Run ID: ERR4769493
Sample name:
Date: 01-04-2023 06:42:44
Number of reads: 223905
Percentage reads mapped: 5.59
Strain: lineage4.9;La1.3
Drug-resistance: Pre-XDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
La1.3 | M.bovis | None | None | 0.07 |
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.99 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 0.92 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrB | 6695 | p.Ile486Leu | missense_variant | 0.93 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
gyrB | 6738 | p.Thr500Asn | missense_variant | 0.91 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761121 | p.Pro439Ser | missense_variant | 0.71 | rifampicin |
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 1.0 | streptomycin |
pncA | 2289073 | p.His57Asp | missense_variant | 1.0 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5287 | c.48T>G | synonymous_variant | 0.67 |
gyrB | 5296 | c.57T>C | synonymous_variant | 1.0 |
gyrB | 5302 | c.63A>G | synonymous_variant | 1.0 |
gyrB | 5308 | c.69G>C | synonymous_variant | 1.0 |
gyrB | 5341 | c.102T>C | synonymous_variant | 1.0 |
gyrB | 5350 | c.111C>G | synonymous_variant | 1.0 |
gyrB | 5353 | c.114T>C | synonymous_variant | 1.0 |
gyrB | 5362 | c.123T>C | synonymous_variant | 1.0 |
gyrB | 5363 | c.124_126delTTAinsCTG | synonymous_variant | 1.0 |
gyrB | 5371 | c.132T>C | synonymous_variant | 1.0 |
gyrB | 5375 | p.Ile46Val | missense_variant | 1.0 |
gyrB | 5386 | c.147G>C | synonymous_variant | 0.75 |
gyrB | 5396 | p.Ala53Ser | missense_variant | 0.75 |
gyrB | 5407 | c.168G>A | synonymous_variant | 0.75 |
gyrB | 5416 | c.177C>G | synonymous_variant | 0.75 |
gyrB | 6170 | p.His311Ile | missense_variant | 0.6 |
gyrB | 6184 | c.945C>G | synonymous_variant | 0.4 |
gyrB | 6446 | p.Ala403Ser | missense_variant | 1.0 |
gyrA | 6655 | c.-647T>C | upstream_gene_variant | 0.67 |
gyrA | 6673 | c.-629A>C | upstream_gene_variant | 0.94 |
gyrA | 6676 | c.-626T>G | upstream_gene_variant | 0.9 |
gyrA | 6685 | c.-617C>A | upstream_gene_variant | 0.93 |
gyrA | 6700 | c.-602T>C | upstream_gene_variant | 0.93 |
gyrA | 6709 | c.-593A>G | upstream_gene_variant | 0.93 |
gyrB | 6710 | p.Ala491Ser | missense_variant | 0.93 |
gyrB | 6716 | p.Ile493Leu | missense_variant | 0.93 |
gyrA | 6724 | c.-578G>C | upstream_gene_variant | 0.93 |
gyrB | 6725 | p.Val496Thr | missense_variant | 0.93 |
gyrA | 6730 | c.-572A>G | upstream_gene_variant | 0.94 |
gyrA | 6742 | c.-560A>G | upstream_gene_variant | 0.91 |
gyrA | 6745 | c.-557T>C | upstream_gene_variant | 0.91 |
gyrA | 6775 | c.-527G>C | upstream_gene_variant | 0.92 |
gyrA | 6793 | c.-509T>C | upstream_gene_variant | 0.92 |
gyrB | 6798 | p.Gly520Ala | missense_variant | 0.92 |
gyrA | 6808 | c.-494C>G | upstream_gene_variant | 0.93 |
gyrA | 6826 | c.-476G>C | upstream_gene_variant | 0.8 |
gyrA | 8486 | c.1185T>C | synonymous_variant | 0.75 |
gyrA | 8489 | c.1188A>G | synonymous_variant | 0.75 |
gyrA | 8495 | c.1194C>G | synonymous_variant | 0.75 |
gyrA | 8498 | c.1197C>T | synonymous_variant | 0.75 |
gyrA | 8504 | c.1203G>C | synonymous_variant | 0.75 |
gyrA | 8516 | c.1215T>C | synonymous_variant | 0.75 |
gyrA | 8519 | c.1218A>C | synonymous_variant | 0.75 |
gyrA | 8528 | c.1227G>C | synonymous_variant | 0.75 |
gyrA | 8529 | p.Ala410Arg | missense_variant | 0.75 |
gyrA | 8536 | p.Glu412Ala | missense_variant | 0.75 |
gyrA | 8546 | c.1245T>C | synonymous_variant | 0.75 |
gyrA | 8548 | p.Ile416Thr | missense_variant | 0.75 |
gyrA | 8552 | c.1251C>G | synonymous_variant | 0.75 |
gyrA | 8555 | c.1254G>C | synonymous_variant | 0.75 |
gyrA | 8556 | p.Ala419Thr | missense_variant | 0.75 |
gyrA | 8561 | c.1260A>C | synonymous_variant | 0.75 |
gyrA | 8567 | p.Ile422Met | missense_variant | 0.88 |
gyrA | 8569 | p.Glu423Gly | missense_variant | 0.88 |
gyrA | 8589 | p.Ile430Val | missense_variant | 1.0 |
gyrA | 8598 | p.Gln433Asp | missense_variant | 1.0 |
gyrA | 8603 | c.1302A>C | synonymous_variant | 1.0 |
gyrA | 8611 | p.Asp437Ala | missense_variant | 1.0 |
gyrA | 8619 | c.1318T>C | synonymous_variant | 0.86 |
gyrA | 8624 | c.1323G>C | synonymous_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 760953 | p.Ile383Val | missense_variant | 0.67 |
rpoB | 760958 | c.1152G>C | synonymous_variant | 0.67 |
rpoB | 760965 | p.Met387Leu | missense_variant | 1.0 |
rpoB | 760973 | c.1167G>C | synonymous_variant | 1.0 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 1.0 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 1.0 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 1.0 |
rpoB | 760997 | c.1191G>C | synonymous_variant | 1.0 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.6 |
rpoB | 761129 | c.1323G>C | synonymous_variant | 0.71 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 0.71 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.78 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.83 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.98 |
rpoB | 761174 | c.1368T>C | synonymous_variant | 0.98 |
rpoB | 761180 | c.1374A>T | synonymous_variant | 0.98 |
rpoB | 761183 | c.1377T>C | synonymous_variant | 0.98 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.98 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.98 |
rpoB | 761198 | c.1392G>C | synonymous_variant | 0.98 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.99 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 1.0 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 1.0 |
rpoB | 761252 | c.1446C>G | synonymous_variant | 1.0 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 1.0 |
rpoB | 761258 | c.1452G>A | synonymous_variant | 1.0 |
rpoB | 761261 | c.1455G>C | synonymous_variant | 1.0 |
rpoB | 761264 | c.1458C>G | synonymous_variant | 1.0 |
rpoB | 761273 | c.1467T>C | synonymous_variant | 1.0 |
rpoB | 761294 | c.1488G>C | synonymous_variant | 1.0 |
rpoB | 761300 | c.1494G>C | synonymous_variant | 1.0 |
rpoB | 761303 | c.1497G>C | synonymous_variant | 1.0 |
rpoB | 761306 | c.1500C>G | synonymous_variant | 1.0 |
rpoB | 761315 | c.1509C>T | synonymous_variant | 0.89 |
rpoB | 761318 | c.1512G>T | synonymous_variant | 1.0 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 1.0 |
rpoB | 761330 | c.1524G>C | synonymous_variant | 0.85 |
rpoB | 761516 | c.1710G>C | synonymous_variant | 0.4 |
rpoB | 761531 | c.1725C>G | synonymous_variant | 0.5 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.6 |
rpoB | 761555 | c.1749G>C | synonymous_variant | 0.71 |
rpoB | 761564 | c.1758G>C | synonymous_variant | 0.86 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.75 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.75 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.75 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.67 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.6 |
rpoB | 761615 | c.1809A>G | synonymous_variant | 0.6 |
rpoB | 761633 | c.1827G>C | synonymous_variant | 0.75 |
rpoB | 761912 | c.2106T>C | synonymous_variant | 0.4 |
rpoB | 761916 | p.Asp704Asn | missense_variant | 0.62 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.92 |
rpoB | 761951 | c.2145G>C | synonymous_variant | 0.93 |
rpoB | 761955 | p.Ile717Phe | missense_variant | 0.93 |
rpoB | 761998 | c.2193_2195delGTC | disruptive_inframe_deletion | 0.97 |
rpoB | 762005 | c.2200_2201insAGC | disruptive_inframe_insertion | 0.97 |
rpoB | 762009 | p.Leu735Met | missense_variant | 0.97 |
rpoB | 762014 | c.2208C>G | synonymous_variant | 0.97 |
rpoB | 762017 | c.2211A>G | synonymous_variant | 0.97 |
rpoB | 762020 | p.Glu738Asp | missense_variant | 0.97 |
rpoB | 762024 | p.Val740Ile | missense_variant | 0.97 |
rpoB | 762053 | c.2247T>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 | 762101 | c.2295C>G | synonymous_variant | 0.94 |
rpoB | 762104 | p.Asp766Glu | missense_variant | 0.93 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.83 |
rpoB | 762117 | p.Ser771Gly | missense_variant | 0.67 |
rpoB | 762122 | p.Asp772Glu | missense_variant | 0.67 |
rpoB | 762125 | p.Glu773Asp | missense_variant | 0.67 |
rpoB | 762126 | p.Val774Met | missense_variant | 0.67 |
rpoB | 762132 | p.Ala776Lys | missense_variant | 0.67 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.67 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.67 |
rpoB | 762146 | p.Glu780Asp | missense_variant | 0.75 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.86 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.89 |
rpoB | 762173 | p.Glu789Asp | missense_variant | 0.88 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.89 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.91 |
rpoB | 762197 | c.2391C>G | synonymous_variant | 0.91 |
rpoB | 762209 | c.2403C>G | synonymous_variant | 0.91 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.94 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.94 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.94 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 1.0 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.94 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.92 |
rpoB | 762296 | c.2490G>C | synonymous_variant | 0.91 |
rpoB | 762297 | p.Leu831Met | missense_variant | 0.91 |
rpoB | 762300 | p.Lys832Arg | missense_variant | 0.91 |
rpoB | 762308 | c.2502G>C | synonymous_variant | 0.91 |
rpoB | 762317 | c.2511A>G | 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 | 762350 | c.2544C>G | synonymous_variant | 1.0 |
rpoB | 762362 | p.Glu852Asp | missense_variant | 1.0 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 1.0 |
rpoB | 762426 | p.Ser874Gln | missense_variant | 1.0 |
rpoC | 762434 | c.-936T>C | upstream_gene_variant | 1.0 |
rpoB | 762441 | p.Leu879Met | missense_variant | 1.0 |
rpoC | 762452 | c.-918G>C | upstream_gene_variant | 1.0 |
rpoC | 762455 | c.-915C>T | upstream_gene_variant | 0.93 |
rpoC | 762470 | c.-900G>C | upstream_gene_variant | 1.0 |
rpoB | 762489 | p.Val895Gln | missense_variant | 1.0 |
rpoC | 762503 | c.-867G>C | upstream_gene_variant | 1.0 |
rpoC | 762509 | c.-861T>G | upstream_gene_variant | 1.0 |
rpoB | 762510 | p.Ala902Pro | missense_variant | 1.0 |
rpoC | 762527 | c.-843G>C | upstream_gene_variant | 1.0 |
rpoC | 762533 | c.-837T>C | upstream_gene_variant | 1.0 |
rpoB | 762534 | p.Ile910Leu | missense_variant | 1.0 |
rpoC | 762537 | c.-833T>C | upstream_gene_variant | 1.0 |
rpoC | 762560 | c.-810A>C | upstream_gene_variant | 1.0 |
rpoC | 762563 | c.-807G>A | upstream_gene_variant | 1.0 |
rpoB | 762579 | p.Ile925Val | missense_variant | 1.0 |
rpoC | 762782 | c.-588T>C | upstream_gene_variant | 0.73 |
rpoB | 762795 | p.Asp997Asn | missense_variant | 0.85 |
rpoC | 762800 | c.-570C>G | upstream_gene_variant | 0.85 |
rpoC | 762812 | c.-558C>G | upstream_gene_variant | 0.85 |
rpoB | 762813 | p.Met1003Gln | missense_variant | 0.85 |
rpoC | 762818 | c.-552C>G | upstream_gene_variant | 0.85 |
rpoB | 762819 | p.Phe1005Ile | missense_variant | 0.85 |
rpoC | 762827 | c.-543G>C | upstream_gene_variant | 0.86 |
rpoC | 762831 | c.-539_-538delAGinsTC | upstream_gene_variant | 0.86 |
rpoC | 762836 | c.-534C>T | upstream_gene_variant | 0.88 |
rpoB | 762850 | p.Tyr1015Phe | missense_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 | 762878 | p.Ile1024Met | missense_variant | 0.97 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.97 |
rpoB | 762905 | p.Asp1033Glu | missense_variant | 0.98 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.98 |
rpoC | 762926 | c.-444C>G | upstream_gene_variant | 0.96 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.96 |
rpoC | 762947 | c.-423C>G | upstream_gene_variant | 0.98 |
rpoC | 762965 | c.-405T>C | upstream_gene_variant | 0.97 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 0.97 |
rpoC | 762980 | c.-390T>C | upstream_gene_variant | 0.97 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.97 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.97 |
rpoB | 763005 | p.Cys1067Val | missense_variant | 0.95 |
rpoC | 763022 | c.-348C>G | upstream_gene_variant | 0.99 |
rpoC | 763025 | c.-345C>T | upstream_gene_variant | 0.99 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.99 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.99 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.98 |
rpoB | 763074 | p.Thr1090Val | missense_variant | 0.98 |
rpoC | 763088 | c.-282C>G | upstream_gene_variant | 0.98 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.98 |
rpoC | 763109 | c.-261C>G | upstream_gene_variant | 0.95 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.97 |
rpoB | 763118 | p.Glu1104Asp | missense_variant | 0.94 |
rpoB | 763130 | p.Glu1108Asp | missense_variant | 0.93 |
rpoC | 763133 | c.-237G>C | upstream_gene_variant | 0.92 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.92 |
rpoC | 763142 | c.-228C>G | upstream_gene_variant | 0.92 |
rpoC | 763160 | c.-210G>C | upstream_gene_variant | 0.89 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.85 |
rpoC | 763169 | c.-201A>G | upstream_gene_variant | 0.83 |
rpoC | 763172 | c.-198G>C | upstream_gene_variant | 0.83 |
rpoC | 763200 | c.-170C>T | upstream_gene_variant | 0.6 |
rpoC | 763444 | p.Tyr25* | stop_gained | 0.67 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.93 |
rpoC | 763462 | c.93G>C | synonymous_variant | 0.94 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.97 |
rpoC | 763507 | c.138G>C | synonymous_variant | 0.94 |
rpoC | 763517 | p.Lys50Arg | missense_variant | 0.95 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.95 |
rpoC | 763531 | c.162G>C | synonymous_variant | 0.96 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.96 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.96 |
rpoC | 763550 | p.Tyr61Ala | missense_variant | 0.96 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.97 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.97 |
rpoC | 763619 | p.Arg84Lys | missense_variant | 0.97 |
rpoC | 763622 | p.Ala85Ser | missense_variant | 0.98 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.98 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.98 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.98 |
rpoC | 763660 | c.291T>G | synonymous_variant | 1.0 |
rpoC | 763669 | c.300C>G | synonymous_variant | 1.0 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.98 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.97 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.97 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.97 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.97 |
rpoC | 763709 | c.340C>T | synonymous_variant | 0.95 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.95 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.95 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.93 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.9 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.89 |
rpoC | 763765 | c.396T>G | synonymous_variant | 0.6 |
rpoC | 763768 | c.399C>G | synonymous_variant | 0.6 |
rpoC | 763769 | p.Tyr134Asn | missense_variant | 0.6 |
rpoC | 763772 | p.Val135Ile | missense_variant | 0.6 |
rpoC | 763783 | c.414G>C | synonymous_variant | 0.6 |
rpoC | 764115 | p.Gly249Glu | missense_variant | 1.0 |
rpoC | 764119 | p.Glu250Asp | missense_variant | 1.0 |
rpoC | 764131 | c.762T>C | synonymous_variant | 1.0 |
rpoC | 764133 | p.Ala255Gly | missense_variant | 1.0 |
rpoC | 764143 | c.774G>C | synonymous_variant | 1.0 |
rpoC | 764147 | p.Ser260Ala | missense_variant | 1.0 |
rpoC | 764157 | p.Lys263Thr | missense_variant | 0.88 |
rpoC | 764165 | p.Glu266Arg | missense_variant | 0.88 |
rpoC | 764177 | p.Ile270Leu | missense_variant | 0.88 |
rpoC | 764181 | p.Asp271Ala | missense_variant | 0.88 |
rpoC | 764188 | c.819A>G | synonymous_variant | 0.88 |
rpoC | 764197 | c.828G>T | synonymous_variant | 0.88 |
rpoC | 764200 | c.831G>C | synonymous_variant | 0.88 |
rpoC | 764203 | c.834G>C | synonymous_variant | 0.88 |
rpoC | 764206 | p.Asp279Glu | missense_variant | 0.88 |
rpoC | 764207 | p.Val280Thr | missense_variant | 0.88 |
rpoC | 764215 | c.846A>C | synonymous_variant | 0.92 |
rpoC | 764216 | p.Asn283Asp | missense_variant | 0.92 |
rpoC | 764227 | c.858G>C | synonymous_variant | 0.96 |
rpoC | 764239 | c.870T>G | synonymous_variant | 0.97 |
rpoC | 764254 | c.885G>C | synonymous_variant | 0.97 |
rpoC | 764263 | c.894G>C | synonymous_variant | 0.96 |
rpoC | 764266 | c.897T>C | synonymous_variant | 0.96 |
rpoC | 764269 | c.900G>C | synonymous_variant | 0.96 |
rpoC | 764277 | p.Gln303Leu | missense_variant | 0.96 |
rpoC | 764291 | p.Ser308Asp | missense_variant | 0.96 |
rpoC | 764297 | p.Met310Ala | missense_variant | 0.96 |
rpoC | 764301 | p.Gly311Ala | missense_variant | 1.0 |
rpoC | 764308 | c.939G>C | synonymous_variant | 1.0 |
rpoC | 764315 | p.Ala316Cys | missense_variant | 1.0 |
rpoC | 764365 | c.996C>T | synonymous_variant | 1.0 |
rpoC | 764371 | c.1002G>T | synonymous_variant | 1.0 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 1.0 |
rpoC | 764383 | c.1014C>G | synonymous_variant | 1.0 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 1.0 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 1.0 |
rpoC | 764410 | c.1041G>C | synonymous_variant | 1.0 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 1.0 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 1.0 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 1.0 |
rpoC | 764435 | c.1066_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 | 0.85 |
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 | 764500 | c.1131C>G | synonymous_variant | 1.0 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 1.0 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 1.0 |
rpoC | 764536 | c.1167G>T | synonymous_variant | 1.0 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 1.0 |
rpoC | 764548 | c.1179G>T | synonymous_variant | 1.0 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 1.0 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 1.0 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.99 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.99 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 0.99 |
rpoC | 764611 | c.1242G>C | synonymous_variant | 0.99 |
rpoC | 764623 | c.1254C>G | synonymous_variant | 0.99 |
rpoC | 764632 | c.1263T>A | synonymous_variant | 0.99 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.98 |
rpoC | 764660 | p.Val431Ile | missense_variant | 0.98 |
rpoC | 764695 | c.1326T>C | synonymous_variant | 0.97 |
rpoC | 764713 | c.1344G>C | synonymous_variant | 0.95 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.95 |
rpoC | 764731 | c.1362G>C | synonymous_variant | 0.96 |
rpoC | 764737 | c.1368G>C | synonymous_variant | 0.95 |
rpoC | 764744 | p.Arg459Glu | missense_variant | 0.88 |
rpoC | 764749 | c.1380G>C | synonymous_variant | 0.86 |
rpoC | 764754 | p.Asp462Ala | missense_variant | 0.86 |
rpoC | 764756 | p.Leu463Lys | missense_variant | 0.86 |
rpoC | 764760 | p.Asn464Ser | missense_variant | 0.86 |
rpoC | 764762 | p.His465Tyr | missense_variant | 0.86 |
rpoC | 764780 | c.1411_1413delAGCinsTCG | synonymous_variant | 0.89 |
rpoC | 764797 | c.1428G>C | synonymous_variant | 0.9 |
rpoC | 764813 | p.Gln482Glu | missense_variant | 1.0 |
rpoC | 764818 | c.1449G>C | synonymous_variant | 1.0 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 1.0 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 1.0 |
rpoC | 764833 | c.1464A>G | synonymous_variant | 1.0 |
rpoC | 764836 | p.Glu489Asp | missense_variant | 1.0 |
rpoC | 764843 | p.Ala492Thr | missense_variant | 1.0 |
rpoC | 764847 | p.Glu493Gly | missense_variant | 1.0 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 1.0 |
rpoC | 764863 | c.1494G>C | synonymous_variant | 0.95 |
rpoC | 764869 | c.1500C>T | synonymous_variant | 0.82 |
rpoC | 764872 | c.1503A>C | synonymous_variant | 0.95 |
rpoC | 764887 | c.1518G>C | synonymous_variant | 0.95 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.95 |
rpoC | 764893 | c.1524T>C | synonymous_variant | 0.96 |
rpoC | 764911 | c.1542A>C | synonymous_variant | 0.95 |
rpoC | 764912 | p.Met515Val | missense_variant | 0.95 |
rpoC | 764917 | c.1548G>C | synonymous_variant | 0.95 |
rpoC | 764920 | c.1551G>C | synonymous_variant | 0.95 |
rpoC | 764923 | c.1554A>G | synonymous_variant | 0.96 |
rpoC | 764935 | c.1566T>C | synonymous_variant | 0.97 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.96 |
rpoC | 764952 | p.Val528Ala | missense_variant | 0.96 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.97 |
rpoC | 764983 | c.1614T>C | synonymous_variant | 0.98 |
rpoC | 765004 | c.1635G>C | synonymous_variant | 0.97 |
rpoC | 765007 | c.1638T>G | synonymous_variant | 0.97 |
rpoC | 765008 | c.1639T>C | synonymous_variant | 0.97 |
rpoC | 765011 | c.1642_1643delAGinsTC | synonymous_variant | 0.97 |
rpoC | 765016 | c.1647C>G | synonymous_variant | 1.0 |
rpoC | 765019 | c.1650A>G | synonymous_variant | 1.0 |
rpoC | 765034 | c.1665T>C | synonymous_variant | 1.0 |
rpoC | 765040 | c.1671T>C | synonymous_variant | 1.0 |
rpoC | 765041 | c.1672T>C | synonymous_variant | 1.0 |
rpoC | 765047 | c.1678T>C | synonymous_variant | 1.0 |
rpoC | 765055 | c.1686C>G | synonymous_variant | 1.0 |
rpoC | 765076 | c.1707A>G | synonymous_variant | 1.0 |
rpoC | 765079 | c.1710T>C | synonymous_variant | 1.0 |
rpoC | 765082 | c.1713G>A | synonymous_variant | 1.0 |
rpoC | 765083 | p.Arg572Lys | missense_variant | 1.0 |
rpoC | 765089 | c.1720T>C | synonymous_variant | 1.0 |
rpoC | 765103 | c.1734G>A | synonymous_variant | 1.0 |
rpoC | 765115 | c.1746G>C | synonymous_variant | 1.0 |
rpoC | 765121 | c.1752G>C | synonymous_variant | 1.0 |
rpoC | 765129 | p.Tyr587Phe | missense_variant | 1.0 |
rpoC | 766291 | c.2922G>C | synonymous_variant | 1.0 |
rpoC | 766297 | c.2928G>C | synonymous_variant | 1.0 |
rpoC | 766309 | c.2940G>C | synonymous_variant | 1.0 |
rpoC | 766331 | p.Leu988Met | missense_variant | 0.93 |
rpoC | 766345 | c.2976T>C | synonymous_variant | 0.97 |
rpoC | 766348 | c.2979A>G | synonymous_variant | 0.97 |
rpoC | 766354 | c.2985C>G | synonymous_variant | 0.97 |
rpoC | 766363 | c.2994G>C | synonymous_variant | 0.97 |
rpoC | 766369 | c.3000C>G | synonymous_variant | 0.97 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.97 |
rpoC | 766393 | c.3024C>G | synonymous_variant | 0.93 |
rpoC | 766408 | c.3039C>T | synonymous_variant | 0.97 |
rpoC | 766423 | c.3054T>C | synonymous_variant | 0.96 |
rpoC | 766432 | c.3063T>C | synonymous_variant | 0.95 |
rpoC | 766434 | p.Glu1022Gly | missense_variant | 0.94 |
rpoC | 766447 | c.3078T>C | synonymous_variant | 0.93 |
rpoC | 766459 | c.3090G>A | synonymous_variant | 0.86 |
rpoC | 766462 | c.3093G>C | synonymous_variant | 0.83 |
rpoC | 767002 | c.3633G>C | synonymous_variant | 0.86 |
rpoC | 767008 | c.3639G>C | synonymous_variant | 0.92 |
rpoC | 767020 | c.3651C>G | synonymous_variant | 1.0 |
rpoC | 767023 | c.3654C>T | synonymous_variant | 0.92 |
rpoC | 767038 | c.3669G>C | synonymous_variant | 0.92 |
rpoC | 767041 | c.3672G>C | synonymous_variant | 0.92 |
rpoC | 767044 | c.3675G>C | synonymous_variant | 0.92 |
rpoC | 767056 | c.3687C>G | synonymous_variant | 0.92 |
rpoC | 767059 | c.3690T>C | synonymous_variant | 0.92 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.92 |
rpoC | 767071 | c.3702C>G | synonymous_variant | 0.92 |
rpoC | 767074 | c.3705T>C | synonymous_variant | 0.92 |
rpoC | 767077 | c.3708G>C | synonymous_variant | 0.92 |
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 | 767104 | c.3735C>G | synonymous_variant | 1.0 |
rpoC | 767106 | p.Asn1246Ile | missense_variant | 1.0 |
rpoC | 767110 | c.3741T>C | synonymous_variant | 1.0 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 1.0 |
rpoC | 767152 | c.3783T>C | synonymous_variant | 1.0 |
rpoC | 767155 | c.3786C>G | synonymous_variant | 1.0 |
rpoC | 767158 | c.3789T>C | synonymous_variant | 1.0 |
rpoC | 767162 | p.Asn1265Ser | missense_variant | 1.0 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.67 |
rpsL | 781763 | c.204C>G | synonymous_variant | 0.75 |
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 | 781817 | c.258G>A | synonymous_variant | 1.0 |
rpsL | 781829 | c.270G>C | synonymous_variant | 1.0 |
rpsL | 781832 | c.273T>G | synonymous_variant | 1.0 |
rpsL | 781835 | c.276T>C | synonymous_variant | 1.0 |
rpsL | 781838 | c.279G>C | synonymous_variant | 1.0 |
rpsL | 781851 | p.Ile98Val | missense_variant | 1.0 |
rpsL | 781859 | c.300T>C | 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 | 781877 | c.318T>C | synonymous_variant | 0.67 |
rpsL | 781884 | p.Asn109Asp | missense_variant | 0.67 |
rplC | 800621 | c.-188G>A | upstream_gene_variant | 0.67 |
rplC | 800633 | c.-176T>C | upstream_gene_variant | 0.92 |
rplC | 800648 | c.-161A>G | upstream_gene_variant | 0.94 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.94 |
rplC | 800672 | c.-137G>C | upstream_gene_variant | 0.94 |
rplC | 800693 | c.-116A>C | upstream_gene_variant | 1.0 |
rplC | 800702 | c.-107G>C | upstream_gene_variant | 0.94 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.94 |
rplC | 800714 | c.-95C>T | upstream_gene_variant | 0.94 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.94 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.94 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.94 |
rplC | 800726 | c.-83G>C | upstream_gene_variant | 0.94 |
rplC | 800744 | c.-65G>T | upstream_gene_variant | 0.89 |
rplC | 800768 | c.-41C>G | upstream_gene_variant | 0.82 |
rplC | 800769 | c.-40_-39delAGinsTC | upstream_gene_variant | 0.81 |
rplC | 800786 | c.-23C>T | upstream_gene_variant | 0.5 |
rrs | 1471850 | n.7_8delTT | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471918 | n.73A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471925 | n.80T>C | 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 | 1471938 | n.93T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471972 | n.127T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471979 | n.134T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472028 | n.183A>G | non_coding_transcript_exon_variant | 0.99 |
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 | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472123 | n.278A>G | 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 | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472225 | n.380C>G | 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 | 1472299 | n.455_462delCCGGGTTC | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472309 | n.464C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472311 | n.467_470delGGAT | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472325 | n.480G>A | 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 | 0.99 |
rrs | 1472450 | n.605A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472451 | n.606C>G | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472461 | n.616G>C | 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 | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472530 | n.685G>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 | 1.0 |
rrs | 1472685 | n.840G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472686 | n.841G>C | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472690 | n.845C>T | 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 | 0.99 |
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 | 1472837 | n.992C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472840 | n.995A>G | 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 | 1472850 | n.1005T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472857 | n.1012A>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 | 0.99 |
rrs | 1472874 | n.1029C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472875 | n.1030T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472878 | n.1033G>A | non_coding_transcript_exon_variant | 0.99 |
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 | 1472993 | n.1148G>A | 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 | 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 | 1.0 |
rrs | 1473123 | n.1278A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473283 | n.1438T>C | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1473390 | n.-268A>T | upstream_gene_variant | 0.33 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473899 | n.242A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473922 | n.265A>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1473923 | n.266C>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474112 | n.455T>C | 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 | 0.99 |
rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474178 | n.522dupC | 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 | 1474285 | n.630_631delTC | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474289 | n.632C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474351 | n.694G>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474399 | n.742G>A | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474400 | n.743_744insA | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474403 | n.746G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474405 | n.748A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474407 | n.752_776delGGCGACCCACACGCGCATACGCGCG | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474438 | n.781A>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474439 | n.782A>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474451 | n.794T>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474487 | n.830G>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474497 | n.840G>A | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474506 | n.849C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474507 | n.850G>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474517 | n.860C>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474552 | n.895C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474628 | n.971C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474640 | n.983C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474658 | n.1001A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474722 | n.1065T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474798 | n.1141C>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474801 | n.1144G>A | non_coding_transcript_exon_variant | 0.99 |
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 | 0.99 |
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 | 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 | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474921 | n.1264C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474934 | n.1277C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475116 | n.1459G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475120 | n.1463G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475538 | n.1881T>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475542 | n.1885A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475544 | n.1887A>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475550 | n.1893A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475659 | n.2002G>A | 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 | 1475758 | n.2101A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475759 | n.2102C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475761 | n.2106_2110delCAAGG | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475769 | n.2112_2113insTTTGCCGGCC | non_coding_transcript_exon_variant | 0.99 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475902 | n.2245T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 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 | 1476035 | n.2378G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476087 | n.2430C>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>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 | 1476116 | n.2459A>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 | 1476165 | n.2508T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 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 | 0.99 |
rrl | 1476276 | n.2619C>A | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.99 |
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 | 1476523 | n.2867delC | 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 | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476608 | n.2951C>T | 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 | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476661 | n.3004A>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476665 | n.3008T>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476666 | n.3009C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476670 | n.3013A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476728 | n.3071T>C | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1833668 | p.Ile43Val | missense_variant | 0.71 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.71 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 0.71 |
rpsA | 1833682 | c.141C>T | synonymous_variant | 0.71 |
rpsA | 1833685 | c.144G>C | synonymous_variant | 0.71 |
rpsA | 1833688 | c.147C>T | synonymous_variant | 0.73 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.76 |
rpsA | 1833697 | c.156C>G | synonymous_variant | 0.79 |
rpsA | 1833718 | c.177C>G | synonymous_variant | 0.85 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.85 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.88 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.86 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.86 |
rpsA | 1833760 | c.219C>T | synonymous_variant | 0.91 |
rpsA | 1833770 | p.Asn77Asp | missense_variant | 0.91 |
rpsA | 1833778 | c.237C>G | synonymous_variant | 0.92 |
rpsA | 1833781 | c.240T>C | synonymous_variant | 0.91 |
rpsA | 1833782 | p.Ser81Glu | missense_variant | 0.91 |
rpsA | 1833797 | p.Val86Ile | missense_variant | 0.95 |
rpsA | 1833802 | p.Glu87Asp | missense_variant | 0.95 |
rpsA | 1833811 | c.270G>C | synonymous_variant | 0.96 |
rpsA | 1833829 | c.288A>G | synonymous_variant | 0.96 |
rpsA | 1833832 | c.291G>A | synonymous_variant | 0.96 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.97 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.96 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.97 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.97 |
rpsA | 1833859 | c.318C>T | synonymous_variant | 0.97 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.98 |
rpsA | 1833894 | p.Ala118Asp | missense_variant | 0.98 |
rpsA | 1833914 | p.Ala125Pro | missense_variant | 0.97 |
rpsA | 1833921 | p.Lys127Thr | missense_variant | 0.95 |
rpsA | 1833925 | c.384C>T | synonymous_variant | 0.95 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.95 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.96 |
rpsA | 1833961 | c.420C>G | synonymous_variant | 0.97 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.97 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.96 |
rpsA | 1833988 | c.447C>G | synonymous_variant | 0.96 |
rpsA | 1833991 | c.450C>G | synonymous_variant | 0.95 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.95 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.95 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.94 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.94 |
rpsA | 1834040 | p.Lys167Gln | missense_variant | 0.95 |
rpsA | 1834046 | p.Ile169Leu | missense_variant | 0.94 |
rpsA | 1834054 | c.513C>G | synonymous_variant | 0.94 |
rpsA | 1834093 | c.552G>C | synonymous_variant | 0.97 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.97 |
rpsA | 1834105 | c.564C>T | synonymous_variant | 0.96 |
rpsA | 1834108 | c.567C>G | synonymous_variant | 0.96 |
rpsA | 1834114 | c.573G>C | synonymous_variant | 0.96 |
rpsA | 1834135 | c.594G>C | synonymous_variant | 1.0 |
rpsA | 1834139 | c.598_599delAGinsTC | synonymous_variant | 1.0 |
rpsA | 1834151 | p.Asn204His | missense_variant | 1.0 |
rpsA | 1834154 | p.Asn205Gln | missense_variant | 1.0 |
rpsA | 1834157 | c.616T>C | synonymous_variant | 1.0 |
rpsA | 1834162 | c.621A>G | synonymous_variant | 1.0 |
rpsA | 1834165 | c.624A>G | synonymous_variant | 1.0 |
rpsA | 1834167 | c.628_629delAC | frameshift_variant | 1.0 |
rpsA | 1834172 | c.631_632insGG | frameshift_variant | 1.0 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834183 | c.642T>C | synonymous_variant | 1.0 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 1.0 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.97 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 1.0 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 1.0 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 1.0 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 1.0 |
rpsA | 1834252 | c.711C>T | synonymous_variant | 1.0 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 1.0 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 1.0 |
rpsA | 1834276 | c.735C>T | synonymous_variant | 1.0 |
rpsA | 1834279 | c.738C>T | synonymous_variant | 1.0 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.93 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.93 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.93 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.83 |
rpsA | 1834333 | p.Asp264Glu | missense_variant | 0.75 |
rpsA | 1834384 | c.843A>G | synonymous_variant | 0.5 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.5 |
rpsA | 1834397 | p.His286Val | missense_variant | 0.5 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.5 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.5 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.6 |
rpsA | 1834432 | c.891G>C | synonymous_variant | 0.71 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.95 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.92 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.94 |
rpsA | 1834486 | c.945G>A | synonymous_variant | 0.82 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.97 |
rpsA | 1834504 | c.963G>C | synonymous_variant | 0.98 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.97 |
rpsA | 1834534 | c.993C>G | synonymous_variant | 0.97 |
rpsA | 1834537 | p.Glu332Asp | missense_variant | 0.96 |
rpsA | 1834540 | c.999G>C | synonymous_variant | 0.96 |
rpsA | 1834543 | c.1002C>G | synonymous_variant | 0.96 |
rpsA | 1834550 | p.Val337Ile | missense_variant | 0.98 |
rpsA | 1834555 | c.1014T>C | synonymous_variant | 0.96 |
rpsA | 1834556 | p.Ala339Thr | missense_variant | 0.98 |
rpsA | 1834567 | p.Asp342Glu | missense_variant | 0.98 |
rpsA | 1834570 | p.Asp343Glu | missense_variant | 0.98 |
rpsA | 1834573 | c.1032G>C | synonymous_variant | 0.99 |
rpsA | 1834603 | p.Glu354Asp | missense_variant | 0.98 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.97 |
rpsA | 1834612 | c.1071G>C | synonymous_variant | 0.97 |
rpsA | 1834618 | c.1077G>C | synonymous_variant | 0.95 |
rpsA | 1834619 | c.1078T>C | synonymous_variant | 0.97 |
rpsA | 1834627 | c.1086C>G | synonymous_variant | 0.97 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.97 |
rpsA | 1834637 | p.Asn366Asp | missense_variant | 0.97 |
rpsA | 1834647 | p.Tyr369Phe | missense_variant | 0.97 |
rpsA | 1834667 | p.Ala376Thr | missense_variant | 0.98 |
rpsA | 1834683 | p.Ala381Gly | missense_variant | 1.0 |
rpsA | 1834687 | c.1146C>T | synonymous_variant | 1.0 |
rpsA | 1834688 | c.1147_1148delAGinsTC | synonymous_variant | 1.0 |
rpsA | 1834720 | c.1179C>G | synonymous_variant | 0.97 |
rpsA | 1834732 | c.1191T>C | synonymous_variant | 0.94 |
rpsA | 1834735 | c.1194C>G | synonymous_variant | 0.94 |
rpsA | 1834738 | c.1197A>G | synonymous_variant | 0.94 |
rpsA | 1834747 | c.1206A>G | synonymous_variant | 0.92 |
rpsA | 1834751 | p.Leu404Met | missense_variant | 0.88 |
rpsA | 1834759 | c.1218A>C | synonymous_variant | 0.88 |
rpsA | 1834765 | c.1224A>G | synonymous_variant | 0.88 |
rpsA | 1834767 | p.Lys409Thr | missense_variant | 0.88 |
rpsA | 1834778 | p.Glu413Gln | missense_variant | 0.5 |
rpsA | 1834786 | c.1245A>G | synonymous_variant | 0.86 |
rpsA | 1834789 | c.1248T>C | synonymous_variant | 0.86 |
rpsA | 1834792 | c.1251G>T | synonymous_variant | 0.86 |
rpsA | 1834804 | c.1263C>G | synonymous_variant | 0.5 |
katG | 2156025 | c.87C>A | synonymous_variant | 1.0 |
PPE35 | 2168814 | c.1798dupA | frameshift_variant | 1.0 |
folC | 2747074 | c.525G>C | synonymous_variant | 1.0 |
folC | 2747086 | c.513A>C | synonymous_variant | 0.67 |
folC | 2747089 | c.510G>C | synonymous_variant | 0.67 |
folC | 2747101 | c.498G>A | synonymous_variant | 0.5 |
folC | 2747107 | c.492G>C | synonymous_variant | 0.5 |
folC | 2747110 | c.489T>C | synonymous_variant | 0.5 |
folC | 2747120 | p.Phe160Tyr | missense_variant | 0.5 |
folC | 2747122 | c.477G>C | synonymous_variant | 0.5 |
folC | 2747128 | c.471G>C | synonymous_variant | 0.5 |
thyA | 3073857 | c.615C>T | synonymous_variant | 1.0 |
thyA | 3073863 | c.609T>C | synonymous_variant | 1.0 |
thyA | 3073888 | p.Ser195Glu | 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 | 3073917 | c.555C>G | synonymous_variant | 1.0 |
thyA | 3073920 | c.552C>G | synonymous_variant | 1.0 |
thyA | 3073925 | c.547T>C | synonymous_variant | 1.0 |
thyA | 3073929 | c.543T>C | synonymous_variant | 1.0 |
thyA | 3073933 | c.538_539delAGinsTC | synonymous_variant | 1.0 |
thyA | 3073953 | c.519T>C | 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 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.67 |
rpoA | 3877824 | p.Glu228Ala | missense_variant | 0.67 |
rpoA | 3877827 | p.Val227Glu | missense_variant | 0.67 |
rpoA | 3877836 | c.672A>G | synonymous_variant | 0.71 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.75 |
rpoA | 3877842 | c.666A>C | synonymous_variant | 0.75 |
rpoA | 3877854 | c.652_654delTTGinsCTC | synonymous_variant | 0.75 |
rpoA | 3877860 | c.648C>G | synonymous_variant | 0.86 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.86 |
rpoA | 3877875 | c.633T>C | synonymous_variant | 0.86 |
rpoA | 3877886 | p.Leu208Met | missense_variant | 0.75 |
rpoA | 3877887 | c.621G>C | synonymous_variant | 0.75 |
rpoA | 3877905 | c.603A>C | synonymous_variant | 0.75 |
rpoA | 3877908 | c.600T>C | synonymous_variant | 0.75 |
rpoA | 3877914 | c.594C>G | synonymous_variant | 0.75 |
rpoA | 3877926 | p.Leu194Ile | missense_variant | 0.86 |
rpoA | 3877931 | p.Ile193Val | missense_variant | 0.86 |
clpC1 | 4038556 | p.Ile717Val | missense_variant | 0.5 |
clpC1 | 4038560 | p.Asp715Glu | missense_variant | 0.6 |
clpC1 | 4038584 | c.2121G>C | synonymous_variant | 0.67 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.6 |
clpC1 | 4038710 | c.1995G>C | synonymous_variant | 0.5 |
clpC1 | 4038713 | c.1992T>C | synonymous_variant | 0.5 |
clpC1 | 4038719 | c.1986G>C | synonymous_variant | 0.69 |
clpC1 | 4038725 | c.1980C>G | synonymous_variant | 0.78 |
clpC1 | 4038743 | p.Thr654Val | missense_variant | 0.82 |
clpC1 | 4038756 | p.Gly650Ala | missense_variant | 0.86 |
clpC1 | 4038758 | c.1947C>T | synonymous_variant | 0.88 |
clpC1 | 4038767 | c.1938G>C | synonymous_variant | 0.89 |
clpC1 | 4038770 | c.1935C>T | synonymous_variant | 0.89 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.9 |
clpC1 | 4038791 | c.1914G>C | synonymous_variant | 0.82 |
clpC1 | 4038794 | p.Ser637Thr | missense_variant | 0.82 |
clpC1 | 4038811 | p.Gln632Lys | missense_variant | 0.89 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.89 |
clpC1 | 4038815 | c.1890G>C | synonymous_variant | 0.82 |
clpC1 | 4038842 | c.1863G>C | synonymous_variant | 0.97 |
clpC1 | 4038845 | c.1860G>C | synonymous_variant | 0.97 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 0.97 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.99 |
clpC1 | 4038905 | c.1800A>C | synonymous_variant | 0.98 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.98 |
clpC1 | 4038911 | c.1794G>T | synonymous_variant | 0.98 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.98 |
clpC1 | 4038917 | c.1788C>T | synonymous_variant | 0.98 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 0.98 |
clpC1 | 4038926 | c.1779G>C | synonymous_variant | 0.98 |
clpC1 | 4038932 | c.1773G>C | synonymous_variant | 0.99 |
clpC1 | 4038941 | c.1764G>C | synonymous_variant | 1.0 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 1.0 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 1.0 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 1.0 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 1.0 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 1.0 |
clpC1 | 4038980 | c.1725C>T | synonymous_variant | 1.0 |
clpC1 | 4038983 | p.Asp574Glu | missense_variant | 1.0 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 1.0 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 1.0 |
clpC1 | 4039001 | p.Asn568Ala | missense_variant | 1.0 |
clpC1 | 4039007 | c.1698G>C | synonymous_variant | 0.93 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.98 |
clpC1 | 4039025 | c.1680C>G | synonymous_variant | 0.97 |
clpC1 | 4039037 | c.1668T>C | synonymous_variant | 0.93 |
clpC1 | 4039064 | c.1641C>T | synonymous_variant | 0.93 |
clpC1 | 4039067 | c.1638G>C | synonymous_variant | 0.93 |
clpC1 | 4039079 | c.1626C>G | synonymous_variant | 0.86 |
clpC1 | 4039085 | c.1620A>G | synonymous_variant | 0.75 |
clpC1 | 4039091 | c.1614G>C | synonymous_variant | 0.62 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.4 |
clpC1 | 4039499 | c.1206G>C | synonymous_variant | 0.86 |
clpC1 | 4039507 | p.Ile400Val | missense_variant | 0.86 |
clpC1 | 4039508 | c.1197G>C | synonymous_variant | 0.86 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.86 |
clpC1 | 4039526 | c.1179G>T | synonymous_variant | 0.86 |
clpC1 | 4039547 | p.Ala386Ser | missense_variant | 0.83 |
clpC1 | 4039553 | c.1152C>G | synonymous_variant | 0.83 |
clpC1 | 4039559 | c.1146C>G | synonymous_variant | 0.83 |
clpC1 | 4039562 | c.1143C>G | synonymous_variant | 0.83 |
clpC1 | 4039565 | c.1140G>C | synonymous_variant | 0.83 |
clpC1 | 4039570 | p.Met379Leu | missense_variant | 0.83 |
clpC1 | 4039575 | p.Ala377Gln | missense_variant | 0.83 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.67 |
clpC1 | 4039580 | c.1125C>G | synonymous_variant | 0.83 |
clpC1 | 4039586 | c.1119G>C | synonymous_variant | 0.83 |
clpC1 | 4039592 | c.1113G>C | synonymous_variant | 1.0 |
clpC1 | 4039598 | c.1107C>T | synonymous_variant | 1.0 |
clpC1 | 4039602 | p.Ala368Gln | missense_variant | 1.0 |
clpC1 | 4039611 | p.Arg365Lys | missense_variant | 1.0 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 1.0 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 1.0 |
clpC1 | 4039714 | p.Tyr331His | missense_variant | 1.0 |
clpC1 | 4039724 | c.981A>G | 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 | 4039790 | c.915C>G | synonymous_variant | 1.0 |
clpC1 | 4039805 | c.900C>T | synonymous_variant | 0.82 |
clpC1 | 4039817 | c.888A>T | synonymous_variant | 1.0 |
clpC1 | 4039820 | c.885T>C | 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 | 4039850 | c.855T>C | synonymous_variant | 1.0 |
clpC1 | 4039865 | c.840T>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 | 4039916 | c.789T>C | synonymous_variant | 0.95 |
clpC1 | 4039928 | c.775_777delAGCinsTCG | synonymous_variant | 0.93 |
clpC1 | 4039934 | c.771G>C | synonymous_variant | 0.93 |
clpC1 | 4039937 | c.768G>C | synonymous_variant | 0.93 |
clpC1 | 4039946 | c.759A>T | synonymous_variant | 0.95 |
clpC1 | 4039955 | c.750G>T | synonymous_variant | 0.9 |
clpC1 | 4039960 | p.Thr249Ser | missense_variant | 0.88 |
clpC1 | 4039964 | c.741C>G | synonymous_variant | 0.88 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.83 |
clpC1 | 4039982 | c.723G>C | synonymous_variant | 0.83 |
clpC1 | 4039988 | c.717C>G | synonymous_variant | 0.8 |
clpC1 | 4039994 | p.Glu237Arg | missense_variant | 0.75 |
clpC1 | 4039998 | p.Gly236Asn | missense_variant | 0.75 |
clpC1 | 4040002 | p.His235Asn | missense_variant | 0.75 |
clpC1 | 4040010 | p.Ala232Asp | missense_variant | 0.8 |
clpC1 | 4040013 | p.Gln231Leu | missense_variant | 0.8 |
clpC1 | 4040015 | c.690G>C | synonymous_variant | 0.8 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.8 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.82 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.85 |
clpC1 | 4040045 | c.660C>G | synonymous_variant | 0.86 |
clpC1 | 4040063 | c.642G>C | synonymous_variant | 0.77 |
clpC1 | 4040087 | c.618G>C | synonymous_variant | 0.92 |
clpC1 | 4040090 | c.615T>G | synonymous_variant | 0.83 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.83 |
clpC1 | 4040107 | p.Val200Ile | missense_variant | 1.0 |
clpC1 | 4040108 | c.597G>C | synonymous_variant | 0.8 |
clpC1 | 4040134 | p.Ile191Val | missense_variant | 1.0 |
clpC1 | 4040135 | c.570C>G | synonymous_variant | 1.0 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 1.0 |
clpC1 | 4040147 | c.558A>G | synonymous_variant | 1.0 |
clpC1 | 4040153 | c.552A>G | synonymous_variant | 1.0 |
clpC1 | 4040291 | c.414G>C | synonymous_variant | 0.67 |
clpC1 | 4040306 | c.399G>C | synonymous_variant | 0.7 |
clpC1 | 4040309 | p.Thr132Pro | missense_variant | 0.7 |
clpC1 | 4040315 | p.Glu130Asp | missense_variant | 0.7 |
clpC1 | 4040324 | c.381G>C | synonymous_variant | 0.7 |
clpC1 | 4040354 | c.351A>G | synonymous_variant | 1.0 |
clpC1 | 4040357 | c.348T>C | synonymous_variant | 0.9 |
clpC1 | 4040363 | c.342A>C | synonymous_variant | 0.9 |
clpC1 | 4040369 | c.336C>G | synonymous_variant | 0.9 |
clpC1 | 4040375 | c.330G>C | synonymous_variant | 0.9 |
clpC1 | 4040380 | c.325T>C | synonymous_variant | 0.9 |
clpC1 | 4040381 | c.324T>C | synonymous_variant | 0.9 |
clpC1 | 4040387 | c.318A>G | synonymous_variant | 0.9 |
clpC1 | 4040393 | c.312G>C | synonymous_variant | 0.9 |
clpC1 | 4040402 | p.Asn101Lys | missense_variant | 0.89 |
clpC1 | 4040411 | c.294T>C | synonymous_variant | 0.8 |
clpC1 | 4040420 | c.285G>C | synonymous_variant | 0.67 |
clpC1 | 4040423 | c.282A>G | synonymous_variant | 0.67 |
clpC1 | 4040426 | c.279T>C | synonymous_variant | 0.67 |
embC | 4241384 | p.Pro508Thr | missense_variant | 1.0 |
embA | 4242970 | c.-263C>T | upstream_gene_variant | 1.0 |
embB | 4249640 | c.3127T>C | synonymous_variant | 1.0 |
aftB | 4267858 | p.Ile327Val | missense_variant | 1.0 |
aftB | 4269351 | c.-515C>T | upstream_gene_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |