Run ID: DRR185024
Sample name:
Date: 31-03-2023 07:24:10
Number of reads: 606503
Percentage reads mapped: 40.38
Strain: lineage2.2.2
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 1.0 |
lineage2.2.2 | East-Asian (Beijing) | Beijing-RD105/RD207 | RD105;RD207 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.24 | streptomycin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.48 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.48 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.29 | kanamycin, capreomycin, aminoglycosides, amikacin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575974 | p.Glu209Asp | missense_variant | 0.17 |
mshA | 576689 | p.Tyr448Asn | missense_variant | 0.11 |
rpoB | 762023 | c.2217C>T | synonymous_variant | 0.15 |
rpoB | 762030 | p.Thr742Ser | missense_variant | 0.17 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.19 |
rpoB | 762056 | c.2250G>A | synonymous_variant | 0.19 |
rpoB | 762057 | p.Ile751Val | missense_variant | 0.19 |
rpoB | 762068 | c.2262C>T | synonymous_variant | 0.19 |
rpoB | 762080 | c.2274G>C | synonymous_variant | 0.19 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.18 |
rpoB | 762089 | c.2283G>A | synonymous_variant | 0.19 |
rpoB | 762098 | c.2292C>T | synonymous_variant | 0.19 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.2 |
rpoB | 762119 | c.2313C>G | synonymous_variant | 0.18 |
rpoB | 762120 | p.Asp772Pro | missense_variant | 0.18 |
rpoB | 762125 | p.Glu773Asp | missense_variant | 0.18 |
rpoB | 762127 | p.Val774Ala | missense_variant | 0.17 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 0.17 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.17 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.17 |
rpoB | 762146 | p.Glu780Asp | missense_variant | 0.17 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.17 |
rpoB | 762152 | c.2346C>A | synonymous_variant | 0.17 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.17 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.16 |
rpoB | 762170 | c.2364C>A | synonymous_variant | 0.16 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.16 |
rpoB | 762177 | p.Arg791Thr | missense_variant | 0.16 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.16 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 0.16 |
rpoB | 762233 | c.2427G>T | synonymous_variant | 0.13 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.11 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763528 | c.159G>T | synonymous_variant | 0.12 |
rpoC | 763558 | c.189C>A | synonymous_variant | 0.12 |
rpoC | 763570 | c.201G>A | synonymous_variant | 0.13 |
rpoC | 763597 | c.228G>A | synonymous_variant | 0.12 |
rpoC | 763621 | c.252C>T | synonymous_variant | 0.12 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.14 |
rpoC | 763652 | p.Ile95Leu | missense_variant | 0.16 |
rpoC | 763660 | c.291T>C | synonymous_variant | 0.16 |
rpoC | 763666 | c.297G>T | synonymous_variant | 0.19 |
rpoC | 763672 | c.303C>G | synonymous_variant | 0.19 |
rpoC | 763705 | c.336G>A | synonymous_variant | 0.15 |
rpoC | 763708 | c.339G>T | synonymous_variant | 0.15 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.15 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.16 |
rpoC | 763726 | c.357C>T | synonymous_variant | 0.14 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.11 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.11 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.15 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.15 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 0.15 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.15 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.15 |
rpoC | 764602 | c.1233C>A | synonymous_variant | 0.2 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 0.2 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.19 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.19 |
rpoC | 764635 | c.1266C>G | synonymous_variant | 0.24 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.25 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.25 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 0.28 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.29 |
rpoC | 764678 | p.Lys437His | missense_variant | 0.29 |
rpoC | 764705 | p.Leu446Thr | missense_variant | 0.3 |
rpoC | 764731 | c.1362G>C | synonymous_variant | 0.27 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.23 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.24 |
rpoC | 764755 | c.1386C>T | synonymous_variant | 0.24 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.23 |
rpoC | 764767 | c.1398G>T | synonymous_variant | 0.23 |
rpoC | 764780 | c.1411_1413delAGCinsTCG | synonymous_variant | 0.22 |
rpoC | 764797 | c.1428G>C | synonymous_variant | 0.2 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.19 |
rpoC | 764808 | p.Arg480His | missense_variant | 0.17 |
rpoC | 764812 | c.1443C>G | synonymous_variant | 0.17 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.17 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.17 |
rpoC | 764843 | p.Ala492Thr | missense_variant | 0.14 |
rpoC | 764854 | c.1485G>C | synonymous_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781406 | c.-154_-153insC | upstream_gene_variant | 1.0 |
Rv1258c | 1406569 | p.Val258Leu | missense_variant | 0.12 |
Rv1258c | 1406672 | c.669G>T | synonymous_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471889 | n.44G>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1471935 | n.91_94delACTC | non_coding_transcript_exon_variant | 0.17 |
rrs | 1471967 | n.122G>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1471972 | n.127T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1471979 | n.134T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1471980 | n.135G>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1471981 | n.136C>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1471983 | n.138C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472023 | n.178G>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472030 | n.185G>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472031 | n.186G>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472034 | n.189T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472041 | n.196C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472042 | n.197T>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472043 | n.198T>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472054 | n.210_212delCGC | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472062 | n.217G>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472065 | n.220G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472067 | n.222G>C | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472068 | n.223T>G | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472148 | n.303T>C | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472223 | n.378C>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472228 | n.383G>C | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472245 | n.400C>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472251 | n.406G>C | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472279 | n.434T>G | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472293 | n.448C>A | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472297 | n.453_465delGTCCGGGTTCTCT | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472337 | n.492C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472380 | n.535G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472427 | n.582T>G | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472431 | n.586G>A | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472434 | n.589_590insC | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472437 | n.592T>C | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472438 | n.594delC | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472443 | n.598A>G | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472448 | n.603T>G | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472451 | n.606C>A | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472452 | n.607G>C | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472460 | n.615T>G | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472461 | n.616G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472464 | n.619A>C | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472473 | n.628G>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472474 | n.629C>G | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472476 | n.631A>G | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472484 | n.639A>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472496 | n.651T>A | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472506 | n.661A>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472572 | n.727T>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472591 | n.746G>A | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472596 | n.751G>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472614 | n.769G>T | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472665 | n.820G>A | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472695 | n.850C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472836 | n.991G>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472851 | n.1006A>G | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472854 | n.1009G>A | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472856 | n.1011T>C | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472861 | n.1016G>C | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472865 | n.1020C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472868 | n.1024delG | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472871 | n.1027_1028insAG | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472874 | n.1029C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472875 | n.1030T>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472982 | n.1137G>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.47 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.58 |
rrs | 1473047 | n.1202C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.65 |
rrs | 1473091 | n.1246G>A | non_coding_transcript_exon_variant | 0.66 |
rrs | 1473093 | n.1248C>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473094 | n.1249T>G | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473099 | n.1254T>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473100 | n.1255G>C | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1473109 | n.1264T>G | non_coding_transcript_exon_variant | 0.68 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.7 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.65 |
rrs | 1473147 | n.1302G>T | non_coding_transcript_exon_variant | 0.66 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473157 | n.1312C>T | non_coding_transcript_exon_variant | 0.65 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1473164 | n.1319C>A | non_coding_transcript_exon_variant | 0.7 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.54 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.46 |
rrs | 1473280 | n.1435G>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473283 | n.1438T>C | non_coding_transcript_exon_variant | 0.34 |
rrs | 1473291 | n.1446G>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473298 | n.1453A>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473305 | n.1460G>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1473871 | n.214T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474164 | n.507C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474171 | n.514C>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474202 | n.545T>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474263 | n.606G>A | non_coding_transcript_exon_variant | 0.39 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1474287 | n.630T>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474290 | n.633T>C | non_coding_transcript_exon_variant | 0.39 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474351 | n.694G>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474354 | n.697C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474355 | n.698A>G | non_coding_transcript_exon_variant | 0.37 |
rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 0.37 |
rrl | 1474359 | n.702C>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.39 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1474402 | n.745T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474437 | n.782_784delATA | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474444 | n.787G>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474451 | n.794T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474454 | n.797G>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474476 | n.819C>G | non_coding_transcript_exon_variant | 0.61 |
rrl | 1474483 | n.826C>G | non_coding_transcript_exon_variant | 0.61 |
rrl | 1474496 | n.839C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474520 | n.863A>C | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474551 | n.894G>C | non_coding_transcript_exon_variant | 0.49 |
rrl | 1474558 | n.901G>T | non_coding_transcript_exon_variant | 0.49 |
rrl | 1474584 | n.927C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474627 | n.970G>A | non_coding_transcript_exon_variant | 0.46 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474640 | n.983C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1474676 | n.1019T>C | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474692 | n.1035G>A | non_coding_transcript_exon_variant | 0.49 |
rrl | 1474694 | n.1037C>T | non_coding_transcript_exon_variant | 0.49 |
rrl | 1474716 | n.1059A>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474717 | n.1060A>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474734 | n.1077G>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474751 | n.1094G>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474777 | n.1120T>C | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474783 | n.1126G>A | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.49 |
rrl | 1474806 | n.1149A>C | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474822 | n.1165G>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474905 | n.1248T>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475649 | n.1992A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475650 | n.1993A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475655 | n.1998T>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475672 | n.2015C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475696 | n.2039T>A | non_coding_transcript_exon_variant | 0.39 |
rrl | 1475697 | n.2040C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475703 | n.2046A>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.65 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.66 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475963 | n.2306G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.63 |
rrl | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475989 | n.2332T>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475990 | n.2333G>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475997 | n.2340A>G | non_coding_transcript_exon_variant | 0.58 |
rrl | 1475998 | n.2341C>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476019 | n.2362G>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476026 | n.2369T>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476040 | n.2383C>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476077 | n.2420T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476079 | n.2422G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476082 | n.2425T>G | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476085 | n.2429_2430delGC | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476095 | n.2438C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476105 | n.2450delA | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476130 | n.2473G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476165 | n.2508T>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476234 | n.2577G>A | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476251 | n.2594T>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476255 | n.2598A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476267 | n.2610G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476268 | n.2611A>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476275 | n.2618T>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476276 | n.2619C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476288 | n.2631T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476534 | n.2877A>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.49 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476572 | n.2915G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.15 |
rpsA | 1833909 | p.Asp123Ala | missense_variant | 1.0 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.17 |
rpsA | 1834228 | c.687C>T | synonymous_variant | 0.16 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.15 |
rpsA | 1834240 | c.699T>A | synonymous_variant | 0.17 |
rpsA | 1834243 | c.702G>C | synonymous_variant | 0.17 |
rpsA | 1834246 | c.705G>C | synonymous_variant | 0.17 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.18 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.18 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.17 |
rpsA | 1834279 | c.738C>T | synonymous_variant | 0.16 |
rpsA | 1834286 | p.Ser249Gly | missense_variant | 0.14 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.14 |
rpsA | 1834298 | p.Gln253Thr | missense_variant | 0.12 |
rpsA | 1834303 | c.762T>G | synonymous_variant | 0.13 |
rpsA | 1834327 | c.786G>C | synonymous_variant | 0.13 |
rpsA | 1834354 | c.813G>C | synonymous_variant | 0.13 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.13 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.13 |
rpsA | 1834375 | c.834G>C | synonymous_variant | 0.13 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.13 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918034 | p.Val32Gly | missense_variant | 0.5 |
ndh | 2102214 | p.Ser277Pro | missense_variant | 0.1 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2222540 | p.Gly209Ser | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518608 | p.Met165Thr | missense_variant | 0.14 |
ahpC | 2726399 | c.207C>T | synonymous_variant | 0.15 |
ribD | 2987172 | p.Ser112Cys | missense_variant | 1.0 |
ribD | 2987185 | p.Gln116Leu | missense_variant | 1.0 |
Rv2752c | 3065369 | p.Gln275* | stop_gained | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
rpoA | 3877903 | p.Ile202Thr | missense_variant | 0.13 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.11 |
clpC1 | 4039775 | c.930G>C | synonymous_variant | 0.11 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.11 |
clpC1 | 4039781 | c.924G>C | synonymous_variant | 0.14 |
clpC1 | 4039790 | c.915C>T | synonymous_variant | 0.18 |
clpC1 | 4039796 | c.909C>T | synonymous_variant | 0.21 |
clpC1 | 4039805 | c.900C>T | synonymous_variant | 0.29 |
clpC1 | 4039808 | c.897G>A | synonymous_variant | 0.29 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.3 |
clpC1 | 4039826 | c.879C>G | synonymous_variant | 0.3 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 0.3 |
clpC1 | 4039838 | p.Leu289Ile | missense_variant | 0.33 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.32 |
clpC1 | 4039853 | c.852G>C | synonymous_variant | 0.32 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.3 |
clpC1 | 4039875 | p.Asn277Arg | missense_variant | 0.28 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.32 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.32 |
clpC1 | 4039907 | c.798G>A | synonymous_variant | 0.32 |
clpC1 | 4039929 | c.775_776delAGinsTC | synonymous_variant | 0.28 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.28 |
clpC1 | 4039937 | c.768G>C | synonymous_variant | 0.26 |
clpC1 | 4039946 | c.759A>T | synonymous_variant | 0.23 |
clpC1 | 4039949 | c.756G>C | synonymous_variant | 0.23 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.23 |
clpC1 | 4039955 | c.750G>C | synonymous_variant | 0.23 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.23 |
clpC1 | 4039976 | p.Lys243Thr | missense_variant | 0.2 |
clpC1 | 4039982 | p.Thr241Ile | missense_variant | 0.17 |
clpC1 | 4039994 | c.711G>A | synonymous_variant | 0.17 |
clpC1 | 4040002 | p.His235Asn | missense_variant | 0.17 |
clpC1 | 4040003 | c.702G>C | synonymous_variant | 0.17 |
clpC1 | 4040012 | c.693G>A | synonymous_variant | 0.18 |
clpC1 | 4040015 | c.690G>A | synonymous_variant | 0.18 |
clpC1 | 4040018 | c.687G>C | synonymous_variant | 0.18 |
clpC1 | 4040272 | p.Tyr145His | missense_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embB | 4247818 | c.1305C>T | synonymous_variant | 0.13 |
aftB | 4267321 | p.Asp506Asn | missense_variant | 0.17 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
ethA | 4328452 | c.-979C>T | upstream_gene_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |
gid | 4408469 | c.-267T>C | upstream_gene_variant | 0.11 |