Run ID: ERR4819706
Sample name:
Date: 01-04-2023 16:15:36
Number of reads: 1902268
Percentage reads mapped: 81.57
Strain: lineage4.3.4.2
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.4 | Euro-American (LAM) | LAM | RD174 | 1.0 |
lineage4.3.4.2 | Euro-American (LAM) | LAM1;LAM4;LAM11 | RD174 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761127 | p.Ser441Ala | missense_variant | 0.24 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.18 | streptomycin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.25 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.12 | kanamycin, capreomycin, aminoglycosides, amikacin |
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
inhA | 1674481 | p.Ser94Ala | missense_variant | 1.0 | isoniazid, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6817 | c.-485G>A | upstream_gene_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.33 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.12 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.17 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.17 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.17 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.17 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.17 |
rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 0.16 |
rpoB | 761096 | c.1290G>C | synonymous_variant | 0.17 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.17 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.19 |
rpoB | 761123 | c.1317G>T | synonymous_variant | 0.19 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 0.22 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.24 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.19 |
rpoB | 761159 | c.1353G>C | synonymous_variant | 0.21 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.23 |
rpoB | 761174 | c.1368T>C | synonymous_variant | 0.16 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.15 |
rpoB | 761186 | p.Glu460Asp | missense_variant | 0.14 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.12 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.13 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.14 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 0.12 |
rpoB | 762212 | c.2406G>C | synonymous_variant | 0.13 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.12 |
rpoB | 762234 | p.Pro810Ser | missense_variant | 0.12 |
rpoB | 762239 | c.2433G>A | synonymous_variant | 0.12 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.12 |
rpoC | 763043 | c.-327G>C | upstream_gene_variant | 0.11 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.11 |
rpoC | 763531 | c.162G>C | synonymous_variant | 0.12 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.11 |
rpoC | 763552 | p.Tyr61* | stop_gained | 0.11 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.16 |
rpoC | 763578 | p.Phe70Tyr | missense_variant | 0.15 |
rpoC | 763598 | p.Arg77Ser | missense_variant | 0.13 |
rpoC | 763657 | p.Glu96Asp | missense_variant | 0.12 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.11 |
rpoC | 763666 | c.297G>C | synonymous_variant | 0.12 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.16 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.15 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.12 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.12 |
rpoC | 763718 | p.Leu117Val | missense_variant | 0.12 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.12 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.2 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.19 |
rpoC | 764503 | c.1134G>T | synonymous_variant | 0.2 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.19 |
rpoC | 764512 | c.1143G>C | synonymous_variant | 0.21 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.25 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.26 |
rpoC | 764543 | p.Thr392Ala | missense_variant | 0.25 |
rpoC | 764548 | c.1179G>T | synonymous_variant | 0.22 |
rpoC | 764551 | c.1182G>C | synonymous_variant | 0.24 |
rpoC | 764573 | p.Leu402Ile | missense_variant | 0.32 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 0.32 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.31 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.33 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.37 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 0.38 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.35 |
rpoC | 764632 | c.1263T>A | synonymous_variant | 0.3 |
rpoC | 764647 | c.1278C>T | synonymous_variant | 0.27 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.27 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.26 |
rpoC | 764656 | c.1287C>G | synonymous_variant | 0.25 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.26 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.23 |
rpoC | 764678 | p.Lys437Gln | missense_variant | 0.23 |
rpoC | 764683 | c.1314G>C | synonymous_variant | 0.22 |
rpoC | 764692 | c.1323C>T | synonymous_variant | 0.22 |
rpoC | 764705 | p.Leu446Ala | missense_variant | 0.19 |
rpoC | 764713 | c.1344G>C | synonymous_variant | 0.17 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304848 | p.Asn640Tyr | missense_variant | 0.29 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472412 | n.567A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472416 | n.571C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472427 | n.582T>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472436 | n.591G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472437 | n.592T>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472449 | n.604C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472450 | n.605A>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472451 | n.606C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472462 | n.617T>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472473 | n.628G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472474 | n.629C>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472476 | n.631A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472484 | n.639A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472496 | n.651T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472513 | n.668T>C | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472549 | n.704G>A | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472597 | n.752G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472686 | n.841G>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472690 | n.845C>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472779 | n.934G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472828 | n.983T>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 | 0.43 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.49 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.49 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.51 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473101 | n.1256C>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.65 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.65 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473305 | n.1460G>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1473384 | n.-274A>G | upstream_gene_variant | 0.41 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474271 | n.614A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474272 | n.615C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474275 | n.618T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474454 | n.797G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474483 | n.826C>T | non_coding_transcript_exon_variant | 0.5 |
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 | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474497 | n.840G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474506 | n.849C>T | non_coding_transcript_exon_variant | 0.67 |
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 | 1.0 |
rrl | 1474528 | n.871T>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474529 | n.872A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474540 | n.883T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474541 | n.884G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474551 | n.894G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 1.0 |
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 | 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 | 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>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474832 | n.1175A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475751 | n.2094C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475752 | n.2095C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475756 | n.2099T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475758 | n.2101A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475760 | n.2103C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475764 | n.2107A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475764 | n.2107A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475765 | n.2108A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476130 | n.2473G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476165 | n.2508T>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476179 | n.2522C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476194 | n.2537A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476204 | n.2547C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476207 | n.2550T>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476253 | n.2596A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476267 | n.2610G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476276 | n.2619C>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476297 | n.2640C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476299 | n.2642C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476300 | n.2643G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.67 |
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 | 1476308 | n.2651G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476542 | n.2885T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.5 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.12 |
rpsA | 1833667 | c.126C>T | synonymous_variant | 0.13 |
rpsA | 1833668 | p.Ile43Val | missense_variant | 0.12 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.11 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 0.11 |
rpsA | 1833685 | c.144G>C | synonymous_variant | 0.1 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.11 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.11 |
rpsA | 1833724 | c.183C>T | synonymous_variant | 0.11 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.11 |
rpsA | 1833732 | p.Pro64Leu | missense_variant | 0.12 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.12 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.12 |
rpsA | 1833764 | p.Asp75Asn | missense_variant | 0.12 |
rpsA | 1833970 | c.429G>T | synonymous_variant | 0.15 |
rpsA | 1833976 | c.435C>T | synonymous_variant | 0.12 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.13 |
rpsA | 1833994 | c.453G>C | synonymous_variant | 0.12 |
rpsA | 1833997 | c.456G>C | synonymous_variant | 0.11 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.12 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.11 |
rpsA | 1834024 | c.483G>C | synonymous_variant | 0.11 |
rpsA | 1834025 | p.Gln162Ala | missense_variant | 0.11 |
rpsA | 1834040 | p.Lys167Gln | missense_variant | 0.13 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.11 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.14 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.13 |
rpsA | 1834264 | c.723G>T | synonymous_variant | 0.11 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.16 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.16 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.16 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.16 |
rpsA | 1834312 | c.771G>A | synonymous_variant | 0.16 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.2 |
rpsA | 1834345 | c.804C>T | synonymous_variant | 0.14 |
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 | 0.15 |
rpsA | 1834360 | c.819G>C | synonymous_variant | 0.15 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.15 |
rpsA | 1834366 | c.825A>C | synonymous_variant | 0.15 |
rpsA | 1834375 | c.834G>C | synonymous_variant | 0.15 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.15 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.12 |
rpsA | 1834397 | p.His286Ala | missense_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612009 | p.Ala370Thr | missense_variant | 1.0 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
embC | 4239763 | c.-100C>T | upstream_gene_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |