Run ID: ERR4819307
Sample name:
Date: 01-04-2023 16:02:19
Number of reads: 238803
Percentage reads mapped: 25.99
Strain: lineage4
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761127 | p.Ser441Ala | missense_variant | 0.5 | rifampicin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.58 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5049 | c.-191A>G | upstream_gene_variant | 0.22 |
gyrB | 5872 | c.633G>A | synonymous_variant | 0.33 |
gyrA | 7625 | c.324G>C | synonymous_variant | 0.67 |
gyrA | 7628 | c.327G>C | synonymous_variant | 0.67 |
gyrA | 7631 | c.330G>C | synonymous_variant | 0.67 |
gyrA | 7633 | p.Asp111Ala | missense_variant | 0.67 |
gyrA | 7643 | c.342C>T | synonymous_variant | 0.67 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 576500 | p.Ile385Leu | missense_variant | 0.25 |
rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 0.5 |
rpoB | 761096 | c.1290G>C | synonymous_variant | 0.6 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.6 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 0.5 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.5 |
rpoB | 761534 | c.1728G>C | synonymous_variant | 0.67 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.67 |
rpoB | 761557 | p.Ala584Gly | missense_variant | 0.67 |
rpoB | 761562 | p.Ala586Ser | missense_variant | 0.67 |
rpoB | 761565 | p.Met587Leu | missense_variant | 0.67 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.67 |
rpoB | 761600 | c.1794T>C | synonymous_variant | 0.75 |
rpoB | 761800 | p.Arg665Gln | missense_variant | 0.67 |
rpoB | 762024 | p.Val740Ile | missense_variant | 0.8 |
rpoB | 762038 | c.2232C>T | synonymous_variant | 0.33 |
rpoB | 762051 | p.His749Tyr | missense_variant | 0.83 |
rpoB | 762057 | p.Ile751Val | missense_variant | 0.83 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.83 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.83 |
rpoB | 762071 | p.Asp755Glu | missense_variant | 0.83 |
rpoB | 762080 | c.2274G>C | synonymous_variant | 0.83 |
rpoB | 762085 | p.Ala760Glu | missense_variant | 0.71 |
rpoB | 762089 | c.2283G>A | synonymous_variant | 0.71 |
rpoB | 762092 | c.2286G>A | synonymous_variant | 0.43 |
rpoB | 762104 | c.2298C>T | synonymous_variant | 0.43 |
rpoB | 762110 | c.2304G>C | synonymous_variant | 0.67 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.75 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 0.67 |
rpoB | 762200 | c.2394C>T | synonymous_variant | 0.33 |
rpoB | 762218 | c.2412T>A | synonymous_variant | 0.6 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.83 |
rpoB | 762234 | p.Pro810Ser | missense_variant | 0.83 |
rpoB | 762239 | c.2433G>A | synonymous_variant | 0.83 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.83 |
rpoB | 762248 | c.2442G>A | synonymous_variant | 0.6 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.67 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.67 |
rpoC | 762944 | c.-426C>T | upstream_gene_variant | 0.5 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.4 |
rpoB | 763038 | p.Thr1078Ala | missense_variant | 0.42 |
rpoC | 763043 | c.-327G>C | upstream_gene_variant | 0.45 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.54 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.56 |
rpoB | 763077 | p.Val1091Thr | missense_variant | 0.56 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.44 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.44 |
rpoB | 763119 | p.Asn1105Asp | missense_variant | 0.44 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.5 |
rpoC | 763133 | c.-237G>C | upstream_gene_variant | 0.5 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.38 |
rpoC | 763615 | c.246G>C | synonymous_variant | 0.5 |
rpoC | 763622 | p.Ala85Ser | missense_variant | 0.5 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.57 |
rpoC | 763647 | p.Gly93Ala | missense_variant | 0.3 |
rpoC | 763654 | c.285C>T | synonymous_variant | 0.18 |
rpoC | 763655 | p.Glu96Lys | missense_variant | 0.27 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.3 |
rpoC | 763666 | c.297G>C | synonymous_variant | 0.27 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.17 |
rpoC | 763672 | c.303C>G | synonymous_variant | 0.25 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.17 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.15 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.62 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.77 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.7 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.7 |
rpoC | 763718 | p.Leu117Val | missense_variant | 0.7 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.7 |
rpoC | 763724 | p.Asp119Asn | missense_variant | 0.7 |
rpoC | 763729 | c.360G>C | synonymous_variant | 0.7 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.7 |
rpoC | 763735 | c.366G>C | synonymous_variant | 0.7 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.64 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.7 |
rpoC | 763772 | p.Val135Met | missense_variant | 0.5 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.25 |
rpoC | 764410 | c.1041G>C | synonymous_variant | 0.25 |
rpoC | 764424 | p.Asn352Thr | missense_variant | 0.5 |
rpoC | 764428 | c.1059G>A | synonymous_variant | 1.0 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 1.0 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 1.0 |
rpoC | 764435 | c.1066_1068delAGGinsCGC | synonymous_variant | 1.0 |
rpoC | 764441 | p.Ile358Leu | missense_variant | 0.67 |
rpoC | 764446 | p.Asp359Glu | missense_variant | 0.67 |
rpoC | 764455 | c.1086G>C | synonymous_variant | 0.67 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.67 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.8 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.67 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.57 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.4 |
rpoC | 764503 | c.1134G>T | synonymous_variant | 0.4 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.4 |
rpoC | 764512 | c.1143G>C | synonymous_variant | 0.4 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.4 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.4 |
rpoC | 764647 | c.1278C>T | synonymous_variant | 0.4 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.5 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.5 |
rpoC | 764656 | c.1287C>T | synonymous_variant | 0.5 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.5 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.5 |
rpoC | 764678 | p.Lys437Gln | missense_variant | 0.5 |
rpoC | 764692 | c.1323C>T | synonymous_variant | 0.67 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.4 |
rpoC | 764713 | c.1344G>C | synonymous_variant | 0.4 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 766985 | p.Val1206Met | missense_variant | 0.5 |
rpoC | 767020 | c.3651C>G | synonymous_variant | 0.67 |
rpoC | 767023 | c.3654C>T | synonymous_variant | 0.67 |
rpoC | 767038 | c.3669G>C | synonymous_variant | 0.8 |
rpoC | 767044 | c.3675G>C | synonymous_variant | 0.8 |
rpoC | 767263 | c.3894T>C | synonymous_variant | 0.25 |
mmpL5 | 776126 | c.2355C>T | synonymous_variant | 0.67 |
mmpL5 | 777525 | p.Gly319Val | missense_variant | 0.29 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.75 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.75 |
rpsL | 781766 | c.207C>T | synonymous_variant | 0.5 |
rpsL | 781769 | c.210G>A | synonymous_variant | 0.33 |
rpsL | 781781 | c.222G>C | synonymous_variant | 0.33 |
rpsL | 781796 | p.Met79Ile | missense_variant | 0.57 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.67 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.57 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.57 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.57 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.5 |
fbiC | 1303685 | p.Ser252Phe | missense_variant | 0.29 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472068 | n.223T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472130 | n.285G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472338 | n.493A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472840 | n.995A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472875 | n.1030T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.65 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.65 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473291 | n.1446G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473294 | n.1449A>G | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473300 | n.1455C>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1473384 | n.-274A>G | upstream_gene_variant | 0.43 |
rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473922 | n.265A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473923 | n.266C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474393 | n.736A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474402 | n.745T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474558 | n.901G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474584 | n.927C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474831 | n.1174A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474832 | n.1175A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474881 | n.1224A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475104 | n.1447T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475109 | n.1452C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475124 | n.1467A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475137 | n.1480A>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475171 | n.1514C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475172 | n.1515A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475175 | n.1518G>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475188 | n.1531C>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475879 | n.2222T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476229 | n.2572C>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476326 | n.2669T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476523 | n.2866T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476528 | n.2871A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476542 | n.2885T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476548 | n.2891T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.22 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 0.22 |
rpsA | 1833684 | p.Arg48Gln | missense_variant | 0.22 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.33 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.4 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.5 |
rpsA | 1833732 | p.Pro64Leu | missense_variant | 0.5 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.5 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.5 |
rpsA | 1833764 | p.Asp75Asn | missense_variant | 0.67 |
rpsA | 1834216 | c.675C>T | synonymous_variant | 0.4 |
rpsA | 1834228 | c.687C>T | synonymous_variant | 0.67 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.67 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.5 |
rpsA | 1834246 | c.705G>T | synonymous_variant | 0.5 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.57 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.7 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.7 |
rpsA | 1834294 | c.753G>T | synonymous_variant | 0.44 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.44 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.5 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.57 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.57 |
rpsA | 1834312 | c.771G>A | synonymous_variant | 0.57 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.5 |
rpsA | 1834345 | c.804C>T | synonymous_variant | 0.44 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.38 |
katG | 2154145 | p.Asp656Gly | missense_variant | 0.22 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ribD | 2987487 | p.Pro217Thr | missense_variant | 0.18 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449581 | p.Val360Met | missense_variant | 0.2 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568464 | p.Asp72Glu | missense_variant | 0.25 |
Rv3236c | 3612805 | c.312T>A | synonymous_variant | 0.17 |
fbiA | 3640453 | c.-90C>T | upstream_gene_variant | 0.67 |
fbiB | 3642054 | p.Arg174Cys | missense_variant | 0.4 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4249147 | c.2634C>T | synonymous_variant | 0.2 |
embB | 4249387 | c.2874G>A | synonymous_variant | 0.5 |
aftB | 4269618 | c.-782C>T | upstream_gene_variant | 0.29 |
ethA | 4326266 | p.Cys403Tyr | missense_variant | 0.22 |
ethA | 4327518 | c.-45G>A | upstream_gene_variant | 0.5 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407547 | p.Ala219Val | missense_variant | 0.25 |
gid | 4408024 | p.Glu60Gly | missense_variant | 0.2 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |