Run ID: SRR4033549
Sample name:
Date: 04-04-2023 06:10:06
Number of reads: 1341117
Percentage reads mapped: 81.76
Strain: lineage2.2.2
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 0.99 |
lineage2.2.2 | East-Asian (Beijing) | Beijing-RD105/RD207 | RD105;RD207 | 0.96 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.33 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.26 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.13 | kanamycin, capreomycin, aminoglycosides, amikacin |
katG | 2155388 | c.723delC | frameshift_variant | 0.13 | isoniazid |
ethA | 4326333 | p.Ala381Pro | missense_variant | 1.0 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8896 | p.Asp532Val | missense_variant | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491027 | p.Asn82Thr | missense_variant | 0.13 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 760206 | p.Ile134Val | missense_variant | 0.11 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.12 |
rpoB | 760244 | c.438G>C | synonymous_variant | 0.1 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.1 |
rpoB | 761799 | p.Arg665Trp | missense_variant | 0.13 |
rpoB | 761961 | p.Pro719Ser | missense_variant | 0.13 |
rpoB | 762030 | p.Thr742Ser | missense_variant | 0.13 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.11 |
rpoB | 762057 | p.Ile751Val | missense_variant | 0.1 |
rpoB | 762065 | c.2259T>G | synonymous_variant | 0.11 |
rpoB | 762098 | c.2292C>G | synonymous_variant | 0.11 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.12 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.13 |
rpoB | 762308 | c.2502G>A | synonymous_variant | 0.11 |
rpoB | 762487 | p.Pro894Leu | missense_variant | 0.12 |
rpoC | 762551 | c.-819C>A | upstream_gene_variant | 0.11 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.14 |
rpoC | 762887 | c.-483G>C | upstream_gene_variant | 0.15 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.18 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 0.22 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.2 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.2 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.13 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.12 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763044 | p.Gln1080Lys | missense_variant | 0.11 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.14 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.14 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.13 |
rpoB | 763130 | p.Glu1108Asp | missense_variant | 0.13 |
rpoB | 763131 | p.Pro1109Ser | missense_variant | 0.13 |
rpoC | 763142 | c.-228C>G | upstream_gene_variant | 0.12 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.12 |
rpoC | 763157 | c.-213G>C | upstream_gene_variant | 0.1 |
rpoC | 763618 | c.249C>G | synonymous_variant | 0.18 |
rpoC | 763622 | p.Ala85Ser | missense_variant | 0.17 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.17 |
rpoC | 763660 | c.291T>C | synonymous_variant | 0.15 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.19 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.15 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.14 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.14 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.16 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.16 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 0.12 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801137 | p.Ser110Asn | missense_variant | 0.12 |
Rv1258c | 1406722 | p.Gly207Trp | missense_variant | 0.15 |
embR | 1416485 | p.Ala288Glu | missense_variant | 0.12 |
embR | 1417294 | c.54A>C | synonymous_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472148 | n.303T>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472496 | n.651T>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472583 | n.738T>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472674 | n.829T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472685 | n.840G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472701 | n.856T>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473122 | n.1277T>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.41 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.24 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.1 |
rrl | 1474201 | n.544T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474202 | n.545T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474280 | n.623C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474281 | n.624A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474476 | n.819C>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474483 | n.826C>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474528 | n.871T>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474529 | n.872A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474540 | n.883T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474541 | n.884G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474551 | n.894G>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474558 | n.901G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474583 | n.926C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474627 | n.970G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474709 | n.1053delT | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474714 | n.1058delT | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.39 |
rrl | 1474777 | n.1120T>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475060 | n.1404delC | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475065 | n.1408G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475067 | n.1410A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475068 | n.1411A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475076 | n.1419C>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475078 | n.1421T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475079 | n.1422T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475081 | n.1424C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475104 | n.1447T>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475113 | n.1456C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475116 | n.1459G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475124 | n.1467A>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475129 | n.1472G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475174 | n.1517C>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475176 | n.1519G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475602 | n.1945G>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475604 | n.1950_1951delAT | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475608 | n.1951T>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475621 | n.1964T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475649 | n.1992A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475655 | n.1998T>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475752 | n.2095C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1475756 | n.2099T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475764 | n.2107A>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475776 | n.2119G>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.37 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.37 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.41 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475997 | n.2340A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476179 | n.2522C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476523 | n.2866T>C | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.49 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.49 |
rrl | 1476661 | n.3004A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476665 | n.3008T>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476668 | n.3011C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476675 | n.3018C>G | non_coding_transcript_exon_variant | 0.15 |
fabG1 | 1673962 | p.Asn175Asp | missense_variant | 0.13 |
rpsA | 1833646 | c.105T>C | synonymous_variant | 0.14 |
rpsA | 1833667 | c.126C>G | synonymous_variant | 0.17 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.19 |
rpsA | 1833685 | c.144G>C | synonymous_variant | 0.17 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.19 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.15 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.15 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.11 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.11 |
rpsA | 1834009 | c.468C>T | synonymous_variant | 0.12 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.19 |
rpsA | 1834024 | c.483G>C | synonymous_variant | 0.25 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.22 |
rpsA | 1834034 | p.Ile165Val | missense_variant | 0.22 |
rpsA | 1834054 | c.513C>G | synonymous_variant | 0.23 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.19 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834210 | c.669C>T | synonymous_variant | 0.17 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.18 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 0.2 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.18 |
rpsA | 1834243 | c.702G>C | synonymous_variant | 0.18 |
tlyA | 1917872 | c.-68T>G | upstream_gene_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102350 | c.693G>A | synonymous_variant | 0.18 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155248 | c.864C>A | synonymous_variant | 0.13 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.23 |
Rv1979c | 2221939 | p.Arg409Gln | missense_variant | 1.0 |
Rv1979c | 2222976 | c.189C>T | synonymous_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518601 | p.Gly163Trp | missense_variant | 0.13 |
eis | 2714668 | c.659_664delCCGACG | disruptive_inframe_deletion | 0.15 |
folC | 2746386 | p.His405Asn | missense_variant | 0.14 |
ribD | 2986962 | p.Arg42Trp | missense_variant | 0.13 |
thyX | 3067660 | p.His96Asn | missense_variant | 0.12 |
thyX | 3067802 | c.144C>A | synonymous_variant | 0.18 |
thyX | 3068036 | c.-92delC | upstream_gene_variant | 0.15 |
thyA | 3074064 | c.407delG | frameshift_variant | 0.17 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087095 | c.277delA | frameshift_variant | 0.1 |
fbiD | 3339222 | c.105C>A | synonymous_variant | 0.22 |
Rv3083 | 3448384 | c.-120_-119insCC | upstream_gene_variant | 0.12 |
Rv3083 | 3449106 | c.603C>T | synonymous_variant | 0.15 |
Rv3083 | 3449676 | c.1173C>A | synonymous_variant | 0.15 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
clpC1 | 4038163 | c.2542C>A | synonymous_variant | 0.29 |
clpC1 | 4039541 | c.1164C>G | synonymous_variant | 0.1 |
clpC1 | 4039562 | c.1143C>G | synonymous_variant | 0.11 |
clpC1 | 4039568 | p.Met379Ile | missense_variant | 0.1 |
clpC1 | 4039580 | c.1125C>G | synonymous_variant | 0.1 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.12 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 0.1 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.14 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.15 |
clpC1 | 4040036 | c.669C>G | synonymous_variant | 0.17 |
embC | 4240424 | p.Arg188Ser | missense_variant | 0.18 |
embC | 4241036 | c.1174C>T | synonymous_variant | 0.14 |
embC | 4242423 | p.Trp854* | stop_gained | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243274 | c.42C>A | synonymous_variant | 0.15 |
embA | 4243370 | c.138G>A | synonymous_variant | 0.13 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4246192 | c.2964delC | frameshift_variant | 0.14 |
embA | 4246390 | p.Asp1053Val | missense_variant | 0.12 |
embB | 4249333 | c.2820C>A | synonymous_variant | 0.12 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407766 | p.Thr146Lys | missense_variant | 0.13 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |