Run ID: ERR4821057
Sample name:
Date: 01-04-2023 17:02:16
Number of reads: 310802
Percentage reads mapped: 46.02
Strain: lineage4
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.8 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.75 | kanamycin, capreomycin, aminoglycosides, amikacin |
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5774 | c.539delT | frameshift_variant | 0.18 |
gyrA | 6811 | c.-491C>T | upstream_gene_variant | 0.29 |
gyrA | 6841 | c.-461T>C | upstream_gene_variant | 0.25 |
gyrA | 6844 | c.-458T>C | upstream_gene_variant | 0.29 |
gyrB | 6851 | p.Gln538Met | missense_variant | 0.29 |
gyrA | 6859 | c.-443T>C | upstream_gene_variant | 0.29 |
gyrB | 6860 | p.Ser541Arg | missense_variant | 0.29 |
gyrA | 6869 | c.-433T>C | upstream_gene_variant | 0.4 |
gyrA | 6872 | c.-430T>C | upstream_gene_variant | 0.33 |
gyrA | 6878 | c.-424T>C | upstream_gene_variant | 0.33 |
gyrA | 6881 | c.-421T>C | upstream_gene_variant | 0.33 |
gyrA | 6898 | c.-404G>C | upstream_gene_variant | 0.29 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
mshA | 575279 | c.-69C>A | upstream_gene_variant | 0.22 |
rpoB | 760982 | c.1176G>T | synonymous_variant | 0.33 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.33 |
rpoB | 760988 | c.1182C>G | synonymous_variant | 0.33 |
rpoB | 760991 | c.1185G>T | synonymous_variant | 0.33 |
rpoB | 760997 | c.1191G>C | synonymous_variant | 0.5 |
rpoB | 761006 | c.1200C>G | synonymous_variant | 0.5 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.4 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.42 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.45 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.38 |
rpoB | 761064 | p.Ala420Ser | missense_variant | 0.38 |
rpoB | 761097 | p.Ser431Cys | missense_variant | 0.2 |
rpoB | 762030 | p.Thr742Ser | missense_variant | 0.33 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.25 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.2 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.2 |
rpoB | 762084 | p.Ala760Pro | missense_variant | 0.22 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.22 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.33 |
rpoB | 762122 | p.Asp772Glu | missense_variant | 0.29 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.6 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.5 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.5 |
rpoB | 762278 | c.2472C>T | synonymous_variant | 0.33 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.4 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.4 |
rpoB | 762297 | p.Leu831Met | missense_variant | 0.5 |
rpoC | 762842 | c.-528G>A | upstream_gene_variant | 0.22 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.29 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.3 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 0.5 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.55 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.46 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.46 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.47 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.5 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.39 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.38 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.36 |
rpoB | 763005 | p.Cys1067Val | missense_variant | 0.25 |
rpoB | 763014 | p.Met1070Leu | missense_variant | 0.29 |
rpoB | 763017 | p.Gln1071Glu | missense_variant | 0.33 |
rpoC | 763022 | c.-348C>G | upstream_gene_variant | 0.37 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.41 |
rpoB | 763038 | p.Thr1078Ala | missense_variant | 0.44 |
rpoC | 763053 | c.-317_-315delTTGinsCTC | upstream_gene_variant | 0.38 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.36 |
rpoC | 763082 | c.-288C>A | upstream_gene_variant | 0.5 |
rpoC | 763088 | c.-282C>G | upstream_gene_variant | 0.44 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.45 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.23 |
rpoC | 763142 | c.-228C>G | upstream_gene_variant | 0.17 |
rpoC | 763507 | c.138G>C | synonymous_variant | 0.4 |
rpoC | 763528 | c.159G>T | synonymous_variant | 0.6 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.6 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.5 |
rpoC | 763570 | c.201G>A | synonymous_variant | 0.33 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.5 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.6 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.25 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.36 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.33 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.29 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.38 |
rpoC | 763708 | c.339G>T | synonymous_variant | 0.25 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.38 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.38 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.38 |
rpoC | 763729 | c.360G>C | synonymous_variant | 0.38 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.18 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.2 |
rpoC | 763795 | p.Glu142Asp | missense_variant | 0.2 |
rpoC | 764338 | p.Glu323Asp | missense_variant | 0.25 |
rpoC | 764344 | c.975C>T | synonymous_variant | 0.25 |
rpoC | 764357 | c.988_990delCTCinsTTG | synonymous_variant | 0.29 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.5 |
rpoC | 764371 | c.1002G>T | synonymous_variant | 0.4 |
rpoC | 764377 | c.1008C>G | synonymous_variant | 0.4 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 0.36 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.5 |
rpoC | 764428 | c.1059G>A | synonymous_variant | 0.5 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.44 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.44 |
rpoC | 764435 | c.1066_1068delAGGinsCGT | synonymous_variant | 0.44 |
rpoC | 764441 | p.Ile358Leu | missense_variant | 0.5 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.67 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.67 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.67 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.67 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.8 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.67 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.29 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.29 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.29 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.29 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.38 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 0.38 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.38 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.5 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.6 |
rpoC | 764644 | c.1275G>C | synonymous_variant | 0.62 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.57 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.29 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.4 |
rpoC | 764692 | c.1323C>T | synonymous_variant | 0.33 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.22 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.33 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.33 |
rpoC | 764759 | p.Asn464Asp | missense_variant | 0.3 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.6 |
rpoC | 764780 | c.1411_1413delAGCinsTCG | synonymous_variant | 0.33 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.33 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.25 |
rpoC | 764812 | c.1443C>G | synonymous_variant | 0.2 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.2 |
rpoC | 764843 | p.Ala492Thr | missense_variant | 0.18 |
rpoC | 766318 | p.Met983Ile | missense_variant | 0.13 |
rpoC | 767210 | p.Ala1281Thr | missense_variant | 0.22 |
rpoC | 767318 | c.3949T>C | stop_lost&splice_region_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776759 | c.1722C>T | synonymous_variant | 0.2 |
mmpL5 | 777586 | p.Tyr299Asn | missense_variant | 0.14 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781658 | c.99A>C | synonymous_variant | 0.14 |
rpsL | 781709 | c.150G>C | synonymous_variant | 0.11 |
rpsL | 781715 | c.156T>G | synonymous_variant | 0.11 |
rpsL | 781721 | c.162C>T | synonymous_variant | 0.12 |
rpsL | 781749 | p.Thr64Ala | missense_variant | 0.15 |
rpsL | 781796 | p.Met79Ile | missense_variant | 0.38 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.3 |
rpsL | 781808 | c.249C>T | synonymous_variant | 0.3 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.3 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.3 |
rpsL | 781829 | c.270G>C | synonymous_variant | 0.36 |
rpsL | 781832 | c.273T>G | synonymous_variant | 0.27 |
rpsL | 781838 | c.279G>C | synonymous_variant | 0.3 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.31 |
rpsL | 781860 | p.Ser101Ala | missense_variant | 0.23 |
rpsL | 781865 | c.306G>C | synonymous_variant | 0.31 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.29 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.31 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
embR | 1416427 | c.921G>A | synonymous_variant | 0.2 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472148 | n.303T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472297 | n.453_465delGTCCGGGTTCTCT | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472337 | n.492C>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472368 | n.523A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473094 | n.1249T>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473127 | n.1282G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473201 | n.1356A>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473202 | n.1357C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1473844 | n.187C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473870 | n.213G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473871 | n.214T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473887 | n.230T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473888 | n.231T>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474201 | n.544T>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474266 | n.609T>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474496 | n.839C>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474636 | n.979A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474709 | n.1053delT | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474714 | n.1058delT | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474717 | n.1060A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474751 | n.1094G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474869 | n.1212G>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474936 | n.1279C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474938 | n.1281G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475740 | n.2083G>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475747 | n.2090A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475758 | n.2101A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475764 | n.2107A>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475765 | n.2108A>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475781 | n.2124T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475788 | n.2131C>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476251 | n.2594T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476266 | n.2609G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476288 | n.2631T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476368 | n.2711T>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.6 |
fabG1 | 1673252 | c.-188C>T | upstream_gene_variant | 0.29 |
rpsA | 1833884 | c.345delC | frameshift_variant | 0.17 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.2 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.33 |
rpsA | 1833955 | c.414G>C | synonymous_variant | 0.38 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.3 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.4 |
rpsA | 1833991 | c.450C>G | synonymous_variant | 0.5 |
rpsA | 1833997 | c.456G>C | synonymous_variant | 0.44 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.56 |
rpsA | 1834012 | c.471G>T | synonymous_variant | 0.4 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.45 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.3 |
rpsA | 1834046 | p.Ile169Val | missense_variant | 0.2 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.22 |
rpsA | 1834210 | c.669C>T | synonymous_variant | 0.25 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.25 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 0.27 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.27 |
rpsA | 1834246 | c.705G>C | synonymous_variant | 0.36 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.33 |
rpsA | 1834255 | c.714C>G | synonymous_variant | 0.33 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.38 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.38 |
rpsA | 1834294 | c.753G>T | synonymous_variant | 0.45 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.38 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.43 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.5 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.5 |
rpsA | 1834312 | c.771G>A | synonymous_variant | 0.5 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.6 |
rpsA | 1834354 | c.813G>T | synonymous_variant | 0.6 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 0.5 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102781 | p.Asn88Asp | missense_variant | 0.22 |
ndh | 2102833 | c.210G>T | synonymous_variant | 0.12 |
PPE35 | 2168864 | c.1749G>T | synonymous_variant | 0.4 |
Rv1979c | 2223233 | c.-69G>C | upstream_gene_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289551 | c.-310C>A | upstream_gene_variant | 0.2 |
eis | 2715029 | p.Ala102Thr | missense_variant | 0.5 |
folC | 2747008 | c.591C>A | synonymous_variant | 0.2 |
thyX | 3068062 | c.-117A>G | upstream_gene_variant | 0.18 |
thyA | 3073969 | p.Ala168Val | missense_variant | 0.22 |
ald | 3087484 | p.Ala222Val | missense_variant | 0.2 |
whiB7 | 3568629 | c.51T>A | synonymous_variant | 0.17 |
alr | 3840751 | p.Glu224Lys | missense_variant | 0.2 |
rpoA | 3877920 | c.588G>C | synonymous_variant | 0.33 |
rpoA | 3877926 | p.Leu194Val | missense_variant | 0.33 |
clpC1 | 4038588 | p.Arg706His | missense_variant | 0.25 |
clpC1 | 4038662 | c.2043T>C | synonymous_variant | 0.25 |
clpC1 | 4039550 | c.1155G>C | synonymous_variant | 0.18 |
clpC1 | 4039554 | p.Thr384Asn | missense_variant | 0.17 |
clpC1 | 4039556 | p.Ala383Val | missense_variant | 0.17 |
clpC1 | 4039570 | p.Met379Leu | missense_variant | 0.22 |
clpC1 | 4039574 | c.1131G>C | synonymous_variant | 0.25 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.25 |
clpC1 | 4039588 | p.Ser373Thr | missense_variant | 0.25 |
clpC1 | 4039589 | c.1116G>C | synonymous_variant | 0.25 |
clpC1 | 4039592 | c.1113G>C | synonymous_variant | 0.2 |
clpC1 | 4039601 | c.1104G>A | synonymous_variant | 0.3 |
clpC1 | 4039610 | c.1095G>T | synonymous_variant | 0.3 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.33 |
clpC1 | 4039622 | c.1083C>T | synonymous_variant | 0.25 |
clpC1 | 4039714 | p.Tyr331His | missense_variant | 0.6 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.5 |
clpC1 | 4039742 | c.963C>T | synonymous_variant | 0.4 |
clpC1 | 4039748 | c.957G>C | synonymous_variant | 0.4 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.4 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.4 |
clpC1 | 4039766 | c.939T>C | synonymous_variant | 0.4 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.4 |
clpC1 | 4039773 | p.Lys311Met | missense_variant | 0.4 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.4 |
clpC1 | 4039787 | c.918G>C | synonymous_variant | 0.36 |
clpC1 | 4039790 | c.915C>G | synonymous_variant | 0.3 |
clpC1 | 4039814 | c.891C>G | synonymous_variant | 0.2 |
clpC1 | 4039817 | c.888A>T | synonymous_variant | 0.18 |
clpC1 | 4039820 | c.885T>C | synonymous_variant | 0.18 |
clpC1 | 4039916 | c.789T>C | synonymous_variant | 0.12 |
clpC1 | 4039928 | c.775_777delAGCinsTCG | synonymous_variant | 0.17 |
clpC1 | 4039934 | c.771G>C | synonymous_variant | 0.17 |
clpC1 | 4039946 | c.759A>G | synonymous_variant | 0.2 |
clpC1 | 4039949 | c.756G>C | synonymous_variant | 0.2 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.2 |
clpC1 | 4039955 | c.750G>C | synonymous_variant | 0.25 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.22 |
clpC1 | 4039994 | p.Glu237Asp | missense_variant | 0.22 |
embC | 4239717 | c.-146C>T | upstream_gene_variant | 0.14 |
embC | 4239745 | c.-118C>A | upstream_gene_variant | 0.13 |
embC | 4239970 | c.108G>T | synonymous_variant | 0.13 |
embC | 4241284 | c.1422G>A | synonymous_variant | 0.22 |
embC | 4241644 | c.1782G>T | synonymous_variant | 0.5 |
embC | 4241998 | c.2136G>T | synonymous_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242784 | c.-449G>T | upstream_gene_variant | 0.2 |
embA | 4243965 | p.Arg245Trp | missense_variant | 0.22 |
embA | 4244003 | c.771G>A | synonymous_variant | 0.33 |
embB | 4248077 | p.Asn522Tyr | missense_variant | 0.18 |
embB | 4248673 | c.2160G>A | synonymous_variant | 0.14 |
embB | 4248810 | p.Pro766Gln | missense_variant | 0.29 |
aftB | 4267170 | p.Gln556Arg | missense_variant | 0.12 |
ethA | 4326074 | p.Leu467His | missense_variant | 0.22 |
ethR | 4326700 | c.-849C>T | upstream_gene_variant | 0.25 |
ethR | 4327803 | p.Met85Ile | missense_variant | 0.2 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |