Run ID: ERR4821811
Sample name:
Date: 01-04-2023 17:27:53
Number of reads: 40047
Percentage reads mapped: 3.05
Strain: lineage4.9
Drug-resistance: RR-TB
| 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 |
|---|---|---|---|---|---|
| rpoB | 761116 | p.Asn437Thr | missense_variant | 1.0 | rifampicin |
| Gene | Chromosome position | Mutation | Type | Estimated fraction |
|---|---|---|---|---|
| rpoB | 760187 | c.381G>C | synonymous_variant | 1.0 |
| rpoB | 760207 | p.Ile134Thr | missense_variant | 1.0 |
| rpoB | 760215 | p.Asn137Glu | missense_variant | 1.0 |
| rpoB | 760233 | c.427_429delAGTinsTCC | synonymous_variant | 1.0 |
| rpoB | 760244 | c.438G>C | synonymous_variant | 1.0 |
| rpoB | 760253 | c.447T>C | synonymous_variant | 1.0 |
| rpoB | 760263 | p.Met153Leu | missense_variant | 1.0 |
| rpoB | 760274 | p.Glu156Asp | missense_variant | 1.0 |
| rpoB | 760968 | p.Ser388Ala | missense_variant | 1.0 |
| rpoB | 760973 | c.1167G>T | synonymous_variant | 1.0 |
| rpoB | 760985 | c.1179G>C | synonymous_variant | 1.0 |
| rpoB | 760991 | c.1185G>T | synonymous_variant | 1.0 |
| rpoB | 761003 | c.1197C>G | synonymous_variant | 1.0 |
| rpoB | 761006 | c.1200C>G | synonymous_variant | 1.0 |
| rpoB | 761015 | c.1209G>C | synonymous_variant | 1.0 |
| rpoB | 761027 | c.1221A>G | synonymous_variant | 1.0 |
| rpoB | 761037 | c.1231T>C | synonymous_variant | 1.0 |
| rpoB | 761057 | c.1251G>C | synonymous_variant | 1.0 |
| rpoB | 761064 | p.Ala420Ser | missense_variant | 1.0 |
| rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 1.0 |
| rpoB | 761102 | c.1296A>G | synonymous_variant | 1.0 |
| rpoB | 761537 | c.1731C>G | synonymous_variant | 1.0 |
| rpoB | 761555 | c.1749G>C | synonymous_variant | 1.0 |
| rpoB | 761558 | c.1752C>G | synonymous_variant | 1.0 |
| rpoB | 761564 | c.1758G>C | synonymous_variant | 1.0 |
| rpoB | 761570 | c.1764T>C | synonymous_variant | 1.0 |
| rpoB | 761603 | c.1797C>G | synonymous_variant | 1.0 |
| rpoB | 761606 | c.1800C>G | synonymous_variant | 1.0 |
| rpoB | 761948 | c.2142G>C | synonymous_variant | 1.0 |
| rpoB | 761955 | p.Ile717Phe | missense_variant | 1.0 |
| rpoB | 761973 | p.His723Tyr | missense_variant | 1.0 |
| rpoB | 761999 | c.2193G>C | synonymous_variant | 1.0 |
| rpoB | 762003 | p.Asn733Gln | missense_variant | 1.0 |
| rpoB | 762008 | c.2202C>G | synonymous_variant | 1.0 |
| rpoB | 762014 | c.2208C>G | synonymous_variant | 1.0 |
| rpoB | 762015 | p.Glu737Gln | missense_variant | 1.0 |
| rpoB | 762020 | p.Glu738Asp | missense_variant | 1.0 |
| rpoB | 762026 | c.2220G>C | synonymous_variant | 1.0 |
| rpoB | 762030 | p.Thr742Ser | missense_variant | 1.0 |
| rpoB | 762053 | c.2247T>C | synonymous_variant | 1.0 |
| rpoB | 762057 | p.Ile751Val | missense_variant | 1.0 |
| rpoB | 762062 | c.2256T>C | synonymous_variant | 1.0 |
| rpoB | 762065 | c.2259T>C | synonymous_variant | 1.0 |
| rpoB | 762068 | c.2262C>T | synonymous_variant | 1.0 |
| rpoB | 762084 | p.Ala760Pro | missense_variant | 1.0 |
| rpoB | 762101 | c.2295C>G | synonymous_variant | 1.0 |
| rpoB | 762114 | p.Ile770Val | missense_variant | 1.0 |
| rpoB | 762122 | p.Asp772Glu | missense_variant | 1.0 |
| rpoB | 762128 | c.2322G>C | synonymous_variant | 1.0 |
| rpoB | 762131 | c.2325C>G | synonymous_variant | 1.0 |
| rpoB | 762140 | c.2334G>C | synonymous_variant | 1.0 |
| rpoB | 762143 | c.2337T>C | synonymous_variant | 1.0 |
| rpoB | 762149 | c.2343G>C | synonymous_variant | 1.0 |
| rpoB | 762156 | p.Val784Ile | missense_variant | 1.0 |
| rpoB | 762167 | c.2361T>C | synonymous_variant | 1.0 |
| rpoB | 762224 | c.2418C>G | synonymous_variant | 1.0 |
| rpoB | 762233 | c.2427G>C | synonymous_variant | 1.0 |
| rpoB | 762254 | c.2448T>C | synonymous_variant | 1.0 |
| rpoB | 762257 | c.2451C>G | synonymous_variant | 1.0 |
| rpoB | 762278 | c.2472C>T | synonymous_variant | 1.0 |
| rpoB | 762284 | c.2478G>C | synonymous_variant | 1.0 |
| rpoB | 762287 | c.2481C>T | synonymous_variant | 1.0 |
| rpoB | 762293 | c.2487T>C | synonymous_variant | 1.0 |
| rpoB | 762317 | c.2511A>G | synonymous_variant | 1.0 |
| rpoC | 762383 | c.-987C>G | upstream_gene_variant | 1.0 |
| rpoB | 762387 | p.Glu861Gln | missense_variant | 1.0 |
| rpoC | 762398 | c.-972T>C | upstream_gene_variant | 1.0 |
| rpoC | 762401 | c.-969G>C | upstream_gene_variant | 1.0 |
| rpoC | 762404 | c.-966T>C | upstream_gene_variant | 1.0 |
| rpoC | 762410 | c.-960T>G | upstream_gene_variant | 1.0 |
| rpoC | 762416 | c.-954A>G | upstream_gene_variant | 1.0 |
| rpoB | 762426 | p.Ser874Thr | missense_variant | 1.0 |
| rpoC | 762443 | c.-927G>C | upstream_gene_variant | 1.0 |
| rpoC | 762446 | c.-924C>T | upstream_gene_variant | 1.0 |
| rpoC | 762470 | c.-900G>C | upstream_gene_variant | 1.0 |
| rpoB | 762474 | p.Gly890Ser | missense_variant | 1.0 |
| rpoC | 762491 | c.-879T>C | upstream_gene_variant | 1.0 |
| rpoC | 762509 | c.-861T>G | upstream_gene_variant | 1.0 |
| rpoB | 762511 | p.Ala902Glu | missense_variant | 1.0 |
| rpoC | 762527 | c.-843G>C | upstream_gene_variant | 1.0 |
| rpoC | 762866 | c.-504C>G | upstream_gene_variant | 1.0 |
| rpoB | 762879 | p.Met1025Leu | missense_variant | 1.0 |
| rpoC | 762899 | c.-471G>C | upstream_gene_variant | 1.0 |
| rpoB | 762909 | p.Ile1035Leu | missense_variant | 1.0 |
| rpoC | 762920 | c.-450C>T | upstream_gene_variant | 1.0 |
| rpoC | 762923 | c.-447C>G | upstream_gene_variant | 1.0 |
| rpoC | 762929 | c.-441G>C | upstream_gene_variant | 1.0 |
| rpoC | 762936 | c.-434_-432delTCGinsAGC | upstream_gene_variant | 1.0 |
| rpoC | 762962 | c.-408C>T | upstream_gene_variant | 1.0 |
| rpoC | 762971 | c.-399G>C | upstream_gene_variant | 1.0 |
| rpoC | 762980 | c.-390T>C | upstream_gene_variant | 1.0 |
| rpoC | 762989 | c.-381G>C | upstream_gene_variant | 1.0 |
| rpoC | 763103 | c.-267G>C | upstream_gene_variant | 1.0 |
| rpoC | 763115 | c.-255T>C | upstream_gene_variant | 1.0 |
| rpoC | 763127 | c.-243G>C | upstream_gene_variant | 1.0 |
| rpoC | 763136 | c.-234C>G | upstream_gene_variant | 1.0 |
| rpoC | 763139 | c.-231C>T | upstream_gene_variant | 1.0 |
| rpoC | 763148 | c.-222G>C | upstream_gene_variant | 1.0 |
| rpoC | 763160 | c.-210G>C | upstream_gene_variant | 1.0 |
| rpoB | 763161 | p.Leu1119Ile | missense_variant | 1.0 |
| rpoC | 763166 | c.-204A>G | upstream_gene_variant | 1.0 |
| rpoC | 763169 | c.-201A>G | upstream_gene_variant | 1.0 |
| rpoB | 763170 | p.Leu1122Met | missense_variant | 1.0 |
| rpoC | 763181 | c.-189G>C | upstream_gene_variant | 1.0 |
| rpoC | 763393 | c.24T>C | synonymous_variant | 1.0 |
| rpoC | 763399 | c.30C>G | synonymous_variant | 1.0 |
| rpoC | 763402 | c.33C>A | synonymous_variant | 1.0 |
| rpoC | 763408 | c.39T>C | synonymous_variant | 1.0 |
| rpoC | 763414 | c.45T>C | synonymous_variant | 1.0 |
| rpoC | 763420 | c.51G>T | synonymous_variant | 1.0 |
| rpoC | 763423 | p.Glu18Asp | missense_variant | 1.0 |
| rpoC | 763430 | c.61_63delAGGinsCGC | synonymous_variant | 1.0 |
| rpoC | 763435 | c.66A>G | synonymous_variant | 1.0 |
| rpoC | 763441 | c.72C>G | synonymous_variant | 1.0 |
| rpoC | 763442 | p.Tyr25His | missense_variant | 1.0 |
| rpoC | 763456 | c.87A>G | synonymous_variant | 1.0 |
| rpoC | 763468 | c.99G>C | synonymous_variant | 1.0 |
| rpoC | 763483 | c.114G>C | synonymous_variant | 1.0 |
| rpoC | 763486 | c.117T>C | synonymous_variant | 1.0 |
| rpoC | 763492 | c.123G>C | synonymous_variant | 1.0 |
| rpoC | 763504 | c.135C>A | synonymous_variant | 1.0 |
| rpoC | 763507 | c.138G>C | synonymous_variant | 1.0 |
| 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 | 763570 | c.201G>C | synonymous_variant | 1.0 |
| rpoC | 763573 | c.204G>C | synonymous_variant | 1.0 |
| rpoC | 763594 | c.225C>T | synonymous_variant | 1.0 |
| rpoC | 763633 | c.264T>C | synonymous_variant | 1.0 |
| rpoC | 763660 | c.291T>G | synonymous_variant | 1.0 |
| rpoC | 763663 | c.294C>A | synonymous_variant | 1.0 |
| rpoC | 763666 | c.297G>C | synonymous_variant | 1.0 |
| rpoC | 763696 | c.327T>C | synonymous_variant | 1.0 |
| rpoC | 763699 | c.330G>C | synonymous_variant | 1.0 |
| rpoC | 763705 | c.336G>C | synonymous_variant | 1.0 |
| rpoC | 763714 | c.345G>C | synonymous_variant | 1.0 |
| rpoC | 763717 | c.348T>C | synonymous_variant | 1.0 |
| rpoC | 763723 | c.354G>C | synonymous_variant | 1.0 |
| rpoC | 763732 | c.363C>G | synonymous_variant | 1.0 |
| rpoC | 763751 | p.Ile128Val | missense_variant | 1.0 |
| rpoC | 763765 | c.396T>G | synonymous_variant | 1.0 |
| rpoC | 763768 | c.399C>G | synonymous_variant | 1.0 |
| rpoC | 763942 | c.573C>G | synonymous_variant | 1.0 |
| rpoC | 763947 | p.Ala193Val | missense_variant | 1.0 |
| rpoC | 763951 | c.582G>C | synonymous_variant | 1.0 |
| rpoC | 763960 | c.591T>G | synonymous_variant | 1.0 |
| rpoC | 763966 | p.Asp199Glu | missense_variant | 1.0 |
| rpoC | 763971 | p.Gly201Ala | missense_variant | 1.0 |
| rpoC | 763985 | p.Arg206Lys | missense_variant | 1.0 |
| rpoC | 763996 | c.627T>C | synonymous_variant | 1.0 |
| rpoC | 764002 | c.633C>G | synonymous_variant | 1.0 |
| rpoC | 764311 | c.942C>G | synonymous_variant | 1.0 |
| rpoC | 764315 | p.Ala316Cys | missense_variant | 1.0 |
| rpoC | 764338 | p.Glu323Asp | missense_variant | 1.0 |
| rpoC | 764344 | c.975C>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>G | synonymous_variant | 1.0 |
| rpoC | 764380 | c.1011G>C | synonymous_variant | 1.0 |
| rpoC | 764387 | c.1018T>C | synonymous_variant | 1.0 |
| rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 1.0 |
| rpoC | 764410 | c.1041G>C | synonymous_variant | 1.0 |
| rpoC | 764434 | c.1065A>G | synonymous_variant | 1.0 |
| rpoC | 764435 | c.1066_1068delAGGinsCGT | 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 | 1.0 |
| rpoC | 764458 | c.1089G>C | synonymous_variant | 1.0 |
| rpoC | 764461 | c.1092A>G | synonymous_variant | 1.0 |
| rpoC | 764470 | c.1101C>G | synonymous_variant | 1.0 |
| rpoC | 764491 | c.1122G>C | synonymous_variant | 1.0 |
| rpoC | 764497 | c.1128A>G | synonymous_variant | 1.0 |
| rpoC | 764498 | p.Ser377Ala | missense_variant | 1.0 |
| rpoC | 764503 | c.1134G>C | synonymous_variant | 1.0 |
| rpoC | 764509 | c.1140G>C | synonymous_variant | 1.0 |
| rpoC | 764521 | c.1152T>C | synonymous_variant | 1.0 |
| rpoC | 764536 | c.1167G>T | synonymous_variant | 0.93 |
| rpoC | 764539 | c.1170C>G | synonymous_variant | 1.0 |
| 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 | 764605 | c.1236G>C | synonymous_variant | 1.0 |
| rpoC | 764632 | c.1263T>C | synonymous_variant | 1.0 |
| rpoC | 764646 | p.Gly426Ala | missense_variant | 1.0 |
| rpoC | 764650 | c.1281G>T | synonymous_variant | 1.0 |
| rpoC | 764653 | c.1284G>C | synonymous_variant | 1.0 |
| rpoC | 764656 | c.1287C>G | synonymous_variant | 1.0 |
| rpoC | 764662 | c.1293G>C | synonymous_variant | 1.0 |
| rpoC | 764677 | c.1308C>G | synonymous_variant | 1.0 |
| rpoC | 764705 | p.Leu446Ala | missense_variant | 1.0 |
| rpoC | 764746 | c.1377G>C | synonymous_variant | 1.0 |
| rpoC | 764752 | c.1383G>C | synonymous_variant | 1.0 |
| rpoC | 764758 | c.1389C>G | synonymous_variant | 1.0 |
| rpoC | 764764 | c.1395T>C | synonymous_variant | 1.0 |
| rpoC | 764797 | c.1428G>C | synonymous_variant | 1.0 |
| rpoC | 764858 | c.1489T>C | synonymous_variant | 1.0 |
| rpoC | 764869 | c.1500C>T | synonymous_variant | 1.0 |
| rpoC | 764872 | c.1503A>G | synonymous_variant | 1.0 |
| rpoC | 764875 | c.1506C>G | synonymous_variant | 1.0 |
| rpoC | 764878 | c.1509C>G | synonymous_variant | 1.0 |
| rpoC | 764887 | c.1518G>C | synonymous_variant | 1.0 |
| rpoC | 764888 | c.1519_1521delTTGinsCTC | synonymous_variant | 1.0 |
| rpoC | 764902 | c.1533C>G | synonymous_variant | 1.0 |
| rpoC | 764911 | c.1542A>G | synonymous_variant | 1.0 |
| rpoC | 764912 | p.Met515Leu | missense_variant | 1.0 |
| rpoC | 764920 | c.1551G>C | synonymous_variant | 1.0 |
| rpoC | 764923 | c.1554A>G | synonymous_variant | 1.0 |
| rpoC | 766309 | c.2940G>C | synonymous_variant | 1.0 |
| rpoC | 766312 | c.2943T>G | synonymous_variant | 1.0 |
| rpoC | 766316 | p.Met983Leu | missense_variant | 1.0 |
| rpoC | 766345 | c.2976T>C | synonymous_variant | 1.0 |
| rpoC | 766348 | c.2979A>G | synonymous_variant | 1.0 |
| rpoC | 766361 | p.Val998Ile | missense_variant | 1.0 |
| rpoC | 766375 | c.3006C>G | synonymous_variant | 1.0 |
| rpoC | 766381 | c.3012C>T | synonymous_variant | 1.0 |
| rpoC | 766384 | c.3015A>G | synonymous_variant | 1.0 |
| rpoC | 766402 | c.3033C>G | synonymous_variant | 1.0 |
| rpoC | 766408 | c.3039C>T | synonymous_variant | 1.0 |
| rpsL | 781754 | c.195G>C | synonymous_variant | 1.0 |
| rpsL | 781763 | c.204C>G | synonymous_variant | 1.0 |
| rpsL | 781766 | c.207C>T | synonymous_variant | 1.0 |
| rpsL | 781772 | c.213C>T | synonymous_variant | 1.0 |
| rpsL | 781796 | p.Met79Ile | missense_variant | 1.0 |
| rpsL | 781802 | c.243G>C | synonymous_variant | 1.0 |
| rpsL | 781808 | c.249C>T | synonymous_variant | 1.0 |
| rpsL | 781811 | c.252C>T | synonymous_variant | 1.0 |
| rpsL | 781817 | c.258G>T | synonymous_variant | 1.0 |
| rpsL | 781832 | c.273T>G | synonymous_variant | 1.0 |
| rpsL | 781838 | c.279G>T | synonymous_variant | 1.0 |
| rpsL | 781859 | c.300T>C | synonymous_variant | 1.0 |
| rpsL | 781862 | c.303G>C | synonymous_variant | 1.0 |
| rpsL | 781865 | c.306G>C | synonymous_variant | 1.0 |
| rpsL | 781868 | c.309T>C | synonymous_variant | 1.0 |
| rpsL | 781877 | c.318T>C | synonymous_variant | 1.0 |
| rpsL | 781892 | c.333A>G | synonymous_variant | 1.0 |
| rpsL | 781898 | c.339A>T | synonymous_variant | 1.0 |
| rpsL | 781907 | c.348T>C | synonymous_variant | 1.0 |
| rpsL | 781916 | c.357T>C | synonymous_variant | 1.0 |
| rplC | 800612 | c.-197A>G | upstream_gene_variant | 1.0 |
| rplC | 800615 | c.-194G>C | upstream_gene_variant | 1.0 |
| rplC | 800618 | c.-191T>A | upstream_gene_variant | 1.0 |
| rplC | 800633 | c.-176T>C | upstream_gene_variant | 1.0 |
| rplC | 800643 | c.-166_-164delCGCinsAAG | upstream_gene_variant | 1.0 |
| rplC | 800648 | c.-161A>G | upstream_gene_variant | 1.0 |
| rplC | 800654 | c.-155T>C | upstream_gene_variant | 1.0 |
| rplC | 800672 | c.-137G>C | upstream_gene_variant | 1.0 |
| rplC | 800693 | c.-116A>C | upstream_gene_variant | 1.0 |
| rplC | 800702 | c.-107G>T | upstream_gene_variant | 1.0 |
| rplC | 800703 | c.-106T>C | upstream_gene_variant | 1.0 |
| rplC | 800715 | c.-94A>C | upstream_gene_variant | 1.0 |
| rplC | 800720 | c.-89T>C | upstream_gene_variant | 1.0 |
| rplC | 800723 | c.-86C>G | upstream_gene_variant | 1.0 |
| rplC | 800729 | c.-80G>C | upstream_gene_variant | 1.0 |
| rplC | 800742 | c.-67G>T | upstream_gene_variant | 1.0 |
| rplC | 800747 | c.-62C>G | upstream_gene_variant | 1.0 |
| rplC | 800754 | c.-55_-53delATCinsCTG | upstream_gene_variant | 1.0 |
| rplC | 800762 | c.-47T>C | upstream_gene_variant | 1.0 |
| rplC | 800769 | c.-40A>G | upstream_gene_variant | 1.0 |
| rrs | 1471969 | n.124T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471985 | n.140T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471991 | n.146T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471997 | n.152T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471998 | n.153G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472005 | n.160T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472023 | n.178G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472025 | n.182delC | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472034 | n.189_190insC | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472068 | n.223T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472069 | n.224G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472148 | n.303T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472425 | n.580T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472486 | n.641A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472494 | n.649A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472496 | n.651T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472507 | n.662C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472571 | n.726G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472583 | n.738T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472673 | n.828T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472674 | n.829T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472675 | n.830T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 1.0 |
| 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 | 1472685 | n.840G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472686 | n.841G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472687 | n.842A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472793 | n.948A>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472803 | n.958T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472825 | n.980G>A | 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 | 1472873 | n.1028C>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 | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472958 | n.1113A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472988 | n.1143T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473026 | n.1181T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473062 | n.1217T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473068 | n.1223A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473089 | n.1244A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473091 | n.1246G>A | non_coding_transcript_exon_variant | 1.0 |
