Run ID: SRR18003030
Sample name:
Date: 03-04-2023 19:14:50
Number of reads: 1113073
Percentage reads mapped: 33.51
Strain: lineage2.2.1
Drug-resistance: Pre-XDR-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 | 1.0 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7582 | p.Asp94Gly | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761127 | p.Ser441Ala | missense_variant | 0.28 | rifampicin |
rpoB | 761155 | p.Ser450Tyr | missense_variant | 0.21 | rifampicin |
rpoB | 761196 | p.Leu464Met | missense_variant | 0.27 | rifampicin |
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.72 | streptomycin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.27 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.94 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.91 | kanamycin, capreomycin, aminoglycosides, amikacin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9194 | c.1893G>A | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 575927 | p.Pro194Ser | missense_variant | 0.13 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.33 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 761001 | p.Thr399Ala | missense_variant | 0.1 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 0.27 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.27 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 0.23 |
rpoB | 761150 | c.1344A>T | synonymous_variant | 0.26 |
rpoB | 761159 | c.1353G>T | synonymous_variant | 0.21 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.26 |
rpoB | 761168 | c.1362C>T | synonymous_variant | 0.22 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.22 |
rpoB | 761186 | p.Glu460Asp | missense_variant | 0.21 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.24 |
rpoB | 761192 | c.1386C>A | synonymous_variant | 0.21 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.26 |
rpoB | 761201 | c.1395G>A | synonymous_variant | 0.23 |
rpoB | 761204 | c.1398C>T | synonymous_variant | 0.25 |
rpoB | 761207 | c.1401C>A | synonymous_variant | 0.22 |
rpoB | 761219 | c.1413G>C | synonymous_variant | 0.28 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.24 |
rpoB | 761243 | c.1437G>C | synonymous_variant | 0.17 |
rpoB | 761246 | c.1440C>T | synonymous_variant | 0.21 |
rpoB | 761600 | c.1794T>A | synonymous_variant | 0.18 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763055 | p.Leu1083Phe | missense_variant | 0.12 |
rpoC | 763058 | c.-312C>G | upstream_gene_variant | 0.12 |
rpoB | 763059 | p.Ile1085Val | missense_variant | 0.12 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.12 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.22 |
rpoC | 763578 | p.Phe70Tyr | missense_variant | 0.16 |
rpoC | 763585 | c.216C>G | synonymous_variant | 0.25 |
rpoC | 763589 | p.Ile74Val | missense_variant | 0.29 |
rpoC | 763606 | c.237C>G | synonymous_variant | 0.29 |
rpoC | 763609 | c.240C>G | synonymous_variant | 0.29 |
rpoC | 763615 | c.246G>C | synonymous_variant | 0.33 |
rpoC | 763622 | p.Ala85Ser | missense_variant | 0.37 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.35 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.28 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.33 |
rpoC | 763647 | p.Gly93Ala | missense_variant | 0.25 |
rpoC | 763655 | p.Glu96Lys | missense_variant | 0.24 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.29 |
rpoC | 763663 | c.294C>G | synonymous_variant | 0.24 |
rpoC | 763672 | c.303C>G | synonymous_variant | 0.22 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.21 |
rpoC | 763699 | c.330G>C | synonymous_variant | 0.17 |
rpoC | 763708 | c.339G>T | synonymous_variant | 0.17 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.12 |
rpoC | 764185 | c.816C>T | synonymous_variant | 0.13 |
rpoC | 764560 | c.1191T>G | synonymous_variant | 0.11 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.12 |
rpoC | 764722 | c.1353G>C | synonymous_variant | 0.42 |
rpoC | 764731 | c.1362G>C | synonymous_variant | 0.4 |
rpoC | 764737 | c.1368G>C | synonymous_variant | 0.41 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.5 |
rpoC | 764755 | p.Asp462Glu | missense_variant | 0.5 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.5 |
rpoC | 764760 | p.Asn464Ser | missense_variant | 0.5 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.5 |
rpoC | 764767 | c.1398G>T | synonymous_variant | 0.49 |
rpoC | 764776 | c.1407C>T | synonymous_variant | 0.5 |
rpoC | 764797 | c.1428G>T | synonymous_variant | 0.56 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.59 |
rpoC | 764804 | p.Gln479Phe | missense_variant | 0.59 |
rpoC | 764812 | c.1443C>G | synonymous_variant | 0.57 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.61 |
rpoC | 764818 | c.1449G>T | synonymous_variant | 0.59 |
rpoC | 764827 | c.1458G>T | synonymous_variant | 0.62 |
rpoC | 764830 | c.1461C>G | synonymous_variant | 0.56 |
rpoC | 764839 | c.1470C>T | synonymous_variant | 0.54 |
rpoC | 764854 | c.1485G>C | synonymous_variant | 0.5 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.46 |
rpoC | 764869 | c.1500C>T | synonymous_variant | 0.32 |
rpoC | 764875 | c.1506C>T | synonymous_variant | 0.18 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800897 | p.Lys30Arg | missense_variant | 0.12 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471845 | n.-1G>A | upstream_gene_variant | 0.17 |
rrs | 1471979 | n.134T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472080 | n.235G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472282 | n.437T>G | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472284 | n.439C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472293 | n.448C>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472297 | n.453_465delGTCCGGGTTCTCT | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472332 | n.487A>G | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472333 | n.488G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472338 | n.493A>G | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472396 | n.551A>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472426 | n.581T>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472438 | n.593T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472439 | n.594C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472447 | n.602C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472450 | n.605A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472451 | n.606C>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472461 | n.616G>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472462 | n.617T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472476 | n.631A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472496 | n.651T>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472513 | n.668T>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472549 | n.704G>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472597 | n.752G>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472674 | n.829T>G | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472675 | n.830T>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473270 | n.1425G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473305 | n.1460G>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474124 | n.467G>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474125 | n.468C>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474130 | n.473C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474141 | n.484G>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474142 | n.485C>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474155 | n.498G>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474164 | n.507C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474171 | n.514C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474182 | n.525C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474183 | n.526T>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474185 | n.528G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474199 | n.542G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474202 | n.545T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474275 | n.618T>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474280 | n.623C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474281 | n.624A>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474284 | n.631_633delCCT | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474293 | n.637_651delCCTCTCCGGAGGAGG | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474316 | n.659T>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474317 | n.660G>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474353 | n.696A>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474354 | n.697C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474383 | n.726G>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1474454 | n.797G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474476 | n.819C>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474496 | n.839C>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.79 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.81 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474558 | n.901G>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474584 | n.927C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474627 | n.970G>A | non_coding_transcript_exon_variant | 0.87 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1474674 | n.1017A>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474675 | n.1018C>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1474676 | n.1019T>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474694 | n.1037C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474709 | n.1053_1056delTGGT | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474717 | n.1060_1061insGTGAG | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474723 | n.1066G>A | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474734 | n.1077G>A | non_coding_transcript_exon_variant | 0.87 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1474751 | n.1094G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474777 | n.1120T>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.79 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474783 | n.1126G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474802 | n.1145T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1474830 | n.1173A>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474831 | n.1174A>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474837 | n.1180A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474883 | n.1226T>C | non_coding_transcript_exon_variant | 0.81 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475124 | n.1467A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475171 | n.1514C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475672 | n.2015C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475673 | n.2016T>C | non_coding_transcript_exon_variant | 0.72 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475751 | n.2094C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475752 | n.2095C>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475758 | n.2101A>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1475963 | n.2306G>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475993 | n.2336C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475998 | n.2341C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476040 | n.2383C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476076 | n.2419A>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476110 | n.2453G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476130 | n.2473G>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476195 | n.2538C>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476253 | n.2596A>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476297 | n.2640C>A | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476299 | n.2642C>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476300 | n.2643G>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476308 | n.2651G>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476528 | n.2871A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476586 | n.2929C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476594 | n.2937C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476603 | n.2946G>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476613 | n.2956G>A | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476624 | n.2967T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476628 | n.2971T>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.69 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.26 |
rpsA | 1833955 | c.414G>C | synonymous_variant | 0.32 |
rpsA | 1833970 | c.429G>T | synonymous_variant | 0.28 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.4 |
