Run ID: SRR1173330
Sample name:
Date: 03-04-2023 03:21:54
Number of reads: 187554
Percentage reads mapped: 62.43
Strain: lineage4
Drug-resistance: Pre-XDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7570 | p.Ala90Val | missense_variant | 0.8 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761110 | p.Asp435Gly | missense_variant | 1.0 | rifampicin |
rpoB | 761161 | p.Leu452Pro | missense_variant | 0.83 | rifampicin |
rrs | 1473246 | n.1401A>G | non_coding_transcript_exon_variant | 0.86 | kanamycin, capreomycin, aminoglycosides, amikacin |
fabG1 | 1673432 | c.-8T>A | upstream_gene_variant | 1.0 | isoniazid |
katG | 2155168 | p.Ser315Thr | missense_variant | 0.67 | isoniazid |
pncA | 2288785 | c.456dupC | frameshift_variant | 1.0 | pyrazinamide, pyrazinamide |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6518 | p.Val427Met | missense_variant | 1.0 |
gyrA | 6949 | c.-353A>G | upstream_gene_variant | 0.4 |
gyrA | 6952 | c.-350C>G | upstream_gene_variant | 0.4 |
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 | 7006 | c.-296T>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 |
gyrA | 7015 | c.-287G>A | upstream_gene_variant | 0.67 |
gyrA | 7018 | c.-284G>A | upstream_gene_variant | 0.5 |
gyrB | 7023 | p.Leu595Gln | missense_variant | 0.5 |
gyrA | 7186 | c.-116C>G | upstream_gene_variant | 0.25 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7622 | c.321C>T | synonymous_variant | 0.33 |
gyrA | 7625 | c.324G>C | synonymous_variant | 0.33 |
gyrA | 7631 | c.330G>C | synonymous_variant | 0.33 |
gyrA | 7637 | c.336C>G | synonymous_variant | 0.33 |
gyrA | 7652 | c.351C>T | synonymous_variant | 0.4 |
gyrA | 7658 | c.357A>C | synonymous_variant | 0.5 |
gyrA | 7763 | c.462T>C | synonymous_variant | 0.56 |
gyrA | 7775 | c.474C>A | synonymous_variant | 0.5 |
gyrA | 7781 | c.480G>C | synonymous_variant | 0.44 |
gyrA | 7784 | c.483A>G | synonymous_variant | 0.33 |
gyrA | 7790 | c.489G>C | synonymous_variant | 0.25 |
gyrA | 7793 | c.492G>C | synonymous_variant | 0.25 |
gyrA | 7796 | c.495G>C | synonymous_variant | 0.25 |
gyrA | 7799 | c.498A>G | synonymous_variant | 0.25 |
gyrA | 7814 | c.513C>G | synonymous_variant | 0.29 |
gyrA | 7823 | c.522G>C | synonymous_variant | 0.25 |
gyrA | 7832 | c.531G>T | synonymous_variant | 0.29 |
gyrA | 7835 | c.534A>C | synonymous_variant | 0.29 |
gyrA | 7853 | c.552C>G | synonymous_variant | 0.29 |
gyrA | 7859 | c.558A>G | synonymous_variant | 0.33 |
gyrA | 7865 | c.564T>C | synonymous_variant | 0.33 |
gyrA | 7886 | c.585T>C | synonymous_variant | 0.33 |
gyrA | 8040 | p.Gly247Ser | missense_variant | 1.0 |
gyrA | 8168 | c.867A>G | synonymous_variant | 0.4 |
gyrA | 8177 | c.876A>C | synonymous_variant | 0.4 |
gyrA | 8198 | c.897T>C | synonymous_variant | 0.29 |
gyrA | 8207 | c.906T>C | synonymous_variant | 0.29 |
gyrA | 8219 | c.918T>C | synonymous_variant | 0.33 |
gyrA | 8225 | c.924T>C | synonymous_variant | 0.5 |
gyrA | 8234 | c.933T>C | synonymous_variant | 0.33 |
gyrA | 8237 | c.936A>G | synonymous_variant | 0.33 |
gyrA | 8247 | p.Ile316Val | missense_variant | 0.29 |
gyrA | 8264 | c.963T>C | synonymous_variant | 0.25 |
gyrA | 8267 | c.966G>C | synonymous_variant | 0.25 |
gyrA | 8270 | c.969G>C | synonymous_variant | 0.33 |
gyrA | 8276 | c.975G>A | synonymous_variant | 0.38 |
gyrA | 8283 | p.Ile328Leu | missense_variant | 0.38 |
gyrA | 8288 | c.987T>C | synonymous_variant | 0.38 |
gyrA | 8294 | c.993T>C | synonymous_variant | 0.38 |
gyrA | 8324 | c.1023T>C | synonymous_variant | 0.33 |
gyrA | 8330 | c.1029C>G | synonymous_variant | 0.29 |
gyrA | 8339 | c.1038A>G | synonymous_variant | 0.4 |
gyrA | 8340 | p.Ala347Ser | missense_variant | 0.4 |
gyrA | 9252 | p.Val651Ile | missense_variant | 0.67 |
gyrA | 9284 | c.1983T>C | synonymous_variant | 0.56 |
gyrA | 9291 | c.1990C>T | synonymous_variant | 0.5 |
gyrA | 9296 | c.1995T>C | synonymous_variant | 0.62 |
gyrA | 9299 | c.1998G>C | synonymous_variant | 0.62 |
gyrA | 9300 | p.Ala667Ser | missense_variant | 0.62 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9308 | p.Asp669Glu | missense_variant | 0.62 |
gyrA | 9323 | c.2022C>G | synonymous_variant | 0.6 |
gyrA | 9335 | c.2034G>C | synonymous_variant | 0.67 |
fgd1 | 490812 | c.30A>G | synonymous_variant | 0.5 |
fgd1 | 490815 | c.33G>C | synonymous_variant | 0.5 |
fgd1 | 490827 | c.45C>T | synonymous_variant | 0.75 |
fgd1 | 490848 | c.66A>G | synonymous_variant | 0.6 |
fgd1 | 490851 | c.69A>T | synonymous_variant | 0.6 |
fgd1 | 490868 | p.Ala29Gly | missense_variant | 0.75 |
fgd1 | 490887 | c.105G>A | synonymous_variant | 1.0 |
fgd1 | 490890 | c.108C>G | synonymous_variant | 0.67 |
fgd1 | 490905 | c.123T>C | synonymous_variant | 0.5 |
fgd1 | 490948 | p.Ser56Ala | missense_variant | 0.4 |
fgd1 | 490974 | c.192T>C | synonymous_variant | 0.43 |
fgd1 | 490977 | c.195C>G | synonymous_variant | 0.43 |
fgd1 | 490980 | p.Asn66Lys | missense_variant | 0.43 |
fgd1 | 490984 | p.Leu68Ile | missense_variant | 0.5 |
fgd1 | 490987 | p.Leu69Thr | missense_variant | 0.5 |
fgd1 | 490998 | c.216T>C | synonymous_variant | 0.67 |
fgd1 | 491001 | c.219G>C | synonymous_variant | 0.67 |
fgd1 | 491007 | c.225G>C | synonymous_variant | 0.57 |
fgd1 | 491013 | c.231C>G | synonymous_variant | 0.57 |
fgd1 | 491144 | p.Ala121Asp | missense_variant | 0.33 |
fgd1 | 491151 | c.369G>A | synonymous_variant | 0.33 |
fgd1 | 491181 | c.399T>C | synonymous_variant | 0.5 |
fgd1 | 491184 | c.402A>G | synonymous_variant | 0.5 |
fgd1 | 491191 | p.Gly137Arg | missense_variant | 0.43 |
fgd1 | 491194 | c.412_414delCTAinsTTG | synonymous_variant | 0.5 |
fgd1 | 491202 | c.420G>C | synonymous_variant | 0.5 |
fgd1 | 491203 | p.Gln141Glu | missense_variant | 0.5 |
fgd1 | 491212 | p.Ser144Arg | missense_variant | 0.5 |
fgd1 | 491217 | c.435T>C | synonymous_variant | 0.5 |
fgd1 | 491232 | c.450T>C | synonymous_variant | 0.4 |
fgd1 | 491241 | p.Asp153Glu | missense_variant | 0.5 |
fgd1 | 491526 | c.744T>C | synonymous_variant | 0.33 |
fgd1 | 491535 | c.753G>C | synonymous_variant | 0.4 |
fgd1 | 491542 | c.760T>C | synonymous_variant | 0.4 |
fgd1 | 491547 | c.765A>C | synonymous_variant | 0.4 |
fgd1 | 491550 | c.768T>C | synonymous_variant | 0.4 |
fgd1 | 491553 | c.771G>A | synonymous_variant | 0.33 |
fgd1 | 491601 | c.819T>C | synonymous_variant | 0.4 |
fgd1 | 491610 | c.828A>G | synonymous_variant | 0.5 |
fgd1 | 491616 | c.834A>G | synonymous_variant | 0.67 |
mshA | 575536 | c.189T>C | synonymous_variant | 0.25 |
mshA | 575542 | c.195C>A | synonymous_variant | 0.25 |
mshA | 575561 | p.Met72Val | missense_variant | 0.22 |
mshA | 575569 | c.222A>G | synonymous_variant | 0.22 |
mshA | 575571 | p.Ser75Thr | missense_variant | 0.22 |
mshA | 575576 | c.229C>T | synonymous_variant | 0.25 |
mshA | 575581 | c.234C>T | synonymous_variant | 0.25 |
mshA | 575587 | c.240C>G | synonymous_variant | 0.22 |
mshA | 575590 | c.243T>C | synonymous_variant | 0.22 |
mshA | 575623 | c.276C>G | synonymous_variant | 0.18 |
mshA | 575713 | c.366G>A | synonymous_variant | 0.33 |
mshA | 575719 | c.372C>T | synonymous_variant | 0.43 |
mshA | 575734 | c.387T>G | synonymous_variant | 0.5 |
mshA | 575737 | c.390T>C | synonymous_variant | 0.5 |
mshA | 575746 | c.399C>G | synonymous_variant | 0.29 |
mshA | 575749 | c.402C>A | synonymous_variant | 0.29 |
mshA | 575752 | c.405G>C | synonymous_variant | 0.29 |
mshA | 575755 | c.408G>A | synonymous_variant | 0.33 |
mshA | 575756 | c.409C>T | synonymous_variant | 0.33 |
mshA | 575770 | c.423G>A | synonymous_variant | 0.29 |
mshA | 575771 | p.Val142Ser | missense_variant | 0.29 |
mshA | 575779 | c.432A>G | synonymous_variant | 0.29 |
mshA | 575782 | c.435G>C | synonymous_variant | 0.38 |
mshA | 575809 | c.462C>T | synonymous_variant | 0.29 |
mshA | 575812 | c.465C>T | synonymous_variant | 0.29 |
ccsA | 620412 | c.522T>C | synonymous_variant | 0.4 |
ccsA | 620415 | c.525T>C | synonymous_variant | 0.4 |
ccsA | 620421 | c.531G>C | synonymous_variant | 0.4 |
ccsA | 620424 | c.534G>C | synonymous_variant | 0.4 |
rpoB | 760040 | c.234T>C | synonymous_variant | 0.22 |
rpoB | 760046 | c.240G>C | synonymous_variant | 0.25 |
rpoB | 760060 | p.Tyr85Leu | missense_variant | 0.25 |
rpoB | 760067 | c.261G>C | synonymous_variant | 0.29 |
rpoB | 760070 | c.264T>G | synonymous_variant | 0.33 |
rpoB | 760091 | c.285G>C | synonymous_variant | 0.33 |
rpoB | 760101 | c.295T>C | synonymous_variant | 0.4 |
rpoB | 760112 | c.306T>C | synonymous_variant | 0.5 |
rpoB | 760118 | c.312T>G | synonymous_variant | 0.5 |
rpoB | 760121 | c.315T>C | synonymous_variant | 0.67 |
rpoB | 760283 | c.477G>C | synonymous_variant | 0.5 |
rpoB | 760298 | c.492G>C | synonymous_variant | 0.5 |
rpoB | 760307 | c.501T>C | synonymous_variant | 0.5 |
rpoB | 760310 | c.504G>C | synonymous_variant | 0.5 |
rpoB | 760328 | c.522G>C | synonymous_variant | 0.6 |
rpoB | 760331 | c.525G>C | synonymous_variant | 0.6 |
rpoB | 760340 | c.534G>T | synonymous_variant | 0.4 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.5 |
rpoB | 760370 | c.564C>G | synonymous_variant | 0.5 |
rpoB | 760472 | c.666C>T | synonymous_variant | 0.33 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.33 |
rpoB | 760481 | c.675G>C | synonymous_variant | 0.33 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.29 |
rpoB | 760522 | p.Ser239Asn | missense_variant | 0.33 |
rpoB | 760532 | c.726T>C | synonymous_variant | 0.29 |
rpoB | 760533 | p.Val243Thr | missense_variant | 0.29 |
rpoB | 760541 | c.735G>C | synonymous_variant | 0.29 |
rpoB | 760547 | c.741G>C | synonymous_variant | 0.25 |
rpoB | 760563 | p.Arg253Met | missense_variant | 0.25 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.29 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.67 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.5 |
rpoB | 760670 | c.864G>C | synonymous_variant | 0.5 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.4 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.4 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.4 |
rpoB | 760715 | c.909C>G | synonymous_variant | 0.33 |
rpoB | 760718 | c.912C>T | synonymous_variant | 0.33 |
rpoB | 760724 | c.918T>C | synonymous_variant | 0.29 |
rpoB | 760730 | c.924T>C | synonymous_variant | 0.25 |
rpoB | 760805 | c.999G>C | synonymous_variant | 0.33 |
rpoB | 760817 | c.1011A>G | synonymous_variant | 0.33 |
rpoB | 760820 | c.1014T>C | synonymous_variant | 0.33 |
rpoB | 760826 | c.1020C>G | synonymous_variant | 0.33 |
rpoB | 760830 | c.1024T>C | synonymous_variant | 0.33 |
rpoB | 760841 | c.1035T>C | synonymous_variant | 0.33 |
rpoB | 760845 | p.Thr347Pro | missense_variant | 0.33 |
rpoB | 760859 | c.1053T>C | synonymous_variant | 0.4 |
rpoB | 760862 | c.1056G>C | synonymous_variant | 0.4 |
rpoB | 760869 | p.Val355Ile | missense_variant | 0.4 |
rpoB | 760886 | c.1080A>G | synonymous_variant | 0.4 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.4 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 0.5 |
rpoB | 760931 | c.1125C>G | synonymous_variant | 0.5 |
rpoB | 760934 | c.1128C>T | synonymous_variant | 0.5 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.5 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.57 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.57 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.57 |
rpoB | 761006 | c.1200C>G | synonymous_variant | 0.6 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.43 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.43 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.43 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.43 |
rpoB | 761219 | c.1413G>C | synonymous_variant | 0.43 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.5 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.57 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.5 |
rpoB | 761306 | c.1500C>G | synonymous_variant | 0.4 |
rpoB | 761510 | c.1704T>C | synonymous_variant | 0.6 |
rpoB | 761531 | c.1725C>G | synonymous_variant | 0.5 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.5 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.43 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.43 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.43 |
rpoB | 761588 | c.1782C>T | synonymous_variant | 0.38 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.33 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.33 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.33 |
rpoB | 761675 | c.1869G>C | synonymous_variant | 0.4 |
rpoB | 761720 | c.1914C>G | synonymous_variant | 0.23 |
rpoB | 761732 | c.1926C>G | synonymous_variant | 0.23 |
rpoB | 761735 | c.1929C>G | synonymous_variant | 0.23 |
rpoB | 761747 | c.1941G>C | synonymous_variant | 0.23 |
rpoB | 761750 | c.1944G>C | synonymous_variant | 0.29 |
rpoB | 761765 | c.1959T>C | synonymous_variant | 0.36 |
rpoB | 761772 | p.His656Ala | missense_variant | 0.27 |
rpoB | 761778 | p.Asn658Asp | missense_variant | 0.36 |
rpoB | 761791 | p.Arg662His | missense_variant | 0.33 |
rpoB | 761813 | c.2007T>C | synonymous_variant | 0.38 |
rpoB | 761815 | p.Ala670Glu | missense_variant | 0.38 |
rpoB | 761834 | c.2028T>C | synonymous_variant | 0.5 |
rpoB | 761848 | p.Cys681Ser | missense_variant | 0.5 |
rpoB | 761852 | c.2046C>G | synonymous_variant | 0.5 |
rpoB | 761858 | c.2052G>C | synonymous_variant | 0.43 |
rpoB | 761873 | c.2067A>C | synonymous_variant | 0.5 |
rpoB | 761906 | c.2100C>G | synonymous_variant | 0.5 |
rpoB | 761909 | c.2103T>C | synonymous_variant | 0.67 |
rpoB | 761912 | c.2106T>C | synonymous_variant | 0.67 |
rpoB | 761915 | p.Asp703Glu | missense_variant | 0.67 |
rpoB | 761916 | p.Asp704Asn | missense_variant | 0.67 |
rpoB | 762008 | c.2202C>T | synonymous_variant | 0.4 |
rpoB | 762014 | c.2208C>T | synonymous_variant | 0.33 |
rpoB | 762017 | c.2211A>G | synonymous_variant | 0.33 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.33 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.33 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.33 |
rpoB | 762206 | c.2400C>G | synonymous_variant | 0.5 |
rpoC | 762434 | c.-936T>C | upstream_gene_variant | 0.5 |
rpoC | 762449 | c.-921C>A | upstream_gene_variant | 0.5 |
rpoC | 762467 | c.-903C>T | upstream_gene_variant | 0.5 |
rpoC | 762488 | c.-882G>C | upstream_gene_variant | 0.5 |
rpoB | 762489 | p.Val895Gln | missense_variant | 0.5 |
rpoC | 762509 | c.-861T>G | upstream_gene_variant | 0.4 |
rpoB | 762510 | p.Ala902Pro | missense_variant | 0.4 |
rpoC | 762521 | c.-849C>T | upstream_gene_variant | 0.4 |
rpoC | 762857 | c.-513C>G | upstream_gene_variant | 0.33 |
rpoC | 762860 | c.-510G>C | upstream_gene_variant | 0.33 |
rpoC | 762863 | c.-507T>C | upstream_gene_variant | 0.4 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.67 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.83 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.83 |
rpoC | 763013 | c.-357C>G | upstream_gene_variant | 0.83 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.56 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 0.56 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.5 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.44 |
rpoC | 763067 | c.-303C>G | upstream_gene_variant | 0.38 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.38 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.38 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.29 |
rpoB | 763123 | p.Ile1106Thr | missense_variant | 0.8 |
rpoC | 763402 | c.33C>G | synonymous_variant | 0.57 |
rpoC | 763411 | c.42T>G | synonymous_variant | 0.71 |
rpoC | 763414 | c.45T>C | synonymous_variant | 0.71 |
rpoC | 763441 | c.72C>T | synonymous_variant | 0.75 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.75 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.83 |
rpoC | 763486 | c.117T>G | synonymous_variant | 0.83 |
rpoC | 763492 | c.123G>C | synonymous_variant | 1.0 |
rpoC | 763528 | c.159G>A | synonymous_variant | 1.0 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.67 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.75 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.67 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.75 |
rpoC | 763603 | c.234C>T | synonymous_variant | 0.75 |
rpoC | 763606 | c.237C>T | synonymous_variant | 0.75 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.75 |
rpoC | 763657 | c.288G>A | synonymous_variant | 0.75 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.8 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.5 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.5 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.5 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.4 |
rpoC | 764083 | c.714A>G | synonymous_variant | 0.25 |
rpoC | 764098 | c.729A>G | synonymous_variant | 0.25 |
rpoC | 764101 | c.732C>G | synonymous_variant | 0.3 |
rpoC | 764102 | p.Val245Ile | missense_variant | 0.3 |
rpoC | 764112 | p.Tyr248Phe | missense_variant | 0.33 |
rpoC | 764116 | c.747C>T | synonymous_variant | 0.33 |
rpoC | 764131 | c.762T>C | synonymous_variant | 0.44 |
rpoC | 764338 | c.969G>A | synonymous_variant | 0.33 |
rpoC | 764353 | c.984G>C | synonymous_variant | 0.33 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.4 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.29 |
rpoC | 764381 | c.1012_1013delTCinsAG | synonymous_variant | 0.29 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 0.25 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.38 |
rpoC | 764419 | c.1050C>G | synonymous_variant | 0.5 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.5 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.5 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.5 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.4 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.4 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.4 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.4 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.5 |
rpoC | 764489 | c.1120C>T | synonymous_variant | 0.4 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.25 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.33 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.33 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.33 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.38 |
rpoC | 764650 | c.1281G>C | synonymous_variant | 0.29 |
rpoC | 764651 | c.1282_1284delTCGinsAGC | synonymous_variant | 0.33 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.33 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.57 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.67 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.67 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.33 |
rpoC | 764872 | c.1503A>G | synonymous_variant | 0.33 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.33 |
rpoC | 764932 | c.1563C>A | synonymous_variant | 0.33 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.29 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.43 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 765529 | c.2160C>T | synonymous_variant | 0.67 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 1.0 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.67 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.5 |
rpoC | 765580 | c.2211G>C | synonymous_variant | 0.6 |
rpoC | 765613 | p.His748Gln | missense_variant | 0.29 |
rpoC | 765625 | c.2256C>G | synonymous_variant | 0.25 |
rpoC | 765628 | c.2259G>C | synonymous_variant | 0.33 |
rpoC | 765631 | p.Asp754Glu | missense_variant | 0.33 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.62 |
rpoC | 765734 | c.2365T>C | synonymous_variant | 0.5 |
rpoC | 765739 | c.2370G>T | synonymous_variant | 0.5 |
rpoC | 765751 | c.2382C>G | synonymous_variant | 0.44 |
rpoC | 765753 | p.Asp795Ala | missense_variant | 0.38 |
rpoC | 765772 | c.2403C>G | synonymous_variant | 0.29 |
rpoC | 765784 | c.2415C>G | synonymous_variant | 0.29 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 0.4 |
rpoC | 765850 | c.2481G>C | synonymous_variant | 0.43 |
rpoC | 765883 | c.2514C>G | synonymous_variant | 0.44 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.4 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.4 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.29 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.33 |
rpoC | 766010 | c.2641_2642delTCinsAG | synonymous_variant | 0.5 |
rpoC | 766021 | c.2652G>C | synonymous_variant | 0.43 |
rpoC | 766027 | c.2658G>C | synonymous_variant | 0.33 |
rpoC | 766043 | p.Gln892Glu | missense_variant | 0.33 |
rpoC | 766054 | c.2685C>G | synonymous_variant | 0.33 |
rpoC | 766084 | c.2715A>G | synonymous_variant | 0.33 |
rpoC | 766096 | c.2727G>C | synonymous_variant | 0.5 |
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 | 766573 | c.3204T>C | synonymous_variant | 1.0 |
rpoC | 766582 | c.3213C>G | synonymous_variant | 0.67 |
rpoC | 766583 | p.Gly1072Ser | missense_variant | 0.67 |
rpoC | 766591 | c.3222A>G | synonymous_variant | 0.75 |
rpoC | 766594 | c.3225G>C | synonymous_variant | 0.75 |
rpoC | 766597 | c.3228C>G | synonymous_variant | 0.75 |
rpoC | 766607 | p.Ile1080Leu | missense_variant | 0.6 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 0.67 |
rpoC | 766864 | c.3495G>C | synonymous_variant | 0.67 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.33 |
rpoC | 766933 | c.3564A>G | synonymous_variant | 0.22 |
rpoC | 766945 | c.3576A>G | synonymous_variant | 0.22 |
mmpL5 | 775966 | p.Ala839Ser | missense_variant | 0.33 |
mmpL5 | 775975 | c.2506T>C | synonymous_variant | 0.29 |
mmpL5 | 775981 | p.Leu834Met | missense_variant | 0.29 |
mmpL5 | 775997 | c.2484T>C | synonymous_variant | 0.4 |
mmpL5 | 776695 | p.Val596Ile | missense_variant | 0.22 |
mmpL5 | 776738 | c.1743C>T | synonymous_variant | 0.22 |
mmpL5 | 777101 | c.1380C>G | synonymous_variant | 0.5 |
mmpL5 | 777110 | c.1371T>G | synonymous_variant | 0.5 |
mmpL5 | 777115 | p.Met456Leu | missense_variant | 0.5 |
mmpL5 | 777116 | c.1365C>T | synonymous_variant | 0.5 |
mmpL5 | 777133 | p.Val450Ile | missense_variant | 0.5 |
mmpL5 | 777158 | c.1323C>G | synonymous_variant | 0.5 |
mmpL5 | 777164 | c.1317C>G | synonymous_variant | 0.5 |
mmpL5 | 777170 | c.1311T>C | synonymous_variant | 0.5 |
mmpL5 | 777176 | p.Glu435Asp | missense_variant | 0.67 |
mmpL5 | 777191 | c.1290C>G | synonymous_variant | 0.67 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.33 |
rpsL | 781742 | c.183C>T | synonymous_variant | 0.43 |
rpsL | 781748 | c.189C>G | synonymous_variant | 0.43 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.38 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.38 |
rpsL | 781772 | c.213C>A | synonymous_variant | 0.5 |
rpsL | 781808 | c.249C>T | synonymous_variant | 0.33 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.33 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.5 |
rpsL | 781838 | c.279G>C | synonymous_variant | 0.33 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.33 |
rpsL | 781865 | c.306G>C | synonymous_variant | 0.33 |
fbiC | 1303489 | c.559C>T | synonymous_variant | 0.5 |
fbiC | 1303497 | c.567G>A | synonymous_variant | 0.5 |
fbiC | 1303501 | c.571C>T | synonymous_variant | 0.5 |
fbiC | 1303509 | c.579G>C | synonymous_variant | 0.5 |
fbiC | 1303512 | c.582T>C | synonymous_variant | 0.5 |
fbiC | 1303521 | c.591C>T | synonymous_variant | 0.5 |
fbiC | 1303530 | c.600G>A | synonymous_variant | 0.5 |
fbiC | 1303534 | p.Ser202Ala | missense_variant | 0.5 |
fbiC | 1303539 | c.609G>C | synonymous_variant | 0.5 |
fbiC | 1303545 | c.615A>G | synonymous_variant | 0.6 |
fbiC | 1303575 | c.645G>C | synonymous_variant | 0.5 |
fbiC | 1303590 | c.660A>G | synonymous_variant | 0.33 |
fbiC | 1303602 | c.672A>G | synonymous_variant | 0.33 |
fbiC | 1303605 | c.675C>G | synonymous_variant | 0.33 |
fbiC | 1303608 | c.678G>A | synonymous_variant | 0.33 |
fbiC | 1303614 | c.684C>T | synonymous_variant | 0.33 |
fbiC | 1303617 | c.687C>G | synonymous_variant | 0.33 |
fbiC | 1303632 | c.702T>G | synonymous_variant | 0.43 |
fbiC | 1303854 | c.924T>C | synonymous_variant | 0.4 |
fbiC | 1303860 | c.930A>C | synonymous_variant | 0.5 |
fbiC | 1303884 | c.954T>G | synonymous_variant | 0.6 |
fbiC | 1303905 | c.975G>C | synonymous_variant | 0.75 |
fbiC | 1303909 | p.Pro327Ser | missense_variant | 0.75 |
fbiC | 1303914 | c.984C>G | synonymous_variant | 0.75 |
fbiC | 1303920 | c.990C>T | synonymous_variant | 0.75 |
fbiC | 1304097 | c.1167G>C | synonymous_variant | 0.33 |
fbiC | 1304127 | c.1197A>G | synonymous_variant | 0.4 |
fbiC | 1304132 | p.Ala401Gly | missense_variant | 0.4 |
fbiC | 1304142 | c.1212G>C | synonymous_variant | 0.4 |
fbiC | 1304808 | c.1878C>G | synonymous_variant | 0.5 |
fbiC | 1304811 | c.1881C>G | synonymous_variant | 0.5 |
fbiC | 1304817 | c.1887T>C | synonymous_variant | 0.5 |
fbiC | 1304829 | c.1899T>C | synonymous_variant | 0.5 |
fbiC | 1304832 | c.1902C>T | synonymous_variant | 0.4 |
fbiC | 1304853 | c.1923C>T | synonymous_variant | 0.5 |
fbiC | 1304856 | c.1926C>G | synonymous_variant | 0.5 |
fbiC | 1304869 | c.1939C>T | synonymous_variant | 0.43 |
fbiC | 1304875 | p.Ile649Val | missense_variant | 0.43 |
fbiC | 1304883 | p.Glu651Asp | missense_variant | 0.33 |
fbiC | 1304891 | p.Ile654Thr | missense_variant | 0.6 |
fbiC | 1304893 | p.Gly655Ser | missense_variant | 0.6 |
fbiC | 1304907 | c.1977C>G | synonymous_variant | 0.5 |
fbiC | 1304910 | c.1980G>C | synonymous_variant | 0.5 |
fbiC | 1304916 | c.1986T>C | synonymous_variant | 0.5 |
fbiC | 1304928 | c.1998T>C | synonymous_variant | 0.67 |
fbiC | 1304937 | c.2007G>C | synonymous_variant | 0.67 |
fbiC | 1304958 | c.2028T>G | synonymous_variant | 1.0 |
fbiC | 1304983 | c.2053C>T | synonymous_variant | 0.67 |
atpE | 1461170 | c.126A>G | synonymous_variant | 0.4 |
atpE | 1461185 | c.141G>T | synonymous_variant | 0.29 |
atpE | 1461197 | c.153A>G | synonymous_variant | 0.29 |
atpE | 1461219 | c.175T>C | synonymous_variant | 0.29 |
atpE | 1461233 | c.189A>C | synonymous_variant | 0.33 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1471932 | n.87A>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1471969 | n.124T>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473756 | n.99G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1473986 | n.329T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1473987 | n.330G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474009 | n.352A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474012 | n.355C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474093 | n.436G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474099 | n.442G>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474291 | n.635_649delTTCCTCTCCGGAGGA | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.6 |
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>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474823 | n.1166C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474904 | n.1247G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474956 | n.1299C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474960 | n.1303C>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474963 | n.1306G>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474964 | n.1307T>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474965 | n.1308G>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474970 | n.1313G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475006 | n.1349A>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475088 | n.1431A>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475199 | n.1542G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475206 | n.1549C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475209 | n.1552G>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475249 | n.1592T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475252 | n.1595C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1475266 | n.1609T>C | non_coding_transcript_exon_variant | 0.55 |
rrl | 1475267 | n.1610G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475275 | n.1618C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475276 | n.1619T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475291 | n.1634A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475313 | n.1656G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475369 | n.1712G>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475402 | n.1745C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475436 | n.1779C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475765 | n.2111delG | non_coding_transcript_exon_variant | 0.55 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476056 | n.2399G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476214 | n.2557G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476689 | n.3032A>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476690 | n.3033C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476693 | n.3036G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476695 | n.3038T>A | non_coding_transcript_exon_variant | 0.2 |
fabG1 | 1674079 | p.Pro214Ala | missense_variant | 0.33 |
inhA | 1674879 | c.678T>C | synonymous_variant | 0.2 |
inhA | 1674900 | c.699G>A | synonymous_variant | 0.25 |
inhA | 1674903 | c.702T>C | synonymous_variant | 0.22 |
inhA | 1674904 | p.Ala235Pro | missense_variant | 0.22 |
inhA | 1674909 | c.708G>A | synonymous_variant | 0.25 |
rpsA | 1833554 | p.Thr5Ala | missense_variant | 0.25 |
rpsA | 1833568 | c.27G>C | synonymous_variant | 0.29 |
rpsA | 1833589 | c.48A>T | synonymous_variant | 0.18 |
rpsA | 1833595 | c.54T>C | synonymous_variant | 0.18 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.33 |
rpsA | 1833667 | c.126C>G | synonymous_variant | 0.33 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.67 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 1.0 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.5 |
rpsA | 1833940 | c.399C>G | synonymous_variant | 0.6 |
rpsA | 1833971 | c.430C>T | synonymous_variant | 0.5 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.75 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.6 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.5 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.5 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.25 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.2 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.33 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.36 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.43 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.5 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.67 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.67 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 1.0 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.5 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.33 |
rpsA | 1834510 | c.969C>T | synonymous_variant | 0.4 |
rpsA | 1834513 | c.972C>G | synonymous_variant | 0.5 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.57 |
rpsA | 1834540 | c.999G>C | synonymous_variant | 0.5 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.5 |
rpsA | 1834732 | c.1191T>C | synonymous_variant | 0.33 |
rpsA | 1834733 | p.Ala398Ser | missense_variant | 0.33 |
rpsA | 1834738 | c.1197A>G | synonymous_variant | 0.33 |
rpsA | 1834753 | c.1212T>C | synonymous_variant | 0.5 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102671 | c.372T>G | synonymous_variant | 0.5 |
ndh | 2102680 | c.363T>C | synonymous_variant | 0.5 |
ndh | 2102686 | c.357G>C | synonymous_variant | 0.4 |
ndh | 2102695 | c.348C>T | synonymous_variant | 0.4 |
katG | 2155704 | c.408C>G | synonymous_variant | 0.67 |
katG | 2155716 | c.396T>G | synonymous_variant | 0.67 |
Rv1979c | 2223051 | p.Glu38Asp | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518696 | c.582C>G | synonymous_variant | 0.4 |
kasA | 2518702 | c.588C>T | synonymous_variant | 0.4 |
kasA | 2518705 | c.591T>C | synonymous_variant | 0.4 |
kasA | 2518711 | c.597A>G | synonymous_variant | 0.33 |
kasA | 2518714 | c.600A>C | synonymous_variant | 0.33 |
kasA | 2518732 | c.618C>G | synonymous_variant | 0.25 |
kasA | 2518744 | c.630C>T | synonymous_variant | 0.25 |
kasA | 2518747 | c.633C>G | synonymous_variant | 0.25 |
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 | 2519107 | c.993T>C | synonymous_variant | 1.0 |
kasA | 2519108 | p.Asp332Gln | missense_variant | 1.0 |
kasA | 2519122 | c.1008G>C | synonymous_variant | 1.0 |
ahpC | 2726198 | c.6A>T | synonymous_variant | 0.33 |
ahpC | 2726204 | c.12A>G | synonymous_variant | 0.43 |
ahpC | 2726210 | c.18T>C | synonymous_variant | 0.43 |
ahpC | 2726216 | c.24T>C | synonymous_variant | 0.43 |
ahpC | 2726219 | c.27A>G | synonymous_variant | 0.5 |
ahpC | 2726232 | p.Gln14Glu | missense_variant | 0.5 |
ahpC | 2726243 | c.51T>G | synonymous_variant | 0.43 |
ahpC | 2726244 | c.52_54delCTCinsTTG | synonymous_variant | 0.43 |
ahpC | 2726251 | p.Gly20Ala | missense_variant | 0.5 |
ahpC | 2726255 | c.63T>C | synonymous_variant | 0.6 |
ahpC | 2726258 | c.66C>T | synonymous_variant | 0.6 |
ahpC | 2726510 | c.318A>G | synonymous_variant | 0.2 |
ahpC | 2726528 | c.336C>G | synonymous_variant | 0.17 |
ahpC | 2726551 | p.Gln120Leu | missense_variant | 0.15 |
ahpC | 2726556 | p.Ala122Thr | missense_variant | 0.18 |
ahpC | 2726564 | c.372C>G | synonymous_variant | 0.23 |
ahpC | 2726591 | c.399C>G | synonymous_variant | 0.2 |
ahpC | 2726593 | p.Val134Ala | missense_variant | 0.2 |
ahpC | 2726600 | c.408T>C | synonymous_variant | 0.22 |
ahpC | 2726601 | p.Ile137Leu | missense_variant | 0.25 |
ahpC | 2726657 | c.465A>C | synonymous_variant | 0.29 |
Rv2752c | 3064914 | c.1278T>G | synonymous_variant | 0.4 |
Rv2752c | 3065241 | c.951A>C | synonymous_variant | 0.25 |
Rv2752c | 3065824 | p.Pro123Leu | missense_variant | 1.0 |
Rv2752c | 3066018 | c.174T>C | synonymous_variant | 0.33 |
Rv2752c | 3066024 | c.168T>G | synonymous_variant | 0.25 |
Rv2752c | 3066040 | p.Gly51Thr | missense_variant | 0.25 |
Rv2752c | 3066042 | c.150T>C | synonymous_variant | 0.25 |
Rv2752c | 3066045 | c.147T>C | synonymous_variant | 0.22 |
Rv2752c | 3066050 | p.Leu48Met | missense_variant | 0.22 |
Rv2752c | 3066054 | c.138T>G | synonymous_variant | 0.22 |
Rv2752c | 3066066 | c.126T>C | synonymous_variant | 0.17 |
Rv2752c | 3066075 | c.117A>G | synonymous_variant | 0.17 |
thyX | 3067439 | c.507A>G | synonymous_variant | 0.67 |
thyX | 3067442 | c.504C>T | synonymous_variant | 0.67 |
thyX | 3067611 | p.Lys112Thr | missense_variant | 0.29 |
thyX | 3067619 | c.327A>C | synonymous_variant | 0.29 |
thyX | 3067631 | c.315C>G | synonymous_variant | 0.29 |
thyX | 3067634 | c.312C>G | synonymous_variant | 0.29 |
thyX | 3067637 | c.309G>A | synonymous_variant | 0.33 |
thyX | 3067652 | c.294T>C | synonymous_variant | 0.5 |
thyX | 3067661 | c.285C>G | synonymous_variant | 0.5 |
thyX | 3067685 | c.261A>C | synonymous_variant | 0.57 |
thyX | 3067691 | p.Ile85Leu | missense_variant | 0.6 |
thyX | 3067694 | c.252G>C | synonymous_variant | 0.5 |
thyX | 3067718 | c.228C>G | synonymous_variant | 0.5 |
thyX | 3067721 | c.225T>C | synonymous_variant | 0.5 |
thyX | 3067727 | c.219A>C | synonymous_variant | 0.43 |
thyX | 3067736 | c.210C>T | synonymous_variant | 0.43 |
thyX | 3067850 | c.96A>C | synonymous_variant | 0.5 |
thyX | 3067869 | p.Thr26Ser | missense_variant | 0.4 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473809 | c.-198G>C | upstream_gene_variant | 0.33 |
fprA | 3473812 | c.-195G>A | upstream_gene_variant | 0.33 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiB | 3642719 | c.1185T>C | synonymous_variant | 0.33 |
fbiB | 3642731 | c.1197C>G | synonymous_variant | 0.4 |
alr | 3840989 | c.432G>C | synonymous_variant | 0.4 |
alr | 3840994 | p.His143Asp | missense_variant | 0.33 |
alr | 3840995 | c.424_426delTTGinsCTC | synonymous_variant | 0.33 |
alr | 3841001 | c.420A>G | synonymous_variant | 0.29 |
alr | 3841010 | c.411A>G | synonymous_variant | 0.38 |
alr | 3841017 | p.Leu135Glu | missense_variant | 0.38 |
alr | 3841022 | c.399C>G | synonymous_variant | 0.38 |
alr | 3841028 | c.393G>C | synonymous_variant | 0.43 |
alr | 3841033 | p.Val130Ile | missense_variant | 0.43 |
alr | 3841037 | c.384G>C | synonymous_variant | 0.43 |
alr | 3841069 | p.Ile118Phe | missense_variant | 0.44 |
alr | 3841076 | c.345G>A | synonymous_variant | 0.38 |
alr | 3841079 | c.342T>C | synonymous_variant | 0.38 |
alr | 3841100 | c.321A>G | synonymous_variant | 0.29 |
rpoA | 3877494 | p.Glu338Asp | missense_variant | 0.33 |
rpoA | 3877503 | c.1005G>C | synonymous_variant | 0.4 |
rpoA | 3877507 | p.Gly334Ala | missense_variant | 0.4 |
rpoA | 3877515 | c.993G>C | synonymous_variant | 0.5 |
rpoA | 3877553 | p.Glu319Gln | missense_variant | 0.55 |
rpoA | 3877571 | p.Pro313Ala | missense_variant | 0.58 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.58 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.5 |
rpoA | 3877656 | c.852T>G | synonymous_variant | 0.43 |
rpoA | 3877679 | p.Ala277Ser | missense_variant | 0.33 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.29 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.4 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.5 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.5 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.57 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.67 |
rpoA | 3877848 | c.660C>T | synonymous_variant | 0.67 |
rpoA | 3877857 | c.651G>A | synonymous_variant | 0.57 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.5 |
rpoA | 3877875 | c.633T>G | synonymous_variant | 0.57 |
rpoA | 3877878 | c.630G>C | synonymous_variant | 0.57 |
rpoA | 3877890 | c.618C>T | synonymous_variant | 0.57 |
rpoA | 3877896 | c.612G>C | synonymous_variant | 0.5 |
rpoA | 3877900 | p.Ser203Asn | missense_variant | 0.43 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.33 |
rpoA | 3877909 | p.Asn200Ser | missense_variant | 0.33 |
rpoA | 3877920 | c.588G>C | synonymous_variant | 0.4 |
rpoA | 3877923 | c.585C>T | synonymous_variant | 0.4 |
rpoA | 3877926 | c.582G>C | synonymous_variant | 0.4 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.67 |
rpoA | 3877986 | c.522G>C | synonymous_variant | 0.6 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.6 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.5 |
rpoA | 3878022 | c.486T>C | synonymous_variant | 0.5 |
rpoA | 3878028 | c.480G>C | synonymous_variant | 0.5 |
rpoA | 3878031 | c.477T>C | synonymous_variant | 0.33 |
rpoA | 3878040 | c.468T>C | synonymous_variant | 0.4 |
rpoA | 3878094 | c.414C>G | synonymous_variant | 0.29 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.25 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.25 |
rpoA | 3878115 | c.393G>A | synonymous_variant | 0.22 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.22 |
rpoA | 3878130 | c.378C>G | synonymous_variant | 0.29 |
rpoA | 3878157 | c.351C>G | synonymous_variant | 0.33 |
rpoA | 3878163 | c.345C>T | synonymous_variant | 0.4 |
rpoA | 3878169 | c.339G>C | synonymous_variant | 0.5 |
rpoA | 3878172 | c.336G>C | synonymous_variant | 0.5 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 0.75 |
clpC1 | 4038368 | c.2337T>C | synonymous_variant | 0.29 |
clpC1 | 4038388 | c.2317T>C | synonymous_variant | 0.33 |
clpC1 | 4038392 | c.2313C>T | synonymous_variant | 0.33 |
clpC1 | 4038398 | c.2307G>T | synonymous_variant | 0.33 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 0.5 |
clpC1 | 4038407 | c.2298G>C | synonymous_variant | 0.4 |
clpC1 | 4038419 | c.2286T>C | synonymous_variant | 0.4 |
clpC1 | 4038433 | c.2272C>T | synonymous_variant | 0.4 |
clpC1 | 4038434 | c.2271G>A | synonymous_variant | 0.4 |
clpC1 | 4038444 | p.Ala754Lys | missense_variant | 0.67 |
clpC1 | 4038446 | c.2259T>C | synonymous_variant | 0.5 |
clpC1 | 4038456 | p.Val750Glu | missense_variant | 0.4 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.29 |
clpC1 | 4038653 | c.2052C>T | synonymous_variant | 0.25 |
clpC1 | 4038658 | p.Lys683Gln | missense_variant | 0.29 |
clpC1 | 4038661 | p.Ser682Thr | missense_variant | 0.29 |
clpC1 | 4038662 | c.2043T>C | synonymous_variant | 0.29 |
clpC1 | 4038671 | c.2034T>C | synonymous_variant | 0.43 |
clpC1 | 4038683 | c.2022T>C | synonymous_variant | 0.62 |
clpC1 | 4038695 | c.2010C>G | synonymous_variant | 0.57 |
clpC1 | 4038701 | c.2004G>C | synonymous_variant | 0.67 |
clpC1 | 4038704 | c.2001T>C | synonymous_variant | 0.67 |
clpC1 | 4038707 | c.1998C>G | synonymous_variant | 0.67 |
clpC1 | 4038710 | c.1995G>C | synonymous_variant | 0.67 |
clpC1 | 4038713 | c.1992T>C | synonymous_variant | 0.67 |
clpC1 | 4038749 | c.1956C>G | synonymous_variant | 0.5 |
clpC1 | 4038755 | c.1950G>T | synonymous_variant | 0.5 |
clpC1 | 4038770 | c.1935C>T | synonymous_variant | 0.33 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.33 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.29 |
clpC1 | 4038845 | c.1860G>C | synonymous_variant | 0.5 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 0.5 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.4 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.4 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.4 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.4 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.4 |
clpC1 | 4039004 | c.1701C>G | synonymous_variant | 0.4 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.6 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.33 |
clpC1 | 4039103 | c.1602T>C | synonymous_variant | 0.33 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.29 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.29 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.29 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.43 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.43 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.44 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.44 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.38 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.5 |
clpC1 | 4039186 | c.1519C>T | synonymous_variant | 0.5 |
clpC1 | 4039226 | c.1479T>C | synonymous_variant | 0.57 |
clpC1 | 4039229 | c.1476C>G | synonymous_variant | 0.57 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.6 |
clpC1 | 4039556 | c.1149G>C | synonymous_variant | 0.5 |
clpC1 | 4039559 | c.1146C>G | synonymous_variant | 0.5 |
clpC1 | 4039562 | c.1143C>G | synonymous_variant | 0.67 |
clpC1 | 4039565 | c.1140G>T | synonymous_variant | 0.67 |
clpC1 | 4039570 | p.Met379Leu | missense_variant | 0.5 |
clpC1 | 4039576 | p.Ala377Pro | missense_variant | 0.5 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.5 |
clpC1 | 4039589 | c.1116G>C | synonymous_variant | 0.33 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.33 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.43 |
clpC1 | 4039661 | c.1044T>G | synonymous_variant | 0.5 |
clpC1 | 4039664 | c.1041G>C | synonymous_variant | 0.5 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.75 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.67 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.67 |
clpC1 | 4039988 | c.717C>G | synonymous_variant | 0.67 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 0.67 |
embC | 4240693 | c.831T>G | synonymous_variant | 0.5 |
embC | 4240699 | c.837C>G | synonymous_variant | 0.5 |
embC | 4240726 | c.864G>C | synonymous_variant | 0.75 |
embC | 4240780 | c.918T>C | synonymous_variant | 1.0 |
embC | 4240783 | c.921G>C | synonymous_variant | 1.0 |
embC | 4240789 | c.927T>C | synonymous_variant | 1.0 |
embC | 4240819 | c.957A>G | synonymous_variant | 0.6 |
embC | 4240828 | c.966G>A | synonymous_variant | 0.6 |
embC | 4240831 | c.969T>G | synonymous_variant | 0.4 |
embC | 4240996 | c.1134G>C | synonymous_variant | 0.5 |
embC | 4241002 | c.1140G>C | synonymous_variant | 0.5 |
embC | 4241013 | p.Met384Thr | missense_variant | 0.5 |
embC | 4241017 | c.1155T>C | synonymous_variant | 0.5 |
embC | 4241023 | c.1161T>G | synonymous_variant | 0.5 |
embC | 4241032 | c.1170G>C | synonymous_variant | 0.5 |
embC | 4241038 | c.1176G>C | synonymous_variant | 0.5 |
embC | 4241047 | c.1185C>G | synonymous_variant | 0.5 |
embC | 4241050 | c.1188T>G | synonymous_variant | 0.5 |
embC | 4241053 | c.1191G>C | synonymous_variant | 0.67 |
embC | 4241727 | p.Phe622Tyr | missense_variant | 0.29 |
embC | 4241741 | p.Val627Leu | missense_variant | 0.33 |
embC | 4241747 | p.Val629Leu | missense_variant | 0.33 |
embC | 4241750 | p.Leu630Val | missense_variant | 0.33 |
embC | 4241755 | c.1893C>G | synonymous_variant | 0.29 |
embA | 4242742 | c.-491C>G | upstream_gene_variant | 0.4 |
embA | 4242748 | c.-485A>G | upstream_gene_variant | 0.4 |
embA | 4242754 | c.-479G>C | upstream_gene_variant | 0.4 |
embC | 4242764 | p.Val968Leu | missense_variant | 0.4 |
embA | 4242772 | c.-461G>C | upstream_gene_variant | 0.4 |
embC | 4242779 | p.Asn973Asp | missense_variant | 0.5 |
embA | 4242802 | c.-431G>C | upstream_gene_variant | 0.5 |
embA | 4242820 | c.-413G>C | upstream_gene_variant | 0.5 |
embA | 4242823 | c.-410G>C | upstream_gene_variant | 0.5 |
embA | 4245693 | p.Ile821Val | missense_variant | 0.33 |
embB | 4245701 | c.-813G>C | upstream_gene_variant | 0.29 |
embB | 4245704 | c.-810G>C | upstream_gene_variant | 0.29 |
embB | 4245725 | c.-789A>G | upstream_gene_variant | 0.5 |
embB | 4245726 | c.-788T>C | upstream_gene_variant | 0.5 |
embB | 4245737 | c.-777A>C | upstream_gene_variant | 0.4 |
embB | 4245740 | c.-774T>C | upstream_gene_variant | 0.4 |
embB | 4245785 | c.-729G>C | upstream_gene_variant | 0.33 |
embB | 4245845 | c.-669T>C | upstream_gene_variant | 0.5 |
embB | 4245851 | c.-663G>C | upstream_gene_variant | 0.43 |
embB | 4245860 | c.-654C>G | upstream_gene_variant | 0.5 |
embA | 4245885 | p.Asp885Thr | missense_variant | 0.5 |
embA | 4245892 | p.Ile887Thr | missense_variant | 0.5 |
embB | 4245899 | c.-615C>G | upstream_gene_variant | 0.67 |
embB | 4245902 | c.-612G>A | upstream_gene_variant | 0.67 |
embB | 4245905 | c.-609C>G | upstream_gene_variant | 0.67 |
embB | 4245911 | c.-603A>G | upstream_gene_variant | 0.67 |
embB | 4245917 | c.-597G>A | upstream_gene_variant | 0.67 |
embA | 4245930 | p.Gly900Arg | missense_variant | 0.67 |
embB | 4246196 | c.-318C>G | upstream_gene_variant | 0.67 |
embB | 4246205 | c.-309A>G | upstream_gene_variant | 0.67 |
embB | 4246211 | c.-303T>C | upstream_gene_variant | 0.5 |
embB | 4246217 | c.-297G>A | upstream_gene_variant | 0.4 |
embB | 4246220 | c.-294T>C | upstream_gene_variant | 0.4 |
embB | 4246223 | c.-291C>T | upstream_gene_variant | 0.4 |
embA | 4246227 | p.Ile999Val | missense_variant | 0.4 |
embB | 4246235 | c.-279G>A | upstream_gene_variant | 0.33 |
embA | 4246242 | p.Gln1004Gly | missense_variant | 0.33 |
embB | 4246250 | c.-264G>C | upstream_gene_variant | 0.29 |
embB | 4246256 | c.-258G>T | upstream_gene_variant | 0.29 |
embB | 4246259 | c.-255G>C | upstream_gene_variant | 0.38 |
embA | 4246264 | p.His1011Arg | missense_variant | 0.38 |
embB | 4246292 | c.-222A>G | upstream_gene_variant | 0.29 |
embA | 4246305 | p.Ser1025Glu | missense_variant | 0.29 |
embA | 4246308 | p.Thr1026Ala | missense_variant | 0.25 |
embB | 4246316 | c.-198T>G | upstream_gene_variant | 0.38 |
embB | 4246319 | c.-195G>C | upstream_gene_variant | 0.38 |
embA | 4246329 | p.Thr1033Ala | missense_variant | 0.38 |
embB | 4246349 | c.-165C>G | upstream_gene_variant | 0.43 |
embA | 4246359 | p.Ala1043Ser | missense_variant | 0.29 |
embB | 4246367 | c.-147C>T | upstream_gene_variant | 0.25 |
embB | 4248304 | c.1791G>C | synonymous_variant | 0.5 |
embB | 4248316 | c.1803C>G | synonymous_variant | 0.67 |
embB | 4248319 | c.1806A>G | synonymous_variant | 1.0 |
embB | 4248343 | c.1830G>C | synonymous_variant | 0.67 |
embB | 4248350 | c.1837T>C | synonymous_variant | 0.67 |
embB | 4248355 | c.1842A>G | synonymous_variant | 0.67 |
embB | 4248358 | c.1845C>G | synonymous_variant | 0.67 |
embB | 4248361 | c.1848A>C | synonymous_variant | 0.67 |
embB | 4248362 | p.Ser617Ala | missense_variant | 0.67 |
embB | 4248373 | c.1860C>G | synonymous_variant | 0.67 |
embB | 4249417 | c.2904A>G | synonymous_variant | 0.33 |
embB | 4249423 | p.Asp970Glu | missense_variant | 0.33 |
embB | 4249424 | p.Leu971Met | missense_variant | 0.33 |
embB | 4249429 | c.2916C>T | synonymous_variant | 0.33 |
embB | 4249432 | c.2919A>G | synonymous_variant | 0.33 |
embB | 4249441 | c.2928A>G | synonymous_variant | 0.33 |
aftB | 4267604 | c.1233C>G | synonymous_variant | 0.5 |
aftB | 4267607 | c.1230G>A | synonymous_variant | 0.5 |
aftB | 4267622 | c.1215G>C | synonymous_variant | 0.5 |
aftB | 4267625 | c.1212T>C | synonymous_variant | 0.5 |
aftB | 4267628 | c.1209C>G | synonymous_variant | 0.5 |
aftB | 4267634 | p.Arg401His | missense_variant | 0.4 |
aftB | 4267649 | c.1188T>C | synonymous_variant | 0.5 |
aftB | 4267658 | c.1179G>C | synonymous_variant | 0.5 |
aftB | 4267661 | c.1176G>A | synonymous_variant | 0.5 |
aftB | 4267664 | c.1173C>T | synonymous_variant | 0.5 |
aftB | 4267667 | c.1170A>G | synonymous_variant | 0.4 |
aftB | 4267670 | c.1167G>C | synonymous_variant | 0.33 |
aftB | 4268999 | c.-163C>T | upstream_gene_variant | 0.67 |
aftB | 4269006 | c.-170T>C | upstream_gene_variant | 0.67 |
aftB | 4269012 | c.-176G>C | upstream_gene_variant | 0.67 |
aftB | 4269027 | c.-191C>T | upstream_gene_variant | 0.67 |
aftB | 4269033 | c.-197T>C | upstream_gene_variant | 0.5 |
aftB | 4269036 | c.-200C>G | upstream_gene_variant | 0.5 |
aftB | 4269042 | c.-206G>C | upstream_gene_variant | 0.5 |
ubiA | 4269075 | p.Ile253Val | missense_variant | 0.4 |
aftB | 4269081 | c.-245G>C | upstream_gene_variant | 0.4 |
aftB | 4269084 | c.-248G>C | upstream_gene_variant | 0.5 |
ubiA | 4269271 | p.Val188Ala | missense_variant | 1.0 |
ethR | 4327396 | c.-153A>G | upstream_gene_variant | 0.5 |
ethA | 4327399 | p.Asp25Glu | missense_variant | 0.5 |
ethR | 4327423 | c.-126G>C | upstream_gene_variant | 0.67 |
ethR | 4327435 | c.-114T>G | upstream_gene_variant | 0.67 |
ethR | 4327438 | c.-111A>G | upstream_gene_variant | 0.67 |
ethA | 4327452 | p.Val8Leu | missense_variant | 0.67 |
ethR | 4327453 | c.-96A>G | upstream_gene_variant | 0.67 |
ethR | 4327459 | c.-90G>A | upstream_gene_variant | 1.0 |
ethA | 4328463 | c.-990G>C | upstream_gene_variant | 0.5 |
ethA | 4328467 | c.-994G>T | upstream_gene_variant | 0.5 |
ethA | 4328470 | c.-998_-997delAGinsGC | upstream_gene_variant | 0.5 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |