Run ID: ERR4816417
Sample name:
Date: 01-04-2023 14:25:03
Number of reads: 50610
Percentage reads mapped: 9.0
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 | 1.0 |
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 | 0.77 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6745 | c.-557T>C | upstream_gene_variant | 1.0 |
gyrA | 6751 | c.-551G>C | upstream_gene_variant | 1.0 |
gyrA | 6760 | c.-542G>C | upstream_gene_variant | 1.0 |
gyrA | 6772 | c.-530C>A | upstream_gene_variant | 0.5 |
gyrA | 6775 | c.-527G>C | upstream_gene_variant | 1.0 |
gyrB | 6784 | p.Asp515Glu | missense_variant | 1.0 |
gyrA | 6787 | c.-515G>A | upstream_gene_variant | 1.0 |
gyrA | 6796 | c.-506C>T | upstream_gene_variant | 0.5 |
gyrB | 6797 | p.Gly520Lys | missense_variant | 1.0 |
gyrA | 6808 | c.-494C>G | upstream_gene_variant | 0.8 |
gyrB | 6812 | p.His525Asp | missense_variant | 0.8 |
gyrA | 6835 | c.-467C>T | upstream_gene_variant | 0.8 |
gyrA | 6841 | c.-461T>C | upstream_gene_variant | 0.4 |
gyrA | 6844 | c.-458T>G | upstream_gene_variant | 0.67 |
rpoB | 762197 | c.2391C>G | synonymous_variant | 0.8 |
rpoB | 762200 | c.2394C>T | synonymous_variant | 0.8 |
rpoB | 762228 | c.2422C>T | synonymous_variant | 0.78 |
rpoB | 762233 | c.2427G>T | synonymous_variant | 1.0 |
rpoB | 762239 | c.2433G>A | synonymous_variant | 1.0 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 1.0 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 1.0 |
rpoB | 762284 | c.2478G>T | synonymous_variant | 0.62 |
rpoB | 762290 | c.2484C>T | synonymous_variant | 1.0 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 1.0 |
rpoB | 762296 | c.2490G>C | synonymous_variant | 0.75 |
rpoB | 762297 | p.Leu831Met | missense_variant | 0.75 |
rpoB | 762305 | c.2499G>T | synonymous_variant | 0.6 |
rpoB | 762352 | p.Arg849Leu | missense_variant | 1.0 |
rpoC | 762971 | c.-399G>T | upstream_gene_variant | 1.0 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.83 |
rpoC | 762995 | c.-375G>C | upstream_gene_variant | 0.83 |
rpoB | 763005 | p.Cys1067Val | missense_variant | 0.83 |
rpoC | 763013 | c.-357C>A | upstream_gene_variant | 0.86 |
rpoC | 763022 | c.-348C>T | upstream_gene_variant | 0.75 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.75 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.25 |
rpoC | 763053 | c.-317_-315delTTGinsCTT | upstream_gene_variant | 0.7 |
rpoB | 763074 | p.Thr1090Val | missense_variant | 0.57 |
rpoC | 763079 | c.-291C>A | upstream_gene_variant | 0.67 |
rpoC | 763088 | c.-282C>G | upstream_gene_variant | 0.67 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.67 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 1.0 |
rpoC | 763109 | c.-261C>G | upstream_gene_variant | 1.0 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 1.0 |
rpoC | 763492 | c.123G>C | synonymous_variant | 0.5 |
rpoC | 763507 | c.138G>C | synonymous_variant | 0.5 |
rpoC | 763528 | c.159G>C | 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 | 763550 | p.Tyr61Ala | missense_variant | 1.0 |
rpoC | 763570 | c.201G>C | synonymous_variant | 1.0 |
rpoC | 763578 | p.Phe70Tyr | missense_variant | 0.8 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.67 |
rpoC | 763600 | c.231C>T | synonymous_variant | 0.57 |
rpoC | 763609 | c.240C>T | synonymous_variant | 0.71 |
rpoC | 763615 | c.246G>C | synonymous_variant | 0.57 |
rpoC | 763619 | p.Arg84Lys | missense_variant | 0.71 |
rpoC | 763622 | p.Ala85Ser | missense_variant | 0.71 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.82 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.83 |
rpoC | 763666 | c.297G>T | synonymous_variant | 0.83 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.82 |
rpoC | 763672 | c.303C>A | synonymous_variant | 0.82 |
rpoC | 763696 | c.327T>C | synonymous_variant | 1.0 |
rpoC | 763699 | c.330G>T | synonymous_variant | 1.0 |
rpoC | 763702 | c.333C>T | synonymous_variant | 1.0 |
rpoC | 763705 | c.336G>C | synonymous_variant | 1.0 |
rpoC | 763708 | c.339G>C | synonymous_variant | 1.0 |
rpoC | 763709 | c.340C>T | synonymous_variant | 1.0 |
rpoC | 763714 | c.345G>C | synonymous_variant | 1.0 |
rpoC | 763717 | c.348T>C | synonymous_variant | 1.0 |
rpoC | 763732 | c.363C>A | synonymous_variant | 1.0 |
rpoC | 764326 | c.957G>T | synonymous_variant | 1.0 |
rpoC | 764329 | c.960C>T | synonymous_variant | 1.0 |
rpoC | 764335 | c.966G>T | synonymous_variant | 1.0 |
rpoC | 764339 | c.970C>T | synonymous_variant | 1.0 |
rpoC | 764359 | c.990C>G | synonymous_variant | 1.0 |
rpoC | 764365 | c.996C>T | synonymous_variant | 1.0 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 1.0 |
rpoC | 764377 | c.1008C>T | synonymous_variant | 1.0 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 1.0 |
rpoC | 764383 | c.1014C>G | synonymous_variant | 1.0 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 1.0 |
rpoC | 764392 | c.1023C>T | synonymous_variant | 1.0 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 1.0 |
rpoC | 764410 | c.1041G>T | synonymous_variant | 1.0 |
rpoC | 764422 | c.1053C>T | synonymous_variant | 1.0 |
rpoC | 764428 | c.1059G>T | synonymous_variant | 1.0 |
rpoC | 764920 | c.1551G>T | synonymous_variant | 1.0 |
rpoC | 764923 | c.1554A>G | synonymous_variant | 1.0 |
rpoC | 764926 | c.1557C>T | synonymous_variant | 1.0 |
rpoC | 764932 | c.1563C>T | synonymous_variant | 1.0 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 1.0 |
rpoC | 764952 | p.Val528Ala | missense_variant | 1.0 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 1.0 |
rpoC | 765119 | p.Gly584Arg | missense_variant | 1.0 |
rpoC | 767106 | p.Asn1246Ile | missense_variant | 1.0 |
rpoC | 767110 | c.3741T>C | synonymous_variant | 1.0 |
rpoC | 767113 | c.3744G>C | synonymous_variant | 1.0 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 1.0 |
rpoC | 767125 | c.3756G>C | synonymous_variant | 1.0 |
rpoC | 767134 | c.3765C>T | synonymous_variant | 1.0 |
rpsL | 781682 | c.123T>C | synonymous_variant | 1.0 |
rplC | 800669 | c.-140G>T | upstream_gene_variant | 1.0 |
