Run ID: ERR5311077
Sample name:
Date: 01-04-2023 22:30:31
Number of reads: 1486757
Percentage reads mapped: 50.58
Strain: La1.8.1
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
La1 | M.bovis | None | None | 1.0 |
La1.8 | M.bovis | None | None | 1.0 |
La1.8.1 | M.bovis | None | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761196 | p.Leu464Met | missense_variant | 0.19 | rifampicin |
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.94 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.97 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.89 | kanamycin, capreomycin, aminoglycosides, amikacin |
pncA | 2289073 | p.His57Asp | missense_variant | 1.0 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5752 | c.513G>A | synonymous_variant | 1.0 |
gyrA | 6406 | c.-896C>T | upstream_gene_variant | 1.0 |
gyrB | 6446 | p.Ala403Ser | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8032 | p.Tyr244Ser | missense_variant | 0.17 |
gyrA | 8285 | c.984C>T | synonymous_variant | 1.0 |
gyrA | 8741 | c.1440C>T | synonymous_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9217 | p.Asp639Ala | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.12 |
rpoB | 760940 | c.1134G>C | synonymous_variant | 0.13 |
rpoB | 760944 | p.Gln380Glu | missense_variant | 0.14 |
rpoB | 760953 | p.Ile383Val | missense_variant | 0.13 |
rpoB | 760958 | c.1152G>C | synonymous_variant | 0.13 |
rpoB | 760960 | p.Val385Ala | missense_variant | 0.13 |
rpoB | 760965 | p.Met387Leu | missense_variant | 0.13 |
rpoB | 760970 | c.1164G>C | synonymous_variant | 0.13 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.17 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.17 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.22 |
rpoB | 760997 | c.1191G>T | synonymous_variant | 0.32 |
rpoB | 761003 | c.1197C>G | synonymous_variant | 0.38 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.48 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 0.44 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.42 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.38 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.39 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.41 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.4 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.4 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.41 |
rpoB | 761063 | c.1257C>A | synonymous_variant | 0.45 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.46 |
rpoB | 761087 | c.1281C>G | synonymous_variant | 0.46 |
rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 0.46 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.46 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.5 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 0.52 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.52 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.39 |
rpoB | 761159 | c.1353G>T | synonymous_variant | 0.25 |
rpoB | 761162 | c.1356G>T | synonymous_variant | 0.18 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.18 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.19 |
rpoB | 761171 | c.1365C>T | synonymous_variant | 0.2 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.21 |
rpoB | 761186 | p.Glu460Asp | missense_variant | 0.21 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.21 |
rpoB | 761192 | c.1386C>A | synonymous_variant | 0.21 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.2 |
rpoB | 761201 | c.1395G>A | synonymous_variant | 0.19 |
rpoB | 761207 | c.1401C>A | synonymous_variant | 0.18 |
rpoB | 761213 | c.1407G>T | synonymous_variant | 0.18 |
rpoB | 761222 | c.1416G>C | synonymous_variant | 0.17 |
rpoB | 761231 | c.1425C>A | synonymous_variant | 0.17 |
rpoB | 761234 | c.1428G>T | synonymous_variant | 0.16 |
rpoB | 761243 | c.1437G>C | synonymous_variant | 0.17 |
rpoB | 762849 | p.Tyr1015Asp | missense_variant | 0.18 |
rpoB | 762855 | p.Val1017Ile | missense_variant | 0.18 |
rpoB | 762858 | p.Thr1018Ser | missense_variant | 0.17 |
rpoC | 762863 | c.-507T>C | upstream_gene_variant | 0.17 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.18 |
rpoC | 762887 | c.-483G>C | upstream_gene_variant | 0.18 |
rpoC | 762914 | c.-456C>T | upstream_gene_variant | 0.17 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 0.17 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.17 |
rpoC | 762938 | c.-432G>C | upstream_gene_variant | 0.15 |
rpoC | 762947 | c.-423C>G | upstream_gene_variant | 0.16 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763453 | c.84C>T | synonymous_variant | 0.19 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.29 |
rpoC | 763465 | c.96G>A | synonymous_variant | 0.36 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.41 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.48 |
rpoC | 763492 | c.123G>T | synonymous_variant | 0.49 |
rpoC | 763507 | c.138G>C | synonymous_variant | 0.57 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.67 |
rpoC | 763532 | p.Thr55Ser | missense_variant | 0.65 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.68 |
rpoC | 763558 | c.189C>T | synonymous_variant | 0.67 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.65 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.64 |
rpoC | 763600 | c.231C>G | synonymous_variant | 0.62 |
rpoC | 763603 | c.234C>T | synonymous_variant | 0.6 |
rpoC | 763609 | c.240C>T | synonymous_variant | 0.57 |
rpoC | 763615 | c.246G>C | synonymous_variant | 0.55 |
rpoC | 763624 | c.255C>A | synonymous_variant | 0.52 |
rpoC | 763630 | c.261G>C | synonymous_variant | 0.51 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.52 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.53 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.42 |
rpoC | 763666 | c.297G>C | synonymous_variant | 0.38 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.36 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.34 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.29 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.27 |
rpoC | 763705 | c.336G>C | synonymous_variant | 0.29 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.3 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.31 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.31 |
rpoC | 763720 | c.351G>C | synonymous_variant | 0.31 |
rpoC | 763723 | c.354G>T | synonymous_variant | 0.31 |
rpoC | 763732 | c.363C>A | synonymous_variant | 0.3 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.3 |
rpoC | 763747 | c.378G>A | synonymous_variant | 0.28 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.25 |
rpoC | 763756 | c.387C>T | synonymous_variant | 0.24 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.15 |
rpoC | 764353 | c.984G>C | synonymous_variant | 0.21 |
rpoC | 764359 | c.990C>G | synonymous_variant | 0.19 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.21 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 0.23 |
rpoC | 764377 | c.1008C>G | synonymous_variant | 0.22 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.22 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 0.23 |
rpoC | 764398 | c.1029G>C | synonymous_variant | 0.23 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.24 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.19 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.19 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.19 |
rpoC | 764435 | c.1066_1068delAGGinsCGC | synonymous_variant | 0.19 |
rpoC | 764441 | p.Ile358Leu | missense_variant | 0.19 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.2 |
rpoC | 764455 | c.1086G>C | synonymous_variant | 0.28 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.26 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.24 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.19 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 0.19 |
rpoC | 764503 | c.1134G>T | synonymous_variant | 0.19 |
rpoC | 764507 | p.Ala380Ser | missense_variant | 0.18 |
rpoC | 764512 | c.1143G>C | synonymous_variant | 0.18 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.22 |
rpoC | 764536 | c.1167G>T | synonymous_variant | 0.28 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.31 |
rpoC | 764548 | c.1179G>A | synonymous_variant | 0.33 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.31 |
rpoC | 764572 | c.1203G>C | synonymous_variant | 0.28 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.28 |
rpoC | 764576 | c.1207_1208delTCinsAG | synonymous_variant | 0.28 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.28 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.28 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.37 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 0.41 |
rpoC | 764611 | c.1242G>C | synonymous_variant | 0.4 |
rpoC | 764620 | c.1251G>C | synonymous_variant | 0.46 |
rpoC | 764623 | c.1254C>G | synonymous_variant | 0.49 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.52 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.51 |
rpoC | 764635 | c.1266C>T | synonymous_variant | 0.51 |
rpoC | 764644 | c.1275G>C | synonymous_variant | 0.5 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.52 |
rpoC | 764653 | c.1284G>T | synonymous_variant | 0.52 |
rpoC | 764656 | c.1287C>G | synonymous_variant | 0.51 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.42 |
rpoC | 764692 | c.1323C>T | synonymous_variant | 0.4 |
rpoC | 764695 | c.1326T>C | synonymous_variant | 0.39 |
rpoC | 764701 | c.1332C>G | synonymous_variant | 0.41 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.44 |
rpoC | 764722 | c.1353G>C | synonymous_variant | 0.49 |
rpoC | 764746 | c.1377G>C | synonymous_variant | 0.46 |
rpoC | 764752 | c.1383G>T | synonymous_variant | 0.43 |
rpoC | 764761 | c.1392C>T | synonymous_variant | 0.28 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.24 |
rpoC | 764767 | c.1398G>C | synonymous_variant | 0.23 |
rpoC | 764780 | c.1411_1413delAGCinsTCG | synonymous_variant | 0.14 |
rpoC | 764788 | c.1419G>A | synonymous_variant | 0.15 |
rpoC | 764791 | c.1422C>G | synonymous_variant | 0.14 |
rpoC | 764797 | c.1428G>C | synonymous_variant | 0.14 |
rpoC | 764806 | p.Gln479His | missense_variant | 0.14 |
rpoC | 764812 | c.1443C>G | synonymous_variant | 0.15 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.15 |
rpoC | 764818 | c.1449G>C | synonymous_variant | 0.15 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.18 |
rpoC | 764837 | p.Val490Ile | missense_variant | 0.17 |
rpoC | 764843 | p.Ala492Thr | missense_variant | 0.17 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.12 |
rpoC | 764932 | c.1563C>A | synonymous_variant | 0.13 |
rpoC | 764935 | c.1566T>C | synonymous_variant | 0.12 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.12 |
rpoC | 764953 | c.1584G>T | synonymous_variant | 0.13 |
rpoC | 764958 | p.Glu530Gly | missense_variant | 0.14 |
rpoC | 764962 | c.1593G>C | synonymous_variant | 0.2 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.2 |
rpoC | 764971 | c.1602C>T | synonymous_variant | 0.2 |
rpoC | 764983 | c.1614T>C | synonymous_variant | 0.19 |
rpoC | 764995 | c.1626C>A | synonymous_variant | 0.16 |
rpoC | 764998 | c.1629G>C | synonymous_variant | 0.15 |
rpoC | 765007 | c.1638T>G | synonymous_variant | 0.15 |
rpoC | 765008 | c.1639T>C | synonymous_variant | 0.15 |
rpoC | 765014 | p.Ala549Pro | missense_variant | 0.14 |
rpoC | 765034 | c.1665T>C | synonymous_variant | 0.16 |
rpoC | 765040 | c.1671T>C | synonymous_variant | 0.15 |
rpoC | 765041 | c.1672T>C | synonymous_variant | 0.15 |
rpoC | 765047 | c.1678T>C | synonymous_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781851 | p.Ile98Val | missense_variant | 0.14 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.15 |
rpsL | 781901 | c.342C>T | synonymous_variant | 0.16 |
rpsL | 781907 | c.348T>C | synonymous_variant | 0.15 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472338 | n.493A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472340 | n.495C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472389 | n.544G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472476 | n.631A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472495 | n.650C>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472582 | n.737G>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472674 | n.829T>G | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472675 | n.830T>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473026 | n.1181T>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473122 | n.1277T>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1473393 | n.-265A>T | upstream_gene_variant | 0.12 |
rrl | 1473833 | n.176_177insT | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473871 | n.214T>C | non_coding_transcript_exon_variant | 0.47 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473888 | n.231T>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473899 | n.242A>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473922 | n.265A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474153 | n.496C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474155 | n.498G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474164 | n.507C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474166 | n.509G>A | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474185 | n.528G>A | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474201 | n.544T>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474202 | n.545T>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474249 | n.592G>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474281 | n.624A>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474286 | n.629_630insAG | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474289 | n.632C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474290 | n.633T>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474291 | n.634T>A | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474294 | n.638_652delCTCTCCGGAGGAGGG | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474316 | n.659T>C | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1474353 | n.696A>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1474354 | n.697C>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.87 |
rrl | 1474381 | n.724T>A | non_coding_transcript_exon_variant | 0.85 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474413 | n.756A>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474414 | n.757C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474415 | n.758C>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474416 | n.761_784delCACGCGCATACGCGCGTGTGAATA | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474450 | n.793T>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474454 | n.797G>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474466 | n.809G>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474496 | n.839C>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474583 | n.926C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474664 | n.1007G>A | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474709 | n.1053_1056delTGGT | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474717 | n.1060_1061insGTGAG | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474722 | n.1065T>C | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474723 | n.1066G>A | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474751 | n.1094G>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474777 | n.1120T>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474783 | n.1126G>A | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474869 | n.1212G>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.84 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474945 | n.1288C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475060 | n.1404delC | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475065 | n.1408G>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475067 | n.1410A>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475068 | n.1411A>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475076 | n.1419C>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475078 | n.1421T>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475079 | n.1422T>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475081 | n.1424C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1475093 | n.1436C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1475104 | n.1447T>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1475108 | n.1451C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1475111 | n.1454G>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1475116 | n.1459G>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1475119 | n.1462C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1475124 | n.1467A>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1475129 | n.1472G>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1475515 | n.1858G>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475538 | n.1881T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475548 | n.1891C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475649 | n.1992A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475655 | n.1998T>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475783 | n.2126T>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.93 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1475963 | n.2306G>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475996 | n.2339T>A | non_coding_transcript_exon_variant | 0.79 |
rrl | 1475997 | n.2340A>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1475998 | n.2341C>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476024 | n.2367T>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476025 | n.2368G>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476033 | n.2376T>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476045 | n.2388G>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476056 | n.2399G>A | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476058 | n.2401T>C | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476076 | n.2419A>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476079 | n.2422G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476080 | n.2423T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476081 | n.2424A>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476095 | n.2438C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476104 | n.2447T>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476105 | n.2448G>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476113 | n.2456T>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476130 | n.2473G>A | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476165 | n.2508T>A | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476251 | n.2594T>A | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476308 | n.2651G>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476523 | n.2866T>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476586 | n.2929C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476594 | n.2937C>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476596 | n.2939C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476601 | n.2944G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476603 | n.2946G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476613 | n.2956G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476629 | n.2972C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.4 |
rpsA | 1833970 | c.429G>T | synonymous_variant | 0.18 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.21 |
rpsA | 1833991 | c.450C>A | synonymous_variant | 0.28 |
rpsA | 1833994 | c.453G>C | synonymous_variant | 0.28 |
rpsA | 1833997 | c.456G>C | synonymous_variant | 0.28 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.28 |
rpsA | 1834012 | c.471G>T | synonymous_variant | 0.28 |
rpsA | 1834024 | c.483G>C | synonymous_variant | 0.3 |
rpsA | 1834025 | p.Gln162Ala | missense_variant | 0.32 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.29 |
rpsA | 1834039 | c.498C>T | synonymous_variant | 0.3 |
rpsA | 1834040 | p.Lys167Gln | missense_variant | 0.3 |
rpsA | 1834043 | p.Glu168Lys | missense_variant | 0.3 |
rpsA | 1834051 | c.510G>A | synonymous_variant | 0.35 |
rpsA | 1834057 | c.516G>A | synonymous_variant | 0.36 |
rpsA | 1834090 | c.549G>T | synonymous_variant | 0.33 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.26 |
rpsA | 1834105 | c.564C>T | synonymous_variant | 0.19 |
rpsA | 1834114 | c.573G>C | synonymous_variant | 0.15 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.12 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.12 |
rpsA | 1834294 | c.753G>T | synonymous_variant | 0.17 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.17 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.19 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.19 |
rpsA | 1834312 | c.771G>A | synonymous_variant | 0.19 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.26 |
rpsA | 1834333 | p.Asp264Glu | missense_variant | 0.27 |
rpsA | 1834340 | p.Met267Leu | missense_variant | 0.24 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.25 |
rpsA | 1834354 | c.813G>T | synonymous_variant | 0.22 |
rpsA | 1834360 | c.819G>C | synonymous_variant | 0.23 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.23 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.21 |
rpsA | 1834375 | c.834G>T | synonymous_variant | 0.26 |
rpsA | 1834378 | c.837T>G | synonymous_variant | 0.26 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.23 |
rpsA | 1834395 | p.Arg285Gln | missense_variant | 0.21 |
rpsA | 1834397 | p.His286Thr | missense_variant | 0.21 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.24 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.17 |
rpsA | 1834427 | p.Ile296Val | missense_variant | 0.19 |
rpsA | 1834438 | c.897C>T | synonymous_variant | 0.22 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.22 |
rpsA | 1834859 | p.Ala440Thr | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102193 | p.Arg284Trp | missense_variant | 1.0 |
ndh | 2103173 | c.-132delG | upstream_gene_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155503 | c.609C>T | synonymous_variant | 1.0 |
katG | 2156025 | c.87C>A | synonymous_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168011 | p.Ser868Arg | missense_variant | 1.0 |
PPE35 | 2168319 | p.Thr765Ile | missense_variant | 1.0 |
PPE35 | 2168814 | c.1798dupA | frameshift_variant | 1.0 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
eis | 2715125 | p.Thr70Ala | missense_variant | 1.0 |
ald | 3086728 | c.-92C>T | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087084 | c.266delA | frameshift_variant | 1.0 |
Rv3083 | 3448783 | p.Val94Ile | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474427 | p.Val141Ile | missense_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
Rv3236c | 3613251 | c.-135C>T | upstream_gene_variant | 1.0 |
rpoA | 3878630 | c.-124delC | upstream_gene_variant | 1.0 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 1.0 |
clpC1 | 4040273 | c.432T>C | synonymous_variant | 0.13 |
clpC1 | 4040276 | c.429C>G | synonymous_variant | 0.15 |
clpC1 | 4040291 | c.414G>C | synonymous_variant | 0.18 |
clpC1 | 4040303 | c.402G>C | synonymous_variant | 0.18 |
clpC1 | 4040306 | c.399G>T | synonymous_variant | 0.17 |
clpC1 | 4040310 | p.Thr132Asn | missense_variant | 0.17 |
clpC1 | 4040312 | c.393G>T | synonymous_variant | 0.17 |
clpC1 | 4040315 | p.Glu130Asp | missense_variant | 0.17 |
clpC1 | 4040318 | c.387C>G | synonymous_variant | 0.17 |
clpC1 | 4040324 | c.381G>C | synonymous_variant | 0.17 |
clpC1 | 4040348 | c.357G>A | synonymous_variant | 0.17 |
clpC1 | 4040351 | c.354C>T | synonymous_variant | 0.17 |
clpC1 | 4040363 | c.342A>C | synonymous_variant | 0.17 |
clpC1 | 4040375 | c.330G>C | synonymous_variant | 0.17 |
clpC1 | 4040380 | c.325T>C | synonymous_variant | 0.16 |
clpC1 | 4040381 | c.324T>C | synonymous_variant | 0.16 |
clpC1 | 4040387 | c.318A>G | synonymous_variant | 0.17 |
clpC1 | 4040390 | c.315C>G | synonymous_variant | 0.17 |
clpC1 | 4040393 | c.312G>C | synonymous_variant | 0.19 |
clpC1 | 4040408 | c.297C>A | synonymous_variant | 0.13 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242970 | c.-263C>T | upstream_gene_variant | 1.0 |
embA | 4244220 | c.988C>T | synonymous_variant | 1.0 |
embB | 4246551 | p.Asn13Ser | missense_variant | 1.0 |
embB | 4246864 | c.351C>T | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
aftB | 4267858 | p.Ile327Val | missense_variant | 1.0 |
aftB | 4269351 | c.-515C>T | upstream_gene_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |