Run ID: ERR4817131
Sample name:
Date: 01-04-2023 14:49:15
Number of reads: 202983
Percentage reads mapped: 47.61
Strain:
Drug-resistance: Pre-XDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7572 | p.Ser91Ala | missense_variant | 0.29 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761127 | p.Ser441Ala | missense_variant | 0.3 | rifampicin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.59 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7547 | c.246C>T | synonymous_variant | 0.25 |
gyrA | 7559 | c.258G>C | synonymous_variant | 0.25 |
gyrA | 7571 | c.270G>T | synonymous_variant | 0.25 |
gyrA | 7584 | p.Ser95Ala | missense_variant | 0.29 |
gyrA | 7589 | c.288G>C | synonymous_variant | 0.29 |
gyrA | 7591 | p.Val97Ala | missense_variant | 0.29 |
gyrA | 7596 | p.Met99Leu | missense_variant | 0.33 |
gyrA | 7600 | p.Ala100Val | missense_variant | 0.33 |
gyrA | 7625 | c.324G>C | synonymous_variant | 0.33 |
gyrA | 7628 | c.327G>C | synonymous_variant | 0.33 |
gyrA | 7631 | c.330G>C | synonymous_variant | 0.33 |
gyrA | 7633 | p.Asp111Ala | missense_variant | 0.33 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 576751 | p.Lys468Asn | missense_variant | 0.29 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.29 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.38 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.38 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.29 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.38 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.33 |
rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 0.33 |
rpoB | 761096 | c.1290G>C | synonymous_variant | 0.38 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.38 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.38 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 0.3 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.3 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.17 |
rpoB | 761159 | c.1353G>C | synonymous_variant | 0.17 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.17 |
rpoB | 761174 | c.1368T>C | synonymous_variant | 0.17 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.22 |
rpoB | 762071 | p.Asp755Glu | missense_variant | 0.25 |
rpoB | 762080 | c.2274G>C | synonymous_variant | 0.29 |
rpoB | 762085 | p.Ala760Glu | missense_variant | 0.29 |
rpoB | 762089 | c.2283G>A | synonymous_variant | 0.29 |
rpoB | 762092 | c.2286G>A | synonymous_variant | 0.29 |
rpoB | 762110 | c.2304G>C | synonymous_variant | 0.33 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.33 |
rpoB | 762122 | p.Asp772Glu | missense_variant | 0.4 |
rpoB | 762125 | c.2319G>A | synonymous_variant | 0.33 |
rpoB | 762126 | p.Val774Ser | missense_variant | 0.33 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.33 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.33 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.33 |
rpoB | 762181 | p.Asp792Ala | missense_variant | 0.4 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.5 |
rpoB | 762191 | c.2385C>T | synonymous_variant | 0.4 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 0.6 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.5 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.4 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.5 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.5 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.31 |
rpoC | 762887 | c.-483G>C | upstream_gene_variant | 0.15 |
rpoC | 762896 | c.-474G>C | upstream_gene_variant | 0.14 |
rpoC | 762902 | c.-468C>T | upstream_gene_variant | 0.13 |
rpoC | 762911 | c.-459C>T | upstream_gene_variant | 0.12 |
rpoC | 762917 | c.-453C>T | upstream_gene_variant | 0.13 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.13 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.15 |
rpoC | 762944 | c.-426C>T | upstream_gene_variant | 0.15 |
rpoC | 762956 | c.-414G>T | upstream_gene_variant | 0.18 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.2 |
rpoC | 762980 | c.-390T>C | upstream_gene_variant | 0.2 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.22 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.22 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.22 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763578 | p.Phe70Tyr | missense_variant | 0.25 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.25 |
rpoC | 763648 | c.279C>T | synonymous_variant | 0.33 |
rpoC | 763657 | p.Glu96Asp | missense_variant | 0.33 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.25 |
rpoC | 763666 | c.297G>C | synonymous_variant | 0.25 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.22 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.36 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.38 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.36 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.36 |
rpoC | 763718 | p.Leu117Val | missense_variant | 0.38 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.33 |
rpoC | 763724 | p.Asp119Asn | missense_variant | 0.36 |
rpoC | 763729 | c.360G>C | synonymous_variant | 0.4 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.4 |
rpoC | 763735 | c.366G>C | synonymous_variant | 0.44 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.4 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.4 |
rpoC | 763772 | p.Val135Met | missense_variant | 0.5 |
rpoC | 764446 | p.Asp359Glu | missense_variant | 0.29 |
rpoC | 764455 | c.1086G>C | synonymous_variant | 0.33 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.33 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.33 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.75 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.75 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.75 |
rpoC | 764503 | c.1134G>T | synonymous_variant | 0.75 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.67 |
rpoC | 764512 | c.1143G>C | synonymous_variant | 0.75 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.78 |
rpoC | 764524 | c.1155C>T | synonymous_variant | 0.4 |
rpoC | 764530 | c.1161C>T | synonymous_variant | 0.45 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.6 |
rpoC | 764543 | p.Thr392Ala | missense_variant | 0.56 |
rpoC | 764548 | c.1179G>T | synonymous_variant | 0.43 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.55 |
rpoC | 764573 | p.Leu402Ile | missense_variant | 0.55 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 0.6 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.6 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.6 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.7 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 0.7 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.67 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.4 |
rpoC | 764647 | c.1278C>T | synonymous_variant | 0.4 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.4 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.4 |
rpoC | 764656 | c.1287C>T | synonymous_variant | 0.4 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.5 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.6 |
rpoC | 764678 | p.Lys437Gln | missense_variant | 0.6 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.86 |
rpoC | 764713 | c.1344G>C | synonymous_variant | 0.83 |
rpoC | 764731 | c.1362G>C | synonymous_variant | 0.83 |
rpoC | 764737 | c.1368G>C | synonymous_variant | 0.83 |
rpoC | 764746 | c.1377G>C | synonymous_variant | 0.83 |
rpoC | 764752 | c.1383G>T | synonymous_variant | 0.83 |
rpoC | 764755 | p.Asp462Glu | missense_variant | 0.8 |
rpoC | 764756 | p.Leu463Lys | missense_variant | 0.8 |
rpoC | 764762 | p.His465Tyr | missense_variant | 0.8 |
rpoC | 764774 | p.Ile469Val | missense_variant | 0.67 |
rpoC | 764780 | p.Ser471Ala | missense_variant | 0.67 |
rpoC | 764793 | p.Met475Lys | missense_variant | 0.67 |
rpoC | 764797 | c.1428G>C | synonymous_variant | 0.67 |
rpoC | 764813 | p.Gln482Glu | missense_variant | 0.6 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 0.5 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.33 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776829 | p.His551Pro | missense_variant | 0.25 |
mmpL5 | 777156 | p.Arg442Gln | missense_variant | 0.25 |
mmpL5 | 777226 | p.Asn419Tyr | missense_variant | 0.33 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406613 | p.Glu243Ala | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472068 | n.223T>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472279 | n.434T>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472295 | n.451_466delAGGTCCGGGTTCTCTC | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472338 | n.493A>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472379 | n.534T>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472389 | n.544G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472498 | n.653C>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472513 | n.668T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472686 | n.841G>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472687 | n.842_843insC | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472687 | n.843dupT | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472690 | n.845C>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472958 | n.1113A>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472974 | n.1129A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472988 | n.1143T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.39 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473129 | n.1284C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.61 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473148 | n.1303G>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473163 | n.1318C>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473262 | n.1417T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473270 | n.1425G>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.76 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473314 | n.1469A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1473384 | n.-274A>G | upstream_gene_variant | 0.82 |
rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474264 | n.607T>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474266 | n.609T>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474275 | n.618T>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474282 | n.625G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474285 | n.630_631delTC | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474294 | n.637C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474295 | n.638C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474296 | n.640_650delCTCCGGAGGAG | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474326 | n.669T>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474355 | n.698A>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474454 | n.797G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474466 | n.809G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474487 | n.830G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474517 | n.860C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474552 | n.895C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474583 | n.926C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474637 | n.980C>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474643 | n.986A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 0.88 |
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 | 1474687 | n.1030C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474692 | n.1035G>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474706 | n.1049G>A | non_coding_transcript_exon_variant | 0.62 |
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 | 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 | 0.81 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475187 | n.1530C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475188 | n.1531C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475751 | n.2094C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475752 | n.2095C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475758 | n.2101A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475760 | n.2103C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475764 | n.2107A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475765 | n.2108A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475902 | n.2245T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476164 | n.2507A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476179 | n.2522C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476194 | n.2537A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476204 | n.2547C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476207 | n.2550T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476235 | n.2578A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476263 | n.2606C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476267 | n.2610G>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476276 | n.2619C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476297 | n.2640C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476298 | n.2641C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476300 | n.2643G>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476542 | n.2885T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476580 | n.2923G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.29 |
rpsA | 1833668 | p.Ile43Val | missense_variant | 0.29 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.2 |
rpsA | 1833685 | c.144G>C | synonymous_variant | 0.25 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.25 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 0.33 |
rpsA | 1834201 | c.660C>T | synonymous_variant | 0.29 |
rpsA | 1834207 | c.666C>T | synonymous_variant | 0.29 |
rpsA | 1834210 | c.669C>T | synonymous_variant | 0.29 |
rpsA | 1834213 | c.672G>C | synonymous_variant | 0.29 |
rpsA | 1834219 | c.678C>T | synonymous_variant | 0.29 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.29 |
rpsA | 1834228 | c.687C>T | synonymous_variant | 0.29 |
rpsA | 1834231 | c.690T>G | synonymous_variant | 0.29 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.33 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.33 |
rpsA | 1834246 | c.705G>T | synonymous_variant | 0.4 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.4 |
rpsA | 1834258 | c.717G>A | synonymous_variant | 0.33 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.58 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.45 |
rpsA | 1834285 | c.744G>C | synonymous_variant | 0.12 |
rpsA | 1834288 | c.747C>A | synonymous_variant | 0.12 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.5 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.5 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.36 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.43 |
rpsA | 1834312 | c.771G>A | synonymous_variant | 0.43 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.23 |
rpsA | 1834345 | c.804C>T | synonymous_variant | 0.17 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.18 |
rpsA | 1834354 | c.813G>C | synonymous_variant | 0.22 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 0.22 |
rpsA | 1834360 | c.819G>C | synonymous_variant | 0.2 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.2 |
rpsA | 1834375 | c.834G>C | synonymous_variant | 0.18 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.18 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155144 | p.Asn323Ser | missense_variant | 0.2 |
Rv1979c | 2222732 | c.432delT | frameshift_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.33 |
pepQ | 2860260 | c.159G>T | synonymous_variant | 0.29 |
Rv2752c | 3065764 | p.Tyr143Phe | missense_variant | 0.33 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339273 | c.156T>G | synonymous_variant | 0.2 |
Rv3083 | 3449182 | p.Ser227Thr | missense_variant | 0.4 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474303 | c.297C>T | synonymous_variant | 0.33 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242959 | c.-274C>T | upstream_gene_variant | 0.25 |
embA | 4245090 | p.Gly620Cys | missense_variant | 0.33 |
embB | 4249195 | c.2682C>A | synonymous_variant | 1.0 |
aftB | 4268129 | c.708T>C | synonymous_variant | 0.17 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4408175 | p.Ala10Pro | missense_variant | 1.0 |