Run ID: SRR1175052
Sample name:
Date: 03-04-2023 03:36:51
Number of reads: 138175
Percentage reads mapped: 5.75
Strain: lineage4.9
Drug-resistance: HR-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 |
|---|---|---|---|---|---|
| katG | 2155694 | p.Ser140Gly | missense_variant | 1.0 | isoniazid |
| Gene | Chromosome position | Mutation | Type | Estimated fraction |
|---|---|---|---|---|
| gyrB | 6115 | c.876A>G | synonymous_variant | 1.0 |
| gyrB | 6122 | p.Ala295Asn | missense_variant | 1.0 |
| gyrB | 6127 | c.888G>C | synonymous_variant | 1.0 |
| gyrB | 6130 | c.891T>C | synonymous_variant | 1.0 |
| gyrB | 6133 | c.894G>C | synonymous_variant | 1.0 |
| gyrB | 6169 | c.930C>G | synonymous_variant | 1.0 |
| gyrB | 6190 | c.951A>G | synonymous_variant | 1.0 |
| gyrB | 6193 | c.954G>A | synonymous_variant | 1.0 |
| gyrB | 6196 | c.957C>T | synonymous_variant | 1.0 |
| gyrB | 6749 | p.Ala504Ser | missense_variant | 1.0 |
| gyrA | 6760 | c.-542G>C | upstream_gene_variant | 1.0 |
| gyrB | 6764 | p.Leu509Phe | missense_variant | 1.0 |
| gyrA | 6769 | c.-533C>T | 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 | 6794 | p.Ile519Leu | missense_variant | 1.0 |
| gyrB | 6798 | p.Gly520Ala | missense_variant | 1.0 |
| gyrA | 6803 | c.-499C>T | upstream_gene_variant | 1.0 |
| gyrA | 6841 | c.-461T>C | upstream_gene_variant | 1.0 |
| gyrA | 6844 | c.-458T>C | upstream_gene_variant | 1.0 |
| gyrA | 7171 | c.-131C>G | upstream_gene_variant | 1.0 |
| gyrA | 7178 | c.-124T>C | upstream_gene_variant | 1.0 |
| gyrA | 7198 | c.-104C>G | upstream_gene_variant | 1.0 |
| gyrB | 7209 | p.Asp657Ala | missense_variant | 1.0 |
| gyrA | 7213 | c.-89G>C | upstream_gene_variant | 1.0 |
| gyrA | 7216 | c.-86G>T | upstream_gene_variant | 1.0 |
| gyrB | 7220 | p.Ser661Gly | missense_variant | 1.0 |
| gyrA | 7225 | c.-77T>C | upstream_gene_variant | 1.0 |
| gyrB | 7229 | p.Thr664Ala | missense_variant | 1.0 |
| gyrA | 7841 | c.540C>T | synonymous_variant | 1.0 |
| gyrA | 7859 | c.558A>C | synonymous_variant | 1.0 |
| gyrA | 7865 | c.564T>C | synonymous_variant | 1.0 |
| gyrA | 7884 | p.Arg195Asn | missense_variant | 1.0 |
| gyrA | 7890 | p.Leu197Val | missense_variant | 1.0 |
| gyrA | 7901 | c.600G>C | synonymous_variant | 1.0 |
| gyrA | 7904 | c.603G>C | synonymous_variant | 1.0 |
| gyrA | 7924 | p.His208Pro | missense_variant | 1.0 |
| gyrA | 7928 | c.627C>T | synonymous_variant | 1.0 |
| gyrA | 7937 | p.Glu212Asp | missense_variant | 1.0 |
| gyrA | 8792 | c.1491G>C | synonymous_variant | 1.0 |
| gyrA | 8807 | p.Asp502Glu | missense_variant | 1.0 |
| gyrA | 8810 | c.1509A>C | synonymous_variant | 1.0 |
| gyrA | 8816 | c.1515C>G | synonymous_variant | 1.0 |
| gyrA | 8818 | p.Ser506Asn | missense_variant | 1.0 |
| gyrA | 8829 | c.1528_1530delTTGinsCTC | synonymous_variant | 1.0 |
| gyrA | 8837 | c.1536C>G | synonymous_variant | 1.0 |
| gyrA | 8849 | c.1548C>G | synonymous_variant | 1.0 |
| gyrA | 8852 | c.1551T>C | synonymous_variant | 1.0 |
| gyrA | 8858 | c.1557T>G | synonymous_variant | 1.0 |
| gyrA | 8867 | c.1566A>G | synonymous_variant | 1.0 |
| gyrA | 8870 | c.1569G>C | synonymous_variant | 1.0 |
| gyrA | 8873 | c.1572A>C | synonymous_variant | 1.0 |
| gyrA | 8897 | c.1596T>C | synonymous_variant | 1.0 |
| gyrA | 8900 | c.1599G>C | synonymous_variant | 1.0 |
| gyrA | 8903 | c.1602T>C | synonymous_variant | 1.0 |
| gyrA | 8915 | c.1614A>G | synonymous_variant | 1.0 |
| gyrA | 8930 | c.1629C>T | synonymous_variant | 1.0 |
| gyrA | 8939 | c.1638T>C | synonymous_variant | 1.0 |
| gyrA | 8942 | c.1641G>C | synonymous_variant | 1.0 |
| gyrA | 8945 | c.1644G>T | synonymous_variant | 1.0 |
| gyrA | 8946 | c.1645T>C | synonymous_variant | 1.0 |
| gyrA | 8969 | c.1668G>C | synonymous_variant | 1.0 |
| rpoB | 760130 | p.Asp108Glu | missense_variant | 1.0 |
| rpoB | 760139 | c.333A>C | synonymous_variant | 1.0 |
| rpoB | 760140 | p.Pro112Ser | missense_variant | 1.0 |
| rpoB | 760143 | p.Val113Ile | missense_variant | 1.0 |
| rpoB | 760157 | c.351A>G | synonymous_variant | 1.0 |
| rpoB | 760172 | c.366G>C | synonymous_variant | 1.0 |
| rpoB | 760176 | p.Ala124Ser | missense_variant | 1.0 |
| rpoB | 760181 | c.375T>G | synonymous_variant | 1.0 |
| rpoB | 760184 | c.378A>G | synonymous_variant | 1.0 |
| rpoB | 760223 | c.417T>C | synonymous_variant | 1.0 |
| rpoB | 760233 | c.427_429delAGTinsTCG | synonymous_variant | 1.0 |
| rpoB | 760253 | c.447T>C | synonymous_variant | 1.0 |
| rpoB | 760256 | p.Asp150Glu | missense_variant | 1.0 |
| rpoB | 760274 | p.Glu156Asp | missense_variant | 1.0 |
| rpoB | 760282 | p.Thr159Ser | missense_variant | 1.0 |
| rpoB | 760298 | c.492G>C | synonymous_variant | 1.0 |
| rpoB | 760307 | c.501T>C | synonymous_variant | 1.0 |
| rpoB | 760310 | c.504G>C | synonymous_variant | 1.0 |
| rpoB | 760313 | c.507G>C | synonymous_variant | 1.0 |
| rpoB | 760325 | c.519G>C | synonymous_variant | 1.0 |
| rpoB | 760328 | c.522G>C | synonymous_variant | 1.0 |
| rpoB | 760340 | c.534_535insC | frameshift_variant | 1.0 |
| rpoB | 760361 | c.555T>C | synonymous_variant | 1.0 |
| rpoB | 760368 | p.Ser188Ala | missense_variant | 1.0 |
| rpoB | 760376 | p.Asp190Glu | missense_variant | 1.0 |
| rpoB | 760382 | c.576G>C | synonymous_variant | 1.0 |
| rpoB | 760388 | c.582C>T | synonymous_variant | 1.0 |
| rpoB | 760389 | p.Ser195Ala | missense_variant | 1.0 |
| rpoB | 760415 | c.609C>T | synonymous_variant | 1.0 |
| rpoB | 760430 | c.624T>C | synonymous_variant | 1.0 |
| rpoB | 760434 | p.Val210Ile | missense_variant | 1.0 |
| rpoB | 760460 | c.654G>C | synonymous_variant | 1.0 |
| rpoB | 760475 | c.669A>G | synonymous_variant | 1.0 |
| rpoB | 760481 | c.675G>C | synonymous_variant | 1.0 |
| rpoB | 760484 | c.678A>G | synonymous_variant | 1.0 |
| rpoB | 760502 | c.696C>G | synonymous_variant | 1.0 |
| rpoB | 760503 | p.Lys233Gln | missense_variant | 1.0 |
| rpoB | 760508 | c.702G>C | synonymous_variant | 1.0 |
| rpoB | 760511 | c.705G>C | synonymous_variant | 1.0 |
| rpoB | 760515 | p.Trp237Val | missense_variant | 1.0 |
| rpoB | 760521 | p.Ser239Arg | missense_variant | 1.0 |
| rpoB | 760527 | p.Gln241Glu | missense_variant | 1.0 |
| rpoB | 760532 | c.726T>C | synonymous_variant | 1.0 |
| rpoB | 760534 | p.Val243Ala | missense_variant | 1.0 |
| rpoB | 760547 | c.741G>T | synonymous_variant | 1.0 |
| rpoB | 760616 | p.Asp270Glu | missense_variant | 1.0 |
| rpoB | 760617 | p.Ile271Val | missense_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>C | synonymous_variant | 1.0 |
| rpoB | 760664 | c.858G>C | synonymous_variant | 1.0 |
| rpoB | 760665 | p.Gln287Glu | missense_variant | 1.0 |
| rpoB | 760669 | p.Thr288Ser | missense_variant | 1.0 |
| rpoB | 760673 | c.867G>C | synonymous_variant | 1.0 |
| rpoB | 760674 | c.868T>C | synonymous_variant | 1.0 |
| rpoB | 760679 | c.873A>G | synonymous_variant | 1.0 |
| rpoB | 760683 | p.Leu293Met | missense_variant | 1.0 |
| rpoB | 760712 | c.906G>C | synonymous_variant | 1.0 |
| rpoB | 760889 | c.1083C>T | synonymous_variant | 1.0 |
| rpoB | 760916 | c.1110C>T | synonymous_variant | 0.9 |
| rpoB | 760925 | c.1119T>C | synonymous_variant | 0.92 |
| rpoB | 760928 | c.1122G>C | synonymous_variant | 0.92 |
| rpoB | 760946 | c.1140A>G | synonymous_variant | 0.96 |
| rpoB | 760959 | p.Val385Leu | missense_variant | 1.0 |
| rpoB | 760964 | c.1158C>T | synonymous_variant | 1.0 |
| rpoB | 760965 | p.Met387Leu | missense_variant | 1.0 |
| rpoB | 760982 | c.1176G>C | synonymous_variant | 1.0 |
| rpoB | 760991 | c.1185G>T | synonymous_variant | 1.0 |
| rpoB | 761014 | p.Val403Ala | missense_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 | 761057 | c.1251G>C | synonymous_variant | 1.0 |
| rpoB | 761060 | c.1254C>G | synonymous_variant | 1.0 |
| rpoB | 761063 | c.1257C>G | synonymous_variant | 1.0 |
| rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 1.0 |
| rpoB | 761102 | c.1296A>G | synonymous_variant | 1.0 |
| rpoB | 761132 | c.1326G>T | synonymous_variant | 0.96 |
| rpoB | 761133 | c.1327T>C | synonymous_variant | 1.0 |
| rpoB | 761150 | c.1344A>C | synonymous_variant | 1.0 |
| rpoB | 761165 | c.1359G>C | synonymous_variant | 0.96 |
| rpoB | 761168 | c.1362C>G | synonymous_variant | 0.96 |
| rpoB | 761178 | c.1372_1374delTCAinsAGC | synonymous_variant | 1.0 |
| rpoB | 761189 | c.1383T>C | synonymous_variant | 1.0 |
| rpoB | 761195 | c.1389G>C | synonymous_variant | 1.0 |
| rpoB | 761198 | c.1392G>C | synonymous_variant | 1.0 |
| rpoB | 761204 | c.1398C>G | synonymous_variant | 1.0 |
| rpoB | 761234 | c.1428G>C | synonymous_variant | 1.0 |
| rpoB | 761243 | c.1437G>C | synonymous_variant | 1.0 |
| rpoB | 761249 | c.1443A>G | synonymous_variant | 1.0 |
| rpoB | 761255 | c.1449T>G | synonymous_variant | 1.0 |
| rpoB | 761258 | c.1452G>A | synonymous_variant | 1.0 |
| rpoB | 761261 | c.1455G>C | synonymous_variant | 0.96 |
| rpoB | 761264 | c.1458C>G | synonymous_variant | 1.0 |
| rpoB | 761273 | c.1467T>C | synonymous_variant | 1.0 |
| rpoB | 761282 | c.1476C>T | synonymous_variant | 1.0 |
| rpoB | 761285 | c.1479G>A | synonymous_variant | 1.0 |
| rpoB | 761288 | c.1482G>C | synonymous_variant | 1.0 |
| rpoB | 761300 | c.1494G>A | synonymous_variant | 1.0 |
| rpoB | 761303 | c.1497G>C | synonymous_variant | 1.0 |
| rpoB | 761318 | c.1512G>C | synonymous_variant | 1.0 |
| rpoB | 761327 | c.1521A>G | synonymous_variant | 1.0 |
| rpoB | 761348 | c.1542C>G | synonymous_variant | 1.0 |
| rpoB | 761355 | p.Val517Lys | missense_variant | 1.0 |
| rpoB | 761360 | c.1554T>C | synonymous_variant | 1.0 |
| rpoB | 761362 | p.Ser519Thr | missense_variant | 1.0 |
| rpoB | 761367 | p.Glu521Gln | missense_variant | 1.0 |
| rpoB | 761374 | p.Val523Glu | missense_variant | 1.0 |
| rpoB | 761379 | p.Leu525Met | missense_variant | 1.0 |
| rpoB | 761403 | p.His533Tyr | missense_variant | 1.0 |
| rpoB | 761525 | p.Met573Ile | missense_variant | 1.0 |
| rpoB | 761534 | c.1728G>A | synonymous_variant | 1.0 |
| rpoB | 761537 | c.1731C>G | synonymous_variant | 1.0 |
| rpoB | 761555 | c.1749G>C | synonymous_variant | 1.0 |
| rpoB | 761558 | c.1752C>G | synonymous_variant | 1.0 |
| rpoB | 761570 | c.1764T>C | synonymous_variant | 1.0 |
| rpoB | 761573 | c.1767C>G | synonymous_variant | 1.0 |
| rpoB | 761594 | c.1788C>G | synonymous_variant | 1.0 |
| rpoB | 761600 | c.1794T>C | synonymous_variant | 1.0 |
| rpoB | 761603 | c.1797C>G | synonymous_variant | 1.0 |
| rpoB | 761606 | c.1800C>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 | 761649 | c.1843_1844delAGinsTC | synonymous_variant | 1.0 |
| rpoB | 761655 | p.Ala617Ser | missense_variant | 1.0 |
| rpoB | 761666 | c.1860G>C | synonymous_variant | 1.0 |
| rpoB | 761675 | c.1869G>C | synonymous_variant | 1.0 |
| rpoB | 761873 | c.2067A>G | synonymous_variant | 1.0 |
| rpoB | 761892 | p.Ile696Leu | missense_variant | 1.0 |
| rpoB | 761906 | c.2100C>G | synonymous_variant | 1.0 |
| rpoB | 761909 | c.2103T>C | synonymous_variant | 1.0 |
| rpoB | 761912 | c.2106T>C | synonymous_variant | 1.0 |
| rpoB | 761915 | c.2109C>T | synonymous_variant | 1.0 |
| rpoB | 761916 | p.Asp704Gln | missense_variant | 1.0 |
| rpoB | 761948 | c.2142G>C | synonymous_variant | 0.95 |
| rpoB | 761954 | c.2148C>G | synonymous_variant | 0.95 |
| rpoB | 761972 | c.2166C>T | synonymous_variant | 0.93 |
| rpoB | 762026 | c.2220G>C | synonymous_variant | 1.0 |
| rpoB | 762051 | p.His749Tyr | missense_variant | 1.0 |
| rpoB | 762065 | c.2259T>C | 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 | 762131 | c.2325C>G | synonymous_variant | 1.0 |
| rpoB | 762137 | c.2331C>T | synonymous_variant | 1.0 |
| rpoB | 762140 | c.2334G>C | synonymous_variant | 1.0 |
| rpoB | 762143 | c.2337T>C | synonymous_variant | 1.0 |
| rpoB | 762149 | c.2343G>C | synonymous_variant | 1.0 |
| rpoB | 762158 | c.2352G>C | synonymous_variant | 1.0 |
| rpoB | 762167 | c.2361T>C | synonymous_variant | 1.0 |
| rpoB | 762176 | c.2370T>C | synonymous_variant | 0.97 |
| rpoB | 762185 | c.2379G>C | synonymous_variant | 0.97 |
| rpoB | 762209 | c.2403C>G | synonymous_variant | 1.0 |
| rpoB | 762218 | c.2412T>C | synonymous_variant | 1.0 |
| rpoB | 762233 | c.2427G>C | synonymous_variant | 1.0 |
| rpoB | 762251 | c.2445G>C | synonymous_variant | 1.0 |
| rpoB | 762254 | c.2448T>C | synonymous_variant | 1.0 |
| rpoB | 762257 | c.2451C>G | synonymous_variant | 1.0 |
| rpoB | 762266 | c.2460T>C | synonymous_variant | 1.0 |
| rpoB | 762275 | c.2469C>G | synonymous_variant | 1.0 |
| rpoB | 762293 | c.2487T>C | synonymous_variant | 1.0 |
| rpoB | 762314 | c.2508C>T | synonymous_variant | 1.0 |
| rpoB | 762317 | c.2511A>G | synonymous_variant | 1.0 |
| rpoB | 762318 | p.Ser838Thr | missense_variant | 1.0 |
| rpoC | 762452 | c.-918G>C | upstream_gene_variant | 1.0 |
| rpoC | 762470 | c.-900G>C | upstream_gene_variant | 1.0 |
| rpoC | 762485 | c.-885G>T | upstream_gene_variant | 1.0 |
| rpoB | 762489 | p.Val895Gln | missense_variant | 1.0 |
| rpoC | 762509 | c.-861T>G | upstream_gene_variant | 1.0 |
| rpoB | 762510 | p.Ala902Pro | missense_variant | 1.0 |
| rpoC | 762527 | c.-843G>C | 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 | 762812 | c.-558C>G | upstream_gene_variant | 1.0 |
| rpoB | 762814 | p.Met1003Thr | missense_variant | 1.0 |
| rpoC | 762818 | c.-552C>G | upstream_gene_variant | 1.0 |
| rpoC | 762827 | c.-543G>C | upstream_gene_variant | 1.0 |
| rpoC | 762831 | c.-539_-538delAGinsTC | upstream_gene_variant | 1.0 |
| rpoB | 762858 | p.Thr1018Ser | missense_variant | 1.0 |
| rpoC | 762863 | c.-507T>C | upstream_gene_variant | 1.0 |
| rpoB | 762881 | p.Met1025Ile | missense_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>A | upstream_gene_variant | 1.0 |
| rpoC | 762959 | c.-411G>C | upstream_gene_variant | 1.0 |
| rpoC | 762971 | c.-399G>C | upstream_gene_variant | 1.0 |
| rpoC | 762980 | c.-390T>C | upstream_gene_variant | 1.0 |
| rpoC | 762989 | c.-381G>T | upstream_gene_variant | 1.0 |
| rpoC | 762995 | c.-375G>T | upstream_gene_variant | 1.0 |
| rpoC | 763013 | c.-357C>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 | 763067 | c.-303C>G | upstream_gene_variant | 1.0 |
| rpoC | 763070 | c.-300T>C | upstream_gene_variant | 1.0 |
| rpoB | 763074 | p.Thr1090Val | missense_variant | 1.0 |
| rpoC | 763085 | c.-285C>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 | 763139 | c.-231C>T | upstream_gene_variant | 1.0 |
| rpoC | 763148 | c.-222G>C | upstream_gene_variant | 1.0 |
| rpoC | 763160 | c.-210G>T | upstream_gene_variant | 1.0 |
| rpoC | 763166 | c.-204A>G | upstream_gene_variant | 1.0 |
| rpoC | 763169 | c.-201A>G | upstream_gene_variant | 1.0 |
| rpoC | 763172 | c.-198G>C | upstream_gene_variant | 1.0 |
| rpoC | 763181 | c.-189G>C | upstream_gene_variant | 1.0 |
| rpoC | 763187 | c.-183C>G | upstream_gene_variant | 1.0 |
| rpoC | 763193 | c.-177C>G | upstream_gene_variant | 0.8 |
| rpoC | 763202 | c.-168A>C | upstream_gene_variant | 0.67 |
| rpoC | 763441 | c.72C>G | synonymous_variant | 1.0 |
| rpoC | 763444 | c.75T>C | synonymous_variant | 1.0 |
| rpoC | 763456 | c.87A>G | synonymous_variant | 1.0 |
| rpoC | 763468 | c.99G>C | synonymous_variant | 1.0 |
| rpoC | 763486 | c.117T>G | synonymous_variant | 1.0 |
| rpoC | 763528 | c.159G>A | synonymous_variant | 1.0 |
| rpoC | 763546 | c.177A>G | synonymous_variant | 0.98 |
| rpoC | 763570 | c.201G>C | synonymous_variant | 0.99 |
| rpoC | 763619 | p.Arg84Lys | missense_variant | 1.0 |
| rpoC | 763633 | c.264T>C | 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 | 763669 | c.300C>G | synonymous_variant | 1.0 |
| rpoC | 763687 | c.318C>T | synonymous_variant | 1.0 |
| rpoC | 763703 | c.334_336delTCGinsAGC | synonymous_variant | 1.0 |
| rpoC | 763711 | c.342G>C | synonymous_variant | 1.0 |
| rpoC | 763714 | c.345G>C | synonymous_variant | 1.0 |
| rpoC | 763717 | c.348T>C | synonymous_variant | 1.0 |
| rpoC | 763723 | c.354G>C | synonymous_variant | 1.0 |
| rpoC | 763732 | c.363C>G | synonymous_variant | 1.0 |
| rpoC | 763741 | c.372C>T | synonymous_variant | 1.0 |
| rpoC | 763744 | c.375G>C | synonymous_variant | 1.0 |
| rpoC | 763765 | c.396T>C | synonymous_variant | 1.0 |
| rpoC | 764320 | c.951C>G | synonymous_variant | 1.0 |
| rpoC | 764344 | c.975C>T | synonymous_variant | 1.0 |
| rpoC | 764353 | c.984G>T | synonymous_variant | 1.0 |
| rpoC | 764371 | c.1002G>T | synonymous_variant | 1.0 |
| rpoC | 764380 | c.1011G>C | synonymous_variant | 1.0 |
| rpoC | 764383 | c.1014C>G | synonymous_variant | 1.0 |
| rpoC | 764387 | c.1018T>C | synonymous_variant | 1.0 |
| rpoC | 764396 | c.1027C>T | synonymous_variant | 1.0 |
| rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.95 |
| rpoC | 764410 | c.1041G>C | 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 | 764446 | c.1077T>C | synonymous_variant | 1.0 |
| rpoC | 764452 | c.1083T>A | 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 | 764500 | c.1131C>G | synonymous_variant | 1.0 |
| rpoC | 764506 | c.1137C>T | synonymous_variant | 1.0 |
| rpoC | 764521 | c.1152T>C | synonymous_variant | 1.0 |
| rpoC | 764527 | c.1158C>T | synonymous_variant | 1.0 |
| rpoC | 764536 | c.1167G>T | synonymous_variant | 1.0 |
| rpoC | 764539 | c.1170C>G | synonymous_variant | 1.0 |
| rpoC | 764544 | p.Thr392Asn | missense_variant | 1.0 |
| rpoC | 764548 | c.1179G>C | synonymous_variant | 1.0 |
| rpoC | 764566 | c.1197C>G | synonymous_variant | 1.0 |
| rpoC | 764575 | c.1206T>G | synonymous_variant | 1.0 |
| rpoC | 764576 | c.1207_1208delTCinsAG | synonymous_variant | 1.0 |
| rpoC | 764611 | c.1242G>C | synonymous_variant | 1.0 |
| rpoC | 764632 | c.1263T>C | synonymous_variant | 1.0 |
| rpoC | 764650 | c.1281G>C | synonymous_variant | 1.0 |
| rpoC | 764656 | c.1287C>G | synonymous_variant | 1.0 |
| rpoC | 764662 | c.1293G>C | synonymous_variant | 1.0 |
| rpoC | 764701 | c.1332C>G | 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 | 764763 | p.His465Leu | missense_variant | 1.0 |
| rpoC | 764780 | c.1411_1413delAGCinsTCG | synonymous_variant | 1.0 |
| rpoC | 764797 | c.1428G>C | synonymous_variant | 1.0 |
| rpoC | 764803 | c.1434C>T | synonymous_variant | 1.0 |
| rpoC | 764812 | c.1443C>G | synonymous_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 | 764830 | c.1461C>G | synonymous_variant | 1.0 |
| rpoC | 764857 | c.1488G>T | synonymous_variant | 1.0 |
| rpoC | 764858 | c.1489T>C | synonymous_variant | 1.0 |
| rpoC | 764869 | c.1500C>T | synonymous_variant | 1.0 |
| rpoC | 764872 | c.1503A>G | synonymous_variant | 1.0 |
| rpoC | 764875 | c.1506C>G | synonymous_variant | 1.0 |
| rpoC | 764878 | c.1509C>G | synonymous_variant | 0.95 |
| rpoC | 764887 | c.1518G>C | synonymous_variant | 1.0 |
| rpoC | 764888 | c.1519T>C | synonymous_variant | 1.0 |
| rpoC | 764893 | c.1524T>C | synonymous_variant | 1.0 |
| rpoC | 764911 | c.1542A>G | synonymous_variant | 1.0 |
| rpoC | 764912 | p.Met515Gln | missense_variant | 1.0 |
| rpoC | 764923 | c.1554A>G | synonymous_variant | 1.0 |
| rpoC | 764935 | c.1566T>C | synonymous_variant | 0.96 |
| rpoC | 764948 | c.1579T>C | synonymous_variant | 1.0 |
| rpoC | 764962 | c.1593G>T | synonymous_variant | 1.0 |
| rpoC | 764983 | c.1614T>C | synonymous_variant | 1.0 |
| rpoC | 764995 | c.1626C>T | synonymous_variant | 1.0 |
| rpoC | 765395 | c.2026C>T | synonymous_variant | 1.0 |
| rpoC | 765405 | p.Leu679Pro | missense_variant | 1.0 |
| rpoC | 765408 | p.Gly680Asp | missense_variant | 1.0 |
| rpoC | 765412 | c.2043T>C | synonymous_variant | 1.0 |
| rpoC | 765425 | p.Lys686Glu | missense_variant | 1.0 |
| rpoC | 765435 | p.His689Pro | missense_variant | 1.0 |
| rpoC | 765443 | p.Val692Arg | missense_variant | 1.0 |
| rpoC | 765453 | p.Ala695Val | missense_variant | 1.0 |
| rpoC | 765466 | c.2097C>T | synonymous_variant | 0.97 |
| rpoC | 765493 | c.2124G>C | synonymous_variant | 0.96 |
| rpoC | 765499 | c.2130C>G | synonymous_variant | 0.96 |
| rpoC | 765508 | c.2139C>G | synonymous_variant | 0.96 |
| rpoC | 765525 | p.Ala719Val | missense_variant | 0.8 |
| rpoC | 765541 | c.2172C>G | synonymous_variant | 0.75 |
| rpoC | 765835 | c.2466C>T | synonymous_variant | 1.0 |
| rpoC | 765856 | c.2487T>C | synonymous_variant | 1.0 |
| rpoC | 765875 | p.Val836Ile | missense_variant | 1.0 |
| rpoC | 765886 | c.2517C>G | synonymous_variant | 1.0 |
| rpoC | 765892 | c.2523T>C | synonymous_variant | 1.0 |
| rpoC | 765904 | c.2535C>G | synonymous_variant | 1.0 |
| rpoC | 765908 | p.Leu847Ala | missense_variant | 1.0 |
| rpoC | 765928 | c.2559C>G | synonymous_variant | 1.0 |
| rpoC | 765937 | c.2568T>C | synonymous_variant | 1.0 |
| rpoC | 765940 | c.2571A>C | synonymous_variant | 1.0 |
| rpoC | 765946 | c.2577C>T | synonymous_variant | 1.0 |
| rpoC | 765947 | c.2578T>C | synonymous_variant | 1.0 |
| rpoC | 765952 | c.2583G>C | synonymous_variant | 1.0 |
| rpoC | 765958 | c.2589C>G | synonymous_variant | 1.0 |
| rpoC | 765962 | c.2593T>C | synonymous_variant | 1.0 |
| rpoC | 766333 | c.2964G>C | synonymous_variant | 1.0 |
| rpoC | 766348 | c.2979A>G | synonymous_variant | 1.0 |
| rpoC | 766361 | p.Val998Ile | missense_variant | 1.0 |
| rpoC | 766366 | c.2997C>G | synonymous_variant | 1.0 |
| rpoC | 766369 | c.3000C>G | synonymous_variant | 1.0 |
| rpoC | 766375 | c.3006C>G | synonymous_variant | 1.0 |
| rpoC | 766381 | c.3012C>T | synonymous_variant | 1.0 |
| rpoC | 766384 | c.3015A>G | synonymous_variant | 1.0 |
| rpoC | 766432 | c.3063T>C | synonymous_variant | 1.0 |
| rpoC | 766435 | p.Glu1022Asp | missense_variant | 1.0 |
| rpoC | 766765 | c.3396A>C | synonymous_variant | 1.0 |
| rpoC | 766774 | c.3405T>C | synonymous_variant | 1.0 |
| rpoC | 766775 | p.Arg1136Asn | missense_variant | 1.0 |
| rpoC | 766783 | c.3414C>G | synonymous_variant | 1.0 |
| rpoC | 766799 | p.Ala1144Arg | missense_variant | 1.0 |
| rpoC | 766804 | c.3435A>G | synonymous_variant | 1.0 |
| rpoC | 766807 | c.3438T>C | synonymous_variant | 1.0 |
| rpoC | 766835 | p.Val1156Thr | missense_variant | 1.0 |
| rpoC | 766843 | c.3474T>G | synonymous_variant | 1.0 |
| rpoC | 766858 | c.3489C>T | synonymous_variant | 1.0 |
| rpoC | 766861 | c.3492G>C | synonymous_variant | 1.0 |
| rpoC | 766879 | c.3510G>C | synonymous_variant | 1.0 |
| rpoC | 766951 | c.3582G>C | synonymous_variant | 1.0 |
| rpoC | 766963 | c.3594T>C | synonymous_variant | 1.0 |
| rpoC | 766969 | c.3600C>G | synonymous_variant | 1.0 |
| rpoC | 766973 | p.Ala1202Ser | missense_variant | 1.0 |
| rpoC | 766978 | c.3609C>T | synonymous_variant | 1.0 |
| rpoC | 766981 | c.3612T>C | synonymous_variant | 1.0 |
| rpoC | 766990 | c.3621G>C | synonymous_variant | 1.0 |
| rpoC | 766996 | c.3627C>T | synonymous_variant | 1.0 |
| rpoC | 767002 | c.3633G>T | synonymous_variant | 1.0 |
| rpoC | 767008 | c.3639G>C | synonymous_variant | 1.0 |
| rpoC | 767059 | c.3690T>G | synonymous_variant | 1.0 |
| rpoC | 767062 | c.3693C>T | synonymous_variant | 1.0 |
| rpoC | 767065 | c.3696G>C | synonymous_variant | 1.0 |
| rpoC | 767074 | c.3705T>C | synonymous_variant | 1.0 |
| rpoC | 767080 | c.3711G>C | synonymous_variant | 1.0 |
| rpoC | 767087 | p.Cys1240Ser | missense_variant | 1.0 |
| rpoC | 767098 | c.3729T>C | synonymous_variant | 1.0 |
| rpoC | 767103 | c.3735_3738delCAAC | frameshift_variant | 1.0 |
| rpoC | 767110 | c.3741_3742insGGGC | frameshift_variant | 1.0 |
| rpoC | 767119 | c.3750A>G | synonymous_variant | 1.0 |
| rpoC | 767134 | c.3765C>T | synonymous_variant | 1.0 |
| rpoC | 767140 | c.3771G>C | synonymous_variant | 1.0 |
| rpsL | 781622 | c.63C>G | synonymous_variant | 1.0 |
| rpsL | 781628 | c.69T>C | synonymous_variant | 1.0 |
| rpsL | 781631 | c.72G>C | synonymous_variant | 1.0 |
| rpsL | 781643 | c.84G>C | synonymous_variant | 1.0 |
| rpsL | 781655 | c.96T>C | synonymous_variant | 1.0 |
| rpsL | 781658 | c.99A>G | synonymous_variant | 1.0 |
| rpsL | 781679 | c.120C>G | synonymous_variant | 1.0 |
| rpsL | 781682 | c.123T>C | synonymous_variant | 1.0 |
| rpsL | 781700 | c.141G>C | synonymous_variant | 1.0 |
| rpsL | 781706 | c.147T>G | synonymous_variant | 1.0 |
| rpsL | 781709 | c.150G>T | synonymous_variant | 1.0 |
| rpsL | 781715 | c.156T>C | synonymous_variant | 1.0 |
| rpsL | 781721 | c.162C>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 | 781763 | c.204C>G | synonymous_variant | 1.0 |
| rpsL | 781772 | c.213C>T | 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 | 781841 | c.282C>T | synonymous_variant | 1.0 |
| rpsL | 781845 | p.Lys96Arg | missense_variant | 1.0 |
| rpsL | 781859 | c.300T>C | synonymous_variant | 1.0 |
| rpsL | 781865 | c.306G>C | synonymous_variant | 1.0 |
| rpsL | 781868 | c.309T>C | synonymous_variant | 1.0 |
| rpsL | 781871 | c.312G>C | synonymous_variant | 1.0 |
| rpsL | 781884 | p.Asn109Asp | missense_variant | 1.0 |
| rpsL | 781892 | c.333A>G | synonymous_variant | 1.0 |
| rplC | 800693 | c.-116A>G | upstream_gene_variant | 1.0 |
| rplC | 800702 | c.-107G>A | 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 | 800738 | c.-71T>C | upstream_gene_variant | 1.0 |
| rplC | 800747 | c.-62C>G | upstream_gene_variant | 1.0 |
| rplC | 800762 | c.-47T>C | upstream_gene_variant | 1.0 |
| fbiC | 1303492 | c.562T>C | synonymous_variant | 1.0 |
| fbiC | 1303503 | c.573G>C | synonymous_variant | 1.0 |
| fbiC | 1303512 | c.582T>C | synonymous_variant | 1.0 |
| fbiC | 1303520 | p.Ser197Thr | missense_variant | 1.0 |
| fbiC | 1303525 | p.Ser199Glu | missense_variant | 1.0 |
| fbiC | 1303533 | p.Met201Ile | missense_variant | 1.0 |
| fbiC | 1303534 | p.Ser202Asn | missense_variant | 1.0 |
| fbiC | 1303545 | c.615A>G | synonymous_variant | 1.0 |
| fbiC | 1303548 | c.618G>C | synonymous_variant | 1.0 |
| fbiC | 1303551 | c.621G>C | synonymous_variant | 1.0 |
| fbiC | 1303581 | c.651G>C | synonymous_variant | 0.75 |
| fbiC | 1304547 | c.1617C>G | synonymous_variant | 1.0 |
| fbiC | 1304562 | c.1632G>C | synonymous_variant | 1.0 |
| fbiC | 1304567 | p.Phe546Tyr | missense_variant | 1.0 |
| fbiC | 1304574 | c.1644C>G | synonymous_variant | 1.0 |
| fbiC | 1304580 | c.1650T>G | synonymous_variant | 1.0 |
| fbiC | 1304610 | c.1680C>G | synonymous_variant | 1.0 |
| fbiC | 1304613 | c.1683T>C | synonymous_variant | 1.0 |
| fbiC | 1304619 | c.1689G>A | synonymous_variant | 1.0 |
| fbiC | 1304625 | c.1695C>T | synonymous_variant | 1.0 |
| fbiC | 1304637 | c.1707G>A | synonymous_variant | 1.0 |
| fbiC | 1304640 | c.1710A>C | synonymous_variant | 1.0 |
| fbiC | 1304646 | c.1716T>C | synonymous_variant | 1.0 |
| fbiC | 1304684 | p.Ala585Gly | missense_variant | 1.0 |
| fbiC | 1304691 | c.1761G>T | synonymous_variant | 1.0 |
| fbiC | 1304694 | c.1764A>G | synonymous_variant | 1.0 |
| fbiC | 1304703 | c.1773C>G | synonymous_variant | 1.0 |
| fbiC | 1304707 | p.Val593Leu | missense_variant | 1.0 |
| fbiC | 1304715 | c.1785G>C | synonymous_variant | 1.0 |
| fbiC | 1304724 | c.1794A>G | synonymous_variant | 1.0 |
| fbiC | 1304727 | c.1797A>G | synonymous_variant | 1.0 |
| fbiC | 1304742 | c.1812T>C | synonymous_variant | 1.0 |
| fbiC | 1304751 | c.1821C>G | synonymous_variant | 1.0 |
| fbiC | 1304757 | c.1827A>G | synonymous_variant | 1.0 |
| fbiC | 1304763 | c.1833C>G | synonymous_variant | 1.0 |
| fbiC | 1304769 | c.1839C>A | synonymous_variant | 1.0 |
| rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471929 | n.84C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471930 | n.85G>C | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1471931 | n.86G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471932 | n.87A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471978 | n.133C>T | 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 | 1471996 | n.151C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472017 | n.172C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472023 | n.178G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472030 | n.185G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472032 | n.187G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472033 | n.188A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472034 | n.189T>C | 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 | 1472043 | n.198T>G | 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 | 1472070 | n.225G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472075 | n.230A>G | 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 | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.98 |
| rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.98 |
| rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.98 |
| rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.9 |
| rrs | 1472438 | n.593T>C | non_coding_transcript_exon_variant | 0.8 |
| rrs | 1472439 | n.594C>T | non_coding_transcript_exon_variant | 0.8 |
| rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 0.97 |
| rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472497 | n.652G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472680 | n.835C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472686 | n.841G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472690 | n.845C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472836 | n.991G>A | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472840 | n.995A>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472841 | n.996G>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 | 0.46 |
| rrs | 1472849 | n.1004C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472858 | n.1013G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472859 | n.1014G>A | 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 | 1472873 | n.1028C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472874 | n.1029C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472875 | n.1030T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.98 |
| rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472958 | n.1113A>G | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472960 | n.1115G>A | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472986 | n.1141C>T | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472988 | n.1143T>C | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1473081 | n.1236C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473082 | n.1237G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.98 |
| rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.98 |
| rrs | 1473129 | n.1284C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473130 | n.1285G>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 | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473294 | n.1449A>G | non_coding_transcript_exon_variant | 0.43 |
| rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473391 | n.-267C>A | upstream_gene_variant | 1.0 |
| rrl | 1473668 | n.11C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473670 | n.13A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473677 | n.20C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473678 | n.21A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473679 | n.22T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473694 | n.37C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473696 | n.39T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473698 | n.41G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473699 | n.42A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473719 | n.62G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473724 | n.67T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473731 | n.74T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473732 | n.75G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473743 | n.86C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473750 | n.93C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473756 | n.99G>T | non_coding_transcript_exon_variant | 0.93 |
| rrl | 1473757 | n.100T>G | non_coding_transcript_exon_variant | 0.93 |
| rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.93 |
| rrl | 1473768 | n.111A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473793 | n.136G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473822 | n.165A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473827 | n.170_171insCC | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473836 | n.179A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473844 | n.187C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473870 | n.213G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473887 | n.230_231insA | 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 | 1473918 | n.261C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473922 | n.265A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473923 | n.266C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473936 | n.279A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473939 | n.282C>T | 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 | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474186 | n.529A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474201 | n.544T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474202 | n.545T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474264 | n.607T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474265 | n.608G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474266 | n.609T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474286 | n.629C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474306 | n.649A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474309 | n.652G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 0.98 |
| rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474353 | n.696A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474354 | n.697C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474355 | n.698A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474356 | n.699T>A | non_coding_transcript_exon_variant | 0.98 |
| rrl | 1474359 | n.702C>G | non_coding_transcript_exon_variant | 0.98 |
| rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474374 | n.718dupG | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474413 | n.756A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474495 | n.838G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474496 | n.839C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474498 | n.841G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474505 | n.848C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474508 | n.851C>G | 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 | 1474552 | n.895C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474627 | n.970G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1474692 | n.1035G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474709 | n.1053_1056delTGGT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474717 | n.1060_1061insGTGAG | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 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 | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474825 | n.1168G>A | 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>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474901 | n.1244A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474952 | n.1296delC | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475009 | n.1352G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475016 | n.1359C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475020 | n.1363G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475031 | n.1374G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475060 | n.1404delC | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475065 | n.1408G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475076 | n.1419C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475081 | n.1424C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475113 | n.1456C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475116 | n.1459G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475199 | n.1542G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475422 | n.1765A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475427 | n.1772delG | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475436 | n.1779C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475443 | n.1786G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475460 | n.1803A>G | 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 | 1475481 | n.1824C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475482 | n.1825A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475483 | n.1826C>T | 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 | 1475538 | n.1881T>A | 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 | 1475550 | n.1893A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475571 | n.1914A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475602 | n.1945G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475649 | n.1992A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475655 | n.1998T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475707 | n.2050T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475757 | n.2101_2102insTCA | non_coding_transcript_exon_variant | 0.34 |
| rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.99 |
| 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 | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476033 | n.2376T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476088 | n.2431A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476105 | n.2450delA | 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 | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 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 | 1476251 | n.2594T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476297 | n.2640C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476298 | n.2641C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476300 | n.2643G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476524 | n.2867_2868insT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476603 | n.2946G>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>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476661 | n.3004A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476665 | n.3008T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476666 | n.3009C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476675 | n.3018C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476690 | n.3033_3034insCA | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476699 | n.3042A>G | non_coding_transcript_exon_variant | 1.0 |
| rpsA | 1833583 | c.42C>T | synonymous_variant | 0.88 |
| 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 | 1833607 | c.66T>C | synonymous_variant | 1.0 |
| rpsA | 1833616 | c.75A>C | synonymous_variant | 1.0 |
| rpsA | 1833619 | c.78A>C | synonymous_variant | 1.0 |
| rpsA | 1833623 | p.Lys28Ser | missense_variant | 1.0 |
| rpsA | 1833673 | c.132C>G | synonymous_variant | 0.91 |
| rpsA | 1833676 | c.135A>G | synonymous_variant | 0.91 |
| rpsA | 1833679 | c.138G>C | synonymous_variant | 0.91 |
| rpsA | 1833682 | c.141C>T | synonymous_variant | 0.91 |
| rpsA | 1833685 | c.144G>C | synonymous_variant | 0.91 |
| rpsA | 1833694 | c.153G>T | synonymous_variant | 0.91 |
| rpsA | 1833697 | c.156C>G | synonymous_variant | 0.91 |
| rpsA | 1833700 | c.159C>T | synonymous_variant | 0.91 |
| rpsA | 1833721 | c.180A>G | synonymous_variant | 0.95 |
| rpsA | 1833727 | c.186G>C | synonymous_variant | 0.94 |
| rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.92 |
| rpsA | 1833742 | c.201A>G | synonymous_variant | 0.9 |
| rpsA | 1833748 | c.207C>G | synonymous_variant | 0.89 |
| rpsA | 1833760 | c.219C>T | synonymous_variant | 1.0 |
| rpsA | 1833790 | c.249T>C | synonymous_variant | 1.0 |
| rpsA | 1833808 | c.267G>C | synonymous_variant | 1.0 |
| rpsA | 1833811 | c.270G>T | synonymous_variant | 1.0 |
| rpsA | 1833829 | c.288A>G | synonymous_variant | 1.0 |
| rpsA | 1833832 | c.291G>A | synonymous_variant | 1.0 |
| rpsA | 1833838 | c.297G>C | synonymous_variant | 1.0 |
| rpsA | 1833844 | c.303C>T | synonymous_variant | 1.0 |
| rpsA | 1833847 | c.306C>G | synonymous_variant | 1.0 |
| rpsA | 1833850 | c.309C>G | synonymous_variant | 1.0 |
| rpsA | 1833856 | c.315A>G | synonymous_variant | 1.0 |
| rpsA | 1833862 | c.321G>T | synonymous_variant | 0.97 |
| rpsA | 1833894 | p.Ala118Glu | missense_variant | 1.0 |
| rpsA | 1833905 | p.Lys122Arg | 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 | 1833985 | c.444G>C | synonymous_variant | 1.0 |
| rpsA | 1833988 | c.447C>G | synonymous_variant | 1.0 |
| rpsA | 1833991 | c.450C>G | 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 | 1834030 | c.489C>G | synonymous_variant | 1.0 |
| rpsA | 1834046 | p.Ile169Val | missense_variant | 1.0 |
| rpsA | 1834069 | c.528G>C | synonymous_variant | 1.0 |
| rpsA | 1834093 | c.552G>C | synonymous_variant | 0.97 |
| rpsA | 1834099 | c.558C>G | synonymous_variant | 0.97 |
| rpsA | 1834102 | c.561T>C | synonymous_variant | 0.97 |
| rpsA | 1834114 | c.573G>C | synonymous_variant | 0.96 |
| rpsA | 1834123 | c.582C>G | synonymous_variant | 0.95 |
| rpsA | 1834135 | c.594G>C | synonymous_variant | 1.0 |
| rpsA | 1834150 | c.609G>C | synonymous_variant | 1.0 |
| rpsA | 1834222 | c.681T>C | synonymous_variant | 1.0 |
| rpsA | 1834231 | c.690T>C | synonymous_variant | 1.0 |
| rpsA | 1834234 | c.693G>C | synonymous_variant | 1.0 |
| rpsA | 1834240 | c.699T>C | synonymous_variant | 1.0 |
| rpsA | 1834249 | c.708T>C | synonymous_variant | 1.0 |
| rpsA | 1834255 | c.714C>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 | 1834285 | c.744G>C | synonymous_variant | 1.0 |
| rpsA | 1834294 | c.753G>C | synonymous_variant | 1.0 |
| rpsA | 1834303 | c.762T>G | synonymous_variant | 1.0 |
| rpsA | 1834306 | c.765T>C | 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>C | synonymous_variant | 1.0 |
| rpsA | 1834361 | c.820_822delTTGinsCTC | synonymous_variant | 1.0 |
| rpsA | 1834366 | c.825A>G | synonymous_variant | 1.0 |
| rpsA | 1834396 | c.855G>C | synonymous_variant | 1.0 |
| rpsA | 1834399 | p.His286Gln | missense_variant | 1.0 |
| rpsA | 1834411 | c.870T>C | synonymous_variant | 1.0 |
| rpsA | 1834423 | c.882G>C | synonymous_variant | 1.0 |
| rpsA | 1834451 | c.910_912delTTGinsCTC | synonymous_variant | 0.98 |
| rpsA | 1834456 | c.915T>G | synonymous_variant | 1.0 |
| rpsA | 1834465 | c.924T>C | synonymous_variant | 1.0 |
| rpsA | 1834468 | c.927A>C | synonymous_variant | 1.0 |
| rpsA | 1834474 | c.933C>G | synonymous_variant | 1.0 |
| rpsA | 1834477 | c.936C>T | synonymous_variant | 1.0 |
| rpsA | 1834489 | c.948T>C | synonymous_variant | 1.0 |
| rpsA | 1834513 | c.972C>G | synonymous_variant | 1.0 |
| rpsA | 1834543 | c.1002C>G | synonymous_variant | 1.0 |
| rpsA | 1834546 | c.1005T>C | synonymous_variant | 1.0 |
| rpsA | 1834552 | c.1011G>A | synonymous_variant | 1.0 |
| rpsA | 1834555 | c.1014T>G | synonymous_variant | 1.0 |
| rpsA | 1834558 | c.1017C>T | synonymous_variant | 1.0 |
| rpsA | 1834561 | c.1020C>G | synonymous_variant | 1.0 |
| rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.96 |
| rpsA | 1834619 | c.1078T>C | synonymous_variant | 0.96 |
| rpsA | 1834627 | c.1086C>G | synonymous_variant | 0.96 |
| rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.96 |
| rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.96 |
| rpsA | 1834667 | p.Ala376Ser | missense_variant | 1.0 |
| rpsA | 1834690 | c.1149T>C | synonymous_variant | 0.98 |
| rpsA | 1834732 | c.1191T>C | synonymous_variant | 1.0 |
| rpsA | 1834738 | c.1197A>G | synonymous_variant | 1.0 |
| rpsA | 1834747 | c.1206A>G | synonymous_variant | 1.0 |
| rpsA | 1834753 | c.1212T>C | synonymous_variant | 1.0 |
| katG | 2155632 | c.480A>C | synonymous_variant | 1.0 |
| katG | 2155641 | p.Lys157Ala | missense_variant | 1.0 |
| katG | 2155655 | p.Lys153Gln | missense_variant | 1.0 |
| katG | 2155661 | p.Val151Ile | missense_variant | 1.0 |
| katG | 2155674 | c.438G>C | synonymous_variant | 1.0 |
| katG | 2155680 | c.432G>C | synonymous_variant | 1.0 |
| katG | 2155683 | c.429G>A | synonymous_variant | 1.0 |
| katG | 2155691 | c.421T>C | synonymous_variant | 1.0 |
| katG | 2155716 | c.396T>C | synonymous_variant | 1.0 |
| katG | 2155722 | c.390G>C | synonymous_variant | 1.0 |
| katG | 2155737 | c.375C>G | synonymous_variant | 1.0 |
| katG | 2155741 | p.Gly124His | missense_variant | 1.0 |
| katG | 2155749 | c.363C>T | synonymous_variant | 1.0 |
| katG | 2155765 | p.His116Ser | missense_variant | 1.0 |
| katG | 2155773 | c.339C>T | synonymous_variant | 1.0 |
| katG | 2155785 | c.327T>C | synonymous_variant | 1.0 |
| katG | 2155796 | p.Ala106Ser | missense_variant | 1.0 |
| katG | 2155806 | c.306T>C | synonymous_variant | 1.0 |
| katG | 2155812 | c.300G>C | synonymous_variant | 1.0 |
| katG | 2155815 | c.297G>T | synonymous_variant | 1.0 |
| katG | 2155823 | p.His97Asn | missense_variant | 1.0 |
| kasA | 2517917 | c.-198G>C | upstream_gene_variant | 1.0 |
| kasA | 2517921 | c.-194_-192delACCinsGTG | upstream_gene_variant | 1.0 |
| kasA | 2517945 | c.-170A>G | upstream_gene_variant | 1.0 |
| kasA | 2517950 | c.-165C>G | upstream_gene_variant | 1.0 |
| kasA | 2517968 | c.-147T>C | upstream_gene_variant | 1.0 |
| kasA | 2517974 | c.-141T>C | upstream_gene_variant | 1.0 |
| kasA | 2517983 | c.-132T>C | upstream_gene_variant | 1.0 |
| kasA | 2517987 | c.-128_-126delGTTinsACC | upstream_gene_variant | 1.0 |
| ahpC | 2726567 | c.375C>G | synonymous_variant | 1.0 |
| ahpC | 2726579 | c.387T>C | synonymous_variant | 1.0 |
| ahpC | 2726582 | c.390G>C | synonymous_variant | 1.0 |
| ahpC | 2726585 | c.393C>T | synonymous_variant | 1.0 |
| ahpC | 2726588 | c.396C>T | synonymous_variant | 1.0 |
| ahpC | 2726593 | p.Val134Ala | missense_variant | 1.0 |
| ahpC | 2726600 | c.408T>C | synonymous_variant | 1.0 |
| ahpC | 2726612 | c.420C>G | synonymous_variant | 1.0 |
| ahpC | 2726633 | c.441C>G | synonymous_variant | 1.0 |
| ahpC | 2726638 | p.Ala149Val | missense_variant | 1.0 |
| ahpC | 2726645 | c.453C>G | synonymous_variant | 1.0 |
| ahpC | 2726648 | c.456T>C | synonymous_variant | 1.0 |
| ahpC | 2726654 | c.462G>C | synonymous_variant | 1.0 |
| ahpC | 2726657 | c.465A>C | synonymous_variant | 1.0 |
| thyX | 3067328 | c.618G>C | synonymous_variant | 1.0 |
| thyX | 3067344 | p.Ser201Thr | missense_variant | 1.0 |
| thyX | 3067346 | c.600C>G | synonymous_variant | 1.0 |
| thyX | 3067355 | p.Ala197Gly | missense_variant | 1.0 |
| thyX | 3067364 | c.582C>T | synonymous_variant | 1.0 |
| thyX | 3067376 | c.570G>T | synonymous_variant | 1.0 |
| thyX | 3067379 | c.567C>T | synonymous_variant | 1.0 |
| thyX | 3067406 | c.540A>G | synonymous_variant | 1.0 |
| thyX | 3067409 | c.537C>G | synonymous_variant | 1.0 |
| thyX | 3067418 | c.528C>G | synonymous_variant | 1.0 |
| thyX | 3067421 | c.525G>C | synonymous_variant | 1.0 |
| thyX | 3067429 | p.Ala173Ser | missense_variant | 1.0 |
| thyX | 3067430 | c.516C>G | synonymous_variant | 1.0 |
| thyX | 3067436 | c.510C>G | synonymous_variant | 1.0 |
| thyX | 3067439 | c.507A>G | synonymous_variant | 0.75 |
| thyX | 3067442 | c.504C>G | synonymous_variant | 0.75 |
| thyX | 3067445 | c.501C>G | synonymous_variant | 0.75 |
| thyX | 3067451 | c.495G>A | synonymous_variant | 0.75 |
| thyX | 3067457 | c.489C>G | synonymous_variant | 0.75 |
| thyX | 3067463 | c.483C>T | synonymous_variant | 0.75 |
| thyA | 3073989 | c.483T>C | synonymous_variant | 1.0 |
| thyA | 3073995 | c.477G>C | synonymous_variant | 1.0 |
| thyA | 3073999 | p.Arg158Lys | missense_variant | 1.0 |
| thyA | 3074004 | p.Asp156Glu | missense_variant | 1.0 |
| thyA | 3074028 | c.444G>C | synonymous_variant | 1.0 |
| thyA | 3074031 | c.441T>C | synonymous_variant | 1.0 |
| thyA | 3074037 | c.435C>G | synonymous_variant | 1.0 |
| thyA | 3074053 | p.Arg140Gln | missense_variant | 1.0 |
| thyA | 3074055 | p.Glu139Gly | missense_variant | 1.0 |
| thyA | 3074061 | c.411A>G | synonymous_variant | 1.0 |
| thyA | 3074076 | c.396C>G | synonymous_variant | 1.0 |
| fbiA | 3640701 | p.Ile53Met | missense_variant | 1.0 |
| fbiB | 3640707 | c.-828G>C | upstream_gene_variant | 1.0 |
| fbiA | 3640708 | p.Leu56Val | missense_variant | 1.0 |
| fbiB | 3640713 | c.-822T>G | upstream_gene_variant | 1.0 |
| fbiA | 3640714 | p.Val58Ile | missense_variant | 1.0 |
| fbiB | 3640722 | c.-813G>C | upstream_gene_variant | 1.0 |
| fbiB | 3640725 | c.-810T>C | upstream_gene_variant | 1.0 |
| fbiB | 3640734 | c.-801C>G | upstream_gene_variant | 1.0 |
| fbiB | 3640743 | c.-792T>C | upstream_gene_variant | 1.0 |
| fbiB | 3640746 | c.-789C>G | upstream_gene_variant | 1.0 |
| fbiA | 3640759 | p.Val73Ile | missense_variant | 1.0 |
| fbiA | 3640765 | p.Pro75Thr | missense_variant | 1.0 |
| fbiA | 3640768 | p.Gln76Glu | missense_variant | 1.0 |
| rpoA | 3877553 | p.Glu319Gln | missense_variant | 1.0 |
| rpoA | 3877557 | c.951C>G | synonymous_variant | 1.0 |
| rpoA | 3877560 | c.948C>T | synonymous_variant | 1.0 |
| rpoA | 3877569 | p.Pro313Ala | missense_variant | 1.0 |
| rpoA | 3877587 | c.921A>G | synonymous_variant | 1.0 |
| rpoA | 3877593 | c.915C>T | synonymous_variant | 1.0 |
| rpoA | 3877599 | p.Gln303Gly | missense_variant | 1.0 |
| rpoA | 3877611 | p.Ile299Val | missense_variant | 1.0 |
| rpoA | 3877629 | c.879C>G | synonymous_variant | 1.0 |
| rpoA | 3877656 | c.852T>C | synonymous_variant | 0.98 |
| rpoA | 3877665 | c.843C>G | synonymous_variant | 0.98 |
| rpoA | 3877668 | c.840A>G | synonymous_variant | 0.96 |
| rpoA | 3877674 | c.834C>T | synonymous_variant | 0.98 |
| rpoA | 3877685 | c.823C>T | synonymous_variant | 0.98 |
| rpoA | 3877686 | c.822A>G | synonymous_variant | 0.98 |
| rpoA | 3877692 | c.816G>C | synonymous_variant | 0.98 |
| rpoA | 3877704 | c.804G>T | synonymous_variant | 0.97 |
| rpoA | 3877728 | c.780C>G | synonymous_variant | 0.95 |
| rpoA | 3877734 | c.774G>C | synonymous_variant | 1.0 |
| rpoA | 3877737 | c.771G>C | synonymous_variant | 1.0 |
| rpoA | 3877743 | p.Asp255Glu | missense_variant | 1.0 |
| rpoA | 3877749 | c.759C>T | synonymous_variant | 1.0 |
| rpoA | 3877752 | p.Asp252Glu | missense_variant | 1.0 |
| rpoA | 3877803 | c.705G>C | synonymous_variant | 0.67 |
| rpoA | 3877818 | c.690A>G | synonymous_variant | 0.75 |
| rpoA | 3877836 | c.672A>G | synonymous_variant | 0.83 |
| rpoA | 3877842 | c.666A>T | synonymous_variant | 0.83 |
| rpoA | 3877854 | c.652_654delTTGinsCTC | synonymous_variant | 0.83 |
| rpoA | 3877866 | c.642G>C | synonymous_variant | 0.88 |
| rpoA | 3877872 | c.636C>T | synonymous_variant | 0.9 |
| rpoA | 3877875 | c.633T>C | synonymous_variant | 0.9 |
| rpoA | 3877887 | c.621G>C | synonymous_variant | 0.91 |
| rpoA | 3877893 | c.615C>G | synonymous_variant | 0.88 |
| rpoA | 3877898 | p.Pro204Ala | missense_variant | 1.0 |
| rpoA | 3877900 | p.Ser203Thr | missense_variant | 1.0 |
| rpoA | 3877905 | c.603A>C | synonymous_variant | 1.0 |
| rpoA | 3877908 | c.600T>C | synonymous_variant | 1.0 |
| rpoA | 3877926 | c.582G>C | synonymous_variant | 1.0 |
| rpoA | 3877929 | p.Ile193Val | missense_variant | 1.0 |
| rpoA | 3877935 | p.Lys191Arg | missense_variant | 1.0 |
| rpoA | 3877938 | c.570C>T | synonymous_variant | 1.0 |
| rpoA | 3877962 | c.546G>C | synonymous_variant | 0.88 |
| rpoA | 3877971 | p.Asp179Glu | missense_variant | 0.75 |
| rpoA | 3877974 | c.534G>C | synonymous_variant | 0.75 |
| rpoA | 3878082 | c.426T>G | synonymous_variant | 0.83 |
| rpoA | 3878102 | p.Val136Ile | missense_variant | 1.0 |
| rpoA | 3878103 | c.405A>G | synonymous_variant | 1.0 |
| rpoA | 3878106 | c.402G>C | synonymous_variant | 1.0 |
| rpoA | 3878118 | c.390T>C | synonymous_variant | 1.0 |
| rpoA | 3878124 | c.384G>C | synonymous_variant | 1.0 |
| rpoA | 3878127 | c.381G>C | synonymous_variant | 1.0 |
| rpoA | 3878130 | c.378C>G | synonymous_variant | 1.0 |
| rpoA | 3878141 | p.Met123Leu | missense_variant | 1.0 |
| rpoA | 3878143 | p.Gly122Asp | missense_variant | 1.0 |
| rpoA | 3878145 | c.363C>G | synonymous_variant | 1.0 |
| rpoA | 3878148 | c.360C>T | synonymous_variant | 1.0 |
| rpoA | 3878157 | c.351C>G | synonymous_variant | 1.0 |
| rpoA | 3878163 | c.345C>T | synonymous_variant | 1.0 |
| rpoA | 3878169 | c.339G>T | synonymous_variant | 1.0 |
| rpoA | 3878172 | c.336G>C | synonymous_variant | 1.0 |
| rpoA | 3878185 | p.Gly108Ala | missense_variant | 1.0 |
| rpoA | 3878188 | p.Ala107Gly | missense_variant | 1.0 |
| rpoA | 3878193 | c.315T>C | synonymous_variant | 1.0 |
| rpoA | 3878197 | p.Glu104Ala | missense_variant | 1.0 |
| rpoA | 3878202 | c.306G>C | synonymous_variant | 1.0 |
| rpoA | 3878217 | p.Leu97Val | missense_variant | 1.0 |
| rpoA | 3878244 | c.264G>A | synonymous_variant | 1.0 |
| rpoA | 3878251 | c.256_257delTCinsAG | synonymous_variant | 1.0 |
| rpoA | 3878253 | c.255G>C | synonymous_variant | 1.0 |
| rpoA | 3878259 | c.249G>C | synonymous_variant | 1.0 |
| rpoA | 3878264 | p.Ser82Gly | missense_variant | 1.0 |
| rpoA | 3878271 | c.237T>C | synonymous_variant | 1.0 |
| rpoA | 3878346 | c.162T>C | synonymous_variant | 1.0 |
| rpoA | 3878358 | c.150C>G | 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 | 3878379 | c.129G>C | synonymous_variant | 1.0 |
| rpoA | 3878385 | c.123C>G | synonymous_variant | 0.75 |
| rpoA | 3878391 | c.117T>G | synonymous_variant | 0.75 |
| rpoA | 3878400 | c.108T>C | synonymous_variant | 0.75 |
| rpoA | 3878406 | c.102G>C | synonymous_variant | 0.75 |
| rpoA | 3878409 | c.99C>G | synonymous_variant | 0.75 |
| rpoA | 3878421 | c.87A>C | synonymous_variant | 0.8 |
| clpC1 | 4038499 | p.Ser736Gly | missense_variant | 1.0 |
| clpC1 | 4038508 | c.2197C>T | synonymous_variant | 1.0 |
| clpC1 | 4038509 | c.2196C>T | synonymous_variant | 1.0 |
| clpC1 | 4038519 | p.Arg729Glu | missense_variant | 1.0 |
| clpC1 | 4038530 | p.Glu725Asp | missense_variant | 1.0 |
| clpC1 | 4038559 | p.Ile716Val | missense_variant | 1.0 |
| clpC1 | 4038569 | c.2136C>T | synonymous_variant | 1.0 |
| clpC1 | 4038575 | c.2130C>G | synonymous_variant | 1.0 |
| clpC1 | 4038584 | c.2121G>C | synonymous_variant | 1.0 |
| clpC1 | 4038596 | c.2109A>G | synonymous_variant | 1.0 |
| clpC1 | 4038623 | c.2082A>G | synonymous_variant | 1.0 |
| clpC1 | 4038640 | p.Asp689Asn | missense_variant | 1.0 |
| clpC1 | 4038677 | p.Pro676Ala | missense_variant | 1.0 |
| clpC1 | 4038683 | c.2022T>G | synonymous_variant | 1.0 |
| clpC1 | 4038692 | c.2013C>G | synonymous_variant | 1.0 |
| clpC1 | 4038695 | c.2010C>G | synonymous_variant | 1.0 |
| clpC1 | 4038704 | c.2001T>C | synonymous_variant | 1.0 |
| clpC1 | 4038707 | c.1998C>G | synonymous_variant | 1.0 |
| clpC1 | 4038710 | c.1995G>C | synonymous_variant | 1.0 |
| clpC1 | 4038713 | c.1992T>C | synonymous_variant | 1.0 |
| clpC1 | 4038740 | c.1965G>C | synonymous_variant | 1.0 |
| clpC1 | 4038749 | c.1956C>T | synonymous_variant | 1.0 |
| clpC1 | 4038755 | c.1950G>T | synonymous_variant | 1.0 |
| clpC1 | 4038767 | c.1938G>C | synonymous_variant | 1.0 |
| clpC1 | 4038773 | c.1932T>C | synonymous_variant | 1.0 |
| clpC1 | 4038782 | c.1923G>C | synonymous_variant | 1.0 |
| clpC1 | 4038790 | c.1915C>T | synonymous_variant | 1.0 |
| clpC1 | 4038795 | p.Ser637Thr | missense_variant | 1.0 |
| clpC1 | 4038810 | p.Gln632Pro | missense_variant | 1.0 |
| clpC1 | 4038812 | c.1893T>C | synonymous_variant | 1.0 |
| clpC1 | 4038815 | c.1890G>T | synonymous_variant | 1.0 |
| clpC1 | 4038839 | c.1866G>C | synonymous_variant | 1.0 |
| clpC1 | 4038842 | c.1863G>C | synonymous_variant | 1.0 |
| clpC1 | 4038845 | c.1860G>C | synonymous_variant | 1.0 |
| clpC1 | 4038860 | c.1845G>C | synonymous_variant | 1.0 |
| clpC1 | 4038878 | c.1827A>G | synonymous_variant | 1.0 |
| clpC1 | 4038890 | p.Glu605Asp | missense_variant | 1.0 |
| clpC1 | 4038896 | c.1809C>G | synonymous_variant | 1.0 |
| clpC1 | 4038905 | c.1800A>C | synonymous_variant | 1.0 |
| clpC1 | 4038911 | c.1794G>T | synonymous_variant | 1.0 |
| clpC1 | 4038914 | c.1791G>C | synonymous_variant | 1.0 |
| clpC1 | 4038923 | c.1782A>C | synonymous_variant | 1.0 |
| clpC1 | 4038941 | c.1764G>C | synonymous_variant | 1.0 |
| clpC1 | 4038953 | c.1752A>G | synonymous_variant | 1.0 |
| clpC1 | 4038956 | c.1749T>C | synonymous_variant | 1.0 |
| clpC1 | 4038965 | c.1740T>C | synonymous_variant | 1.0 |
| clpC1 | 4038971 | c.1734T>C | synonymous_variant | 1.0 |
| clpC1 | 4038974 | c.1731T>C | synonymous_variant | 1.0 |
| clpC1 | 4038986 | p.Asp573Glu | missense_variant | 1.0 |
| clpC1 | 4038989 | c.1716T>C | synonymous_variant | 1.0 |
| clpC1 | 4038997 | c.1708T>C | synonymous_variant | 1.0 |
| clpC1 | 4039004 | c.1701C>G | synonymous_variant | 1.0 |
| clpC1 | 4039022 | c.1683A>G | synonymous_variant | 1.0 |
| clpC1 | 4039031 | c.1674T>C | synonymous_variant | 1.0 |
| clpC1 | 4039067 | c.1638G>C | synonymous_variant | 1.0 |
| clpC1 | 4039073 | c.1632C>T | synonymous_variant | 1.0 |
| clpC1 | 4039082 | c.1623C>T | 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>C | synonymous_variant | 1.0 |
| clpC1 | 4039106 | c.1599G>C | synonymous_variant | 1.0 |
| clpC1 | 4039112 | c.1593C>G | synonymous_variant | 1.0 |
| clpC1 | 4039116 | p.Lys530Arg | missense_variant | 1.0 |
| clpC1 | 4039118 | c.1587C>G | synonymous_variant | 1.0 |
| clpC1 | 4039121 | c.1584T>C | synonymous_variant | 1.0 |
| clpC1 | 4039124 | c.1581C>G | 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 | 4039181 | c.1522_1524delTTGinsCTC | synonymous_variant | 1.0 |
| clpC1 | 4039187 | c.1518G>T | synonymous_variant | 1.0 |
| clpC1 | 4039190 | c.1515C>T | 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 | 4039226 | c.1479T>C | synonymous_variant | 1.0 |
| clpC1 | 4039258 | p.Gln483Glu | missense_variant | 1.0 |
| clpC1 | 4039430 | c.1275T>C | synonymous_variant | 1.0 |
| clpC1 | 4039442 | c.1263A>T | synonymous_variant | 1.0 |
| clpC1 | 4039448 | c.1257A>G | synonymous_variant | 1.0 |
| clpC1 | 4039454 | c.1251A>G | synonymous_variant | 1.0 |
| clpC1 | 4039463 | c.1242C>G | synonymous_variant | 1.0 |
| clpC1 | 4039466 | c.1239T>C | synonymous_variant | 1.0 |
| clpC1 | 4039469 | c.1236T>C | synonymous_variant | 1.0 |
| clpC1 | 4039472 | c.1233G>C | synonymous_variant | 1.0 |
| clpC1 | 4039478 | c.1227G>C | synonymous_variant | 1.0 |
| clpC1 | 4039481 | c.1224T>G | synonymous_variant | 1.0 |
| clpC1 | 4039487 | c.1218G>C | synonymous_variant | 1.0 |
| clpC1 | 4039517 | c.1188C>G | synonymous_variant | 1.0 |
| clpC1 | 4039532 | c.1173C>T | synonymous_variant | 0.94 |
| clpC1 | 4039541 | c.1164C>G | synonymous_variant | 1.0 |
| clpC1 | 4039544 | c.1161C>T | synonymous_variant | 1.0 |
| clpC1 | 4039553 | c.1152C>G | synonymous_variant | 0.86 |
| clpC1 | 4039559 | c.1146C>G | synonymous_variant | 0.83 |
| clpC1 | 4039562 | c.1143C>T | synonymous_variant | 0.83 |
| clpC1 | 4039565 | p.Val380Ala | missense_variant | 1.0 |
| clpC1 | 4039570 | p.Met379Leu | missense_variant | 1.0 |
| clpC1 | 4039574 | c.1131G>C | synonymous_variant | 1.0 |
| clpC1 | 4039577 | c.1128T>C | synonymous_variant | 1.0 |
| clpC1 | 4039586 | c.1119G>C | synonymous_variant | 1.0 |
| clpC1 | 4039602 | p.Ala368Gln | missense_variant | 1.0 |
| clpC1 | 4039610 | c.1095G>C | synonymous_variant | 1.0 |
| clpC1 | 4039616 | c.1089G>C | synonymous_variant | 1.0 |
| clpC1 | 4039622 | c.1083C>T | synonymous_variant | 1.0 |
| clpC1 | 4039654 | p.Thr351Ser | missense_variant | 1.0 |
| clpC1 | 4039661 | c.1044T>G | synonymous_variant | 1.0 |
| clpC1 | 4039670 | c.1035G>C | synonymous_variant | 0.94 |
| clpC1 | 4039694 | c.1011G>C | synonymous_variant | 1.0 |
| clpC1 | 4039724 | c.981A>G | synonymous_variant | 1.0 |
| clpC1 | 4039733 | c.972G>C | synonymous_variant | 0.87 |
| 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 | 4039778 | c.927A>G | synonymous_variant | 1.0 |
| clpC1 | 4039787 | c.918G>C | synonymous_variant | 1.0 |
| clpC1 | 4039790 | c.915C>G | synonymous_variant | 1.0 |
| clpC1 | 4039796 | c.909C>T | synonymous_variant | 1.0 |
| clpC1 | 4039802 | c.903G>C | synonymous_variant | 1.0 |
| clpC1 | 4039817 | c.888A>C | synonymous_variant | 1.0 |
| clpC1 | 4039820 | c.885T>C | synonymous_variant | 1.0 |
| clpC1 | 4039823 | c.882T>G | synonymous_variant | 1.0 |
| clpC1 | 4039835 | c.869_870insT | frameshift_variant | 1.0 |
| clpC1 | 4039850 | c.855T>C | synonymous_variant | 1.0 |
| clpC1 | 4039856 | c.849C>T | synonymous_variant | 1.0 |
| clpC1 | 4039898 | c.807C>G | synonymous_variant | 1.0 |
| clpC1 | 4039904 | c.801A>G | synonymous_variant | 1.0 |
| clpC1 | 4039907 | c.798G>A | synonymous_variant | 1.0 |
| clpC1 | 4039916 | c.789T>C | synonymous_variant | 1.0 |
| clpC1 | 4039931 | c.774T>C | synonymous_variant | 1.0 |
| clpC1 | 4039934 | c.771G>C | synonymous_variant | 1.0 |
| clpC1 | 4039946 | c.759A>T | synonymous_variant | 1.0 |
| clpC1 | 4039949 | c.756G>C | synonymous_variant | 1.0 |
| clpC1 | 4039952 | c.753T>C | synonymous_variant | 1.0 |
| clpC1 | 4039958 | c.747G>C | synonymous_variant | 1.0 |
| clpC1 | 4039988 | c.717C>G | synonymous_variant | 1.0 |
| clpC1 | 4039991 | c.714G>T | synonymous_variant | 1.0 |
| clpC1 | 4039994 | p.Glu237Asn | missense_variant | 1.0 |
| clpC1 | 4040001 | p.His235Ser | missense_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>C | synonymous_variant | 1.0 |
| clpC1 | 4040024 | c.681A>G | synonymous_variant | 1.0 |
| clpC1 | 4040027 | c.678C>G | synonymous_variant | 1.0 |
| clpC1 | 4040033 | c.672G>C | synonymous_variant | 1.0 |
| clpC1 | 4040036 | c.669C>G | synonymous_variant | 1.0 |
| clpC1 | 4040051 | c.654C>G | synonymous_variant | 1.0 |
| clpC1 | 4040069 | c.636G>C | synonymous_variant | 1.0 |
| clpC1 | 4040087 | c.618G>C | synonymous_variant | 1.0 |
| clpC1 | 4040090 | c.615T>G | synonymous_variant | 1.0 |
| clpC1 | 4040105 | c.600C>G | synonymous_variant | 1.0 |
| clpC1 | 4040117 | c.588A>G | synonymous_variant | 1.0 |
| clpC1 | 4040135 | c.570C>G | synonymous_variant | 1.0 |
| clpC1 | 4040267 | c.438A>G | synonymous_variant | 1.0 |
| clpC1 | 4040273 | c.432T>A | synonymous_variant | 1.0 |
| clpC1 | 4040279 | c.426C>G | synonymous_variant | 1.0 |
| clpC1 | 4040300 | c.405C>T | synonymous_variant | 1.0 |
| clpC1 | 4040306 | p.Arg133Ser | missense_variant | 1.0 |
| clpC1 | 4040310 | p.Thr132Asn | missense_variant | 1.0 |
| clpC1 | 4040315 | p.Glu130Asp | missense_variant | 1.0 |
| clpC1 | 4040330 | c.375C>G | synonymous_variant | 1.0 |
| clpC1 | 4040336 | c.369G>C | synonymous_variant | 1.0 |
| clpC1 | 4040348 | c.357G>C | synonymous_variant | 1.0 |
| clpC1 | 4040354 | c.351A>G | synonymous_variant | 1.0 |
| clpC1 | 4040408 | c.297C>T | synonymous_variant | 1.0 |
| clpC1 | 4040411 | c.294T>C | synonymous_variant | 1.0 |
| clpC1 | 4040426 | c.279T>C | synonymous_variant | 1.0 |
| clpC1 | 4040431 | c.274T>C | synonymous_variant | 1.0 |
| clpC1 | 4040441 | c.264C>G | synonymous_variant | 1.0 |
| clpC1 | 4040444 | c.261C>G | synonymous_variant | 1.0 |
| clpC1 | 4040450 | c.255A>G | synonymous_variant | 1.0 |
| clpC1 | 4040459 | c.246C>G | synonymous_variant | 1.0 |
| clpC1 | 4040462 | c.243C>T | synonymous_variant | 1.0 |
| clpC1 | 4040465 | c.240T>C | synonymous_variant | 1.0 |
| clpC1 | 4040471 | c.234T>C | synonymous_variant | 1.0 |
| clpC1 | 4040480 | c.225T>C | synonymous_variant | 1.0 |
| clpC1 | 4040501 | c.204C>G | synonymous_variant | 1.0 |
| clpC1 | 4040516 | c.189C>G | synonymous_variant | 1.0 |
| clpC1 | 4040522 | c.183T>C | synonymous_variant | 1.0 |
| clpC1 | 4040531 | p.Gly58Ala | missense_variant | 1.0 |
| clpC1 | 4040537 | c.168G>C | synonymous_variant | 1.0 |
| clpC1 | 4040546 | c.159G>C | synonymous_variant | 1.0 |
| clpC1 | 4040551 | c.154T>C | synonymous_variant | 1.0 |
| clpC1 | 4040561 | c.144A>G | synonymous_variant | 1.0 |
| clpC1 | 4040606 | c.99T>C | synonymous_variant | 1.0 |
| clpC1 | 4040633 | c.72C>T | synonymous_variant | 1.0 |
| clpC1 | 4040644 | c.61A>C | synonymous_variant | 0.67 |
| clpC1 | 4040645 | c.60C>A | synonymous_variant | 0.67 |
| clpC1 | 4040648 | c.57G>A | synonymous_variant | 0.67 |
| clpC1 | 4040654 | c.51G>A | synonymous_variant | 0.67 |
| clpC1 | 4040657 | c.48T>G | synonymous_variant | 0.67 |
| clpC1 | 4040674 | c.31A>C | synonymous_variant | 0.67 |
| clpC1 | 4040678 | c.27C>G | synonymous_variant | 0.67 |
| clpC1 | 4040690 | c.15T>C | synonymous_variant | 0.67 |
| clpC1 | 4040693 | c.12A>G | synonymous_variant | 0.67 |
