Run ID: ERR736831
Sample name:
Date: 02-04-2023 04:19:47
Number of reads: 195633
Percentage reads mapped: 3.69
Strain: lineage4.9
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrB | 6738 | p.Thr500Asn | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
gyrA | 7572 | p.Ser91Ala | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
katG | 2155163 | p.Ile317Leu | missense_variant | 1.0 | isoniazid |
katG | 2155693 | p.Ser140Asn | missense_variant | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5329 | c.90C>G | synonymous_variant | 1.0 |
gyrB | 5341 | c.102T>C | synonymous_variant | 1.0 |
gyrB | 5347 | c.108G>C | synonymous_variant | 1.0 |
gyrB | 5363 | c.124_126delTTAinsCTG | synonymous_variant | 1.0 |
gyrB | 5371 | c.132T>C | synonymous_variant | 1.0 |
gyrB | 5374 | c.135C>G | synonymous_variant | 1.0 |
gyrB | 5377 | c.138T>C | synonymous_variant | 1.0 |
gyrB | 5386 | c.147G>C | synonymous_variant | 1.0 |
gyrB | 5396 | p.Ala53Ser | missense_variant | 1.0 |
gyrB | 5419 | c.180T>A | synonymous_variant | 1.0 |
gyrB | 6074 | p.Ser279Thr | missense_variant | 1.0 |
gyrB | 6082 | c.843G>A | synonymous_variant | 1.0 |
gyrB | 6091 | c.852G>C | synonymous_variant | 1.0 |
gyrB | 6098 | p.Val287Leu | missense_variant | 1.0 |
gyrB | 6104 | p.Ile289Val | missense_variant | 1.0 |
gyrB | 6115 | c.876A>G | synonymous_variant | 1.0 |
gyrB | 6122 | p.Ala295Ser | missense_variant | 1.0 |
gyrB | 6127 | c.888G>T | synonymous_variant | 1.0 |
gyrB | 6130 | c.891T>C | synonymous_variant | 1.0 |
gyrB | 6133 | c.894G>C | synonymous_variant | 1.0 |
gyrB | 6184 | c.945C>G | synonymous_variant | 1.0 |
gyrB | 6203 | p.Ser322Ala | missense_variant | 1.0 |
gyrB | 6214 | c.975G>C | synonymous_variant | 1.0 |
gyrB | 6215 | p.Ser326Thr | missense_variant | 1.0 |
gyrB | 6223 | c.984G>C | synonymous_variant | 1.0 |
gyrB | 6242 | p.Arg335Lys | missense_variant | 1.0 |
gyrB | 6250 | c.1011A>C | synonymous_variant | 1.0 |
gyrB | 6251 | p.Leu338Ile | missense_variant | 1.0 |
gyrB | 6259 | p.Asp340Glu | missense_variant | 1.0 |
gyrB | 6266 | p.Pro343Gly | missense_variant | 1.0 |
gyrB | 6286 | c.1047T>C | synonymous_variant | 1.0 |
gyrB | 6295 | c.1056A>G | synonymous_variant | 1.0 |
gyrB | 6312 | p.Ile358Ser | missense_variant | 1.0 |
gyrB | 6313 | c.1075_1077delTCG | conservative_inframe_deletion | 1.0 |
gyrA | 6319 | c.-983G>C | upstream_gene_variant | 1.0 |
gyrB | 6326 | p.Ser363Gly | missense_variant | 1.0 |
gyrA | 6331 | c.-971A>G | upstream_gene_variant | 1.0 |
gyrA | 6362 | c.-940T>C | upstream_gene_variant | 1.0 |
gyrB | 6663 | p.Phe475Tyr | missense_variant | 1.0 |
gyrA | 6673 | c.-629A>C | upstream_gene_variant | 1.0 |
gyrA | 6676 | c.-626T>G | upstream_gene_variant | 1.0 |
gyrA | 6700 | c.-602T>C | upstream_gene_variant | 1.0 |
gyrA | 6703 | c.-599G>C | upstream_gene_variant | 1.0 |
gyrA | 6709 | c.-593A>G | upstream_gene_variant | 1.0 |
gyrA | 6715 | c.-587C>T | upstream_gene_variant | 1.0 |
gyrB | 6722 | p.Arg495Lys | missense_variant | 1.0 |
gyrA | 6727 | c.-575G>C | upstream_gene_variant | 1.0 |
gyrA | 6730 | c.-572A>C | upstream_gene_variant | 1.0 |
gyrA | 6742 | c.-560A>G | upstream_gene_variant | 1.0 |
gyrA | 6745 | c.-557T>C | upstream_gene_variant | 1.0 |
gyrB | 6749 | p.Ala504Ser | missense_variant | 1.0 |
gyrA | 6760 | c.-542G>C | upstream_gene_variant | 1.0 |
gyrB | 6764 | p.Leu509Phe | missense_variant | 1.0 |
gyrA | 6775 | c.-527G>C | upstream_gene_variant | 1.0 |
gyrA | 6793 | c.-509T>C | upstream_gene_variant | 1.0 |
gyrB | 6797 | p.Gly520Ser | missense_variant | 1.0 |
gyrA | 6808 | c.-494C>G | upstream_gene_variant | 1.0 |
gyrA | 6811 | c.-491C>T | upstream_gene_variant | 1.0 |
gyrA | 6841 | c.-461T>C | upstream_gene_variant | 0.94 |
gyrA | 6844 | c.-458T>C | upstream_gene_variant | 0.94 |
gyrA | 6853 | c.-449A>G | upstream_gene_variant | 0.94 |
gyrA | 6856 | c.-446T>C | upstream_gene_variant | 0.93 |
gyrA | 6859 | c.-443T>C | upstream_gene_variant | 0.93 |
gyrA | 6869 | c.-433T>C | upstream_gene_variant | 0.92 |
gyrA | 6872 | c.-430T>C | upstream_gene_variant | 0.9 |
gyrA | 6877 | c.-425G>C | upstream_gene_variant | 0.88 |
gyrA | 6878 | c.-424T>C | upstream_gene_variant | 0.88 |
gyrA | 6881 | c.-421T>C | upstream_gene_variant | 0.88 |
gyrA | 6889 | c.-413G>T | upstream_gene_variant | 0.88 |
gyrA | 6898 | c.-404G>T | upstream_gene_variant | 0.8 |
gyrA | 6949 | c.-353A>G | upstream_gene_variant | 0.67 |
gyrA | 6952 | c.-350C>G | upstream_gene_variant | 0.67 |
gyrA | 6967 | c.-335T>C | upstream_gene_variant | 0.75 |
gyrB | 6970 | p.Asp577Glu | missense_variant | 0.75 |
gyrA | 6976 | c.-326A>G | upstream_gene_variant | 0.75 |
gyrA | 6982 | c.-320A>C | upstream_gene_variant | 0.75 |
gyrA | 6994 | c.-308C>G | upstream_gene_variant | 0.75 |
gyrA | 6997 | c.-305G>A | upstream_gene_variant | 0.75 |
gyrA | 7124 | c.-178_-176delTCGinsAGT | upstream_gene_variant | 1.0 |
gyrA | 7129 | c.-173T>C | upstream_gene_variant | 1.0 |
gyrA | 7132 | c.-170T>G | upstream_gene_variant | 1.0 |
gyrA | 7136 | c.-166_-164delTTGinsCTT | upstream_gene_variant | 1.0 |
gyrA | 7151 | c.-151C>T | upstream_gene_variant | 1.0 |
gyrA | 7162 | c.-140C>G | upstream_gene_variant | 1.0 |
gyrA | 7168 | c.-134C>G | upstream_gene_variant | 1.0 |
gyrA | 7184 | c.-118_-117delTCinsAG | upstream_gene_variant | 1.0 |
gyrB | 7187 | p.Ile650Val | missense_variant | 1.0 |
gyrA | 7207 | c.-95C>G | upstream_gene_variant | 1.0 |
gyrB | 7210 | p.Asp657Glu | missense_variant | 1.0 |
gyrA | 7213 | c.-89G>C | upstream_gene_variant | 1.0 |
gyrA | 7216 | c.-86G>C | upstream_gene_variant | 1.0 |
gyrA | 7225 | c.-77T>C | upstream_gene_variant | 1.0 |
gyrA | 7246 | c.-56T>C | upstream_gene_variant | 1.0 |
gyrA | 7249 | c.-53T>C | upstream_gene_variant | 1.0 |
gyrA | 7343 | c.42G>C | synonymous_variant | 1.0 |
gyrA | 7344 | p.Ile15Val | missense_variant | 1.0 |
gyrA | 7355 | c.54T>C | synonymous_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7366 | p.Gln22Leu | missense_variant | 1.0 |
gyrA | 7377 | p.Arg26Asn | missense_variant | 1.0 |
gyrA | 7391 | c.90C>T | synonymous_variant | 1.0 |
gyrA | 7394 | c.93T>C | synonymous_variant | 1.0 |
gyrA | 7427 | c.126G>C | synonymous_variant | 1.0 |
gyrA | 7442 | c.141G>C | synonymous_variant | 1.0 |
gyrA | 7445 | c.144C>G | synonymous_variant | 1.0 |
gyrA | 7451 | c.150C>G | synonymous_variant | 1.0 |
gyrA | 7464 | p.Val55Ile | missense_variant | 1.0 |
gyrA | 7547 | c.246C>T | synonymous_variant | 1.0 |
gyrA | 7569 | p.Ala90Ser | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7587 | c.286C>T | synonymous_variant | 1.0 |
gyrA | 7607 | c.306C>G | synonymous_variant | 1.0 |
gyrA | 7611 | p.Ser104Ala | missense_variant | 1.0 |
gyrA | 7614 | p.Leu105Met | missense_variant | 1.0 |
gyrA | 7619 | c.318C>T | synonymous_variant | 1.0 |
gyrA | 7859 | c.558A>G | synonymous_variant | 1.0 |
gyrA | 7865 | c.564T>C | synonymous_variant | 1.0 |
gyrA | 7880 | c.579C>T | synonymous_variant | 1.0 |
gyrA | 7884 | p.Arg195Thr | missense_variant | 1.0 |
gyrA | 7892 | c.591G>C | synonymous_variant | 1.0 |
gyrA | 7901 | c.600G>C | synonymous_variant | 1.0 |
gyrA | 7902 | p.Val201Ile | missense_variant | 1.0 |
gyrA | 7906 | p.Phe202Tyr | missense_variant | 1.0 |
gyrA | 7919 | p.Glu206Asp | missense_variant | 1.0 |
gyrA | 7922 | c.621T>C | synonymous_variant | 1.0 |
gyrA | 7937 | c.636A>G | synonymous_variant | 1.0 |
gyrA | 8315 | c.1014G>A | synonymous_variant | 1.0 |
gyrA | 8324 | c.1023T>C | synonymous_variant | 1.0 |
gyrA | 8327 | c.1026C>T | synonymous_variant | 1.0 |
gyrA | 8339 | c.1038A>G | synonymous_variant | 1.0 |
gyrA | 8340 | p.Ala347Ser | missense_variant | 1.0 |
gyrA | 8354 | c.1053G>C | synonymous_variant | 1.0 |
gyrA | 8369 | c.1068G>C | synonymous_variant | 1.0 |
gyrA | 8372 | c.1071G>C | synonymous_variant | 1.0 |
gyrA | 8382 | p.Leu361Met | missense_variant | 1.0 |
gyrA | 8434 | p.Thr378Arg | missense_variant | 1.0 |
gyrA | 8440 | p.Arg380Leu | missense_variant | 1.0 |
gyrA | 8453 | c.1152A>C | synonymous_variant | 1.0 |
gyrA | 8454 | p.Asn385Glu | missense_variant | 1.0 |
gyrA | 8462 | c.1161A>G | synonymous_variant | 1.0 |
gyrA | 8471 | c.1170T>C | synonymous_variant | 1.0 |
gyrA | 8486 | c.1185T>C | synonymous_variant | 1.0 |
gyrA | 8489 | c.1188A>G | synonymous_variant | 1.0 |
gyrA | 8495 | c.1194C>G | synonymous_variant | 1.0 |
gyrA | 8516 | c.1215T>C | synonymous_variant | 1.0 |
gyrA | 8519 | c.1218A>G | synonymous_variant | 1.0 |
gyrA | 8767 | p.Arg489Lys | missense_variant | 1.0 |
gyrA | 8769 | p.His490Tyr | missense_variant | 1.0 |
gyrA | 8780 | p.Asp493Glu | missense_variant | 1.0 |
gyrA | 8786 | c.1485T>C | synonymous_variant | 1.0 |
gyrA | 8791 | p.Arg497Gln | missense_variant | 1.0 |
gyrA | 8796 | p.Ile499Val | missense_variant | 1.0 |
gyrA | 8799 | p.Ala500Ser | missense_variant | 1.0 |
gyrA | 8810 | c.1509A>C | synonymous_variant | 1.0 |
gyrA | 8816 | c.1515C>G | synonymous_variant | 1.0 |
gyrA | 8817 | p.Ser506Ala | missense_variant | 1.0 |
gyrA | 8829 | c.1528T>C | synonymous_variant | 1.0 |
gyrA | 8843 | c.1542G>A | synonymous_variant | 1.0 |
gyrA | 8849 | c.1548C>G | synonymous_variant | 1.0 |
gyrA | 8852 | c.1551T>C | synonymous_variant | 1.0 |
gyrA | 8858 | c.1557T>G | synonymous_variant | 1.0 |
gyrA | 8867 | c.1566A>G | synonymous_variant | 1.0 |
gyrA | 8870 | c.1569G>C | synonymous_variant | 1.0 |
gyrA | 8873 | c.1572A>C | synonymous_variant | 0.97 |
gyrA | 8900 | c.1599G>C | synonymous_variant | 1.0 |
gyrA | 8903 | c.1602T>C | synonymous_variant | 1.0 |
gyrA | 8909 | c.1608C>T | synonymous_variant | 1.0 |
gyrA | 8915 | c.1614A>G | synonymous_variant | 1.0 |
gyrA | 8918 | c.1617C>T | synonymous_variant | 1.0 |
gyrA | 8939 | c.1638T>C | synonymous_variant | 1.0 |
gyrA | 8945 | c.1644G>C | synonymous_variant | 1.0 |
gyrA | 8946 | c.1645_1647delTTGinsCTC | synonymous_variant | 1.0 |
gyrA | 8967 | p.Ala556Lys | missense_variant | 1.0 |
gyrA | 8979 | p.Val560Met | missense_variant | 1.0 |
gyrA | 9208 | p.Lys636Arg | missense_variant | 1.0 |
gyrA | 9230 | c.1929T>C | synonymous_variant | 1.0 |
gyrA | 9234 | c.1933_1935delTCGinsAGC | synonymous_variant | 1.0 |
gyrA | 9242 | c.1941A>C | synonymous_variant | 1.0 |
gyrA | 9248 | c.1947G>C | synonymous_variant | 1.0 |
gyrA | 9254 | c.1953C>G | synonymous_variant | 1.0 |
gyrA | 9257 | c.1956C>T | synonymous_variant | 1.0 |
gyrA | 9267 | p.Asn656Glu | missense_variant | 1.0 |
gyrA | 9275 | c.1974G>A | synonymous_variant | 1.0 |
gyrA | 9276 | c.1975C>T | synonymous_variant | 1.0 |
gyrA | 9284 | c.1983T>C | synonymous_variant | 1.0 |
gyrA | 9293 | c.1992G>C | synonymous_variant | 1.0 |
gyrA | 9296 | c.1995T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491514 | p.Asn244Lys | missense_variant | 1.0 |
fgd1 | 491526 | c.744T>C | synonymous_variant | 1.0 |
fgd1 | 491532 | c.750G>T | synonymous_variant | 1.0 |
fgd1 | 491542 | c.760_762delTTGinsCTC | synonymous_variant | 1.0 |
fgd1 | 491547 | c.765A>C | synonymous_variant | 1.0 |
fgd1 | 491550 | c.768T>G | synonymous_variant | 1.0 |
fgd1 | 491569 | p.Asp263Thr | missense_variant | 1.0 |
fgd1 | 491590 | p.Lys270Ala | missense_variant | 1.0 |
fgd1 | 491601 | c.819T>C | synonymous_variant | 1.0 |
fgd1 | 491610 | c.828A>C | synonymous_variant | 1.0 |
fgd1 | 491616 | c.834A>G | synonymous_variant | 1.0 |
mshA | 575795 | p.Ile150Leu | missense_variant | 1.0 |
mshA | 575818 | c.471G>T | synonymous_variant | 1.0 |
mshA | 575821 | c.474G>C | synonymous_variant | 1.0 |
mshA | 575824 | c.477T>C | synonymous_variant | 1.0 |
mshA | 575840 | p.Ala165Thr | missense_variant | 1.0 |
mshA | 575843 | c.496_498delCGCinsAGG | synonymous_variant | 1.0 |
mshA | 575851 | c.504C>G | synonymous_variant | 1.0 |
mshA | 575855 | p.Ala170Arg | missense_variant | 1.0 |
mshA | 575864 | c.517T>C | synonymous_variant | 1.0 |
mshA | 575878 | c.531A>G | synonymous_variant | 1.0 |
mshA | 575884 | c.537G>C | synonymous_variant | 1.0 |
mshA | 575890 | c.543C>G | synonymous_variant | 1.0 |
mshA | 575893 | c.546C>G | synonymous_variant | 1.0 |
rpoB | 760046 | c.240G>C | synonymous_variant | 1.0 |
rpoB | 760049 | c.243A>G | synonymous_variant | 1.0 |
rpoB | 760059 | p.Tyr85Glu | missense_variant | 1.0 |
rpoB | 760067 | c.261G>C | synonymous_variant | 1.0 |
rpoB | 760070 | c.264T>C | synonymous_variant | 1.0 |
rpoB | 760091 | c.285G>C | synonymous_variant | 1.0 |
rpoB | 760094 | c.288G>C | synonymous_variant | 1.0 |
rpoB | 760101 | c.295T>C | synonymous_variant | 1.0 |
rpoB | 760106 | c.300G>C | synonymous_variant | 1.0 |
rpoB | 760112 | c.306T>C | synonymous_variant | 1.0 |
rpoB | 760118 | c.312T>G | synonymous_variant | 1.0 |
rpoB | 760121 | c.315T>C | synonymous_variant | 1.0 |
rpoB | 760127 | p.Asp107Glu | missense_variant | 1.0 |
rpoB | 760130 | p.Asp108Glu | missense_variant | 1.0 |
rpoB | 760139 | c.333A>C | synonymous_variant | 1.0 |
rpoB | 760140 | p.Pro112Ser | missense_variant | 1.0 |
rpoB | 760143 | p.Val113Ile | missense_variant | 1.0 |
rpoB | 760148 | c.342C>T | synonymous_variant | 1.0 |
rpoB | 760175 | c.369C>T | synonymous_variant | 1.0 |
rpoB | 760184 | c.378A>G | synonymous_variant | 1.0 |
rpoB | 760185 | c.379C>T | synonymous_variant | 1.0 |
rpoB | 760193 | c.387C>G | synonymous_variant | 1.0 |
rpoB | 760196 | c.390C>G | synonymous_variant | 1.0 |
rpoB | 760199 | c.393C>G | synonymous_variant | 1.0 |
rpoB | 760235 | c.429T>C | synonymous_variant | 1.0 |
rpoB | 760244 | c.438G>C | synonymous_variant | 1.0 |
rpoB | 760256 | c.450C>T | synonymous_variant | 1.0 |
rpoB | 760274 | p.Glu156Asp | missense_variant | 1.0 |
rpoB | 760298 | c.492G>C | synonymous_variant | 1.0 |
rpoB | 760307 | c.501T>G | synonymous_variant | 0.9 |
rpoB | 760310 | c.504G>T | synonymous_variant | 0.86 |
rpoB | 760424 | c.618C>G | synonymous_variant | 1.0 |
rpoB | 760430 | c.624T>C | synonymous_variant | 1.0 |
rpoB | 760436 | c.630C>G | synonymous_variant | 1.0 |
rpoB | 760454 | c.648C>G | synonymous_variant | 1.0 |
rpoB | 760457 | c.651C>T | synonymous_variant | 1.0 |
rpoB | 760475 | c.669A>G | synonymous_variant | 1.0 |
rpoB | 760481 | c.675G>C | synonymous_variant | 1.0 |
rpoB | 760484 | c.678A>G | synonymous_variant | 1.0 |
rpoB | 760502 | c.696C>G | synonymous_variant | 1.0 |
rpoB | 760514 | c.708C>G | synonymous_variant | 0.87 |
rpoB | 760522 | p.Ser239Thr | missense_variant | 0.88 |
rpoB | 760527 | p.Gln241Glu | missense_variant | 0.88 |
rpoB | 760532 | c.726T>C | synonymous_variant | 1.0 |
rpoB | 760541 | c.735G>C | synonymous_variant | 1.0 |
rpoB | 760547 | c.741G>C | synonymous_variant | 1.0 |
rpoB | 760563 | p.Arg253Met | missense_variant | 1.0 |
rpoB | 760571 | c.765G>C | synonymous_variant | 1.0 |
rpoB | 760591 | p.Val262Ala | missense_variant | 1.0 |
rpoB | 760595 | c.789C>T | synonymous_variant | 1.0 |
rpoB | 760596 | p.Thr264Gln | missense_variant | 1.0 |
rpoB | 760611 | c.805T>C | synonymous_variant | 1.0 |
rpoB | 760640 | c.834C>T | synonymous_variant | 0.99 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.98 |
rpoB | 760652 | c.846C>G | synonymous_variant | 0.81 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.98 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.98 |
rpoB | 760670 | c.864G>C | synonymous_variant | 0.98 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.98 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.98 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.98 |
rpoB | 760715 | c.909C>G | synonymous_variant | 0.97 |
rpoB | 760721 | c.915C>G | synonymous_variant | 0.64 |
rpoB | 760724 | c.918T>C | synonymous_variant | 0.96 |
rpoB | 760730 | c.924T>C | synonymous_variant | 0.94 |
rpoB | 760734 | p.Val310Ile | missense_variant | 0.94 |
rpoB | 760865 | c.1059C>T | synonymous_variant | 1.0 |
rpoB | 760877 | c.1071G>C | synonymous_variant | 1.0 |
rpoB | 760887 | p.Thr361Val | missense_variant | 1.0 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 1.0 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 1.0 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.82 |
rpoB | 760965 | p.Met387Leu | missense_variant | 1.0 |
rpoB | 760970 | c.1164G>C | synonymous_variant | 0.8 |
rpoB | 760973 | c.1167G>C | synonymous_variant | 0.8 |
rpoB | 760982 | c.1176G>T | synonymous_variant | 0.81 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 1.0 |
rpoB | 761006 | c.1200C>T | synonymous_variant | 1.0 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 1.0 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 1.0 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.91 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 1.0 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 1.0 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 1.0 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 1.0 |
rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 1.0 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 1.0 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 1.0 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 1.0 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 1.0 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 1.0 |
rpoB | 761162 | c.1356G>C | synonymous_variant | 1.0 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.94 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.94 |
rpoB | 761171 | c.1365C>T | 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>T | synonymous_variant | 1.0 |
rpoB | 761201 | c.1395G>A | synonymous_variant | 1.0 |
rpoB | 761213 | c.1407G>C | 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 | 761258 | c.1452G>A | synonymous_variant | 1.0 |
rpoB | 761261 | c.1455G>C | synonymous_variant | 0.98 |
rpoB | 761264 | c.1458C>G | synonymous_variant | 1.0 |
rpoB | 761273 | c.1467T>C | synonymous_variant | 1.0 |
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 | 1.0 |
rpoB | 761341 | p.Lys512Arg | missense_variant | 0.93 |
rpoB | 761345 | c.1539G>C | synonymous_variant | 0.92 |
rpoB | 761355 | p.Val517Arg | missense_variant | 1.0 |
rpoB | 761360 | c.1554T>C | synonymous_variant | 1.0 |
rpoB | 761362 | p.Ser519Thr | missense_variant | 1.0 |
rpoB | 761370 | p.Ile522Val | missense_variant | 1.0 |
rpoB | 761375 | c.1569G>C | synonymous_variant | 1.0 |
rpoB | 761393 | c.1587G>A | synonymous_variant | 1.0 |
rpoB | 761510 | c.1704T>C | synonymous_variant | 1.0 |
rpoB | 761516 | c.1710G>C | synonymous_variant | 1.0 |
rpoB | 761521 | p.Tyr572Phe | missense_variant | 0.55 |
rpoB | 761528 | c.1722C>T | synonymous_variant | 0.56 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 1.0 |
rpoB | 761540 | c.1734C>T | synonymous_variant | 0.39 |
rpoB | 761555 | c.1749G>C | synonymous_variant | 1.0 |
rpoB | 761558 | c.1752C>G | synonymous_variant | 1.0 |
rpoB | 761561 | c.1755C>G | synonymous_variant | 1.0 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 1.0 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 1.0 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 1.0 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 1.0 |
rpoB | 761615 | c.1809A>G | synonymous_variant | 1.0 |
rpoB | 761627 | c.1821C>T | synonymous_variant | 1.0 |
rpoB | 761633 | c.1827G>C | synonymous_variant | 1.0 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 1.0 |
rpoB | 761643 | p.Val613Ile | missense_variant | 1.0 |
rpoB | 761649 | c.1843_1844delAGinsTC | synonymous_variant | 1.0 |
rpoB | 761657 | c.1851C>G | synonymous_variant | 1.0 |
rpoB | 761661 | p.Leu619Ile | missense_variant | 1.0 |
rpoB | 761666 | c.1860G>C | synonymous_variant | 1.0 |
rpoB | 761906 | c.2100C>G | synonymous_variant | 1.0 |
rpoB | 761909 | c.2103T>C | synonymous_variant | 1.0 |
rpoB | 761912 | c.2106T>C | synonymous_variant | 1.0 |
rpoB | 761916 | p.Asp704Asn | missense_variant | 1.0 |
rpoB | 761921 | c.2115C>T | synonymous_variant | 1.0 |
rpoB | 761930 | c.2124G>C | synonymous_variant | 1.0 |
rpoB | 761931 | c.2125C>T | synonymous_variant | 1.0 |
rpoB | 761936 | c.2130C>T | synonymous_variant | 1.0 |
rpoB | 761954 | c.2148C>G | synonymous_variant | 1.0 |
rpoB | 761972 | c.2166C>T | synonymous_variant | 1.0 |
rpoB | 762002 | c.2196C>G | synonymous_variant | 1.0 |
rpoB | 762003 | p.Asn733Gln | missense_variant | 1.0 |
rpoB | 762008 | c.2202C>G | synonymous_variant | 1.0 |
rpoB | 762009 | c.2203C>T | synonymous_variant | 1.0 |
rpoB | 762014 | c.2208C>G | synonymous_variant | 1.0 |
rpoB | 762017 | c.2211A>G | synonymous_variant | 1.0 |
rpoB | 762018 | p.Glu738Gln | missense_variant | 1.0 |
rpoB | 762029 | c.2223C>G | synonymous_variant | 1.0 |
rpoB | 762038 | c.2232C>T | synonymous_variant | 1.0 |
rpoB | 762041 | c.2235C>T | synonymous_variant | 1.0 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 1.0 |
rpoB | 762068 | c.2262C>T | synonymous_variant | 1.0 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 1.0 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 1.0 |
rpoB | 762089 | c.2283G>A | synonymous_variant | 0.99 |
rpoB | 762113 | c.2307C>T | synonymous_variant | 1.0 |
rpoB | 762114 | p.Ile770Val | missense_variant | 1.0 |
rpoB | 762122 | c.2316C>T | synonymous_variant | 1.0 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 0.37 |
rpoB | 762134 | c.2328C>G | synonymous_variant | 1.0 |
rpoB | 762137 | c.2331C>T | synonymous_variant | 1.0 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 1.0 |
rpoB | 762149 | c.2343G>T | synonymous_variant | 1.0 |
rpoB | 762170 | c.2364C>G | synonymous_variant | 1.0 |
rpoB | 762176 | c.2370T>G | synonymous_variant | 1.0 |
rpoB | 762179 | c.2373C>T | synonymous_variant | 1.0 |
rpoB | 762200 | c.2394C>T | synonymous_variant | 1.0 |
rpoB | 762209 | c.2403C>G | synonymous_variant | 1.0 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 1.0 |
rpoB | 762239 | c.2433G>A | synonymous_variant | 0.46 |
rpoB | 762249 | c.2443C>T | synonymous_variant | 1.0 |
rpoB | 762254 | c.2448T>G | synonymous_variant | 1.0 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 1.0 |
rpoB | 762266 | c.2460T>G | synonymous_variant | 1.0 |
rpoB | 762287 | c.2481C>G | synonymous_variant | 1.0 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 1.0 |
rpoB | 762297 | c.2491C>T | synonymous_variant | 1.0 |
rpoB | 762308 | c.2502G>C | synonymous_variant | 1.0 |
rpoB | 762314 | c.2508C>T | synonymous_variant | 1.0 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 1.0 |
rpoB | 762335 | c.2529C>T | synonymous_variant | 1.0 |
rpoB | 762338 | c.2532T>C | synonymous_variant | 1.0 |
rpoB | 762347 | c.2541T>C | synonymous_variant | 1.0 |
rpoB | 762353 | c.2547C>G | synonymous_variant | 1.0 |
rpoB | 762362 | p.Glu852Asp | missense_variant | 1.0 |
rpoB | 762368 | p.Glu854Asp | missense_variant | 1.0 |
rpoB | 762369 | c.2563T>C | synonymous_variant | 1.0 |
rpoB | 762375 | p.Ala857Pro | missense_variant | 0.97 |
rpoC | 762398 | c.-972T>G | upstream_gene_variant | 1.0 |
rpoC | 762410 | c.-960T>G | upstream_gene_variant | 1.0 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 1.0 |
rpoB | 762426 | p.Ser874Gln | missense_variant | 1.0 |
rpoC | 762443 | c.-927G>C | upstream_gene_variant | 1.0 |
rpoC | 762446 | c.-924C>G | 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 |
rpoC | 762488 | c.-882G>C | upstream_gene_variant | 1.0 |
rpoB | 762489 | p.Val895Thr | missense_variant | 1.0 |
rpoC | 762512 | c.-858C>G | upstream_gene_variant | 0.84 |
rpoC | 762518 | c.-852C>T | upstream_gene_variant | 1.0 |
rpoC | 762527 | c.-843G>C | upstream_gene_variant | 1.0 |
rpoC | 762533 | c.-837T>C | upstream_gene_variant | 1.0 |
rpoC | 762536 | c.-834T>C | upstream_gene_variant | 1.0 |
rpoC | 762537 | c.-833_-831delTTGinsCTC | upstream_gene_variant | 1.0 |
rpoC | 762551 | c.-819C>T | upstream_gene_variant | 1.0 |
rpoC | 762836 | c.-534C>T | upstream_gene_variant | 1.0 |
rpoC | 762857 | c.-513C>G | upstream_gene_variant | 1.0 |
rpoB | 762858 | p.Thr1018Ala | missense_variant | 1.0 |
rpoC | 762863 | c.-507T>G | upstream_gene_variant | 1.0 |
rpoC | 762866 | c.-504C>T | upstream_gene_variant | 1.0 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 1.0 |
rpoC | 762885 | c.-485C>T | upstream_gene_variant | 0.45 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 1.0 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 1.0 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 1.0 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 1.0 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 1.0 |
rpoC | 762989 | c.-381G>T | upstream_gene_variant | 1.0 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 1.0 |
rpoC | 763049 | c.-321G>A | upstream_gene_variant | 1.0 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 1.0 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 1.0 |
rpoB | 763074 | p.Thr1090Val | missense_variant | 1.0 |
rpoC | 763082 | c.-288C>T | upstream_gene_variant | 1.0 |
rpoC | 763088 | c.-282C>G | upstream_gene_variant | 1.0 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 1.0 |
rpoC | 763100 | c.-270G>A | upstream_gene_variant | 1.0 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 1.0 |
rpoC | 763139 | c.-231C>T | upstream_gene_variant | 1.0 |
rpoC | 763142 | c.-228C>G | upstream_gene_variant | 1.0 |
rpoC | 763145 | c.-225G>A | upstream_gene_variant | 1.0 |
rpoC | 763157 | c.-213G>C | upstream_gene_variant | 1.0 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 1.0 |
rpoC | 763172 | c.-198G>C | upstream_gene_variant | 1.0 |
rpoC | 763196 | c.-174G>A | upstream_gene_variant | 1.0 |
rpoC | 763202 | c.-168A>G | upstream_gene_variant | 1.0 |
rpoC | 763206 | c.-164_-162delAGTinsTCC | upstream_gene_variant | 0.97 |
rpoC | 763214 | c.-156T>C | upstream_gene_variant | 1.0 |
rpoC | 763226 | c.-144A>G | upstream_gene_variant | 1.0 |
rpoC | 763238 | c.-132T>C | upstream_gene_variant | 1.0 |
rpoC | 763259 | c.-111G>C | upstream_gene_variant | 1.0 |
rpoC | 763268 | c.-102C>G | upstream_gene_variant | 1.0 |
rpoC | 763274 | c.-96G>C | upstream_gene_variant | 1.0 |
rpoC | 763277 | c.-93A>C | upstream_gene_variant | 1.0 |
rpoC | 763283 | c.-87T>C | upstream_gene_variant | 1.0 |
rpoC | 763375 | c.6C>A | synonymous_variant | 1.0 |
rpoC | 763402 | c.33C>G | synonymous_variant | 1.0 |
rpoC | 763408 | c.39T>C | synonymous_variant | 1.0 |
rpoC | 763411 | c.42T>C | synonymous_variant | 1.0 |
rpoC | 763414 | c.45T>C | 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_63delAGGinsCGT | synonymous_variant | 1.0 |
rpoC | 763435 | c.66A>G | synonymous_variant | 1.0 |
rpoC | 763444 | c.75T>C | synonymous_variant | 1.0 |
rpoC | 763453 | c.84C>G | synonymous_variant | 1.0 |
rpoC | 763456 | c.87A>G | synonymous_variant | 1.0 |
rpoC | 763468 | c.99G>C | synonymous_variant | 1.0 |
rpoC | 763486 | c.117T>C | synonymous_variant | 1.0 |
rpoC | 763528 | c.159G>T | synonymous_variant | 1.0 |
rpoC | 763531 | c.162G>C | synonymous_variant | 1.0 |
rpoC | 763534 | c.165T>C | synonymous_variant | 1.0 |
rpoC | 763537 | c.168C>G | synonymous_variant | 1.0 |
rpoC | 763546 | c.177A>G | synonymous_variant | 1.0 |
rpoC | 763570 | c.201G>C | synonymous_variant | 1.0 |
rpoC | 763573 | c.204G>C | synonymous_variant | 1.0 |
rpoC | 763594 | c.225C>T | synonymous_variant | 1.0 |
rpoC | 763603 | c.234C>T | synonymous_variant | 1.0 |
rpoC | 763618 | c.249C>T | synonymous_variant | 1.0 |
rpoC | 763633 | c.264T>C | synonymous_variant | 1.0 |
rpoC | 763636 | c.267T>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>T | synonymous_variant | 1.0 |
rpoC | 763669 | c.300C>G | synonymous_variant | 1.0 |
rpoC | 763696 | c.327T>C | synonymous_variant | 1.0 |
rpoC | 763702 | c.333C>G | 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 | 763723 | c.354G>C | synonymous_variant | 1.0 |
rpoC | 763732 | c.363C>G | synonymous_variant | 1.0 |
rpoC | 763741 | c.372C>T | synonymous_variant | 1.0 |
rpoC | 763765 | c.396T>C | synonymous_variant | 1.0 |
rpoC | 763774 | c.405G>C | synonymous_variant | 1.0 |
rpoC | 763778 | p.Thr137Val | missense_variant | 1.0 |
rpoC | 763781 | p.Ser138Ala | missense_variant | 1.0 |
rpoC | 763796 | p.Met143Leu | missense_variant | 1.0 |
rpoC | 763801 | c.432C>G | synonymous_variant | 1.0 |
rpoC | 763807 | c.438T>C | synonymous_variant | 1.0 |
rpoC | 763813 | c.444C>G | synonymous_variant | 1.0 |
rpoC | 763831 | c.462A>G | synonymous_variant | 1.0 |
rpoC | 763888 | c.519G>C | synonymous_variant | 0.67 |
rpoC | 763891 | c.522G>C | synonymous_variant | 0.67 |
rpoC | 763894 | c.525A>G | synonymous_variant | 0.8 |
rpoC | 763900 | c.531G>C | synonymous_variant | 0.92 |
rpoC | 763930 | c.561G>A | synonymous_variant | 0.95 |
rpoC | 763940 | p.Ala191Ser | missense_variant | 0.95 |
rpoC | 763945 | c.576T>C | synonymous_variant | 0.95 |
rpoC | 763947 | p.Ala193Val | missense_variant | 0.95 |
rpoC | 763951 | c.582G>C | synonymous_variant | 0.9 |
rpoC | 763960 | c.591T>C | synonymous_variant | 0.85 |
rpoC | 763961 | p.Arg198Lys | missense_variant | 0.89 |
rpoC | 763978 | c.609C>T | synonymous_variant | 0.97 |
rpoC | 763991 | p.Ile208Leu | missense_variant | 0.97 |
rpoC | 763996 | c.627T>C | synonymous_variant | 0.97 |
rpoC | 764002 | c.633C>G | synonymous_variant | 0.96 |
rpoC | 764005 | c.636G>C | synonymous_variant | 0.96 |
rpoC | 764011 | c.642T>C | synonymous_variant | 0.96 |
rpoC | 764024 | c.655T>C | synonymous_variant | 0.97 |
rpoC | 764029 | p.Glu220Asp | missense_variant | 0.97 |
rpoC | 764032 | p.Asp221Glu | missense_variant | 0.97 |
rpoC | 764040 | p.Ser224Asn | missense_variant | 0.97 |
rpoC | 764044 | c.675T>C | synonymous_variant | 0.97 |
rpoC | 764071 | c.702G>C | synonymous_variant | 1.0 |
rpoC | 764083 | c.714A>G | synonymous_variant | 1.0 |
rpoC | 764084 | p.Asn239Val | missense_variant | 1.0 |
rpoC | 764098 | c.729A>G | synonymous_variant | 1.0 |
rpoC | 764101 | c.732C>G | synonymous_variant | 1.0 |
rpoC | 764131 | c.762T>C | synonymous_variant | 1.0 |
rpoC | 764134 | c.765C>G | synonymous_variant | 1.0 |
rpoC | 764164 | p.Ile265Met | missense_variant | 1.0 |
rpoC | 764169 | p.Asn267Ser | missense_variant | 1.0 |
rpoC | 764182 | p.Asp271Glu | missense_variant | 1.0 |
rpoC | 764188 | c.819A>G | synonymous_variant | 1.0 |
rpoC | 764203 | c.834G>C | synonymous_variant | 1.0 |
rpoC | 764206 | p.Asp279Glu | missense_variant | 1.0 |
rpoC | 764207 | p.Val280Thr | missense_variant | 1.0 |
rpoC | 764215 | c.846A>C | synonymous_variant | 1.0 |
rpoC | 764217 | p.Asn283Thr | missense_variant | 1.0 |
rpoC | 764227 | c.858G>C | synonymous_variant | 1.0 |
rpoC | 764239 | c.870T>G | synonymous_variant | 1.0 |
rpoC | 764245 | c.876C>G | synonymous_variant | 1.0 |
rpoC | 764257 | c.888G>C | synonymous_variant | 1.0 |
rpoC | 764263 | c.894G>C | synonymous_variant | 1.0 |
rpoC | 764266 | c.897T>C | synonymous_variant | 1.0 |
rpoC | 764274 | c.908_909insGGCCA | frameshift_variant | 1.0 |
rpoC | 764279 | c.911_915delAGTCG | frameshift_variant | 1.0 |
rpoC | 764320 | c.951C>T | synonymous_variant | 1.0 |
rpoC | 764353 | c.984G>T | 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 | 764387 | c.1018T>C | synonymous_variant | 1.0 |
rpoC | 764404 | c.1035C>T | 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_1068delAGGinsCGA | synonymous_variant | 1.0 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 1.0 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 1.0 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 1.0 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 1.0 |
rpoC | 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 | 764509 | c.1140G>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>A | synonymous_variant | 1.0 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 1.0 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 1.0 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 0.98 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.98 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.98 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 1.0 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 1.0 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 1.0 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 1.0 |
rpoC | 764746 | c.1377G>C | synonymous_variant | 0.98 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.98 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 1.0 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 1.0 |
rpoC | 764780 | c.1411_1413delAGCinsTCG | synonymous_variant | 1.0 |
rpoC | 764791 | c.1422C>G | synonymous_variant | 1.0 |
rpoC | 764803 | c.1434C>G | synonymous_variant | 1.0 |
rpoC | 764809 | c.1440C>G | synonymous_variant | 1.0 |
rpoC | 764812 | c.1443C>G | synonymous_variant | 1.0 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 1.0 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 1.0 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 1.0 |
rpoC | 764848 | c.1479G>A | synonymous_variant | 1.0 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 1.0 |
rpoC | 764869 | c.1500C>T | synonymous_variant | 1.0 |
rpoC | 764872 | c.1503A>G | synonymous_variant | 1.0 |
rpoC | 764887 | c.1518G>C | synonymous_variant | 1.0 |
rpoC | 764888 | c.1519_1521delTTGinsCTC | synonymous_variant | 1.0 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 1.0 |
rpoC | 764912 | p.Met515Gln | missense_variant | 1.0 |
rpoC | 764935 | c.1566T>C | synonymous_variant | 1.0 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 1.0 |
rpoC | 764953 | c.1584G>C | synonymous_variant | 1.0 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 1.0 |
rpoC | 765469 | c.2100G>C | synonymous_variant | 1.0 |
rpoC | 765481 | c.2112C>T | synonymous_variant | 1.0 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 1.0 |
rpoC | 765544 | c.2175C>G | synonymous_variant | 1.0 |
rpoC | 765547 | c.2178C>T | synonymous_variant | 1.0 |
rpoC | 765548 | c.2179_2180delAGinsTC | synonymous_variant | 1.0 |
rpoC | 765562 | c.2193G>C | synonymous_variant | 1.0 |
rpoC | 765569 | p.Ala734Ser | missense_variant | 1.0 |
rpoC | 765580 | c.2211G>C | synonymous_variant | 1.0 |
rpoC | 765718 | p.Asp783Glu | missense_variant | 1.0 |
rpoC | 765728 | p.Gln787Lys | missense_variant | 1.0 |
rpoC | 765734 | c.2365T>C | synonymous_variant | 1.0 |
rpoC | 765739 | c.2370G>C | synonymous_variant | 1.0 |
rpoC | 765741 | p.Glu791Ala | missense_variant | 1.0 |
rpoC | 765751 | c.2382C>G | synonymous_variant | 1.0 |
rpoC | 765753 | p.Asp795Ala | missense_variant | 1.0 |
rpoC | 765772 | c.2403C>G | synonymous_variant | 1.0 |
rpoC | 765784 | c.2415C>G | synonymous_variant | 1.0 |
rpoC | 765793 | c.2424C>G | synonymous_variant | 1.0 |
rpoC | 765796 | c.2427C>T | synonymous_variant | 1.0 |
rpoC | 765811 | c.2442T>C | synonymous_variant | 1.0 |
rpoC | 765814 | c.2445A>T | synonymous_variant | 1.0 |
rpoC | 765817 | c.2448G>C | synonymous_variant | 1.0 |
rpoC | 765820 | c.2451G>C | synonymous_variant | 1.0 |
rpoC | 765844 | c.2475C>G | synonymous_variant | 1.0 |
rpoC | 765871 | c.2502T>G | synonymous_variant | 1.0 |
rpoC | 765875 | p.Val836Ile | missense_variant | 1.0 |
rpoC | 765904 | c.2535C>G | synonymous_variant | 1.0 |
rpoC | 765907 | c.2538G>T | synonymous_variant | 1.0 |
rpoC | 765940 | c.2571A>T | synonymous_variant | 1.0 |
rpoC | 765946 | c.2577C>T | synonymous_variant | 1.0 |
rpoC | 765947 | c.2578T>C | synonymous_variant | 1.0 |
rpoC | 765952 | c.2583G>C | synonymous_variant | 1.0 |
rpoC | 765962 | c.2593T>C | synonymous_variant | 1.0 |
rpoC | 765979 | c.2610C>G | synonymous_variant | 1.0 |
rpoC | 765982 | c.2613C>T | synonymous_variant | 1.0 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 1.0 |
rpoC | 766009 | c.2640G>C | synonymous_variant | 1.0 |
rpoC | 766012 | c.2643C>G | synonymous_variant | 1.0 |
rpoC | 766021 | c.2652G>C | synonymous_variant | 1.0 |
rpoC | 766039 | c.2670C>T | synonymous_variant | 1.0 |
rpoC | 766043 | p.Gln892Gly | missense_variant | 1.0 |
rpoC | 766261 | c.2892G>C | synonymous_variant | 1.0 |
rpoC | 766270 | c.2901G>C | synonymous_variant | 1.0 |
rpoC | 766273 | c.2904T>C | synonymous_variant | 1.0 |
rpoC | 766274 | p.Ala969Thr | missense_variant | 1.0 |
rpoC | 766280 | p.Ser971Gly | missense_variant | 1.0 |
rpoC | 766309 | c.2940G>C | synonymous_variant | 1.0 |
rpoC | 766312 | c.2943T>C | synonymous_variant | 1.0 |
rpoC | 766321 | c.2952C>G | synonymous_variant | 1.0 |
rpoC | 766348 | c.2979A>G | synonymous_variant | 1.0 |
rpoC | 766357 | c.2988C>T | synonymous_variant | 1.0 |
rpoC | 766363 | c.2994G>C | synonymous_variant | 1.0 |
rpoC | 766369 | c.3000C>G | synonymous_variant | 1.0 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 1.0 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 1.0 |
rpoC | 766390 | c.3021C>T | synonymous_variant | 1.0 |
rpoC | 766408 | c.3039C>T | synonymous_variant | 1.0 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 1.0 |
rpoC | 766429 | c.3061_3062insCTG | disruptive_inframe_insertion | 1.0 |
rpoC | 766435 | p.Glu1022Asp | missense_variant | 1.0 |
rpoC | 766447 | c.3078T>C | synonymous_variant | 1.0 |
rpoC | 766480 | c.3111C>G | synonymous_variant | 1.0 |
rpoC | 766483 | c.3114G>C | synonymous_variant | 1.0 |
rpoC | 766486 | c.3117A>G | synonymous_variant | 1.0 |
rpoC | 766490 | p.Arg1041Lys | missense_variant | 1.0 |
rpoC | 766504 | c.3135G>C | synonymous_variant | 1.0 |
rpoC | 766513 | p.Asp1048Glu | missense_variant | 1.0 |
rpoC | 766517 | p.Thr1050Ser | missense_variant | 1.0 |
rpoC | 766522 | c.3153C>T | synonymous_variant | 1.0 |
rpoC | 766525 | c.3156G>C | synonymous_variant | 1.0 |
rpoC | 766528 | c.3159T>G | synonymous_variant | 1.0 |
rpoC | 766534 | c.3165C>G | synonymous_variant | 1.0 |
rpoC | 766542 | p.Gly1058Asp | missense_variant | 1.0 |
rpoC | 766546 | p.Glu1059Asp | missense_variant | 1.0 |
rpoC | 766549 | c.3180G>C | synonymous_variant | 1.0 |
rpoC | 766568 | p.Val1067Ile | missense_variant | 1.0 |
rpoC | 766573 | c.3204T>G | synonymous_variant | 1.0 |
rpoC | 766576 | c.3207C>T | synonymous_variant | 1.0 |
rpoC | 766582 | c.3213C>T | synonymous_variant | 1.0 |
rpoC | 766585 | c.3216T>C | synonymous_variant | 1.0 |
rpoC | 766588 | c.3219G>A | synonymous_variant | 1.0 |
rpoC | 766591 | c.3222A>G | synonymous_variant | 1.0 |
rpoC | 766594 | c.3225G>T | synonymous_variant | 1.0 |
rpoC | 766607 | p.Ile1080Leu | missense_variant | 1.0 |
rpoC | 766612 | c.3243C>G | synonymous_variant | 1.0 |
rpoC | 766624 | c.3255G>T | synonymous_variant | 1.0 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 1.0 |
rpoC | 766651 | c.3282T>C | synonymous_variant | 1.0 |
rpoC | 766652 | p.Ser1095Thr | missense_variant | 1.0 |
rpoC | 766657 | c.3288A>G | synonymous_variant | 1.0 |
rpoC | 766660 | c.3291G>C | synonymous_variant | 1.0 |
rpoC | 766661 | p.Val1098Leu | missense_variant | 1.0 |
rpoC | 766672 | c.3303T>C | synonymous_variant | 1.0 |
rpoC | 766675 | c.3306C>T | synonymous_variant | 1.0 |
rpoC | 766690 | c.3321G>C | synonymous_variant | 1.0 |
rpoC | 766700 | c.3331C>T | synonymous_variant | 1.0 |
rpoC | 766703 | p.Met1112Leu | missense_variant | 1.0 |
rpoC | 766712 | p.Ser1115Ala | missense_variant | 1.0 |
rpoC | 766717 | c.3348C>G | synonymous_variant | 1.0 |
rpoC | 766720 | c.3351C>T | synonymous_variant | 1.0 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 1.0 |
rpoC | 766776 | p.Arg1136His | missense_variant | 1.0 |
rpoC | 766798 | c.3429C>G | synonymous_variant | 1.0 |
rpoC | 766799 | p.Ala1144Ser | missense_variant | 1.0 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 1.0 |
rpoC | 766837 | c.3468G>C | synonymous_variant | 1.0 |
rpoC | 766843 | c.3474T>G | synonymous_variant | 1.0 |
rpoC | 766858 | c.3489C>T | synonymous_variant | 1.0 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 1.0 |
rpoC | 766867 | c.3498C>G | synonymous_variant | 1.0 |
rpoC | 766883 | p.Ser1172Ala | missense_variant | 1.0 |
rpoC | 766894 | c.3525T>C | synonymous_variant | 1.0 |
rpoC | 766895 | c.3526T>C | synonymous_variant | 1.0 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 1.0 |
rpoC | 766909 | c.3540G>C | synonymous_variant | 1.0 |
rpoC | 766911 | p.Ile1181Thr | missense_variant | 1.0 |
rpoC | 766915 | p.Asp1182Glu | missense_variant | 1.0 |
rpoC | 766921 | c.3552G>C | synonymous_variant | 1.0 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 1.0 |
rpoC | 766975 | c.3606C>G | synonymous_variant | 1.0 |
rpoC | 766978 | c.3609C>T | synonymous_variant | 1.0 |
rpoC | 766981 | c.3612T>C | synonymous_variant | 1.0 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 1.0 |
rpoC | 767002 | c.3633G>C | synonymous_variant | 1.0 |
rpoC | 767044 | c.3675G>C | synonymous_variant | 1.0 |
rpoC | 767059 | c.3690T>C | synonymous_variant | 1.0 |
rpoC | 767060 | c.3691_3693delCGCinsAGG | synonymous_variant | 1.0 |
rpoC | 767065 | c.3696G>T | synonymous_variant | 1.0 |
rpoC | 767071 | c.3702C>G | synonymous_variant | 1.0 |
rpoC | 767074 | c.3705T>C | synonymous_variant | 1.0 |
rpoC | 767093 | c.3724_3725delAGinsTC | synonymous_variant | 1.0 |
rpoC | 767098 | c.3729T>C | synonymous_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 | 767180 | p.Ala1271Gln | missense_variant | 1.0 |
rpoC | 767191 | c.3822C>G | synonymous_variant | 1.0 |
rpsL | 781558 | c.-2A>C | upstream_gene_variant | 1.0 |
rpsL | 781559 | c.-1G>T | upstream_gene_variant | 1.0 |
rpsL | 781572 | p.Gln5Asn | missense_variant | 1.0 |
rpsL | 781595 | c.36T>C | synonymous_variant | 1.0 |
rpsL | 781598 | c.39G>C | synonymous_variant | 1.0 |
rpsL | 781605 | p.Ile16Val | missense_variant | 1.0 |
rpsL | 781608 | p.Ser17Ala | missense_variant | 1.0 |
rpsL | 781614 | p.Val19Thr | missense_variant | 1.0 |
rpsL | 781628 | c.69T>C | synonymous_variant | 1.0 |
rpsL | 781637 | c.78C>G | synonymous_variant | 1.0 |
rpsL | 781655 | c.96T>C | synonymous_variant | 1.0 |
rpsL | 781658 | c.99A>G | synonymous_variant | 1.0 |
rpsL | 781679 | c.120C>G | synonymous_variant | 1.0 |
rpsL | 781682 | c.123T>C | synonymous_variant | 1.0 |
rpsL | 781700 | c.141G>C | synonymous_variant | 1.0 |
rpsL | 781706 | c.147T>G | synonymous_variant | 1.0 |
rpsL | 781709 | c.150G>C | synonymous_variant | 1.0 |
rpsL | 781715 | c.156T>C | synonymous_variant | 1.0 |
rpsL | 781754 | c.195G>C | synonymous_variant | 1.0 |
rpsL | 781760 | c.201T>C | synonymous_variant | 1.0 |
rpsL | 781763 | c.204C>G | synonymous_variant | 1.0 |
rpsL | 781772 | c.213C>G | synonymous_variant | 1.0 |
rpsL | 781793 | c.234G>C | synonymous_variant | 1.0 |
rpsL | 781802 | c.243G>C | synonymous_variant | 1.0 |
rpsL | 781814 | c.255C>T | synonymous_variant | 1.0 |
rpsL | 781817 | c.258G>T | synonymous_variant | 1.0 |
rpsL | 781829 | c.270G>C | synonymous_variant | 1.0 |
rpsL | 781832 | c.273T>C | synonymous_variant | 1.0 |
rpsL | 781838 | c.279G>T | synonymous_variant | 1.0 |
rpsL | 781841 | c.282C>T | synonymous_variant | 1.0 |
rpsL | 781853 | c.294C>T | synonymous_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>T | synonymous_variant | 1.0 |
rpsL | 781880 | c.321C>G | synonymous_variant | 1.0 |
rpsL | 781892 | c.333A>G | synonymous_variant | 1.0 |
rpsL | 781898 | c.339A>C | synonymous_variant | 1.0 |
rpsL | 781907 | c.348T>C | synonymous_variant | 1.0 |
rpsL | 781916 | c.357T>C | synonymous_variant | 1.0 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 1.0 |
rplC | 800610 | c.-199_-197delCTAinsTTG | upstream_gene_variant | 1.0 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 1.0 |
rplC | 800633 | c.-176T>C | upstream_gene_variant | 1.0 |
rplC | 800645 | c.-164C>T | upstream_gene_variant | 1.0 |
rplC | 800648 | c.-161A>G | upstream_gene_variant | 1.0 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.83 |
rplC | 800672 | c.-137G>C | upstream_gene_variant | 1.0 |
rplC | 800690 | c.-119C>T | upstream_gene_variant | 0.95 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.95 |
rplC | 800702 | c.-107G>C | upstream_gene_variant | 0.95 |
rplC | 800703 | c.-106_-104delTTGinsCTT | upstream_gene_variant | 0.95 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.95 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.95 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.95 |
rplC | 800735 | c.-74C>G | upstream_gene_variant | 0.95 |
rplC | 800738 | c.-71T>G | upstream_gene_variant | 0.95 |
rplC | 800762 | c.-47T>G | upstream_gene_variant | 0.94 |
fbiC | 1303488 | c.558G>C | synonymous_variant | 1.0 |
fbiC | 1303492 | c.562T>C | synonymous_variant | 1.0 |
fbiC | 1303512 | c.582T>C | synonymous_variant | 1.0 |
fbiC | 1303519 | c.589_590delAGinsTC | synonymous_variant | 1.0 |
fbiC | 1303525 | p.Ser199Glu | missense_variant | 1.0 |
fbiC | 1303533 | p.Met201Ile | missense_variant | 1.0 |
fbiC | 1303534 | p.Ser202Ala | missense_variant | 1.0 |
fbiC | 1303545 | c.615A>G | synonymous_variant | 1.0 |
fbiC | 1303556 | p.Pro209Gln | missense_variant | 1.0 |
fbiC | 1303560 | c.630G>C | synonymous_variant | 1.0 |
fbiC | 1303581 | c.651G>C | synonymous_variant | 1.0 |
fbiC | 1304559 | p.Glu543Asp | missense_variant | 1.0 |
fbiC | 1304562 | c.1632G>C | synonymous_variant | 1.0 |
fbiC | 1304567 | p.Phe546Tyr | missense_variant | 1.0 |
fbiC | 1304574 | c.1644C>G | synonymous_variant | 1.0 |
fbiC | 1304580 | c.1650T>G | synonymous_variant | 1.0 |
fbiC | 1304599 | p.Ile557Val | missense_variant | 1.0 |
fbiC | 1304613 | c.1683T>G | synonymous_variant | 1.0 |
fbiC | 1304619 | c.1689G>C | synonymous_variant | 1.0 |
fbiC | 1304640 | c.1710A>C | synonymous_variant | 1.0 |
fbiC | 1304646 | c.1716T>C | synonymous_variant | 1.0 |
fbiC | 1304652 | c.1722C>G | synonymous_variant | 1.0 |
fbiC | 1304727 | c.1797A>C | synonymous_variant | 1.0 |
fbiC | 1304742 | c.1812T>C | synonymous_variant | 1.0 |
fbiC | 1304748 | c.1818T>C | synonymous_variant | 1.0 |
fbiC | 1304754 | p.Glu608Asp | missense_variant | 1.0 |
fbiC | 1304757 | c.1827A>G | synonymous_variant | 1.0 |
fbiC | 1304769 | c.1839C>G | synonymous_variant | 1.0 |
fbiC | 1304775 | c.1845C>G | synonymous_variant | 1.0 |
fbiC | 1304778 | c.1848T>C | synonymous_variant | 1.0 |
fbiC | 1304784 | c.1854T>G | synonymous_variant | 1.0 |
fbiC | 1304790 | c.1860C>G | synonymous_variant | 1.0 |
fbiC | 1304797 | p.Ala623Gln | missense_variant | 0.86 |
fbiC | 1304808 | c.1878C>G | synonymous_variant | 0.75 |
fbiC | 1304811 | c.1881C>G | synonymous_variant | 0.75 |
fbiC | 1305339 | c.2409C>G | synonymous_variant | 1.0 |
fbiC | 1305348 | c.2418C>T | synonymous_variant | 1.0 |
fbiC | 1305361 | c.2431C>T | synonymous_variant | 1.0 |
fbiC | 1305381 | c.2451G>C | synonymous_variant | 1.0 |
fbiC | 1305390 | c.2460C>G | synonymous_variant | 1.0 |
fbiC | 1305396 | c.2466C>G | synonymous_variant | 1.0 |
fbiC | 1305397 | p.Glu823Gln | missense_variant | 1.0 |
fbiC | 1305405 | c.2475A>C | synonymous_variant | 1.0 |
fbiC | 1305417 | c.2487C>G | synonymous_variant | 1.0 |
fbiC | 1305423 | c.2493T>C | synonymous_variant | 1.0 |
fbiC | 1305432 | c.2502C>G | synonymous_variant | 1.0 |
fbiC | 1305434 | p.Ala835Glu | missense_variant | 1.0 |
rrs | 1471914 | n.69A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471918 | n.73A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471922 | n.78delT | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471931 | n.87delA | 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 | 1471943 | n.98T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471978 | n.133C>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1471979 | n.134T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472062 | n.217G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472068 | n.223T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472070 | n.225G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472148 | n.303T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472328 | n.483G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472416 | n.571C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472422 | n.577T>C | 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 | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472456 | n.611T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472467 | n.622G>T | 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 | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472597 | n.752G>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 | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472836 | n.991G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472840 | n.995A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472844 | n.999C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472845 | n.1000G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472847 | n.1002G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472849 | n.1004C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472850 | n.1005T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472855 | n.1011_1012insGT | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472873 | n.1028C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472875 | n.1030T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472958 | n.1113A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472971 | n.1126G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472988 | n.1143T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473026 | n.1181T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.98 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473696 | n.39T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473698 | n.41G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473699 | n.42A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473717 | n.60G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473731 | n.74T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473756 | n.99G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473757 | n.100T>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1473758 | n.101G>A | non_coding_transcript_exon_variant | 0.99 |
rrl | 1473788 | n.131A>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1473807 | n.150T>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1473812 | n.155G>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1473814 | n.157A>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1473815 | n.158T>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1473844 | n.187C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1473870 | n.213G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473871 | n.214T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1473922 | n.265A>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1473923 | n.266C>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1473934 | n.277G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474112 | n.455T>G | 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 | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474186 | n.529A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474201 | n.544T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474264 | n.607T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474265 | n.608G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474266 | n.609T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474286 | n.630dupT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474293 | n.637_646delCCTCTCCGGA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474306 | n.649A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474308 | n.653_654delTG | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474350 | n.693G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474351 | n.694G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474354 | n.697C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474355 | n.698A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474359 | n.702C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474402 | n.745T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474413 | n.756A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474496 | n.839C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474627 | n.970G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474664 | n.1007G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474666 | n.1009T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474670 | n.1013C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474679 | n.1022G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474684 | n.1027T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474687 | n.1030C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474710 | n.1053T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474711 | n.1054G>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474803 | n.1146G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474830 | n.1173A>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 | 0.99 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474953 | n.1297delA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475028 | n.1371G>C | 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 | 1475060 | n.1404delC | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475065 | n.1408G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475067 | n.1410A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475076 | n.1419C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475079 | n.1422T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475081 | n.1424C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475113 | n.1456C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475116 | n.1459G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475406 | n.1749T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475422 | n.1765A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475443 | n.1786G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475460 | n.1803A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475475 | n.1818C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475479 | n.1822C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475481 | n.1824C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475482 | n.1825A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475532 | n.1875A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475538 | n.1881T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475550 | n.1893A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475602 | n.1945G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475639 | n.1982C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475649 | n.1992A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475655 | n.1998T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475735 | n.2078T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475758 | n.2101A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475760 | n.2103C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475762 | n.2105G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475764 | n.2107A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475765 | n.2108A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475769 | n.2113_2114insCG | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475791 | n.2134A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.99 |
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 | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476032 | n.2375C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476033 | n.2376T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476046 | n.2389G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476047 | n.2390G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476058 | n.2401T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476076 | n.2419A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476088 | n.2431A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476105 | n.2450delA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476160 | n.2503T>C | 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 | 1476221 | n.2564T>C | 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 | 1476255 | n.2598A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476297 | n.2640C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476298 | n.2641C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476300 | n.2643G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 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 | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476596 | n.2939C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476601 | n.2944G>A | 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 | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476661 | n.3004A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476665 | n.3008T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476666 | n.3009C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476675 | n.3018C>G | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1833571 | c.30A>G | synonymous_variant | 1.0 |
rpsA | 1833589 | c.48A>C | synonymous_variant | 1.0 |
rpsA | 1833595 | c.54T>C | synonymous_variant | 1.0 |
rpsA | 1833596 | p.Ser19Ala | missense_variant | 1.0 |
rpsA | 1833604 | c.63C>T | synonymous_variant | 1.0 |
rpsA | 1833607 | c.66T>C | synonymous_variant | 1.0 |
rpsA | 1833616 | c.75A>C | synonymous_variant | 1.0 |
rpsA | 1833619 | c.78A>C | synonymous_variant | 1.0 |
rpsA | 1833623 | p.Lys28Ala | missense_variant | 1.0 |
rpsA | 1833646 | c.105T>C | synonymous_variant | 1.0 |
rpsA | 1833664 | c.123C>A | synonymous_variant | 1.0 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 1.0 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 1.0 |
rpsA | 1833682 | c.141C>T | synonymous_variant | 1.0 |
rpsA | 1833685 | c.144G>C | synonymous_variant | 1.0 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 1.0 |
rpsA | 1833697 | c.156C>G | synonymous_variant | 1.0 |
rpsA | 1833709 | c.168C>T | synonymous_variant | 1.0 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 1.0 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 1.0 |
rpsA | 1833739 | c.198C>T | synonymous_variant | 1.0 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 1.0 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 1.0 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 1.0 |
rpsA | 1833793 | c.252C>T | synonymous_variant | 1.0 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 1.0 |
rpsA | 1833808 | c.267G>T | synonymous_variant | 1.0 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 1.0 |
rpsA | 1833829 | c.288A>G | synonymous_variant | 1.0 |
rpsA | 1833832 | c.291G>A | synonymous_variant | 1.0 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 1.0 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 1.0 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 1.0 |
rpsA | 1833850 | c.309C>G | synonymous_variant | 1.0 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 1.0 |
rpsA | 1833859 | c.318C>G | synonymous_variant | 1.0 |
rpsA | 1833877 | c.336C>G | synonymous_variant | 1.0 |
rpsA | 1833894 | p.Ala118Glu | missense_variant | 1.0 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 1.0 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 1.0 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 1.0 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 1.0 |
rpsA | 1833991 | c.450C>G | synonymous_variant | 1.0 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 1.0 |
rpsA | 1834009 | c.468C>G | synonymous_variant | 1.0 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 1.0 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 1.0 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 1.0 |
rpsA | 1834024 | c.483G>C | synonymous_variant | 1.0 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 1.0 |
rpsA | 1834034 | p.Ile165Val | missense_variant | 1.0 |
rpsA | 1834090 | c.549G>C | synonymous_variant | 1.0 |
rpsA | 1834096 | c.555G>C | synonymous_variant | 1.0 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 1.0 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834186 | c.645C>G | synonymous_variant | 1.0 |
rpsA | 1834189 | c.648G>C | synonymous_variant | 1.0 |
rpsA | 1834213 | c.672G>C | synonymous_variant | 1.0 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 1.0 |
rpsA | 1834225 | c.684C>G | synonymous_variant | 1.0 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 1.0 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 1.0 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 1.0 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 1.0 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 1.0 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 1.0 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 1.0 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 1.0 |
rpsA | 1834307 | p.Asp256Asn | missense_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 | 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 | 1834396 | c.855G>T | synonymous_variant | 1.0 |
rpsA | 1834399 | p.His286Gln | missense_variant | 1.0 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 1.0 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 1.0 |
rpsA | 1834451 | c.910_912delTTGinsCTC | synonymous_variant | 1.0 |
rpsA | 1834465 | c.924T>C | synonymous_variant | 1.0 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 1.0 |
rpsA | 1834489 | c.948T>C | synonymous_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>C | synonymous_variant | 1.0 |
rpsA | 1834555 | c.1014T>G | synonymous_variant | 1.0 |
rpsA | 1834606 | c.1065C>T | synonymous_variant | 1.0 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 1.0 |
rpsA | 1834619 | c.1078T>C | synonymous_variant | 1.0 |
rpsA | 1834622 | c.1081_1083delTCGinsAGC | synonymous_variant | 1.0 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 1.0 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 1.0 |
rpsA | 1834649 | p.Thr370His | missense_variant | 1.0 |
rpsA | 1834653 | p.Glu371Ala | missense_variant | 1.0 |
rpsA | 1834667 | p.Ala376Ser | missense_variant | 1.0 |
rpsA | 1834690 | c.1149T>C | synonymous_variant | 1.0 |
rpsA | 1834732 | c.1191T>C | synonymous_variant | 1.0 |
rpsA | 1834733 | p.Ala398Pro | missense_variant | 1.0 |
rpsA | 1834738 | p.Glu399Asp | missense_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 |
rpsA | 1834765 | p.Glu408Asp | missense_variant | 1.0 |
rpsA | 1834776 | p.Ala412Glu | missense_variant | 1.0 |
rpsA | 1834780 | c.1239A>G | synonymous_variant | 1.0 |
rpsA | 1834788 | p.Ala416Gly | missense_variant | 1.0 |
rpsA | 1834792 | c.1251G>C | synonymous_variant | 1.0 |
rpsA | 1834804 | c.1263C>G | synonymous_variant | 1.0 |
rpsA | 1834810 | c.1269C>T | synonymous_variant | 1.0 |
rpsA | 1834813 | c.1272G>C | synonymous_variant | 1.0 |
rpsA | 1834844 | p.Phe435Ile | missense_variant | 1.0 |
katG | 2155080 | c.1032G>C | synonymous_variant | 1.0 |
katG | 2155108 | p.Ile335Asn | missense_variant | 1.0 |
katG | 2155112 | p.Glu334Gln | missense_variant | 1.0 |
katG | 2155113 | c.999C>G | synonymous_variant | 1.0 |
katG | 2155119 | p.Ser331Gly | missense_variant | 1.0 |
katG | 2155126 | p.Asp329Gly | missense_variant | 1.0 |
katG | 2155131 | c.981A>G | synonymous_variant | 1.0 |
katG | 2155134 | c.978G>C | synonymous_variant | 1.0 |
katG | 2155137 | c.975G>C | synonymous_variant | 1.0 |
katG | 2155144 | p.Asn323Ser | missense_variant | 1.0 |
katG | 2155152 | c.960A>C | synonymous_variant | 1.0 |
katG | 2155176 | c.936G>C | synonymous_variant | 1.0 |
katG | 2155626 | c.486G>C | synonymous_variant | 1.0 |
katG | 2155632 | c.480A>C | synonymous_variant | 1.0 |
katG | 2155637 | p.Leu159Ile | missense_variant | 1.0 |
katG | 2155641 | p.Lys157Asn | missense_variant | 1.0 |
katG | 2155655 | p.Lys153Gln | missense_variant | 1.0 |
katG | 2155673 | c.439C>T | synonymous_variant | 1.0 |
katG | 2155691 | c.421T>C | synonymous_variant | 1.0 |
katG | 2155695 | c.417C>G | synonymous_variant | 1.0 |
katG | 2155704 | c.408C>G | synonymous_variant | 1.0 |
katG | 2155716 | c.396T>G | synonymous_variant | 1.0 |
katG | 2155728 | c.384G>T | synonymous_variant | 1.0 |
katG | 2155747 | p.Ala122Gly | missense_variant | 1.0 |
katG | 2155765 | p.His116Ser | missense_variant | 1.0 |
katG | 2155782 | c.330C>G | synonymous_variant | 1.0 |
katG | 2155785 | c.327T>C | synonymous_variant | 1.0 |
kasA | 2517917 | c.-198G>T | upstream_gene_variant | 1.0 |
kasA | 2517941 | c.-174C>G | upstream_gene_variant | 1.0 |
kasA | 2517950 | c.-165C>T | upstream_gene_variant | 1.0 |
kasA | 2517959 | c.-156C>T | upstream_gene_variant | 1.0 |
kasA | 2517962 | c.-153C>G | upstream_gene_variant | 1.0 |
kasA | 2518723 | p.Glu203Asp | missense_variant | 1.0 |
kasA | 2518727 | p.Leu205Val | missense_variant | 1.0 |
kasA | 2518732 | c.618C>G | synonymous_variant | 1.0 |
kasA | 2518745 | p.Ser211Thr | missense_variant | 1.0 |
kasA | 2518756 | c.642G>C | synonymous_variant | 1.0 |
kasA | 2518763 | c.649_651delTCGinsAGC | synonymous_variant | 1.0 |
kasA | 2518780 | p.Glu222Asp | missense_variant | 1.0 |
kasA | 2518783 | c.669T>G | synonymous_variant | 1.0 |
kasA | 2518784 | p.Glu224Lys | missense_variant | 1.0 |
kasA | 2518787 | p.Arg225Gly | missense_variant | 1.0 |
kasA | 2518795 | c.681C>G | synonymous_variant | 1.0 |
kasA | 2518798 | c.684G>T | synonymous_variant | 1.0 |
kasA | 2518825 | c.711T>C | synonymous_variant | 1.0 |
kasA | 2518828 | c.714G>C | synonymous_variant | 1.0 |
kasA | 2518840 | c.726C>G | synonymous_variant | 1.0 |
ahpC | 2726234 | p.Gln14His | missense_variant | 0.67 |
ahpC | 2726243 | c.51T>G | synonymous_variant | 1.0 |
ahpC | 2726244 | p.Leu18Val | missense_variant | 1.0 |
ahpC | 2726264 | c.72C>G | synonymous_variant | 1.0 |
ahpC | 2726276 | c.84C>T | synonymous_variant | 1.0 |
ahpC | 2726277 | p.Lys29Gln | missense_variant | 1.0 |
ahpC | 2726287 | p.Gly32Asp | missense_variant | 1.0 |
ahpC | 2726301 | p.Thr37Arg | missense_variant | 1.0 |
ahpC | 2726312 | c.120T>C | synonymous_variant | 1.0 |
ahpC | 2726318 | p.Glu42Asp | missense_variant | 1.0 |
ahpC | 2726322 | p.Pro44Ala | missense_variant | 1.0 |
ahpC | 2726337 | p.Val49Ile | missense_variant | 1.0 |
ahpC | 2726342 | c.150G>C | synonymous_variant | 1.0 |
ahpC | 2726348 | c.156T>C | synonymous_variant | 1.0 |
ahpC | 2726357 | c.165A>G | synonymous_variant | 1.0 |
ahpC | 2726366 | c.174G>C | synonymous_variant | 1.0 |
ahpC | 2726378 | c.186T>G | synonymous_variant | 1.0 |
ahpC | 2726390 | c.198G>C | synonymous_variant | 1.0 |
ahpC | 2726397 | p.Ser69Gly | missense_variant | 1.0 |
ahpC | 2726408 | c.216T>C | synonymous_variant | 1.0 |
ahpC | 2726414 | c.222G>A | synonymous_variant | 1.0 |
ahpC | 2726567 | c.375C>G | synonymous_variant | 1.0 |
ahpC | 2726579 | c.387T>C | synonymous_variant | 1.0 |
ahpC | 2726582 | c.390G>C | synonymous_variant | 1.0 |
ahpC | 2726593 | p.Val134Ala | missense_variant | 1.0 |
ahpC | 2726600 | c.408T>C | synonymous_variant | 1.0 |
ahpC | 2726604 | p.Val138Ile | missense_variant | 1.0 |
ahpC | 2726612 | c.420C>G | synonymous_variant | 1.0 |
ahpC | 2726636 | c.444G>C | synonymous_variant | 1.0 |
ahpC | 2726638 | p.Ala149Val | missense_variant | 1.0 |
ahpC | 2726645 | c.453C>G | synonymous_variant | 1.0 |
ahpC | 2726657 | c.465A>C | synonymous_variant | 1.0 |
ahpC | 2726669 | c.477T>C | synonymous_variant | 1.0 |
ahpC | 2726675 | c.483A>G | synonymous_variant | 1.0 |
ahpC | 2726681 | c.489A>T | synonymous_variant | 1.0 |
ahpC | 2726696 | c.504C>G | synonymous_variant | 1.0 |
ahpC | 2726717 | c.525A>C | synonymous_variant | 1.0 |
ahpC | 2726723 | c.531C>T | synonymous_variant | 1.0 |
ahpC | 2726727 | p.Arg179Lys | missense_variant | 1.0 |
ahpC | 2726741 | c.549G>C | synonymous_variant | 1.0 |
folC | 2747312 | p.Thr96Ile | missense_variant | 1.0 |
folC | 2747314 | c.285A>G | synonymous_variant | 1.0 |
folC | 2747329 | c.270C>T | synonymous_variant | 1.0 |
folC | 2747343 | p.Val86Leu | missense_variant | 1.0 |
folC | 2747347 | c.252G>C | synonymous_variant | 1.0 |
folC | 2747355 | p.Val82Ile | missense_variant | 1.0 |
folC | 2747359 | c.238_240delCGCinsAGG | synonymous_variant | 1.0 |
folC | 2747362 | p.Ala79Thr | missense_variant | 1.0 |
folC | 2747395 | c.204T>C | synonymous_variant | 1.0 |
folC | 2747401 | c.198G>C | synonymous_variant | 1.0 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 1.0 |
rpoA | 3877590 | c.918G>C | synonymous_variant | 1.0 |
rpoA | 3877596 | c.912G>C | synonymous_variant | 1.0 |
rpoA | 3877600 | p.Gln303Ala | missense_variant | 1.0 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 1.0 |
rpoA | 3877617 | c.891G>C | synonymous_variant | 1.0 |
rpoA | 3877638 | c.870T>C | synonymous_variant | 1.0 |
rpoA | 3877650 | c.858C>T | synonymous_variant | 1.0 |
rpoA | 3877656 | c.852T>G | synonymous_variant | 1.0 |
rpoA | 3877662 | c.846C>T | synonymous_variant | 1.0 |
rpoA | 3877665 | c.843C>G | synonymous_variant | 1.0 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 1.0 |
rpoA | 3877677 | c.831G>C | synonymous_variant | 1.0 |
rpoA | 3877680 | c.828G>C | synonymous_variant | 1.0 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 1.0 |
rpoA | 3877704 | c.804G>T | synonymous_variant | 1.0 |
rpoA | 3877734 | c.774G>C | synonymous_variant | 1.0 |
rpoA | 3877737 | c.771G>C | synonymous_variant | 1.0 |
rpoA | 3877740 | c.768G>C | synonymous_variant | 1.0 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 1.0 |
rpoA | 3877752 | p.Asp252Glu | missense_variant | 1.0 |
rpoA | 3877764 | p.Ala248Gly | missense_variant | 1.0 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 1.0 |
rpoA | 3877773 | c.735G>C | synonymous_variant | 1.0 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 1.0 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 1.0 |
rpoA | 3877785 | c.723C>G | synonymous_variant | 1.0 |
rpoA | 3877800 | c.708G>C | synonymous_variant | 1.0 |
rpoA | 3877803 | c.705G>C | synonymous_variant | 1.0 |
rpoA | 3877821 | c.687C>A | synonymous_variant | 1.0 |
rpoA | 3877824 | c.684G>A | synonymous_variant | 1.0 |
rpoA | 3877833 | c.675C>G | synonymous_variant | 1.0 |
rpoA | 3877836 | c.672A>G | synonymous_variant | 1.0 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 1.0 |
rpoA | 3877842 | c.666A>C | synonymous_variant | 1.0 |
rpoA | 3877854 | c.652_654delTTGinsCTC | synonymous_variant | 1.0 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 1.0 |
rpoA | 3877875 | c.633T>G | synonymous_variant | 1.0 |
rpoA | 3877881 | c.627G>C | synonymous_variant | 1.0 |
rpoA | 3877884 | c.624G>C | synonymous_variant | 1.0 |
rpoA | 3877893 | c.615C>G | synonymous_variant | 1.0 |
rpoA | 3877898 | p.Pro204Ala | missense_variant | 1.0 |
rpoA | 3877905 | c.603A>C | synonymous_variant | 1.0 |
rpoA | 3877908 | c.600T>C | synonymous_variant | 1.0 |
rpoA | 3877932 | c.576G>C | synonymous_variant | 1.0 |
rpoA | 3877936 | p.Lys191Arg | missense_variant | 1.0 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 1.0 |
rpoA | 3877965 | c.543C>T | synonymous_variant | 1.0 |
rpoA | 3877968 | c.540C>G | synonymous_variant | 1.0 |
rpoA | 3877971 | p.Asp179Glu | missense_variant | 1.0 |
rpoA | 3877974 | c.534G>C | synonymous_variant | 1.0 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 1.0 |
rpoA | 3877992 | c.516C>G | synonymous_variant | 1.0 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 1.0 |
rpoA | 3878010 | c.498C>G | synonymous_variant | 1.0 |
rpoA | 3878016 | c.492C>G | synonymous_variant | 1.0 |
rpoA | 3878019 | c.489A>G | synonymous_variant | 1.0 |
rpoA | 3878064 | c.444G>C | synonymous_variant | 1.0 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 1.0 |
rpoA | 3878079 | c.429C>T | synonymous_variant | 1.0 |
rpoA | 3878082 | c.426T>C | synonymous_variant | 1.0 |
rpoA | 3878102 | p.Val136Ile | missense_variant | 1.0 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 1.0 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 1.0 |
rpoA | 3878127 | c.381G>C | synonymous_variant | 1.0 |
rpoA | 3878130 | c.378C>G | synonymous_variant | 1.0 |
rpoA | 3878143 | p.Gly122Asp | missense_variant | 1.0 |
rpoA | 3878145 | c.363C>G | synonymous_variant | 1.0 |
rpoA | 3878202 | c.306G>C | synonymous_variant | 1.0 |
rpoA | 3878205 | c.303T>C | synonymous_variant | 1.0 |
rpoA | 3878217 | p.Leu97Val | missense_variant | 1.0 |
rpoA | 3878226 | c.282C>G | synonymous_variant | 1.0 |
rpoA | 3878247 | c.261G>C | synonymous_variant | 1.0 |
rpoA | 3878250 | c.258C>G | synonymous_variant | 1.0 |
rpoA | 3878253 | c.255G>C | synonymous_variant | 1.0 |
rpoA | 3878256 | c.252G>C | synonymous_variant | 1.0 |
rpoA | 3878264 | p.Ser82Gly | missense_variant | 1.0 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 1.0 |
rpoA | 3878283 | p.Glu75Asp | missense_variant | 1.0 |
rpoA | 3878295 | c.213A>G | synonymous_variant | 1.0 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 1.0 |
rpoA | 3878301 | c.207C>G | synonymous_variant | 1.0 |
rpoA | 3878304 | c.204G>C | synonymous_variant | 1.0 |
rpoA | 3878310 | c.198G>T | synonymous_variant | 1.0 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 1.0 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 1.0 |
clpC1 | 4038350 | c.2355C>G | synonymous_variant | 1.0 |
clpC1 | 4038356 | c.2349T>C | synonymous_variant | 1.0 |
clpC1 | 4038359 | c.2346A>G | synonymous_variant | 1.0 |
clpC1 | 4038368 | c.2337T>C | synonymous_variant | 1.0 |
clpC1 | 4038383 | c.2322G>C | synonymous_variant | 1.0 |
clpC1 | 4038388 | c.2317T>C | synonymous_variant | 1.0 |
clpC1 | 4038392 | c.2311_2313delCGCinsAGG | synonymous_variant | 1.0 |
clpC1 | 4038398 | c.2307G>T | synonymous_variant | 1.0 |
clpC1 | 4038401 | c.2302_2304delTTGinsCTC | synonymous_variant | 1.0 |
clpC1 | 4038407 | c.2298G>C | synonymous_variant | 1.0 |
clpC1 | 4038474 | p.Ser744Asn | missense_variant | 1.0 |
clpC1 | 4038479 | c.2226C>G | synonymous_variant | 1.0 |
clpC1 | 4038485 | p.Gly740Thr | missense_variant | 1.0 |
clpC1 | 4038494 | c.2211G>C | synonymous_variant | 1.0 |
clpC1 | 4038499 | p.Ser736Gly | missense_variant | 1.0 |
clpC1 | 4038512 | c.2193C>G | synonymous_variant | 1.0 |
clpC1 | 4038519 | p.Arg729Glu | missense_variant | 1.0 |
clpC1 | 4038523 | p.Ile728Val | missense_variant | 1.0 |
clpC1 | 4038529 | p.Glu726Gln | missense_variant | 1.0 |
clpC1 | 4038534 | p.Arg724Asn | missense_variant | 1.0 |
clpC1 | 4038539 | c.2166G>C | synonymous_variant | 1.0 |
clpC1 | 4038557 | p.Ile716Val | missense_variant | 1.0 |
clpC1 | 4038587 | c.2118C>G | synonymous_variant | 1.0 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 1.0 |
clpC1 | 4038620 | p.Gln695Leu | missense_variant | 1.0 |
clpC1 | 4038623 | c.2082A>G | synonymous_variant | 1.0 |
clpC1 | 4038640 | p.Asp689Asn | missense_variant | 1.0 |
clpC1 | 4038674 | c.2031C>G | synonymous_variant | 1.0 |
clpC1 | 4038677 | p.Pro676Ala | missense_variant | 1.0 |
clpC1 | 4038683 | c.2022T>G | synonymous_variant | 1.0 |
clpC1 | 4038692 | c.2013C>G | synonymous_variant | 1.0 |
clpC1 | 4038701 | c.2004G>C | synonymous_variant | 1.0 |
clpC1 | 4038704 | c.2001T>C | synonymous_variant | 1.0 |
clpC1 | 4038707 | c.1998C>G | synonymous_variant | 1.0 |
clpC1 | 4038710 | c.1995G>C | synonymous_variant | 1.0 |
clpC1 | 4038713 | c.1992T>C | synonymous_variant | 1.0 |
clpC1 | 4038725 | c.1980C>G | synonymous_variant | 1.0 |
clpC1 | 4038743 | c.1962G>C | synonymous_variant | 1.0 |
clpC1 | 4038746 | c.1959C>G | synonymous_variant | 1.0 |
clpC1 | 4038755 | c.1950G>C | synonymous_variant | 1.0 |
clpC1 | 4038764 | c.1941C>G | synonymous_variant | 1.0 |
clpC1 | 4038767 | c.1938G>C | synonymous_variant | 1.0 |
clpC1 | 4038770 | c.1935C>T | synonymous_variant | 1.0 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 1.0 |
clpC1 | 4038779 | c.1924_1926delCTCinsTTG | synonymous_variant | 1.0 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 1.0 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 1.0 |
clpC1 | 4038795 | p.Ser637Thr | missense_variant | 1.0 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 1.0 |
clpC1 | 4038815 | c.1890G>C | synonymous_variant | 1.0 |
clpC1 | 4038842 | c.1863G>C | synonymous_variant | 0.74 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 1.0 |
clpC1 | 4038863 | c.1842G>A | synonymous_variant | 0.29 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 1.0 |
clpC1 | 4038890 | c.1815G>A | synonymous_variant | 1.0 |
clpC1 | 4038905 | c.1800A>C | synonymous_variant | 1.0 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.73 |
clpC1 | 4038911 | c.1794G>T | synonymous_variant | 1.0 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.79 |
clpC1 | 4038917 | c.1788C>T | synonymous_variant | 1.0 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 1.0 |
clpC1 | 4038932 | c.1773G>T | synonymous_variant | 1.0 |
clpC1 | 4038941 | c.1764G>C | synonymous_variant | 1.0 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 1.0 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 1.0 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 1.0 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 1.0 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 1.0 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 1.0 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 1.0 |
clpC1 | 4039004 | c.1701C>G | synonymous_variant | 1.0 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 1.0 |
clpC1 | 4039037 | c.1668T>C | synonymous_variant | 1.0 |
clpC1 | 4039067 | c.1638G>C | synonymous_variant | 1.0 |
clpC1 | 4039073 | c.1632C>T | synonymous_variant | 1.0 |
clpC1 | 4039079 | c.1626C>G | synonymous_variant | 1.0 |
clpC1 | 4039085 | c.1620A>G | synonymous_variant | 1.0 |
clpC1 | 4039091 | c.1614G>C | synonymous_variant | 1.0 |
clpC1 | 4039097 | c.1608G>T | synonymous_variant | 1.0 |
clpC1 | 4039103 | c.1602T>C | synonymous_variant | 1.0 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 1.0 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 1.0 |
clpC1 | 4039124 | c.1581C>G | synonymous_variant | 1.0 |
clpC1 | 4039133 | c.1572C>G | synonymous_variant | 1.0 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 1.0 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 1.0 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 1.0 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 1.0 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 1.0 |
clpC1 | 4039181 | c.1522_1524delTTGinsCTC | synonymous_variant | 1.0 |
clpC1 | 4039187 | c.1518G>T | synonymous_variant | 1.0 |
clpC1 | 4039199 | p.Ala502Glu | missense_variant | 1.0 |
clpC1 | 4039238 | p.Gly489Ala | missense_variant | 1.0 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 1.0 |
clpC1 | 4039277 | c.1428C>G | synonymous_variant | 1.0 |
clpC1 | 4039280 | c.1425G>C | synonymous_variant | 1.0 |
clpC1 | 4039286 | c.1419T>G | synonymous_variant | 1.0 |
clpC1 | 4039289 | c.1416T>C | synonymous_variant | 1.0 |
clpC1 | 4039292 | c.1413C>T | synonymous_variant | 1.0 |
clpC1 | 4039295 | c.1410A>C | synonymous_variant | 1.0 |
clpC1 | 4039310 | c.1395A>G | synonymous_variant | 1.0 |
clpC1 | 4039313 | c.1392C>G | synonymous_variant | 1.0 |
clpC1 | 4039319 | c.1386T>C | synonymous_variant | 1.0 |
clpC1 | 4039382 | c.1323C>G | synonymous_variant | 1.0 |
clpC1 | 4039391 | c.1314T>G | synonymous_variant | 1.0 |
clpC1 | 4039394 | c.1311G>C | synonymous_variant | 1.0 |
clpC1 | 4039397 | c.1308A>G | synonymous_variant | 1.0 |
clpC1 | 4039409 | c.1296T>C | synonymous_variant | 1.0 |
clpC1 | 4039412 | c.1293T>C | synonymous_variant | 1.0 |
clpC1 | 4039427 | p.Glu426Asp | missense_variant | 1.0 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 1.0 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 1.0 |
clpC1 | 4039448 | c.1257A>G | synonymous_variant | 1.0 |
clpC1 | 4039454 | c.1251A>T | synonymous_variant | 1.0 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 1.0 |
clpC1 | 4039472 | c.1233G>C | synonymous_variant | 1.0 |
clpC1 | 4039481 | c.1224T>G | synonymous_variant | 1.0 |
clpC1 | 4039484 | c.1221T>C | synonymous_variant | 1.0 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 1.0 |
clpC1 | 4039553 | c.1152C>G | synonymous_variant | 1.0 |
clpC1 | 4039556 | c.1149G>C | synonymous_variant | 1.0 |
clpC1 | 4039559 | c.1146C>G | synonymous_variant | 1.0 |
clpC1 | 4039570 | p.Met379Leu | missense_variant | 1.0 |
clpC1 | 4039574 | p.Ala377Gly | missense_variant | 0.97 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 1.0 |
clpC1 | 4039586 | c.1119G>C | synonymous_variant | 1.0 |
clpC1 | 4039589 | c.1116G>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 | 4039634 | p.Glu357Asn | missense_variant | 1.0 |
clpC1 | 4039649 | c.1056G>C | synonymous_variant | 1.0 |
clpC1 | 4039652 | c.1053G>C | synonymous_variant | 1.0 |
clpC1 | 4039661 | c.1044T>C | synonymous_variant | 1.0 |
clpC1 | 4039682 | c.1023C>G | synonymous_variant | 1.0 |
clpC1 | 4039694 | c.1011G>T | synonymous_variant | 1.0 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 1.0 |
clpC1 | 4039733 | c.972G>C | synonymous_variant | 1.0 |
clpC1 | 4039739 | c.966C>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 | 4039793 | c.912C>G | synonymous_variant | 1.0 |
clpC1 | 4039802 | c.903G>C | synonymous_variant | 1.0 |
clpC1 | 4039814 | c.891C>G | synonymous_variant | 1.0 |
clpC1 | 4039817 | c.888A>C | synonymous_variant | 1.0 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 1.0 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 1.0 |
clpC1 | 4039832 | c.873C>G | synonymous_variant | 1.0 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 1.0 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 1.0 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 1.0 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 1.0 |
clpC1 | 4039907 | c.798G>A | synonymous_variant | 1.0 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 1.0 |
clpC1 | 4039937 | c.768G>C | synonymous_variant | 1.0 |
clpC1 | 4039943 | c.762G>C | synonymous_variant | 1.0 |
clpC1 | 4039946 | c.759A>C | synonymous_variant | 1.0 |
clpC1 | 4039955 | c.750G>C | synonymous_variant | 1.0 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 1.0 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 1.0 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 1.0 |
clpC1 | 4040002 | p.His235Asn | missense_variant | 1.0 |
clpC1 | 4040003 | c.702G>C | synonymous_variant | 1.0 |
clpC1 | 4040018 | c.687G>C | synonymous_variant | 1.0 |
clpC1 | 4040021 | c.684A>G | synonymous_variant | 1.0 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 1.0 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 1.0 |
clpC1 | 4040048 | c.657C>T | synonymous_variant | 0.98 |
clpC1 | 4040087 | c.618G>C | synonymous_variant | 1.0 |
clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 1.0 |
clpC1 | 4040117 | c.588A>G | synonymous_variant | 1.0 |
clpC1 | 4040124 | p.Glu194Ser | missense_variant | 1.0 |
clpC1 | 4040141 | c.564C>T | 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 | 4040156 | p.Met183Leu | missense_variant | 1.0 |
clpC1 | 4040162 | c.543G>C | synonymous_variant | 1.0 |
clpC1 | 4040166 | p.Ala180Gln | missense_variant | 1.0 |
clpC1 | 4040168 | c.537G>C | synonymous_variant | 1.0 |
clpC1 | 4040171 | c.534C>G | synonymous_variant | 1.0 |
clpC1 | 4040180 | c.525C>T | synonymous_variant | 1.0 |
clpC1 | 4040330 | c.375C>G | synonymous_variant | 1.0 |
clpC1 | 4040342 | c.363C>G | synonymous_variant | 1.0 |
clpC1 | 4040345 | c.360C>G | synonymous_variant | 1.0 |
clpC1 | 4040354 | c.351A>G | synonymous_variant | 1.0 |
clpC1 | 4040357 | c.348T>C | synonymous_variant | 1.0 |
clpC1 | 4040363 | c.342A>T | synonymous_variant | 1.0 |
clpC1 | 4040366 | c.339C>T | synonymous_variant | 1.0 |
clpC1 | 4040375 | c.330G>C | synonymous_variant | 1.0 |
clpC1 | 4040380 | c.325T>C | synonymous_variant | 1.0 |
clpC1 | 4040381 | c.324T>C | synonymous_variant | 1.0 |
clpC1 | 4040387 | c.318A>G | synonymous_variant | 1.0 |
clpC1 | 4040393 | c.312G>T | synonymous_variant | 1.0 |
clpC1 | 4040408 | c.297C>T | synonymous_variant | 1.0 |
clpC1 | 4040411 | c.294T>G | synonymous_variant | 1.0 |
clpC1 | 4040426 | c.279T>C | synonymous_variant | 1.0 |
clpC1 | 4040429 | c.274_276delTTGinsCTT | synonymous_variant | 1.0 |
clpC1 | 4040441 | c.264C>G | synonymous_variant | 1.0 |
clpC1 | 4040444 | c.261C>G | synonymous_variant | 1.0 |
clpC1 | 4040450 | c.255A>G | synonymous_variant | 1.0 |
clpC1 | 4040459 | c.246C>G | synonymous_variant | 1.0 |
clpC1 | 4040465 | c.240T>C | synonymous_variant | 1.0 |
clpC1 | 4040471 | c.234T>C | synonymous_variant | 1.0 |
clpC1 | 4040477 | c.228G>T | synonymous_variant | 1.0 |
clpC1 | 4040480 | c.225T>C | synonymous_variant | 1.0 |
clpC1 | 4040486 | c.219G>C | synonymous_variant | 1.0 |
clpC1 | 4040516 | c.189C>G | synonymous_variant | 1.0 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 1.0 |
clpC1 | 4040531 | c.174T>C | synonymous_variant | 1.0 |
clpC1 | 4040539 | c.166C>T | synonymous_variant | 1.0 |
clpC1 | 4040543 | c.162C>T | synonymous_variant | 1.0 |
clpC1 | 4040546 | c.159G>C | synonymous_variant | 1.0 |
clpC1 | 4040549 | c.154_156delTTGinsCTC | synonymous_variant | 1.0 |
clpC1 | 4040561 | c.144A>G | synonymous_variant | 1.0 |
clpC1 | 4040570 | c.135C>G | synonymous_variant | 1.0 |
clpC1 | 4040573 | c.132T>C | synonymous_variant | 1.0 |
clpC1 | 4040579 | c.126A>G | synonymous_variant | 1.0 |
embC | 4240729 | c.867C>G | synonymous_variant | 1.0 |
embC | 4240758 | p.Thr299Asn | missense_variant | 1.0 |
embC | 4240765 | c.903C>G | synonymous_variant | 1.0 |
embC | 4240768 | c.906G>C | synonymous_variant | 1.0 |
embC | 4240771 | c.909G>C | synonymous_variant | 1.0 |
embC | 4240776 | p.Glu305Gly | missense_variant | 1.0 |
embC | 4240780 | c.918T>C | synonymous_variant | 1.0 |
ubiA | 4268994 | p.Arg280Gly | missense_variant | 1.0 |
ubiA | 4269006 | p.Asp276Glu | missense_variant | 1.0 |
ubiA | 4269025 | p.Leu270Glu | missense_variant | 1.0 |
aftB | 4269030 | c.-194C>G | upstream_gene_variant | 1.0 |
aftB | 4269042 | c.-206G>C | upstream_gene_variant | 1.0 |
aftB | 4269051 | c.-215C>T | upstream_gene_variant | 1.0 |
aftB | 4269054 | c.-218G>C | upstream_gene_variant | 1.0 |
aftB | 4269075 | c.-239T>C | upstream_gene_variant | 1.0 |
ubiA | 4269084 | p.Val250Ile | missense_variant | 1.0 |
kasA | 2518878 | c.765_*835del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |