Run ID: ERR4188213
Sample name:
Date: 01-04-2023 04:57:49
Number of reads: 880605
Percentage reads mapped: 21.57
Strain: La1.8.1
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
La1 | M.bovis | None | None | 1.0 |
La1.8 | M.bovis | None | None | 1.0 |
La1.8.1 | M.bovis | None | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2154154 | p.Leu653Pro | missense_variant | 0.14 | isoniazid |
pncA | 2289073 | p.His57Asp | missense_variant | 1.0 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5752 | c.513G>A | synonymous_variant | 1.0 |
gyrA | 6406 | c.-896C>T | upstream_gene_variant | 0.95 |
gyrB | 6446 | p.Ala403Ser | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8285 | c.984C>T | synonymous_variant | 1.0 |
gyrA | 8741 | c.1440C>T | synonymous_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9217 | p.Asp639Ala | missense_variant | 0.96 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763477 | c.108C>T | synonymous_variant | 0.27 |
rpoC | 763478 | c.109_111delCGCinsAGG | synonymous_variant | 0.26 |
rpoC | 763484 | c.115_117delCTTinsTTG | synonymous_variant | 0.28 |
rpoC | 763498 | c.129G>A | synonymous_variant | 0.3 |
rpoC | 763501 | p.Asp44Glu | missense_variant | 0.32 |
rpoC | 763505 | c.136C>T | synonymous_variant | 0.31 |
rpoC | 763519 | c.150G>A | synonymous_variant | 0.33 |
rpoC | 763522 | c.153C>A | synonymous_variant | 0.33 |
rpoC | 763528 | c.159G>T | synonymous_variant | 0.32 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.33 |
rpoC | 763535 | p.Arg56Lys | missense_variant | 0.31 |
rpoC | 763550 | p.Tyr61His | missense_variant | 0.39 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.44 |
rpoC | 763573 | c.204G>T | synonymous_variant | 0.44 |
rpoC | 763578 | p.Phe70Tyr | missense_variant | 0.44 |
rpoC | 763582 | c.213G>A | synonymous_variant | 0.47 |
rpoC | 763586 | p.Ile73Val | missense_variant | 0.47 |
rpoC | 763589 | p.Ile74Val | missense_variant | 0.47 |
rpoC | 763597 | p.Glu76Asp | missense_variant | 0.42 |
rpoC | 763615 | c.246G>T | synonymous_variant | 0.3 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.22 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.24 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.23 |
rpoC | 763648 | c.279C>G | synonymous_variant | 0.23 |
rpoC | 763651 | c.282C>T | synonymous_variant | 0.23 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.23 |
rpoC | 763663 | c.294C>T | synonymous_variant | 0.23 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.23 |
rpoC | 763672 | c.303C>A | synonymous_variant | 0.23 |
rpoC | 763673 | p.Thr102Ser | missense_variant | 0.23 |
rpoC | 764353 | c.984G>T | synonymous_variant | 0.16 |
rpoC | 764359 | c.990C>T | synonymous_variant | 0.42 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 0.52 |
rpoC | 764377 | c.1008C>G | synonymous_variant | 0.54 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.54 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 0.65 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.61 |
rpoC | 764410 | c.1041G>C | synonymous_variant | 0.67 |
rpoC | 764419 | c.1050C>G | synonymous_variant | 0.71 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.74 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.74 |
rpoC | 764435 | c.1066A>C | synonymous_variant | 0.74 |
rpoC | 764441 | p.Ile358Leu | missense_variant | 0.73 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.73 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.74 |
rpoC | 764461 | p.Glu364Asp | missense_variant | 0.77 |
rpoC | 764470 | c.1101C>T | synonymous_variant | 0.77 |
rpoC | 764471 | p.Asn368Gln | missense_variant | 0.76 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 0.82 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.82 |
rpoC | 764513 | p.Phe382Ile | missense_variant | 0.8 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.81 |
rpoC | 764536 | c.1167G>T | synonymous_variant | 0.81 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.8 |
rpoC | 764548 | c.1179G>A | synonymous_variant | 0.83 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.83 |
rpoC | 764575 | c.1206T>C | synonymous_variant | 0.84 |
rpoC | 764576 | c.1207_1208delTCinsAG | synonymous_variant | 0.84 |
rpoC | 764579 | p.Asp404His | missense_variant | 0.82 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.83 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 0.77 |
rpoC | 764614 | c.1245G>A | synonymous_variant | 0.77 |
rpoC | 764623 | c.1254C>T | synonymous_variant | 0.75 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.75 |
rpoC | 764644 | c.1275G>C | synonymous_variant | 0.67 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.57 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.56 |
rpoC | 764656 | c.1287C>T | synonymous_variant | 0.55 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.51 |
rpoC | 764672 | p.Gln435Ser | missense_variant | 0.36 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.36 |
rpoC | 764681 | p.Leu438Met | missense_variant | 0.34 |
rpoC | 764684 | p.His439Tyr | missense_variant | 0.33 |
rpoC | 764695 | c.1326T>C | synonymous_variant | 0.33 |
rpoC | 764701 | c.1332C>G | synonymous_variant | 0.3 |
rpoC | 764705 | p.Leu446Glu | missense_variant | 0.28 |
rpoC | 764713 | c.1344G>C | synonymous_variant | 0.28 |
rpoC | 764731 | c.1362G>T | synonymous_variant | 0.23 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472100 | n.255T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472101 | n.256G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472379 | n.534T>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472518 | n.673G>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472544 | n.699C>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472579 | n.734G>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472669 | n.824_825insCGG | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472676 | n.832_840delCTTCCTTGG | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472697 | n.852T>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472700 | n.855C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472708 | n.863T>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472733 | n.888G>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472742 | n.897C>G | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472779 | n.934G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472786 | n.941C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472953 | n.1107_1108insAG | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472970 | n.1125C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472971 | n.1127delT | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472974 | n.1129A>G | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472975 | n.1130T>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472977 | n.1132G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472982 | n.1137G>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472987 | n.1142G>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472988 | n.1143T>A | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472992 | n.1147A>C | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473002 | n.1157G>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473004 | n.1159T>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473008 | n.1163C>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473009 | n.1164T>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473053 | n.1208T>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473062 | n.1217T>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473068 | n.1223A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473070 | n.1225G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473093 | n.1248C>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473094 | n.1249T>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473099 | n.1254T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473122 | n.1277T>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473127 | n.1282G>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473128 | n.1283C>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473147 | n.1302G>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473150 | n.1305T>G | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473161 | n.1316A>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473164 | n.1319C>G | non_coding_transcript_exon_variant | 0.54 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473179 | n.1334C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474228 | n.571T>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474232 | n.575C>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474239 | n.582G>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474467 | n.810A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474758 | n.1101G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474790 | n.1133C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474798 | n.1141C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474804 | n.1147C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474844 | n.1187G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474866 | n.1209C>A | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474869 | n.1212G>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474902 | n.1245T>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474913 | n.1256T>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474920 | n.1263G>A | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474927 | n.1271delC | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474931 | n.1274G>A | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474938 | n.1281G>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475154 | n.1497C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475167 | n.1510T>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475696 | n.2039T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475703 | n.2046A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475707 | n.2050T>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475713 | n.2056C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475716 | n.2059A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475747 | n.2090A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475751 | n.2094C>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475756 | n.2100_2101insGGGGAA | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475761 | n.2106_2113delCAAGGGTG | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475781 | n.2124T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475782 | n.2125T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475783 | n.2126T>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475843 | n.2186G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475849 | n.2192G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476141 | n.2484A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476165 | n.2508T>C | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476181 | n.2524A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476195 | n.2538C>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476196 | n.2539C>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476204 | n.2547C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476210 | n.2553G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476211 | n.2554G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476212 | n.2555T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476214 | n.2557G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476215 | n.2558C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476229 | n.2572C>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476297 | n.2640C>A | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476512 | n.2855C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476577 | n.2920T>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476595 | n.2938C>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476621 | n.2964C>A | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476624 | n.2967T>A | non_coding_transcript_exon_variant | 0.47 |
rpsA | 1834166 | p.Gly209Arg | missense_variant | 1.0 |
rpsA | 1834859 | p.Ala440Thr | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102193 | p.Arg284Trp | missense_variant | 1.0 |
ndh | 2103173 | c.-132delG | upstream_gene_variant | 1.0 |
katG | 2153942 | p.Phe724Ile | missense_variant | 0.17 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155503 | c.609C>T | synonymous_variant | 1.0 |
katG | 2156025 | c.87C>A | synonymous_variant | 1.0 |
katG | 2156162 | c.-51G>A | upstream_gene_variant | 0.14 |
katG | 2156207 | c.-96T>C | upstream_gene_variant | 0.13 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168011 | p.Ser868Arg | missense_variant | 1.0 |
PPE35 | 2168319 | p.Thr765Ile | missense_variant | 1.0 |
PPE35 | 2168814 | c.1798dupA | frameshift_variant | 1.0 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
eis | 2715125 | p.Thr70Ala | missense_variant | 1.0 |
ald | 3086728 | c.-92C>T | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087084 | c.266delA | frameshift_variant | 1.0 |
Rv3083 | 3448783 | p.Val94Ile | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474427 | p.Val141Ile | missense_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
rpoA | 3878630 | c.-124delC | upstream_gene_variant | 1.0 |
ddn | 3986916 | p.Asn25Asp | missense_variant | 0.11 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242970 | c.-263C>T | upstream_gene_variant | 1.0 |
embA | 4244220 | c.988C>T | synonymous_variant | 1.0 |
embB | 4246551 | p.Asn13Ser | missense_variant | 1.0 |
embB | 4246625 | p.Phe38Leu | missense_variant | 0.11 |
embB | 4246864 | c.351C>T | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
aftB | 4267858 | p.Ile327Val | missense_variant | 1.0 |
aftB | 4269351 | c.-515C>T | upstream_gene_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4408237 | c.-35C>A | upstream_gene_variant | 1.0 |