Run ID: ERR4769433
Sample name:
Date: 01-04-2023 06:40:27
Number of reads: 74708
Percentage reads mapped: 3.5
Strain: lineage4.9
Drug-resistance: Pre-XDR-TB
| Drug | Resistance | Supporting mutations |
|---|
| Lineage | Family | Main Spoligotype | RDs | Frequency |
|---|---|---|---|---|
| lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
| lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 0.99 |
| Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
|---|---|---|---|---|---|
| gyrB | 6695 | p.Ile486Leu | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
| rpoB | 761121 | p.Pro439Ser | missense_variant | 1.0 | rifampicin |
| 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 | 6709 | c.-593A>G | upstream_gene_variant | 1.0 |
| gyrA | 6712 | c.-590G>C | upstream_gene_variant | 1.0 |
| gyrB | 6716 | p.Ile493Leu | missense_variant | 1.0 |
| gyrA | 6724 | c.-578G>C | upstream_gene_variant | 1.0 |
| gyrA | 6730 | c.-572A>G | upstream_gene_variant | 1.0 |
| gyrB | 6737 | p.Thr500Ala | missense_variant | 1.0 |
| gyrA | 6742 | c.-560A>G | upstream_gene_variant | 1.0 |
| gyrA | 6745 | c.-557T>G | upstream_gene_variant | 1.0 |
| gyrA | 6751 | c.-551G>C | upstream_gene_variant | 1.0 |
| gyrA | 6760 | c.-542G>C | upstream_gene_variant | 1.0 |
| gyrA | 6772 | c.-530C>G | upstream_gene_variant | 1.0 |
| gyrA | 6775 | c.-527G>C | upstream_gene_variant | 1.0 |
| gyrB | 6779 | p.His514Asn | missense_variant | 1.0 |
| gyrB | 6784 | p.Asp515Glu | missense_variant | 1.0 |
| gyrA | 6793 | c.-509T>C | upstream_gene_variant | 1.0 |
| gyrB | 6797 | p.Gly520Ser | missense_variant | 1.0 |
| gyrA | 6805 | c.-497G>C | upstream_gene_variant | 1.0 |
| gyrA | 6808 | c.-494C>T | upstream_gene_variant | 1.0 |
| gyrA | 6826 | c.-476G>C | upstream_gene_variant | 1.0 |
| rpoB | 760389 | c.583_584delAGinsTC | synonymous_variant | 1.0 |
| rpoB | 760400 | c.594G>C | synonymous_variant | 1.0 |
| rpoB | 760407 | c.601_602delAGinsTC | synonymous_variant | 1.0 |
| rpoB | 760418 | c.612G>C | synonymous_variant | 1.0 |
| rpoB | 760430 | c.624T>C | synonymous_variant | 1.0 |
| rpoB | 760436 | c.630C>G | synonymous_variant | 1.0 |
| rpoB | 760460 | c.654G>C | synonymous_variant | 1.0 |
| rpoB | 760475 | c.669A>G | synonymous_variant | 1.0 |
| rpoB | 760481 | c.675G>C | synonymous_variant | 1.0 |
| rpoB | 760484 | c.678A>G | synonymous_variant | 1.0 |
| rpoB | 760496 | c.690G>C | synonymous_variant | 1.0 |
| rpoB | 760508 | c.702G>C | synonymous_variant | 1.0 |
| rpoB | 760511 | c.705G>C | synonymous_variant | 1.0 |
| rpoB | 760522 | p.Ser239Thr | missense_variant | 1.0 |
| rpoB | 760532 | c.726T>C | synonymous_variant | 1.0 |
| rpoB | 760533 | p.Val243Gln | missense_variant | 1.0 |
| rpoB | 760541 | c.735G>C | synonymous_variant | 1.0 |
| rpoB | 760547 | c.741G>C | synonymous_variant | 1.0 |
| rpoB | 761072 | p.Lys422Asn | missense_variant | 1.0 |
| rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 1.0 |
| rpoB | 761097 | c.1291_1292delAGinsTC | synonymous_variant | 1.0 |
| rpoB | 761102 | c.1296A>G | synonymous_variant | 1.0 |
| rpoB | 761132 | c.1326G>T | synonymous_variant | 1.0 |
| rpoB | 761133 | c.1327T>C | synonymous_variant | 1.0 |
| rpoB | 761147 | c.1341C>T | synonymous_variant | 1.0 |
| rpoB | 761150 | c.1344A>T | synonymous_variant | 1.0 |
| rpoB | 761153 | c.1347G>C | synonymous_variant | 1.0 |
| rpoB | 761156 | c.1350G>C | synonymous_variant | 1.0 |
| rpoB | 761159 | c.1353G>C | 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 | 761180 | c.1374A>C | synonymous_variant | 1.0 |
| rpoB | 761189 | c.1383T>C | synonymous_variant | 1.0 |
| rpoB | 761195 | c.1389G>C | synonymous_variant | 1.0 |
| rpoB | 761196 | p.Leu464Ile | missense_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 | 761255 | c.1449T>G | synonymous_variant | 1.0 |
| rpoB | 761261 | c.1455G>T | synonymous_variant | 1.0 |
| rpoB | 761264 | c.1458C>G | synonymous_variant | 1.0 |
| rpoB | 761558 | c.1752C>G | synonymous_variant | 1.0 |
| rpoB | 761564 | c.1758G>C | synonymous_variant | 0.67 |
| rpoB | 761573 | c.1767C>G | synonymous_variant | 1.0 |
| rpoB | 761579 | c.1773G>C | synonymous_variant | 1.0 |
| rpoB | 761612 | c.1806G>T | synonymous_variant | 1.0 |
| rpoB | 761615 | c.1809A>C | synonymous_variant | 1.0 |
| rpoB | 761627 | c.1821C>T | synonymous_variant | 1.0 |
| rpoB | 761645 | c.1839C>G | synonymous_variant | 1.0 |
| rpoB | 761648 | c.1842T>C | synonymous_variant | 1.0 |
| rpoB | 761669 | c.1863C>T | synonymous_variant | 1.0 |
| rpoB | 761675 | c.1869G>C | synonymous_variant | 1.0 |
| rpoB | 761951 | c.2145G>C | synonymous_variant | 1.0 |
| rpoB | 761954 | c.2148C>G | synonymous_variant | 1.0 |
| rpoB | 761955 | p.Ile717Phe | missense_variant | 1.0 |
| rpoB | 761972 | c.2166C>T | synonymous_variant | 1.0 |
| rpoB | 761987 | c.2181C>T | synonymous_variant | 1.0 |
| rpoB | 761998 | c.2193_2195delGTC | disruptive_inframe_deletion | 1.0 |
| rpoB | 762005 | c.2200_2201insAGC | disruptive_inframe_insertion | 1.0 |
| rpoB | 762009 | p.Leu735Val | missense_variant | 1.0 |
| rpoB | 762014 | c.2208C>G | synonymous_variant | 1.0 |
| rpoB | 762017 | c.2211A>G | synonymous_variant | 1.0 |
| rpoB | 762024 | p.Val740Ile | missense_variant | 1.0 |
| rpoB | 762053 | c.2247T>C | synonymous_variant | 1.0 |
| rpoB | 762062 | c.2256T>C | synonymous_variant | 1.0 |
| rpoB | 762065 | c.2259T>C | synonymous_variant | 1.0 |
| rpoB | 762080 | c.2274G>C | synonymous_variant | 1.0 |
