Run ID: SRR6982239
Sample name:
Date: 04-04-2023 18:31:33
Number of reads: 763917
Percentage reads mapped: 57.55
Strain: lineage4.1.1.3
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.1 | Euro-American (X-type) | X1;X2;X3 | None | 1.0 |
lineage4.1.1.3 | Euro-American (X-type) | X1;X3 | RD193 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2155693 | p.Ser140Asn | missense_variant | 0.14 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.11 |
rpoB | 761138 | c.1332C>G | synonymous_variant | 0.11 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 0.12 |
rpoB | 761150 | c.1344A>T | synonymous_variant | 0.12 |
rpoB | 761154 | p.Ser450Asn | missense_variant | 0.12 |
rpoB | 761162 | c.1356G>C | synonymous_variant | 0.11 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.11 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.12 |
rpoB | 761171 | c.1365C>T | synonymous_variant | 0.12 |
rpoB | 761177 | c.1371G>C | synonymous_variant | 0.11 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.11 |
rpoB | 761189 | c.1383T>G | synonymous_variant | 0.12 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.11 |
rpoB | 761198 | c.1392G>C | synonymous_variant | 0.11 |
rpoB | 762209 | c.2403C>G | synonymous_variant | 0.15 |
rpoB | 762212 | c.2406G>C | synonymous_variant | 0.11 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.11 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.11 |
rpoB | 762236 | c.2430G>C | synonymous_variant | 0.11 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.11 |
rpoB | 762251 | c.2445G>C | synonymous_variant | 0.11 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.12 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.11 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.11 |
rpoC | 762866 | c.-504C>G | upstream_gene_variant | 0.12 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.17 |
rpoC | 762887 | c.-483G>C | upstream_gene_variant | 0.2 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.23 |
rpoB | 762909 | p.Ile1035Leu | missense_variant | 0.22 |
rpoC | 762920 | c.-450C>G | upstream_gene_variant | 0.22 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.21 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.21 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.22 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 0.23 |
rpoC | 762980 | c.-390T>C | upstream_gene_variant | 0.24 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.22 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.21 |
rpoB | 763005 | p.Cys1067Val | missense_variant | 0.21 |
rpoC | 763013 | c.-357C>G | upstream_gene_variant | 0.26 |
rpoB | 763014 | p.Met1070Leu | missense_variant | 0.27 |
rpoB | 763017 | p.Gln1071Glu | missense_variant | 0.27 |
rpoC | 763022 | c.-348C>G | upstream_gene_variant | 0.29 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.24 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.24 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.2 |
rpoB | 763038 | p.Thr1078Ala | missense_variant | 0.22 |
rpoC | 763043 | c.-327G>C | upstream_gene_variant | 0.26 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.28 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.21 |
rpoC | 763088 | c.-282C>G | upstream_gene_variant | 0.2 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.18 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.19 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.19 |
rpoC | 763127 | c.-243G>T | upstream_gene_variant | 0.13 |
rpoC | 763133 | c.-237G>C | upstream_gene_variant | 0.13 |
rpoC | 763462 | c.93G>C | synonymous_variant | 0.16 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.19 |
rpoC | 763483 | c.114G>C | synonymous_variant | 0.18 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.16 |
rpoC | 763492 | c.123G>C | synonymous_variant | 0.18 |
rpoC | 763504 | c.135C>A | synonymous_variant | 0.18 |
rpoC | 763507 | c.138G>C | synonymous_variant | 0.21 |
rpoC | 763528 | c.159G>T | synonymous_variant | 0.22 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.27 |
rpoC | 763537 | c.168C>G | synonymous_variant | 0.27 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.22 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.21 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.21 |
rpoC | 763615 | c.246G>C | synonymous_variant | 0.17 |
rpoC | 763618 | c.249C>T | synonymous_variant | 0.19 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.19 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.25 |
rpoC | 763666 | c.297G>T | synonymous_variant | 0.23 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.15 |
rpoC | 763699 | c.330G>C | synonymous_variant | 0.14 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.14 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.14 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.13 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.14 |
rpoC | 763720 | c.351G>C | synonymous_variant | 0.13 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.14 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.15 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.12 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.11 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 0.11 |
rpoC | 764512 | c.1143G>C | synonymous_variant | 0.13 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.16 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.16 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.16 |
rpoC | 764545 | c.1176C>G | synonymous_variant | 0.16 |
rpoC | 764548 | c.1179G>C | synonymous_variant | 0.16 |
rpoC | 764551 | c.1182G>C | synonymous_variant | 0.16 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.18 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.2 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.22 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.22 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.21 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 0.26 |
rpoC | 764611 | c.1242G>C | synonymous_variant | 0.25 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.22 |
rpoC | 764635 | c.1266C>G | synonymous_variant | 0.22 |
rpoC | 764644 | c.1275G>C | synonymous_variant | 0.2 |
rpoC | 764646 | p.Gly426Ala | missense_variant | 0.21 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.21 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.21 |
rpoC | 764656 | c.1287C>G | synonymous_variant | 0.22 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.24 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 0.25 |
rpoC | 764701 | c.1332C>G | synonymous_variant | 0.25 |
rpoC | 764705 | p.Leu446Ala | missense_variant | 0.23 |
rpoC | 764722 | c.1353G>C | synonymous_variant | 0.23 |
rpoC | 764746 | c.1377G>C | synonymous_variant | 0.21 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.22 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.22 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.2 |
rpoC | 764872 | c.1503A>G | synonymous_variant | 0.1 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 766312 | c.2943T>C | synonymous_variant | 0.11 |
rpoC | 766316 | p.Met983Leu | missense_variant | 0.11 |
rpoC | 766351 | c.2982C>G | synonymous_variant | 0.11 |
rpoC | 766361 | p.Val998Ile | missense_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776107 | p.Leu792Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472148 | n.303T>C | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472293 | n.448C>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472297 | n.453_465delGTCCGGGTTCTCT | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472338 | n.493A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472425 | n.580T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472431 | n.586G>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472437 | n.592T>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472439 | n.594C>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472446 | n.601T>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472450 | n.605A>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472451 | n.606C>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472460 | n.615T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472461 | n.616G>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472462 | n.617T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472466 | n.621C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472467 | n.622G>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472473 | n.628G>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472486 | n.641A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472494 | n.649A>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472496 | n.651T>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472507 | n.662C>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472508 | n.663T>C | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472571 | n.726G>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472583 | n.738T>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472673 | n.828T>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472674 | n.829T>A | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472675 | n.830T>A | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472793 | n.948A>C | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472803 | n.958T>C | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472836 | n.991G>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472840 | n.995A>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472844 | n.999C>A | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472845 | n.1000G>A | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472848 | n.1003T>G | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472850 | n.1005T>C | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472857 | n.1012A>G | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472859 | n.1014G>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472862 | n.1017T>C | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472863 | n.1018T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472873 | n.1028C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472875 | n.1030T>G | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472958 | n.1113A>G | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472968 | n.1125_1128delCGTA | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472974 | n.1129_1130insGCCCCTTCGGGGG | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472977 | n.1132G>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472988 | n.1143T>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472996 | n.1151T>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473026 | n.1181T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1473062 | n.1217T>G | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473068 | n.1223A>G | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473089 | n.1244A>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473091 | n.1246G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473120 | n.1275C>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473122 | n.1277T>A | non_coding_transcript_exon_variant | 0.77 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.76 |
rrs | 1473201 | n.1356A>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473202 | n.1357C>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.61 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.59 |
rrs | 1473283 | n.1438T>C | non_coding_transcript_exon_variant | 0.59 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.54 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1473658 | n.1T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473696 | n.39T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473698 | n.41G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473699 | n.42A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473702 | n.45G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473724 | n.67T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473725 | n.68G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473731 | n.74T>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474179 | n.522C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474186 | n.529A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474232 | n.575C>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474239 | n.582G>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474483 | n.826C>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474497 | n.840G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474507 | n.850G>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 | 0.13 |
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 | 0.16 |
rrl | 1474551 | n.894G>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474558 | n.901G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474628 | n.971C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474651 | n.995delT | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474660 | n.1003G>A | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474662 | n.1005C>G | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474676 | n.1019T>C | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474688 | n.1031G>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474690 | n.1033C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474709 | n.1053_1056delTGGT | non_coding_transcript_exon_variant | 0.59 |
rrl | 1474717 | n.1060_1061insGTGAG | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474722 | n.1065T>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1474751 | n.1094G>A | non_coding_transcript_exon_variant | 0.63 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474777 | n.1120T>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.65 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1474783 | n.1126G>A | non_coding_transcript_exon_variant | 0.65 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1474801 | n.1144G>A | non_coding_transcript_exon_variant | 0.65 |
rrl | 1474802 | n.1145T>C | non_coding_transcript_exon_variant | 0.66 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 0.68 |
rrl | 1474896 | n.1239A>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.37 |
rrl | 1475129 | n.1472G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475171 | n.1514C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475175 | n.1518G>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475649 | n.1992A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475655 | n.1998T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475696 | n.2039T>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1475703 | n.2046A>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475740 | n.2083G>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475747 | n.2090A>G | non_coding_transcript_exon_variant | 0.58 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475758 | n.2101A>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1475760 | n.2103C>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1475761 | n.2105delG | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.61 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475781 | n.2124T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475788 | n.2131C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475882 | n.2225C>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1475883 | n.2226A>G | non_coding_transcript_exon_variant | 0.72 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475902 | n.2245T>C | non_coding_transcript_exon_variant | 0.72 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.73 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1475982 | n.2325G>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476015 | n.2358G>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476025 | n.2368G>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476035 | n.2378_2379insC | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476058 | n.2401T>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476071 | n.2414C>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476076 | n.2419A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476081 | n.2424A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476082 | n.2425T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476087 | n.2430C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476088 | n.2431A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476097 | n.2440C>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476100 | n.2443A>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476103 | n.2446C>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476105 | n.2450delA | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476113 | n.2456T>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476126 | n.2469C>T | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476130 | n.2473G>A | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476165 | n.2508T>A | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476255 | n.2598A>G | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476297 | n.2640C>G | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476298 | n.2641C>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476300 | n.2643G>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476528 | n.2871A>G | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476529 | n.2872A>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476596 | n.2939C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476601 | n.2944G>A | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476628 | n.2971T>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.45 |
rpsA | 1833952 | c.411C>T | synonymous_variant | 0.12 |
rpsA | 1833955 | c.414G>C | synonymous_variant | 0.12 |
rpsA | 1833973 | c.432G>C | synonymous_variant | 0.13 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.13 |
rpsA | 1833985 | c.444G>C | synonymous_variant | 0.15 |
rpsA | 1833988 | c.447C>G | synonymous_variant | 0.15 |
rpsA | 1833994 | c.453G>C | synonymous_variant | 0.15 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.13 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.11 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.11 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155674 | c.438G>C | synonymous_variant | 0.14 |
katG | 2155680 | c.432G>C | synonymous_variant | 0.16 |
katG | 2155689 | c.421_423delTTGinsCTC | synonymous_variant | 0.14 |
katG | 2155696 | p.Ala139Gly | missense_variant | 0.15 |
katG | 2155704 | c.408C>G | synonymous_variant | 0.14 |
katG | 2155716 | c.396T>C | synonymous_variant | 0.15 |
katG | 2155722 | c.390G>C | synonymous_variant | 0.16 |
katG | 2155728 | c.384G>C | synonymous_variant | 0.13 |
katG | 2155735 | p.Met126Gln | missense_variant | 0.12 |
katG | 2155741 | p.Gly124Ala | missense_variant | 0.12 |
katG | 2155743 | c.369G>C | synonymous_variant | 0.12 |
katG | 2155746 | c.366C>G | synonymous_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289989 | c.-748C>A | 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 |
clpC1 | 4039670 | p.Val345Ile | missense_variant | 0.15 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.14 |
clpC1 | 4039697 | c.1008C>G | synonymous_variant | 0.13 |
clpC1 | 4039709 | p.Ile332Leu | missense_variant | 0.13 |
clpC1 | 4039714 | p.Tyr331His | missense_variant | 0.13 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.14 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.11 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.12 |
clpC1 | 4039853 | c.852G>C | synonymous_variant | 0.12 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.18 |
clpC1 | 4039875 | p.Asn277Arg | missense_variant | 0.18 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.2 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.19 |
clpC1 | 4039929 | c.775_776delAGinsTC | synonymous_variant | 0.17 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.17 |
clpC1 | 4039934 | c.771G>C | synonymous_variant | 0.16 |
clpC1 | 4039945 | p.Ser254Ala | missense_variant | 0.16 |
clpC1 | 4039946 | c.759A>C | synonymous_variant | 0.16 |
clpC1 | 4039949 | c.756G>C | synonymous_variant | 0.16 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.17 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.17 |
clpC1 | 4039967 | p.Gln246His | missense_variant | 0.16 |
clpC1 | 4039982 | c.723G>C | synonymous_variant | 0.17 |
clpC1 | 4040000 | p.His235Lys | missense_variant | 0.18 |
clpC1 | 4040003 | c.702G>C | synonymous_variant | 0.18 |
clpC1 | 4040018 | c.687G>C | synonymous_variant | 0.19 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.19 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.18 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.19 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.16 |
clpC1 | 4040063 | c.642G>C | synonymous_variant | 0.16 |
clpC1 | 4040084 | c.621C>T | synonymous_variant | 0.14 |
clpC1 | 4040087 | c.618G>C | synonymous_variant | 0.14 |
clpC1 | 4040090 | c.615T>C | synonymous_variant | 0.13 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4244809 | p.Phe526Tyr | missense_variant | 0.12 |
embB | 4249408 | c.2895G>A | synonymous_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |