Run ID: ERR4818785
Sample name:
Date: 01-04-2023 15:45:03
Number of reads: 606734
Percentage reads mapped: 77.63
Strain: lineage4.1.2.1
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 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761127 | p.Ser441Ala | missense_variant | 0.31 | rifampicin |
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.13 | streptomycin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.42 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7171 | c.-131C>T | upstream_gene_variant | 0.18 |
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 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
mshA | 576120 | p.Ala258Glu | missense_variant | 0.14 |
mshA | 576394 | c.1047G>A | synonymous_variant | 0.11 |
mshA | 576482 | p.Val379Ile | missense_variant | 0.25 |
ccsA | 619831 | c.-60T>G | upstream_gene_variant | 0.25 |
ccsA | 620029 | c.139C>T | synonymous_variant | 0.14 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 761030 | c.1224G>C | synonymous_variant | 0.22 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.2 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.2 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.21 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.21 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.22 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.22 |
rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 0.22 |
rpoB | 761096 | c.1290G>C | synonymous_variant | 0.22 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.24 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.28 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 0.27 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.31 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 0.21 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.23 |
rpoB | 761159 | c.1353G>C | synonymous_variant | 0.23 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.31 |
rpoB | 762026 | c.2220G>C | synonymous_variant | 0.17 |
rpoB | 762051 | p.His749Tyr | missense_variant | 0.15 |
rpoB | 762057 | p.Ile751Val | missense_variant | 0.15 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.15 |
rpoB | 762071 | p.Asp755Glu | missense_variant | 0.14 |
rpoB | 762080 | c.2274G>C | synonymous_variant | 0.18 |
rpoB | 762085 | p.Ala760Glu | missense_variant | 0.2 |
rpoB | 762089 | c.2283G>A | synonymous_variant | 0.2 |
rpoB | 762092 | c.2286G>A | synonymous_variant | 0.2 |
rpoB | 762110 | c.2304G>C | synonymous_variant | 0.21 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.22 |
rpoB | 762122 | p.Asp772Glu | missense_variant | 0.12 |
rpoB | 762125 | c.2319G>A | synonymous_variant | 0.12 |
rpoB | 762126 | p.Val774Ser | missense_variant | 0.12 |
rpoB | 762134 | c.2328C>T | synonymous_variant | 0.25 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.25 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.25 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.24 |
rpoB | 762173 | c.2367G>A | synonymous_variant | 0.12 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.14 |
rpoB | 762177 | p.Arg791Thr | missense_variant | 0.14 |
rpoB | 762181 | p.Asp792Ala | missense_variant | 0.14 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.15 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 0.15 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.18 |
rpoB | 762234 | p.Pro810Ser | missense_variant | 0.17 |
rpoB | 762239 | c.2433G>A | synonymous_variant | 0.15 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.15 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.14 |
rpoC | 763043 | c.-327G>C | upstream_gene_variant | 0.11 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.11 |
rpoC | 763067 | c.-303C>G | upstream_gene_variant | 0.11 |
rpoB | 763068 | p.Asp1088Tyr | missense_variant | 0.11 |
rpoB | 763077 | p.Val1091Thr | missense_variant | 0.12 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.11 |
rpoC | 763615 | c.246G>C | synonymous_variant | 0.11 |
rpoC | 763622 | p.Ala85Ser | missense_variant | 0.11 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.1 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.14 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.19 |
rpoC | 764503 | c.1134G>T | synonymous_variant | 0.15 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.19 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.12 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.12 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.12 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.12 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.14 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.12 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 0.13 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.14 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.11 |
rpoC | 764647 | c.1278C>T | synonymous_variant | 0.1 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.1 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.1 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.22 |
rpoC | 764678 | p.Lys437Gln | missense_variant | 0.22 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.24 |
rpoC | 764713 | c.1344G>C | synonymous_variant | 0.29 |
rpoC | 764731 | c.1362G>C | synonymous_variant | 0.22 |
rpoC | 764737 | c.1368G>C | synonymous_variant | 0.22 |
rpoC | 764746 | c.1377G>C | synonymous_variant | 0.21 |
rpoC | 764752 | c.1383G>T | synonymous_variant | 0.17 |
rpoC | 764755 | p.Asp462Glu | missense_variant | 0.17 |
rpoC | 764756 | p.Leu463Lys | missense_variant | 0.17 |
rpoC | 764762 | p.His465Tyr | missense_variant | 0.17 |
rpoC | 764774 | p.Ile469Val | missense_variant | 0.21 |
rpoC | 764780 | p.Ser471Ala | missense_variant | 0.22 |
rpoC | 764793 | p.Met475Lys | missense_variant | 0.21 |
rpoC | 764797 | c.1428G>C | synonymous_variant | 0.21 |
rpoC | 764813 | p.Gln482Glu | missense_variant | 0.2 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 778714 | c.-234T>G | upstream_gene_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800789 | c.-20G>A | upstream_gene_variant | 0.11 |
rplC | 800815 | p.Arg3* | stop_gained | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472068 | n.223T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472597 | n.752G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472686 | n.841G>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472958 | n.1113A>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472974 | n.1129A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472988 | n.1143T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.51 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473101 | n.1256C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.72 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473314 | n.1469A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1473384 | n.-274A>G | upstream_gene_variant | 0.55 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474393 | n.736A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474402 | n.745T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474448 | n.791T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 0.89 |
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 | 0.89 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474634 | n.977T>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474637 | n.980C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474643 | n.986A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474658 | n.1001A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474692 | n.1035G>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474706 | n.1049G>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474734 | n.1077G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474734 | n.1077G>C | non_coding_transcript_exon_variant | 1.0 |
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>C | 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 | 0.5 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475758 | n.2101A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475774 | n.2117C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475783 | n.2126T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476267 | n.2610G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476276 | n.2619C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476295 | n.2638C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476306 | n.2649A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476307 | n.2650A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476311 | n.2654G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476523 | n.2866T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476528 | n.2871A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.2 |
rpsA | 1833530 | c.-12C>T | upstream_gene_variant | 0.12 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.1 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.2 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.21 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.16 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.16 |
rpsA | 1834312 | c.771G>A | synonymous_variant | 0.17 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.17 |
rpsA | 1834345 | c.804C>T | synonymous_variant | 0.15 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.15 |
rpsA | 1834354 | c.813G>C | synonymous_variant | 0.15 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 0.14 |
rpsA | 1834360 | c.819G>C | synonymous_variant | 0.14 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.14 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.13 |
rpsA | 1834375 | c.834G>C | synonymous_variant | 0.14 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.14 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.17 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2169182 | c.1431G>T | synonymous_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289993 | c.-752C>T | upstream_gene_variant | 0.12 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
eis | 2714967 | p.Glu122Asp | missense_variant | 0.22 |
eis | 2715332 | p.Val1Met | missense_variant | 0.11 |
folC | 2746434 | p.Gly389Arg | missense_variant | 0.13 |
folC | 2746864 | c.735G>A | synonymous_variant | 0.11 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449013 | c.510C>T | synonymous_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 1.0 |
alr | 3841568 | c.-148G>A | upstream_gene_variant | 1.0 |
alr | 3841570 | c.-151delA | upstream_gene_variant | 1.0 |
alr | 3841574 | c.-154T>G | upstream_gene_variant | 1.0 |
alr | 3841578 | c.-158G>T | upstream_gene_variant | 1.0 |
alr | 3841582 | c.-162A>G | upstream_gene_variant | 1.0 |
alr | 3841584 | c.-164C>A | upstream_gene_variant | 1.0 |
alr | 3841589 | c.-170delG | upstream_gene_variant | 1.0 |
rpoA | 3878387 | p.Thr41Ala | missense_variant | 0.11 |
clpC1 | 4038501 | p.Ile735Thr | missense_variant | 0.1 |
embC | 4241451 | p.Ser530Trp | missense_variant | 0.13 |
embC | 4242401 | p.Arg847Ser | missense_variant | 0.18 |
embA | 4242628 | c.-605C>T | upstream_gene_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4246101 | c.2873dupC | frameshift_variant | 0.11 |
aftB | 4267089 | p.Thr583Asn | missense_variant | 1.0 |
aftB | 4268447 | c.390G>T | synonymous_variant | 0.12 |
ethA | 4326379 | c.1095G>C | synonymous_variant | 0.12 |
ethR | 4327957 | p.Leu137Val | missense_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338598 | c.-77G>T | upstream_gene_variant | 0.13 |