Run ID: ERR4816548
Sample name:
Date: 01-04-2023 14:29:33
Number of reads: 659195
Percentage reads mapped: 26.96
Strain: lineage4.5
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.5 | Euro-American | H;T | RD122 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761196 | p.Leu464Met | missense_variant | 0.18 | rifampicin |
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
katG | 2154347 | p.Pro589Thr | missense_variant | 0.18 | isoniazid |
embB | 4247619 | p.Val369Ala | missense_variant | 0.22 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6763 | c.-539G>A | upstream_gene_variant | 0.2 |
gyrA | 6766 | c.-536G>T | upstream_gene_variant | 0.2 |
gyrA | 6775 | c.-527G>T | upstream_gene_variant | 0.2 |
gyrA | 6793 | c.-509T>C | upstream_gene_variant | 0.18 |
gyrB | 6797 | p.Gly520Ser | missense_variant | 0.18 |
gyrA | 6808 | c.-494C>G | upstream_gene_variant | 0.2 |
gyrB | 7261 | p.Asp674Glu | missense_variant | 0.17 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7892 | c.591G>A | synonymous_variant | 1.0 |
gyrA | 8261 | c.960C>G | synonymous_variant | 0.12 |
gyrA | 8264 | c.963T>C | synonymous_variant | 0.12 |
gyrA | 8270 | c.969G>C | synonymous_variant | 0.19 |
gyrA | 8283 | p.Ile328Leu | missense_variant | 0.33 |
gyrA | 8288 | c.987T>C | synonymous_variant | 0.4 |
gyrA | 8294 | c.993T>C | synonymous_variant | 0.43 |
gyrA | 8316 | p.Thr339Tyr | missense_variant | 0.38 |
gyrA | 8320 | p.Ser340Asn | missense_variant | 0.4 |
gyrA | 8324 | c.1023T>C | synonymous_variant | 0.38 |
gyrA | 8329 | p.Ala343Val | missense_variant | 0.38 |
gyrA | 8339 | c.1038A>G | synonymous_variant | 0.42 |
gyrA | 8343 | p.Ile348Leu | missense_variant | 0.4 |
gyrA | 8354 | c.1053G>C | synonymous_variant | 0.35 |
gyrA | 8375 | c.1074G>C | synonymous_variant | 0.25 |
gyrA | 8382 | p.Leu361Met | missense_variant | 0.24 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
ccsA | 620029 | c.139C>T | synonymous_variant | 1.0 |
rpoB | 760130 | p.Asp108Glu | missense_variant | 0.25 |
rpoB | 760139 | c.333A>C | synonymous_variant | 0.25 |
rpoB | 760140 | p.Pro112Ser | missense_variant | 0.26 |
rpoB | 760148 | p.Asp114Glu | missense_variant | 0.25 |
rpoB | 760157 | c.351A>G | synonymous_variant | 0.38 |
rpoB | 760181 | c.375T>G | synonymous_variant | 0.53 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.53 |
rpoB | 760206 | p.Ile134Val | missense_variant | 0.47 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.48 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.48 |
rpoB | 760244 | c.438G>C | synonymous_variant | 0.62 |
rpoB | 760253 | c.447T>C | synonymous_variant | 0.56 |
rpoB | 760262 | c.456G>C | synonymous_variant | 0.5 |
rpoB | 760263 | p.Met153Val | missense_variant | 0.5 |
rpoB | 760274 | p.Glu156Asp | missense_variant | 0.59 |
rpoB | 760298 | c.492G>C | synonymous_variant | 0.57 |
rpoB | 760310 | c.504G>C | synonymous_variant | 0.57 |
rpoB | 760313 | c.507G>C | synonymous_variant | 0.54 |
rpoB | 760316 | c.510C>G | synonymous_variant | 0.53 |
rpoB | 760317 | c.511_512delAGinsTC | synonymous_variant | 0.53 |
rpoB | 760325 | c.519G>C | synonymous_variant | 0.53 |
rpoB | 760340 | c.534G>C | synonymous_variant | 0.54 |
rpoB | 760353 | p.Glu183Gln | missense_variant | 0.36 |
rpoB | 760356 | p.Thr184Ala | missense_variant | 0.35 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.42 |
rpoB | 760370 | c.564C>G | synonymous_variant | 0.31 |
rpoB | 760398 | p.Val198Ile | missense_variant | 0.3 |
rpoB | 760403 | c.597C>T | synonymous_variant | 0.3 |
rpoB | 760412 | c.606C>G | synonymous_variant | 0.55 |
rpoB | 760415 | c.609C>T | synonymous_variant | 0.55 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.73 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.57 |
rpoB | 760481 | c.675G>C | synonymous_variant | 0.55 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.52 |
rpoB | 760502 | c.696C>G | synonymous_variant | 0.33 |
rpoB | 760508 | c.702G>C | synonymous_variant | 0.3 |
rpoB | 760511 | c.705G>C | synonymous_variant | 0.26 |
rpoB | 760598 | c.792C>G | synonymous_variant | 0.12 |
rpoB | 760611 | c.805T>C | synonymous_variant | 0.32 |
rpoB | 760634 | c.828T>C | synonymous_variant | 0.39 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.39 |
rpoB | 760652 | c.846C>G | synonymous_variant | 0.37 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.37 |
rpoB | 760659 | c.853_855delTCAinsAGC | synonymous_variant | 0.37 |
rpoB | 760673 | c.867G>C | synonymous_variant | 0.37 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.33 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.33 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.33 |
rpoB | 760697 | p.Glu297Asp | missense_variant | 0.2 |
rpoB | 760916 | c.1110C>T | synonymous_variant | 0.25 |
rpoB | 760919 | c.1113C>T | synonymous_variant | 0.25 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.25 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.33 |
rpoB | 760965 | p.Met387Leu | missense_variant | 0.36 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.25 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.27 |
rpoB | 760988 | c.1182C>G | synonymous_variant | 0.24 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.24 |
rpoB | 760997 | c.1191G>C | synonymous_variant | 0.24 |
rpoB | 761003 | c.1197C>G | synonymous_variant | 0.24 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.2 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.2 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 0.21 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.22 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 0.25 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.24 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.21 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.21 |
rpoB | 761171 | c.1365C>T | synonymous_variant | 0.2 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.19 |
rpoB | 761192 | c.1386C>G | synonymous_variant | 0.19 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.17 |
rpoB | 761201 | p.Glu465Asp | missense_variant | 0.18 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.16 |
rpoB | 761540 | c.1734C>G | synonymous_variant | 0.16 |
rpoB | 761552 | c.1746G>C | synonymous_variant | 0.15 |
rpoB | 761558 | c.1752C>G | synonymous_variant | 0.15 |
rpoB | 761564 | c.1758G>C | synonymous_variant | 0.14 |
rpoB | 761603 | c.1797C>G | synonymous_variant | 0.22 |
rpoB | 761612 | c.1806G>T | synonymous_variant | 0.21 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.21 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.21 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.32 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.3 |
rpoB | 762080 | c.2274G>C | synonymous_variant | 0.27 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.29 |
rpoB | 762099 | c.2293_2295delCGCinsAGG | synonymous_variant | 0.39 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.49 |
rpoB | 762122 | p.Asp772Glu | missense_variant | 0.55 |
rpoB | 762125 | p.Glu773Asp | missense_variant | 0.5 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 0.54 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.57 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.58 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.62 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.62 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.64 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.68 |
rpoB | 762209 | c.2403C>G | synonymous_variant | 0.71 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.65 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.72 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.72 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.71 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.68 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.69 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.67 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.63 |
rpoB | 762318 | p.Ser838Thr | missense_variant | 0.63 |
rpoB | 762329 | c.2523G>C | synonymous_variant | 0.65 |
rpoB | 762338 | c.2532T>C | synonymous_variant | 0.59 |
rpoB | 762341 | c.2535G>C | synonymous_variant | 0.52 |
rpoB | 762347 | c.2541T>C | synonymous_variant | 0.5 |
rpoB | 762359 | p.Asp851Glu | missense_variant | 0.45 |
rpoB | 762362 | p.Glu852Asp | missense_variant | 0.43 |
rpoB | 762369 | c.2563T>C | synonymous_variant | 0.38 |
rpoC | 762374 | c.-996G>C | upstream_gene_variant | 0.35 |
rpoB | 762375 | p.Ala857Pro | missense_variant | 0.32 |
rpoC | 762380 | c.-990T>C | upstream_gene_variant | 0.3 |
rpoC | 762392 | c.-978G>C | upstream_gene_variant | 0.17 |
rpoC | 762836 | c.-534C>T | upstream_gene_variant | 0.16 |
rpoC | 762857 | c.-513C>G | upstream_gene_variant | 0.32 |
rpoB | 762858 | p.Thr1018Ala | missense_variant | 0.32 |
rpoC | 762863 | c.-507T>C | upstream_gene_variant | 0.32 |
rpoB | 762878 | p.Ile1024Met | missense_variant | 0.48 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.48 |
rpoB | 762894 | p.Leu1030Met | missense_variant | 0.52 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 0.62 |
rpoC | 762920 | c.-450C>G | upstream_gene_variant | 0.64 |
rpoC | 762926 | c.-444C>G | upstream_gene_variant | 0.64 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.63 |
rpoC | 762947 | c.-423C>G | upstream_gene_variant | 0.57 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.61 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.61 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.57 |
rpoC | 762995 | c.-375G>C | upstream_gene_variant | 0.59 |
rpoC | 763013 | c.-357C>G | upstream_gene_variant | 0.53 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.39 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 0.38 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.37 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.33 |
rpoC | 763053 | c.-317_-315delTTGinsCTC | upstream_gene_variant | 0.15 |
rpoC | 763465 | c.96G>A | synonymous_variant | 0.13 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.2 |
rpoC | 763483 | c.114G>C | synonymous_variant | 0.32 |
rpoC | 763486 | c.117T>G | synonymous_variant | 0.3 |
rpoC | 763504 | c.135C>A | synonymous_variant | 0.42 |
rpoC | 763507 | c.138G>C | synonymous_variant | 0.52 |
rpoC | 763528 | c.159G>T | synonymous_variant | 0.58 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.62 |
rpoC | 763537 | c.168C>G | synonymous_variant | 0.63 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.69 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.79 |
rpoC | 763603 | c.234C>T | synonymous_variant | 0.8 |
rpoC | 763606 | c.237C>T | synonymous_variant | 0.8 |
rpoC | 763615 | c.246G>C | synonymous_variant | 0.77 |
rpoC | 763618 | c.249C>G | synonymous_variant | 0.77 |
rpoC | 763621 | c.252C>T | synonymous_variant | 0.77 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.76 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.7 |
rpoC | 763666 | c.297G>C | synonymous_variant | 0.68 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.63 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.67 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.57 |
rpoC | 763711 | c.342G>C | synonymous_variant | 0.52 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.51 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.52 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.46 |
rpoC | 763765 | c.396T>G | synonymous_variant | 0.39 |
rpoC | 763768 | c.399C>G | synonymous_variant | 0.39 |
rpoC | 764098 | c.729A>G | synonymous_variant | 0.15 |
rpoC | 764099 | c.730_732delCTCinsTTG | synonymous_variant | 0.15 |
rpoC | 764110 | c.741C>T | synonymous_variant | 0.27 |
rpoC | 764131 | c.762T>C | synonymous_variant | 0.36 |
rpoC | 764133 | p.Ala255Gly | missense_variant | 0.36 |
rpoC | 764143 | c.774G>C | synonymous_variant | 0.33 |
rpoC | 764147 | p.Ser260Ala | missense_variant | 0.36 |
rpoC | 764162 | p.Ile265Ala | missense_variant | 0.42 |
rpoC | 764168 | p.Asn267Asp | missense_variant | 0.33 |
rpoC | 764177 | p.Ile270Val | missense_variant | 0.36 |
rpoC | 764188 | c.819A>G | synonymous_variant | 0.27 |
rpoC | 764195 | p.Ser276Ala | missense_variant | 0.2 |
rpoC | 764338 | c.969G>A | synonymous_variant | 0.32 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.46 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 0.46 |
rpoC | 764383 | c.1014C>G | synonymous_variant | 0.41 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 0.41 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.5 |
rpoC | 764410 | c.1041G>C | synonymous_variant | 0.54 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.48 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.46 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.43 |
rpoC | 764435 | c.1066_1068delAGGinsCGA | synonymous_variant | 0.43 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.5 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.5 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.5 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.5 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.5 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.44 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.56 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.69 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.69 |
rpoC | 764533 | c.1164C>A | synonymous_variant | 0.69 |
rpoC | 764536 | c.1167G>T | synonymous_variant | 0.65 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.65 |
rpoC | 764542 | c.1173C>G | synonymous_variant | 0.65 |
rpoC | 764548 | c.1179G>T | synonymous_variant | 0.65 |
rpoC | 764551 | c.1182G>C | synonymous_variant | 0.65 |
rpoC | 764554 | c.1185C>T | synonymous_variant | 0.67 |
rpoC | 764560 | c.1191T>G | synonymous_variant | 0.68 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.68 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.67 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.65 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 0.77 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.74 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.67 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.77 |
rpoC | 764644 | c.1275G>C | synonymous_variant | 0.77 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.77 |
rpoC | 764660 | p.Val431Ile | missense_variant | 0.7 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 0.72 |
rpoC | 764701 | c.1332C>G | synonymous_variant | 0.61 |
rpoC | 764705 | p.Leu446Asp | missense_variant | 0.59 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.56 |
rpoC | 764737 | c.1368G>C | synonymous_variant | 0.44 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.38 |
rpoC | 764780 | c.1411_1412delAGinsTC | synonymous_variant | 0.18 |
rpoC | 764896 | c.1527C>T | synonymous_variant | 0.24 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.25 |
rpoC | 764912 | p.Met515Gln | missense_variant | 0.24 |
rpoC | 764935 | c.1566T>C | synonymous_variant | 0.25 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.25 |
rpoC | 764953 | c.1584G>C | synonymous_variant | 0.26 |
rpoC | 764956 | c.1587T>C | synonymous_variant | 0.3 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.29 |
rpoC | 764971 | c.1602C>G | synonymous_variant | 0.29 |
rpoC | 765813 | p.Arg815Gln | missense_variant | 0.15 |
rpoC | 766588 | p.Glu1073Asp | missense_variant | 0.17 |
rpoC | 766957 | p.Glu1196Asp | missense_variant | 0.17 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.4 |
rpoC | 767008 | c.3639G>C | synonymous_variant | 0.62 |
rpoC | 767015 | p.Ala1216Thr | missense_variant | 0.59 |
rpoC | 767020 | c.3651C>G | synonymous_variant | 0.57 |
rpoC | 767038 | c.3669G>C | synonymous_variant | 0.56 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.54 |
rpoC | 767062 | c.3693C>T | synonymous_variant | 0.48 |
rpoC | 767065 | c.3696G>C | synonymous_variant | 0.48 |
rpoC | 767074 | c.3705T>C | synonymous_variant | 0.4 |
rpoC | 767077 | c.3708G>C | synonymous_variant | 0.38 |
rpoC | 767087 | p.Cys1240Gly | missense_variant | 0.33 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776922 | p.Ala520Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781751 | c.192G>C | synonymous_variant | 0.28 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.26 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.22 |
rpsL | 781763 | c.204C>G | synonymous_variant | 0.25 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.38 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.39 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.38 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.35 |
rpsL | 781829 | c.270G>C | synonymous_variant | 0.38 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.43 |
rpsL | 781838 | c.279G>C | synonymous_variant | 0.45 |
rpsL | 781851 | p.Ile98Val | missense_variant | 0.48 |
rpsL | 781865 | c.306G>C | synonymous_variant | 0.6 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.56 |
rpsL | 781877 | c.318T>C | synonymous_variant | 0.57 |
rpsL | 781880 | c.321C>G | synonymous_variant | 0.48 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.43 |
rpsL | 781898 | c.339A>G | synonymous_variant | 0.43 |
rpsL | 781907 | c.348T>G | synonymous_variant | 0.42 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.35 |
rpsL | 781933 | c.374G>A | splice_region_variant&stop_retained_variant | 0.29 |
rplC | 800672 | c.-137G>C | upstream_gene_variant | 0.24 |
rplC | 800690 | c.-119C>T | upstream_gene_variant | 0.33 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.4 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.42 |
rplC | 800715 | c.-94_-92delATCinsGTG | upstream_gene_variant | 0.47 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.5 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.47 |
rplC | 800735 | c.-74C>G | upstream_gene_variant | 0.38 |
rplC | 800738 | c.-71T>C | upstream_gene_variant | 0.38 |
rplC | 800762 | c.-47T>G | upstream_gene_variant | 0.21 |
rplC | 800771 | c.-38C>T | upstream_gene_variant | 0.21 |
rplC | 800780 | c.-29C>G | upstream_gene_variant | 0.24 |
fbiC | 1305191 | p.Ala754Val | missense_variant | 0.2 |