rplC | 800672 | c.-137G>C | upstream_gene_variant | 1.0 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.67 |
rplC | 800702 | c.-107G>C | upstream_gene_variant | 0.67 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.67 |
rplC | 800711 | c.-98C>T | upstream_gene_variant | 0.67 |
rplC | 800714 | c.-95C>T | upstream_gene_variant | 0.67 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.67 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 1.0 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 1.0 |
rplC | 800726 | c.-83G>C | upstream_gene_variant | 1.0 |
rplC | 800741 | c.-68C>T | upstream_gene_variant | 1.0 |
rrs | 1471922 | n.78delT | non_coding_transcript_exon_variant | 0.96 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.79 |
rrs | 1471926 | n.81C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1471928 | n.83T>G | non_coding_transcript_exon_variant | 0.78 |
rrs | 1471985 | n.140T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1471996 | n.151C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472026 | n.181C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472069 | n.224G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472123 | n.278A>G | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472278 | n.433C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472279 | n.434T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472330 | n.485G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472412 | n.567A>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472431 | n.586G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472438 | n.593T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472439 | n.594C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472447 | n.602C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472484 | n.639A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472504 | n.659A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472505 | n.660G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472574 | n.729T>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472669 | n.824_825insA | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472836 | n.991G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472874 | n.1029C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472875 | n.1030T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472970 | n.1128A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472974 | n.1129A>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472977 | n.1133dupT | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473026 | n.1181T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473089 | n.1244A>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473091 | n.1246G>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473099 | n.1254T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 1.0 |
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 | 1473120 | n.1275C>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473123 | n.1278A>G | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473129 | n.1284C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473132 | n.1287T>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1473135 | n.1290C>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473202 | n.1357C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473292 | n.1447G>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473293 | n.1448G>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473346 | n.1501G>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473365 | n.1520C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1473697 | n.40C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473698 | n.41G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473699 | n.42A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473700 | n.43G>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1473718 | n.61G>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1473719 | n.62G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473728 | n.71A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473731 | n.74T>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1473743 | n.86C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473750 | n.93C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473751 | n.94C>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473752 | n.95G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473884 | n.227C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473888 | n.231T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473889 | n.232G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473896 | n.239C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473899 | n.242A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473911 | n.254G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473918 | n.261C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473922 | n.265A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473923 | n.266C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474124 | n.467G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474130 | n.473C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474142 | n.485C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474143 | n.486T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474253 | n.596A>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474263 | n.606G>A | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474351 | n.694G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474495 | n.838G>A | 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 | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474517 | n.860C>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474527 | n.870T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474542 | n.885A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474634 | n.977T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474658 | n.1001A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474663 | n.1006C>T | 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 | 0.83 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474751 | n.1094G>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474784 | n.1127C>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474798 | n.1141C>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474803 | n.1146G>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474825 | n.1168G>A | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474837 | n.1180A>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474901 | n.1244A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474921 | n.1264C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475171 | n.1514C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475175 | n.1518G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475176 | n.1519G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475499 | n.1842C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475499 | n.1842C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475522 | n.1865A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475525 | n.1868G>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475526 | n.1869C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475542 | n.1885A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475544 | n.1887A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475550 | n.1893A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475562 | n.1905C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475688 | n.2031G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475696 | n.2039T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475703 | n.2046A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475704 | n.2047C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475713 | n.2056C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475757 | n.2101_2104delACCC | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1475892 | n.2235A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1475902 | n.2245T>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1475916 | n.2259C>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 | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475993 | n.2336C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476031 | n.2374C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476033 | n.2376T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476034 | n.2377C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476040 | n.2383C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476046 | n.2389G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476080 | n.2423T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476085 | n.2428G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.94 |
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 | 0.92 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.96 |
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 | 1476251 | n.2594T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476298 | n.2641C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476300 | n.2643G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476307 | n.2650A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476309 | n.2652G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476535 | n.2878G>A | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476580 | n.2923G>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476592 | n.2935G>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476605 | n.2948C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476624 | n.2967T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1833709 | c.168C>A | synonymous_variant | 1.0 |
rpsA | 1833727 | c.186G>T | synonymous_variant | 1.0 |
rpsA | 1833733 | c.192C>T | synonymous_variant | 1.0 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 1.0 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 1.0 |
rpsA | 1834003 | c.462G>A | synonymous_variant | 1.0 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 1.0 |
rpsA | 1834015 | c.474G>T | synonymous_variant | 1.0 |
rpsA | 1834025 | p.Gln162Glu | missense_variant | 1.0 |
rpsA | 1834030 | c.489C>A | synonymous_variant | 0.67 |
rpsA | 1834036 | c.495C>T | synonymous_variant | 1.0 |
rpsA | 1834040 | p.Lys167Gln | missense_variant | 1.0 |
rpsA | 1834046 | p.Ile169Leu | missense_variant | 1.0 |
rpsA | 1834051 | p.Glu170Asp | missense_variant | 1.0 |
clpC1 | 4038356 | c.2349T>C | synonymous_variant | 1.0 |
clpC1 | 4038359 | c.2346A>G | synonymous_variant | 1.0 |
clpC1 | 4038365 | p.Glu780Asp | missense_variant | 1.0 |
clpC1 | 4038368 | c.2337T>C | synonymous_variant | 1.0 |
clpC1 | 4038374 | c.2331C>T | synonymous_variant | 1.0 |
clpC1 | 4038383 | c.2322G>C | synonymous_variant | 1.0 |
clpC1 | 4038395 | c.2310C>T | synonymous_variant | 1.0 |
clpC1 | 4038398 | c.2307G>T | synonymous_variant | 1.0 |
clpC1 | 4038401 | c.2302_2304delTTGinsCTC | synonymous_variant | 1.0 |
clpC1 | 4038404 | c.2301G>A | synonymous_variant | 1.0 |
clpC1 | 4038419 | c.2286T>C | synonymous_variant | 1.0 |
clpC1 | 4038424 | p.Lys761Gln | missense_variant | 1.0 |
clpC1 | 4038529 | p.Glu726Gln | missense_variant | 0.6 |
clpC1 | 4038539 | c.2166G>C | synonymous_variant | 0.6 |
clpC1 | 4038554 | p.Ile717Val | missense_variant | 0.6 |
clpC1 | 4038559 | p.Ile716Val | missense_variant | 0.6 |
clpC1 | 4038563 | c.2142C>T | synonymous_variant | 0.6 |
clpC1 | 4038569 | c.2136C>T | synonymous_variant | 0.6 |
clpC1 | 4038575 | c.2130C>G | synonymous_variant | 0.6 |
clpC1 | 4038584 | c.2121G>C | synonymous_variant | 0.6 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.75 |
clpC1 | 4039004 | c.1701C>T | synonymous_variant | 1.0 |
clpC1 | 4039012 | p.Ala565Ser | missense_variant | 1.0 |
clpC1 | 4039016 | c.1689C>G | synonymous_variant | 1.0 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 1.0 |
clpC1 | 4039034 | c.1671C>G | synonymous_variant | 1.0 |
whiB6 | 4338384 | c.138C>T | synonymous_variant | 0.5 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |