Run ID: ERR4818393
Sample name:
Date: 01-04-2023 15:31:54
Number of reads: 301760
Percentage reads mapped: 32.77
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 | 0.8 | rifampicin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.22 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5466 | p.Glu76Gly | missense_variant | 0.5 |
gyrB | 6170 | p.His311Thr | missense_variant | 0.5 |
gyrB | 6175 | c.936G>A | synonymous_variant | 0.5 |
gyrB | 6183 | p.Thr315Met | missense_variant | 0.5 |
gyrB | 6190 | c.951A>G | synonymous_variant | 0.5 |
gyrB | 6196 | c.957C>T | synonymous_variant | 0.5 |
gyrB | 6204 | p.Ser322Thr | missense_variant | 0.5 |
gyrB | 6211 | c.972G>C | synonymous_variant | 0.5 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8453 | c.1152A>C | synonymous_variant | 0.67 |
gyrA | 8462 | c.1161A>T | synonymous_variant | 0.67 |
gyrA | 8465 | c.1164C>G | synonymous_variant | 0.67 |
gyrA | 8471 | c.1170T>C | synonymous_variant | 0.67 |
gyrA | 8472 | c.1171C>T | synonymous_variant | 0.67 |
gyrA | 8480 | c.1179C>T | synonymous_variant | 0.67 |
gyrA | 8486 | c.1185T>C | synonymous_variant | 0.67 |
gyrA | 8516 | c.1215T>C | synonymous_variant | 0.5 |
gyrA | 8519 | c.1218A>C | synonymous_variant | 0.5 |
gyrA | 8520 | c.1219C>T | synonymous_variant | 0.5 |
gyrA | 8528 | c.1227G>C | synonymous_variant | 0.4 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 761030 | c.1224G>C | synonymous_variant | 0.4 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.4 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.5 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.5 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.5 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.56 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.65 |
rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 0.69 |
rpoB | 761096 | c.1290G>C | synonymous_variant | 0.73 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.73 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.73 |
rpoB | 761126 | c.1320G>C | synonymous_variant | 0.18 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 0.78 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.78 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 0.38 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.75 |
rpoB | 761159 | c.1353G>C | synonymous_variant | 0.67 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.67 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 1.0 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 1.0 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.67 |
rpoB | 762024 | p.Val740Ile | missense_variant | 0.43 |
rpoB | 762051 | p.His749Tyr | missense_variant | 0.45 |
rpoB | 762057 | p.Ile751Val | missense_variant | 0.42 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.38 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.36 |
rpoB | 762071 | p.Asp755Glu | missense_variant | 0.33 |
rpoB | 762080 | c.2274G>C | synonymous_variant | 0.35 |
rpoB | 762085 | p.Ala760Glu | missense_variant | 0.35 |
rpoB | 762089 | c.2283G>A | synonymous_variant | 0.35 |
rpoB | 762110 | c.2304G>C | synonymous_variant | 0.4 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.31 |
rpoB | 762122 | p.Asp772Glu | missense_variant | 0.18 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.27 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.3 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.33 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.25 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.4 |
rpoB | 762177 | p.Arg791Thr | missense_variant | 0.4 |
rpoB | 762181 | p.Asp792Ala | missense_variant | 0.5 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.5 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 0.67 |
rpoB | 762200 | c.2394C>T | synonymous_variant | 0.44 |
rpoB | 762212 | c.2406G>C | synonymous_variant | 0.57 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.57 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.71 |
rpoB | 762234 | p.Pro810Ser | missense_variant | 0.68 |
rpoB | 762239 | c.2433G>A | synonymous_variant | 0.7 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.7 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.7 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.25 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.55 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763022 | c.-348C>A | upstream_gene_variant | 0.38 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.44 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763038 | p.Thr1078Ala | missense_variant | 0.73 |
rpoC | 763043 | c.-327G>C | upstream_gene_variant | 0.77 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.76 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.76 |
rpoB | 763077 | p.Val1091Ser | missense_variant | 0.76 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.7 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.58 |
rpoB | 763119 | p.Asn1105Asp | missense_variant | 0.58 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.53 |
rpoC | 763133 | c.-237G>C | upstream_gene_variant | 0.55 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.29 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.17 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.18 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.22 |
rpoC | 763492 | c.123G>C | synonymous_variant | 0.22 |
rpoC | 763496 | p.Lys43Arg | missense_variant | 0.22 |
rpoC | 763511 | p.Cys48Gly | missense_variant | 0.33 |
rpoC | 763517 | p.Lys50Gln | missense_variant | 0.43 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.5 |
rpoC | 763531 | c.162G>C | synonymous_variant | 0.5 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.5 |
rpoC | 763555 | c.186C>T | synonymous_variant | 0.67 |
rpoC | 763666 | c.297G>C | synonymous_variant | 0.4 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.56 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.72 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.72 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.67 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.67 |
rpoC | 763718 | p.Leu117Val | missense_variant | 0.67 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.67 |
rpoC | 763724 | p.Asp119Asn | missense_variant | 0.67 |
rpoC | 763729 | c.360G>C | synonymous_variant | 0.67 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.67 |
rpoC | 763735 | c.366G>C | synonymous_variant | 0.67 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.63 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.63 |
rpoC | 763772 | p.Val135Met | missense_variant | 0.59 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.33 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.56 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.64 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.64 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.54 |
rpoC | 764503 | c.1134G>T | synonymous_variant | 0.87 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.31 |
rpoC | 764512 | c.1143G>C | synonymous_variant | 0.9 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.9 |
rpoC | 764530 | c.1161C>T | synonymous_variant | 0.57 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.88 |
rpoC | 764543 | p.Thr392Ala | missense_variant | 0.84 |
rpoC | 764548 | c.1179G>T | synonymous_variant | 0.79 |
rpoC | 764551 | c.1182G>C | synonymous_variant | 0.33 |
rpoC | 764573 | p.Leu402Ile | missense_variant | 0.81 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 0.81 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.81 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.81 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.39 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.88 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 0.87 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.87 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.23 |
rpoC | 764632 | c.1263T>A | synonymous_variant | 0.74 |
rpoC | 764647 | c.1278C>T | synonymous_variant | 0.72 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.76 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.78 |
rpoC | 764656 | c.1287C>T | synonymous_variant | 0.72 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.72 |
rpoC | 764677 | c.1308C>A | synonymous_variant | 0.71 |
rpoC | 764678 | p.Lys437Gln | missense_variant | 0.75 |
rpoC | 764683 | c.1314G>C | synonymous_variant | 0.62 |
rpoC | 764692 | c.1323C>T | synonymous_variant | 0.69 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.4 |
rpoC | 767279 | c.3912delC | frameshift_variant | 0.22 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781745 | c.186G>A | synonymous_variant | 0.33 |
rpsL | 781748 | c.189C>G | synonymous_variant | 0.42 |
rpsL | 781751 | c.192G>C | synonymous_variant | 0.75 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.75 |
rpsL | 781766 | c.207C>T | synonymous_variant | 0.77 |
rpsL | 781796 | p.Met79Ile | missense_variant | 0.76 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.76 |
rpsL | 781805 | c.246G>T | synonymous_variant | 0.59 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.72 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.68 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.68 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.61 |
rpsL | 781835 | c.276T>C | synonymous_variant | 0.44 |
rpsL | 781841 | c.282C>T | synonymous_variant | 0.56 |
rpsL | 781845 | p.Lys96Arg | missense_variant | 0.38 |
rpsL | 781851 | p.Ile98Val | missense_variant | 0.36 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.27 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.27 |
rplC | 800943 | c.135C>T | synonymous_variant | 0.22 |
Rv1258c | 1406530 | p.Gly271Ser | missense_variant | 0.29 |
Rv1258c | 1406935 | p.Gly136Ser | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472068 | n.223T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472513 | n.668T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472549 | n.704G>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472840 | n.995A>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472875 | n.1030T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473101 | n.1256C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 1.0 |
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 | 0.63 |
rrs | 1473122 | n.1281delA | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473122 | n.1278A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473294 | n.1449A>G | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473300 | n.1455C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1473384 | n.-274A>G | upstream_gene_variant | 0.75 |
rrl | 1473390 | n.-268A>C | upstream_gene_variant | 0.67 |
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 | 1.0 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474275 | n.618T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474326 | n.669T>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474355 | n.698A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474582 | n.925T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474615 | n.958A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474637 | n.980C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474643 | n.986A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474692 | n.1035G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474706 | n.1049G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474831 | n.1174A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474832 | n.1175A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475104 | n.1447T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475109 | n.1452C>T | 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 | 1.0 |
rrl | 1475715 | n.2058G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475756 | n.2099T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475767 | n.2110_2111insT | non_coding_transcript_exon_variant | 0.93 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475974 | n.2317A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476594 | n.2937C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476603 | n.2946G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 1.0 |
rpsA | 1833667 | c.126C>T | synonymous_variant | 1.0 |
rpsA | 1833668 | p.Ile43Val | missense_variant | 1.0 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 1.0 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 1.0 |
rpsA | 1833684 | p.Arg48His | missense_variant | 1.0 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.71 |
rpsA | 1833700 | c.159C>T | synonymous_variant | 0.71 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.71 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.71 |
rpsA | 1833732 | p.Pro64Leu | missense_variant | 0.57 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.5 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.5 |
rpsA | 1833764 | p.Asp75Asn | missense_variant | 0.67 |
rpsA | 1834189 | c.648G>C | synonymous_variant | 0.33 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 0.64 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.79 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.88 |
rpsA | 1834246 | c.705G>T | synonymous_variant | 0.28 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.93 |
rpsA | 1834258 | c.717G>A | synonymous_variant | 0.4 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.93 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.92 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.92 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.92 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.88 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.88 |
rpsA | 1834312 | c.771G>A | synonymous_variant | 0.88 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 1.0 |
rpsA | 1834345 | c.804C>T | synonymous_variant | 0.9 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.86 |
rpsA | 1834354 | c.813G>T | synonymous_variant | 0.8 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.8 |
rpsA | 1834600 | c.1059G>C | synonymous_variant | 0.33 |
rpsA | 1834606 | c.1065C>T | synonymous_variant | 0.33 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.33 |
rpsA | 1834612 | c.1071G>C | synonymous_variant | 0.4 |
rpsA | 1834618 | c.1077G>C | synonymous_variant | 0.22 |
rpsA | 1834619 | c.1078T>C | synonymous_variant | 0.22 |
rpsA | 1834624 | c.1083G>C | synonymous_variant | 0.22 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.22 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.22 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2222758 | p.Val136Ala | missense_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
pepQ | 2860006 | p.Gly138Asp | missense_variant | 0.2 |
Rv2752c | 3066050 | p.Leu48Met | missense_variant | 0.33 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiB | 3642163 | p.Thr210Ser | missense_variant | 0.2 |
alr | 3840230 | c.1191T>C | synonymous_variant | 0.29 |
ddn | 3986754 | c.-90T>C | upstream_gene_variant | 0.18 |
clpC1 | 4038378 | p.Thr776Ser | missense_variant | 0.22 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.67 |
clpC1 | 4039994 | p.Glu237Asp | missense_variant | 0.2 |
clpC1 | 4040009 | c.696C>G | synonymous_variant | 0.23 |
clpC1 | 4040015 | c.690G>T | synonymous_variant | 0.23 |
clpC1 | 4040018 | c.687G>C | synonymous_variant | 0.23 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.25 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.23 |
clpC1 | 4040036 | c.669C>G | synonymous_variant | 0.25 |
clpC1 | 4040042 | c.663C>T | synonymous_variant | 0.25 |
clpC1 | 4040066 | c.639G>C | synonymous_variant | 0.25 |
clpC1 | 4040081 | c.624C>G | synonymous_variant | 0.27 |
clpC1 | 4040087 | c.618G>C | synonymous_variant | 0.3 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242999 | p.Ala1046Val | missense_variant | 0.33 |
embA | 4246435 | p.Gln1068Arg | missense_variant | 0.22 |
embB | 4248193 | c.1680C>A | synonymous_variant | 0.15 |
aftB | 4268250 | c.586delG | frameshift_variant | 0.22 |
ubiA | 4269117 | p.Glu239Asp | missense_variant | 0.29 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |