Run ID: ERR4814841
Sample name:
Date: 01-04-2023 13:31:18
Number of reads: 300936
Percentage reads mapped: 72.11
Strain: lineage4.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.57 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8694 | c.1393C>T | synonymous_variant | 1.0 |
gyrA | 9024 | p.Arg575Trp | missense_variant | 0.2 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491162 | p.Glu127Val | missense_variant | 0.29 |
rpoB | 761030 | c.1224G>C | synonymous_variant | 0.29 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.25 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.25 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.25 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.25 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.25 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.22 |
rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 0.2 |
rpoB | 761096 | c.1290G>C | synonymous_variant | 0.2 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.2 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.2 |
rpoB | 761150 | c.1344A>T | synonymous_variant | 0.2 |
rpoB | 761159 | c.1353G>C | synonymous_variant | 0.18 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.18 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.25 |
rpoB | 762057 | p.Ile751Val | missense_variant | 0.25 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.29 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.29 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.2 |
rpoB | 762110 | c.2304G>C | synonymous_variant | 0.18 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.2 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.25 |
rpoC | 763648 | c.279C>T | synonymous_variant | 0.29 |
rpoC | 763657 | p.Glu96Asp | missense_variant | 0.29 |
rpoC | 763660 | c.291T>C | synonymous_variant | 0.21 |
rpoC | 763666 | c.297G>C | synonymous_variant | 0.31 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.23 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.33 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.27 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.27 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.25 |
rpoC | 763718 | p.Leu117Val | missense_variant | 0.25 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.27 |
rpoC | 763724 | p.Asp119Asn | missense_variant | 0.27 |
rpoC | 763729 | c.360G>C | synonymous_variant | 0.3 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.33 |
rpoC | 763735 | c.366G>C | synonymous_variant | 0.3 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.33 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.33 |
rpoC | 763772 | p.Val135Met | missense_variant | 0.33 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.17 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.15 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.21 |
rpoC | 764503 | c.1134G>T | synonymous_variant | 0.2 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.2 |
rpoC | 764512 | c.1143G>C | synonymous_variant | 0.2 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.19 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.2 |
rpoC | 764542 | c.1173C>T | synonymous_variant | 0.14 |
rpoC | 764543 | p.Thr392Ala | missense_variant | 0.15 |
rpoC | 764548 | c.1179G>C | synonymous_variant | 0.14 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.12 |
rpoC | 764573 | p.Leu402Ile | missense_variant | 0.12 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 0.12 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.12 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.12 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.25 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.22 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 0.33 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.29 |
rpoC | 764623 | c.1254C>G | synonymous_variant | 0.14 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.27 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.18 |
rpoC | 764635 | c.1266C>G | synonymous_variant | 0.11 |
rpoC | 764644 | c.1275G>T | synonymous_variant | 0.11 |
rpoC | 764647 | c.1278C>T | synonymous_variant | 0.11 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.18 |
rpoC | 764656 | c.1287C>A | synonymous_variant | 0.13 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.24 |
rpoC | 764664 | p.Val432Gly | missense_variant | 0.12 |
rpoC | 764671 | c.1302G>C | synonymous_variant | 0.11 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.11 |
rpoC | 764678 | p.Lys437Gln | missense_variant | 0.12 |
rpoC | 764692 | c.1323C>T | synonymous_variant | 0.11 |
rpoC | 764703 | p.Lys445Ser | missense_variant | 0.12 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.25 |
rpoC | 764713 | c.1344G>C | synonymous_variant | 0.23 |
rpoC | 764731 | c.1362G>C | synonymous_variant | 0.25 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765575 | p.Val736Met | missense_variant | 0.18 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776198 | c.2283C>T | synonymous_variant | 0.17 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781865 | c.306G>C | synonymous_variant | 0.22 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.22 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.22 |
rpsL | 781877 | c.318T>C | synonymous_variant | 0.22 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.25 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.25 |
rpsL | 781916 | c.357T>C | synonymous_variant | 0.2 |
rplC | 800758 | c.-51A>C | upstream_gene_variant | 0.17 |
embR | 1416232 | p.Cys372Gly | missense_variant | 0.14 |
embR | 1416259 | c.1089G>C | synonymous_variant | 0.14 |
embR | 1416262 | c.1086G>C | synonymous_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472687 | n.843dupT | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.59 |
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 | 0.42 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472958 | n.1113A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472974 | n.1129A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472988 | n.1143T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.47 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1473034 | n.1189A>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.37 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.68 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.65 |
rrs | 1473101 | n.1256C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.65 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.72 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.7 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.65 |
rrs | 1473148 | n.1303G>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473163 | n.1318C>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.65 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1473262 | n.1417T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1473384 | n.-274A>G | upstream_gene_variant | 0.25 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474634 | n.977T>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474692 | n.1035G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474706 | n.1049G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474717 | n.1060A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474734 | n.1077G>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474831 | n.1174A>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474832 | n.1175A>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.91 |
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 | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475756 | n.2099T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475767 | n.2110_2111insT | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.55 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476207 | n.2550T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476255 | n.2598A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476267 | n.2610G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476276 | n.2619C>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476295 | n.2638C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476306 | n.2649A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476307 | n.2650A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476311 | n.2654G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476467 | n.2810A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476523 | n.2866T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476528 | n.2871A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.67 |
rpsA | 1833628 | c.87G>C | synonymous_variant | 0.5 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.75 |
rpsA | 1833667 | c.126C>T | synonymous_variant | 0.6 |
rpsA | 1833668 | p.Ile43Val | missense_variant | 0.6 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.6 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 0.6 |
rpsA | 1833684 | p.Arg48His | missense_variant | 0.33 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.5 |
rpsA | 1833700 | c.159C>T | synonymous_variant | 0.29 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.18 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.27 |
rpsA | 1833732 | p.Pro64Leu | missense_variant | 0.27 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.18 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.25 |
rpsA | 1833764 | p.Asp75Asn | missense_variant | 0.15 |
rpsA | 1833770 | p.Asn77Asp | missense_variant | 0.21 |
rpsA | 1833775 | p.Glu78Asp | missense_variant | 0.14 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.15 |
rpsA | 1833994 | c.453G>C | synonymous_variant | 0.18 |
rpsA | 1834009 | c.468C>T | synonymous_variant | 0.22 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.22 |
rpsA | 1834040 | p.Lys167Arg | missense_variant | 0.25 |
rpsA | 1834093 | c.552G>C | synonymous_variant | 0.17 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.22 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.22 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 1.0 |
rpsA | 1834354 | c.813G>C | synonymous_variant | 0.22 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.22 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.25 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.22 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.22 |
rpsA | 1834395 | p.Arg285Gln | missense_variant | 0.25 |
rpsA | 1834398 | p.His286Pro | missense_variant | 0.22 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102401 | c.642T>C | synonymous_variant | 0.67 |
PPE35 | 2170229 | c.384A>G | synonymous_variant | 0.5 |
PPE35 | 2170232 | c.381T>A | synonymous_variant | 0.5 |
PPE35 | 2170238 | c.375T>G | synonymous_variant | 0.5 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475346 | p.Leu447Arg | missense_variant | 1.0 |
Rv3236c | 3612515 | p.Arg201His | missense_variant | 1.0 |
clpC1 | 4038465 | p.Met747Thr | missense_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embB | 4249408 | c.2895G>A | synonymous_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408031 | p.Leu58Phe | missense_variant | 1.0 |