Run ID: ERR4817037
Sample name:
Date: 01-04-2023 14:46:07
Number of reads: 30426
Percentage reads mapped: 26.56
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 |
|---|---|---|---|---|---|
| embB | 4247588 | p.Leu359Ile | missense_variant | 1.0 | ethambutol |
| Gene | Chromosome position | Mutation | Type | Estimated fraction |
|---|---|---|---|---|
| gyrB | 6196 | c.957C>T | 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 | 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 | 6811 | c.-491C>T | upstream_gene_variant | 1.0 |
| gyrA | 6952 | c.-350C>G | upstream_gene_variant | 1.0 |
| gyrA | 6967 | c.-335T>C | upstream_gene_variant | 1.0 |
| gyrA | 6973 | c.-329G>C | upstream_gene_variant | 1.0 |
| gyrA | 6982 | c.-320A>C | upstream_gene_variant | 1.0 |
| gyrA | 7007 | c.-295C>T | upstream_gene_variant | 1.0 |
| gyrA | 7010 | c.-292C>T | upstream_gene_variant | 1.0 |
| gyrB | 7023 | p.Leu595Gln | missense_variant | 1.0 |
| gyrA | 7033 | c.-269G>C | upstream_gene_variant | 1.0 |
| gyrB | 7051 | p.Glu604Asp | missense_variant | 1.0 |
| gyrA | 7066 | c.-236G>C | upstream_gene_variant | 1.0 |
| gyrA | 7078 | c.-224A>C | upstream_gene_variant | 1.0 |
| gyrA | 7084 | c.-218A>G | upstream_gene_variant | 1.0 |
| gyrA | 7090 | c.-212C>T | upstream_gene_variant | 1.0 |
| gyrA | 7093 | c.-209T>G | upstream_gene_variant | 1.0 |
| gyrA | 7099 | c.-203G>A | upstream_gene_variant | 1.0 |
| gyrA | 7637 | c.336C>G | synonymous_variant | 1.0 |
| gyrA | 7652 | c.351C>T | synonymous_variant | 1.0 |
| gyrA | 7658 | c.357A>G | synonymous_variant | 1.0 |
| gyrA | 7664 | c.363T>C | synonymous_variant | 1.0 |
| gyrA | 7673 | c.372G>A | synonymous_variant | 1.0 |
| gyrA | 7683 | c.382_384delAGGinsCGC | synonymous_variant | 1.0 |
| gyrA | 7694 | c.393A>G | synonymous_variant | 1.0 |
| gyrA | 7697 | c.396C>G | synonymous_variant | 1.0 |
| gyrA | 7710 | c.409_411delTTGinsCTC | synonymous_variant | 1.0 |
| gyrA | 7721 | c.420G>A | synonymous_variant | 1.0 |
| gyrA | 7725 | c.424C>T | synonymous_variant | 1.0 |
| gyrA | 7728 | c.427_429delAGGinsCGC | synonymous_variant | 1.0 |
| gyrA | 7739 | c.438C>T | synonymous_variant | 1.0 |
| gyrA | 7763 | c.462T>C | synonymous_variant | 1.0 |
| gyrA | 7784 | c.483A>G | synonymous_variant | 1.0 |
| gyrA | 8051 | c.750C>G | synonymous_variant | 1.0 |
| gyrA | 8054 | c.753T>C | synonymous_variant | 1.0 |
| gyrA | 8057 | c.756A>G | synonymous_variant | 1.0 |
| gyrA | 8069 | c.768T>C | synonymous_variant | 1.0 |
| gyrA | 8078 | c.777A>G | synonymous_variant | 1.0 |
| gyrA | 8090 | c.789C>A | synonymous_variant | 1.0 |
| gyrA | 8096 | c.795T>A | synonymous_variant | 1.0 |
| gyrA | 8099 | c.798T>C | synonymous_variant | 1.0 |
| gyrA | 8106 | c.805C>T | 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 | 8189 | c.888G>C | synonymous_variant | 1.0 |
| gyrA | 8198 | c.897T>C | synonymous_variant | 1.0 |
| gyrA | 8207 | c.906T>C | synonymous_variant | 1.0 |
| gyrA | 8219 | c.918T>C | synonymous_variant | 1.0 |
| gyrA | 8225 | c.924T>C | synonymous_variant | 1.0 |
| gyrA | 8234 | c.933T>C | synonymous_variant | 1.0 |
| gyrA | 8237 | c.936A>G | synonymous_variant | 1.0 |
| gyrA | 8247 | p.Ile316Val | missense_variant | 1.0 |
| gyrA | 8264 | c.963T>C | synonymous_variant | 1.0 |
| gyrA | 8267 | c.966G>C | synonymous_variant | 1.0 |
| gyrA | 8270 | c.969G>T | synonymous_variant | 1.0 |
| gyrA | 8276 | c.975G>A | synonymous_variant | 1.0 |
| gyrA | 8283 | p.Ile328Leu | missense_variant | 1.0 |
| gyrA | 8288 | c.987T>C | synonymous_variant | 1.0 |
| gyrA | 8294 | c.993T>C | synonymous_variant | 1.0 |
| gyrA | 8324 | c.1023T>C | synonymous_variant | 1.0 |
| gyrA | 8453 | c.1152A>C | synonymous_variant | 1.0 |
| gyrA | 8459 | c.1158G>A | synonymous_variant | 1.0 |
| gyrA | 8462 | c.1161A>C | synonymous_variant | 1.0 |
| gyrA | 8465 | c.1164C>G | synonymous_variant | 1.0 |
| gyrA | 8471 | c.1170T>C | synonymous_variant | 1.0 |
| gyrA | 8472 | c.1171C>T | synonymous_variant | 1.0 |
| gyrA | 8480 | c.1179C>A | synonymous_variant | 1.0 |
| gyrA | 8486 | c.1185T>C | synonymous_variant | 1.0 |
| gyrA | 8489 | c.1188A>G | synonymous_variant | 1.0 |
| gyrA | 8504 | c.1203G>C | synonymous_variant | 1.0 |
| gyrA | 8516 | c.1215T>C | synonymous_variant | 1.0 |
| gyrA | 8519 | c.1218A>C | synonymous_variant | 1.0 |
| gyrA | 8520 | c.1219C>T | synonymous_variant | 1.0 |
| gyrA | 8528 | c.1227G>C | synonymous_variant | 1.0 |
| gyrA | 8543 | c.1242C>G | synonymous_variant | 1.0 |
| gyrA | 8546 | c.1245T>C | synonymous_variant | 1.0 |
| gyrA | 8553 | c.1252C>A | synonymous_variant | 1.0 |
| gyrA | 8818 | p.Ser506Asn | missense_variant | 1.0 |
| gyrA | 8828 | c.1527T>C | synonymous_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 | 8933 | c.1632G>C | synonymous_variant | 1.0 |
| gyrA | 8946 | c.1645_1647delTTGinsCTC | synonymous_variant | 1.0 |
| gyrA | 8966 | c.1665C>G | synonymous_variant | 1.0 |
| gyrA | 8967 | p.Ala556Arg | missense_variant | 1.0 |
| gyrA | 8987 | c.1686C>A | synonymous_variant | 1.0 |
| gyrA | 8990 | c.1689C>G | synonymous_variant | 1.0 |
| gyrA | 8996 | c.1695T>C | synonymous_variant | 1.0 |
| gyrA | 8998 | p.Leu566Trp | missense_variant | 1.0 |
| gyrA | 9017 | c.1716C>G | synonymous_variant | 1.0 |
| gyrA | 9023 | c.1722A>G | synonymous_variant | 1.0 |
| gyrA | 9029 | c.1728T>C | synonymous_variant | 1.0 |
| gyrA | 9032 | c.1731T>C | synonymous_variant | 1.0 |
| gyrA | 9050 | p.Asp583Glu | missense_variant | 1.0 |
| gyrA | 9051 | c.1750T>C | synonymous_variant | 1.0 |
| fgd1 | 490896 | c.114C>T | synonymous_variant | 1.0 |
| fgd1 | 490905 | c.123T>C | synonymous_variant | 0.75 |
| fgd1 | 490911 | c.129T>G | synonymous_variant | 0.75 |
| fgd1 | 490917 | c.135C>G | synonymous_variant | 0.75 |
| fgd1 | 490921 | p.Gln47Glu | missense_variant | 0.75 |
| fgd1 | 490929 | c.147C>G | synonymous_variant | 0.75 |
| fgd1 | 490932 | c.150T>C | synonymous_variant | 0.75 |
| fgd1 | 490948 | p.Ser56Ala | missense_variant | 0.75 |
| fgd1 | 490962 | c.180T>G | synonymous_variant | 0.75 |
| fgd1 | 490974 | c.192T>C | synonymous_variant | 0.75 |
| fgd1 | 490977 | c.195C>G | synonymous_variant | 0.75 |
