Run ID: ERR4821176
Sample name:
Date: 01-04-2023 17:06:13
Number of reads: 716236
Percentage reads mapped: 88.34
Strain: lineage2.2.1
Drug-resistance: Pre-XDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 0.99 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7572 | p.Ser91Ala | missense_variant | 0.13 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761127 | p.Ser441Ala | missense_variant | 0.11 | rifampicin |
rpoB | 761196 | p.Leu464Met | missense_variant | 0.12 | rifampicin |
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.23 | streptomycin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.29 | streptomycin |
embB | 4247622 | p.Leu370Arg | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6458 | p.Val407Met | missense_variant | 0.25 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7547 | c.246C>T | synonymous_variant | 0.17 |
gyrA | 7559 | c.258G>T | synonymous_variant | 0.14 |
gyrA | 7571 | c.270G>C | synonymous_variant | 0.13 |
gyrA | 7584 | p.Ser95Ala | missense_variant | 0.11 |
gyrA | 7589 | c.288G>C | synonymous_variant | 0.11 |
gyrA | 7591 | p.Val97Ala | missense_variant | 0.11 |
gyrA | 7596 | p.Met99Leu | missense_variant | 0.12 |
gyrA | 7600 | p.Ala100Val | missense_variant | 0.12 |
gyrA | 7625 | c.324G>C | synonymous_variant | 0.11 |
gyrA | 7628 | c.327G>C | synonymous_variant | 0.11 |
gyrA | 7631 | c.330G>C | synonymous_variant | 0.11 |
gyrA | 7633 | p.Asp111Ala | missense_variant | 0.11 |
gyrA | 7643 | c.342C>T | synonymous_variant | 0.11 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490928 | p.Gly49Asp | missense_variant | 0.14 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576751 | p.Lys468Asn | missense_variant | 0.12 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 759686 | c.-121G>T | upstream_gene_variant | 0.22 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 0.11 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.11 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.11 |
rpoB | 761159 | c.1353G>C | synonymous_variant | 0.12 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.12 |
rpoB | 761174 | c.1368T>C | synonymous_variant | 0.12 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.11 |
rpoB | 761183 | c.1377T>C | synonymous_variant | 0.12 |
rpoB | 761186 | p.Glu460Asp | missense_variant | 0.12 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.12 |
rpoB | 761192 | c.1386C>G | synonymous_variant | 0.12 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.12 |
rpoB | 761201 | c.1395G>A | synonymous_variant | 0.11 |
rpoB | 761207 | c.1401C>A | synonymous_variant | 0.12 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.12 |
rpoB | 761219 | c.1413G>C | synonymous_variant | 0.12 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763043 | c.-327G>C | upstream_gene_variant | 0.14 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.13 |
rpoB | 763078 | p.Val1091Ala | missense_variant | 0.11 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.1 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.12 |
rpoC | 763657 | p.Glu96Asp | missense_variant | 0.12 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.13 |
rpoC | 763666 | c.297G>C | synonymous_variant | 0.14 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.12 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.14 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.12 |
rpoC | 764353 | c.984G>T | synonymous_variant | 0.12 |
rpoC | 764359 | c.990C>G | synonymous_variant | 0.18 |
rpoC | 764371 | c.1002G>T | synonymous_variant | 0.18 |
rpoC | 764377 | c.1008C>G | synonymous_variant | 0.16 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.16 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 0.16 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.16 |
rpoC | 764410 | c.1041G>C | synonymous_variant | 0.15 |
rpoC | 764424 | p.Asn352Thr | missense_variant | 0.18 |
rpoC | 764428 | c.1059G>A | synonymous_variant | 0.18 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.18 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.18 |
rpoC | 764435 | c.1066_1068delAGGinsCGA | synonymous_variant | 0.18 |
rpoC | 764441 | p.Ile358Leu | missense_variant | 0.17 |
rpoC | 764446 | p.Asp359Glu | missense_variant | 0.16 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.16 |
rpoC | 764455 | c.1086G>C | synonymous_variant | 0.15 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.18 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.18 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.27 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.29 |
rpoC | 764503 | c.1134G>T | synonymous_variant | 0.21 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.23 |
rpoC | 764512 | c.1143G>C | synonymous_variant | 0.19 |
rpoC | 764530 | c.1161C>T | synonymous_variant | 0.2 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.21 |
rpoC | 764543 | p.Thr392Ala | missense_variant | 0.19 |
rpoC | 764548 | c.1179G>C | synonymous_variant | 0.18 |
rpoC | 764551 | c.1182G>C | synonymous_variant | 0.16 |
rpoC | 764573 | p.Leu402Ile | missense_variant | 0.2 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 0.2 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.19 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.18 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.21 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 0.21 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.2 |
rpoC | 764632 | c.1263T>A | synonymous_variant | 0.12 |
rpoC | 764647 | c.1278C>T | synonymous_variant | 0.12 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.12 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.13 |
rpoC | 764656 | c.1287C>T | synonymous_variant | 0.13 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776682 | p.Leu600Pro | missense_variant | 0.11 |
mmpL5 | 777189 | p.Tyr431Cys | missense_variant | 0.1 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303016 | p.Val29Gly | missense_variant | 0.29 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472513 | n.668T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472549 | n.704G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472597 | n.752G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472686 | n.841G>T | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472690 | n.845C>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472786 | n.941C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472787 | n.942A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472803 | n.958T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.52 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.77 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.66 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.61 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.77 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.84 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.84 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.7 |
rrs | 1473294 | n.1449A>G | non_coding_transcript_exon_variant | 0.66 |
rrs | 1473300 | n.1455C>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.75 |
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 | 1474717 | n.1060A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474734 | n.1077G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474736 | n.1079C>T | 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 | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.9 |
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>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476523 | n.2866T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476542 | n.2885T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.2 |
rpsA | 1833844 | c.303C>A | synonymous_variant | 0.11 |
rpsA | 1833970 | c.429G>T | synonymous_variant | 0.11 |
rpsA | 1833991 | c.450C>T | synonymous_variant | 0.11 |
rpsA | 1834009 | c.468C>T | synonymous_variant | 0.14 |
rpsA | 1834040 | p.Lys167Arg | missense_variant | 0.13 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 0.17 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.24 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.18 |
rpsA | 1834246 | c.705G>T | synonymous_variant | 0.2 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.19 |
rpsA | 1834258 | c.717G>A | synonymous_variant | 0.17 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.16 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.16 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.18 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.18 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.2 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.17 |
rpsA | 1834312 | c.771G>A | synonymous_variant | 0.17 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.19 |
rpsA | 1834345 | c.804C>T | synonymous_variant | 0.11 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.13 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.12 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.13 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.14 |
rpsA | 1834427 | p.Ile296Val | missense_variant | 0.1 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.1 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.14 |
rpsA | 1834861 | c.1320G>A | synonymous_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155124 | p.Asn330Asp | missense_variant | 0.14 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169821 | c.792C>T | synonymous_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519320 | p.Phe402Leu | missense_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
Rv3236c | 3613293 | c.-177G>T | upstream_gene_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
aftB | 4266972 | p.Gly622Asp | missense_variant | 0.13 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268746 | p.Gly31* | stop_gained | 0.17 |
ethA | 4326676 | p.Ser266Arg | missense_variant | 1.0 |
ethA | 4327181 | p.Ile98Thr | missense_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.95 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |