Run ID: SRR3675266
Sample name:
Date: 04-04-2023 05:24:50
Number of reads: 25624
Percentage reads mapped: 9.43
Strain: lineage4.9
Drug-resistance: Sensitive
| 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 |
|---|
| Gene | Chromosome position | Mutation | Type | Estimated fraction |
|---|---|---|---|---|
| gyrB | 6100 | c.861G>A | synonymous_variant | 1.0 |
| gyrB | 6115 | c.876A>G | synonymous_variant | 1.0 |
| gyrB | 6121 | c.882C>T | synonymous_variant | 1.0 |
| gyrB | 6127 | c.888G>C | synonymous_variant | 1.0 |
| gyrB | 6133 | c.894G>C | synonymous_variant | 1.0 |
| gyrB | 6136 | c.897G>A | synonymous_variant | 1.0 |
| gyrB | 6151 | c.912C>T | synonymous_variant | 1.0 |
| gyrB | 6172 | c.933C>T | synonymous_variant | 1.0 |
| gyrB | 6184 | c.945C>T | synonymous_variant | 1.0 |
| gyrB | 6193 | c.954G>A | synonymous_variant | 1.0 |
| gyrB | 6196 | c.957C>T | synonymous_variant | 1.0 |
| gyrB | 6202 | c.963C>T | synonymous_variant | 1.0 |
| gyrB | 6203 | p.Ser322Ala | missense_variant | 1.0 |
| gyrB | 6214 | c.975G>C | synonymous_variant | 1.0 |
| gyrB | 6223 | c.984G>C | synonymous_variant | 1.0 |
| gyrB | 6229 | c.990G>A | synonymous_variant | 1.0 |
| gyrA | 6673 | c.-629A>C | upstream_gene_variant | 1.0 |
| gyrA | 6676 | c.-626T>G | upstream_gene_variant | 1.0 |
| gyrA | 6700 | c.-602T>C | upstream_gene_variant | 1.0 |
| gyrA | 6703 | c.-599G>C | upstream_gene_variant | 1.0 |
| gyrA | 6706 | c.-596G>A | upstream_gene_variant | 1.0 |
| gyrA | 6709 | c.-593A>G | upstream_gene_variant | 1.0 |
| gyrA | 6712 | c.-590G>C | upstream_gene_variant | 1.0 |
| gyrA | 6727 | c.-575G>T | upstream_gene_variant | 1.0 |
| gyrA | 6728 | c.-574_-572delCTAinsTTG | upstream_gene_variant | 1.0 |
| gyrA | 6739 | c.-563C>T | upstream_gene_variant | 1.0 |
| gyrA | 6745 | c.-557T>C | upstream_gene_variant | 1.0 |
| gyrA | 6763 | c.-539G>C | upstream_gene_variant | 1.0 |
| gyrA | 6772 | c.-530C>G | upstream_gene_variant | 1.0 |
| gyrA | 6775 | c.-527G>C | upstream_gene_variant | 1.0 |
| gyrA | 6793 | c.-509T>C | upstream_gene_variant | 1.0 |
| gyrB | 6798 | p.Gly520Ala | missense_variant | 1.0 |
| gyrA | 6808 | c.-494C>G | upstream_gene_variant | 1.0 |
| gyrB | 7051 | p.Glu604Asp | missense_variant | 1.0 |
| gyrA | 7060 | c.-242T>C | upstream_gene_variant | 1.0 |
| gyrA | 7066 | c.-236G>T | upstream_gene_variant | 1.0 |
| gyrA | 7078 | c.-224A>G | upstream_gene_variant | 1.0 |
| gyrA | 7081 | c.-221T>C | upstream_gene_variant | 1.0 |
| gyrA | 7084 | c.-218A>G | upstream_gene_variant | 1.0 |
| gyrA | 7090 | c.-212C>T | upstream_gene_variant | 1.0 |
| gyrA | 7093 | c.-209T>C | upstream_gene_variant | 1.0 |
| gyrA | 7100 | c.-202T>C | upstream_gene_variant | 1.0 |
| gyrA | 7123 | c.-179C>G | upstream_gene_variant | 1.0 |
| gyrA | 7126 | c.-176G>C | upstream_gene_variant | 1.0 |
| gyrA | 7129 | c.-173T>G | upstream_gene_variant | 1.0 |
| gyrA | 7132 | c.-170T>C | upstream_gene_variant | 1.0 |
| gyrA | 7135 | c.-167G>A | upstream_gene_variant | 1.0 |
| gyrA | 7136 | c.-166T>C | upstream_gene_variant | 1.0 |
| gyrA | 7141 | c.-161T>G | upstream_gene_variant | 1.0 |
| gyrA | 7144 | c.-158A>G | upstream_gene_variant | 1.0 |
| gyrA | 7150 | c.-152G>A | upstream_gene_variant | 1.0 |
| gyrA | 7153 | c.-149G>C | upstream_gene_variant | 1.0 |
| gyrA | 7168 | c.-134C>G | upstream_gene_variant | 1.0 |
| gyrA | 7178 | c.-124T>C | upstream_gene_variant | 1.0 |
| gyrA | 7186 | c.-116C>G | upstream_gene_variant | 1.0 |
| gyrA | 7189 | c.-113C>T | upstream_gene_variant | 1.0 |
| gyrA | 7198 | c.-104C>T | upstream_gene_variant | 1.0 |
| gyrA | 7391 | c.90C>T | synonymous_variant | 1.0 |
| gyrA | 7394 | c.93T>C | synonymous_variant | 1.0 |
| gyrA | 7397 | c.96G>C | synonymous_variant | 1.0 |
| gyrA | 7403 | c.102C>T | synonymous_variant | 1.0 |
| gyrA | 7412 | c.111C>G | synonymous_variant | 1.0 |
| gyrA | 7421 | c.120G>C | synonymous_variant | 1.0 |
| gyrA | 7424 | c.123G>C | synonymous_variant | 1.0 |
| gyrA | 7427 | c.126G>C | synonymous_variant | 1.0 |
| gyrA | 7433 | c.132G>C | synonymous_variant | 1.0 |
| gyrA | 7439 | c.138C>T | synonymous_variant | 1.0 |
| gyrA | 7442 | c.141G>C | synonymous_variant | 1.0 |
| gyrA | 7451 | c.150C>A | synonymous_variant | 1.0 |
| gyrA | 7457 | c.156T>C | synonymous_variant | 1.0 |
| gyrA | 7463 | c.162G>C | synonymous_variant | 1.0 |
| gyrA | 7466 | c.165G>C | synonymous_variant | 1.0 |
| gyrA | 7469 | c.168C>G | synonymous_variant | 1.0 |
| gyrA | 7472 | c.171T>C | synonymous_variant | 1.0 |
| gyrA | 7475 | c.174A>G | synonymous_variant | 1.0 |
| gyrA | 7480 | p.Phe60Tyr | missense_variant | 1.0 |
| gyrA | 7484 | c.183T>C | synonymous_variant | 1.0 |
| gyrA | 7499 | c.198G>C | synonymous_variant | 1.0 |
| gyrA | 7511 | c.210C>T | synonymous_variant | 1.0 |
| gyrA | 8831 | p.Leu510Phe | missense_variant | 1.0 |
| gyrA | 8837 | c.1536C>G | synonymous_variant | 1.0 |
| gyrA | 8846 | c.1545C>T | synonymous_variant | 1.0 |
| gyrA | 8852 | c.1551T>C | synonymous_variant | 1.0 |
| gyrA | 8858 | c.1557T>C | synonymous_variant | 1.0 |
| gyrA | 8870 | c.1569G>C | synonymous_variant | 1.0 |
| gyrA | 8873 | c.1572A>G | synonymous_variant | 1.0 |
| gyrA | 8897 | c.1596T>C | synonymous_variant | 1.0 |
| gyrA | 8903 | c.1602T>C | synonymous_variant | 1.0 |
| gyrA | 8915 | c.1614A>G | synonymous_variant | 1.0 |
| gyrA | 8942 | c.1641G>C | synonymous_variant | 1.0 |
| gyrA | 8945 | c.1644G>C | synonymous_variant | 1.0 |
| gyrA | 8946 | c.1645T>C | synonymous_variant | 1.0 |
| gyrA | 8967 | p.Ala556Lys | missense_variant | 1.0 |
| gyrA | 8978 | c.1677C>T | synonymous_variant | 1.0 |
| gyrA | 8987 | c.1686C>G | synonymous_variant | 1.0 |
| gyrA | 8990 | c.1689C>G | synonymous_variant | 1.0 |
| gyrA | 8993 | c.1692C>T | synonymous_variant | 1.0 |
| gyrA | 8996 | c.1695T>C | synonymous_variant | 1.0 |
| gyrA | 8998 | p.Leu566Trp | missense_variant | 1.0 |
| gyrA | 9018 | p.Gln573Lys | missense_variant | 1.0 |
| gyrA | 9023 | c.1722A>C | synonymous_variant | 1.0 |
| gyrA | 9026 | c.1725G>C | synonymous_variant | 1.0 |
| gyrA | 9029 | c.1728T>C | synonymous_variant | 1.0 |
| gyrA | 9032 | c.1731T>C | synonymous_variant | 1.0 |
| gyrA | 9035 | c.1734G>C | synonymous_variant | 1.0 |
| gyrA | 9044 | c.1743C>G | synonymous_variant | 1.0 |
| gyrA | 9047 | c.1746C>T | synonymous_variant | 1.0 |
| gyrA | 9062 | c.1761C>T | synonymous_variant | 1.0 |
| gyrA | 9063 | p.Ser588Ala | missense_variant | 1.0 |
| gyrA | 9068 | c.1767G>C | synonymous_variant | 1.0 |
| gyrA | 9071 | c.1770G>C | synonymous_variant | 1.0 |
| gyrA | 9080 | c.1779G>C | synonymous_variant | 1.0 |
| gyrA | 9089 | c.1788G>C | synonymous_variant | 1.0 |
| gyrA | 9095 | c.1794C>T | synonymous_variant | 1.0 |
| gyrA | 9099 | c.1798_1800delTTAinsCTG | synonymous_variant | 1.0 |
| fgd1 | 491097 | c.315G>C | synonymous_variant | 1.0 |
| fgd1 | 491112 | c.330G>C | synonymous_variant | 1.0 |
| fgd1 | 491115 | c.333G>C | synonymous_variant | 1.0 |
| fgd1 | 491121 | c.339A>G | synonymous_variant | 1.0 |
| fgd1 | 491137 | p.Glu119Ile | missense_variant | 1.0 |
| fgd1 | 491144 | p.Ala121Glu | missense_variant | 1.0 |
| fgd1 | 491166 | c.384G>T | synonymous_variant | 1.0 |
| fgd1 | 491172 | c.390C>G | synonymous_variant | 1.0 |
| fgd1 | 491184 | c.402A>G | synonymous_variant | 1.0 |
| rpoB | 760130 | p.Asp108Glu | missense_variant | 1.0 |
| rpoB | 760139 | c.333A>G | synonymous_variant | 1.0 |
| rpoB | 760181 | c.375T>C | synonymous_variant | 1.0 |
| rpoB | 760184 | c.378A>G | synonymous_variant | 1.0 |
| rpoB | 760196 | c.390C>G | synonymous_variant | 1.0 |
| rpoB | 760608 | c.802C>T | synonymous_variant | 1.0 |
| rpoB | 760611 | c.805T>C | synonymous_variant | 1.0 |
| rpoB | 760634 | c.828T>C | synonymous_variant | 1.0 |
| rpoB | 760646 | c.840C>G | synonymous_variant | 1.0 |
| rpoB | 760655 | c.849A>G | synonymous_variant | 1.0 |
| rpoB | 760661 | c.855A>G | synonymous_variant | 1.0 |
| rpoB | 760668 | p.Thr288Ala | missense_variant | 1.0 |
| rpoB | 760674 | c.868T>C | synonymous_variant | 1.0 |
| rpoB | 760679 | c.873A>G | synonymous_variant | 1.0 |
| rpoB | 760683 | c.877T>C | synonymous_variant | 1.0 |
| rpoB | 760805 | c.999G>C | synonymous_variant | 1.0 |
| rpoB | 760817 | c.1011A>G | synonymous_variant | 1.0 |
| rpoB | 760820 | c.1014T>C | synonymous_variant | 1.0 |
| rpoB | 760826 | c.1020C>G | synonymous_variant | 1.0 |
| rpoB | 760830 | c.1024T>C | synonymous_variant | 1.0 |
| rpoB | 760841 | c.1035T>C | synonymous_variant | 1.0 |
| rpoB | 760858 | p.Val351Ala | missense_variant | 1.0 |
| rpoB | 760862 | c.1056G>C | synonymous_variant | 1.0 |
| rpoB | 760865 | c.1059C>T | synonymous_variant | 1.0 |
| rpoB | 760886 | p.Glu360Asp | missense_variant | 1.0 |
| rpoB | 760887 | p.Thr361Val | missense_variant | 1.0 |
| rpoB | 760910 | c.1104C>T | synonymous_variant | 1.0 |
| rpoB | 760916 | c.1110C>T | synonymous_variant | 1.0 |
| rpoB | 760928 | c.1122G>C | synonymous_variant | 1.0 |
| rpoB | 760943 | c.1137C>T | synonymous_variant | 1.0 |
| rpoB | 760946 | c.1140A>G | synonymous_variant | 1.0 |
| rpoB | 760965 | p.Met387Leu | missense_variant | 1.0 |
| rpoB | 760970 | c.1164G>C | synonymous_variant | 1.0 |
| rpoB | 760973 | c.1167G>T | synonymous_variant | 1.0 |
| rpoB | 760982 | c.1176G>C | synonymous_variant | 1.0 |
| rpoB | 760985 | c.1179G>C | synonymous_variant | 1.0 |
| rpoB | 760988 | c.1182C>G | synonymous_variant | 1.0 |
| rpoB | 760991 | c.1185G>T | synonymous_variant | 1.0 |
| rpoB | 760997 | c.1191G>C | 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>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 | 761063 | c.1257C>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 | 761573 | c.1767C>G | synonymous_variant | 1.0 |
| rpoB | 761579 | c.1773G>C | synonymous_variant | 1.0 |
| rpoB | 761612 | c.1806G>T | synonymous_variant | 1.0 |
| rpoB | 761636 | c.1830G>T | synonymous_variant | 1.0 |
| rpoB | 761645 | c.1839C>G | synonymous_variant | 1.0 |
| rpoB | 761657 | c.1851C>T | synonymous_variant | 1.0 |
| rpoB | 761666 | c.1860G>C | synonymous_variant | 1.0 |
| rpoB | 761669 | c.1863C>T | synonymous_variant | 1.0 |
| rpoB | 762038 | c.2232C>T | synonymous_variant | 1.0 |
| rpoB | 762047 | c.2241G>A | synonymous_variant | 1.0 |
| rpoB | 762053 | c.2247T>C | synonymous_variant | 1.0 |
| rpoB | 762056 | c.2250G>A | synonymous_variant | 1.0 |
| rpoB | 762065 | c.2259T>G | synonymous_variant | 1.0 |
| rpoB | 762083 | c.2277T>C | synonymous_variant | 1.0 |
| rpoB | 762086 | c.2280G>C | synonymous_variant | 1.0 |
| rpoB | 762101 | c.2295C>G | synonymous_variant | 1.0 |
| rpoB | 762114 | p.Ile770Val | missense_variant | 1.0 |
| rpoB | 762122 | c.2316C>T | synonymous_variant | 1.0 |
| rpoB | 762296 | c.2490G>C | synonymous_variant | 1.0 |
| rpoB | 762317 | c.2511A>G | synonymous_variant | 1.0 |
| rpoB | 762323 | c.2517C>A | synonymous_variant | 1.0 |
| rpoB | 762329 | c.2523G>C | synonymous_variant | 1.0 |
| rpoB | 762338 | c.2532T>C | synonymous_variant | 1.0 |
| rpoB | 762341 | c.2535G>C | synonymous_variant | 1.0 |
| rpoB | 762347 | c.2541T>C | synonymous_variant | 1.0 |
| rpoB | 762350 | c.2544C>G | synonymous_variant | 1.0 |
| rpoB | 762353 | c.2547C>T | synonymous_variant | 1.0 |
| rpoB | 762356 | p.Glu850Asp | missense_variant | 1.0 |
| rpoB | 762362 | p.Glu852Asp | missense_variant | 1.0 |
| rpoB | 762368 | p.Glu854Asp | missense_variant | 1.0 |
| rpoB | 762369 | c.2563T>C | synonymous_variant | 1.0 |
| rpoC | 762374 | c.-996G>T | upstream_gene_variant | 1.0 |
| rpoC | 762380 | c.-990T>C | upstream_gene_variant | 1.0 |
| rpoC | 762383 | c.-987C>G | upstream_gene_variant | 1.0 |
| rpoC | 762386 | c.-984C>T | upstream_gene_variant | 1.0 |
| rpoC | 762392 | c.-978G>C | upstream_gene_variant | 1.0 |
| rpoC | 762395 | c.-975G>T | upstream_gene_variant | 1.0 |
| rpoC | 762398 | c.-972T>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 |
| rpoC | 762449 | c.-921C>A | upstream_gene_variant | 1.0 |
| rpoC | 762452 | c.-918G>C | upstream_gene_variant | 1.0 |
| rpoC | 762470 | c.-900G>C | upstream_gene_variant | 1.0 |
| rpoC | 762488 | c.-882G>C | upstream_gene_variant | 1.0 |
| rpoC | 762491 | c.-879T>C | upstream_gene_variant | 1.0 |
| rpoC | 762509 | c.-861T>G | upstream_gene_variant | 1.0 |
| rpoB | 762510 | p.Ala902Pro | missense_variant | 1.0 |
| rpoC | 762515 | c.-855C>T | upstream_gene_variant | 1.0 |
| rpoC | 762533 | c.-837T>C | upstream_gene_variant | 1.0 |
| rpoC | 762536 | c.-834T>C | upstream_gene_variant | 1.0 |
| rpoC | 762537 | c.-833T>C | upstream_gene_variant | 1.0 |
| rpoC | 762551 | c.-819C>T | upstream_gene_variant | 1.0 |
| rpoC | 762830 | c.-540C>T | upstream_gene_variant | 1.0 |
| rpoC | 762857 | c.-513C>G | upstream_gene_variant | 1.0 |
| rpoC | 762860 | c.-510G>C | upstream_gene_variant | 1.0 |
| rpoC | 762863 | c.-507T>C | upstream_gene_variant | 1.0 |
| rpoC | 762866 | c.-504C>T | upstream_gene_variant | 1.0 |
| rpoB | 762879 | p.Met1025Leu | missense_variant | 1.0 |
| rpoC | 762894 | c.-476C>T | upstream_gene_variant | 1.0 |
| rpoC | 762899 | c.-471G>C | upstream_gene_variant | 1.0 |
| rpoC | 762917 | c.-453C>G | upstream_gene_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 | 762959 | c.-411G>C | upstream_gene_variant | 1.0 |
| rpoC | 762962 | c.-408C>T | upstream_gene_variant | 1.0 |
| rpoC | 762995 | c.-375G>T | upstream_gene_variant | 1.0 |
| rpoC | 763031 | c.-339T>G | upstream_gene_variant | 1.0 |
| rpoC | 763034 | c.-336C>G | upstream_gene_variant | 1.0 |
| rpoC | 763040 | c.-330C>G | upstream_gene_variant | 1.0 |
| rpoC | 763070 | c.-300T>C | upstream_gene_variant | 1.0 |
| rpoC | 763082 | c.-288C>T | upstream_gene_variant | 1.0 |
| rpoC | 763088 | c.-282C>G | upstream_gene_variant | 1.0 |
| rpoC | 763094 | c.-276G>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>T | upstream_gene_variant | 1.0 |
| rpoC | 763145 | c.-225G>A | upstream_gene_variant | 1.0 |
| rpoC | 763157 | c.-213G>T | upstream_gene_variant | 1.0 |
| rpoC | 763166 | c.-204A>G | upstream_gene_variant | 1.0 |
| rpoC | 763172 | c.-198G>C | upstream_gene_variant | 1.0 |
| rpoC | 763193 | c.-177C>G | upstream_gene_variant | 1.0 |
| rpoC | 763202 | c.-168A>G | upstream_gene_variant | 1.0 |
| rpoC | 763205 | c.-165G>C | upstream_gene_variant | 1.0 |
| rpoB | 763207 | p.Ser1134Lys | missense_variant | 1.0 |
| rpoC | 763214 | c.-156T>C | upstream_gene_variant | 1.0 |
| rpoC | 763217 | c.-153G>C | upstream_gene_variant | 1.0 |
| rpoC | 763220 | c.-150G>C | upstream_gene_variant | 1.0 |
| rpoC | 763226 | c.-144A>G | upstream_gene_variant | 1.0 |
| rpoB | 763227 | p.Leu1141Met | missense_variant | 1.0 |
| rpoB | 763235 | p.Glu1143Asp | missense_variant | 1.0 |
| rpoC | 763238 | c.-132T>C | upstream_gene_variant | 1.0 |
| rpoB | 763241 | p.Glu1145Asp | missense_variant | 1.0 |
| rpoC | 763259 | c.-111G>C | upstream_gene_variant | 1.0 |
| rpoC | 763262 | c.-108C>T | upstream_gene_variant | 1.0 |
| rpoC | 763265 | c.-105G>C | upstream_gene_variant | 1.0 |
| rpoC | 763268 | c.-102C>G | upstream_gene_variant | 1.0 |
| rpoC | 763283 | c.-87T>C | upstream_gene_variant | 1.0 |
| rpoC | 763528 | c.159G>A | synonymous_variant | 1.0 |
| rpoC | 763531 | c.162G>T | synonymous_variant | 1.0 |
| rpoC | 763546 | c.177A>G | synonymous_variant | 1.0 |
| rpoC | 763570 | c.201G>C | synonymous_variant | 1.0 |
| rpoC | 763594 | c.225C>T | synonymous_variant | 1.0 |
| rpoC | 763633 | c.264T>C | synonymous_variant | 1.0 |
| rpoC | 763657 | c.288G>A | synonymous_variant | 1.0 |
| rpoC | 763660 | c.291T>G | synonymous_variant | 1.0 |
| rpoC | 763666 | c.297G>C | synonymous_variant | 1.0 |
| rpoC | 763669 | c.300C>G | synonymous_variant | 1.0 |
| rpoC | 763675 | c.306C>G | synonymous_variant | 1.0 |
| rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 1.0 |
| rpoC | 764428 | c.1059G>C | synonymous_variant | 1.0 |
| rpoC | 764431 | c.1062G>C | synonymous_variant | 1.0 |
| rpoC | 764434 | c.1065A>G | synonymous_variant | 1.0 |
| rpoC | 764435 | c.1066_1068delAGGinsCGA | synonymous_variant | 1.0 |
| rpoC | 764458 | c.1089G>C | synonymous_variant | 1.0 |
| rpoC | 764461 | c.1092A>G | synonymous_variant | 1.0 |
| rpoC | 764497 | c.1128A>G | synonymous_variant | 1.0 |
| rpoC | 764510 | c.1141C>T | synonymous_variant | 1.0 |
| rpoC | 764524 | c.1155C>G | synonymous_variant | 1.0 |
| rpoC | 764530 | c.1161C>G | synonymous_variant | 1.0 |
| rpoC | 764534 | c.1165C>A | synonymous_variant | 1.0 |
| rpoC | 764539 | c.1170C>T | synonymous_variant | 1.0 |
| rpoC | 764542 | c.1173C>T | synonymous_variant | 1.0 |
| rpoC | 764545 | c.1176C>A | synonymous_variant | 1.0 |
| rpoC | 764560 | c.1191T>C | synonymous_variant | 1.0 |
| rpoC | 764575 | c.1206T>G | synonymous_variant | 1.0 |
| rpoC | 764611 | c.1242G>T | synonymous_variant | 1.0 |
| rpoC | 764626 | c.1257C>T | synonymous_variant | 1.0 |
| rpoC | 764632 | c.1263T>C | synonymous_variant | 1.0 |
| rpoC | 764650 | c.1281G>T | synonymous_variant | 1.0 |
| rpoC | 764668 | c.1299C>T | synonymous_variant | 1.0 |
| rpoC | 764692 | c.1323C>T | synonymous_variant | 1.0 |
| rpoC | 764713 | c.1344G>T | synonymous_variant | 1.0 |
| rpoC | 764716 | c.1347G>C | synonymous_variant | 1.0 |
| rpoC | 764746 | c.1377G>T | 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 | 764791 | c.1422C>G | synonymous_variant | 1.0 |
| rpoC | 764803 | c.1434C>T | synonymous_variant | 1.0 |
| rpoC | 764809 | c.1440C>T | synonymous_variant | 1.0 |
| rpoC | 764810 | p.Pro481Ala | missense_variant | 1.0 |
| rpoC | 764815 | c.1446A>G | synonymous_variant | 1.0 |
| rpoC | 764824 | c.1455T>C | synonymous_variant | 1.0 |
| rpoC | 764827 | c.1458G>C | synonymous_variant | 1.0 |
| rpoC | 764858 | c.1489T>C | synonymous_variant | 1.0 |
| rpoC | 764869 | c.1500C>T | synonymous_variant | 1.0 |
| rpoC | 764875 | c.1506C>A | synonymous_variant | 1.0 |
| rpoC | 764887 | c.1518G>C | synonymous_variant | 1.0 |
| rpoC | 764888 | c.1519T>C | synonymous_variant | 1.0 |
| rpoC | 764911 | c.1542A>G | synonymous_variant | 1.0 |
| rpoC | 764912 | p.Met515Gln | missense_variant | 1.0 |
| rpoC | 764932 | c.1563C>A | synonymous_variant | 1.0 |
| rpoC | 764948 | c.1579_1581delTTGinsCTC | synonymous_variant | 1.0 |
| rpoC | 764968 | c.1599T>C | synonymous_variant | 1.0 |
| rpoC | 765004 | c.1635G>C | synonymous_variant | 1.0 |
| rpoC | 765403 | c.2034G>C | synonymous_variant | 1.0 |
| rpoC | 765405 | p.Leu679His | missense_variant | 1.0 |
| rpoC | 765409 | c.2040T>G | synonymous_variant | 1.0 |
| rpoC | 765421 | c.2052C>G | synonymous_variant | 1.0 |
| rpoC | 765449 | p.Ala694Ser | missense_variant | 1.0 |
| rpoC | 765875 | p.Val836Ile | missense_variant | 1.0 |
| rpoC | 765907 | c.2538G>T | synonymous_variant | 1.0 |
| rpoC | 765910 | c.2541G>C | synonymous_variant | 1.0 |
| rpoC | 765928 | c.2559C>G | synonymous_variant | 1.0 |
| rpoC | 765940 | c.2571A>T | synonymous_variant | 1.0 |
| rpoC | 765947 | c.2578T>C | synonymous_variant | 1.0 |
| rpoC | 765962 | c.2593_2595delTTGinsCTT | synonymous_variant | 1.0 |
| rpoC | 765967 | c.2598C>T | synonymous_variant | 1.0 |
| rpoC | 765973 | c.2604C>G | synonymous_variant | 1.0 |
| rpoC | 765979 | c.2610C>G | synonymous_variant | 1.0 |
| rpoC | 765982 | c.2613C>T | synonymous_variant | 1.0 |
| rpoC | 765994 | c.2625A>T | synonymous_variant | 1.0 |
| rpoC | 766003 | c.2634G>C | synonymous_variant | 1.0 |
| rpoC | 766009 | c.2640G>C | synonymous_variant | 1.0 |
| rpoC | 766012 | c.2643C>G | synonymous_variant | 1.0 |
| rpoC | 766021 | c.2652G>C | synonymous_variant | 1.0 |
| rpoC | 766570 | c.3201T>C | synonymous_variant | 1.0 |
| rpoC | 766573 | c.3204T>G | synonymous_variant | 1.0 |
| rpoC | 766594 | c.3225G>T | synonymous_variant | 1.0 |
| rpoC | 766607 | p.Ile1080Leu | missense_variant | 1.0 |
| rpoC | 766996 | c.3627C>T | synonymous_variant | 1.0 |
| rpoC | 767002 | c.3633G>C | synonymous_variant | 1.0 |
| rpoC | 767008 | c.3639G>A | synonymous_variant | 1.0 |
| rpoC | 767023 | c.3654C>T | synonymous_variant | 1.0 |
| rpoC | 767044 | c.3675G>C | synonymous_variant | 1.0 |
| rpoC | 767080 | c.3711G>C | synonymous_variant | 1.0 |
| rpoC | 767095 | c.3726C>T | synonymous_variant | 1.0 |
| rpoC | 767098 | c.3729T>C | synonymous_variant | 1.0 |
| rpoC | 767104 | c.3735C>G | synonymous_variant | 1.0 |
| rpoC | 767107 | c.3738C>T | synonymous_variant | 1.0 |
| rpoC | 767119 | c.3750A>G | synonymous_variant | 1.0 |
| rpoC | 767125 | c.3756G>C | synonymous_variant | 1.0 |
| rpsL | 781802 | c.243G>C | synonymous_variant | 0.67 |
| rpsL | 781814 | c.255C>T | synonymous_variant | 0.75 |
| rpsL | 781817 | c.258G>T | synonymous_variant | 0.75 |
| rpsL | 781829 | c.270G>C | synonymous_variant | 0.75 |
| rpsL | 781832 | c.273T>C | synonymous_variant | 0.67 |
| rpsL | 781859 | c.300T>C | synonymous_variant | 1.0 |
| rpsL | 781868 | c.309T>C | synonymous_variant | 1.0 |
| rpsL | 781871 | c.312G>C | synonymous_variant | 1.0 |
| rpsL | 781877 | c.318T>A | 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 |
| rpsL | 781929 | p.Gly124Ser | missense_variant | 1.0 |
| rpsL | 781933 | c.374G>A | splice_region_variant&stop_retained_variant | 1.0 |
| rplC | 800621 | c.-188G>A | upstream_gene_variant | 0.67 |
| rplC | 800633 | c.-176T>C | upstream_gene_variant | 1.0 |
| rplC | 800639 | c.-170C>T | 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 | 800672 | c.-137G>C | upstream_gene_variant | 1.0 |
| rplC | 800690 | c.-119C>T | upstream_gene_variant | 1.0 |
| rplC | 800693 | c.-116A>C | upstream_gene_variant | 1.0 |
| rplC | 800703 | c.-106_-104delTTGinsCTC | 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 | 800735 | c.-74C>G | upstream_gene_variant | 1.0 |
| rplC | 800762 | c.-47T>G | upstream_gene_variant | 1.0 |
| atpE | 1461101 | c.57T>A | synonymous_variant | 1.0 |
| atpE | 1461113 | c.69C>T | synonymous_variant | 1.0 |
| atpE | 1461132 | p.Val30Ile | missense_variant | 1.0 |
| atpE | 1461146 | c.102G>T | synonymous_variant | 1.0 |
| atpE | 1461149 | c.105T>G | synonymous_variant | 1.0 |
| rrs | 1471922 | n.78delT | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471931 | n.87delA | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471934 | n.89A>G | 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 | 1472030 | n.185G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472031 | n.186G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472032 | n.187G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472033 | n.188A>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472035 | n.190G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472040 | n.195T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472041 | n.196C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472042 | n.197T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472043 | n.198T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472050 | n.205G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472061 | n.216A>T | non_coding_transcript_exon_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 | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472380 | n.535G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472846 | n.1001C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472847 | n.1002G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472848 | n.1003T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472860 | n.1015C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472861 | n.1016G>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 | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472978 | n.1133T>C | 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 | 1473082 | n.1237G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473099 | n.1254T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473105 | n.1260G>A | 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 | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.92 |
| rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473129 | n.1284C>T | 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 | 1473288 | n.1443C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473291 | n.1446G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473707 | n.50T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473717 | n.60G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473731 | n.74T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473746 | n.89T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473756 | n.99G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473770 | n.113T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473812 | n.155G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473814 | n.157A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473815 | n.158T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473829 | n.172G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473831 | n.174G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473832 | n.175C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473839 | n.182G>A | 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>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473923 | n.266C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473924 | n.267_268insT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473937 | n.280C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473943 | n.286G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473945 | n.288T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473946 | n.289A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473950 | n.293G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474030 | n.373G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474044 | n.387C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474051 | n.394T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474054 | n.397T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474056 | n.399T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474061 | n.404T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474074 | n.417C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474089 | n.432C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474093 | n.436G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474100 | n.443C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474103 | n.446A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474106 | n.449_450insCT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474109 | n.453_454delAT | 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 | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474181 | n.524_525insT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474184 | n.527C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474185 | n.529delA | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474263 | n.606G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474282 | n.625G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474315 | n.658A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474413 | n.756A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474415 | n.759_781delCACACGCGCATACGCGCGTGTGA | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474507 | n.850G>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 | 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>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474640 | n.983C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474717 | n.1060A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474722 | n.1065T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474743 | n.1086T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474803 | n.1146G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475061 | n.1406delA | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475076 | n.1419C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475120 | n.1463G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475129 | n.1472G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475202 | n.1545G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475209 | n.1552G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475220 | n.1563G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475443 | n.1786G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475475 | n.1818C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475479 | n.1822C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475505 | n.1848G>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 | 1475573 | n.1916G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475659 | n.2002G>A | 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 | 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 | 1475989 | n.2332T>C | 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 | 1476085 | n.2428G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476088 | n.2431A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476103 | n.2446C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476105 | n.2448G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476106 | n.2449A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476114 | n.2457T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476115 | n.2458T>C | 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 | 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 | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476251 | n.2594T>C | 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 | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 1.0 |
| rpsA | 1833547 | c.6G>A | synonymous_variant | 1.0 |
| rpsA | 1833589 | c.48A>C | synonymous_variant | 1.0 |
| rpsA | 1833595 | c.54T>G | synonymous_variant | 1.0 |
| rpsA | 1833596 | p.Ser19Ala | missense_variant | 1.0 |
| rpsA | 1833604 | c.63C>T | synonymous_variant | 1.0 |
| rpsA | 1833616 | c.75A>T | synonymous_variant | 1.0 |
| rpsA | 1833619 | c.78A>C | synonymous_variant | 1.0 |
| rpsA | 1833625 | c.84A>G | synonymous_variant | 1.0 |
| rpsA | 1833664 | c.123C>G | synonymous_variant | 1.0 |
| rpsA | 1833676 | c.135A>G | synonymous_variant | 1.0 |
| rpsA | 1833679 | c.138G>T | synonymous_variant | 1.0 |
| rpsA | 1833685 | c.144G>C | synonymous_variant | 1.0 |
| rpsA | 1833691 | c.150G>A | synonymous_variant | 1.0 |
| rpsA | 1833694 | c.153G>T | synonymous_variant | 1.0 |
| rpsA | 1833697 | c.156C>T | synonymous_variant | 1.0 |
| rpsA | 1833700 | c.159C>T | 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>G | synonymous_variant | 1.0 |
| rpsA | 1833734 | p.Ala65Ser | missense_variant | 1.0 |
| rpsA | 1833742 | c.201A>G | synonymous_variant | 1.0 |
| rpsA | 1833745 | c.204G>C | synonymous_variant | 1.0 |
| rpsA | 1833748 | c.207C>G | synonymous_variant | 1.0 |
| rpsA | 1833760 | c.219C>T | synonymous_variant | 1.0 |
| rpsA | 1833787 | c.246C>G | synonymous_variant | 1.0 |
| rpsA | 1833790 | c.249T>C | synonymous_variant | 1.0 |
| rpsA | 1833802 | c.261A>G | synonymous_variant | 1.0 |
| rpsA | 1833811 | c.270G>T | synonymous_variant | 1.0 |
| rpsA | 1833823 | c.282G>A | 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 | 1833847 | c.306C>G | synonymous_variant | 1.0 |
| rpsA | 1833856 | c.315A>G | synonymous_variant | 1.0 |
| rpsA | 1833862 | c.321G>T | synonymous_variant | 1.0 |
| rpsA | 1833874 | c.333T>G | synonymous_variant | 1.0 |
| rpsA | 1833886 | c.345C>G | synonymous_variant | 1.0 |
| rpsA | 1833894 | p.Ala118Glu | missense_variant | 1.0 |
| rpsA | 1833928 | c.387G>C | synonymous_variant | 1.0 |
| rpsA | 1833949 | c.408T>C | synonymous_variant | 1.0 |
| rpsA | 1833961 | c.420C>G | synonymous_variant | 1.0 |
| rpsA | 1833970 | c.429G>T | synonymous_variant | 1.0 |
| rpsA | 1833979 | c.438T>C | synonymous_variant | 1.0 |
| rpsA | 1833991 | c.450C>G | synonymous_variant | 1.0 |
| rpsA | 1834000 | c.459G>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 | 1834021 | c.480C>T | synonymous_variant | 1.0 |
| rpsA | 1834030 | c.489C>G | synonymous_variant | 1.0 |
| rpsA | 1834033 | c.492C>T | synonymous_variant | 1.0 |
| rpsA | 1834073 | p.Lys178Arg | missense_variant | 1.0 |
| rpsA | 1834228 | c.687C>A | synonymous_variant | 1.0 |
| rpsA | 1834231 | c.690T>G | synonymous_variant | 1.0 |
| rpsA | 1834234 | c.693G>T | synonymous_variant | 1.0 |
| rpsA | 1834240 | c.699T>C | synonymous_variant | 1.0 |
| rpsA | 1834246 | c.705G>T | synonymous_variant | 1.0 |
| rpsA | 1834249 | c.708T>C | synonymous_variant | 1.0 |
| rpsA | 1834252 | c.711C>G | synonymous_variant | 1.0 |
| rpsA | 1834261 | c.720A>G | synonymous_variant | 1.0 |
| rpsA | 1834264 | c.723G>C | synonymous_variant | 1.0 |
| rpsA | 1834279 | c.738C>T | synonymous_variant | 1.0 |
| rpsA | 1834294 | c.753G>T | synonymous_variant | 1.0 |
| rpsA | 1834297 | c.756C>T | synonymous_variant | 1.0 |
| rpsA | 1834303 | c.762T>G | synonymous_variant | 1.0 |
| rpsA | 1834306 | c.765T>C | synonymous_variant | 1.0 |
| rpsA | 1834327 | c.786G>T | synonymous_variant | 1.0 |
| rpsA | 1834357 | c.816T>C | synonymous_variant | 1.0 |
| rpsA | 1834366 | c.825A>G | synonymous_variant | 1.0 |
| rpsA | 1834375 | c.834G>C | synonymous_variant | 1.0 |
| rpsA | 1834396 | c.855G>C | synonymous_variant | 1.0 |
| rpsA | 1834411 | c.870T>G | synonymous_variant | 1.0 |
| rpsA | 1834414 | c.873C>T | synonymous_variant | 1.0 |
| rpsA | 1834417 | c.876G>C | synonymous_variant | 1.0 |
| rpsA | 1834420 | c.879C>T | synonymous_variant | 1.0 |
| rpsA | 1834423 | c.882G>C | synonymous_variant | 1.0 |
| rpsA | 1834429 | c.888C>T | synonymous_variant | 1.0 |
| rpsA | 1834438 | c.897C>T | 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 | 1834477 | c.936C>T | synonymous_variant | 1.0 |
| rpsA | 1834489 | c.948T>C | synonymous_variant | 1.0 |
| rpsA | 1834606 | c.1065C>T | synonymous_variant | 1.0 |
| rpsA | 1834609 | c.1068T>C | synonymous_variant | 1.0 |
| rpsA | 1834619 | c.1078T>C | synonymous_variant | 1.0 |
| rpsA | 1834622 | c.1081_1083delTCGinsAGC | synonymous_variant | 1.0 |
| rpsA | 1834633 | c.1092A>G | synonymous_variant | 1.0 |
| rpsA | 1834639 | c.1098T>C | synonymous_variant | 1.0 |
| rpsA | 1834645 | c.1104C>T | synonymous_variant | 1.0 |
| rpsA | 1834666 | c.1125G>C | synonymous_variant | 1.0 |
| rpsA | 1834667 | p.Ala376Ser | missense_variant | 1.0 |
| rpsA | 1834690 | c.1149T>C | synonymous_variant | 1.0 |
| rpsA | 1834700 | p.Gln387Ala | missense_variant | 1.0 |
| rpsA | 1834705 | c.1164C>G | synonymous_variant | 1.0 |
| rpsA | 1834720 | c.1179C>G | synonymous_variant | 1.0 |
| rpsA | 1834732 | c.1191T>C | synonymous_variant | 1.0 |
| rpsA | 1834738 | c.1197A>G | synonymous_variant | 1.0 |
| rpsA | 1834753 | c.1212T>C | synonymous_variant | 1.0 |
| rpsA | 1834759 | c.1218A>C | synonymous_variant | 1.0 |
| rpsA | 1834765 | p.Glu408Asp | missense_variant | 1.0 |
| rpsA | 1834774 | c.1233C>T | synonymous_variant | 1.0 |
| rpsA | 1834776 | p.Ala412Glu | missense_variant | 1.0 |
| rpsA | 1834780 | c.1239A>G | synonymous_variant | 1.0 |
| rpsA | 1834789 | c.1248T>C | synonymous_variant | 1.0 |
| rpsA | 1834813 | c.1272G>T | synonymous_variant | 1.0 |
| kasA | 2517917 | c.-198G>C | upstream_gene_variant | 1.0 |
| kasA | 2517941 | c.-174C>G | upstream_gene_variant | 1.0 |
| kasA | 2517953 | c.-162C>T | upstream_gene_variant | 1.0 |
| rpoA | 3877542 | c.966C>A | synonymous_variant | 1.0 |
| rpoA | 3877545 | c.963G>T | synonymous_variant | 1.0 |
| rpoA | 3877554 | c.954G>A | synonymous_variant | 1.0 |
| rpoA | 3877560 | c.948C>T | synonymous_variant | 1.0 |
| rpoA | 3877563 | c.945C>T | synonymous_variant | 1.0 |
| rpoA | 3877569 | p.Pro313Thr | missense_variant | 1.0 |
| rpoA | 3877587 | c.921A>G | synonymous_variant | 1.0 |
| rpoA | 3877593 | c.915C>T | synonymous_variant | 1.0 |
| rpoA | 3877614 | c.894G>A | synonymous_variant | 1.0 |
| rpoA | 3877620 | c.888G>A | synonymous_variant | 1.0 |
| rpoA | 3877638 | c.870T>C | synonymous_variant | 1.0 |
| rpoA | 3877656 | c.852T>G | synonymous_variant | 1.0 |
| rpoA | 3877665 | c.843C>G | synonymous_variant | 1.0 |
| rpoA | 3877677 | c.831G>C | synonymous_variant | 1.0 |
| rpoA | 3877680 | c.828G>C | synonymous_variant | 1.0 |
| rpoA | 3877686 | c.822A>G | synonymous_variant | 1.0 |
| rpoA | 3877692 | c.816G>C | synonymous_variant | 1.0 |
| rpoA | 3877704 | c.804G>T | synonymous_variant | 1.0 |
| rpoA | 3877728 | c.780C>G | synonymous_variant | 1.0 |
| rpoA | 3877731 | c.777G>C | synonymous_variant | 1.0 |
| rpoA | 3877734 | c.774G>C | synonymous_variant | 1.0 |
| rpoA | 3877737 | c.771G>C | synonymous_variant | 1.0 |
| rpoA | 3877743 | c.765T>C | synonymous_variant | 1.0 |
| rpoA | 3877749 | c.759C>T | synonymous_variant | 1.0 |
| rpoA | 3877752 | p.Asp252Glu | missense_variant | 1.0 |
| rpoA | 3877755 | c.753C>T | synonymous_variant | 1.0 |
| rpoA | 3877758 | c.750G>C | synonymous_variant | 1.0 |
| rpoA | 3877764 | c.744C>A | synonymous_variant | 1.0 |
| rpoA | 3877770 | c.738A>G | synonymous_variant | 1.0 |
| rpoA | 3877773 | c.735G>C | synonymous_variant | 1.0 |
| rpoA | 3877776 | c.732T>C | synonymous_variant | 1.0 |
| rpoA | 3877782 | c.726T>C | synonymous_variant | 1.0 |
| rpoA | 3877797 | c.711G>A | synonymous_variant | 1.0 |
| rpoA | 3877815 | c.693C>T | synonymous_variant | 1.0 |
| rpoA | 3877818 | c.690A>G | synonymous_variant | 1.0 |
| rpoA | 3877848 | c.660C>T | synonymous_variant | 1.0 |
| rpoA | 3877856 | c.652T>C | synonymous_variant | 1.0 |
| rpoA | 3877875 | c.633T>C | synonymous_variant | 1.0 |
| rpoA | 3877896 | c.612G>A | synonymous_variant | 1.0 |
| rpoA | 3877905 | c.603A>G | synonymous_variant | 1.0 |
| rpoA | 3877908 | c.600T>C | synonymous_variant | 1.0 |
| rpoA | 3877920 | c.588G>C | synonymous_variant | 1.0 |
| rpoA | 3877923 | c.585C>T | synonymous_variant | 1.0 |
| rpoA | 3877929 | p.Ile193Val | 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>T | synonymous_variant | 1.0 |
| rpoA | 3877977 | p.Lys177Asn | missense_variant | 1.0 |
| rpoA | 3877989 | c.519A>G | synonymous_variant | 1.0 |
| rpoA | 3878001 | c.507A>G | synonymous_variant | 1.0 |
| rpoA | 3878019 | c.489A>C | synonymous_variant | 1.0 |
| rpoA | 3878022 | c.486T>C | synonymous_variant | 1.0 |
| rpoA | 3878025 | c.483C>T | synonymous_variant | 1.0 |
| rpoA | 3878028 | c.480G>T | synonymous_variant | 1.0 |
| rpoA | 3878031 | c.477T>C | synonymous_variant | 1.0 |
| rpoA | 3878034 | c.474A>G | synonymous_variant | 1.0 |
| rpoA | 3878046 | c.462T>C | synonymous_variant | 1.0 |
| rpoA | 3878050 | p.Arg153Lys | missense_variant | 1.0 |
| rpoA | 3878055 | c.453A>G | synonymous_variant | 1.0 |
| rpoA | 3878061 | c.447G>C | synonymous_variant | 1.0 |
| rpoA | 3878070 | c.438T>C | synonymous_variant | 1.0 |
| rpoA | 3878073 | c.435C>T | synonymous_variant | 1.0 |
| rpoA | 3878079 | c.429C>T | synonymous_variant | 1.0 |
| rpoA | 3878118 | c.390T>C | synonymous_variant | 1.0 |
| rpoA | 3878130 | c.378C>G | synonymous_variant | 1.0 |
| rpoA | 3878142 | p.Gly122Asp | missense_variant | 1.0 |
| rpoA | 3878160 | c.348C>G | synonymous_variant | 1.0 |
| rpoA | 3878163 | c.345C>T | synonymous_variant | 1.0 |
| rpoA | 3878169 | c.339G>C | synonymous_variant | 1.0 |
| rpoA | 3878184 | c.324C>T | synonymous_variant | 1.0 |
| rpoA | 3878193 | c.315T>C | synonymous_variant | 1.0 |
| rpoA | 3878196 | p.Glu104Ala | missense_variant | 1.0 |
| rpoA | 3878205 | c.303T>C | synonymous_variant | 1.0 |
| rpoA | 3878217 | c.291A>G | synonymous_variant | 1.0 |
| rpoA | 3878259 | c.249G>C | synonymous_variant | 1.0 |
| rpoA | 3878271 | c.237T>C | synonymous_variant | 1.0 |
| rpoA | 3878283 | p.Glu75Asp | missense_variant | 1.0 |
| rpoA | 3878292 | c.216T>C | synonymous_variant | 1.0 |
| rpoA | 3878298 | c.210A>G | synonymous_variant | 1.0 |
| rpoA | 3878301 | c.207C>G | synonymous_variant | 1.0 |
| rpoA | 3878310 | c.198G>T | synonymous_variant | 1.0 |
| rpoA | 3878313 | c.195G>C | synonymous_variant | 1.0 |
| rpoA | 3878322 | c.186A>G | synonymous_variant | 1.0 |
| rpoA | 3878331 | c.177A>G | synonymous_variant | 1.0 |
| rpoA | 3878337 | c.171T>C | synonymous_variant | 1.0 |
| rpoA | 3878343 | c.165C>T | synonymous_variant | 1.0 |
| rpoA | 3878346 | c.162T>C | synonymous_variant | 1.0 |
| rpoA | 3878364 | c.144A>C | synonymous_variant | 1.0 |
| rpoA | 3878367 | c.141C>G | synonymous_variant | 1.0 |
| rpoA | 3878370 | c.138T>C | synonymous_variant | 1.0 |
| rpoA | 3878373 | c.135G>C | synonymous_variant | 1.0 |
| rpoA | 3878381 | c.127C>T | synonymous_variant | 1.0 |
| rpoA | 3878391 | c.117T>G | synonymous_variant | 1.0 |
| rpoA | 3878400 | c.108T>C | synonymous_variant | 1.0 |
| clpC1 | 4038749 | c.1956C>A | synonymous_variant | 1.0 |
| clpC1 | 4038755 | c.1950G>C | synonymous_variant | 1.0 |
| clpC1 | 4038767 | c.1938G>C | synonymous_variant | 1.0 |
| clpC1 | 4038770 | c.1935C>T | synonymous_variant | 1.0 |
| clpC1 | 4038773 | c.1932T>C | synonymous_variant | 1.0 |
| clpC1 | 4038782 | c.1923G>T | synonymous_variant | 1.0 |
| clpC1 | 4038790 | c.1915C>T | synonymous_variant | 1.0 |
| clpC1 | 4038795 | p.Ser637Thr | missense_variant | 1.0 |
| clpC1 | 4038812 | c.1893T>C | synonymous_variant | 1.0 |
| clpC1 | 4038815 | c.1890G>T | synonymous_variant | 1.0 |
| clpC1 | 4038838 | c.1867C>T | synonymous_variant | 1.0 |
| clpC1 | 4038845 | c.1858_1860delTCGinsAGC | synonymous_variant | 1.0 |
| clpC1 | 4038860 | c.1845G>C | synonymous_variant | 1.0 |
| clpC1 | 4038878 | c.1827A>G | synonymous_variant | 1.0 |
| clpC1 | 4039046 | c.1659C>G | synonymous_variant | 1.0 |
| clpC1 | 4039070 | c.1635G>C | synonymous_variant | 1.0 |
| clpC1 | 4039077 | p.Lys543Arg | missense_variant | 1.0 |
| clpC1 | 4039079 | c.1626C>G | synonymous_variant | 1.0 |
| clpC1 | 4039085 | c.1620A>G | synonymous_variant | 1.0 |
| clpC1 | 4039091 | c.1614G>T | synonymous_variant | 1.0 |
| clpC1 | 4039097 | c.1608G>T | synonymous_variant | 1.0 |
| clpC1 | 4039103 | c.1602T>C | synonymous_variant | 1.0 |
| clpC1 | 4039106 | c.1599G>C | synonymous_variant | 1.0 |
| clpC1 | 4039121 | c.1584T>C | synonymous_variant | 1.0 |
| clpC1 | 4039142 | c.1563A>G | synonymous_variant | 1.0 |
| clpC1 | 4039145 | c.1560G>C | synonymous_variant | 1.0 |
| clpC1 | 4039169 | p.Glu512Asp | missense_variant | 1.0 |
| clpC1 | 4039172 | c.1533A>G | synonymous_variant | 1.0 |
| clpC1 | 4039178 | c.1527G>C | synonymous_variant | 1.0 |
| clpC1 | 4039183 | c.1522T>C | synonymous_variant | 1.0 |
| clpC1 | 4039190 | c.1515C>T | synonymous_variant | 1.0 |
| clpC1 | 4039196 | c.1509G>A | synonymous_variant | 1.0 |
| clpC1 | 4039199 | p.Ala502Glu | missense_variant | 1.0 |
| clpC1 | 4039208 | c.1497C>G | synonymous_variant | 1.0 |
| clpC1 | 4039220 | c.1485G>C | synonymous_variant | 1.0 |
| clpC1 | 4039391 | c.1314T>C | synonymous_variant | 0.75 |
| clpC1 | 4039409 | c.1296T>C | synonymous_variant | 0.75 |
| clpC1 | 4039412 | c.1293T>G | synonymous_variant | 0.75 |
| clpC1 | 4039415 | p.Glu430Asp | missense_variant | 0.75 |
| clpC1 | 4039418 | c.1287C>G | synonymous_variant | 0.8 |
| clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.8 |
| clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.83 |
| 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 | 4039478 | c.1227G>C | synonymous_variant | 1.0 |
| clpC1 | 4039481 | c.1224T>C | synonymous_variant | 1.0 |
| clpC1 | 4039487 | c.1218G>C | synonymous_variant | 1.0 |
| clpC1 | 4039522 | c.1183C>T | synonymous_variant | 1.0 |
| clpC1 | 4039528 | c.1177C>A | synonymous_variant | 1.0 |
| clpC1 | 4039541 | c.1164C>G | synonymous_variant | 1.0 |
| clpC1 | 4039544 | c.1161C>T | synonymous_variant | 1.0 |
| clpC1 | 4039559 | c.1146C>G | synonymous_variant | 1.0 |
| clpC1 | 4039565 | c.1140G>T | synonymous_variant | 1.0 |
| clpC1 | 4039649 | c.1056G>C | synonymous_variant | 1.0 |
| clpC1 | 4039661 | c.1044T>C | synonymous_variant | 1.0 |
| clpC1 | 4039682 | c.1023C>G | synonymous_variant | 1.0 |
| clpC1 | 4039694 | c.1011G>C | synonymous_variant | 1.0 |
| clpC1 | 4039724 | c.981A>G | synonymous_variant | 1.0 |
| clpC1 | 4039733 | c.972G>A | synonymous_variant | 1.0 |
| clpC1 | 4039739 | c.966C>G | synonymous_variant | 1.0 |
| clpC1 | 4039742 | c.963C>T | 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 | 4039763 | c.942C>T | synonymous_variant | 1.0 |
| clpC1 | 4039769 | c.936C>G | synonymous_variant | 1.0 |
| clpC1 | 4039778 | c.927A>G | synonymous_variant | 1.0 |
| clpC1 | 4039793 | c.912C>G | synonymous_variant | 1.0 |
| clpC1 | 4039814 | c.891C>G | synonymous_variant | 1.0 |
| clpC1 | 4039817 | c.888A>C | synonymous_variant | 1.0 |
| clpC1 | 4039820 | c.885T>G | synonymous_variant | 1.0 |
| clpC1 | 4039826 | c.879C>G | synonymous_variant | 1.0 |
| clpC1 | 4039831 | c.874T>C | synonymous_variant | 1.0 |
| clpC1 | 4039832 | c.873C>G | synonymous_variant | 1.0 |
| clpC1 | 4039850 | c.855T>C | synonymous_variant | 1.0 |
| clpC1 | 4039868 | c.837C>T | synonymous_variant | 1.0 |
| clpC1 | 4039913 | c.792C>T | synonymous_variant | 1.0 |
| clpC1 | 4039931 | c.774T>C | 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>G | synonymous_variant | 1.0 |
| clpC1 | 4039952 | c.753T>C | synonymous_variant | 1.0 |
| clpC1 | 4039957 | c.748C>T | synonymous_variant | 1.0 |
| clpC1 | 4039958 | c.747G>C | synonymous_variant | 1.0 |
| clpC1 | 4039964 | c.741C>G | synonymous_variant | 1.0 |
| clpC1 | 4039975 | p.Asp244Asn | missense_variant | 1.0 |
| clpC1 | 4039979 | c.726C>G | synonymous_variant | 1.0 |
| clpC1 | 4039982 | c.723G>A | synonymous_variant | 1.0 |
| clpC1 | 4040009 | c.696C>G | synonymous_variant | 1.0 |
| clpC1 | 4040015 | c.690G>C | synonymous_variant | 1.0 |
| clpC1 | 4040021 | c.684A>T | synonymous_variant | 1.0 |
| clpC1 | 4040024 | c.681A>G | synonymous_variant | 1.0 |
| clpC1 | 4040033 | c.672G>C | synonymous_variant | 1.0 |
| clpC1 | 4040048 | c.657C>T | synonymous_variant | 1.0 |
| clpC1 | 4040087 | c.618G>C | synonymous_variant | 1.0 |
| clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 1.0 |
| clpC1 | 4040093 | c.612C>G | synonymous_variant | 1.0 |
| clpC1 | 4040267 | c.438A>G | synonymous_variant | 1.0 |
| clpC1 | 4040276 | c.427_429delTCCinsAGT | synonymous_variant | 1.0 |
| clpC1 | 4040291 | c.414G>C | synonymous_variant | 1.0 |
| clpC1 | 4040300 | c.405C>T | synonymous_variant | 1.0 |
| clpC1 | 4040309 | c.396C>T | synonymous_variant | 1.0 |
| clpC1 | 4040333 | c.372G>C | synonymous_variant | 1.0 |
| clpC1 | 4040342 | c.363C>A | synonymous_variant | 1.0 |
| clpC1 | 4040348 | c.357G>T | synonymous_variant | 1.0 |
| clpC1 | 4040354 | c.351A>G | synonymous_variant | 1.0 |
| clpC1 | 4040357 | c.348T>C | synonymous_variant | 1.0 |
| clpC1 | 4040363 | c.342A>C | synonymous_variant | 1.0 |
| clpC1 | 4040366 | c.339C>T | synonymous_variant | 1.0 |
| clpC1 | 4040369 | c.336C>G | synonymous_variant | 1.0 |
| clpC1 | 4040375 | c.330G>C | synonymous_variant | 1.0 |
| clpC1 | 4040380 | c.325T>C | synonymous_variant | 1.0 |
| clpC1 | 4040381 | c.324T>C | synonymous_variant | 1.0 |
| clpC1 | 4040387 | c.318A>G | synonymous_variant | 1.0 |
| clpC1 | 4040393 | c.312G>C | synonymous_variant | 1.0 |
| clpC1 | 4040480 | c.225T>C | synonymous_variant | 1.0 |
| clpC1 | 4040495 | c.210C>T | synonymous_variant | 1.0 |
| clpC1 | 4040522 | c.183T>C | synonymous_variant | 1.0 |
| clpC1 | 4040531 | c.174T>G | synonymous_variant | 1.0 |
| clpC1 | 4040546 | c.159G>C | synonymous_variant | 1.0 |
| clpC1 | 4040558 | c.147G>C | synonymous_variant | 1.0 |
| clpC1 | 4040561 | c.144A>G | synonymous_variant | 1.0 |
| clpC1 | 4040573 | c.132T>C | synonymous_variant | 1.0 |
| clpC1 | 4040579 | c.126A>G | synonymous_variant | 1.0 |
| clpC1 | 4040582 | c.123G>C | synonymous_variant | 1.0 |
| clpC1 | 4040585 | c.120A>G | synonymous_variant | 1.0 |
| clpC1 | 4040597 | c.108C>T | synonymous_variant | 1.0 |
| clpC1 | 4040600 | c.103_105delTTAinsCTG | synonymous_variant | 1.0 |
| clpC1 | 4040603 | c.102T>G | synonymous_variant | 1.0 |
| clpC1 | 4040606 | c.99T>C | synonymous_variant | 1.0 |
| panD | 4044138 | c.144T>C | synonymous_variant | 1.0 |
| panD | 4044150 | c.132A>C | synonymous_variant | 1.0 |
| panD | 4044156 | c.126A>G | synonymous_variant | 1.0 |
| panD | 4044167 | c.115C>T | synonymous_variant | 1.0 |
| panD | 4044171 | c.111C>T | synonymous_variant | 1.0 |
| panD | 4044174 | c.108C>T | synonymous_variant | 1.0 |
| panD | 4044180 | p.Asp34Glu | missense_variant | 1.0 |
| panD | 4044186 | c.94_96delTTGinsCTC | synonymous_variant | 1.0 |
| panD | 4044189 | c.93C>T | synonymous_variant | 1.0 |
| panD | 4044194 | p.Ala30Pro | missense_variant | 1.0 |
| panD | 4044195 | c.87T>C | synonymous_variant | 1.0 |
| panD | 4044219 | c.63C>T | synonymous_variant | 1.0 |
| panD | 4044232 | p.Cys17His | missense_variant | 1.0 |
| panD | 4044234 | c.48C>G | synonymous_variant | 1.0 |
| panD | 4044249 | c.33C>T | synonymous_variant | 1.0 |