Rv1258c | 1406101 | p.Pro414Ser | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472123 | n.278A>G | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472148 | n.303T>C | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472296 | n.454_458delTCCGG | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472305 | n.461_467delTCTCTCG | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472315 | n.470_471insAC | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472426 | n.581T>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472473 | n.628G>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472474 | n.629C>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472494 | n.649A>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472496 | n.651T>G | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472583 | n.738T>A | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472675 | n.830T>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472678 | n.833T>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472685 | n.840G>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472686 | n.841G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472687 | n.842A>C | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472843 | n.998_999insT | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472847 | n.1002G>C | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472849 | n.1005delT | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472857 | n.1012A>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472860 | n.1015C>G | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472861 | n.1016G>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472873 | n.1028C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472959 | n.1114T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1473094 | n.1249T>G | non_coding_transcript_exon_variant | 0.65 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.72 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473129 | n.1284C>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1473147 | n.1302G>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473164 | n.1319C>G | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.65 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.61 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473283 | n.1438T>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473292 | n.1447_1448insA | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473300 | n.1455C>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.59 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473788 | n.131A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1473793 | n.136G>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473794 | n.137A>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473801 | n.144T>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473802 | n.145C>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1473807 | n.150T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1473814 | n.157A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473815 | n.158T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473822 | n.165A>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1473830 | n.173T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473832 | n.175C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1473833 | n.176_177insT | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1473886 | n.229A>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1473888 | n.231T>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473922 | n.265A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1473923 | n.266C>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474163 | n.506C>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.61 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1474186 | n.529A>G | non_coding_transcript_exon_variant | 0.61 |
rrl | 1474201 | n.544T>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474202 | n.545T>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.65 |
rrl | 1474220 | n.563G>A | non_coding_transcript_exon_variant | 0.61 |
rrl | 1474271 | n.614A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474275 | n.618T>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474349 | n.692A>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474353 | n.696A>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474354 | n.697C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474355 | n.698A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474359 | n.702C>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474406 | n.749T>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.39 |
rrl | 1474627 | n.970G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474628 | n.971C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474629 | n.972G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474638 | n.981C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474640 | n.983C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474643 | n.986A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474658 | n.1001A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474676 | n.1019T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474777 | n.1120T>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474779 | n.1122G>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474798 | n.1141C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474806 | n.1149A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.39 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474825 | n.1168G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474830 | n.1173A>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474901 | n.1244A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474928 | n.1271C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475088 | n.1431A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475113 | n.1456C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1475115 | n.1458A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475116 | n.1459G>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1475153 | n.1496A>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1475171 | n.1514C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475538 | n.1881T>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475542 | n.1885A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475544 | n.1887A>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475550 | n.1893A>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475571 | n.1914A>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475688 | n.2031G>A | non_coding_transcript_exon_variant | 0.39 |
rrl | 1475696 | n.2039T>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475703 | n.2046A>T | non_coding_transcript_exon_variant | 0.51 |
rrl | 1475707 | n.2050T>G | non_coding_transcript_exon_variant | 0.51 |
rrl | 1475713 | n.2056C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475740 | n.2083G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.66 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475788 | n.2131C>G | non_coding_transcript_exon_variant | 0.68 |
rrl | 1475880 | n.2223C>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.65 |
rrl | 1475883 | n.2226A>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.65 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1475902 | n.2245T>C | non_coding_transcript_exon_variant | 0.65 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.49 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1475990 | n.2333G>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.49 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476032 | n.2375C>G | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476033 | n.2376T>G | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476040 | n.2383C>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476046 | n.2389G>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476076 | n.2419A>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476081 | n.2424A>G | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476082 | n.2425T>C | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476087 | n.2430C>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476095 | n.2438C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476103 | n.2446C>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476105 | n.2450delA | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476110 | n.2453G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476196 | n.2539C>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476204 | n.2547C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476255 | n.2598A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.49 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476300 | n.2643G>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476301 | n.2644A>G | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476528 | n.2871A>G | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476534 | n.2877A>C | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476645 | n.2988A>G | non_coding_transcript_exon_variant | 0.24 |
rpsA | 1833628 | c.87G>C | synonymous_variant | 0.15 |
rpsA | 1833649 | c.108C>T | synonymous_variant | 0.15 |
rpsA | 1833667 | c.126C>G | synonymous_variant | 0.14 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.14 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 0.17 |
rpsA | 1833685 | c.144G>T | synonymous_variant | 0.21 |
rpsA | 1833691 | c.150G>A | synonymous_variant | 0.13 |
rpsA | 1833697 | c.156C>G | synonymous_variant | 0.13 |
rpsA | 1833709 | c.168C>T | synonymous_variant | 0.19 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.24 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.21 |
rpsA | 1833730 | c.189C>T | synonymous_variant | 0.16 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.16 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.18 |
rpsA | 1833769 | c.228C>G | synonymous_variant | 0.19 |
rpsA | 1833771 | p.Asn77Thr | missense_variant | 0.18 |
rpsA | 1833829 | c.288A>G | synonymous_variant | 0.19 |
rpsA | 1833832 | c.291G>A | synonymous_variant | 0.24 |
rpsA | 1833838 | c.297G>T | synonymous_variant | 0.23 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.23 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.31 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.3 |
rpsA | 1833862 | c.321G>C | synonymous_variant | 0.33 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.39 |
rpsA | 1833886 | c.345C>G | synonymous_variant | 0.4 |
rpsA | 1833894 | p.Ala118Glu | missense_variant | 0.41 |
rpsA | 1833914 | p.Ala125Pro | missense_variant | 0.44 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.44 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.49 |
rpsA | 1833955 | c.414G>C | synonymous_variant | 0.51 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.52 |
rpsA | 1833973 | c.432G>C | synonymous_variant | 0.54 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.54 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.61 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.6 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.61 |
rpsA | 1834034 | p.Ile165Val | missense_variant | 0.57 |
rpsA | 1834040 | p.Lys167Arg | missense_variant | 0.51 |
rpsA | 1834046 | p.Ile169Leu | missense_variant | 0.51 |
rpsA | 1834093 | c.552G>C | synonymous_variant | 0.36 |
rpsA | 1834110 | p.Trp190Tyr | missense_variant | 0.18 |
rpsA | 1834172 | p.Ile211Val | missense_variant | 0.14 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.13 |
rpsA | 1834183 | c.642T>C | synonymous_variant | 0.16 |
rpsA | 1834189 | c.648G>C | synonymous_variant | 0.21 |
rpsA | 1834210 | c.669C>T | synonymous_variant | 0.31 |
rpsA | 1834219 | c.678C>G | synonymous_variant | 0.26 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.27 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 0.29 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.3 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.39 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.47 |
rpsA | 1834255 | c.714C>G | synonymous_variant | 0.56 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.56 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.57 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.46 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.43 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.43 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.42 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.42 |
rpsA | 1834318 | c.777C>G | synonymous_variant | 0.44 |
rpsA | 1834327 | c.786G>C | synonymous_variant | 0.41 |
rpsA | 1834333 | p.Asp264Glu | missense_variant | 0.38 |
rpsA | 1834336 | c.795C>G | synonymous_variant | 0.34 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.21 |
rpsA | 1834396 | c.855G>T | synonymous_variant | 0.25 |
rpsA | 1834399 | p.His286Gln | missense_variant | 0.32 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.4 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.41 |
rpsA | 1834451 | c.910_912delTTGinsCTC | synonymous_variant | 0.48 |
rpsA | 1834456 | c.915T>C | synonymous_variant | 0.46 |
rpsA | 1834465 | c.924T>C | synonymous_variant | 0.46 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.48 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.45 |
rpsA | 1834670 | p.Lys377Gln | missense_variant | 0.2 |
rpsA | 1834686 | p.Asp382Ala | missense_variant | 0.18 |
rpsA | 1834688 | p.Ser383Glu | missense_variant | 0.18 |
rpsA | 1834716 | p.Phe392Tyr | missense_variant | 0.16 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103101 | c.-59C>A | upstream_gene_variant | 1.0 |
katG | 2154228 | p.Val628Leu | missense_variant | 0.15 |
katG | 2154246 | c.1866T>G | synonymous_variant | 0.21 |
katG | 2154249 | c.1863C>G | synonymous_variant | 0.21 |
katG | 2154252 | p.Ser620Thr | missense_variant | 0.21 |
katG | 2154255 | c.1857C>G | synonymous_variant | 0.2 |
katG | 2154261 | c.1851T>G | synonymous_variant | 0.18 |
katG | 2154281 | p.Leu611Ile | missense_variant | 0.19 |
katG | 2154286 | p.Met609Ala | missense_variant | 0.2 |
katG | 2154297 | c.1815G>C | synonymous_variant | 0.22 |
katG | 2154302 | c.1810T>C | synonymous_variant | 0.24 |
katG | 2155601 | p.Cys171Arg | missense_variant | 0.19 |
katG | 2155608 | c.504C>G | synonymous_variant | 0.18 |
katG | 2155617 | p.Ile165Met | missense_variant | 0.18 |
katG | 2155626 | c.486G>C | synonymous_variant | 0.18 |
katG | 2155632 | c.480A>G | synonymous_variant | 0.14 |
katG | 2155636 | p.Leu159Ile | missense_variant | 0.21 |
katG | 2155659 | c.453C>G | synonymous_variant | 0.39 |
katG | 2155674 | c.438G>T | synonymous_variant | 0.25 |
katG | 2155677 | c.435C>T | synonymous_variant | 0.26 |
katG | 2155691 | c.421T>C | synonymous_variant | 0.33 |
katG | 2155696 | p.Ala139Val | missense_variant | 0.3 |
katG | 2155704 | c.408C>G | synonymous_variant | 0.33 |
katG | 2155716 | c.396T>C | synonymous_variant | 0.35 |
katG | 2155722 | c.390G>C | synonymous_variant | 0.38 |
katG | 2155728 | c.384G>C | synonymous_variant | 0.33 |
PPE35 | 2167781 | c.2832C>T | synonymous_variant | 0.18 |
PPE35 | 2168908 | p.Thr569Ser | missense_variant | 0.13 |
PPE35 | 2170568 | p.Ile15Met | missense_variant | 1.0 |
Rv1979c | 2222371 | p.Ala265Glu | missense_variant | 0.2 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288760 | p.Ala161Val | missense_variant | 0.12 |
kasA | 2517921 | c.-194A>G | upstream_gene_variant | 0.13 |
kasA | 2517934 | c.-181A>T | upstream_gene_variant | 0.17 |
kasA | 2517941 | c.-174C>G | upstream_gene_variant | 0.15 |
kasA | 2517950 | c.-165C>G | upstream_gene_variant | 0.18 |
Rv2752c | 3064865 | p.Pro443Thr | missense_variant | 0.18 |
Rv2752c | 3067117 | c.-926C>T | upstream_gene_variant | 0.12 |
thyX | 3067619 | c.327A>G | synonymous_variant | 0.33 |
thyX | 3067625 | c.321C>G | synonymous_variant | 0.29 |
thyX | 3067631 | c.315C>A | synonymous_variant | 0.33 |
thyX | 3067640 | c.306G>A | synonymous_variant | 0.33 |
thyX | 3067652 | c.294T>C | synonymous_variant | 0.33 |
thyX | 3067679 | p.Cys89Val | missense_variant | 0.26 |
thyX | 3067694 | c.252G>C | synonymous_variant | 0.24 |
thyX | 3067697 | c.249C>G | synonymous_variant | 0.24 |
thyX | 3067709 | c.237G>C | synonymous_variant | 0.14 |
thyA | 3073863 | c.609T>C | synonymous_variant | 0.21 |
thyA | 3073874 | p.Ile200Val | missense_variant | 0.18 |
thyA | 3073878 | p.Glu198Asp | missense_variant | 0.2 |
thyA | 3073888 | p.Ser195Glu | missense_variant | 0.18 |
thyA | 3073892 | c.580T>C | synonymous_variant | 0.2 |
thyA | 3073893 | c.579C>A | synonymous_variant | 0.2 |
thyA | 3073897 | p.Ala192Val | missense_variant | 0.19 |
thyA | 3073903 | p.Ala190Asp | missense_variant | 0.24 |
thyA | 3073908 | p.Met188Ile | missense_variant | 0.24 |
thyA | 3073920 | c.552C>G | synonymous_variant | 0.25 |
thyA | 3073925 | c.547T>C | synonymous_variant | 0.21 |
thyA | 3073926 | c.546G>C | synonymous_variant | 0.21 |
thyA | 3073929 | c.543T>C | synonymous_variant | 0.2 |
thyA | 3073935 | c.537C>G | synonymous_variant | 0.26 |
thyA | 3073953 | c.519T>C | synonymous_variant | 0.24 |
thyA | 3073959 | c.513T>C | synonymous_variant | 0.25 |
thyA | 3073968 | c.504C>G | synonymous_variant | 0.31 |
thyA | 3073977 | c.495A>G | synonymous_variant | 0.29 |
thyA | 3073983 | c.489C>G | synonymous_variant | 0.28 |
thyA | 3073993 | c.478_479delAGinsTC | synonymous_variant | 0.24 |
thyA | 3073999 | p.Arg158Gln | missense_variant | 0.22 |
thyA | 3074001 | c.471C>G | synonymous_variant | 0.21 |
thyA | 3074004 | c.468T>C | synonymous_variant | 0.21 |
thyA | 3074031 | c.441T>C | synonymous_variant | 0.29 |
thyA | 3074034 | c.438T>C | synonymous_variant | 0.29 |
thyA | 3074037 | c.435C>G | synonymous_variant | 0.26 |
thyA | 3074053 | p.Arg140Gln | missense_variant | 0.23 |
thyA | 3074056 | p.Glu139Pro | missense_variant | 0.23 |
thyA | 3074058 | c.414C>T | synonymous_variant | 0.23 |
thyA | 3074061 | p.Glu137Asp | missense_variant | 0.23 |
thyA | 3074065 | p.Gly136Ala | missense_variant | 0.23 |
thyA | 3074076 | c.396C>G | synonymous_variant | 0.23 |
thyA | 3074079 | c.393G>C | synonymous_variant | 0.25 |
thyA | 3074091 | c.381C>G | synonymous_variant | 0.25 |
thyA | 3074100 | c.372T>C | synonymous_variant | 0.25 |
ald | 3087279 | p.Gly154Trp | missense_variant | 0.13 |
ald | 3087917 | c.1098C>T | synonymous_variant | 0.17 |
fbiD | 3339324 | c.207G>C | synonymous_variant | 0.22 |
Rv3083 | 3448480 | c.-24G>T | upstream_gene_variant | 0.2 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474813 | p.Phe269Leu | missense_variant | 0.2 |
alr | 3841251 | p.Gly57Val | missense_variant | 0.2 |
rpoA | 3877656 | c.852T>C | synonymous_variant | 0.32 |
rpoA | 3877667 | p.Ser281Ala | missense_variant | 0.32 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.32 |
rpoA | 3877672 | p.Thr279Ser | missense_variant | 0.32 |
rpoA | 3877679 | p.Ala277Ser | missense_variant | 0.33 |
rpoA | 3877680 | c.828G>C | synonymous_variant | 0.33 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.32 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.33 |
rpoA | 3877695 | c.813C>G | synonymous_variant | 0.35 |
rpoA | 3877701 | p.Val269Ile | missense_variant | 0.32 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.23 |
rpoA | 3877856 | c.652T>C | synonymous_variant | 0.33 |
rpoA | 3877863 | c.645G>C | synonymous_variant | 0.42 |
rpoA | 3877875 | c.633T>G | synonymous_variant | 0.55 |
rpoA | 3877884 | p.Leu208Val | missense_variant | 0.55 |
rpoA | 3877887 | c.621G>C | synonymous_variant | 0.5 |
rpoA | 3877899 | p.Ser203Thr | missense_variant | 0.38 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.38 |
rpoA | 3877908 | p.Asn200Pro | missense_variant | 0.4 |
rpoA | 3877950 | c.558C>G | synonymous_variant | 0.54 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.4 |
rpoA | 3877965 | c.543C>G | synonymous_variant | 0.36 |
rpoA | 3877971 | p.Asp179Glu | missense_variant | 0.31 |
rpoA | 3877974 | c.534G>C | synonymous_variant | 0.29 |
rpoA | 3877983 | c.525C>G | synonymous_variant | 0.28 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.33 |
rpoA | 3877992 | c.516C>G | synonymous_variant | 0.33 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.36 |
rpoA | 3878082 | c.426T>C | synonymous_variant | 0.23 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.33 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.33 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.28 |
rpoA | 3878128 | p.Thr127Trp | missense_variant | 0.25 |
rpoA | 3878141 | p.Met123Leu | missense_variant | 0.22 |
rpoA | 3878142 | p.Gly122Asp | missense_variant | 0.22 |
rpoA | 3878145 | c.363C>G | synonymous_variant | 0.22 |
rpoA | 3878160 | c.348C>G | synonymous_variant | 0.29 |
rpoA | 3878163 | c.345C>T | synonymous_variant | 0.3 |
rpoA | 3878175 | c.333G>C | synonymous_variant | 0.24 |
rpoA | 3878184 | p.Gly108Ala | missense_variant | 0.14 |
rpoA | 3878187 | c.321C>G | synonymous_variant | 0.13 |
rpoA | 3878202 | c.306G>C | synonymous_variant | 0.21 |
rpoA | 3878205 | c.303T>C | synonymous_variant | 0.21 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.25 |
rpoA | 3878232 | c.276G>C | synonymous_variant | 0.3 |
rpoA | 3878247 | c.261G>C | synonymous_variant | 0.25 |
rpoA | 3878259 | c.249G>C | synonymous_variant | 0.26 |
rpoA | 3878262 | p.Ser82Glu | missense_variant | 0.26 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.25 |
rpoA | 3878295 | c.213A>G | synonymous_variant | 0.19 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.16 |
rpoA | 3878301 | c.207C>G | synonymous_variant | 0.17 |
rpoA | 3878307 | c.201C>G | synonymous_variant | 0.18 |
rpoA | 3878310 | c.198G>C | synonymous_variant | 0.19 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 0.18 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.14 |
rpoA | 3878575 | c.-68C>T | upstream_gene_variant | 1.0 |
clpC1 | 4038318 | p.Pro796Leu | missense_variant | 1.0 |
clpC1 | 4038725 | c.1980C>G | synonymous_variant | 0.24 |
clpC1 | 4038740 | c.1965G>C | synonymous_variant | 0.35 |
clpC1 | 4038755 | c.1950G>T | synonymous_variant | 0.46 |
clpC1 | 4038764 | c.1941C>G | synonymous_variant | 0.48 |
clpC1 | 4038767 | c.1938G>C | synonymous_variant | 0.46 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.46 |
clpC1 | 4038782 | c.1923G>T | synonymous_variant | 0.48 |
clpC1 | 4038794 | p.Ser637Thr | missense_variant | 0.55 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.57 |
clpC1 | 4038815 | c.1890G>C | synonymous_variant | 0.57 |
clpC1 | 4038839 | c.1866G>C | synonymous_variant | 0.5 |
clpC1 | 4038849 | p.Phe619Tyr | missense_variant | 0.15 |
clpC1 | 4038855 | p.Lys617Thr | missense_variant | 0.16 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 0.43 |
clpC1 | 4038863 | c.1842G>C | synonymous_variant | 0.43 |
clpC1 | 4038867 | p.Lys613Ala | missense_variant | 0.16 |
clpC1 | 4038875 | c.1830C>G | synonymous_variant | 0.15 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.67 |
clpC1 | 4038881 | c.1824C>T | synonymous_variant | 0.67 |
clpC1 | 4038885 | p.Gly607Ala | missense_variant | 0.16 |
clpC1 | 4038905 | c.1800A>C | synonymous_variant | 0.58 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.42 |
clpC1 | 4038911 | c.1794G>T | synonymous_variant | 0.48 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.48 |
clpC1 | 4038917 | c.1788C>T | synonymous_variant | 0.58 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 0.52 |
clpC1 | 4038932 | c.1773G>C | synonymous_variant | 0.54 |
clpC1 | 4038939 | p.Phe589Tyr | missense_variant | 0.54 |
clpC1 | 4038941 | c.1764G>C | synonymous_variant | 0.54 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.58 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.58 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.67 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.61 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.6 |
clpC1 | 4038986 | p.Asp573Glu | missense_variant | 0.63 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.66 |
clpC1 | 4039004 | c.1701C>G | synonymous_variant | 0.63 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.66 |
clpC1 | 4039064 | c.1641C>T | synonymous_variant | 0.7 |
clpC1 | 4039067 | c.1638G>C | synonymous_variant | 0.68 |
clpC1 | 4039079 | c.1626C>G | synonymous_variant | 0.64 |
clpC1 | 4039085 | c.1620A>G | synonymous_variant | 0.58 |
clpC1 | 4039091 | c.1614G>C | synonymous_variant | 0.6 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.56 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.56 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.5 |
clpC1 | 4039117 | p.Lys530Gln | missense_variant | 0.44 |
clpC1 | 4039118 | c.1587C>G | synonymous_variant | 0.44 |
clpC1 | 4039121 | c.1584T>G | synonymous_variant | 0.48 |
clpC1 | 4039133 | c.1572C>G | synonymous_variant | 0.59 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.48 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.48 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.36 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.36 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.37 |
clpC1 | 4039181 | c.1522_1524delTTGinsCTC | synonymous_variant | 0.39 |
clpC1 | 4039187 | c.1518G>T | synonymous_variant | 0.41 |
clpC1 | 4039190 | c.1515C>G | synonymous_variant | 0.39 |
clpC1 | 4039193 | c.1512C>G | synonymous_variant | 0.37 |
clpC1 | 4039199 | p.Ala502Glu | missense_variant | 0.39 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.16 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.21 |
clpC1 | 4039448 | c.1257A>G | synonymous_variant | 0.24 |
clpC1 | 4039454 | c.1251A>T | synonymous_variant | 0.27 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 0.29 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.29 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.33 |
clpC1 | 4039472 | c.1233G>C | synonymous_variant | 0.31 |
clpC1 | 4039478 | c.1227G>C | synonymous_variant | 0.4 |
clpC1 | 4039481 | c.1224T>G | synonymous_variant | 0.4 |
clpC1 | 4039484 | c.1221T>C | synonymous_variant | 0.4 |
clpC1 | 4039487 | c.1218G>A | synonymous_variant | 0.44 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.59 |
clpC1 | 4039524 | p.Phe394Tyr | missense_variant | 0.59 |
clpC1 | 4039541 | c.1164C>G | synonymous_variant | 0.7 |
clpC1 | 4039561 | p.Ala382Ser | missense_variant | 0.66 |
clpC1 | 4039565 | c.1140G>C | synonymous_variant | 0.66 |
clpC1 | 4039570 | p.Met379Leu | missense_variant | 0.64 |
clpC1 | 4039571 | c.1134G>A | synonymous_variant | 0.64 |
clpC1 | 4039576 | p.Ala377Ser | missense_variant | 0.66 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.66 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.68 |
clpC1 | 4039622 | c.1083C>T | synonymous_variant | 0.75 |
clpC1 | 4039649 | p.Val352Leu | missense_variant | 0.75 |
clpC1 | 4039654 | p.Thr351Ser | missense_variant | 0.78 |
clpC1 | 4039661 | c.1044T>C | synonymous_variant | 0.77 |
clpC1 | 4039670 | p.Val345Ile | missense_variant | 0.71 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.45 |
clpC1 | 4039727 | p.Asp326Glu | missense_variant | 0.42 |
clpC1 | 4039739 | c.966C>G | synonymous_variant | 0.33 |
clpC1 | 4039742 | c.963C>T | synonymous_variant | 0.29 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.23 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.14 |
clpC1 | 4039829 | c.874_876delTTGinsCTC | synonymous_variant | 0.14 |
clpC1 | 4039838 | c.867G>C | synonymous_variant | 0.15 |
clpC1 | 4039874 | p.Asn277Lys | missense_variant | 0.17 |
clpC1 | 4039889 | c.816G>C | synonymous_variant | 0.27 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.29 |
clpC1 | 4039901 | c.804C>G | synonymous_variant | 0.29 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.3 |
clpC1 | 4039907 | c.798G>A | synonymous_variant | 0.29 |
clpC1 | 4039925 | c.780C>G | synonymous_variant | 0.21 |
clpC1 | 4039928 | c.775_777delAGCinsTCG | synonymous_variant | 0.21 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.22 |
clpC1 | 4039937 | c.768G>C | synonymous_variant | 0.25 |
clpC1 | 4039946 | c.759A>C | synonymous_variant | 0.26 |
clpC1 | 4039949 | c.756G>C | synonymous_variant | 0.25 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.32 |
clpC1 | 4039973 | p.Asp244Glu | missense_variant | 0.49 |
clpC1 | 4040000 | p.His235Lys | missense_variant | 0.56 |
clpC1 | 4040003 | c.702G>C | synonymous_variant | 0.55 |
clpC1 | 4040010 | p.Ala232Asn | missense_variant | 0.58 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.67 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.7 |
clpC1 | 4040036 | c.669C>G | synonymous_variant | 0.68 |
clpC1 | 4040042 | c.663C>T | synonymous_variant | 0.68 |
clpC1 | 4040048 | c.657C>T | synonymous_variant | 0.71 |
clpC1 | 4040066 | c.639G>C | synonymous_variant | 0.65 |
clpC1 | 4040087 | c.618G>C | synonymous_variant | 0.38 |
clpC1 | 4040090 | c.615T>G | synonymous_variant | 0.36 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.33 |
clpC1 | 4040108 | c.597G>C | synonymous_variant | 0.24 |
clpC1 | 4040117 | c.588A>G | synonymous_variant | 0.29 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.22 |
clpC1 | 4040273 | c.432T>C | synonymous_variant | 0.17 |
clpC1 | 4040279 | c.426C>G | synonymous_variant | 0.2 |
clpC1 | 4040282 | c.423G>C | synonymous_variant | 0.2 |
clpC1 | 4040288 | p.Ile139Leu | missense_variant | 0.2 |
clpC1 | 4040303 | c.402G>C | synonymous_variant | 0.25 |
clpC1 | 4040306 | c.399G>C | synonymous_variant | 0.24 |
clpC1 | 4040310 | p.Thr132Asn | missense_variant | 0.22 |
clpC1 | 4040315 | p.Glu130Asp | missense_variant | 0.24 |
clpC1 | 4040318 | c.387C>G | synonymous_variant | 0.24 |
clpC1 | 4040324 | c.381G>C | synonymous_variant | 0.3 |
clpC1 | 4040345 | c.360C>G | synonymous_variant | 0.3 |
clpC1 | 4040348 | c.357G>C | synonymous_variant | 0.3 |
clpC1 | 4040354 | c.351A>G | synonymous_variant | 0.27 |
clpC1 | 4040363 | c.342A>C | synonymous_variant | 0.23 |
clpC1 | 4040375 | c.330G>C | synonymous_variant | 0.14 |
panD | 4044213 | c.69C>G | synonymous_variant | 0.12 |
embC | 4240743 | p.Asp294Val | missense_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245795 | p.Ala855Thr | missense_variant | 0.13 |
ubiA | 4269257 | p.Tyr193His | missense_variant | 0.12 |
ethA | 4326367 | c.1107C>T | synonymous_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408176 | c.27T>C | synonymous_variant | 0.15 |