Run ID: ERR4821214
Sample name:
Date: 01-04-2023 17:07:37
Number of reads: 664404
Percentage reads mapped: 45.11
Strain:
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 1.0 |
lineage1.2.1.2 | Indo-Oceanic | NA | RD239 | 0.98 |
lineage1.2.1.2.1 | Indo-Oceanic | NA | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761127 | p.Ser441Ala | missense_variant | 0.25 | rifampicin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.55 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9260 | c.1959G>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575368 | c.21T>C | synonymous_variant | 1.0 |
ccsA | 620449 | c.560delT | frameshift_variant | 0.22 |
rpoB | 761030 | c.1224G>C | synonymous_variant | 0.25 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.22 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.22 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.22 |
rpoB | 761057 | c.1251G>T | synonymous_variant | 0.22 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.33 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.31 |
rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 0.33 |
rpoB | 761096 | c.1290G>C | synonymous_variant | 0.33 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.27 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.31 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 0.23 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.23 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.15 |
rpoB | 761159 | c.1353G>C | synonymous_variant | 0.15 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.15 |
rpoB | 762024 | p.Val740Ile | missense_variant | 0.29 |
rpoB | 762051 | p.His749Tyr | missense_variant | 0.3 |
rpoB | 762057 | p.Ile751Val | missense_variant | 0.32 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.35 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.38 |
rpoB | 762071 | p.Asp755Glu | missense_variant | 0.33 |
rpoB | 762080 | c.2274G>C | synonymous_variant | 0.4 |
rpoB | 762085 | p.Ala760Glu | missense_variant | 0.46 |
rpoB | 762089 | c.2283G>A | synonymous_variant | 0.43 |
rpoB | 762092 | c.2286G>A | synonymous_variant | 0.36 |
rpoB | 762110 | c.2304G>C | synonymous_variant | 0.36 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.33 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.36 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.33 |
rpoB | 762234 | p.Pro810Ser | missense_variant | 0.33 |
rpoB | 762239 | c.2433G>A | synonymous_variant | 0.38 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.3 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.3 |
rpoB | 762858 | p.Thr1018Ser | missense_variant | 0.15 |
rpoC | 762863 | c.-507T>C | upstream_gene_variant | 0.15 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.23 |
rpoC | 762887 | c.-483G>C | upstream_gene_variant | 0.15 |
rpoC | 762893 | c.-477C>T | upstream_gene_variant | 0.13 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.2 |
rpoC | 762926 | c.-444C>G | upstream_gene_variant | 0.17 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.27 |
rpoC | 762938 | c.-432G>C | upstream_gene_variant | 0.17 |
rpoC | 762947 | c.-423C>G | upstream_gene_variant | 0.12 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.21 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 0.25 |
rpoC | 762980 | c.-390T>C | upstream_gene_variant | 0.13 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.14 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.23 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.15 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763038 | p.Thr1078Ala | missense_variant | 0.15 |
rpoC | 763043 | c.-327G>C | upstream_gene_variant | 0.15 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.27 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.24 |
rpoB | 763077 | p.Val1091Thr | missense_variant | 0.25 |
rpoC | 763085 | c.-285C>A | upstream_gene_variant | 0.12 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.27 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.31 |
rpoB | 763119 | p.Asn1105Asp | missense_variant | 0.33 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.31 |
rpoC | 763133 | c.-237G>C | upstream_gene_variant | 0.17 |
rpoC | 763531 | c.162G>C | synonymous_variant | 1.0 |
rpoC | 763550 | p.Tyr61Ala | missense_variant | 0.11 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.18 |
rpoC | 763578 | p.Phe70Tyr | missense_variant | 0.17 |
rpoC | 763622 | p.Ala85Ser | missense_variant | 0.13 |
rpoC | 763642 | c.273G>T | synonymous_variant | 0.12 |
rpoC | 763648 | c.279C>T | synonymous_variant | 0.17 |
rpoC | 763654 | c.285C>T | synonymous_variant | 0.16 |
rpoC | 763657 | p.Glu96Asp | missense_variant | 0.18 |
rpoC | 763666 | c.297G>C | synonymous_variant | 0.17 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.19 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.41 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.33 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.41 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.4 |
rpoC | 763718 | p.Leu117Val | missense_variant | 0.39 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.26 |
rpoC | 763724 | p.Asp119Asn | missense_variant | 0.26 |
rpoC | 763729 | c.360G>C | synonymous_variant | 0.39 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.31 |
rpoC | 763735 | c.366G>C | synonymous_variant | 0.29 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.33 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.43 |
rpoC | 763772 | p.Val135Met | missense_variant | 0.32 |
rpoC | 763781 | p.Ser138Ala | missense_variant | 0.18 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.44 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.44 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.47 |
rpoC | 764503 | c.1134G>T | synonymous_variant | 0.4 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.44 |
rpoC | 764512 | c.1143G>C | synonymous_variant | 0.41 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.41 |
rpoC | 764524 | c.1155C>T | synonymous_variant | 0.35 |
rpoC | 764530 | c.1161C>T | synonymous_variant | 0.33 |
rpoC | 764533 | c.1164C>T | synonymous_variant | 0.33 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.3 |
rpoC | 764543 | p.Thr392Ala | missense_variant | 0.32 |
rpoC | 764548 | c.1179G>T | synonymous_variant | 0.4 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.39 |
rpoC | 764573 | p.Leu402Ile | missense_variant | 0.14 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 0.14 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.13 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.14 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.5 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 0.54 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.61 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.65 |
rpoC | 764647 | c.1278C>T | synonymous_variant | 0.66 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.65 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.68 |
rpoC | 764656 | c.1287C>T | synonymous_variant | 0.65 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.68 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.64 |
rpoC | 764678 | p.Lys437Gln | missense_variant | 0.64 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.54 |
rpoC | 764713 | c.1344G>C | synonymous_variant | 0.53 |
rpoC | 764731 | c.1362G>C | synonymous_variant | 0.6 |
rpoC | 764737 | c.1368G>C | synonymous_variant | 0.38 |
rpoC | 764746 | c.1377G>C | synonymous_variant | 0.25 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.29 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.83 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 778320 | p.Glu54Gly | missense_variant | 0.15 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781616 | c.57C>G | synonymous_variant | 0.13 |
rpsL | 781623 | p.Ala22Pro | missense_variant | 0.14 |
rpsL | 781628 | c.69T>G | synonymous_variant | 0.14 |
rpsL | 781638 | c.79_80delAGinsTC | synonymous_variant | 0.12 |
rpsL | 781643 | c.84G>C | synonymous_variant | 0.12 |
rpsL | 781652 | c.93T>C | synonymous_variant | 0.13 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.14 |
rpsL | 781658 | c.99A>G | synonymous_variant | 0.14 |
rpsL | 781682 | c.123T>G | synonymous_variant | 0.13 |
rpsL | 781703 | c.144G>T | synonymous_variant | 0.18 |
rpsL | 781706 | c.147T>G | synonymous_variant | 0.18 |
rpsL | 781709 | c.150G>A | synonymous_variant | 0.18 |
rpsL | 781796 | p.Met79Ile | missense_variant | 0.27 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.25 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.25 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.24 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.24 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.29 |
rpsL | 781835 | c.276T>C | synonymous_variant | 0.29 |
rpsL | 781841 | c.282C>T | synonymous_variant | 0.29 |
rpsL | 781845 | p.Lys96Arg | missense_variant | 0.23 |
rpsL | 781851 | p.Ile98Val | missense_variant | 0.23 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.25 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.25 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.15 |
rplC | 800667 | c.-142_-140delTCGinsAGC | upstream_gene_variant | 0.14 |
rplC | 800672 | c.-137G>C | upstream_gene_variant | 0.15 |
fbiC | 1302821 | c.-110G>A | upstream_gene_variant | 1.0 |
fbiC | 1305128 | p.Thr733Ile | missense_variant | 0.12 |
Rv1258c | 1406312 | c.1029T>C | synonymous_variant | 1.0 |
Rv1258c | 1406943 | c.397_398insGC | frameshift_variant | 0.13 |
Rv1258c | 1406946 | p.Ala132Gly | missense_variant | 0.12 |
Rv1258c | 1406948 | c.391_392delGC | frameshift_variant | 0.13 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
embR | 1417119 | p.Ser77Pro | missense_variant | 0.13 |
atpE | 1460907 | c.-138T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472068 | n.223T>G | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472338 | n.493A>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472412 | n.567A>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472416 | n.571C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472427 | n.582T>G | non_coding_transcript_exon_variant | 0.6 |
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 | 0.67 |
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 | 0.67 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.67 |
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 | 0.43 |
rrs | 1472513 | n.668T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472549 | n.704G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472687 | n.843dupT | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472840 | n.995A>G | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472875 | n.1030T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472974 | n.1129A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.74 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.98 |
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 | 0.77 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.76 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.87 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473262 | n.1417T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473314 | n.1469A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1473384 | n.-274A>G | upstream_gene_variant | 0.5 |
rrl | 1474163 | n.506C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474164 | n.507C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474271 | n.614A>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474272 | n.615C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474275 | n.618T>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474468 | n.811G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474476 | n.819C>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474479 | n.822A>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474483 | n.826C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.77 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474529 | n.872A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474551 | n.894G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474634 | n.977T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474637 | n.980C>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474640 | n.983C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474643 | n.986A>G | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474692 | n.1035G>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474706 | n.1049G>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474734 | n.1077G>A | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474753 | n.1096delA | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474766 | n.1109A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474777 | n.1120T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474783 | n.1126G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474785 | n.1128T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1474802 | n.1145T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474831 | n.1174A>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474832 | n.1175A>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1474837 | n.1180A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474852 | n.1195T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475104 | n.1447T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475124 | n.1467A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475171 | n.1514C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475499 | n.1842C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475518 | n.1861A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475521 | n.1864T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475526 | n.1869C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475529 | n.1872A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475532 | n.1875A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475538 | n.1881T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475548 | n.1891C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475549 | n.1892T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475703 | n.2046A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475715 | n.2058G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475754 | n.2097G>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475756 | n.2099T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475774 | n.2117C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.53 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475995 | n.2338G>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475998 | n.2341C>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476000 | n.2343G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476164 | n.2507A>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476165 | n.2508T>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476179 | n.2522C>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476187 | n.2530T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476194 | n.2537A>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476204 | n.2547C>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476207 | n.2550T>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476235 | n.2578A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476523 | n.2866T>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476528 | n.2871A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476542 | n.2885T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476594 | n.2937C>A | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476603 | n.2946G>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476661 | n.3004A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476665 | n.3008T>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476668 | n.3011C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476675 | n.3018C>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476682 | n.3026delT | non_coding_transcript_exon_variant | 0.22 |
inhA | 1674162 | c.-40C>T | upstream_gene_variant | 1.0 |
inhA | 1674497 | p.Pro99Leu | missense_variant | 0.15 |
rpsA | 1834183 | c.642T>C | synonymous_variant | 0.15 |
rpsA | 1834189 | c.648G>T | synonymous_variant | 0.33 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 0.38 |
rpsA | 1834228 | c.687C>T | synonymous_variant | 0.46 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 0.38 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.53 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.48 |
rpsA | 1834246 | c.705G>T | synonymous_variant | 0.58 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.58 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.62 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.61 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.55 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.55 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.52 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.5 |
rpsA | 1834312 | c.771G>A | synonymous_variant | 0.52 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.54 |
rpsA | 1834345 | c.804C>T | synonymous_variant | 0.44 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.38 |
rpsA | 1834354 | c.813G>C | synonymous_variant | 0.31 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 0.29 |
rpsA | 1834360 | c.819G>C | synonymous_variant | 0.29 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.29 |
rpsA | 1834366 | c.825A>C | synonymous_variant | 0.31 |
rpsA | 1834375 | c.834G>C | synonymous_variant | 0.29 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.31 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.29 |
rpsA | 1834395 | p.Arg285Gln | missense_variant | 0.29 |
rpsA | 1834397 | p.His286Ala | missense_variant | 0.27 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.35 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.21 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.2 |
rpsA | 1834427 | p.Ile296Val | missense_variant | 0.2 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.2 |
rpsA | 1834451 | c.910_912delTTGinsCTC | synonymous_variant | 0.18 |
rpsA | 1834456 | c.915T>C | synonymous_variant | 0.19 |
rpsA | 1834459 | c.918G>C | synonymous_variant | 0.19 |
rpsA | 1834465 | c.924T>C | synonymous_variant | 0.19 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.19 |
rpsA | 1834477 | c.936C>T | synonymous_variant | 0.2 |
rpsA | 1834486 | p.Glu315Asp | missense_variant | 0.19 |
rpsA | 1834607 | p.Arg356Cys | missense_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102050 | c.993T>C | synonymous_variant | 0.11 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2154843 | c.1269T>C | synonymous_variant | 0.15 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169074 | c.1539T>C | synonymous_variant | 0.25 |
Rv1979c | 2221756 | p.Ile470Thr | missense_variant | 0.11 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2222750 | c.415C>T | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2519048 | p.Gly312Ser | missense_variant | 1.0 |
eis | 2715524 | c.-192G>A | upstream_gene_variant | 0.17 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
ribD | 2986947 | p.Asp37Asn | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086987 | p.Gln56His | missense_variant | 0.17 |
fbiD | 3339417 | c.300A>G | synonymous_variant | 1.0 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474344 | p.Asn113Ser | missense_variant | 0.18 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3474806 | p.Met267Thr | missense_variant | 0.11 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
whiB7 | 3568488 | c.191delG | frameshift_variant | 1.0 |
fbiB | 3640557 | c.-978T>C | upstream_gene_variant | 1.0 |
clpC1 | 4038826 | p.Ile627Val | missense_variant | 0.12 |
clpC1 | 4038830 | c.1875C>T | synonymous_variant | 0.13 |
clpC1 | 4038836 | c.1869G>C | synonymous_variant | 0.13 |
clpC1 | 4038839 | c.1866G>C | synonymous_variant | 0.14 |
clpC1 | 4038842 | c.1863G>C | synonymous_variant | 0.12 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 0.12 |
clpC1 | 4038872 | c.1833C>G | synonymous_variant | 0.13 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.21 |
clpC1 | 4038881 | c.1824C>T | synonymous_variant | 0.14 |
clpC1 | 4038884 | c.1821C>T | synonymous_variant | 0.14 |
clpC1 | 4038890 | p.Glu605Asp | missense_variant | 0.17 |
clpC1 | 4038896 | c.1809C>T | synonymous_variant | 0.15 |
clpC1 | 4038905 | c.1800A>C | synonymous_variant | 0.13 |
clpC1 | 4039814 | c.891C>G | synonymous_variant | 0.2 |
clpC1 | 4039817 | c.888A>T | synonymous_variant | 0.2 |
clpC1 | 4039820 | c.885T>C | synonymous_variant | 0.2 |
clpC1 | 4039823 | c.882T>G | synonymous_variant | 0.2 |
clpC1 | 4039829 | c.874_876delTTGinsCTC | synonymous_variant | 0.27 |
clpC1 | 4039838 | p.Leu289Ile | missense_variant | 0.25 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.17 |
clpC1 | 4039853 | c.852G>C | synonymous_variant | 0.17 |
clpC1 | 4039856 | p.Ile283Met | missense_variant | 0.17 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.25 |
clpC1 | 4039874 | p.Asn277Lys | missense_variant | 0.18 |
clpC1 | 4039881 | p.Glu275Gly | missense_variant | 0.15 |
clpC1 | 4040063 | c.642G>C | synonymous_variant | 0.25 |
clpC1 | 4040066 | c.639G>C | synonymous_variant | 0.25 |
clpC1 | 4040090 | c.615T>C | synonymous_variant | 0.29 |
clpC1 | 4040117 | c.588A>G | synonymous_variant | 0.22 |
clpC1 | 4040125 | p.Glu194Gln | missense_variant | 0.2 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embC | 4242210 | p.Glu783Gly | missense_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243580 | c.348G>A | synonymous_variant | 1.0 |
embA | 4244420 | c.1188G>C | synonymous_variant | 1.0 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4247578 | c.1065G>A | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4248609 | p.Ile699Thr | missense_variant | 0.18 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ubiA | 4269864 | c.-32delG | upstream_gene_variant | 1.0 |
whiB6 | 4338361 | p.Arg54Gln | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |