Run ID: ERR4816755
Sample name:
Date: 01-04-2023 14:36:49
Number of reads: 1395934
Percentage reads mapped: 45.59
Strain: lineage4.1.1.3
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 0.99 |
lineage4.1.1 | Euro-American (X-type) | X1;X2;X3 | None | 1.0 |
lineage4.1.1.3 | Euro-American (X-type) | X1;X3 | RD193 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5157 | c.-83C>T | upstream_gene_variant | 0.13 |
gyrB | 5484 | p.Arg82Leu | missense_variant | 0.18 |
gyrB | 5713 | c.476delA | frameshift_variant | 0.13 |
gyrA | 6439 | c.-863C>T | upstream_gene_variant | 0.17 |
gyrA | 6523 | c.-779G>T | upstream_gene_variant | 0.14 |
gyrB | 6567 | p.Ala443Gly | missense_variant | 0.12 |
gyrB | 6836 | p.Ala533Ser | missense_variant | 0.17 |
gyrB | 6849 | p.Gly537Val | missense_variant | 0.17 |
gyrB | 6966 | p.Ser576Ile | missense_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7522 | p.Ala74Asp | missense_variant | 0.12 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7686 | c.388_389delAC | frameshift_variant | 0.14 |
gyrA | 7966 | p.Arg222Leu | missense_variant | 0.15 |
gyrA | 8706 | p.Leu469Met | missense_variant | 0.22 |
gyrA | 8738 | c.1437G>A | synonymous_variant | 0.14 |
gyrA | 8748 | p.Leu483Ile | missense_variant | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490595 | c.-188G>A | upstream_gene_variant | 0.14 |
fgd1 | 490799 | p.Leu6Pro | missense_variant | 0.11 |
mshA | 575582 | c.236delT | frameshift_variant | 0.11 |
mshA | 575588 | p.Arg81Ser | missense_variant | 0.12 |
mshA | 575649 | p.Val101Ala | missense_variant | 0.14 |
mshA | 576104 | p.Arg253Ser | missense_variant | 0.17 |
mshA | 576113 | c.766C>A | synonymous_variant | 0.17 |
ccsA | 619984 | p.Leu32Val | missense_variant | 0.12 |
ccsA | 620157 | c.267G>T | synonymous_variant | 0.15 |
ccsA | 620661 | c.771C>A | synonymous_variant | 0.17 |
ccsA | 620743 | p.Ala285Ser | missense_variant | 0.2 |
rpoB | 760232 | p.Lys142Asn | missense_variant | 0.17 |
rpoB | 760722 | p.Gly306Cys | missense_variant | 0.15 |
rpoB | 761016 | p.Glu404* | stop_gained | 0.22 |
rpoB | 761364 | p.Asp520Tyr | missense_variant | 0.18 |
rpoB | 761403 | p.His533Asn | missense_variant | 0.14 |
rpoB | 761896 | p.Ala697Asp | missense_variant | 0.2 |
rpoB | 762870 | p.Met1022Val | missense_variant | 0.1 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.14 |
rpoB | 762888 | p.His1028Ala | missense_variant | 0.2 |
rpoC | 762896 | c.-474G>C | upstream_gene_variant | 0.13 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.13 |
rpoC | 762917 | c.-453C>T | upstream_gene_variant | 0.13 |
rpoC | 762920 | c.-450C>G | upstream_gene_variant | 0.27 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.25 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.17 |
rpoC | 763067 | c.-303C>G | upstream_gene_variant | 0.1 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.22 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.18 |
rpoC | 763453 | c.84C>G | synonymous_variant | 0.1 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.15 |
rpoC | 763462 | c.93G>C | synonymous_variant | 0.1 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.11 |
rpoC | 763486 | c.117T>G | synonymous_variant | 0.16 |
rpoC | 763492 | c.123G>C | synonymous_variant | 0.11 |
rpoC | 763504 | c.135C>G | synonymous_variant | 0.11 |
rpoC | 763507 | c.138G>C | synonymous_variant | 0.13 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.19 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.22 |
rpoC | 764326 | c.957G>C | synonymous_variant | 0.14 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.14 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 0.14 |
rpoC | 764377 | c.1008C>G | synonymous_variant | 0.15 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.2 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 0.24 |
rpoC | 764401 | c.1032C>T | synonymous_variant | 0.16 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.21 |
rpoC | 764410 | c.1041G>C | synonymous_variant | 0.12 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.14 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.13 |
rpoC | 764435 | c.1066A>C | synonymous_variant | 0.13 |
rpoC | 764443 | p.Ile358Met | missense_variant | 0.11 |
rpoC | 764446 | p.Asp359Glu | missense_variant | 0.17 |
rpoC | 764450 | p.Gly361Arg | missense_variant | 0.19 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.13 |
rpoC | 764461 | p.Glu364Asp | missense_variant | 0.21 |
rpoC | 764471 | p.Asn368Arg | missense_variant | 0.15 |
rpoC | 764479 | c.1110G>A | synonymous_variant | 0.15 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.12 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.15 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.17 |
rpoC | 764530 | c.1161C>T | synonymous_variant | 0.14 |
rpoC | 764536 | c.1167G>T | synonymous_variant | 0.12 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.12 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.14 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.23 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.22 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.22 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 0.17 |
rpoC | 764611 | c.1242G>C | synonymous_variant | 0.22 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.31 |
rpoC | 764644 | c.1275G>C | synonymous_variant | 0.17 |
rpoC | 764650 | c.1281G>C | synonymous_variant | 0.13 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.18 |
rpoC | 764664 | p.Val432Ala | missense_variant | 0.12 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.14 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765527 | p.Gly720Ser | missense_variant | 0.12 |
rpoC | 765553 | c.2184C>A | synonymous_variant | 0.14 |
rpoC | 765610 | p.Asp747Glu | missense_variant | 0.14 |
rpoC | 765832 | p.Lys821Asn | missense_variant | 0.12 |
rpoC | 765947 | c.2578T>C | synonymous_variant | 0.11 |
rpoC | 766363 | c.2994G>C | synonymous_variant | 0.12 |
rpoC | 766369 | c.3000C>G | synonymous_variant | 0.18 |
rpoC | 766402 | c.3033C>T | synonymous_variant | 0.2 |
rpoC | 766716 | p.Ala1116Val | missense_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776609 | p.Met624Ile | missense_variant | 0.14 |
mmpL5 | 777157 | c.1324C>A | synonymous_variant | 0.2 |
mmpS5 | 778554 | p.Val118Phe | missense_variant | 0.2 |
mmpL5 | 779112 | c.-632G>T | upstream_gene_variant | 0.12 |
mmpR5 | 779186 | p.Gly66Val | missense_variant | 0.13 |
mmpS5 | 779652 | c.-747G>T | upstream_gene_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781668 | p.Val37Met | missense_variant | 0.15 |
rplC | 800700 | c.-109C>A | upstream_gene_variant | 0.14 |
rplC | 801231 | c.423C>A | synonymous_variant | 0.17 |
rplC | 801236 | p.Ala143Val | missense_variant | 0.14 |
fbiC | 1303264 | p.Gly112Ser | missense_variant | 0.14 |
fbiC | 1304751 | c.1821C>T | synonymous_variant | 0.13 |
fbiC | 1304752 | p.Glu608* | stop_gained | 0.13 |
fbiC | 1304789 | p.Ala620Asp | missense_variant | 0.13 |
Rv1258c | 1406677 | p.Leu222Met | missense_variant | 0.12 |
Rv1258c | 1407505 | c.-165G>T | upstream_gene_variant | 0.12 |
embR | 1416222 | p.Phe376Leu | missense_variant | 0.35 |
embR | 1416232 | p.Cys372Gly | missense_variant | 0.38 |
embR | 1416259 | c.1089G>C | synonymous_variant | 0.33 |
embR | 1416262 | c.1086G>C | synonymous_variant | 0.15 |
embR | 1416502 | p.Met282Ile | missense_variant | 0.14 |
embR | 1416568 | c.780G>C | synonymous_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472094 | n.249T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472120 | n.275G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472146 | n.301G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472210 | n.365A>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472235 | n.390G>C | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472242 | n.397C>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472303 | n.458G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472338 | n.493A>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472374 | n.529T>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472379 | n.534T>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472380 | n.535G>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472382 | n.537G>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472389 | n.544G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472390 | n.545T>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472391 | n.546C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472412 | n.567A>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472415 | n.570T>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472583 | n.738T>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472659 | n.814G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472664 | n.819A>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472714 | n.869A>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472715 | n.870C>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472716 | n.871C>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472754 | n.909G>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472827 | n.982G>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472887 | n.1042G>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472936 | n.1091C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472951 | n.1106T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472963 | n.1118G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472982 | n.1137G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472988 | n.1143T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472996 | n.1151T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473002 | n.1157G>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473004 | n.1159T>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473008 | n.1163C>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473009 | n.1164T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473026 | n.1181T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473044 | n.1199C>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473091 | n.1246G>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473100 | n.1255G>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473109 | n.1264T>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473122 | n.1277T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473128 | n.1283C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473179 | n.1334C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.53 |
rrs | 1473195 | n.1350T>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473207 | n.1362C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473248 | n.1403G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473249 | n.1404T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473255 | n.1410A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.77 |
rrs | 1473260 | n.1415G>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473282 | n.1437C>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473283 | n.1438T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473288 | n.1443C>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473291 | n.1446_1447insC | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473314 | n.1469A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473319 | n.1474C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473324 | n.1479G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473414 | n.-244G>T | upstream_gene_variant | 0.12 |
rrl | 1473756 | n.99G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473768 | n.111A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474201 | n.544T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474202 | n.545T>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474234 | n.577G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474237 | n.580A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474476 | n.819C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474483 | n.826C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474496 | n.839C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474507 | n.850G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474529 | n.872A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474534 | n.877G>A | 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 | 0.29 |
rrl | 1474551 | n.894G>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474558 | n.901G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474583 | n.926C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474584 | n.927C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474601 | n.944C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474638 | n.981C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474639 | n.982G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474664 | n.1007G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474717 | n.1060A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474777 | n.1120T>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474869 | n.1212G>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474938 | n.1281G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475460 | n.1803A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475481 | n.1824C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475482 | n.1825A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475508 | n.1851A>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475544 | n.1887A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475752 | n.2095C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475756 | n.2101_2108delACCCGCAA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475768 | n.2111G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475769 | n.2112_2113insTCGGCC | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475874 | n.2217C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475892 | n.2235A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476141 | n.2484A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476251 | n.2594T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476297 | n.2640C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476298 | n.2641C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476300 | n.2643G>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476366 | n.2709A>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476374 | n.2717T>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476455 | n.2798C>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476515 | n.2858C>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 | 0.5 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.5 |
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 | 0.5 |
inhA | 1674472 | p.Val91Met | missense_variant | 0.15 |
inhA | 1674818 | p.Ala206Glu | missense_variant | 0.14 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.14 |
rpsA | 1833697 | c.156C>G | synonymous_variant | 0.14 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.17 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.14 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.14 |
rpsA | 1833737 | p.Arg66Ser | missense_variant | 0.17 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.24 |
rpsA | 1833766 | c.225C>T | synonymous_variant | 0.15 |
rpsA | 1833770 | p.Asn77Gly | missense_variant | 0.2 |
rpsA | 1833780 | c.240_242delTTC | disruptive_inframe_deletion | 0.22 |
rpsA | 1833785 | c.244_245insAGA | disruptive_inframe_insertion | 0.18 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.18 |
rpsA | 1833802 | p.Glu87Asp | missense_variant | 0.13 |
rpsA | 1833808 | c.267G>C | synonymous_variant | 0.12 |
rpsA | 1833811 | c.270G>C | synonymous_variant | 0.12 |
rpsA | 1833829 | c.288A>G | synonymous_variant | 0.12 |
rpsA | 1833910 | c.369C>T | synonymous_variant | 0.18 |
rpsA | 1833955 | c.414G>C | synonymous_variant | 0.1 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.11 |
rpsA | 1833991 | c.450C>G | synonymous_variant | 0.14 |
rpsA | 1834034 | p.Ile165Val | missense_variant | 0.13 |
rpsA | 1834040 | p.Lys167Gln | missense_variant | 0.1 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.11 |
rpsA | 1834090 | c.549G>C | synonymous_variant | 0.11 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.12 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.11 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.11 |
tlyA | 1917943 | p.Ala2Ser | missense_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918282 | p.Tyr115His | missense_variant | 0.1 |
ndh | 2102290 | p.Asp251Ala | missense_variant | 0.15 |
ndh | 2102367 | p.Ala226Thr | missense_variant | 0.17 |
ndh | 2102804 | p.Arg80Leu | missense_variant | 0.12 |
ndh | 2102983 | c.60C>A | synonymous_variant | 0.13 |
katG | 2154838 | p.Arg425Ile | missense_variant | 0.13 |
katG | 2154991 | p.Ser374Tyr | missense_variant | 0.13 |
katG | 2155081 | p.Thr344Met | missense_variant | 0.33 |
katG | 2155271 | p.Ala281Ser | missense_variant | 0.22 |
katG | 2155719 | c.393G>C | synonymous_variant | 0.11 |
katG | 2156096 | p.Pro6Ser | missense_variant | 1.0 |
PPE35 | 2168328 | p.Pro762Arg | missense_variant | 0.17 |
PPE35 | 2168722 | p.Ala631Ser | missense_variant | 0.25 |
PPE35 | 2169521 | c.1092G>A | synonymous_variant | 0.17 |
PPE35 | 2170416 | p.Ala66Val | missense_variant | 0.13 |
PPE35 | 2170556 | c.57G>T | synonymous_variant | 0.15 |
Rv1979c | 2221761 | c.1404C>T | synonymous_variant | 0.17 |
Rv1979c | 2222212 | p.Ala318Val | missense_variant | 0.17 |
Rv1979c | 2222718 | c.447G>A | synonymous_variant | 0.22 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv1979c | 2223319 | c.-155C>A | upstream_gene_variant | 0.14 |
pncA | 2290041 | c.-800C>A | upstream_gene_variant | 0.15 |
pncA | 2290123 | c.-882G>T | upstream_gene_variant | 0.13 |
eis | 2714704 | p.Gly210Glu | missense_variant | 0.15 |
eis | 2715496 | c.-164C>T | upstream_gene_variant | 1.0 |
ahpC | 2726245 | p.Leu18Arg | missense_variant | 0.11 |
ahpC | 2726257 | p.Asp22Gly | missense_variant | 0.11 |
ahpC | 2726691 | c.502delC | frameshift_variant | 0.12 |
folC | 2746684 | c.915C>A | synonymous_variant | 0.17 |
folC | 2746715 | p.Gly295Asp | missense_variant | 0.13 |
folC | 2746893 | p.Arg236Cys | missense_variant | 0.17 |
folC | 2746900 | c.699C>A | synonymous_variant | 0.18 |
folC | 2746916 | p.Pro228Leu | missense_variant | 0.2 |
pepQ | 2859394 | p.Leu342* | stop_gained | 0.12 |
pepQ | 2859439 | p.Gly327Val | missense_variant | 0.17 |
pepQ | 2859619 | p.Gly267Asp | missense_variant | 0.22 |
pepQ | 2859643 | p.Ala259Asp | missense_variant | 0.14 |
pepQ | 2860034 | p.Glu129* | stop_gained | 0.12 |
thyX | 3067760 | c.186G>T | synonymous_variant | 0.12 |
thyX | 3068105 | c.-160C>A | upstream_gene_variant | 0.15 |
thyA | 3073817 | p.Gln219Lys | missense_variant | 0.12 |
thyA | 3074151 | p.Glu107Asp | missense_variant | 0.17 |
thyA | 3074571 | c.-100T>C | upstream_gene_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086925 | p.Gln36Glu | missense_variant | 0.12 |
ald | 3087420 | p.Ile201Val | missense_variant | 0.1 |
fbiD | 3339094 | c.-24G>A | upstream_gene_variant | 0.13 |
fbiD | 3339274 | p.Val53Phe | missense_variant | 0.14 |
fbiD | 3339409 | p.Ala98Thr | missense_variant | 0.2 |
Rv3083 | 3448780 | p.Gly93Ser | missense_variant | 0.2 |
Rv3083 | 3449562 | c.1059G>T | synonymous_variant | 0.33 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474603 | c.597C>A | synonymous_variant | 0.25 |
fprA | 3474997 | p.Gly331Arg | missense_variant | 0.15 |
fprA | 3475371 | c.1365C>A | synonymous_variant | 0.25 |
Rv3236c | 3612037 | c.1079delT | frameshift_variant | 0.12 |
Rv3236c | 3612454 | c.663G>A | synonymous_variant | 0.17 |
Rv3236c | 3612479 | p.Pro213His | missense_variant | 0.17 |
Rv3236c | 3612511 | p.Trp202Cys | missense_variant | 0.18 |
fbiA | 3640344 | c.-199C>T | upstream_gene_variant | 0.18 |
fbiA | 3640525 | c.-18G>T | upstream_gene_variant | 0.25 |
fbiA | 3640976 | p.Ala145Asp | missense_variant | 0.25 |
fbiB | 3642237 | p.Pro235Thr | missense_variant | 0.13 |
fbiB | 3642444 | p.Ala304Thr | missense_variant | 0.12 |
alr | 3840738 | p.Arg228Leu | missense_variant | 0.13 |
alr | 3841034 | p.Gln129His | missense_variant | 0.29 |
alr | 3841211 | c.210C>T | synonymous_variant | 0.13 |
alr | 3841546 | c.-126C>T | upstream_gene_variant | 0.12 |
rpoA | 3878677 | c.-170C>T | upstream_gene_variant | 0.18 |
clpC1 | 4038422 | p.Lys761Asn | missense_variant | 0.2 |
clpC1 | 4039074 | p.Arg544Leu | missense_variant | 0.14 |
clpC1 | 4039487 | c.1218G>C | synonymous_variant | 0.15 |
clpC1 | 4040336 | c.369G>T | synonymous_variant | 0.15 |
panD | 4043990 | p.Ala98Thr | missense_variant | 0.12 |
panD | 4044160 | p.Gly41Val | missense_variant | 0.14 |
embC | 4239676 | c.-187T>A | upstream_gene_variant | 0.18 |
embC | 4239933 | p.Ala24Glu | missense_variant | 0.17 |
embC | 4241677 | c.1815G>A | synonymous_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4244214 | p.Ala328Ser | missense_variant | 0.33 |
embA | 4244233 | p.Ala334Asp | missense_variant | 0.2 |
embA | 4245690 | p.Gly820Arg | missense_variant | 0.13 |
embB | 4246815 | p.Thr101Asn | missense_variant | 0.17 |
embB | 4248673 | c.2160G>A | synonymous_variant | 0.14 |
embB | 4249408 | c.2895G>A | synonymous_variant | 1.0 |
aftB | 4268341 | p.Pro166Thr | missense_variant | 0.15 |
ubiA | 4269062 | p.Ala258Ser | missense_variant | 0.13 |
ethR | 4326952 | c.-597G>A | upstream_gene_variant | 0.14 |
ethR | 4327798 | p.Asp84Tyr | missense_variant | 0.15 |
ethR | 4328012 | p.Ala155Asp | missense_variant | 0.18 |
ethR | 4328101 | p.Ala185Ser | missense_variant | 0.14 |
whiB6 | 4338175 | p.Ala116Glu | missense_variant | 0.13 |
whiB6 | 4338594 | c.-73T>G | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338677 | c.-156G>T | upstream_gene_variant | 0.12 |
gid | 4408085 | p.Glu40Lys | missense_variant | 0.12 |