Run ID: ERR4820266
Sample name:
Date: 01-04-2023 16:35:00
Number of reads: 394169
Percentage reads mapped: 76.29
Strain: lineage3
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761127 | p.Ser441Ala | missense_variant | 0.38 | rifampicin |
rpoB | 761196 | p.Leu464Met | missense_variant | 0.29 | rifampicin |
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.12 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6707 | p.Lys490Glu | missense_variant | 0.18 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7823 | c.522G>A | synonymous_variant | 0.18 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576060 | p.Val238Asp | missense_variant | 0.5 |
ccsA | 620468 | p.Ser193Asn | missense_variant | 0.2 |
ccsA | 620532 | c.642T>G | synonymous_variant | 0.33 |
ccsA | 620694 | c.804C>A | synonymous_variant | 0.4 |
rpoB | 759615 | c.-192A>C | upstream_gene_variant | 0.5 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 759859 | p.Pro18Gln | missense_variant | 0.18 |
rpoB | 760636 | p.Pro277Leu | missense_variant | 0.2 |
rpoB | 761097 | c.1291_1292delAGinsTC | synonymous_variant | 0.25 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.29 |
rpoB | 761123 | c.1317G>C | synonymous_variant | 0.25 |
rpoB | 761126 | c.1320G>C | synonymous_variant | 0.25 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 0.25 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.38 |
rpoB | 761150 | c.1344A>T | synonymous_variant | 0.29 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.33 |
rpoB | 761186 | p.Glu460Asp | missense_variant | 0.29 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.29 |
rpoB | 761201 | c.1395G>A | synonymous_variant | 0.29 |
rpoB | 761207 | c.1401C>A | synonymous_variant | 0.25 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.25 |
rpoB | 761219 | c.1413G>C | synonymous_variant | 0.25 |
rpoB | 761231 | c.1425C>T | synonymous_variant | 0.33 |
rpoB | 761234 | c.1428G>T | synonymous_variant | 0.33 |
rpoB | 762099 | p.Arg765Cys | missense_variant | 0.22 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 0.88 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.12 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.12 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763038 | p.Thr1078Ala | missense_variant | 0.11 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.11 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.12 |
rpoB | 763078 | p.Val1091Ala | missense_variant | 0.12 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.13 |
rpoC | 763507 | c.138G>C | synonymous_variant | 0.18 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.21 |
rpoC | 763531 | c.162G>C | synonymous_variant | 0.21 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.21 |
rpoC | 763537 | c.168C>G | synonymous_variant | 0.2 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.19 |
rpoC | 763550 | p.Tyr61Ala | missense_variant | 0.2 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.12 |
rpoC | 763578 | p.Phe70Tyr | missense_variant | 0.14 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.19 |
rpoC | 763657 | p.Glu96Asp | missense_variant | 0.11 |
rpoC | 763660 | c.291T>C | synonymous_variant | 0.12 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.11 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.11 |
rpoC | 763713 | c.345G>C | synonymous_variant | 0.12 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.11 |
rpoC | 763729 | c.360G>C | synonymous_variant | 0.12 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.12 |
rpoC | 763735 | c.366G>C | synonymous_variant | 0.18 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.13 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.2 |
rpoC | 763772 | p.Val135Met | missense_variant | 0.15 |
rpoC | 763781 | p.Ser138Glu | missense_variant | 0.13 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.15 |
rpoC | 764573 | p.Leu402Ile | missense_variant | 0.15 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 0.15 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.14 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.14 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.29 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.35 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 0.42 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.42 |
rpoC | 764632 | c.1263T>A | synonymous_variant | 0.43 |
rpoC | 764647 | c.1278C>T | synonymous_variant | 0.41 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.42 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.42 |
rpoC | 764656 | c.1287C>G | synonymous_variant | 0.41 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.39 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.35 |
rpoC | 764678 | p.Lys437Gln | missense_variant | 0.32 |
rpoC | 764683 | c.1314G>C | synonymous_variant | 0.32 |
rpoC | 764692 | c.1323C>T | synonymous_variant | 0.32 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.28 |
rpoC | 764731 | c.1362G>C | synonymous_variant | 0.22 |
rpoC | 764737 | c.1368G>C | synonymous_variant | 0.16 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776758 | p.Asp575Asn | missense_variant | 0.22 |
mmpL5 | 776984 | c.1496delT | frameshift_variant | 0.15 |
mmpL5 | 777482 | c.999G>A | synonymous_variant | 0.22 |
mmpR5 | 778448 | c.-542G>A | upstream_gene_variant | 0.33 |
mmpR5 | 779247 | c.262delG | frameshift_variant | 0.12 |
mmpS5 | 779679 | c.-774G>A | upstream_gene_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781490 | c.-70C>T | upstream_gene_variant | 0.13 |
rplC | 800753 | c.-56C>A | upstream_gene_variant | 0.25 |
fbiC | 1303016 | p.Val29Gly | missense_variant | 0.33 |
Rv1258c | 1406102 | c.1239G>A | synonymous_variant | 0.15 |
Rv1258c | 1407224 | c.116delG | frameshift_variant | 0.2 |
embR | 1417314 | p.Asp12His | missense_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471740 | n.-106A>G | upstream_gene_variant | 0.22 |
rrs | 1471762 | n.-84C>T | upstream_gene_variant | 0.33 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472290 | n.445C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472293 | n.448C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472295 | n.450A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472298 | n.453_454insCCTGC | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472314 | n.469A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472330 | n.485G>T | non_coding_transcript_exon_variant | 1.0 |
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 | 1472476 | n.631A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472513 | n.668T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472549 | n.704G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472686 | n.841G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472690 | n.845C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 1.0 |
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 | 0.11 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.63 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.74 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1473262 | n.1417T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.7 |
rrs | 1473283 | n.1438T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473284 | n.1439A>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473300 | n.1455C>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473314 | n.1469A>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473319 | n.1474C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1473384 | n.-274A>G | upstream_gene_variant | 0.6 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474355 | n.698A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474393 | n.736A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474402 | n.745T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474448 | n.791T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 0.8 |
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 | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475754 | n.2097G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475756 | n.2099T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475774 | n.2117C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475866 | n.2209T>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.71 |
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 | 1475892 | n.2235A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.4 |
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 | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476523 | n.2866T>C | non_coding_transcript_exon_variant | 0.83 |
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 | 0.67 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.67 |
inhA | 1673816 | c.-386G>A | upstream_gene_variant | 1.0 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 0.2 |
rpsA | 1834228 | c.687C>T | synonymous_variant | 0.31 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.33 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.3 |
rpsA | 1834246 | c.705G>T | synonymous_variant | 0.38 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.43 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.53 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.56 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.78 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.74 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.74 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.74 |
rpsA | 1834312 | c.771G>A | synonymous_variant | 0.74 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.7 |
rpsA | 1834345 | c.804C>T | synonymous_variant | 0.55 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.55 |
rpsA | 1834354 | c.813G>C | synonymous_variant | 0.48 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 0.45 |
rpsA | 1834360 | c.819G>C | synonymous_variant | 0.45 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.45 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.45 |
rpsA | 1834375 | c.834G>C | synonymous_variant | 0.43 |
rpsA | 1834378 | c.837T>G | synonymous_variant | 0.43 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.38 |
rpsA | 1834394 | c.853_854insA | frameshift_variant | 0.26 |
rpsA | 1834398 | c.858delC | frameshift_variant | 0.22 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.2 |
tlyA | 1917764 | c.-176C>T | upstream_gene_variant | 0.2 |
tlyA | 1917824 | c.-116C>T | upstream_gene_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918683 | c.744C>T | synonymous_variant | 0.25 |
ndh | 2102970 | p.Gly25Ser | missense_variant | 0.25 |
katG | 2154146 | p.Asp656Asn | missense_variant | 0.15 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155964 | p.Gln50Lys | missense_variant | 0.12 |
PPE35 | 2167745 | p.Thr956Arg | missense_variant | 0.13 |
PPE35 | 2167865 | c.2748G>C | synonymous_variant | 0.29 |
PPE35 | 2167868 | c.2745A>C | synonymous_variant | 0.25 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168019 | p.Thr865Ile | missense_variant | 1.0 |
PPE35 | 2168763 | p.Thr617Ile | missense_variant | 0.25 |
PPE35 | 2169269 | c.1344A>G | synonymous_variant | 0.25 |
PPE35 | 2169272 | c.1341C>G | synonymous_variant | 0.25 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.2 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.2 |
PPE35 | 2169441 | p.Ala391Gly | missense_variant | 0.22 |
PPE35 | 2169447 | p.Phe389Thr | missense_variant | 0.22 |
PPE35 | 2170472 | c.141G>A | synonymous_variant | 0.22 |
PPE35 | 2170574 | c.39C>G | synonymous_variant | 0.12 |
PPE35 | 2170577 | c.36G>A | synonymous_variant | 0.12 |
Rv1979c | 2222088 | p.Leu359Phe | missense_variant | 0.18 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
pncA | 2289634 | c.-393A>G | upstream_gene_variant | 0.25 |
kasA | 2518864 | c.750G>C | synonymous_variant | 0.13 |
eis | 2714474 | p.Thr287Ala | missense_variant | 0.12 |
ahpC | 2725981 | c.-212T>C | upstream_gene_variant | 0.25 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726758 | p.Glu189Val | missense_variant | 0.29 |
folC | 2747052 | p.Ala183Thr | missense_variant | 0.18 |
folC | 2747158 | c.441G>T | synonymous_variant | 0.14 |
pepQ | 2859660 | c.759G>A | synonymous_variant | 0.29 |
pepQ | 2860252 | p.Thr56Ile | missense_variant | 0.13 |
ribD | 2987537 | c.699G>A | synonymous_variant | 0.11 |
Rv2752c | 3066258 | c.-67G>A | upstream_gene_variant | 0.2 |
thyX | 3067987 | c.-42C>T | upstream_gene_variant | 1.0 |
thyX | 3068093 | c.-148A>C | upstream_gene_variant | 0.29 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086841 | p.Glu8Lys | missense_variant | 0.2 |
fbiD | 3339468 | c.351G>A | synonymous_variant | 0.2 |
fbiD | 3339498 | c.381G>A | synonymous_variant | 0.2 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474143 | p.Trp46Tyr | missense_variant | 0.17 |
fprA | 3474459 | c.453A>C | synonymous_variant | 0.15 |
fprA | 3474790 | p.Pro262Ser | missense_variant | 0.2 |
rpoA | 3877839 | c.669G>A | synonymous_variant | 0.12 |
clpC1 | 4038440 | c.2265C>A | synonymous_variant | 0.18 |
clpC1 | 4039049 | c.1656C>T | synonymous_variant | 0.22 |
clpC1 | 4039774 | p.Lys311Glu | missense_variant | 0.4 |
clpC1 | 4039827 | p.Val293Asp | missense_variant | 0.29 |
embC | 4239964 | c.102G>A | synonymous_variant | 0.22 |
embC | 4240235 | p.Arg125Trp | missense_variant | 0.17 |
embC | 4240571 | p.Gly237Trp | missense_variant | 0.17 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242454 | c.-779G>A | upstream_gene_variant | 0.67 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4246200 | p.Gln990* | stop_gained | 0.2 |
embB | 4246536 | p.Arg8His | missense_variant | 0.14 |
embB | 4246585 | c.72C>T | synonymous_variant | 0.18 |
embB | 4248963 | p.Ala817Val | missense_variant | 0.5 |
embB | 4249323 | p.Ala937Glu | missense_variant | 0.22 |
aftB | 4268198 | c.639C>T | synonymous_variant | 0.15 |
ethA | 4326582 | p.Asn298Asp | missense_variant | 0.14 |
ethA | 4327364 | p.Lys37Thr | missense_variant | 0.15 |
ethA | 4328318 | c.-845G>A | upstream_gene_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338719 | c.-198T>C | upstream_gene_variant | 0.12 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |