Run ID: ERR4819017
Sample name:
Date: 01-04-2023 15:52:45
Number of reads: 733198
Percentage reads mapped: 41.99
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 | 0.15 | rifampicin |
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.13 | streptomycin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.74 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.3 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.19 | kanamycin, capreomycin, aminoglycosides, amikacin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 7024 | c.1787delA | frameshift_variant | 0.18 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8392 | p.Tyr364Cys | missense_variant | 0.14 |
gyrA | 8405 | p.His368Gln | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.17 |
rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 0.15 |
rpoB | 761097 | c.1291_1292delAGinsTC | synonymous_variant | 0.14 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.18 |
rpoB | 761557 | p.Ala584Gly | missense_variant | 0.11 |
rpoB | 761567 | p.Met587Ile | missense_variant | 0.11 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.11 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.12 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.13 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.14 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.12 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.13 |
rpoB | 762177 | p.Arg791Thr | missense_variant | 0.13 |
rpoB | 762181 | p.Asp792Ala | missense_variant | 0.13 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.19 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 0.17 |
rpoB | 762200 | c.2394C>T | synonymous_variant | 0.2 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.12 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 0.95 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.2 |
rpoC | 762902 | c.-468C>T | upstream_gene_variant | 0.36 |
rpoC | 762911 | c.-459C>T | upstream_gene_variant | 0.41 |
rpoC | 762917 | c.-453C>T | upstream_gene_variant | 0.38 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.36 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.38 |
rpoC | 762944 | c.-426C>T | upstream_gene_variant | 0.32 |
rpoC | 762956 | c.-414G>C | upstream_gene_variant | 0.18 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.24 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.17 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.16 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.13 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.12 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.14 |
rpoB | 763077 | p.Val1091Thr | missense_variant | 0.18 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.18 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.18 |
rpoB | 763119 | p.Asn1105Asp | missense_variant | 0.18 |
rpoC | 763370 | p.Val1Met | missense_variant | 0.13 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.12 |
rpoC | 763531 | c.162G>C | synonymous_variant | 0.12 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.13 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.15 |
rpoC | 763550 | p.Tyr61Ala | missense_variant | 0.13 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.15 |
rpoC | 763578 | p.Phe70Tyr | missense_variant | 0.17 |
rpoC | 763647 | p.Gly93Ala | missense_variant | 0.14 |
rpoC | 763655 | p.Glu96Lys | missense_variant | 0.2 |
rpoC | 763660 | c.291T>C | synonymous_variant | 0.13 |
rpoC | 763666 | c.297G>T | synonymous_variant | 0.13 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.12 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.14 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.27 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.29 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.29 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.28 |
rpoC | 763718 | p.Leu117Val | missense_variant | 0.16 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.24 |
rpoC | 763724 | p.Asp119Asn | missense_variant | 0.24 |
rpoC | 763729 | c.360G>C | synonymous_variant | 0.24 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.18 |
rpoC | 763735 | c.366G>C | synonymous_variant | 0.17 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.2 |
rpoC | 763772 | p.Val135Met | missense_variant | 0.17 |
rpoC | 764321 | p.Pro318Thr | missense_variant | 0.17 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.22 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.17 |
rpoC | 764503 | c.1134G>T | synonymous_variant | 0.18 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.29 |
rpoC | 764512 | c.1143G>C | synonymous_variant | 0.19 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.25 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.25 |
rpoC | 764543 | p.Thr392Ala | missense_variant | 0.18 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.17 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.12 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.12 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.17 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 0.21 |
rpoC | 764611 | c.1242G>C | synonymous_variant | 0.17 |
rpoC | 764623 | c.1254C>G | synonymous_variant | 0.12 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.24 |
rpoC | 764635 | c.1266C>G | synonymous_variant | 0.12 |
rpoC | 764647 | c.1278C>T | synonymous_variant | 0.11 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.14 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.2 |
rpoC | 764656 | c.1287C>T | synonymous_variant | 0.12 |
rpoC | 764692 | c.1323C>T | synonymous_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775675 | p.Trp936Arg | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpR5 | 779342 | p.Ala118Val | missense_variant | 0.17 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781706 | c.147T>G | synonymous_variant | 0.14 |
rpsL | 781751 | c.192G>C | synonymous_variant | 0.18 |
rpsL | 781754 | c.195G>A | synonymous_variant | 0.15 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.27 |
rpsL | 781766 | c.207C>T | synonymous_variant | 0.3 |
rpsL | 781772 | c.213C>T | synonymous_variant | 0.22 |
rpsL | 781796 | p.Met79Ile | missense_variant | 0.4 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.42 |
rpsL | 781805 | c.246G>T | synonymous_variant | 0.32 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.44 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.42 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.42 |
rpsL | 781829 | c.270G>C | synonymous_variant | 0.29 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.44 |
rpsL | 781835 | c.276T>C | synonymous_variant | 0.17 |
rpsL | 781838 | c.279G>T | synonymous_variant | 0.25 |
rpsL | 781841 | c.282C>T | synonymous_variant | 0.19 |
rpsL | 781851 | p.Ile98Val | missense_variant | 0.18 |
fbiC | 1305215 | p.Ser762Asn | missense_variant | 1.0 |
embR | 1416934 | c.414G>A | synonymous_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472496 | n.651T>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472498 | n.653C>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472673 | n.828T>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472674 | n.829T>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472840 | n.995A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.48 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473122 | n.1278A>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473163 | n.1318C>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473270 | n.1425G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1473293 | n.1449delA | non_coding_transcript_exon_variant | 0.52 |
rrs | 1473300 | n.1455C>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473305 | n.1460G>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473319 | n.1474C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473384 | n.-274A>G | upstream_gene_variant | 0.43 |
rrl | 1474130 | n.473C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474164 | n.507C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 0.79 |
rrl | 1474182 | n.525C>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474183 | n.526T>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474185 | n.529delA | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.67 |
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 | 0.67 |
rrl | 1474448 | n.791T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474492 | n.835A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474520 | n.863A>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474525 | n.868A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 0.87 |
rrl | 1474529 | n.872A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474540 | n.883T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474615 | n.958A>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474636 | n.979A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474638 | n.981C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474652 | n.995T>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474658 | n.1001A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474666 | n.1009T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474687 | n.1030C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474692 | n.1035G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474734 | n.1077G>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474774 | n.1117A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474790 | n.1133C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474798 | n.1141C>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474800 | n.1143T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474831 | n.1174A>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474832 | n.1175A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474837 | n.1180A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474883 | n.1226T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474901 | n.1244A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475998 | n.2341C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476179 | n.2522C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476207 | n.2550T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476253 | n.2596A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476523 | n.2866T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476528 | n.2871A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476548 | n.2891T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476594 | n.2937C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476600 | n.2943A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476603 | n.2946G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476628 | n.2971T>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476633 | n.2976A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476664 | n.3007T>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476668 | n.3011C>T | non_coding_transcript_exon_variant | 0.57 |
inhA | 1673568 | c.-634C>A | upstream_gene_variant | 0.2 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 0.1 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.11 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.2 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.14 |
rpsA | 1833732 | p.Pro64Leu | missense_variant | 0.18 |
rpsA | 1833736 | c.195C>T | synonymous_variant | 0.18 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.17 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.12 |
rpsA | 1833952 | c.411C>T | synonymous_variant | 0.12 |
rpsA | 1833955 | c.414G>C | synonymous_variant | 0.12 |
rpsA | 1833961 | c.420C>G | synonymous_variant | 0.12 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.17 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.18 |
rpsA | 1833991 | c.450C>A | synonymous_variant | 0.11 |
rpsA | 1833994 | c.453G>C | synonymous_variant | 0.19 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.12 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 0.2 |
rpsA | 1834219 | c.678C>G | synonymous_variant | 0.14 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.14 |
rpsA | 1834225 | c.684C>G | synonymous_variant | 0.13 |
rpsA | 1834228 | c.687C>T | synonymous_variant | 0.26 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 0.13 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.17 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.17 |
rpsA | 1834246 | c.705G>T | synonymous_variant | 0.27 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.33 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.41 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.41 |
rpsA | 1834285 | c.744G>C | synonymous_variant | 0.11 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.29 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.31 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.31 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.25 |
rpsA | 1834312 | c.771G>A | synonymous_variant | 0.25 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154206 | p.Ala636Thr | missense_variant | 0.12 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
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 |
kasA | 2519057 | p.Thr315Ser | missense_variant | 0.18 |
kasA | 2519062 | c.948T>G | synonymous_variant | 0.22 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
folC | 2746268 | p.Thr444Ile | missense_variant | 1.0 |
pepQ | 2859624 | c.795G>A | synonymous_variant | 0.92 |
pepQ | 2860207 | p.Leu71Arg | missense_variant | 0.12 |
Rv2752c | 3065361 | c.831C>A | synonymous_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568847 | c.-168G>T | upstream_gene_variant | 0.12 |
fbiB | 3640671 | c.-864T>C | upstream_gene_variant | 1.0 |
clpC1 | 4039638 | p.Ile356Thr | missense_variant | 0.14 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.1 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |