Run ID: ERR4188222
Sample name:
Date: 01-04-2023 04:58:02
Number of reads: 422777
Percentage reads mapped: 29.57
Strain: La1.8.1
Drug-resistance: MDR-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 |
---|---|---|---|---|---|
rpoB | 761196 | p.Leu464Met | missense_variant | 0.2 | rifampicin |
katG | 2154569 | p.Arg515Cys | missense_variant | 0.33 | isoniazid |
pncA | 2289073 | p.His57Asp | missense_variant | 1.0 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5172 | c.-68C>T | upstream_gene_variant | 0.2 |
gyrB | 5752 | c.513G>A | synonymous_variant | 1.0 |
gyrA | 6406 | c.-896C>T | upstream_gene_variant | 1.0 |
gyrB | 6446 | p.Ala403Ser | missense_variant | 0.88 |
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 | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576217 | c.870G>A | synonymous_variant | 0.2 |
rpoB | 761138 | c.1332C>G | synonymous_variant | 0.29 |
rpoB | 761150 | c.1344A>T | synonymous_variant | 0.22 |
rpoB | 761162 | c.1356G>C | synonymous_variant | 0.2 |
rpoB | 761165 | c.1359G>T | synonymous_variant | 0.18 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.18 |
rpoB | 761178 | p.Ser458Thr | missense_variant | 0.2 |
rpoB | 761183 | c.1377T>G | synonymous_variant | 0.2 |
rpoB | 761186 | c.1380G>A | synonymous_variant | 0.2 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.2 |
rpoB | 761192 | c.1386C>G | synonymous_variant | 0.2 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.2 |
rpoB | 761201 | c.1395G>A | synonymous_variant | 0.2 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.18 |
rpoB | 761216 | c.1410C>T | synonymous_variant | 0.18 |
rpoB | 761222 | c.1416G>C | synonymous_variant | 0.17 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.14 |
rpoB | 761252 | c.1446C>G | synonymous_variant | 0.14 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.44 |
rpoC | 764410 | c.1041G>C | synonymous_variant | 0.33 |
rpoC | 764419 | c.1050C>G | synonymous_variant | 0.28 |
rpoC | 764428 | c.1059G>T | synonymous_variant | 0.27 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.26 |
rpoC | 764435 | c.1066_1068delAGGinsCGT | synonymous_variant | 0.26 |
rpoC | 764440 | c.1071G>T | synonymous_variant | 0.26 |
rpoC | 764441 | p.Ile358Leu | missense_variant | 0.26 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.24 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.25 |
rpoC | 764461 | p.Glu364Asp | missense_variant | 0.26 |
rpoC | 764470 | c.1101C>A | synonymous_variant | 0.23 |
rpoC | 764471 | p.Asn368Gln | missense_variant | 0.23 |
rpoC | 764494 | c.1125G>A | synonymous_variant | 0.35 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 0.35 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.34 |
rpoC | 764513 | p.Phe382Ile | missense_variant | 0.34 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.36 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.36 |
rpoC | 764536 | c.1167G>T | synonymous_variant | 0.3 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.27 |
rpoC | 764545 | c.1176C>G | synonymous_variant | 0.25 |
rpoC | 764548 | c.1179G>C | synonymous_variant | 0.27 |
rpoC | 764551 | c.1182G>C | synonymous_variant | 0.28 |
rpoC | 764569 | c.1200G>A | synonymous_variant | 0.3 |
rpoC | 764575 | c.1206T>C | synonymous_variant | 0.31 |
rpoC | 764576 | c.1207_1208delTCinsAG | synonymous_variant | 0.31 |
rpoC | 764579 | p.Asp404His | missense_variant | 0.31 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.31 |
rpoC | 764587 | c.1218C>G | synonymous_variant | 0.38 |
rpoC | 764599 | c.1230G>A | synonymous_variant | 0.42 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 0.43 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.42 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.36 |
rpoC | 764644 | c.1275G>C | synonymous_variant | 0.26 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.26 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.27 |
rpoC | 764656 | c.1287C>T | synonymous_variant | 0.29 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.29 |
rpoC | 764668 | c.1299C>A | synonymous_variant | 0.29 |
rpoC | 764672 | p.Gln435Tyr | missense_variant | 0.26 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.28 |
rpoC | 764681 | p.Leu438Met | missense_variant | 0.28 |
rpoC | 764684 | p.His439Tyr | missense_variant | 0.28 |
rpoC | 764695 | c.1326T>C | synonymous_variant | 0.31 |
rpoC | 764701 | c.1332C>G | synonymous_variant | 0.29 |
rpoC | 764705 | p.Leu446Glu | missense_variant | 0.28 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.29 |
rpoC | 764737 | c.1368G>C | synonymous_variant | 0.25 |
rpoC | 765462 | p.Asn698Ser | missense_variant | 0.17 |
rpoC | 766840 | c.3471C>T | synonymous_variant | 0.2 |
rpoC | 767032 | c.3663G>A | synonymous_variant | 0.2 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777422 | c.1059G>T | synonymous_variant | 0.18 |
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 | 1471703 | n.-143T>C | upstream_gene_variant | 0.25 |
rrs | 1472089 | n.244C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472256 | n.411T>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472271 | n.426T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472277 | n.432C>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472379 | n.534T>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472508 | n.663T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472518 | n.673G>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472544 | n.699C>G | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472579 | n.734G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472668 | n.824dupT | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472672 | n.828_838delTTTCCTTCCTT | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472687 | n.842A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472690 | n.845_846insACCCCTCG | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472697 | n.852T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472700 | n.855C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472705 | n.860G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472954 | n.1109T>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472955 | n.1110C>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472958 | n.1113A>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472959 | n.1114T>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472971 | n.1126G>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472975 | n.1130T>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472982 | n.1137G>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472987 | n.1142G>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472988 | n.1143T>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472991 | n.1146G>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472992 | n.1147A>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473002 | n.1157G>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473004 | n.1159T>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473008 | n.1163C>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473009 | n.1164T>C | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473020 | n.1175T>C | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473053 | n.1208T>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1473062 | n.1217T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473068 | n.1223A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473070 | n.1225G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473089 | n.1244A>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473094 | n.1249T>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473099 | n.1254T>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473101 | n.1256C>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473102 | n.1257C>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473107 | n.1262G>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473108 | n.1263G>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473115 | n.1270G>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474768 | n.1111C>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474790 | n.1133C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474798 | n.1141C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474804 | n.1147C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474844 | n.1187G>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474866 | n.1209C>A | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474869 | n.1212G>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474902 | n.1245T>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474913 | n.1256T>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474920 | n.1263G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474927 | n.1271delC | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474931 | n.1274G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475750 | n.2093A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475843 | n.2186G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475849 | n.2192G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475853 | n.2196C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476297 | n.2640C>A | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476512 | n.2855C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476573 | n.2916A>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476577 | n.2920T>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.43 |
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 | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155503 | c.609C>T | synonymous_variant | 1.0 |
katG | 2155546 | p.Asp189Val | missense_variant | 0.15 |
katG | 2156025 | c.87C>A | synonymous_variant | 1.0 |
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 |
PPE35 | 2170066 | p.Ala183Thr | missense_variant | 0.18 |
PPE35 | 2170395 | p.Ala73Val | missense_variant | 0.18 |
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 |
ribD | 2987169 | p.Gln111Lys | missense_variant | 0.3 |
Rv2752c | 3065988 | p.Glu68Asp | 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 | 3448691 | p.Gly63Asp | missense_variant | 0.13 |
Rv3083 | 3448768 | c.267delC | frameshift_variant | 0.14 |
Rv3083 | 3448783 | p.Val94Ile | missense_variant | 1.0 |
Rv3083 | 3449061 | c.558C>T | synonymous_variant | 0.12 |
fprA | 3473948 | c.-59C>T | upstream_gene_variant | 0.22 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474427 | p.Val141Ile | missense_variant | 1.0 |
fprA | 3474942 | c.936G>A | synonymous_variant | 0.15 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 0.83 |
Rv3236c | 3612055 | c.1062G>A | synonymous_variant | 0.12 |
fbiA | 3640567 | p.Gly9Arg | missense_variant | 0.2 |
alr | 3841579 | c.-159C>A | upstream_gene_variant | 0.18 |
ddn | 3986699 | c.-145C>A | upstream_gene_variant | 0.2 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 1.0 |
embC | 4240636 | c.774G>A | synonymous_variant | 0.17 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4240960 | c.1098G>A | synonymous_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242970 | c.-263C>T | upstream_gene_variant | 1.0 |
embC | 4242981 | p.Met1040Thr | missense_variant | 1.0 |
embA | 4244220 | c.988C>T | synonymous_variant | 1.0 |
embB | 4246551 | p.Asn13Ser | missense_variant | 1.0 |
embB | 4246864 | c.351C>T | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4249753 | p.Leu1080Phe | missense_variant | 0.15 |
aftB | 4267858 | p.Ile327Val | missense_variant | 1.0 |
aftB | 4268002 | c.835C>T | synonymous_variant | 0.17 |
aftB | 4269339 | c.-503C>T | upstream_gene_variant | 0.17 |
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 |
ethA | 4327557 | c.-84G>A | upstream_gene_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407774 | c.429C>T | synonymous_variant | 0.14 |