Run ID: ERR4769508
Sample name:
Date: 01-04-2023 06:43:05
Number of reads: 68193
Percentage reads mapped: 2.54
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 |
| rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 1.0 | streptomycin |
| Gene | Chromosome position | Mutation | Type | Estimated fraction |
|---|---|---|---|---|
| gyrB | 5323 | c.84A>G | synonymous_variant | 1.0 |
| gyrB | 5326 | c.87T>C | synonymous_variant | 1.0 |
| gyrB | 5341 | c.102T>C | synonymous_variant | 1.0 |
| rpoB | 760916 | c.1110C>T | synonymous_variant | 1.0 |
| rpoB | 760919 | c.1113C>T | synonymous_variant | 1.0 |
| rpoB | 760925 | c.1119T>C | synonymous_variant | 1.0 |
| rpoB | 760927 | p.Thr374Ser | missense_variant | 1.0 |
| rpoB | 760940 | c.1134G>C | synonymous_variant | 1.0 |
| rpoB | 760946 | c.1140A>G | synonymous_variant | 1.0 |
| rpoB | 760953 | p.Ile383Leu | missense_variant | 1.0 |
| rpoB | 760958 | c.1152G>T | synonymous_variant | 1.0 |
| rpoB | 760959 | p.Val385Thr | missense_variant | 1.0 |
| rpoB | 760965 | p.Met387Leu | missense_variant | 1.0 |
| rpoB | 760968 | p.Ser388Ala | missense_variant | 1.0 |
| rpoB | 760973 | c.1167G>C | synonymous_variant | 1.0 |
| rpoB | 760985 | c.1179G>C | synonymous_variant | 1.0 |
| rpoB | 760991 | c.1185G>C | synonymous_variant | 1.0 |
| rpoB | 761003 | c.1197C>G | 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 | 1.0 |
| rpoB | 761037 | c.1231T>C | synonymous_variant | 1.0 |
| rpoB | 761051 | c.1245G>T | synonymous_variant | 1.0 |
| rpoB | 761054 | c.1248G>C | synonymous_variant | 1.0 |
| rpoB | 761057 | c.1251G>C | synonymous_variant | 1.0 |
| rpoB | 761060 | c.1254C>G | synonymous_variant | 1.0 |
| rpoB | 761063 | c.1257C>G | synonymous_variant | 1.0 |
| rpoB | 761067 | p.Ile421Leu | missense_variant | 1.0 |
| rpoB | 761088 | c.1282_1284delAGCinsTCG | synonymous_variant | 1.0 |
| rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 1.0 |
| rpoB | 761102 | c.1296A>G | synonymous_variant | 1.0 |
| rpoB | 761126 | c.1320G>C | synonymous_variant | 1.0 |
| rpoB | 761132 | c.1326G>C | synonymous_variant | 1.0 |
| rpoB | 761133 | c.1327T>C | synonymous_variant | 1.0 |
| rpoB | 761138 | c.1332C>G | synonymous_variant | 1.0 |
| rpoB | 761147 | c.1341C>T | synonymous_variant | 1.0 |
| rpoB | 761150 | c.1344A>T | synonymous_variant | 1.0 |
| rpoB | 761159 | c.1353G>C | synonymous_variant | 1.0 |
| rpoB | 761162 | c.1356G>C | synonymous_variant | 1.0 |
| rpoB | 761165 | c.1359G>T | synonymous_variant | 1.0 |
| rpoB | 761168 | c.1362C>G | synonymous_variant | 1.0 |
| rpoB | 761180 | c.1374A>G | synonymous_variant | 1.0 |
| rpoB | 761192 | c.1386C>A | synonymous_variant | 1.0 |
| rpoB | 761195 | c.1389G>C | synonymous_variant | 1.0 |
| rpoB | 761196 | p.Leu464Tyr | missense_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>C | synonymous_variant | 1.0 |
| rpoB | 761258 | c.1452G>A | synonymous_variant | 1.0 |
| rpoB | 761261 | c.1455G>C | synonymous_variant | 1.0 |
| rpoB | 761264 | c.1458C>G | synonymous_variant | 1.0 |
| rpoB | 761289 | p.Ser495Ala | missense_variant | 1.0 |
| rpoB | 761292 | p.Val496Ser | missense_variant | 1.0 |
| rpoB | 761299 | p.Ala498Gly | missense_variant | 1.0 |
| rpoB | 761303 | c.1497G>C | synonymous_variant | 1.0 |
| rpoB | 761304 | p.Val500Ile | missense_variant | 1.0 |
| rpoB | 761310 | p.Pro502Ser | missense_variant | 1.0 |
| rpoB | 761322 | p.Ile506Val | missense_variant | 1.0 |
| rpoB | 761327 | c.1521A>G | synonymous_variant | 1.0 |
| rpoB | 761341 | c.1539_1541delGGT | disruptive_inframe_deletion | 1.0 |
| rpoB | 761516 | c.1710G>C | synonymous_variant | 1.0 |
| rpoB | 761537 | c.1731C>G | synonymous_variant | 1.0 |
| 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 | 761565 | p.Met587Leu | missense_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 | 761600 | c.1794T>C | synonymous_variant | 1.0 |
| rpoB | 761603 | c.1797C>G | synonymous_variant | 1.0 |
| rpoB | 761613 | p.Ala603Ser | missense_variant | 1.0 |
| rpoB | 761631 | p.Ala609Ser | missense_variant | 1.0 |
| rpoB | 761636 | c.1830G>C | synonymous_variant | 1.0 |
| rpoB | 761643 | p.Val613Ile | missense_variant | 1.0 |
| rpoB | 761648 | c.1842T>C | synonymous_variant | 1.0 |
| rpoB | 761650 | p.Ser615Asn | missense_variant | 1.0 |
| rpoB | 761654 | p.Glu616Asp | missense_variant | 1.0 |
| rpoB | 761663 | c.1857G>C | synonymous_variant | 1.0 |
