Run ID: ERR4820107
Sample name:
Date: 01-04-2023 16:29:19
Number of reads: 527249
Percentage reads mapped: 38.91
Strain:
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 0.99 |
lineage1.2.1.2 | Indo-Oceanic | NA | RD239 | 0.97 |
lineage1.2.1.2.1 | Indo-Oceanic | NA | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761127 | p.Ser441Ala | missense_variant | 0.31 | rifampicin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.83 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.19 | kanamycin, capreomycin, aminoglycosides, amikacin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9260 | c.1959G>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575368 | c.21T>C | synonymous_variant | 1.0 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.36 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 0.23 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.29 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.21 |
rpoB | 761154 | c.1348_1350delTCGinsAGC | synonymous_variant | 0.21 |
rpoB | 761159 | c.1353G>C | synonymous_variant | 0.14 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.2 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.15 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.18 |
rpoB | 762017 | p.Glu737Asp | missense_variant | 0.13 |
rpoB | 762024 | p.Val740Met | missense_variant | 0.13 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.14 |
rpoB | 762057 | p.Ile751Val | missense_variant | 0.13 |
rpoB | 762110 | c.2304G>C | synonymous_variant | 0.16 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.17 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.17 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.19 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.15 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.23 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 0.12 |
rpoC | 762887 | c.-483G>C | upstream_gene_variant | 0.13 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.12 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.14 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.12 |
rpoC | 762938 | c.-432G>C | upstream_gene_variant | 0.18 |
rpoC | 762980 | c.-390T>C | upstream_gene_variant | 0.2 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.29 |
rpoC | 763067 | c.-303C>G | upstream_gene_variant | 0.22 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.22 |
rpoB | 763077 | p.Val1091Thr | missense_variant | 0.25 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.18 |
rpoC | 763109 | c.-261C>T | upstream_gene_variant | 0.2 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.2 |
rpoB | 763119 | p.Asn1105Asp | missense_variant | 0.2 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.22 |
rpoC | 763133 | c.-237G>C | upstream_gene_variant | 0.22 |
rpoC | 763504 | c.135C>A | synonymous_variant | 0.15 |
rpoC | 763507 | c.138G>C | synonymous_variant | 0.15 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.27 |
rpoC | 763531 | c.162G>C | synonymous_variant | 1.0 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.21 |
rpoC | 763537 | c.168C>G | synonymous_variant | 0.23 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.27 |
rpoC | 763550 | p.Tyr61Ala | missense_variant | 0.33 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.23 |
rpoC | 763578 | p.Phe70Tyr | missense_variant | 0.21 |
rpoC | 763585 | c.216C>G | synonymous_variant | 0.14 |
rpoC | 763598 | p.Arg77Ser | missense_variant | 0.15 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.19 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.18 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.19 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.19 |
rpoC | 763718 | p.Leu117Val | missense_variant | 0.12 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.18 |
rpoC | 763724 | p.Asp119Asn | missense_variant | 0.18 |
rpoC | 763729 | c.360G>C | synonymous_variant | 0.19 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.19 |
rpoC | 763735 | c.366G>C | synonymous_variant | 0.19 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.17 |
rpoC | 763772 | p.Val135Met | missense_variant | 0.17 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpS5 | 779505 | c.-600A>C | upstream_gene_variant | 0.14 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406312 | c.1029T>C | synonymous_variant | 1.0 |
embR | 1416278 | p.Ile357Thr | missense_variant | 0.25 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
atpE | 1460907 | c.-138T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472150 | n.305T>G | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472338 | n.493A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472412 | n.567A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472416 | n.571C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472427 | n.582T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472506 | n.661A>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472513 | n.668T>C | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472958 | n.1113A>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472974 | n.1129A>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472988 | n.1143T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.46 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473089 | n.1244A>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1473101 | n.1256C>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473109 | n.1264T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473116 | n.1271A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1473147 | n.1302G>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473148 | n.1303G>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473150 | n.1305T>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473161 | n.1316A>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473163 | n.1318C>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473164 | n.1319C>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.34 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473248 | n.1403G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473249 | n.1404T>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.84 |
rrs | 1473255 | n.1410A>G | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473260 | n.1415G>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473270 | n.1425G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473300 | n.1455C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473305 | n.1460G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474163 | n.506C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474164 | n.507C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474393 | n.736A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474402 | n.745T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474406 | n.749T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474437 | n.781_782delAA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474448 | n.791T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474492 | n.835A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474520 | n.863A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474525 | n.868A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474540 | n.883T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474658 | n.1001A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474692 | n.1035G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474802 | n.1145T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474831 | n.1174A>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474832 | n.1175A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474837 | n.1180A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475104 | n.1447T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475124 | n.1467A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475171 | n.1514C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475172 | n.1515A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475754 | n.2097G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475756 | n.2099T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475772 | n.2115A>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475774 | n.2117C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475879 | n.2222T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.91 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1475892 | n.2235A>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475902 | n.2245T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476179 | n.2522C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476187 | n.2530T>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476204 | n.2547C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476207 | n.2550T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476235 | n.2578A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476535 | n.2878G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476628 | n.2971T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476633 | n.2976A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476645 | n.2988A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476664 | n.3007T>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476668 | n.3011C>T | non_coding_transcript_exon_variant | 0.67 |
inhA | 1674162 | c.-40C>T | upstream_gene_variant | 1.0 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.15 |
rpsA | 1833732 | p.Pro64Leu | missense_variant | 0.14 |
rpsA | 1833736 | c.195C>T | synonymous_variant | 0.15 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.14 |
rpsA | 1833770 | p.Asn77Asp | missense_variant | 0.17 |
rpsA | 1833776 | p.Val79Ile | missense_variant | 0.15 |
rpsA | 1833781 | c.240T>C | synonymous_variant | 0.15 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.15 |
rpsA | 1833797 | p.Val86Ile | missense_variant | 0.17 |
rpsA | 1833994 | c.453G>C | synonymous_variant | 0.11 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.11 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.2 |
rpsA | 1834034 | p.Ile165Val | missense_variant | 0.2 |
rpsA | 1834040 | p.Lys167Arg | missense_variant | 0.13 |
rpsA | 1834046 | p.Ile169Leu | missense_variant | 0.21 |
rpsA | 1834054 | c.513C>G | synonymous_variant | 0.13 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.15 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 0.12 |
rpsA | 1834210 | c.669C>T | synonymous_variant | 0.14 |
rpsA | 1834219 | c.678C>G | synonymous_variant | 0.14 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.14 |
rpsA | 1834225 | c.684C>G | synonymous_variant | 0.23 |
rpsA | 1834228 | c.687C>T | synonymous_variant | 0.15 |
rpsA | 1834246 | c.705G>T | synonymous_variant | 0.14 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.15 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.15 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.14 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.18 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.22 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.2 |
rpsA | 1834427 | p.Ile296Val | missense_variant | 0.2 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.27 |
rpsA | 1834451 | c.910_912delTTGinsCTC | synonymous_variant | 0.25 |
rpsA | 1834456 | c.915T>C | synonymous_variant | 0.25 |
rpsA | 1834459 | c.918G>C | synonymous_variant | 0.25 |
rpsA | 1834465 | c.924T>C | synonymous_variant | 0.25 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.25 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918704 | c.765A>G | synonymous_variant | 0.2 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290226 | c.-985T>C | upstream_gene_variant | 0.18 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2519048 | p.Gly312Ser | missense_variant | 1.0 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
folC | 2746167 | p.Ala478Ser | missense_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087470 | c.651T>C | synonymous_variant | 0.2 |
fbiD | 3339417 | c.300A>G | synonymous_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 |
whiB7 | 3568488 | c.191delG | frameshift_variant | 1.0 |
fbiB | 3640557 | c.-978T>C | upstream_gene_variant | 1.0 |
fbiB | 3642441 | p.Pro303Ser | missense_variant | 0.2 |
rpoA | 3878108 | p.Leu134Met | missense_variant | 0.29 |
clpC1 | 4038835 | p.Phe624Leu | missense_variant | 0.13 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243580 | c.348G>A | synonymous_variant | 1.0 |
embA | 4244420 | c.1188G>C | synonymous_variant | 1.0 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4247578 | c.1065G>A | synonymous_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 |
ubiA | 4269864 | c.-32delG | upstream_gene_variant | 1.0 |
whiB6 | 4338361 | p.Arg54Gln | missense_variant | 1.0 |
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 |