Run ID: SRR8692790
Sample name:
Date: 13-08-2023 19:09:12
Number of reads: NA
Percentage reads mapped: NA
Strain: lineage4
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761160 | p.Leu452Met | missense_variant | 0.13 | rifampicin |
rplC | 801268 | p.Cys154Arg | missense_variant | 0.64 | linezolid |
ethA | 4326426 | c.1047delT | frameshift_variant | 0.18 | ethionamide, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5270 | p.Glu11* | stop_gained | 0.2 |
gyrB | 5494 | c.255G>A | synonymous_variant | 0.18 |
gyrB | 5504 | p.His89Asn | missense_variant | 0.2 |
gyrB | 5533 | c.294G>A | synonymous_variant | 0.17 |
gyrB | 6057 | p.Ser273Ile | missense_variant | 0.14 |
gyrB | 6125 | p.Gly296Arg | missense_variant | 0.22 |
gyrB | 6160 | c.921C>A | synonymous_variant | 0.25 |
gyrA | 6331 | c.-971A>G | upstream_gene_variant | 0.12 |
gyrB | 6767 | p.Gly510Cys | missense_variant | 0.15 |
gyrA | 7240 | c.-62C>A | upstream_gene_variant | 0.22 |
gyrA | 7412 | c.111C>G | synonymous_variant | 0.29 |
gyrA | 7421 | c.120G>C | synonymous_variant | 0.29 |
gyrA | 7424 | c.123G>T | synonymous_variant | 0.29 |
gyrA | 7427 | c.126G>C | synonymous_variant | 0.33 |
gyrA | 7433 | c.132G>C | synonymous_variant | 0.33 |
gyrA | 7442 | c.141G>C | synonymous_variant | 0.33 |
gyrA | 7451 | c.150C>G | synonymous_variant | 0.33 |
gyrA | 7457 | c.156T>C | synonymous_variant | 0.33 |
gyrA | 7475 | c.174A>C | synonymous_variant | 0.33 |
gyrA | 7480 | p.Phe60Tyr | missense_variant | 0.33 |
gyrA | 7484 | c.183T>C | synonymous_variant | 0.4 |
gyrA | 7487 | c.186C>G | synonymous_variant | 0.4 |
gyrA | 7502 | c.201C>T | synonymous_variant | 0.33 |
gyrA | 7506 | p.Ser69Gly | missense_variant | 0.33 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 0.29 |
gyrA | 7595 | c.294C>G | synonymous_variant | 0.25 |
gyrA | 7607 | c.306C>G | synonymous_variant | 0.25 |
gyrA | 7631 | c.330G>C | synonymous_variant | 0.33 |
gyrA | 7637 | c.336C>T | synonymous_variant | 0.33 |
gyrA | 7658 | c.357A>G | synonymous_variant | 0.43 |
gyrA | 7661 | c.360C>T | synonymous_variant | 0.43 |
gyrA | 7664 | c.363T>C | synonymous_variant | 0.43 |
gyrA | 7670 | c.369A>G | synonymous_variant | 0.43 |
gyrA | 7676 | c.375G>C | synonymous_variant | 0.43 |
gyrA | 7679 | c.378G>C | synonymous_variant | 0.43 |
gyrA | 7683 | c.382_384delAGGinsCGC | synonymous_variant | 0.5 |
gyrA | 7694 | c.393A>G | synonymous_variant | 0.57 |
gyrA | 7700 | c.399G>T | synonymous_variant | 0.57 |
gyrA | 7706 | c.405C>T | synonymous_variant | 0.57 |
gyrA | 7709 | c.408G>A | synonymous_variant | 0.57 |
gyrA | 7710 | c.409T>C | synonymous_variant | 0.57 |
gyrA | 7715 | c.414G>C | synonymous_variant | 0.57 |
gyrA | 7728 | c.427_429delAGGinsCGT | synonymous_variant | 0.6 |
gyrA | 7752 | p.Asp151Asn | missense_variant | 0.71 |
gyrA | 7763 | c.462T>C | synonymous_variant | 0.62 |
gyrA | 7769 | c.468C>T | synonymous_variant | 0.56 |
gyrA | 7775 | c.474C>G | synonymous_variant | 0.5 |
gyrA | 7778 | c.477G>C | synonymous_variant | 0.5 |
gyrA | 7784 | c.483A>G | synonymous_variant | 0.44 |
gyrA | 7796 | c.495G>C | synonymous_variant | 0.4 |
gyrA | 7799 | c.498A>G | synonymous_variant | 0.33 |
gyrA | 7802 | c.501C>G | synonymous_variant | 0.33 |
gyrA | 7804 | p.Ser168Ile | missense_variant | 0.17 |
gyrA | 7814 | c.513C>G | synonymous_variant | 0.31 |
gyrA | 7832 | c.531G>T | synonymous_variant | 0.31 |
gyrA | 7835 | c.534A>G | synonymous_variant | 0.33 |
gyrA | 7841 | c.540C>T | synonymous_variant | 0.27 |
gyrA | 7853 | c.552C>T | synonymous_variant | 0.25 |
gyrA | 7859 | c.558A>C | synonymous_variant | 0.24 |
gyrA | 7865 | c.564T>C | synonymous_variant | 0.22 |
gyrA | 8020 | p.Thr240Asn | missense_variant | 0.2 |
gyrA | 8461 | p.Arg387Leu | missense_variant | 0.22 |
gyrA | 8627 | c.1326C>A | synonymous_variant | 0.12 |
gyrA | 9301 | p.Ala667Asp | missense_variant | 0.18 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 0.27 |
gyrA | 9325 | p.Ser675* | stop_gained | 0.15 |
gyrA | 9372 | p.Arg691Trp | missense_variant | 0.18 |
gyrA | 9502 | p.Arg734Leu | missense_variant | 0.15 |
fgd1 | 491164 | p.Arg128Trp | missense_variant | 0.33 |
fgd1 | 491693 | p.Gly304Val | missense_variant | 0.2 |
fgd1 | 491728 | p.Asp316Asn | missense_variant | 0.25 |
mshA | 575397 | p.Arg17His | missense_variant | 0.17 |
mshA | 575556 | p.Val70Ala | missense_variant | 0.17 |
mshA | 575864 | c.517T>C | synonymous_variant | 0.14 |
mshA | 575905 | c.558G>C | synonymous_variant | 0.12 |
mshA | 575908 | c.561A>C | synonymous_variant | 0.12 |
mshA | 575925 | p.Gly193Ala | missense_variant | 0.12 |
mshA | 575935 | c.588G>C | synonymous_variant | 0.12 |
mshA | 575936 | p.Pro197Ala | missense_variant | 0.12 |
mshA | 575945 | p.Thr200Ser | missense_variant | 0.13 |
mshA | 575953 | c.606G>T | synonymous_variant | 0.15 |
mshA | 575965 | c.618C>G | synonymous_variant | 0.14 |
mshA | 576256 | c.909C>A | synonymous_variant | 0.14 |
mshA | 576605 | p.Ala420Ser | missense_variant | 0.18 |
ccsA | 619781 | c.-110T>C | upstream_gene_variant | 0.15 |
ccsA | 619932 | c.42C>A | synonymous_variant | 0.27 |
ccsA | 620478 | p.Phe196Leu | missense_variant | 0.18 |
ccsA | 620541 | c.651G>T | synonymous_variant | 0.15 |
ccsA | 620557 | p.Gln223Lys | missense_variant | 0.14 |
ccsA | 620563 | p.Leu225Met | missense_variant | 0.15 |
ccsA | 620787 | c.897C>A | synonymous_variant | 0.2 |
rpoB | 760410 | p.Arg202Ser | missense_variant | 0.22 |
rpoB | 760424 | c.618C>A | synonymous_variant | 0.29 |
rpoB | 760541 | c.735G>C | synonymous_variant | 0.22 |
rpoB | 760547 | c.741G>C | synonymous_variant | 0.25 |
rpoB | 760561 | c.757_758delCG | frameshift_variant | 0.25 |
rpoB | 760567 | p.Ser254Trp | missense_variant | 0.25 |
rpoB | 760568 | c.762_763insGC | frameshift_variant | 0.25 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.25 |
rpoB | 760601 | c.795C>T | synonymous_variant | 0.33 |
rpoB | 760611 | c.805T>C | synonymous_variant | 0.3 |
rpoB | 760625 | c.819C>G | synonymous_variant | 0.23 |
rpoB | 760634 | c.828T>C | synonymous_variant | 0.23 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.19 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.2 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.17 |
rpoB | 760670 | c.864G>C | synonymous_variant | 0.12 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.12 |
rpoB | 760715 | c.909C>T | synonymous_variant | 0.12 |
rpoB | 760724 | c.918T>C | synonymous_variant | 0.13 |
rpoB | 760730 | c.924T>C | synonymous_variant | 0.13 |
rpoB | 760815 | p.Glu337* | stop_gained | 0.14 |
rpoB | 761061 | c.1257delC | frameshift_variant | 0.14 |
rpoB | 761171 | c.1365C>T | synonymous_variant | 0.15 |
rpoB | 761469 | p.Val555Phe | missense_variant | 0.13 |
rpoB | 761706 | p.Asp634Asn | missense_variant | 0.2 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.2 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.22 |
rpoC | 763034 | c.-336C>A | upstream_gene_variant | 0.22 |
rpoC | 763049 | c.-321G>A | upstream_gene_variant | 0.2 |
rpoC | 763053 | c.-317_-315delTTGinsCTC | upstream_gene_variant | 0.2 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.25 |
rpoC | 763076 | c.-294C>G | upstream_gene_variant | 0.27 |
rpoC | 763079 | c.-291C>G | upstream_gene_variant | 0.27 |
rpoC | 763082 | c.-288C>T | upstream_gene_variant | 0.3 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.3 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.3 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.3 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.23 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.27 |
rpoC | 763158 | c.-212C>T | upstream_gene_variant | 0.27 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.18 |
rpoC | 763169 | c.-201A>G | upstream_gene_variant | 0.18 |
rpoC | 763181 | c.-189G>C | upstream_gene_variant | 0.18 |
rpoC | 763187 | c.-183C>G | upstream_gene_variant | 0.18 |
rpoC | 763190 | c.-180C>T | upstream_gene_variant | 0.18 |
rpoC | 763274 | c.-96G>T | upstream_gene_variant | 0.22 |
rpoC | 763378 | p.Asp3Glu | missense_variant | 0.25 |
rpoC | 763461 | p.Pro31Leu | missense_variant | 0.14 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.18 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.13 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.17 |
rpoC | 764102 | p.Val245Ile | missense_variant | 0.2 |
rpoC | 764549 | p.Pro394Thr | missense_variant | 0.29 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.12 |
rpoC | 764719 | c.1350G>A | synonymous_variant | 0.15 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.22 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.24 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.24 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.24 |
rpoC | 764800 | c.1431G>A | synonymous_variant | 0.18 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.18 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.18 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.25 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.33 |
rpoC | 765271 | p.Lys634Asn | missense_variant | 0.13 |
rpoC | 765754 | p.Asp795Glu | missense_variant | 0.4 |
rpoC | 765772 | c.2403C>G | synonymous_variant | 0.4 |
rpoC | 765778 | c.2409C>G | synonymous_variant | 0.4 |
rpoC | 765779 | p.Asp804Lys | missense_variant | 0.4 |
rpoC | 765800 | p.Phe811Leu | missense_variant | 0.38 |
rpoC | 765811 | c.2442T>C | synonymous_variant | 0.38 |
rpoC | 765814 | c.2445A>C | synonymous_variant | 0.38 |
rpoC | 765820 | c.2451G>C | synonymous_variant | 0.38 |
rpoC | 765823 | c.2454C>G | synonymous_variant | 0.33 |
rpoC | 765826 | c.2457T>C | synonymous_variant | 0.3 |
rpoC | 765834 | p.Gly822Asp | missense_variant | 0.18 |
rpoC | 765861 | p.Phe831Tyr | missense_variant | 0.33 |
rpoC | 765875 | p.Val836Ile | missense_variant | 0.42 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.38 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.38 |
rpoC | 765898 | c.2529C>T | synonymous_variant | 0.33 |
rpoC | 765934 | c.2565C>T | synonymous_variant | 0.13 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.13 |
rpoC | 765940 | c.2571A>T | synonymous_variant | 0.14 |
rpoC | 765946 | c.2577C>T | synonymous_variant | 0.14 |
rpoC | 765947 | c.2578T>C | synonymous_variant | 0.14 |
rpoC | 765952 | c.2583G>C | synonymous_variant | 0.14 |
rpoC | 765962 | c.2593T>C | synonymous_variant | 0.14 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.14 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.18 |
rpoC | 767002 | c.3633G>C | synonymous_variant | 0.18 |
rpoC | 767014 | c.3645G>C | synonymous_variant | 0.18 |
rpoC | 767023 | c.3654C>T | synonymous_variant | 0.21 |
rpoC | 767035 | c.3666G>C | synonymous_variant | 0.21 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.24 |
rpoC | 767104 | c.3735C>G | synonymous_variant | 0.27 |
rpoC | 767106 | p.Asn1246Met | missense_variant | 0.27 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.25 |
rpoC | 767151 | p.Gly1261Val | missense_variant | 0.17 |
rpoC | 767155 | c.3786C>G | synonymous_variant | 0.17 |
rpoC | 767162 | p.Asn1265Ala | missense_variant | 0.15 |
mmpL5 | 775847 | c.2634G>T | synonymous_variant | 0.17 |
mmpL5 | 775851 | p.Ser877Thr | missense_variant | 0.17 |
mmpL5 | 775856 | c.2625T>C | synonymous_variant | 0.23 |
mmpL5 | 775862 | c.2619G>C | synonymous_variant | 0.15 |
mmpL5 | 775865 | c.2616T>C | synonymous_variant | 0.15 |
mmpL5 | 775885 | p.Ile866Leu | missense_variant | 0.14 |
mmpL5 | 775886 | c.2595A>T | synonymous_variant | 0.14 |
mmpL5 | 775889 | c.2592C>G | synonymous_variant | 0.13 |
mmpL5 | 775909 | p.Leu858Ile | missense_variant | 0.14 |
mmpL5 | 775916 | c.2565T>C | synonymous_variant | 0.14 |
mmpL5 | 775949 | c.2532G>C | synonymous_variant | 0.11 |
mmpL5 | 775955 | p.Ile842Met | missense_variant | 0.12 |
mmpL5 | 775961 | c.2520C>G | synonymous_variant | 0.12 |
mmpL5 | 775981 | p.Leu834Met | missense_variant | 0.13 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.15 |
mmpL5 | 776830 | p.His551Asn | missense_variant | 0.15 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 0.29 |
rpsL | 781506 | c.-54C>T | upstream_gene_variant | 0.2 |
rpsL | 781644 | p.Gln29Lys | missense_variant | 0.17 |
rpsL | 781682 | c.123T>C | synonymous_variant | 0.13 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.12 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.12 |
rpsL | 781736 | p.Ser59Arg | missense_variant | 0.12 |
rpsL | 781737 | p.Gln60Gly | missense_variant | 0.12 |
rpsL | 781742 | c.183C>T | synonymous_variant | 0.14 |
rpsL | 781751 | c.192G>C | synonymous_variant | 0.13 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.13 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.14 |
rpsL | 781769 | c.210G>A | synonymous_variant | 0.14 |
rpsL | 781805 | c.246G>C | synonymous_variant | 0.21 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.21 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.21 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.2 |
rpsL | 781829 | c.270G>C | synonymous_variant | 0.14 |
rpsL | 781832 | c.273T>G | synonymous_variant | 0.13 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.13 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.13 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.13 |
rpsL | 781874 | p.Gln105His | missense_variant | 0.13 |
rpsL | 781875 | p.Gly106Cys | missense_variant | 0.13 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.11 |
rpsL | 781916 | c.357T>G | synonymous_variant | 0.12 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.18 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.15 |
rplC | 800633 | c.-176T>C | upstream_gene_variant | 0.17 |
rplC | 800639 | c.-170C>T | upstream_gene_variant | 0.18 |
rplC | 800655 | c.-154A>G | upstream_gene_variant | 0.18 |
rplC | 801150 | c.342G>T | synonymous_variant | 0.17 |
fbiC | 1303277 | p.Ala116Asp | missense_variant | 0.17 |
fbiC | 1303703 | p.Gly258Asp | missense_variant | 0.2 |
fbiC | 1304695 | p.Trp589Arg | missense_variant | 0.18 |
fbiC | 1304789 | p.Ala620Asp | missense_variant | 0.15 |
Rv1258c | 1406500 | p.Leu281Met | missense_variant | 0.17 |
Rv1258c | 1406686 | p.Val219Ile | missense_variant | 0.92 |
Rv1258c | 1406832 | p.Gly170Val | missense_variant | 0.22 |
Rv1258c | 1407134 | p.Phe69Leu | missense_variant | 0.33 |
embR | 1416249 | p.Asp367Tyr | missense_variant | 0.17 |
embR | 1416533 | p.Gly272Val | missense_variant | 0.15 |
embR | 1416577 | c.771G>A | synonymous_variant | 0.22 |
embR | 1416907 | c.441G>T | synonymous_variant | 0.18 |
embR | 1417259 | p.Ser30* | stop_gained | 0.17 |
rrs | 1471653 | n.-193C>A | upstream_gene_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471674 | n.-172G>A | upstream_gene_variant | 0.15 |
rrs | 1471704 | n.-142C>A | upstream_gene_variant | 0.15 |
rrs | 1471773 | n.-73G>T | upstream_gene_variant | 0.2 |
rrs | 1471866 | n.21C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1471922 | n.78delT | non_coding_transcript_exon_variant | 0.55 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1471931 | n.87delA | non_coding_transcript_exon_variant | 0.6 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.55 |
rrs | 1471979 | n.134T>C | non_coding_transcript_exon_variant | 0.7 |
rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472019 | n.174G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472023 | n.178G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472029 | n.184C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472030 | n.185G>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472033 | n.188A>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472035 | n.190G>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472040 | n.195T>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472043 | n.198T>G | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472176 | n.331G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472317 | n.472G>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472360 | n.515G>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472847 | n.1002G>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472849 | n.1004C>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472850 | n.1005T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472857 | n.1012A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472858 | n.1013G>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472859 | n.1014G>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472860 | n.1015C>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.42 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473814 | n.157A>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473815 | n.158T>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473816 | n.159C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473828 | n.171G>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473829 | n.172G>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473830 | n.173T>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473831 | n.174G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473869 | n.212C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473887 | n.230T>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473888 | n.231T>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473908 | n.251C>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473994 | n.337C>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474135 | n.478G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474185 | n.528G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474498 | n.841G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474505 | n.848C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474552 | n.895C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474694 | n.1037C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474708 | n.1051C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475158 | n.1501C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475187 | n.1530C>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475363 | n.1706C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475369 | n.1712G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475380 | n.1723C>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475381 | n.1724G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475382 | n.1725A>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475395 | n.1738T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475396 | n.1739C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475397 | n.1740G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475402 | n.1745C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475460 | n.1803A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475479 | n.1822C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475544 | n.1887A>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475634 | n.1977G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475759 | n.2102C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475764 | n.2107A>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475775 | n.2118G>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475991 | n.2334T>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475995 | n.2338G>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476056 | n.2399G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476088 | n.2431A>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476095 | n.2438C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476188 | n.2531C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476251 | n.2594T>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476317 | n.2660C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476518 | n.2861G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476529 | n.2872A>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476563 | n.2906G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476583 | n.2926G>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.22 |
fabG1 | 1673910 | p.Lys157Asn | missense_variant | 0.33 |
inhA | 1674620 | p.Pro140His | missense_variant | 0.22 |
inhA | 1674771 | c.570C>G | synonymous_variant | 0.12 |
inhA | 1674774 | c.573A>G | synonymous_variant | 0.19 |
inhA | 1674780 | c.579T>G | synonymous_variant | 0.19 |
inhA | 1674789 | c.588G>C | synonymous_variant | 0.18 |
inhA | 1674795 | c.594G>C | synonymous_variant | 0.24 |
inhA | 1674801 | c.600T>C | synonymous_variant | 0.25 |
inhA | 1674804 | c.603G>C | synonymous_variant | 0.25 |
inhA | 1674810 | c.609C>G | synonymous_variant | 0.27 |
inhA | 1674822 | c.621C>G | synonymous_variant | 0.25 |
inhA | 1674827 | p.Glu209Ala | missense_variant | 0.25 |
inhA | 1674839 | p.Ala213Asp | missense_variant | 0.31 |
inhA | 1674846 | p.Ile215Met | missense_variant | 0.36 |
inhA | 1674848 | p.Gln216Arg | missense_variant | 0.36 |
inhA | 1674858 | c.657G>A | synonymous_variant | 0.4 |
inhA | 1674866 | p.Trp222* | stop_gained | 0.22 |
inhA | 1674879 | c.678T>A | synonymous_variant | 0.44 |
inhA | 1674883 | p.Ile228Val | missense_variant | 0.44 |
inhA | 1674904 | p.Ala235Pro | missense_variant | 0.33 |
inhA | 1674909 | c.708G>C | synonymous_variant | 0.25 |
inhA | 1674915 | c.714C>G | synonymous_variant | 0.33 |
inhA | 1674930 | c.729C>T | synonymous_variant | 0.29 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.14 |
rpsA | 1833760 | c.219C>T | synonymous_variant | 0.14 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.15 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.14 |
rpsA | 1833793 | c.252C>T | synonymous_variant | 0.14 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.14 |
rpsA | 1833808 | c.267G>C | synonymous_variant | 0.14 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 0.14 |
rpsA | 1833829 | c.288A>G | synonymous_variant | 0.15 |
rpsA | 1833832 | c.291G>A | synonymous_variant | 0.15 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.16 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.15 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.15 |
rpsA | 1834090 | c.549G>T | synonymous_variant | 0.18 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.13 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.13 |
rpsA | 1834279 | c.738C>T | synonymous_variant | 0.12 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.12 |
rpsA | 1834299 | p.Gln253Pro | missense_variant | 0.12 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.12 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.12 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.16 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.15 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.15 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.15 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.17 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.14 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.13 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.12 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.18 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.19 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.2 |
rpsA | 1834475 | p.Arg312Ser | missense_variant | 0.17 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.14 |
rpsA | 1834666 | c.1125G>C | synonymous_variant | 0.15 |
rpsA | 1834667 | p.Ala376Ser | missense_variant | 0.15 |
rpsA | 1834690 | c.1149T>C | synonymous_variant | 0.14 |
rpsA | 1834700 | p.Gln387Ala | missense_variant | 0.17 |
rpsA | 1834705 | c.1164C>G | synonymous_variant | 0.18 |
rpsA | 1834732 | c.1191T>C | synonymous_variant | 0.2 |
rpsA | 1834738 | p.Glu399Asp | missense_variant | 0.25 |
rpsA | 1834753 | c.1212T>C | synonymous_variant | 0.29 |
rpsA | 1834759 | c.1218A>C | synonymous_variant | 0.33 |
rpsA | 1834765 | p.Glu408Asp | missense_variant | 0.33 |
tlyA | 1917823 | c.-117C>A | upstream_gene_variant | 0.17 |
tlyA | 1917955 | p.Arg6Ser | missense_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 0.3 |
tlyA | 1917985 | p.Leu16Met | missense_variant | 0.18 |
tlyA | 1918431 | p.Leu164Phe | missense_variant | 0.33 |
tlyA | 1918455 | c.516G>T | synonymous_variant | 0.25 |
tlyA | 1918479 | c.540G>T | synonymous_variant | 0.25 |
ndh | 2101976 | p.Pro356Gln | missense_variant | 0.29 |
ndh | 2102052 | p.Gly331Cys | missense_variant | 0.13 |
ndh | 2102469 | p.Leu192Met | missense_variant | 0.25 |
ndh | 2102564 | p.Arg160Leu | missense_variant | 0.13 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.15 |
katG | 2154864 | c.1248C>A | synonymous_variant | 0.22 |
katG | 2155706 | p.Pro136Ala | missense_variant | 0.13 |
katG | 2155716 | c.396T>C | synonymous_variant | 0.14 |
katG | 2155722 | c.390G>T | synonymous_variant | 0.14 |
katG | 2155728 | c.384G>C | synonymous_variant | 0.14 |
katG | 2155964 | p.Gln50Lys | missense_variant | 0.33 |
PPE35 | 2168560 | p.Ala685Ser | missense_variant | 0.18 |
PPE35 | 2168562 | p.Pro684His | missense_variant | 0.18 |
PPE35 | 2168679 | p.Ser645Ile | missense_variant | 0.14 |
Rv1979c | 2221758 | c.1407A>G | synonymous_variant | 0.18 |
Rv1979c | 2221977 | p.Leu396Phe | missense_variant | 0.15 |
Rv1979c | 2222021 | c.1144C>A | synonymous_variant | 0.2 |
Rv1979c | 2222086 | p.Ala360Glu | missense_variant | 0.18 |
Rv1979c | 2222318 | p.Ala283Ser | missense_variant | 0.2 |
Rv1979c | 2222337 | c.828G>T | synonymous_variant | 0.17 |
Rv1979c | 2222340 | p.Met275Ile | missense_variant | 0.17 |
Rv1979c | 2223056 | p.Gly37Cys | missense_variant | 0.2 |
Rv1979c | 2223213 | c.-49G>T | upstream_gene_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 0.2 |
Rv1979c | 2223321 | c.-157G>T | upstream_gene_variant | 0.2 |
pncA | 2288894 | c.348G>T | synonymous_variant | 0.17 |
pncA | 2289135 | p.Ala36Asp | missense_variant | 0.13 |
pncA | 2289156 | p.Arg29His | missense_variant | 0.14 |
pncA | 2289735 | c.-494C>A | upstream_gene_variant | 0.29 |
kasA | 2517941 | c.-174C>G | upstream_gene_variant | 0.17 |
kasA | 2517950 | c.-165C>G | upstream_gene_variant | 0.17 |
kasA | 2517962 | c.-153C>G | upstream_gene_variant | 0.15 |
kasA | 2517968 | c.-147T>C | upstream_gene_variant | 0.16 |
kasA | 2517974 | c.-141T>C | upstream_gene_variant | 0.16 |
kasA | 2518318 | c.204C>A | synonymous_variant | 0.29 |
eis | 2714221 | p.Ala371Asp | missense_variant | 0.17 |
eis | 2714230 | p.Thr368Lys | missense_variant | 0.15 |
folC | 2746299 | p.Glu434* | stop_gained | 0.17 |
folC | 2746328 | p.Arg424Leu | missense_variant | 0.15 |
folC | 2746749 | p.Gly284Trp | missense_variant | 0.25 |
folC | 2746807 | c.792G>T | synonymous_variant | 0.18 |
folC | 2746842 | p.Asp253Tyr | missense_variant | 0.25 |
folC | 2746892 | p.Arg236Leu | missense_variant | 0.29 |
folC | 2747026 | c.573C>A | synonymous_variant | 0.2 |
folC | 2747065 | c.534C>A | synonymous_variant | 0.22 |
folC | 2747080 | c.519C>A | synonymous_variant | 0.17 |
pepQ | 2859568 | p.Ala284Asp | missense_variant | 0.29 |
pepQ | 2859827 | p.Ala198Thr | missense_variant | 0.2 |
ribD | 2987401 | p.Arg188Leu | missense_variant | 0.14 |
Rv2752c | 3064991 | c.1201C>A | synonymous_variant | 0.13 |
Rv2752c | 3065004 | c.1188G>T | synonymous_variant | 0.13 |
Rv2752c | 3065551 | p.Ser214* | stop_gained | 0.2 |
Rv2752c | 3065979 | c.213T>C | synonymous_variant | 0.18 |
Rv2752c | 3065982 | c.210G>C | synonymous_variant | 0.18 |
Rv2752c | 3065987 | p.Asp69Asn | missense_variant | 0.18 |
Rv2752c | 3065988 | c.204A>G | synonymous_variant | 0.18 |
Rv2752c | 3065993 | p.Val67Ile | missense_variant | 0.18 |
Rv2752c | 3065997 | c.195C>G | synonymous_variant | 0.18 |
Rv2752c | 3066002 | p.Met64Leu | missense_variant | 0.18 |
Rv2752c | 3066006 | c.186G>C | synonymous_variant | 0.17 |
Rv2752c | 3066018 | c.174T>C | synonymous_variant | 0.17 |
Rv2752c | 3066021 | c.171C>G | synonymous_variant | 0.17 |
Rv2752c | 3066024 | c.168T>G | synonymous_variant | 0.17 |
Rv2752c | 3066039 | c.153C>T | synonymous_variant | 0.18 |
Rv2752c | 3066042 | c.150T>C | synonymous_variant | 0.17 |
Rv2752c | 3066045 | c.147T>C | synonymous_variant | 0.15 |
Rv2752c | 3066054 | c.138T>G | synonymous_variant | 0.17 |
Rv2752c | 3066066 | c.126T>C | synonymous_variant | 0.17 |
Rv2752c | 3066069 | c.121_123delTTGinsCTC | synonymous_variant | 0.15 |
Rv2752c | 3066312 | c.-121C>A | upstream_gene_variant | 0.14 |
Rv2752c | 3067019 | c.-828C>A | upstream_gene_variant | 0.29 |
Rv2752c | 3067157 | c.-966G>T | upstream_gene_variant | 0.29 |
thyX | 3067901 | c.45C>A | synonymous_variant | 0.17 |
thyX | 3067989 | c.-44C>A | upstream_gene_variant | 0.18 |
thyA | 3073929 | c.543T>C | synonymous_variant | 0.13 |
thyA | 3073947 | c.525G>C | synonymous_variant | 0.14 |
thyA | 3073953 | c.519T>C | synonymous_variant | 0.14 |
thyA | 3073956 | c.516G>C | synonymous_variant | 0.14 |
thyA | 3073959 | c.513T>C | synonymous_variant | 0.14 |
thyA | 3073968 | c.504C>G | synonymous_variant | 0.18 |
thyA | 3073977 | c.495A>G | synonymous_variant | 0.2 |
thyA | 3073983 | c.489C>G | synonymous_variant | 0.2 |
thyA | 3073989 | c.483T>C | synonymous_variant | 0.18 |
thyA | 3073993 | c.478_479delAGinsTC | synonymous_variant | 0.18 |
thyA | 3073999 | p.Arg158Lys | missense_variant | 0.29 |
thyA | 3074004 | c.468T>C | synonymous_variant | 0.25 |
thyA | 3074031 | c.441T>C | synonymous_variant | 0.22 |
thyA | 3074034 | c.438T>C | synonymous_variant | 0.25 |
thyA | 3074037 | c.435C>G | synonymous_variant | 0.25 |
thyA | 3074046 | c.426G>C | synonymous_variant | 0.2 |
thyA | 3074053 | p.Arg140Gln | missense_variant | 0.2 |
thyA | 3074056 | p.Glu139Pro | missense_variant | 0.2 |
thyA | 3074061 | c.411A>G | synonymous_variant | 0.2 |
thyA | 3074064 | c.408C>T | synonymous_variant | 0.2 |
thyA | 3074316 | p.Phe52Leu | missense_variant | 0.14 |
thyA | 3074322 | c.150C>A | synonymous_variant | 0.14 |
thyA | 3074378 | p.Gln32Lys | missense_variant | 0.15 |
ald | 3086712 | c.-108C>A | upstream_gene_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.18 |
ald | 3086812 | c.-8G>T | upstream_gene_variant | 0.25 |
ald | 3087542 | c.723G>A | synonymous_variant | 0.22 |
ald | 3087577 | p.Ser253* | stop_gained | 0.29 |
ald | 3087698 | c.879G>T | synonymous_variant | 0.2 |
fbiD | 3339014 | c.-104C>A | upstream_gene_variant | 0.17 |
fbiD | 3339029 | c.-89C>A | upstream_gene_variant | 0.18 |
fbiD | 3339051 | c.-67C>A | upstream_gene_variant | 0.22 |
fbiD | 3339088 | c.-30C>A | upstream_gene_variant | 0.2 |
fbiD | 3339472 | p.Ala119Ser | missense_variant | 0.17 |
fbiD | 3339480 | p.Gln121His | missense_variant | 0.2 |
fbiD | 3339488 | p.Glu124Gly | missense_variant | 0.25 |
fbiD | 3339692 | p.Pro192His | missense_variant | 0.18 |
fbiD | 3339754 | p.His213Asn | missense_variant | 0.22 |
Rv3083 | 3448458 | c.-46C>A | upstream_gene_variant | 0.33 |
Rv3083 | 3449009 | p.Trp169Leu | missense_variant | 0.18 |
fprA | 3473854 | c.-153G>T | upstream_gene_variant | 0.13 |
fprA | 3474283 | p.Leu93Ile | missense_variant | 0.15 |
fprA | 3474427 | p.Val141Ile | missense_variant | 0.18 |
fprA | 3474466 | p.Gly154Cys | missense_variant | 0.13 |
fprA | 3475078 | p.Gly358Trp | missense_variant | 0.13 |
fprA | 3475143 | c.1137C>A | synonymous_variant | 0.17 |
fprA | 3475295 | p.Glu430Val | missense_variant | 0.15 |
fprA | 3475329 | c.1323G>T | synonymous_variant | 0.2 |
whiB7 | 3568556 | p.Leu42Met | missense_variant | 0.15 |
Rv3236c | 3611959 | c.1158G>T | stop_lost&splice_region_variant | 0.15 |
Rv3236c | 3612169 | p.Glu316Asp | missense_variant | 0.14 |
Rv3236c | 3612727 | c.390G>T | synonymous_variant | 0.18 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 0.2 |
Rv3236c | 3613251 | c.-135C>T | upstream_gene_variant | 0.13 |
fbiB | 3640656 | c.-879C>T | upstream_gene_variant | 0.25 |
fbiA | 3641044 | p.His168Asn | missense_variant | 0.25 |
fbiA | 3641333 | p.Gly264Val | missense_variant | 0.15 |
fbiB | 3642138 | p.Ala202Thr | missense_variant | 0.25 |
fbiB | 3642806 | c.1272C>A | synonymous_variant | 0.2 |
alr | 3840248 | c.1173C>T | synonymous_variant | 0.22 |
alr | 3840350 | c.1071G>A | synonymous_variant | 0.4 |
alr | 3841128 | p.Leu98Pro | missense_variant | 0.29 |
alr | 3841310 | p.Glu37Asp | missense_variant | 0.22 |
alr | 3841517 | c.-97G>T | upstream_gene_variant | 0.2 |
alr | 3841545 | c.-125G>T | upstream_gene_variant | 0.2 |
rpoA | 3877833 | c.675C>A | synonymous_variant | 0.17 |
rpoA | 3878147 | p.Pro121Thr | missense_variant | 0.22 |
rpoA | 3878487 | c.21C>A | synonymous_variant | 0.29 |
ddn | 3986645 | c.-199G>A | upstream_gene_variant | 0.25 |
ddn | 3986648 | c.-196C>G | upstream_gene_variant | 0.25 |
ddn | 3986659 | c.-185A>G | upstream_gene_variant | 0.29 |
ddn | 3986661 | c.-183C>A | upstream_gene_variant | 0.29 |
ddn | 3986667 | c.-177_-176delCTinsAC | upstream_gene_variant | 0.29 |
ddn | 3986696 | c.-148G>C | upstream_gene_variant | 0.22 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.15 |
clpC1 | 4038605 | c.2100G>A | synonymous_variant | 0.19 |
clpC1 | 4038613 | p.Asn698His | missense_variant | 0.19 |
clpC1 | 4038614 | c.2091C>T | synonymous_variant | 0.19 |
clpC1 | 4038620 | p.Gln695Leu | missense_variant | 0.2 |
clpC1 | 4038623 | c.2082A>G | synonymous_variant | 0.2 |
clpC1 | 4038640 | p.Asp689Asn | missense_variant | 0.28 |
clpC1 | 4038647 | c.2058T>C | synonymous_variant | 0.25 |
clpC1 | 4038650 | c.2055C>T | synonymous_variant | 0.25 |
clpC1 | 4038658 | p.Lys683Gln | missense_variant | 0.24 |
clpC1 | 4038661 | p.Ser682Thr | missense_variant | 0.23 |
clpC1 | 4038662 | c.2043T>C | synonymous_variant | 0.24 |
clpC1 | 4038671 | c.2034T>G | synonymous_variant | 0.26 |
clpC1 | 4038677 | p.Pro676Ala | missense_variant | 0.29 |
clpC1 | 4038683 | c.2022T>C | synonymous_variant | 0.31 |
clpC1 | 4038704 | c.2001T>C | synonymous_variant | 0.25 |
clpC1 | 4038707 | c.1998C>G | synonymous_variant | 0.25 |
clpC1 | 4038710 | c.1995G>C | synonymous_variant | 0.25 |
clpC1 | 4038713 | c.1992T>C | synonymous_variant | 0.25 |
clpC1 | 4038755 | c.1950G>C | synonymous_variant | 0.17 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.15 |
clpC1 | 4038779 | c.1926C>G | synonymous_variant | 0.15 |
clpC1 | 4038899 | c.1806C>A | synonymous_variant | 0.25 |
clpC1 | 4039028 | p.Lys559Asn | missense_variant | 0.22 |
clpC1 | 4039118 | c.1587C>G | synonymous_variant | 0.15 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.15 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.15 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.15 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.22 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.22 |
clpC1 | 4039187 | c.1518G>C | synonymous_variant | 0.18 |
clpC1 | 4039440 | p.Arg422Leu | missense_variant | 0.18 |
clpC1 | 4039718 | c.987C>G | synonymous_variant | 0.12 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.15 |
clpC1 | 4039733 | c.972G>C | synonymous_variant | 0.15 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.17 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.17 |
clpC1 | 4039760 | c.945T>C | synonymous_variant | 0.16 |
clpC1 | 4039766 | c.939T>C | synonymous_variant | 0.16 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.17 |
clpC1 | 4039775 | c.930G>C | synonymous_variant | 0.17 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.17 |
clpC1 | 4039787 | c.916_918delTCGinsAGC | synonymous_variant | 0.16 |
clpC1 | 4039817 | c.888A>T | synonymous_variant | 0.17 |
clpC1 | 4039820 | c.885T>C | synonymous_variant | 0.18 |
clpC1 | 4039823 | c.882T>A | synonymous_variant | 0.18 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 0.2 |
clpC1 | 4039832 | c.873C>G | synonymous_variant | 0.2 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.13 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.24 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.17 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.22 |
clpC1 | 4039934 | c.771G>C | synonymous_variant | 0.25 |
clpC1 | 4039937 | c.768G>C | synonymous_variant | 0.27 |
clpC1 | 4039946 | c.759A>C | synonymous_variant | 0.22 |
clpC1 | 4039949 | c.756G>C | synonymous_variant | 0.21 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.2 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.22 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 0.24 |
clpC1 | 4040015 | c.690G>C | synonymous_variant | 0.19 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.2 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.21 |
clpC1 | 4040030 | c.675C>G | synonymous_variant | 0.2 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.2 |
clpC1 | 4040042 | c.663C>T | synonymous_variant | 0.16 |
clpC1 | 4040087 | c.618G>C | synonymous_variant | 0.12 |
clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 0.12 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.27 |
clpC1 | 4040147 | c.558A>G | synonymous_variant | 0.25 |
clpC1 | 4040153 | c.552A>G | synonymous_variant | 0.23 |
clpC1 | 4040159 | c.546G>C | synonymous_variant | 0.23 |
clpC1 | 4040162 | c.543G>C | synonymous_variant | 0.23 |
clpC1 | 4040165 | c.540G>C | synonymous_variant | 0.23 |
clpC1 | 4040168 | c.537G>C | synonymous_variant | 0.25 |
clpC1 | 4040195 | c.510G>C | synonymous_variant | 0.3 |
clpC1 | 4040200 | c.505T>C | synonymous_variant | 0.3 |
clpC1 | 4040201 | c.504C>A | synonymous_variant | 0.3 |
clpC1 | 4040204 | c.501G>C | synonymous_variant | 0.3 |
clpC1 | 4040207 | c.498T>G | synonymous_variant | 0.3 |
clpC1 | 4040213 | p.Ser164Asn | missense_variant | 0.33 |
clpC1 | 4040228 | c.477G>C | synonymous_variant | 0.33 |
clpC1 | 4040237 | c.468C>T | synonymous_variant | 0.25 |
clpC1 | 4040246 | c.459C>A | synonymous_variant | 0.25 |
clpC1 | 4040458 | p.Arg83Ser | missense_variant | 0.13 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 0.17 |
clpC1 | 4040531 | c.174T>C | synonymous_variant | 0.21 |
clpC1 | 4040537 | c.168G>C | synonymous_variant | 0.21 |
clpC1 | 4040540 | c.165G>C | synonymous_variant | 0.21 |
clpC1 | 4040551 | c.154T>C | synonymous_variant | 0.27 |
clpC1 | 4040558 | c.147G>C | synonymous_variant | 0.29 |
clpC1 | 4040561 | c.144A>G | synonymous_variant | 0.27 |
clpC1 | 4040573 | c.132T>C | synonymous_variant | 0.29 |
clpC1 | 4040579 | c.126A>G | synonymous_variant | 0.27 |
clpC1 | 4040582 | c.123G>C | synonymous_variant | 0.27 |
clpC1 | 4040585 | c.120A>G | synonymous_variant | 0.27 |
clpC1 | 4040588 | c.117T>C | synonymous_variant | 0.25 |
clpC1 | 4040594 | c.111G>C | synonymous_variant | 0.25 |
clpC1 | 4040600 | c.103_105delTTAinsCTC | synonymous_variant | 0.22 |
clpC1 | 4040603 | c.102T>G | synonymous_variant | 0.22 |
clpC1 | 4040606 | c.99T>C | synonymous_variant | 0.21 |
clpC1 | 4040644 | c.61A>C | synonymous_variant | 0.22 |
clpC1 | 4040648 | c.57G>A | synonymous_variant | 0.24 |
panD | 4044207 | c.75G>T | synonymous_variant | 0.22 |
embC | 4240386 | p.Pro175His | missense_variant | 0.14 |
embC | 4241017 | c.1155T>C | synonymous_variant | 0.17 |
embC | 4241023 | c.1161T>G | synonymous_variant | 0.17 |
embC | 4241024 | p.Val388Phe | missense_variant | 0.17 |
embC | 4241035 | c.1173G>C | synonymous_variant | 0.16 |
embC | 4241039 | p.Asp393Asn | missense_variant | 0.16 |
embC | 4241050 | c.1188T>G | synonymous_variant | 0.17 |
embC | 4241056 | c.1194C>G | synonymous_variant | 0.18 |
embC | 4241072 | p.Leu404Val | missense_variant | 0.11 |
embC | 4241107 | c.1245G>C | synonymous_variant | 0.13 |
embC | 4241109 | p.Ala416Gly | missense_variant | 0.13 |
embC | 4241116 | c.1254C>G | synonymous_variant | 0.15 |
embC | 4241634 | p.Gly591Val | missense_variant | 0.17 |
embC | 4241729 | p.Ala623Thr | missense_variant | 0.2 |
embC | 4242492 | p.Arg877Leu | missense_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 0.17 |
embC | 4242962 | p.Gly1034Ser | missense_variant | 0.4 |
embA | 4243182 | c.-51G>T | upstream_gene_variant | 0.4 |
embA | 4244055 | p.Gly275Cys | missense_variant | 0.22 |
embA | 4244073 | p.Ala281Ser | missense_variant | 0.22 |
embA | 4244397 | p.Val389Leu | missense_variant | 0.25 |
embA | 4245387 | p.Ala719Ser | missense_variant | 0.18 |
embA | 4245558 | p.Gly776Arg | missense_variant | 0.22 |
embA | 4245820 | p.Ser863Thr | missense_variant | 0.14 |
embA | 4245840 | p.Val870Thr | missense_variant | 0.13 |
embB | 4245845 | c.-669T>C | upstream_gene_variant | 0.13 |
embA | 4245846 | p.Ser872Ala | missense_variant | 0.12 |
embB | 4245854 | c.-660C>G | upstream_gene_variant | 0.13 |
embA | 4245868 | p.Ser879Phe | missense_variant | 0.14 |
embA | 4245873 | p.Lys881Glu | missense_variant | 0.15 |
embA | 4245892 | p.Ile887Asn | missense_variant | 0.12 |
embB | 4245905 | c.-609C>G | upstream_gene_variant | 0.12 |
embB | 4246788 | p.Pro92Gln | missense_variant | 0.14 |
embB | 4247299 | c.786G>A | synonymous_variant | 0.2 |
embB | 4247758 | c.1245C>A | synonymous_variant | 0.22 |
embB | 4248553 | c.2040C>A | synonymous_variant | 0.25 |
embB | 4248660 | p.Ala716Glu | missense_variant | 0.12 |
embB | 4249484 | p.Gly991Cys | missense_variant | 0.22 |
embB | 4249507 | p.Gln998His | missense_variant | 0.22 |
aftB | 4267070 | c.1767C>A | synonymous_variant | 0.15 |
aftB | 4267215 | p.Gly541Val | missense_variant | 0.22 |
aftB | 4267628 | c.1209C>A | synonymous_variant | 0.15 |
aftB | 4268314 | c.523T>C | synonymous_variant | 0.12 |
aftB | 4268683 | p.Gly52Cys | missense_variant | 0.12 |
ubiA | 4269019 | p.Gly272Val | missense_variant | 0.2 |
ubiA | 4269974 | c.-141C>A | upstream_gene_variant | 0.18 |
ubiA | 4269982 | c.-149T>C | upstream_gene_variant | 0.18 |
ethA | 4326064 | c.1410C>A | synonymous_variant | 0.17 |
ethA | 4326175 | p.Glu433Asp | missense_variant | 0.29 |
ethA | 4326422 | p.Gly351Val | missense_variant | 0.18 |
ethA | 4326750 | p.Asn242Asp | missense_variant | 0.2 |
ethA | 4327013 | p.Ser154* | stop_gained | 0.17 |
ethA | 4327031 | p.Ser148* | stop_gained | 0.18 |
ethR | 4327865 | p.Gly106Val | missense_variant | 0.2 |
gid | 4407780 | c.423G>A | synonymous_variant | 0.33 |
gid | 4408356 | c.-154G>T | upstream_gene_variant | 0.15 |