Run ID: SRR7585435
Sample name:
Date: 04-04-2023 19:47:17
Number of reads: 34862
Percentage reads mapped: 4.53
Strain: lineage4.9
Drug-resistance: Other
| Drug | Resistance | Supporting mutations |
|---|
| Lineage | Family | Main Spoligotype | RDs | Frequency |
|---|---|---|---|---|
| lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
| lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
| Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
|---|---|---|---|---|---|
| rrs | 1472307 | n.462C>T | non_coding_transcript_exon_variant | 1.0 | streptomycin |
| rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.8 | streptomycin |
| rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.67 | kanamycin, capreomycin, aminoglycosides, amikacin |
| rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 1.0 | kanamycin, capreomycin, aminoglycosides, amikacin |
| tlyA | 1918451 | c.513_514delTT | frameshift_variant | 1.0 | capreomycin |
| embB | 4247448 | p.His312Arg | missense_variant | 1.0 | ethambutol |
| Gene | Chromosome position | Mutation | Type | Estimated fraction |
|---|---|---|---|---|
| gyrB | 5809 | c.570C>G | synonymous_variant | 1.0 |
| gyrB | 5812 | c.573C>G | synonymous_variant | 1.0 |
| gyrB | 5824 | c.585A>G | synonymous_variant | 1.0 |
| gyrB | 5827 | c.588G>A | synonymous_variant | 1.0 |
| gyrB | 5849 | c.610C>T | synonymous_variant | 1.0 |
| gyrB | 5863 | c.624G>C | synonymous_variant | 1.0 |
| gyrB | 5873 | c.634A>C | synonymous_variant | 1.0 |
| gyrB | 6238 | c.999G>A | synonymous_variant | 1.0 |
| gyrB | 6242 | p.Arg335Lys | missense_variant | 1.0 |
| gyrB | 6250 | c.1011A>G | synonymous_variant | 1.0 |
| gyrB | 6256 | c.1017G>A | synonymous_variant | 1.0 |
| gyrB | 6268 | c.1029C>G | synonymous_variant | 1.0 |
| gyrB | 6280 | c.1041T>C | synonymous_variant | 1.0 |
| gyrB | 6286 | c.1047T>C | synonymous_variant | 1.0 |
| gyrB | 6289 | c.1050C>T | synonymous_variant | 1.0 |
| gyrB | 6292 | c.1053G>C | synonymous_variant | 1.0 |
| gyrA | 6307 | c.-995T>G | upstream_gene_variant | 1.0 |
| gyrA | 6319 | c.-983G>C | upstream_gene_variant | 1.0 |
| gyrA | 6362 | c.-940T>C | 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 | 6616 | c.-686A>G | upstream_gene_variant | 1.0 |
| gyrA | 6622 | c.-680C>T | upstream_gene_variant | 1.0 |
| 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 | 1.0 |
| gyrA | 6643 | c.-659A>G | upstream_gene_variant | 1.0 |
| gyrA | 6649 | c.-653T>C | upstream_gene_variant | 1.0 |
| gyrA | 6655 | c.-647T>C | upstream_gene_variant | 1.0 |
| gyrA | 6670 | c.-632G>C | upstream_gene_variant | 1.0 |
| gyrA | 6673 | c.-629A>C | upstream_gene_variant | 1.0 |
| gyrA | 6676 | c.-626T>G | upstream_gene_variant | 1.0 |
| gyrA | 6700 | c.-602T>C | upstream_gene_variant | 1.0 |
| gyrA | 6703 | c.-599G>C | upstream_gene_variant | 1.0 |
| gyrA | 6709 | c.-593A>G | upstream_gene_variant | 1.0 |
| gyrA | 6712 | c.-590G>C | upstream_gene_variant | 1.0 |
| gyrA | 6728 | c.-574_-572delCTAinsTTG | upstream_gene_variant | 1.0 |
| gyrA | 8090 | c.789C>A | synonymous_variant | 1.0 |
| gyrA | 8093 | c.792C>T | synonymous_variant | 1.0 |
| gyrA | 8096 | c.795T>A | synonymous_variant | 1.0 |
| gyrA | 8099 | c.798T>C | synonymous_variant | 1.0 |
| gyrA | 8111 | c.810G>C | synonymous_variant | 1.0 |
| gyrA | 8121 | c.820T>C | synonymous_variant | 1.0 |
| gyrA | 8129 | c.828T>C | synonymous_variant | 1.0 |
| gyrA | 8135 | c.834C>G | synonymous_variant | 1.0 |
| gyrA | 8156 | c.855T>C | synonymous_variant | 1.0 |
| gyrA | 8168 | c.867A>G | synonymous_variant | 1.0 |
| gyrA | 8177 | c.876A>C | synonymous_variant | 1.0 |
| gyrA | 8588 | c.1287G>A | synonymous_variant | 1.0 |
| gyrA | 8597 | c.1296C>G | synonymous_variant | 1.0 |
| gyrA | 8603 | c.1302A>G | synonymous_variant | 1.0 |
| gyrA | 8619 | c.1318_1320delTTGinsCTA | synonymous_variant | 1.0 |
| gyrA | 8624 | c.1323G>C | synonymous_variant | 1.0 |
| gyrA | 8636 | c.1335A>C | synonymous_variant | 1.0 |
| gyrA | 8642 | c.1341A>G | synonymous_variant | 1.0 |
| gyrA | 8672 | c.1371A>G | synonymous_variant | 1.0 |
| gyrA | 8678 | c.1377G>A | synonymous_variant | 1.0 |
| gyrA | 8693 | c.1392T>C | synonymous_variant | 1.0 |
| gyrA | 8696 | c.1395G>C | synonymous_variant | 1.0 |
| gyrA | 8699 | c.1398A>G | synonymous_variant | 1.0 |
| gyrA | 8711 | c.1410A>C | synonymous_variant | 1.0 |
| gyrA | 8714 | c.1413A>G | synonymous_variant | 1.0 |
| gyrA | 8729 | c.1428T>C | synonymous_variant | 1.0 |
| gyrA | 8730 | p.Gly477Arg | missense_variant | 1.0 |
| gyrA | 8740 | p.Arg480His | missense_variant | 1.0 |
| gyrA | 8867 | c.1566A>G | synonymous_variant | 1.0 |
| gyrA | 8870 | c.1569G>C | synonymous_variant | 1.0 |
| gyrA | 8873 | c.1572A>C | synonymous_variant | 1.0 |
| gyrA | 8891 | c.1590G>A | synonymous_variant | 1.0 |
| gyrA | 8897 | c.1596T>C | synonymous_variant | 1.0 |
| gyrA | 8903 | c.1602T>C | synonymous_variant | 1.0 |
| gyrA | 8933 | c.1632G>C | synonymous_variant | 1.0 |
| gyrA | 8939 | c.1638T>C | synonymous_variant | 1.0 |
| gyrA | 8942 | c.1641G>C | synonymous_variant | 1.0 |
| gyrA | 8946 | c.1645_1647delTTGinsCTC | synonymous_variant | 1.0 |
| 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 | 9224 | c.1923C>T | synonymous_variant | 1.0 |
| gyrA | 9230 | c.1929T>C | synonymous_variant | 1.0 |
| gyrA | 9233 | c.1932C>G | synonymous_variant | 1.0 |
| gyrA | 9239 | c.1938C>T | synonymous_variant | 1.0 |
| gyrA | 9252 | p.Val651Ile | missense_variant | 1.0 |
| gyrA | 9275 | p.Glu658Asp | missense_variant | 0.33 |
| gyrA | 9284 | c.1983T>C | synonymous_variant | 1.0 |
| gyrA | 9291 | c.1990C>T | synonymous_variant | 1.0 |
| gyrA | 9296 | c.1995T>C | synonymous_variant | 1.0 |
| gyrA | 9299 | c.1998G>C | synonymous_variant | 1.0 |
| gyrA | 9300 | p.Ala667Ser | missense_variant | 1.0 |
| gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
| gyrA | 9308 | p.Asp669Glu | missense_variant | 1.0 |
| gyrA | 9323 | c.2022C>G | synonymous_variant | 1.0 |
| gyrA | 9335 | c.2034G>C | synonymous_variant | 1.0 |
| gyrA | 9365 | c.2064G>A | synonymous_variant | 1.0 |
| gyrA | 9374 | c.2073G>C | synonymous_variant | 1.0 |
| gyrA | 9377 | c.2076A>G | synonymous_variant | 1.0 |
| gyrA | 9383 | c.2082T>G | synonymous_variant | 1.0 |
| gyrA | 9386 | c.2085T>C | synonymous_variant | 1.0 |
| gyrA | 9644 | c.2343T>C | synonymous_variant | 1.0 |
| gyrA | 9650 | c.2349G>C | synonymous_variant | 1.0 |
| gyrA | 9656 | c.2355C>G | synonymous_variant | 1.0 |
| gyrA | 9665 | c.2364A>C | synonymous_variant | 1.0 |
| gyrA | 9666 | p.Arg789Gly | missense_variant | 1.0 |
| gyrA | 9674 | c.2373T>C | synonymous_variant | 1.0 |
| gyrA | 9704 | c.2403T>G | synonymous_variant | 1.0 |
| gyrA | 9708 | c.2407T>C | synonymous_variant | 1.0 |
| gyrA | 9716 | c.2415T>C | synonymous_variant | 1.0 |
| gyrA | 9725 | c.2424G>A | synonymous_variant | 1.0 |
| gyrA | 9727 | p.Gly809Glu | missense_variant | 1.0 |
| gyrA | 9729 | p.Asp810Asn | missense_variant | 1.0 |
| gyrA | 9734 | c.2433A>C | synonymous_variant | 1.0 |
| fgd1 | 490948 | p.Ser56Ala | missense_variant | 1.0 |
| fgd1 | 490962 | c.180T>G | synonymous_variant | 1.0 |
| fgd1 | 490974 | c.192T>C | synonymous_variant | 1.0 |
| fgd1 | 490977 | c.195C>G | synonymous_variant | 1.0 |
| fgd1 | 490980 | p.Asn66Lys | missense_variant | 1.0 |
| fgd1 | 490984 | p.Leu68Ile | missense_variant | 1.0 |
| fgd1 | 490987 | p.Leu69Thr | missense_variant | 1.0 |
| fgd1 | 490998 | c.216T>C | synonymous_variant | 1.0 |
| fgd1 | 491001 | c.219G>C | synonymous_variant | 1.0 |
| fgd1 | 491007 | c.225G>C | synonymous_variant | 1.0 |
| fgd1 | 491013 | c.231C>G | synonymous_variant | 1.0 |
| fgd1 | 491212 | p.Ser144Arg | missense_variant | 1.0 |
| fgd1 | 491217 | c.435T>C | 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 |
| mshA | 575674 | c.327G>C | synonymous_variant | 1.0 |
| mshA | 575695 | c.348C>G | synonymous_variant | 1.0 |
| mshA | 575701 | c.354G>A | synonymous_variant | 1.0 |
| mshA | 575704 | c.357T>G | synonymous_variant | 1.0 |
| mshA | 575705 | c.358T>C | synonymous_variant | 1.0 |
| rpoB | 759812 | c.6A>T | synonymous_variant | 1.0 |
| rpoB | 759817 | p.Ser4Phe | missense_variant | 1.0 |
| rpoB | 759830 | c.24A>G | 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 | 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 | 760283 | c.477G>C | synonymous_variant | 1.0 |
| rpoB | 760298 | c.492G>C | synonymous_variant | 1.0 |
| rpoB | 760307 | c.501T>C | synonymous_variant | 1.0 |
| rpoB | 760310 | c.504G>C | synonymous_variant | 1.0 |
| rpoB | 760328 | c.522G>C | synonymous_variant | 1.0 |
| rpoB | 760331 | c.525G>C | synonymous_variant | 1.0 |
| rpoB | 760340 | c.534G>T | synonymous_variant | 1.0 |
| rpoB | 760646 | c.840C>G | synonymous_variant | 1.0 |
| rpoB | 760655 | c.849A>G | synonymous_variant | 1.0 |
| rpoB | 760661 | c.855A>C | synonymous_variant | 1.0 |
| rpoB | 760715 | c.909C>G | synonymous_variant | 1.0 |
| rpoB | 760718 | c.912C>T | synonymous_variant | 1.0 |
| rpoB | 760724 | c.918T>C | synonymous_variant | 1.0 |
| rpoB | 760730 | c.924T>C | synonymous_variant | 1.0 |
| rpoB | 760751 | c.945G>C | synonymous_variant | 1.0 |
| rpoB | 760757 | c.951T>C | synonymous_variant | 1.0 |
| rpoB | 760759 | p.Val318Ala | missense_variant | 1.0 |
| rpoB | 760769 | c.963C>G | synonymous_variant | 1.0 |
| rpoB | 760775 | c.969G>C | synonymous_variant | 1.0 |
| rpoB | 760776 | c.970_972delTCGinsAGC | synonymous_variant | 1.0 |
| rpoB | 760793 | c.987A>G | synonymous_variant | 1.0 |
| rpoB | 760934 | c.1128C>T | synonymous_variant | 1.0 |
| rpoB | 760946 | c.1140A>G | synonymous_variant | 1.0 |
| rpoB | 760949 | c.1143C>T | synonymous_variant | 1.0 |
| rpoB | 760982 | c.1176G>C | 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 | 0.57 |
| rpoB | 761015 | c.1209G>C | synonymous_variant | 1.0 |
| rpoB | 761021 | c.1215G>C | synonymous_variant | 0.67 |
| 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 | 0.67 |
| rpoB | 761051 | c.1245G>T | synonymous_variant | 0.4 |
| rpoB | 761054 | c.1248G>C | synonymous_variant | 0.4 |
| rpoB | 761057 | c.1251G>C | synonymous_variant | 1.0 |
| rpoB | 761060 | c.1254C>G | synonymous_variant | 0.4 |
| rpoB | 761063 | c.1257C>G | synonymous_variant | 0.4 |
| rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 0.33 |
| rpoB | 761097 | c.1291_1292delAGinsTC | synonymous_variant | 0.33 |
| rpoB | 761102 | c.1296A>G | synonymous_variant | 1.0 |
| rpoB | 761477 | c.1671C>G | synonymous_variant | 1.0 |
| rpoB | 761492 | c.1686G>C | synonymous_variant | 1.0 |
| rpoB | 761510 | c.1704T>C | synonymous_variant | 1.0 |
| rpoB | 761537 | c.1731C>G | synonymous_variant | 1.0 |
| rpoB | 761570 | c.1764T>C | synonymous_variant | 1.0 |
| rpoB | 761573 | c.1767C>G | synonymous_variant | 1.0 |
| rpoB | 761579 | c.1773G>C | synonymous_variant | 1.0 |
| rpoB | 761588 | c.1782C>T | synonymous_variant | 1.0 |
| rpoB | 761792 | c.1986T>C | synonymous_variant | 1.0 |
| rpoB | 761813 | c.2007T>C | synonymous_variant | 1.0 |
| rpoB | 761815 | p.Ala670Glu | missense_variant | 1.0 |
| rpoB | 761955 | p.Ile717Tyr | missense_variant | 1.0 |
| rpoB | 761961 | p.Pro719Ser | missense_variant | 1.0 |
| rpoB | 761974 | p.His723Leu | missense_variant | 1.0 |
| rpoB | 761999 | c.2193G>C | synonymous_variant | 1.0 |
| rpoB | 762003 | p.Asn733Gln | missense_variant | 1.0 |
| rpoB | 762008 | c.2202C>G | synonymous_variant | 1.0 |
| rpoB | 762009 | p.Leu735Met | missense_variant | 1.0 |
| rpoB | 762015 | p.Glu737Ser | missense_variant | 1.0 |
| rpoB | 762810 | p.Ala1002Ser | missense_variant | 0.75 |
| rpoB | 762813 | p.Met1003Val | 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 | 762857 | c.-513C>G | upstream_gene_variant | 1.0 |
| rpoC | 762860 | c.-510G>C | upstream_gene_variant | 0.75 |
| rpoC | 762863 | c.-507T>C | upstream_gene_variant | 1.0 |
| rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.54 |
| rpoB | 762925 | p.Thr1040Ile | missense_variant | 0.31 |
| rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.69 |
| rpoB | 762934 | c.3129_3130insAGCC | frameshift_variant | 0.44 |
| rpoB | 762938 | c.3133_3136delATGA | frameshift_variant | 0.5 |
| rpoC | 762980 | c.-390T>C | upstream_gene_variant | 0.57 |
| rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.8 |
| rpoC | 762989 | c.-381G>C | upstream_gene_variant | 1.0 |
| rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.8 |
| rpoB | 763005 | p.Cys1067Val | missense_variant | 0.8 |
| rpoB | 763014 | p.Met1070Leu | missense_variant | 1.0 |
| rpoC | 763034 | c.-336C>G | upstream_gene_variant | 1.0 |
| rpoC | 763040 | c.-330C>G | upstream_gene_variant | 1.0 |
| rpoC | 763070 | c.-300T>C | upstream_gene_variant | 1.0 |
| rpoC | 763085 | c.-285C>G | upstream_gene_variant | 1.0 |
| rpoC | 763115 | c.-255T>C | upstream_gene_variant | 1.0 |
| rpoC | 763136 | c.-234C>T | upstream_gene_variant | 1.0 |
| rpoC | 763148 | c.-222G>C | upstream_gene_variant | 1.0 |
| rpoC | 763441 | c.72C>T | synonymous_variant | 1.0 |
| rpoC | 763444 | c.75T>C | synonymous_variant | 1.0 |
| rpoC | 763456 | c.87A>G | synonymous_variant | 1.0 |
| rpoC | 763486 | c.117T>G | 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 | 0.67 |
| rpoC | 763573 | c.204G>C | synonymous_variant | 0.67 |
| rpoC | 763594 | c.225C>T | synonymous_variant | 1.0 |
| rpoC | 763696 | c.327T>C | synonymous_variant | 1.0 |
| rpoC | 763702 | c.333C>G | synonymous_variant | 0.5 |
| rpoC | 763714 | c.345G>C | synonymous_variant | 0.5 |
| rpoC | 763717 | c.348T>C | synonymous_variant | 1.0 |
| rpoC | 763723 | c.354G>C | synonymous_variant | 0.5 |
| rpoC | 763732 | c.363C>G | synonymous_variant | 0.5 |
| rpoC | 763741 | c.372C>T | synonymous_variant | 0.5 |
| rpoC | 763744 | c.375G>C | synonymous_variant | 1.0 |
| rpoC | 763765 | c.396T>C | synonymous_variant | 1.0 |
| rpoC | 763774 | c.405G>C | synonymous_variant | 0.75 |
| rpoC | 763807 | c.438T>C | synonymous_variant | 1.0 |
| rpoC | 763816 | c.447C>G | synonymous_variant | 1.0 |
| rpoC | 763835 | p.Ala156Met | missense_variant | 1.0 |
| rpoC | 763853 | p.Val162Ile | missense_variant | 1.0 |
| rpoC | 763858 | c.489A>G | synonymous_variant | 1.0 |
| rpoC | 764083 | c.714A>G | synonymous_variant | 1.0 |
| rpoC | 764112 | p.Tyr248Phe | missense_variant | 1.0 |
| rpoC | 764116 | c.747C>T | synonymous_variant | 1.0 |
| rpoC | 764131 | c.762T>C | synonymous_variant | 1.0 |
| rpoC | 764140 | c.771C>T | synonymous_variant | 1.0 |
| rpoC | 764188 | c.819A>G | synonymous_variant | 1.0 |
| rpoC | 764195 | p.Ser276Ile | missense_variant | 1.0 |
| rpoC | 764203 | c.834G>C | synonymous_variant | 1.0 |
| rpoC | 764206 | c.837T>C | synonymous_variant | 1.0 |
| rpoC | 764215 | c.846A>G | synonymous_variant | 1.0 |
| rpoC | 764236 | c.867G>A | synonymous_variant | 1.0 |
| rpoC | 764248 | c.879C>G | synonymous_variant | 1.0 |
| rpoC | 764257 | c.888G>C | synonymous_variant | 1.0 |
| rpoC | 764266 | c.897T>C | synonymous_variant | 1.0 |
| rpoC | 764269 | c.900G>C | synonymous_variant | 1.0 |
| rpoC | 764272 | c.903G>C | synonymous_variant | 1.0 |
| rpoC | 764278 | c.909A>G | synonymous_variant | 1.0 |
| rpoC | 764405 | c.1036A>C | synonymous_variant | 1.0 |
| rpoC | 764419 | c.1050C>G | synonymous_variant | 0.67 |
| 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 | 764446 | c.1077T>C | synonymous_variant | 1.0 |
| rpoC | 764449 | c.1080G>C | synonymous_variant | 1.0 |
| rpoC | 764452 | c.1083T>C | synonymous_variant | 0.67 |
| rpoC | 764458 | c.1089G>C | synonymous_variant | 1.0 |
| rpoC | 764461 | c.1092A>G | synonymous_variant | 1.0 |
| rpoC | 764489 | c.1120C>T | synonymous_variant | 0.5 |
| rpoC | 764497 | c.1128A>G | synonymous_variant | 1.0 |
| rpoC | 764498 | p.Ser377Ala | missense_variant | 0.5 |
| rpoC | 764507 | p.Ala380Ser | missense_variant | 0.5 |
| rpoC | 764510 | c.1141C>T | synonymous_variant | 0.5 |
| rpoC | 764521 | c.1152T>C | synonymous_variant | 1.0 |
| rpoC | 764527 | c.1158C>T | synonymous_variant | 0.75 |
| rpoC | 764536 | c.1167G>C | synonymous_variant | 1.0 |
| rpoC | 764539 | c.1170C>G | synonymous_variant | 1.0 |
| rpoC | 764566 | c.1197C>G | synonymous_variant | 1.0 |
| rpoC | 764575 | c.1206T>G | synonymous_variant | 1.0 |
| rpoC | 764581 | c.1212T>C | synonymous_variant | 1.0 |
| rpoC | 764593 | c.1224C>T | synonymous_variant | 0.43 |
| rpoC | 764605 | c.1236G>C | synonymous_variant | 0.43 |
| rpoC | 764611 | c.1242G>C | synonymous_variant | 1.0 |
| rpoC | 764632 | c.1263T>C | synonymous_variant | 0.56 |
| rpoC | 764641 | c.1272C>T | synonymous_variant | 0.56 |
| rpoC | 764650 | c.1281G>T | synonymous_variant | 1.0 |
| rpoC | 764651 | c.1282_1284delTCGinsAGC | synonymous_variant | 0.38 |
| rpoC | 764663 | p.Val432Thr | missense_variant | 0.62 |
| rpoC | 764668 | c.1299C>G | synonymous_variant | 0.62 |
| rpoC | 764672 | p.Gln435Glu | missense_variant | 0.62 |
| rpoC | 764683 | c.1314G>C | synonymous_variant | 0.83 |
| rpoC | 764686 | c.1317C>T | synonymous_variant | 0.71 |
| rpoC | 764705 | p.Leu446Lys | missense_variant | 0.5 |
| rpoC | 764716 | c.1347G>C | synonymous_variant | 0.6 |
| rpoC | 764749 | c.1380G>C | synonymous_variant | 0.33 |
| rpoC | 764752 | c.1383G>C | synonymous_variant | 0.67 |
| rpoC | 764764 | c.1395T>C | synonymous_variant | 1.0 |
| rpoC | 764780 | c.1411_1413delAGCinsTCG | synonymous_variant | 0.4 |
| rpoC | 764791 | c.1422C>G | synonymous_variant | 0.4 |
| rpoC | 764797 | c.1428G>C | synonymous_variant | 0.4 |
| rpoC | 764804 | p.Gln479Tyr | missense_variant | 0.4 |
| rpoC | 764809 | c.1440C>T | synonymous_variant | 0.6 |
| rpoC | 764815 | c.1446A>G | synonymous_variant | 1.0 |
| rpoC | 764827 | c.1458G>C | synonymous_variant | 0.8 |
| rpoC | 764858 | c.1489T>C | synonymous_variant | 1.0 |
| rpoC | 764872 | c.1503A>G | synonymous_variant | 1.0 |
| rpoC | 764888 | c.1519T>C | synonymous_variant | 1.0 |
| rpoC | 764911 | c.1542A>G | synonymous_variant | 1.0 |
| rpoC | 764932 | c.1563C>A | synonymous_variant | 0.67 |
| rpoC | 764935 | c.1566T>C | synonymous_variant | 1.0 |
| rpoC | 764948 | c.1579T>C | synonymous_variant | 1.0 |
| rpoC | 764968 | c.1599T>C | synonymous_variant | 1.0 |
| rpoC | 764995 | c.1626C>G | synonymous_variant | 0.83 |
| 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 | 765053 | c.1684_1685delTCinsAG | synonymous_variant | 1.0 |
| rpoC | 765073 | c.1704G>C | synonymous_variant | 1.0 |
| rpoC | 765076 | c.1707A>G | synonymous_variant | 1.0 |
| rpoC | 765079 | c.1710T>G | synonymous_variant | 1.0 |
| rpoC | 765082 | c.1713G>C | synonymous_variant | 1.0 |
| rpoC | 765089 | c.1720T>C | synonymous_variant | 1.0 |
| rpoC | 765103 | c.1734G>T | synonymous_variant | 1.0 |
| rpoC | 765478 | c.2109T>C | synonymous_variant | 1.0 |
| rpoC | 765499 | c.2130C>G | synonymous_variant | 1.0 |
| rpoC | 765529 | c.2160C>T | synonymous_variant | 1.0 |
| rpoC | 765541 | c.2172C>G | synonymous_variant | 1.0 |
| rpoC | 765553 | c.2184C>T | synonymous_variant | 1.0 |
| rpoC | 765556 | c.2187G>C | synonymous_variant | 1.0 |
| rpoC | 765559 | c.2190G>C | synonymous_variant | 1.0 |
| rpoC | 765580 | c.2211G>C | synonymous_variant | 1.0 |
| rpoC | 765613 | p.His748Gln | missense_variant | 1.0 |
| rpoC | 765625 | c.2256C>G | synonymous_variant | 1.0 |
| rpoC | 765631 | p.Asp754Glu | missense_variant | 1.0 |
| rpoC | 765700 | c.2331T>C | synonymous_variant | 1.0 |
| rpoC | 765835 | c.2466C>T | synonymous_variant | 1.0 |
| rpoC | 765850 | c.2481G>C | synonymous_variant | 1.0 |
| rpoC | 765883 | c.2514C>G | synonymous_variant | 1.0 |
| rpoC | 765886 | c.2517C>G | synonymous_variant | 1.0 |
| rpoC | 765892 | c.2523T>C | synonymous_variant | 1.0 |
| rpoC | 765937 | c.2568T>C | synonymous_variant | 1.0 |
| rpoC | 765967 | c.2598C>T | synonymous_variant | 1.0 |
| rpoC | 765982 | c.2613C>G | synonymous_variant | 1.0 |
| rpoC | 765994 | c.2625A>T | synonymous_variant | 1.0 |
| rpoC | 766010 | c.2641_2642delTCinsAG | synonymous_variant | 1.0 |
| rpoC | 766021 | c.2652G>C | synonymous_variant | 1.0 |
| rpoC | 766023 | c.2655delC | frameshift_variant | 0.4 |
| rpoC | 766027 | c.2658G>C | synonymous_variant | 1.0 |
| rpoC | 766030 | c.2661C>G | synonymous_variant | 1.0 |
| rpoC | 766036 | c.2667C>T | synonymous_variant | 1.0 |
| rpoC | 766043 | p.Gln892Glu | missense_variant | 1.0 |
| rpoC | 766054 | c.2685C>G | synonymous_variant | 1.0 |
| rpoC | 766082 | p.Ala905Gln | missense_variant | 1.0 |
| rpoC | 766096 | c.2727G>C | synonymous_variant | 1.0 |
| rpoC | 766129 | c.2760C>G | synonymous_variant | 1.0 |
| rpoC | 766408 | c.3039C>G | synonymous_variant | 1.0 |
| rpoC | 766411 | c.3042C>G | synonymous_variant | 1.0 |
| rpoC | 766426 | c.3057C>T | synonymous_variant | 1.0 |
| rpoC | 766447 | c.3078T>C | synonymous_variant | 1.0 |
| rpoC | 766462 | c.3093G>C | synonymous_variant | 1.0 |
| rpoC | 766483 | c.3114G>C | synonymous_variant | 1.0 |
| rpoC | 766484 | p.Val1039Ile | missense_variant | 1.0 |
| rpoC | 766492 | c.3123T>C | synonymous_variant | 1.0 |
| rpoC | 766630 | c.3261G>C | synonymous_variant | 1.0 |
| rpoC | 766657 | c.3288A>G | synonymous_variant | 1.0 |
| rpoC | 766861 | c.3492G>C | synonymous_variant | 1.0 |
| rpoC | 766864 | c.3495G>C | synonymous_variant | 1.0 |
| rpoC | 766900 | c.3531T>C | synonymous_variant | 1.0 |
| rpoC | 766933 | c.3564A>G | synonymous_variant | 1.0 |
| rpoC | 766945 | c.3576A>G | synonymous_variant | 1.0 |
| rpoC | 766963 | c.3594T>C | synonymous_variant | 1.0 |
| rpoC | 766972 | c.3603G>C | synonymous_variant | 1.0 |
| rpoC | 766996 | c.3627C>T | synonymous_variant | 1.0 |
| rpoC | 767098 | c.3729T>C | synonymous_variant | 1.0 |
| rpoC | 767119 | c.3750A>G | synonymous_variant | 1.0 |
| rpoC | 767134 | c.3765C>A | synonymous_variant | 1.0 |
| rpoC | 767158 | c.3789T>C | synonymous_variant | 1.0 |
| rpoC | 767180 | p.Ala1271Gln | missense_variant | 1.0 |
| rpoC | 767191 | c.3822C>G | 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 |
| rpsL | 781595 | c.36T>C | synonymous_variant | 1.0 |
| rpsL | 781605 | p.Ile16Val | missense_variant | 1.0 |
| rpsL | 781608 | p.Ser17Ala | missense_variant | 1.0 |
| rpsL | 781628 | c.69T>C | synonymous_variant | 1.0 |
| rpsL | 781631 | c.72G>C | synonymous_variant | 1.0 |
| rpsL | 781649 | c.90T>C | synonymous_variant | 1.0 |
| rpsL | 781655 | c.96T>C | synonymous_variant | 1.0 |
| rpsL | 781682 | c.123T>C | synonymous_variant | 1.0 |
| rpsL | 781700 | c.141G>C | synonymous_variant | 1.0 |
| rpsL | 781703 | c.144G>T | synonymous_variant | 1.0 |
| rpsL | 781715 | c.156T>C | synonymous_variant | 1.0 |
| rpsL | 781728 | c.169T>C | synonymous_variant | 1.0 |
| rpsL | 781736 | c.177T>C | synonymous_variant | 1.0 |
| rpsL | 781742 | c.183C>T | synonymous_variant | 1.0 |
| rpsL | 781748 | c.189C>G | synonymous_variant | 1.0 |
| rpsL | 781754 | c.195G>C | synonymous_variant | 1.0 |
| rpsL | 781760 | c.201T>C | synonymous_variant | 1.0 |
| rpsL | 781772 | c.213C>A | synonymous_variant | 1.0 |
| rpsL | 781808 | c.249C>T | synonymous_variant | 1.0 |
| rpsL | 781811 | c.252C>T | synonymous_variant | 1.0 |
| rpsL | 781832 | c.273T>C | synonymous_variant | 1.0 |
| rpsL | 781838 | c.279G>C | synonymous_variant | 1.0 |
| rpsL | 781841 | c.282C>G | synonymous_variant | 1.0 |
| rpsL | 781865 | c.306G>C | synonymous_variant | 1.0 |
| rpsL | 781868 | c.309T>C | synonymous_variant | 1.0 |
| rpsL | 781871 | c.312G>C | synonymous_variant | 1.0 |
| rpsL | 781877 | c.318T>C | synonymous_variant | 1.0 |
| rpsL | 781892 | c.333A>G | synonymous_variant | 1.0 |
| rpsL | 781898 | c.339A>T | synonymous_variant | 1.0 |
| rpsL | 781916 | c.357T>C | synonymous_variant | 1.0 |
| rpsL | 781929 | p.Gly124Ser | missense_variant | 1.0 |
| rplC | 800612 | c.-197A>G | upstream_gene_variant | 1.0 |
| rplC | 800618 | c.-191T>C | upstream_gene_variant | 1.0 |
| rplC | 800627 | c.-182C>T | upstream_gene_variant | 1.0 |
| rplC | 800648 | c.-161A>T | upstream_gene_variant | 1.0 |
| rplC | 800654 | c.-155T>C | upstream_gene_variant | 1.0 |
| rplC | 800693 | c.-116A>G | upstream_gene_variant | 1.0 |
| rplC | 800703 | c.-106T>C | upstream_gene_variant | 1.0 |
| rplC | 800715 | c.-94A>C | upstream_gene_variant | 1.0 |
| rplC | 800720 | c.-89T>C | upstream_gene_variant | 1.0 |
| rplC | 800723 | c.-86C>G | upstream_gene_variant | 1.0 |
| rplC | 800747 | c.-62C>G | upstream_gene_variant | 1.0 |
| rplC | 800771 | c.-38C>T | upstream_gene_variant | 1.0 |
| rplC | 800814 | c.6A>G | synonymous_variant | 1.0 |
| rplC | 800817 | c.9A>T | synonymous_variant | 1.0 |
| rplC | 800844 | c.36T>C | synonymous_variant | 1.0 |
| rplC | 800865 | c.57A>G | synonymous_variant | 1.0 |
| rplC | 800867 | p.Ser20Asn | missense_variant | 1.0 |
| rplC | 800874 | c.66A>G | synonymous_variant | 1.0 |
| rplC | 800875 | p.Val23Ile | missense_variant | 1.0 |
| rplC | 800880 | c.72A>G | synonymous_variant | 1.0 |
| rplC | 800889 | c.81C>G | synonymous_variant | 1.0 |
| rplC | 800892 | c.84G>C | synonymous_variant | 1.0 |
| rplC | 800905 | p.Pro33Thr | missense_variant | 1.0 |
| rplC | 800916 | c.108A>G | synonymous_variant | 1.0 |
| fbiC | 1303998 | c.1068T>G | synonymous_variant | 1.0 |
| fbiC | 1304004 | c.1074A>G | synonymous_variant | 1.0 |
| fbiC | 1304008 | c.1078T>C | synonymous_variant | 1.0 |
| fbiC | 1304022 | c.1092T>C | synonymous_variant | 1.0 |
| fbiC | 1304031 | c.1101C>G | synonymous_variant | 1.0 |
| fbiC | 1304034 | c.1104A>G | synonymous_variant | 1.0 |
| fbiC | 1304040 | c.1110C>G | synonymous_variant | 1.0 |
| fbiC | 1304046 | c.1116C>G | synonymous_variant | 1.0 |
| fbiC | 1304049 | c.1119T>C | 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.1129_1131delCTGinsTTA | synonymous_variant | 1.0 |
| fbiC | 1304064 | c.1134G>C | synonymous_variant | 1.0 |
| fbiC | 1304067 | c.1137G>C | synonymous_variant | 1.0 |
| fbiC | 1304085 | c.1155C>T | synonymous_variant | 1.0 |
| fbiC | 1304091 | p.Asp387Glu | missense_variant | 1.0 |
| fbiC | 1304092 | p.Met388Leu | missense_variant | 1.0 |
| fbiC | 1304097 | c.1167G>C | synonymous_variant | 1.0 |
| rrs | 1471969 | n.124T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.33 |
| rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.25 |
| rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.56 |
| rrs | 1472225 | n.380C>G | non_coding_transcript_exon_variant | 0.67 |
| rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.5 |
| rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.5 |
| rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.5 |
| rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.67 |
| rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.5 |
| rrs | 1472518 | n.673G>C | non_coding_transcript_exon_variant | 0.5 |
| rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.75 |
| rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.5 |
| rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.29 |
| rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.29 |
| rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.29 |
| rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.29 |
| rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.29 |
| rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.67 |
| rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.33 |
| rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.71 |
| rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.78 |
| rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.71 |
| rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.62 |
| rrs | 1472694 | n.849C>G | non_coding_transcript_exon_variant | 0.38 |
| rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.38 |
| rrs | 1472707 | n.862A>G | non_coding_transcript_exon_variant | 0.38 |
| rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.71 |
| rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.3 |
| rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.25 |
| rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.42 |
| rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.42 |
| rrs | 1472770 | n.925C>T | non_coding_transcript_exon_variant | 0.38 |
| rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.5 |
| rrs | 1472786 | n.941C>T | non_coding_transcript_exon_variant | 0.33 |
| rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.57 |
| rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.5 |
| rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.83 |
| rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.62 |
| rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.4 |
| rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.4 |
| rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.33 |
| rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.33 |
| rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.5 |
| rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.6 |
| rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.6 |
| rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.44 |
| rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473147 | n.1302G>A | non_coding_transcript_exon_variant | 0.5 |
| rrs | 1473164 | n.1319C>T | non_coding_transcript_exon_variant | 0.62 |
| rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473179 | n.1334C>T | non_coding_transcript_exon_variant | 0.3 |
| rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.38 |
| rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.38 |
| rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.3 |
| rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.88 |
| rrs | 1473259 | n.1414C>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 |
| rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473833 | n.176_177insT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473844 | n.187C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473870 | n.213G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473871 | n.214T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473887 | n.230T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473888 | n.231T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474093 | n.436G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474099 | n.442G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.75 |
| rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474201 | n.544T>C | non_coding_transcript_exon_variant | 0.67 |
| rrl | 1474202 | n.545T>C | non_coding_transcript_exon_variant | 0.67 |
| rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474281 | n.624A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474316 | n.659T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474353 | n.696A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474354 | n.697C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474376 | n.719T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474383 | n.726G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474450 | n.793T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474454 | n.797G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474466 | n.809G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.67 |
| rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 0.67 |
| rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 0.67 |
| rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.67 |
| rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.67 |
| rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.5 |
| rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.75 |
| rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.5 |
| rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.67 |
| rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.5 |
| rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.29 |
| rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 0.44 |
| rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.44 |
| rrl | 1474751 | n.1094G>A | non_coding_transcript_exon_variant | 0.44 |
| rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.44 |
| rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.5 |
| rrl | 1474777 | n.1120T>C | non_coding_transcript_exon_variant | 0.55 |
| rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.71 |
| rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.71 |
| rrl | 1474783 | n.1126G>A | non_coding_transcript_exon_variant | 0.71 |
| rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.55 |
| rrl | 1474830 | n.1173A>T | non_coding_transcript_exon_variant | 0.55 |
| rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474904 | n.1247G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.43 |
| rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.6 |
| rrl | 1475006 | n.1349A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475088 | n.1431A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475191 | n.1537delC | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475199 | n.1542G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475206 | n.1549C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475209 | n.1552G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475249 | n.1592T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475252 | n.1595C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475659 | n.2002G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475758 | n.2101A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475766 | n.2109G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475791 | n.2134A>G | non_coding_transcript_exon_variant | 0.4 |
| rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.5 |
| rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.5 |
| rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.5 |
| rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.5 |
| rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.44 |
| rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.5 |
| rrl | 1475892 | n.2235A>C | non_coding_transcript_exon_variant | 0.5 |
| rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475963 | n.2306G>A | non_coding_transcript_exon_variant | 0.86 |
| rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.86 |
| rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.83 |
| rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.83 |
| rrl | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 0.83 |
| rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475997 | n.2340A>G | non_coding_transcript_exon_variant | 0.86 |
| rrl | 1475998 | n.2341C>T | non_coding_transcript_exon_variant | 0.83 |
| rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.86 |
| rrl | 1476024 | n.2367T>G | non_coding_transcript_exon_variant | 0.75 |
| rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476089 | n.2432T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476095 | n.2438C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476117 | n.2460G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.6 |
| rrl | 1476165 | n.2508T>A | non_coding_transcript_exon_variant | 0.6 |
| rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.67 |
| rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476214 | n.2557G>T | 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 | 1.0 |
| rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.67 |
| rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.5 |
| rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.5 |
| rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.5 |
| rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.33 |
| rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.67 |
| rrl | 1476308 | n.2651G>T | non_coding_transcript_exon_variant | 0.6 |
| rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.6 |
| rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.6 |
| rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.36 |
| rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.27 |
| rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.42 |
| rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.67 |
| rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.32 |
| rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.58 |
| rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.32 |
| rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.63 |
| rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.3 |
| rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.36 |
| rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.65 |
| rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.35 |
| rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.29 |
| rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.89 |
| rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.88 |
| rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.75 |
| rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.71 |
| rrl | 1476523 | n.2866T>C | non_coding_transcript_exon_variant | 0.67 |
| rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.67 |
| rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.67 |
| rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.67 |
| rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.8 |
| rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.67 |
| rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.67 |
| rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 1.0 |
| inhA | 1674602 | p.Leu134Pro | missense_variant | 1.0 |
| inhA | 1674624 | c.423A>C | synonymous_variant | 1.0 |
| inhA | 1674660 | c.459G>C | synonymous_variant | 1.0 |
| inhA | 1674672 | c.471C>G | synonymous_variant | 1.0 |
| inhA | 1674689 | p.Val163Ala | missense_variant | 0.5 |
| inhA | 1674703 | c.502T>C | synonymous_variant | 1.0 |
| inhA | 1674708 | c.507G>A | synonymous_variant | 1.0 |
| inhA | 1674718 | c.517A>C | synonymous_variant | 1.0 |
| inhA | 1674738 | c.537C>G | synonymous_variant | 1.0 |
| inhA | 1674741 | c.540C>T | synonymous_variant | 1.0 |
| inhA | 1674746 | p.Tyr182Phe | missense_variant | 1.0 |
| inhA | 1674750 | c.549T>C | synonymous_variant | 1.0 |
| inhA | 1674753 | c.552G>C | synonymous_variant | 1.0 |
| inhA | 1674756 | c.555T>C | synonymous_variant | 1.0 |
| inhA | 1674759 | c.558G>C | synonymous_variant | 1.0 |
| inhA | 1674870 | c.669T>C | synonymous_variant | 1.0 |
| inhA | 1674879 | c.678T>C | synonymous_variant | 1.0 |
| inhA | 1674888 | c.687C>G | synonymous_variant | 1.0 |
| inhA | 1674903 | c.702T>C | synonymous_variant | 1.0 |
| inhA | 1674904 | p.Ala235Pro | missense_variant | 1.0 |
| inhA | 1674909 | c.708G>A | synonymous_variant | 1.0 |
| inhA | 1674919 | p.Lys240* | stop_gained | 1.0 |
| inhA | 1674939 | c.738G>A | synonymous_variant | 1.0 |
| inhA | 1674942 | c.741T>G | synonymous_variant | 1.0 |
| inhA | 1674954 | c.753G>C | synonymous_variant | 1.0 |
| inhA | 1674960 | c.759C>G | synonymous_variant | 1.0 |
| inhA | 1674966 | c.765T>C | synonymous_variant | 1.0 |
| inhA | 1674967 | p.Asp256Thr | missense_variant | 1.0 |
| rpsA | 1833568 | c.27G>C | synonymous_variant | 1.0 |
| rpsA | 1833589 | c.48A>T | synonymous_variant | 1.0 |
| rpsA | 1833595 | c.54T>C | synonymous_variant | 1.0 |
| rpsA | 1833661 | c.120A>G | synonymous_variant | 1.0 |
| rpsA | 1833667 | c.126C>G | synonymous_variant | 0.67 |
| rpsA | 1833676 | c.135A>G | synonymous_variant | 0.6 |
| rpsA | 1833679 | c.138G>C | synonymous_variant | 0.6 |
| rpsA | 1833685 | c.144G>C | synonymous_variant | 0.6 |
| rpsA | 1833694 | c.153G>C | synonymous_variant | 0.6 |
| rpsA | 1833697 | c.156C>T | synonymous_variant | 0.6 |
| rpsA | 1833721 | c.180A>G | synonymous_variant | 1.0 |
| rpsA | 1833724 | c.183C>G | synonymous_variant | 0.67 |
| rpsA | 1833727 | c.186G>C | synonymous_variant | 1.0 |
| rpsA | 1833742 | c.201A>G | synonymous_variant | 1.0 |
| rpsA | 1833745 | c.204G>C | synonymous_variant | 0.67 |
| rpsA | 1833748 | c.207C>G | synonymous_variant | 0.67 |
| rpsA | 1833928 | c.387G>C | synonymous_variant | 1.0 |
| rpsA | 1833949 | c.408T>C | synonymous_variant | 0.75 |
| rpsA | 1833955 | c.414G>C | synonymous_variant | 0.75 |
| rpsA | 1833961 | c.420C>G | synonymous_variant | 0.75 |
| rpsA | 1833970 | c.429G>C | synonymous_variant | 1.0 |
| rpsA | 1833973 | c.432G>C | synonymous_variant | 0.75 |
| rpsA | 1833979 | c.438T>C | synonymous_variant | 1.0 |
| rpsA | 1833994 | c.453G>C | synonymous_variant | 0.38 |
| rpsA | 1833997 | c.456G>C | synonymous_variant | 0.38 |
| rpsA | 1834000 | c.459G>C | synonymous_variant | 1.0 |
| rpsA | 1834012 | c.471G>C | synonymous_variant | 0.5 |
| rpsA | 1834021 | c.480C>T | synonymous_variant | 0.5 |
| rpsA | 1834024 | c.483G>C | synonymous_variant | 0.38 |
| rpsA | 1834025 | p.Gln162Ala | missense_variant | 0.38 |
| rpsA | 1834030 | c.489C>G | synonymous_variant | 0.88 |
| rpsA | 1834040 | p.Lys167Gln | missense_variant | 0.38 |
| rpsA | 1834043 | p.Glu168Gln | missense_variant | 0.38 |
| rpsA | 1834210 | c.669C>T | synonymous_variant | 1.0 |
| rpsA | 1834222 | c.681T>C | synonymous_variant | 1.0 |
| rpsA | 1834231 | c.690T>C | synonymous_variant | 1.0 |
| rpsA | 1834234 | c.693G>C | synonymous_variant | 1.0 |
| rpsA | 1834249 | c.708T>C | synonymous_variant | 1.0 |
| rpsA | 1834264 | c.723G>C | synonymous_variant | 1.0 |
| rpsA | 1834303 | c.762T>C | synonymous_variant | 1.0 |
| rpsA | 1834306 | c.765T>C | synonymous_variant | 1.0 |
| rpsA | 1834327 | c.786G>C | synonymous_variant | 0.5 |
| rpsA | 1834336 | c.795C>G | synonymous_variant | 0.43 |
| rpsA | 1834348 | c.807T>C | synonymous_variant | 1.0 |
| rpsA | 1834366 | c.825A>G | synonymous_variant | 1.0 |
| rpsA | 1834395 | p.Arg285His | missense_variant | 0.43 |
| rpsA | 1834398 | p.His286Leu | missense_variant | 0.43 |
| rpsA | 1834411 | c.870T>C | synonymous_variant | 1.0 |
| rpsA | 1834417 | c.876G>C | synonymous_variant | 1.0 |
| rpsA | 1834418 | p.Ile293Leu | missense_variant | 1.0 |
| rpsA | 1834423 | c.882G>C | synonymous_variant | 1.0 |
| rpsA | 1834427 | p.Ile296Val | missense_variant | 1.0 |
| rpsA | 1834451 | c.910_912delTTGinsCTC | synonymous_variant | 1.0 |
| tlyA | 1918382 | p.Val148Ala | missense_variant | 1.0 |
| tlyA | 1918389 | c.450G>C | synonymous_variant | 1.0 |
| tlyA | 1918392 | c.453A>C | synonymous_variant | 1.0 |
| tlyA | 1918417 | c.478T>C | synonymous_variant | 1.0 |
| tlyA | 1918422 | c.483T>C | synonymous_variant | 1.0 |
| tlyA | 1918442 | p.Val168Ala | missense_variant | 1.0 |
| tlyA | 1918446 | c.507A>C | synonymous_variant | 1.0 |
| tlyA | 1918457 | p.Arg173His | missense_variant | 1.0 |
| tlyA | 1918464 | c.525C>G | synonymous_variant | 1.0 |
| tlyA | 1918476 | c.537A>C | synonymous_variant | 1.0 |
| tlyA | 1918477 | p.Leu180Met | missense_variant | 1.0 |
| tlyA | 1918488 | c.549G>A | synonymous_variant | 1.0 |
| tlyA | 1918506 | c.567A>G | synonymous_variant | 1.0 |
| tlyA | 1918509 | c.570T>C | synonymous_variant | 1.0 |
| ndh | 2101723 | c.1320G>C | synonymous_variant | 1.0 |
| ndh | 2101726 | c.1317A>C | synonymous_variant | 1.0 |
| ndh | 2101729 | c.1314G>C | synonymous_variant | 1.0 |
| ndh | 2101732 | c.1311T>C | synonymous_variant | 1.0 |
| ndh | 2101735 | c.1308A>G | synonymous_variant | 1.0 |
| ndh | 2101744 | p.Asp433Glu | missense_variant | 1.0 |
| ndh | 2101756 | c.1287G>C | synonymous_variant | 1.0 |
| ndh | 2101765 | c.1278C>G | synonymous_variant | 1.0 |
| ndh | 2101768 | c.1275C>A | synonymous_variant | 1.0 |
| ndh | 2101771 | c.1272T>G | synonymous_variant | 1.0 |
| ndh | 2101774 | c.1269T>C | synonymous_variant | 1.0 |
| ndh | 2101777 | c.1266C>G | synonymous_variant | 1.0 |
| ndh | 2101783 | c.1260T>A | synonymous_variant | 1.0 |
| ndh | 2101804 | c.1239T>G | synonymous_variant | 1.0 |
| ndh | 2102635 | c.408C>G | synonymous_variant | 1.0 |
| ndh | 2102638 | c.405A>C | synonymous_variant | 1.0 |
| ndh | 2102644 | c.399A>G | synonymous_variant | 1.0 |
| ndh | 2102671 | c.372T>G | synonymous_variant | 1.0 |
| ndh | 2102680 | c.363T>G | synonymous_variant | 1.0 |
| ndh | 2102683 | c.360T>C | synonymous_variant | 1.0 |
| ndh | 2102695 | c.348C>T | synonymous_variant | 1.0 |
| ndh | 2102700 | c.343C>T | synonymous_variant | 1.0 |
| ndh | 2102710 | c.333C>T | synonymous_variant | 1.0 |
| ndh | 2102718 | p.Gln109Glu | missense_variant | 1.0 |
| ndh | 2102728 | c.315T>C | synonymous_variant | 1.0 |
| katG | 2155632 | c.480A>C | synonymous_variant | 1.0 |
| katG | 2155637 | p.Leu159Ile | missense_variant | 1.0 |
| katG | 2155641 | p.Lys157Asn | missense_variant | 1.0 |
| katG | 2155661 | p.Val151Ile | missense_variant | 1.0 |
| katG | 2155680 | c.432G>C | synonymous_variant | 1.0 |
| katG | 2155691 | c.421T>C | synonymous_variant | 1.0 |
| katG | 2155695 | c.417C>G | synonymous_variant | 1.0 |
| katG | 2155704 | c.408C>G | synonymous_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 | 2155740 | p.Gly124Gln | missense_variant | 1.0 |
| katG | 2155743 | c.369G>C | synonymous_variant | 1.0 |
| pncA | 2290009 | c.-768A>C | upstream_gene_variant | 1.0 |
| pncA | 2290015 | c.-774A>C | upstream_gene_variant | 1.0 |
| pncA | 2290024 | c.-783C>G | upstream_gene_variant | 1.0 |
| pncA | 2290030 | c.-791_-789delAATinsCAC | upstream_gene_variant | 1.0 |
| pncA | 2290033 | c.-792C>G | upstream_gene_variant | 1.0 |
| pncA | 2290038 | c.-797G>A | upstream_gene_variant | 1.0 |
| pncA | 2290042 | c.-801T>C | upstream_gene_variant | 1.0 |
| pncA | 2290069 | c.-830_-828delAGCinsGGA | upstream_gene_variant | 1.0 |
| pncA | 2290072 | c.-831T>C | upstream_gene_variant | 1.0 |
| pncA | 2290075 | c.-834C>G | upstream_gene_variant | 1.0 |
| pncA | 2290087 | c.-846T>C | upstream_gene_variant | 1.0 |
| pncA | 2290099 | c.-858C>T | upstream_gene_variant | 1.0 |
| kasA | 2518506 | p.Ala131Glu | missense_variant | 1.0 |
| kasA | 2518519 | c.405G>C | synonymous_variant | 1.0 |
| kasA | 2518528 | c.414C>G | synonymous_variant | 1.0 |
| kasA | 2518540 | c.426T>C | synonymous_variant | 1.0 |
| kasA | 2518561 | c.447T>C | synonymous_variant | 1.0 |
| kasA | 2518567 | c.453G>C | synonymous_variant | 1.0 |
| kasA | 2518570 | c.456G>C | synonymous_variant | 1.0 |
| kasA | 2518574 | p.Ile154Val | missense_variant | 1.0 |
| kasA | 2518579 | c.465T>C | synonymous_variant | 1.0 |
| kasA | 2518588 | c.474T>C | synonymous_variant | 1.0 |
| kasA | 2518591 | c.477G>A | synonymous_variant | 1.0 |
| kasA | 2518603 | c.489G>C | synonymous_variant | 1.0 |
| kasA | 2518609 | p.Met165Ile | missense_variant | 1.0 |
| kasA | 2518624 | c.510C>G | synonymous_variant | 1.0 |
| kasA | 2518639 | c.525G>C | synonymous_variant | 1.0 |
| kasA | 2518672 | c.558G>C | synonymous_variant | 1.0 |
| kasA | 2518678 | c.564C>T | synonymous_variant | 1.0 |
| kasA | 2518684 | c.570C>G | synonymous_variant | 1.0 |
| kasA | 2518693 | c.579C>G | synonymous_variant | 1.0 |
| kasA | 2518696 | c.582C>G | synonymous_variant | 1.0 |
| kasA | 2518702 | c.588C>T | synonymous_variant | 1.0 |
| kasA | 2518705 | c.591T>C | synonymous_variant | 1.0 |
| kasA | 2518711 | c.597A>G | synonymous_variant | 1.0 |
| kasA | 2518714 | c.600A>C | synonymous_variant | 1.0 |
| kasA | 2518732 | c.618C>G | synonymous_variant | 1.0 |
| kasA | 2518744 | c.630C>T | synonymous_variant | 1.0 |
| kasA | 2518747 | c.633C>G | synonymous_variant | 1.0 |
| kasA | 2518768 | c.654C>T | synonymous_variant | 1.0 |
| kasA | 2519062 | c.948T>G | synonymous_variant | 1.0 |
| kasA | 2519068 | c.954C>T | synonymous_variant | 1.0 |
| kasA | 2519072 | p.Ala320Thr | missense_variant | 1.0 |
| kasA | 2519107 | c.993T>C | synonymous_variant | 1.0 |
| kasA | 2519108 | p.Asp332Gln | missense_variant | 1.0 |
| kasA | 2519116 | c.1002C>G | synonymous_variant | 1.0 |
| kasA | 2519122 | c.1008G>C | synonymous_variant | 1.0 |
| kasA | 2519137 | c.1023T>G | synonymous_variant | 1.0 |
| kasA | 2519158 | c.1044C>T | synonymous_variant | 1.0 |
| kasA | 2519167 | c.1053T>G | synonymous_variant | 1.0 |
| kasA | 2519173 | c.1059C>G | synonymous_variant | 1.0 |
| thyX | 3067223 | c.723G>C | synonymous_variant | 1.0 |
| thyX | 3067232 | c.714C>G | synonymous_variant | 1.0 |
| thyX | 3067246 | p.Thr234Ala | missense_variant | 1.0 |
| thyX | 3067249 | p.Thr233Ser | missense_variant | 1.0 |
| thyX | 3067250 | p.Val232Ile | missense_variant | 1.0 |
| thyX | 3067274 | c.672C>G | synonymous_variant | 1.0 |
| thyX | 3067277 | c.669C>G | synonymous_variant | 1.0 |
| thyX | 3067281 | p.Val222Ala | missense_variant | 1.0 |
| thyX | 3067284 | p.Ala221Gly | missense_variant | 1.0 |
| thyX | 3067286 | c.660C>G | synonymous_variant | 1.0 |
| thyX | 3067289 | c.657C>G | synonymous_variant | 1.0 |
| thyX | 3067292 | c.654G>A | synonymous_variant | 1.0 |
| thyX | 3067295 | c.651C>T | synonymous_variant | 1.0 |
| thyX | 3067316 | c.630A>G | synonymous_variant | 1.0 |
| thyX | 3067439 | c.507A>G | synonymous_variant | 1.0 |
| thyX | 3067442 | c.504C>T | synonymous_variant | 1.0 |
| thyX | 3067445 | c.501C>G | synonymous_variant | 1.0 |
| thyX | 3067457 | c.489C>G | synonymous_variant | 1.0 |
| thyX | 3067465 | p.Ile161Val | missense_variant | 1.0 |
| thyX | 3067661 | c.285C>G | synonymous_variant | 1.0 |
| thyX | 3067685 | c.261A>C | synonymous_variant | 1.0 |
| thyX | 3067691 | p.Ile85Leu | missense_variant | 1.0 |
| thyX | 3067694 | c.252G>C | synonymous_variant | 1.0 |
| thyX | 3067718 | c.228C>G | synonymous_variant | 1.0 |
| thyX | 3067721 | c.225T>C | synonymous_variant | 1.0 |
| thyX | 3067727 | c.219A>C | synonymous_variant | 1.0 |
| thyA | 3074112 | c.360C>G | synonymous_variant | 1.0 |
| thyA | 3074127 | c.345G>C | synonymous_variant | 1.0 |
| thyA | 3074130 | c.342G>C | synonymous_variant | 1.0 |
| thyA | 3074154 | c.318T>C | synonymous_variant | 1.0 |
| thyA | 3074157 | c.315C>G | synonymous_variant | 1.0 |
| thyA | 3074160 | c.312A>G | synonymous_variant | 1.0 |
| thyA | 3074163 | p.Ala103Thr | missense_variant | 1.0 |
| thyA | 3074172 | c.300G>C | synonymous_variant | 1.0 |
| thyA | 3074175 | c.297A>G | synonymous_variant | 1.0 |
| thyA | 3074181 | c.291A>G | synonymous_variant | 1.0 |
| thyA | 3074187 | c.285T>C | synonymous_variant | 1.0 |
| thyA | 3074205 | p.Glu89Asp | missense_variant | 1.0 |
| thyA | 3074214 | c.258T>C | synonymous_variant | 1.0 |
| thyA | 3074412 | c.60C>T | synonymous_variant | 1.0 |
| thyA | 3074423 | p.Pro17Ala | missense_variant | 1.0 |
| thyA | 3074427 | c.45T>A | synonymous_variant | 1.0 |
| thyA | 3074431 | p.Thr14Glu | missense_variant | 1.0 |
| thyA | 3074433 | p.Glu13Asp | missense_variant | 1.0 |
| thyA | 3074442 | p.Phe10Leu | missense_variant | 1.0 |
| thyA | 3074445 | c.27C>A | synonymous_variant | 1.0 |
| thyA | 3074448 | c.24G>T | synonymous_variant | 1.0 |
| thyA | 3074463 | c.9A>C | synonymous_variant | 1.0 |
| thyA | 3074470 | p.Val1Pro | missense_variant | 1.0 |
| thyA | 3074477 | c.-6T>C | upstream_gene_variant | 1.0 |
| thyA | 3074482 | c.-11G>A | upstream_gene_variant | 1.0 |
| thyA | 3074490 | c.-19G>A | upstream_gene_variant | 1.0 |
| fbiA | 3640347 | c.-196A>G | upstream_gene_variant | 1.0 |
| fbiA | 3640349 | c.-194A>G | upstream_gene_variant | 1.0 |
| fbiA | 3640350 | c.-193C>T | upstream_gene_variant | 1.0 |
| fbiA | 3640365 | c.-178C>G | upstream_gene_variant | 1.0 |
| fbiA | 3640820 | p.Val93Ala | missense_variant | 1.0 |
| fbiB | 3640827 | c.-708T>C | upstream_gene_variant | 1.0 |
| fbiB | 3640830 | c.-705C>G | upstream_gene_variant | 1.0 |
| fbiB | 3640839 | c.-696C>G | upstream_gene_variant | 1.0 |
| fbiA | 3640850 | p.Glu103Gly | missense_variant | 1.0 |
| fbiB | 3640857 | c.-678G>C | upstream_gene_variant | 1.0 |
| fbiB | 3640866 | c.-669T>C | upstream_gene_variant | 1.0 |
| fbiA | 3640871 | p.Ala110Gly | missense_variant | 1.0 |
| fbiB | 3640878 | c.-657T>C | upstream_gene_variant | 1.0 |
| fbiB | 3640899 | c.-636G>C | upstream_gene_variant | 1.0 |
| fbiA | 3640900 | p.Gln120Asn | missense_variant | 1.0 |
| fbiB | 3640914 | c.-621C>G | upstream_gene_variant | 1.0 |
| rpoA | 3877553 | p.Glu319Gln | missense_variant | 1.0 |
| rpoA | 3877571 | p.Pro313Ala | missense_variant | 1.0 |
| rpoA | 3877587 | c.921A>G | synonymous_variant | 1.0 |
| rpoA | 3877613 | p.Ile299Val | missense_variant | 1.0 |
| rpoA | 3877926 | c.582G>C | synonymous_variant | 1.0 |
| rpoA | 3877989 | c.519A>G | synonymous_variant | 1.0 |
| rpoA | 3878001 | c.507A>G | synonymous_variant | 1.0 |
| rpoA | 3878022 | c.486T>C | synonymous_variant | 1.0 |
| rpoA | 3878028 | c.480G>C | synonymous_variant | 1.0 |
| rpoA | 3878031 | c.477T>C | synonymous_variant | 1.0 |
| rpoA | 3878040 | c.468T>C | synonymous_variant | 1.0 |
| rpoA | 3878043 | c.465G>A | synonymous_variant | 1.0 |
| rpoA | 3878665 | c.-158A>G | upstream_gene_variant | 1.0 |
| rpoA | 3878672 | c.-165A>T | upstream_gene_variant | 1.0 |
| rpoA | 3878683 | c.-176G>C | upstream_gene_variant | 1.0 |
| ddn | 3986645 | c.-199G>A | upstream_gene_variant | 1.0 |
| ddn | 3986646 | c.-198_-196delCTCinsTTG | upstream_gene_variant | 1.0 |
| clpC1 | 4038509 | c.2196C>T | synonymous_variant | 1.0 |
| clpC1 | 4038530 | p.Glu725Asp | missense_variant | 1.0 |
| clpC1 | 4038596 | c.2109A>G | synonymous_variant | 1.0 |
| clpC1 | 4038623 | c.2082A>G | synonymous_variant | 1.0 |
| clpC1 | 4038640 | p.Asp689Asn | missense_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 | 4038671 | c.2034T>C | synonymous_variant | 1.0 |
| clpC1 | 4038683 | c.2022T>C | synonymous_variant | 1.0 |
| clpC1 | 4038695 | c.2010C>G | synonymous_variant | 1.0 |
| clpC1 | 4038701 | c.2004G>C | synonymous_variant | 1.0 |
| clpC1 | 4038704 | c.2001T>C | synonymous_variant | 1.0 |
| clpC1 | 4038707 | c.1998C>G | synonymous_variant | 1.0 |
| clpC1 | 4038710 | c.1995G>C | synonymous_variant | 1.0 |
| clpC1 | 4038713 | c.1992T>C | synonymous_variant | 1.0 |
| clpC1 | 4038770 | c.1935C>T | synonymous_variant | 0.67 |
| clpC1 | 4038773 | c.1932T>C | synonymous_variant | 1.0 |
| clpC1 | 4038782 | c.1923G>C | synonymous_variant | 1.0 |
| clpC1 | 4038812 | c.1893T>C | synonymous_variant | 1.0 |
| clpC1 | 4038845 | c.1860G>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 | 4039064 | c.1641C>T | synonymous_variant | 1.0 |
| clpC1 | 4039097 | c.1608G>C | synonymous_variant | 1.0 |
| clpC1 | 4039103 | c.1602T>C | synonymous_variant | 1.0 |
| clpC1 | 4039106 | c.1599G>C | synonymous_variant | 1.0 |
| clpC1 | 4039112 | c.1593C>G | synonymous_variant | 1.0 |
| clpC1 | 4039121 | c.1584T>C | synonymous_variant | 1.0 |
| clpC1 | 4039274 | c.1431G>C | synonymous_variant | 1.0 |
| clpC1 | 4039286 | c.1419T>C | synonymous_variant | 1.0 |
| clpC1 | 4039409 | c.1296T>C | synonymous_variant | 1.0 |
| clpC1 | 4039412 | c.1293T>G | synonymous_variant | 1.0 |
| clpC1 | 4039415 | p.Glu430Asp | missense_variant | 1.0 |
| clpC1 | 4039430 | c.1275T>C | synonymous_variant | 1.0 |
| clpC1 | 4039442 | c.1263A>G | synonymous_variant | 1.0 |
| clpC1 | 4039826 | c.879C>G | synonymous_variant | 0.67 |
| clpC1 | 4039831 | c.874T>C | synonymous_variant | 1.0 |
| clpC1 | 4039850 | c.855T>C | synonymous_variant | 1.0 |
| clpC1 | 4039865 | c.840T>C | synonymous_variant | 1.0 |
| clpC1 | 4039875 | p.Asn277Arg | missense_variant | 0.4 |
| clpC1 | 4039901 | c.804C>G | synonymous_variant | 0.33 |
| clpC1 | 4039928 | c.775_777delAGCinsTCG | synonymous_variant | 0.67 |
| clpC1 | 4039931 | c.774T>C | synonymous_variant | 1.0 |
| clpC1 | 4039937 | c.768G>C | synonymous_variant | 1.0 |
| clpC1 | 4039946 | c.759A>C | synonymous_variant | 1.0 |
| clpC1 | 4039952 | c.753T>C | synonymous_variant | 1.0 |
| clpC1 | 4039988 | c.717C>G | synonymous_variant | 1.0 |
| clpC1 | 4039991 | c.714G>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 | 0.67 |
| clpC1 | 4040036 | c.669C>G | synonymous_variant | 0.67 |
| clpC1 | 4040090 | c.615T>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 | 4040201 | c.504C>G | synonymous_variant | 1.0 |
| clpC1 | 4040207 | c.498T>G | synonymous_variant | 1.0 |
| clpC1 | 4040210 | c.495G>C | synonymous_variant | 1.0 |
| clpC1 | 4040213 | c.490_492delTCTinsAGC | synonymous_variant | 1.0 |
| clpC1 | 4040225 | c.480A>C | synonymous_variant | 1.0 |
| clpC1 | 4040228 | c.477G>T | synonymous_variant | 1.0 |
| clpC1 | 4040237 | c.468C>T | synonymous_variant | 1.0 |
| clpC1 | 4040246 | c.459C>G | synonymous_variant | 1.0 |
| clpC1 | 4040249 | c.456A>G | synonymous_variant | 1.0 |
| clpC1 | 4040318 | c.387C>G | synonymous_variant | 1.0 |
| clpC1 | 4040330 | c.375C>G | synonymous_variant | 1.0 |
| clpC1 | 4040342 | c.363C>G | synonymous_variant | 1.0 |
| clpC1 | 4040354 | c.351A>G | synonymous_variant | 1.0 |
| clpC1 | 4040363 | c.342A>T | synonymous_variant | 1.0 |
| clpC1 | 4040369 | c.336C>G | synonymous_variant | 1.0 |
| clpC1 | 4040380 | c.325T>C | synonymous_variant | 1.0 |
| clpC1 | 4040381 | c.324T>C | synonymous_variant | 1.0 |
| clpC1 | 4040387 | c.318A>G | synonymous_variant | 1.0 |
| clpC1 | 4040393 | c.312G>C | synonymous_variant | 1.0 |
| clpC1 | 4040411 | c.294T>C | synonymous_variant | 1.0 |
| embC | 4240444 | c.582C>G | synonymous_variant | 1.0 |
| embC | 4240459 | c.597G>C | synonymous_variant | 1.0 |
| embC | 4240462 | c.600G>C | synonymous_variant | 1.0 |
| embC | 4240471 | c.609C>T | synonymous_variant | 1.0 |
| embC | 4240474 | c.612G>C | synonymous_variant | 1.0 |
| embC | 4240475 | p.Ala205Ser | missense_variant | 1.0 |
| embC | 4240484 | p.Ala208Thr | missense_variant | 1.0 |
| embC | 4240489 | c.627A>G | synonymous_variant | 1.0 |
| embC | 4240492 | c.630G>C | synonymous_variant | 1.0 |
| embC | 4240495 | c.633T>G | synonymous_variant | 1.0 |
| embC | 4240505 | p.Ser215Ala | missense_variant | 1.0 |
| embC | 4240512 | p.Ser217Thr | missense_variant | 1.0 |
| embC | 4240516 | c.654G>C | synonymous_variant | 1.0 |
| embC | 4240519 | c.657T>C | synonymous_variant | 1.0 |
| embC | 4241449 | c.1587C>G | synonymous_variant | 1.0 |
| embC | 4241453 | p.Ile531Val | missense_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 |
| embC | 4241496 | p.Ala545Gly | missense_variant | 1.0 |
| embC | 4241500 | c.1638A>C | synonymous_variant | 1.0 |
| embC | 4241501 | p.Ser547Thr | missense_variant | 1.0 |
| embC | 4241506 | c.1644G>C | synonymous_variant | 1.0 |
| embC | 4241518 | c.1656A>G | synonymous_variant | 1.0 |
| embC | 4241521 | c.1659T>C | synonymous_variant | 1.0 |
| embC | 4241530 | c.1668C>A | synonymous_variant | 1.0 |
| embC | 4241536 | c.1674A>G | synonymous_variant | 1.0 |
| embC | 4241539 | c.1677T>C | synonymous_variant | 1.0 |
| embC | 4241545 | c.1683T>C | synonymous_variant | 1.0 |
| embC | 4241548 | c.1686T>C | synonymous_variant | 1.0 |
| embC | 4241551 | c.1689A>G | synonymous_variant | 1.0 |
| embC | 4241567 | p.Ile569Val | missense_variant | 1.0 |
| embC | 4241572 | c.1710C>G | synonymous_variant | 1.0 |
| embC | 4241578 | c.1716G>C | synonymous_variant | 1.0 |
| embC | 4241584 | c.1722T>C | synonymous_variant | 1.0 |
| embC | 4241587 | c.1725C>G | synonymous_variant | 1.0 |
| embC | 4241591 | p.Leu577Val | missense_variant | 1.0 |
| embC | 4241611 | c.1749G>C | synonymous_variant | 1.0 |
| embC | 4241614 | c.1752A>C | synonymous_variant | 1.0 |
| embA | 4244462 | c.1230A>G | synonymous_variant | 1.0 |
| embA | 4244478 | p.Thr416Leu | missense_variant | 1.0 |
| embA | 4244483 | c.1251T>G | synonymous_variant | 1.0 |
| embA | 4244485 | p.Thr418Ser | missense_variant | 1.0 |
| embA | 4244498 | c.1266A>G | synonymous_variant | 1.0 |
| embA | 4244507 | c.1275G>T | synonymous_variant | 1.0 |
| embA | 4244508 | c.1276T>C | synonymous_variant | 1.0 |
| embA | 4244516 | c.1284G>C | synonymous_variant | 1.0 |
| embA | 4244517 | p.Leu429Val | missense_variant | 1.0 |
| embA | 4244523 | p.Pro431Ala | missense_variant | 1.0 |
| embA | 4244531 | c.1299G>C | synonymous_variant | 1.0 |
| embA | 4244534 | c.1302T>C | synonymous_variant | 1.0 |
| embA | 4244537 | c.1305T>G | synonymous_variant | 1.0 |
| embA | 4244543 | c.1311C>G | synonymous_variant | 1.0 |
| embA | 4244547 | p.Ile439Val | missense_variant | 1.0 |
| embA | 4244557 | p.Arg442Thr | missense_variant | 1.0 |
| embA | 4244690 | c.1458G>A | synonymous_variant | 1.0 |
| embA | 4244702 | c.1470C>G | synonymous_variant | 1.0 |
| embA | 4244708 | c.1476C>G | synonymous_variant | 1.0 |
| embA | 4244728 | p.Phe499Cys | missense_variant | 1.0 |
| embA | 4245060 | c.1828T>C | synonymous_variant | 1.0 |
| embA | 4245083 | c.1851A>C | synonymous_variant | 1.0 |
| embA | 4245089 | c.1857G>C | synonymous_variant | 1.0 |
| embA | 4245101 | c.1869G>C | synonymous_variant | 1.0 |
| embA | 4245137 | c.1905T>C | synonymous_variant | 1.0 |
| embA | 4245146 | c.1914G>A | synonymous_variant | 1.0 |
| embA | 4245149 | c.1917C>G | synonymous_variant | 1.0 |
| embA | 4245153 | p.Ile641Val | missense_variant | 1.0 |
| embA | 4245182 | c.1950T>C | synonymous_variant | 1.0 |
| embA | 4245189 | c.1957C>T | synonymous_variant | 1.0 |
| embA | 4245198 | p.Leu656Ile | missense_variant | 1.0 |
| embA | 4245207 | c.1975T>C | synonymous_variant | 1.0 |
| embA | 4245215 | c.1983A>C | synonymous_variant | 1.0 |
| embA | 4245222 | p.Tyr664Gln | missense_variant | 1.0 |
| embA | 4245248 | c.2016G>C | synonymous_variant | 1.0 |
| embA | 4245257 | c.2025A>G | synonymous_variant | 1.0 |
| embA | 4245263 | c.2031A>G | synonymous_variant | 1.0 |
| embB | 4245737 | c.-777A>C | upstream_gene_variant | 1.0 |
| embB | 4245740 | c.-774T>C | upstream_gene_variant | 1.0 |
| embB | 4245764 | c.-750G>C | upstream_gene_variant | 1.0 |
| embA | 4245772 | p.Asn847Thr | missense_variant | 1.0 |
| embB | 4245785 | c.-729G>C | upstream_gene_variant | 1.0 |
| embB | 4245807 | c.-707_-705delTTAinsCTG | upstream_gene_variant | 1.0 |
| embB | 4245812 | c.-702G>C | upstream_gene_variant | 1.0 |
| embA | 4245813 | p.Pro861Ala | missense_variant | 1.0 |
| embA | 4245820 | p.Ser863Thr | missense_variant | 1.0 |
| embB | 4245824 | c.-690G>C | upstream_gene_variant | 1.0 |
| embB | 4245833 | c.-681G>C | upstream_gene_variant | 1.0 |
| embB | 4245842 | c.-672G>C | upstream_gene_variant | 1.0 |
| embB | 4245845 | c.-669T>C | upstream_gene_variant | 1.0 |
| embB | 4245851 | c.-663G>C | upstream_gene_variant | 1.0 |
| embB | 4245860 | c.-654C>G | upstream_gene_variant | 1.0 |
| embB | 4247386 | c.873T>C | synonymous_variant | 1.0 |
| embB | 4247395 | c.882C>G | synonymous_variant | 1.0 |
| embB | 4247401 | c.888T>C | synonymous_variant | 1.0 |
| embB | 4247407 | c.894G>C | synonymous_variant | 1.0 |
| embB | 4247425 | c.912G>C | synonymous_variant | 1.0 |
| embB | 4247434 | c.921C>A | synonymous_variant | 1.0 |
| embB | 4247437 | c.924A>G | synonymous_variant | 1.0 |
| embB | 4247440 | c.927C>G | synonymous_variant | 1.0 |
| embB | 4247446 | c.933C>T | synonymous_variant | 1.0 |
| embB | 4247461 | p.Met316Ile | missense_variant | 1.0 |
| embB | 4247464 | c.951C>G | synonymous_variant | 1.0 |
| embB | 4247470 | c.957T>C | synonymous_variant | 1.0 |
| embB | 4247491 | c.978G>C | synonymous_variant | 1.0 |
| embB | 4247497 | c.984T>C | synonymous_variant | 1.0 |
| embB | 4248007 | c.1494C>G | synonymous_variant | 1.0 |
| embB | 4248011 | p.Ser500Arg | missense_variant | 1.0 |
| embB | 4248014 | p.Thr501Ala | missense_variant | 1.0 |
| embB | 4248035 | p.Val508Ile | missense_variant | 1.0 |
| embB | 4248040 | c.1527C>G | synonymous_variant | 1.0 |
| embB | 4248041 | p.Ala510Thr | missense_variant | 1.0 |
| embB | 4248044 | p.Lys511Ala | missense_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 | 4248343 | c.1830G>C | synonymous_variant | 1.0 |
| embB | 4248350 | c.1837T>C | synonymous_variant | 1.0 |
| embB | 4248355 | c.1842A>G | synonymous_variant | 1.0 |
| embB | 4248358 | c.1845C>G | synonymous_variant | 1.0 |
| embB | 4248361 | c.1848A>C | synonymous_variant | 1.0 |
| embB | 4248362 | p.Ser617Ala | missense_variant | 1.0 |
| embB | 4248373 | c.1860C>G | synonymous_variant | 1.0 |
| embB | 4248386 | c.1873C>A | synonymous_variant | 1.0 |
| embB | 4248407 | p.Leu632Val | missense_variant | 1.0 |
| embB | 4248410 | p.Phe633Leu | missense_variant | 1.0 |
| embB | 4248419 | p.Leu636Met | missense_variant | 1.0 |
| embB | 4248425 | c.1912T>C | synonymous_variant | 1.0 |
| embB | 4248430 | c.1917T>C | synonymous_variant | 1.0 |
| embB | 4248432 | p.Trp640Phe | missense_variant | 1.0 |
| embB | 4248457 | c.1944T>C | synonymous_variant | 1.0 |
| aftB | 4268360 | p.Ser159Ala | missense_variant | 1.0 |
| aftB | 4268386 | c.451T>C | synonymous_variant | 1.0 |
| aftB | 4268393 | c.444G>C | synonymous_variant | 1.0 |
| aftB | 4268396 | c.441T>C | synonymous_variant | 1.0 |
| aftB | 4268404 | c.433T>C | synonymous_variant | 1.0 |
| aftB | 4268406 | p.Val144Ala | missense_variant | 1.0 |
| aftB | 4268410 | c.427C>T | synonymous_variant | 1.0 |
| aftB | 4268411 | c.426G>T | synonymous_variant | 1.0 |
| aftB | 4268417 | c.420G>A | synonymous_variant | 1.0 |
| aftB | 4268426 | c.411C>G | synonymous_variant | 1.0 |
| aftB | 4268444 | c.393C>G | synonymous_variant | 1.0 |
| aftB | 4268450 | c.387A>G | synonymous_variant | 1.0 |
| aftB | 4268455 | p.Val128Leu | missense_variant | 1.0 |
| aftB | 4268462 | c.375T>C | synonymous_variant | 1.0 |
| aftB | 4268465 | c.372A>G | synonymous_variant | 1.0 |
| ethR | 4327396 | c.-153A>G | upstream_gene_variant | 1.0 |
| ethA | 4327399 | p.Asp25Glu | missense_variant | 1.0 |
| ethR | 4327423 | c.-126G>C | upstream_gene_variant | 1.0 |
| ethR | 4327435 | c.-114T>G | upstream_gene_variant | 1.0 |
| ethR | 4327438 | c.-111A>G | upstream_gene_variant | 1.0 |
| ethA | 4327452 | p.Val8Leu | missense_variant | 1.0 |
| ethR | 4327453 | c.-96A>G | upstream_gene_variant | 1.0 |
| ethR | 4327459 | c.-90G>A | upstream_gene_variant | 1.0 |
| ethA | 4328463 | c.-990G>C | upstream_gene_variant | 1.0 |
| ethA | 4328467 | c.-994G>T | upstream_gene_variant | 1.0 |
| ethA | 4328470 | c.-998_-997delAGinsGC | upstream_gene_variant | 1.0 |
