Run ID: ERR4818607
Sample name:
Date: 01-04-2023 15:39:10
Number of reads: 32040
Percentage reads mapped: 31.15
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 | 0.99 |
| Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
|---|
| Gene | Chromosome position | Mutation | Type | Estimated fraction |
|---|---|---|---|---|
| gyrB | 6238 | c.999G>A | synonymous_variant | 1.0 |
| gyrB | 6242 | p.Arg335Lys | missense_variant | 1.0 |
| gyrB | 6247 | c.1008G>A | synonymous_variant | 1.0 |
| gyrB | 6250 | c.1011A>G | synonymous_variant | 1.0 |
| gyrB | 6265 | c.1026C>T | synonymous_variant | 0.75 |
| gyrB | 6280 | c.1041T>C | synonymous_variant | 0.75 |
| gyrB | 6286 | c.1047T>C | synonymous_variant | 0.75 |
| gyrB | 6292 | c.1053G>C | synonymous_variant | 0.75 |
| gyrB | 6295 | c.1056A>G | synonymous_variant | 0.75 |
| gyrB | 6298 | c.1059C>G | synonymous_variant | 0.75 |
| gyrB | 6299 | c.1060C>T | synonymous_variant | 0.75 |
| gyrA | 6307 | c.-995T>G | upstream_gene_variant | 0.6 |
| gyrA | 6310 | c.-992G>C | upstream_gene_variant | 0.6 |
| gyrA | 6319 | c.-983G>C | upstream_gene_variant | 0.67 |
| gyrB | 6326 | p.Ser363Ala | missense_variant | 0.67 |
| gyrA | 6352 | c.-950C>G | upstream_gene_variant | 0.67 |
| gyrA | 6362 | c.-940T>C | upstream_gene_variant | 0.6 |
| gyrA | 6382 | c.-920A>G | upstream_gene_variant | 0.5 |
| gyrA | 6388 | c.-914T>C | upstream_gene_variant | 0.5 |
| gyrA | 6400 | c.-902C>G | upstream_gene_variant | 0.5 |
| gyrA | 6403 | c.-899T>C | upstream_gene_variant | 0.5 |
| gyrA | 6409 | c.-893A>G | upstream_gene_variant | 0.67 |
| gyrA | 6841 | c.-461T>C | upstream_gene_variant | 1.0 |
| gyrA | 6844 | c.-458T>G | upstream_gene_variant | 1.0 |
| gyrA | 6853 | c.-449A>G | upstream_gene_variant | 1.0 |
| gyrA | 6856 | c.-446T>C | upstream_gene_variant | 1.0 |
| gyrA | 6859 | c.-443T>C | upstream_gene_variant | 1.0 |
| gyrA | 6862 | c.-440C>G | upstream_gene_variant | 1.0 |
| gyrA | 6865 | c.-437G>T | upstream_gene_variant | 1.0 |
| gyrA | 6869 | c.-433T>C | upstream_gene_variant | 1.0 |
| gyrA | 6877 | c.-425G>C | upstream_gene_variant | 1.0 |
| gyrA | 6878 | c.-424T>C | upstream_gene_variant | 1.0 |
| gyrA | 6889 | c.-413G>C | upstream_gene_variant | 1.0 |
| gyrA | 6904 | c.-398C>G | upstream_gene_variant | 1.0 |
| gyrA | 6916 | c.-386G>A | upstream_gene_variant | 1.0 |
| gyrA | 6919 | c.-383T>C | upstream_gene_variant | 1.0 |
| gyrA | 6925 | c.-377T>C | upstream_gene_variant | 1.0 |
| gyrA | 6926 | c.-376T>C | upstream_gene_variant | 1.0 |
| gyrA | 6931 | c.-371A>G | upstream_gene_variant | 1.0 |
| gyrA | 6934 | c.-368A>G | upstream_gene_variant | 0.67 |
| gyrA | 6949 | c.-353A>G | upstream_gene_variant | 0.67 |
| gyrA | 6950 | c.-352_-350delCTCinsTTG | upstream_gene_variant | 0.67 |
| gyrA | 7480 | p.Phe60Tyr | missense_variant | 1.0 |
| gyrA | 7484 | c.183T>C | synonymous_variant | 1.0 |
| gyrA | 7490 | c.189C>G | synonymous_variant | 1.0 |
| gyrA | 7496 | c.195C>A | synonymous_variant | 1.0 |
| gyrA | 7523 | c.222C>G | synonymous_variant | 1.0 |
| gyrA | 7532 | c.231T>G | synonymous_variant | 1.0 |
| gyrA | 7559 | c.258G>C | synonymous_variant | 1.0 |
| gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
| gyrA | 7587 | c.286C>T | synonymous_variant | 1.0 |
| gyrA | 7607 | c.306C>G | synonymous_variant | 1.0 |
| gyrA | 7619 | c.318C>G | synonymous_variant | 1.0 |
| gyrA | 7626 | c.325C>T | synonymous_variant | 1.0 |
| gyrA | 7631 | c.330G>C | synonymous_variant | 1.0 |
| gyrA | 7637 | c.336C>G | synonymous_variant | 1.0 |
| gyrA | 7763 | c.462T>G | synonymous_variant | 1.0 |
| gyrA | 7784 | c.483A>G | synonymous_variant | 1.0 |
| gyrA | 7787 | c.486G>A | synonymous_variant | 1.0 |
| gyrA | 7790 | c.489G>A | synonymous_variant | 1.0 |
| gyrA | 7799 | c.498A>G | synonymous_variant | 1.0 |
| gyrA | 7832 | c.531G>C | synonymous_variant | 1.0 |
| gyrA | 7835 | c.534A>C | synonymous_variant | 1.0 |
| gyrA | 7841 | c.540C>T | synonymous_variant | 1.0 |
| gyrA | 7859 | c.558A>G | synonymous_variant | 1.0 |
| gyrA | 7865 | c.564T>C | synonymous_variant | 1.0 |
| gyrA | 7871 | c.570G>C | synonymous_variant | 1.0 |
| gyrA | 7886 | c.585T>C | synonymous_variant | 1.0 |
| gyrA | 7892 | c.591G>C | synonymous_variant | 1.0 |
| gyrA | 7898 | p.Asp199Glu | missense_variant | 1.0 |
| gyrA | 8516 | c.1215T>C | synonymous_variant | 0.67 |
| gyrA | 8519 | c.1218A>G | synonymous_variant | 0.67 |
| gyrA | 8522 | c.1221G>C | synonymous_variant | 0.67 |
| gyrA | 8546 | c.1245T>C | synonymous_variant | 0.67 |
| gyrA | 8555 | c.1254G>A | synonymous_variant | 1.0 |
| gyrA | 8588 | c.1287G>A | synonymous_variant | 1.0 |
| gyrA | 8603 | c.1302A>C | synonymous_variant | 1.0 |
| gyrA | 8714 | c.1413A>G | synonymous_variant | 1.0 |
| gyrA | 8717 | c.1416C>G | synonymous_variant | 1.0 |
| gyrA | 8729 | c.1428T>C | synonymous_variant | 1.0 |
| gyrA | 8732 | c.1431G>C | synonymous_variant | 1.0 |
| gyrA | 8747 | c.1446A>G | synonymous_variant | 1.0 |
| gyrA | 8756 | c.1455A>G | synonymous_variant | 1.0 |
| gyrA | 8762 | c.1461G>C | synonymous_variant | 1.0 |
| gyrA | 8765 | p.Asp488Glu | missense_variant | 1.0 |
| gyrA | 8767 | p.Arg489Lys | missense_variant | 1.0 |
| gyrA | 8783 | c.1482G>T | synonymous_variant | 1.0 |
| gyrA | 8786 | c.1485T>C | synonymous_variant | 1.0 |
| gyrA | 8790 | c.1489C>A | synonymous_variant | 1.0 |
| gyrA | 8796 | p.Ile499Val | missense_variant | 1.0 |
| gyrA | 8810 | c.1509A>C | synonymous_variant | 1.0 |
| gyrA | 8813 | p.Asp504Glu | missense_variant | 1.0 |
| gyrA | 8818 | p.Ser506Asn | missense_variant | 1.0 |
| gyrA | 8829 | c.1528T>C | synonymous_variant | 1.0 |
| gyrA | 8852 | c.1551T>C | synonymous_variant | 1.0 |
| gyrA | 8858 | c.1557T>C | synonymous_variant | 1.0 |
| gyrA | 8867 | c.1566A>G | synonymous_variant | 1.0 |
| gyrA | 8873 | c.1572A>C | synonymous_variant | 1.0 |
| gyrA | 8882 | c.1581G>A | synonymous_variant | 1.0 |
| gyrA | 8900 | c.1599G>C | synonymous_variant | 0.75 |
| gyrA | 8903 | c.1602T>C | synonymous_variant | 0.8 |
| gyrA | 8939 | c.1638T>C | synonymous_variant | 0.75 |
| gyrA | 8942 | c.1641G>C | synonymous_variant | 0.75 |
| gyrA | 8945 | c.1644G>C | synonymous_variant | 0.75 |
| gyrA | 8946 | c.1645_1647delTTGinsCTC | synonymous_variant | 0.75 |
| gyrA | 8967 | p.Ala556Arg | missense_variant | 0.75 |
| gyrA | 8981 | c.1680G>C | synonymous_variant | 0.75 |
| gyrA | 8982 | p.Cys561Ser | missense_variant | 0.75 |
| gyrA | 8987 | c.1686C>G | synonymous_variant | 0.75 |
| gyrA | 8990 | c.1689C>G | synonymous_variant | 0.75 |
| gyrA | 8996 | c.1695T>C | synonymous_variant | 0.75 |
| gyrA | 8998 | p.Leu566Trp | missense_variant | 0.75 |
| gyrA | 9017 | c.1716C>G | synonymous_variant | 0.75 |
| gyrA | 9023 | c.1722A>C | synonymous_variant | 0.67 |
| gyrA | 9026 | c.1725G>C | synonymous_variant | 0.5 |
| gyrA | 9029 | c.1728T>C | synonymous_variant | 0.5 |
| gyrA | 9035 | c.1734G>C | synonymous_variant | 0.5 |
| gyrA | 9191 | c.1890G>C | synonymous_variant | 1.0 |
| gyrA | 9200 | c.1899A>G | synonymous_variant | 1.0 |
| gyrA | 9204 | p.Ser635Thr | missense_variant | 1.0 |
| gyrA | 9215 | c.1914C>G | synonymous_variant | 1.0 |
| gyrA | 9230 | c.1929T>C | synonymous_variant | 1.0 |
| gyrA | 9233 | c.1932C>G | synonymous_variant | 1.0 |
| gyrA | 9242 | c.1941A>C | synonymous_variant | 1.0 |
| gyrA | 9252 | p.Val651Ile | missense_variant | 1.0 |
| gyrA | 9275 | c.1974G>A | synonymous_variant | 1.0 |
| gyrA | 9278 | c.1977G>C | synonymous_variant | 1.0 |
| gyrA | 9284 | c.1983T>C | synonymous_variant | 1.0 |
| gyrA | 9287 | c.1986G>C | synonymous_variant | 1.0 |
| gyrA | 9296 | c.1995T>C | synonymous_variant | 1.0 |
| gyrA | 9300 | p.Ala667Ser | missense_variant | 0.75 |
| gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
| gyrA | 9308 | p.Asp669Glu | missense_variant | 0.6 |
| gyrA | 9329 | c.2028C>G | synonymous_variant | 0.6 |
| gyrA | 9335 | c.2034G>C | synonymous_variant | 0.6 |
| gyrA | 9443 | c.2142G>C | synonymous_variant | 0.33 |
| gyrA | 9452 | c.2151G>T | synonymous_variant | 0.4 |
| gyrA | 9455 | c.2154T>C | synonymous_variant | 0.4 |
| gyrA | 9458 | c.2157A>G | synonymous_variant | 0.5 |
| gyrA | 9467 | c.2166T>C | synonymous_variant | 0.5 |
| gyrA | 9479 | c.2178G>A | synonymous_variant | 0.5 |
| gyrA | 9485 | c.2184A>C | synonymous_variant | 0.5 |
| gyrA | 9488 | c.2187G>C | synonymous_variant | 0.5 |
| gyrA | 9494 | c.2193T>C | synonymous_variant | 0.67 |
| gyrA | 9497 | c.2196G>C | synonymous_variant | 0.67 |
| gyrA | 9500 | c.2199A>G | synonymous_variant | 0.67 |
| gyrA | 9503 | c.2202T>G | synonymous_variant | 0.67 |
| gyrA | 9518 | c.2217A>G | synonymous_variant | 1.0 |
| gyrA | 9521 | c.2220C>T | synonymous_variant | 1.0 |
| gyrA | 9565 | p.Tyr755Phe | missense_variant | 1.0 |
| gyrA | 9572 | c.2271C>T | synonymous_variant | 1.0 |
| fgd1 | 491226 | c.444C>G | synonymous_variant | 1.0 |
| fgd1 | 491232 | c.450T>C | synonymous_variant | 1.0 |
| fgd1 | 491241 | p.Asp153Glu | missense_variant | 1.0 |
| fgd1 | 491244 | c.462T>C | synonymous_variant | 1.0 |
| fgd1 | 491259 | c.477T>C | synonymous_variant | 1.0 |
| fgd1 | 491277 | c.495G>C | synonymous_variant | 1.0 |
| fgd1 | 491283 | p.Asp167Glu | missense_variant | 1.0 |
| fgd1 | 491286 | c.504G>C | synonymous_variant | 1.0 |
| fgd1 | 491296 | p.Val172Ile | missense_variant | 1.0 |
| fgd1 | 491302 | p.Ile174Val | missense_variant | 1.0 |
| fgd1 | 491316 | c.534C>G | synonymous_variant | 1.0 |
| fgd1 | 491322 | c.540G>C | synonymous_variant | 1.0 |
| fgd1 | 491331 | c.549G>A | synonymous_variant | 1.0 |
| mshA | 575156 | c.-192G>C | upstream_gene_variant | 1.0 |
| mshA | 575159 | c.-189C>G | upstream_gene_variant | 1.0 |
| mshA | 575162 | c.-186T>C | upstream_gene_variant | 1.0 |
| ccsA | 620198 | p.Gln103Leu | missense_variant | 1.0 |
| ccsA | 620204 | p.Val105Ala | missense_variant | 1.0 |
| ccsA | 620241 | c.351C>G | synonymous_variant | 1.0 |
| ccsA | 620245 | p.Leu119Met | missense_variant | 1.0 |
| ccsA | 620249 | p.Ser120Cys | missense_variant | 1.0 |
| ccsA | 620256 | c.366C>G | synonymous_variant | 1.0 |
| ccsA | 620257 | p.Ile123Leu | missense_variant | 1.0 |
| ccsA | 620269 | p.Val127Phe | missense_variant | 1.0 |
| ccsA | 620283 | c.393T>C | synonymous_variant | 1.0 |
| ccsA | 620284 | p.Ala132Pro | missense_variant | 1.0 |
| ccsA | 620288 | p.Arg133Gln | missense_variant | 1.0 |
| ccsA | 620295 | c.405G>C | synonymous_variant | 1.0 |
| ccsA | 620319 | c.429C>G | synonymous_variant | 1.0 |
| rpoB | 760059 | p.Tyr85Asp | missense_variant | 1.0 |
| rpoB | 760067 | c.261G>C | synonymous_variant | 1.0 |
| rpoB | 760070 | c.264T>G | synonymous_variant | 1.0 |
| rpoB | 760079 | c.273G>A | synonymous_variant | 1.0 |
| rpoB | 760091 | c.285G>C | synonymous_variant | 1.0 |
| rpoB | 760101 | c.295T>C | synonymous_variant | 1.0 |
| rpoB | 760112 | c.306T>C | synonymous_variant | 1.0 |
| rpoB | 760118 | c.312T>G | synonymous_variant | 1.0 |
| rpoB | 760130 | p.Asp108Glu | missense_variant | 1.0 |
| rpoB | 760136 | c.330G>A | synonymous_variant | 1.0 |
| rpoB | 760139 | c.333A>G | synonymous_variant | 1.0 |
| rpoB | 760142 | c.336C>G | synonymous_variant | 1.0 |
| rpoB | 760181 | c.375T>C | synonymous_variant | 1.0 |
| rpoB | 760184 | c.378A>G | synonymous_variant | 1.0 |
| rpoB | 760223 | c.417T>C | synonymous_variant | 1.0 |
| rpoB | 760235 | c.429T>C | synonymous_variant | 1.0 |
| rpoB | 760253 | c.447T>C | synonymous_variant | 1.0 |
| rpoB | 760283 | c.477G>C | synonymous_variant | 1.0 |
| rpoB | 760307 | c.501T>C | synonymous_variant | 1.0 |
| rpoB | 760310 | c.504G>C | synonymous_variant | 1.0 |
| rpoB | 760313 | c.507G>C | synonymous_variant | 1.0 |
| rpoB | 760340 | c.534G>C | synonymous_variant | 1.0 |
| rpoB | 760343 | c.537G>C | synonymous_variant | 1.0 |
| rpoB | 760361 | c.555T>C | synonymous_variant | 1.0 |
| rpoB | 760376 | p.Asp190Glu | missense_variant | 1.0 |
| rpoB | 760380 | p.Thr192Leu | missense_variant | 1.0 |
| rpoB | 760406 | c.600G>C | synonymous_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 | 760591 | p.Val262Ala | missense_variant | 1.0 |
| rpoB | 760611 | c.805T>C | synonymous_variant | 1.0 |
| rpoB | 760634 | c.828T>C | synonymous_variant | 1.0 |
| rpoB | 760646 | c.840C>A | 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 | 760724 | c.918T>C | synonymous_variant | 1.0 |
| rpoB | 760730 | c.924T>C | synonymous_variant | 1.0 |
| rpoB | 760919 | c.1113C>G | synonymous_variant | 1.0 |
| rpoB | 760925 | c.1119T>C | synonymous_variant | 1.0 |
| rpoB | 760928 | c.1122G>C | synonymous_variant | 1.0 |
| rpoB | 760934 | c.1128C>G | synonymous_variant | 1.0 |
| rpoB | 760946 | c.1140A>G | synonymous_variant | 1.0 |
| rpoB | 760970 | c.1164G>C | synonymous_variant | 1.0 |
| rpoB | 760973 | c.1167G>C | synonymous_variant | 1.0 |
| rpoB | 760982 | c.1176G>C | synonymous_variant | 1.0 |
| rpoB | 760991 | c.1185G>C | synonymous_variant | 1.0 |
| rpoB | 761015 | c.1209G>C | synonymous_variant | 1.0 |
| rpoB | 761027 | c.1221A>G | synonymous_variant | 1.0 |
| rpoB | 761207 | c.1401C>T | synonymous_variant | 1.0 |
| rpoB | 761249 | c.1443A>G | synonymous_variant | 1.0 |
| rpoB | 761255 | c.1449T>G | synonymous_variant | 1.0 |
| rpoB | 761261 | c.1455G>T | synonymous_variant | 1.0 |
| rpoB | 761273 | c.1467T>C | synonymous_variant | 1.0 |
| rpoB | 761312 | c.1506G>C | synonymous_variant | 1.0 |
| rpoB | 761327 | c.1521A>G | synonymous_variant | 1.0 |
| rpoB | 761345 | c.1539G>C | synonymous_variant | 1.0 |
| rpoB | 761346 | p.Val514Ile | missense_variant | 1.0 |
| rpoB | 761999 | c.2193G>C | synonymous_variant | 1.0 |
| rpoB | 762038 | c.2232C>T | synonymous_variant | 1.0 |
| rpoB | 762053 | c.2247T>C | synonymous_variant | 1.0 |
| rpoB | 762065 | c.2259T>C | 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 | 762131 | c.2325C>G | synonymous_variant | 1.0 |
| rpoC | 762917 | c.-453C>G | upstream_gene_variant | 1.0 |
| rpoC | 762929 | c.-441G>C | upstream_gene_variant | 1.0 |
| rpoC | 762962 | c.-408C>T | upstream_gene_variant | 1.0 |
| rpoC | 762995 | c.-375G>C | upstream_gene_variant | 1.0 |
| rpoC | 763028 | c.-342T>C | upstream_gene_variant | 1.0 |
| rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
| rpoC | 763034 | c.-336C>G | upstream_gene_variant | 1.0 |
| rpoC | 763040 | c.-330C>G | upstream_gene_variant | 1.0 |
| rpoC | 763546 | c.177A>G | synonymous_variant | 1.0 |
| rpoC | 763570 | c.201G>C | synonymous_variant | 1.0 |
| rpoC | 763573 | c.204G>C | synonymous_variant | 1.0 |
| rpoC | 763600 | c.231C>T | synonymous_variant | 1.0 |
| rpoC | 763813 | c.444C>G | synonymous_variant | 1.0 |
| rpoC | 763835 | p.Ala156Met | missense_variant | 1.0 |
| rpoC | 763855 | c.486C>T | synonymous_variant | 1.0 |
| rpoC | 763858 | c.489A>G | synonymous_variant | 1.0 |
| rpoC | 763872 | p.Gly168Ala | missense_variant | 1.0 |
| rpoC | 763876 | p.Glu169Asp | missense_variant | 1.0 |
| rpoC | 763879 | c.510A>G | synonymous_variant | 1.0 |
| rpoC | 763888 | c.519G>C | synonymous_variant | 1.0 |
| rpoC | 763894 | c.525A>G | synonymous_variant | 1.0 |
| rpoC | 763912 | c.543G>C | synonymous_variant | 1.0 |
| rpoC | 763945 | c.576T>C | synonymous_variant | 1.0 |
| rpoC | 763951 | c.582G>C | synonymous_variant | 1.0 |
| rpoC | 763960 | c.591T>C | synonymous_variant | 1.0 |
| rpoC | 763991 | p.Ile208Leu | missense_variant | 1.0 |
| rpoC | 763996 | c.627T>G | synonymous_variant | 1.0 |
| rpoC | 764005 | c.636G>C | synonymous_variant | 1.0 |
| rpoC | 764011 | c.642T>C | synonymous_variant | 1.0 |
| rpoC | 764024 | c.655T>C | synonymous_variant | 1.0 |
| rpoC | 764044 | c.675T>C | synonymous_variant | 1.0 |
| rpoC | 764059 | c.690G>C | synonymous_variant | 1.0 |
| rpoC | 764083 | c.714A>G | synonymous_variant | 1.0 |
| rpoC | 764365 | c.996C>T | synonymous_variant | 1.0 |
| rpoC | 764380 | c.1011G>C | synonymous_variant | 1.0 |
| rpoC | 764381 | c.1012_1013delTCinsAG | synonymous_variant | 1.0 |
| rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 1.0 |
| rpoC | 764405 | c.1036A>C | synonymous_variant | 1.0 |
| rpoC | 764410 | c.1041G>C | synonymous_variant | 1.0 |
| rpoC | 764431 | c.1062G>C | synonymous_variant | 1.0 |
| rpoC | 764434 | c.1065A>G | synonymous_variant | 1.0 |
| rpoC | 764695 | c.1326T>G | synonymous_variant | 1.0 |
| rpoC | 764737 | c.1368G>C | synonymous_variant | 1.0 |
| rpoC | 764749 | c.1380G>C | synonymous_variant | 1.0 |
| rpoC | 764752 | c.1383G>C | synonymous_variant | 1.0 |
| rpoC | 764764 | c.1395T>C | synonymous_variant | 1.0 |
| rpoC | 764803 | c.1434C>G | synonymous_variant | 1.0 |
| rpoC | 764809 | c.1440C>T | synonymous_variant | 1.0 |
| rpoC | 764815 | c.1446A>G | synonymous_variant | 1.0 |
| rpoC | 764827 | c.1458G>C | synonymous_variant | 1.0 |
| rpoC | 765277 | c.1908G>A | synonymous_variant | 1.0 |
| rpoC | 765283 | c.1914C>G | synonymous_variant | 1.0 |
| rpoC | 765292 | c.1923G>T | synonymous_variant | 1.0 |
| rpoC | 765298 | c.1929G>C | synonymous_variant | 1.0 |
| rpoC | 765300 | p.Val644Ala | missense_variant | 1.0 |
| rpoC | 765313 | c.1944C>G | synonymous_variant | 1.0 |
| rpoC | 765319 | c.1950A>G | synonymous_variant | 1.0 |
| rpoC | 765326 | p.His653Ala | missense_variant | 1.0 |
| rpoC | 765330 | p.Ser654Asn | missense_variant | 1.0 |
| rpoC | 765421 | c.2052C>G | synonymous_variant | 0.67 |
| rpoC | 765445 | c.2076G>T | synonymous_variant | 0.5 |
| rpoC | 765499 | c.2130C>G | synonymous_variant | 0.6 |
| rpoC | 765505 | c.2136C>G | synonymous_variant | 0.6 |
| rpoC | 765541 | c.2172C>G | synonymous_variant | 0.75 |
| rpoC | 765553 | c.2184C>T | synonymous_variant | 0.75 |
| rpoC | 765556 | c.2187G>C | synonymous_variant | 0.75 |
| rpoC | 765559 | c.2190G>C | synonymous_variant | 0.67 |
| rpoC | 765583 | c.2214G>T | synonymous_variant | 1.0 |
| rpoC | 765625 | c.2256C>G | synonymous_variant | 1.0 |
| rpoC | 765628 | c.2259G>C | synonymous_variant | 1.0 |
| rpoC | 765631 | p.Asp754Glu | missense_variant | 1.0 |
| rpoC | 765655 | c.2286T>C | synonymous_variant | 1.0 |
| rpoC | 765700 | c.2331T>C | synonymous_variant | 1.0 |
| rpoC | 765734 | c.2365T>C | synonymous_variant | 1.0 |
| rpoC | 765739 | c.2370G>C | synonymous_variant | 1.0 |
| rpoC | 765751 | c.2382C>G | synonymous_variant | 1.0 |
| rpoC | 765772 | c.2403C>G | synonymous_variant | 1.0 |
| rpoC | 765784 | c.2415C>G | synonymous_variant | 1.0 |
| rpoC | 765793 | c.2424C>G | synonymous_variant | 1.0 |
| rpoC | 765796 | c.2427C>T | synonymous_variant | 1.0 |
| rpoC | 765811 | c.2442T>C | synonymous_variant | 1.0 |
| rpoC | 765814 | c.2445A>G | synonymous_variant | 1.0 |
| rpoC | 765826 | c.2457T>C | synonymous_variant | 1.0 |
| rpoC | 765883 | c.2514C>G | synonymous_variant | 1.0 |
| rpoC | 765886 | c.2517C>G | synonymous_variant | 1.0 |
| rpoC | 765892 | c.2523T>C | synonymous_variant | 1.0 |
| rpoC | 765937 | c.2568T>C | synonymous_variant | 1.0 |
| rpoC | 765947 | c.2578T>C | synonymous_variant | 1.0 |
| rpoC | 765979 | c.2610C>G | synonymous_variant | 1.0 |
| rpoC | 765982 | c.2613C>T | synonymous_variant | 1.0 |
| rpoC | 766010 | c.2641_2642delTCinsAG | synonymous_variant | 1.0 |
| rpoC | 766522 | c.3153C>G | synonymous_variant | 1.0 |
| rpoC | 766528 | c.3159T>C | synonymous_variant | 1.0 |
| rpoC | 766530 | p.Arg1054Gln | missense_variant | 1.0 |
| rpoC | 766573 | c.3204T>C | synonymous_variant | 1.0 |
| rpoC | 766582 | c.3213C>G | synonymous_variant | 1.0 |
| rpoC | 766583 | p.Gly1072Ser | missense_variant | 1.0 |
| rpoC | 766591 | c.3222A>G | synonymous_variant | 1.0 |
| rpoC | 766594 | c.3225G>C | synonymous_variant | 1.0 |
| rpoC | 766607 | p.Ile1080Leu | missense_variant | 1.0 |
| rpoC | 766630 | c.3261G>T | synonymous_variant | 1.0 |
| rpoC | 766645 | c.3276A>G | synonymous_variant | 1.0 |
| rpoC | 766651 | c.3282T>C | synonymous_variant | 1.0 |
| rpoC | 766657 | c.3288A>G | synonymous_variant | 1.0 |
| rpoC | 766666 | c.3297C>G | synonymous_variant | 1.0 |
| rpoC | 766672 | c.3303T>C | synonymous_variant | 1.0 |
| rpoC | 766708 | c.3339A>G | synonymous_variant | 1.0 |
| rpoC | 766726 | c.3357T>C | synonymous_variant | 1.0 |
| rpoC | 766738 | c.3369G>C | synonymous_variant | 1.0 |
| rpoC | 766765 | c.3396A>C | synonymous_variant | 1.0 |
| rpoC | 766774 | c.3405T>C | synonymous_variant | 1.0 |
| rpoC | 766801 | c.3432C>A | synonymous_variant | 1.0 |
| rpoC | 766804 | c.3435A>G | synonymous_variant | 1.0 |
| rpoC | 766861 | c.3492G>C | synonymous_variant | 1.0 |
| rpoC | 766864 | c.3495G>C | synonymous_variant | 1.0 |
| rpoC | 766882 | c.3513C>T | synonymous_variant | 1.0 |
| rpoC | 766894 | c.3525T>C | synonymous_variant | 1.0 |
| rpoC | 766895 | c.3526T>C | synonymous_variant | 1.0 |
| rpoC | 766900 | c.3531T>C | synonymous_variant | 1.0 |
| rpoC | 766903 | c.3534C>T | synonymous_variant | 1.0 |
| rpoC | 766996 | c.3627C>T | synonymous_variant | 1.0 |
| rpoC | 767002 | c.3633G>C | synonymous_variant | 1.0 |
| rpoC | 767033 | c.3664_3666delTCGinsAGC | synonymous_variant | 1.0 |
| rpoC | 767059 | c.3690T>G | synonymous_variant | 1.0 |
| rpoC | 767062 | c.3693C>G | synonymous_variant | 1.0 |
| rpoC | 767098 | c.3729T>C | synonymous_variant | 1.0 |
| rpoC | 767104 | c.3735C>G | synonymous_variant | 1.0 |
| rpoC | 767105 | p.Asn1246Gln | missense_variant | 1.0 |
| rpoC | 767119 | c.3750A>G | synonymous_variant | 1.0 |
| rpoC | 767134 | c.3765C>A | synonymous_variant | 1.0 |
| rpoC | 767167 | c.3798C>G | synonymous_variant | 1.0 |
| rpoC | 767179 | c.3810C>T | synonymous_variant | 1.0 |
| rpoC | 767180 | p.Ala1271Gln | missense_variant | 1.0 |
| rpoC | 767191 | c.3822C>G | synonymous_variant | 1.0 |
| rpoC | 767203 | c.3834C>T | synonymous_variant | 1.0 |
| rpoC | 767206 | c.3837C>G | synonymous_variant | 1.0 |
| rpoC | 767209 | c.3840T>C | synonymous_variant | 1.0 |
| rpoC | 767212 | c.3843G>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 |
| mmpL5 | 777125 | c.1356C>T | synonymous_variant | 1.0 |
| mmpL5 | 777128 | c.1353A>G | synonymous_variant | 1.0 |
| mmpL5 | 777133 | p.Val450Ile | missense_variant | 1.0 |
| mmpL5 | 777143 | c.1338G>A | synonymous_variant | 1.0 |
| mmpL5 | 777146 | c.1335C>G | synonymous_variant | 1.0 |
| mmpL5 | 777149 | c.1332C>T | synonymous_variant | 1.0 |
| mmpL5 | 777158 | c.1323C>G | synonymous_variant | 1.0 |
| mmpL5 | 777170 | c.1311T>C | synonymous_variant | 1.0 |
| mmpL5 | 777173 | c.1308C>G | synonymous_variant | 1.0 |
| mmpL5 | 777176 | p.Glu435Asp | missense_variant | 1.0 |
| mmpL5 | 777185 | c.1296G>C | synonymous_variant | 1.0 |
| mmpL5 | 777188 | c.1293T>C | synonymous_variant | 1.0 |
| mmpL5 | 777191 | c.1290C>T | synonymous_variant | 1.0 |
| mmpL5 | 777194 | c.1287A>G | synonymous_variant | 1.0 |
| mmpL5 | 777200 | c.1281C>G | synonymous_variant | 1.0 |
| mmpL5 | 777206 | c.1275A>T | synonymous_variant | 1.0 |
| mmpL5 | 777215 | c.1266C>G | synonymous_variant | 1.0 |
| mmpL5 | 777245 | c.1236G>C | synonymous_variant | 1.0 |
| mmpL5 | 777251 | c.1230C>G | synonymous_variant | 1.0 |
| mmpL5 | 777254 | c.1227G>C | synonymous_variant | 1.0 |
| rpsL | 781715 | c.156T>C | synonymous_variant | 1.0 |
| rpsL | 781718 | c.159C>G | synonymous_variant | 1.0 |
| rpsL | 781728 | c.169T>C | synonymous_variant | 1.0 |
| rpsL | 781736 | c.177T>C | 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 | 781808 | c.249C>T | synonymous_variant | 1.0 |
| rpsL | 781811 | c.252C>T | synonymous_variant | 1.0 |
| rpsL | 781817 | c.258G>A | synonymous_variant | 1.0 |
| rpsL | 781820 | c.261G>C | synonymous_variant | 1.0 |
| rpsL | 781892 | c.333A>G | synonymous_variant | 1.0 |
| rpsL | 781898 | c.339A>C | synonymous_variant | 1.0 |
| rpsL | 781916 | c.357T>C | synonymous_variant | 1.0 |
| rpsL | 781929 | p.Gly124Ser | missense_variant | 1.0 |
| rplC | 801367 | p.Ala187Thr | missense_variant | 1.0 |
| rplC | 801396 | c.588T>C | synonymous_variant | 1.0 |
| rplC | 801402 | c.594T>C | synonymous_variant | 1.0 |
| rplC | 801405 | c.597T>C | synonymous_variant | 1.0 |
| rplC | 801420 | c.612A>G | synonymous_variant | 1.0 |
| rplC | 801423 | c.615G>C | synonymous_variant | 1.0 |
| rplC | 801426 | c.618C>G | synonymous_variant | 1.0 |
| rplC | 801438 | c.630T>C | synonymous_variant | 1.0 |
| rplC | 801461 | c.653G>A | splice_region_variant&stop_retained_variant | 1.0 |
| fbiC | 1304778 | c.1848T>C | synonymous_variant | 1.0 |
| fbiC | 1304784 | c.1854T>C | synonymous_variant | 1.0 |
| fbiC | 1304787 | c.1857T>C | synonymous_variant | 1.0 |
| fbiC | 1304808 | c.1878C>G | synonymous_variant | 1.0 |
| fbiC | 1304811 | c.1881C>G | synonymous_variant | 1.0 |
| fbiC | 1304817 | c.1887T>C | synonymous_variant | 1.0 |
| fbiC | 1304826 | c.1896G>C | synonymous_variant | 1.0 |
| fbiC | 1304829 | c.1899T>C | synonymous_variant | 1.0 |
| fbiC | 1304832 | c.1902C>G | synonymous_variant | 1.0 |
| fbiC | 1304847 | c.1917C>G | synonymous_variant | 1.0 |
| fbiC | 1304856 | c.1926C>G | synonymous_variant | 1.0 |
| fbiC | 1304875 | p.Ile649Val | missense_variant | 1.0 |
| fbiC | 1304880 | c.1950C>G | synonymous_variant | 1.0 |
| fbiC | 1304896 | c.1966C>T | synonymous_variant | 1.0 |
| fbiC | 1304916 | c.1986T>C | synonymous_variant | 1.0 |
| fbiC | 1304994 | c.2064A>G | synonymous_variant | 1.0 |
| fbiC | 1304995 | p.Leu689Glu | missense_variant | 1.0 |
| fbiC | 1305006 | p.Glu692Asp | missense_variant | 1.0 |
| atpE | 1461197 | c.153A>G | synonymous_variant | 1.0 |
| atpE | 1461219 | c.175T>C | synonymous_variant | 0.67 |
| atpE | 1461224 | c.180T>C | synonymous_variant | 0.67 |
| atpE | 1461233 | c.189A>C | synonymous_variant | 0.67 |
| rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473899 | n.242A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473937 | n.280C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473944 | n.287G>A | non_coding_transcript_exon_variant | 1.0 |
| fabG1 | 1673710 | p.Leu91Ile | missense_variant | 1.0 |
| inhA | 1673715 | c.-487C>G | upstream_gene_variant | 1.0 |
| fabG1 | 1673716 | p.Ala93Lys | missense_variant | 1.0 |
| inhA | 1673724 | c.-478A>C | upstream_gene_variant | 1.0 |
| inhA | 1673730 | c.-472C>G | upstream_gene_variant | 1.0 |
| fabG1 | 1673733 | p.Met98Ile | missense_variant | 1.0 |
| inhA | 1673748 | c.-454A>G | upstream_gene_variant | 1.0 |
| fabG1 | 1673749 | p.Lys104Arg | missense_variant | 1.0 |
| fabG1 | 1673758 | p.Lys107Glu | missense_variant | 1.0 |
| inhA | 1673772 | c.-430C>G | upstream_gene_variant | 1.0 |
| rpsA | 1833661 | c.120A>G | synonymous_variant | 0.5 |
| rpsA | 1833664 | c.123C>G | synonymous_variant | 0.5 |
| rpsA | 1833667 | c.126C>G | synonymous_variant | 0.5 |
| rpsA | 1833721 | c.180A>G | synonymous_variant | 0.5 |
| rpsA | 1833727 | c.186G>C | synonymous_variant | 0.5 |
| rpsA | 1833742 | c.201A>G | synonymous_variant | 0.67 |
| rpsA | 1833745 | c.204G>C | synonymous_variant | 0.67 |
| rpsA | 1833754 | c.213G>A | synonymous_variant | 0.67 |
| rpsA | 1833760 | c.219C>T | synonymous_variant | 0.67 |
| rpsA | 1833928 | c.387G>C | synonymous_variant | 1.0 |
| rpsA | 1833940 | c.399C>G | synonymous_variant | 1.0 |
| rpsA | 1833970 | c.429G>C | synonymous_variant | 1.0 |
| rpsA | 1833979 | c.438T>C | synonymous_variant | 1.0 |
| rpsA | 1833991 | c.450C>G | synonymous_variant | 1.0 |
| rpsA | 1834000 | c.459G>C | synonymous_variant | 1.0 |
| rpsA | 1834015 | c.474G>C | synonymous_variant | 1.0 |
| rpsA | 1834021 | c.480C>T | synonymous_variant | 1.0 |
| rpsA | 1834030 | c.489C>G | synonymous_variant | 1.0 |
| rpsA | 1834240 | c.699T>C | synonymous_variant | 1.0 |
| rpsA | 1834249 | c.708T>C | synonymous_variant | 1.0 |
| rpsA | 1834261 | c.720A>G | synonymous_variant | 1.0 |
| rpsA | 1834262 | c.721_723delTCGinsAGC | synonymous_variant | 1.0 |
| rpsA | 1834294 | c.753G>C | synonymous_variant | 1.0 |
| rpsA | 1834297 | c.756C>T | synonymous_variant | 1.0 |
| rpsA | 1834303 | c.762T>G | synonymous_variant | 1.0 |
| rpsA | 1834306 | c.765T>C | synonymous_variant | 1.0 |
| rpsA | 1834348 | c.807T>C | synonymous_variant | 1.0 |
| rpsA | 1834351 | c.810G>A | synonymous_variant | 1.0 |
| rpsA | 1834366 | c.825A>G | synonymous_variant | 1.0 |
| rpsA | 1834411 | c.870T>G | synonymous_variant | 1.0 |
| rpsA | 1834417 | c.876G>C | synonymous_variant | 1.0 |
| rpsA | 1834423 | c.882G>C | synonymous_variant | 1.0 |
| rpsA | 1834435 | c.894G>C | synonymous_variant | 1.0 |
| rpsA | 1834451 | c.910T>C | synonymous_variant | 1.0 |
| rpsA | 1834456 | c.915T>G | synonymous_variant | 1.0 |
| rpsA | 1834465 | c.924T>C | synonymous_variant | 1.0 |
| rpsA | 1834468 | c.927A>G | synonymous_variant | 1.0 |
| rpsA | 1834489 | c.948T>C | synonymous_variant | 1.0 |
| rpsA | 1834528 | c.987T>C | synonymous_variant | 1.0 |
| rpsA | 1834540 | c.999G>C | synonymous_variant | 1.0 |
| rpsA | 1834546 | c.1005T>C | synonymous_variant | 1.0 |
| rpsA | 1834555 | c.1014T>C | synonymous_variant | 1.0 |
| rpsA | 1834606 | c.1065C>G | synonymous_variant | 1.0 |
| rpsA | 1834609 | c.1068T>C | synonymous_variant | 1.0 |
| rpsA | 1834633 | c.1092A>G | synonymous_variant | 1.0 |
| rpsA | 1834639 | c.1098T>C | synonymous_variant | 1.0 |
| rpsA | 1834645 | c.1104C>T | synonymous_variant | 1.0 |
| rpsA | 1834690 | c.1149T>C | synonymous_variant | 1.0 |
| rpsA | 1834732 | c.1191T>C | synonymous_variant | 1.0 |
| rpsA | 1834738 | c.1197A>G | synonymous_variant | 1.0 |
| rpsA | 1834753 | c.1212T>C | synonymous_variant | 1.0 |
| rpsA | 1834759 | c.1218A>C | synonymous_variant | 1.0 |
| katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
| kasA | 2518146 | p.Phe11Tyr | missense_variant | 1.0 |
| kasA | 2518174 | c.60A>G | synonymous_variant | 1.0 |
| kasA | 2518187 | p.Ile25Val | missense_variant | 1.0 |
| kasA | 2518190 | p.Ser26Ala | missense_variant | 1.0 |
| kasA | 2518220 | c.106C>T | synonymous_variant | 1.0 |
| kasA | 2518234 | c.120G>A | synonymous_variant | 1.0 |
| kasA | 2518248 | p.Ala45Val | missense_variant | 1.0 |
| kasA | 2518265 | p.Val51Ile | missense_variant | 1.0 |
| kasA | 2518279 | c.165T>C | synonymous_variant | 1.0 |
| kasA | 2518282 | c.168A>G | synonymous_variant | 1.0 |
| kasA | 2518283 | p.Ala57Pro | missense_variant | 1.0 |
| kasA | 2518588 | c.474T>G | synonymous_variant | 1.0 |
| kasA | 2518591 | c.477G>C | synonymous_variant | 1.0 |
| kasA | 2518597 | c.483C>G | synonymous_variant | 1.0 |
| kasA | 2518609 | p.Met165Ile | missense_variant | 1.0 |
| kasA | 2518624 | c.510C>G | synonymous_variant | 1.0 |
| kasA | 2518627 | c.513T>C | synonymous_variant | 1.0 |
| kasA | 2518639 | c.525G>C | synonymous_variant | 1.0 |
| kasA | 2518651 | c.537C>G | synonymous_variant | 1.0 |
| kasA | 2518663 | c.549T>C | synonymous_variant | 1.0 |
| kasA | 2518671 | p.Val186Ala | missense_variant | 1.0 |
| kasA | 2518678 | c.564C>T | synonymous_variant | 1.0 |
| kasA | 2518688 | p.Val192Phe | missense_variant | 1.0 |
| thyX | 3067304 | c.642A>G | synonymous_variant | 1.0 |
| thyX | 3067316 | c.630A>G | synonymous_variant | 1.0 |
| thyX | 3067321 | c.625C>A | synonymous_variant | 1.0 |
| thyX | 3067349 | c.597G>C | synonymous_variant | 1.0 |
| thyX | 3067355 | c.591A>C | synonymous_variant | 1.0 |
| thyX | 3067367 | c.579G>A | 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 |
| ald | 3087767 | c.948G>C | synonymous_variant | 1.0 |
| ald | 3087770 | c.951G>C | synonymous_variant | 1.0 |
| ald | 3087779 | c.960T>C | synonymous_variant | 0.8 |
| ald | 3087781 | p.Val321Ala | missense_variant | 0.8 |
| ald | 3087788 | c.969G>A | synonymous_variant | 0.8 |
| ald | 3087791 | c.972T>G | synonymous_variant | 0.8 |
| ald | 3087799 | p.His327Arg | missense_variant | 0.8 |
| ald | 3087808 | p.Arg330Gln | missense_variant | 0.8 |
| ald | 3087825 | p.Asn336Asp | missense_variant | 1.0 |
| ald | 3087833 | c.1014A>T | synonymous_variant | 1.0 |
| ald | 3087836 | c.1017A>C | synonymous_variant | 1.0 |
| ald | 3087845 | c.1026T>G | synonymous_variant | 1.0 |
| ald | 3087860 | p.Glu347Asp | missense_variant | 1.0 |
| ald | 3087863 | c.1044G>C | synonymous_variant | 1.0 |
| ald | 3087867 | c.1048_1050delTTAinsCTG | synonymous_variant | 1.0 |
| ald | 3087899 | c.1080G>T | synonymous_variant | 1.0 |
| ald | 3087900 | p.Val361Leu | missense_variant | 1.0 |
| fprA | 3473809 | c.-198G>C | upstream_gene_variant | 1.0 |
| fprA | 3473812 | c.-195G>A | upstream_gene_variant | 1.0 |
| fprA | 3473843 | c.-164C>G | upstream_gene_variant | 1.0 |
| fprA | 3474171 | c.165G>C | synonymous_variant | 0.5 |
| fprA | 3474180 | c.174C>G | synonymous_variant | 0.5 |
| fprA | 3474204 | c.198A>G | synonymous_variant | 0.5 |
| fprA | 3474210 | c.204A>G | synonymous_variant | 0.5 |
| fprA | 3474216 | c.210G>C | synonymous_variant | 0.67 |
| fprA | 3474218 | p.Ala71Gly | missense_variant | 0.67 |
| fprA | 3474222 | c.216G>A | synonymous_variant | 0.67 |
| fprA | 3474225 | c.219C>T | synonymous_variant | 0.67 |
| fprA | 3474237 | c.231C>G | synonymous_variant | 0.67 |
| fprA | 3474249 | c.243T>C | synonymous_variant | 0.67 |
| fprA | 3474255 | c.249C>G | synonymous_variant | 0.67 |
| fprA | 3474258 | c.252C>G | synonymous_variant | 0.67 |
| fprA | 3474261 | c.255C>G | synonymous_variant | 0.67 |
| fprA | 3474270 | c.264C>G | synonymous_variant | 0.67 |
| fprA | 3474274 | p.Pro90Ala | missense_variant | 0.67 |
| fprA | 3474278 | p.Gly91Ala | missense_variant | 0.67 |
| fprA | 3474282 | c.276G>A | synonymous_variant | 0.67 |
| fprA | 3474285 | c.279C>G | synonymous_variant | 1.0 |
| fprA | 3474286 | p.Ser94Ala | missense_variant | 1.0 |
| fprA | 3474820 | p.Leu272Met | missense_variant | 0.67 |
| fprA | 3474825 | c.819C>T | synonymous_variant | 0.67 |
| fprA | 3474828 | c.822T>A | synonymous_variant | 0.67 |
| fprA | 3474847 | p.Lys281Asp | missense_variant | 0.67 |
| fprA | 3474850 | p.Arg282Gly | missense_variant | 0.67 |
| fprA | 3474855 | c.849A>G | synonymous_variant | 0.67 |
| fprA | 3474862 | p.Arg286Ser | missense_variant | 0.67 |
| fprA | 3474885 | c.879G>A | synonymous_variant | 0.67 |
| fprA | 3474892 | p.Ser296Thr | missense_variant | 0.67 |
| fprA | 3474899 | p.Gly298Ala | missense_variant | 0.67 |
| fprA | 3474902 | p.Ser299Asn | missense_variant | 0.67 |
| fprA | 3474909 | c.903A>G | synonymous_variant | 0.67 |
| fprA | 3474913 | p.Ala303Ser | missense_variant | 0.67 |
| fprA | 3474930 | c.924C>T | synonymous_variant | 0.67 |
| fprA | 3474948 | c.942A>G | synonymous_variant | 1.0 |
| fprA | 3474950 | p.Ala315Val | missense_variant | 1.0 |
| fprA | 3474960 | c.954C>G | synonymous_variant | 1.0 |
| fprA | 3474966 | c.960G>A | synonymous_variant | 1.0 |
| fbiB | 3641184 | c.-351T>C | upstream_gene_variant | 1.0 |
| fbiB | 3641187 | c.-348T>C | upstream_gene_variant | 1.0 |
| fbiA | 3641200 | p.Ile220Val | missense_variant | 1.0 |
| fbiB | 3641217 | c.-318C>G | upstream_gene_variant | 1.0 |
| fbiB | 3641226 | c.-309G>C | upstream_gene_variant | 1.0 |
| fbiB | 3641235 | c.-300G>C | upstream_gene_variant | 1.0 |
| fbiB | 3641244 | c.-291G>C | upstream_gene_variant | 1.0 |
| fbiA | 3641245 | p.Glu235Ser | missense_variant | 1.0 |
| fbiB | 3641250 | c.-285A>G | upstream_gene_variant | 1.0 |
| fbiB | 3641256 | c.-279A>G | upstream_gene_variant | 1.0 |
| fbiA | 3641260 | p.Ile240Val | missense_variant | 1.0 |
| fbiB | 3641286 | c.-249C>T | upstream_gene_variant | 1.0 |
| fbiA | 3641288 | p.Glu249Gly | missense_variant | 1.0 |
| fbiB | 3641295 | c.-240G>C | upstream_gene_variant | 1.0 |
| fbiA | 3641314 | p.Thr258Ala | missense_variant | 1.0 |
| alr | 3840522 | p.Ile300Thr | missense_variant | 1.0 |
| alr | 3840527 | c.894A>C | synonymous_variant | 1.0 |
| alr | 3840536 | c.885T>C | synonymous_variant | 1.0 |
| alr | 3840547 | p.Gly292Ser | missense_variant | 1.0 |
| alr | 3840551 | c.870G>C | synonymous_variant | 1.0 |
| alr | 3840557 | c.864T>G | synonymous_variant | 1.0 |
| alr | 3840560 | c.861T>C | synonymous_variant | 1.0 |
| alr | 3840566 | c.855A>G | synonymous_variant | 1.0 |
| alr | 3840569 | c.852G>C | synonymous_variant | 1.0 |
| alr | 3840572 | c.849G>A | synonymous_variant | 1.0 |
| alr | 3840578 | c.843T>G | synonymous_variant | 1.0 |
| alr | 3840583 | p.Ala280Pro | missense_variant | 1.0 |
| alr | 3840584 | c.837T>C | synonymous_variant | 1.0 |
| alr | 3840593 | c.828C>G | synonymous_variant | 1.0 |
| alr | 3840620 | c.801T>C | synonymous_variant | 1.0 |
| alr | 3840626 | p.Ala265Glu | missense_variant | 1.0 |
| alr | 3840632 | c.789A>G | synonymous_variant | 1.0 |
| alr | 3840641 | c.780A>G | synonymous_variant | 0.67 |
| alr | 3840644 | c.777G>A | synonymous_variant | 0.67 |
| alr | 3840647 | c.774T>C | synonymous_variant | 0.67 |
| alr | 3840656 | p.Ile255Val | missense_variant | 0.67 |
| alr | 3840662 | c.759G>C | synonymous_variant | 0.67 |
| rpoA | 3877530 | c.978C>T | synonymous_variant | 1.0 |
| rpoA | 3877533 | c.975C>G | synonymous_variant | 1.0 |
| rpoA | 3877545 | c.963G>C | synonymous_variant | 1.0 |
| rpoA | 3877553 | p.Glu319Gln | missense_variant | 1.0 |
| rpoA | 3877557 | c.951C>G | synonymous_variant | 1.0 |
| rpoA | 3877587 | c.921A>G | synonymous_variant | 1.0 |
| rpoA | 3877613 | p.Ile299Val | missense_variant | 1.0 |
| rpoA | 3877656 | c.852T>C | synonymous_variant | 1.0 |
| rpoA | 3877668 | c.840A>G | synonymous_variant | 1.0 |
| rpoA | 3877677 | p.Ala277Ser | missense_variant | 1.0 |
| rpoA | 3877680 | c.828G>C | synonymous_variant | 1.0 |
| rpoA | 3877686 | c.822A>G | synonymous_variant | 1.0 |
| rpoA | 3877692 | c.816G>C | synonymous_variant | 1.0 |
| rpoA | 3877695 | c.813C>G | synonymous_variant | 1.0 |
| rpoA | 3877704 | c.804G>C | synonymous_variant | 1.0 |
| rpoA | 3877728 | c.780C>G | synonymous_variant | 1.0 |
| rpoA | 3877743 | c.765T>C | synonymous_variant | 1.0 |
| rpoA | 3877764 | c.744C>G | synonymous_variant | 1.0 |
| rpoA | 3877770 | c.738A>G | synonymous_variant | 1.0 |
| rpoA | 3877773 | c.735G>C | synonymous_variant | 1.0 |
| rpoA | 3877776 | c.732T>C | synonymous_variant | 1.0 |
| rpoA | 3877782 | c.726T>C | synonymous_variant | 1.0 |
| rpoA | 3877803 | c.705G>T | synonymous_variant | 1.0 |
| rpoA | 3877809 | c.699G>A | synonymous_variant | 1.0 |
| rpoA | 3877818 | c.690A>G | synonymous_variant | 1.0 |
| rpoA | 3878184 | c.324C>T | synonymous_variant | 1.0 |
| rpoA | 3878205 | c.303T>C | synonymous_variant | 1.0 |
| rpoA | 3878217 | c.291A>G | synonymous_variant | 0.67 |
| rpoA | 3878256 | c.252G>C | synonymous_variant | 0.75 |
| rpoA | 3878264 | p.Ser82Gly | missense_variant | 0.75 |
| rpoA | 3878284 | p.Glu75Ala | missense_variant | 0.75 |
| rpoA | 3878292 | c.216T>C | synonymous_variant | 0.8 |
| rpoA | 3878298 | c.210A>G | synonymous_variant | 0.8 |
| rpoA | 3878301 | c.207C>G | synonymous_variant | 0.67 |
| rpoA | 3878309 | p.Pro67Ala | missense_variant | 0.67 |
| rpoA | 3878310 | c.198G>C | synonymous_variant | 0.67 |
| rpoA | 3878313 | c.195G>C | synonymous_variant | 0.67 |
| rpoA | 3878322 | c.186A>G | synonymous_variant | 0.67 |
| rpoA | 3878331 | c.177A>G | synonymous_variant | 0.6 |
| rpoA | 3878334 | c.174T>C | synonymous_variant | 0.6 |
| rpoA | 3878337 | c.171T>C | synonymous_variant | 0.6 |
| rpoA | 3878346 | c.162T>C | synonymous_variant | 0.6 |
| rpoA | 3878364 | c.144A>C | synonymous_variant | 0.5 |
| rpoA | 3878379 | c.129G>C | synonymous_variant | 0.67 |
| rpoA | 3878385 | c.123C>G | synonymous_variant | 0.67 |
| rpoA | 3878388 | c.120C>G | synonymous_variant | 0.67 |
| rpoA | 3878391 | c.117T>C | synonymous_variant | 0.67 |
| clpC1 | 4038671 | c.2034T>C | synonymous_variant | 1.0 |
| clpC1 | 4038683 | c.2022T>C | synonymous_variant | 1.0 |
| clpC1 | 4038755 | c.1950G>C | synonymous_variant | 1.0 |
| clpC1 | 4038770 | c.1935C>G | synonymous_variant | 1.0 |
| clpC1 | 4038773 | c.1932T>C | synonymous_variant | 1.0 |
| clpC1 | 4038782 | c.1923G>C | synonymous_variant | 1.0 |
| clpC1 | 4038790 | c.1915C>T | synonymous_variant | 1.0 |
| clpC1 | 4038812 | c.1893T>C | synonymous_variant | 1.0 |
| clpC1 | 4038839 | p.Val622Ile | missense_variant | 0.5 |
| clpC1 | 4038878 | c.1827A>G | synonymous_variant | 1.0 |
| clpC1 | 4039274 | c.1431G>C | synonymous_variant | 1.0 |
| clpC1 | 4039286 | c.1419T>C | synonymous_variant | 1.0 |
| clpC1 | 4039289 | c.1416T>C | synonymous_variant | 1.0 |
| clpC1 | 4039292 | c.1413C>T | synonymous_variant | 1.0 |
| clpC1 | 4039295 | c.1410A>G | synonymous_variant | 1.0 |
| clpC1 | 4039298 | c.1407T>C | synonymous_variant | 1.0 |
| clpC1 | 4039310 | c.1395A>G | synonymous_variant | 1.0 |
| clpC1 | 4039316 | c.1389G>A | synonymous_variant | 1.0 |
| clpC1 | 4039319 | c.1386T>C | synonymous_variant | 1.0 |
| clpC1 | 4039322 | c.1383T>G | synonymous_variant | 1.0 |
| clpC1 | 4039328 | c.1377A>C | synonymous_variant | 1.0 |
| clpC1 | 4039338 | p.Thr456Gln | missense_variant | 1.0 |
| clpC1 | 4039382 | c.1323C>G | synonymous_variant | 1.0 |
| clpC1 | 4039391 | c.1314T>G | synonymous_variant | 1.0 |
| clpC1 | 4039394 | c.1311G>C | synonymous_variant | 1.0 |
| clpC1 | 4039397 | c.1308A>G | synonymous_variant | 1.0 |
| clpC1 | 4039409 | c.1296T>C | synonymous_variant | 0.75 |
| clpC1 | 4039412 | c.1293T>G | synonymous_variant | 0.75 |
| clpC1 | 4039415 | p.Glu430Asp | missense_variant | 0.75 |
| clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.75 |
| clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.75 |
| clpC1 | 4039454 | c.1251A>G | synonymous_variant | 0.75 |
| clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.6 |
| clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.5 |
| clpC1 | 4039481 | c.1224T>G | synonymous_variant | 0.67 |
| clpC1 | 4039484 | c.1221T>C | synonymous_variant | 0.67 |
| clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.83 |
| clpC1 | 4039547 | c.1158C>G | synonymous_variant | 0.8 |
| clpC1 | 4039556 | c.1149G>C | synonymous_variant | 0.83 |
| clpC1 | 4039570 | p.Met379Leu | missense_variant | 0.8 |
| clpC1 | 4039571 | c.1134G>A | synonymous_variant | 0.8 |
| clpC1 | 4039582 | p.Thr375Ser | missense_variant | 0.8 |
| clpC1 | 4039592 | c.1113G>C | synonymous_variant | 0.75 |
| clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.8 |
| clpC1 | 4039622 | c.1083C>G | synonymous_variant | 1.0 |
| clpC1 | 4039661 | c.1044T>G | synonymous_variant | 1.0 |
| clpC1 | 4039694 | c.1011G>C | synonymous_variant | 1.0 |
| clpC1 | 4039724 | c.981A>G | synonymous_variant | 1.0 |
| clpC1 | 4039733 | c.972G>C | synonymous_variant | 1.0 |
| clpC1 | 4039898 | c.807C>G | synonymous_variant | 1.0 |
| clpC1 | 4039904 | c.801A>G | synonymous_variant | 1.0 |
| clpC1 | 4039929 | c.775_776delAGinsTC | synonymous_variant | 1.0 |
| clpC1 | 4039931 | c.774T>C | synonymous_variant | 1.0 |
| clpC1 | 4039934 | c.771G>C | synonymous_variant | 1.0 |
| clpC1 | 4039946 | c.759A>C | synonymous_variant | 1.0 |
| clpC1 | 4039949 | c.756G>C | synonymous_variant | 1.0 |
| clpC1 | 4039952 | c.753T>C | synonymous_variant | 1.0 |
| clpC1 | 4039979 | c.726C>G | synonymous_variant | 1.0 |
| clpC1 | 4039988 | c.717C>G | synonymous_variant | 1.0 |
| clpC1 | 4039996 | p.Glu237Gln | missense_variant | 1.0 |
| clpC1 | 4040009 | c.696C>G | 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 | 4040084 | c.621C>G | synonymous_variant | 1.0 |
| clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 1.0 |
| clpC1 | 4040093 | c.612C>G | synonymous_variant | 1.0 |
| clpC1 | 4040108 | c.597G>C | synonymous_variant | 1.0 |
| clpC1 | 4040129 | c.576C>G | synonymous_variant | 1.0 |
| clpC1 | 4040144 | c.561G>C | synonymous_variant | 1.0 |
| clpC1 | 4040147 | c.558A>G | synonymous_variant | 1.0 |
| clpC1 | 4040162 | c.543G>C | synonymous_variant | 1.0 |
| clpC1 | 4040165 | c.540G>C | synonymous_variant | 1.0 |
| clpC1 | 4040171 | c.534C>G | synonymous_variant | 1.0 |
| clpC1 | 4040180 | c.525C>G | synonymous_variant | 1.0 |
| clpC1 | 4040213 | c.492T>C | synonymous_variant | 1.0 |
| clpC1 | 4040228 | c.477G>C | synonymous_variant | 1.0 |
| clpC1 | 4040231 | c.474C>G | synonymous_variant | 1.0 |
| clpC1 | 4040240 | c.465C>G | synonymous_variant | 1.0 |
| clpC1 | 4040249 | c.456A>G | synonymous_variant | 1.0 |
| clpC1 | 4040252 | c.453C>G | synonymous_variant | 1.0 |
| clpC1 | 4040267 | c.438A>G | synonymous_variant | 1.0 |
| clpC1 | 4040270 | c.435C>T | synonymous_variant | 1.0 |
| clpC1 | 4040273 | c.432T>C | synonymous_variant | 1.0 |
| clpC1 | 4040277 | c.427_428delTCinsAG | synonymous_variant | 1.0 |
| clpC1 | 4040279 | c.426C>G | synonymous_variant | 1.0 |
| clpC1 | 4040291 | c.414G>C | synonymous_variant | 1.0 |
| clpC1 | 4040324 | c.381G>C | synonymous_variant | 1.0 |
| clpC1 | 4040335 | c.370C>T | synonymous_variant | 1.0 |
| clpC1 | 4040354 | c.351A>G | synonymous_variant | 1.0 |
| clpC1 | 4040522 | c.183T>C | synonymous_variant | 1.0 |
| clpC1 | 4040528 | c.177G>T | synonymous_variant | 1.0 |
| embC | 4240459 | c.597G>C | synonymous_variant | 0.67 |
| embC | 4240474 | c.612G>C | synonymous_variant | 0.67 |
| embC | 4240475 | p.Ala205Thr | missense_variant | 0.67 |
| embC | 4240489 | c.627A>G | synonymous_variant | 0.8 |
| embC | 4240495 | c.633T>C | synonymous_variant | 0.8 |
| embC | 4240512 | p.Ser217Thr | missense_variant | 0.8 |
| embC | 4240514 | p.Val218Ile | missense_variant | 0.8 |
| embC | 4240519 | c.657T>C | synonymous_variant | 0.8 |
| embC | 4240543 | c.681G>C | synonymous_variant | 1.0 |
| embC | 4240545 | p.Pro228Gln | missense_variant | 1.0 |
| embC | 4240558 | c.696C>G | synonymous_variant | 1.0 |
| embC | 4240561 | c.699C>G | synonymous_variant | 1.0 |
| embC | 4241071 | c.1209C>G | synonymous_variant | 1.0 |
| embC | 4241074 | c.1212G>C | synonymous_variant | 1.0 |
| embC | 4241104 | c.1242G>A | synonymous_variant | 1.0 |
| embC | 4241107 | c.1245G>C | synonymous_variant | 1.0 |
| embC | 4241116 | c.1254C>G | synonymous_variant | 1.0 |
| embC | 4241140 | c.1278A>G | synonymous_variant | 1.0 |
| embC | 4241141 | p.Ile427Ala | missense_variant | 1.0 |
| embC | 4241158 | c.1296T>C | synonymous_variant | 1.0 |
| embC | 4241161 | c.1299C>G | synonymous_variant | 1.0 |
| embC | 4241162 | c.1300T>C | synonymous_variant | 1.0 |
| embC | 4241203 | c.1341T>C | synonymous_variant | 1.0 |
| embC | 4241206 | c.1344G>C | synonymous_variant | 1.0 |
| embC | 4241479 | c.1617C>G | synonymous_variant | 1.0 |
| embC | 4241480 | c.1618T>C | synonymous_variant | 1.0 |
| embC | 4241488 | c.1626G>C | synonymous_variant | 1.0 |
| embA | 4242826 | c.-407G>C | upstream_gene_variant | 1.0 |
| embA | 4242838 | c.-395C>G | upstream_gene_variant | 1.0 |
| embA | 4242844 | c.-389A>G | upstream_gene_variant | 1.0 |
| embA | 4242847 | c.-386C>G | upstream_gene_variant | 1.0 |
| embA | 4242859 | c.-374C>T | upstream_gene_variant | 1.0 |
| embA | 4242862 | c.-371A>G | upstream_gene_variant | 1.0 |
| embC | 4242863 | p.Tyr1001Asn | missense_variant | 1.0 |
| embA | 4242880 | c.-353A>G | upstream_gene_variant | 1.0 |
| embA | 4242883 | c.-350C>G | upstream_gene_variant | 1.0 |
| embA | 4242892 | c.-341G>C | upstream_gene_variant | 1.0 |
| embA | 4242907 | c.-326G>T | upstream_gene_variant | 1.0 |
| embA | 4242928 | c.-305A>C | upstream_gene_variant | 1.0 |
| embA | 4242940 | c.-293T>C | upstream_gene_variant | 1.0 |
| embC | 4242941 | p.His1027Asn | missense_variant | 1.0 |
| embA | 4242946 | c.-287T>C | upstream_gene_variant | 1.0 |
| embA | 4242952 | c.-281T>C | upstream_gene_variant | 1.0 |
| embA | 4242959 | c.-274C>T | upstream_gene_variant | 1.0 |
| embC | 4242965 | p.Ile1035Val | missense_variant | 1.0 |
| embA | 4242973 | c.-260G>A | upstream_gene_variant | 1.0 |
| embA | 4245257 | c.2025A>G | synonymous_variant | 1.0 |
| embA | 4245261 | p.Lys677Glu | missense_variant | 1.0 |
| embA | 4245281 | c.2049C>G | synonymous_variant | 1.0 |
| embA | 4245282 | p.Ile684Val | missense_variant | 1.0 |
| embA | 4245285 | c.2053_2055delTTGinsCTC | synonymous_variant | 1.0 |
| embA | 4245290 | c.2058C>G | synonymous_variant | 1.0 |
| embA | 4245293 | c.2061T>G | synonymous_variant | 1.0 |
| embA | 4245299 | c.2067A>C | synonymous_variant | 1.0 |
| embA | 4245315 | p.Val695Thr | missense_variant | 1.0 |
| embA | 4245327 | p.Ala699Ile | missense_variant | 1.0 |
| embA | 4245345 | p.Met705Leu | missense_variant | 1.0 |
| embB | 4245755 | c.-759C>G | upstream_gene_variant | 1.0 |
| embB | 4245764 | c.-750G>C | upstream_gene_variant | 1.0 |
| embA | 4245771 | p.Asn847Ser | missense_variant | 1.0 |
| embB | 4245776 | c.-738G>C | upstream_gene_variant | 1.0 |
| embB | 4245807 | c.-707_-705delTTAinsCTG | upstream_gene_variant | 1.0 |
| embA | 4245820 | p.Ser863Thr | missense_variant | 1.0 |
| embA | 4245834 | p.Leu868Ile | missense_variant | 1.0 |
| embB | 4245839 | c.-675G>C | upstream_gene_variant | 1.0 |
| embB | 4245845 | c.-669T>G | upstream_gene_variant | 1.0 |
| embB | 4245848 | c.-666C>G | upstream_gene_variant | 1.0 |
| embB | 4245851 | c.-663G>C | upstream_gene_variant | 1.0 |
| embA | 4245852 | p.Ala874Thr | missense_variant | 1.0 |
| embB | 4245860 | c.-654C>G | upstream_gene_variant | 1.0 |
| embB | 4245869 | c.-645C>G | upstream_gene_variant | 1.0 |
| embB | 4246262 | c.-252C>T | upstream_gene_variant | 1.0 |
| embA | 4246278 | p.Ala1016Ser | missense_variant | 1.0 |
| embA | 4246290 | p.Leu1020Gly | missense_variant | 1.0 |
| embA | 4246305 | p.Ser1025Glu | missense_variant | 1.0 |
| embA | 4246308 | p.Thr1026Ala | missense_variant | 1.0 |
| embB | 4246316 | c.-198T>G | upstream_gene_variant | 1.0 |
| embB | 4246325 | c.-189G>C | upstream_gene_variant | 1.0 |
| embA | 4246329 | p.Thr1033Leu | missense_variant | 1.0 |
| embA | 4246335 | p.Ala1035Thr | missense_variant | 1.0 |
| embA | 4246338 | p.Leu1036Met | missense_variant | 1.0 |
| embB | 4246355 | c.-159G>C | upstream_gene_variant | 1.0 |
| embA | 4246359 | p.Ala1043Ser | missense_variant | 1.0 |
| embB | 4246373 | c.-141T>C | upstream_gene_variant | 1.0 |
| embB | 4246376 | c.-138G>C | upstream_gene_variant | 1.0 |
| embB | 4246385 | c.-129T>C | upstream_gene_variant | 1.0 |
| embB | 4247386 | c.873T>C | synonymous_variant | 0.67 |
| embB | 4247389 | c.876C>G | synonymous_variant | 0.67 |
| embB | 4247395 | c.882C>G | synonymous_variant | 1.0 |
| embB | 4247401 | c.888T>C | synonymous_variant | 1.0 |
| embB | 4247404 | c.891G>C | synonymous_variant | 1.0 |
| embB | 4247407 | c.894G>C | synonymous_variant | 1.0 |
| embB | 4247437 | c.924A>C | synonymous_variant | 1.0 |
| embB | 4247464 | c.951C>G | synonymous_variant | 1.0 |
| embB | 4247470 | c.957T>C | synonymous_variant | 1.0 |
| embB | 4247497 | c.984T>C | synonymous_variant | 1.0 |
| embB | 4247753 | p.Val414Ile | missense_variant | 0.67 |
| embB | 4247776 | c.1263G>C | synonymous_variant | 0.67 |
| embB | 4247779 | c.1266C>G | synonymous_variant | 0.67 |
| embB | 4247785 | c.1272G>C | synonymous_variant | 0.67 |
| embB | 4247797 | c.1284C>G | synonymous_variant | 0.67 |
| embB | 4247800 | c.1287A>G | synonymous_variant | 0.67 |
| embB | 4247803 | c.1290G>C | synonymous_variant | 0.67 |
| embB | 4247809 | c.1296G>A | synonymous_variant | 0.67 |
| embB | 4247815 | c.1302C>G | synonymous_variant | 0.67 |
| embB | 4247819 | p.Val436Ile | missense_variant | 0.67 |
| aftB | 4269027 | c.-191C>G | upstream_gene_variant | 1.0 |
| aftB | 4269033 | c.-197T>C | upstream_gene_variant | 1.0 |
| aftB | 4269042 | c.-206G>C | upstream_gene_variant | 1.0 |
| aftB | 4269045 | c.-209G>C | upstream_gene_variant | 1.0 |
| ubiA | 4269075 | p.Ile253Val | missense_variant | 1.0 |
| aftB | 4269099 | c.-263G>A | upstream_gene_variant | 1.0 |
| aftB | 4269102 | c.-268_-266delAGCinsTCG | upstream_gene_variant | 1.0 |
| ubiA | 4269107 | p.Tyr243His | missense_variant | 1.0 |
| ubiA | 4269110 | p.Gly242Arg | missense_variant | 1.0 |
| aftB | 4269114 | c.-278C>T | upstream_gene_variant | 1.0 |
| aftB | 4269123 | c.-287T>G | upstream_gene_variant | 1.0 |
| aftB | 4269131 | c.-295C>T | upstream_gene_variant | 1.0 |
| aftB | 4269141 | c.-307_-305delTTGinsCTC | upstream_gene_variant | 1.0 |
| aftB | 4269144 | c.-308C>G | upstream_gene_variant | 1.0 |
| ubiA | 4269164 | p.Leu224Met | missense_variant | 1.0 |
| aftB | 4269165 | c.-329G>C | upstream_gene_variant | 1.0 |
| aftB | 4269201 | c.-365A>G | upstream_gene_variant | 1.0 |
| aftB | 4269207 | c.-371G>C | upstream_gene_variant | 1.0 |
| aftB | 4269639 | c.-803C>G | upstream_gene_variant | 1.0 |
| aftB | 4269646 | c.-811_-810delAGinsTC | upstream_gene_variant | 1.0 |
| aftB | 4269660 | c.-824C>G | upstream_gene_variant | 1.0 |
| ubiA | 4269665 | p.Met57Val | missense_variant | 1.0 |
| ubiA | 4269676 | p.Ser53Thr | missense_variant | 1.0 |
| aftB | 4269678 | c.-842C>G | upstream_gene_variant | 1.0 |
| ubiA | 4269683 | p.Val51Leu | missense_variant | 1.0 |
| ubiA | 4269688 | p.Val49Ala | missense_variant | 1.0 |
| ubiA | 4269695 | p.Asp47Asn | missense_variant | 1.0 |
| ubiA | 4269700 | p.Arg45His | missense_variant | 1.0 |
| aftB | 4269716 | c.-880T>C | upstream_gene_variant | 1.0 |
| ubiA | 4269725 | p.Leu37Val | missense_variant | 1.0 |