| rpoB | 761666 | c.1860G>C | synonymous_variant | 1.0 |
| rpoB | 761675 | c.1869G>C | synonymous_variant | 1.0 |
| rpoB | 761909 | c.2103T>C | synonymous_variant | 1.0 |
| rpoB | 761912 | c.2106T>C | synonymous_variant | 1.0 |
| rpoB | 761918 | p.Asp704Glu | missense_variant | 1.0 |
| rpoB | 761933 | c.2127G>C | synonymous_variant | 1.0 |
| rpoB | 761937 | p.Lys711Ser | missense_variant | 1.0 |
| rpoB | 761945 | c.2139G>C | synonymous_variant | 1.0 |
| rpoB | 761948 | c.2142G>C | synonymous_variant | 1.0 |
| rpoB | 761954 | c.2148C>G | synonymous_variant | 1.0 |
| rpoB | 761955 | p.Ile717Phe | missense_variant | 1.0 |
| rpoB | 761967 | p.Glu721Gln | missense_variant | 1.0 |
| rpoB | 761999 | c.2193G>C | synonymous_variant | 1.0 |
| rpoB | 762002 | c.2196C>G | synonymous_variant | 1.0 |
| rpoB | 762003 | p.Asn733Gln | missense_variant | 1.0 |
| rpoB | 762009 | p.Leu735Val | missense_variant | 1.0 |
| rpoB | 762015 | p.Glu737Gln | missense_variant | 1.0 |
| rpoB | 762020 | p.Glu738Asp | missense_variant | 0.94 |
| rpoB | 762024 | p.Val740Leu | missense_variant | 1.0 |
| rpoB | 762029 | c.2223C>G | synonymous_variant | 1.0 |
| rpoB | 762053 | c.2247T>C | synonymous_variant | 1.0 |
| rpoB | 762057 | p.Ile751Val | missense_variant | 1.0 |
| rpoB | 762062 | c.2256T>C | synonymous_variant | 1.0 |
| rpoB | 762065 | c.2259T>C | synonymous_variant | 1.0 |
| rpoB | 762074 | c.2268C>G | synonymous_variant | 1.0 |
| rpoB | 762083 | c.2277T>C | synonymous_variant | 1.0 |
| rpoB | 762084 | p.Ala760Pro | missense_variant | 1.0 |
| rpoB | 762114 | p.Ile770Val | missense_variant | 0.98 |
| rpoB | 762117 | c.2311_2312delTCinsAG | synonymous_variant | 1.0 |
| rpoB | 762126 | p.Val774Met | missense_variant | 1.0 |
| rpoB | 762140 | c.2334G>C | synonymous_variant | 1.0 |
| rpoB | 762143 | c.2337T>C | synonymous_variant | 1.0 |
| rpoB | 762149 | c.2343G>C | synonymous_variant | 0.98 |
| rpoB | 762156 | p.Val784Ile | missense_variant | 1.0 |
| rpoB | 762176 | c.2370T>G | synonymous_variant | 1.0 |
| rpoB | 762177 | p.Arg791Ser | missense_variant | 1.0 |
| rpoB | 762180 | p.Asp792Asn | missense_variant | 1.0 |
| rpoB | 762185 | c.2379G>C | synonymous_variant | 1.0 |
| rpoB | 762194 | c.2388G>C | synonymous_variant | 1.0 |
| rpoB | 762218 | c.2412T>C | synonymous_variant | 1.0 |
| rpoB | 762233 | c.2427G>C | synonymous_variant | 1.0 |
| rpoB | 762236 | c.2430G>C | synonymous_variant | 1.0 |
| rpoB | 762245 | c.2439G>C | synonymous_variant | 1.0 |
| rpoB | 762251 | c.2445G>C | synonymous_variant | 1.0 |
| rpoB | 762254 | c.2448T>C | synonymous_variant | 1.0 |
| rpoB | 762257 | c.2451C>G | synonymous_variant | 1.0 |
| rpoB | 762275 | c.2469C>G | synonymous_variant | 1.0 |
| rpoB | 762293 | c.2487T>C | synonymous_variant | 1.0 |
| rpoB | 762305 | c.2499G>C | synonymous_variant | 1.0 |
| rpoB | 762317 | c.2511A>G | synonymous_variant | 1.0 |
| rpoB | 762325 | p.Lys840Thr | missense_variant | 1.0 |
| rpoB | 762329 | c.2523G>C | synonymous_variant | 1.0 |
| rpoB | 762336 | p.Ile844Val | missense_variant | 1.0 |
| rpoB | 762369 | c.2563T>C | synonymous_variant | 1.0 |
| rpoB | 762375 | p.Ala857Pro | missense_variant | 1.0 |
| rpoC | 762380 | c.-990T>C | upstream_gene_variant | 1.0 |
| rpoB | 762387 | p.Glu861Gln | missense_variant | 1.0 |
| rpoC | 762398 | c.-972T>C | upstream_gene_variant | 1.0 |
| rpoC | 762401 | c.-969G>C | upstream_gene_variant | 1.0 |
| rpoC | 762404 | c.-966T>C | upstream_gene_variant | 1.0 |
| rpoC | 762407 | c.-963G>C | 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 |
| rpoC | 762443 | c.-927G>C | upstream_gene_variant | 1.0 |
| rpoC | 762449 | c.-921C>A | upstream_gene_variant | 1.0 |
| rpoC | 762452 | c.-918G>C | upstream_gene_variant | 1.0 |
| rpoC | 762470 | c.-900G>C | upstream_gene_variant | 1.0 |
| rpoB | 762474 | p.Gly890Ser | missense_variant | 1.0 |
| rpoB | 762489 | p.Val895Gln | missense_variant | 1.0 |
| rpoC | 762509 | c.-861T>G | upstream_gene_variant | 1.0 |
| rpoB | 762510 | p.Ala902Ser | missense_variant | 1.0 |
| rpoC | 762527 | c.-843G>C | upstream_gene_variant | 1.0 |
| rpoB | 762849 | p.Tyr1015Asp | missense_variant | 1.0 |
| rpoB | 762855 | p.Val1017Ile | missense_variant | 1.0 |
| rpoB | 762858 | p.Thr1018Ser | missense_variant | 1.0 |
| rpoC | 762863 | c.-507T>C | upstream_gene_variant | 1.0 |
| rpoB | 762879 | p.Met1025Leu | missense_variant | 1.0 |