| rpoB | 762083 | c.2277T>C | synonymous_variant | 1.0 |
| rpoB | 762086 | c.2280G>C | synonymous_variant | 1.0 |
| rpoB | 762101 | c.2295C>G | synonymous_variant | 1.0 |
| rpoB | 762104 | p.Asp766Glu | missense_variant | 1.0 |
| rpoB | 762114 | p.Ile770Val | 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 | 762132 | p.Ala776Arg | missense_variant | 1.0 |
| rpoB | 762140 | c.2334G>C | synonymous_variant | 1.0 |
| rpoB | 762143 | c.2337T>C | synonymous_variant | 1.0 |
| rpoB | 762149 | c.2343G>C | synonymous_variant | 1.0 |
| rpoB | 762158 | c.2352G>C | synonymous_variant | 1.0 |
| rpoB | 762173 | p.Glu789Asp | missense_variant | 1.0 |
| rpoB | 762176 | c.2370T>C | synonymous_variant | 1.0 |
| rpoB | 762181 | p.Asp792Ala | missense_variant | 1.0 |
| rpoB | 762185 | c.2379G>C | synonymous_variant | 1.0 |
| rpoB | 762194 | c.2388G>C | synonymous_variant | 1.0 |
| rpoB | 762218 | c.2412T>C | synonymous_variant | 1.0 |
| rpoB | 762233 | c.2427G>C | synonymous_variant | 1.0 |
| rpoB | 762245 | c.2439G>C | synonymous_variant | 1.0 |
| rpoB | 762248 | c.2442G>C | synonymous_variant | 1.0 |
| rpoB | 762254 | c.2448T>C | synonymous_variant | 1.0 |
| rpoB | 762284 | c.2478G>C | 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 | 762314 | c.2508C>T | synonymous_variant | 0.75 |
| rpoC | 762443 | c.-927G>C | upstream_gene_variant | 1.0 |
| rpoC | 762452 | c.-918G>C | upstream_gene_variant | 1.0 |
| rpoC | 762467 | c.-903C>T | upstream_gene_variant | 1.0 |
| rpoC | 762470 | c.-900G>C | upstream_gene_variant | 1.0 |
| rpoB | 762471 | p.Ile889Val | missense_variant | 1.0 |
| rpoC | 762476 | c.-894C>T | upstream_gene_variant | 1.0 |
| rpoB | 762489 | p.Val895Pro | missense_variant | 1.0 |
| rpoB | 762507 | p.Leu901Met | missense_variant | 1.0 |
| rpoB | 762510 | p.Ala902Pro | missense_variant | 1.0 |
| rpoC | 762524 | c.-846G>C | upstream_gene_variant | 1.0 |
| rpoC | 762533 | c.-837T>C | upstream_gene_variant | 1.0 |
| rpoC | 762536 | c.-834T>C | upstream_gene_variant | 1.0 |
| rpoC | 762537 | c.-833_-831delTTGinsCTC | upstream_gene_variant | 1.0 |
| rpoC | 762551 | c.-819C>T | upstream_gene_variant | 1.0 |
| rpoC | 762554 | c.-816G>C | upstream_gene_variant | 1.0 |
| rpoC | 762560 | c.-810A>T | upstream_gene_variant | 1.0 |
| rpoC | 762563 | c.-807G>T | upstream_gene_variant | 1.0 |
| rpoC | 762782 | c.-588T>C | upstream_gene_variant | 0.67 |
| rpoB | 762785 | p.Asp993Glu | missense_variant | 1.0 |
| rpoC | 762788 | c.-582G>C | upstream_gene_variant | 1.0 |
| rpoB | 762789 | p.Leu995Met | missense_variant | 1.0 |
| rpoB | 762795 | p.Asp997Asn | missense_variant | 1.0 |
| rpoB | 762814 | p.Met1003Thr | missense_variant | 1.0 |
| rpoC | 762818 | c.-552C>T | upstream_gene_variant | 1.0 |
| rpoB | 762819 | p.Phe1005Leu | missense_variant | 1.0 |
| rpoC | 762827 | c.-543G>A | upstream_gene_variant | 1.0 |
| rpoC | 762831 | c.-539_-538delAGinsTC | upstream_gene_variant | 1.0 |
| rpoC | 762836 | c.-534C>T | upstream_gene_variant | 1.0 |
| rpoC | 762842 | c.-528G>C | upstream_gene_variant | 1.0 |
| rpoC | 762857 | c.-513C>G | upstream_gene_variant | 1.0 |
| rpoB | 762858 | p.Thr1018Ser | missense_variant | 1.0 |
| rpoC | 762863 | c.-507T>G | upstream_gene_variant | 1.0 |
| rpoB | 762876 | p.Ile1024Leu | missense_variant | 1.0 |
| rpoB | 762879 | p.Met1025Leu | missense_variant | 1.0 |
| rpoC | 762887 | c.-483G>C | upstream_gene_variant | 1.0 |
| rpoB | 762905 | p.Asp1033Glu | missense_variant | 1.0 |
| rpoC | 762929 | c.-441G>C | upstream_gene_variant | 1.0 |
| rpoC | 762938 | c.-432G>C | upstream_gene_variant | 1.0 |
| rpoC | 762959 | c.-411G>C | upstream_gene_variant | 1.0 |
| rpoC | 762971 | c.-399G>C | upstream_gene_variant | 1.0 |
| rpoC | 762989 | c.-381G>C | upstream_gene_variant | 1.0 |
| rpoC | 762995 | c.-375G>T | upstream_gene_variant | 1.0 |
| rpoB | 763005 | p.Cys1067Val | missense_variant | 1.0 |
| rpoC | 763013 | c.-357C>G | upstream_gene_variant | 1.0 |
| rpoC | 763028 | c.-342T>C | upstream_gene_variant | 1.0 |
| rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
| rpoC | 763053 | c.-317T>C | upstream_gene_variant | 1.0 |
| rpoC | 763058 | c.-312C>G | upstream_gene_variant | 1.0 |
| rpoB | 763074 | p.Thr1090Val | missense_variant | 1.0 |
| rpoC | 763085 | c.-285C>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 |
| rpoB | 763130 | p.Glu1108Asp | missense_variant | 1.0 |
| rpoC | 763148 | c.-222G>C | upstream_gene_variant | 1.0 |
| rpoC | 763157 | c.-213G>T | upstream_gene_variant | 1.0 |
| rpoC | 763160 | c.-210G>C | 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 | 763178 | c.-192G>C | upstream_gene_variant | 1.0 |
| rpoC | 763187 | c.-183C>G | upstream_gene_variant | 1.0 |
| rpoC | 763373 | p.Leu2Phe | missense_variant | 1.0 |
| rpoC | 763381 | c.12C>A | synonymous_variant | 1.0 |
| rpoC | 763385 | p.Phe6Leu | missense_variant | 1.0 |
| rpoC | 763393 | p.Asp8Glu | missense_variant | 1.0 |
| rpoC | 763396 | c.27A>G | synonymous_variant | 1.0 |
| rpoC | 763408 | c.39T>C | synonymous_variant | 1.0 |
| rpoC | 763411 | c.42T>G | synonymous_variant | 1.0 |
| rpoC | 763414 | c.45T>C | synonymous_variant | 1.0 |
| rpoC | 763417 | c.48C>T | synonymous_variant | 1.0 |
| rpoC | 763420 | c.51G>C | synonymous_variant | 1.0 |
| rpoC | 763423 | p.Glu18Asp | missense_variant | 1.0 |
| rpoC | 763430 | c.61_63delAGGinsCGC | synonymous_variant | 1.0 |
| rpoC | 763434 | p.Gln22Arg | missense_variant | 0.67 |
| rpoC | 763442 | p.Tyr25Lys | missense_variant | 1.0 |
| rpoC | 763456 | c.87A>G | synonymous_variant | 1.0 |
| rpoC | 763468 | c.99G>C | synonymous_variant | 1.0 |
| rpoC | 763483 | c.114G>C | synonymous_variant | 1.0 |
| rpoC | 763486 | c.117T>C | synonymous_variant | 1.0 |
| rpoC | 763504 | c.135C>T | synonymous_variant | 1.0 |
| rpoC | 763507 | c.138G>C | synonymous_variant | 1.0 |
| rpoC | 763517 | p.Lys50Arg | missense_variant | 1.0 |
| rpoC | 763528 | c.159G>C | synonymous_variant | 1.0 |
| rpoC | 763534 | c.165T>C | synonymous_variant | 1.0 |
| rpoC | 763546 | c.177A>G | synonymous_variant | 0.91 |
| rpoC | 763550 | p.Tyr61Ala | missense_variant | 1.0 |
| rpoC | 763555 | c.186C>T | synonymous_variant | 1.0 |
| rpoC | 763570 | c.201G>C | synonymous_variant | 1.0 |
| rpoC | 763573 | c.204G>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 | 763619 | p.Arg84Lys | missense_variant | 1.0 |
| rpoC | 763622 | p.Ala85Ser | missense_variant | 1.0 |
| rpoC | 763630 | c.261G>C | 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>C | synonymous_variant | 1.0 |
| rpoC | 763669 | c.300C>G | synonymous_variant | 1.0 |
| rpoC | 763675 | c.306C>G | synonymous_variant | 1.0 |
| rpoC | 763702 | c.333C>G | synonymous_variant | 1.0 |
| rpoC | 763705 | c.336G>C | 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 | 763729 | c.360G>C | synonymous_variant | 1.0 |
| rpoC | 763732 | c.363C>G | synonymous_variant | 1.0 |
| rpoC | 763741 | c.372C>T | synonymous_variant | 1.0 |
| rpoC | 763744 | c.375G>C | synonymous_variant | 1.0 |
| rpoC | 763748 | p.Lys127Arg | missense_variant | 1.0 |
| rpoC | 763765 | c.396T>C | synonymous_variant | 1.0 |
| rpoC | 763768 | c.399C>G | synonymous_variant | 1.0 |
| rpoC | 763769 | p.Tyr134Asn | missense_variant | 1.0 |
| rpoC | 763772 | p.Val135Ile | missense_variant | 1.0 |
| rpoC | 763783 | c.414G>C | synonymous_variant | 1.0 |
| rpoC | 763792 | p.Glu141Asp | missense_variant | 1.0 |
| rpoC | 764353 | c.984G>C | synonymous_variant | 1.0 |
| rpoC | 764365 | c.996C>T | synonymous_variant | 1.0 |
| rpoC | 764371 | c.1002G>C | synonymous_variant | 1.0 |
| rpoC | 764380 | c.1011G>C | synonymous_variant | 1.0 |
| rpoC | 764383 | c.1014C>G | synonymous_variant | 1.0 |
| rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 1.0 |
| rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 1.0 |
| rpoC | 764428 | c.1059G>C | synonymous_variant | 1.0 |
| rpoC | 764431 | c.1062G>C | synonymous_variant | 1.0 |
| rpoC | 764434 | c.1065A>G | synonymous_variant | 1.0 |
| rpoC | 764435 | c.1066_1068delAGGinsCGC | synonymous_variant | 1.0 |
| rpoC | 764438 | p.Leu357Met | missense_variant | 1.0 |
| rpoC | 764446 | c.1077T>C | synonymous_variant | 1.0 |
| rpoC | 764449 | c.1080G>C | synonymous_variant | 1.0 |
| rpoC | 764452 | c.1083T>C | synonymous_variant | 1.0 |
| rpoC | 764458 | c.1089G>C | synonymous_variant | 1.0 |
| rpoC | 764461 | c.1092A>G | synonymous_variant | 1.0 |
| rpoC | 764470 | c.1101C>G | synonymous_variant | 1.0 |
| rpoC | 764485 | c.1116G>C | synonymous_variant | 1.0 |
| rpoC | 764497 | c.1128A>G | synonymous_variant | 1.0 |
| rpoC | 764509 | c.1140G>C | synonymous_variant | 1.0 |
| rpoC | 764512 | c.1143G>C | synonymous_variant | 1.0 |
| rpoC | 764521 | c.1152T>C | synonymous_variant | 1.0 |
| rpoC | 764536 | c.1167G>C | synonymous_variant | 0.97 |
| rpoC | 764539 | c.1170C>G | synonymous_variant | 1.0 |
| rpoC | 764548 | c.1179G>A | synonymous_variant | 1.0 |
| rpoC | 764560 | c.1191T>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 | 764581 | c.1212T>C | synonymous_variant | 1.0 |
| rpoC | 764602 | c.1233C>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 | 764632 | c.1263T>C | 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 | 764660 | p.Val431Ile | missense_variant | 0.98 |
| rpoC | 764687 | p.Gln440Glu | missense_variant | 1.0 |
| rpoC | 764692 | c.1323C>T | synonymous_variant | 1.0 |
| rpoC | 764695 | c.1326T>C | synonymous_variant | 1.0 |
| rpoC | 764701 | c.1332C>G | synonymous_variant | 1.0 |
| rpoC | 764731 | c.1362G>T | synonymous_variant | 1.0 |
| rpoC | 764737 | c.1368G>C | synonymous_variant | 1.0 |
| rpoC | 764746 | c.1377G>T | synonymous_variant | 1.0 |
| rpoC | 764755 | p.Asp462Glu | missense_variant | 1.0 |
| rpoC | 764756 | p.Leu463Asn | missense_variant | 1.0 |
| rpoC | 764759 | p.Asn464Asp | missense_variant | 1.0 |
| rpoC | 764762 | p.His465Tyr | missense_variant | 1.0 |
| rpoC | 764780 | c.1411_1412delAGinsTC | synonymous_variant | 1.0 |
| rpoC | 764785 | c.1416C>G | synonymous_variant | 1.0 |
| rpoC | 764797 | c.1428G>C | synonymous_variant | 1.0 |
| rpoC | 764803 | c.1434C>T | synonymous_variant | 1.0 |
| rpoC | 764809 | c.1440C>T | synonymous_variant | 1.0 |
| rpoC | 764813 | p.Gln482Glu | missense_variant | 1.0 |
| rpoC | 764824 | c.1455T>C | synonymous_variant | 1.0 |
| rpoC | 764833 | c.1464A>G | synonymous_variant | 1.0 |
| rpoC | 764838 | p.Val490Ala | missense_variant | 1.0 |
| rpoC | 764857 | c.1488G>C | synonymous_variant | 1.0 |
| rpoC | 764858 | p.Leu497Met | missense_variant | 1.0 |
| rpoC | 764863 | c.1494G>C | synonymous_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 | 764902 | c.1533C>G | synonymous_variant | 1.0 |
| rpoC | 764911 | c.1542A>G | synonymous_variant | 1.0 |
| rpoC | 764913 | p.Met515Lys | missense_variant | 1.0 |
| rpoC | 764917 | c.1548G>C | synonymous_variant | 1.0 |
| rpoC | 764920 | c.1551G>C | 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 | 765007 | c.1638T>G | synonymous_variant | 1.0 |
| rpoC | 765892 | c.2523T>C | synonymous_variant | 1.0 |
| rpoC | 765902 | p.Thr845Ser | missense_variant | 1.0 |
| rpoC | 765907 | c.2538G>C | synonymous_variant | 1.0 |
| rpoC | 765921 | p.Ile851Asn | missense_variant | 1.0 |
| rpoC | 765926 | p.Thr853Ser | missense_variant | 1.0 |
| rpoC | 765934 | c.2565C>T | synonymous_variant | 1.0 |
| rpoC | 765935 | p.Ala856Ser | missense_variant | 1.0 |
| rpoC | 765940 | c.2571A>T | synonymous_variant | 1.0 |
| rpoC | 765947 | c.2578T>C | synonymous_variant | 1.0 |
| rpoC | 765952 | c.2583G>C | synonymous_variant | 1.0 |
| rpoC | 765955 | c.2586C>T | synonymous_variant | 1.0 |
| rpoC | 765962 | c.2593T>C | synonymous_variant | 1.0 |
| rpoC | 765967 | c.2598C>T | synonymous_variant | 1.0 |
| rpoC | 765994 | c.2625A>T | synonymous_variant | 1.0 |
| rpoC | 766000 | c.2631G>C | synonymous_variant | 1.0 |
| rpoC | 766003 | c.2634G>C | synonymous_variant | 1.0 |
| rpoC | 766009 | c.2640G>C | synonymous_variant | 1.0 |
| rpoC | 766010 | p.Ser881Ala | missense_variant | 1.0 |
| rpoC | 766018 | c.2649C>T | synonymous_variant | 1.0 |
| rpoC | 766021 | c.2652G>C | synonymous_variant | 1.0 |
| rpoC | 766027 | c.2658G>C | synonymous_variant | 0.86 |
| rpoC | 766034 | p.His889Asp | missense_variant | 0.83 |
| rpoC | 766328 | p.Lys987Gln | missense_variant | 0.75 |
| rpoC | 766345 | c.2976T>C | synonymous_variant | 0.91 |
| rpoC | 766348 | c.2979A>G | synonymous_variant | 0.91 |
| rpoC | 766363 | c.2994G>C | synonymous_variant | 0.91 |
| rpoC | 766375 | c.3006C>G | synonymous_variant | 1.0 |
| rpoC | 766381 | c.3012C>T | synonymous_variant | 1.0 |
| rpoC | 766384 | c.3015A>G | synonymous_variant | 1.0 |
| rpoC | 766408 | c.3039C>T | synonymous_variant | 1.0 |
| rpoC | 766426 | c.3057C>T | synonymous_variant | 1.0 |
| rpoC | 766434 | p.Glu1022Gly | missense_variant | 1.0 |
| rpoC | 766447 | c.3078T>C | synonymous_variant | 1.0 |
| rpoC | 766453 | c.3084G>C | synonymous_variant | 1.0 |
| rpoC | 766456 | c.3087C>G | synonymous_variant | 1.0 |
| rpoC | 766459 | c.3090G>T | synonymous_variant | 1.0 |
| rpoC | 766462 | c.3093G>C | synonymous_variant | 1.0 |
| rpoC | 766483 | c.3114G>C | synonymous_variant | 1.0 |
| rpoC | 767008 | c.3639G>C | synonymous_variant | 1.0 |
| rpoC | 767020 | c.3651C>G | 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 | 767044 | c.3675G>C | synonymous_variant | 1.0 |
| rpoC | 767059 | c.3690T>G | synonymous_variant | 1.0 |
| rpoC | 767062 | c.3693C>T | synonymous_variant | 1.0 |
| rpoC | 767065 | c.3696G>C | synonymous_variant | 1.0 |
| rpoC | 767074 | c.3705T>C | synonymous_variant | 1.0 |
| rpoC | 767077 | c.3708G>C | synonymous_variant | 1.0 |
| rpoC | 767087 | p.Cys1240Lys | missense_variant | 1.0 |
| rpoC | 767093 | c.3724_3725delAGinsTC | synonymous_variant | 1.0 |
| rpoC | 767098 | c.3729T>C | synonymous_variant | 1.0 |
| rpoC | 767099 | p.Lys1244Gln | missense_variant | 1.0 |
| rpoC | 767106 | p.Asn1246Ile | missense_variant | 1.0 |
| rpoC | 767110 | c.3741T>C | synonymous_variant | 1.0 |
| rpoC | 767113 | c.3744G>C | synonymous_variant | 1.0 |
| rpoC | 767119 | c.3750A>G | synonymous_variant | 1.0 |
| rpoC | 767134 | c.3765C>T | synonymous_variant | 1.0 |
| rrs | 1471852 | n.7T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 0.98 |
| rrs | 1471925 | n.81_82insAAGCTTGC | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471928 | n.84_85delCG | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471932 | n.87A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472028 | n.183A>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472029 | n.185_194delGGGATGCATG | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472057 | n.212C>T | 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 | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472150 | n.305T>G | 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 | 1472225 | n.380C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472286 | n.441C>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.97 |
| rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472297 | n.453_461delGTCCGGGTT | 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 | 0.97 |
| rrs | 1472312 | n.468_470delGAT | 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>T | 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 | 1472447 | n.602C>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 | 1472489 | n.644A>T | 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 | 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 | 1.0 |
| rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472685 | n.840G>A | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472686 | n.841G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472690 | n.845C>T | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.99 |
| 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 | 0.99 |
| rrs | 1472840 | n.995A>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472844 | n.999C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472845 | n.1000G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472846 | n.1001C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472848 | n.1003T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472859 | n.1014G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472861 | n.1016G>C | 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 | 0.99 |
| rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.99 |
| 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 | 1473089 | n.1244A>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473091 | n.1246G>C | non_coding_transcript_exon_variant | 0.98 |
| rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.98 |
| rrs | 1473094 | n.1249T>C | non_coding_transcript_exon_variant | 0.98 |
| rrs | 1473099 | n.1254T>G | non_coding_transcript_exon_variant | 0.98 |
| rrs | 1473100 | n.1255G>C | non_coding_transcript_exon_variant | 0.98 |
| rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.98 |
| rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.98 |
| rrs | 1473109 | n.1264T>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 | 0.98 |
| rrs | 1473119 | n.1274_1275insG | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473122 | n.1277T>C | non_coding_transcript_exon_variant | 0.98 |
| rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473132 | n.1287T>C | non_coding_transcript_exon_variant | 0.98 |
| rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.99 |
| 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 | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1473391 | n.-267C>T | upstream_gene_variant | 1.0 |
| rrl | 1473676 | n.19G>A | non_coding_transcript_exon_variant | 0.67 |
| rrl | 1473697 | n.40C>G | non_coding_transcript_exon_variant | 0.75 |
| rrl | 1473698 | n.41G>C | non_coding_transcript_exon_variant | 0.75 |
| rrl | 1473699 | n.42A>T | non_coding_transcript_exon_variant | 0.75 |
| rrl | 1473701 | n.44A>G | non_coding_transcript_exon_variant | 0.75 |
| rrl | 1473718 | n.61G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473719 | n.62G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473728 | n.71A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473731 | n.74T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473743 | n.86C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473750 | n.93C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474135 | n.478G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474182 | n.525C>A | non_coding_transcript_exon_variant | 0.97 |
| rrl | 1474183 | n.526T>G | 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 | 1474200 | n.545delT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474293 | n.637_651delCCTCTCCGGAGGAGG | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474310 | n.655delG | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474328 | n.671T>G | 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 | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474384 | n.727C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474399 | n.742G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474447 | n.790G>A | 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 | 1474496 | n.839C>A | non_coding_transcript_exon_variant | 0.98 |
| rrl | 1474497 | n.840G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474517 | n.860C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1474633 | n.977_981delTCACC | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474640 | n.983_984insTTACT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474722 | n.1065T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474723 | n.1066G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474751 | n.1094G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474798 | n.1141C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474803 | n.1146G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.99 |
| 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 | 1474920 | n.1263G>A | 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 | 1474953 | n.1296C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475027 | n.1370G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475031 | n.1374G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475033 | n.1376G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475057 | n.1400G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475061 | n.1404C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475062 | n.1405A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475063 | n.1406A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475076 | n.1419C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475088 | n.1431A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475094 | n.1437C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475108 | n.1451C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475110 | n.1454_1457delGGCC | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475118 | n.1461C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475120 | n.1463_1464insTCTT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475499 | n.1842C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475514 | n.1857G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475542 | n.1885A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475544 | n.1887A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475550 | n.1893A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475672 | n.2015C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475703 | n.2046A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475704 | n.2047C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475757 | n.2100_2101insGTG | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475760 | n.2103C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 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 | 0.99 |
| 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 | 1476024 | n.2367T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476025 | n.2368G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476028 | n.2372_2375delAACC | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476034 | n.2377_2378insACAT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476046 | n.2389G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476048 | n.2391G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476049 | n.2392C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476080 | n.2423T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476089 | n.2432T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476090 | n.2434dupT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476097 | n.2440C>T | non_coding_transcript_exon_variant | 1.0 |
| 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>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476105 | n.2450delA | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476110 | n.2453G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476113 | n.2456T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476116 | n.2459A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476297 | n.2640C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476298 | n.2641C>A | 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 | 1476307 | n.2650A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476309 | n.2652G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476533 | n.2876G>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 | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476607 | n.2950C>G | 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 | 0.89 |
| 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 | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476661 | n.3004A>G | non_coding_transcript_exon_variant | 1.0 |
| rpsA | 1833649 | c.108C>T | synonymous_variant | 0.83 |
| rpsA | 1833661 | c.120A>G | synonymous_variant | 0.83 |
| rpsA | 1833668 | p.Ile43Val | missense_variant | 0.83 |
| rpsA | 1833676 | c.135A>G | synonymous_variant | 1.0 |
| rpsA | 1833679 | c.138G>C | synonymous_variant | 1.0 |
| rpsA | 1833685 | c.144G>C | synonymous_variant | 1.0 |
| rpsA | 1833694 | c.153G>T | synonymous_variant | 1.0 |
| rpsA | 1833697 | c.156C>T | synonymous_variant | 1.0 |
| rpsA | 1833721 | c.180A>G | synonymous_variant | 0.92 |
| 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 | 0.92 |
| rpsA | 1833760 | c.219C>T | synonymous_variant | 0.93 |
| rpsA | 1833769 | c.228C>G | synonymous_variant | 1.0 |
| rpsA | 1833770 | p.Asn77Asp | missense_variant | 1.0 |
| rpsA | 1833781 | c.240T>C | synonymous_variant | 1.0 |
| rpsA | 1833782 | p.Ser81Glu | missense_variant | 1.0 |
| rpsA | 1833790 | c.249T>C | synonymous_variant | 1.0 |
| rpsA | 1833794 | p.Glu85Gln | missense_variant | 1.0 |
| rpsA | 1833797 | p.Val86Ile | missense_variant | 1.0 |
| rpsA | 1833802 | p.Glu87Asp | missense_variant | 1.0 |
| rpsA | 1833805 | c.264C>A | synonymous_variant | 1.0 |
| rpsA | 1833811 | c.270G>C | synonymous_variant | 1.0 |
| rpsA | 1833829 | c.288A>G | synonymous_variant | 1.0 |
| rpsA | 1833835 | c.294C>T | synonymous_variant | 1.0 |
| rpsA | 1833838 | c.297G>C | synonymous_variant | 1.0 |
| rpsA | 1833841 | c.300C>G | synonymous_variant | 1.0 |
| rpsA | 1833856 | c.315A>G | synonymous_variant | 1.0 |
| rpsA | 1833862 | c.321G>A | synonymous_variant | 1.0 |
| rpsA | 1833874 | c.333T>C | synonymous_variant | 1.0 |
| rpsA | 1833884 | p.Thr115Ala | missense_variant | 1.0 |
| rpsA | 1833894 | p.Ala118Glu | 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 | 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 | 1833988 | c.447C>G | synonymous_variant | 1.0 |
| rpsA | 1833994 | c.453G>C | synonymous_variant | 1.0 |
| rpsA | 1833997 | c.456G>C | synonymous_variant | 1.0 |
| rpsA | 1834000 | c.459G>C | synonymous_variant | 1.0 |
| rpsA | 1834009 | c.468C>T | synonymous_variant | 1.0 |
| rpsA | 1834012 | c.471G>C | synonymous_variant | 1.0 |
| rpsA | 1834015 | c.474G>C | synonymous_variant | 1.0 |
| rpsA | 1834025 | p.Gln162Asp | missense_variant | 1.0 |
| rpsA | 1834030 | c.489C>G | synonymous_variant | 1.0 |
| rpsA | 1834040 | p.Lys167Gln | missense_variant | 1.0 |
| rpsA | 1834046 | p.Ile169Leu | missense_variant | 1.0 |
| rpsA | 1834054 | c.513C>A | synonymous_variant | 1.0 |
| rpsA | 1834076 | p.Asn179His | missense_variant | 1.0 |
| rpsA | 1834093 | c.552G>C | 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 | 0.8 |
| rpsA | 1834189 | c.648G>C | synonymous_variant | 1.0 |
| rpsA | 1834195 | c.654G>C | synonymous_variant | 1.0 |
| rpsA | 1834213 | c.672G>C | synonymous_variant | 1.0 |
| rpsA | 1834234 | c.693G>C | synonymous_variant | 0.94 |
| 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 | 1834261 | c.720A>G | synonymous_variant | 1.0 |
| rpsA | 1834264 | c.723G>C | synonymous_variant | 1.0 |
| rpsA | 1834288 | c.747C>T | synonymous_variant | 1.0 |
| rpsA | 1834294 | c.753G>T | synonymous_variant | 1.0 |
| rpsA | 1834298 | p.Gln253Thr | 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>C | synonymous_variant | 1.0 |
| rpsA | 1834339 | c.798C>T | synonymous_variant | 1.0 |
| rpsA | 1834340 | p.Met267Leu | missense_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 | 1834369 | c.828C>G | synonymous_variant | 1.0 |
| rpsA | 1834378 | c.837T>C | synonymous_variant | 1.0 |
| rpsA | 1834384 | c.843A>G | synonymous_variant | 1.0 |
| rpsA | 1834396 | c.855G>C | synonymous_variant | 1.0 |
| rpsA | 1834397 | p.His286Val | missense_variant | 1.0 |
| rpsA | 1834411 | c.870T>C | synonymous_variant | 1.0 |
| rpsA | 1834417 | c.876G>T | synonymous_variant | 1.0 |
| rpsA | 1834418 | p.Ile293Val | missense_variant | 1.0 |
| rpsA | 1834423 | c.882G>C | synonymous_variant | 1.0 |
| rpsA | 1834432 | c.891G>C | synonymous_variant | 1.0 |
| rpsA | 1834451 | c.910_912delTTGinsCTC | synonymous_variant | 1.0 |
| rpsA | 1834456 | c.915T>C | synonymous_variant | 1.0 |
| rpsA | 1834465 | c.924T>C | synonymous_variant | 0.92 |
| rpsA | 1834468 | c.927A>G | synonymous_variant | 1.0 |
| rpsA | 1834489 | c.948T>C | synonymous_variant | 1.0 |
| rpsA | 1834501 | c.960G>C | synonymous_variant | 1.0 |
| rpsA | 1834504 | c.963G>C | synonymous_variant | 1.0 |
| rpsA | 1834523 | p.Glu328Gln | missense_variant | 1.0 |
| rpsA | 1834528 | c.987T>C | synonymous_variant | 1.0 |
| rpsA | 1834534 | c.993C>G | synonymous_variant | 1.0 |
| rpsA | 1834540 | c.999G>C | synonymous_variant | 1.0 |
| rpsA | 1834543 | c.1002C>G | synonymous_variant | 1.0 |
| rpsA | 1834546 | c.1005T>C | synonymous_variant | 1.0 |
| rpsA | 1834552 | c.1011G>T | synonymous_variant | 1.0 |
| rpsA | 1834555 | c.1014T>C | synonymous_variant | 1.0 |
| rpsA | 1834556 | p.Ala339Thr | missense_variant | 1.0 |
| rpsA | 1834565 | p.Asp342Gln | missense_variant | 1.0 |
| rpsA | 1834570 | p.Asp343Glu | missense_variant | 1.0 |
| rpsA | 1834573 | c.1032G>C | synonymous_variant | 1.0 |
| rpsA | 1834600 | c.1059G>C | synonymous_variant | 1.0 |
| rpsA | 1834606 | c.1065C>T | synonymous_variant | 1.0 |
| rpsA | 1834612 | c.1071G>C | synonymous_variant | 1.0 |
| rpsA | 1834618 | c.1077G>C | synonymous_variant | 1.0 |
| rpsA | 1834619 | c.1078T>C | synonymous_variant | 1.0 |
| rpsA | 1834624 | c.1083G>C | synonymous_variant | 1.0 |
| rpsA | 1834633 | c.1092A>G | synonymous_variant | 1.0 |
| rpsA | 1834637 | p.Asn366Asp | missense_variant | 0.95 |
| rpsA | 1834654 | p.Glu371Asp | missense_variant | 1.0 |
| rpsA | 1834667 | p.Ala376Ser | missense_variant | 1.0 |
| rpsA | 1834688 | c.1147_1149delAGTinsTCC | synonymous_variant | 1.0 |
| rpsA | 1834720 | c.1179C>G | synonymous_variant | 1.0 |
| rpsA | 1834732 | c.1191T>C | synonymous_variant | 1.0 |
| rpsA | 1834733 | p.Ala398Pro | missense_variant | 1.0 |
| rpsA | 1834738 | c.1197A>G | synonymous_variant | 1.0 |
| rpsA | 1834747 | c.1206A>G | synonymous_variant | 1.0 |
| rpsA | 1834753 | c.1212T>C | synonymous_variant | 1.0 |
| rpsA | 1834759 | c.1218A>C | synonymous_variant | 1.0 |
| thyX | 3067373 | c.573C>G | synonymous_variant | 1.0 |
| thyX | 3067391 | c.555G>C | synonymous_variant | 1.0 |
| thyX | 3067394 | c.552G>C | synonymous_variant | 1.0 |
| thyX | 3067405 | p.Thr181Ser | missense_variant | 1.0 |
| thyX | 3067427 | c.519G>C | synonymous_variant | 1.0 |
| thyX | 3067439 | c.507A>G | synonymous_variant | 1.0 |
| clpC1 | 4038740 | c.1965G>C | synonymous_variant | 1.0 |
| clpC1 | 4038743 | p.Thr654Ile | missense_variant | 1.0 |
| clpC1 | 4038755 | c.1950G>C | synonymous_variant | 1.0 |
| clpC1 | 4038767 | c.1938G>T | synonymous_variant | 1.0 |
| clpC1 | 4038770 | c.1935C>T | synonymous_variant | 1.0 |
| clpC1 | 4038773 | c.1932T>C | synonymous_variant | 1.0 |
| clpC1 | 4038791 | c.1914G>C | synonymous_variant | 1.0 |
| clpC1 | 4038795 | p.Ser637Thr | missense_variant | 1.0 |
| clpC1 | 4038803 | c.1902C>T | synonymous_variant | 1.0 |
| clpC1 | 4038811 | p.Gln632Lys | missense_variant | 1.0 |
| clpC1 | 4038812 | c.1893T>C | synonymous_variant | 1.0 |
| clpC1 | 4038815 | c.1890G>C | synonymous_variant | 1.0 |
| clpC1 | 4038836 | c.1869G>C | synonymous_variant | 1.0 |
| clpC1 | 4038842 | c.1863G>C | synonymous_variant | 1.0 |
| clpC1 | 4038845 | c.1860G>C | synonymous_variant | 1.0 |
| clpC1 | 4038857 | c.1848C>T | synonymous_variant | 1.0 |
| clpC1 | 4038860 | c.1845G>C | synonymous_variant | 1.0 |
| clpC1 | 4038863 | c.1842G>C | synonymous_variant | 1.0 |
| clpC1 | 4038878 | c.1827A>G | synonymous_variant | 1.0 |
| clpC1 | 4038905 | c.1800A>C | synonymous_variant | 1.0 |
| clpC1 | 4038911 | c.1794G>C | synonymous_variant | 1.0 |
| clpC1 | 4038923 | c.1782A>C | synonymous_variant | 1.0 |
| clpC1 | 4038926 | c.1779G>A | synonymous_variant | 1.0 |
| clpC1 | 4038929 | c.1776G>C | synonymous_variant | 1.0 |
| clpC1 | 4038932 | c.1773G>C | synonymous_variant | 1.0 |
| clpC1 | 4038941 | c.1764G>C | synonymous_variant | 1.0 |
| clpC1 | 4038953 | c.1752A>G | synonymous_variant | 1.0 |
| clpC1 | 4038965 | c.1740T>C | synonymous_variant | 1.0 |
| clpC1 | 4038971 | c.1734T>C | synonymous_variant | 1.0 |
| clpC1 | 4038974 | c.1731T>C | synonymous_variant | 1.0 |
| clpC1 | 4038977 | c.1728G>C | synonymous_variant | 1.0 |
| clpC1 | 4038983 | c.1722C>T | synonymous_variant | 1.0 |
| clpC1 | 4038986 | p.Asp573Glu | missense_variant | 1.0 |
| clpC1 | 4038989 | c.1716T>C | synonymous_variant | 1.0 |
| clpC1 | 4038995 | c.1708_1710delTTGinsCTC | synonymous_variant | 1.0 |
| clpC1 | 4039001 | p.Asn568Glu | missense_variant | 1.0 |
| clpC1 | 4039010 | c.1695G>C | synonymous_variant | 1.0 |
| clpC1 | 4039016 | c.1689C>G | synonymous_variant | 1.0 |
| clpC1 | 4039022 | c.1683A>G | synonymous_variant | 1.0 |
| clpC1 | 4039034 | c.1671C>G | synonymous_variant | 1.0 |
| clpC1 | 4039061 | c.1644G>C | synonymous_variant | 0.96 |
| clpC1 | 4039064 | c.1641C>T | synonymous_variant | 1.0 |
| clpC1 | 4039067 | c.1638G>C | synonymous_variant | 1.0 |
| clpC1 | 4039070 | c.1635G>C | synonymous_variant | 1.0 |
| clpC1 | 4039073 | c.1632C>T | synonymous_variant | 1.0 |
| clpC1 | 4039079 | c.1626C>G | synonymous_variant | 0.96 |
| clpC1 | 4039085 | c.1620A>G | synonymous_variant | 1.0 |
| clpC1 | 4039091 | c.1614G>C | synonymous_variant | 1.0 |
| clpC1 | 4039094 | c.1611C>G | synonymous_variant | 1.0 |
| clpC1 | 4039097 | c.1608G>C | synonymous_variant | 1.0 |
| clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.96 |
| clpC1 | 4039115 | p.Lys530Arg | missense_variant | 0.96 |
| clpC1 | 4039121 | c.1584T>C | synonymous_variant | 1.0 |
| clpC1 | 4039136 | p.Asp523Glu | missense_variant | 0.97 |
| clpC1 | 4039139 | p.Glu522Asp | missense_variant | 0.97 |
| 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 | 0.97 |
| clpC1 | 4039169 | p.Glu512Asp | missense_variant | 1.0 |
| clpC1 | 4039172 | c.1533A>G | synonymous_variant | 1.0 |
| clpC1 | 4039178 | c.1527G>C | synonymous_variant | 1.0 |
| clpC1 | 4039183 | c.1522T>C | synonymous_variant | 1.0 |
| clpC1 | 4039187 | c.1518G>T | synonymous_variant | 0.93 |
| clpC1 | 4039190 | p.Thr505Ser | missense_variant | 1.0 |
| clpC1 | 4039195 | p.Thr504Ser | missense_variant | 0.93 |
| clpC1 | 4039199 | p.Ala502Glu | missense_variant | 1.0 |
| clpC1 | 4039226 | c.1479T>C | synonymous_variant | 0.92 |
| clpC1 | 4039236 | p.Asn490Ser | missense_variant | 0.92 |
| clpC1 | 4039241 | c.1464G>C | synonymous_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 | 4039487 | c.1218G>C | synonymous_variant | 1.0 |
| clpC1 | 4039499 | c.1206G>C | synonymous_variant | 1.0 |
| clpC1 | 4039507 | p.Ile400Val | missense_variant | 1.0 |
| clpC1 | 4039508 | c.1197G>C | synonymous_variant | 1.0 |
| clpC1 | 4039517 | c.1188C>G | synonymous_variant | 1.0 |
| clpC1 | 4039526 | c.1179G>T | synonymous_variant | 1.0 |
| clpC1 | 4039549 | p.Ala386Ser | missense_variant | 1.0 |
| clpC1 | 4039550 | c.1155G>C | synonymous_variant | 1.0 |
| clpC1 | 4039554 | p.Thr384Asn | missense_variant | 1.0 |
| clpC1 | 4039565 | p.Val380Ala | missense_variant | 1.0 |
| clpC1 | 4039570 | p.Met379Leu | missense_variant | 1.0 |
| clpC1 | 4039571 | c.1134G>C | synonymous_variant | 1.0 |
| clpC1 | 4039574 | p.Ala377Gly | missense_variant | 1.0 |
| clpC1 | 4039577 | c.1128T>C | synonymous_variant | 1.0 |
| clpC1 | 4039586 | c.1119G>C | synonymous_variant | 1.0 |
| clpC1 | 4039592 | c.1113G>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 | 4039631 | c.1074C>T | synonymous_variant | 1.0 |
| clpC1 | 4039643 | p.His354Met | missense_variant | 1.0 |
| clpC1 | 4039649 | c.1056G>C | synonymous_variant | 1.0 |
| clpC1 | 4039652 | p.Thr351Ser | missense_variant | 1.0 |
| clpC1 | 4039655 | c.1050G>C | synonymous_variant | 1.0 |
| clpC1 | 4039661 | p.Gly348Pro | missense_variant | 1.0 |
| clpC1 | 4039664 | c.1041G>C | synonymous_variant | 1.0 |
| clpC1 | 4039682 | c.1023C>T | synonymous_variant | 1.0 |
| clpC1 | 4039685 | c.1020C>T | synonymous_variant | 1.0 |
| clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.95 |
| clpC1 | 4039714 | p.Tyr331His | missense_variant | 0.96 |
| clpC1 | 4039724 | c.981A>G | synonymous_variant | 1.0 |
| clpC1 | 4039727 | c.978C>T | 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 | 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 | 4039784 | p.Ile307Leu | missense_variant | 1.0 |
| clpC1 | 4039787 | c.918G>C | synonymous_variant | 1.0 |
| clpC1 | 4039817 | c.888A>T | synonymous_variant | 1.0 |
| clpC1 | 4039820 | c.885T>G | synonymous_variant | 1.0 |
| clpC1 | 4039823 | c.882T>C | synonymous_variant | 1.0 |
| clpC1 | 4039831 | c.874T>C | synonymous_variant | 1.0 |
| clpC1 | 4039838 | p.Leu289Ile | missense_variant | 1.0 |
| clpC1 | 4039850 | c.855T>C | synonymous_variant | 1.0 |
| clpC1 | 4039871 | p.Thr278Gln | missense_variant | 1.0 |
| clpC1 | 4039898 | c.807C>G | synonymous_variant | 1.0 |
| clpC1 | 4039904 | c.801A>G | synonymous_variant | 1.0 |
| clpC1 | 4039982 | c.723G>C | synonymous_variant | 1.0 |
| clpC1 | 4039991 | c.714G>C | 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 | 4040012 | p.Gln231Leu | missense_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 | 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 | 4040063 | c.642G>C | synonymous_variant | 1.0 |
| clpC1 | 4040066 | c.639G>C | synonymous_variant | 1.0 |
| clpC1 | 4040084 | c.621C>T | synonymous_variant | 1.0 |
| clpC1 | 4040087 | c.618G>T | synonymous_variant | 1.0 |
| clpC1 | 4040090 | c.615T>G | synonymous_variant | 1.0 |
| clpC1 | 4040107 | p.Val200Ile | missense_variant | 1.0 |
| clpC1 | 4040108 | c.597G>C | synonymous_variant | 1.0 |
| clpC1 | 4040117 | c.588A>G | synonymous_variant | 1.0 |
| clpC1 | 4040126 | c.579C>T | synonymous_variant | 1.0 |
| clpC1 | 4040134 | p.Ile191Val | missense_variant | 1.0 |
| clpC1 | 4040144 | c.561G>C | synonymous_variant | 1.0 |
| clpC1 | 4040147 | c.558A>G | synonymous_variant | 1.0 |
| clpC1 | 4040153 | p.Glu184Asp | missense_variant | 1.0 |
| clpC1 | 4040157 | p.Met183Arg | missense_variant | 1.0 |
| clpC1 | 4040159 | c.546G>C | synonymous_variant | 1.0 |
| clpC1 | 4040166 | p.Ala180Gln | missense_variant | 1.0 |
| clpC1 | 4040195 | c.510G>C | synonymous_variant | 1.0 |
