Run ID: SRR16156775
Sample name:
Date: 03-04-2023 16:39:52
Number of reads: 117604
Percentage reads mapped: 4.56
Strain: lineage4.9
Drug-resistance: Other
| 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 |
|---|---|---|---|---|---|
| gyrB | 6695 | p.Ile486Leu | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
| gyrB | 6738 | p.Thr500Asn | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
| rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 1.0 | streptomycin |
| Gene | Chromosome position | Mutation | Type | Estimated fraction |
|---|---|---|---|---|
| gyrA | 6700 | c.-602T>C | upstream_gene_variant | 1.0 |
| gyrA | 6712 | c.-590G>A | upstream_gene_variant | 1.0 |
| gyrB | 6718 | p.Ile493Met | missense_variant | 1.0 |
| gyrA | 6721 | c.-581C>T | upstream_gene_variant | 1.0 |
| gyrB | 6722 | p.Arg495Lys | missense_variant | 1.0 |
| gyrA | 6730 | c.-572A>G | upstream_gene_variant | 1.0 |
| gyrA | 6742 | c.-560A>G | upstream_gene_variant | 1.0 |
| gyrA | 6745 | c.-557T>C | upstream_gene_variant | 1.0 |
| gyrA | 6751 | c.-551G>C | upstream_gene_variant | 1.0 |
| gyrA | 6754 | c.-548C>T | upstream_gene_variant | 1.0 |
| gyrA | 6757 | c.-545C>T | upstream_gene_variant | 1.0 |
| gyrA | 6763 | c.-539G>C | upstream_gene_variant | 1.0 |
| gyrA | 6766 | c.-536G>T | upstream_gene_variant | 1.0 |
| gyrA | 6769 | c.-533C>T | upstream_gene_variant | 1.0 |
| gyrA | 6775 | c.-527G>T | upstream_gene_variant | 1.0 |
| gyrA | 6793 | c.-509T>C | upstream_gene_variant | 1.0 |
| gyrB | 6797 | p.Gly520Lys | missense_variant | 1.0 |
| gyrA | 6808 | c.-494C>T | upstream_gene_variant | 1.0 |
| gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
| rpoB | 761150 | c.1344A>C | synonymous_variant | 1.0 |
| rpoB | 761156 | c.1350G>T | synonymous_variant | 1.0 |
| rpoB | 761165 | c.1359G>T | synonymous_variant | 1.0 |
| rpoB | 761168 | c.1362C>G | synonymous_variant | 1.0 |
| rpoB | 761174 | c.1368T>C | synonymous_variant | 1.0 |
| rpoB | 761180 | c.1374A>C | synonymous_variant | 1.0 |
| rpoB | 761189 | c.1383T>C | synonymous_variant | 1.0 |
| rpoB | 761192 | c.1386C>T | synonymous_variant | 1.0 |
| rpoB | 761195 | c.1389G>C | synonymous_variant | 1.0 |
| rpoB | 761213 | c.1407G>T | synonymous_variant | 0.67 |
| rpoB | 761222 | c.1416G>T | synonymous_variant | 1.0 |
| rpoB | 761234 | c.1428G>C | synonymous_variant | 1.0 |
| rpoB | 761246 | c.1440C>T | synonymous_variant | 1.0 |
| rpoB | 761249 | c.1443A>G | synonymous_variant | 1.0 |
| rpoB | 761252 | c.1446C>T | synonymous_variant | 1.0 |
| rpoB | 761261 | c.1455G>T | synonymous_variant | 1.0 |
| rpoB | 761264 | c.1458C>G | synonymous_variant | 1.0 |
| rpoB | 761270 | c.1464C>T | synonymous_variant | 1.0 |
| rpoB | 761930 | c.2124G>A | synonymous_variant | 1.0 |
| rpoB | 761936 | c.2130C>T | synonymous_variant | 1.0 |
| rpoB | 761951 | c.2145G>T | synonymous_variant | 1.0 |
| rpoB | 761955 | p.Ile717Phe | missense_variant | 1.0 |
| rpoB | 761969 | c.2163G>A | synonymous_variant | 1.0 |
| rpoB | 761990 | c.2184G>C | synonymous_variant | 1.0 |
| rpoB | 762000 | p.Ser732Asn | missense_variant | 1.0 |
| rpoB | 762003 | p.Asn733Gln | missense_variant | 1.0 |
| rpoB | 762009 | p.Leu735Met | missense_variant | 1.0 |
| rpoB | 762014 | c.2208C>T | synonymous_variant | 1.0 |
| rpoB | 762017 | c.2211A>G | synonymous_variant | 1.0 |
| rpoB | 762026 | c.2220G>T | synonymous_variant | 1.0 |
| rpoB | 762029 | c.2223C>G | synonymous_variant | 1.0 |
| rpoB | 762051 | p.His749Tyr | missense_variant | 1.0 |
| rpoB | 762059 | c.2253C>T | synonymous_variant | 1.0 |
| rpoB | 762062 | c.2256T>C | synonymous_variant | 1.0 |
| rpoB | 762065 | c.2259T>C | synonymous_variant | 1.0 |
| rpoB | 762083 | c.2277T>C | synonymous_variant | 1.0 |
| rpoB | 762084 | p.Ala760Pro | missense_variant | 1.0 |
| rpoB | 762107 | c.2301C>T | synonymous_variant | 1.0 |
| rpoB | 762110 | c.2304G>T | synonymous_variant | 1.0 |
| rpoB | 762114 | p.Ile770Val | missense_variant | 1.0 |
| rpoB | 762117 | p.Ser771Gly | missense_variant | 1.0 |
| rpoB | 762122 | p.Asp772Glu | missense_variant | 1.0 |
| rpoB | 762125 | p.Glu773Asp | missense_variant | 1.0 |
| rpoB | 762128 | c.2322G>C | synonymous_variant | 1.0 |
| rpoB | 762131 | c.2325C>G | synonymous_variant | 1.0 |
| rpoB | 762134 | c.2328C>T | synonymous_variant | 1.0 |
| rpoB | 762143 | c.2337T>C | synonymous_variant | 1.0 |
| rpoB | 762146 | c.2340G>A | synonymous_variant | 1.0 |
| rpoB | 762149 | c.2343G>C | synonymous_variant | 1.0 |
| rpoB | 762152 | c.2346C>T | synonymous_variant | 1.0 |
| rpoB | 762158 | c.2352G>C | synonymous_variant | 1.0 |
| rpoB | 762167 | c.2361T>C | synonymous_variant | 1.0 |
| rpoB | 762170 | c.2364C>G | synonymous_variant | 1.0 |
| rpoB | 762173 | p.Glu789Asp | missense_variant | 0.94 |
| rpoB | 762176 | c.2370T>C | synonymous_variant | 1.0 |
| rpoB | 762185 | c.2379G>C | synonymous_variant | 1.0 |
| rpoB | 762200 | c.2394C>T | synonymous_variant | 1.0 |
| rpoB | 762221 | c.2415G>A | synonymous_variant | 1.0 |
| rpoB | 762233 | c.2427G>T | synonymous_variant | 1.0 |
| rpoB | 762239 | c.2433G>A | synonymous_variant | 1.0 |
| rpoB | 762245 | c.2439G>C | synonymous_variant | 1.0 |
| rpoB | 762254 | c.2448T>C | synonymous_variant | 1.0 |
| rpoB | 762284 | c.2478G>T | synonymous_variant | 1.0 |
| rpoB | 762290 | c.2484C>T | synonymous_variant | 1.0 |
| rpoB | 762293 | c.2487T>C | synonymous_variant | 1.0 |
| rpoB | 762296 | c.2490G>C | synonymous_variant | 1.0 |
| rpoB | 762297 | p.Leu831Met | missense_variant | 1.0 |
| rpoB | 762317 | c.2511A>G | synonymous_variant | 1.0 |
| rpoB | 762318 | p.Ser838Thr | missense_variant | 1.0 |
| rpoB | 762323 | c.2517C>T | synonymous_variant | 1.0 |
| rpoB | 762329 | c.2523G>C | synonymous_variant | 1.0 |
| rpoB | 762336 | p.Ile844Val | missense_variant | 1.0 |
| rpoB | 762341 | c.2535G>C | synonymous_variant | 1.0 |
| rpoB | 762347 | c.2541T>C | synonymous_variant | 1.0 |
| rpoB | 762353 | c.2547C>T | synonymous_variant | 1.0 |
| rpoB | 762359 | c.2553C>T | synonymous_variant | 1.0 |
| rpoB | 762362 | p.Glu852Asp | missense_variant | 1.0 |
| rpoB | 762832 | p.Ser1009Thr | missense_variant | 1.0 |
| rpoC | 762842 | c.-528G>C | upstream_gene_variant | 1.0 |
| rpoC | 762857 | c.-513C>T | upstream_gene_variant | 1.0 |
| rpoB | 762858 | p.Thr1018Ala | missense_variant | 1.0 |
| rpoC | 762863 | c.-507T>G | upstream_gene_variant | 1.0 |
| rpoB | 762878 | p.Ile1024Met | missense_variant | 1.0 |
| rpoB | 762879 | p.Met1025Leu | missense_variant | 1.0 |
| rpoC | 762899 | c.-471G>C | upstream_gene_variant | 1.0 |
| rpoB | 762905 | p.Asp1033Glu | missense_variant | 1.0 |
| rpoC | 762917 | c.-453C>T | upstream_gene_variant | 1.0 |
| rpoC | 762926 | c.-444C>T | upstream_gene_variant | 1.0 |
| rpoC | 762929 | c.-441G>T | upstream_gene_variant | 1.0 |
| rpoC | 762932 | c.-438G>T | upstream_gene_variant | 1.0 |
| rpoC | 762938 | c.-432G>C | upstream_gene_variant | 1.0 |
| rpoC | 762944 | c.-426C>T | upstream_gene_variant | 1.0 |
| rpoC | 762962 | c.-408C>T | upstream_gene_variant | 1.0 |
| rpoC | 762971 | c.-399G>A | upstream_gene_variant | 1.0 |
| rpoC | 762989 | c.-381G>C | upstream_gene_variant | 1.0 |
| rpoC | 762995 | c.-375G>T | upstream_gene_variant | 1.0 |
| rpoB | 763005 | p.Cys1067Val | missense_variant | 1.0 |
| rpoC | 763013 | c.-357C>A | upstream_gene_variant | 1.0 |
| rpoC | 763022 | c.-348C>A | upstream_gene_variant | 1.0 |
| rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
| rpoC | 763052 | c.-318G>C | upstream_gene_variant | 1.0 |
| rpoC | 763053 | c.-317T>C | upstream_gene_variant | 1.0 |
| rpoC | 763070 | c.-300T>C | upstream_gene_variant | 1.0 |
| rpoB | 763074 | p.Thr1090Val | missense_variant | 1.0 |
| rpoC | 763079 | c.-291C>T | upstream_gene_variant | 1.0 |
| rpoC | 763082 | c.-288C>T | upstream_gene_variant | 1.0 |
| rpoC | 763085 | c.-285C>T | upstream_gene_variant | 1.0 |
| rpoC | 763088 | c.-282C>G | upstream_gene_variant | 1.0 |
| rpoC | 763109 | c.-261C>G | upstream_gene_variant | 1.0 |
| rpoC | 763115 | c.-255T>C | upstream_gene_variant | 1.0 |
| rpoB | 763130 | p.Glu1108Asp | missense_variant | 1.0 |
| rpoC | 763133 | c.-237G>T | upstream_gene_variant | 1.0 |
| rpoC | 763136 | c.-234C>T | upstream_gene_variant | 1.0 |
| rpoC | 763142 | c.-228C>G | upstream_gene_variant | 1.0 |
| rpoC | 763148 | c.-222G>C | upstream_gene_variant | 1.0 |
| rpoC | 763157 | c.-213G>C | upstream_gene_variant | 1.0 |
| rpoC | 763160 | c.-210G>T | upstream_gene_variant | 1.0 |
| rpoC | 763163 | c.-207C>G | 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 | 763187 | c.-183C>G | upstream_gene_variant | 1.0 |
| rpoC | 763375 | c.6C>G | synonymous_variant | 1.0 |
| rpoC | 763387 | c.18C>T | synonymous_variant | 1.0 |
| rpoC | 763396 | c.27A>G | synonymous_variant | 1.0 |
| rpoC | 763399 | c.30C>T | synonymous_variant | 1.0 |
| rpoC | 763408 | c.39T>C | synonymous_variant | 1.0 |
| rpoC | 763411 | c.42T>A | synonymous_variant | 1.0 |
| rpoC | 763414 | c.45T>G | synonymous_variant | 1.0 |
| rpoC | 763417 | c.48C>T | synonymous_variant | 1.0 |
| rpoC | 763423 | p.Glu18Asp | missense_variant | 1.0 |
| rpoC | 763430 | c.61_63delAGGinsCGT | synonymous_variant | 1.0 |
| rpoC | 763434 | p.Gln22Arg | missense_variant | 1.0 |
| rpoC | 763442 | p.Tyr25Arg | missense_variant | 1.0 |
| rpoC | 763456 | c.87A>G | synonymous_variant | 1.0 |
| rpoC | 763462 | c.93G>T | synonymous_variant | 1.0 |
| rpoC | 763465 | c.96G>A | synonymous_variant | 1.0 |
| rpoC | 763468 | c.99G>C | synonymous_variant | 1.0 |
| rpoC | 763471 | c.102C>T | synonymous_variant | 1.0 |
| rpoC | 763483 | c.114G>C | synonymous_variant | 1.0 |
| rpoC | 763486 | c.117T>G | synonymous_variant | 1.0 |
| rpoC | 763517 | p.Lys50Arg | missense_variant | 1.0 |
| rpoC | 763522 | c.153C>T | synonymous_variant | 1.0 |
| rpoC | 763528 | c.159G>C | synonymous_variant | 1.0 |
| rpoC | 763531 | c.162G>C | synonymous_variant | 1.0 |
| rpoC | 763534 | c.165T>C | synonymous_variant | 1.0 |
| rpoC | 763546 | c.177A>G | synonymous_variant | 1.0 |
| rpoC | 763549 | c.180C>T | synonymous_variant | 1.0 |
| rpoC | 763550 | p.Tyr61Gly | missense_variant | 1.0 |
| rpoC | 763555 | c.186C>T | synonymous_variant | 1.0 |
| rpoC | 763570 | c.201G>C | synonymous_variant | 1.0 |
| rpoC | 763578 | p.Phe70Tyr | missense_variant | 1.0 |
| rpoC | 763594 | c.225C>T | synonymous_variant | 1.0 |
| rpoC | 763603 | c.234C>T | synonymous_variant | 1.0 |
| rpoC | 763609 | c.240C>T | synonymous_variant | 1.0 |
| rpoC | 763619 | p.Arg84Lys | missense_variant | 1.0 |
| rpoC | 763622 | p.Ala85Ser | missense_variant | 1.0 |
| rpoC | 763630 | c.261G>T | synonymous_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>G | synonymous_variant | 1.0 |
| rpoC | 763666 | c.297G>A | synonymous_variant | 1.0 |
| rpoC | 763696 | c.327T>C | synonymous_variant | 1.0 |
| rpoC | 763705 | c.336G>T | synonymous_variant | 1.0 |
| rpoC | 763708 | c.339G>C | synonymous_variant | 1.0 |
| rpoC | 763714 | c.345G>C | synonymous_variant | 1.0 |
| rpoC | 763717 | c.348T>C | synonymous_variant | 1.0 |
| rpoC | 763732 | c.363C>T | synonymous_variant | 1.0 |
| rpoC | 763741 | c.372C>T | synonymous_variant | 1.0 |
| rpoC | 763747 | c.378G>A | synonymous_variant | 1.0 |
| rpoC | 763765 | c.396T>C | synonymous_variant | 1.0 |
| rpoC | 763769 | p.Tyr134Asn | missense_variant | 1.0 |
| rpoC | 763772 | p.Val135Ile | missense_variant | 1.0 |
| rpoC | 763783 | c.414G>T | synonymous_variant | 1.0 |
| rpoC | 763786 | c.417C>G | synonymous_variant | 1.0 |
| rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 1.0 |
| rpoC | 764410 | c.1041G>A | synonymous_variant | 1.0 |
| rpoC | 764428 | c.1059G>C | synonymous_variant | 1.0 |
| rpoC | 764470 | c.1101C>G | synonymous_variant | 1.0 |
| rpoC | 764485 | c.1116G>C | synonymous_variant | 1.0 |
| rpoC | 764497 | c.1128A>G | synonymous_variant | 1.0 |
| rpoC | 764503 | c.1134G>C | synonymous_variant | 1.0 |
| rpoC | 764509 | c.1140G>A | synonymous_variant | 1.0 |
| rpoC | 764521 | c.1152T>C | synonymous_variant | 1.0 |
| rpoC | 764524 | c.1155C>T | synonymous_variant | 1.0 |
| rpoC | 764527 | c.1158C>T | 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 | 764542 | c.1173C>T | synonymous_variant | 1.0 |
| rpoC | 764548 | c.1179G>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 | 764578 | c.1209C>T | synonymous_variant | 1.0 |
| rpoC | 764587 | c.1218C>G | synonymous_variant | 1.0 |
| rpoC | 764593 | c.1224C>T | synonymous_variant | 1.0 |
| rpoC | 764605 | c.1236G>C | synonymous_variant | 1.0 |
| rpoC | 764611 | c.1242G>C | synonymous_variant | 1.0 |
| rpoC | 764623 | c.1254C>G | synonymous_variant | 1.0 |
| rpoC | 764626 | c.1257C>T | synonymous_variant | 1.0 |
| rpoC | 764635 | c.1266C>G | synonymous_variant | 1.0 |
| rpoC | 764644 | c.1275G>C | synonymous_variant | 1.0 |
| rpoC | 764650 | c.1281G>T | synonymous_variant | 1.0 |
| rpoC | 764653 | c.1284G>C | synonymous_variant | 1.0 |
| rpoC | 764656 | c.1287C>G | synonymous_variant | 1.0 |
| rpoC | 764659 | c.1290C>T | synonymous_variant | 1.0 |
| rpoC | 764660 | p.Val431Ile | missense_variant | 1.0 |
| rpoC | 764668 | c.1299C>T | synonymous_variant | 1.0 |
| rpoC | 764677 | c.1308C>G | synonymous_variant | 1.0 |
| rpoC | 764692 | c.1323C>T | synonymous_variant | 1.0 |
| rpoC | 764701 | c.1332C>G | synonymous_variant | 1.0 |
| rpoC | 764713 | c.1344G>T | synonymous_variant | 1.0 |
| rpoC | 764746 | c.1377G>C | synonymous_variant | 1.0 |
| rpoC | 764764 | c.1395T>C | synonymous_variant | 1.0 |
| rpoC | 764780 | c.1411_1412delAGinsTC | synonymous_variant | 1.0 |
| rpoC | 764803 | c.1434C>T | synonymous_variant | 1.0 |
| rpoC | 764813 | p.Gln482Glu | missense_variant | 1.0 |
| rpoC | 764824 | c.1455T>C | synonymous_variant | 1.0 |
| rpoC | 764830 | c.1461C>G | synonymous_variant | 1.0 |
| rpoC | 764838 | p.Val490Ala | missense_variant | 1.0 |
| rpoC | 764845 | c.1476C>G | synonymous_variant | 1.0 |
| rpoC | 764858 | p.Leu497Met | missense_variant | 1.0 |
| rpoC | 764869 | c.1500C>T | synonymous_variant | 1.0 |
| rpoC | 764875 | c.1506C>G | synonymous_variant | 1.0 |
| rpoC | 764887 | c.1518G>C | synonymous_variant | 1.0 |
| rpoC | 764888 | c.1519T>C | synonymous_variant | 1.0 |
| rpoC | 764896 | c.1527C>T | synonymous_variant | 1.0 |
| rpoC | 764911 | c.1542A>G | synonymous_variant | 1.0 |
| rpoC | 764914 | p.Met515Ile | missense_variant | 1.0 |
| rpoC | 764920 | c.1551G>T | synonymous_variant | 1.0 |
| rpoC | 764923 | c.1554A>G | synonymous_variant | 1.0 |
| rpoC | 764926 | c.1557C>T | synonymous_variant | 1.0 |
| rpoC | 764935 | c.1566T>C | synonymous_variant | 1.0 |
| rpoC | 764948 | c.1579T>C | synonymous_variant | 1.0 |
| rpoC | 764952 | p.Val528Ala | missense_variant | 1.0 |
| rpoC | 764962 | c.1593G>C | synonymous_variant | 1.0 |
| rpoC | 764968 | c.1599T>C | synonymous_variant | 1.0 |
| rpoC | 764971 | c.1602C>G | synonymous_variant | 1.0 |
| rpoC | 764995 | c.1626C>T | synonymous_variant | 1.0 |
| rpoC | 764998 | c.1629G>T | synonymous_variant | 1.0 |
| rpoC | 765007 | c.1638T>G | synonymous_variant | 1.0 |
| rpoC | 765008 | c.1639T>C | synonymous_variant | 1.0 |
| rpoC | 765011 | c.1642_1643delAGinsTC | synonymous_variant | 0.97 |
| rpoC | 765016 | c.1647C>A | synonymous_variant | 1.0 |
| rpoC | 765019 | c.1650A>G | 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 | 765050 | p.Ser561Ala | missense_variant | 1.0 |
| rpoC | 765061 | c.1692C>T | synonymous_variant | 1.0 |
| rpoC | 765064 | c.1695C>T | synonymous_variant | 1.0 |
| rpoC | 765070 | c.1701G>T | synonymous_variant | 1.0 |
| rpoC | 765079 | c.1710T>C | synonymous_variant | 1.0 |
| rpoC | 765082 | c.1713G>T | synonymous_variant | 1.0 |
| rpoC | 765083 | p.Arg572Lys | missense_variant | 1.0 |
| rpoC | 765088 | c.1719G>A | synonymous_variant | 1.0 |
| rpoC | 765089 | c.1720T>C | synonymous_variant | 1.0 |
| rpoC | 765094 | c.1725C>T | synonymous_variant | 1.0 |
| rpoC | 765103 | c.1734G>T | synonymous_variant | 1.0 |
| rpoC | 765121 | c.1752G>C | synonymous_variant | 1.0 |
| rpoC | 766787 | p.Glu1140Lys | missense_variant | 0.67 |
| rpoC | 766800 | p.Ala1144Asp | missense_variant | 0.67 |
| rpoC | 766804 | c.3435A>G | synonymous_variant | 0.67 |
| rpoC | 766811 | p.Ser1148Ala | missense_variant | 0.67 |
| rpoC | 766835 | p.Val1156Ile | missense_variant | 1.0 |
| rpoC | 766843 | c.3474T>G | synonymous_variant | 1.0 |
| rpoC | 766861 | c.3492G>C | synonymous_variant | 1.0 |
| rpoC | 767011 | c.3642G>C | synonymous_variant | 1.0 |
| rpoC | 767023 | p.Asp1218Glu | missense_variant | 1.0 |
| rpoC | 767026 | c.3657G>C | synonymous_variant | 1.0 |
| rpoC | 767035 | c.3666G>C | synonymous_variant | 1.0 |
| rpoC | 767038 | c.3669G>C | synonymous_variant | 1.0 |
| rpoC | 767041 | c.3672G>C | synonymous_variant | 1.0 |
| rpoC | 767068 | c.3699G>C | synonymous_variant | 1.0 |
| rpoC | 767071 | c.3702C>G | synonymous_variant | 1.0 |
| rpoC | 767074 | c.3705T>C | synonymous_variant | 1.0 |
| rpoC | 767077 | c.3708G>T | synonymous_variant | 1.0 |
| rpoC | 767080 | c.3711G>T | synonymous_variant | 1.0 |
| rpoC | 767098 | c.3729T>C | synonymous_variant | 1.0 |
| rpoC | 767104 | c.3735C>G | synonymous_variant | 1.0 |
| rpoC | 767106 | p.Asn1246Ile | missense_variant | 1.0 |
| rpoC | 767119 | c.3750A>G | synonymous_variant | 1.0 |
| rpoC | 767134 | c.3765C>T | synonymous_variant | 1.0 |
| rpoC | 767155 | c.3786C>G | synonymous_variant | 1.0 |
| rpsL | 781793 | c.234G>C | synonymous_variant | 1.0 |
| rpsL | 781802 | c.243G>C | synonymous_variant | 1.0 |
| rpsL | 781805 | c.246G>C | synonymous_variant | 1.0 |
| rpsL | 781811 | c.252C>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>G | synonymous_variant | 1.0 |
| rpsL | 781838 | c.279G>T | synonymous_variant | 1.0 |
| rpsL | 781841 | c.282C>T | synonymous_variant | 1.0 |
| rpsL | 781851 | p.Ile98Val | missense_variant | 1.0 |
| rpsL | 781856 | c.297C>T | synonymous_variant | 1.0 |
| rpsL | 781862 | c.303G>C | synonymous_variant | 1.0 |
| rpsL | 781865 | c.306G>C | synonymous_variant | 1.0 |
| rpsL | 781868 | c.309T>C | synonymous_variant | 1.0 |
| rpsL | 781871 | c.312G>C | synonymous_variant | 1.0 |
| rpsL | 781880 | c.321C>T | synonymous_variant | 1.0 |
| rpsL | 781884 | p.Asn109Asp | missense_variant | 1.0 |
| rpsL | 781892 | c.333A>G | synonymous_variant | 1.0 |
| rpsL | 781901 | c.342C>T | synonymous_variant | 1.0 |
| rpsL | 781902 | c.343_344delAGinsTC | synonymous_variant | 1.0 |
| rpsL | 781907 | c.348T>C | synonymous_variant | 1.0 |
| rpsL | 781929 | p.Gly124Cys | missense_variant | 1.0 |
| rplC | 800633 | c.-176T>C | upstream_gene_variant | 1.0 |
| rplC | 800648 | c.-161A>T | upstream_gene_variant | 1.0 |
| rplC | 800654 | c.-155T>C | upstream_gene_variant | 1.0 |
| rplC | 800672 | c.-137G>C | upstream_gene_variant | 1.0 |
| rplC | 800681 | c.-128C>T | upstream_gene_variant | 1.0 |
| rplC | 800690 | c.-119C>T | upstream_gene_variant | 1.0 |
| rplC | 800693 | c.-116A>G | upstream_gene_variant | 1.0 |
| rplC | 800702 | c.-107G>T | upstream_gene_variant | 1.0 |
| rplC | 800703 | c.-106T>C | upstream_gene_variant | 1.0 |
| rplC | 800714 | c.-95C>T | 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>A | upstream_gene_variant | 1.0 |
| rplC | 800726 | c.-83G>C | upstream_gene_variant | 1.0 |
| rplC | 800744 | c.-65G>C | upstream_gene_variant | 1.0 |
| rplC | 800759 | c.-50C>T | upstream_gene_variant | 1.0 |
| rplC | 800786 | c.-23C>T | upstream_gene_variant | 1.0 |
| rrs | 1471850 | n.5G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471852 | n.7T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471922 | n.78delT | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471978 | n.133C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472027 | n.184_188delCGGGA | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472037 | n.192A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472038 | n.193_194insTA | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472041 | n.196C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472042 | n.197_198insG | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472054 | n.210_212delCGC | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472062 | n.217G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472068 | n.223T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472069 | n.224G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472070 | n.225G>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 | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472278 | n.433C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472279 | n.434T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472287 | n.442C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472293 | n.448C>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472309 | n.464C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472311 | n.466C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472313 | n.469_470delAT | 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 | 1472330 | n.485G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472438 | n.593T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472439 | n.594C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472450 | n.605A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472451 | n.606C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472461 | n.616G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472462 | n.617T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472688 | n.843_844insTC | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472836 | n.991G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472840 | n.995A>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472843 | n.998_999insT | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472846 | n.1002delG | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472849 | n.1004C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472850 | n.1005T>C | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472855 | n.1011_1012insGT | 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 | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472958 | n.1113A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472988 | n.1143T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473089 | n.1244A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 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 | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.97 |
| rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473283 | n.1438T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473292 | n.1447G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473293 | n.1448G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.37 |
| rrl | 1474112 | n.455T>A | 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 | 1474161 | n.504A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474182 | n.525C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474185 | n.529delA | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474199 | n.542G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474202 | n.545T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474275 | n.618T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474284 | n.631_633delCCT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474293 | n.637_648delCCTCTCCGGAGG | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474308 | n.651G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474309 | n.653delT | 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 | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 0.59 |
| rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474372 | n.717_718insTGT | non_coding_transcript_exon_variant | 0.93 |
| rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.91 |
| rrl | 1474390 | n.733C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474440 | n.783T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474451 | n.794T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474487 | n.830G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474507 | n.850G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474517 | n.860C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474537 | n.880G>A | 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 | 1474628 | n.971C>T | non_coding_transcript_exon_variant | 0.88 |
| 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 | 1474709 | n.1053_1056delTGGT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474717 | n.1060_1061insGTCAG | 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 | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474753 | n.1096A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474754 | n.1097C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474784 | n.1127C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474798 | n.1141C>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 | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474837 | n.1180A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474901 | n.1244A>G | 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 | 1474921 | n.1264C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474944 | n.1287G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474951 | n.1294C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475137 | n.1480A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475170 | n.1513A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475171 | n.1514C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475696 | n.2039T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475703 | n.2046A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475902 | n.2245T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476032 | n.2375C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476033 | n.2376T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476035 | n.2378G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476040 | n.2383C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476046 | n.2389G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476060 | n.2403T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476080 | n.2423T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476091 | n.2434_2435insG | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476100 | n.2443A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476103 | n.2446C>G | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476105 | n.2450delA | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476113 | n.2456T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 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 | 1476252 | n.2595T>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 | 1476267 | n.2610G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476276 | n.2619C>A | 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>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 | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476534 | n.2877A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476535 | n.2878G>A | 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 | 1476572 | n.2915G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476584 | n.2927C>G | non_coding_transcript_exon_variant | 0.98 |
| rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476595 | n.2938C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476600 | n.2943A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476602 | n.2945G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476624 | n.2967T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476625 | n.2968C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476628 | n.2971T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 1.0 |
| rpsA | 1833649 | c.108C>T | synonymous_variant | 1.0 |
| rpsA | 1833655 | c.114C>T | synonymous_variant | 1.0 |
| rpsA | 1833661 | c.120A>G | synonymous_variant | 1.0 |
| rpsA | 1833664 | c.123C>T | synonymous_variant | 1.0 |
| rpsA | 1833668 | p.Ile43Val | missense_variant | 1.0 |
| rpsA | 1833676 | c.135A>G | synonymous_variant | 1.0 |
| rpsA | 1833679 | c.138G>C | synonymous_variant | 1.0 |
| rpsA | 1833682 | c.141C>T | synonymous_variant | 1.0 |
| rpsA | 1833684 | p.Arg48His | missense_variant | 1.0 |
| rpsA | 1833694 | c.153G>C | synonymous_variant | 1.0 |
| rpsA | 1833697 | c.156C>G | synonymous_variant | 1.0 |
| rpsA | 1833700 | c.159C>G | synonymous_variant | 1.0 |
| rpsA | 1833709 | c.168C>A | synonymous_variant | 1.0 |
| rpsA | 1833718 | c.177C>G | synonymous_variant | 1.0 |
| rpsA | 1833721 | c.180A>G | synonymous_variant | 1.0 |
| rpsA | 1833724 | c.183C>T | synonymous_variant | 1.0 |
| rpsA | 1833727 | c.186G>C | synonymous_variant | 1.0 |
| rpsA | 1833733 | c.192C>T | synonymous_variant | 1.0 |
| rpsA | 1833734 | p.Ala65Ser | missense_variant | 1.0 |
| rpsA | 1833742 | c.201A>G | synonymous_variant | 1.0 |
| rpsA | 1833748 | c.207C>G | synonymous_variant | 1.0 |
| rpsA | 1833805 | c.264C>T | synonymous_variant | 1.0 |
| rpsA | 1833811 | c.270G>T | synonymous_variant | 1.0 |
| rpsA | 1833823 | c.282G>A | 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 | 1833841 | c.300C>G | synonymous_variant | 1.0 |
| rpsA | 1833847 | c.306C>G | synonymous_variant | 1.0 |
| rpsA | 1833856 | c.315A>G | synonymous_variant | 1.0 |
| rpsA | 1833859 | c.318C>T | synonymous_variant | 0.98 |
| rpsA | 1833862 | c.321G>A | synonymous_variant | 1.0 |
| rpsA | 1833874 | c.333T>C | synonymous_variant | 1.0 |
| rpsA | 1833877 | c.336C>T | synonymous_variant | 1.0 |
| rpsA | 1833886 | c.345C>G | synonymous_variant | 1.0 |
| rpsA | 1833894 | p.Ala118Glu | missense_variant | 1.0 |
| rpsA | 1833902 | p.Glu121Lys | missense_variant | 1.0 |
| rpsA | 1833907 | p.Lys122Asn | missense_variant | 1.0 |
| rpsA | 1833910 | p.Asp123Glu | missense_variant | 1.0 |
| rpsA | 1833914 | p.Ala125Pro | missense_variant | 1.0 |
| rpsA | 1833921 | p.Lys127Thr | missense_variant | 1.0 |
| rpsA | 1833925 | c.384C>T | synonymous_variant | 1.0 |
| rpsA | 1833928 | c.387G>C | synonymous_variant | 1.0 |
| rpsA | 1833949 | c.408T>C | synonymous_variant | 1.0 |
| rpsA | 1833961 | c.420C>G | synonymous_variant | 1.0 |
| rpsA | 1833970 | c.429G>C | synonymous_variant | 1.0 |
| rpsA | 1833979 | c.438T>C | synonymous_variant | 1.0 |
| rpsA | 1833994 | c.453G>C | synonymous_variant | 0.99 |
| rpsA | 1834009 | c.468C>T | synonymous_variant | 1.0 |
| rpsA | 1834012 | c.471G>T | synonymous_variant | 1.0 |
| rpsA | 1834015 | c.474G>T | synonymous_variant | 1.0 |
| rpsA | 1834040 | p.Lys167Gln | missense_variant | 1.0 |
| rpsA | 1834076 | p.Asn179His | missense_variant | 1.0 |
| rpsA | 1834090 | c.549G>T | synonymous_variant | 1.0 |
| rpsA | 1834102 | c.561T>C | synonymous_variant | 1.0 |
| rpsA | 1834108 | c.567C>A | synonymous_variant | 1.0 |
| rpsA | 1834114 | c.573G>C | synonymous_variant | 1.0 |
| rpsA | 1834135 | c.594G>C | synonymous_variant | 1.0 |
| rpsA | 1834139 | c.598_599delAGinsTC | synonymous_variant | 1.0 |
| rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
| rpsA | 1834183 | c.642T>C | synonymous_variant | 1.0 |
| rpsA | 1834186 | c.645C>T | synonymous_variant | 1.0 |
| rpsA | 1834189 | c.648G>C | synonymous_variant | 1.0 |
| rpsA | 1834195 | c.654G>C | synonymous_variant | 1.0 |
| rpsA | 1834213 | c.672G>A | synonymous_variant | 1.0 |
| rpsA | 1834234 | c.693G>C | synonymous_variant | 1.0 |
| rpsA | 1834240 | c.699T>C | synonymous_variant | 1.0 |
| rpsA | 1834246 | c.705G>T | synonymous_variant | 1.0 |
| rpsA | 1834249 | c.708T>C | synonymous_variant | 1.0 |
| rpsA | 1834256 | p.Glu239Gln | missense_variant | 1.0 |
| rpsA | 1834261 | c.720A>G | synonymous_variant | 1.0 |
| rpsA | 1834264 | c.723G>C | synonymous_variant | 1.0 |
| rpsA | 1834294 | c.753G>T | synonymous_variant | 1.0 |
| rpsA | 1834298 | p.Gln253Ala | missense_variant | 1.0 |
| rpsA | 1834303 | c.762T>C | synonymous_variant | 1.0 |
| rpsA | 1834306 | c.765T>C | synonymous_variant | 1.0 |
| rpsA | 1834327 | c.786G>T | synonymous_variant | 1.0 |
| rpsA | 1834405 | c.864C>A | synonymous_variant | 1.0 |
| rpsA | 1834411 | c.870T>C | synonymous_variant | 1.0 |
| rpsA | 1834417 | c.876G>C | synonymous_variant | 1.0 |
| rpsA | 1834420 | c.879C>T | synonymous_variant | 1.0 |
| rpsA | 1834423 | c.882G>T | synonymous_variant | 1.0 |
| rpsA | 1834451 | c.910T>C | synonymous_variant | 1.0 |
| rpsA | 1834465 | c.924T>C | synonymous_variant | 1.0 |
| rpsA | 1834489 | c.948T>C | synonymous_variant | 1.0 |
| rpsA | 1834504 | c.963G>T | synonymous_variant | 1.0 |
| rpsA | 1834528 | c.987T>C | synonymous_variant | 1.0 |
| rpsA | 1834540 | c.999G>T | synonymous_variant | 1.0 |
| rpsA | 1834543 | c.1002C>G | synonymous_variant | 1.0 |
| rpsA | 1834552 | c.1011G>T | synonymous_variant | 1.0 |
| rpsA | 1834557 | p.Ala339Gly | missense_variant | 1.0 |
| rpsA | 1834561 | c.1020C>T | synonymous_variant | 1.0 |
| rpsA | 1834565 | p.Asp342Gln | missense_variant | 1.0 |
| rpsA | 1834573 | c.1032G>A | synonymous_variant | 1.0 |
| rpsA | 1834606 | c.1065C>T | synonymous_variant | 1.0 |
| rpsA | 1834609 | c.1068T>C | synonymous_variant | 1.0 |
| rpsA | 1834612 | c.1071G>C | synonymous_variant | 1.0 |
| rpsA | 1834618 | c.1077G>C | synonymous_variant | 0.97 |
| rpsA | 1834619 | c.1078T>C | synonymous_variant | 1.0 |
| rpsA | 1834624 | c.1083G>C | synonymous_variant | 1.0 |
| rpsA | 1834627 | c.1086C>G | synonymous_variant | 1.0 |
| rpsA | 1834633 | c.1092A>G | synonymous_variant | 1.0 |
| rpsA | 1834636 | c.1095C>T | synonymous_variant | 1.0 |
| rpsA | 1834637 | p.Asn366Asp | missense_variant | 1.0 |
| rpsA | 1834667 | p.Ala376Ser | missense_variant | 0.96 |
| rpsA | 1834684 | c.1143C>T | synonymous_variant | 0.95 |
| rpsA | 1834688 | c.1147_1149delAGTinsTCC | synonymous_variant | 0.95 |
| rpsA | 1834720 | c.1179C>G | synonymous_variant | 0.92 |
| thyA | 3073857 | c.615C>T | synonymous_variant | 1.0 |
| thyA | 3073863 | c.609T>C | synonymous_variant | 1.0 |
| thyA | 3073887 | p.Ser195Asp | missense_variant | 1.0 |
| thyA | 3073892 | c.580T>C | synonymous_variant | 1.0 |
| thyA | 3073896 | c.576C>G | synonymous_variant | 1.0 |
| thyA | 3073902 | p.Ala190Gln | missense_variant | 1.0 |
| thyA | 3073908 | p.Met188Phe | missense_variant | 1.0 |
| thyA | 3073920 | c.552C>G | synonymous_variant | 1.0 |
| thyA | 3073925 | c.547T>C | synonymous_variant | 1.0 |
| thyA | 3073928 | p.Ala182Ser | missense_variant | 1.0 |
| thyA | 3073929 | c.543T>C | synonymous_variant | 1.0 |
| thyA | 3073944 | c.528C>T | synonymous_variant | 1.0 |
| thyA | 3073959 | c.513T>C | synonymous_variant | 1.0 |
| thyA | 3073964 | p.Leu170Met | missense_variant | 1.0 |
| thyA | 3073968 | c.504C>G | synonymous_variant | 1.0 |
| thyA | 3073977 | c.495A>G | synonymous_variant | 1.0 |
| thyA | 3073983 | c.489C>G | synonymous_variant | 1.0 |
| thyA | 3073989 | c.483T>C | synonymous_variant | 1.0 |
| clpC1 | 4038704 | c.2001T>C | synonymous_variant | 1.0 |
| clpC1 | 4038710 | c.1995G>C | synonymous_variant | 1.0 |
| clpC1 | 4038713 | c.1992T>C | synonymous_variant | 1.0 |
| clpC1 | 4038722 | c.1983G>C | synonymous_variant | 1.0 |
| clpC1 | 4038744 | p.Thr654Met | missense_variant | 1.0 |
| clpC1 | 4038755 | c.1950G>C | synonymous_variant | 1.0 |
| clpC1 | 4038764 | c.1941C>G | synonymous_variant | 1.0 |
| clpC1 | 4038767 | c.1938G>C | synonymous_variant | 1.0 |
| clpC1 | 4038770 | c.1935C>T | synonymous_variant | 1.0 |
| clpC1 | 4038773 | c.1932T>C | synonymous_variant | 1.0 |
| clpC1 | 4038776 | c.1929G>A | synonymous_variant | 1.0 |
| clpC1 | 4038779 | c.1924_1926delCTCinsTTG | synonymous_variant | 1.0 |
| clpC1 | 4038795 | p.Ser637Thr | missense_variant | 1.0 |
| clpC1 | 4038810 | p.Gln632Thr | missense_variant | 1.0 |
| clpC1 | 4038812 | c.1893T>C | synonymous_variant | 1.0 |
| clpC1 | 4038815 | c.1890G>C | synonymous_variant | 1.0 |
| clpC1 | 4038845 | c.1860G>T | synonymous_variant | 1.0 |
| clpC1 | 4038851 | c.1854G>A | synonymous_variant | 1.0 |
| clpC1 | 4038860 | c.1845G>C | synonymous_variant | 1.0 |
| clpC1 | 4038863 | c.1842G>C | synonymous_variant | 1.0 |
| clpC1 | 4038875 | c.1830C>G | synonymous_variant | 1.0 |
| clpC1 | 4038878 | c.1827A>G | synonymous_variant | 1.0 |
| clpC1 | 4038884 | c.1821C>T | synonymous_variant | 1.0 |
| clpC1 | 4038890 | p.Glu605Asp | missense_variant | 1.0 |
| clpC1 | 4038908 | c.1797C>G | synonymous_variant | 1.0 |
| clpC1 | 4038911 | c.1794G>T | synonymous_variant | 1.0 |
| clpC1 | 4038917 | c.1788C>T | synonymous_variant | 1.0 |
| clpC1 | 4038923 | c.1782A>G | synonymous_variant | 1.0 |
| clpC1 | 4038926 | c.1779G>C | synonymous_variant | 1.0 |
| clpC1 | 4038929 | c.1776G>C | synonymous_variant | 1.0 |
| clpC1 | 4038932 | c.1773G>A | synonymous_variant | 1.0 |
| clpC1 | 4038935 | c.1770C>G | synonymous_variant | 1.0 |
| clpC1 | 4038942 | p.Arg588Lys | missense_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>G | synonymous_variant | 1.0 |
| clpC1 | 4038983 | c.1722C>T | synonymous_variant | 1.0 |
| clpC1 | 4038989 | c.1716T>C | synonymous_variant | 1.0 |
| clpC1 | 4038997 | c.1708T>C | synonymous_variant | 1.0 |
| clpC1 | 4039001 | p.Asn568Glu | missense_variant | 1.0 |
| clpC1 | 4039010 | c.1695G>A | synonymous_variant | 1.0 |
| clpC1 | 4039016 | c.1689C>G | synonymous_variant | 1.0 |
| clpC1 | 4039022 | c.1683A>G | synonymous_variant | 1.0 |
| clpC1 | 4039025 | c.1680C>T | synonymous_variant | 1.0 |
| clpC1 | 4039034 | c.1671C>G | synonymous_variant | 1.0 |
| clpC1 | 4039064 | c.1641C>T | synonymous_variant | 1.0 |
| clpC1 | 4039067 | c.1638G>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>C | synonymous_variant | 1.0 |
| clpC1 | 4039097 | c.1608G>C | synonymous_variant | 1.0 |
| clpC1 | 4039103 | c.1602T>C | synonymous_variant | 1.0 |
| clpC1 | 4039106 | c.1599G>C | synonymous_variant | 1.0 |
| clpC1 | 4039115 | p.Lys530Arg | missense_variant | 1.0 |
| clpC1 | 4039121 | c.1584T>C | synonymous_variant | 1.0 |
| clpC1 | 4039136 | c.1569C>T | synonymous_variant | 1.0 |
| clpC1 | 4039139 | p.Glu522Asp | missense_variant | 1.0 |
| clpC1 | 4039142 | c.1563A>G | synonymous_variant | 1.0 |
| clpC1 | 4039145 | c.1560G>C | synonymous_variant | 1.0 |
| clpC1 | 4039154 | c.1551G>C | synonymous_variant | 1.0 |
| clpC1 | 4039169 | p.Glu512Asp | missense_variant | 1.0 |
| clpC1 | 4039178 | p.Arg509His | missense_variant | 1.0 |
| clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.95 |
| clpC1 | 4039187 | c.1518G>C | synonymous_variant | 1.0 |
| clpC1 | 4039195 | p.Thr504Ser | missense_variant | 1.0 |
| clpC1 | 4039199 | p.Ala502Glu | missense_variant | 1.0 |
| clpC1 | 4039220 | c.1485G>C | synonymous_variant | 1.0 |
| clpC1 | 4039226 | c.1479T>C | synonymous_variant | 1.0 |
| clpC1 | 4039236 | p.Asn490Thr | missense_variant | 1.0 |
| clpC1 | 4039243 | p.Leu488Met | missense_variant | 1.0 |
| clpC1 | 4039244 | c.1461G>C | synonymous_variant | 1.0 |
| clpC1 | 4039262 | p.Asp481Glu | missense_variant | 1.0 |
| clpC1 | 4039266 | p.Asp480Gly | missense_variant | 1.0 |
| clpC1 | 4039268 | c.1437C>G | synonymous_variant | 1.0 |
| clpC1 | 4039274 | c.1431G>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>G | synonymous_variant | 1.0 |
| clpC1 | 4039628 | c.1077C>T | synonymous_variant | 1.0 |
| clpC1 | 4039637 | p.Ile356Val | missense_variant | 1.0 |
| clpC1 | 4039643 | p.His354Leu | missense_variant | 1.0 |
| clpC1 | 4039652 | p.Thr351Ser | missense_variant | 1.0 |
| clpC1 | 4039655 | c.1050G>T | synonymous_variant | 1.0 |
| clpC1 | 4039661 | p.Gly348Pro | missense_variant | 1.0 |
| clpC1 | 4039664 | c.1041G>T | synonymous_variant | 1.0 |
| clpC1 | 4039670 | c.1035G>A | synonymous_variant | 1.0 |
| clpC1 | 4039697 | c.1008C>T | synonymous_variant | 1.0 |
| clpC1 | 4039700 | c.1005C>T | synonymous_variant | 1.0 |
| clpC1 | 4039714 | p.Tyr331His | missense_variant | 1.0 |
| clpC1 | 4039724 | c.981A>G | synonymous_variant | 1.0 |
| clpC1 | 4039730 | c.975C>G | synonymous_variant | 1.0 |
| clpC1 | 4039733 | c.972G>C | synonymous_variant | 1.0 |
| clpC1 | 4039742 | c.963C>T | synonymous_variant | 1.0 |
| clpC1 | 4039748 | c.957G>C | synonymous_variant | 1.0 |
| clpC1 | 4039751 | c.954A>G | synonymous_variant | 1.0 |
| clpC1 | 4039757 | c.948A>G | synonymous_variant | 1.0 |
| clpC1 | 4039760 | c.945T>C | synonymous_variant | 1.0 |
| clpC1 | 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.916_918delTCGinsAGC | synonymous_variant | 1.0 |
| clpC1 | 4039793 | c.912C>T | synonymous_variant | 1.0 |
| clpC1 | 4039805 | c.900C>T | synonymous_variant | 1.0 |
| clpC1 | 4039814 | c.891C>T | synonymous_variant | 1.0 |
| clpC1 | 4039817 | c.888A>T | synonymous_variant | 1.0 |
| clpC1 | 4039820 | c.885T>A | synonymous_variant | 1.0 |
| clpC1 | 4039823 | c.882T>C | synonymous_variant | 1.0 |
| clpC1 | 4039829 | c.874_876delTTGinsCTC | synonymous_variant | 1.0 |
| clpC1 | 4039838 | p.Leu289Ile | missense_variant | 1.0 |
| clpC1 | 4039856 | c.849C>T | synonymous_variant | 1.0 |
| clpC1 | 4039865 | c.840T>C | synonymous_variant | 1.0 |
| clpC1 | 4039871 | p.Thr278Gln | missense_variant | 1.0 |
| clpC1 | 4039886 | c.819C>G | synonymous_variant | 1.0 |
| clpC1 | 4039898 | c.807C>G | synonymous_variant | 1.0 |
| clpC1 | 4039904 | c.801A>G | synonymous_variant | 1.0 |
| clpC1 | 4039910 | c.795C>T | synonymous_variant | 1.0 |
| clpC1 | 4039929 | c.775_776delAGinsTC | synonymous_variant | 1.0 |
| clpC1 | 4039943 | c.762G>C | synonymous_variant | 1.0 |
| clpC1 | 4039946 | c.759A>C | synonymous_variant | 1.0 |
| clpC1 | 4039951 | c.754C>T | synonymous_variant | 1.0 |
| clpC1 | 4039952 | c.753T>C | synonymous_variant | 1.0 |
| clpC1 | 4039958 | p.Thr249Ser | missense_variant | 1.0 |
| clpC1 | 4039964 | c.741C>G | synonymous_variant | 1.0 |
| clpC1 | 4039973 | c.732C>T | synonymous_variant | 1.0 |
| clpC1 | 4039979 | c.726C>G | synonymous_variant | 1.0 |
| clpC1 | 4039982 | c.723G>T | synonymous_variant | 1.0 |
| clpC1 | 4039988 | c.717C>G | synonymous_variant | 1.0 |
| clpC1 | 4039996 | p.Glu237Lys | missense_variant | 1.0 |
| clpC1 | 4040002 | p.His235Asn | missense_variant | 1.0 |
| clpC1 | 4040003 | c.702G>C | synonymous_variant | 1.0 |
| clpC1 | 4040010 | p.Ala232Asp | missense_variant | 1.0 |
| clpC1 | 4040013 | p.Gln231Leu | missense_variant | 1.0 |
| clpC1 | 4040021 | c.684A>G | synonymous_variant | 1.0 |
| clpC1 | 4040024 | c.681A>G | synonymous_variant | 1.0 |
| clpC1 | 4040030 | c.675C>G | synonymous_variant | 1.0 |
| clpC1 | 4040033 | c.672G>C | synonymous_variant | 1.0 |
| clpC1 | 4040042 | c.663C>T | synonymous_variant | 1.0 |
| clpC1 | 4040045 | c.660C>G | synonymous_variant | 1.0 |
| clpC1 | 4040048 | c.657C>T | synonymous_variant | 1.0 |
| clpC1 | 4040066 | c.639G>A | 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 | 4040105 | c.600C>A | synonymous_variant | 1.0 |
| clpC1 | 4040108 | c.597G>C | synonymous_variant | 1.0 |
| clpC1 | 4040117 | c.588A>G | synonymous_variant | 1.0 |
| clpC1 | 4040120 | p.Lys195Asn | missense_variant | 1.0 |
| clpC1 | 4040288 | c.417C>T | synonymous_variant | 1.0 |
| clpC1 | 4040291 | c.414G>A | synonymous_variant | 1.0 |
| clpC1 | 4040306 | c.399G>C | synonymous_variant | 1.0 |
| clpC1 | 4040311 | p.Thr132Ser | missense_variant | 1.0 |
| clpC1 | 4040315 | p.Glu130Asp | missense_variant | 1.0 |
| clpC1 | 4040318 | c.387C>G | synonymous_variant | 1.0 |
| clpC1 | 4040321 | c.384C>T | synonymous_variant | 1.0 |
| clpC1 | 4040342 | c.363C>G | synonymous_variant | 1.0 |
| clpC1 | 4040345 | c.360C>G | synonymous_variant | 1.0 |
| clpC1 | 4040363 | c.342A>C | synonymous_variant | 1.0 |
| clpC1 | 4040380 | c.325T>C | synonymous_variant | 1.0 |
| clpC1 | 4040381 | c.324T>C | synonymous_variant | 1.0 |
| clpC1 | 4040387 | c.318A>G | synonymous_variant | 1.0 |
| clpC1 | 4040393 | c.312G>C | synonymous_variant | 1.0 |
| clpC1 | 4040402 | p.Asn101Lys | missense_variant | 1.0 |
| clpC1 | 4040411 | c.294T>G | synonymous_variant | 1.0 |