| rpoC | 762899 | c.-471G>C | upstream_gene_variant | 1.0 |
| rpoC | 762920 | c.-450C>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 | 762956 | c.-414G>C | upstream_gene_variant | 1.0 |
| rpoC | 762962 | c.-408C>T | upstream_gene_variant | 1.0 |
| rpoC | 762983 | c.-387C>A | upstream_gene_variant | 1.0 |
| rpoC | 762989 | c.-381G>C | upstream_gene_variant | 1.0 |
| rpoC | 762995 | c.-375G>T | upstream_gene_variant | 1.0 |
| rpoB | 763005 | p.Cys1067Val | missense_variant | 1.0 |
| 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 |
| rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
| rpoC | 763034 | c.-336C>G | upstream_gene_variant | 1.0 |
| rpoB | 763038 | p.Thr1078Ala | missense_variant | 1.0 |
| rpoC | 763052 | c.-318G>C | upstream_gene_variant | 1.0 |
| rpoC | 763053 | c.-317T>C | upstream_gene_variant | 1.0 |
| rpoC | 763067 | c.-303C>G | 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.Val1091Leu | missense_variant | 1.0 |
| rpoC | 763082 | c.-288C>A | upstream_gene_variant | 1.0 |
| rpoC | 763094 | c.-276G>C | upstream_gene_variant | 1.0 |
| rpoC | 763103 | c.-267G>C | upstream_gene_variant | 1.0 |
| rpoC | 763453 | c.84C>G | synonymous_variant | 1.0 |
| rpoC | 763456 | c.87A>G | synonymous_variant | 1.0 |
| rpoC | 763462 | c.93G>C | synonymous_variant | 1.0 |
| rpoC | 763486 | c.117T>C | synonymous_variant | 1.0 |
| rpoC | 763492 | c.123G>C | synonymous_variant | 1.0 |
| rpoC | 763496 | p.Lys43Arg | missense_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>T | synonymous_variant | 1.0 |
| rpoC | 763573 | c.204G>C | synonymous_variant | 1.0 |
| rpoC | 763621 | c.252C>T | synonymous_variant | 0.97 |
| rpoC | 763622 | p.Ala85Ser | missense_variant | 1.0 |
| rpoC | 763642 | c.273G>C | synonymous_variant | 1.0 |
| rpoC | 763648 | c.279C>A | synonymous_variant | 1.0 |
| rpoC | 763660 | c.291T>C | synonymous_variant | 1.0 |
| rpoC | 763666 | c.297G>T | synonymous_variant | 1.0 |
| rpoC | 763702 | c.333C>G | synonymous_variant | 1.0 |
| rpoC | 763703 | c.334_336delTCGinsAGC | synonymous_variant | 1.0 |
| rpoC | 763708 | c.339G>T | synonymous_variant | 1.0 |
| rpoC | 763711 | c.342G>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 | 763729 | c.360G>C | synonymous_variant | 1.0 |
| rpoC | 763732 | c.363C>T | synonymous_variant | 1.0 |
| rpoC | 763744 | c.375G>C | synonymous_variant | 1.0 |
| rpoC | 763751 | p.Ile128Val | missense_variant | 1.0 |
| rpoC | 763765 | c.396T>C | synonymous_variant | 1.0 |
| rpoC | 763768 | c.399C>G | synonymous_variant | 1.0 |
| rpoC | 763772 | p.Val135Met | missense_variant | 1.0 |
| rpoC | 764353 | c.984G>C | synonymous_variant | 1.0 |
| rpoC | 764365 | c.996C>T | synonymous_variant | 1.0 |
| rpoC | 764371 | c.1002G>C | synonymous_variant | 1.0 |
| rpoC | 764380 | c.1011G>C | synonymous_variant | 1.0 |
| rpoC | 764381 | c.1012_1013delTCinsAG | synonymous_variant | 1.0 |
| rpoC | 764387 | c.1018T>C | synonymous_variant | 1.0 |
| rpoC | 764398 | c.1029G>C | synonymous_variant | 1.0 |
| rpoC | 764404 | c.1035C>T | synonymous_variant | 1.0 |
| rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 1.0 |
| rpoC | 764410 | c.1041G>C | synonymous_variant | 1.0 |
| rpoC | 764431 | c.1062G>C | synonymous_variant | 1.0 |
| rpoC | 764434 | c.1065A>G | synonymous_variant | 0.96 |
| rpoC | 764435 | c.1066_1068delAGGinsCGC | 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 | 764452 | c.1083T>C | synonymous_variant | 1.0 |
| rpoC | 764461 | c.1092A>G | synonymous_variant | 1.0 |
| rpoC | 764491 | c.1122G>C | 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 | 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 | 764566 | c.1197C>G | synonymous_variant | 1.0 |
| rpoC | 764573 | p.Leu402Ile | missense_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>C | synonymous_variant | 1.0 |
| rpoC | 764611 | c.1242G>T | synonymous_variant | 1.0 |
| 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 | 764701 | c.1332C>G | synonymous_variant | 1.0 |
| rpoC | 764706 | p.Leu446Gln | missense_variant | 1.0 |
| rpoC | 764714 | p.Leu449Ile | missense_variant | 1.0 |
| rpoC | 764737 | c.1368G>C | synonymous_variant | 1.0 |
| rpoC | 764752 | c.1383G>C | synonymous_variant | 1.0 |
| rpoC | 764755 | c.1386C>T | synonymous_variant | 0.98 |
| rpoC | 764764 | c.1395T>C | synonymous_variant | 1.0 |
| rpoC | 764767 | c.1398G>T | synonymous_variant | 1.0 |
| rpoC | 764780 | c.1411_1412delAGinsTC | synonymous_variant | 1.0 |
| rpoC | 764791 | c.1422C>G | synonymous_variant | 1.0 |
| rpoC | 764824 | c.1455T>C | synonymous_variant | 1.0 |
| rpoC | 764827 | c.1458G>C | synonymous_variant | 1.0 |
| rpoC | 764854 | c.1485G>T | synonymous_variant | 1.0 |
| rpoC | 764858 | c.1489T>C | synonymous_variant | 1.0 |
| rpoC | 764863 | c.1494G>C | synonymous_variant | 1.0 |
| rpoC | 764869 | c.1500C>T | synonymous_variant | 1.0 |
| rpoC | 764878 | c.1509C>T | synonymous_variant | 1.0 |
| rpoC | 764887 | c.1518G>T | synonymous_variant | 1.0 |
| rpoC | 764888 | c.1519T>C | synonymous_variant | 0.95 |
| rpoC | 764893 | c.1524T>C | synonymous_variant | 1.0 |
| rpoC | 764902 | c.1533C>G | synonymous_variant | 1.0 |
| rpoC | 764911 | c.1542A>G | synonymous_variant | 1.0 |
| rpoC | 764912 | p.Met515Gln | missense_variant | 1.0 |
| rpoC | 764918 | p.Val517Ile | missense_variant | 1.0 |
| rpoC | 764923 | c.1554A>G | synonymous_variant | 1.0 |
| rpoC | 764935 | c.1566T>C | synonymous_variant | 1.0 |
| rpoC | 764939 | p.Leu524Ile | missense_variant | 1.0 |
| rpoC | 764948 | c.1579_1581delTTGinsCTC | synonymous_variant | 1.0 |
| rpoC | 764956 | c.1587T>C | synonymous_variant | 1.0 |
| rpoC | 764957 | p.Glu530Ser | missense_variant | 1.0 |
| rpoC | 764968 | c.1599T>C | synonymous_variant | 1.0 |
| rpoC | 764998 | c.1629G>C | synonymous_variant | 1.0 |
| rpsL | 781754 | c.195G>C | synonymous_variant | 1.0 |
| rpsL | 781760 | c.201T>C | synonymous_variant | 1.0 |
| rpsL | 781766 | c.207C>T | synonymous_variant | 1.0 |
| rpsL | 781772 | c.213C>T | synonymous_variant | 1.0 |
| rpsL | 781796 | p.Met79Ile | missense_variant | 1.0 |
| rpsL | 781802 | c.243G>C | synonymous_variant | 1.0 |
| rpsL | 781817 | c.258G>T | synonymous_variant | 1.0 |
| rpsL | 781829 | c.270G>C | synonymous_variant | 1.0 |
| rpsL | 781832 | c.273T>G | synonymous_variant | 1.0 |
| rpsL | 781838 | c.279G>C | synonymous_variant | 1.0 |
| rpsL | 781841 | c.282C>T | synonymous_variant | 1.0 |
| rpsL | 781856 | c.297C>T | synonymous_variant | 1.0 |
| rpsL | 781859 | c.300T>C | synonymous_variant | 1.0 |
| rpsL | 781860 | p.Ser101Ala | missense_variant | 1.0 |
| rpsL | 781868 | c.309T>C | synonymous_variant | 1.0 |
| rpsL | 781871 | c.312G>C | synonymous_variant | 1.0 |
| rpsL | 781885 | p.Asn109Ser | missense_variant | 1.0 |
| rpsL | 781892 | c.333A>G | synonymous_variant | 1.0 |
| rpsL | 781898 | c.339A>T | synonymous_variant | 1.0 |
| rpsL | 781916 | c.357T>G | synonymous_variant | 1.0 |
| rrs | 1471914 | n.69A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472069 | n.224G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472108 | n.263C>T | 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 | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472235 | n.390G>C | non_coding_transcript_exon_variant | 0.98 |
| rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.98 |
| rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472287 | n.442C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472297 | n.453_465delGTCCGGGTTCTCT | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472315 | n.470T>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 | 1472327 | n.482G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472337 | n.492C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472380 | n.535G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472412 | n.567A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472493 | n.648T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472494 | n.649A>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472495 | n.650C>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472496 | n.651T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472507 | n.662C>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472508 | n.663T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472571 | n.726G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472582 | n.737G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472583 | n.738T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472585 | n.740A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472655 | n.810G>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 | 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 | 1472697 | n.852T>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 | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472791 | n.946G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472836 | n.991G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 0.88 |
| 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 | 1472974 | n.1129A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472987 | n.1142G>A | 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 | 1473065 | n.1220C>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473099 | n.1254T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473105 | n.1260G>A | 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 | 1.0 |
| rrs | 1473122 | n.1277T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473262 | n.1417T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473314 | n.1469A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 1.0 |
| 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 | 1474201 | n.544T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474202 | n.545T>A | 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 | 1474263 | n.606G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474281 | n.624A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474306 | n.649A>T | non_coding_transcript_exon_variant | 0.97 |
| rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474316 | n.659T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474351 | n.694G>T | 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 | 1474356 | n.699T>C | 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 | 1474373 | n.717dupT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474376 | n.719T>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 | 1474444 | n.787G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474450 | n.793T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474454 | n.797G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474476 | n.819C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474483 | n.826C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474534 | n.877G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474551 | n.894G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474558 | n.901G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474734 | n.1077G>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 | 1474777 | n.1120T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474800 | n.1143T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474801 | n.1144G>T | 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 | 1474831 | n.1174A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474917 | n.1260G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474934 | n.1277C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474935 | n.1278A>T | 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 | 1475080 | n.1423G>T | 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 | 1475104 | n.1447T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475108 | n.1451C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475111 | n.1454G>A | 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 | 1475119 | n.1462C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475124 | n.1467A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475129 | n.1472G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475458 | n.1801C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475460 | n.1803A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475479 | n.1822C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475481 | n.1825delA | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475485 | n.1828C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475526 | n.1869C>A | 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 | 1475544 | n.1887A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475548 | n.1891C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475549 | n.1892T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475550 | n.1893A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475602 | n.1945G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475649 | n.1992A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475652 | n.1998_2001delTGAG | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475659 | n.2002_2003insCCCA | 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 | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475747 | n.2090A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475752 | n.2095C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475775 | n.2118G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475776 | n.2119G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475781 | n.2124T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475880 | n.2223C>G | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1475881 | n.2224T>G | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1475882 | n.2225C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475952 | n.2295A>G | 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 | 1475993 | n.2336C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476000 | n.2343G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476032 | n.2375C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476033 | n.2376T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476046 | n.2389G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476056 | n.2399G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476076 | n.2419A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476082 | n.2425T>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 | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.98 |
| rrl | 1476248 | n.2591G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476251 | n.2594T>C | 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 | 1476259 | n.2602C>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 | 1476288 | n.2631T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476296 | n.2639C>T | 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 | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476506 | n.2849T>C | 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 | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 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 | 0.91 |
| rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.91 |
| rrl | 1476596 | n.2939C>T | non_coding_transcript_exon_variant | 0.91 |
| rrl | 1476601 | n.2944G>A | non_coding_transcript_exon_variant | 0.91 |
| rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.91 |
| rrl | 1476608 | n.2951C>T | non_coding_transcript_exon_variant | 0.91 |
| rrl | 1476613 | n.2956G>A | non_coding_transcript_exon_variant | 0.91 |
| rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.91 |
| rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.91 |
| rrl | 1476628 | n.2971T>G | non_coding_transcript_exon_variant | 0.91 |
| rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.91 |
| rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.91 |
| rrl | 1476631 | n.2974G>T | non_coding_transcript_exon_variant | 0.91 |
| rpsA | 1833625 | c.84A>G | synonymous_variant | 1.0 |
| rpsA | 1833628 | c.87G>C | synonymous_variant | 1.0 |
| rpsA | 1833646 | c.105T>C | synonymous_variant | 1.0 |
| rpsA | 1833649 | c.108C>T | synonymous_variant | 1.0 |
| rpsA | 1833661 | p.Glu40Asp | missense_variant | 1.0 |
| rpsA | 1833676 | c.135A>G | synonymous_variant | 1.0 |
| rpsA | 1833679 | c.138G>C | synonymous_variant | 1.0 |
| rpsA | 1833682 | c.141C>T | synonymous_variant | 1.0 |
| rpsA | 1833685 | c.144G>T | synonymous_variant | 1.0 |
| rpsA | 1833694 | c.153G>C | 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 | 1833739 | c.198C>G | synonymous_variant | 1.0 |
| rpsA | 1833742 | c.201A>G | synonymous_variant | 1.0 |
| rpsA | 1833770 | p.Asn77His | missense_variant | 1.0 |
| rpsA | 1833781 | c.240T>C | synonymous_variant | 1.0 |
| rpsA | 1833784 | c.243C>G | synonymous_variant | 1.0 |
| rpsA | 1833790 | c.249T>C | synonymous_variant | 1.0 |
| rpsA | 1833795 | p.Glu85Ala | missense_variant | 1.0 |
| rpsA | 1833802 | c.261A>G | synonymous_variant | 1.0 |
| rpsA | 1833808 | c.267G>C | synonymous_variant | 1.0 |
| rpsA | 1833811 | c.270G>C | synonymous_variant | 1.0 |
| rpsA | 1833815 | p.Thr92Gln | missense_variant | 1.0 |
| rpsA | 1833829 | c.288A>G | synonymous_variant | 1.0 |
| rpsA | 1833835 | c.294C>G | synonymous_variant | 1.0 |
| rpsA | 1833838 | c.297G>T | synonymous_variant | 1.0 |
| rpsA | 1833841 | c.300C>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 | 1833874 | c.333T>C | synonymous_variant | 1.0 |
| rpsA | 1833884 | p.Thr115Asp | missense_variant | 1.0 |
| rpsA | 1833893 | p.Ala118Lys | missense_variant | 1.0 |
| rpsA | 1833896 | p.Leu119Ile | missense_variant | 1.0 |
| rpsA | 1833904 | p.Glu121Asp | missense_variant | 1.0 |
| rpsA | 1833905 | p.Lys122Glu | missense_variant | 1.0 |
| rpsA | 1833912 | p.Glu124Gly | missense_variant | 1.0 |
| rpsA | 1833915 | p.Ala125Val | missense_variant | 1.0 |
| rpsA | 1833920 | p.Lys127Glu | missense_variant | 1.0 |
| rpsA | 1833928 | c.387G>C | synonymous_variant | 1.0 |
| rpsA | 1833949 | c.408T>C | synonymous_variant | 1.0 |
| rpsA | 1833955 | c.414G>C | 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 | 1833991 | c.450C>G | synonymous_variant | 1.0 |
| rpsA | 1833997 | c.456G>C | synonymous_variant | 1.0 |
| rpsA | 1834000 | c.459G>C | synonymous_variant | 1.0 |
| rpsA | 1834009 | c.468C>T | synonymous_variant | 1.0 |
| rpsA | 1834012 | c.471G>C | synonymous_variant | 1.0 |
| rpsA | 1834015 | c.474G>C | synonymous_variant | 1.0 |
| rpsA | 1834025 | p.Gln162Ala | missense_variant | 1.0 |
| rpsA | 1834030 | c.489C>G | synonymous_variant | 1.0 |
| rpsA | 1834034 | p.Ile165Val | missense_variant | 1.0 |
| rpsA | 1834040 | p.Lys167Gln | missense_variant | 1.0 |
| rpsA | 1834043 | p.Glu168Lys | missense_variant | 1.0 |
| rpsA | 1834046 | p.Ile169Leu | missense_variant | 1.0 |
| rpsA | 1834054 | c.513C>G | synonymous_variant | 1.0 |
| rpsA | 1834069 | c.528G>C | synonymous_variant | 1.0 |
| rpsA | 1834093 | c.552G>C | synonymous_variant | 1.0 |
| rpsA | 1834099 | c.558C>G | synonymous_variant | 1.0 |
| rpsA | 1834105 | c.564C>T | synonymous_variant | 1.0 |
| rpsA | 1834114 | c.573G>C | synonymous_variant | 1.0 |
| rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
| rpsA | 1834183 | c.642T>C | synonymous_variant | 1.0 |
| rpsA | 1834189 | c.648G>C | synonymous_variant | 1.0 |
| rpsA | 1834192 | c.651C>G | synonymous_variant | 1.0 |
| rpsA | 1834210 | c.669C>T | synonymous_variant | 1.0 |
| rpsA | 1834222 | c.681T>C | synonymous_variant | 1.0 |
| rpsA | 1834240 | c.699T>A | synonymous_variant | 1.0 |
| rpsA | 1834243 | c.702G>C | synonymous_variant | 1.0 |
| rpsA | 1834246 | c.705G>C | synonymous_variant | 1.0 |
| rpsA | 1834249 | c.708T>C | synonymous_variant | 1.0 |
| rpsA | 1834255 | c.714C>G | synonymous_variant | 1.0 |
| rpsA | 1834261 | c.720A>G | synonymous_variant | 1.0 |
| rpsA | 1834294 | c.753G>C | synonymous_variant | 1.0 |
| rpsA | 1834303 | c.762T>G | synonymous_variant | 1.0 |
| rpsA | 1834306 | c.765T>C | synonymous_variant | 1.0 |
| rpsA | 1834318 | c.777C>G | synonymous_variant | 1.0 |
| rpsA | 1834327 | c.786G>C | 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 | 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>G | synonymous_variant | 1.0 |
| rpsA | 1834384 | c.843A>G | synonymous_variant | 1.0 |
| rpsA | 1834387 | c.846C>T | synonymous_variant | 1.0 |
| rpsA | 1834395 | p.Arg285Gln | missense_variant | 1.0 |
| rpsA | 1834408 | c.867C>G | synonymous_variant | 1.0 |
| rpsA | 1834411 | c.870T>C | synonymous_variant | 1.0 |
| rpsA | 1834415 | p.Ala292Gln | missense_variant | 1.0 |
| rpsA | 1834423 | c.882G>C | synonymous_variant | 1.0 |
| rpsA | 1834432 | c.891G>C | synonymous_variant | 0.97 |
| rpsA | 1834451 | c.910_912delTTGinsCTC | synonymous_variant | 1.0 |
| rpsA | 1834456 | c.915T>C | synonymous_variant | 1.0 |
| rpsA | 1834468 | c.927A>G | synonymous_variant | 1.0 |
| rpsA | 1834474 | c.933C>G | synonymous_variant | 1.0 |
| rpsA | 1834489 | c.948T>C | synonymous_variant | 1.0 |
| rpsA | 1834513 | c.972C>G | synonymous_variant | 1.0 |
| rpsA | 1834519 | c.978G>C | synonymous_variant | 1.0 |
| rpsA | 1834538 | p.Val333Ile | 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>C | synonymous_variant | 1.0 |
| rpsA | 1834554 | c.1014_1015delTG | frameshift_variant | 1.0 |
| rpsA | 1834558 | c.1017_1018insAG | frameshift_variant | 1.0 |
| rpsA | 1834568 | p.Asp343Ser | missense_variant | 1.0 |
| rpsA | 1834572 | p.Ala344Val | missense_variant | 1.0 |
| rpsA | 1834583 | p.Val348Ile | missense_variant | 1.0 |
| rpsA | 1834600 | c.1059G>C | synonymous_variant | 1.0 |
| rpsA | 1834606 | c.1065C>T | synonymous_variant | 1.0 |
| rpsA | 1834609 | c.1068T>C | synonymous_variant | 1.0 |
| rpsA | 1834612 | c.1071G>C | synonymous_variant | 1.0 |
| rpsA | 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 |
| rpoA | 3877809 | p.Glu233Asp | missense_variant | 1.0 |
| rpoA | 3877818 | c.690A>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>G | synonymous_variant | 1.0 |
| rpoA | 3877845 | c.663G>C | synonymous_variant | 1.0 |
| rpoA | 3877856 | c.652T>C | synonymous_variant | 1.0 |
| rpoA | 3877875 | c.633T>C | synonymous_variant | 1.0 |
| rpoA | 3877886 | p.Leu208Met | missense_variant | 1.0 |
| rpoA | 3877887 | c.621G>C | synonymous_variant | 1.0 |
| rpoA | 3877899 | p.Ser203Leu | missense_variant | 1.0 |
| rpoA | 3877905 | c.603A>G | synonymous_variant | 1.0 |
| rpoA | 3877908 | p.Asn200Arg | missense_variant | 1.0 |
| rpoA | 3877920 | c.588G>C | synonymous_variant | 1.0 |
| rpoA | 3877926 | p.Leu194Ile | missense_variant | 1.0 |
| rpoA | 3877932 | c.576G>C | synonymous_variant | 1.0 |
| rpoA | 3877962 | c.546G>T | synonymous_variant | 1.0 |
| rpoA | 3877965 | c.543C>T | synonymous_variant | 1.0 |
| rpoA | 3877971 | p.Asp179Glu | missense_variant | 1.0 |
| rpoA | 3877974 | c.534G>C | synonymous_variant | 1.0 |
| clpC1 | 4039487 | c.1218G>C | synonymous_variant | 1.0 |
| clpC1 | 4039498 | p.Ile403Val | missense_variant | 1.0 |
| clpC1 | 4039499 | c.1206G>C | synonymous_variant | 1.0 |
| clpC1 | 4039508 | c.1197G>C | synonymous_variant | 1.0 |
| clpC1 | 4039532 | p.Asn391Ser | missense_variant | 1.0 |
| clpC1 | 4039553 | c.1152C>G | synonymous_variant | 1.0 |
| clpC1 | 4039559 | c.1146C>G | synonymous_variant | 1.0 |
| clpC1 | 4039564 | p.Ala381Ser | missense_variant | 1.0 |
| clpC1 | 4039565 | c.1140G>C | synonymous_variant | 1.0 |
| clpC1 | 4039568 | p.Met379Leu | missense_variant | 1.0 |
| clpC1 | 4039575 | p.Ala377Glu | missense_variant | 1.0 |
| clpC1 | 4039577 | c.1128T>C | synonymous_variant | 1.0 |
| clpC1 | 4039588 | p.Ser373Thr | missense_variant | 1.0 |
| clpC1 | 4039610 | c.1095G>C | synonymous_variant | 1.0 |
| clpC1 | 4039616 | c.1089G>C | synonymous_variant | 1.0 |
| clpC1 | 4039631 | p.Ile358Met | missense_variant | 1.0 |
| clpC1 | 4039640 | c.1065C>G | synonymous_variant | 1.0 |
| clpC1 | 4039647 | p.Glu353Ala | missense_variant | 1.0 |
| clpC1 | 4039649 | p.Val352Ile | missense_variant | 1.0 |
| clpC1 | 4039654 | p.Thr351Ser | missense_variant | 1.0 |
| clpC1 | 4039661 | p.Gly348Ala | missense_variant | 1.0 |
| clpC1 | 4039664 | c.1041G>C | synonymous_variant | 1.0 |
| clpC1 | 4039670 | p.Val345Ile | missense_variant | 1.0 |
| clpC1 | 4039697 | c.1008C>G | synonymous_variant | 1.0 |
| clpC1 | 4039711 | p.Ile332Phe | missense_variant | 1.0 |
| clpC1 | 4039714 | p.Tyr331His | missense_variant | 1.0 |
| clpC1 | 4039724 | c.981A>G | synonymous_variant | 1.0 |
| clpC1 | 4039736 | c.969C>G | synonymous_variant | 1.0 |
| clpC1 | 4040063 | c.642G>C | synonymous_variant | 1.0 |
| clpC1 | 4040066 | c.639G>C | synonymous_variant | 1.0 |
| clpC1 | 4040087 | c.618G>C | synonymous_variant | 1.0 |
| clpC1 | 4040090 | c.615T>G | synonymous_variant | 1.0 |
| clpC1 | 4040105 | c.600C>G | synonymous_variant | 1.0 |
| clpC1 | 4040108 | c.597G>C | synonymous_variant | 1.0 |
| clpC1 | 4040117 | c.588A>G | synonymous_variant | 1.0 |
| clpC1 | 4040126 | c.579C>T | synonymous_variant | 1.0 |
| clpC1 | 4040129 | c.576C>G | synonymous_variant | 1.0 |
| clpC1 | 4040144 | c.561G>C | synonymous_variant | 1.0 |
| clpC1 | 4040147 | c.558A>G | synonymous_variant | 1.0 |
| clpC1 | 4040153 | c.552A>G | synonymous_variant | 1.0 |
| clpC1 | 4040156 | p.Met183Arg | missense_variant | 1.0 |
| clpC1 | 4040159 | c.546G>C | synonymous_variant | 1.0 |
| clpC1 | 4040162 | c.543G>T | synonymous_variant | 1.0 |
| clpC1 | 4040166 | p.Ala180Gln | missense_variant | 1.0 |
| clpC1 | 4040180 | c.525C>T | synonymous_variant | 1.0 |
| clpC1 | 4040357 | c.348T>C | synonymous_variant | 1.0 |
| clpC1 | 4040363 | c.342A>C | 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>C | synonymous_variant | 1.0 |
| clpC1 | 4040403 | p.Asn101Ser | missense_variant | 1.0 |
| clpC1 | 4040411 | c.294T>C | synonymous_variant | 1.0 |
| clpC1 | 4040423 | c.282A>G | synonymous_variant | 1.0 |
| clpC1 | 4040429 | c.274_276delTTGinsCTC | synonymous_variant | 1.0 |
| clpC1 | 4040435 | c.270G>C | synonymous_variant | 1.0 |
| clpC1 | 4040450 | c.255A>G | synonymous_variant | 1.0 |
| clpC1 | 4040456 | c.249C>T | synonymous_variant | 1.0 |
| clpC1 | 4040459 | c.246C>G | synonymous_variant | 1.0 |
| clpC1 | 4040462 | c.243C>T | 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>C | synonymous_variant | 1.0 |
| clpC1 | 4040480 | c.223_225delTCTinsAGC | synonymous_variant | 1.0 |
