Run ID: ERR4798139
Sample name:
Date: 01-04-2023 08:09:04
Number of reads: 2127162
Percentage reads mapped: 86.75
Strain: lineage1.1.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 0.97 |
lineage1.1 | Indo-Oceanic | EAI3;EAI4;EAI5;EAI6 | RD239 | 1.0 |
lineage1.1.2 | Indo-Oceanic | EAI3;EAI5 | RD239 | 0.98 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6112 | p.Met291Ile | missense_variant | 0.98 |
gyrB | 6124 | c.885C>T | synonymous_variant | 0.97 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8452 | p.Ala384Val | missense_variant | 0.89 |
gyrA | 8786 | c.1485T>C | synonymous_variant | 0.13 |
gyrA | 8813 | c.1512C>T | synonymous_variant | 0.14 |
gyrA | 8818 | p.Ser506Asn | missense_variant | 0.14 |
gyrA | 8870 | c.1569G>C | synonymous_variant | 0.13 |
gyrA | 8897 | c.1596T>C | synonymous_variant | 0.13 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 0.98 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575884 | c.537G>C | synonymous_variant | 0.14 |
mshA | 575887 | c.540G>T | synonymous_variant | 0.14 |
mshA | 575893 | c.546C>G | synonymous_variant | 0.14 |
mshA | 575896 | c.549G>T | synonymous_variant | 0.14 |
mshA | 575905 | c.558G>C | synonymous_variant | 0.14 |
mshA | 575914 | c.567C>G | synonymous_variant | 0.13 |
mshA | 575926 | c.579A>G | synonymous_variant | 0.13 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.29 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.14 |
rpoB | 760634 | c.828T>C | synonymous_variant | 0.12 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.15 |
rpoB | 761097 | c.1291_1292delAGinsTC | synonymous_variant | 0.15 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.15 |
rpoB | 761129 | c.1323G>C | synonymous_variant | 0.17 |
rpoB | 761133 | c.1327_1329delTTGinsCTC | synonymous_variant | 0.17 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.17 |
rpoB | 761165 | c.1359G>A | synonymous_variant | 0.16 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.17 |
rpoB | 761171 | c.1365C>T | synonymous_variant | 0.17 |
rpoB | 761180 | c.1374A>G | synonymous_variant | 0.15 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.14 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.14 |
rpoB | 761252 | c.1446C>T | synonymous_variant | 0.16 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.16 |
rpoB | 761264 | c.1458C>G | synonymous_variant | 0.14 |
rpoB | 761282 | c.1476C>G | synonymous_variant | 0.16 |
rpoB | 761286 | c.1480C>T | synonymous_variant | 0.17 |
rpoB | 761300 | c.1494G>A | synonymous_variant | 0.19 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.19 |
rpoB | 761354 | c.1548C>T | synonymous_variant | 0.25 |
rpoB | 761360 | c.1554T>C | synonymous_variant | 0.22 |
rpoB | 761363 | c.1557C>T | synonymous_variant | 0.22 |
rpoB | 761367 | p.Glu521Gln | missense_variant | 0.21 |
rpoB | 761374 | p.Val523Asp | missense_variant | 0.2 |
rpoB | 761378 | c.1572C>T | synonymous_variant | 0.2 |
rpoB | 761393 | c.1587G>A | synonymous_variant | 0.19 |
rpoB | 761408 | c.1602G>C | synonymous_variant | 0.16 |
rpoB | 761414 | c.1608A>G | synonymous_variant | 0.15 |
rpoC | 762758 | c.-612G>C | upstream_gene_variant | 0.14 |
rpoC | 762782 | c.-588T>C | upstream_gene_variant | 0.14 |
rpoC | 762788 | c.-582G>C | upstream_gene_variant | 0.14 |
rpoB | 762789 | p.Leu995Met | missense_variant | 0.14 |
rpoC | 762794 | c.-576C>G | upstream_gene_variant | 0.14 |
rpoB | 762795 | p.Asp997Asn | missense_variant | 0.14 |
rpoC | 762800 | c.-570C>A | upstream_gene_variant | 0.15 |
rpoC | 762812 | c.-558C>G | upstream_gene_variant | 0.16 |
rpoB | 762814 | p.Met1003Arg | missense_variant | 0.16 |
rpoC | 762818 | c.-552C>G | upstream_gene_variant | 0.16 |
rpoC | 762824 | c.-546C>T | upstream_gene_variant | 0.16 |
rpoC | 762827 | c.-543G>C | upstream_gene_variant | 0.17 |
rpoC | 762833 | c.-537C>T | upstream_gene_variant | 0.17 |
rpoC | 762836 | c.-534C>G | upstream_gene_variant | 0.17 |
rpoC | 762857 | c.-513C>G | upstream_gene_variant | 0.19 |
rpoC | 762860 | c.-510G>C | upstream_gene_variant | 0.19 |
rpoC | 762890 | c.-480C>T | upstream_gene_variant | 0.16 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.15 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.15 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.14 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.16 |
rpoC | 763082 | c.-288C>G | upstream_gene_variant | 0.2 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.2 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.15 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.14 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.16 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.14 |
rpoC | 763884 | p.Ala172Val | missense_variant | 0.91 |
rpoC | 763886 | c.517C>A | synonymous_variant | 0.91 |
rpoC | 763969 | c.600C>T | synonymous_variant | 0.17 |
rpoC | 763978 | c.609C>T | synonymous_variant | 0.2 |
rpoC | 763991 | p.Ile208Leu | missense_variant | 0.17 |
rpoC | 763996 | c.627T>C | synonymous_variant | 0.17 |
rpoC | 764002 | c.633C>G | synonymous_variant | 0.18 |
rpoC | 764005 | c.636G>C | synonymous_variant | 0.18 |
rpoC | 764011 | c.642T>C | synonymous_variant | 0.17 |
rpoC | 764024 | c.655_657delTTGinsCTC | synonymous_variant | 0.16 |
rpoC | 764040 | p.Ser224Thr | missense_variant | 0.15 |
rpoC | 764044 | c.675T>G | synonymous_variant | 0.15 |
rpoC | 764059 | c.690G>C | synonymous_variant | 0.16 |
rpoC | 764083 | c.714A>G | synonymous_variant | 0.14 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.15 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.14 |
rpoC | 764554 | c.1185C>T | synonymous_variant | 0.18 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.15 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 0.15 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.18 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.16 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.17 |
rpoC | 764737 | c.1368G>C | synonymous_variant | 0.14 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.14 |
rpoC | 764782 | c.1413C>T | synonymous_variant | 0.16 |
rpoC | 764797 | c.1428G>C | synonymous_variant | 0.15 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.14 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 0.14 |
rpoC | 765040 | c.1671T>C | synonymous_variant | 0.14 |
rpoC | 765047 | c.1678T>C | synonymous_variant | 0.13 |
rpoC | 765052 | c.1683C>G | synonymous_variant | 0.14 |
rpoC | 765053 | p.Ser562Thr | missense_variant | 0.14 |
rpoC | 765171 | p.Pro601Leu | missense_variant | 1.0 |
rpoC | 765370 | c.2001G>C | synonymous_variant | 0.14 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.13 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.16 |
rpoC | 765547 | c.2178C>A | synonymous_variant | 0.15 |
rpoC | 765728 | p.Gln787Lys | missense_variant | 0.16 |
rpoC | 765734 | c.2365T>C | synonymous_variant | 0.16 |
rpoC | 765739 | c.2370G>T | synonymous_variant | 0.16 |
rpoC | 765751 | c.2382C>G | synonymous_variant | 0.14 |
rpoC | 765753 | p.Asp795Ala | missense_variant | 0.13 |
rpoC | 765772 | c.2403C>G | synonymous_variant | 0.14 |
rpoC | 765787 | c.2418C>T | synonymous_variant | 0.14 |
rpoC | 765793 | c.2424C>G | synonymous_variant | 0.14 |
rpoC | 765796 | c.2427C>T | synonymous_variant | 0.14 |
rpoC | 765811 | c.2442T>C | synonymous_variant | 0.14 |
rpoC | 765844 | c.2475C>T | synonymous_variant | 0.14 |
rpoC | 765850 | c.2481G>C | synonymous_variant | 0.14 |
rpoC | 766366 | c.2997C>T | synonymous_variant | 0.13 |
rpoC | 766369 | c.3000C>G | synonymous_variant | 0.13 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.14 |
rpoC | 766390 | c.3021C>T | synonymous_variant | 0.15 |
rpoC | 766408 | c.3039C>T | synonymous_variant | 0.13 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.15 |
rpoC | 766447 | c.3078T>C | synonymous_variant | 0.14 |
rpoC | 766657 | c.3288A>G | synonymous_variant | 0.16 |
rpoC | 766666 | c.3297C>T | synonymous_variant | 0.14 |
rpoC | 766672 | c.3303T>C | synonymous_variant | 0.13 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.14 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.16 |
rpoC | 766978 | c.3609C>A | synonymous_variant | 0.18 |
rpoC | 766981 | c.3612T>C | synonymous_variant | 0.18 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.22 |
rpoC | 767033 | c.3664_3666delTCGinsAGT | synonymous_variant | 0.24 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.23 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.22 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.22 |
rpoC | 767107 | c.3738C>T | synonymous_variant | 0.22 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.18 |
rpoC | 767134 | c.3765C>A | synonymous_variant | 0.19 |
rpoC | 767152 | c.3783T>G | synonymous_variant | 0.14 |
rpoC | 767158 | c.3789T>A | synonymous_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 0.99 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.13 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.16 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.16 |
rpsL | 781916 | c.357T>C | synonymous_variant | 0.18 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.2 |
rpsL | 781933 | c.374G>A | splice_region_variant&stop_retained_variant | 0.19 |
rplC | 801222 | c.414T>C | synonymous_variant | 0.13 |
rplC | 801246 | c.438C>T | synonymous_variant | 0.15 |
rplC | 801252 | c.444G>C | synonymous_variant | 0.16 |
rplC | 801255 | c.447C>T | synonymous_variant | 0.17 |
rplC | 801267 | c.459A>T | synonymous_variant | 0.17 |
rplC | 801270 | c.462T>C | synonymous_variant | 0.16 |
rplC | 801276 | c.468G>T | synonymous_variant | 0.15 |
rplC | 801279 | c.471G>A | synonymous_variant | 0.15 |
rplC | 801285 | c.477G>C | synonymous_variant | 0.14 |
rplC | 801288 | c.480G>C | synonymous_variant | 0.14 |
fbiC | 1303377 | p.Asp149Glu | missense_variant | 0.99 |
fbiC | 1304502 | c.1572G>A | synonymous_variant | 0.15 |
fbiC | 1304520 | c.1590A>G | synonymous_variant | 0.16 |
fbiC | 1304526 | c.1596T>G | synonymous_variant | 0.16 |
fbiC | 1304538 | c.1608C>A | synonymous_variant | 0.16 |
fbiC | 1304544 | c.1614T>C | synonymous_variant | 0.16 |
fbiC | 1304545 | p.Val539Thr | missense_variant | 0.17 |
fbiC | 1304550 | c.1620C>T | synonymous_variant | 0.17 |
fbiC | 1304559 | p.Glu543Asp | missense_variant | 0.18 |
fbiC | 1304562 | c.1632G>C | synonymous_variant | 0.18 |
fbiC | 1304565 | c.1635C>G | synonymous_variant | 0.18 |
fbiC | 1304568 | c.1638T>C | synonymous_variant | 0.18 |
fbiC | 1304574 | c.1644C>G | synonymous_variant | 0.18 |
fbiC | 1304580 | c.1650T>C | synonymous_variant | 0.15 |
fbiC | 1304937 | c.2007G>C | synonymous_variant | 0.14 |
fbiC | 1304946 | c.2016G>C | synonymous_variant | 0.14 |
fbiC | 1304958 | c.2028T>G | synonymous_variant | 0.12 |
Rv1258c | 1406503 | p.Val280Leu | missense_variant | 1.0 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473668 | n.11C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473676 | n.19G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1473707 | n.50T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473797 | n.140G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473813 | n.156C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473861 | n.205dupC | non_coding_transcript_exon_variant | 0.88 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473887 | n.230T>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473888 | n.231T>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1473937 | n.280C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473943 | n.286G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474627 | n.970G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475062 | n.1405A>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475999 | n.2342G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476032 | n.2375C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476033 | n.2376T>C | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476034 | n.2377C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476035 | n.2378G>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476045 | n.2388G>A | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476047 | n.2390G>A | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476077 | n.2420T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476089 | n.2432T>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476095 | n.2438C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476104 | n.2448delG | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476256 | n.2599A>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476580 | n.2923G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476595 | n.2938C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476602 | n.2945G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476608 | n.2951C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.16 |
inhA | 1674801 | c.600T>C | synonymous_variant | 0.13 |
inhA | 1674813 | c.612C>T | synonymous_variant | 0.14 |
inhA | 1674816 | c.615T>C | synonymous_variant | 0.14 |
inhA | 1674846 | p.Ile215Met | missense_variant | 0.15 |
inhA | 1674870 | c.669T>C | synonymous_variant | 0.12 |
rpsA | 1833589 | c.48A>T | synonymous_variant | 0.14 |
rpsA | 1833595 | c.54T>G | synonymous_variant | 0.15 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.13 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.14 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.14 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.14 |
rpsA | 1834423 | c.882G>T | synonymous_variant | 0.14 |
rpsA | 1834432 | c.891G>T | synonymous_variant | 0.13 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.13 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.12 |
rpsA | 1834606 | c.1065C>T | synonymous_variant | 0.14 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.14 |
rpsA | 1834612 | c.1071G>A | synonymous_variant | 0.14 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.15 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167983 | p.Gly877Asp | missense_variant | 1.0 |
PPE35 | 2169636 | p.Ser326Thr | missense_variant | 1.0 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2518594 | c.480C>G | synonymous_variant | 0.14 |
kasA | 2518606 | c.492G>C | synonymous_variant | 0.15 |
kasA | 2518609 | p.Met165Ile | missense_variant | 0.15 |
kasA | 2518618 | c.504G>A | synonymous_variant | 0.2 |
kasA | 2518621 | c.507G>C | synonymous_variant | 0.2 |
kasA | 2518624 | c.510C>G | synonymous_variant | 0.2 |
kasA | 2518627 | c.513T>C | synonymous_variant | 0.21 |
kasA | 2518639 | c.525G>C | synonymous_variant | 0.3 |
kasA | 2518642 | c.528A>G | synonymous_variant | 0.29 |
kasA | 2518645 | c.531G>C | synonymous_variant | 0.29 |
kasA | 2518651 | c.537C>G | synonymous_variant | 0.31 |
kasA | 2518657 | c.543G>C | synonymous_variant | 0.3 |
kasA | 2518663 | c.549T>C | synonymous_variant | 0.26 |
kasA | 2518672 | c.558G>C | synonymous_variant | 0.24 |
kasA | 2518678 | c.564C>T | synonymous_variant | 0.24 |
kasA | 2518687 | p.Asp191Glu | missense_variant | 0.21 |
kasA | 2518711 | c.597A>G | synonymous_variant | 0.23 |
kasA | 2518717 | c.603C>G | synonymous_variant | 0.23 |
kasA | 2518747 | c.633C>G | synonymous_variant | 0.24 |
kasA | 2518778 | p.Glu222Gln | missense_variant | 0.14 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
ahpC | 2726090 | c.-103C>T | upstream_gene_variant | 1.0 |
ribD | 2987449 | p.Glu204Ala | missense_variant | 1.0 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 1.0 |
Rv2752c | 3066390 | c.-199C>G | upstream_gene_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.15 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.18 |
rpoA | 3877857 | c.651G>A | synonymous_variant | 0.15 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.15 |
rpoA | 3878022 | c.486T>C | synonymous_variant | 0.14 |
rpoA | 3878025 | c.483C>T | synonymous_variant | 0.15 |
rpoA | 3878028 | c.480G>C | synonymous_variant | 0.15 |
rpoA | 3878031 | c.477T>C | synonymous_variant | 0.15 |
rpoA | 3878043 | c.465G>C | synonymous_variant | 0.15 |
rpoA | 3878046 | c.462T>C | synonymous_variant | 0.15 |
rpoA | 3878049 | c.459G>T | synonymous_variant | 0.15 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.22 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.22 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.21 |
rpoA | 3878073 | c.435C>T | synonymous_variant | 0.21 |
rpoA | 3878076 | c.432C>T | synonymous_variant | 0.22 |
rpoA | 3878079 | c.429C>T | synonymous_variant | 0.22 |
rpoA | 3878082 | c.426T>C | synonymous_variant | 0.21 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.24 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.25 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.24 |
rpoA | 3878126 | c.382C>T | synonymous_variant | 0.23 |
rpoA | 3878130 | c.378C>G | synonymous_variant | 0.21 |
rpoA | 3878157 | c.351C>G | synonymous_variant | 0.17 |
rpoA | 3878169 | c.339G>C | synonymous_variant | 0.17 |
rpoA | 3878184 | c.324C>T | synonymous_variant | 0.16 |
rpoA | 3878187 | c.321C>G | synonymous_variant | 0.16 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.17 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.14 |
rpoA | 3878247 | c.261G>C | synonymous_variant | 0.15 |
rpoA | 3878262 | p.Ser82Gly | missense_variant | 0.18 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.23 |
rpoA | 3878283 | p.Glu75Asp | missense_variant | 0.24 |
rpoA | 3878295 | c.213A>G | synonymous_variant | 0.22 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.22 |
rpoA | 3878304 | c.204G>C | synonymous_variant | 0.21 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 0.22 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.24 |
rpoA | 3878331 | c.177A>G | synonymous_variant | 0.23 |
rpoA | 3878334 | c.174T>C | synonymous_variant | 0.22 |
rpoA | 3878337 | c.171T>C | synonymous_variant | 0.22 |
rpoA | 3878355 | c.153C>G | synonymous_variant | 0.2 |
rpoA | 3878364 | c.144A>C | synonymous_variant | 0.18 |
rpoA | 3878385 | c.123C>G | synonymous_variant | 0.2 |
rpoA | 3878391 | c.117T>G | synonymous_variant | 0.19 |
rpoA | 3878403 | c.105C>T | synonymous_variant | 0.14 |
clpC1 | 4038647 | c.2058T>G | synonymous_variant | 0.14 |
clpC1 | 4038658 | p.Lys683Gln | missense_variant | 0.15 |
clpC1 | 4038661 | p.Ser682Thr | missense_variant | 0.15 |
clpC1 | 4038662 | c.2043T>C | synonymous_variant | 0.14 |
clpC1 | 4038671 | c.2034T>C | synonymous_variant | 0.21 |
clpC1 | 4038683 | c.2022T>C | synonymous_variant | 0.22 |
clpC1 | 4038692 | c.2013C>G | synonymous_variant | 0.21 |
clpC1 | 4038695 | c.2010C>G | synonymous_variant | 0.21 |
clpC1 | 4038698 | c.2007C>T | synonymous_variant | 0.21 |
clpC1 | 4038701 | c.2004G>C | synonymous_variant | 0.21 |
clpC1 | 4038704 | c.2001T>C | synonymous_variant | 0.21 |
clpC1 | 4038713 | c.1992T>C | synonymous_variant | 0.21 |
clpC1 | 4038740 | c.1965G>C | synonymous_variant | 0.2 |
clpC1 | 4038749 | c.1956C>T | synonymous_variant | 0.17 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.19 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 0.17 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.13 |
clpC1 | 4038845 | c.1860G>C | synonymous_variant | 0.14 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 0.13 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.15 |
clpC1 | 4038884 | c.1821C>T | synonymous_variant | 0.14 |
clpC1 | 4038905 | c.1800A>C | synonymous_variant | 0.15 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.15 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.15 |
clpC1 | 4038923 | c.1780_1782delCTAinsTTG | synonymous_variant | 0.14 |
clpC1 | 4039124 | c.1581C>T | synonymous_variant | 0.14 |
clpC1 | 4039328 | c.1377A>C | synonymous_variant | 0.13 |
clpC1 | 4039338 | p.Thr456Gln | missense_variant | 0.15 |
clpC1 | 4039553 | c.1152C>A | synonymous_variant | 0.15 |
clpC1 | 4039556 | c.1149G>C | synonymous_variant | 0.14 |
clpC1 | 4040267 | c.438A>G | synonymous_variant | 0.15 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 0.89 |
clpC1 | 4040546 | c.159G>T | synonymous_variant | 0.14 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 0.95 |
embC | 4241567 | p.Ile569Val | missense_variant | 0.14 |
embC | 4241587 | c.1725C>G | synonymous_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243848 | p.Val206Met | missense_variant | 1.0 |
embB | 4245785 | c.-729G>C | upstream_gene_variant | 0.14 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
aftB | 4268156 | c.681C>T | synonymous_variant | 0.94 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ethA | 4326654 | p.Glu274Lys | missense_variant | 1.0 |
whiB6 | 4338224 | c.297delC | frameshift_variant | 1.0 |
whiB6 | 4338301 | p.Gly74Glu | missense_variant | 0.99 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |