Run ID: ERR4821143
Sample name:
Date: 01-04-2023 17:05:02
Number of reads: 41042
Percentage reads mapped: 3.1
Strain: lineage4.9
Drug-resistance: RR-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 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761127 | p.Ser441Ala | missense_variant | 1.0 | rifampicin |
rpsL | 781821 | p.Lys88Arg | missense_variant | 1.0 | streptomycin |
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.71 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.83 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 1.0 | kanamycin, capreomycin, aminoglycosides, amikacin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
rpoB | 760169 | p.Met121Ile | missense_variant | 1.0 |
rpoB | 760172 | c.366G>C | synonymous_variant | 1.0 |
rpoB | 760181 | c.375T>G | synonymous_variant | 1.0 |
rpoB | 760184 | c.378A>G | synonymous_variant | 1.0 |
rpoB | 760199 | c.393C>G | synonymous_variant | 0.86 |
rpoB | 760208 | c.402C>T | synonymous_variant | 0.89 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.82 |
rpoB | 760263 | p.Met153Leu | missense_variant | 0.89 |
rpoB | 760275 | p.Lys157Arg | missense_variant | 0.78 |
rpoB | 760283 | c.477G>C | synonymous_variant | 0.78 |
rpoB | 760298 | c.492G>C | synonymous_variant | 0.71 |
rpoB | 760415 | c.609C>T | synonymous_variant | 1.0 |
rpoB | 760418 | c.612G>C | synonymous_variant | 1.0 |
rpoB | 760424 | c.618C>G | synonymous_variant | 1.0 |
rpoB | 760430 | c.624T>C | synonymous_variant | 1.0 |
rpoB | 760433 | p.Asp209Glu | missense_variant | 1.0 |
rpoB | 760434 | p.Val210Ile | missense_variant | 1.0 |
rpoB | 760970 | c.1164G>C | synonymous_variant | 1.0 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 1.0 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 1.0 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 1.0 |
rpoB | 760997 | c.1191G>C | synonymous_variant | 1.0 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 1.0 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 1.0 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 1.0 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 1.0 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 1.0 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 1.0 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 1.0 |
rpoB | 761064 | p.Ala420Ser | missense_variant | 1.0 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 1.0 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 1.0 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 1.0 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 1.0 |
rpoB | 761147 | c.1341C>G | synonymous_variant | 1.0 |
rpoB | 761252 | c.1446C>T | synonymous_variant | 0.67 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.67 |
rpoB | 761258 | c.1452G>A | synonymous_variant | 0.67 |
rpoB | 761261 | c.1455G>C | synonymous_variant | 0.67 |
rpoB | 761264 | c.1458C>G | synonymous_variant | 0.67 |
rpoB | 761273 | c.1467T>C | synonymous_variant | 0.67 |
rpoB | 761282 | c.1476C>T | synonymous_variant | 0.67 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 1.0 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 1.0 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 1.0 |
rpoB | 762084 | p.Ala760Pro | missense_variant | 1.0 |
rpoB | 762098 | c.2292C>T | synonymous_variant | 1.0 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 1.0 |
rpoB | 762114 | p.Ile770Val | missense_variant | 1.0 |
rpoB | 762122 | p.Asp772Glu | missense_variant | 1.0 |
rpoB | 762128 | c.2322G>C | synonymous_variant | 1.0 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 1.0 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 1.0 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 1.0 |
rpoB | 762156 | p.Val784Ile | missense_variant | 1.0 |
rpoB | 762170 | c.2364C>A | synonymous_variant | 1.0 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 1.0 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 1.0 |
rpoB | 762189 | p.Ile795Leu | missense_variant | 1.0 |
rpoB | 762209 | c.2403C>G | synonymous_variant | 1.0 |
rpoB | 762212 | c.2406G>C | synonymous_variant | 1.0 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 1.0 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 1.0 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 1.0 |
rpoB | 762275 | c.2469C>T | synonymous_variant | 1.0 |
rpoB | 762278 | c.2472C>T | synonymous_variant | 1.0 |
rpoB | 762284 | c.2478G>T | synonymous_variant | 1.0 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 1.0 |
rpoB | 762297 | p.Leu831Met | missense_variant | 1.0 |
rpoB | 762305 | c.2499G>C | synonymous_variant | 1.0 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 1.0 |
rpoB | 762318 | p.Ser838Thr | missense_variant | 1.0 |
rpoB | 762325 | p.Lys840Thr | missense_variant | 1.0 |
rpoB | 762329 | c.2523G>C | synonymous_variant | 1.0 |
rpoC | 762827 | c.-543G>T | upstream_gene_variant | 0.75 |
rpoC | 762831 | c.-539_-538delAGinsTC | upstream_gene_variant | 0.75 |
rpoC | 762839 | c.-531G>A | upstream_gene_variant | 0.83 |
rpoB | 762849 | p.Tyr1015Glu | missense_variant | 0.83 |
rpoC | 762857 | c.-513C>G | upstream_gene_variant | 1.0 |
rpoB | 762858 | p.Thr1018Ser | missense_variant | 1.0 |
rpoC | 762863 | c.-507T>G | upstream_gene_variant | 0.88 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.93 |
rpoC | 762885 | c.-485C>T | upstream_gene_variant | 0.93 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.95 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.96 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.96 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 0.95 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.95 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.94 |
rpoB | 763005 | p.Cys1067Val | missense_variant | 0.89 |
rpoB | 763014 | p.Met1070Leu | missense_variant | 1.0 |
rpoB | 763017 | p.Gln1071Glu | missense_variant | 1.0 |
rpoC | 763022 | c.-348C>G | upstream_gene_variant | 1.0 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 1.0 |
rpoB | 763038 | p.Thr1078Ala | missense_variant | 1.0 |
rpoC | 763053 | c.-317_-315delTTGinsCTC | upstream_gene_variant | 1.0 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 1.0 |
rpoB | 763075 | p.Thr1090Ile | missense_variant | 1.0 |
rpoB | 763077 | p.Val1091Asn | missense_variant | 1.0 |
rpoC | 763088 | c.-282C>A | upstream_gene_variant | 1.0 |
rpoC | 763094 | c.-276G>T | upstream_gene_variant | 1.0 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 1.0 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 1.0 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 1.0 |
rpoC | 763160 | c.-210G>C | upstream_gene_variant | 1.0 |
rpoB | 763161 | p.Leu1119Ile | missense_variant | 1.0 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 1.0 |
rpoB | 763170 | p.Leu1122Met | missense_variant | 1.0 |
rpoC | 763181 | c.-189G>C | upstream_gene_variant | 1.0 |
rpoC | 763199 | c.-171G>C | upstream_gene_variant | 1.0 |
rpoC | 763462 | c.93G>C | synonymous_variant | 1.0 |
rpoC | 763465 | c.96G>A | synonymous_variant | 1.0 |
rpoC | 763468 | c.99G>C | synonymous_variant | 1.0 |
rpoC | 763483 | c.114G>C | synonymous_variant | 1.0 |
rpoC | 763486 | c.117T>C | synonymous_variant | 1.0 |
rpoC | 763492 | c.123G>C | synonymous_variant | 1.0 |
rpoC | 763507 | c.138G>C | synonymous_variant | 1.0 |
rpoC | 763528 | c.159G>C | synonymous_variant | 1.0 |
rpoC | 763531 | c.162G>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>A | synonymous_variant | 1.0 |
rpoC | 763573 | c.204G>C | synonymous_variant | 1.0 |
rpoC | 763594 | c.225C>T | synonymous_variant | 1.0 |
rpoC | 763600 | c.231C>G | synonymous_variant | 1.0 |
rpoC | 763603 | c.234C>T | synonymous_variant | 1.0 |
rpoC | 763609 | c.240C>T | synonymous_variant | 1.0 |
rpoC | 763615 | c.246G>C | synonymous_variant | 1.0 |
rpoC | 763618 | c.249C>T | synonymous_variant | 1.0 |
rpoC | 763621 | c.252C>T | synonymous_variant | 1.0 |
rpoC | 763622 | p.Ala85Ser | missense_variant | 1.0 |
rpoC | 763625 | p.Lys86Ala | missense_variant | 1.0 |
rpoC | 763633 | c.264T>C | synonymous_variant | 1.0 |
rpoC | 763660 | c.291T>C | synonymous_variant | 1.0 |
rpoC | 763669 | c.300C>G | synonymous_variant | 1.0 |
rpoC | 763708 | c.339G>C | synonymous_variant | 1.0 |
rpoC | 763709 | c.340C>T | synonymous_variant | 1.0 |
rpoC | 763714 | c.345G>T | synonymous_variant | 1.0 |
rpoC | 763717 | c.348T>C | synonymous_variant | 1.0 |
rpoC | 763723 | c.354G>C | synonymous_variant | 1.0 |
rpoC | 763729 | c.360G>C | synonymous_variant | 1.0 |
rpoC | 763751 | p.Ile128Val | missense_variant | 1.0 |
rpoC | 763765 | c.396T>G | synonymous_variant | 1.0 |
rpoC | 763768 | c.399C>G | synonymous_variant | 1.0 |
rpoC | 763772 | p.Val135Met | missense_variant | 1.0 |
rpoC | 763786 | c.417C>T | synonymous_variant | 1.0 |
rpoC | 764320 | c.951C>G | synonymous_variant | 1.0 |
rpoC | 764326 | c.957G>C | synonymous_variant | 1.0 |
rpoC | 764338 | p.Glu323Asp | missense_variant | 1.0 |
rpoC | 764359 | c.990C>G | synonymous_variant | 1.0 |
rpoC | 764362 | c.993C>T | synonymous_variant | 1.0 |
rpoC | 764365 | c.996C>T | synonymous_variant | 1.0 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 1.0 |
rpoC | 764377 | c.1008C>G | synonymous_variant | 1.0 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 1.0 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 1.0 |
rpoC | 764398 | c.1029G>C | synonymous_variant | 1.0 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 1.0 |
rpoC | 764410 | c.1041G>C | synonymous_variant | 1.0 |
rpoC | 764429 | c.1060C>T | synonymous_variant | 1.0 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 1.0 |
rpoC | 764435 | c.1066_1068delAGGinsCGA | synonymous_variant | 1.0 |
rpoC | 764441 | p.Ile358Leu | missense_variant | 1.0 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 1.0 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 1.0 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 1.0 |
rpoC | 764489 | c.1120C>T | synonymous_variant | 1.0 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 1.0 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 1.0 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 1.0 |
rpoC | 764507 | p.Ala380Ser | missense_variant | 1.0 |
rpoC | 764512 | c.1143G>C | synonymous_variant | 1.0 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 1.0 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 1.0 |
rpoC | 764530 | c.1161C>T | synonymous_variant | 1.0 |
rpoC | 764536 | c.1167G>T | synonymous_variant | 1.0 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 1.0 |
rpoC | 764548 | c.1179G>A | synonymous_variant | 1.0 |
rpoC | 764554 | c.1185C>T | synonymous_variant | 1.0 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 1.0 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 1.0 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 1.0 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 1.0 |
rpoC | 764582 | p.Leu405Met | missense_variant | 1.0 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 1.0 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 1.0 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 1.0 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 1.0 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 1.0 |
rpoC | 764644 | c.1275G>C | synonymous_variant | 1.0 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 1.0 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 1.0 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 1.0 |
rpoC | 764692 | c.1323C>T | synonymous_variant | 1.0 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 1.0 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 1.0 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 1.0 |
rpoC | 764756 | c.1387_1389delCTCinsTTG | synonymous_variant | 1.0 |
rpoC | 764759 | p.Asn464Asp | missense_variant | 1.0 |
rpoC | 764762 | p.His465Tyr | missense_variant | 1.0 |
rpoC | 764780 | c.1411_1413delAGCinsTCG | synonymous_variant | 1.0 |
rpoC | 764793 | p.Met475Lys | missense_variant | 1.0 |
rpoC | 764797 | c.1428G>C | synonymous_variant | 1.0 |
rpoC | 764843 | p.Ala492Arg | missense_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 | 764878 | c.1509C>G | synonymous_variant | 1.0 |
rpoC | 764887 | c.1518G>T | synonymous_variant | 1.0 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 1.0 |
rpoC | 766309 | c.2940G>C | synonymous_variant | 1.0 |
rpoC | 766312 | c.2943T>C | synonymous_variant | 1.0 |
rpoC | 766316 | p.Met983Leu | missense_variant | 1.0 |
rpoC | 766348 | c.2979A>G | synonymous_variant | 1.0 |
rpoC | 766361 | p.Val998Ile | missense_variant | 1.0 |
rpoC | 766366 | c.2997C>G | synonymous_variant | 1.0 |
rpoC | 766375 | c.3006C>G | synonymous_variant | 1.0 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 1.0 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 1.0 |
rpsL | 781643 | c.84G>C | synonymous_variant | 1.0 |
rpsL | 781649 | c.90T>A | synonymous_variant | 1.0 |
rpsL | 781652 | c.93T>C | synonymous_variant | 1.0 |
rpsL | 781655 | c.96T>C | synonymous_variant | 1.0 |
rpsL | 781658 | c.99A>G | synonymous_variant | 1.0 |
rpsL | 781670 | c.111G>T | synonymous_variant | 1.0 |
rpsL | 781679 | c.120C>G | synonymous_variant | 1.0 |
rpsL | 781682 | c.123T>C | synonymous_variant | 1.0 |
rpsL | 781709 | c.150G>T | synonymous_variant | 1.0 |
rpsL | 781715 | c.156T>C | synonymous_variant | 1.0 |
rpsL | 781738 | p.Gln60Arg | missense_variant | 1.0 |
rpsL | 781740 | c.182_183insAT | frameshift_variant | 1.0 |
rpsL | 781751 | c.192G>C | synonymous_variant | 1.0 |
rpsL | 781760 | c.201T>C | synonymous_variant | 1.0 |
rpsL | 781803 | p.Val82Ile | missense_variant | 1.0 |
rpsL | 781811 | c.252C>T | synonymous_variant | 1.0 |
rpsL | 781817 | c.258G>T | synonymous_variant | 1.0 |
rpsL | 781832 | c.273T>G | synonymous_variant | 1.0 |
rpsL | 781868 | c.309T>C | synonymous_variant | 1.0 |
rpsL | 781871 | c.312G>C | synonymous_variant | 1.0 |
rpsL | 781892 | c.333A>G | synonymous_variant | 1.0 |
rpsL | 781896 | p.Ala113Ser | missense_variant | 1.0 |
rpsL | 781902 | c.343_344delAGinsTC | synonymous_variant | 1.0 |
rpsL | 781916 | c.357T>G | synonymous_variant | 1.0 |
rpsL | 781921 | p.Lys121Met | missense_variant | 1.0 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472084 | n.239C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472130 | n.285G>A | 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 | 0.9 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472278 | n.433C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472279 | n.434T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472290 | n.445C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472297 | n.453_454delGT | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472301 | n.457_461delGGGTT | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472309 | n.464C>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472311 | n.466C>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472314 | n.469A>G | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472582 | n.737G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472583 | n.738T>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472597 | n.752G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472673 | n.828T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472677 | n.832C>A | 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 | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473082 | n.1237G>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473118 | n.1275dupC | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473126 | n.1282_1283delGC | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473130 | n.1285_1286insA | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473201 | n.1356A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473202 | n.1357C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473278 | n.1433T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473291 | n.1446G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473300 | n.1455C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473822 | n.165A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473832 | n.175C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473833 | n.176_177insT | 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 | 1473888 | n.231T>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 | 1.0 |
rrl | 1474201 | n.544T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474283 | n.626A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474488 | n.831G>T | 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 | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474540 | n.883T>G | 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 | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474676 | n.1019T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474709 | n.1053_1056delTGGT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474717 | n.1060_1061insGTGAG | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474752 | n.1096delA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474790 | n.1133C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474830 | n.1173A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474832 | n.1175A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474869 | n.1212G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475696 | n.2039T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475697 | n.2040C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475702 | n.2045G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475703 | n.2046A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475740 | n.2083G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475747 | n.2090A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475767 | n.2110G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475781 | n.2124T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475788 | n.2131C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476025 | n.2368G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476076 | n.2419A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476081 | n.2424A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476082 | n.2425T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476088 | n.2431A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476089 | n.2432T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476092 | n.2435A>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476103 | n.2446C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476105 | n.2450delA | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476110 | n.2453G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476165 | n.2508T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476368 | n.2711T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476586 | n.2929C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476613 | n.2956G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476614 | n.2957A>T | 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 | 1476631 | n.2974G>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476661 | n.3004A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476663 | n.3006C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476664 | n.3007T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476665 | n.3008T>G | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1833635 | p.Tyr32His | missense_variant | 1.0 |
rpsA | 1833646 | c.105T>C | synonymous_variant | 1.0 |
rpsA | 1833664 | c.123C>T | synonymous_variant | 1.0 |
rpsA | 1833665 | p.Thr42Val | missense_variant | 1.0 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 1.0 |
rpsA | 1833679 | c.138G>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>G | synonymous_variant | 1.0 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 1.0 |
rpsA | 1833724 | c.183C>T | synonymous_variant | 1.0 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 1.0 |
rpsA | 1833730 | c.189C>T | synonymous_variant | 1.0 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 1.0 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 1.0 |
rpsA | 1833770 | p.Asn77Gly | missense_variant | 1.0 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.91 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.9 |
rpsA | 1833793 | c.252C>T | synonymous_variant | 0.9 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.88 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 0.83 |
rpsA | 1833815 | p.Thr92Gln | missense_variant | 0.8 |
rpsA | 1833829 | c.288A>G | synonymous_variant | 0.8 |
rpsA | 1833832 | c.291G>A | synonymous_variant | 0.75 |
rpsA | 1833835 | c.294C>T | synonymous_variant | 0.75 |
rpsA | 1833838 | c.297G>A | synonymous_variant | 0.75 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.75 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.75 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.75 |
rpsA | 1833862 | c.321G>T | synonymous_variant | 0.75 |
rpsA | 1833940 | c.399C>T | synonymous_variant | 1.0 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 1.0 |
rpsA | 1833961 | c.420C>G | synonymous_variant | 1.0 |
rpsA | 1833970 | c.429G>T | synonymous_variant | 1.0 |
rpsA | 1833976 | c.435C>T | synonymous_variant | 1.0 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 1.0 |
rpsA | 1833988 | c.447C>G | synonymous_variant | 1.0 |
rpsA | 1833994 | c.453G>C | synonymous_variant | 1.0 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 1.0 |
rpsA | 1834009 | c.468C>T | synonymous_variant | 1.0 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 1.0 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 1.0 |
rpsA | 1834033 | c.492C>T | synonymous_variant | 1.0 |
rpsA | 1834034 | p.Ile165Val | missense_variant | 1.0 |
rpsA | 1834093 | c.552G>C | synonymous_variant | 1.0 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 1.0 |
rpsA | 1834105 | c.564C>T | synonymous_variant | 1.0 |
rpsA | 1834114 | c.573G>C | synonymous_variant | 1.0 |
rpsA | 1834189 | c.648G>C | synonymous_variant | 1.0 |
rpsA | 1834210 | c.669C>T | synonymous_variant | 1.0 |
rpsA | 1834219 | c.678C>G | synonymous_variant | 1.0 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 1.0 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 1.0 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 1.0 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 1.0 |
rpsA | 1834252 | c.711C>G | synonymous_variant | 1.0 |
rpsA | 1834259 | c.718_720delCTAinsTTG | synonymous_variant | 1.0 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 1.0 |
rpsA | 1834286 | c.745_746delTCinsAG | synonymous_variant | 1.0 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 1.0 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 1.0 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 1.0 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.8 |
rpsA | 1834310 | p.Glu257Pro | missense_variant | 1.0 |
rpsA | 1834336 | c.795C>G | synonymous_variant | 1.0 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 1.0 |
rpsA | 1834354 | c.813G>C | synonymous_variant | 1.0 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 1.0 |
rpsA | 1834360 | c.819G>C | synonymous_variant | 1.0 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 1.0 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 1.0 |
rpsA | 1834369 | c.828C>G | synonymous_variant | 1.0 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 1.0 |
rpsA | 1834395 | p.Arg285Gln | missense_variant | 1.0 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 1.0 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 1.0 |
rpsA | 1834423 | c.882G>T | synonymous_variant | 1.0 |
rpsA | 1834427 | p.Ile296Val | missense_variant | 1.0 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 1.0 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 1.0 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 1.0 |
rpsA | 1834474 | c.933C>G | synonymous_variant | 1.0 |
rpsA | 1834483 | c.942G>A | synonymous_variant | 1.0 |
rpsA | 1834486 | p.Glu315Asp | missense_variant | 1.0 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 1.0 |
rpsA | 1834517 | c.976C>T | synonymous_variant | 1.0 |
rpsA | 1834534 | c.993C>G | synonymous_variant | 1.0 |
rpsA | 1834538 | p.Val333Leu | missense_variant | 1.0 |
rpsA | 1834543 | c.1002C>G | synonymous_variant | 1.0 |
rpsA | 1834546 | p.Asp335Glu | missense_variant | 1.0 |
rpsA | 1834552 | c.1011G>T | synonymous_variant | 1.0 |
rpsA | 1834555 | c.1014T>C | synonymous_variant | 1.0 |
rpsA | 1834556 | p.Ala339Thr | missense_variant | 1.0 |
rpsA | 1834561 | c.1020C>T | synonymous_variant | 1.0 |
rpsA | 1834565 | p.Asp342Gln | missense_variant | 1.0 |
rpsA | 1834571 | p.Ala344Ile | missense_variant | 1.0 |
rpsA | 1834574 | p.Met345Phe | missense_variant | 1.0 |
rpsA | 1834606 | c.1065C>T | synonymous_variant | 1.0 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 1.0 |
rpsA | 1834612 | c.1071G>C | synonymous_variant | 1.0 |
rpsA | 1834619 | c.1078T>C | synonymous_variant | 1.0 |
rpsA | 1834627 | c.1086C>G | synonymous_variant | 1.0 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 1.0 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 1.0 |
katG | 2154048 | p.Lys688Asn | missense_variant | 1.0 |
alr | 3840861 | p.Ala187Val | missense_variant | 1.0 |
rpoA | 3877636 | p.Gln291Ala | missense_variant | 0.67 |
rpoA | 3877656 | c.850_852delCTTinsTTG | synonymous_variant | 1.0 |
rpoA | 3877667 | p.Ser281Ala | missense_variant | 1.0 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 1.0 |
rpoA | 3877672 | p.Thr279Ser | missense_variant | 1.0 |
rpoA | 3877680 | c.828G>C | synonymous_variant | 1.0 |
rpoA | 3877683 | c.825G>C | synonymous_variant | 1.0 |
rpoA | 3877689 | c.819C>T | synonymous_variant | 1.0 |
rpoA | 3877695 | c.813C>T | synonymous_variant | 1.0 |
rpoA | 3877701 | p.Val269Ile | missense_variant | 1.0 |
rpoA | 3877704 | p.Gly268Ala | missense_variant | 1.0 |
rpoA | 3877731 | c.777G>C | synonymous_variant | 1.0 |
rpoA | 3877734 | c.774G>C | synonymous_variant | 1.0 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 1.0 |
rpoA | 3877752 | p.Asp252Glu | missense_variant | 1.0 |
rpoA | 3877848 | c.660C>T | synonymous_variant | 0.67 |
rpoA | 3877856 | c.652T>C | synonymous_variant | 0.75 |
rpoA | 3877872 | c.636C>T | synonymous_variant | 1.0 |
rpoA | 3877875 | c.633T>C | synonymous_variant | 1.0 |
rpoA | 3877878 | c.630G>C | synonymous_variant | 1.0 |
rpoA | 3877881 | c.627G>C | synonymous_variant | 1.0 |
rpoA | 3877886 | p.Leu208Met | missense_variant | 1.0 |
rpoA | 3877900 | p.Ser203Ala | missense_variant | 1.0 |
rpoA | 3877905 | p.Ser201Ala | missense_variant | 1.0 |
rpoA | 3877908 | c.600T>C | synonymous_variant | 1.0 |
rpoA | 3877923 | c.585C>T | synonymous_variant | 1.0 |
rpoA | 3877926 | p.Leu194Val | missense_variant | 1.0 |
rpoA | 3877962 | c.546G>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 | p.Lys173Ala | missense_variant | 1.0 |
rpoA | 3877992 | c.516C>G | synonymous_variant | 1.0 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 1.0 |
rpoA | 3878013 | c.495T>C | synonymous_variant | 1.0 |
rpoA | 3878019 | c.489A>G | synonymous_variant | 1.0 |
rpoA | 3878295 | c.213A>G | synonymous_variant | 1.0 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 1.0 |
rpoA | 3878310 | p.Val66Ile | missense_variant | 1.0 |
rpoA | 3878318 | p.Thr64Ser | missense_variant | 1.0 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 1.0 |
rpoA | 3878329 | p.Leu60Gln | missense_variant | 1.0 |
rpoA | 3878331 | c.177A>G | synonymous_variant | 1.0 |
rpoA | 3878342 | p.Ile56Val | missense_variant | 1.0 |
rpoA | 3878346 | p.Ile54Leu | missense_variant | 1.0 |
rpoA | 3878358 | c.150C>G | synonymous_variant | 1.0 |
rpoA | 3878364 | c.144A>C | synonymous_variant | 1.0 |
rpoA | 3878367 | c.141C>G | synonymous_variant | 1.0 |
rpoA | 3878370 | c.138T>C | synonymous_variant | 1.0 |
rpoA | 3878373 | c.135G>C | synonymous_variant | 1.0 |
rpoA | 3878397 | c.111G>C | synonymous_variant | 1.0 |
rpoA | 3878400 | c.108T>C | synonymous_variant | 1.0 |
rpoA | 3878406 | c.102G>C | synonymous_variant | 1.0 |
rpoA | 3878409 | c.99C>G | synonymous_variant | 1.0 |
rpoA | 3878421 | c.87A>T | synonymous_variant | 1.0 |
rpoA | 3878424 | c.84G>C | synonymous_variant | 1.0 |
rpoA | 3878436 | c.72A>G | synonymous_variant | 1.0 |
rpoA | 3878442 | c.66G>C | synonymous_variant | 1.0 |
rpoA | 3878449 | p.Gln20Arg | missense_variant | 1.0 |
rpoA | 3878451 | c.57C>G | synonymous_variant | 1.0 |
rpoA | 3878454 | c.54A>T | synonymous_variant | 1.0 |
rpoA | 3878465 | p.Thr15Ser | missense_variant | 1.0 |
clpC1 | 4038845 | c.1860G>C | synonymous_variant | 1.0 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 1.0 |
clpC1 | 4038869 | c.1836G>A | synonymous_variant | 1.0 |
clpC1 | 4038875 | c.1830C>G | synonymous_variant | 1.0 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 1.0 |
clpC1 | 4038884 | c.1821C>T | synonymous_variant | 1.0 |
clpC1 | 4038890 | c.1815G>A | synonymous_variant | 1.0 |
clpC1 | 4038905 | c.1800A>G | synonymous_variant | 1.0 |
clpC1 | 4038914 | p.Ala597Ser | missense_variant | 1.0 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 1.0 |
clpC1 | 4039487 | c.1218G>C | synonymous_variant | 1.0 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 1.0 |
clpC1 | 4039524 | p.Phe394His | missense_variant | 1.0 |
clpC1 | 4039552 | p.Leu385Met | missense_variant | 1.0 |
clpC1 | 4039554 | p.Thr384Asn | missense_variant | 1.0 |
clpC1 | 4039556 | p.Ala383Val | missense_variant | 1.0 |
clpC1 | 4039559 | c.1146C>G | synonymous_variant | 1.0 |
clpC1 | 4039562 | p.Ala381Gly | missense_variant | 1.0 |
clpC1 | 4039570 | p.Met379Leu | missense_variant | 1.0 |
clpC1 | 4039574 | c.1131G>C | synonymous_variant | 1.0 |
clpC1 | 4039588 | p.Ser373Thr | missense_variant | 1.0 |
clpC1 | 4039601 | c.1104G>C | synonymous_variant | 1.0 |
clpC1 | 4039604 | c.1101G>A | synonymous_variant | 1.0 |
clpC1 | 4039616 | c.1089G>T | synonymous_variant | 1.0 |
clpC1 | 4039622 | c.1083C>T | synonymous_variant | 1.0 |
clpC1 | 4039628 | c.1077C>G | synonymous_variant | 1.0 |
clpC1 | 4039642 | p.Thr355Ala | missense_variant | 1.0 |
clpC1 | 4039647 | p.Glu353Pro | missense_variant | 1.0 |
clpC1 | 4039649 | p.Val352Ile | missense_variant | 1.0 |
clpC1 | 4039652 | c.1053G>C | synonymous_variant | 1.0 |
clpC1 | 4039661 | p.Gly348Gln | missense_variant | 1.0 |
clpC1 | 4039670 | p.Val345Ile | missense_variant | 1.0 |
clpC1 | 4039682 | c.1023C>G | synonymous_variant | 1.0 |
clpC1 | 4039714 | p.Tyr331His | missense_variant | 1.0 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 1.0 |
clpC1 | 4039727 | c.978C>T | synonymous_variant | 0.78 |
clpC1 | 4039730 | c.975C>G | synonymous_variant | 0.78 |
clpC1 | 4039739 | c.966C>G | synonymous_variant | 0.67 |
clpC1 | 4039742 | c.963C>T | synonymous_variant | 0.6 |
clpC1 | 4039748 | c.957G>C | synonymous_variant | 0.5 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.5 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.5 |
clpC1 | 4039793 | c.912C>T | synonymous_variant | 0.78 |
clpC1 | 4039796 | c.909C>T | synonymous_variant | 0.78 |
clpC1 | 4039817 | c.888A>T | synonymous_variant | 0.8 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.8 |
clpC1 | 4039826 | c.879C>G | synonymous_variant | 0.78 |
clpC1 | 4039829 | c.874_876delTTGinsCTC | synonymous_variant | 0.88 |
clpC1 | 4039832 | c.873C>T | synonymous_variant | 0.78 |
clpC1 | 4039838 | p.Leu289Ile | missense_variant | 0.8 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.85 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 1.0 |
clpC1 | 4039875 | p.Asn277Arg | missense_variant | 1.0 |
clpC1 | 4039889 | c.816G>C | synonymous_variant | 1.0 |
clpC1 | 4039898 | c.805_807delCTCinsTTG | synonymous_variant | 0.88 |
clpC1 | 4039901 | c.804C>G | synonymous_variant | 1.0 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 1.0 |
clpC1 | 4039925 | c.780C>T | synonymous_variant | 1.0 |
clpC1 | 4039934 | c.771G>C | synonymous_variant | 1.0 |
clpC1 | 4039937 | c.768G>T | synonymous_variant | 1.0 |
clpC1 | 4039949 | c.756G>C | synonymous_variant | 1.0 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 1.0 |
clpC1 | 4039955 | c.750G>C | synonymous_variant | 1.0 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 1.0 |
clpC1 | 4039967 | p.Gln246His | missense_variant | 1.0 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.93 |
clpC1 | 4039994 | p.Glu237Asp | missense_variant | 1.0 |
clpC1 | 4039997 | c.708C>T | synonymous_variant | 1.0 |
clpC1 | 4040001 | p.His235Arg | missense_variant | 1.0 |
clpC1 | 4040010 | p.Ala232Asp | missense_variant | 0.92 |
clpC1 | 4040013 | p.Gln231Ala | missense_variant | 1.0 |
clpC1 | 4040015 | c.690G>T | synonymous_variant | 1.0 |
clpC1 | 4040018 | c.687G>A | synonymous_variant | 1.0 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 1.0 |
clpC1 | 4040027 | c.678C>G | synonymous_variant | 1.0 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 1.0 |
clpC1 | 4040042 | c.663C>T | synonymous_variant | 1.0 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 1.0 |
clpC1 | 4040066 | c.639G>C | synonymous_variant | 1.0 |
clpC1 | 4040089 | c.616C>A | synonymous_variant | 1.0 |
clpC1 | 4040090 | c.615T>C | synonymous_variant | 1.0 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 1.0 |
clpC1 | 4040117 | c.588A>G | synonymous_variant | 1.0 |
clpC1 | 4040273 | c.432T>C | synonymous_variant | 1.0 |
clpC1 | 4040281 | p.Leu142Val | missense_variant | 1.0 |
clpC1 | 4040291 | c.414G>C | synonymous_variant | 1.0 |
clpC1 | 4040306 | c.399G>C | synonymous_variant | 1.0 |
clpC1 | 4040309 | p.Thr132Ser | missense_variant | 1.0 |
clpC1 | 4040315 | p.Glu130Asp | missense_variant | 1.0 |
clpC1 | 4040326 | p.Leu127Met | missense_variant | 1.0 |
clpC1 | 4040336 | c.369G>C | synonymous_variant | 1.0 |
clpC1 | 4040348 | c.357G>C | synonymous_variant | 1.0 |
clpC1 | 4040354 | c.351A>G | synonymous_variant | 1.0 |