rpsA | 1833991 | c.450C>A | synonymous_variant | 0.3 |
rpsA | 1833994 | c.453G>C | synonymous_variant | 0.43 |
rpsA | 1833997 | c.456G>C | synonymous_variant | 0.28 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.4 |
rpsA | 1834012 | c.471G>T | synonymous_variant | 0.32 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.41 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.14 |
rpsA | 1834024 | c.483G>C | synonymous_variant | 0.43 |
rpsA | 1834025 | p.Gln162Ala | missense_variant | 0.29 |
rpsA | 1834033 | c.492C>T | synonymous_variant | 0.15 |
rpsA | 1834034 | p.Ile165Val | missense_variant | 0.15 |
rpsA | 1834040 | p.Lys167Arg | missense_variant | 0.46 |
rpsA | 1834043 | p.Glu168Gln | missense_variant | 0.3 |
rpsA | 1834046 | p.Ile169Leu | missense_variant | 0.44 |
rpsA | 1834051 | c.510G>A | synonymous_variant | 0.29 |
rpsA | 1834054 | c.513C>T | synonymous_variant | 0.28 |
rpsA | 1834060 | c.519C>T | synonymous_variant | 0.28 |
rpsA | 1834090 | c.549G>T | synonymous_variant | 0.16 |
rpsA | 1834093 | c.552G>T | synonymous_variant | 0.19 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.11 |
rpsA | 1834285 | c.744G>C | synonymous_variant | 0.14 |
rpsA | 1834294 | c.753G>T | synonymous_variant | 0.15 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.15 |
rpsA | 1834305 | c.765_767delTGA | disruptive_inframe_deletion | 0.14 |
rpsA | 1834310 | p.Glu257Gln | missense_variant | 0.14 |
rpsA | 1834312 | c.771_772insCCC | conservative_inframe_insertion | 0.14 |
rpsA | 1834333 | p.Asp264Glu | missense_variant | 0.12 |
rpsA | 1834336 | c.795C>G | synonymous_variant | 0.12 |
rpsA | 1834340 | p.Met267Leu | missense_variant | 0.12 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.12 |
rpsA | 1834354 | c.813G>C | synonymous_variant | 0.12 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 0.12 |
rpsA | 1834360 | c.819G>C | synonymous_variant | 0.12 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.13 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.12 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102955 | p.Ala30Thr | missense_variant | 0.18 |
ndh | 2102976 | p.Gly23Arg | missense_variant | 0.17 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170110 | p.Phe168Tyr | missense_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289559 | c.-318T>G | upstream_gene_variant | 1.0 |
kasA | 2517966 | c.-149G>A | upstream_gene_variant | 0.13 |
folC | 2747615 | c.-17C>T | upstream_gene_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
rpoA | 3878567 | c.-60C>G | upstream_gene_variant | 0.25 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.27 |
clpC1 | 4039714 | p.Tyr331His | missense_variant | 0.31 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.3 |
clpC1 | 4039730 | c.975C>G | synonymous_variant | 0.29 |
clpC1 | 4039733 | c.972G>C | synonymous_variant | 0.3 |
clpC1 | 4039739 | c.966C>A | synonymous_variant | 0.29 |
clpC1 | 4039742 | c.963C>T | synonymous_variant | 0.3 |
clpC1 | 4039748 | c.957G>C | synonymous_variant | 0.33 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.32 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.33 |
clpC1 | 4039760 | c.945T>C | synonymous_variant | 0.33 |
clpC1 | 4039763 | c.942C>A | synonymous_variant | 0.33 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.34 |
clpC1 | 4039773 | p.Lys311Met | missense_variant | 0.33 |
clpC1 | 4039775 | c.930G>C | synonymous_variant | 0.31 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.33 |
clpC1 | 4039781 | c.924G>C | synonymous_variant | 0.33 |
clpC1 | 4039787 | c.918G>C | synonymous_variant | 0.42 |
clpC1 | 4039799 | c.906C>T | synonymous_variant | 0.38 |
clpC1 | 4039808 | c.897G>A | synonymous_variant | 0.4 |
clpC1 | 4039817 | c.888A>T | synonymous_variant | 0.48 |
clpC1 | 4039820 | c.885T>C | synonymous_variant | 0.46 |
clpC1 | 4039826 | c.879C>G | synonymous_variant | 0.37 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 0.42 |
clpC1 | 4039838 | p.Leu289Ile | missense_variant | 0.3 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.35 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.4 |
clpC1 | 4039873 | p.Thr278Ser | missense_variant | 0.37 |
clpC1 | 4039875 | p.Asn277Arg | missense_variant | 0.42 |
clpC1 | 4039877 | c.828C>T | synonymous_variant | 0.44 |
clpC1 | 4039886 | c.819C>G | synonymous_variant | 0.49 |
clpC1 | 4039889 | c.816G>C | synonymous_variant | 0.49 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.48 |
clpC1 | 4039919 | c.786C>T | synonymous_variant | 0.5 |
clpC1 | 4039929 | c.775_776delAGinsTC | synonymous_variant | 0.47 |
clpC1 | 4039934 | c.771G>C | synonymous_variant | 0.49 |
clpC1 | 4039940 | c.765G>C | synonymous_variant | 0.47 |
clpC1 | 4039943 | c.762G>C | synonymous_variant | 0.44 |
clpC1 | 4039946 | c.759A>C | synonymous_variant | 0.52 |
clpC1 | 4039949 | c.756G>C | synonymous_variant | 0.53 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.55 |
clpC1 | 4039964 | c.741C>G | synonymous_variant | 0.57 |
clpC1 | 4039967 | p.Gln246His | missense_variant | 0.56 |
clpC1 | 4039973 | c.732C>T | synonymous_variant | 0.55 |
clpC1 | 4039982 | c.723G>C | synonymous_variant | 0.54 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 0.56 |
clpC1 | 4039994 | p.Glu237Asp | missense_variant | 0.56 |
clpC1 | 4039997 | c.708C>T | synonymous_variant | 0.52 |
clpC1 | 4040015 | c.690G>C | synonymous_variant | 0.51 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.45 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.42 |
clpC1 | 4040027 | c.678C>T | synonymous_variant | 0.39 |
clpC1 | 4040030 | c.675C>G | synonymous_variant | 0.4 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.43 |
clpC1 | 4040042 | c.663C>T | synonymous_variant | 0.42 |
clpC1 | 4040045 | c.660C>G | synonymous_variant | 0.44 |
clpC1 | 4040048 | c.657C>T | synonymous_variant | 0.45 |
clpC1 | 4040069 | c.636G>C | synonymous_variant | 0.44 |
clpC1 | 4040087 | c.618G>C | synonymous_variant | 0.39 |
clpC1 | 4040096 | c.609G>T | synonymous_variant | 0.36 |
clpC1 | 4040108 | c.597G>C | synonymous_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.17 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.17 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.17 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.2 |
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 | 4407927 | p.Glu92Asp | missense_variant | 1.0 |