Run ID: SRR6044952
Sample name:
Date: 04-04-2023 11:50:11
Number of reads: 58303
Percentage reads mapped: 3.8
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 | 761127 | p.Ser441Ala | missense_variant | 1.0 | rifampicin |
| rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 1.0 | streptomycin |
| rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 1.0 | kanamycin, capreomycin, aminoglycosides, amikacin |
| rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 1.0 | kanamycin, capreomycin, aminoglycosides, amikacin |
| Gene | Chromosome position | Mutation | Type | Estimated fraction |
|---|---|---|---|---|
| gyrB | 6148 | c.909C>G | synonymous_variant | 1.0 |
| gyrB | 6150 | p.Phe304Tyr | missense_variant | 1.0 |
| gyrB | 6160 | c.921C>G | synonymous_variant | 1.0 |
| gyrB | 6169 | c.930C>T | synonymous_variant | 1.0 |
| gyrB | 6190 | c.951A>G | synonymous_variant | 1.0 |
| gyrA | 6362 | c.-940T>C | upstream_gene_variant | 1.0 |
| gyrB | 6371 | p.Thr378Ser | missense_variant | 1.0 |
| rpoB | 760916 | c.1110C>T | synonymous_variant | 1.0 |
| rpoB | 760920 | p.Leu372Ile | missense_variant | 1.0 |
| rpoB | 760925 | c.1119T>C | synonymous_variant | 1.0 |
| rpoB | 760926 | p.Thr374Ala | missense_variant | 1.0 |
| rpoB | 760931 | c.1125C>G | synonymous_variant | 1.0 |
| rpoB | 760944 | p.Gln380Glu | missense_variant | 1.0 |
| rpoB | 760958 | c.1152G>C | synonymous_variant | 1.0 |
| rpoB | 760959 | p.Val385Thr | missense_variant | 1.0 |
| rpoB | 760965 | p.Met387Leu | missense_variant | 1.0 |
| rpoB | 760970 | c.1164G>C | synonymous_variant | 1.0 |
| rpoB | 760973 | c.1167G>C | synonymous_variant | 1.0 |
| rpoB | 760982 | c.1176G>C | synonymous_variant | 1.0 |
| rpoB | 760988 | c.1182C>G | synonymous_variant | 1.0 |
| rpoB | 760991 | c.1185G>C | synonymous_variant | 1.0 |
| rpoB | 761015 | c.1209G>C | synonymous_variant | 1.0 |
| rpoB | 761027 | c.1221A>G | synonymous_variant | 1.0 |
| rpoB | 761030 | c.1224G>C | synonymous_variant | 1.0 |
| rpoB | 761036 | c.1230G>C | synonymous_variant | 1.0 |
| rpoB | 761037 | c.1231T>C | synonymous_variant | 1.0 |
| rpoB | 761051 | c.1245G>T | synonymous_variant | 1.0 |
| rpoB | 761054 | c.1248G>C | synonymous_variant | 1.0 |
| rpoB | 761060 | c.1254C>G | synonymous_variant | 1.0 |
| rpoB | 761084 | c.1278C>A | synonymous_variant | 1.0 |
| rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 1.0 |
| rpoB | 761097 | c.1291_1292delAGinsTC | synonymous_variant | 1.0 |
| rpoB | 761102 | c.1296A>G | synonymous_variant | 1.0 |
| rpoB | 761126 | c.1320G>C | synonymous_variant | 1.0 |
| rpoB | 761132 | c.1326G>T | synonymous_variant | 1.0 |
| rpoB | 761133 | c.1327T>C | synonymous_variant | 1.0 |
| rpoB | 761150 | c.1344A>C | synonymous_variant | 1.0 |
| rpoB | 761153 | c.1347G>C | synonymous_variant | 1.0 |
| rpoB | 761156 | c.1350G>C | synonymous_variant | 1.0 |
| rpoB | 761165 | c.1359G>C | synonymous_variant | 1.0 |
| rpoB | 761219 | c.1413G>C | synonymous_variant | 1.0 |
| rpoB | 761234 | c.1428G>C | synonymous_variant | 1.0 |
| rpoB | 761249 | c.1443A>G | synonymous_variant | 1.0 |
| rpoB | 761261 | c.1455G>C | synonymous_variant | 1.0 |
| rpoB | 761262 | p.Pro486Ser | missense_variant | 1.0 |
| rpoB | 761288 | c.1482G>C | synonymous_variant | 1.0 |
| rpoB | 761289 | p.Ser495Ala | missense_variant | 1.0 |
| rpoB | 761292 | p.Val496Thr | missense_variant | 1.0 |
| rpoB | 761303 | c.1497G>C | synonymous_variant | 1.0 |
| rpoB | 761304 | p.Val500Ile | missense_variant | 1.0 |
| rpoB | 761327 | c.1521A>G | synonymous_variant | 1.0 |
| rpoB | 761333 | c.1527G>C | synonymous_variant | 1.0 |
| rpoB | 761345 | c.1539G>C | synonymous_variant | 1.0 |
| rpoB | 761348 | c.1542C>G | synonymous_variant | 1.0 |
| rpoB | 761521 | p.Tyr572Phe | missense_variant | 1.0 |
| rpoB | 761534 | c.1728G>C | synonymous_variant | 1.0 |
| rpoB | 761537 | c.1731C>G | synonymous_variant | 1.0 |
| rpoB | 761564 | c.1758G>C | synonymous_variant | 1.0 |
| rpoB | 761565 | p.Met587Leu | missense_variant | 1.0 |
| rpoB | 761570 | c.1764T>C | synonymous_variant | 1.0 |
| rpoB | 761573 | c.1767C>G | synonymous_variant | 1.0 |
| rpoB | 761575 | p.Phe590Tyr | missense_variant | 1.0 |
| rpoB | 761579 | c.1773G>C | synonymous_variant | 1.0 |
| rpoB | 761600 | c.1794T>C | synonymous_variant | 1.0 |
| rpoB | 761603 | c.1797C>G | synonymous_variant | 1.0 |
| rpoB | 761612 | c.1806G>C | synonymous_variant | 1.0 |
| rpoB | 761615 | c.1809A>C | synonymous_variant | 1.0 |
| rpoB | 761627 | c.1821C>T | synonymous_variant | 1.0 |
| rpoB | 761633 | c.1827G>C | synonymous_variant | 1.0 |
| rpoB | 762209 | c.2403C>G | synonymous_variant | 1.0 |
| rpoB | 762212 | c.2406G>C | synonymous_variant | 1.0 |
| rpoB | 762218 | c.2412T>C | synonymous_variant | 1.0 |
| rpoB | 762233 | c.2427G>C | synonymous_variant | 1.0 |
| rpoB | 762236 | c.2430G>C | synonymous_variant | 1.0 |
| rpoB | 762245 | c.2439G>C | synonymous_variant | 1.0 |
| rpoB | 762254 | c.2448T>C | synonymous_variant | 1.0 |
| rpoB | 762266 | c.2460T>C | synonymous_variant | 1.0 |
| rpoB | 762273 | p.Ala823Ser | missense_variant | 1.0 |
| rpoB | 762293 | c.2487T>C | synonymous_variant | 1.0 |
| rpoB | 762296 | c.2490G>C | synonymous_variant | 1.0 |
| rpoB | 762299 | c.2493G>C | synonymous_variant | 1.0 |
| rpoB | 762308 | c.2502G>C | synonymous_variant | 1.0 |
| rpoB | 762317 | c.2511A>G | synonymous_variant | 1.0 |
| rpoB | 762325 | p.Lys840Thr | missense_variant | 1.0 |
| rpoB | 762849 | p.Tyr1015Asp | missense_variant | 1.0 |
| rpoB | 762858 | p.Thr1018Ser | missense_variant | 1.0 |
| rpoC | 762863 | c.-507T>G | upstream_gene_variant | 1.0 |
| rpoB | 762870 | p.Met1022Gln | missense_variant | 1.0 |
| rpoB | 762879 | p.Met1025Leu | missense_variant | 1.0 |
| rpoC | 762887 | c.-483G>C | upstream_gene_variant | 1.0 |
| rpoC | 762929 | c.-441G>T | upstream_gene_variant | 1.0 |
| rpoC | 762938 | c.-432G>C | upstream_gene_variant | 1.0 |
| rpoC | 762980 | c.-390T>C | upstream_gene_variant | 1.0 |
| rpoC | 762983 | c.-387C>T | upstream_gene_variant | 1.0 |
| rpoC | 762989 | c.-381G>C | upstream_gene_variant | 1.0 |
| rpoC | 762995 | c.-375G>T | upstream_gene_variant | 1.0 |
| rpoB | 763005 | p.Cys1067Val | missense_variant | 1.0 |
| rpoC | 763013 | c.-357C>G | upstream_gene_variant | 1.0 |
| rpoB | 763014 | p.Met1070Leu | missense_variant | 1.0 |
| rpoB | 763017 | p.Gln1071Glu | missense_variant | 1.0 |
| rpoC | 763022 | c.-348C>G | upstream_gene_variant | 1.0 |
| rpoC | 763028 | c.-342T>C | upstream_gene_variant | 1.0 |
| rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
| rpoC | 763444 | c.75T>C | synonymous_variant | 1.0 |
| rpoC | 763456 | c.87A>G | synonymous_variant | 1.0 |
| rpoC | 763465 | c.96G>A | 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 | 763505 | c.136C>T | synonymous_variant | 1.0 |
| 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 | 1.0 |
| rpoC | 763578 | p.Phe70Tyr | missense_variant | 1.0 |
| rpoC | 763609 | c.240C>G | synonymous_variant | 1.0 |
| rpoC | 763615 | c.246G>C | synonymous_variant | 1.0 |
| rpoC | 763618 | c.249C>G | synonymous_variant | 1.0 |
| rpoC | 763621 | c.252C>T | synonymous_variant | 1.0 |
| rpoC | 763642 | c.273G>C | synonymous_variant | 1.0 |
| rpoC | 763660 | c.291T>C | synonymous_variant | 1.0 |
| rpoC | 763666 | c.297G>T | synonymous_variant | 1.0 |
| rpoC | 763672 | c.303C>G | synonymous_variant | 1.0 |
| rpoC | 763696 | c.327T>C | synonymous_variant | 1.0 |
| rpoC | 763699 | c.330G>T | 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 | 763729 | c.360G>C | synonymous_variant | 1.0 |
| rpoC | 763732 | c.363C>G | synonymous_variant | 1.0 |
| rpoC | 763735 | c.366G>C | synonymous_variant | 1.0 |
| rpoC | 763744 | c.375G>C | 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 | 763772 | p.Val135Met | missense_variant | 1.0 |
| rpoC | 763780 | c.411C>G | synonymous_variant | 1.0 |
| rpoC | 764308 | c.939G>C | synonymous_variant | 1.0 |
| rpoC | 764311 | c.942C>G | synonymous_variant | 1.0 |
| rpoC | 764347 | c.978G>C | synonymous_variant | 1.0 |
| rpoC | 764359 | c.990C>G | synonymous_variant | 1.0 |
| rpoC | 764365 | c.996C>T | 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.1018_1020delTTGinsCTC | synonymous_variant | 1.0 |
| rpoC | 764398 | c.1029G>C | synonymous_variant | 1.0 |
| rpoC | 764404 | c.1035C>T | synonymous_variant | 1.0 |
| rpoC | 764405 | c.1036_1038delAGGinsCGT | synonymous_variant | 1.0 |
| rpoC | 764428 | c.1059G>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 | 764455 | c.1086G>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 | 764485 | c.1116G>C | synonymous_variant | 1.0 |
| rpoC | 764497 | c.1128A>G | synonymous_variant | 1.0 |
| rpoC | 764498 | p.Ser377Ala | missense_variant | 1.0 |
| rpoC | 764507 | p.Ala380Ser | missense_variant | 1.0 |
| rpoC | 764521 | c.1152T>C | synonymous_variant | 1.0 |
| rpoC | 764524 | c.1155C>T | synonymous_variant | 1.0 |
| rpoC | 764536 | c.1167G>T | synonymous_variant | 1.0 |
| rpoC | 764545 | c.1176C>G | synonymous_variant | 1.0 |
| rpoC | 764548 | c.1179G>T | synonymous_variant | 1.0 |
| rpoC | 764561 | p.Pro398Ala | missense_variant | 1.0 |
| rpoC | 764566 | c.1197C>G | synonymous_variant | 1.0 |
| rpoC | 764572 | c.1203G>C | 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 | 764587 | c.1218C>G | synonymous_variant | 1.0 |
| rpoC | 764602 | c.1233C>A | synonymous_variant | 1.0 |
| rpoC | 764605 | c.1236G>C | synonymous_variant | 1.0 |
| rpoC | 764611 | c.1242G>T | synonymous_variant | 1.0 |
| rpoC | 764623 | c.1254C>G | synonymous_variant | 1.0 |
| rpoC | 764635 | c.1266C>G | synonymous_variant | 1.0 |
| rpoC | 764644 | c.1275G>C | synonymous_variant | 1.0 |
| rpoC | 764647 | c.1278C>T | synonymous_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 | 764665 | c.1296C>G | synonymous_variant | 1.0 |
| rpoC | 764677 | c.1308C>G | synonymous_variant | 1.0 |
| rpoC | 764706 | p.Leu446Gln | missense_variant | 1.0 |
| rpoC | 764746 | c.1377G>T | synonymous_variant | 1.0 |
| rpoC | 764758 | c.1389C>G | synonymous_variant | 1.0 |
| rpoC | 764764 | c.1395T>C | synonymous_variant | 1.0 |
| rpoC | 764780 | c.1411_1412delAGinsTC | synonymous_variant | 1.0 |
| rpoC | 764804 | p.Gln479Tyr | missense_variant | 1.0 |
| rpoC | 764812 | c.1443C>G | synonymous_variant | 1.0 |
| rpoC | 764815 | c.1446A>G | synonymous_variant | 1.0 |
| rpoC | 764818 | c.1449G>C | synonymous_variant | 1.0 |
| rpoC | 764824 | c.1455T>C | synonymous_variant | 1.0 |
| rpoC | 764830 | c.1461C>G | synonymous_variant | 1.0 |
| rpoC | 764843 | p.Ala492Thr | missense_variant | 1.0 |
| rpoC | 764854 | c.1485G>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 | 764887 | c.1518G>T | synonymous_variant | 1.0 |
| rpoC | 764888 | c.1519T>C | synonymous_variant | 1.0 |
| rpoC | 764893 | c.1524T>C | 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.Met515Gln | missense_variant | 1.0 |
| rpoC | 764917 | c.1548G>T | synonymous_variant | 1.0 |
| rpoC | 764923 | c.1554A>G | synonymous_variant | 1.0 |
| rpoC | 764935 | c.1566T>C | synonymous_variant | 1.0 |
| rpoC | 764948 | c.1579_1581delTTGinsCTC | synonymous_variant | 1.0 |
| rpoC | 764956 | c.1587T>C | synonymous_variant | 1.0 |
| rpoC | 764958 | p.Glu530Gly | missense_variant | 1.0 |
| rpoC | 764968 | c.1599T>C | synonymous_variant | 1.0 |
| rpoC | 765888 | p.Phe840Tyr | missense_variant | 1.0 |
| rpoC | 765902 | p.Thr845Ser | missense_variant | 1.0 |
| rpoC | 765923 | p.Asn852Ala | missense_variant | 1.0 |
| rpoC | 765934 | c.2565C>T | synonymous_variant | 1.0 |
| rpoC | 765937 | c.2568T>C | synonymous_variant | 1.0 |
| rpoC | 765946 | c.2577C>T | synonymous_variant | 1.0 |
| rpoC | 765947 | c.2578_2580delTTGinsCTC | synonymous_variant | 1.0 |
| rpoC | 765962 | c.2593T>C | synonymous_variant | 0.83 |
| rpoC | 765967 | c.2598C>T | synonymous_variant | 1.0 |
| rpoC | 765974 | p.Asp869Asn | missense_variant | 1.0 |
| rpoC | 765979 | c.2610C>G | synonymous_variant | 1.0 |
| rpoC | 765994 | c.2625A>T | synonymous_variant | 1.0 |
| rpoC | 766009 | c.2640G>C | synonymous_variant | 1.0 |
| rpoC | 766012 | c.2643C>G | synonymous_variant | 1.0 |
| rpoC | 766034 | p.His889Ser | missense_variant | 1.0 |
| rpoC | 766384 | c.3015A>G | synonymous_variant | 1.0 |
| rpoC | 766390 | c.3021C>T | synonymous_variant | 1.0 |
| rpsL | 781751 | c.192G>C | synonymous_variant | 1.0 |
| rpsL | 781754 | c.195G>C | synonymous_variant | 1.0 |
| rpsL | 781760 | c.201T>C | synonymous_variant | 1.0 |
| rpsL | 781793 | c.234G>C | synonymous_variant | 1.0 |
| rpsL | 781796 | p.Met79Ile | missense_variant | 1.0 |
| rpsL | 781802 | c.243G>C | synonymous_variant | 1.0 |
| rpsL | 781814 | c.255C>T | synonymous_variant | 1.0 |
| rpsL | 781817 | c.258G>T | synonymous_variant | 1.0 |
| rpsL | 781829 | c.270G>C | synonymous_variant | 1.0 |
| rpsL | 781832 | c.273T>C | synonymous_variant | 1.0 |
| rpsL | 781838 | c.279G>C | synonymous_variant | 1.0 |
| rpsL | 781851 | p.Ile98Val | missense_variant | 1.0 |
| rplC | 800627 | c.-182C>T | upstream_gene_variant | 1.0 |
| rplC | 800633 | c.-176T>C | upstream_gene_variant | 1.0 |
| rplC | 800645 | c.-164C>G | 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 | 800667 | c.-142_-140delTCGinsAGC | upstream_gene_variant | 1.0 |
| rplC | 800672 | c.-137G>C | upstream_gene_variant | 1.0 |
| rplC | 800693 | c.-116A>G | upstream_gene_variant | 1.0 |
| rplC | 800703 | c.-106T>C | upstream_gene_variant | 1.0 |
| rplC | 800720 | c.-89T>C | upstream_gene_variant | 1.0 |
| rplC | 800729 | c.-80G>C | upstream_gene_variant | 1.0 |
| rplC | 800733 | c.-76_-74delACCinsGCT | upstream_gene_variant | 1.0 |
| rplC | 800738 | c.-71T>C | upstream_gene_variant | 1.0 |
| rplC | 800742 | c.-67G>T | upstream_gene_variant | 1.0 |
| rplC | 800753 | c.-56C>T | upstream_gene_variant | 1.0 |
| rplC | 800754 | c.-55A>C | upstream_gene_variant | 1.0 |
| rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472113 | n.268T>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 | 1472225 | n.380C>A | 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 | 1472289 | n.444T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472293 | n.448C>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472297 | n.453_465delGTCCGGGTTCTCT | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472338 | n.493A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472496 | n.651T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472498 | n.653C>T | 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 | 1.0 |
| rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472607 | n.762G>A | 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>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472674 | n.829T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472675 | n.830T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472790 | n.945T>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 | 1472840 | n.995A>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472845 | n.1000G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472846 | n.1001C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472848 | n.1003T>G | 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 | 1472859 | n.1014G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472861 | n.1016G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472863 | n.1020_1021dupCC | 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 | 1.0 |
| rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472955 | n.1110C>T | 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 | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473035 | n.1190G>A | 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 | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473082 | n.1237G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473089 | n.1244A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473093 | n.1248C>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 | 1473115 | n.1270G>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 | 1473129 | n.1284C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473147 | n.1302G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473164 | n.1319C>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 1.0 |
| 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 | 1473290 | n.1445C>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 | 1474111 | n.454T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474124 | n.467G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474125 | n.468C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474135 | n.478G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474141 | n.484G>C | 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 | 1474155 | n.498G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474164 | n.507C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474181 | n.524C>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 | 1474202 | n.545T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474275 | n.618T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474280 | n.623C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474365 | n.708G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474384 | n.727C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 1.0 |
| 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 | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 0.43 |
| 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 | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474633 | n.977_981delTCACC | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474640 | n.983_984insTTGCT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474692 | n.1035G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474708 | n.1051_1052insA | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474711 | n.1054G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474712 | n.1055G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474713 | n.1056T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474716 | n.1059A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474717 | n.1060A>G | 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 | 1474777 | n.1120T>C | 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 | 1474782 | n.1125G>A | 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 | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474830 | n.1173A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474831 | n.1174A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475488 | n.1831G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475515 | n.1858G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475526 | n.1869C>A | 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 | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475548 | n.1891C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475549 | n.1892T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475672 | n.2015C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475673 | n.2016T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475757 | n.2100_2101insG | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475760 | n.2105_2106delGC | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475764 | n.2107A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475765 | n.2108A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475769 | n.2112_2113insC | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475778 | n.2121G>A | non_coding_transcript_exon_variant | 0.76 |
| rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475899 | n.2242G>A | 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 | 1475963 | n.2306G>A | non_coding_transcript_exon_variant | 1.0 |
| 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 | 1.0 |
| rrl | 1475998 | n.2341C>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>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476033 | n.2376T>A | 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 | 1476076 | n.2419A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476130 | n.2473G>A | 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>A | 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 | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476250 | n.2593C>G | 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 | 1.0 |
| rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476308 | n.2651G>T | 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 | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476481 | n.2824T>C | 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 | 1476519 | n.2862C>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 | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476534 | n.2877A>T | 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 | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476583 | n.2926G>A | 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 | 1476586 | n.2929C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476613 | n.2956G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476614 | n.2957A>T | 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 | 1476630 | n.2973A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476631 | n.2974G>T | non_coding_transcript_exon_variant | 1.0 |
| rpsA | 1833952 | c.411C>T | synonymous_variant | 1.0 |
| rpsA | 1833955 | c.414G>C | synonymous_variant | 1.0 |
| rpsA | 1833961 | c.420C>G | synonymous_variant | 1.0 |
| rpsA | 1833970 | c.429G>C | synonymous_variant | 1.0 |
| rpsA | 1833979 | c.438T>C | synonymous_variant | 1.0 |
| rpsA | 1833988 | c.447C>G | synonymous_variant | 1.0 |
| rpsA | 1833994 | c.453G>C | synonymous_variant | 1.0 |
| rpsA | 1833997 | c.456G>C | synonymous_variant | 1.0 |
| rpsA | 1834009 | c.468C>T | 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 | 1834025 | p.Gln162Ala | missense_variant | 1.0 |
| rpsA | 1834030 | c.489C>G | synonymous_variant | 1.0 |
| rpsA | 1834040 | p.Lys167Gln | missense_variant | 1.0 |
| rpsA | 1834043 | p.Glu168Gln | missense_variant | 1.0 |
| rpsA | 1834046 | p.Ile169Leu | missense_variant | 1.0 |
| rpsA | 1834102 | c.561T>C | synonymous_variant | 1.0 |
| rpsA | 1834105 | c.564C>T | synonymous_variant | 1.0 |
| rpsA | 1834108 | c.567C>A | synonymous_variant | 1.0 |
| rpsA | 1834114 | c.573G>C | synonymous_variant | 1.0 |
| rpsA | 1834210 | c.669C>T | synonymous_variant | 1.0 |
| rpsA | 1834219 | c.678C>G | synonymous_variant | 1.0 |
| rpsA | 1834222 | c.681T>C | synonymous_variant | 1.0 |
| rpsA | 1834225 | c.684C>G | synonymous_variant | 1.0 |
| rpsA | 1834228 | c.687C>T | 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 | 1834252 | c.711C>A | synonymous_variant | 0.29 |
| 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 | 1834307 | p.Asp256Gln | missense_variant | 1.0 |
| rpsA | 1834312 | c.771G>A | synonymous_variant | 1.0 |
| rpsA | 1834321 | c.780C>G | synonymous_variant | 1.0 |
| rpsA | 1834327 | c.786G>C | synonymous_variant | 1.0 |
| rpsA | 1834330 | c.789C>G | synonymous_variant | 1.0 |
| rpsA | 1834336 | c.795C>G | synonymous_variant | 1.0 |
| rpsA | 1834348 | c.807T>C | synonymous_variant | 1.0 |
| rpsA | 1834354 | c.813G>C | synonymous_variant | 1.0 |
| rpsA | 1834357 | c.816T>G | synonymous_variant | 1.0 |
| rpsA | 1834360 | c.819G>C | synonymous_variant | 1.0 |
| rpsA | 1834361 | c.820T>C | synonymous_variant | 1.0 |
| rpsA | 1834366 | c.825A>G | synonymous_variant | 1.0 |
| rpsA | 1834451 | c.910T>C | synonymous_variant | 1.0 |
| rpsA | 1834459 | c.918G>C | synonymous_variant | 1.0 |
| rpsA | 1834465 | c.924T>C | synonymous_variant | 1.0 |
| rpsA | 1834468 | c.927A>G | synonymous_variant | 1.0 |
| rpsA | 1834474 | c.933C>G | synonymous_variant | 1.0 |
| rpsA | 1834486 | p.Glu315Asp | missense_variant | 1.0 |
| rpsA | 1834489 | c.948T>C | synonymous_variant | 1.0 |
| rpoA | 3877635 | p.Gln291Ala | missense_variant | 1.0 |
| rpoA | 3877656 | p.Leu284Met | missense_variant | 1.0 |
| rpoA | 3877667 | p.Ser281Ala | missense_variant | 1.0 |
| rpoA | 3877668 | c.840A>G | synonymous_variant | 1.0 |
| rpoA | 3877673 | p.Thr279Ser | missense_variant | 1.0 |
| rpoA | 3877674 | c.834C>T | synonymous_variant | 1.0 |
| rpoA | 3877677 | p.Ala277Gly | missense_variant | 1.0 |
| rpoA | 3877683 | c.825G>C | synonymous_variant | 1.0 |
| rpoA | 3877686 | c.822A>G | synonymous_variant | 1.0 |
| rpoA | 3877689 | c.819C>T | synonymous_variant | 1.0 |
| rpoA | 3877696 | p.Thr271Ser | missense_variant | 1.0 |
| rpoA | 3877701 | p.Val269Ile | missense_variant | 1.0 |
| rpoA | 3877704 | c.804G>C | synonymous_variant | 1.0 |
| rpoA | 3877734 | c.774G>C | synonymous_variant | 1.0 |
| rpoA | 3877739 | p.Thr257Ser | missense_variant | 1.0 |
| rpoA | 3877743 | p.Asp255Glu | missense_variant | 1.0 |
| rpoA | 3877746 | c.762G>C | synonymous_variant | 1.0 |
| rpoA | 3877752 | p.Asp252Glu | missense_variant | 1.0 |
| rpoA | 3877758 | c.750G>C | synonymous_variant | 1.0 |
| rpoA | 3877926 | c.582G>C | synonymous_variant | 1.0 |
| rpoA | 3877932 | c.576G>C | synonymous_variant | 1.0 |
| rpoA | 3877959 | c.549C>G | synonymous_variant | 1.0 |
| rpoA | 3877962 | c.546G>T | synonymous_variant | 1.0 |
| rpoA | 3877971 | p.Asp179Glu | missense_variant | 1.0 |
| rpoA | 3877977 | p.Lys177Arg | missense_variant | 1.0 |
| rpoA | 3877981 | p.Tyr176Phe | missense_variant | 1.0 |
| rpoA | 3877989 | c.519A>G | synonymous_variant | 1.0 |
| rpoA | 3877998 | c.510G>C | synonymous_variant | 1.0 |
| rpoA | 3878001 | c.507A>T | synonymous_variant | 1.0 |
| clpC1 | 4038824 | p.Ile627Val | missense_variant | 1.0 |
| clpC1 | 4038833 | p.Phe624Leu | missense_variant | 0.4 |
| clpC1 | 4038836 | c.1869G>C | synonymous_variant | 0.6 |
| clpC1 | 4038845 | c.1860G>C | synonymous_variant | 1.0 |
| clpC1 | 4038860 | c.1845G>C | synonymous_variant | 1.0 |
| clpC1 | 4038863 | c.1842G>C | synonymous_variant | 1.0 |
| clpC1 | 4038872 | c.1833C>G | synonymous_variant | 1.0 |
| clpC1 | 4038875 | c.1830C>G | synonymous_variant | 1.0 |
| clpC1 | 4038878 | c.1827A>G | synonymous_variant | 1.0 |
| clpC1 | 4038899 | c.1806C>G | synonymous_variant | 1.0 |
| clpC1 | 4038905 | c.1800A>C | synonymous_variant | 1.0 |
| clpC1 | 4039487 | c.1218G>C | synonymous_variant | 1.0 |
| clpC1 | 4039508 | c.1197G>C | synonymous_variant | 1.0 |
| clpC1 | 4039517 | c.1188C>G | synonymous_variant | 1.0 |
| clpC1 | 4039670 | p.Val345Ile | missense_variant | 1.0 |
| clpC1 | 4039673 | c.1032G>C | synonymous_variant | 1.0 |
| clpC1 | 4039685 | c.1020C>G | synonymous_variant | 0.5 |
| clpC1 | 4039694 | c.1011G>C | synonymous_variant | 1.0 |
| clpC1 | 4039714 | p.Tyr331His | missense_variant | 1.0 |
| clpC1 | 4039724 | c.981A>G | synonymous_variant | 1.0 |
| clpC1 | 4039730 | c.975C>G | synonymous_variant | 1.0 |
| clpC1 | 4039733 | c.972G>C | synonymous_variant | 1.0 |
| clpC1 | 4039748 | c.957G>C | synonymous_variant | 1.0 |
| clpC1 | 4039751 | c.954A>G | synonymous_variant | 1.0 |
| clpC1 | 4039757 | c.948A>G | synonymous_variant | 1.0 |
| clpC1 | 4039760 | c.945T>C | synonymous_variant | 1.0 |
| clpC1 | 4039766 | c.939T>C | synonymous_variant | 1.0 |
| clpC1 | 4039769 | c.936C>G | synonymous_variant | 1.0 |
| clpC1 | 4039773 | p.Lys311Met | missense_variant | 1.0 |
| clpC1 | 4039775 | c.930G>C | synonymous_variant | 1.0 |
| clpC1 | 4039778 | c.927A>G | synonymous_variant | 1.0 |
| clpC1 | 4039781 | c.924G>C | synonymous_variant | 1.0 |
| clpC1 | 4039817 | c.888A>T | synonymous_variant | 1.0 |
| clpC1 | 4039820 | c.885T>C | synonymous_variant | 1.0 |
| clpC1 | 4039826 | c.879C>G | synonymous_variant | 1.0 |
| clpC1 | 4039829 | c.874_876delTTGinsCTC | synonymous_variant | 1.0 |
| clpC1 | 4039838 | p.Leu289Ile | missense_variant | 1.0 |
| clpC1 | 4039850 | c.855T>C | synonymous_variant | 1.0 |
| clpC1 | 4039865 | c.840T>G | synonymous_variant | 1.0 |
| clpC1 | 4039875 | 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 | 4039934 | c.771G>C | synonymous_variant | 1.0 |
| clpC1 | 4039943 | c.762G>C | synonymous_variant | 1.0 |
| clpC1 | 4039946 | c.759A>C | synonymous_variant | 1.0 |
| clpC1 | 4039949 | c.756G>C | synonymous_variant | 1.0 |
| clpC1 | 4039952 | c.753T>C | synonymous_variant | 1.0 |
| clpC1 | 4039979 | c.726C>G | synonymous_variant | 1.0 |
| clpC1 | 4039982 | c.723G>C | synonymous_variant | 1.0 |
| clpC1 | 4039988 | c.717C>G | synonymous_variant | 1.0 |
| clpC1 | 4039991 | c.714G>C | synonymous_variant | 1.0 |
| clpC1 | 4039994 | p.Glu237Asp | missense_variant | 1.0 |
| clpC1 | 4039997 | c.708C>A | synonymous_variant | 1.0 |
| clpC1 | 4040001 | p.His235Arg | missense_variant | 1.0 |
| clpC1 | 4040003 | c.702G>C | synonymous_variant | 1.0 |
| clpC1 | 4040018 | c.687G>C | synonymous_variant | 1.0 |
| clpC1 | 4040021 | c.684A>C | synonymous_variant | 1.0 |
| clpC1 | 4040024 | c.681A>G | synonymous_variant | 1.0 |
| clpC1 | 4040027 | c.678C>G | synonymous_variant | 1.0 |
| clpC1 | 4040030 | c.675C>G | synonymous_variant | 1.0 |
| clpC1 | 4040033 | c.672G>C | synonymous_variant | 1.0 |
| clpC1 | 4040045 | c.660C>G | synonymous_variant | 1.0 |
| clpC1 | 4040069 | c.636G>C | synonymous_variant | 1.0 |
| clpC1 | 4040657 | c.48T>C | synonymous_variant | 1.0 |
| clpC1 | 4040663 | c.42C>G | synonymous_variant | 1.0 |
| clpC1 | 4040669 | c.36C>G | synonymous_variant | 1.0 |
| clpC1 | 4040674 | c.31A>C | synonymous_variant | 1.0 |
| clpC1 | 4040690 | c.15T>C | synonymous_variant | 1.0 |
| clpC1 | 4040693 | c.12A>C | synonymous_variant | 1.0 |
