Run ID: ERR4816100
Sample name:
Date: 01-04-2023 14:14:31
Number of reads: 2349731
Percentage reads mapped: 75.28
Strain: lineage4.1.3;lineage4.1.2.1;lineage1.1.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.66 |
lineage1 | Indo-Oceanic | EAI | RD239 | 0.35 |
lineage4.1 | Euro-American | T;X;H | None | 0.6 |
lineage1.1 | Indo-Oceanic | EAI3;EAI4;EAI5;EAI6 | RD239 | 0.36 |
lineage4.1.3 | Euro-American | T;X;H | None | 0.49 |
lineage1.1.2 | Indo-Oceanic | EAI3;EAI5 | RD239 | 0.4 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 0.08 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6112 | p.Met291Ile | missense_variant | 0.34 |
gyrB | 6124 | c.885C>T | synonymous_variant | 0.35 |
gyrA | 6670 | c.-632G>C | upstream_gene_variant | 0.13 |
gyrA | 6676 | c.-626T>G | upstream_gene_variant | 0.13 |
gyrA | 6730 | c.-572A>G | upstream_gene_variant | 0.13 |
gyrA | 6760 | c.-542G>C | upstream_gene_variant | 0.14 |
gyrA | 6764 | c.-538C>T | upstream_gene_variant | 0.13 |
gyrA | 6772 | c.-530C>G | upstream_gene_variant | 0.14 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7394 | c.93T>C | synonymous_variant | 0.13 |
gyrA | 7442 | c.141G>C | synonymous_variant | 0.14 |
gyrA | 7457 | c.156T>C | synonymous_variant | 0.16 |
gyrA | 7480 | p.Phe60Tyr | missense_variant | 0.14 |
gyrA | 7484 | c.183T>C | synonymous_variant | 0.14 |
gyrA | 7490 | c.189C>G | synonymous_variant | 0.13 |
gyrA | 7496 | c.195C>G | synonymous_variant | 0.16 |
gyrA | 7499 | c.198G>C | synonymous_variant | 0.17 |
gyrA | 7523 | c.222C>G | synonymous_variant | 0.16 |
gyrA | 7526 | c.225G>C | synonymous_variant | 0.17 |
gyrA | 7532 | c.231T>G | synonymous_variant | 0.18 |
gyrA | 7559 | c.258G>A | synonymous_variant | 0.15 |
gyrA | 7571 | c.270G>C | synonymous_variant | 0.22 |
gyrA | 7574 | c.273G>C | synonymous_variant | 0.16 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 0.99 |
gyrA | 8435 | c.1134C>G | synonymous_variant | 0.35 |
gyrA | 8452 | p.Ala384Val | missense_variant | 0.32 |
gyrA | 8897 | c.1596T>C | synonymous_variant | 0.16 |
gyrA | 8915 | c.1614A>G | synonymous_variant | 0.15 |
gyrA | 8924 | c.1623C>T | synonymous_variant | 0.14 |
gyrA | 9122 | c.1821C>A | synonymous_variant | 0.12 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 0.59 |
gyrA | 9182 | c.1881T>C | synonymous_variant | 0.14 |
gyrA | 9191 | c.1890G>C | synonymous_variant | 0.14 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491173 | c.391C>A | synonymous_variant | 0.13 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.33 |
mshA | 575376 | p.Ser10Leu | missense_variant | 0.32 |
ccsA | 620688 | c.798G>C | synonymous_variant | 0.15 |
rpoB | 760112 | c.306T>C | synonymous_variant | 0.14 |
rpoB | 760115 | c.309C>T | synonymous_variant | 0.13 |
rpoB | 760118 | c.312T>G | synonymous_variant | 0.16 |
rpoB | 760121 | c.315T>C | synonymous_variant | 0.16 |
rpoB | 760130 | p.Asp108Glu | missense_variant | 0.19 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.16 |
rpoB | 760196 | c.390C>G | synonymous_variant | 0.21 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.18 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.14 |
rpoB | 760283 | c.477G>C | synonymous_variant | 0.16 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.14 |
rpoB | 760522 | p.Ser239Asn | missense_variant | 0.14 |
rpoB | 760634 | c.828T>C | synonymous_variant | 0.14 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.14 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.13 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.14 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.14 |
rpoB | 760887 | p.Thr361Ala | missense_variant | 0.13 |
rpoB | 760910 | c.1104C>T | synonymous_variant | 0.15 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 0.13 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.16 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 0.16 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.16 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.18 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.19 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.22 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.29 |
rpoB | 761129 | c.1323G>C | synonymous_variant | 0.13 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.16 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.12 |
rpoB | 761219 | c.1413G>C | synonymous_variant | 0.17 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.24 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.23 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.18 |
rpoB | 761306 | c.1500C>G | synonymous_variant | 0.16 |
rpoB | 761312 | c.1506G>C | synonymous_variant | 0.19 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.27 |
rpoB | 761330 | c.1524G>C | synonymous_variant | 0.16 |
rpoB | 761354 | c.1548C>T | synonymous_variant | 0.17 |
rpoB | 761360 | c.1554T>C | synonymous_variant | 0.22 |
rpoB | 761362 | p.Ser519Thr | missense_variant | 0.23 |
rpoB | 761373 | p.Val523His | missense_variant | 0.19 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.21 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.21 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.22 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.2 |
rpoB | 761612 | c.1806G>T | synonymous_variant | 0.16 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.25 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.21 |
rpoB | 761645 | c.1839C>G | synonymous_variant | 0.19 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.19 |
rpoB | 762008 | c.2202C>T | synonymous_variant | 0.16 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.19 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.15 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.15 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.15 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.15 |
rpoC | 762989 | c.-381G>A | upstream_gene_variant | 0.14 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.2 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.43 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.25 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.24 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.15 |
rpoC | 763088 | c.-282C>G | upstream_gene_variant | 0.15 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.17 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.26 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.14 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.2 |
rpoC | 763142 | c.-228C>G | upstream_gene_variant | 0.15 |
rpoC | 763157 | c.-213G>T | upstream_gene_variant | 0.14 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.14 |
rpoC | 763402 | c.33C>G | synonymous_variant | 0.18 |
rpoC | 763411 | c.42T>G | synonymous_variant | 0.18 |
rpoC | 763414 | c.45T>C | synonymous_variant | 0.18 |
rpoC | 763441 | c.72C>T | synonymous_variant | 0.19 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.19 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.2 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.17 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.18 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.17 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.14 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.21 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.18 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.19 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.17 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.15 |
rpoC | 763884 | p.Ala172Val | missense_variant | 0.52 |
rpoC | 763886 | c.517C>A | synonymous_variant | 0.55 |
rpoC | 764257 | c.888G>C | synonymous_variant | 0.2 |
rpoC | 764266 | c.897T>C | synonymous_variant | 0.16 |
rpoC | 764269 | c.900G>C | synonymous_variant | 0.17 |
rpoC | 764278 | c.909A>G | synonymous_variant | 0.15 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.15 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.14 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.21 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.18 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.18 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.18 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.2 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.19 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.24 |
rpoC | 764506 | c.1137C>T | synonymous_variant | 0.24 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.22 |
rpoC | 764530 | c.1161C>T | synonymous_variant | 0.17 |
rpoC | 764536 | c.1167G>T | synonymous_variant | 0.16 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.23 |
rpoC | 764548 | c.1179G>A | synonymous_variant | 0.17 |
rpoC | 764554 | c.1185C>T | synonymous_variant | 0.24 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.28 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.27 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 0.2 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.22 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.13 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.23 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.24 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.22 |
rpoC | 764635 | c.1266C>T | synonymous_variant | 0.18 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.24 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.26 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.3 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.14 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.25 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.17 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.21 |
rpoC | 764875 | c.1506C>A | synonymous_variant | 0.13 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.15 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.14 |
rpoC | 764932 | c.1563C>A | synonymous_variant | 0.17 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.17 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.17 |
rpoC | 765019 | c.1650A>G | synonymous_variant | 0.15 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 0.61 |
rpoC | 765171 | p.Pro601Leu | missense_variant | 0.31 |
rpoC | 765352 | c.1983G>C | synonymous_variant | 0.16 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.2 |
rpoC | 765529 | c.2160C>T | synonymous_variant | 0.15 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.14 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.14 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.15 |
rpoC | 765559 | c.2190G>C | synonymous_variant | 0.15 |
rpoC | 765580 | c.2211G>C | synonymous_variant | 0.13 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.18 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.14 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.15 |
rpoC | 766390 | c.3021C>T | synonymous_variant | 0.13 |
rpoC | 766607 | p.Ile1080Leu | missense_variant | 0.14 |
rpoC | 766630 | c.3261G>C | synonymous_variant | 0.15 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.17 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.62 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781421 | c.-139C>A | upstream_gene_variant | 0.55 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.16 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.18 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.18 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.18 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.18 |
rpsL | 781916 | c.357T>C | synonymous_variant | 0.17 |
fbiC | 1303818 | c.888C>G | synonymous_variant | 0.21 |
fbiC | 1303836 | c.906G>C | synonymous_variant | 0.22 |
fbiC | 1303845 | c.915C>G | synonymous_variant | 0.22 |
fbiC | 1303846 | p.Phe306Val | missense_variant | 0.22 |
fbiC | 1303854 | c.924T>C | synonymous_variant | 0.22 |
fbiC | 1303860 | c.930A>C | synonymous_variant | 0.22 |
fbiC | 1303884 | c.954T>G | synonymous_variant | 0.17 |
fbiC | 1304610 | c.1680C>T | synonymous_variant | 0.54 |
fbiC | 1304856 | c.1926C>G | synonymous_variant | 0.18 |
fbiC | 1304869 | c.1939C>T | synonymous_variant | 0.12 |
fbiC | 1304928 | c.1998T>C | synonymous_variant | 0.12 |
fbiC | 1304958 | c.2028T>G | synonymous_variant | 0.18 |
fbiC | 1304983 | c.2053C>T | synonymous_variant | 0.23 |
fbiC | 1304994 | c.2064A>G | synonymous_variant | 0.16 |
fbiC | 1304995 | p.Leu689Met | missense_variant | 0.16 |
fbiC | 1305006 | c.2076A>G | synonymous_variant | 0.15 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 0.26 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473123 | n.1278A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1473660 | n.3G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473943 | n.286G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474181 | n.524_525insT | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474184 | n.527C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474185 | n.529delA | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474282 | n.625G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474803 | n.1146G>A | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.37 |
rrl | 1475061 | n.1406delA | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475076 | n.1419C>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1475120 | n.1463G>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475129 | n.1472G>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475249 | n.1592T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475291 | n.1634A>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475313 | n.1656G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475402 | n.1745C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475406 | n.1749T>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475443 | n.1786G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475475 | n.1818C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475479 | n.1822C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476295 | n.2638C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476311 | n.2654G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.14 |
inhA | 1674589 | p.Met130Leu | missense_variant | 0.13 |
inhA | 1674660 | c.459G>C | synonymous_variant | 0.15 |
inhA | 1674703 | c.502T>C | synonymous_variant | 0.15 |
inhA | 1674708 | c.507G>A | synonymous_variant | 0.16 |
inhA | 1674718 | c.517A>C | synonymous_variant | 0.17 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.16 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.18 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.2 |
rpsA | 1833874 | c.333T>G | synonymous_variant | 0.13 |
rpsA | 1833886 | c.345C>G | synonymous_variant | 0.19 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.24 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.16 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.19 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.15 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.19 |
rpsA | 1834074 | p.Lys178Arg | missense_variant | 0.13 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.14 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.13 |
rpsA | 1834498 | c.957C>T | synonymous_variant | 0.14 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.21 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 0.3 |
PPE35 | 2167983 | p.Gly877Asp | missense_variant | 0.34 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 0.41 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 0.46 |
kasA | 2518696 | c.582C>G | synonymous_variant | 0.14 |
kasA | 2518702 | c.588C>T | synonymous_variant | 0.14 |
kasA | 2518711 | c.597A>G | synonymous_variant | 0.15 |
kasA | 2518714 | c.600A>C | synonymous_variant | 0.13 |
kasA | 2518777 | c.663C>T | synonymous_variant | 0.14 |
kasA | 2518825 | c.711T>C | synonymous_variant | 0.21 |
kasA | 2519062 | c.948T>G | synonymous_variant | 0.16 |
kasA | 2519068 | c.954C>T | synonymous_variant | 0.14 |
kasA | 2519072 | p.Ala320Thr | missense_variant | 0.15 |
kasA | 2519107 | c.993T>C | synonymous_variant | 0.17 |
kasA | 2519108 | p.Asp332Gln | missense_variant | 0.17 |
kasA | 2519116 | c.1002C>G | synonymous_variant | 0.17 |
kasA | 2519122 | c.1008G>C | synonymous_variant | 0.19 |
kasA | 2519137 | c.1023T>G | synonymous_variant | 0.19 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 0.29 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 0.47 |
Rv2752c | 3066376 | c.-185C>T | upstream_gene_variant | 0.14 |
thyX | 3067316 | c.630A>G | synonymous_variant | 0.14 |
thyX | 3067391 | c.555G>C | synonymous_variant | 0.13 |
thyX | 3067394 | c.552G>C | synonymous_variant | 0.12 |
thyX | 3067439 | c.507A>G | synonymous_variant | 0.19 |
thyX | 3067445 | c.501C>G | synonymous_variant | 0.2 |
thyX | 3067457 | c.489C>G | synonymous_variant | 0.25 |
thyX | 3067465 | p.Ile161Val | missense_variant | 0.25 |
thyX | 3067475 | c.471A>G | synonymous_variant | 0.25 |
thyX | 3067490 | c.456C>G | synonymous_variant | 0.25 |
thyX | 3067493 | c.453A>G | synonymous_variant | 0.28 |
thyX | 3067515 | p.Ser144Thr | missense_variant | 0.25 |
thyX | 3067718 | c.228C>G | synonymous_variant | 0.14 |
thyX | 3067721 | c.225T>C | synonymous_variant | 0.14 |
thyA | 3074175 | c.297A>G | synonymous_variant | 0.13 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.98 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 0.47 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 0.98 |
fprA | 3474597 | c.591C>A | synonymous_variant | 0.37 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 0.44 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.15 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.17 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.18 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.18 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.2 |
rpoA | 3877785 | c.723C>A | synonymous_variant | 0.14 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.2 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.15 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.15 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.13 |
rpoA | 3878578 | c.-71C>A | upstream_gene_variant | 0.5 |
clpC1 | 4038388 | c.2317T>C | synonymous_variant | 0.13 |
clpC1 | 4038530 | p.Glu725Asp | missense_variant | 0.15 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.2 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.15 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.16 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.16 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.14 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.14 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.16 |
clpC1 | 4039064 | c.1641C>T | synonymous_variant | 0.15 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.14 |
clpC1 | 4039338 | p.Thr456Gln | missense_variant | 0.15 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.17 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.18 |
clpC1 | 4039934 | c.771G>C | synonymous_variant | 0.14 |
clpC1 | 4039943 | c.762G>C | synonymous_variant | 0.15 |
clpC1 | 4039946 | c.759A>G | synonymous_variant | 0.16 |
clpC1 | 4039949 | c.756G>C | synonymous_variant | 0.15 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.22 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.2 |
clpC1 | 4039964 | c.741C>G | synonymous_variant | 0.18 |
clpC1 | 4039975 | p.Asp244Asn | missense_variant | 0.14 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.25 |
clpC1 | 4039982 | c.723G>A | synonymous_variant | 0.16 |
clpC1 | 4039988 | c.717C>G | synonymous_variant | 0.13 |
clpC1 | 4040000 | c.705C>T | synonymous_variant | 0.15 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.14 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.16 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.15 |
clpC1 | 4040105 | c.600C>G | synonymous_variant | 0.15 |
clpC1 | 4040267 | c.438A>G | synonymous_variant | 0.15 |
clpC1 | 4040291 | c.414G>C | synonymous_variant | 0.13 |
clpC1 | 4040330 | c.375C>G | synonymous_variant | 0.14 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 0.27 |
embC | 4240671 | p.Thr270Ile | missense_variant | 0.44 |
embC | 4241042 | p.Asn394Asp | missense_variant | 0.39 |
embC | 4241611 | c.1749G>C | synonymous_variant | 0.18 |
embC | 4241614 | c.1752A>C | synonymous_variant | 0.15 |
embC | 4241727 | p.Phe622Tyr | missense_variant | 0.15 |
embC | 4241741 | p.Val627Leu | missense_variant | 0.14 |
embC | 4241747 | p.Val629Leu | missense_variant | 0.15 |
embC | 4241750 | p.Leu630Val | missense_variant | 0.14 |
embC | 4241755 | c.1893C>G | synonymous_variant | 0.14 |
embC | 4241770 | c.1908T>C | synonymous_variant | 0.14 |
embC | 4241791 | c.1929G>C | synonymous_variant | 0.13 |
embC | 4241794 | c.1932C>G | synonymous_variant | 0.13 |
embC | 4241797 | c.1935C>T | synonymous_variant | 0.12 |
embC | 4241809 | c.1947A>C | synonymous_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 0.69 |
embA | 4243848 | p.Val206Met | missense_variant | 0.43 |
embA | 4245137 | c.1905T>C | synonymous_variant | 0.13 |
embA | 4245149 | c.1917C>G | synonymous_variant | 0.15 |
embA | 4245182 | c.1950T>C | synonymous_variant | 0.14 |
embA | 4245969 | p.Pro913Ser | missense_variant | 0.45 |
embB | 4247356 | c.843C>T | synonymous_variant | 0.53 |
embB | 4247470 | c.957T>C | synonymous_variant | 0.14 |
embB | 4247491 | c.978G>C | synonymous_variant | 0.14 |
embB | 4247646 | p.Glu378Ala | missense_variant | 0.38 |
embB | 4247893 | c.1380C>T | synonymous_variant | 0.16 |
embB | 4247899 | p.Met462Ile | missense_variant | 0.17 |
embB | 4247905 | c.1392G>C | synonymous_variant | 0.16 |
embB | 4247940 | p.Leu476Trp | missense_variant | 0.14 |
embB | 4247945 | c.1432T>C | synonymous_variant | 0.15 |
embB | 4247951 | p.Ser480Ala | missense_variant | 0.14 |
embB | 4247956 | c.1443G>C | synonymous_variant | 0.15 |
aftB | 4268683 | p.Gly52Ser | missense_variant | 0.53 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 0.4 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 0.31 |
whiB6 | 4338441 | p.Tyr27* | stop_gained | 0.37 |
whiB6 | 4338449 | p.Ala25Pro | missense_variant | 0.39 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 0.24 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.28 |
gid | 4407873 | c.330G>T | synonymous_variant | 0.26 |