Run ID: ERR2512606
Sample name:
Date: 31-03-2023 19:08:40
Number of reads: 935418
Percentage reads mapped: 77.62
Strain: lineage3
Drug-resistance: MDR-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 | 761109 | p.Asp435Asn | missense_variant | 0.25 | rifampicin |
rpoB | 761127 | p.Ser441Ala | missense_variant | 0.24 | rifampicin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.14 | streptomycin |
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491259 | c.477T>C | synonymous_variant | 0.11 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.13 |
rpoB | 761030 | c.1224G>T | synonymous_variant | 0.17 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.2 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.25 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.24 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.25 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.25 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.26 |
rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 0.26 |
rpoB | 761096 | c.1290G>C | synonymous_variant | 0.25 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.25 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.26 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 0.23 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.23 |
rpoB | 761150 | c.1344A>T | synonymous_variant | 0.19 |
rpoB | 761159 | c.1353G>C | synonymous_variant | 0.2 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.21 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.13 |
rpoB | 762026 | c.2220G>C | synonymous_variant | 0.13 |
rpoB | 762050 | c.2244G>A | synonymous_variant | 0.16 |
rpoB | 762051 | p.His749Tyr | missense_variant | 0.16 |
rpoB | 762057 | p.Ile751Val | missense_variant | 0.16 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.19 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.22 |
rpoB | 762071 | p.Asp755Glu | missense_variant | 0.24 |
rpoB | 762080 | c.2274G>C | synonymous_variant | 0.23 |
rpoB | 762085 | p.Ala760Glu | missense_variant | 0.27 |
rpoB | 762089 | c.2283G>A | synonymous_variant | 0.27 |
rpoB | 762110 | c.2304G>C | synonymous_variant | 0.24 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.24 |
rpoB | 762122 | p.Asp772Glu | missense_variant | 0.22 |
rpoB | 762125 | c.2319G>A | synonymous_variant | 0.22 |
rpoB | 762126 | p.Val774Ser | missense_variant | 0.23 |
rpoB | 762134 | c.2328C>A | synonymous_variant | 0.24 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.24 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.24 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.18 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.11 |
rpoB | 762177 | p.Arg791Thr | missense_variant | 0.11 |
rpoB | 762181 | p.Asp792Ala | missense_variant | 0.1 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.13 |
rpoB | 762188 | c.2382C>T | synonymous_variant | 0.13 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 0.14 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoB | 763017 | p.Gln1071Glu | missense_variant | 0.1 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.12 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763038 | p.Thr1078Ala | missense_variant | 0.14 |
rpoC | 763043 | c.-327G>C | upstream_gene_variant | 0.14 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.14 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.19 |
rpoC | 763578 | p.Phe70Tyr | missense_variant | 0.2 |
rpoC | 763598 | p.Arg77Lys | missense_variant | 0.22 |
rpoC | 763606 | c.237C>T | synonymous_variant | 0.17 |
rpoC | 763615 | c.246G>C | synonymous_variant | 0.15 |
rpoC | 763618 | c.249C>T | synonymous_variant | 0.15 |
rpoC | 763622 | p.Ala85Ser | missense_variant | 0.15 |
rpoC | 763625 | p.Lys86Arg | missense_variant | 0.14 |
rpoC | 763630 | c.261G>C | synonymous_variant | 0.14 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.14 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.16 |
rpoC | 763648 | c.279C>T | synonymous_variant | 0.19 |
rpoC | 763657 | p.Glu96Asp | missense_variant | 0.23 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.23 |
rpoC | 763666 | c.297G>C | synonymous_variant | 0.24 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.23 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.22 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.18 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.11 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.12 |
rpoC | 763781 | p.Ser138Ala | missense_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpR5 | 779311 | p.Ile108Val | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1305456 | c.2526C>T | synonymous_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472068 | n.223T>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472513 | n.668T>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472549 | n.704G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472690 | n.845C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472958 | n.1113A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472974 | n.1129A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472988 | n.1143T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.7 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.87 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.77 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1473288 | n.1443C>G | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473289 | n.1444_1445insTTTG | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473293 | n.1449delA | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473300 | n.1455C>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.74 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1473384 | n.-274A>G | upstream_gene_variant | 0.65 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474658 | n.1001A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474692 | n.1035G>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474706 | n.1049G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474734 | n.1077G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474734 | n.1077G>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474831 | n.1174A>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474832 | n.1175A>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476224 | n.2567A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476255 | n.2598A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476281 | n.2624T>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476297 | n.2640C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476298 | n.2641C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476303 | n.2646T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476307 | n.2650A>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476523 | n.2866T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476542 | n.2885T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476594 | n.2937C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.12 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.13 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.13 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.14 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.14 |
rpsA | 1834312 | c.771G>A | synonymous_variant | 0.13 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.18 |
rpsA | 1834345 | c.804C>T | synonymous_variant | 0.19 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.17 |
rpsA | 1834354 | c.813G>C | synonymous_variant | 0.16 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 0.15 |
rpsA | 1834360 | c.819G>C | synonymous_variant | 0.14 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.13 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.13 |
rpsA | 1834375 | c.834G>C | synonymous_variant | 0.13 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.13 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.16 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.15 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.12 |
rpsA | 1834427 | p.Ile296Val | missense_variant | 0.11 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155865 | p.Val83Leu | missense_variant | 1.0 |
PPE35 | 2167745 | c.2868C>G | synonymous_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 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
Rv2752c | 3064830 | c.1362C>T | synonymous_variant | 0.18 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086891 | c.72G>A | synonymous_variant | 0.11 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
embC | 4241613 | p.Thr584Lys | missense_variant | 0.14 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407797 | p.Ser136Pro | missense_variant | 1.0 |