Run ID: ERR3439265
Sample name:
Date: 01-04-2023 02:00:28
Number of reads: 42120
Percentage reads mapped: 3.01
Strain: lineage4.9
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.99 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.38 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.67 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.67 | kanamycin, capreomycin, aminoglycosides, amikacin |
pncA | 2289073 | p.His57Asp | missense_variant | 1.0 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
rpoB | 760982 | c.1176G>C | synonymous_variant | 1.0 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 1.0 |
rpoB | 760997 | c.1191G>C | synonymous_variant | 1.0 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 1.0 |
rpoB | 762003 | p.Asn733Gln | missense_variant | 1.0 |
rpoB | 762017 | c.2211A>G | synonymous_variant | 1.0 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 1.0 |
rpoB | 762114 | p.Ile770Val | missense_variant | 1.0 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 1.0 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 1.0 |
rpoB | 762209 | c.2403C>G | synonymous_variant | 0.67 |
rpoB | 762212 | c.2406G>C | synonymous_variant | 0.67 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.5 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.67 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.67 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 1.0 |
rpoC | 762896 | c.-474G>C | upstream_gene_variant | 0.67 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 1.0 |
rpoB | 762912 | p.His1036Asn | missense_variant | 0.67 |
rpoC | 762917 | c.-453C>T | upstream_gene_variant | 0.67 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 1.0 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 1.0 |
rpoC | 762932 | c.-438G>C | upstream_gene_variant | 0.67 |
rpoC | 762947 | c.-423C>G | upstream_gene_variant | 0.67 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 0.6 |
rpoC | 762983 | c.-387C>A | upstream_gene_variant | 0.5 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 1.0 |
rpoB | 763005 | p.Cys1067Val | missense_variant | 1.0 |
rpoC | 763013 | c.-357C>A | upstream_gene_variant | 1.0 |
rpoB | 763014 | p.Met1070Leu | missense_variant | 0.5 |
rpoB | 763017 | p.Gln1071Glu | missense_variant | 1.0 |
rpoC | 763022 | c.-348C>G | upstream_gene_variant | 0.67 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763053 | c.-317_-315delTTGinsCTC | upstream_gene_variant | 1.0 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 1.0 |
rpoB | 763075 | p.Thr1090Ile | missense_variant | 1.0 |
rpoC | 763088 | c.-282C>G | upstream_gene_variant | 1.0 |
rpoC | 763444 | c.75T>C | synonymous_variant | 1.0 |
rpoC | 763456 | c.87A>G | synonymous_variant | 1.0 |
rpoC | 763468 | c.99G>C | synonymous_variant | 1.0 |
rpoC | 763486 | c.117T>C | synonymous_variant | 1.0 |
rpoC | 763492 | c.123G>C | synonymous_variant | 1.0 |
rpoC | 763496 | p.Lys43Arg | missense_variant | 0.5 |
rpoC | 763528 | c.159G>T | synonymous_variant | 1.0 |
rpoC | 763531 | c.162G>C | synonymous_variant | 1.0 |
rpoC | 763534 | c.165T>C | synonymous_variant | 1.0 |
rpoC | 763537 | c.168C>G | synonymous_variant | 1.0 |
rpoC | 763546 | c.177A>G | synonymous_variant | 1.0 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.83 |
rpoC | 763578 | p.Phe70Tyr | missense_variant | 0.33 |
rpoC | 763600 | c.231C>G | synonymous_variant | 0.4 |
rpoC | 763603 | c.234C>T | synonymous_variant | 0.6 |
rpoC | 763609 | c.240C>G | synonymous_variant | 0.33 |
rpoC | 763615 | c.246G>C | synonymous_variant | 1.0 |
rpoC | 763622 | p.Ala85Ser | missense_variant | 0.75 |
rpoC | 763633 | c.264T>C | synonymous_variant | 1.0 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.5 |
rpoC | 763660 | c.291T>C | synonymous_variant | 1.0 |
rpoC | 763672 | c.303C>G | synonymous_variant | 0.67 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.67 |
rpoC | 763711 | c.342G>C | synonymous_variant | 0.67 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.67 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.67 |
rpoC | 763729 | c.360G>C | synonymous_variant | 0.67 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.67 |
rpoC | 764338 | p.Glu323Asp | missense_variant | 1.0 |
rpoC | 764353 | c.984G>C | synonymous_variant | 1.0 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 0.75 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.5 |
rpoC | 764383 | c.1014C>G | synonymous_variant | 0.5 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 1.0 |
rpoC | 764398 | c.1029G>C | synonymous_variant | 0.5 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 1.0 |
rpoC | 764410 | c.1041G>C | synonymous_variant | 0.5 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.8 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 1.0 |
rpoC | 764435 | c.1066_1068delAGGinsCGC | synonymous_variant | 1.0 |
rpoC | 764441 | p.Ile358Leu | missense_variant | 1.0 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 1.0 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.6 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 1.0 |
rpoC | 764455 | c.1086G>C | synonymous_variant | 0.4 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.4 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 1.0 |
rpoC | 764477 | p.Glu370* | stop_gained | 0.4 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 1.0 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 1.0 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 1.0 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 1.0 |
rpoC | 764548 | c.1179G>C | synonymous_variant | 0.4 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.67 |
rpoC | 764561 | p.Pro398Ala | missense_variant | 0.4 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.8 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 1.0 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 1.0 |
rpoC | 764582 | p.Leu405Met | missense_variant | 1.0 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.33 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 0.67 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.25 |
rpoC | 764623 | c.1254C>G | synonymous_variant | 0.62 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 1.0 |
rpoC | 764635 | c.1266C>G | synonymous_variant | 0.22 |
rpoC | 764644 | c.1275G>C | synonymous_variant | 0.8 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 1.0 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.2 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.33 |
rpoC | 764701 | c.1332C>G | synonymous_variant | 0.43 |
rpoC | 764705 | p.Leu446Ala | missense_variant | 0.67 |
rpoC | 764751 | p.Val461Asp | missense_variant | 0.6 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 1.0 |
rpoC | 764780 | c.1411_1412delAGinsTC | synonymous_variant | 1.0 |
rpoC | 764797 | c.1428G>C | synonymous_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472287 | n.442C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472293 | n.448C>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472297 | n.453_465delGTCCGGGTTCTCT | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472312 | n.467_468insA | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 0.67 |
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 | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472338 | n.493A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472571 | n.726G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472754 | n.909G>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472836 | n.991G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472837 | n.992C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472838 | n.993A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472840 | n.995A>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472844 | n.999C>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472847 | n.1002G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472849 | n.1004C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472850 | n.1005T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472857 | n.1012A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472860 | n.1015C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472863 | n.1018T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472875 | n.1030T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472878 | n.1033G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473097 | n.1252G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.4 |
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 | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473135 | n.1290C>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473147 | n.1302G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473164 | n.1319C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473283 | n.1438T>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473289 | n.1444T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473324 | n.1479G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474450 | n.793T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474454 | n.797G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474466 | n.809G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474583 | n.926C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474627 | n.970G>A | non_coding_transcript_exon_variant | 1.0 |
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>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474709 | n.1053_1056delTGGT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474717 | n.1060_1061insGTGAG | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474723 | n.1066G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474751 | n.1094G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474777 | n.1120T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474783 | n.1126G>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474790 | n.1133C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474799 | n.1142G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474830 | n.1173A>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474831 | n.1174A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474917 | n.1260G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475692 | n.2035G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475752 | n.2095C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475766 | n.2109G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475776 | n.2119G>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.58 |
rrl | 1475880 | n.2223C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475881 | n.2224T>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475882 | n.2225C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.72 |
rrl | 1475892 | n.2235A>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.77 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475963 | n.2306G>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475997 | n.2340A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475998 | n.2341C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476165 | n.2508T>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476308 | n.2651G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476316 | n.2659G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476322 | n.2665C>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476368 | n.2711T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476381 | n.2724G>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476523 | n.2866T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476528 | n.2871A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476529 | n.2872A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1833668 | p.Ile43Val | missense_variant | 0.67 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.67 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 0.67 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.67 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 1.0 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 1.0 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 1.0 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.67 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.5 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.5 |
rpsA | 1834024 | c.483G>C | synonymous_variant | 0.5 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.5 |
rpsA | 1834034 | p.Ile165Val | missense_variant | 0.5 |
rpsA | 1834040 | p.Lys167Gln | missense_variant | 0.5 |
rpsA | 1834046 | p.Ile169Leu | missense_variant | 0.5 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.5 |
rpsA | 1834108 | c.567C>G | synonymous_variant | 0.5 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 1.0 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 1.0 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 1.0 |
rpsA | 1834243 | c.702G>C | synonymous_variant | 1.0 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 1.0 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 1.0 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 1.0 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 1.0 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 1.0 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 1.0 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.67 |
rpsA | 1834312 | p.Glu257Asp | missense_variant | 0.67 |
rpsA | 1834318 | c.777C>G | synonymous_variant | 0.67 |
rpsA | 1834327 | c.786G>C | synonymous_variant | 1.0 |
rpsA | 1834340 | p.Met267Leu | missense_variant | 0.67 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ald | 3087084 | c.266delA | frameshift_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 1.0 |
clpC1 | 4039916 | c.789T>C | synonymous_variant | 0.67 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.67 |
clpC1 | 4039937 | p.Val256Ile | missense_variant | 0.67 |
clpC1 | 4039940 | c.765G>C | synonymous_variant | 0.67 |
clpC1 | 4039946 | c.759A>C | synonymous_variant | 0.67 |
clpC1 | 4039949 | c.756G>C | synonymous_variant | 0.67 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.67 |
clpC1 | 4039955 | c.750G>C | synonymous_variant | 0.67 |
clpC1 | 4039966 | p.Leu247Val | missense_variant | 0.67 |
clpC1 | 4040000 | p.His235Lys | missense_variant | 0.67 |
clpC1 | 4040003 | c.702G>C | synonymous_variant | 0.67 |
clpC1 | 4040009 | c.696C>G | synonymous_variant | 0.67 |
clpC1 | 4040018 | c.687G>C | synonymous_variant | 0.67 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.67 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.67 |
clpC1 | 4040030 | c.675C>G | synonymous_variant | 0.67 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.67 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.67 |
embB | 4246864 | c.351C>T | synonymous_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |