymous_variant | 1.0 |
| rpoC | 764257 | c.888G>C | synonymous_variant | 1.0 |
| rpoC | 764263 | c.894G>C | synonymous_variant | 1.0 |
| rpoC | 764266 | c.897T>C | synonymous_variant | 1.0 |
| rpoC | 764296 | c.927G>C | synonymous_variant | 1.0 |
| rpoC | 764320 | c.951C>T | synonymous_variant | 1.0 |
| rpoC | 764329 | c.960C>T | synonymous_variant | 1.0 |
| rpoC | 764365 | c.996C>T | synonymous_variant | 1.0 |
| rpoC | 764371 | c.1002G>T | synonymous_variant | 1.0 |
| rpoC | 764380 | c.1011G>C | synonymous_variant | 1.0 |
| rpoC | 764387 | c.1018T>C | synonymous_variant | 1.0 |
| rpoC | 764401 | c.1032C>T | 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 | 764509 | c.1140G>C | synonymous_variant | 1.0 |
| rpoC | 764521 | c.1152T>C | synonymous_variant | 1.0 |
| rpoC | 764533 | c.1164C>T | synonymous_variant | 1.0 |
| rpoC | 764536 | c.1167G>T | synonymous_variant | 1.0 |
| rpoC | 764539 | c.1170C>G | synonymous_variant | 1.0 |
| rpoC | 764554 | c.1185C>T | synonymous_variant | 1.0 |
| rpoC | 764560 | c.1191T>C | synonymous_variant | 1.0 |
| rpoC | 764566 | c.1197C>G | synonymous_variant | 1.0 |
| rpoC | 764575 | c.1206T>G | synonymous_variant | 1.0 |
| rpoC | 764578 | c.1209C>G | synonymous_variant | 0.95 |
| rpoC | 764593 | c.1224C>T | synonymous_variant | 1.0 |
| rpoC | 764626 | c.1257C>T | synonymous_variant | 1.0 |
| rpoC | 764632 | c.1263T>C | synonymous_variant | 1.0 |
| rpoC | 764644 | c.1275G>C | synonymous_variant | 1.0 |
| rpoC | 764650 | c.1281G>T | synonymous_variant | 1.0 |
| rpoC | 764656 | c.1287C>T | synonymous_variant | 1.0 |
| rpoC | 764662 | c.1293G>C | synonymous_variant | 1.0 |
| rpoC | 764668 | c.1299C>T | synonymous_variant | 1.0 |
| rpoC | 764677 | c.1308C>G | synonymous_variant | 1.0 |
| rpoC | 764680 | c.1311G>A | synonymous_variant | 1.0 |
| rpoC | 764692 | c.1323C>T | synonymous_variant | 1.0 |
| rpoC | 764746 | c.1377G>C | synonymous_variant | 1.0 |
| 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 | 764780 | c.1411_1412delAGinsTC | synonymous_variant | 1.0 |
| rpoC | 764791 | c.1422C>G | synonymous_variant | 1.0 |
| rpoC | 764803 | c.1434C>G | synonymous_variant | 1.0 |
| rpoC | 764809 | c.1440C>G | synonymous_variant | 1.0 |
| rpoC | 764812 | c.1443C>G | synonymous_variant | 1.0 |
| rpoC | 764815 | c.1446A>G | synonymous_variant | 1.0 |
| rpoC | 764827 | c.1458G>C | synonymous_variant | 1.0 |
| rpoC | 764848 | c.1479G>A | synonymous_variant | 1.0 |
| rpoC | 764858 | c.1489T>C | synonymous_variant | 1.0 |
| rpoC | 764863 | c.1494G>C | synonymous_variant | 1.0 |
| rpoC | 764869 | c.1500C>T | synonymous_variant | 1.0 |
| rpoC | 764872 | c.1503A>G | synonymous_variant | 1.0 |
| rpoC | 764887 | c.1518G>T | synonymous_variant | 1.0 |
| rpoC | 764888 | c.1519T>C | synonymous_variant | 1.0 |
| rpoC | 764893 | c.1524T>C | synonymous_variant | 1.0 |
| rpoC | 764911 | c.1542A>G | synonymous_variant | 1.0 |
| rpoC | 764912 | p.Met515Gln | missense_variant | 1.0 |
| rpoC | 764926 | c.1557C>T | synonymous_variant | 1.0 |
| rpoC | 764935 | c.1566T>C | synonymous_variant | 1.0 |
| rpoC | 764939 | c.1570C>T | synonymous_variant | 1.0 |
| rpoC | 764948 | c.1579T>C | synonymous_variant | 1.0 |
| rpoC | 764968 | c.1599T>C | synonymous_variant | 1.0 |
| rpoC | 765403 | c.2034G>C | synonymous_variant | 1.0 |
| rpoC | 765404 | p.Leu679Gly | missense_variant | 1.0 |
| rpoC | 765408 | p.Gly680Asp | missense_variant | 1.0 |
| rpoC | 765412 | c.2043T>C | synonymous_variant | 1.0 |
| rpoC | 765425 | p.Lys686Glu | missense_variant | 1.0 |
| rpoC | 765435 | p.His689Pro | missense_variant | 1.0 |
| rpoC | 765443 | p.Val692Arg | missense_variant | 1.0 |
| rpoC | 765451 | c.2082C>G | synonymous_variant | 1.0 |
| rpoC | 765452 | p.Ala695Thr | missense_variant | 1.0 |
| rpoC | 765466 | c.2097C>T | synonymous_variant | 1.0 |
| rpoC | 765469 | c.2100G>C | synonymous_variant | 1.0 |
| rpoC | 765478 | c.2109T>C | synonymous_variant | 1.0 |
| rpoC | 765499 | c.2130C>G | synonymous_variant | 1.0 |
| rpoC | 765508 | c.2139C>G | synonymous_variant | 1.0 |
| rpoC | 765526 | c.2157C>G | synonymous_variant | 1.0 |
| rpoC | 765718 | p.Asp783Glu | missense_variant | 1.0 |
| rpoC | 765728 | p.Gln787Lys | missense_variant | 1.0 |
| rpoC | 765734 | c.2365T>C | synonymous_variant | 1.0 |
| rpoC | 765741 | p.Glu791Ala | missense_variant | 1.0 |
| rpoC | 765751 | c.2382C>G | synonymous_variant | 1.0 |
| rpoC | 765753 | p.Asp795Ala | missense_variant | 1.0 |
| rpoC | 765772 | c.2403C>G | synonymous_variant | 1.0 |
| rpoC | 765784 | c.2415C>G | synonymous_variant | 1.0 |
| rpoC | 765796 | c.2427C>T | synonymous_variant | 1.0 |
| rpoC | 765811 | c.2442T>C | synonymous_variant | 1.0 |
| rpoC | 765817 | c.2448G>C | synonymous_variant | 1.0 |
| rpoC | 765835 | c.2466C>T | synonymous_variant | 1.0 |
| rpoC | 765871 | c.2502T>G | synonymous_variant | 1.0 |
| rpoC | 765875 | p.Val836Ile | missense_variant | 1.0 |
| rpoC | 765898 | c.2529C>T | synonymous_variant | 1.0 |
| rpoC | 765904 | c.2535C>G | synonymous_variant | 1.0 |
| rpoC | 765908 | c.2539C>T | synonymous_variant | 1.0 |
| rpoC | 765934 | c.2565C>T | synonymous_variant | 1.0 |
| rpoC | 765937 | c.2568T>G | 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 | 765952 | c.2583G>C | synonymous_variant | 1.0 |
| rpoC | 765962 | c.2593T>C | synonymous_variant | 1.0 |
| rpoC | 765979 | c.2610C>G | synonymous_variant | 1.0 |
| rpoC | 765982 | c.2613C>T | synonymous_variant | 1.0 |
| rpoC | 765994 | c.2625A>T | synonymous_variant | 1.0 |
| rpoC | 766009 | c.2640G>T | synonymous_variant | 1.0 |
| rpoC | 766012 | c.2643C>G | synonymous_variant | 1.0 |
| rpoC | 766018 | c.2649C>T | synonymous_variant | 1.0 |
| rpoC | 766021 | c.2652G>C | synonymous_variant | 1.0 |
| rpoC | 766039 | c.2670C>T | synonymous_variant | 1.0 |
| rpoC | 766321 | c.2952C>G | synonymous_variant | 1.0 |
| rpoC | 766336 | c.2967C>G | synonymous_variant | 1.0 |
| rpoC | 766339 | c.2970C>T | synonymous_variant | 1.0 |
| rpoC | 766348 | c.2979A>G | synonymous_variant | 1.0 |
| rpoC | 766357 | c.2988C>T | synonymous_variant | 1.0 |
| rpoC | 766363 | c.2994G>C | 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 | 766425 | c.3056_3057insTGT | disruptive_inframe_insertion | 1.0 |
| rpoC | 766428 | p.Val1020Ala | missense_variant | 1.0 |
| rpoC | 766435 | p.Glu1022Asp | missense_variant | 1.0 |
| rpoC | 766456 | c.3087C>G | synonymous_variant | 1.0 |
| rpoC | 766459 | c.3090G>T | synonymous_variant | 1.0 |
| rpoC | 766471 | c.3102G>C | synonymous_variant | 1.0 |
| rpoC | 766483 | c.3114G>T | synonymous_variant | 1.0 |
| rpoC | 766486 | c.3117A>G | synonymous_variant | 1.0 |
| rpoC | 766489 | c.3120G>C | synonymous_variant | 1.0 |
| rpoC | 766490 | p.Arg1041Lys | missense_variant | 1.0 |
| rpoC | 766513 | p.Asp1048Glu | missense_variant | 1.0 |
| rpoC | 766516 | c.3147C>T | synonymous_variant | 1.0 |
| rpoC | 766517 | p.Thr1050Ser | missense_variant | 1.0 |
| rpoC | 766525 | c.3156G>A | synonymous_variant | 1.0 |
| rpoC | 766528 | c.3159T>G | synonymous_variant | 1.0 |
| rpoC | 766534 | c.3165C>G | synonymous_variant | 1.0 |
| rpoC | 766542 | p.Gly1058Asp | missense_variant | 1.0 |
| rpoC | 766546 | p.Glu1059Asp | missense_variant | 1.0 |
| rpoC | 766549 | c.3180G>C | synonymous_variant | 1.0 |
| rpoC | 766568 | p.Val1067Ile | missense_variant | 1.0 |
| rpoC | 766573 | c.3204T>G | synonymous_variant | 1.0 |
| rpoC | 766582 | c.3213C>T | synonymous_variant | 1.0 |
| rpoC | 766588 | p.Glu1073Asp | missense_variant | 1.0 |
| rpoC | 766607 | p.Ile1080Leu | missense_variant | 1.0 |
| rpoC | 766618 | c.3249G>T | synonymous_variant | 1.0 |
| rpoC | 766630 | c.3261G>C | synonymous_variant | 1.0 |
| rpoC | 766645 | p.Glu1092Asp | missense_variant | 1.0 |
| rpoC | 766651 | c.3282T>C | synonymous_variant | 1.0 |
| rpoC | 766652 | p.Ser1095Thr | missense_variant | 1.0 |
| rpoC | 766657 | c.3288A>G | synonymous_variant | 1.0 |
| rpoC | 766660 | c.3291G>T | synonymous_variant | 1.0 |
| rpoC | 766661 | p.Val1098Leu | missense_variant | 1.0 |
| rpoC | 766666 | c.3297C>G | synonymous_variant | 1.0 |
| rpoC | 766672 | c.3303T>C | synonymous_variant | 1.0 |
| rpoC | 766690 | c.3321G>C | synonymous_variant | 1.0 |
| rpoC | 766703 | p.Met1112Leu | missense_variant | 1.0 |
| rpoC | 766711 | c.3342C>T | synonymous_variant | 1.0 |
| rpoC | 766712 | p.Ser1115Ala | missense_variant | 1.0 |
| rpoC | 766717 | c.3348C>G | synonymous_variant | 1.0 |
| rpoC | 766726 | c.3357T>C | synonymous_variant | 1.0 |
| rpoC | 766742 | p.Gln1125Met | missense_variant | 1.0 |
| rpoC | 766747 | c.3378C>T | synonymous_variant | 1.0 |
| rpoC | 766753 | c.3384C>G | synonymous_variant | 1.0 |
| rpoC | 766754 | p.Glu1129Gln | missense_variant | 1.0 |
| rpoC | 766765 | c.3396A>C | synonymous_variant | 1.0 |
| rpoC | 766774 | c.3405T>C | synonymous_variant | 1.0 |
| rpoC | 766776 | p.Arg1136His | missense_variant | 1.0 |
| rpoC | 766798 | c.3429C>G | synonymous_variant | 1.0 |
| rpoC | 766799 | p.Ala1144Ser | missense_variant | 1.0 |
| rpoC | 766804 | c.3435A>G | synonymous_variant | 1.0 |
| rpoC | 766813 | c.3444G>C | synonymous_variant | 1.0 |
| rpoC | 766837 | c.3468G>C | synonymous_variant | 1.0 |
| rpoC | 766843 | c.3474T>C | synonymous_variant | 1.0 |
| rpoC | 766846 | c.3477C>G | synonymous_variant | 1.0 |
| rpoC | 766858 | c.3489C>T | synonymous_variant | 1.0 |
| rpoC | 766861 | c.3492G>C | synonymous_variant | 1.0 |
| rpoC | 766867 | c.3498C>G | synonymous_variant | 1.0 |
| rpoC | 766879 | c.3510G>C | synonymous_variant | 1.0 |
| rpoC | 766885 | c.3516G>C | synonymous_variant | 1.0 |
| rpoC | 766888 | c.3519G>C | synonymous_variant | 1.0 |
| rpoC | 766894 | c.3525T>C | synonymous_variant | 1.0 |
| rpoC | 766895 | c.3526T>C | synonymous_variant | 1.0 |
| rpoC | 766900 | c.3531T>C | synonymous_variant | 1.0 |
| rpoC | 766903 | c.3534C>T | synonymous_variant | 1.0 |
| rpoC | 766909 | c.3540G>C | synonymous_variant | 1.0 |
| rpoC | 766911 | p.Ile1181Thr | missense_variant | 1.0 |
| rpoC | 766915 | p.Asp1182Glu | missense_variant | 1.0 |
| rpoC | 766918 | c.3549C>G | synonymous_variant | 1.0 |
| rpoC | 766960 | c.3591C>T | synonymous_variant | 1.0 |
| rpoC | 766969 | c.3600C>G | synonymous_variant | 1.0 |
| rpoC | 766972 | c.3603G>C | synonymous_variant | 1.0 |
| rpoC | 766975 | c.3606C>G | synonymous_variant | 1.0 |
| rpoC | 766978 | c.3609C>T | synonymous_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 | 767023 | c.3654C>T | synonymous_variant | 1.0 |
| rpoC | 767044 | c.3675G>C | synonymous_variant | 1.0 |
| rpoC | 767059 | c.3690T>C | synonymous_variant | 1.0 |
| rpoC | 767062 | c.3693C>A | synonymous_variant | 1.0 |
| rpoC | 767065 | c.3696G>C | synonymous_variant | 1.0 |
| rpoC | 767071 | c.3702C>G | synonymous_variant | 1.0 |
| rpoC | 767080 | c.3711G>C | synonymous_variant | 1.0 |
| rpoC | 767093 | c.3724_3725delAGinsTC | synonymous_variant | 1.0 |
| rpoC | 767098 | c.3729T>C | synonymous_variant | 1.0 |
| rpoC | 767106 | p.Asn1246Ile | missense_variant | 1.0 |
| rpoC | 767113 | c.3744G>C | synonymous_variant | 1.0 |
| rpoC | 767119 | c.3750A>G | synonymous_variant | 1.0 |
| rpoC | 767134 | c.3765C>T | synonymous_variant | 1.0 |
| rpoC | 767138 | c.3769C>T | synonymous_variant | 1.0 |
| rpoC | 767167 | c.3798C>G | synonymous_variant | 1.0 |
| rpoC | 767176 | c.3807C>T | synonymous_variant | 1.0 |
| rpoC | 767180 | p.Ala1271Gln | missense_variant | 1.0 |
| rpoC | 767185 | c.3816G>T | synonymous_variant | 1.0 |
| rpoC | 767191 | c.3822C>G | synonymous_variant | 1.0 |
| rpoC | 767203 | c.3834C>T | synonymous_variant | 1.0 |
| rpoC | 767206 | c.3837C>T | synonymous_variant | 1.0 |
| rpoC | 767209 | c.3840T>C | synonymous_variant | 1.0 |
| rpoC | 767219 | p.Thr1284Ala | missense_variant | 1.0 |
| rpsL | 781558 | c.-2A>C | upstream_gene_variant | 1.0 |
| rpsL | 781559 | c.-1G>T | upstream_gene_variant | 1.0 |
| rpsL | 781572 | p.Gln5Asn | missense_variant | 1.0 |
| rpsL | 781595 | c.36T>C | synonymous_variant | 1.0 |
| rpsL | 781598 | c.39G>C | synonymous_variant | 1.0 |
| rpsL | 781605 | p.Ile16Val | missense_variant | 1.0 |
| rpsL | 781637 | c.78C>G | 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 | 781679 | c.120C>G | synonymous_variant | 1.0 |
| rpsL | 781682 | c.123T>C | synonymous_variant | 1.0 |
| rpsL | 781700 | c.141G>C | synonymous_variant | 1.0 |
| rpsL | 781703 | c.144G>C | synonymous_variant | 1.0 |
| rpsL | 781706 | c.147T>G | synonymous_variant | 1.0 |
| rpsL | 781709 | c.150G>T | synonymous_variant | 1.0 |
| rpsL | 781728 | c.170_171insCGCCT | frameshift_variant | 1.0 |
| rpsL | 781733 | c.174G>C | synonymous_variant | 1.0 |
| rpsL | 781736 | c.177T>C | synonymous_variant | 1.0 |
| rpsL | 781754 | c.195G>C | synonymous_variant | 1.0 |
| rpsL | 781760 | c.201T>C | synonymous_variant | 1.0 |
| rpsL | 781763 | c.204C>G | synonymous_variant | 0.83 |
| rpsL | 781766 | c.207C>T | synonymous_variant | 1.0 |
| rpsL | 781793 | c.234G>C | synonymous_variant | 0.8 |
| rpsL | 781802 | c.243G>C | synonymous_variant | 1.0 |
| rpsL | 781805 | c.246G>C | synonymous_variant | 0.8 |
| rpsL | 781814 | c.255C>T | synonymous_variant | 0.88 |
| rpsL | 781817 | c.258G>T | synonymous_variant | 1.0 |
| rpsL | 781829 | c.270G>T | synonymous_variant | 0.71 |
| rpsL | 781832 | c.273T>C | synonymous_variant | 1.0 |
| rpsL | 781838 | c.279G>T | synonymous_variant | 0.71 |
| rpsL | 781841 | c.282C>T | synonymous_variant | 1.0 |
| rpsL | 781856 | c.297C>T | synonymous_variant | 1.0 |
| rpsL | 781859 | c.300T>A | synonymous_variant | 1.0 |
| rpsL | 781862 | c.303G>C | synonymous_variant | 1.0 |
| rpsL | 781865 | c.306G>C | synonymous_variant | 1.0 |
| rpsL | 781868 | c.309T>C | synonymous_variant | 1.0 |
| rpsL | 781871 | c.312G>T | synonymous_variant | 1.0 |
| rpsL | 781877 | c.318T>C | synonymous_variant | 1.0 |
| rpsL | 781880 | c.321C>G | synonymous_variant | 1.0 |
| rpsL | 781892 | c.333A>G | synonymous_variant | 1.0 |
| rpsL | 781898 | c.339A>C | synonymous_variant | 1.0 |
| rpsL | 781916 | c.357T>C | synonymous_variant | 1.0 |
| rpsL | 781929 | p.Gly124Ser | missense_variant | 1.0 |
| rplC | 800633 | c.-176T>C | upstream_gene_variant | 1.0 |
| rplC | 800645 | c.-164C>T | 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 | 800672 | c.-137G>C | upstream_gene_variant | 1.0 |
| rplC | 800690 | c.-119C>T | upstream_gene_variant | 1.0 |
| rplC | 800693 | c.-116A>G | upstream_gene_variant | 1.0 |
| rplC | 800703 | c.-106T>C | upstream_gene_variant | 1.0 |
| rplC | 800715 | c.-94A>C | upstream_gene_variant | 1.0 |
| rplC | 800720 | c.-89T>C | upstream_gene_variant | 1.0 |
| rplC | 800723 | c.-86C>G | upstream_gene_variant | 1.0 |
| rplC | 800735 | c.-74C>G | upstream_gene_variant | 1.0 |
| rplC | 800738 | c.-71T>C | upstream_gene_variant | 1.0 |
| rplC | 800762 | c.-47T>G | upstream_gene_variant | 1.0 |
| rrs | 1471914 | n.69A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471918 | n.73A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471932 | n.87A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471938 | n.93T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471943 | n.98T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471978 | n.133C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471979 | n.134T>C | 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 | 1472023 | n.178G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472030 | n.185G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472033 | n.188A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472034 | n.189T>C | 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 | 1472043 | n.198T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472057 | n.212C>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472062 | n.217G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472068 | n.223T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472070 | n.225G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.94 |
| rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472148 | n.303T>C | non_coding_transcript_exon_variant | 0.86 |
| rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.88 |
| rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472286 | n.441C>A | 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 | 1472328 | n.483G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472416 | n.571C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472425 | n.580T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472437 | n.592T>A | 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 | 1472456 | n.611T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472467 | n.622G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472473 | n.628G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472486 | n.641A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472516 | n.671C>T | non_coding_transcript_exon_variant | 0.93 |
| rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.94 |
| rrs | 1472597 | n.752G>A | non_coding_transcript_exon_variant | 0.75 |
| rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 0.76 |
| rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 0.91 |
| rrs | 1472836 | n.991G>A | non_coding_transcript_exon_variant | 0.89 |
| rrs | 1472840 | n.995A>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472844 | n.999C>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472845 | n.1000G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472847 | n.1002G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472849 | n.1004C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472850 | n.1005T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472855 | n.1011_1012insGT | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472873 | n.1028C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472875 | n.1030T>G | non_coding_transcript_exon_variant | 0.88 |
| rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472953 | n.1108G>A | 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 | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473026 | n.1181T>C | non_coding_transcript_exon_variant | 0.82 |
| rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473104 | n.1259C>T | 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 | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473668 | n.11C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473673 | n.16G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473677 | n.20C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473678 | n.21A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473679 | n.22T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473696 | n.39T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473698 | n.41G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473699 | n.42A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473756 | n.99G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473757 | n.100T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473788 | n.131A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473807 | n.150T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473815 | n.158T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473822 | n.165A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473832 | n.175C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473833 | n.176_177insT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473844 | n.187C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473870 | n.213G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473871 | n.214T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473887 | n.230T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473888 | n.231T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473922 | n.265A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473923 | n.266C>G | 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 | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474186 | n.529A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474201 | n.544T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474266 | n.609T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474284 | n.631_633delCCT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474293 | n.637_651delCCTCTCCGGAGGAGG | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474359 | n.702C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474402 | n.745T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474496 | n.839C>A | non_coding_transcript_exon_variant | 0.71 |
| rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.71 |
| rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.78 |
| rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.78 |
| rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.86 |
| rrl | 1474627 | n.970G>A | non_coding_transcript_exon_variant | 0.86 |
| rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.88 |
| rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.89 |
| rrl | 1474664 | n.1007G>T | non_coding_transcript_exon_variant | 0.75 |
| rrl | 1474666 | n.1009T>G | non_coding_transcript_exon_variant | 0.75 |
| rrl | 1474670 | n.1013C>G | non_coding_transcript_exon_variant | 0.75 |
| rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.75 |
| rrl | 1474679 | n.1022G>C | non_coding_transcript_exon_variant | 0.67 |
| rrl | 1474684 | n.1027T>C | non_coding_transcript_exon_variant | 0.67 |
| rrl | 1474687 | n.1030C>A | non_coding_transcript_exon_variant | 0.67 |
| rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474753 | n.1097delC | 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 | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474837 | n.1180A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474904 | n.1247G>C | 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 | 1475060 | n.1404delC | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475065 | n.1408G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475067 | n.1410A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475076 | n.1419C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475079 | n.1422T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475081 | n.1424C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475113 | n.1456C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475116 | n.1459G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475291 | n.1634A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475298 | n.1643delG | 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 | 1475339 | n.1682T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475340 | n.1683A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475361 | n.1704G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475363 | n.1706C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475369 | n.1712G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475376 | n.1719A>C | non_coding_transcript_exon_variant | 0.8 |
| rrl | 1475380 | n.1723C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475394 | n.1740_1743delGCTC | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475404 | n.1747A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475406 | n.1749_1750insGTGG | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475422 | n.1765A>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 | 1475460 | n.1803A>G | 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 | 1475481 | n.1824C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475482 | n.1825A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475532 | n.1875A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475538 | n.1881T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475550 | n.1893A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475555 | n.1898T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475602 | n.1945G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475617 | n.1960C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475633 | n.1976G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475636 | n.1979A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475638 | n.1981C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475639 | n.1982C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475649 | n.1992A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475655 | n.1998T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475735 | n.2078T>C | non_coding_transcript_exon_variant | 0.67 |
| rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 0.67 |
| rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475767 | n.2110_2111insT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.67 |
| rrl | 1475791 | n.2134A>G | non_coding_transcript_exon_variant | 0.5 |
| rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475892 | n.2235A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475916 | n.2259C>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 | 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>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476058 | n.2401T>C | 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.2450delA | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476110 | n.2453G>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 | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.86 |
| rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.8 |
| rrl | 1476251 | n.2594T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.8 |
| rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.75 |
| rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.75 |
| rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.5 |
| rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.5 |
| rrl | 1476297 | n.2640C>G | non_coding_transcript_exon_variant | 0.67 |
| rrl | 1476298 | n.2641C>G | non_coding_transcript_exon_variant | 0.5 |
| rrl | 1476300 | n.2643G>A | non_coding_transcript_exon_variant | 0.5 |
| rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.71 |
| rrl | 1476423 | n.2766T>C | non_coding_transcript_exon_variant | 0.76 |
| rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.96 |
| rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476597 | n.2940G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.91 |
| rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476661 | n.3004A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476665 | n.3008T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476666 | n.3009C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476675 | n.3018C>G | non_coding_transcript_exon_variant | 1.0 |
| rpsA | 1833557 | p.Val6Ile | missense_variant | 1.0 |
| rpsA | 1833571 | c.30A>G | synonymous_variant | 1.0 |
| rpsA | 1833586 | c.45C>T | synonymous_variant | 1.0 |
| rpsA | 1833589 | c.48A>C | synonymous_variant | 1.0 |
| rpsA | 1833595 | c.54T>C | synonymous_variant | 1.0 |
| rpsA | 1833596 | p.Ser19Ala | missense_variant | 1.0 |
| rpsA | 1833607 | c.66T>C | synonymous_variant | 1.0 |
| rpsA | 1833616 | c.75A>C | synonymous_variant | 1.0 |
| rpsA | 1833619 | c.78A>C | synonymous_variant | 1.0 |
| rpsA | 1833623 | p.Lys28Ala | missense_variant | 1.0 |
| rpsA | 1833646 | c.105T>C | synonymous_variant | 1.0 |
| rpsA | 1833652 | c.111C>T | synonymous_variant | 1.0 |
| rpsA | 1833664 | c.123C>A | synonymous_variant | 1.0 |
| rpsA | 1833676 | c.135A>G | synonymous_variant | 1.0 |
| rpsA | 1833679 | c.138G>C | synonymous_variant | 1.0 |
| rpsA | 1833682 | c.141C>T | synonymous_variant | 1.0 |
| rpsA | 1833685 | c.144G>T | synonymous_variant | 1.0 |
| rpsA | 1833694 | c.153G>C | synonymous_variant | 1.0 |
| rpsA | 1833697 | c.156C>G | synonymous_variant | 1.0 |
| rpsA | 1833721 | c.180A>G | 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 | 1833742 | c.201A>G | synonymous_variant | 1.0 |
| rpsA | 1833745 | c.204G>C | 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 | 1833793 | c.252C>T | synonymous_variant | 1.0 |
| rpsA | 1833799 | c.258C>G | synonymous_variant | 1.0 |
| rpsA | 1833802 | c.261A>G | synonymous_variant | 1.0 |
| rpsA | 1833805 | c.264C>G | synonymous_variant | 1.0 |
| rpsA | 1833808 | c.267G>C | synonymous_variant | 1.0 |
| rpsA | 1833811 | c.270G>C | synonymous_variant | 1.0 |
| rpsA | 1833820 | c.279G>A | synonymous_variant | 1.0 |
| rpsA | 1833832 | c.291G>A | synonymous_variant | 1.0 |
| rpsA | 1833838 | c.297G>C | synonymous_variant | 1.0 |
| rpsA | 1833841 | c.300C>G | synonymous_variant | 1.0 |
| rpsA | 1833847 | c.306C>G | synonymous_variant | 1.0 |
| rpsA | 1833850 | c.309C>G | synonymous_variant | 1.0 |
| rpsA | 1833856 | c.315A>G | synonymous_variant | 1.0 |
| rpsA | 1833859 | c.318C>G | synonymous_variant | 1.0 |
| rpsA | 1833874 | c.333T>C | synonymous_variant | 1.0 |
| rpsA | 1833877 | c.336C>G | synonymous_variant | 1.0 |
| rpsA | 1833894 | p.Ala118Glu | missense_variant | 1.0 |
| rpsA | 1833919 | c.378C>T | synonymous_variant | 1.0 |
| rpsA | 1833920 | p.Lys127Arg | missense_variant | 1.0 |
| rpsA | 1833928 | c.387G>T | synonymous_variant | 1.0 |
| rpsA | 1833931 | c.390C>G | synonymous_variant | 1.0 |
| rpsA | 1833949 | c.408T>C | synonymous_variant | 1.0 |
| rpsA | 1833952 | c.411C>T | synonymous_variant | 1.0 |
| rpsA | 1833964 | c.423C>T | synonymous_variant | 1.0 |
| rpsA | 1833970 | c.429G>T | synonymous_variant | 1.0 |
| rpsA | 1833976 | c.435C>T | synonymous_variant | 1.0 |
| rpsA | 1833979 | c.438T>C | 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 | 1834033 | c.492C>T | synonymous_variant | 1.0 |
| rpsA | 1834034 | p.Ile165Val | missense_variant | 1.0 |
| rpsA | 1834054 | c.513C>G | synonymous_variant | 1.0 |
| rpsA | 1834087 | c.546C>T | synonymous_variant | 1.0 |
| rpsA | 1834093 | c.552G>T | synonymous_variant | 1.0 |
| rpsA | 1834102 | c.561T>G | synonymous_variant | 1.0 |
| rpsA | 1834105 | c.564C>T | synonymous_variant | 1.0 |
| rpsA | 1834108 | c.567C>A | synonymous_variant | 1.0 |
| rpsA | 1834151 | p.Asn204His | missense_variant | 1.0 |
| rpsA | 1834172 | p.Ile211Val | missense_variant | 1.0 |
| rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
| rpsA | 1834186 | c.645C>G | synonymous_variant | 1.0 |
| rpsA | 1834189 | c.648G>C | synonymous_variant | 1.0 |
| rpsA | 1834195 | c.654G>C | synonymous_variant | 1.0 |
| rpsA | 1834213 | c.672G>C | synonymous_variant | 1.0 |
| rpsA | 1834222 | c.681T>C | synonymous_variant | 1.0 |
| rpsA | 1834225 | c.684C>G | synonymous_variant | 1.0 |
| rpsA | 1834234 | c.693G>C | synonymous_variant | 1.0 |
| rpsA | 1834249 | c.708T>C | synonymous_variant | 1.0 |
| rpsA | 1834261 | c.720A>G | synonymous_variant | 1.0 |
| rpsA | 1834264 | c.723G>C | synonymous_variant | 1.0 |
| rpsA | 1834294 | c.753G>C | synonymous_variant | 1.0 |
| rpsA | 1834298 | p.Gln253Glu | missense_variant | 1.0 |
| rpsA | 1834303 | c.762T>G | synonymous_variant | 1.0 |
| rpsA | 1834306 | c.765T>C | synonymous_variant | 1.0 |
| rpsA | 1834307 | p.Asp256Asn | missense_variant | 1.0 |
| rpsA | 1834318 | c.777C>G | synonymous_variant | 0.97 |
| rpsA | 1834333 | c.792C>T | synonymous_variant | 0.96 |
| rpsA | 1834340 | p.Met267Leu | missense_variant | 0.96 |
| rpsA | 1834345 | c.804C>T | synonymous_variant | 0.95 |
| rpsA | 1834348 | c.807T>C | synonymous_variant | 1.0 |
| rpsA | 1834354 | c.813G>C | synonymous_variant | 1.0 |
| rpsA | 1834357 | c.816T>C | synonymous_variant | 0.95 |
| rpsA | 1834361 | c.820T>C | synonymous_variant | 1.0 |
| rpsA | 1834366 | c.825A>G | synonymous_variant | 1.0 |
| rpsA | 1834369 | c.828C>G | synonymous_variant | 1.0 |
| rpsA | 1834375 | c.834G>C | synonymous_variant | 1.0 |
| rpsA | 1834378 | c.837T>C | synonymous_variant | 1.0 |
| rpsA | 1834387 | c.846C>T | synonymous_variant | 0.96 |
| rpsA | 1834399 | p.His286Gln | missense_variant | 0.95 |
| rpsA | 1834411 | c.870T>C | synonymous_variant | 1.0 |
| rpsA | 1834451 | c.910T>C | synonymous_variant | 1.0 |
| rpsA | 1834468 | c.927A>G | synonymous_variant | 1.0 |
| rpsA | 1834474 | c.933C>G | synonymous_variant | 1.0 |
| rpsA | 1834483 | c.942G>A | synonymous_variant | 1.0 |
| rpsA | 1834489 | c.948T>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>C | synonymous_variant | 1.0 |
| rpsA | 1834555 | c.1014T>G | synonymous_variant | 1.0 |
| rpsA | 1834561 | c.1020C>G | synonymous_variant | 1.0 |
| rpsA | 1834606 | c.1065C>G | synonymous_variant | 1.0 |
| rpsA | 1834609 | c.1068T>C | synonymous_variant | 1.0 |
| rpsA | 1834612 | c.1071G>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 | 1834650 | p.Thr370Ser | missense_variant | 1.0 |
| rpsA | 1834652 | p.Glu371Pro | missense_variant | 1.0 |
| rpsA | 1834663 | c.1122C>T | synonymous_variant | 1.0 |
| rpsA | 1834667 | p.Ala376Ser | missense_variant | 1.0 |
| rpsA | 1834678 | c.1137C>T | synonymous_variant | 1.0 |
| rpsA | 1834690 | c.1149T>C | synonymous_variant | 1.0 |
| rpsA | 1834732 | c.1191T>C | synonymous_variant | 1.0 |
| rpsA | 1834733 | p.Ala398Pro | missense_variant | 1.0 |
| rpsA | 1834738 | c.1197A>G | synonymous_variant | 1.0 |
| rpsA | 1834753 | c.1212T>C | synonymous_variant | 1.0 |
| rpsA | 1834759 | c.1218A>C | synonymous_variant | 1.0 |
| rpsA | 1834765 | c.1224A>G | synonymous_variant | 1.0 |
| rpsA | 1834774 | c.1233C>G | synonymous_variant | 1.0 |
| rpsA | 1834776 | p.Ala412Glu | missense_variant | 1.0 |
| rpsA | 1834780 | c.1239A>G | synonymous_variant | 1.0 |
| rpsA | 1834785 | c.1244_1245insG | frameshift_variant | 1.0 |
| rpsA | 1834788 | c.1248delT | frameshift_variant | 1.0 |
| rpsA | 1834792 | c.1251G>C | synonymous_variant | 1.0 |
| rpsA | 1834810 | c.1269C>G | synonymous_variant | 1.0 |
| kasA | 2517941 | c.-174C>G | upstream_gene_variant | 1.0 |
| kasA | 2517962 | c.-153C>G | upstream_gene_variant | 1.0 |
| kasA | 2517968 | c.-147T>A | upstream_gene_variant | 1.0 |
| kasA | 2517972 | c.-143_-141delCGTinsAAG | upstream_gene_variant | 1.0 |
| kasA | 2517980 | c.-135C>G | upstream_gene_variant | 1.0 |
| kasA | 2517988 | c.-127_-126delTTinsCC | upstream_gene_variant | 1.0 |
| ahpC | 2726561 | c.369T>C | synonymous_variant | 1.0 |
| ahpC | 2726570 | c.378C>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 | 2726638 | p.Ala149Val | missense_variant | 1.0 |
| ahpC | 2726645 | c.453C>G | synonymous_variant | 1.0 |
| ahpC | 2726654 | c.462G>C | synonymous_variant | 1.0 |
| ahpC | 2726663 | c.471C>T | synonymous_variant | 1.0 |
| ahpC | 2726669 | c.477T>C | synonymous_variant | 1.0 |
| ahpC | 2726675 | c.483A>G | synonymous_variant | 1.0 |
| ahpC | 2726681 | c.489A>G | synonymous_variant | 1.0 |
| ahpC | 2726687 | c.495C>G | synonymous_variant | 1.0 |
| ahpC | 2726696 | c.504C>G | synonymous_variant | 1.0 |
| ahpC | 2726705 | c.513C>T | synonymous_variant | 1.0 |
| ahpC | 2726717 | c.525A>G | synonymous_variant | 1.0 |
| pepQ | 2859690 | c.729C>G | synonymous_variant | 1.0 |
| pepQ | 2859697 | p.Lys241Arg | missense_variant | 1.0 |
| pepQ | 2859702 | c.715_717delTTGinsCTC | synonymous_variant | 1.0 |
| pepQ | 2859735 | c.684G>C | synonymous_variant | 1.0 |
| pepQ | 2859739 | p.Ala227Gly | missense_variant | 1.0 |
| pepQ | 2859746 | p.Leu225Val | missense_variant | 1.0 |
| pepQ | 2859747 | c.672C>G | synonymous_variant | 1.0 |
| pepQ | 2859756 | c.663C>T | synonymous_variant | 1.0 |
| rpoA | 3877613 | p.Ile299Val | missense_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 | 3877662 | c.846C>T | synonymous_variant | 1.0 |
| rpoA | 3877665 | c.843C>G | synonymous_variant | 1.0 |
| rpoA | 3877674 | c.834C>G | synonymous_variant | 1.0 |
| rpoA | 3877677 | c.831G>C | 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 | 3877737 | c.771G>C | synonymous_variant | 1.0 |
| rpoA | 3877749 | c.759C>T | synonymous_variant | 1.0 |
| rpoA | 3877752 | p.Asp252Glu | missense_variant | 1.0 |
| rpoA | 3877764 | p.Ala248Gly | missense_variant | 1.0 |
| rpoA | 3877770 | c.738A>C | synonymous_variant | 1.0 |
| rpoA | 3877773 | c.735G>C | synonymous_variant | 1.0 |
| rpoA | 3877776 | c.732T>C | synonymous_variant | 1.0 |
| rpoA | 3877785 | c.723C>G | synonymous_variant | 1.0 |
| rpoA | 3877800 | c.708G>C | synonymous_variant | 1.0 |
| rpoA | 3877803 | c.705G>C | synonymous_variant | 1.0 |
| rpoA | 3877818 | c.690A>G | synonymous_variant | 1.0 |
| rpoA | 3877833 | c.675C>G | synonymous_variant | 1.0 |
| rpoA | 3877839 | c.669G>T | synonymous_variant | 1.0 |
| rpoA | 3877842 | c.666A>C | synonymous_variant | 1.0 |
| rpoA | 3877856 | c.652T>C | synonymous_variant | 1.0 |
| rpoA | 3877866 | c.642G>C | synonymous_variant | 1.0 |
| rpoA | 3877875 | c.633T>G | synonymous_variant | 1.0 |
| rpoA | 3877881 | c.627G>T | synonymous_variant | 1.0 |
| rpoA | 3877884 | c.624G>C | synonymous_variant | 1.0 |
| rpoA | 3877893 | c.615C>G | synonymous_variant | 1.0 |
| rpoA | 3877898 | p.Pro204Ala | missense_variant | 1.0 |
| rpoA | 3877905 | c.603A>C | synonymous_variant | 1.0 |
| rpoA | 3877908 | c.600T>C | synonymous_variant | 1.0 |
| rpoA | 3877932 | c.576G>C | synonymous_variant | 1.0 |
| rpoA | 3877936 | p.Lys191Arg | missense_variant | 1.0 |
| rpoA | 3877938 | c.570C>T | synonymous_variant | 1.0 |
| rpoA | 3877962 | c.546G>C | synonymous_variant | 1.0 |
| rpoA | 3877971 | p.Asp179Glu | missense_variant | 1.0 |
| rpoA | 3877989 | c.519A>G | synonymous_variant | 1.0 |
| rpoA | 3878067 | c.441C>T | 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 | 3878102 | p.Val136Ile | missense_variant | 1.0 |
| rpoA | 3878103 | c.405A>G | synonymous_variant | 1.0 |
| rpoA | 3878106 | c.402G>C | synonymous_variant | 1.0 |
| rpoA | 3878118 | c.390T>C | synonymous_variant | 1.0 |
| rpoA | 3878127 | c.381G>C | synonymous_variant | 1.0 |
| rpoA | 3878142 | p.Gly122Asp | missense_variant | 1.0 |
| rpoA | 3878157 | p.Thr117Val | missense_variant | 1.0 |
| rpoA | 3878160 | c.348C>G | synonymous_variant | 1.0 |
| rpoA | 3878163 | c.345C>T | synonymous_variant | 1.0 |
| rpoA | 3878181 | c.327C>T | synonymous_variant | 1.0 |
| rpoA | 3878193 | c.315T>C | synonymous_variant | 1.0 |
| rpoA | 3878196 | p.Glu104Val | missense_variant | 1.0 |
| rpoA | 3878199 | c.309T>C | synonymous_variant | 1.0 |
| rpoA | 3878202 | c.306G>C | synonymous_variant | 1.0 |
| rpoA | 3878217 | c.291A>G | synonymous_variant | 1.0 |
| rpoA | 3878256 | c.252G>C | synonymous_variant | 1.0 |
| rpoA | 3878262 | p.Ser82Gly | missense_variant | 1.0 |
| rpoA | 3878271 | c.237T>C | synonymous_variant | 1.0 |
| rpoA | 3878283 | p.Glu75Asp | missense_variant | 1.0 |
| rpoA | 3878295 | c.213A>G | 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>C | 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 | 3878346 | c.162T>C | synonymous_variant | 1.0 |
| rpoA | 3878355 | c.153C>G | synonymous_variant | 1.0 |
| ddn | 3986645 | c.-199G>A | upstream_gene_variant | 1.0 |
| clpC1 | 4038725 | c.1980C>G | synonymous_variant | 1.0 |
| clpC1 | 4038740 | c.1965G>C | synonymous_variant | 1.0 |
| clpC1 | 4038755 | c.1950G>C | synonymous_variant | 1.0 |
| clpC1 | 4038767 | c.1938G>C | synonymous_variant | 1.0 |
| clpC1 | 4038773 | c.1932T>C | synonymous_variant | 1.0 |
| clpC1 | 4038779 | c.1926C>G | synonymous_variant | 1.0 |
| clpC1 | 4038791 | c.1914G>C | synonymous_variant | 1.0 |
| clpC1 | 4038795 | p.Ser637Thr | missense_variant | 1.0 |
| clpC1 | 4038815 | c.1890G>A | synonymous_variant | 1.0 |
| clpC1 | 4038878 | c.1827A>G | synonymous_variant | 1.0 |
| clpC1 | 4038905 | c.1800A>C | synonymous_variant | 1.0 |
| clpC1 | 4038908 | c.1797C>G | synonymous_variant | 1.0 |
| clpC1 | 4038911 | c.1794G>T | synonymous_variant | 1.0 |
| clpC1 | 4038914 | c.1791G>C | synonymous_variant | 1.0 |
| clpC1 | 4038917 | c.1788C>T | synonymous_variant | 1.0 |
| clpC1 | 4038923 | c.1782A>G | synonymous_variant | 1.0 |
| clpC1 | 4038932 | c.1773G>C | synonymous_variant | 1.0 |
| clpC1 | 4038941 | c.1764G>C | synonymous_variant | 1.0 |
| clpC1 | 4038944 | c.1761C>T | synonymous_variant | 1.0 |
| clpC1 | 4038953 | c.1752A>G | synonymous_variant | 1.0 |
| clpC1 | 4038962 | c.1743C>T | synonymous_variant | 1.0 |
| clpC1 | 4038965 | c.1740T>C | synonymous_variant | 1.0 |
| clpC1 | 4038971 | c.1734T>C | synonymous_variant | 1.0 |
| clpC1 | 4038974 | c.1731T>C | synonymous_variant | 1.0 |
| clpC1 | 4038977 | c.1728G>C | synonymous_variant | 1.0 |
| clpC1 | 4038980 | c.1725C>T | synonymous_variant | 1.0 |
| clpC1 | 4038997 | c.1708T>C | synonymous_variant | 1.0 |
| clpC1 | 4039004 | c.1701C>G | synonymous_variant | 1.0 |
| clpC1 | 4039022 | c.1683A>G | synonymous_variant | 1.0 |
| clpC1 | 4039067 | c.1638G>C | synonymous_variant | 1.0 |
| clpC1 | 4039073 | c.1632C>T | synonymous_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>C | synonymous_variant | 1.0 |
| clpC1 | 4039097 | c.1608G>T | synonymous_variant | 0.95 |
| clpC1 | 4039106 | c.1599G>C | synonymous_variant | 1.0 |
| clpC1 | 4039112 | c.1593C>G | synonymous_variant | 1.0 |
| clpC1 | 4039121 | c.1584T>C | synonymous_variant | 1.0 |
| clpC1 | 4039142 | c.1563A>G | synonymous_variant | 1.0 |
| clpC1 | 4039145 | c.1560G>T | synonymous_variant | 1.0 |
| clpC1 | 4039169 | c.1536A>G | synonymous_variant | 1.0 |
| clpC1 | 4039172 | c.1533A>G | synonymous_variant | 1.0 |
| clpC1 | 4039178 | c.1527G>T | synonymous_variant | 1.0 |
| clpC1 | 4039181 | c.1522_1524delTTGinsCTC | synonymous_variant | 1.0 |
| clpC1 | 4039199 | p.Ala502Glu | missense_variant | 1.0 |
| clpC1 | 4039239 | p.Gly489Ala | missense_variant | 1.0 |
| clpC1 | 4039274 | c.1431G>C | synonymous_variant | 1.0 |
| clpC1 | 4039277 | c.1428C>G | synonymous_variant | 1.0 |
| clpC1 | 4039280 | c.1425G>A | synonymous_variant | 1.0 |
| clpC1 | 4039286 | c.1419T>G | synonymous_variant | 1.0 |
| clpC1 | 4039292 | c.1413C>T | synonymous_variant | 1.0 |
| clpC1 | 4039295 | c.1410A>G | synonymous_variant | 1.0 |
| clpC1 | 4039310 | c.1395A>G | synonymous_variant | 1.0 |
| clpC1 | 4039313 | c.1392C>G | synonymous_variant | 1.0 |
| clpC1 | 4039319 | c.1386T>C | synonymous_variant | 1.0 |
| clpC1 | 4039322 | c.1383T>C | synonymous_variant | 1.0 |
| clpC1 | 4039327 | p.Gln460Lys | missense_variant | 1.0 |
| clpC1 | 4039328 | c.1377A>C | synonymous_variant | 1.0 |
| clpC1 | 4039337 | p.Thr456Gln | missense_variant | 1.0 |
| clpC1 | 4039347 | p.Arg453Gln | missense_variant | 1.0 |
| clpC1 | 4039360 | p.Ser449Arg | missense_variant | 1.0 |
| clpC1 | 4039382 | c.1323C>G | synonymous_variant | 1.0 |
| clpC1 | 4039391 | c.1314T>G | synonymous_variant | 1.0 |
| clpC1 | 4039394 | c.1311G>C | synonymous_variant | 1.0 |
| clpC1 | 4039397 | c.1308A>G | synonymous_variant | 1.0 |
| clpC1 | 4039409 | c.1296T>C | synonymous_variant | 1.0 |
| clpC1 | 4039412 | c.1293T>G | synonymous_variant | 1.0 |
| clpC1 | 4039427 | p.Glu426Asp | missense_variant | 1.0 |
| clpC1 | 4039430 | c.1275T>C | synonymous_variant | 1.0 |
| clpC1 | 4039436 | c.1269G>A | synonymous_variant | 1.0 |
| clpC1 | 4039442 | c.1263A>G | synonymous_variant | 1.0 |
| clpC1 | 4039448 | c.1257A>G | synonymous_variant | 1.0 |
| clpC1 | 4039454 | c.1251A>G | synonymous_variant | 1.0 |
| clpC1 | 4039463 | c.1242C>G | synonymous_variant | 1.0 |
| clpC1 | 4039466 | c.1239T>C | synonymous_variant | 1.0 |
| clpC1 | 4039472 | c.1233G>C | synonymous_variant | 1.0 |
| clpC1 | 4039481 | c.1224T>C | synonymous_variant | 1.0 |
| clpC1 | 4039487 | c.1218G>C | synonymous_variant | 1.0 |
| clpC1 | 4039517 | c.1188C>G | synonymous_variant | 1.0 |
| clpC1 | 4039526 | c.1179G>C | synonymous_variant | 1.0 |
| clpC1 | 4039553 | c.1152C>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>T | synonymous_variant | 1.0 |
| clpC1 | 4039616 | c.1089G>C | synonymous_variant | 1.0 |
| clpC1 | 4039622 | c.1083C>T | synonymous_variant | 1.0 |
| clpC1 | 4039634 | p.Glu357Asn | missense_variant | 1.0 |
| clpC1 | 4039649 | c.1056G>C | synonymous_variant | 1.0 |
| clpC1 | 4039652 | c.1053G>C | synonymous_variant | 1.0 |
| clpC1 | 4039661 | c.1044T>C | synonymous_variant | 1.0 |
| clpC1 | 4039694 | c.1011G>C | synonymous_variant | 1.0 |
| clpC1 | 4039724 | c.981A>G | synonymous_variant | 1.0 |
| clpC1 | 4039733 | c.972G>C | synonymous_variant | 1.0 |
| clpC1 | 4039739 | c.966C>G | synonymous_variant | 1.0 |
| clpC1 | 4039748 | c.957G>C | synonymous_variant | 1.0 |
| clpC1 | 4039751 | c.954A>G | synonymous_variant | 1.0 |
| clpC1 | 4039760 | c.945T>C | synonymous_variant | 1.0 |
| clpC1 | 4039763 | c.942C>T | synonymous_variant | 1.0 |
| clpC1 | 4039766 | c.939T>C | synonymous_variant | 1.0 |
| clpC1 | 4039769 | c.936C>G | synonymous_variant | 1.0 |
| clpC1 | 4039778 | c.927A>G | synonymous_variant | 1.0 |
| clpC1 | 4039787 | c.918G>C | synonymous_variant | 1.0 |
| clpC1 | 4039796 | c.909C>T | synonymous_variant | 1.0 |
| clpC1 | 4039805 | c.900C>T | synonymous_variant | 1.0 |
| clpC1 | 4039814 | c.891C>A | synonymous_variant | 1.0 |
| clpC1 | 4039817 | c.888A>T | synonymous_variant | 1.0 |
| clpC1 | 4039820 | c.885T>G | synonymous_variant | 1.0 |
| clpC1 | 4039823 | c.882T>C | synonymous_variant | 1.0 |
| clpC1 | 4039831 | c.874T>C | synonymous_variant | 1.0 |
| clpC1 | 4039832 | c.873C>G | synonymous_variant | 1.0 |
| clpC1 | 4039850 | c.855T>C | synonymous_variant | 1.0 |
| clpC1 | 4039865 | c.840T>C | synonymous_variant | 1.0 |
| clpC1 | 4039898 | c.807C>G | synonymous_variant | 1.0 |
| clpC1 | 4039901 | c.804C>G | synonymous_variant | 1.0 |
| clpC1 | 4039904 | c.801A>G | synonymous_variant | 1.0 |
| clpC1 | 4039907 | c.798G>A | synonymous_variant | 1.0 |
| clpC1 | 4039913 | c.792C>T | synonymous_variant | 1.0 |
| clpC1 | 4039937 | c.768G>C | synonymous_variant | 1.0 |
| clpC1 | 4039943 | c.762G>C | synonymous_variant | 1.0 |
| clpC1 | 4039946 | c.759A>T | synonymous_variant | 1.0 |
| clpC1 | 4039952 | c.753T>C | synonymous_variant | 1.0 |
| clpC1 | 4039955 | c.750G>C | synonymous_variant | 1.0 |
| clpC1 | 4039958 | c.747G>C | synonymous_variant | 1.0 |
| clpC1 | 4039979 | c.726C>G | synonymous_variant | 1.0 |
| clpC1 | 4039991 | c.714G>T | synonymous_variant | 1.0 |
| clpC1 | 4040000 | p.His235Asn | missense_variant | 1.0 |
| clpC1 | 4040003 | c.702G>C | synonymous_variant | 1.0 |
| clpC1 | 4040021 | c.684A>T | synonymous_variant | 1.0 |
| clpC1 | 4040024 | c.681A>G | synonymous_variant | 1.0 |
| clpC1 | 4040027 | c.678C>G | synonymous_variant | 1.0 |
| clpC1 | 4040030 | c.675C>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 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 1.0 |
| clpC1 | 4040117 | c.588A>G | synonymous_variant | 1.0 |
| clpC1 | 4040120 | c.585G>A | synonymous_variant | 1.0 |
| clpC1 | 4040124 | p.Glu194Ser | missense_variant | 1.0 |
| clpC1 | 4040135 | c.570C>G | synonymous_variant | 1.0 |
| clpC1 | 4040267 | c.438A>G | synonymous_variant | 1.0 |
| clpC1 | 4040273 | c.432T>G | 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 | 4040303 | c.402G>T | synonymous_variant | 1.0 |
| clpC1 | 4040310 | p.Thr132Asn | missense_variant | 1.0 |
| clpC1 | 4040315 | p.Glu130Asp | missense_variant | 1.0 |
| clpC1 | 4040321 | c.384C>T | synonymous_variant | 1.0 |
| clpC1 | 4040330 | c.375C>G | synonymous_variant | 1.0 |
| clpC1 | 4040342 | c.363C>G | synonymous_variant | 1.0 |
| clpC1 | 4040345 | c.360C>G | synonymous_variant | 1.0 |
| clpC1 | 4040348 | c.357G>T | synonymous_variant | 1.0 |
| clpC1 | 4040354 | c.351A>G | synonymous_variant | 1.0 |
| clpC1 | 4040357 | c.348T>C | synonymous_variant | 1.0 |
| clpC1 | 4040363 | c.342A>T | synonymous_variant | 1.0 |
| clpC1 | 4040375 | c.330G>C | synonymous_variant | 1.0 |
| clpC1 | 4040380 | c.325T>C | synonymous_variant | 1.0 |
| clpC1 | 4040381 | c.324T>C | synonymous_variant | 1.0 |
| clpC1 | 4040393 | c.312G>C | synonymous_variant | 1.0 |
| clpC1 | 4040411 | c.294T>C | synonymous_variant | 1.0 |
| clpC1 | 4040423 | c.282A>G | 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 | 4040447 | c.258G>A | synonymous_variant | 1.0 |
| clpC1 | 4040450 | c.255A>G | synonymous_variant | 1.0 |
| clpC1 | 4040456 | c.249C>G | synonymous_variant | 1.0 |
| clpC1 | 4040459 | c.246C>G | synonymous_variant | 1.0 |
| clpC1 | 4040465 | c.240T>C | synonymous_variant | 1.0 |
| clpC1 | 4040474 | c.231C>T | synonymous_variant | 1.0 |
| clpC1 | 4040477 | c.228G>T | synonymous_variant | 1.0 |
| clpC1 | 4040480 | c.225T>C | synonymous_variant | 1.0 |
| clpC1 | 4040483 | c.222G>C | synonymous_variant | 1.0 |
| clpC1 | 4040522 | c.183T>C | synonymous_variant | 1.0 |
| clpC1 | 4040525 | c.180C>T | synonymous_variant | 1.0 |
| clpC1 | 4040531 | c.174T>C | synonymous_variant | 1.0 |
| clpC1 | 4040546 | c.159G>T | synonymous_variant | 1.0 |
| clpC1 | 4040549 | c.154_156delTTGinsCTC | synonymous_variant | 1.0 |
| clpC1 | 4040561 | c.144A>C | synonymous_variant | 1.0 |
| clpC1 | 4040570 | c.135C>G | synonymous_variant | 1.0 |
| clpC1 | 4040573 | c.132T>C | synonymous_variant | 1.0 |
| clpC1 | 4040576 | c.129C>A | 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 | 4040597 | c.108C>G | synonymous_variant | 1.0 |
| clpC1 | 4040600 | c.105A>G | synonymous_variant | 1.0 |
| clpC1 | 4040603 | c.102T>G | synonymous_variant | 1.0 |
| clpC1 | 4040606 | c.99T>C | synonymous_variant | 1.0 |
| clpC1 | 4040644 | c.61A>C | synonymous_variant | 1.0 |
| clpC1 | 4040657 | c.48T>C | synonymous_variant | 1.0 |