| 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>T | non_coding_transcript_exon_variant | 1.0 |
| 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 | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473201 | n.1356A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473202 | n.1357C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473283 | n.1438T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473300 | n.1455C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473679 | n.22T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473696 | n.39T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473698 | n.41G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473699 | n.42A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473702 | n.45G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473724 | n.67T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473731 | n.74T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473735 | n.78T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473743 | n.86C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473756 | n.99G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473757 | n.100T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473765 | n.108A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473768 | n.111A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473887 | n.230T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473888 | n.231T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473898 | n.241C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473908 | n.251C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473917 | n.260G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473922 | n.265A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473923 | n.266C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474133 | n.476T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474135 | n.478G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474141 | n.484G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474142 | n.485C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474153 | n.496C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474166 | n.509G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474167 | n.510T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474179 | n.522C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474186 | n.529A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474232 | n.575C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474239 | n.582G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474317 | n.660G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474349 | n.692A>T | non_coding_transcript_exon_variant | 1.0 |
| 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 | 1474359 | n.702C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474381 | n.724T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474402 | n.745T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474406 | n.749T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474528 | n.871T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474529 | n.872A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474540 | n.883T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474541 | n.884G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474551 | n.894G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474558 | n.901G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474628 | n.971C>T | 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 | 1474651 | n.995delT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474660 | n.1003G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474662 | n.1005C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474676 | n.1019T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474688 | n.1031G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474690 | n.1033C>T | 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 | 1474722 | n.1065T>C | 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 | 1474751 | n.1094G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474777 | n.1120T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474783 | n.1126G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474945 | n.1288C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475129 | n.1472G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475171 | n.1514C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475175 | n.1518G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475188 | n.1531C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475196 | n.1539T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475499 | n.1842C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475508 | n.1851A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475518 | n.1861A>T | non_coding_transcript_exon_variant | 0.97 |
| rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475532 | n.1875A>G | 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 | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475649 | n.1992A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475655 | n.1998T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475696 | n.2039T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475703 | n.2046A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475740 | n.2083G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475747 | n.2090A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475758 | n.2101A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475760 | n.2103C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475761 | n.2105delG | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.97 |
| rrl | 1475781 | n.2124T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475788 | n.2131C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475882 | n.2225C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475883 | n.2226A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475902 | n.2245T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475982 | n.2325G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476032 | n.2375C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476033 | n.2376T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476046 | n.2389G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476047 | n.2390G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476076 | n.2419A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476126 | n.2469C>T | 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 | 1.0 |
| rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 1.0 |
| 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 | 1476204 | n.2547C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476205 | n.2548A>C | 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 | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476255 | n.2598A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476256 | n.2599A>G | 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 | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476297 | n.2640C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476298 | n.2641C>G | 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 | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 1.0 |
| 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 | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476524 | n.2867C>T | 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 | 1.0 |
| rrl | 1476529 | n.2872A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476573 | n.2916A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476596 | n.2939C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476601 | n.2944G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476628 | n.2971T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476661 | n.3004A>G | non_coding_transcript_exon_variant | 1.0 |
| rpsA | 1833646 | c.105T>C | synonymous_variant | 1.0 |
| rpsA | 1833661 | p.Glu40Asp | missense_variant | 1.0 |
| rpsA | 1833665 | p.Thr42Val | missense_variant | 1.0 |
| rpsA | 1833673 | c.132C>G | synonymous_variant | 1.0 |
| rpsA | 1833676 | c.135A>G | synonymous_variant | 1.0 |
| rpsA | 1833679 | c.138G>C | synonymous_variant | 1.0 |
| rpsA | 1833694 | c.153G>C | synonymous_variant | 1.0 |
| rpsA | 1833697 | c.156C>G | synonymous_variant | 1.0 |
| rpsA | 1833709 | c.168C>T | synonymous_variant | 1.0 |
| rpsA | 1833724 | c.183C>T | synonymous_variant | 1.0 |
| rpsA | 1833727 | c.186G>C | synonymous_variant | 1.0 |
| rpsA | 1833733 | c.192C>T | synonymous_variant | 1.0 |
| rpsA | 1833734 | p.Ala65Ser | missense_variant | 1.0 |
| rpsA | 1833739 | c.198C>A | synonymous_variant | 1.0 |
| rpsA | 1833742 | c.201A>G | synonymous_variant | 1.0 |
| rpsA | 1833748 | c.207C>G | synonymous_variant | 1.0 |
| rpsA | 1833769 | c.228C>G | synonymous_variant | 1.0 |
| rpsA | 1833781 | c.240T>C | synonymous_variant | 1.0 |
| rpsA | 1833782 | p.Ser81Ala | missense_variant | 1.0 |
| rpsA | 1833797 | p.Val86Ile | missense_variant | 1.0 |
| rpsA | 1833802 | c.261A>G | synonymous_variant | 1.0 |
| rpsA | 1833808 | c.267G>C | synonymous_variant | 1.0 |
| rpsA | 1833811 | c.270G>C | synonymous_variant | 1.0 |
| rpsA | 1833815 | p.Thr92Gln | missense_variant | 1.0 |
| rpsA | 1833829 | c.288A>G | synonymous_variant | 1.0 |
| rpsA | 1833832 | c.291G>A | synonymous_variant | 1.0 |
| rpsA | 1833838 | c.297G>C | synonymous_variant | 1.0 |
| rpsA | 1833841 | c.300C>G | synonymous_variant | 1.0 |
| rpsA | 1833850 | c.309C>G | synonymous_variant | 1.0 |
| rpsA | 1833856 | c.315A>G | synonymous_variant | 1.0 |
| rpsA | 1833862 | c.321G>C | synonymous_variant | 1.0 |
| rpsA | 1833893 | p.Ala118Lys | missense_variant | 1.0 |
| rpsA | 1833896 | p.Leu119Ile | missense_variant | 1.0 |
| rpsA | 1833904 | c.363G>A | synonymous_variant | 1.0 |
| rpsA | 1833905 | p.Lys122Glu | missense_variant | 1.0 |
| rpsA | 1833910 | c.371_372delAG | frameshift_variant | 1.0 |
| rpsA | 1833915 | c.374_375insAT | frameshift_variant | 1.0 |
| rpsA | 1833921 | p.Lys127Thr | missense_variant | 1.0 |
| rpsA | 1833925 | c.384C>T | synonymous_variant | 1.0 |
| rpsA | 1833928 | c.387G>C | synonymous_variant | 1.0 |
| rpsA | 1833949 | c.408T>C | synonymous_variant | 1.0 |
| rpsA | 1833955 | c.414G>C | synonymous_variant | 1.0 |
| rpsA | 1833970 | c.429G>T | synonymous_variant | 1.0 |
| rpsA | 1833976 | c.435C>T | synonymous_variant | 1.0 |
| rpsA | 1833979 | c.438T>C | synonymous_variant | 1.0 |
| rpsA | 1833985 | c.444G>C | synonymous_variant | 1.0 |
| rpsA | 1833988 | c.447C>G | synonymous_variant | 1.0 |
| rpsA | 1833994 | c.453G>C | synonymous_variant | 1.0 |
| rpsA | 1834000 | c.459G>C | synonymous_variant | 1.0 |
| rpsA | 1834012 | c.471G>C | synonymous_variant | 1.0 |
| rpsA | 1834015 | c.474G>C | synonymous_variant | 1.0 |
| rpsA | 1834024 | c.483G>C | synonymous_variant | 1.0 |
| rpsA | 1834030 | c.489C>G | synonymous_variant | 1.0 |
| rpsA | 1834034 | p.Ile165Val | missense_variant | 1.0 |
| rpsA | 1834046 | p.Ile169Leu | missense_variant | 1.0 |
| rpsA | 1834093 | c.552G>C | synonymous_variant | 1.0 |
| rpsA | 1834096 | c.555G>C | synonymous_variant | 1.0 |
| rpsA | 1834102 | c.561T>C | synonymous_variant | 1.0 |
| rpsA | 1834189 | c.648G>C | synonymous_variant | 1.0 |
| rpsA | 1834195 | c.654G>C | synonymous_variant | 1.0 |
| rpsA | 1834213 | c.672G>C | synonymous_variant | 1.0 |
| rpsA | 1834222 | c.681T>C | synonymous_variant | 1.0 |
| rpsA | 1834225 | c.684C>G | synonymous_variant | 1.0 |
| rpsA | 1834231 | c.690T>C | synonymous_variant | 1.0 |
| rpsA | 1834246 | c.705G>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 | 1834285 | c.744G>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 | 1834306 | c.765T>C | synonymous_variant | 1.0 |
| rpsA | 1834307 | p.Asp256Gln | missense_variant | 1.0 |
| rpsA | 1834318 | c.777C>G | synonymous_variant | 1.0 |
| rpsA | 1834327 | c.786G>C | synonymous_variant | 1.0 |
| rpsA | 1834330 | c.789C>G | synonymous_variant | 1.0 |
| rpsA | 1834348 | c.807T>C | synonymous_variant | 1.0 |
| rpsA | 1834378 | c.837T>C | synonymous_variant | 1.0 |
| rpsA | 1834395 | p.Arg285Gln | missense_variant | 1.0 |
| rpsA | 1834399 | p.His286Gln | missense_variant | 1.0 |
| rpsA | 1834411 | c.870T>C | synonymous_variant | 1.0 |
| rpsA | 1834415 | p.Ala292Gln | missense_variant | 1.0 |
| rpsA | 1834423 | c.882G>C | synonymous_variant | 1.0 |
| rpsA | 1834427 | p.Ile296Val | missense_variant | 1.0 |
| rpsA | 1834435 | c.894G>C | synonymous_variant | 1.0 |
| rpsA | 1834447 | c.906C>G | synonymous_variant | 1.0 |
| rpsA | 1834451 | c.910T>C | synonymous_variant | 1.0 |
| rpsA | 1834456 | c.915T>G | synonymous_variant | 1.0 |
| rpsA | 1834468 | c.927A>G | synonymous_variant | 1.0 |
| rpsA | 1834480 | c.939C>G | synonymous_variant | 1.0 |
| rpsA | 1834483 | p.Glu314Asp | missense_variant | 1.0 |
| rpsA | 1834489 | c.948T>C | synonymous_variant | 1.0 |
| rpsA | 1834504 | c.963G>C | synonymous_variant | 1.0 |
| rpsA | 1834528 | c.987T>C | synonymous_variant | 1.0 |
| rpoA | 3877920 | c.588G>C | synonymous_variant | 1.0 |
| rpoA | 3877926 | p.Leu194Val | missense_variant | 1.0 |
| rpoA | 3877962 | c.546G>T | synonymous_variant | 1.0 |
| rpoA | 3877971 | p.Asp179Glu | missense_variant | 1.0 |
| rpoA | 3877974 | c.534G>C | synonymous_variant | 1.0 |
| rpoA | 3877989 | c.519A>G | synonymous_variant | 1.0 |
| rpoA | 3877995 | c.513G>C | synonymous_variant | 1.0 |
| rpoA | 3878001 | c.507A>G | synonymous_variant | 1.0 |
| rpoA | 3878013 | c.495T>C | synonymous_variant | 1.0 |
| rpoA | 3878019 | c.489A>G | synonymous_variant | 1.0 |
| rpoA | 3878022 | c.486T>C | synonymous_variant | 1.0 |
| clpC1 | 4039442 | c.1263A>G | synonymous_variant | 1.0 |
| clpC1 | 4039448 | c.1257A>G | synonymous_variant | 1.0 |
| clpC1 | 4039454 | c.1251A>T | synonymous_variant | 1.0 |
| clpC1 | 4039463 | c.1242C>G | synonymous_variant | 1.0 |
| clpC1 | 4039466 | c.1239T>C | synonymous_variant | 1.0 |
| clpC1 | 4039469 | c.1236T>C | synonymous_variant | 1.0 |
| clpC1 | 4039472 | c.1233G>C | synonymous_variant | 1.0 |
| clpC1 | 4039481 | p.Ala408Ser | missense_variant | 1.0 |
| clpC1 | 4039484 | c.1221T>C | synonymous_variant | 1.0 |
| clpC1 | 4039487 | c.1218G>C | synonymous_variant | 1.0 |
| clpC1 | 4039508 | c.1197G>C | synonymous_variant | 1.0 |
| clpC1 | 4039616 | c.1089G>C | synonymous_variant | 1.0 |
| clpC1 | 4039647 | p.Glu353Pro | missense_variant | 1.0 |
| clpC1 | 4039651 | p.Val352Leu | missense_variant | 1.0 |
| clpC1 | 4039654 | p.Thr351Ser | missense_variant | 1.0 |
| clpC1 | 4039661 | p.Gly348Ala | missense_variant | 1.0 |
| clpC1 | 4039664 | c.1041G>C | synonymous_variant | 1.0 |
| clpC1 | 4039670 | p.Val345Ile | missense_variant | 1.0 |
| clpC1 | 4039673 | c.1032G>C | synonymous_variant | 1.0 |
| clpC1 | 4039694 | c.1011G>C | synonymous_variant | 1.0 |
| clpC1 | 4039709 | p.Ile332Leu | missense_variant | 1.0 |
| clpC1 | 4039817 | c.888A>C | synonymous_variant | 1.0 |
| clpC1 | 4039820 | c.885T>G | synonymous_variant | 1.0 |
| clpC1 | 4039831 | c.874T>C | synonymous_variant | 1.0 |
| clpC1 | 4039850 | c.855T>C | synonymous_variant | 1.0 |
| clpC1 | 4039865 | c.840T>C | synonymous_variant | 1.0 |
| clpC1 | 4039871 | c.834C>G | synonymous_variant | 1.0 |
| clpC1 | 4039874 | p.Asn277Arg | missense_variant | 1.0 |
| clpC1 | 4039898 | c.807C>G | synonymous_variant | 1.0 |
| clpC1 | 4039904 | c.801A>G | synonymous_variant | 1.0 |
| clpC1 | 4039929 | c.775_776delAGinsTC | synonymous_variant | 1.0 |
| clpC1 | 4039931 | c.774T>C | synonymous_variant | 1.0 |
| clpC1 | 4039934 | c.771G>C | synonymous_variant | 1.0 |
| clpC1 | 4039937 | c.768G>C | synonymous_variant | 1.0 |
| clpC1 | 4039945 | p.Ser254Ala | missense_variant | 1.0 |
| clpC1 | 4039946 | c.759A>C | synonymous_variant | 1.0 |
| clpC1 | 4039952 | c.753T>C | synonymous_variant | 1.0 |
| clpC1 | 4039958 | c.747G>C | synonymous_variant | 1.0 |
| clpC1 | 4039967 | p.Gln246His | missense_variant | 1.0 |
| clpC1 | 4039982 | c.723G>C | synonymous_variant | 1.0 |
| clpC1 | 4040000 | p.His235Lys | missense_variant | 1.0 |
| clpC1 | 4040003 | c.702G>C | synonymous_variant | 1.0 |
| clpC1 | 4040021 | c.684A>C | synonymous_variant | 1.0 |
| clpC1 | 4040024 | c.681A>G | synonymous_variant | 1.0 |
| clpC1 | 4040033 | c.672G>C | synonymous_variant | 1.0 |
| clpC1 | 4040063 | c.642G>C | synonymous_variant | 1.0 |
| clpC1 | 4040081 | c.624C>G | synonymous_variant | 1.0 |
| clpC1 | 4040084 | c.621C>T | synonymous_variant | 1.0 |
| clpC1 | 4040087 | c.618G>C | synonymous_variant | 1.0 |
| clpC1 | 4040090 | c.615T>C | synonymous_variant | 1.0 |
| clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.92 |
| clpC1 | 4040096 | c.609G>C | synonymous_variant | 0.92 |
| clpC1 | 4040117 | c.588A>G | synonymous_variant | 1.0 |
| clpC1 | 4040129 | c.576C>G | synonymous_variant | 1.0 |
| clpC1 | 4040147 | c.558A>G | synonymous_variant | 1.0 |
| clpC1 | 4040563 | p.Ser48Ala | missense_variant | 1.0 |
| clpC1 | 4040567 | c.138C>T | synonymous_variant | 1.0 |
| clpC1 | 4040573 | c.132T>C | synonymous_variant | 1.0 |
| clpC1 | 4040576 | c.129C>T | synonymous_variant | 1.0 |
| clpC1 | 4040579 | c.126A>G | synonymous_variant | 1.0 |
| clpC1 | 4040582 | c.123G>T | synonymous_variant | 1.0 |
| clpC1 | 4040588 | c.117T>C | synonymous_variant | 1.0 |
| clpC1 | 4040600 | c.103_105delTTAinsCTG | synonymous_variant | 1.0 |
| clpC1 | 4040606 | c.99T>C | synonymous_variant | 1.0 |
