Run ID: SRR6046259
Sample name:
Date: 04-04-2023 12:13:55
Number of reads: 57708
Percentage reads mapped: 7.5
Strain: lineage4.9
Drug-resistance: Sensitive
| 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 | 1.0 |
| Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
|---|
| Gene | Chromosome position | Mutation | Type | Estimated fraction |
|---|---|---|---|---|
| gyrB | 6160 | c.921C>G | synonymous_variant | 1.0 |
| gyrB | 6196 | c.957C>T | synonymous_variant | 1.0 |
| gyrB | 6200 | c.962_963insTG | frameshift_variant | 1.0 |
| gyrB | 6205 | c.967_969delGCG | conservative_inframe_deletion | 1.0 |
| gyrB | 6215 | p.Ser326Thr | missense_variant | 1.0 |
| gyrB | 6223 | c.984G>C | synonymous_variant | 1.0 |
| gyrB | 6238 | c.999G>A | synonymous_variant | 1.0 |
| gyrB | 6242 | p.Arg335Lys | missense_variant | 1.0 |
| gyrB | 6248 | p.Leu337Met | missense_variant | 1.0 |
| gyrB | 6253 | c.1014G>T | synonymous_variant | 1.0 |
| gyrB | 6259 | p.Asp340Glu | missense_variant | 1.0 |
| gyrB | 6266 | p.Pro343Thr | missense_variant | 1.0 |
| gyrB | 6286 | c.1047T>C | synonymous_variant | 1.0 |
| gyrB | 6292 | c.1053G>T | synonymous_variant | 1.0 |
| gyrB | 6295 | c.1056A>G | synonymous_variant | 1.0 |
| gyrA | 6307 | c.-995T>G | upstream_gene_variant | 1.0 |
| gyrA | 6310 | c.-992G>C | upstream_gene_variant | 1.0 |
| gyrA | 6316 | c.-986G>C | upstream_gene_variant | 1.0 |
| gyrA | 6550 | c.-752A>T | upstream_gene_variant | 1.0 |
| gyrA | 6551 | c.-751T>C | upstream_gene_variant | 1.0 |
| gyrA | 6565 | c.-737G>C | upstream_gene_variant | 1.0 |
| gyrA | 6571 | c.-731T>C | upstream_gene_variant | 1.0 |
| gyrA | 6583 | c.-719G>C | upstream_gene_variant | 1.0 |
| gyrA | 6586 | c.-716T>C | upstream_gene_variant | 1.0 |
| gyrA | 6598 | c.-704C>G | upstream_gene_variant | 1.0 |
| gyrA | 6610 | c.-692C>G | upstream_gene_variant | 1.0 |
| gyrA | 6613 | c.-689A>G | upstream_gene_variant | 1.0 |
| gyrA | 6622 | c.-680C>T | upstream_gene_variant | 1.0 |
| gyrA | 6628 | c.-674C>G | upstream_gene_variant | 0.88 |
| gyrA | 6634 | c.-668T>C | upstream_gene_variant | 1.0 |
| gyrA | 6637 | c.-665T>G | upstream_gene_variant | 1.0 |
| gyrA | 6640 | c.-662A>G | upstream_gene_variant | 0.75 |
| gyrA | 6643 | c.-659A>G | upstream_gene_variant | 1.0 |
| gyrA | 6652 | c.-650C>G | upstream_gene_variant | 0.44 |
| 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 | 6700 | c.-602T>C | upstream_gene_variant | 1.0 |
| gyrA | 6703 | c.-599G>C | upstream_gene_variant | 1.0 |
| gyrA | 6706 | c.-596G>A | upstream_gene_variant | 0.88 |
| gyrA | 6709 | c.-593A>G | upstream_gene_variant | 1.0 |
| gyrA | 6712 | c.-590G>C | upstream_gene_variant | 1.0 |
| gyrA | 6727 | c.-575G>T | upstream_gene_variant | 0.88 |
| gyrA | 6730 | c.-572A>G | upstream_gene_variant | 1.0 |
| gyrA | 6739 | c.-563C>G | upstream_gene_variant | 0.83 |
| gyrA | 6745 | c.-557T>C | upstream_gene_variant | 1.0 |
| gyrA | 6751 | c.-551G>C | upstream_gene_variant | 1.0 |
| gyrA | 6760 | c.-542G>C | upstream_gene_variant | 1.0 |
| gyrA | 6763 | c.-539G>T | upstream_gene_variant | 1.0 |
| gyrA | 6775 | c.-527G>T | upstream_gene_variant | 1.0 |
| gyrB | 6794 | p.Ile519Leu | missense_variant | 1.0 |
| gyrB | 6798 | p.Gly520Ala | missense_variant | 1.0 |
| gyrA | 6808 | c.-494C>G | upstream_gene_variant | 1.0 |
| gyrA | 6811 | c.-491C>T | upstream_gene_variant | 1.0 |
| gyrA | 6824 | c.-478C>T | upstream_gene_variant | 1.0 |
| gyrA | 6841 | c.-461T>C | upstream_gene_variant | 1.0 |
| gyrA | 6844 | c.-458T>C | upstream_gene_variant | 1.0 |
| gyrA | 6853 | c.-449A>G | upstream_gene_variant | 1.0 |
| gyrA | 6856 | c.-446T>C | upstream_gene_variant | 1.0 |
| gyrA | 6859 | c.-443T>C | upstream_gene_variant | 1.0 |
| gyrA | 6869 | c.-433T>C | upstream_gene_variant | 1.0 |
| gyrA | 6872 | c.-430T>C | upstream_gene_variant | 1.0 |
| gyrA | 6877 | c.-425G>A | 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 | 6889 | c.-413G>C | upstream_gene_variant | 1.0 |
| gyrA | 6916 | c.-386G>C | upstream_gene_variant | 1.0 |
| gyrA | 6919 | c.-383T>C | upstream_gene_variant | 1.0 |
| gyrB | 6924 | p.Phe562Tyr | missense_variant | 1.0 |
| gyrA | 6926 | c.-376T>C | upstream_gene_variant | 1.0 |
| gyrA | 6931 | c.-371A>C | upstream_gene_variant | 1.0 |
| gyrA | 6934 | c.-368A>G | upstream_gene_variant | 1.0 |
| gyrA | 7150 | c.-152G>C | upstream_gene_variant | 0.67 |
| gyrA | 7168 | c.-134C>G | upstream_gene_variant | 0.75 |
| gyrA | 7171 | c.-131C>T | upstream_gene_variant | 0.75 |
| gyrA | 7178 | c.-124T>C | upstream_gene_variant | 1.0 |
| gyrA | 7198 | c.-104C>T | upstream_gene_variant | 0.67 |
| gyrB | 7210 | p.Asp657Glu | missense_variant | 1.0 |
| gyrA | 7213 | c.-89G>C | upstream_gene_variant | 1.0 |
| gyrA | 7216 | c.-86G>C | upstream_gene_variant | 1.0 |
| gyrA | 7225 | c.-77T>C | upstream_gene_variant | 1.0 |
| gyrA | 7553 | c.252C>T | synonymous_variant | 1.0 |
| gyrA | 7569 | p.Ala90Thr | missense_variant | 1.0 |
| gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
| gyrA | 7592 | c.291G>C | synonymous_variant | 1.0 |
| gyrA | 7595 | c.294C>G | synonymous_variant | 0.75 |
| gyrA | 7607 | c.306C>G | synonymous_variant | 1.0 |
| gyrA | 7625 | c.324G>C | synonymous_variant | 1.0 |
| gyrA | 7631 | c.330G>C | synonymous_variant | 1.0 |
| gyrA | 7637 | c.336C>G | synonymous_variant | 0.67 |
| gyrA | 7658 | c.357A>G | synonymous_variant | 1.0 |
| gyrA | 7661 | c.360C>T | synonymous_variant | 0.67 |
| gyrA | 7664 | c.363T>C | synonymous_variant | 1.0 |
| gyrA | 7667 | c.366C>T | synonymous_variant | 1.0 |
| gyrA | 7670 | c.369A>T | synonymous_variant | 1.0 |
| gyrA | 7676 | c.375G>C | synonymous_variant | 1.0 |
| gyrA | 7688 | c.387C>T | 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 | 7793 | c.492G>C | synonymous_variant | 1.0 |
| gyrA | 7799 | c.498A>G | synonymous_variant | 1.0 |
| gyrA | 7814 | c.513C>G | synonymous_variant | 1.0 |
| gyrA | 7821 | c.520C>T | synonymous_variant | 1.0 |
| gyrA | 7829 | c.528C>T | synonymous_variant | 1.0 |
| gyrA | 7832 | c.531G>T | synonymous_variant | 1.0 |
| gyrA | 7835 | c.534A>C | synonymous_variant | 1.0 |
| gyrA | 7847 | c.546G>C | synonymous_variant | 1.0 |
| gyrA | 7853 | c.552C>G | synonymous_variant | 1.0 |
| gyrA | 7859 | c.558A>C | synonymous_variant | 1.0 |
| gyrA | 7865 | c.564T>C | synonymous_variant | 1.0 |
| gyrA | 7868 | p.Ile189Met | missense_variant | 1.0 |
| gyrA | 7880 | c.579C>T | synonymous_variant | 1.0 |
| gyrA | 7886 | c.585T>C | synonymous_variant | 1.0 |
| gyrA | 8792 | c.1491G>C | synonymous_variant | 1.0 |
| gyrA | 8799 | p.Ala500Pro | missense_variant | 1.0 |
| gyrA | 8810 | c.1509A>C | synonymous_variant | 1.0 |
| gyrA | 8816 | c.1515C>G | synonymous_variant | 1.0 |
| gyrA | 8817 | p.Ser506Ala | missense_variant | 1.0 |
| gyrA | 8829 | c.1528T>C | synonymous_variant | 1.0 |
| gyrA | 8843 | c.1542G>A | synonymous_variant | 1.0 |
| gyrA | 8846 | p.Asp515Glu | missense_variant | 1.0 |
| gyrA | 8849 | c.1548C>G | synonymous_variant | 1.0 |
| gyrA | 8852 | c.1551T>C | synonymous_variant | 1.0 |
| gyrA | 8855 | c.1554C>G | synonymous_variant | 1.0 |
| gyrA | 8858 | c.1557T>G | synonymous_variant | 1.0 |
| gyrA | 8870 | c.1569G>C | synonymous_variant | 1.0 |
| gyrA | 8873 | c.1572A>C | synonymous_variant | 1.0 |
| gyrA | 8885 | c.1584C>A | synonymous_variant | 1.0 |
| gyrA | 8888 | c.1587C>G | synonymous_variant | 1.0 |
| gyrA | 8892 | p.Thr531Ser | missense_variant | 1.0 |
| gyrA | 8915 | c.1614A>G | synonymous_variant | 1.0 |
| gyrA | 8918 | c.1617C>T | synonymous_variant | 1.0 |
| gyrA | 8921 | c.1620C>T | synonymous_variant | 1.0 |
| gyrA | 8930 | c.1629C>G | synonymous_variant | 1.0 |
| gyrA | 8942 | c.1641G>C | synonymous_variant | 1.0 |
| gyrA | 8945 | c.1644G>C | synonymous_variant | 1.0 |
| gyrA | 8946 | c.1645_1647delTTGinsCTC | synonymous_variant | 1.0 |
| gyrA | 8951 | c.1650G>A | synonymous_variant | 1.0 |
| gyrA | 8967 | p.Ala556Arg | missense_variant | 1.0 |
| gyrA | 8981 | c.1680G>C | synonymous_variant | 1.0 |
| gyrA | 8982 | p.Cys561Ser | missense_variant | 1.0 |
| gyrA | 8993 | c.1692C>T | synonymous_variant | 1.0 |
| gyrA | 8996 | c.1695T>C | synonymous_variant | 1.0 |
| gyrA | 8998 | p.Leu566Trp | missense_variant | 1.0 |
| gyrA | 9023 | c.1722A>C | synonymous_variant | 1.0 |
| gyrA | 9029 | c.1728T>C | synonymous_variant | 1.0 |
| gyrA | 9032 | c.1731T>C | synonymous_variant | 1.0 |
| gyrA | 9035 | c.1734G>C | synonymous_variant | 1.0 |
| gyrA | 9044 | c.1743C>G | synonymous_variant | 1.0 |
| gyrA | 9050 | p.Asp583Glu | missense_variant | 1.0 |
| gyrA | 9051 | c.1750T>C | synonymous_variant | 1.0 |
| gyrA | 9056 | c.1755C>G | synonymous_variant | 1.0 |
| gyrA | 9062 | c.1761C>G | synonymous_variant | 1.0 |
| gyrA | 9065 | c.1764C>G | synonymous_variant | 1.0 |
| gyrA | 9071 | c.1770G>C | synonymous_variant | 1.0 |
| gyrA | 9080 | c.1779G>C | synonymous_variant | 1.0 |
| gyrA | 9089 | c.1788G>C | synonymous_variant | 1.0 |
| gyrA | 9092 | c.1791C>G | synonymous_variant | 1.0 |
| gyrA | 9099 | c.1798_1800delTTAinsCTG | synonymous_variant | 1.0 |
| gyrA | 9119 | c.1818A>G | synonymous_variant | 1.0 |
| gyrA | 9128 | c.1827C>G | synonymous_variant | 1.0 |
| gyrA | 9267 | p.Asn656Gly | missense_variant | 1.0 |
| gyrA | 9278 | c.1977G>C | synonymous_variant | 1.0 |
| gyrA | 9284 | c.1983T>C | synonymous_variant | 1.0 |
| gyrA | 9296 | c.1995T>C | synonymous_variant | 1.0 |
| gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
| gyrA | 9308 | p.Asp669Glu | missense_variant | 1.0 |
| gyrA | 9320 | c.2019G>C | synonymous_variant | 1.0 |
| gyrA | 9335 | c.2034G>C | synonymous_variant | 1.0 |
| gyrA | 9341 | c.2040C>G | synonymous_variant | 1.0 |
| gyrA | 9353 | c.2052G>C | synonymous_variant | 1.0 |
| gyrA | 9356 | c.2055G>C | synonymous_variant | 1.0 |
| gyrA | 9368 | c.2067G>A | synonymous_variant | 1.0 |
| gyrA | 9377 | c.2076A>G | synonymous_variant | 1.0 |
| gyrA | 9383 | c.2082T>C | synonymous_variant | 1.0 |
| gyrA | 9386 | c.2085T>G | synonymous_variant | 1.0 |
| gyrA | 9395 | c.2094G>C | synonymous_variant | 1.0 |
| gyrA | 9401 | c.2100G>A | synonymous_variant | 1.0 |
| fgd1 | 491491 | p.Pro237Thr | missense_variant | 0.75 |
| fgd1 | 491496 | c.714C>T | synonymous_variant | 0.75 |
| fgd1 | 491508 | c.726A>G | synonymous_variant | 1.0 |
| fgd1 | 491509 | c.727T>C | synonymous_variant | 1.0 |
| fgd1 | 491512 | p.Asn244Glu | missense_variant | 1.0 |
| fgd1 | 491523 | c.741G>C | synonymous_variant | 0.75 |
| fgd1 | 491526 | c.744T>C | synonymous_variant | 1.0 |
| fgd1 | 491542 | c.760T>C | synonymous_variant | 1.0 |
| fgd1 | 491547 | c.765A>C | synonymous_variant | 1.0 |
| fgd1 | 491550 | c.768T>C | synonymous_variant | 1.0 |
| fgd1 | 491560 | p.His260Thr | missense_variant | 0.8 |
| fgd1 | 491564 | p.Ser261Asn | missense_variant | 0.8 |
| fgd1 | 491569 | p.Asp263His | missense_variant | 0.8 |
| fgd1 | 491578 | p.Ile266Leu | missense_variant | 0.8 |
| fgd1 | 491601 | c.819T>C | synonymous_variant | 1.0 |
| fgd1 | 491603 | p.Ala274Glu | missense_variant | 0.8 |
| fgd1 | 491610 | c.828A>C | synonymous_variant | 1.0 |
| fgd1 | 491616 | c.834A>G | synonymous_variant | 1.0 |
| fgd1 | 491620 | p.Ile280Val | missense_variant | 1.0 |
| mshA | 575689 | c.342G>C | synonymous_variant | 1.0 |
| mshA | 575692 | c.345G>C | synonymous_variant | 1.0 |
| mshA | 575695 | c.348C>G | synonymous_variant | 1.0 |
| mshA | 575704 | c.357T>G | synonymous_variant | 1.0 |
| mshA | 575705 | c.358_360delTTGinsCTC | synonymous_variant | 1.0 |
| mshA | 575713 | c.366G>A | synonymous_variant | 1.0 |
| mshA | 575734 | c.387T>G | synonymous_variant | 1.0 |
| mshA | 575737 | c.390T>C | synonymous_variant | 1.0 |
| mshA | 575740 | c.393G>C | synonymous_variant | 1.0 |
| mshA | 575744 | p.Ala133Thr | missense_variant | 1.0 |
| mshA | 575749 | c.402C>G | synonymous_variant | 1.0 |
| mshA | 575752 | c.405G>C | synonymous_variant | 1.0 |
| mshA | 575755 | c.408G>A | synonymous_variant | 1.0 |
| mshA | 575761 | c.414C>G | synonymous_variant | 1.0 |
| mshA | 575770 | c.423G>C | synonymous_variant | 1.0 |
| mshA | 575771 | p.Val142Asn | missense_variant | 1.0 |
| mshA | 575782 | c.435G>C | synonymous_variant | 1.0 |
| mshA | 575809 | c.462C>T | synonymous_variant | 1.0 |
| mshA | 575816 | c.469C>T | synonymous_variant | 1.0 |
| mshA | 575821 | c.474G>C | synonymous_variant | 1.0 |
| mshA | 575851 | c.504C>G | synonymous_variant | 1.0 |
| mshA | 575857 | c.510G>C | synonymous_variant | 1.0 |
| mshA | 575864 | c.517T>C | synonymous_variant | 1.0 |
| mshA | 575878 | c.531A>C | synonymous_variant | 1.0 |
| ccsA | 620598 | c.708C>G | synonymous_variant | 1.0 |
| ccsA | 620607 | c.717T>C | synonymous_variant | 1.0 |
| ccsA | 620619 | c.729G>C | synonymous_variant | 1.0 |
| ccsA | 620625 | c.735A>C | synonymous_variant | 1.0 |
| ccsA | 620631 | c.741T>C | synonymous_variant | 1.0 |
| ccsA | 620649 | c.759A>G | synonymous_variant | 1.0 |
| ccsA | 620652 | c.762C>G | synonymous_variant | 1.0 |
| ccsA | 620661 | c.771C>G | synonymous_variant | 1.0 |
| rpoB | 760181 | c.375T>C | synonymous_variant | 1.0 |
| rpoB | 760184 | c.378A>G | synonymous_variant | 1.0 |
| rpoB | 760196 | c.390C>G | synonymous_variant | 1.0 |
| rpoB | 760223 | c.417T>C | 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 | 0.83 |
| rpoB | 760274 | c.468G>A | synonymous_variant | 0.8 |
| rpoB | 760283 | c.477G>C | synonymous_variant | 1.0 |
| rpoB | 760298 | c.492G>C | synonymous_variant | 1.0 |
| rpoB | 760310 | c.504G>C | synonymous_variant | 1.0 |
| rpoB | 760316 | c.510C>G | synonymous_variant | 1.0 |
| rpoB | 760317 | c.511_512delAGinsTC | synonymous_variant | 0.67 |
| 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>C | synonymous_variant | 1.0 |
| rpoB | 760353 | p.Glu183Ser | missense_variant | 0.71 |
| rpoB | 760358 | c.552C>G | synonymous_variant | 0.71 |
| rpoB | 760361 | c.555T>C | synonymous_variant | 1.0 |
| rpoB | 760376 | p.Asp190Glu | missense_variant | 1.0 |
| rpoB | 760406 | c.600G>C | synonymous_variant | 1.0 |
| rpoB | 760407 | p.Ser201Gly | missense_variant | 1.0 |
| rpoB | 760415 | c.609C>T | synonymous_variant | 1.0 |
| rpoB | 760424 | c.618C>G | synonymous_variant | 1.0 |
| rpoB | 760430 | c.624T>C | synonymous_variant | 1.0 |
| rpoB | 760460 | c.654G>C | synonymous_variant | 1.0 |
| rpoB | 760475 | c.669A>G | synonymous_variant | 1.0 |
| rpoB | 760478 | c.672C>T | synonymous_variant | 0.9 |
| rpoB | 760481 | c.675G>C | synonymous_variant | 1.0 |
| rpoB | 760484 | c.678A>G | synonymous_variant | 1.0 |
| rpoB | 760487 | c.681G>C | synonymous_variant | 1.0 |
| rpoB | 760493 | c.687C>G | synonymous_variant | 1.0 |
| rpoB | 760502 | c.696C>G | synonymous_variant | 1.0 |
| rpoB | 760511 | c.705G>C | synonymous_variant | 1.0 |
| rpoB | 760522 | p.Ser239Asn | missense_variant | 1.0 |
| rpoB | 760532 | c.726T>C | synonymous_variant | 1.0 |
| rpoB | 760533 | p.Val243Thr | missense_variant | 1.0 |
| rpoB | 760541 | c.735G>C | synonymous_variant | 1.0 |
| rpoB | 760547 | c.741G>C | synonymous_variant | 1.0 |
| rpoB | 760563 | p.Arg253Met | missense_variant | 1.0 |
| rpoB | 760591 | p.Val262Ala | missense_variant | 1.0 |
| rpoB | 760596 | p.Thr264Pro | missense_variant | 1.0 |
| rpoB | 760611 | c.805T>C | synonymous_variant | 1.0 |
| rpoB | 760616 | c.810C>T | synonymous_variant | 1.0 |
| rpoB | 760634 | c.828T>C | synonymous_variant | 1.0 |
| rpoB | 760643 | c.837G>A | synonymous_variant | 1.0 |
| rpoB | 760646 | c.840C>G | synonymous_variant | 1.0 |
| rpoB | 760649 | c.843G>C | synonymous_variant | 1.0 |
| rpoB | 760655 | c.849A>G | synonymous_variant | 1.0 |
| rpoB | 760661 | c.855A>C | synonymous_variant | 1.0 |
| rpoB | 760670 | c.864G>C | synonymous_variant | 1.0 |
| rpoB | 760674 | c.868T>C | synonymous_variant | 1.0 |
| rpoB | 760679 | c.873A>G | synonymous_variant | 1.0 |
| rpoB | 760683 | c.877T>C | synonymous_variant | 1.0 |
| rpoB | 760721 | c.915C>G | synonymous_variant | 1.0 |
| rpoB | 760730 | c.924T>C | synonymous_variant | 1.0 |
| rpoB | 760751 | c.945G>C | synonymous_variant | 1.0 |
| rpoB | 760755 | p.His317Asn | missense_variant | 1.0 |
| rpoB | 760760 | c.954C>G | synonymous_variant | 1.0 |
| rpoB | 760764 | p.Glu320Lys | missense_variant | 1.0 |
| rpoB | 760769 | c.963C>G | synonymous_variant | 1.0 |
| rpoB | 760776 | c.970_972delTCGinsAGC | synonymous_variant | 1.0 |
| rpoB | 760796 | c.990A>G | synonymous_variant | 1.0 |
| rpoB | 760800 | p.Val332Ile | missense_variant | 1.0 |
| rpoB | 760805 | c.999G>C | synonymous_variant | 1.0 |
| rpoB | 760808 | c.1002C>G | synonymous_variant | 1.0 |
| rpoB | 760916 | c.1110C>T | synonymous_variant | 1.0 |
| rpoB | 760919 | c.1113C>T | synonymous_variant | 1.0 |
| rpoB | 760928 | c.1122G>C | synonymous_variant | 1.0 |
| rpoB | 760946 | c.1140A>G | synonymous_variant | 1.0 |
| rpoB | 760965 | p.Met387Leu | missense_variant | 1.0 |
| rpoB | 760970 | c.1164G>C | synonymous_variant | 1.0 |
| rpoB | 760973 | c.1167G>T | synonymous_variant | 1.0 |
| rpoB | 760982 | c.1176G>T | synonymous_variant | 1.0 |
| rpoB | 760985 | c.1179G>C | synonymous_variant | 1.0 |
| rpoB | 760991 | c.1185G>C | synonymous_variant | 1.0 |
| rpoB | 761006 | c.1200C>G | synonymous_variant | 1.0 |
| rpoB | 761015 | c.1209G>C | synonymous_variant | 1.0 |
| rpoB | 761027 | c.1221A>G | synonymous_variant | 1.0 |
| rpoB | 761036 | c.1230G>C | synonymous_variant | 1.0 |
| rpoB | 761037 | c.1231T>C | synonymous_variant | 1.0 |
| rpoB | 761051 | c.1245G>T | synonymous_variant | 1.0 |
| rpoB | 761054 | c.1248G>C | synonymous_variant | 1.0 |
| rpoB | 761057 | c.1251G>C | synonymous_variant | 1.0 |
| rpoB | 761060 | c.1254C>G | synonymous_variant | 1.0 |
| rpoB | 761063 | c.1257C>G | synonymous_variant | 1.0 |
| rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 1.0 |
| rpoB | 761102 | c.1296A>G | synonymous_variant | 1.0 |
| rpoB | 761132 | c.1326G>T | synonymous_variant | 1.0 |
| rpoB | 761133 | c.1327T>C | synonymous_variant | 1.0 |
| rpoB | 761150 | c.1344A>C | synonymous_variant | 1.0 |
| rpoB | 761159 | c.1353G>A | synonymous_variant | 0.71 |
| rpoB | 761165 | c.1359G>C | 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 | 761183 | c.1377T>C | synonymous_variant | 1.0 |
| rpoB | 761273 | c.1467T>C | synonymous_variant | 1.0 |
| rpoB | 761282 | c.1476C>T | synonymous_variant | 1.0 |
| rpoB | 761318 | c.1512G>C | synonymous_variant | 1.0 |
| rpoB | 761345 | c.1539G>C | synonymous_variant | 1.0 |
| rpoB | 761354 | c.1548C>T | synonymous_variant | 1.0 |
| rpoB | 761360 | c.1554T>C | synonymous_variant | 1.0 |
| rpoB | 761362 | p.Ser519Thr | missense_variant | 1.0 |
| rpoB | 761366 | c.1560C>T | synonymous_variant | 1.0 |
| rpoB | 761373 | p.Val523His | missense_variant | 1.0 |
| rpoB | 761381 | c.1575G>C | synonymous_variant | 0.67 |
| rpoB | 761393 | c.1587G>A | synonymous_variant | 0.67 |
| rpoB | 761408 | c.1602G>C | synonymous_variant | 1.0 |
| rpoB | 761561 | c.1755C>G | synonymous_variant | 1.0 |
| rpoB | 761564 | c.1758G>C | synonymous_variant | 0.67 |
| rpoB | 761570 | c.1764T>C | synonymous_variant | 1.0 |
| rpoB | 761573 | c.1767C>G | synonymous_variant | 1.0 |
| rpoB | 761579 | c.1773G>C | synonymous_variant | 1.0 |
| rpoB | 761606 | c.1800C>G | synonymous_variant | 1.0 |
| rpoB | 761612 | c.1806G>T | synonymous_variant | 1.0 |
| rpoB | 761615 | c.1809A>C | synonymous_variant | 1.0 |
| rpoB | 761636 | c.1830G>T | synonymous_variant | 1.0 |
| rpoB | 761645 | c.1839C>G | synonymous_variant | 1.0 |
| rpoB | 761648 | c.1842T>C | synonymous_variant | 0.5 |
| rpoB | 761657 | c.1851C>A | synonymous_variant | 1.0 |
| rpoB | 761660 | c.1854G>T | synonymous_variant | 0.5 |
| rpoB | 761663 | c.1857G>C | synonymous_variant | 0.67 |
| rpoB | 761666 | c.1860G>C | synonymous_variant | 0.67 |
| rpoB | 761675 | c.1869G>T | synonymous_variant | 1.0 |
| rpoB | 761687 | c.1881C>T | synonymous_variant | 1.0 |
| rpoB | 761690 | c.1884G>C | synonymous_variant | 1.0 |
| rpoB | 761693 | c.1887G>C | synonymous_variant | 1.0 |
| rpoB | 761699 | c.1893C>T | synonymous_variant | 1.0 |
| rpoB | 761705 | c.1899C>T | synonymous_variant | 1.0 |
| rpoB | 761711 | c.1905C>G | synonymous_variant | 1.0 |
| rpoB | 761714 | c.1908C>T | synonymous_variant | 1.0 |
| rpoB | 761930 | c.2124G>C | synonymous_variant | 1.0 |
| rpoB | 761936 | c.2130C>T | synonymous_variant | 1.0 |
| rpoB | 761948 | c.2142G>C | synonymous_variant | 1.0 |
| rpoB | 761954 | c.2148C>G | synonymous_variant | 1.0 |
| rpoB | 761969 | c.2163G>A | synonymous_variant | 1.0 |
| rpoB | 762002 | c.2196C>G | synonymous_variant | 0.86 |
| rpoB | 762003 | p.Asn733Gln | missense_variant | 0.86 |
| rpoB | 762014 | c.2208C>T | synonymous_variant | 1.0 |
| rpoB | 762017 | c.2211A>G | synonymous_variant | 1.0 |
| rpoB | 762026 | c.2220G>C | synonymous_variant | 1.0 |
| rpoB | 762029 | c.2223C>G | synonymous_variant | 1.0 |
| rpoB | 762032 | c.2226C>G | synonymous_variant | 1.0 |
| rpoB | 762035 | c.2229G>C | synonymous_variant | 1.0 |
| rpoB | 762053 | c.2247T>C | synonymous_variant | 1.0 |
| rpoB | 762065 | c.2259T>C | synonymous_variant | 1.0 |
| rpoB | 762078 | c.2272C>T | synonymous_variant | 1.0 |
| rpoB | 762083 | c.2277T>C | synonymous_variant | 1.0 |
| rpoB | 762086 | c.2280G>C | synonymous_variant | 1.0 |
| rpoB | 762101 | c.2295C>G | synonymous_variant | 1.0 |
| rpoB | 762114 | p.Ile770Val | missense_variant | 1.0 |
| rpoB | 762122 | c.2316C>T | synonymous_variant | 1.0 |
| rpoB | 762131 | c.2325C>G | synonymous_variant | 1.0 |
| rpoB | 762137 | c.2331C>T | synonymous_variant | 1.0 |
| rpoB | 762140 | c.2334G>C | synonymous_variant | 1.0 |
| rpoB | 762143 | c.2337T>C | synonymous_variant | 1.0 |
| rpoB | 762149 | c.2343G>C | synonymous_variant | 1.0 |
| rpoB | 762156 | p.Val784Ile | missense_variant | 1.0 |
| rpoB | 762167 | c.2361T>C | synonymous_variant | 1.0 |
| rpoB | 762176 | c.2370T>C | synonymous_variant | 1.0 |
| rpoB | 762185 | c.2379G>C | synonymous_variant | 1.0 |
| rpoB | 762194 | c.2388G>C | synonymous_variant | 1.0 |
| rpoB | 762218 | c.2412T>C | synonymous_variant | 1.0 |
| rpoB | 762233 | c.2427G>C | synonymous_variant | 1.0 |
| rpoB | 762236 | c.2430G>C | synonymous_variant | 1.0 |
| rpoB | 762245 | c.2439G>C | synonymous_variant | 1.0 |
| rpoB | 762281 | c.2475G>A | synonymous_variant | 1.0 |
| rpoB | 762284 | c.2478G>C | synonymous_variant | 1.0 |
| rpoB | 762293 | c.2487T>C | synonymous_variant | 1.0 |
| rpoB | 762317 | c.2511A>G | synonymous_variant | 1.0 |
| rpoB | 762329 | c.2523G>C | synonymous_variant | 1.0 |
| rpoB | 762338 | c.2532T>C | synonymous_variant | 1.0 |
| rpoB | 762341 | c.2535G>C | synonymous_variant | 1.0 |
| rpoB | 762347 | c.2541T>C | synonymous_variant | 1.0 |
| rpoB | 762359 | c.2553C>T | synonymous_variant | 1.0 |
| rpoB | 762362 | p.Glu852Asp | missense_variant | 1.0 |
| rpoB | 762369 | c.2563T>C | synonymous_variant | 1.0 |
| rpoC | 762395 | c.-975G>C | upstream_gene_variant | 1.0 |
| rpoC | 762398 | c.-972T>C | upstream_gene_variant | 1.0 |
| rpoC | 762401 | c.-969G>C | upstream_gene_variant | 1.0 |
| rpoC | 762404 | c.-966T>C | upstream_gene_variant | 1.0 |
| rpoC | 762410 | c.-960T>C | upstream_gene_variant | 1.0 |
| rpoC | 762416 | c.-954A>G | upstream_gene_variant | 1.0 |
| rpoC | 762434 | c.-936T>C | upstream_gene_variant | 1.0 |
| rpoC | 762443 | c.-927G>C | upstream_gene_variant | 1.0 |
| rpoC | 762449 | c.-921C>A | upstream_gene_variant | 1.0 |
| rpoC | 762452 | c.-918G>C | upstream_gene_variant | 1.0 |
| rpoC | 762470 | c.-900G>C | upstream_gene_variant | 1.0 |
| rpoB | 762489 | p.Val895Ile | missense_variant | 1.0 |
| rpoC | 762503 | c.-867G>C | upstream_gene_variant | 1.0 |
| rpoC | 762509 | c.-861T>G | upstream_gene_variant | 1.0 |
| rpoB | 762511 | p.Ala902Glu | missense_variant | 1.0 |
| rpoC | 762521 | c.-849C>G | upstream_gene_variant | 1.0 |
| rpoC | 762524 | c.-846G>C | 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 | 762537 | c.-833T>C | upstream_gene_variant | 1.0 |
| rpoC | 762545 | c.-825C>G | upstream_gene_variant | 1.0 |
| rpoC | 762551 | c.-819C>T | upstream_gene_variant | 1.0 |
| rpoB | 762795 | p.Asp997Asn | missense_variant | 1.0 |
| rpoB | 762814 | p.Met1003Asn | missense_variant | 1.0 |
| rpoC | 762818 | c.-552C>G | upstream_gene_variant | 1.0 |
| rpoC | 762827 | c.-543G>C | upstream_gene_variant | 1.0 |
| rpoC | 762833 | c.-537C>T | upstream_gene_variant | 1.0 |
| rpoC | 762836 | c.-534C>T | upstream_gene_variant | 1.0 |
| rpoC | 762839 | c.-531G>A | upstream_gene_variant | 1.0 |
| rpoC | 762857 | c.-513C>G | upstream_gene_variant | 1.0 |
| rpoC | 762863 | c.-507T>C | upstream_gene_variant | 1.0 |
| rpoB | 762879 | p.Met1025Leu | missense_variant | 1.0 |
| rpoC | 762894 | c.-476C>T | upstream_gene_variant | 1.0 |
| rpoC | 762899 | c.-471G>C | upstream_gene_variant | 1.0 |
| rpoC | 762917 | c.-453C>G | upstream_gene_variant | 1.0 |
| rpoC | 762929 | c.-441G>T | upstream_gene_variant | 1.0 |
| rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.94 |
| rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.94 |
| rpoC | 762983 | c.-387C>T | upstream_gene_variant | 1.0 |
| rpoC | 762989 | c.-381G>A | upstream_gene_variant | 0.94 |
| rpoC | 762995 | c.-375G>T | upstream_gene_variant | 1.0 |
| rpoC | 763028 | c.-342T>C | upstream_gene_variant | 1.0 |
| rpoC | 763031 | c.-339T>G | upstream_gene_variant | 1.0 |
| rpoC | 763034 | c.-336C>G | upstream_gene_variant | 1.0 |
| rpoC | 763040 | c.-330C>G | upstream_gene_variant | 1.0 |
| rpoC | 763052 | c.-318G>C | upstream_gene_variant | 1.0 |
| rpoC | 763070 | c.-300T>C | upstream_gene_variant | 1.0 |
| rpoC | 763094 | c.-276G>C | upstream_gene_variant | 1.0 |
| rpoC | 763115 | c.-255T>C | upstream_gene_variant | 1.0 |
| rpoC | 763127 | c.-243G>C | upstream_gene_variant | 1.0 |
| rpoC | 763142 | c.-228C>G | upstream_gene_variant | 1.0 |
| rpoC | 763160 | c.-210G>C | upstream_gene_variant | 1.0 |
| rpoC | 763166 | c.-204A>G | upstream_gene_variant | 1.0 |
| rpoC | 763363 | c.-7G>A | upstream_gene_variant | 1.0 |
| rpoC | 763405 | c.36C>T | synonymous_variant | 1.0 |
| rpoC | 763408 | c.39T>C | synonymous_variant | 1.0 |
| rpoC | 763411 | c.42T>C | synonymous_variant | 1.0 |
| rpoC | 763414 | c.45T>C | synonymous_variant | 1.0 |
| rpoC | 763417 | c.48C>T | synonymous_variant | 1.0 |
| rpoC | 763423 | p.Glu18Asp | missense_variant | 1.0 |
| rpoC | 763430 | c.61_63delAGGinsCGC | synonymous_variant | 1.0 |
| rpoC | 763433 | p.Gln22Asn | missense_variant | 1.0 |
| rpoC | 763443 | p.Tyr25Phe | missense_variant | 1.0 |
| rpoC | 763468 | c.99G>C | synonymous_variant | 1.0 |
| rpoC | 763486 | c.117T>C | synonymous_variant | 1.0 |
| rpoC | 763492 | c.123G>A | synonymous_variant | 1.0 |
| rpoC | 763528 | c.159G>A | synonymous_variant | 1.0 |
| rpoC | 763546 | c.177A>G | synonymous_variant | 1.0 |
| rpoC | 763570 | c.201G>C | synonymous_variant | 1.0 |
| rpoC | 763594 | c.225C>T | synonymous_variant | 0.91 |
| rpoC | 763621 | c.252C>T | synonymous_variant | 0.86 |
| rpoC | 763633 | c.264T>C | synonymous_variant | 1.0 |
| rpoC | 763651 | c.282C>T | synonymous_variant | 1.0 |
| rpoC | 763657 | c.288G>A | synonymous_variant | 1.0 |
| rpoC | 763660 | c.291T>G | synonymous_variant | 1.0 |
| rpoC | 763666 | c.297G>A | synonymous_variant | 1.0 |
| rpoC | 763675 | c.306C>G | synonymous_variant | 1.0 |
| rpoC | 763696 | c.327T>C | synonymous_variant | 1.0 |
| rpoC | 763699 | c.330G>T | synonymous_variant | 1.0 |
| rpoC | 763702 | c.333C>G | synonymous_variant | 1.0 |
| rpoC | 763705 | c.336G>C | synonymous_variant | 1.0 |
| rpoC | 763708 | c.339G>C | synonymous_variant | 1.0 |
| rpoC | 763714 | c.345G>C | synonymous_variant | 1.0 |
| rpoC | 763717 | c.348T>C | synonymous_variant | 1.0 |
| rpoC | 763732 | c.363C>G | synonymous_variant | 1.0 |
| rpoC | 763741 | c.372C>T | synonymous_variant | 1.0 |
| rpoC | 763744 | c.375G>C | synonymous_variant | 1.0 |
| rpoC | 763747 | c.378G>A | synonymous_variant | 1.0 |
| rpoC | 763765 | c.396T>C | synonymous_variant | 1.0 |
| rpoC | 763774 | c.405G>C | synonymous_variant | 1.0 |
| rpoC | 763991 | p.Ile208Leu | missense_variant | 1.0 |
| rpoC | 764002 | c.633C>T | synonymous_variant | 1.0 |
| rpoC | 764005 | c.636G>C | synonymous_variant | 1.0 |
| rpoC | 764023 | c.654G>T | 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.Ser224Thr | missense_variant | 1.0 |
| rpoC | 764044 | c.675T>G | synonymous_variant | 1.0 |
| rpoC | 764059 | c.690G>C | synonymous_variant | 1.0 |
| rpoC | 764060 | p.Pro231Val | missense_variant | 1.0 |
| rpoC | 764083 | c.714A>G | synonymous_variant | 1.0 |
| rpoC | 764098 | c.729A>G | synonymous_variant | 1.0 |
| rpoC | 764099 | p.Leu244Ile | missense_variant | 0.86 |
| rpoC | 764131 | c.762T>C | synonymous_variant | 1.0 |
| rpoC | 764134 | c.765C>G | synonymous_variant | 1.0 |
| rpoC | 764153 | p.Gln262Lys | missense_variant | 0.8 |
| rpoC | 764161 | c.792G>C | 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 | 764283 | c.916_917delGG | frameshift_variant | 1.0 |
| rpoC | 764296 | c.927G>C | synonymous_variant | 1.0 |
| rpoC | 764320 | c.951C>T | synonymous_variant | 1.0 |
| rpoC | 764353 | c.984G>C | synonymous_variant | 1.0 |
| rpoC | 764365 | c.996C>T | synonymous_variant | 1.0 |
| rpoC | 764380 | c.1011G>C | synonymous_variant | 1.0 |
| rpoC | 764387 | c.1018T>C | synonymous_variant | 1.0 |
| rpoC | 764395 | c.1026C>T | synonymous_variant | 0.75 |
| rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 1.0 |
| rpoC | 764428 | c.1059G>C | synonymous_variant | 1.0 |
| rpoC | 764431 | c.1062G>C | synonymous_variant | 1.0 |
| rpoC | 764434 | c.1065A>G | synonymous_variant | 1.0 |
| rpoC | 764435 | c.1066_1068delAGGinsCGA | synonymous_variant | 1.0 |
| rpoC | 764446 | c.1077T>C | synonymous_variant | 0.8 |
| rpoC | 764449 | c.1080G>C | synonymous_variant | 0.67 |
| rpoC | 764455 | c.1086G>C | synonymous_variant | 0.8 |
| rpoC | 764458 | c.1089G>C | synonymous_variant | 1.0 |
| rpoC | 764461 | c.1092A>G | synonymous_variant | 1.0 |
| rpoC | 764491 | c.1122G>T | synonymous_variant | 0.4 |
| rpoC | 764497 | c.1128A>G | synonymous_variant | 1.0 |
| rpoC | 764500 | c.1131C>G | synonymous_variant | 1.0 |
| rpoC | 764521 | c.1152T>C | synonymous_variant | 1.0 |
| rpoC | 764524 | c.1155C>T | synonymous_variant | 0.5 |
| rpoC | 764527 | c.1158C>T | synonymous_variant | 1.0 |
| rpoC | 764530 | c.1161C>T | synonymous_variant | 1.0 |
| rpoC | 764533 | c.1164C>A | synonymous_variant | 0.5 |
| rpoC | 764536 | c.1167G>T | synonymous_variant | 1.0 |
| rpoC | 764539 | c.1170C>G | synonymous_variant | 0.43 |
| rpoC | 764542 | c.1173C>T | synonymous_variant | 0.38 |
| rpoC | 764545 | c.1176C>G | synonymous_variant | 0.62 |
| rpoC | 764548 | c.1179G>A | synonymous_variant | 0.38 |
| rpoC | 764575 | c.1206T>G | synonymous_variant | 1.0 |
| rpoC | 764602 | c.1233C>T | synonymous_variant | 0.8 |
| rpoC | 764605 | c.1236G>C | synonymous_variant | 0.8 |
| rpoC | 764611 | c.1242G>T | synonymous_variant | 1.0 |
| rpoC | 764626 | c.1257C>T | synonymous_variant | 0.92 |
| rpoC | 764632 | c.1263T>C | synonymous_variant | 1.0 |
| rpoC | 764650 | c.1281G>T | synonymous_variant | 1.0 |
| rpoC | 764662 | c.1293G>C | synonymous_variant | 0.73 |
| rpoC | 764701 | c.1332C>G | synonymous_variant | 0.8 |
| rpoC | 764713 | c.1344G>T | synonymous_variant | 0.9 |
| rpoC | 764716 | c.1347G>C | synonymous_variant | 0.91 |
| rpoC | 764746 | c.1377G>T | synonymous_variant | 1.0 |
| rpoC | 764752 | c.1383G>C | synonymous_variant | 1.0 |
| rpoC | 764755 | c.1386C>T | synonymous_variant | 0.76 |
| rpoC | 764758 | c.1389C>G | synonymous_variant | 1.0 |
| rpoC | 764764 | c.1395T>C | synonymous_variant | 1.0 |
| rpoC | 764797 | c.1428G>C | synonymous_variant | 0.79 |
| rpoC | 764803 | c.1434C>T | synonymous_variant | 1.0 |
| rpoC | 764809 | c.1440C>T | synonymous_variant | 0.93 |
| rpoC | 764815 | c.1446A>G | synonymous_variant | 1.0 |
| rpoC | 764827 | c.1458G>C | synonymous_variant | 1.0 |
| rpoC | 764858 | c.1489T>C | synonymous_variant | 1.0 |
| rpoC | 764869 | c.1500C>T | synonymous_variant | 1.0 |
| rpoC | 764875 | c.1506C>A | synonymous_variant | 1.0 |
| rpoC | 764887 | c.1518G>C | synonymous_variant | 0.83 |
| rpoC | 764888 | c.1519_1521delTTGinsCTC | synonymous_variant | 0.83 |
| rpoC | 764911 | c.1542A>G | synonymous_variant | 1.0 |
| rpoC | 764912 | p.Met515Gln | missense_variant | 1.0 |
| rpoC | 764923 | c.1554A>G | synonymous_variant | 1.0 |
| rpoC | 764935 | c.1566T>C | synonymous_variant | 1.0 |
| rpoC | 764948 | c.1579T>C | synonymous_variant | 1.0 |
| rpoC | 764953 | c.1584G>C | synonymous_variant | 1.0 |
| rpoC | 764956 | c.1587T>C | synonymous_variant | 1.0 |
| rpoC | 764968 | c.1599T>C | synonymous_variant | 1.0 |
| rpoC | 765004 | c.1635G>T | synonymous_variant | 1.0 |
| rpoC | 765007 | c.1638T>G | synonymous_variant | 1.0 |
| rpoC | 765008 | c.1639T>C | synonymous_variant | 1.0 |
| rpoC | 765011 | c.1642_1643delAGinsTC | synonymous_variant | 1.0 |
| rpoC | 765016 | c.1647C>G | synonymous_variant | 1.0 |
| rpoC | 765019 | c.1650A>G | synonymous_variant | 1.0 |
| rpoC | 765034 | c.1665T>C | synonymous_variant | 1.0 |
| rpoC | 765040 | c.1671T>C | synonymous_variant | 1.0 |
| rpoC | 765041 | c.1672T>C | synonymous_variant | 1.0 |
| rpoC | 765047 | c.1678T>C | synonymous_variant | 1.0 |
| rpoC | 765055 | c.1686C>G | synonymous_variant | 1.0 |
| rpoC | 765070 | c.1701G>C | synonymous_variant | 1.0 |
| rpoC | 765376 | c.2007C>T | synonymous_variant | 1.0 |
| rpoC | 765379 | c.2010G>C | synonymous_variant | 1.0 |
| rpoC | 765385 | p.Met672Ile | missense_variant | 1.0 |
| rpoC | 765404 | p.Leu679Lys | missense_variant | 1.0 |
| rpoC | 765407 | p.Gly680Ser | missense_variant | 1.0 |
| rpoC | 765412 | c.2043T>C | synonymous_variant | 1.0 |
| rpoC | 765415 | c.2046G>C | synonymous_variant | 1.0 |
| rpoC | 765431 | p.Met688Gln | missense_variant | 1.0 |
| rpoC | 765445 | c.2076G>C | synonymous_variant | 1.0 |
| rpoC | 765451 | c.2082C>G | synonymous_variant | 1.0 |
| rpoC | 765454 | c.2085C>G | synonymous_variant | 1.0 |
| rpoC | 765466 | c.2097C>T | synonymous_variant | 1.0 |
| rpoC | 765469 | c.2100G>C | synonymous_variant | 1.0 |
| rpoC | 765529 | c.2160C>A | synonymous_variant | 1.0 |
| rpoC | 765533 | p.Tyr722His | missense_variant | 1.0 |
| rpoC | 765769 | p.Ile800Met | missense_variant | 1.0 |
| rpoC | 765772 | c.2403C>G | synonymous_variant | 1.0 |
| rpoC | 765778 | c.2409C>G | synonymous_variant | 1.0 |
| rpoC | 765779 | p.Asp804Lys | missense_variant | 1.0 |
| rpoC | 765790 | c.2421C>T | synonymous_variant | 1.0 |
| rpoC | 765793 | c.2424C>G | synonymous_variant | 1.0 |
| rpoC | 765800 | p.Phe811Leu | missense_variant | 1.0 |
| rpoC | 765811 | c.2442T>C | synonymous_variant | 1.0 |
| rpoC | 765814 | c.2445A>C | synonymous_variant | 1.0 |
| rpoC | 765817 | c.2448G>C | synonymous_variant | 1.0 |
| rpoC | 765826 | c.2457T>C | synonymous_variant | 1.0 |
| rpoC | 765844 | c.2475C>G | synonymous_variant | 1.0 |
| rpoC | 765856 | c.2487T>C | synonymous_variant | 1.0 |
| rpoC | 765861 | p.Phe831Tyr | missense_variant | 1.0 |
| rpoC | 765871 | c.2502T>C | synonymous_variant | 1.0 |
| rpoC | 765874 | c.2505G>C | synonymous_variant | 1.0 |
| rpoC | 765875 | p.Val836Ile | missense_variant | 1.0 |
| rpoC | 765886 | c.2517C>G | synonymous_variant | 1.0 |
| rpoC | 765892 | c.2523T>C | synonymous_variant | 1.0 |
| rpoC | 765904 | c.2535C>G | synonymous_variant | 1.0 |
| rpoC | 765934 | c.2565C>T | synonymous_variant | 1.0 |
| rpoC | 765937 | c.2568T>C | synonymous_variant | 1.0 |
| rpoC | 765940 | c.2571A>T | synonymous_variant | 1.0 |
| rpoC | 765946 | c.2577C>T | synonymous_variant | 1.0 |
| rpoC | 765947 | c.2578T>C | synonymous_variant | 1.0 |
| rpoC | 765952 | c.2583G>C | synonymous_variant | 1.0 |
| rpoC | 765962 | c.2593T>C | synonymous_variant | 1.0 |
| rpoC | 765967 | c.2598C>T | synonymous_variant | 1.0 |
| rpoC | 765973 | c.2604C>T | 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 | 766012 | c.2643C>G | synonymous_variant | 1.0 |
| rpoC | 766027 | c.2658G>T | synonymous_variant | 1.0 |
| rpoC | 766043 | p.Gln892Thr | missense_variant | 1.0 |
| rpoC | 766207 | c.2838T>C | synonymous_variant | 1.0 |
| rpoC | 766212 | p.Glu948Ala | missense_variant | 1.0 |
| rpoC | 766216 | c.2847T>C | synonymous_variant | 1.0 |
| rpoC | 766222 | c.2853T>C | synonymous_variant | 1.0 |
| rpoC | 766226 | c.2857T>C | synonymous_variant | 1.0 |
| rpoC | 766234 | c.2865T>C | synonymous_variant | 1.0 |
| rpoC | 766240 | c.2871T>C | synonymous_variant | 1.0 |
| rpoC | 766249 | c.2880C>G | synonymous_variant | 1.0 |
| rpoC | 766255 | c.2886G>C | synonymous_variant | 1.0 |
| rpoC | 766258 | c.2889T>C | synonymous_variant | 1.0 |
| rpoC | 766261 | c.2892G>C | synonymous_variant | 1.0 |
| rpoC | 766270 | c.2901G>T | synonymous_variant | 1.0 |
| rpoC | 766273 | c.2904T>C | synonymous_variant | 1.0 |
| rpoC | 766274 | p.Ala969Thr | missense_variant | 1.0 |
| rpoC | 766279 | c.2910C>G | synonymous_variant | 1.0 |
| rpoC | 766280 | p.Ser971Gly | missense_variant | 1.0 |
| rpoC | 766291 | c.2922G>C | synonymous_variant | 0.8 |
| rpoC | 766297 | c.2928G>C | synonymous_variant | 0.83 |
| rpoC | 766309 | c.2940G>C | synonymous_variant | 1.0 |
| rpoC | 766315 | c.2946C>G | synonymous_variant | 1.0 |
| rpoC | 766348 | c.2979A>G | synonymous_variant | 1.0 |
| rpoC | 766363 | c.2994G>C | synonymous_variant | 1.0 |
| rpoC | 766369 | c.3000C>G | synonymous_variant | 1.0 |
| rpoC | 766381 | c.3012C>T | synonymous_variant | 1.0 |
| rpoC | 766384 | c.3015A>G | synonymous_variant | 1.0 |
| rpoC | 766393 | c.3024C>G | synonymous_variant | 1.0 |
| rpoC | 766408 | c.3039C>T | synonymous_variant | 1.0 |
| rpoC | 766432 | c.3063T>C | synonymous_variant | 1.0 |
| rpoC | 766435 | p.Glu1022Asp | missense_variant | 1.0 |
| rpoC | 766459 | c.3090G>C | synonymous_variant | 1.0 |
| rpoC | 766462 | c.3093G>C | synonymous_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 | 766633 | c.3264G>C | synonymous_variant | 1.0 |
| rpoC | 766645 | p.Glu1092Asp | missense_variant | 1.0 |
| rpoC | 766651 | c.3282T>C | synonymous_variant | 1.0 |
| rpoC | 766652 | c.3283_3284delTCinsAG | synonymous_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 | 766667 | p.Ser1100Thr | missense_variant | 1.0 |
| rpoC | 766672 | c.3303T>C | synonymous_variant | 1.0 |
| rpoC | 766678 | c.3309C>T | synonymous_variant | 1.0 |
| rpoC | 766686 | p.Glu1106Val | missense_variant | 1.0 |
| rpoC | 766693 | c.3324C>G | synonymous_variant | 1.0 |
| rpoC | 766714 | c.3345G>C | synonymous_variant | 0.8 |
| rpoC | 766726 | c.3357T>C | synonymous_variant | 1.0 |
| rpoC | 766733 | c.3364C>T | synonymous_variant | 0.67 |
| rpoC | 766738 | c.3369G>C | synonymous_variant | 1.0 |
| rpoC | 766741 | c.3372G>C | synonymous_variant | 1.0 |
| rpoC | 766742 | p.Gln1125Met | missense_variant | 1.0 |
| rpoC | 766750 | c.3381C>G | synonymous_variant | 1.0 |
| rpoC | 766763 | p.Ile1132Val | missense_variant | 0.67 |
| rpoC | 766771 | c.3402G>C | synonymous_variant | 1.0 |
| rpoC | 766774 | c.3405T>C | synonymous_variant | 1.0 |
| rpoC | 766775 | p.Arg1136Asn | missense_variant | 1.0 |
| rpoC | 766801 | c.3432C>T | synonymous_variant | 1.0 |
| rpoC | 766804 | c.3435A>G | synonymous_variant | 1.0 |
| rpoC | 767023 | c.3654C>T | synonymous_variant | 1.0 |
| rpoC | 767026 | c.3657G>C | synonymous_variant | 1.0 |
| rpoC | 767038 | c.3669G>A | synonymous_variant | 0.75 |
| rpoC | 767059 | c.3690T>G | synonymous_variant | 0.75 |
| rpoC | 767062 | c.3693C>T | synonymous_variant | 0.75 |
| rpoC | 767068 | c.3699G>C | synonymous_variant | 0.75 |
| rpoC | 767098 | c.3729T>C | synonymous_variant | 1.0 |
| rpoC | 767104 | c.3735C>G | synonymous_variant | 1.0 |
| rpoC | 767105 | p.Asn1246Leu | missense_variant | 0.75 |
| rpoC | 767163 | p.Asn1265Ser | missense_variant | 1.0 |
| rpoC | 767180 | p.Ala1271Gln | missense_variant | 1.0 |
| rpoC | 767191 | c.3822C>G | synonymous_variant | 1.0 |
| rpoC | 767197 | c.3828G>A | synonymous_variant | 1.0 |
| rpoC | 767203 | c.3834C>T | synonymous_variant | 1.0 |
| rpoC | 767206 | c.3837C>G | synonymous_variant | 1.0 |
| rpoC | 767209 | c.3840T>C | synonymous_variant | 1.0 |
| rpoC | 767221 | c.3852C>G | synonymous_variant | 1.0 |
| rpoC | 767230 | c.3861G>C | synonymous_variant | 1.0 |
| rpoC | 767233 | c.3864T>C | synonymous_variant | 1.0 |
| rpoC | 767263 | c.3894T>C | synonymous_variant | 1.0 |
| rpoC | 767264 | p.Ala1299Gln | missense_variant | 1.0 |
| mmpL5 | 775751 | c.2730C>T | synonymous_variant | 1.0 |
| mmpL5 | 775763 | c.2718T>C | synonymous_variant | 1.0 |
| mmpL5 | 775769 | c.2712C>G | synonymous_variant | 1.0 |
| mmpL5 | 775808 | c.2673C>G | synonymous_variant | 1.0 |
| mmpL5 | 775817 | c.2664T>C | synonymous_variant | 1.0 |
| mmpL5 | 775826 | c.2655G>T | synonymous_variant | 1.0 |
| mmpL5 | 775829 | c.2652C>G | synonymous_variant | 1.0 |
| mmpL5 | 775834 | p.Ala883Ser | missense_variant | 1.0 |
| mmpL5 | 775838 | c.2643G>C | synonymous_variant | 0.5 |
| mmpL5 | 775841 | c.2640G>C | synonymous_variant | 0.5 |
| mmpL5 | 775844 | c.2637G>C | synonymous_variant | 1.0 |
| mmpL5 | 775847 | c.2634G>T | synonymous_variant | 1.0 |
| mmpL5 | 775856 | c.2625T>C | synonymous_variant | 1.0 |
| mmpL5 | 775865 | c.2616T>C | synonymous_variant | 1.0 |
| mmpL5 | 775885 | p.Ile866Leu | missense_variant | 0.5 |
| mmpL5 | 775886 | c.2595A>G | synonymous_variant | 1.0 |
| mmpL5 | 775909 | p.Leu858Phe | missense_variant | 0.91 |
| mmpL5 | 775913 | p.Ala856Ser | missense_variant | 0.42 |
| mmpL5 | 775916 | c.2565T>G | synonymous_variant | 1.0 |
| mmpL5 | 775940 | c.2541C>T | synonymous_variant | 0.71 |
| mmpL5 | 775961 | c.2520C>G | synonymous_variant | 0.95 |
| mmpL5 | 775975 | c.2506T>C | synonymous_variant | 1.0 |
| mmpL5 | 775981 | p.Leu834Met | missense_variant | 1.0 |
| mmpL5 | 776000 | p.Leu827Ile | missense_variant | 0.89 |
| mmpL5 | 776009 | c.2472A>G | synonymous_variant | 0.94 |
| mmpL5 | 776030 | c.2451G>C | synonymous_variant | 0.93 |
| mmpL5 | 776055 | p.Val809Ala | missense_variant | 0.6 |
| mmpL5 | 776068 | p.Val805Ile | missense_variant | 0.57 |
| mmpL5 | 776072 | c.2409C>G | synonymous_variant | 1.0 |
| mmpL5 | 776075 | c.2406C>G | synonymous_variant | 0.8 |
| mmpL5 | 776081 | c.2400G>C | synonymous_variant | 0.8 |
| mmpL5 | 776099 | p.Thr794Leu | missense_variant | 1.0 |
| rpsL | 781549 | c.-11A>G | upstream_gene_variant | 1.0 |
| rpsL | 781559 | c.-1G>C | upstream_gene_variant | 1.0 |
| rpsL | 781595 | c.36T>C | synonymous_variant | 1.0 |
| rpsL | 781598 | c.39G>C | synonymous_variant | 1.0 |
| rpsL | 781608 | p.Ser17Ala | missense_variant | 1.0 |
| rpsL | 781628 | c.69T>C | synonymous_variant | 1.0 |
| rpsL | 781631 | c.72G>C | synonymous_variant | 1.0 |
| rpsL | 781649 | c.90T>C | synonymous_variant | 1.0 |
| rpsL | 781652 | c.93T>A | synonymous_variant | 1.0 |
| rpsL | 781658 | c.99A>G | synonymous_variant | 1.0 |
| rpsL | 781664 | c.105C>T | synonymous_variant | 1.0 |
| rpsL | 781682 | c.123T>C | synonymous_variant | 1.0 |
| rpsL | 781703 | c.144G>A | synonymous_variant | 1.0 |
| rpsL | 781709 | c.150G>C | synonymous_variant | 1.0 |
| rpsL | 781715 | c.156T>C | synonymous_variant | 1.0 |
| rpsL | 781718 | c.159C>G | synonymous_variant | 1.0 |
| rpsL | 781724 | c.165G>C | synonymous_variant | 1.0 |
| rpsL | 781728 | c.169T>C | synonymous_variant | 1.0 |
| rpsL | 781733 | c.174G>C | synonymous_variant | 1.0 |
| rpsL | 781735 | p.Ser59Thr | missense_variant | 1.0 |
| rpsL | 781748 | c.189C>G | synonymous_variant | 1.0 |
| rpsL | 781751 | c.192G>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 | 1.0 |
| rpsL | 781805 | c.246G>C | synonymous_variant | 1.0 |
| rpsL | 781814 | c.255C>T | synonymous_variant | 1.0 |
| rpsL | 781817 | c.258G>T | synonymous_variant | 1.0 |
| rpsL | 781832 | c.273T>G | synonymous_variant | 1.0 |
| rplC | 800612 | c.-197A>G | upstream_gene_variant | 1.0 |
| rplC | 800618 | c.-191T>G | upstream_gene_variant | 1.0 |
| rplC | 800628 | c.-181_-179delGTGinsATC | upstream_gene_variant | 0.67 |
| rplC | 800633 | c.-176T>C | upstream_gene_variant | 1.0 |
| rplC | 800645 | c.-164C>G | upstream_gene_variant | 0.8 |
| rplC | 800648 | c.-161A>C | upstream_gene_variant | 1.0 |
| rplC | 800666 | c.-143C>T | upstream_gene_variant | 0.71 |
| rplC | 800693 | c.-116A>C | upstream_gene_variant | 1.0 |
| rplC | 800702 | c.-107G>A | upstream_gene_variant | 1.0 |
| rplC | 800703 | c.-106_-104delTTGinsCTC | upstream_gene_variant | 1.0 |
| rplC | 800715 | c.-94A>C | upstream_gene_variant | 1.0 |
| rplC | 800723 | c.-86C>G | upstream_gene_variant | 1.0 |
| rplC | 800744 | c.-65G>C | upstream_gene_variant | 1.0 |
| rplC | 800745 | c.-64_-62delCTCinsTTG | upstream_gene_variant | 0.67 |
| rplC | 800759 | c.-50C>T | upstream_gene_variant | 1.0 |
| rplC | 800762 | c.-47T>G | upstream_gene_variant | 1.0 |
| fbiC | 1303794 | c.864A>G | synonymous_variant | 1.0 |
| fbiC | 1303818 | c.888C>G | synonymous_variant | 1.0 |
| fbiC | 1303914 | c.984C>G | synonymous_variant | 1.0 |
| fbiC | 1303929 | c.999G>C | synonymous_variant | 1.0 |
| fbiC | 1303938 | c.1008C>T | synonymous_variant | 1.0 |
| fbiC | 1304022 | c.1092T>C | synonymous_variant | 1.0 |
| fbiC | 1304034 | c.1104A>G | synonymous_variant | 0.67 |
| fbiC | 1304049 | c.1119T>G | synonymous_variant | 1.0 |
| fbiC | 1304050 | c.1120T>C | synonymous_variant | 1.0 |
| fbiC | 1304058 | c.1128G>A | synonymous_variant | 1.0 |
| fbiC | 1304059 | c.1129C>T | synonymous_variant | 0.67 |
| fbiC | 1304064 | c.1134G>A | synonymous_variant | 1.0 |
| fbiC | 1304066 | p.Ala379Asp | missense_variant | 1.0 |
| fbiC | 1304085 | c.1155C>T | synonymous_variant | 1.0 |
| fbiC | 1304092 | p.Met388Leu | missense_variant | 1.0 |
| fbiC | 1304109 | c.1179C>G | synonymous_variant | 0.67 |
| fbiC | 1304133 | c.1203G>C | synonymous_variant | 1.0 |
| fbiC | 1304137 | p.Ala403Ser | missense_variant | 1.0 |
| fbiC | 1304465 | p.Gly512Asp | missense_variant | 1.0 |
| fbiC | 1304472 | c.1542T>C | synonymous_variant | 1.0 |
| fbiC | 1304478 | c.1548G>C | synonymous_variant | 1.0 |
| fbiC | 1304481 | c.1551T>G | synonymous_variant | 1.0 |
| fbiC | 1304490 | c.1560C>T | synonymous_variant | 1.0 |
| fbiC | 1304493 | p.Asp521Glu | missense_variant | 1.0 |
| fbiC | 1304515 | p.Ala529Thr | missense_variant | 1.0 |
| fbiC | 1304520 | c.1590A>G | synonymous_variant | 1.0 |
| fbiC | 1304526 | c.1596T>C | synonymous_variant | 1.0 |
| fbiC | 1304527 | p.Asp533Asn | missense_variant | 1.0 |
| fbiC | 1304533 | c.1603T>C | synonymous_variant | 1.0 |
| fbiC | 1304539 | p.Arg537Met | missense_variant | 1.0 |
| fbiC | 1304544 | p.Asp538Glu | missense_variant | 1.0 |
| fbiC | 1304547 | c.1617C>T | synonymous_variant | 1.0 |
| fbiC | 1304559 | p.Glu543Asp | missense_variant | 1.0 |
| fbiC | 1304565 | c.1635C>G | synonymous_variant | 1.0 |
| fbiC | 1304567 | p.Phe546Tyr | missense_variant | 1.0 |
| fbiC | 1304571 | c.1641G>C | synonymous_variant | 1.0 |
| fbiC | 1304574 | c.1644C>G | synonymous_variant | 1.0 |
| fbiC | 1304580 | c.1650T>C | synonymous_variant | 1.0 |
| fbiC | 1304613 | c.1683T>C | synonymous_variant | 1.0 |
| fbiC | 1304619 | c.1689G>C | synonymous_variant | 1.0 |
| fbiC | 1304640 | c.1710A>C | synonymous_variant | 1.0 |
| fbiC | 1304652 | c.1722C>G | synonymous_variant | 1.0 |
| fbiC | 1304658 | c.1728C>T | synonymous_variant | 1.0 |
| fbiC | 1304660 | p.Tyr577Phe | missense_variant | 1.0 |
| fbiC | 1304664 | c.1734G>A | synonymous_variant | 1.0 |
| fbiC | 1304670 | c.1740G>C | synonymous_variant | 1.0 |
| fbiC | 1304671 | p.Val581Thr | missense_variant | 1.0 |
| fbiC | 1304676 | c.1746A>C | synonymous_variant | 1.0 |
| fbiC | 1304694 | c.1764A>G | synonymous_variant | 1.0 |
| fbiC | 1304700 | c.1770G>A | synonymous_variant | 1.0 |
| fbiC | 1304703 | c.1773C>G | synonymous_variant | 1.0 |
| fbiC | 1304715 | c.1785G>C | synonymous_variant | 1.0 |
| fbiC | 1304724 | c.1794A>G | synonymous_variant | 1.0 |
| fbiC | 1304727 | c.1797A>C | synonymous_variant | 1.0 |
| fbiC | 1304748 | c.1818T>C | synonymous_variant | 1.0 |
| fbiC | 1304751 | c.1821C>T | synonymous_variant | 1.0 |
| fbiC | 1304757 | c.1827A>G | synonymous_variant | 1.0 |
| fbiC | 1304760 | c.1830G>T | synonymous_variant | 1.0 |
| Rv1258c | 1406297 | c.1044A>C | synonymous_variant | 1.0 |
| Rv1258c | 1406318 | p.Ala341Pro | missense_variant | 1.0 |
| Rv1258c | 1406321 | c.1020A>C | synonymous_variant | 1.0 |
| Rv1258c | 1406324 | c.1017G>C | synonymous_variant | 1.0 |
| Rv1258c | 1406327 | c.1014G>C | synonymous_variant | 1.0 |
| Rv1258c | 1406333 | p.Ile336Met | missense_variant | 1.0 |
| Rv1258c | 1406336 | c.1005G>C | synonymous_variant | 1.0 |
| Rv1258c | 1406345 | c.996T>C | synonymous_variant | 1.0 |
| Rv1258c | 1406355 | p.Gln329Ala | missense_variant | 1.0 |
| Rv1258c | 1406360 | c.981C>G | synonymous_variant | 1.0 |
| Rv1258c | 1406363 | c.978A>G | synonymous_variant | 1.0 |
| Rv1258c | 1406381 | c.960G>C | synonymous_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.81delC | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471931 | n.87delA | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471938 | n.93T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472023 | n.178G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472028 | n.183A>G | non_coding_transcript_exon_variant | 0.77 |
| rrs | 1472030 | n.185G>A | non_coding_transcript_exon_variant | 0.77 |
| rrs | 1472031 | n.186G>T | non_coding_transcript_exon_variant | 0.77 |
| rrs | 1472033 | n.188A>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472035 | n.190G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472040 | n.195T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472041 | n.196C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472042 | n.197T>G | non_coding_transcript_exon_variant | 0.79 |
| rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472337 | n.492C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472380 | n.535G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472456 | n.611T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472846 | n.1001C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472848 | n.1003T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472860 | n.1015C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472861 | n.1016G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472873 | n.1028C>T | non_coding_transcript_exon_variant | 0.88 |
| rrs | 1472951 | n.1106T>C | non_coding_transcript_exon_variant | 0.89 |
| rrs | 1472953 | n.1108G>A | non_coding_transcript_exon_variant | 0.89 |
| rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.88 |
| rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.87 |
| rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.93 |
| rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.92 |
| rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.92 |
| rrs | 1473053 | n.1208T>C | non_coding_transcript_exon_variant | 0.6 |
| rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473099 | n.1254T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 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 | 0.91 |
| rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473656 | n.-1delT | upstream_gene_variant | 1.0 |
| rrl | 1473668 | n.11C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473673 | n.16G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473697 | n.40C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473717 | n.60G>A | non_coding_transcript_exon_variant | 0.92 |
| rrl | 1473731 | n.74T>A | non_coding_transcript_exon_variant | 0.92 |
| rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473813 | n.156C>T | non_coding_transcript_exon_variant | 0.94 |
| rrl | 1473815 | n.158T>C | non_coding_transcript_exon_variant | 0.88 |
| rrl | 1473823 | n.166T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473836 | n.179A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473876 | n.219G>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 | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474185 | n.528G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474186 | n.529A>G | 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 | 1474286 | n.630_639delTCCTTTTCCT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474304 | n.647G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474306 | n.649A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474412 | n.756_768delACCCACACGCGCA | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474428 | n.771C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474429 | n.772G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474431 | n.774G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474434 | n.777_778insAAGGG | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474437 | n.781_782delAA | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474552 | n.895C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474629 | n.972G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474709 | n.1053delT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474714 | n.1058delT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474720 | n.1063C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474753 | n.1096A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.92 |
| rrl | 1474803 | n.1146G>A | non_coding_transcript_exon_variant | 0.92 |
| rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.93 |
| rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 0.86 |
| rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475425 | n.1768G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475430 | n.1773T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475436 | n.1779C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475544 | n.1887A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475573 | n.1916G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475576 | n.1919C>T | non_coding_transcript_exon_variant | 0.75 |
| rrl | 1475596 | n.1939G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475764 | n.2107A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.92 |
| rrl | 1475995 | n.2338G>A | non_coding_transcript_exon_variant | 0.79 |
| rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476032 | n.2375C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476033 | n.2376T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476034 | n.2377C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476040 | n.2383C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476045 | n.2388G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476046 | n.2389G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476088 | n.2431A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476095 | n.2438C>T | non_coding_transcript_exon_variant | 0.9 |
| rrl | 1476103 | n.2446C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476105 | n.2448G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476106 | n.2449A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.71 |
| rrl | 1476251 | n.2594T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.72 |
| rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476529 | n.2872A>G | non_coding_transcript_exon_variant | 0.96 |
| rrl | 1476540 | n.2883C>T | non_coding_transcript_exon_variant | 0.96 |
| rrl | 1476583 | n.2926G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.96 |
| rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.96 |
| rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476664 | n.3007T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476665 | n.3008T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476666 | n.3009C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476674 | n.3017T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476679 | n.3022T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476690 | n.3033C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476692 | n.3035T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476693 | n.3036G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476716 | n.3059A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476723 | n.3066T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476725 | n.3068C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476726 | n.3069A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476731 | n.3074G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476732 | n.3075T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476740 | n.3083G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476744 | n.3087G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476746 | n.3089T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476750 | n.3093T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476757 | n.3100T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476759 | n.3102T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476770 | n.3113T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476771 | n.3114G>A | non_coding_transcript_exon_variant | 1.0 |
| inhA | 1673505 | c.-697A>T | upstream_gene_variant | 1.0 |
| inhA | 1673535 | c.-667A>G | upstream_gene_variant | 1.0 |
| inhA | 1673538 | c.-664G>A | upstream_gene_variant | 0.67 |
| inhA | 1673547 | c.-655T>C | upstream_gene_variant | 1.0 |
| inhA | 1673550 | c.-652C>T | upstream_gene_variant | 0.5 |
| inhA | 1673556 | c.-646C>T | upstream_gene_variant | 1.0 |
| inhA | 1673565 | c.-637G>C | upstream_gene_variant | 0.4 |
| inhA | 1673580 | c.-622T>C | upstream_gene_variant | 0.75 |
| inhA | 1673583 | c.-619A>C | upstream_gene_variant | 1.0 |
| inhA | 1673589 | c.-613A>C | upstream_gene_variant | 1.0 |
| inhA | 1673592 | c.-610G>C | upstream_gene_variant | 1.0 |
| inhA | 1673595 | c.-607A>C | upstream_gene_variant | 1.0 |
| fabG1 | 1673596 | p.Lys53Asp | missense_variant | 1.0 |
| inhA | 1673601 | c.-601G>A | upstream_gene_variant | 1.0 |
| inhA | 1673607 | c.-595T>C | upstream_gene_variant | 1.0 |
| inhA | 1673610 | c.-592C>T | upstream_gene_variant | 1.0 |
| inhA | 1673616 | c.-586A>G | upstream_gene_variant | 1.0 |
| fabG1 | 1673633 | p.Ser65Asn | missense_variant | 1.0 |
| fabG1 | 1673644 | p.Asp69Asn | missense_variant | 1.0 |
| inhA | 1673649 | c.-553C>T | upstream_gene_variant | 1.0 |
| inhA | 1673658 | c.-544G>C | upstream_gene_variant | 1.0 |
| inhA | 1673660 | c.-542C>A | upstream_gene_variant | 1.0 |
| inhA | 1673664 | c.-538A>C | upstream_gene_variant | 1.0 |
| inhA | 1673667 | c.-535A>G | upstream_gene_variant | 1.0 |
| inhA | 1673679 | c.-523T>C | upstream_gene_variant | 1.0 |
| inhA | 1673691 | c.-511G>A | upstream_gene_variant | 1.0 |
| fabG1 | 1673755 | p.Glu106Gln | missense_variant | 1.0 |
| fabG1 | 1673760 | p.Lys107Asn | missense_variant | 1.0 |
| fabG1 | 1673767 | p.Asn110Asp | missense_variant | 1.0 |
| fabG1 | 1673797 | p.Ala120Thr | missense_variant | 1.0 |
| inhA | 1673802 | c.-400A>G | upstream_gene_variant | 1.0 |
| inhA | 1673808 | c.-394A>G | upstream_gene_variant | 1.0 |
| fabG1 | 1673829 | p.Asn130Lys | missense_variant | 1.0 |
| fabG1 | 1673830 | p.Lys131Arg | missense_variant | 1.0 |
| inhA | 1673838 | c.-364T>G | upstream_gene_variant | 1.0 |
| inhA | 1673841 | c.-361A>G | upstream_gene_variant | 1.0 |
| fabG1 | 1673844 | p.Met135Ile | missense_variant | 1.0 |
| inhA | 1673847 | c.-355A>C | upstream_gene_variant | 1.0 |
| fabG1 | 1673849 | p.Phe137Tyr | missense_variant | 1.0 |
| inhA | 1673853 | c.-349A>C | upstream_gene_variant | 1.0 |
| inhA | 1673868 | c.-334C>G | upstream_gene_variant | 1.0 |
| fabG1 | 1673870 | p.Ser144Met | missense_variant | 1.0 |
| inhA | 1673883 | c.-319C>T | upstream_gene_variant | 1.0 |
| inhA | 1673901 | c.-301A>G | upstream_gene_variant | 1.0 |
| fabG1 | 1673905 | p.Ser156Ala | missense_variant | 1.0 |
| inhA | 1674471 | c.270G>C | synonymous_variant | 1.0 |
| inhA | 1674480 | c.279T>C | synonymous_variant | 1.0 |
| inhA | 1674483 | c.282G>C | synonymous_variant | 1.0 |
| inhA | 1674486 | c.285T>C | synonymous_variant | 1.0 |
| inhA | 1674489 | c.288G>C | synonymous_variant | 1.0 |
| inhA | 1674507 | c.306G>A | synonymous_variant | 1.0 |
| inhA | 1674531 | c.330C>T | synonymous_variant | 1.0 |
| inhA | 1674537 | c.336C>G | synonymous_variant | 1.0 |
| inhA | 1674542 | p.Ala114Glu | missense_variant | 1.0 |
| inhA | 1674549 | c.348G>C | synonymous_variant | 1.0 |
| inhA | 1674550 | p.Ser117Ala | missense_variant | 1.0 |
| inhA | 1674555 | c.354G>A | synonymous_variant | 1.0 |
| inhA | 1674561 | c.360C>T | synonymous_variant | 1.0 |
| inhA | 1674570 | c.369G>C | synonymous_variant | 1.0 |
| inhA | 1674573 | c.372G>C | synonymous_variant | 1.0 |
| inhA | 1674585 | c.384T>G | synonymous_variant | 1.0 |
| inhA | 1674589 | p.Met130Leu | missense_variant | 1.0 |
| inhA | 1674597 | c.396G>A | synonymous_variant | 1.0 |
| inhA | 1674600 | c.399G>T | synonymous_variant | 1.0 |
| inhA | 1674601 | p.Leu134Val | missense_variant | 1.0 |
| inhA | 1674651 | c.450C>T | synonymous_variant | 1.0 |
| inhA | 1674656 | p.Ser152Thr | missense_variant | 1.0 |
| inhA | 1674660 | c.459G>C | synonymous_variant | 1.0 |
| inhA | 1674771 | c.570C>T | synonymous_variant | 1.0 |
| inhA | 1674780 | c.579T>G | synonymous_variant | 1.0 |
| inhA | 1674789 | c.588G>A | synonymous_variant | 1.0 |
| rpsA | 1833539 | c.-3A>C | upstream_gene_variant | 1.0 |
| rpsA | 1833540 | c.-2A>T | upstream_gene_variant | 1.0 |
| rpsA | 1833547 | c.6G>A | synonymous_variant | 1.0 |
| rpsA | 1833550 | c.9T>C | synonymous_variant | 1.0 |
| rpsA | 1833578 | p.Val13Ile | missense_variant | 1.0 |
| rpsA | 1833586 | c.45C>T | synonymous_variant | 1.0 |
| rpsA | 1833589 | c.48A>T | synonymous_variant | 1.0 |
| rpsA | 1833595 | c.54T>G | synonymous_variant | 1.0 |
| rpsA | 1833596 | p.Ser19Ala | missense_variant | 1.0 |
| rpsA | 1833604 | c.63C>T | synonymous_variant | 1.0 |
| rpsA | 1833607 | c.66T>C | synonymous_variant | 1.0 |
| rpsA | 1833608 | p.Leu23Met | missense_variant | 1.0 |
| rpsA | 1833619 | c.78A>C | synonymous_variant | 1.0 |
| rpsA | 1833625 | c.84A>G | synonymous_variant | 1.0 |
| rpsA | 1833628 | c.87G>C | synonymous_variant | 1.0 |
| rpsA | 1833634 | c.93G>A | synonymous_variant | 1.0 |
| rpsA | 1833664 | c.123C>G | synonymous_variant | 1.0 |
| rpsA | 1833676 | c.135A>G | synonymous_variant | 1.0 |
| rpsA | 1833685 | c.144G>C | synonymous_variant | 1.0 |
| rpsA | 1833688 | c.147C>T | synonymous_variant | 0.88 |
| rpsA | 1833694 | c.153G>C | synonymous_variant | 1.0 |
| rpsA | 1833697 | c.156C>G | synonymous_variant | 1.0 |
| rpsA | 1833703 | c.162C>T | synonymous_variant | 1.0 |
| rpsA | 1833718 | c.177C>A | synonymous_variant | 0.88 |
| rpsA | 1833724 | c.183C>G | synonymous_variant | 1.0 |
| rpsA | 1833727 | c.186G>T | synonymous_variant | 1.0 |
| rpsA | 1833733 | c.192C>T | synonymous_variant | 1.0 |
| rpsA | 1833734 | p.Ala65Ser | missense_variant | 1.0 |
| rpsA | 1833739 | c.198C>T | synonymous_variant | 1.0 |
| rpsA | 1833742 | c.201A>G | synonymous_variant | 1.0 |
| rpsA | 1833745 | c.204G>C | synonymous_variant | 1.0 |
| rpsA | 1833748 | c.207C>G | synonymous_variant | 1.0 |
| rpsA | 1833772 | c.231C>T | synonymous_variant | 1.0 |
| rpsA | 1833778 | c.237C>T | synonymous_variant | 1.0 |
| rpsA | 1833781 | c.240T>G | synonymous_variant | 1.0 |
| rpsA | 1833790 | c.249T>C | synonymous_variant | 1.0 |
| rpsA | 1833793 | c.252C>T | synonymous_variant | 1.0 |
| rpsA | 1833811 | c.270G>T | 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 | 1833856 | c.315A>G | synonymous_variant | 1.0 |
| rpsA | 1833859 | c.318C>T | synonymous_variant | 1.0 |
| rpsA | 1833862 | c.321G>T | synonymous_variant | 1.0 |
| rpsA | 1833874 | c.333T>C | synonymous_variant | 1.0 |
| rpsA | 1833886 | c.345C>G | synonymous_variant | 1.0 |
| rpsA | 1833894 | p.Ala118Glu | missense_variant | 1.0 |
| rpsA | 1833928 | c.387G>C | synonymous_variant | 1.0 |
| rpsA | 1833949 | c.408T>C | synonymous_variant | 1.0 |
| rpsA | 1833970 | c.429G>T | synonymous_variant | 1.0 |
| rpsA | 1833973 | c.432G>C | synonymous_variant | 0.71 |
| rpsA | 1833976 | c.435C>T | synonymous_variant | 0.71 |
| rpsA | 1833979 | c.438T>C | synonymous_variant | 1.0 |
| rpsA | 1833985 | c.444G>T | synonymous_variant | 0.9 |
| rpsA | 1833988 | c.447C>T | synonymous_variant | 0.8 |
| rpsA | 1833997 | c.456G>C | synonymous_variant | 0.89 |
| rpsA | 1834000 | c.459G>C | synonymous_variant | 1.0 |
| rpsA | 1834012 | c.471G>C | synonymous_variant | 0.91 |
| rpsA | 1834015 | c.474G>T | synonymous_variant | 1.0 |
| rpsA | 1834021 | c.480C>T | synonymous_variant | 1.0 |
| rpsA | 1834030 | c.489C>G | synonymous_variant | 1.0 |
| rpsA | 1834051 | c.510G>A | synonymous_variant | 1.0 |
| rpsA | 1834054 | c.513C>G | synonymous_variant | 1.0 |
| rpsA | 1834097 | c.556_557delTCinsAG | synonymous_variant | 0.88 |
| rpsA | 1834102 | c.561T>C | synonymous_variant | 1.0 |
| rpsA | 1834150 | c.609G>C | synonymous_variant | 1.0 |
| rpsA | 1834153 | c.612T>C | synonymous_variant | 1.0 |
| rpsA | 1834154 | p.Asn205Gln | missense_variant | 1.0 |
| rpsA | 1834157 | c.616_618delTTGinsCTC | synonymous_variant | 1.0 |
| rpsA | 1834162 | c.621A>G | synonymous_variant | 1.0 |
| rpsA | 1834165 | c.624A>G | synonymous_variant | 1.0 |
| rpsA | 1834168 | c.627C>T | synonymous_variant | 0.75 |
| rpsA | 1834169 | p.Thr210Ala | missense_variant | 1.0 |
| rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
| rpsA | 1834189 | c.648G>C | synonymous_variant | 1.0 |
| rpsA | 1834213 | c.672G>A | synonymous_variant | 0.86 |
| rpsA | 1834231 | c.690T>C | synonymous_variant | 1.0 |
| rpsA | 1834234 | c.693G>C | synonymous_variant | 1.0 |
| rpsA | 1834240 | c.699T>C | synonymous_variant | 1.0 |
| rpsA | 1834249 | c.708T>C | synonymous_variant | 1.0 |
| rpsA | 1834252 | c.711C>T | synonymous_variant | 0.89 |
| rpsA | 1834261 | c.720A>G | synonymous_variant | 1.0 |
| rpsA | 1834264 | c.723G>C | synonymous_variant | 1.0 |
| rpsA | 1834294 | c.753G>T | synonymous_variant | 0.82 |
| rpsA | 1834306 | c.765T>C | synonymous_variant | 1.0 |
| rpsA | 1834348 | c.807T>C | synonymous_variant | 1.0 |
| rpsA | 1834361 | c.820T>C | synonymous_variant | 1.0 |
| rpsA | 1834366 | c.825A>G | synonymous_variant | 1.0 |
| rpsA | 1834375 | c.834G>A | synonymous_variant | 1.0 |
| rpsA | 1834387 | c.846C>T | synonymous_variant | 0.88 |
| rpsA | 1834396 | c.855G>C | synonymous_variant | 1.0 |
| rpsA | 1834411 | c.870T>G | synonymous_variant | 1.0 |
| rpsA | 1834414 | c.873C>T | synonymous_variant | 0.82 |
| rpsA | 1834417 | c.876G>C | synonymous_variant | 0.88 |
| rpsA | 1834438 | c.897C>T | synonymous_variant | 0.61 |
| rpsA | 1834451 | c.910T>C | synonymous_variant | 1.0 |
| rpsA | 1834459 | c.918G>C | synonymous_variant | 0.89 |
| rpsA | 1834468 | c.927A>G | synonymous_variant | 1.0 |
| rpsA | 1834483 | c.942G>A | synonymous_variant | 1.0 |
| rpsA | 1834489 | c.948T>C | synonymous_variant | 1.0 |
| rpsA | 1834522 | c.981C>T | synonymous_variant | 0.38 |
| rpsA | 1834528 | c.987T>C | synonymous_variant | 1.0 |
| rpsA | 1834543 | c.1002C>G | synonymous_variant | 1.0 |
| rpsA | 1834552 | c.1011G>T | synonymous_variant | 1.0 |
| rpsA | 1834591 | c.1050C>T | synonymous_variant | 0.78 |
| rpsA | 1834606 | c.1065C>T | synonymous_variant | 0.67 |
| rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.33 |
| 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 | 1834654 | c.1113G>A | synonymous_variant | 0.89 |
| rpsA | 1834667 | p.Ala376Ser | missense_variant | 1.0 |
| rpsA | 1834690 | c.1149T>C | synonymous_variant | 1.0 |
| rpsA | 1834700 | p.Gln387Ala | missense_variant | 1.0 |
| rpsA | 1834720 | c.1179C>G | synonymous_variant | 1.0 |
| rpsA | 1834732 | c.1191T>C | synonymous_variant | 1.0 |
| rpsA | 1834738 | c.1197A>G | synonymous_variant | 1.0 |
| rpsA | 1834751 | c.1210_1212delCTTinsTTG | synonymous_variant | 1.0 |
| rpsA | 1834756 | c.1215G>A | synonymous_variant | 1.0 |
| rpsA | 1834759 | c.1218A>C | synonymous_variant | 1.0 |
| rpsA | 1834765 | p.Glu408Asp | missense_variant | 1.0 |
| rpsA | 1834775 | p.Ala412Thr | missense_variant | 1.0 |
| rpsA | 1834780 | c.1239A>G | synonymous_variant | 1.0 |
| rpsA | 1834786 | c.1245A>G | synonymous_variant | 1.0 |
| rpsA | 1834789 | c.1248T>C | synonymous_variant | 1.0 |
| rpsA | 1834810 | c.1269C>T | synonymous_variant | 1.0 |
| rpsA | 1834813 | c.1272G>C | synonymous_variant | 1.0 |
| rpsA | 1834819 | c.1278G>A | synonymous_variant | 1.0 |
| rpsA | 1834829 | p.Ala430Thr | missense_variant | 1.0 |
| rpsA | 1834852 | c.1311C>A | synonymous_variant | 1.0 |
| rpsA | 1834855 | c.1314C>A | synonymous_variant | 1.0 |
| katG | 2155601 | p.Cys171Arg | missense_variant | 1.0 |
| katG | 2155605 | c.507C>T | synonymous_variant | 1.0 |
| katG | 2155610 | p.Ala168Thr | missense_variant | 1.0 |
| katG | 2155614 | c.498T>C | synonymous_variant | 1.0 |
| katG | 2155617 | c.495T>C | synonymous_variant | 1.0 |
| katG | 2155626 | c.486G>C | synonymous_variant | 1.0 |
| katG | 2155632 | c.480A>G | synonymous_variant | 1.0 |
| katG | 2155635 | c.477C>G | synonymous_variant | 1.0 |
| katG | 2155638 | p.Lys158Asn | missense_variant | 1.0 |
| katG | 2155661 | p.Val151Ile | missense_variant | 1.0 |
| katG | 2155674 | c.438G>C | synonymous_variant | 1.0 |
| katG | 2155680 | c.432G>C | synonymous_variant | 1.0 |
| katG | 2155691 | c.421T>C | synonymous_variant | 1.0 |
| katG | 2155696 | p.Ala139Val | missense_variant | 1.0 |
| katG | 2155716 | c.396T>G | synonymous_variant | 1.0 |
| katG | 2155722 | c.390G>C | synonymous_variant | 1.0 |
| katG | 2155728 | c.384G>C | synonymous_variant | 1.0 |
| katG | 2155737 | c.375C>T | synonymous_variant | 1.0 |
| katG | 2155742 | p.Gly124Arg | missense_variant | 1.0 |
| katG | 2155743 | c.369G>A | synonymous_variant | 1.0 |
| katG | 2155747 | p.Ala122Gly | missense_variant | 1.0 |
| katG | 2155752 | c.360C>T | synonymous_variant | 1.0 |
| katG | 2155764 | p.His116Glu | missense_variant | 1.0 |
| katG | 2155769 | p.Ile115Val | missense_variant | 1.0 |
| katG | 2155770 | c.342C>G | synonymous_variant | 1.0 |
| katG | 2155779 | c.333C>T | synonymous_variant | 1.0 |
| katG | 2155782 | c.330C>G | synonymous_variant | 1.0 |
| katG | 2155785 | c.327T>C | synonymous_variant | 1.0 |
| katG | 2155796 | p.Ala106Ser | missense_variant | 1.0 |
| katG | 2155805 | p.Ile103Val | missense_variant | 1.0 |
| katG | 2155806 | c.306T>C | synonymous_variant | 1.0 |
| katG | 2155815 | c.297G>T | synonymous_variant | 1.0 |
| katG | 2155828 | p.Tyr95Phe | missense_variant | 1.0 |
| kasA | 2517926 | c.-189G>A | upstream_gene_variant | 1.0 |
| kasA | 2517941 | c.-174C>G | upstream_gene_variant | 1.0 |
| kasA | 2517953 | c.-162C>T | upstream_gene_variant | 1.0 |
| kasA | 2517962 | c.-153C>T | upstream_gene_variant | 1.0 |
| kasA | 2517968 | c.-147T>C | upstream_gene_variant | 1.0 |
| kasA | 2517971 | c.-144G>T | upstream_gene_variant | 1.0 |
| kasA | 2517974 | c.-141T>C | upstream_gene_variant | 1.0 |
| kasA | 2517980 | c.-135C>T | upstream_gene_variant | 1.0 |
| kasA | 2517989 | c.-126T>C | upstream_gene_variant | 1.0 |
| kasA | 2518636 | c.522C>G | synonymous_variant | 1.0 |
| kasA | 2518642 | c.528A>G | synonymous_variant | 1.0 |
| kasA | 2518645 | c.531G>C | synonymous_variant | 1.0 |
| kasA | 2518651 | c.537C>A | synonymous_variant | 1.0 |
| kasA | 2518657 | c.543G>C | synonymous_variant | 1.0 |
| kasA | 2518663 | c.549T>C | synonymous_variant | 1.0 |
| kasA | 2518672 | c.558G>C | synonymous_variant | 1.0 |
| kasA | 2518678 | c.564C>T | synonymous_variant | 1.0 |
| kasA | 2518687 | c.573C>T | synonymous_variant | 1.0 |
| kasA | 2518688 | p.Val192Phe | missense_variant | 1.0 |
| kasA | 2518702 | c.588C>T | synonymous_variant | 1.0 |
| kasA | 2518708 | c.594C>G | synonymous_variant | 1.0 |
| kasA | 2518714 | c.600A>T | synonymous_variant | 1.0 |
| kasA | 2518715 | p.Pro201Val | missense_variant | 1.0 |
| kasA | 2518723 | c.609G>A | synonymous_variant | 1.0 |
| kasA | 2518732 | c.618C>G | synonymous_variant | 1.0 |
| kasA | 2518747 | c.633C>G | synonymous_variant | 1.0 |
| Rv2752c | 3065142 | c.1050A>C | synonymous_variant | 1.0 |
| Rv2752c | 3065150 | p.Val348Ile | missense_variant | 1.0 |
| Rv2752c | 3065157 | c.1035G>A | synonymous_variant | 1.0 |
| Rv2752c | 3065166 | c.1026C>G | synonymous_variant | 1.0 |
| Rv2752c | 3065173 | p.Leu340Gln | missense_variant | 1.0 |
| Rv2752c | 3065181 | c.1011G>C | synonymous_variant | 1.0 |
| Rv2752c | 3065186 | c.1006T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065187 | p.Val335Ile | missense_variant | 1.0 |
| Rv2752c | 3065193 | c.999C>G | synonymous_variant | 1.0 |
| Rv2752c | 3065199 | c.993T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065202 | p.Ala330Asp | missense_variant | 1.0 |
| Rv2752c | 3065205 | c.987T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065229 | c.963G>C | synonymous_variant | 1.0 |
| Rv2752c | 3065232 | c.960T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065241 | c.951A>G | synonymous_variant | 1.0 |
| Rv2752c | 3066066 | c.126T>C | synonymous_variant | 1.0 |
| Rv2752c | 3066071 | c.121T>C | synonymous_variant | 1.0 |
| Rv2752c | 3066075 | c.117A>G | synonymous_variant | 1.0 |
| Rv2752c | 3066084 | c.108C>T | synonymous_variant | 1.0 |
| Rv2752c | 3066096 | c.96G>C | synonymous_variant | 1.0 |
| Rv2752c | 3066118 | p.Asn25Ser | missense_variant | 1.0 |
| Rv2752c | 3066123 | c.69C>A | synonymous_variant | 1.0 |
| thyX | 3067817 | c.129C>T | synonymous_variant | 1.0 |
| thyX | 3067826 | c.120C>A | synonymous_variant | 1.0 |
| thyX | 3067835 | c.111G>A | synonymous_variant | 1.0 |
| thyX | 3067843 | c.103C>T | synonymous_variant | 1.0 |
| thyX | 3067849 | p.Pro33Ala | missense_variant | 1.0 |
| thyX | 3067850 | c.96A>C | synonymous_variant | 1.0 |
| thyX | 3067869 | p.Thr26Ser | missense_variant | 1.0 |
| thyX | 3067877 | c.69G>C | synonymous_variant | 1.0 |
| thyX | 3067883 | c.63C>T | synonymous_variant | 1.0 |
| thyX | 3067886 | c.60A>C | synonymous_variant | 1.0 |
| thyX | 3067889 | c.57C>A | synonymous_variant | 1.0 |
| thyX | 3067894 | c.52T>C | synonymous_variant | 1.0 |
| thyX | 3067898 | p.Asp16Glu | missense_variant | 1.0 |
| thyX | 3067919 | c.27G>C | synonymous_variant | 1.0 |
| thyA | 3073863 | c.609T>C | synonymous_variant | 1.0 |
| thyA | 3073889 | p.Ser195Ala | missense_variant | 1.0 |
| thyA | 3073892 | c.580T>C | synonymous_variant | 1.0 |
| thyA | 3073902 | c.570C>G | synonymous_variant | 1.0 |
| thyA | 3073917 | c.555C>G | synonymous_variant | 0.75 |
| thyA | 3073920 | c.552C>G | synonymous_variant | 1.0 |
| thyA | 3073929 | c.543T>C | synonymous_variant | 0.8 |
| thyA | 3073950 | c.522G>A | synonymous_variant | 0.86 |
| thyA | 3073953 | c.519T>C | synonymous_variant | 1.0 |
| thyA | 3073956 | c.516G>C | synonymous_variant | 1.0 |
| thyA | 3073959 | c.513T>C | synonymous_variant | 1.0 |
| thyA | 3073977 | c.495A>G | synonymous_variant | 1.0 |
| thyA | 3073980 | c.492C>T | synonymous_variant | 1.0 |
| thyA | 3073983 | c.489C>T | synonymous_variant | 1.0 |
| thyA | 3074004 | c.468T>C | synonymous_variant | 1.0 |
| thyA | 3074031 | c.441T>C | synonymous_variant | 1.0 |
| thyA | 3074037 | c.435C>G | synonymous_variant | 1.0 |
| thyA | 3074045 | c.427C>T | synonymous_variant | 1.0 |
| thyA | 3074053 | p.Arg140Gln | missense_variant | 1.0 |
| thyA | 3074055 | p.Glu139Pro | missense_variant | 1.0 |
| thyA | 3074058 | c.414C>T | synonymous_variant | 1.0 |
| thyA | 3074061 | c.411A>G | synonymous_variant | 1.0 |
| thyA | 3074070 | c.402C>T | synonymous_variant | 1.0 |
| thyA | 3074082 | c.390G>C | synonymous_variant | 1.0 |
| thyA | 3074089 | p.Ile128Asn | missense_variant | 1.0 |
| thyA | 3074097 | c.375C>G | synonymous_variant | 1.0 |
| thyA | 3074103 | c.369C>G | synonymous_variant | 1.0 |
| thyA | 3074120 | c.352T>C | synonymous_variant | 1.0 |
| thyA | 3074123 | p.Asp117Asn | missense_variant | 1.0 |
| thyA | 3074127 | c.345G>A | synonymous_variant | 1.0 |
| thyA | 3074130 | c.342G>C | synonymous_variant | 1.0 |
| thyA | 3074133 | c.339C>T | synonymous_variant | 1.0 |
| thyA | 3074220 | c.252A>C | synonymous_variant | 1.0 |
| thyA | 3074244 | c.228A>C | synonymous_variant | 1.0 |
| thyA | 3074248 | p.His75Arg | missense_variant | 1.0 |
| thyA | 3074253 | p.His73Gln | missense_variant | 1.0 |
| thyA | 3074262 | c.210T>C | synonymous_variant | 1.0 |
| thyA | 3074265 | p.Ile69Val | missense_variant | 1.0 |
| thyA | 3074268 | c.204T>C | synonymous_variant | 1.0 |
| rpoA | 3877569 | p.Pro313Ala | missense_variant | 1.0 |
| rpoA | 3877587 | c.921A>G | synonymous_variant | 1.0 |
| rpoA | 3877590 | c.918G>C | synonymous_variant | 0.67 |
| rpoA | 3877593 | c.915C>T | synonymous_variant | 1.0 |
| rpoA | 3877602 | c.906C>T | synonymous_variant | 0.67 |
| rpoA | 3877617 | c.891G>C | synonymous_variant | 1.0 |
| rpoA | 3877638 | c.870T>C | synonymous_variant | 1.0 |
| rpoA | 3877656 | c.852T>G | synonymous_variant | 1.0 |
| rpoA | 3877662 | c.846C>T | synonymous_variant | 1.0 |
| rpoA | 3877668 | c.840A>G | synonymous_variant | 1.0 |
| rpoA | 3877671 | c.837C>G | synonymous_variant | 1.0 |
| rpoA | 3877677 | c.831G>C | synonymous_variant | 1.0 |
| rpoA | 3877683 | c.825G>C | synonymous_variant | 1.0 |
| rpoA | 3877686 | c.822A>G | synonymous_variant | 1.0 |
| rpoA | 3877704 | c.804G>T | synonymous_variant | 1.0 |
| rpoA | 3877728 | c.780C>G | synonymous_variant | 1.0 |
| rpoA | 3877734 | c.774G>C | synonymous_variant | 1.0 |
| rpoA | 3877749 | c.759C>T | synonymous_variant | 1.0 |
| rpoA | 3877764 | c.744C>G | synonymous_variant | 1.0 |
| rpoA | 3877776 | c.732T>C | synonymous_variant | 1.0 |
| rpoA | 3877782 | c.726T>C | synonymous_variant | 1.0 |
| rpoA | 3877818 | c.690A>G | synonymous_variant | 1.0 |
| rpoA | 3877829 | p.Val227Ile | missense_variant | 1.0 |
| rpoA | 3877848 | c.660C>T | synonymous_variant | 1.0 |
| rpoA | 3877857 | c.651G>A | synonymous_variant | 1.0 |
| rpoA | 3877875 | c.633T>C | synonymous_variant | 1.0 |
| rpoA | 3877881 | c.627G>C | synonymous_variant | 1.0 |
| rpoA | 3877893 | c.615C>T | synonymous_variant | 1.0 |
| rpoA | 3877900 | p.Ser203Thr | missense_variant | 1.0 |
| rpoA | 3877905 | c.603A>G | synonymous_variant | 1.0 |
| rpoA | 3877908 | c.600T>C | synonymous_variant | 1.0 |
| rpoA | 3877920 | c.588G>C | synonymous_variant | 1.0 |
| rpoA | 3877926 | c.582G>C | synonymous_variant | 1.0 |
| rpoA | 3877929 | c.579C>T | synonymous_variant | 1.0 |
| rpoA | 3877962 | c.546G>C | synonymous_variant | 1.0 |
| rpoA | 3877968 | c.540C>G | synonymous_variant | 1.0 |
| rpoA | 3877971 | p.Asp179Glu | missense_variant | 1.0 |
| rpoA | 3877974 | c.534G>C | synonymous_variant | 1.0 |
| rpoA | 3877989 | c.519A>G | synonymous_variant | 1.0 |
| rpoA | 3877992 | c.516C>G | synonymous_variant | 1.0 |
| rpoA | 3878001 | c.507A>G | synonymous_variant | 1.0 |
| rpoA | 3878019 | c.489A>G | synonymous_variant | 1.0 |
| rpoA | 3878022 | c.486T>C | synonymous_variant | 1.0 |
| rpoA | 3878025 | c.483C>T | synonymous_variant | 1.0 |
| rpoA | 3878028 | c.480G>C | synonymous_variant | 1.0 |
| rpoA | 3878031 | c.477T>C | synonymous_variant | 1.0 |
| rpoA | 3878046 | c.462T>C | synonymous_variant | 1.0 |
| rpoA | 3878050 | p.Arg153Lys | missense_variant | 1.0 |
| rpoA | 3878055 | c.453A>G | synonymous_variant | 1.0 |
| rpoA | 3878061 | c.447G>C | synonymous_variant | 1.0 |
| rpoA | 3878064 | c.444G>C | synonymous_variant | 1.0 |
| rpoA | 3878070 | c.438T>C | synonymous_variant | 1.0 |
| rpoA | 3878076 | c.432C>T | synonymous_variant | 1.0 |
| rpoA | 3878088 | c.420C>G | 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.Gly122Glu | missense_variant | 0.86 |
| rpoA | 3878163 | c.345C>T | synonymous_variant | 0.89 |
| rpoA | 3878181 | c.327C>T | synonymous_variant | 0.89 |
| rpoA | 3878184 | c.324C>G | synonymous_variant | 0.44 |
| rpoA | 3878187 | c.321C>G | synonymous_variant | 0.89 |
| rpoA | 3878193 | c.315T>C | synonymous_variant | 1.0 |
| rpoA | 3878205 | c.303T>C | synonymous_variant | 1.0 |
| rpoA | 3878217 | c.291A>G | synonymous_variant | 1.0 |
| rpoA | 3878244 | c.264G>A | synonymous_variant | 1.0 |
| rpoA | 3878247 | c.261G>C | synonymous_variant | 1.0 |
| rpoA | 3878250 | c.258C>G | synonymous_variant | 1.0 |
| rpoA | 3878256 | c.252G>C | synonymous_variant | 1.0 |
| rpoA | 3878264 | p.Ser82Gly | missense_variant | 1.0 |
| rpoA | 3878271 | c.237T>C | synonymous_variant | 1.0 |
| rpoA | 3878274 | c.234G>C | synonymous_variant | 1.0 |
| rpoA | 3878283 | p.Glu75Asp | missense_variant | 1.0 |
| rpoA | 3878292 | c.216T>C | synonymous_variant | 1.0 |
| rpoA | 3878298 | c.210A>G | synonymous_variant | 1.0 |
| rpoA | 3878304 | c.204G>T | synonymous_variant | 1.0 |
| rpoA | 3878307 | c.201C>G | 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>G | synonymous_variant | 1.0 |
| rpoA | 3878334 | c.174T>C | synonymous_variant | 1.0 |
| rpoA | 3878337 | c.171T>C | synonymous_variant | 1.0 |
| rpoA | 3878346 | c.162T>C | synonymous_variant | 1.0 |
| rpoA | 3878358 | c.150C>G | synonymous_variant | 1.0 |
| rpoA | 3878361 | c.147G>A | synonymous_variant | 1.0 |
| rpoA | 3878364 | c.144A>C | synonymous_variant | 1.0 |
| rpoA | 3878367 | c.141C>G | synonymous_variant | 1.0 |
| rpoA | 3878370 | c.138T>C | synonymous_variant | 1.0 |
| rpoA | 3878373 | c.135G>C | synonymous_variant | 1.0 |
| rpoA | 3878385 | c.123C>G | synonymous_variant | 1.0 |
| rpoA | 3878391 | c.117T>G | synonymous_variant | 1.0 |
| rpoA | 3878400 | c.108T>C | synonymous_variant | 1.0 |
| rpoA | 3878403 | c.105C>T | synonymous_variant | 1.0 |
| rpoA | 3878406 | c.102G>C | synonymous_variant | 1.0 |
| rpoA | 3878433 | c.75G>C | synonymous_variant | 1.0 |
| rpoA | 3878436 | c.72A>G | synonymous_variant | 1.0 |
| rpoA | 3878442 | c.66G>C | synonymous_variant | 1.0 |
| ddn | 3986646 | c.-198_-196delCTCinsATG | upstream_gene_variant | 1.0 |
| ddn | 3986655 | c.-189A>T | upstream_gene_variant | 1.0 |
| ddn | 3986661 | c.-183C>A | upstream_gene_variant | 1.0 |
| ddn | 3986667 | c.-177_-176delCTinsAC | upstream_gene_variant | 1.0 |
| ddn | 3986672 | c.-172G>A | upstream_gene_variant | 1.0 |
| clpC1 | 4038254 | c.2451G>C | synonymous_variant | 1.0 |
| clpC1 | 4038269 | p.Pro812Ala | missense_variant | 1.0 |
| clpC1 | 4038272 | c.2433T>C | synonymous_variant | 1.0 |
| clpC1 | 4038275 | c.2430A>G | synonymous_variant | 1.0 |
| clpC1 | 4038278 | c.2427T>C | synonymous_variant | 1.0 |
| clpC1 | 4038293 | c.2412G>C | synonymous_variant | 1.0 |
| clpC1 | 4038302 | c.2403C>G | synonymous_variant | 1.0 |
| clpC1 | 4038308 | c.2397G>C | synonymous_variant | 1.0 |
| clpC1 | 4038317 | c.2388G>C | synonymous_variant | 1.0 |
| clpC1 | 4038320 | c.2385G>C | synonymous_variant | 1.0 |
| clpC1 | 4038325 | p.Val794Ile | missense_variant | 1.0 |
| clpC1 | 4038329 | p.Glu792Asp | missense_variant | 1.0 |
| clpC1 | 4038335 | c.2368_2370delCTCinsTTG | synonymous_variant | 1.0 |
| clpC1 | 4038368 | c.2337T>C | synonymous_variant | 1.0 |
| clpC1 | 4038388 | c.2317T>C | synonymous_variant | 1.0 |
| clpC1 | 4038395 | c.2310C>T | synonymous_variant | 1.0 |
| clpC1 | 4038398 | c.2307G>T | synonymous_variant | 1.0 |
| clpC1 | 4038541 | c.2164C>T | synonymous_variant | 1.0 |
| clpC1 | 4038575 | c.2130C>G | synonymous_variant | 0.8 |
| clpC1 | 4038623 | c.2082A>G | synonymous_variant | 1.0 |
| clpC1 | 4038640 | p.Asp689Asn | missense_variant | 1.0 |
| clpC1 | 4038647 | c.2058T>C | synonymous_variant | 1.0 |
| clpC1 | 4038653 | c.2052C>T | synonymous_variant | 1.0 |
| clpC1 | 4038658 | p.Lys683Gln | missense_variant | 1.0 |
| clpC1 | 4038661 | p.Ser682Thr | missense_variant | 1.0 |
| clpC1 | 4038662 | c.2043T>C | synonymous_variant | 1.0 |
| clpC1 | 4038668 | c.2037G>C | synonymous_variant | 0.8 |
| clpC1 | 4038674 | c.2031C>T | synonymous_variant | 1.0 |
| clpC1 | 4038679 | p.Pro676Ala | missense_variant | 1.0 |
| clpC1 | 4038683 | c.2022T>C | synonymous_variant | 1.0 |
| clpC1 | 4038692 | c.2013C>G | synonymous_variant | 0.83 |
| clpC1 | 4038698 | c.2007C>T | synonymous_variant | 1.0 |
| clpC1 | 4038701 | c.2004G>C | synonymous_variant | 1.0 |
| clpC1 | 4038704 | c.2001T>C | synonymous_variant | 1.0 |
| clpC1 | 4038713 | c.1992T>C | synonymous_variant | 1.0 |
| clpC1 | 4038740 | c.1965G>C | synonymous_variant | 1.0 |
| clpC1 | 4038755 | c.1950G>T | synonymous_variant | 1.0 |
| clpC1 | 4038758 | c.1947C>T | synonymous_variant | 0.86 |
| clpC1 | 4038764 | c.1941C>G | synonymous_variant | 0.86 |
| clpC1 | 4038767 | c.1938G>C | synonymous_variant | 1.0 |
| clpC1 | 4038770 | c.1935C>T | synonymous_variant | 0.86 |
| clpC1 | 4038773 | c.1932T>C | synonymous_variant | 1.0 |
| clpC1 | 4038776 | c.1929G>A | synonymous_variant | 0.86 |
| clpC1 | 4038779 | c.1926C>G | synonymous_variant | 0.86 |
| clpC1 | 4038795 | p.Ser637Thr | missense_variant | 1.0 |
| clpC1 | 4038812 | c.1893T>C | synonymous_variant | 1.0 |
| clpC1 | 4038863 | c.1842G>C | synonymous_variant | 1.0 |
| clpC1 | 4038878 | c.1827A>G | synonymous_variant | 1.0 |
| clpC1 | 4038890 | c.1815G>A | synonymous_variant | 1.0 |
| clpC1 | 4038905 | c.1800A>C | synonymous_variant | 0.78 |
| clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.78 |
| clpC1 | 4038911 | c.1794G>T | synonymous_variant | 0.78 |
| clpC1 | 4038914 | c.1791G>C | synonymous_variant | 1.0 |
| clpC1 | 4038917 | c.1788C>T | synonymous_variant | 0.78 |
| clpC1 | 4038923 | c.1782A>G | synonymous_variant | 1.0 |
| clpC1 | 4038941 | c.1764G>C | synonymous_variant | 1.0 |
| clpC1 | 4038953 | c.1752A>G | synonymous_variant | 1.0 |
| clpC1 | 4038956 | c.1749T>C | synonymous_variant | 1.0 |
| clpC1 | 4038965 | c.1740T>C | synonymous_variant | 1.0 |
| clpC1 | 4038971 | c.1734T>C | synonymous_variant | 1.0 |
| clpC1 | 4038974 | c.1731T>C | synonymous_variant | 1.0 |
| clpC1 | 4038989 | c.1716T>C | 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 | 4039046 | c.1659C>T | synonymous_variant | 0.91 |
| clpC1 | 4039073 | c.1632C>T | synonymous_variant | 1.0 |
| clpC1 | 4039085 | c.1620A>G | synonymous_variant | 1.0 |
| clpC1 | 4039091 | c.1614G>T | synonymous_variant | 1.0 |
| clpC1 | 4039097 | c.1608G>C | synonymous_variant | 1.0 |
| clpC1 | 4039106 | c.1599G>C | synonymous_variant | 1.0 |
| clpC1 | 4039169 | p.Glu512Asp | missense_variant | 1.0 |
| clpC1 | 4039178 | c.1527G>C | synonymous_variant | 1.0 |
| clpC1 | 4039183 | c.1522T>C | synonymous_variant | 1.0 |
| clpC1 | 4039199 | p.Ala502Glu | missense_variant | 1.0 |
| clpC1 | 4039208 | c.1497C>G | synonymous_variant | 1.0 |
| clpC1 | 4039220 | c.1485G>C | synonymous_variant | 1.0 |
| clpC1 | 4039241 | c.1464G>C | synonymous_variant | 1.0 |
| clpC1 | 4039250 | c.1455C>G | synonymous_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>C | synonymous_variant | 1.0 |
| clpC1 | 4039286 | c.1419T>G | synonymous_variant | 1.0 |
| clpC1 | 4039292 | c.1413C>T | synonymous_variant | 1.0 |
| clpC1 | 4039298 | c.1407T>C | synonymous_variant | 1.0 |
| clpC1 | 4039313 | c.1392C>G | synonymous_variant | 1.0 |
| clpC1 | 4039319 | c.1386T>C | synonymous_variant | 1.0 |
| clpC1 | 4039328 | c.1377A>T | synonymous_variant | 1.0 |
| clpC1 | 4039337 | c.1368A>G | synonymous_variant | 1.0 |
| clpC1 | 4039346 | c.1359G>C | synonymous_variant | 1.0 |
| clpC1 | 4039358 | p.Ser449Asn | missense_variant | 0.67 |
| clpC1 | 4039376 | c.1329C>T | synonymous_variant | 0.67 |
| 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 | 4039403 | c.1302G>A | synonymous_variant | 0.8 |
| clpC1 | 4039409 | c.1296T>C | synonymous_variant | 1.0 |
| clpC1 | 4039412 | c.1293T>G | synonymous_variant | 1.0 |
| clpC1 | 4039415 | p.Glu430Asp | missense_variant | 1.0 |
| clpC1 | 4039430 | c.1275T>C | synonymous_variant | 1.0 |
| clpC1 | 4039436 | c.1269G>A | synonymous_variant | 0.8 |
| clpC1 | 4039442 | c.1263A>G | synonymous_variant | 1.0 |
| clpC1 | 4039454 | c.1251A>T | synonymous_variant | 1.0 |
| clpC1 | 4039463 | c.1242C>G | synonymous_variant | 1.0 |
| clpC1 | 4039466 | c.1239T>C | synonymous_variant | 1.0 |
| clpC1 | 4039469 | c.1236T>C | synonymous_variant | 1.0 |
| clpC1 | 4039472 | c.1233G>T | synonymous_variant | 1.0 |
| clpC1 | 4039484 | c.1221T>C | synonymous_variant | 0.78 |
| clpC1 | 4039517 | c.1188C>G | synonymous_variant | 1.0 |
| clpC1 | 4039522 | c.1183C>T | synonymous_variant | 0.83 |
| clpC1 | 4039553 | c.1152C>G | synonymous_variant | 0.86 |
| clpC1 | 4039565 | c.1140G>C | synonymous_variant | 1.0 |
| clpC1 | 4039568 | p.Met379Ile | missense_variant | 1.0 |
| clpC1 | 4039574 | p.Ala377Gly | missense_variant | 1.0 |
| clpC1 | 4039577 | c.1128T>C | synonymous_variant | 1.0 |
| clpC1 | 4039589 | c.1116G>C | synonymous_variant | 0.75 |
| clpC1 | 4039592 | c.1113G>C | synonymous_variant | 0.8 |
| clpC1 | 4039601 | c.1104G>A | synonymous_variant | 0.8 |
| clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.88 |
| clpC1 | 4039616 | c.1089G>C | synonymous_variant | 1.0 |
| clpC1 | 4039622 | c.1083C>T | synonymous_variant | 1.0 |
| clpC1 | 4039637 | p.Ile356Val | missense_variant | 0.82 |
| clpC1 | 4039664 | c.1041G>C | synonymous_variant | 1.0 |
| clpC1 | 4039670 | c.1035G>C | synonymous_variant | 1.0 |
| clpC1 | 4039673 | c.1032G>C | synonymous_variant | 0.91 |
| clpC1 | 4039688 | c.1017G>A | synonymous_variant | 0.89 |
| clpC1 | 4039694 | c.1011G>C | synonymous_variant | 1.0 |
| clpC1 | 4039724 | c.981A>G | synonymous_variant | 1.0 |
| clpC1 | 4039742 | c.963C>T | synonymous_variant | 1.0 |
| clpC1 | 4039751 | c.954A>G | synonymous_variant | 1.0 |
| clpC1 | 4039865 | c.840T>C | synonymous_variant | 1.0 |
| clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.88 |
| clpC1 | 4039913 | c.792C>T | synonymous_variant | 1.0 |
| clpC1 | 4039931 | c.774T>C | synonymous_variant | 1.0 |
| clpC1 | 4039934 | c.771G>A | synonymous_variant | 1.0 |
| clpC1 | 4039946 | c.759A>T | synonymous_variant | 1.0 |
| clpC1 | 4039949 | c.756G>C | synonymous_variant | 1.0 |
| clpC1 | 4039952 | c.753T>C | synonymous_variant | 1.0 |
| clpC1 | 4039955 | c.750G>T | synonymous_variant | 1.0 |
| clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.93 |
| clpC1 | 4039982 | c.723G>A | synonymous_variant | 0.93 |
| clpC1 | 4039994 | p.Glu237Asp | missense_variant | 1.0 |
| clpC1 | 4039997 | c.708C>G | synonymous_variant | 1.0 |
| clpC1 | 4040015 | c.690G>C | synonymous_variant | 1.0 |
| clpC1 | 4040021 | c.684A>C | synonymous_variant | 1.0 |
| clpC1 | 4040024 | c.681A>G | synonymous_variant | 1.0 |
| clpC1 | 4040033 | c.672G>C | synonymous_variant | 1.0 |
| clpC1 | 4040036 | c.669C>G | synonymous_variant | 1.0 |
| clpC1 | 4040057 | c.648C>T | synonymous_variant | 1.0 |
| clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 1.0 |
| clpC1 | 4040093 | c.612C>G | synonymous_variant | 1.0 |
| clpC1 | 4040096 | c.609G>C | synonymous_variant | 1.0 |
| clpC1 | 4040105 | c.600C>G | synonymous_variant | 1.0 |
| clpC1 | 4040138 | c.567G>C | synonymous_variant | 1.0 |
| clpC1 | 4040246 | c.459C>A | synonymous_variant | 1.0 |
| clpC1 | 4040255 | p.Ala150Thr | missense_variant | 1.0 |
| clpC1 | 4040267 | c.438A>G | synonymous_variant | 1.0 |
| clpC1 | 4040277 | c.427_428delTCinsAG | synonymous_variant | 1.0 |
| clpC1 | 4040279 | c.426C>G | synonymous_variant | 1.0 |
| clpC1 | 4040291 | c.414G>C | synonymous_variant | 1.0 |
| clpC1 | 4040303 | c.402G>C | synonymous_variant | 0.83 |
| clpC1 | 4040312 | c.393G>C | synonymous_variant | 0.71 |
| clpC1 | 4040324 | c.381G>T | synonymous_variant | 0.29 |
| clpC1 | 4040333 | c.372G>C | synonymous_variant | 0.71 |
| clpC1 | 4040348 | c.357G>C | synonymous_variant | 0.6 |
| clpC1 | 4040357 | c.348T>C | synonymous_variant | 1.0 |
| clpC1 | 4040360 | c.345G>A | synonymous_variant | 0.67 |
| clpC1 | 4040363 | c.342A>T | synonymous_variant | 0.33 |
| clpC1 | 4040369 | c.336C>G | synonymous_variant | 1.0 |
| clpC1 | 4040375 | c.330G>C | synonymous_variant | 1.0 |
| clpC1 | 4040380 | c.325T>C | synonymous_variant | 1.0 |
| clpC1 | 4040387 | c.318A>G | synonymous_variant | 1.0 |
| clpC1 | 4040393 | c.312G>C | synonymous_variant | 1.0 |
| clpC1 | 4040411 | c.294T>C | synonymous_variant | 1.0 |
| clpC1 | 4040420 | c.285G>T | synonymous_variant | 0.82 |
| clpC1 | 4040423 | c.282A>G | synonymous_variant | 1.0 |
| clpC1 | 4040431 | c.274T>C | synonymous_variant | 1.0 |
| clpC1 | 4040432 | c.271_273delAGCinsTCG | synonymous_variant | 0.82 |
| clpC1 | 4040450 | c.255A>G | synonymous_variant | 1.0 |
| clpC1 | 4040459 | c.246C>G | synonymous_variant | 1.0 |
| clpC1 | 4040465 | c.240T>C | synonymous_variant | 1.0 |
| clpC1 | 4040468 | c.237G>C | synonymous_variant | 1.0 |
| clpC1 | 4040471 | c.234T>C | synonymous_variant | 1.0 |
| clpC1 | 4040477 | c.228G>T | synonymous_variant | 0.92 |
| clpC1 | 4040480 | c.225T>C | synonymous_variant | 1.0 |
| clpC1 | 4040522 | c.183T>C | synonymous_variant | 1.0 |
| clpC1 | 4040531 | c.174T>C | synonymous_variant | 0.89 |
| clpC1 | 4040546 | c.159G>C | synonymous_variant | 1.0 |
| clpC1 | 4040549 | c.154_156delTTGinsCTT | synonymous_variant | 1.0 |
| clpC1 | 4040558 | c.147G>C | synonymous_variant | 1.0 |
| clpC1 | 4040561 | c.144A>C | synonymous_variant | 1.0 |
| clpC1 | 4040573 | c.132T>A | 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 | 4040594 | c.111G>C | synonymous_variant | 1.0 |
| clpC1 | 4040600 | c.103_105delTTAinsCTG | synonymous_variant | 1.0 |
| clpC1 | 4040603 | c.102T>G | synonymous_variant | 1.0 |
| clpC1 | 4040606 | c.99T>C | synonymous_variant | 1.0 |
| clpC1 | 4040618 | c.87C>G | synonymous_variant | 1.0 |
| clpC1 | 4040644 | c.61A>C | synonymous_variant | 1.0 |
| clpC1 | 4040648 | c.57G>A | synonymous_variant | 1.0 |
| clpC1 | 4040654 | c.51G>A | synonymous_variant | 1.0 |
| embC | 4241074 | c.1212G>C | synonymous_variant | 1.0 |
| embC | 4241095 | c.1233C>T | synonymous_variant | 1.0 |
| embC | 4241101 | c.1239G>C | synonymous_variant | 1.0 |
| embC | 4241109 | p.Ala416Gly | missense_variant | 1.0 |
| embC | 4241134 | c.1272G>C | synonymous_variant | 1.0 |
| embC | 4241140 | c.1278A>G | synonymous_variant | 1.0 |
| embC | 4241162 | c.1300T>C | synonymous_variant | 1.0 |
| embC | 4241584 | c.1722T>C | synonymous_variant | 1.0 |
| embC | 4241587 | c.1725C>G | synonymous_variant | 1.0 |
| embC | 4241614 | c.1752A>C | synonymous_variant | 1.0 |
| embB | 4247446 | c.933C>T | synonymous_variant | 1.0 |
| embB | 4247464 | c.951C>G | synonymous_variant | 1.0 |
| embB | 4247470 | c.957T>C | synonymous_variant | 1.0 |
| embB | 4247476 | c.963C>G | synonymous_variant | 1.0 |
| embB | 4247500 | c.987C>G | synonymous_variant | 1.0 |
| embB | 4247511 | p.Tyr333Phe | missense_variant | 1.0 |
| embB | 4247988 | p.Val492Ala | missense_variant | 1.0 |
| embB | 4247992 | c.1479G>A | synonymous_variant | 1.0 |
| embB | 4248007 | c.1494C>A | synonymous_variant | 1.0 |
| embB | 4248028 | c.1515C>G | synonymous_variant | 1.0 |
| embB | 4248035 | p.Val508Ile | missense_variant | 1.0 |
| embB | 4248041 | p.Ala510Thr | missense_variant | 1.0 |
| embB | 4248044 | p.Lys511Ala | missense_variant | 1.0 |
| embB | 4248052 | c.1539G>A | synonymous_variant | 1.0 |
| embB | 4248055 | c.1542G>C | synonymous_variant | 1.0 |
| embB | 4248064 | c.1551G>C | synonymous_variant | 1.0 |
| embB | 4248070 | c.1557T>C | synonymous_variant | 1.0 |
| embB | 4248085 | c.1572T>C | synonymous_variant | 1.0 |
| embB | 4248097 | c.1584C>G | synonymous_variant | 1.0 |
| embB | 4248106 | c.1593C>G | synonymous_variant | 1.0 |
| embB | 4248118 | c.1605T>A | synonymous_variant | 1.0 |
| embB | 4248133 | c.1620C>G | synonymous_variant | 1.0 |
| embB | 4248142 | c.1629T>C | synonymous_variant | 1.0 |
| embB | 4248143 | c.1630T>C | synonymous_variant | 1.0 |
| embB | 4248157 | c.1644A>G | synonymous_variant | 1.0 |
| embB | 4248158 | p.Cys549Ser | missense_variant | 1.0 |
| embB | 4248172 | c.1659G>C | synonymous_variant | 1.0 |
| embB | 4248173 | p.Val554Met | missense_variant | 1.0 |
| embB | 4248190 | c.1677G>C | synonymous_variant | 1.0 |
| embB | 4248199 | c.1686A>G | synonymous_variant | 1.0 |
| embB | 4248202 | c.1689T>C | synonymous_variant | 1.0 |
| embB | 4248206 | p.Ser565Gly | missense_variant | 1.0 |
| embB | 4248211 | c.1698G>A | synonymous_variant | 1.0 |
| embB | 4248214 | c.1701C>G | synonymous_variant | 1.0 |
| embB | 4248225 | p.Ala571Val | missense_variant | 1.0 |
| embB | 4248232 | c.1719G>C | synonymous_variant | 1.0 |
| embB | 4248242 | p.Val577Ile | missense_variant | 1.0 |
| embB | 4248257 | p.Met582Val | missense_variant | 1.0 |
| embB | 4248277 | c.1764G>C | synonymous_variant | 1.0 |
| embB | 4248280 | c.1767C>G | synonymous_variant | 1.0 |
| embB | 4248286 | c.1773G>A | synonymous_variant | 1.0 |
| embB | 4248295 | c.1782C>T | synonymous_variant | 1.0 |
| embB | 4248304 | c.1791G>T | synonymous_variant | 1.0 |
