Run ID: ERR4814396
Sample name:
Date: 01-04-2023 13:16:27
Number of reads: 4510221
Percentage reads mapped: 86.83
Strain: lineage4.1.1.3
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.1 | Euro-American (X-type) | X1;X2;X3 | None | 1.0 |
lineage4.1.1.3 | Euro-American (X-type) | X1;X3 | RD193 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6655 | c.-647T>C | upstream_gene_variant | 0.1 |
gyrA | 6673 | c.-629A>C | upstream_gene_variant | 0.14 |
gyrA | 6676 | c.-626T>G | upstream_gene_variant | 0.13 |
gyrA | 6703 | c.-599G>C | upstream_gene_variant | 0.12 |
gyrA | 6712 | c.-590G>C | upstream_gene_variant | 0.1 |
gyrA | 6739 | c.-563C>T | upstream_gene_variant | 0.11 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7559 | c.258G>C | synonymous_variant | 0.11 |
gyrA | 7565 | c.264C>T | synonymous_variant | 0.12 |
gyrA | 7574 | c.273G>C | synonymous_variant | 0.12 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8330 | c.1029C>G | synonymous_variant | 0.11 |
gyrA | 8339 | c.1038A>G | synonymous_variant | 0.11 |
gyrA | 8837 | c.1536C>G | synonymous_variant | 0.14 |
gyrA | 8846 | c.1545C>T | synonymous_variant | 0.16 |
gyrA | 8852 | c.1551T>C | synonymous_variant | 0.16 |
gyrA | 8858 | c.1557T>C | synonymous_variant | 0.17 |
gyrA | 8870 | c.1569G>C | synonymous_variant | 0.16 |
gyrA | 8873 | c.1572A>G | synonymous_variant | 0.15 |
gyrA | 8897 | c.1596T>C | synonymous_variant | 0.22 |
gyrA | 8903 | c.1602T>C | synonymous_variant | 0.2 |
gyrA | 8915 | c.1614A>G | synonymous_variant | 0.19 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9437 | c.2136G>A | synonymous_variant | 1.0 |
rpoB | 760079 | c.273G>A | synonymous_variant | 0.13 |
rpoB | 760091 | c.285G>C | synonymous_variant | 0.12 |
rpoB | 760101 | c.295T>C | synonymous_variant | 0.12 |
rpoB | 760111 | p.Ser102Cys | missense_variant | 0.13 |
rpoB | 760118 | c.312T>G | synonymous_variant | 0.12 |
rpoB | 760121 | c.315T>C | synonymous_variant | 0.11 |
rpoB | 760139 | c.333A>G | synonymous_variant | 0.12 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.1 |
rpoB | 760400 | c.594G>C | synonymous_variant | 0.14 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.14 |
rpoB | 760407 | p.Ser201Gly | missense_variant | 0.15 |
rpoB | 760415 | c.609C>T | synonymous_variant | 0.2 |
rpoB | 760418 | c.612G>C | synonymous_variant | 0.2 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.23 |
rpoB | 760460 | c.654G>C | synonymous_variant | 0.2 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.21 |
rpoB | 760481 | c.675G>C | synonymous_variant | 0.22 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.21 |
rpoB | 760502 | c.696C>G | synonymous_variant | 0.15 |
rpoB | 760541 | c.735G>C | synonymous_variant | 0.13 |
rpoB | 760571 | c.765G>C | synonymous_variant | 0.12 |
rpoB | 760588 | p.Thr261Ile | missense_variant | 0.13 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.13 |
rpoB | 760595 | c.789C>T | synonymous_variant | 0.13 |
rpoB | 760596 | p.Thr264Pro | missense_variant | 0.13 |
rpoB | 760608 | c.802C>T | synonymous_variant | 0.15 |
rpoB | 760611 | c.805T>C | synonymous_variant | 0.14 |
rpoB | 760634 | c.828T>C | synonymous_variant | 0.18 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.17 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.17 |
rpoB | 760661 | c.855A>G | synonymous_variant | 0.15 |
rpoB | 760668 | p.Thr288Ala | missense_variant | 0.14 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.12 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.13 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.13 |
rpoB | 760841 | c.1035T>C | synonymous_variant | 0.13 |
rpoB | 760858 | p.Val351Ala | missense_variant | 0.13 |
rpoB | 760862 | c.1056G>C | synonymous_variant | 0.13 |
rpoB | 760865 | c.1059C>T | synonymous_variant | 0.12 |
rpoB | 760886 | p.Glu360Asp | missense_variant | 0.13 |
rpoB | 760887 | p.Thr361Val | missense_variant | 0.13 |
rpoB | 760910 | c.1104C>T | synonymous_variant | 0.12 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.12 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.12 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.12 |
rpoB | 761063 | c.1257C>G | synonymous_variant | 0.12 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.16 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.13 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.14 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 0.11 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.11 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.11 |
rpoB | 761273 | c.1467T>C | synonymous_variant | 0.12 |
rpoB | 761564 | c.1758G>C | synonymous_variant | 0.11 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.11 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.11 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.13 |
rpoB | 761612 | c.1806G>T | synonymous_variant | 0.19 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.2 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.19 |
rpoB | 761645 | c.1839C>G | synonymous_variant | 0.15 |
rpoB | 761657 | c.1851C>T | synonymous_variant | 0.17 |
rpoB | 761990 | c.2184G>C | synonymous_variant | 0.12 |
rpoB | 762008 | c.2202C>T | synonymous_variant | 0.14 |
rpoB | 762038 | c.2232C>T | synonymous_variant | 0.12 |
rpoB | 762047 | c.2241G>A | synonymous_variant | 0.13 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.13 |
rpoB | 762056 | c.2250G>A | synonymous_variant | 0.12 |
rpoB | 762065 | c.2259T>G | synonymous_variant | 0.12 |
rpoB | 762158 | c.2352G>C | synonymous_variant | 0.1 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.1 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.12 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.13 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 0.14 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.14 |
rpoB | 762236 | c.2430G>C | synonymous_variant | 0.15 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.16 |
rpoB | 762275 | c.2469C>T | synonymous_variant | 0.14 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.14 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.13 |
rpoB | 762296 | c.2490G>C | synonymous_variant | 0.11 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 0.13 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.12 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.1 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.11 |
rpoC | 763082 | c.-288C>T | upstream_gene_variant | 0.12 |
rpoC | 763088 | c.-282C>G | upstream_gene_variant | 0.11 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.13 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.18 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.23 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.2 |
rpoC | 763657 | c.288G>A | synonymous_variant | 0.16 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.15 |
rpoC | 763666 | c.297G>C | synonymous_variant | 0.16 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.19 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.19 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.12 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.11 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.11 |
rpoC | 763711 | c.342G>C | synonymous_variant | 0.11 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.11 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.11 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.11 |
rpoC | 763732 | c.363C>A | synonymous_variant | 0.14 |
rpoC | 764407 | p.Arg346Ser | missense_variant | 0.12 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.1 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.1 |
rpoC | 764692 | c.1323C>T | synonymous_variant | 0.14 |
rpoC | 764713 | c.1344G>T | synonymous_variant | 0.13 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.13 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.12 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.11 |
rpoC | 764791 | c.1422C>G | synonymous_variant | 0.12 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.13 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.12 |
rpoC | 764810 | p.Pro481Ala | missense_variant | 0.12 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.11 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 0.14 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.16 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.17 |
rpoC | 764869 | c.1500C>T | synonymous_variant | 0.15 |
rpoC | 764875 | c.1506C>A | synonymous_variant | 0.14 |
rpoC | 764887 | c.1518G>C | synonymous_variant | 0.14 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.14 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.12 |
rpoC | 764912 | p.Met515Leu | missense_variant | 0.11 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765403 | c.2034G>C | synonymous_variant | 0.12 |
rpoC | 765405 | p.Leu679His | missense_variant | 0.12 |
rpoC | 765409 | c.2040T>G | synonymous_variant | 0.11 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.16 |
rpoC | 765875 | p.Val836Ile | missense_variant | 0.12 |
rpoC | 765886 | c.2517C>T | synonymous_variant | 0.12 |
rpoC | 765907 | c.2538G>T | synonymous_variant | 0.12 |
rpoC | 765910 | c.2541G>C | synonymous_variant | 0.12 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.1 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.13 |
rpoC | 767002 | c.3633G>C | synonymous_variant | 0.15 |
rpoC | 767008 | c.3639G>A | synonymous_variant | 0.13 |
rpoC | 767023 | c.3654C>T | synonymous_variant | 0.16 |
rpoC | 767044 | c.3675G>C | synonymous_variant | 0.18 |
rpoC | 767080 | c.3711G>C | synonymous_variant | 0.14 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.19 |
rpoC | 767104 | c.3735C>G | synonymous_variant | 0.17 |
rpoC | 767107 | c.3738C>T | synonymous_variant | 0.2 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.16 |
rpoC | 767125 | c.3756G>C | synonymous_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.1 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.12 |
rpsL | 781829 | c.270G>C | synonymous_variant | 0.12 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.12 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.19 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.2 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.17 |
rpsL | 781877 | c.318T>A | synonymous_variant | 0.16 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.12 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.11 |
rpsL | 781907 | c.348T>C | synonymous_variant | 0.1 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471922 | n.78delT | non_coding_transcript_exon_variant | 0.13 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1471931 | n.87delA | non_coding_transcript_exon_variant | 0.13 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1471985 | n.140T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473082 | n.1237G>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473099 | n.1254T>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473129 | n.1284C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473288 | n.1443C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473291 | n.1446G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473717 | n.60G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473731 | n.74T>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1473746 | n.89T>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1473756 | n.99G>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473767 | n.110G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473770 | n.113T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473812 | n.155G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1473814 | n.157A>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473815 | n.158T>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473829 | n.172G>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473831 | n.174G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473832 | n.175C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473839 | n.182G>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474717 | n.1060A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474722 | n.1065T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474743 | n.1086T>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474803 | n.1146G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475475 | n.1818C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475479 | n.1822C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.33 |
rpsA | 1833823 | c.282G>A | synonymous_variant | 0.11 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.11 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.11 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.13 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.13 |
rpsA | 1833862 | c.321G>T | synonymous_variant | 0.13 |
rpsA | 1833874 | c.333T>G | synonymous_variant | 0.12 |
rpsA | 1833886 | c.345C>G | synonymous_variant | 0.13 |
rpsA | 1833894 | p.Ala118Glu | missense_variant | 0.13 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.14 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.14 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155296 | c.816C>T | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2517941 | c.-174C>G | upstream_gene_variant | 0.1 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087225 | p.Val136Leu | missense_variant | 1.0 |
fbiD | 3339178 | p.Ala21Thr | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474197 | p.Ser64Thr | missense_variant | 1.0 |
fprA | 3474504 | c.498G>A | synonymous_variant | 1.0 |
rpoA | 3877638 | c.870T>C | synonymous_variant | 0.1 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.14 |
rpoA | 3877908 | c.600T>C | synonymous_variant | 0.16 |
rpoA | 3877920 | c.588G>C | synonymous_variant | 0.15 |
rpoA | 3877923 | c.585C>T | synonymous_variant | 0.15 |
rpoA | 3877929 | p.Ile193Val | missense_variant | 0.12 |
rpoA | 3878259 | c.249G>C | synonymous_variant | 0.11 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.12 |
rpoA | 3878283 | p.Glu75Asp | missense_variant | 0.12 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.12 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.11 |
clpC1 | 4038838 | c.1867C>T | synonymous_variant | 0.13 |
clpC1 | 4038845 | c.1858_1860delTCGinsAGC | synonymous_variant | 0.13 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 0.14 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.13 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.11 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.14 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.13 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.13 |
clpC1 | 4039046 | c.1659C>G | synonymous_variant | 0.12 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.11 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.13 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.16 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.17 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.21 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.21 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.22 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.22 |
clpC1 | 4039190 | c.1515C>T | synonymous_variant | 0.2 |
clpC1 | 4039196 | c.1509G>A | synonymous_variant | 0.18 |
clpC1 | 4039199 | p.Ala502Glu | missense_variant | 0.18 |
clpC1 | 4039208 | c.1497C>G | synonymous_variant | 0.16 |
clpC1 | 4039220 | c.1485G>C | synonymous_variant | 0.15 |
clpC1 | 4039454 | c.1251A>G | synonymous_variant | 0.12 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.13 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.13 |
clpC1 | 4039472 | c.1233G>C | synonymous_variant | 0.13 |
clpC1 | 4039478 | c.1227G>C | synonymous_variant | 0.13 |
clpC1 | 4039481 | c.1224T>C | synonymous_variant | 0.14 |
clpC1 | 4039487 | c.1218G>C | synonymous_variant | 0.17 |
clpC1 | 4039522 | c.1183C>T | synonymous_variant | 0.19 |
clpC1 | 4039528 | c.1177C>A | synonymous_variant | 0.2 |
clpC1 | 4039541 | c.1164C>G | synonymous_variant | 0.15 |
clpC1 | 4039544 | c.1161C>T | synonymous_variant | 0.12 |
clpC1 | 4039622 | c.1083C>T | synonymous_variant | 0.12 |
clpC1 | 4039649 | c.1056G>C | synonymous_variant | 0.15 |
clpC1 | 4039661 | c.1044T>C | synonymous_variant | 0.17 |
clpC1 | 4039682 | c.1023C>G | synonymous_variant | 0.16 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.16 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.12 |
clpC1 | 4039748 | c.957G>C | synonymous_variant | 0.11 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.11 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.11 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.14 |
clpC1 | 4039793 | c.912C>G | synonymous_variant | 0.13 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.11 |
clpC1 | 4040015 | c.690G>C | synonymous_variant | 0.1 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.12 |
clpC1 | 4040048 | c.657C>T | synonymous_variant | 0.13 |
clpC1 | 4040546 | c.159G>C | synonymous_variant | 0.11 |
clpC1 | 4040558 | c.147G>C | synonymous_variant | 0.11 |
clpC1 | 4040561 | c.144A>G | synonymous_variant | 0.11 |
clpC1 | 4040573 | c.132T>C | synonymous_variant | 0.14 |
clpC1 | 4040579 | c.126A>G | synonymous_variant | 0.12 |
clpC1 | 4040582 | c.123G>C | synonymous_variant | 0.12 |
clpC1 | 4040585 | c.120A>G | synonymous_variant | 0.13 |
embC | 4239763 | c.-100C>T | upstream_gene_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embB | 4249408 | c.2895G>A | synonymous_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |