Run ID: SRR1184308
Sample name:
Date: 03-04-2023 05:18:08
Number of reads: 73137
Percentage reads mapped: 3.02
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 | 6323 | p.Val362Leu | missense_variant | 0.75 |
| gyrB | 6326 | p.Ser363Gly | missense_variant | 0.75 |
| gyrA | 6331 | c.-971A>G | upstream_gene_variant | 0.75 |
| gyrA | 6352 | c.-950C>G | upstream_gene_variant | 0.75 |
| gyrA | 6362 | c.-940T>C | upstream_gene_variant | 1.0 |
| gyrA | 6373 | c.-929C>G | upstream_gene_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>C | synonymous_variant | 1.0 |
| rpoB | 760997 | c.1191G>C | synonymous_variant | 1.0 |
| rpoB | 761015 | c.1209G>C | synonymous_variant | 1.0 |
| rpoB | 761027 | c.1221A>G | synonymous_variant | 1.0 |
| rpoB | 761036 | c.1230G>C | synonymous_variant | 1.0 |
| rpoB | 761037 | c.1231T>C | synonymous_variant | 1.0 |
| rpoB | 761057 | c.1251G>C | synonymous_variant | 1.0 |
| rpoB | 761064 | p.Ala420Ser | missense_variant | 1.0 |
| rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 1.0 |
| rpoB | 761102 | c.1296A>G | synonymous_variant | 1.0 |
| rpoB | 761132 | c.1326G>T | synonymous_variant | 1.0 |
| rpoB | 761133 | c.1327_1329delTTGinsCTC | synonymous_variant | 1.0 |
| rpoB | 761150 | c.1344A>C | synonymous_variant | 1.0 |
| rpoB | 761159 | c.1353G>T | synonymous_variant | 1.0 |
| rpoB | 761162 | c.1356G>C | synonymous_variant | 1.0 |
| rpoB | 761165 | c.1359G>C | synonymous_variant | 1.0 |
| rpoB | 761168 | c.1362C>G | synonymous_variant | 1.0 |
| rpoB | 761171 | c.1365C>T | synonymous_variant | 1.0 |
| rpoB | 761177 | c.1371G>C | synonymous_variant | 1.0 |
| rpoB | 761180 | c.1374A>C | synonymous_variant | 1.0 |
| rpoB | 761189 | c.1383T>G | synonymous_variant | 1.0 |
| rpoB | 761195 | c.1389G>C | synonymous_variant | 1.0 |
| rpoB | 761196 | p.Leu464Phe | missense_variant | 1.0 |
| rpoB | 761207 | c.1401C>A | synonymous_variant | 1.0 |
| rpoB | 761222 | c.1416G>C | synonymous_variant | 1.0 |
| rpoB | 761231 | c.1425C>A | synonymous_variant | 1.0 |
| rpoB | 761234 | c.1428G>C | synonymous_variant | 1.0 |
| rpoB | 761249 | c.1443A>G | synonymous_variant | 1.0 |
| rpoB | 761516 | c.1710G>C | synonymous_variant | 1.0 |
| rpoB | 761537 | c.1731C>G | synonymous_variant | 1.0 |
| rpoB | 761552 | c.1746G>C | synonymous_variant | 1.0 |
| rpoB | 761555 | c.1749G>C | synonymous_variant | 1.0 |
| rpoB | 761570 | c.1764T>C | synonymous_variant | 1.0 |
| rpoB | 761612 | c.1806G>C | synonymous_variant | 1.0 |
| rpoB | 761615 | c.1809A>G | synonymous_variant | 1.0 |
| rpoB | 761622 | p.Gln606Met | missense_variant | 1.0 |
| rpoB | 761627 | c.1821C>G | synonymous_variant | 1.0 |
| rpoB | 761642 | c.1836_1837insATCAA | frameshift_variant | 1.0 |
| rpoB | 761645 | c.1842_1846delTAGCG | frameshift_variant | 1.0 |
| rpoB | 761666 | c.1860G>C | synonymous_variant | 1.0 |
| rpoB | 761675 | c.1869G>C | synonymous_variant | 1.0 |
| rpoB | 761972 | c.2166C>T | synonymous_variant | 1.0 |
| rpoB | 762002 | c.2196C>G | synonymous_variant | 1.0 |
| rpoB | 762003 | p.Asn733Gln | missense_variant | 1.0 |
| rpoB | 762011 | c.2205G>C | synonymous_variant | 1.0 |
| rpoB | 762014 | c.2208C>G | synonymous_variant | 1.0 |
| rpoB | 762015 | p.Glu737Gln | missense_variant | 1.0 |
| rpoB | 762020 | p.Glu738Asp | missense_variant | 1.0 |
| rpoB | 762026 | c.2220G>C | synonymous_variant | 1.0 |
| rpoB | 762030 | p.Thr742Ser | missense_variant | 1.0 |
| rpoB | 762053 | c.2247T>C | synonymous_variant | 1.0 |
| rpoB | 762057 | p.Ile751Val | missense_variant | 1.0 |
| rpoB | 762062 | c.2256T>C | synonymous_variant | 1.0 |
| rpoB | 762065 | c.2259T>C | synonymous_variant | 1.0 |
| rpoB | 762068 | c.2262C>T | synonymous_variant | 1.0 |
| rpoB | 762080 | c.2274G>C | synonymous_variant | 1.0 |
| rpoB | 762083 | c.2277T>C | synonymous_variant | 1.0 |
| rpoB | 762084 | p.Ala760Pro | missense_variant | 1.0 |
| rpoB | 762101 | c.2295C>G | synonymous_variant | 1.0 |
| rpoB | 762114 | p.Ile770Val | missense_variant | 1.0 |
| rpoB | 762122 | p.Asp772Glu | missense_variant | 1.0 |
| rpoB | 762128 | c.2322G>C | synonymous_variant | 1.0 |
| rpoB | 762140 | c.2334G>C | synonymous_variant | 1.0 |
| rpoB | 762143 | c.2337T>C | synonymous_variant | 1.0 |
| rpoB | 762149 | c.2343G>C | synonymous_variant | 1.0 |
| rpoB | 762156 | p.Val784Ile | missense_variant | 1.0 |
| rpoB | 762161 | c.2355C>T | synonymous_variant | 1.0 |
| rpoB | 762175 | c.2369_2370insCG | frameshift_variant | 1.0 |
| rpoB | 762179 | c.2374_2375delGA | frameshift_variant | 1.0 |
| rpoB | 762185 | c.2379G>T | synonymous_variant | 1.0 |
| rpoB | 762194 | c.2388G>C | synonymous_variant | 1.0 |
| rpoB | 762209 | c.2403C>G | synonymous_variant | 1.0 |
| rpoB | 762212 | c.2406G>C | synonymous_variant | 1.0 |
| rpoB | 762233 | c.2427G>C | synonymous_variant | 1.0 |
| rpoB | 762236 | c.2430G>C | synonymous_variant | 1.0 |
| rpoB | 762245 | c.2439G>C | synonymous_variant | 1.0 |
| rpoB | 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 | 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 |
| rpoC | 762443 | c.-927G>C | upstream_gene_variant | 1.0 |
| rpoC | 762452 | c.-918G>T | upstream_gene_variant | 1.0 |
| rpoC | 762470 | c.-900G>C | upstream_gene_variant | 1.0 |
| rpoB | 762474 | p.Gly890Ser | missense_variant | 1.0 |
| rpoB | 762489 | p.Val895Ile | missense_variant | 1.0 |
| rpoC | 762509 | c.-861T>G | upstream_gene_variant | 1.0 |
| rpoB | 762511 | p.Ala902Glu | missense_variant | 1.0 |
| rpoC | 762863 | c.-507T>C | upstream_gene_variant | 1.0 |
| rpoB | 762868 | p.Tyr1021Phe | missense_variant | 0.75 |
| rpoB | 762879 | p.Met1025Leu | missense_variant | 0.89 |
| rpoC | 762899 | c.-471G>C | upstream_gene_variant | 1.0 |
| rpoB | 762909 | p.Ile1035Leu | missense_variant | 0.96 |
| rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.96 |
| rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.96 |
| rpoC | 762929 | c.-441G>C | upstream_gene_variant | 1.0 |
| rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.96 |
| rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.93 |
| rpoC | 762989 | c.-381G>C | upstream_gene_variant | 1.0 |
| rpoC | 762995 | c.-375G>T | upstream_gene_variant | 1.0 |
| rpoC | 763094 | c.-276G>C | upstream_gene_variant | 1.0 |
| rpoC | 763103 | c.-267G>C | upstream_gene_variant | 1.0 |
| rpoC | 763115 | c.-255T>C | upstream_gene_variant | 1.0 |
| rpoC | 763127 | c.-243G>C | upstream_gene_variant | 1.0 |
| rpoC | 763133 | c.-237G>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>C | upstream_gene_variant | 1.0 |
| rpoB | 763161 | p.Leu1119Ile | missense_variant | 1.0 |
| rpoC | 763166 | c.-204A>G | upstream_gene_variant | 1.0 |
| rpoB | 763170 | p.Leu1122Met | missense_variant | 1.0 |
| rpoC | 763181 | c.-189G>C | upstream_gene_variant | 1.0 |
| rpoC | 763193 | c.-177C>G | upstream_gene_variant | 1.0 |
| rpoC | 763444 | c.75T>C | synonymous_variant | 1.0 |
| rpoC | 763450 | c.81G>A | 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>C | synonymous_variant | 1.0 |
| rpoC | 763492 | c.123G>C | synonymous_variant | 1.0 |
| rpoC | 763504 | c.135C>A | synonymous_variant | 1.0 |
| rpoC | 763507 | c.138G>C | synonymous_variant | 1.0 |
| rpoC | 763528 | c.159G>T | synonymous_variant | 1.0 |
| rpoC | 763534 | c.165T>C | synonymous_variant | 1.0 |
| rpoC | 763537 | c.168C>G | synonymous_variant | 1.0 |
| rpoC | 763546 | c.177A>G | synonymous_variant | 1.0 |
| rpoC | 763570 | c.201G>T | synonymous_variant | 1.0 |
| rpoC | 763573 | c.204G>C | synonymous_variant | 1.0 |
| rpoC | 763615 | c.246G>C | synonymous_variant | 1.0 |
| rpoC | 763618 | c.249C>T | synonymous_variant | 1.0 |
| rpoC | 763666 | c.297G>T | synonymous_variant | 1.0 |
| rpoC | 763669 | c.300C>T | synonymous_variant | 1.0 |
| rpoC | 763696 | c.327T>C | synonymous_variant | 1.0 |
| rpoC | 763699 | c.330G>T | synonymous_variant | 1.0 |
| rpoC | 763708 | c.339G>C | synonymous_variant | 1.0 |
| rpoC | 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 | 763729 | c.360G>C | synonymous_variant | 1.0 |
| rpoC | 763732 | c.363C>G | synonymous_variant | 1.0 |
| rpoC | 763747 | c.378G>A | synonymous_variant | 1.0 |
| rpoC | 763751 | p.Ile128Val | missense_variant | 1.0 |
| rpoC | 763765 | c.396T>C | synonymous_variant | 1.0 |
| rpoC | 763768 | c.399C>G | synonymous_variant | 1.0 |
| rpoC | 764338 | p.Glu323Asp | missense_variant | 1.0 |
| rpoC | 764344 | c.975C>T | synonymous_variant | 1.0 |
| rpoC | 764359 | c.990C>G | synonymous_variant | 1.0 |
| rpoC | 764365 | c.996C>T | synonymous_variant | 1.0 |
| rpoC | 764371 | c.1002G>C | synonymous_variant | 1.0 |
| rpoC | 764377 | c.1008C>G | synonymous_variant | 1.0 |
| rpoC | 764380 | c.1011G>C | synonymous_variant | 1.0 |
| rpoC | 764387 | c.1018T>C | synonymous_variant | 1.0 |
| rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 1.0 |
| rpoC | 764428 | c.1059G>C | synonymous_variant | 1.0 |
| rpoC | 764434 | c.1065A>G | synonymous_variant | 1.0 |
| rpoC | 764435 | c.1066_1068delAGGinsCGC | synonymous_variant | 1.0 |
| rpoC | 764440 | c.1071G>C | synonymous_variant | 1.0 |
| rpoC | 764441 | p.Ile358Leu | missense_variant | 1.0 |
| rpoC | 764446 | c.1077T>C | synonymous_variant | 1.0 |
| rpoC | 764449 | c.1080G>C | synonymous_variant | 1.0 |
| rpoC | 764458 | c.1089G>C | synonymous_variant | 1.0 |
| rpoC | 764461 | c.1092A>G | synonymous_variant | 1.0 |
| rpoC | 764470 | c.1101C>G | synonymous_variant | 1.0 |
| rpoC | 764485 | c.1116G>C | synonymous_variant | 1.0 |
| rpoC | 764491 | c.1122G>C | synonymous_variant | 1.0 |
| rpoC | 764497 | c.1128A>G | synonymous_variant | 1.0 |
| rpoC | 764498 | p.Ser377Ala | missense_variant | 1.0 |
| rpoC | 764503 | c.1134G>C | synonymous_variant | 1.0 |
| rpoC | 764521 | c.1152T>C | synonymous_variant | 1.0 |
| rpoC | 764533 | c.1164C>T | synonymous_variant | 1.0 |
| rpoC | 764536 | c.1167G>T | synonymous_variant | 1.0 |
| rpoC | 764539 | c.1170C>G | synonymous_variant | 1.0 |
| rpoC | 764548 | c.1179G>T | synonymous_variant | 1.0 |
| rpoC | 764551 | c.1182G>C | synonymous_variant | 1.0 |
| rpoC | 764563 | c.1194G>C | synonymous_variant | 1.0 |
| rpoC | 764566 | c.1197C>G | synonymous_variant | 1.0 |
| rpoC | 764572 | c.1203G>C | synonymous_variant | 1.0 |
| rpoC | 764575 | c.1206T>G | synonymous_variant | 1.0 |
| rpoC | 764576 | c.1207_1208delTCinsAG | synonymous_variant | 1.0 |
| rpoC | 764581 | c.1212T>C | synonymous_variant | 1.0 |
| rpoC | 764582 | p.Leu405Met | missense_variant | 1.0 |
| rpoC | 764605 | c.1236G>C | synonymous_variant | 1.0 |
| rpoC | 764611 | c.1242G>T | synonymous_variant | 1.0 |
| rpoC | 764614 | c.1245G>A | synonymous_variant | 1.0 |
| rpoC | 764620 | c.1251G>C | synonymous_variant | 1.0 |
| rpoC | 764632 | c.1263T>C | synonymous_variant | 1.0 |
| rpoC | 764635 | c.1266C>G | synonymous_variant | 1.0 |
| rpoC | 764644 | c.1275G>C | synonymous_variant | 1.0 |
| rpoC | 764646 | p.Gly426Ala | missense_variant | 1.0 |
| rpoC | 764650 | c.1281G>T | synonymous_variant | 1.0 |
| rpoC | 764653 | c.1284G>C | synonymous_variant | 1.0 |
| rpoC | 764656 | c.1287C>G | synonymous_variant | 1.0 |
| rpoC | 764662 | c.1293G>C | synonymous_variant | 1.0 |
| rpoC | 764668 | c.1299C>T | synonymous_variant | 1.0 |
| rpoC | 764701 | c.1332C>G | synonymous_variant | 1.0 |
| rpoC | 764705 | p.Leu446Ala | missense_variant | 1.0 |
| rpoC | 764722 | c.1353G>C | synonymous_variant | 1.0 |
| rpoC | 764746 | c.1377G>C | synonymous_variant | 1.0 |
| rpoC | 764758 | c.1389C>G | synonymous_variant | 1.0 |
| rpoC | 764764 | c.1395T>C | synonymous_variant | 1.0 |
| rpoC | 764780 | c.1411_1413delAGCinsTCG | synonymous_variant | 1.0 |
| rpoC | 764797 | c.1428G>C | synonymous_variant | 1.0 |
| rpoC | 764968 | c.1599T>C | synonymous_variant | 1.0 |
| rpoC | 764971 | c.1602C>G | synonymous_variant | 1.0 |
| rpoC | 765007 | c.1638T>G | synonymous_variant | 1.0 |
| rpoC | 765008 | c.1639_1641delTTGinsCTC | synonymous_variant | 1.0 |
| rpoC | 765011 | c.1642_1643delAGinsTC | synonymous_variant | 1.0 |
| rpoC | 765016 | c.1647C>G | synonymous_variant | 1.0 |
| rpoC | 765019 | c.1650A>G | synonymous_variant | 1.0 |
| rpoC | 765034 | c.1665T>C | synonymous_variant | 1.0 |
| rpoC | 765040 | c.1671T>C | synonymous_variant | 1.0 |
| rpoC | 765041 | c.1672T>C | synonymous_variant | 1.0 |
| rpoC | 765047 | c.1678T>C | synonymous_variant | 1.0 |
| rpoC | 765055 | c.1686C>G | synonymous_variant | 1.0 |
| rpoC | 766309 | c.2940G>A | synonymous_variant | 0.5 |
| rpoC | 766315 | c.2946C>G | synonymous_variant | 0.5 |
| rpoC | 766316 | p.Met983Leu | missense_variant | 0.5 |
| rpoC | 766348 | c.2979A>G | synonymous_variant | 0.67 |
| rpoC | 766351 | c.2982C>G | synonymous_variant | 0.67 |
| rpoC | 766361 | p.Val998Ile | missense_variant | 0.67 |
| rpoC | 766381 | c.3012C>T | synonymous_variant | 0.75 |
| rpoC | 766384 | c.3015A>G | synonymous_variant | 0.75 |
| rpoC | 766390 | c.3021C>T | synonymous_variant | 1.0 |
| rpoC | 766402 | c.3033C>G | synonymous_variant | 1.0 |
| rpoC | 766964 | p.Glu1199His | missense_variant | 1.0 |
| rpoC | 766972 | c.3603G>C | synonymous_variant | 1.0 |
| rpoC | 766973 | p.Ala1202Ser | missense_variant | 1.0 |
| rpoC | 766985 | p.Val1206Gln | missense_variant | 1.0 |
| rpoC | 766996 | c.3627C>T | synonymous_variant | 1.0 |
| rpoC | 767008 | c.3639G>C | synonymous_variant | 1.0 |
| rpoC | 767014 | c.3645G>C | synonymous_variant | 1.0 |
| rpoC | 767023 | p.Asp1218Glu | missense_variant | 1.0 |
| rpoC | 767044 | c.3675G>C | synonymous_variant | 1.0 |
| rpoC | 767056 | c.3687C>G | synonymous_variant | 0.67 |
| 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 | 781766 | c.207C>T | synonymous_variant | 1.0 |
| rpsL | 781772 | c.213C>A | synonymous_variant | 1.0 |
| rpsL | 781793 | c.234G>C | synonymous_variant | 1.0 |
| rpsL | 781796 | p.Met79Ile | missense_variant | 1.0 |
| rpsL | 781802 | c.243G>C | synonymous_variant | 1.0 |
| rpsL | 781808 | c.249C>T | synonymous_variant | 1.0 |
| rpsL | 781811 | c.252C>T | synonymous_variant | 1.0 |
| rpsL | 781817 | c.258G>T | synonymous_variant | 1.0 |
| rpsL | 781832 | c.273T>G | synonymous_variant | 1.0 |
| rpsL | 781838 | c.279G>T | synonymous_variant | 1.0 |
| rpsL | 781841 | c.282C>T | synonymous_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 | 781892 | c.333A>G | synonymous_variant | 1.0 |
| rpsL | 781898 | c.339A>C | synonymous_variant | 1.0 |
| rpsL | 781907 | c.348T>C | synonymous_variant | 1.0 |
| rpsL | 781916 | c.357T>C | synonymous_variant | 1.0 |
| rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.88 |
| rplC | 800615 | c.-194G>C | upstream_gene_variant | 0.88 |
| rplC | 800633 | c.-176T>C | upstream_gene_variant | 0.89 |
| rplC | 800643 | c.-166_-164delCGCinsAAG | upstream_gene_variant | 1.0 |
| rplC | 800648 | c.-161A>G | upstream_gene_variant | 1.0 |
| rplC | 800654 | c.-155T>C | upstream_gene_variant | 1.0 |
| rplC | 800669 | c.-140G>T | upstream_gene_variant | 1.0 |
| rplC | 800672 | c.-137G>C | upstream_gene_variant | 1.0 |
| rplC | 800693 | c.-116A>C | upstream_gene_variant | 1.0 |
| rplC | 800702 | c.-107G>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 | 800735 | c.-74C>G | upstream_gene_variant | 1.0 |
| rplC | 800742 | c.-67G>T | upstream_gene_variant | 1.0 |
| rplC | 800747 | c.-62C>G | upstream_gene_variant | 1.0 |
| rplC | 800753 | c.-56C>T | upstream_gene_variant | 1.0 |
| rplC | 800754 | c.-55A>C | upstream_gene_variant | 1.0 |
| rplC | 800762 | c.-47T>C | upstream_gene_variant | 1.0 |
| rplC | 800769 | c.-40A>G | upstream_gene_variant | 1.0 |
| rrs | 1471969 | n.124T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471980 | n.135G>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 | 1471991 | n.146T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471997 | n.152T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471998 | n.153G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472005 | n.160T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472068 | n.223T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472069 | n.224G>A | 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 | 1472148 | n.303T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472338 | n.493A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472425 | n.580T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472431 | n.586G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.91 |
| rrs | 1472507 | n.662C>T | non_coding_transcript_exon_variant | 0.96 |
| rrs | 1472508 | n.663T>C | non_coding_transcript_exon_variant | 0.97 |
| rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472571 | n.726G>A | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472582 | n.737G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472660 | n.815T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472690 | n.845C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472714 | n.869A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472779 | n.934G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472793 | n.948A>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472803 | n.958T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473026 | n.1181T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473062 | n.1217T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473068 | n.1223A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473089 | n.1244A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473091 | n.1246G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473109 | n.1264T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473120 | n.1275C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473122 | n.1277T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473179 | n.1334C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473201 | n.1356A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473202 | n.1357C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473283 | n.1438T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473391 | n.-267C>T | upstream_gene_variant | 1.0 |
| rrl | 1473666 | n.9G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473668 | n.11C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473679 | n.22T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473696 | n.39T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473698 | n.41G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473699 | n.42A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473702 | n.45G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473724 | n.67T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473725 | n.68G>A | 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 | 1473735 | n.78T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473752 | n.95G>A | 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 | 1473765 | n.108A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473768 | n.111A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473870 | n.213G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473871 | n.214T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473887 | n.230T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473888 | n.231T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473898 | n.241C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474133 | n.476T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474135 | n.478G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474141 | n.485delC | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474153 | n.496C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474166 | n.509G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474179 | n.522C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474186 | n.529A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1474232 | n.575C>G | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1474239 | n.582G>C | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1474275 | n.618T>G | non_coding_transcript_exon_variant | 0.86 |
| rrl | 1474280 | n.623C>G | non_coding_transcript_exon_variant | 0.8 |
| rrl | 1474281 | n.624A>G | non_coding_transcript_exon_variant | 0.8 |
| rrl | 1474316 | n.659T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474317 | n.660G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474351 | n.694G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474354 | n.697C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474355 | n.698A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474359 | n.702C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474381 | n.724T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474402 | n.745T>C | non_coding_transcript_exon_variant | 0.95 |
| rrl | 1474406 | n.749T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474413 | n.756A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474483 | n.826C>G | non_coding_transcript_exon_variant | 0.8 |
| rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.8 |
| rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 0.8 |
| rrl | 1474497 | n.840G>A | non_coding_transcript_exon_variant | 0.8 |
| rrl | 1474506 | n.849C>T | non_coding_transcript_exon_variant | 0.8 |
| rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.8 |
| rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.8 |
| rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 0.75 |
| rrl | 1474528 | n.871T>A | non_coding_transcript_exon_variant | 0.75 |
| rrl | 1474529 | n.872A>G | non_coding_transcript_exon_variant | 0.75 |
| rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.75 |
| rrl | 1474540 | n.883T>C | non_coding_transcript_exon_variant | 0.75 |
| rrl | 1474541 | n.884G>T | non_coding_transcript_exon_variant | 0.67 |
| rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 0.75 |
| rrl | 1474551 | n.894G>C | non_coding_transcript_exon_variant | 0.75 |
| rrl | 1474558 | n.901G>T | non_coding_transcript_exon_variant | 0.8 |
| rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474628 | n.971C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474651 | n.995delT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474660 | n.1003G>A | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1474662 | n.1005C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474676 | n.1019T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474688 | n.1031G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474690 | n.1033C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474709 | n.1053_1056delTGGT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474717 | n.1060_1061insGTGAG | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474722 | n.1065T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474751 | n.1094G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474777 | n.1120T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474783 | n.1126G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474801 | n.1144G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474802 | n.1145T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474933 | n.1276A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474934 | n.1277C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474945 | n.1288C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475175 | n.1518G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475486 | n.1829A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475499 | n.1842C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475508 | n.1851A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475532 | n.1875A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475542 | n.1885A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475544 | n.1887A>T | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475649 | n.1992A>G | non_coding_transcript_exon_variant | 0.98 |
| rrl | 1475655 | n.1998T>C | non_coding_transcript_exon_variant | 0.98 |
| rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1475696 | n.2039T>C | non_coding_transcript_exon_variant | 0.98 |
| rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.98 |
| rrl | 1475703 | n.2046A>G | non_coding_transcript_exon_variant | 0.98 |
| rrl | 1475740 | n.2083G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475747 | n.2090A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475758 | n.2101A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475781 | n.2124T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475788 | n.2131C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475883 | n.2226A>G | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475902 | n.2245T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475982 | n.2325G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.97 |
| rrl | 1476032 | n.2375C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476033 | n.2376T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476046 | n.2389G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476058 | n.2401T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476076 | n.2419A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476081 | n.2424A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476126 | n.2469C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476130 | n.2473G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476165 | n.2508T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 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>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476255 | n.2598A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476297 | n.2640C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476298 | n.2641C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476300 | n.2643G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476529 | n.2872A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476530 | n.2873C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 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 | 0.99 |
| rrl | 1476596 | n.2939C>T | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476601 | n.2944G>A | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476661 | n.3004A>G | non_coding_transcript_exon_variant | 0.94 |
| rrl | 1476665 | n.3008T>G | non_coding_transcript_exon_variant | 0.88 |
| rpsA | 1833646 | c.105T>C | synonymous_variant | 1.0 |
| rpsA | 1833658 | c.117C>T | synonymous_variant | 1.0 |
| rpsA | 1833661 | p.Glu40Asp | missense_variant | 1.0 |
| rpsA | 1833664 | c.123C>T | synonymous_variant | 1.0 |
| rpsA | 1833665 | p.Thr42Val | missense_variant | 1.0 |
| rpsA | 1833676 | c.135A>G | synonymous_variant | 1.0 |
| rpsA | 1833679 | c.138G>T | synonymous_variant | 1.0 |
| rpsA | 1833694 | c.153G>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 | 1833769 | c.228C>G | synonymous_variant | 1.0 |
| rpsA | 1833862 | c.321G>T | synonymous_variant | 1.0 |
| rpsA | 1833893 | p.Ala118Lys | missense_variant | 1.0 |
| rpsA | 1833896 | p.Leu119Ile | missense_variant | 1.0 |
| rpsA | 1833904 | c.363G>A | synonymous_variant | 1.0 |
| rpsA | 1833905 | p.Lys122Glu | missense_variant | 1.0 |
| rpsA | 1833910 | c.371_372delAG | frameshift_variant | 1.0 |
| rpsA | 1833915 | c.374_375insAT | frameshift_variant | 1.0 |
| rpsA | 1833921 | p.Lys127Thr | missense_variant | 1.0 |
| rpsA | 1833925 | c.384C>T | synonymous_variant | 1.0 |
| rpsA | 1833928 | c.387G>C | synonymous_variant | 1.0 |
| rpsA | 1833952 | c.411C>T | synonymous_variant | 1.0 |
| rpsA | 1833955 | c.414G>C | synonymous_variant | 1.0 |
| rpsA | 1833970 | c.429G>C | synonymous_variant | 1.0 |
| rpsA | 1833973 | c.432G>C | 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 | 1833997 | c.456G>C | 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>T | synonymous_variant | 1.0 |
| rpsA | 1834015 | c.474G>C | synonymous_variant | 1.0 |
| rpsA | 1834024 | c.483G>C | synonymous_variant | 1.0 |
| rpsA | 1834034 | p.Ile165Val | missense_variant | 1.0 |
| rpsA | 1834046 | p.Ile169Leu | missense_variant | 1.0 |
| rpsA | 1834054 | c.513C>G | synonymous_variant | 1.0 |
| rpsA | 1834093 | c.552G>C | synonymous_variant | 1.0 |
| rpsA | 1834102 | c.561T>C | synonymous_variant | 1.0 |
| rpsA | 1834114 | c.573G>C | synonymous_variant | 1.0 |
| rpsA | 1834189 | c.648G>C | synonymous_variant | 1.0 |
| rpsA | 1834210 | c.669C>T | synonymous_variant | 1.0 |
| rpsA | 1834213 | c.672G>C | synonymous_variant | 1.0 |
| rpsA | 1834219 | c.678C>G | synonymous_variant | 1.0 |
| rpsA | 1834225 | c.684C>G | synonymous_variant | 1.0 |
| rpsA | 1834231 | c.690T>C | synonymous_variant | 1.0 |
| rpsA | 1834234 | c.693G>C | synonymous_variant | 1.0 |
| rpsA | 1834243 | c.702G>C | synonymous_variant | 1.0 |
| rpsA | 1834249 | c.708T>C | synonymous_variant | 1.0 |
| rpsA | 1834261 | c.720A>G | synonymous_variant | 1.0 |
| rpsA | 1834264 | c.723G>C | synonymous_variant | 1.0 |
| rpsA | 1834285 | c.744G>C | synonymous_variant | 1.0 |
| rpsA | 1834294 | c.753G>C | synonymous_variant | 1.0 |
| rpsA | 1834298 | p.Gln253Glu | missense_variant | 1.0 |
| rpsA | 1834303 | c.762T>C | synonymous_variant | 1.0 |
| rpsA | 1834307 | p.Asp256Gln | missense_variant | 1.0 |
| rpsA | 1834312 | c.771G>A | synonymous_variant | 1.0 |
| rpsA | 1834327 | c.786G>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 | 1834360 | c.819G>C | synonymous_variant | 1.0 |
| rpsA | 1834361 | c.820T>C | synonymous_variant | 1.0 |
| rpsA | 1834366 | c.825A>G | synonymous_variant | 1.0 |
| rpsA | 1834378 | c.837T>G | synonymous_variant | 0.8 |
| rpsA | 1834395 | p.Arg285Gln | missense_variant | 0.83 |
| rpsA | 1834399 | p.His286Gln | missense_variant | 0.83 |
| rpsA | 1834411 | c.870T>G | synonymous_variant | 0.83 |
| rpsA | 1834415 | p.Ala292Gln | missense_variant | 0.83 |
| rpsA | 1834423 | c.882G>T | synonymous_variant | 0.83 |
| rpsA | 1834427 | p.Ile296Val | missense_variant | 1.0 |
| rpsA | 1834432 | c.891G>C | synonymous_variant | 1.0 |
| rpsA | 1834438 | c.897C>T | synonymous_variant | 1.0 |
| rpsA | 1834451 | c.910_912delTTGinsCTC | synonymous_variant | 1.0 |
| rpsA | 1834468 | c.927A>G | synonymous_variant | 1.0 |
| rpsA | 1834483 | p.Glu314Asp | missense_variant | 1.0 |
| rpsA | 1834489 | c.948T>C | synonymous_variant | 1.0 |
| rpsA | 1834498 | c.957C>T | synonymous_variant | 1.0 |
| rpsA | 1834504 | c.963G>C | synonymous_variant | 1.0 |
| rpsA | 1834528 | c.987T>C | synonymous_variant | 1.0 |
| rpsA | 1834534 | c.993C>G | synonymous_variant | 1.0 |
| folC | 2747007 | p.Ser198Cys | missense_variant | 1.0 |
| folC | 2747031 | p.Pro190Thr | missense_variant | 1.0 |
| folC | 2747032 | p.Ala189Ser | missense_variant | 1.0 |
| folC | 2747037 | p.Asn188Asp | missense_variant | 1.0 |
| folC | 2747059 | p.Arg180Thr | missense_variant | 1.0 |
| folC | 2747062 | c.537A>C | synonymous_variant | 1.0 |
| folC | 2747074 | c.525G>C | synonymous_variant | 1.0 |
| folC | 2747083 | c.516G>C | synonymous_variant | 1.0 |
| folC | 2747086 | c.513A>G | synonymous_variant | 1.0 |
| folC | 2747089 | c.510G>C | synonymous_variant | 1.0 |
| folC | 2747107 | c.492G>C | synonymous_variant | 1.0 |
| folC | 2747110 | c.489T>C | synonymous_variant | 1.0 |
| ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
| rpoA | 3877926 | p.Leu194Val | missense_variant | 1.0 |
| rpoA | 3877962 | c.546G>T | synonymous_variant | 0.86 |
| rpoA | 3877968 | c.540C>G | synonymous_variant | 0.83 |
| rpoA | 3877971 | p.Asp179Glu | missense_variant | 0.83 |
| rpoA | 3877974 | c.534G>C | synonymous_variant | 0.83 |
| rpoA | 3877983 | c.525C>G | synonymous_variant | 0.83 |
| rpoA | 3877986 | c.522G>C | synonymous_variant | 0.83 |
| rpoA | 3877989 | c.519A>G | synonymous_variant | 0.83 |
| rpoA | 3878001 | c.507A>G | synonymous_variant | 0.83 |
| rpoA | 3878013 | c.495T>C | synonymous_variant | 0.67 |
| 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 | 4038899 | c.1806C>G | synonymous_variant | 1.0 |
| clpC1 | 4038905 | c.1800A>T | synonymous_variant | 1.0 |
| clpC1 | 4038911 | c.1794G>C | synonymous_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>A | synonymous_variant | 1.0 |
| clpC1 | 4039100 | c.1605C>G | synonymous_variant | 1.0 |
| clpC1 | 4039106 | c.1599G>C | synonymous_variant | 1.0 |
| clpC1 | 4039112 | c.1593C>G | synonymous_variant | 1.0 |
| clpC1 | 4039117 | p.Lys530Gln | missense_variant | 1.0 |
| clpC1 | 4039118 | c.1587C>G | synonymous_variant | 1.0 |
| clpC1 | 4039123 | p.Val528Leu | missense_variant | 1.0 |
| clpC1 | 4039132 | p.Val525Ile | missense_variant | 1.0 |
| clpC1 | 4039418 | c.1287C>G | synonymous_variant | 1.0 |
| clpC1 | 4039430 | c.1275T>C | synonymous_variant | 1.0 |
| clpC1 | 4039442 | c.1263A>C | 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 | 4039481 | p.Ala408Ser | missense_variant | 1.0 |
| clpC1 | 4039484 | c.1221T>C | synonymous_variant | 1.0 |
| clpC1 | 4039487 | c.1218G>C | synonymous_variant | 1.0 |
| clpC1 | 4039517 | c.1188C>G | synonymous_variant | 1.0 |
| clpC1 | 4039526 | c.1179G>C | synonymous_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 | 4039647 | p.Glu353Pro | missense_variant | 1.0 |
| clpC1 | 4039651 | p.Val352Leu | missense_variant | 1.0 |
| clpC1 | 4039654 | p.Thr351Ser | missense_variant | 1.0 |
| clpC1 | 4039661 | p.Gly348Ala | missense_variant | 1.0 |
| clpC1 | 4039664 | c.1041G>C | synonymous_variant | 1.0 |
| clpC1 | 4039670 | p.Val345Ile | missense_variant | 1.0 |
| clpC1 | 4039682 | c.1023C>T | synonymous_variant | 1.0 |
| clpC1 | 4039694 | c.1011G>C | synonymous_variant | 1.0 |
| clpC1 | 4039697 | c.1008C>G | synonymous_variant | 1.0 |
| clpC1 | 4039709 | p.Ile332Leu | missense_variant | 1.0 |
| clpC1 | 4039714 | p.Tyr331His | missense_variant | 1.0 |
| clpC1 | 4039808 | c.897G>A | synonymous_variant | 1.0 |
| clpC1 | 4039817 | c.888A>C | synonymous_variant | 1.0 |
| clpC1 | 4039820 | c.885T>G | synonymous_variant | 1.0 |
| clpC1 | 4039831 | c.874T>C | synonymous_variant | 1.0 |
| clpC1 | 4039832 | c.873C>G | synonymous_variant | 1.0 |
| clpC1 | 4039850 | c.855T>C | synonymous_variant | 1.0 |
| clpC1 | 4039865 | c.840T>C | synonymous_variant | 1.0 |
| clpC1 | 4039875 | p.Asn277Arg | missense_variant | 1.0 |
| clpC1 | 4039889 | c.816G>C | synonymous_variant | 1.0 |
| clpC1 | 4039898 | c.807C>G | synonymous_variant | 1.0 |
| clpC1 | 4039967 | p.Gln246His | missense_variant | 1.0 |
| clpC1 | 4039982 | c.723G>C | synonymous_variant | 1.0 |
| clpC1 | 4040000 | p.His235Lys | missense_variant | 1.0 |
| clpC1 | 4040003 | c.702G>C | synonymous_variant | 1.0 |
| clpC1 | 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 | 4040036 | c.669C>G | synonymous_variant | 1.0 |
| clpC1 | 4040057 | c.648C>T | synonymous_variant | 1.0 |
| clpC1 | 4040063 | c.642G>C | synonymous_variant | 1.0 |
| clpC1 | 4040081 | c.624C>G | synonymous_variant | 1.0 |
| clpC1 | 4040084 | c.621C>G | synonymous_variant | 1.0 |
| clpC1 | 4040087 | c.618G>C | synonymous_variant | 1.0 |
| clpC1 | 4040090 | c.615T>C | synonymous_variant | 1.0 |
| clpC1 | 4040093 | c.612C>G | synonymous_variant | 1.0 |
| clpC1 | 4040117 | c.588A>G | synonymous_variant | 1.0 |
| clpC1 | 4040129 | c.576C>G | synonymous_variant | 1.0 |
| clpC1 | 4040144 | c.561G>C | synonymous_variant | 1.0 |
| clpC1 | 4040147 | c.558A>G | synonymous_variant | 1.0 |
