Run ID: ERR7821126
Sample name:
Date: 02-04-2023 06:21:13
Number of reads: 1582829
Percentage reads mapped: 88.51
Strain: lineage1.1.3.2
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 |
lineage1.1.3 | Indo-Oceanic | EAI6 | RD239 | 1.0 |
lineage1.1.3.2 | Indo-Oceanic | NA | RD239 | 0.97 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrA | 7147 | c.-155G>C | upstream_gene_variant | 0.13 |
gyrA | 7165 | c.-137C>G | upstream_gene_variant | 0.17 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8188 | p.Leu296Pro | missense_variant | 1.0 |
gyrA | 8452 | p.Ala384Val | missense_variant | 0.95 |
gyrA | 8672 | c.1371A>G | synonymous_variant | 0.14 |
gyrA | 8967 | p.Ala556Arg | missense_variant | 0.17 |
gyrA | 8978 | c.1677C>T | synonymous_variant | 0.19 |
gyrA | 8987 | c.1686C>G | synonymous_variant | 0.18 |
gyrA | 8990 | c.1689C>G | synonymous_variant | 0.2 |
gyrA | 8996 | c.1695T>C | synonymous_variant | 0.2 |
gyrA | 8998 | p.Leu566Trp | missense_variant | 0.2 |
gyrA | 9017 | c.1716C>G | synonymous_variant | 0.18 |
gyrA | 9023 | c.1722A>C | synonymous_variant | 0.19 |
gyrA | 9029 | c.1728T>C | synonymous_variant | 0.22 |
gyrA | 9050 | c.1749C>T | synonymous_variant | 0.17 |
gyrA | 9051 | c.1750_1752delTTGinsCTT | synonymous_variant | 0.15 |
gyrA | 9056 | c.1755C>G | synonymous_variant | 0.16 |
gyrA | 9065 | c.1764C>G | synonymous_variant | 0.15 |
gyrA | 9074 | c.1773G>T | synonymous_variant | 0.16 |
gyrA | 9080 | c.1779G>T | synonymous_variant | 0.15 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9267 | p.Asn656Gly | missense_variant | 0.16 |
gyrA | 9293 | c.1992G>C | synonymous_variant | 0.17 |
gyrA | 9296 | c.1995T>C | synonymous_variant | 0.18 |
gyrA | 9299 | c.1998G>C | synonymous_variant | 0.16 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.18 |
ccsA | 619695 | c.-196G>A | upstream_gene_variant | 0.95 |
rpoB | 760547 | c.741G>T | synonymous_variant | 0.16 |
rpoB | 760973 | c.1167G>C | synonymous_variant | 0.15 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.15 |
rpoB | 761003 | c.1197C>G | synonymous_variant | 0.17 |
rpoB | 761006 | c.1200C>G | synonymous_variant | 0.16 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.18 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 0.19 |
rpoB | 761027 | c.1221A>C | synonymous_variant | 0.22 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.21 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.21 |
rpoB | 761097 | p.Ser431Cys | missense_variant | 0.14 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.16 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.16 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 0.16 |
rpoB | 761150 | c.1344A>T | synonymous_variant | 0.16 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.15 |
rpoB | 761171 | c.1365C>T | synonymous_variant | 0.15 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.16 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.14 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.15 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.15 |
rpoB | 761510 | c.1704T>C | synonymous_variant | 0.14 |
rpoB | 761531 | c.1725C>G | synonymous_variant | 0.2 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.21 |
rpoB | 761561 | c.1755C>G | synonymous_variant | 0.24 |
rpoB | 761564 | c.1758G>C | synonymous_variant | 0.27 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.28 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.26 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.27 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.22 |
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 | 0.23 |
rpoB | 761645 | c.1839C>G | synonymous_variant | 0.2 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.19 |
rpoB | 761657 | c.1851C>G | synonymous_variant | 0.18 |
rpoB | 761669 | c.1863C>T | synonymous_variant | 0.16 |
rpoB | 761675 | c.1869G>T | synonymous_variant | 0.19 |
rpoB | 761870 | p.Asp688Glu | missense_variant | 0.16 |
rpoB | 761873 | c.2067A>G | synonymous_variant | 0.17 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.16 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.16 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.16 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.18 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.16 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.18 |
rpoB | 762122 | c.2316C>T | synonymous_variant | 0.2 |
rpoB | 762129 | c.2323_2325delCTCinsTTG | synonymous_variant | 0.17 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.2 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.21 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.3 |
rpoB | 762221 | c.2415G>A | synonymous_variant | 0.25 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.24 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.17 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.17 |
rpoB | 762284 | c.2478G>T | synonymous_variant | 0.17 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.15 |
rpoB | 762296 | c.2490G>C | synonymous_variant | 0.14 |
rpoB | 762297 | c.2491C>T | synonymous_variant | 0.14 |
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 | 0.16 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.16 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.13 |
rpoC | 763441 | c.72C>T | synonymous_variant | 0.16 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.16 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.2 |
rpoC | 763486 | c.117T>G | synonymous_variant | 0.16 |
rpoC | 763492 | c.123G>C | synonymous_variant | 0.17 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.16 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.18 |
rpoC | 763570 | c.201G>T | synonymous_variant | 0.21 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.2 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.21 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.22 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.21 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.23 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.2 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.2 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.19 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.2 |
rpoC | 763884 | p.Ala172Val | missense_variant | 0.9 |
rpoC | 763886 | c.517C>A | synonymous_variant | 0.89 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.15 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.17 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.13 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.14 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.14 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.17 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.16 |
rpoC | 765171 | p.Pro601Leu | missense_variant | 1.0 |
rpoC | 765230 | p.Ala621Thr | missense_variant | 0.98 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.15 |
rpoC | 765493 | c.2124G>C | synonymous_variant | 0.19 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.19 |
rpoC | 765508 | c.2139C>G | synonymous_variant | 0.19 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.23 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.18 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.17 |
rpoC | 765562 | c.2193G>C | synonymous_variant | 0.14 |
rpoC | 765580 | c.2211G>C | synonymous_variant | 0.15 |
rpoC | 765583 | c.2214G>C | synonymous_variant | 0.15 |
rpoC | 765592 | c.2223C>T | synonymous_variant | 0.15 |
rpoC | 765613 | p.His748Gln | missense_variant | 0.16 |
rpoC | 765622 | p.Glu751Asp | missense_variant | 0.13 |
rpoC | 765694 | c.2325G>C | synonymous_variant | 0.16 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.18 |
rpoC | 765734 | c.2365T>C | synonymous_variant | 0.26 |
rpoC | 765739 | c.2370G>T | synonymous_variant | 0.24 |
rpoC | 765751 | c.2382C>G | synonymous_variant | 0.21 |
rpoC | 765753 | p.Asp795Ala | missense_variant | 0.21 |
rpoC | 765772 | c.2403C>G | synonymous_variant | 0.18 |
rpoC | 765778 | c.2409C>G | synonymous_variant | 0.19 |
rpoC | 765793 | c.2424C>G | synonymous_variant | 0.15 |
rpoC | 765811 | c.2442T>G | synonymous_variant | 0.16 |
rpoC | 765826 | c.2457T>C | synonymous_variant | 0.15 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 0.16 |
rpoC | 765883 | c.2514C>G | synonymous_variant | 0.16 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.16 |
rpoC | 766312 | c.2943T>G | synonymous_variant | 0.13 |
rpoC | 766408 | c.3039C>T | synonymous_variant | 0.13 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.14 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.18 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.22 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.22 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 0.18 |
rpoC | 766864 | c.3495G>C | synonymous_variant | 0.19 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.15 |
rpoC | 767009 | p.Ser1214Arg | missense_variant | 0.15 |
rpoC | 767014 | c.3645G>C | synonymous_variant | 0.16 |
rpoC | 767033 | c.3664_3666delTCGinsAGT | synonymous_variant | 0.25 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.28 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.28 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.23 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.24 |
rpoC | 767134 | c.3765C>A | synonymous_variant | 0.21 |
rpoC | 767167 | c.3798C>G | synonymous_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776288 | c.2193C>G | synonymous_variant | 1.0 |
mmpS5 | 778701 | p.Ile69Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.17 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.15 |
rpsL | 781769 | c.210G>A | synonymous_variant | 0.15 |
rpsL | 781808 | c.249C>T | synonymous_variant | 0.15 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.15 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.14 |
rpsL | 781838 | c.279G>C | synonymous_variant | 0.16 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.13 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.14 |
rplC | 800690 | c.-119C>T | upstream_gene_variant | 0.22 |
rplC | 800693 | c.-116A>C | upstream_gene_variant | 0.21 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.18 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.18 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.15 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.16 |
rplC | 800738 | c.-71T>C | upstream_gene_variant | 0.14 |
rplC | 800747 | c.-62C>G | upstream_gene_variant | 0.15 |
rplC | 801166 | p.Gly120Ser | missense_variant | 0.9 |
fbiC | 1303740 | c.810C>T | synonymous_variant | 0.15 |
fbiC | 1303746 | c.816T>C | synonymous_variant | 0.14 |
fbiC | 1303752 | c.822A>G | synonymous_variant | 0.15 |
fbiC | 1303755 | c.825T>C | synonymous_variant | 0.15 |
fbiC | 1303761 | c.831T>C | synonymous_variant | 0.19 |
fbiC | 1303785 | c.855G>C | synonymous_variant | 0.22 |
fbiC | 1303788 | c.858T>C | synonymous_variant | 0.22 |
fbiC | 1303789 | p.Ile287Val | missense_variant | 0.22 |
fbiC | 1303794 | c.864A>G | synonymous_variant | 0.19 |
fbiC | 1303800 | c.870G>T | synonymous_variant | 0.22 |
fbiC | 1303818 | c.888C>G | synonymous_variant | 0.24 |
fbiC | 1303846 | p.Phe306Val | missense_variant | 0.19 |
fbiC | 1303854 | c.924T>C | synonymous_variant | 0.19 |
fbiC | 1303860 | c.930A>C | synonymous_variant | 0.19 |
fbiC | 1303869 | c.939T>C | synonymous_variant | 0.19 |
fbiC | 1303881 | c.951G>C | synonymous_variant | 0.21 |
fbiC | 1303884 | c.954T>G | synonymous_variant | 0.22 |
fbiC | 1303890 | c.960G>A | synonymous_variant | 0.2 |
fbiC | 1303897 | c.967C>T | synonymous_variant | 0.23 |
fbiC | 1303905 | c.975G>C | synonymous_variant | 0.16 |
fbiC | 1303908 | c.978C>G | synonymous_variant | 0.16 |
fbiC | 1303913 | p.Gly328Ala | missense_variant | 0.15 |
fbiC | 1303947 | c.1017T>G | synonymous_variant | 0.16 |
fbiC | 1303948 | p.Gly340Arg | missense_variant | 0.16 |
fbiC | 1303956 | c.1026A>G | synonymous_variant | 0.16 |
fbiC | 1303961 | p.Arg344Leu | missense_variant | 0.14 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473813 | n.156C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1473839 | n.182G>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1473971 | n.314G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473981 | n.324_325insT | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474009 | n.352A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474012 | n.355C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474036 | n.379G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474040 | n.383G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474054 | n.397T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474823 | n.1166C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475006 | n.1349A>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475028 | n.1371G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475638 | n.1981C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475659 | n.2002G>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.17 |
inhA | 1674690 | c.489C>G | synonymous_variant | 0.17 |
inhA | 1674703 | c.502T>C | synonymous_variant | 0.17 |
inhA | 1674708 | c.507G>A | synonymous_variant | 0.18 |
inhA | 1674718 | c.517A>C | synonymous_variant | 0.14 |
inhA | 1674729 | c.528G>C | synonymous_variant | 0.17 |
inhA | 1674883 | p.Ile228Val | missense_variant | 0.91 |
rpsA | 1833595 | c.54T>G | synonymous_variant | 0.16 |
rpsA | 1833667 | c.126C>G | synonymous_variant | 0.15 |
rpsA | 1833703 | c.162C>T | synonymous_variant | 0.17 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.16 |
rpsA | 1833940 | c.399C>G | synonymous_variant | 0.18 |
rpsA | 1833971 | c.430C>T | synonymous_variant | 0.17 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.17 |
rpsA | 1833997 | c.456G>C | synonymous_variant | 0.18 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.2 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.18 |
rpsA | 1834294 | c.753G>T | synonymous_variant | 0.14 |
rpsA | 1834297 | c.756C>G | synonymous_variant | 0.14 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.19 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 0.18 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.19 |
rpsA | 1834369 | c.828C>G | synonymous_variant | 0.19 |
rpsA | 1834375 | c.834G>A | synonymous_variant | 0.17 |
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 |
katG | 2154917 | p.Glu399Lys | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167983 | p.Gly877Asp | missense_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.21 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.19 |
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 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 1.0 |
thyX | 3067349 | c.597G>C | synonymous_variant | 0.13 |
thyX | 3067355 | c.591A>G | synonymous_variant | 0.14 |
thyX | 3067817 | c.129C>T | synonymous_variant | 0.96 |
ald | 3086788 | c.-32T>C | upstream_gene_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 |
fbiB | 3642173 | c.639G>A | synonymous_variant | 1.0 |
rpoA | 3877542 | c.966C>T | synonymous_variant | 0.17 |
rpoA | 3877553 | p.Glu319Gln | missense_variant | 0.19 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.21 |
rpoA | 3877599 | c.909G>A | synonymous_variant | 0.18 |
rpoA | 3877656 | c.852T>C | synonymous_variant | 0.16 |
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 | 0.17 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.2 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.2 |
rpoA | 3877857 | c.651G>A | synonymous_variant | 0.26 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.25 |
rpoA | 3877872 | c.636C>T | synonymous_variant | 0.27 |
rpoA | 3877875 | c.633T>C | synonymous_variant | 0.29 |
rpoA | 3877896 | c.612G>C | synonymous_variant | 0.23 |
rpoA | 3877900 | p.Ser203Asn | missense_variant | 0.2 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.19 |
rpoA | 3877909 | p.Asn200Ser | missense_variant | 0.17 |
rpoA | 3877920 | c.588G>C | synonymous_variant | 0.17 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.13 |
rpoA | 3877965 | c.543C>T | synonymous_variant | 0.14 |
rpoA | 3878076 | c.432C>T | synonymous_variant | 0.14 |
rpoA | 3878082 | c.426T>C | synonymous_variant | 0.15 |
rpoA | 3878094 | c.414C>G | synonymous_variant | 0.18 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.17 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.14 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.16 |
rpoA | 3878687 | c.-180A>C | upstream_gene_variant | 1.0 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.14 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.16 |
clpC1 | 4038911 | c.1794G>C | synonymous_variant | 0.16 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 0.15 |
clpC1 | 4038932 | c.1773G>C | synonymous_variant | 0.15 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.15 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.17 |
clpC1 | 4039034 | c.1671C>G | synonymous_variant | 0.18 |
clpC1 | 4039037 | c.1668T>C | synonymous_variant | 0.17 |
clpC1 | 4039064 | c.1641C>T | synonymous_variant | 0.17 |
clpC1 | 4039094 | c.1611C>G | synonymous_variant | 0.17 |
clpC1 | 4039103 | c.1602T>C | synonymous_variant | 0.15 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.15 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.15 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.17 |
clpC1 | 4040042 | c.663C>T | synonymous_variant | 0.17 |
clpC1 | 4040048 | c.657C>T | synonymous_variant | 0.18 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 0.97 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 0.86 |
embC | 4241047 | c.1185C>A | synonymous_variant | 0.14 |
embC | 4241050 | c.1188T>G | synonymous_variant | 0.14 |
embC | 4241053 | c.1191G>C | synonymous_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243848 | p.Val206Met | missense_variant | 1.0 |
embA | 4244612 | c.1380C>G | synonymous_variant | 0.16 |
embA | 4244615 | c.1383G>C | synonymous_variant | 0.17 |
embA | 4244619 | c.1387T>C | synonymous_variant | 0.17 |
embA | 4244631 | p.Thr467Leu | missense_variant | 0.15 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338613 | c.-92G>A | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407780 | c.423G>A | synonymous_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 0.96 |
Rv3083 | 3432818 | c.-15685_*836del | transcript_ablation | 1.0 |