| fgd1 | 490980 | p.Asn66Lys | missense_variant | 0.75 |
| fgd1 | 490983 | c.201G>C | synonymous_variant | 0.75 |
| fgd1 | 490984 | p.Leu68Ile | missense_variant | 0.75 |
| fgd1 | 490987 | p.Leu69Thr | missense_variant | 0.75 |
| fgd1 | 490998 | c.216T>C | synonymous_variant | 0.75 |
| fgd1 | 491001 | c.219G>C | synonymous_variant | 0.75 |
| fgd1 | 491007 | c.225G>C | synonymous_variant | 0.75 |
| fgd1 | 491013 | c.231C>G | synonymous_variant | 0.75 |
| fgd1 | 491130 | c.348C>G | synonymous_variant | 1.0 |
| fgd1 | 491144 | p.Ala121Asp | missense_variant | 1.0 |
| fgd1 | 491151 | c.369G>A | synonymous_variant | 0.67 |
| fgd1 | 491181 | c.399T>C | synonymous_variant | 0.75 |
| fgd1 | 491184 | c.402A>G | synonymous_variant | 0.75 |
| fgd1 | 491191 | p.Gly137Arg | missense_variant | 0.75 |
| fgd1 | 491194 | c.412_414delCTAinsTTG | synonymous_variant | 0.75 |
| fgd1 | 491202 | c.420G>C | synonymous_variant | 0.75 |
| fgd1 | 491203 | p.Gln141Glu | missense_variant | 0.75 |
| fgd1 | 491212 | p.Ser144Arg | missense_variant | 0.75 |
| fgd1 | 491217 | c.435T>C | synonymous_variant | 0.75 |
| fgd1 | 491232 | c.450T>C | synonymous_variant | 0.75 |
| fgd1 | 491241 | p.Asp153Glu | missense_variant | 0.8 |
| fgd1 | 491244 | c.462T>C | synonymous_variant | 0.8 |
| fgd1 | 491259 | c.477T>G | synonymous_variant | 0.8 |
| fgd1 | 491349 | c.567T>C | synonymous_variant | 1.0 |
| fgd1 | 491364 | c.582T>C | synonymous_variant | 1.0 |
| fgd1 | 491367 | c.585G>C | synonymous_variant | 1.0 |
| mshA | 575623 | c.276C>G | synonymous_variant | 1.0 |
| mshA | 575629 | c.282A>G | synonymous_variant | 1.0 |
| mshA | 575632 | c.285G>C | synonymous_variant | 1.0 |
| mshA | 575635 | c.288A>C | synonymous_variant | 1.0 |
| mshA | 575638 | c.291T>C | synonymous_variant | 1.0 |
| mshA | 575641 | c.294A>G | synonymous_variant | 1.0 |
| mshA | 575647 | c.300G>C | synonymous_variant | 1.0 |
| mshA | 575649 | p.Val101Ala | missense_variant | 1.0 |
| mshA | 575659 | c.312A>G | synonymous_variant | 1.0 |
| mshA | 575662 | c.315C>G | synonymous_variant | 1.0 |
| mshA | 575665 | c.318G>A | 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 |
| mshA | 575713 | c.366G>A | synonymous_variant | 1.0 |
| mshA | 575719 | c.372C>T | synonymous_variant | 1.0 |
| mshA | 575734 | c.387T>G | synonymous_variant | 1.0 |
| mshA | 575737 | c.390T>C | synonymous_variant | 1.0 |
| ccsA | 620346 | c.456C>A | synonymous_variant | 1.0 |
| ccsA | 620362 | p.Ala158Thr | missense_variant | 1.0 |
| ccsA | 620367 | c.477T>C | synonymous_variant | 1.0 |
| ccsA | 620373 | c.483C>G | synonymous_variant | 1.0 |
| ccsA | 620376 | c.486G>C | synonymous_variant | 1.0 |
| ccsA | 620385 | c.495G>C | synonymous_variant | 1.0 |
| ccsA | 620388 | c.498A>G | synonymous_variant | 1.0 |
| ccsA | 620389 | c.499C>T | synonymous_variant | 1.0 |
| ccsA | 620412 | c.522T>C | synonymous_variant | 1.0 |
| ccsA | 620415 | c.525T>C | synonymous_variant | 1.0 |
| ccsA | 620424 | c.534G>C | synonymous_variant | 1.0 |
| ccsA | 620433 | c.543C>G | synonymous_variant | 1.0 |
| ccsA | 620436 | c.546T>A | synonymous_variant | 1.0 |
| ccsA | 620439 | c.549T>C | synonymous_variant | 1.0 |
| ccsA | 620445 | c.555A>G | synonymous_variant | 1.0 |
| ccsA | 620460 | c.570T>G | synonymous_variant | 1.0 |
| ccsA | 620461 | p.Val191Ile | missense_variant | 1.0 |
| ccsA | 620710 | p.Val274Ile | missense_variant | 1.0 |
| ccsA | 620718 | c.828G>C | synonymous_variant | 1.0 |
| ccsA | 620721 | c.831G>C | synonymous_variant | 1.0 |
| rpoB | 760406 | c.600G>C | synonymous_variant | 1.0 |
| rpoB | 760412 | c.606C>G | synonymous_variant | 1.0 |
| rpoB | 760424 | c.618C>G | synonymous_variant | 1.0 |
| rpoB | 760430 | c.624T>C | synonymous_variant | 1.0 |
| rpoB | 760475 | c.669A>G | synonymous_variant | 1.0 |
| rpoB | 760481 | c.675G>C | synonymous_variant | 1.0 |
| rpoB | 760484 | c.678A>G | synonymous_variant | 1.0 |
| rpoB | 760522 | p.Ser239Asn | missense_variant | 1.0 |
| rpoB | 760532 | c.726T>C | synonymous_variant | 1.0 |
| rpoB | 760533 | p.Val243Thr | missense_variant | 1.0 |
| rpoB | 760541 | c.735G>C | synonymous_variant | 1.0 |
| rpoB | 760547 | c.741G>C | synonymous_variant | 1.0 |
| rpoB | 760563 | p.Arg253Met | missense_variant | 1.0 |
| rpoB | 760591 | p.Val262Ala | missense_variant | 1.0 |
| rpoB | 760611 | c.805T>C | 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 | 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 | 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 | 760886 | c.1080A>G | synonymous_variant | 1.0 |
| rpoB | 760889 | c.1083C>T | 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>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 | 1.0 |
| rpoB | 761015 | c.1209G>C | synonymous_variant | 1.0 |
| rpoB | 761021 | c.1215G>C | 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 | 761606 | c.1800C>G | synonymous_variant | 1.0 |
| rpoB | 761612 | c.1806G>C | synonymous_variant | 1.0 |
| rpoB | 761615 | c.1809A>C | synonymous_variant | 1.0 |
| rpoB | 761636 | c.1830G>T | synonymous_variant | 1.0 |
| rpoB | 761639 | c.1833G>A | synonymous_variant | 1.0 |
| rpoB | 761765 | c.1959T>C | synonymous_variant | 1.0 |
| rpoB | 761772 | p.His656Ala | missense_variant | 1.0 |
| rpoB | 761778 | p.Asn658Asp | missense_variant | 1.0 |
| rpoB | 761791 | p.Arg662His | missense_variant | 1.0 |
| rpoB | 761813 | c.2007T>C | synonymous_variant | 1.0 |
| rpoB | 761815 | p.Ala670Glu | missense_variant | 1.0 |
| rpoB | 761834 | c.2028T>C | synonymous_variant | 1.0 |
| rpoB | 761848 | p.Cys681Ser | missense_variant | 1.0 |
| rpoB | 761852 | c.2046C>G | synonymous_variant | 1.0 |
| rpoB | 761858 | c.2052G>C | synonymous_variant | 1.0 |
| rpoB | 761873 | c.2067A>C | synonymous_variant | 1.0 |
| rpoB | 761885 | c.2079T>C | synonymous_variant | 1.0 |
| rpoB | 761906 | c.2100C>G | synonymous_variant | 1.0 |
| rpoB | 761909 | c.2103T>C | synonymous_variant | 1.0 |
| rpoB | 761912 | c.2106T>C | synonymous_variant | 1.0 |
| rpoB | 761915 | p.Asp703Glu | missense_variant | 1.0 |
| rpoB | 761916 | p.Asp704Asn | missense_variant | 1.0 |
| rpoB | 761948 | c.2142G>C | synonymous_variant | 1.0 |
| rpoB | 761954 | c.2148C>G | synonymous_variant | 1.0 |
| rpoB | 762008 | c.2202C>T | synonymous_variant | 1.0 |
| rpoB | 762014 | c.2208C>T | synonymous_variant | 1.0 |
| rpoB | 762017 | c.2211A>G | synonymous_variant | 1.0 |
| rpoB | 762053 | c.2247T>C | synonymous_variant | 1.0 |
| rpoB | 762062 | c.2256T>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 | 0.8 |
| rpoB | 762140 | c.2334G>C | synonymous_variant | 1.0 |
| rpoB | 762143 | c.2337T>C | synonymous_variant | 1.0 |
| rpoB | 762149 | c.2343G>C | synonymous_variant | 1.0 |
| rpoB | 762167 | c.2361T>C | synonymous_variant | 1.0 |
| rpoB | 762176 | c.2370T>C | synonymous_variant | 1.0 |
| rpoB | 762185 | c.2379G>C | synonymous_variant | 1.0 |
| rpoB | 762206 | c.2400C>G | synonymous_variant | 1.0 |
| rpoB | 762233 | c.2427G>C | synonymous_variant | 1.0 |
| rpoB | 762246 | c.2440C>T | synonymous_variant | 1.0 |
| rpoB | 762254 | c.2448T>G | synonymous_variant | 1.0 |
| rpoB | 762257 | c.2451C>G | synonymous_variant | 1.0 |
| rpoB | 762266 | c.2460T>C | synonymous_variant | 1.0 |
| rpoB | 762293 | c.2487T>C | synonymous_variant | 1.0 |
| rpoB | 762338 | c.2532T>C | synonymous_variant | 1.0 |
| rpoB | 762347 | c.2541T>C | synonymous_variant | 1.0 |
| rpoB | 762362 | p.Glu852Asp | missense_variant | 1.0 |
| rpoB | 762369 | c.2563T>C | synonymous_variant | 1.0 |
| rpoC | 762398 | c.-972T>C | upstream_gene_variant | 1.0 |
| rpoC | 762401 | c.-969G>C | upstream_gene_variant | 1.0 |
| rpoC | 762404 | c.-966T>C | upstream_gene_variant | 1.0 |
| rpoC | 762410 | c.-960T>C | upstream_gene_variant | 1.0 |
| rpoC | 762416 | c.-954A>G | upstream_gene_variant | 1.0 |
| rpoC | 762419 | c.-951C>G | upstream_gene_variant | 1.0 |
| rpoC | 762434 | c.-936T>C | upstream_gene_variant | 1.0 |
| rpoB | 762729 | p.Gln975Lys | missense_variant | 1.0 |
| rpoB | 762736 | p.Ala977Glu | missense_variant | 1.0 |
| rpoB | 762744 | p.Gln980Ala | missense_variant | 1.0 |
| rpoB | 762750 | p.Leu982Met | missense_variant | 1.0 |
| rpoC | 762753 | c.-617T>C | upstream_gene_variant | 1.0 |
| rpoC | 762758 | c.-612G>C | upstream_gene_variant | 1.0 |
| rpoC | 762782 | c.-588T>C | upstream_gene_variant | 1.0 |
| rpoB | 762785 | p.Asp993Glu | missense_variant | 1.0 |
| rpoC | 762788 | c.-582G>C | upstream_gene_variant | 1.0 |
| rpoB | 762789 | p.Leu995Met | missense_variant | 1.0 |
| rpoC | 762794 | c.-576C>G | upstream_gene_variant | 1.0 |
| rpoB | 762799 | p.Ala998Gly | missense_variant | 1.0 |
| rpoB | 762810 | p.Ala1002Ser | missense_variant | 1.0 |
| 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 | 762929 | c.-441G>C | upstream_gene_variant | 1.0 |
| rpoC | 762989 | c.-381G>C | upstream_gene_variant | 1.0 |
| rpoC | 763013 | c.-357C>G | upstream_gene_variant | 1.0 |
| rpoC | 763028 | c.-342T>C | upstream_gene_variant | 1.0 |
| rpoC | 763031 | c.-339T>G | upstream_gene_variant | 1.0 |
| rpoC | 763034 | c.-336C>G | upstream_gene_variant | 1.0 |
| rpoC | 763040 | c.-330C>G | upstream_gene_variant | 1.0 |
| rpoC | 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 | 763158 | c.-212C>T | upstream_gene_variant | 1.0 |
| rpoC | 763166 | c.-204A>G | upstream_gene_variant | 1.0 |
| rpoC | 763190 | c.-180C>T | upstream_gene_variant | 1.0 |
| rpoC | 763202 | c.-168A>G | upstream_gene_variant | 1.0 |
| rpoC | 763205 | c.-165G>C | upstream_gene_variant | 1.0 |
| rpoC | 763206 | c.-164_-162delAGTinsTCG | upstream_gene_variant | 1.0 |
| rpoC | 763214 | c.-156T>C | upstream_gene_variant | 1.0 |
| rpoC | 763226 | c.-144A>G | upstream_gene_variant | 1.0 |
| rpoC | 763227 | c.-143C>T | upstream_gene_variant | 1.0 |
| rpoC | 763238 | c.-132T>C | upstream_gene_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 | 1.0 |
| rpoC | 763573 | c.204G>C | synonymous_variant | 1.0 |
| rpoC | 763594 | c.225C>T | synonymous_variant | 1.0 |
| rpoC | 763633 | c.264T>C | synonymous_variant | 1.0 |
| rpoC | 763636 | c.267T>C | synonymous_variant | 1.0 |
| rpoC | 763660 | c.291T>G | synonymous_variant | 1.0 |
| rpoC | 763675 | c.306C>G | synonymous_variant | 1.0 |
| rpoC | 763696 | c.327T>C | synonymous_variant | 1.0 |
| rpoC | 763702 | c.333C>G | synonymous_variant | 1.0 |
| rpoC | 763717 | c.348T>C | synonymous_variant | 1.0 |
| rpoC | 763723 | c.354G>C | synonymous_variant | 1.0 |
| rpoC | 763732 | c.363C>G | synonymous_variant | 1.0 |
| rpoC | 763741 | c.372C>T | synonymous_variant | 1.0 |
| rpoC | 763744 | c.375G>C | synonymous_variant | 1.0 |
| rpoC | 763765 | c.396T>C | synonymous_variant | 1.0 |
| rpoC | 763774 | c.405G>C | synonymous_variant | 1.0 |
| rpoC | 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 | 763872 | p.Gly168Ala | missense_variant | 1.0 |
| rpoC | 763876 | p.Glu169Asp | missense_variant | 1.0 |
| rpoC | 763877 | c.508_510delCTAinsTTG | synonymous_variant | 1.0 |
| rpoC | 763888 | c.519G>C | synonymous_variant | 1.0 |
| rpoC | 763891 | c.522G>C | synonymous_variant | 1.0 |
| rpoC | 763894 | c.525A>G | synonymous_variant | 1.0 |
| rpoC | 763900 | c.531G>C | synonymous_variant | 1.0 |
| rpoC | 763936 | c.567C>G | synonymous_variant | 1.0 |
| rpoC | 763945 | c.576T>C | synonymous_variant | 1.0 |
| rpoC | 763951 | c.582G>C | synonymous_variant | 1.0 |
| rpoC | 764059 | c.690G>T | synonymous_variant | 1.0 |
| rpoC | 764083 | c.714A>G | synonymous_variant | 1.0 |
| rpoC | 764098 | c.729A>G | synonymous_variant | 1.0 |
| rpoC | 764101 | c.732C>G | synonymous_variant | 1.0 |
| rpoC | 764102 | p.Val245Ile | missense_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 | 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 | 764338 | c.969G>A | synonymous_variant | 1.0 |
| rpoC | 764353 | c.984G>C | synonymous_variant | 1.0 |
| rpoC | 764489 | c.1120C>T | synonymous_variant | 1.0 |
| rpoC | 764497 | c.1128A>G | synonymous_variant | 1.0 |
| rpoC | 764510 | c.1141C>T | synonymous_variant | 1.0 |
| rpoC | 764527 | c.1158C>T | synonymous_variant | 1.0 |
| rpoC | 764536 | c.1167G>C | synonymous_variant | 1.0 |
| rpoC | 764539 | c.1170C>G | synonymous_variant | 1.0 |
| rpoC | 764554 | c.1185C>T | synonymous_variant | 1.0 |
| rpoC | 764560 | c.1191T>C | synonymous_variant | 1.0 |
| rpoC | 764566 | c.1197C>G | synonymous_variant | 1.0 |
| rpoC | 764575 | c.1206T>G | synonymous_variant | 1.0 |
| rpoC | 764581 | c.1212T>C | synonymous_variant | 1.0 |
| rpoC | 764593 | c.1224C>T | synonymous_variant | 1.0 |
| rpoC | 764611 | c.1242G>T | synonymous_variant | 1.0 |
| rpoC | 764650 | c.1281G>C | synonymous_variant | 1.0 |
| rpoC | 764651 | c.1282_1284delTCGinsAGC | synonymous_variant | 1.0 |
| rpoC | 764752 | c.1383G>C | synonymous_variant | 1.0 |
| rpoC | 764764 | c.1395T>C | 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 | 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 | 764995 | c.1626C>G | synonymous_variant | 1.0 |
| rpoC | 765019 | c.1650A>G | synonymous_variant | 1.0 |
| rpoC | 765034 | c.1665T>C | synonymous_variant | 1.0 |
| rpoC | 765040 | c.1671T>C | synonymous_variant | 1.0 |
| rpoC | 765041 | c.1672T>C | synonymous_variant | 1.0 |
| rpoC | 765047 | c.1678T>C | synonymous_variant | 1.0 |
| rpoC | 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 | 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 | 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 | 766522 | c.3153C>G | synonymous_variant | 1.0 |
| rpoC | 766528 | c.3159T>C | synonymous_variant | 1.0 |
| rpoC | 766531 | c.3162G>C | synonymous_variant | 1.0 |
| rpoC | 766540 | p.Asp1057Glu | missense_variant | 1.0 |
| rpoC | 766549 | c.3180G>C | synonymous_variant | 1.0 |
| rpoC | 766972 | c.3603G>C | synonymous_variant | 1.0 |
| rpoC | 766996 | c.3627C>T | synonymous_variant | 1.0 |
| rpoC | 767009 | c.3640_3642delTCGinsAGC | synonymous_variant | 1.0 |
| rpoC | 767014 | c.3645G>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>A | 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 |
| rpoC | 767263 | c.3894T>C | synonymous_variant | 1.0 |
| rpoC | 767264 | p.Ala1299Gln | missense_variant | 1.0 |
| rpoC | 767275 | c.3906T>C | synonymous_variant | 1.0 |
| rpoC | 767278 | c.3909T>C | synonymous_variant | 1.0 |
| rpoC | 767281 | c.3912C>G | synonymous_variant | 1.0 |
| rpoC | 767284 | c.3915C>T | synonymous_variant | 1.0 |
| rpoC | 767288 | c.3919C>T | synonymous_variant | 1.0 |
| rpoC | 767317 | c.3948C>G | synonymous_variant | 1.0 |
| mmpL5 | 775921 | c.2560C>T | synonymous_variant | 1.0 |
| mmpL5 | 775937 | c.2544G>C | synonymous_variant | 0.67 |
| mmpL5 | 775975 | c.2506T>C | synonymous_variant | 1.0 |
| mmpL5 | 775981 | p.Leu834Met | missense_variant | 1.0 |
| mmpL5 | 776009 | c.2472A>G | synonymous_variant | 1.0 |
| mmpL5 | 776030 | c.2451G>A | synonymous_variant | 1.0 |
| mmpL5 | 776053 | c.2428T>C | synonymous_variant | 1.0 |
| mmpL5 | 776056 | p.Val809Leu | missense_variant | 1.0 |
| mmpL5 | 776060 | c.2421C>G | synonymous_variant | 1.0 |
| mmpL5 | 777101 | c.1380C>G | synonymous_variant | 1.0 |
| mmpL5 | 777110 | c.1371T>G | synonymous_variant | 1.0 |
| mmpL5 | 777115 | p.Met456Leu | missense_variant | 1.0 |
| mmpL5 | 777116 | c.1365C>T | synonymous_variant | 1.0 |
| mmpL5 | 777133 | p.Val450Ile | missense_variant | 1.0 |
| mmpL5 | 777139 | c.1342C>T | synonymous_variant | 1.0 |
| mmpL5 | 777158 | c.1323C>G | synonymous_variant | 1.0 |
| mmpL5 | 777164 | c.1317C>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 | 777191 | c.1290C>G | synonymous_variant | 1.0 |
| mmpL5 | 777194 | c.1287A>G | synonymous_variant | 1.0 |
| mmpL5 | 777206 | c.1275A>G | synonymous_variant | 1.0 |
| mmpL5 | 777212 | p.Ala423Thr | missense_variant | 1.0 |
| mmpL5 | 777215 | c.1266C>G | synonymous_variant | 1.0 |
| mmpL5 | 777218 | c.1263G>A | 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>G | 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 |
| fbiC | 1303755 | c.825T>C | synonymous_variant | 1.0 |
| fbiC | 1303761 | c.831T>C | synonymous_variant | 1.0 |
| fbiC | 1303785 | c.855G>C | synonymous_variant | 1.0 |
| fbiC | 1303789 | p.Ile287Val | missense_variant | 1.0 |
| fbiC | 1303797 | c.867A>G | synonymous_variant | 1.0 |
| fbiC | 1303818 | c.888C>G | synonymous_variant | 1.0 |
| fbiC | 1303836 | c.906G>C | synonymous_variant | 1.0 |
| fbiC | 1303845 | c.915C>G | synonymous_variant | 1.0 |
| fbiC | 1303846 | p.Phe306Val | missense_variant | 1.0 |
| fbiC | 1303854 | c.924T>C | synonymous_variant | 1.0 |
| fbiC | 1303860 | c.930A>C | synonymous_variant | 1.0 |
| fbiC | 1303866 | p.Glu312Asp | missense_variant | 0.5 |
| fbiC | 1303884 | c.954T>G | synonymous_variant | 1.0 |
| fbiC | 1303905 | c.975G>C | synonymous_variant | 1.0 |
| fbiC | 1303914 | c.984C>G | synonymous_variant | 1.0 |
| fbiC | 1304526 | c.1596T>G | synonymous_variant | 1.0 |
| fbiC | 1304535 | c.1605G>A | synonymous_variant | 1.0 |
| fbiC | 1304544 | c.1614T>C | synonymous_variant | 1.0 |
| fbiC | 1304545 | p.Val539Thr | missense_variant | 1.0 |
| fbiC | 1304553 | c.1623C>T | synonymous_variant | 1.0 |
| fbiC | 1304559 | p.Glu543Asp | missense_variant | 1.0 |
| fbiC | 1304565 | c.1635C>G | synonymous_variant | 1.0 |
| fbiC | 1304568 | c.1638T>C | synonymous_variant | 1.0 |
| fbiC | 1304580 | c.1650T>C | synonymous_variant | 1.0 |
| fbiC | 1304613 | c.1683T>C | synonymous_variant | 1.0 |
| fbiC | 1304634 | c.1704C>G | synonymous_variant | 1.0 |
| fbiC | 1304640 | c.1710A>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 | 1304829 | c.1899T>C | synonymous_variant | 1.0 |
| fbiC | 1304832 | c.1902C>T | synonymous_variant | 1.0 |
| fbiC | 1304853 | c.1923C>T | synonymous_variant | 1.0 |
| fbiC | 1304856 | c.1926C>G | synonymous_variant | 1.0 |
| fbiC | 1304869 | c.1939C>T | synonymous_variant | 1.0 |
| fbiC | 1304875 | p.Ile649Val | missense_variant | 1.0 |
| fbiC | 1304883 | p.Glu651Asp | missense_variant | 1.0 |
| fbiC | 1304891 | p.Ile654Thr | missense_variant | 1.0 |
| fbiC | 1304893 | p.Gly655Ser | missense_variant | 1.0 |
| fbiC | 1304907 | c.1977C>G | synonymous_variant | 1.0 |
| fbiC | 1304910 | c.1980G>C | synonymous_variant | 1.0 |
| fbiC | 1304916 | c.1986T>C | synonymous_variant | 1.0 |
| fbiC | 1304928 | c.1998T>C | synonymous_variant | 1.0 |
| fbiC | 1304937 | c.2007G>C | synonymous_variant | 1.0 |
| rrs | 1471647 | n.-199G>A | upstream_gene_variant | 0.67 |
| rrs | 1471648 | n.-198A>G | upstream_gene_variant | 0.67 |
| rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
| rrs | 1471665 | n.-181G>A | upstream_gene_variant | 0.67 |
| rrs | 1471668 | n.-178G>A | upstream_gene_variant | 0.67 |
| rrs | 1471673 | n.-172delG | upstream_gene_variant | 0.67 |
| rrs | 1471681 | n.-164_-159delGCAAGC | upstream_gene_variant | 0.67 |
| rrs | 1473290 | n.1445C>T | 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 | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476689 | n.3032A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476690 | n.3033C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476693 | n.3036G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476695 | n.3038T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476716 | n.3059A>C | non_coding_transcript_exon_variant | 1.0 |
| inhA | 1673547 | c.-655T>C | upstream_gene_variant | 1.0 |
| inhA | 1673568 | c.-634C>G | upstream_gene_variant | 1.0 |
| inhA | 1673574 | c.-628C>G | upstream_gene_variant | 1.0 |
| inhA | 1673580 | c.-622T>G | upstream_gene_variant | 1.0 |
| inhA | 1673589 | c.-613A>G | upstream_gene_variant | 1.0 |
| inhA | 1673591 | c.-611C>T | upstream_gene_variant | 1.0 |
| inhA | 1673595 | c.-607A>C | upstream_gene_variant | 1.0 |
| fabG1 | 1673596 | p.Lys53Glu | missense_variant | 1.0 |
| inhA | 1673602 | c.-600C>T | upstream_gene_variant | 1.0 |
| inhA | 1673607 | c.-595T>C | upstream_gene_variant | 1.0 |
| fabG1 | 1673615 | p.Glu59Val | missense_variant | 1.0 |
| inhA | 1673619 | c.-583T>C | upstream_gene_variant | 1.0 |
| fabG1 | 1673633 | p.Ser65Asn | missense_variant | 1.0 |
| fabG1 | 1673637 | p.Asp66Glu | missense_variant | 1.0 |
| fabG1 | 1673641 | p.Val68Ile | missense_variant | 1.0 |
| inhA | 1673646 | c.-556T>C | upstream_gene_variant | 1.0 |
| fabG1 | 1673657 | p.Thr73Lys | missense_variant | 1.0 |
| inhA | 1673660 | c.-542C>A | upstream_gene_variant | 1.0 |
| inhA | 1673664 | c.-538A>C | upstream_gene_variant | 1.0 |
| inhA | 1673667 | c.-535A>G | upstream_gene_variant | 1.0 |
| inhA | 1674537 | c.336C>G | synonymous_variant | 1.0 |
| inhA | 1674542 | p.Ala114Glu | missense_variant | 1.0 |
| inhA | 1674546 | c.345T>C | synonymous_variant | 1.0 |
| inhA | 1674549 | c.348G>C | synonymous_variant | 1.0 |
| inhA | 1674555 | c.354G>A | synonymous_variant | 1.0 |
| inhA | 1674561 | c.360C>T | synonymous_variant | 1.0 |
| inhA | 1674582 | c.381T>C | synonymous_variant | 1.0 |
| inhA | 1674585 | c.384T>C | synonymous_variant | 1.0 |
| inhA | 1674589 | p.Met130Leu | missense_variant | 1.0 |
| inhA | 1674601 | p.Leu134Thr | missense_variant | 1.0 |
| inhA | 1674624 | c.423A>C | synonymous_variant | 1.0 |
| inhA | 1674660 | c.459G>C | 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 | 1.0 |
| rpsA | 1833721 | c.180A>G | synonymous_variant | 1.0 |
| rpsA | 1833724 | c.183C>G | synonymous_variant | 1.0 |
| 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 | 1.0 |
| rpsA | 1833748 | c.207C>G | synonymous_variant | 1.0 |
| rpsA | 1833802 | c.261A>G | synonymous_variant | 1.0 |
| rpsA | 1833811 | c.270G>T | synonymous_variant | 1.0 |
| rpsA | 1833838 | c.297G>C | synonymous_variant | 1.0 |
| rpsA | 1833841 | c.300C>G | synonymous_variant | 1.0 |
| rpsA | 1833847 | c.306C>G | synonymous_variant | 1.0 |
| rpsA | 1833856 | c.315A>G | synonymous_variant | 1.0 |
| rpsA | 1833886 | c.345C>G | synonymous_variant | 1.0 |
| rpsA | 1833928 | c.387G>C | synonymous_variant | 1.0 |
| rpsA | 1833940 | c.399C>G | synonymous_variant | 1.0 |
| rpsA | 1834303 | c.762T>C | synonymous_variant | 1.0 |
| rpsA | 1834306 | c.765T>C | synonymous_variant | 1.0 |
| rpsA | 1834396 | c.855G>C | synonymous_variant | 1.0 |
| rpsA | 1834411 | c.870T>C | synonymous_variant | 1.0 |
| rpsA | 1834417 | c.876G>C | synonymous_variant | 1.0 |
| rpsA | 1834423 | c.882G>C | synonymous_variant | 1.0 |
| rpsA | 1834540 | c.999G>C | synonymous_variant | 1.0 |
| rpsA | 1834546 | c.1005T>C | synonymous_variant | 1.0 |
| rpsA | 1834555 | c.1014T>G | synonymous_variant | 1.0 |
| rpsA | 1834609 | c.1068T>C | synonymous_variant | 1.0 |
| rpsA | 1834618 | c.1077G>C | synonymous_variant | 1.0 |
| rpsA | 1834690 | c.1149T>C | synonymous_variant | 1.0 |
| rpsA | 1834732 | c.1191T>C | synonymous_variant | 1.0 |
| rpsA | 1834733 | p.Ala398Ser | missense_variant | 1.0 |
| rpsA | 1834738 | c.1197A>G | synonymous_variant | 1.0 |
| rpsA | 1834753 | c.1212T>C | synonymous_variant | 1.0 |
| rpsA | 1834765 | p.Glu408Asp | missense_variant | 1.0 |
| rpsA | 1834775 | p.Ala412Thr | missense_variant | 1.0 |
| rpsA | 1834780 | c.1239A>G | synonymous_variant | 1.0 |
| rpsA | 1834786 | c.1245A>G | synonymous_variant | 1.0 |
| rpsA | 1834789 | c.1248T>C | synonymous_variant | 1.0 |
| rpsA | 1834792 | c.1251G>C | synonymous_variant | 1.0 |
| tlyA | 1917908 | c.-32C>G | upstream_gene_variant | 1.0 |
| tlyA | 1917929 | c.-11T>C | upstream_gene_variant | 1.0 |
| tlyA | 1917937 | c.-3_-2insC | upstream_gene_variant | 1.0 |
| tlyA | 1917940 | p.Val1Met | missense_variant | 1.0 |
| tlyA | 1917943 | p.Ala2Ser | missense_variant | 1.0 |
| tlyA | 1917951 | c.12T>C | synonymous_variant | 1.0 |
| tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
| tlyA | 1917975 | c.36C>G | synonymous_variant | 0.67 |
| tlyA | 1917981 | c.42G>C | synonymous_variant | 0.67 |
| tlyA | 1917990 | c.51G>C | synonymous_variant | 0.67 |
| tlyA | 1917993 | c.54A>G | synonymous_variant | 0.67 |
| tlyA | 1917996 | c.57A>G | synonymous_variant | 0.67 |
| tlyA | 1918002 | c.63A>G | synonymous_variant | 0.67 |
| ndh | 2101912 | c.1131G>C | synonymous_variant | 1.0 |
| ndh | 2101920 | c.1123A>C | synonymous_variant | 1.0 |
| ndh | 2101924 | c.1119T>G | synonymous_variant | 1.0 |
| ndh | 2101939 | c.1104A>G | synonymous_variant | 1.0 |
| ndh | 2101951 | c.1092C>T | synonymous_variant | 1.0 |
| kasA | 2518825 | c.711T>C | synonymous_variant | 1.0 |
| kasA | 2518864 | c.750G>C | synonymous_variant | 1.0 |
| kasA | 2518879 | c.765A>G | synonymous_variant | 1.0 |
| kasA | 2518885 | c.771T>C | synonymous_variant | 1.0 |
| kasA | 2518898 | c.784T>C | synonymous_variant | 1.0 |
| kasA | 2518906 | c.792A>G | synonymous_variant | 1.0 |
| kasA | 2518910 | p.Leu266Met | missense_variant | 1.0 |
| kasA | 2518921 | c.807T>C | synonymous_variant | 1.0 |
| kasA | 2518936 | c.822C>G | synonymous_variant | 1.0 |
| kasA | 2518939 | c.825T>C | synonymous_variant | 1.0 |
| kasA | 2518942 | c.828T>C | synonymous_variant | 1.0 |
| kasA | 2518951 | c.837G>C | synonymous_variant | 1.0 |
| kasA | 2518954 | c.840C>G | synonymous_variant | 1.0 |
| ahpC | 2726579 | c.387T>C | synonymous_variant | 1.0 |
| ahpC | 2726591 | c.399C>G | synonymous_variant | 1.0 |
| ahpC | 2726593 | p.Val134Ala | missense_variant | 1.0 |
| ahpC | 2726600 | c.408T>C | synonymous_variant | 1.0 |
| ahpC | 2726601 | p.Ile137Leu | missense_variant | 1.0 |
| ahpC | 2726638 | p.Ala149Val | missense_variant | 1.0 |
| ahpC | 2726645 | c.453C>G | synonymous_variant | 1.0 |
| ahpC | 2726657 | c.465A>C | synonymous_variant | 1.0 |
| ahpC | 2726669 | p.Asp159Glu | missense_variant | 1.0 |
| ahpC | 2726672 | c.480G>A | synonymous_variant | 1.0 |
| ahpC | 2726675 | c.483A>G | synonymous_variant | 1.0 |
| ahpC | 2726681 | c.489A>C | synonymous_variant | 1.0 |
| ahpC | 2726687 | c.495C>G | synonymous_variant | 1.0 |
| ahpC | 2726693 | c.501C>G | synonymous_variant | 1.0 |
| ahpC | 2726696 | c.504C>G | synonymous_variant | 1.0 |
| ahpC | 2726717 | c.525A>G | synonymous_variant | 1.0 |
| Rv2752c | 3064914 | c.1278T>G | synonymous_variant | 1.0 |
| Rv2752c | 3064926 | c.1264_1266delTTGinsCTC | synonymous_variant | 1.0 |
| Rv2752c | 3064932 | c.1260T>C | synonymous_variant | 1.0 |
| Rv2752c | 3064935 | c.1257A>G | synonymous_variant | 1.0 |
| Rv2752c | 3064941 | p.Gln417Glu | missense_variant | 1.0 |
| Rv2752c | 3064947 | c.1245A>G | synonymous_variant | 1.0 |
| Rv2752c | 3064956 | p.Ser412Arg | missense_variant | 1.0 |
| Rv2752c | 3064962 | c.1230C>G | synonymous_variant | 1.0 |
| Rv2752c | 3064973 | p.Ala407Ser | missense_variant | 1.0 |
| Rv2752c | 3064974 | c.1218T>C | synonymous_variant | 1.0 |
| Rv2752c | 3064995 | c.1197C>G | synonymous_variant | 1.0 |
| Rv2752c | 3064998 | c.1194A>G | synonymous_variant | 1.0 |
| Rv2752c | 3065007 | c.1185G>C | synonymous_variant | 1.0 |
| Rv2752c | 3065013 | c.1179G>C | synonymous_variant | 1.0 |
| Rv2752c | 3065018 | p.Asn392His | missense_variant | 1.0 |
| Rv2752c | 3065022 | c.1170G>C | synonymous_variant | 1.0 |
| Rv2752c | 3065028 | p.Val388Ile | missense_variant | 1.0 |
| Rv2752c | 3065040 | c.1152C>G | synonymous_variant | 1.0 |
| Rv2752c | 3065048 | c.1144C>T | synonymous_variant | 1.0 |
| Rv2752c | 3065146 | p.Phe349Tyr | missense_variant | 1.0 |
| Rv2752c | 3065151 | c.1041G>C | synonymous_variant | 1.0 |
| Rv2752c | 3065183 | p.Ser337Ala | missense_variant | 1.0 |
| Rv2752c | 3065186 | c.1006T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065190 | p.Ile334Val | missense_variant | 1.0 |
| Rv2752c | 3065196 | c.996T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065202 | c.990T>G | synonymous_variant | 1.0 |
| Rv2752c | 3065205 | c.987T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065210 | c.982T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065223 | c.969T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065229 | c.963G>C | synonymous_variant | 1.0 |
| Rv2752c | 3065232 | c.960T>C | synonymous_variant | 1.0 |
| Rv2752c | 3065241 | c.951A>G | synonymous_variant | 1.0 |
| Rv2752c | 3065262 | c.930G>A | synonymous_variant | 1.0 |
| Rv2752c | 3065268 | c.924A>G | synonymous_variant | 1.0 |
| Rv2752c | 3065288 | c.904T>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 | 3067325 | c.621A>G | synonymous_variant | 1.0 |
| thyX | 3067349 | c.597G>C | synonymous_variant | 1.0 |
| thyX | 3067445 | c.501C>G | synonymous_variant | 1.0 |
| thyX | 3067457 | c.489C>G | synonymous_variant | 1.0 |
| thyX | 3067462 | c.484C>T | synonymous_variant | 1.0 |
| thyX | 3067465 | p.Ile161Val | missense_variant | 1.0 |
| thyX | 3067475 | c.471A>G | synonymous_variant | 1.0 |
| thyX | 3067490 | c.456C>G | synonymous_variant | 1.0 |
| thyX | 3067493 | c.453A>G | synonymous_variant | 1.0 |
| thyX | 3067515 | p.Ser144Thr | missense_variant | 1.0 |
| thyX | 3067530 | p.Ala139Ser | missense_variant | 1.0 |
| thyX | 3067545 | p.Glu134Ala | missense_variant | 1.0 |
| thyX | 3067549 | p.Thr133Ala | missense_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 |
| thyX | 3067736 | p.Phe70Leu | missense_variant | 1.0 |
| thyX | 3067739 | c.207T>C | synonymous_variant | 1.0 |
| thyX | 3067754 | c.192C>T | synonymous_variant | 1.0 |
| thyX | 3067761 | p.Arg62Lys | missense_variant | 1.0 |
| thyX | 3067765 | p.Leu61Ile | missense_variant | 1.0 |
| thyX | 3067772 | c.174C>G | synonymous_variant | 1.0 |
| thyX | 3067781 | c.165C>G | synonymous_variant | 1.0 |
| thyX | 3067793 | c.153T>C | synonymous_variant | 1.0 |
| thyX | 3067799 | c.147G>A | synonymous_variant | 1.0 |
| thyX | 3067802 | c.144C>G | synonymous_variant | 1.0 |
| thyX | 3067814 | c.132T>C | synonymous_variant | 1.0 |
| thyX | 3067850 | c.96A>C | synonymous_variant | 1.0 |
| thyX | 3067869 | p.Thr26Ser | missense_variant | 1.0 |
| thyX | 3067874 | c.72C>G | synonymous_variant | 1.0 |
| thyX | 3067883 | c.63C>G | synonymous_variant | 1.0 |
| thyX | 3067886 | c.60A>C | synonymous_variant | 1.0 |
| thyX | 3067889 | c.57C>G | synonymous_variant | 1.0 |
| thyX | 3067898 | p.Asp16Glu | missense_variant | 1.0 |
| thyA | 3074079 | c.393G>C | synonymous_variant | 1.0 |
| thyA | 3074097 | c.375C>G | synonymous_variant | 1.0 |
| thyA | 3074100 | p.Asp124Asn | missense_variant | 1.0 |
| thyA | 3074106 | c.366T>C | synonymous_variant | 1.0 |
| fprA | 3474081 | c.75C>G | synonymous_variant | 1.0 |
| fprA | 3474088 | p.Thr28Ala | missense_variant | 1.0 |
| fprA | 3474091 | p.Thr29Ser | missense_variant | 1.0 |
| fprA | 3474094 | p.Glu30Gln | missense_variant | 1.0 |
| fprA | 3474100 | p.Leu32Ile | missense_variant | 1.0 |
| fprA | 3474105 | c.99C>T | synonymous_variant | 1.0 |
| fprA | 3474106 | p.Met34Val | missense_variant | 1.0 |
| fprA | 3474114 | c.108C>T | synonymous_variant | 1.0 |
| fprA | 3474130 | c.124_126delTTGinsCTC | synonymous_variant | 1.0 |
| fprA | 3474135 | c.129G>C | synonymous_variant | 1.0 |
| fprA | 3474138 | c.132T>C | synonymous_variant | 1.0 |
| fprA | 3474141 | c.135C>G | synonymous_variant | 1.0 |
| fprA | 3474162 | c.156G>C | synonymous_variant | 1.0 |
| fprA | 3474171 | c.165G>C | synonymous_variant | 1.0 |
| fprA | 3474177 | c.171C>T | synonymous_variant | 1.0 |
| fprA | 3474180 | c.174C>G | synonymous_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 | 3877656 | c.852T>G | synonymous_variant | 1.0 |
| rpoA | 3877668 | c.840A>G | synonymous_variant | 1.0 |
| rpoA | 3877679 | p.Ala277Ser | missense_variant | 1.0 |
| rpoA | 3877686 | c.822A>G | synonymous_variant | 1.0 |
| rpoA | 3877692 | c.816G>C | synonymous_variant | 1.0 |
| rpoA | 3877776 | c.732T>C | synonymous_variant | 1.0 |
| rpoA | 3877782 | c.726T>C | synonymous_variant | 1.0 |
| rpoA | 3877791 | c.717C>G | synonymous_variant | 1.0 |
| rpoA | 3877818 | c.690A>G | synonymous_variant | 1.0 |
| rpoA | 3877839 | c.669G>C | synonymous_variant | 1.0 |
| rpoA | 3877857 | c.651G>A | synonymous_variant | 1.0 |
| rpoA | 3877866 | c.642G>C | synonymous_variant | 1.0 |
| rpoA | 3877875 | c.633T>G | synonymous_variant | 1.0 |
| rpoA | 3877878 | c.630G>C | synonymous_variant | 1.0 |
| rpoA | 3877890 | c.618C>T | synonymous_variant | 1.0 |
| clpC1 | 4038302 | c.2403C>G | synonymous_variant | 1.0 |
| clpC1 | 4038308 | c.2397G>T | synonymous_variant | 1.0 |
| clpC1 | 4038314 | c.2391T>C | synonymous_variant | 1.0 |
| clpC1 | 4038317 | c.2388G>C | synonymous_variant | 1.0 |
| clpC1 | 4038320 | c.2385G>C | synonymous_variant | 1.0 |
| clpC1 | 4038356 | c.2349T>C | synonymous_variant | 1.0 |
| clpC1 | 4038419 | c.2286T>C | synonymous_variant | 1.0 |
| clpC1 | 4038433 | c.2272C>T | synonymous_variant | 1.0 |
| clpC1 | 4038434 | c.2271G>A | synonymous_variant | 1.0 |
| clpC1 | 4038444 | p.Ala754Lys | missense_variant | 1.0 |
| clpC1 | 4038446 | c.2259T>C | synonymous_variant | 1.0 |
| clpC1 | 4038456 | p.Val750Glu | missense_variant | 1.0 |
| clpC1 | 4038460 | p.Leu749Met | missense_variant | 1.0 |
| clpC1 | 4038486 | p.Gly740Asn | missense_variant | 1.0 |
| clpC1 | 4038489 | p.Ala739Gly | missense_variant | 1.0 |
| clpC1 | 4038494 | c.2211G>C | synonymous_variant | 1.0 |
| clpC1 | 4038497 | p.Ser736Gln | missense_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 | 4038749 | c.1956C>G | synonymous_variant | 1.0 |
| clpC1 | 4038755 | c.1950G>T | synonymous_variant | 1.0 |
| clpC1 | 4038770 | c.1935C>T | synonymous_variant | 1.0 |
| 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 | 4038860 | c.1845G>C | synonymous_variant | 1.0 |
| clpC1 | 4038878 | c.1827A>G | synonymous_variant | 1.0 |
| clpC1 | 4038908 | c.1797C>G | synonymous_variant | 1.0 |
| clpC1 | 4038914 | c.1791G>C | synonymous_variant | 1.0 |
| clpC1 | 4038923 | c.1780_1782delCTAinsTTG | synonymous_variant | 1.0 |
| clpC1 | 4038953 | c.1752A>G | synonymous_variant | 1.0 |
| clpC1 | 4038956 | c.1749T>C | synonymous_variant | 1.0 |
| clpC1 | 4038965 | c.1740T>C | synonymous_variant | 1.0 |
| clpC1 | 4038971 | c.1734T>C | synonymous_variant | 1.0 |
| clpC1 | 4038974 | c.1731T>C | synonymous_variant | 1.0 |
| clpC1 | 4038989 | c.1716T>C | synonymous_variant | 1.0 |
| clpC1 | 4038997 | c.1708T>C | synonymous_variant | 1.0 |
| clpC1 | 4039004 | c.1701C>G | synonymous_variant | 1.0 |
| clpC1 | 4039112 | c.1593C>G | synonymous_variant | 1.0 |
| clpC1 | 4039121 | c.1584T>C | synonymous_variant | 1.0 |
| clpC1 | 4039142 | c.1563A>G | synonymous_variant | 1.0 |
| clpC1 | 4039145 | c.1560G>C | synonymous_variant | 1.0 |
| clpC1 | 4039169 | p.Glu512Asp | missense_variant | 1.0 |
| clpC1 | 4039172 | c.1533A>G | synonymous_variant | 1.0 |
| clpC1 | 4039178 | c.1527G>C | synonymous_variant | 1.0 |
| clpC1 | 4039183 | c.1522T>C | synonymous_variant | 1.0 |
| clpC1 | 4039186 | c.1519C>T | synonymous_variant | 1.0 |
| clpC1 | 4039226 | c.1479T>C | synonymous_variant | 1.0 |
| clpC1 | 4039274 | c.1431G>C | synonymous_variant | 1.0 |
| clpC1 | 4039286 | c.1419T>C | synonymous_variant | 1.0 |
| clpC1 | 4039295 | c.1410A>C | synonymous_variant | 1.0 |
| clpC1 | 4039298 | c.1407T>C | synonymous_variant | 1.0 |
| clpC1 | 4039319 | c.1386T>C | synonymous_variant | 1.0 |
| clpC1 | 4039322 | c.1383T>C | synonymous_variant | 1.0 |
| clpC1 | 4039328 | c.1377A>C | synonymous_variant | 1.0 |
| clpC1 | 4039331 | c.1374C>G | synonymous_variant | 1.0 |
| clpC1 | 4039337 | p.Thr456Gln | missense_variant | 1.0 |
| clpC1 | 4039349 | c.1356C>T | synonymous_variant | 1.0 |
| clpC1 | 4039352 | c.1353C>G | synonymous_variant | 1.0 |
| clpC1 | 4039364 | c.1341C>G | synonymous_variant | 1.0 |
| clpC1 | 4039391 | c.1314T>G | 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 | 4039517 | c.1188C>G | synonymous_variant | 1.0 |
| clpC1 | 4039556 | c.1149G>C | synonymous_variant | 1.0 |
| clpC1 | 4039559 | c.1146C>G | synonymous_variant | 1.0 |
| clpC1 | 4039562 | c.1143C>G | synonymous_variant | 1.0 |
| clpC1 | 4039565 | c.1140G>C | synonymous_variant | 1.0 |
| clpC1 | 4039570 | p.Met379Leu | missense_variant | 1.0 |
| clpC1 | 4039576 | p.Ala377Pro | missense_variant | 1.0 |
| clpC1 | 4039577 | c.1128T>C | synonymous_variant | 1.0 |
| clpC1 | 4039589 | c.1116G>C | synonymous_variant | 1.0 |
| clpC1 | 4039610 | c.1095G>C | synonymous_variant | 1.0 |
| clpC1 | 4039616 | c.1089G>C | synonymous_variant | 1.0 |
| clpC1 | 4039817 | c.888A>C | synonymous_variant | 1.0 |
| clpC1 | 4039820 | c.885T>G | synonymous_variant | 1.0 |
| clpC1 | 4039826 | c.879C>G | synonymous_variant | 1.0 |
| 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 | 4039898 | c.807C>G | synonymous_variant | 1.0 |
| clpC1 | 4039928 | c.775_777delAGCinsTCG | synonymous_variant | 1.0 |
| 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 | 4039982 | c.723G>A | 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 | 1.0 |
| clpC1 | 4040036 | c.669C>G | synonymous_variant | 1.0 |
| embC | 4241047 | c.1185C>G | synonymous_variant | 1.0 |
| embC | 4241050 | c.1188T>G | synonymous_variant | 1.0 |
| embC | 4241053 | c.1191G>C | synonymous_variant | 1.0 |
| embC | 4241394 | p.Lys511Ser | 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>G | 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 | 4242764 | p.Val968Leu | missense_variant | 0.67 |
| embA | 4242772 | c.-461G>C | upstream_gene_variant | 0.75 |
| embC | 4242779 | p.Asn973Asp | missense_variant | 0.75 |
| embC | 4242791 | p.Ala977Ser | missense_variant | 1.0 |
| embA | 4242796 | c.-437G>C | upstream_gene_variant | 1.0 |
| embA | 4242799 | c.-434T>C | upstream_gene_variant | 1.0 |
| embA | 4242802 | c.-431G>C | upstream_gene_variant | 1.0 |
| embA | 4242820 | c.-413G>C | upstream_gene_variant | 1.0 |
| embA | 4242823 | c.-410G>C | upstream_gene_variant | 1.0 |
| embA | 4242832 | c.-401A>C | upstream_gene_variant | 1.0 |
| embA | 4242838 | c.-395C>G | upstream_gene_variant | 1.0 |
| embA | 4242841 | c.-392C>T | upstream_gene_variant | 1.0 |
| embA | 4242844 | c.-389A>G | upstream_gene_variant | 1.0 |
| embA | 4242847 | c.-386C>A | 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 | 4242883 | c.-350C>G | upstream_gene_variant | 1.0 |
| embA | 4244582 | c.1350T>C | synonymous_variant | 0.75 |
| embA | 4244585 | c.1353A>G | synonymous_variant | 0.75 |
| embA | 4244611 | p.Ala460Gly | missense_variant | 0.75 |
| embA | 4244616 | p.Ala462Ser | missense_variant | 0.75 |
| embA | 4244619 | c.1387_1389delTTGinsCTC | synonymous_variant | 0.75 |
| embA | 4244625 | p.Leu465Val | missense_variant | 0.75 |
| embA | 4244631 | p.Thr467Leu | missense_variant | 0.75 |
| embA | 4244645 | c.1413T>C | synonymous_variant | 1.0 |
| embA | 4244648 | c.1416G>C | synonymous_variant | 1.0 |
| embA | 4244649 | p.Asp473Ser | missense_variant | 1.0 |
| embA | 4244670 | p.Ala480Leu | missense_variant | 1.0 |
| embA | 4244675 | c.1443A>G | synonymous_variant | 1.0 |
| embA | 4244678 | c.1446G>C | synonymous_variant | 1.0 |
| embA | 4244681 | c.1449A>C | synonymous_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 | 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 |
| embA | 4245282 | p.Ile684Val | missense_variant | 1.0 |
| embA | 4245285 | c.2053T>C | synonymous_variant | 1.0 |
| embA | 4245290 | c.2058C>G | synonymous_variant | 1.0 |
| embA | 4245293 | c.2061T>G | synonymous_variant | 1.0 |
| embA | 4245296 | c.2064G>C | synonymous_variant | 1.0 |
| embA | 4245299 | c.2067A>G | synonymous_variant | 1.0 |
| embA | 4245315 | p.Val695Thr | missense_variant | 1.0 |
| embA | 4245328 | p.Ala699Val | missense_variant | 1.0 |
| embA | 4245335 | c.2103A>G | synonymous_variant | 0.8 |
| embA | 4245340 | p.Gly703Ala | missense_variant | 0.8 |
| embA | 4245345 | p.Met705Leu | missense_variant | 0.8 |
| embA | 4245348 | p.Ala706Thr | missense_variant | 0.8 |
| embA | 4245355 | p.Ala708Gly | missense_variant | 0.8 |
| embA | 4245368 | c.2136T>C | synonymous_variant | 0.75 |
| embA | 4245377 | c.2145T>C | synonymous_variant | 0.67 |
| embB | 4245659 | c.-855C>G | upstream_gene_variant | 1.0 |
| embB | 4245674 | c.-840A>C | upstream_gene_variant | 1.0 |
| embB | 4245677 | c.-837G>C | upstream_gene_variant | 1.0 |
| embA | 4245693 | p.Ile821Val | missense_variant | 1.0 |
| embB | 4245701 | c.-813G>C | upstream_gene_variant | 1.0 |
| embB | 4245704 | c.-810G>C | upstream_gene_variant | 1.0 |
| embB | 4245725 | c.-789A>G | upstream_gene_variant | 1.0 |
| embB | 4245726 | c.-788T>C | upstream_gene_variant | 1.0 |
| embB | 4245737 | c.-777A>C | upstream_gene_variant | 1.0 |
| embB | 4245740 | c.-774T>C | upstream_gene_variant | 1.0 |
| embB | 4247491 | c.978G>C | synonymous_variant | 1.0 |
| embB | 4247497 | c.984T>C | synonymous_variant | 1.0 |
| embB | 4247512 | c.999T>C | synonymous_variant | 1.0 |
| embB | 4247539 | c.1026T>C | synonymous_variant | 1.0 |
| embB | 4247554 | c.1041T>C | synonymous_variant | 1.0 |
| embB | 4247566 | c.1053C>A | synonymous_variant | 1.0 |
| embB | 4247572 | c.1059A>G | synonymous_variant | 1.0 |
| embB | 4247579 | p.Ala356Phe | missense_variant | 1.0 |
| embB | 4247587 | c.1074G>A | synonymous_variant | 1.0 |
| embB | 4247603 | c.1090C>T | synonymous_variant | 1.0 |
| embB | 4247611 | c.1098G>T | synonymous_variant | 1.0 |
| embB | 4247614 | c.1101T>C | synonymous_variant | 1.0 |
| embB | 4247746 | c.1233C>T | synonymous_variant | 1.0 |
| embB | 4247761 | c.1248T>C | synonymous_variant | 1.0 |
| embB | 4247773 | c.1260G>A | synonymous_variant | 1.0 |
| embB | 4247776 | c.1263G>T | synonymous_variant | 1.0 |
| embB | 4247797 | c.1284C>G | synonymous_variant | 1.0 |
| embB | 4247800 | c.1287A>T | synonymous_variant | 1.0 |
| embB | 4247803 | c.1290G>C | synonymous_variant | 1.0 |
| embB | 4247815 | c.1302C>G | synonymous_variant | 1.0 |
| embB | 4247819 | p.Val436Ile | missense_variant | 1.0 |
| embB | 4247830 | c.1317A>G | synonymous_variant | 1.0 |
| embB | 4247836 | c.1323A>G | synonymous_variant | 1.0 |
| embB | 4247839 | c.1326G>C | synonymous_variant | 1.0 |
| embB | 4247866 | c.1353G>C | synonymous_variant | 1.0 |
| embB | 4247875 | c.1362G>C | synonymous_variant | 1.0 |
| embB | 4247876 | c.1363C>T | synonymous_variant | 1.0 |
| embB | 4247881 | c.1368G>C | synonymous_variant | 1.0 |
| embB | 4247887 | c.1374C>T | synonymous_variant | 1.0 |
| embB | 4247893 | c.1380C>T | synonymous_variant | 1.0 |
| embB | 4247932 | c.1419C>G | synonymous_variant | 1.0 |
| embB | 4247940 | p.Leu476Trp | missense_variant | 1.0 |
| embB | 4247945 | c.1432T>C | synonymous_variant | 1.0 |
| embB | 4247951 | p.Ser480Ala | missense_variant | 1.0 |
| embB | 4247956 | c.1443G>C | synonymous_variant | 1.0 |
| embB | 4247974 | c.1461C>G | 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 | 4248130 | c.1617G>C | synonymous_variant | 1.0 |
| embB | 4248142 | c.1629T>C | synonymous_variant | 1.0 |
| embB | 4248143 | c.1630T>C | synonymous_variant | 1.0 |
| embB | 4248157 | c.1644A>G | synonymous_variant | 1.0 |
| embB | 4248172 | c.1659G>C | synonymous_variant | 1.0 |
| embB | 4248199 | c.1686A>G | synonymous_variant | 1.0 |
| embB | 4248200 | p.Ile563Val | missense_variant | 1.0 |
| embB | 4248205 | c.1692C>G | synonymous_variant | 1.0 |
| embB | 4248206 | p.Ser565Gly | missense_variant | 1.0 |
| embB | 4248220 | c.1707A>C | synonymous_variant | 1.0 |
