Run ID: ERR4815079
Sample name:
Date: 01-04-2023 13:39:30
Number of reads: 583149
Percentage reads mapped: 46.7
Strain: lineage3
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761127 | p.Ser441Ala | missense_variant | 0.26 | rifampicin |
rpoB | 761196 | p.Leu464Met | missense_variant | 0.21 | rifampicin |
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.7 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.84 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.7 | kanamycin, capreomycin, aminoglycosides, amikacin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6316 | c.-986G>C | upstream_gene_variant | 0.24 |
gyrB | 6323 | p.Val362Leu | missense_variant | 0.21 |
gyrA | 6326 | c.-976_-975delAGinsTC | upstream_gene_variant | 0.21 |
gyrA | 6331 | c.-971A>G | upstream_gene_variant | 0.24 |
gyrB | 6364 | p.Leu375Phe | missense_variant | 0.12 |
gyrB | 6371 | p.Thr378Ser | missense_variant | 0.12 |
gyrB | 6416 | c.1180delC | frameshift_variant | 0.17 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7430 | p.Glu43Asp | missense_variant | 0.14 |
gyrA | 7457 | c.156T>C | synonymous_variant | 0.12 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9135 | p.Ile612Phe | missense_variant | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491027 | p.Asn82Thr | missense_variant | 0.23 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576784 | c.1437C>T | synonymous_variant | 0.22 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.18 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 760692 | p.Lys296Glu | missense_variant | 0.17 |
rpoB | 760916 | c.1110C>T | synonymous_variant | 0.22 |
rpoB | 760920 | p.Leu372Ile | missense_variant | 0.22 |
rpoB | 760926 | p.Thr374Ala | missense_variant | 0.18 |
rpoB | 760931 | c.1125C>G | synonymous_variant | 0.15 |
rpoB | 760973 | c.1167G>C | synonymous_variant | 0.14 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.13 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.14 |
rpoB | 760988 | c.1182C>G | synonymous_variant | 0.14 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.13 |
rpoB | 760997 | c.1191G>C | synonymous_variant | 0.13 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.17 |
rpoB | 761027 | c.1221A>C | synonymous_variant | 0.22 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.24 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.24 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.19 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.19 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.19 |
rpoB | 761063 | c.1257C>G | synonymous_variant | 0.19 |
rpoB | 761088 | c.1282_1284delAGCinsTCG | synonymous_variant | 0.27 |
rpoB | 761097 | c.1291_1292delAGinsTC | synonymous_variant | 0.26 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.26 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 0.26 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.26 |
rpoB | 761138 | c.1332C>G | synonymous_variant | 0.26 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.31 |
rpoB | 761156 | c.1350G>C | synonymous_variant | 0.28 |
rpoB | 761162 | c.1356G>C | synonymous_variant | 0.27 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.23 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.24 |
rpoB | 761174 | c.1368T>C | synonymous_variant | 0.24 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.2 |
rpoB | 761183 | c.1377T>C | synonymous_variant | 0.2 |
rpoB | 761186 | p.Glu460Asp | missense_variant | 0.24 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.21 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.24 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.19 |
rpoB | 761963 | c.2157G>C | synonymous_variant | 0.18 |
rpoB | 761974 | p.His723Leu | missense_variant | 0.18 |
rpoB | 762003 | p.Asn733Gln | missense_variant | 0.33 |
rpoB | 762009 | p.Leu735Met | missense_variant | 0.35 |
rpoB | 762015 | p.Glu737Ser | missense_variant | 0.32 |
rpoB | 762026 | c.2220G>C | synonymous_variant | 0.42 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.41 |
rpoB | 762057 | p.Ile751Val | missense_variant | 0.39 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.44 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.43 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.32 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.34 |
rpoB | 762110 | c.2304G>C | synonymous_variant | 0.14 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.13 |
rpoB | 762122 | p.Asp772Glu | missense_variant | 0.13 |
rpoB | 762426 | p.Ser874Thr | missense_variant | 0.15 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoB | 762441 | p.Leu879Met | missense_variant | 0.23 |
rpoC | 762452 | c.-918G>C | upstream_gene_variant | 0.23 |
rpoC | 762470 | c.-900G>C | upstream_gene_variant | 0.18 |
rpoB | 762474 | p.Gly890Ser | missense_variant | 0.18 |
rpoB | 762489 | p.Val895Leu | missense_variant | 0.15 |
rpoC | 762509 | c.-861T>G | upstream_gene_variant | 0.17 |
rpoC | 762512 | c.-858C>G | upstream_gene_variant | 0.17 |
rpoC | 762827 | c.-543G>C | upstream_gene_variant | 0.17 |
rpoB | 762832 | p.Ser1009Thr | missense_variant | 0.25 |
rpoB | 762849 | p.Tyr1015Asp | missense_variant | 0.24 |
rpoC | 762857 | c.-513C>G | upstream_gene_variant | 0.21 |
rpoB | 762858 | p.Thr1018Ser | missense_variant | 0.21 |
rpoC | 762863 | c.-507T>G | upstream_gene_variant | 0.21 |
rpoB | 762878 | p.Ile1024Met | missense_variant | 0.25 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.25 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.29 |
rpoC | 762926 | c.-444C>G | upstream_gene_variant | 0.26 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.23 |
rpoC | 762947 | c.-423C>G | upstream_gene_variant | 0.16 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 0.12 |
rpoC | 762980 | c.-390T>C | upstream_gene_variant | 0.12 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763483 | c.114G>C | synonymous_variant | 0.12 |
rpoC | 763486 | c.117T>G | synonymous_variant | 0.12 |
rpoC | 763504 | c.135C>A | synonymous_variant | 0.18 |
rpoC | 763507 | c.138G>C | synonymous_variant | 0.26 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.26 |
rpoC | 763531 | c.162G>C | synonymous_variant | 0.26 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.26 |
rpoC | 763537 | c.168C>T | synonymous_variant | 0.25 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.26 |
rpoC | 763550 | p.Tyr61Ala | missense_variant | 0.26 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.35 |
rpoC | 763622 | p.Ala85Ser | missense_variant | 0.41 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.41 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.41 |
rpoC | 763639 | p.Glu90Asp | missense_variant | 0.42 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.44 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.5 |
rpoC | 763663 | c.294C>T | synonymous_variant | 0.5 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.46 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.44 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.4 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.36 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.35 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.29 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.24 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.23 |
rpoC | 763765 | c.396T>G | synonymous_variant | 0.23 |
rpoC | 763768 | c.399C>G | synonymous_variant | 0.21 |
rpoC | 763772 | p.Val135Met | missense_variant | 0.19 |
rpoC | 764308 | c.939G>C | synonymous_variant | 0.13 |
rpoC | 764344 | c.975C>T | synonymous_variant | 0.29 |
rpoC | 764359 | c.990C>G | synonymous_variant | 0.35 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 0.38 |
rpoC | 764377 | c.1008C>G | synonymous_variant | 0.38 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.43 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 0.46 |
rpoC | 764404 | c.1035C>T | synonymous_variant | 0.46 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.48 |
rpoC | 764419 | c.1050C>T | synonymous_variant | 0.64 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.64 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.63 |
rpoC | 764435 | c.1066A>C | synonymous_variant | 0.65 |
rpoC | 764441 | p.Ile358Leu | missense_variant | 0.72 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.58 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.58 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.56 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.57 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.58 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.62 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.62 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 0.67 |
rpoC | 764507 | p.Ala380Ser | missense_variant | 0.69 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.66 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.69 |
rpoC | 764542 | c.1173C>G | synonymous_variant | 0.69 |
rpoC | 764548 | c.1179G>C | synonymous_variant | 0.76 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.72 |
rpoC | 764575 | c.1206T>C | synonymous_variant | 0.68 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.71 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.72 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.74 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.65 |
rpoC | 764635 | c.1266C>G | synonymous_variant | 0.64 |
rpoC | 764650 | c.1281G>C | synonymous_variant | 0.63 |
rpoC | 764665 | c.1296C>G | synonymous_variant | 0.58 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 0.55 |
rpoC | 764671 | c.1302G>C | synonymous_variant | 0.57 |
rpoC | 764695 | c.1326T>C | synonymous_variant | 0.52 |
rpoC | 764701 | c.1332C>G | synonymous_variant | 0.51 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.5 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.4 |
rpoC | 764749 | c.1380G>C | synonymous_variant | 0.4 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.38 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.36 |
rpoC | 764780 | c.1411_1412delAGinsTC | synonymous_variant | 0.41 |
rpoC | 764804 | p.Gln479Phe | missense_variant | 0.3 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.26 |
rpoC | 764812 | c.1443C>G | synonymous_variant | 0.26 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.26 |
rpoC | 764818 | c.1449G>C | synonymous_variant | 0.26 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 0.26 |
rpoC | 764833 | c.1464A>G | synonymous_variant | 0.26 |
rpoC | 764843 | p.Ala492Thr | missense_variant | 0.29 |
rpoC | 764857 | c.1488G>C | synonymous_variant | 0.28 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.26 |
rpoC | 764872 | c.1503A>C | synonymous_variant | 0.3 |
rpoC | 764887 | c.1518G>T | synonymous_variant | 0.32 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.25 |
rpoC | 764893 | c.1524T>C | synonymous_variant | 0.29 |
rpoC | 766877 | p.Ser1170Thr | missense_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777136 | p.Met449Leu | missense_variant | 0.2 |
mmpL5 | 777142 | p.Val447Met | missense_variant | 0.2 |
mmpL5 | 777159 | c.1321delG | frameshift_variant | 0.25 |
mmpL5 | 777166 | p.Ser439Ala | missense_variant | 0.25 |
mmpL5 | 777167 | p.Phe438Leu | missense_variant | 0.25 |
mmpL5 | 777170 | c.1310_1311insC | frameshift_variant | 0.25 |
mmpL5 | 777173 | c.1308C>G | synonymous_variant | 0.25 |
mmpL5 | 777176 | p.Glu435Asp | missense_variant | 0.25 |
mmpL5 | 777179 | c.1302G>C | synonymous_variant | 0.25 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.15 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.15 |
rpsL | 781796 | p.Met79Ile | missense_variant | 0.15 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.13 |
rpsL | 781805 | c.246G>C | synonymous_variant | 0.14 |
Rv1258c | 1407084 | p.Val86Gly | missense_variant | 0.2 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471967 | n.122G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1471972 | n.127T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1471980 | n.135G>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1471981 | n.136C>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472389 | n.544G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472674 | n.829T>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472686 | n.841G>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472973 | n.1128A>C | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472974 | n.1129A>G | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.47 |
rrs | 1473022 | n.1177G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473026 | n.1181T>C | non_coding_transcript_exon_variant | 0.59 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473089 | n.1244A>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473122 | n.1277T>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.68 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473317 | n.1472G>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1473844 | n.187C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473870 | n.213G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473871 | n.214T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1473887 | n.230T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473888 | n.231T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473899 | n.242A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474124 | n.467G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474125 | n.468C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474133 | n.476T>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474141 | n.484G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474142 | n.485C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474155 | n.498G>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474164 | n.507C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474186 | n.529A>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474202 | n.545T>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474263 | n.606G>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474275 | n.618T>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474280 | n.623C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474281 | n.624A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474291 | n.635_649delTTCCTCTCCGGAGGA | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474316 | n.659T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474317 | n.660G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474354 | n.697C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474359 | n.702C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474381 | n.724T>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474627 | n.970G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474662 | n.1005C>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474688 | n.1031G>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474710 | n.1053T>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474711 | n.1054_1055insAA | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474714 | n.1058delT | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474717 | n.1060A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474751 | n.1094G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474777 | n.1120T>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474784 | n.1127C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474830 | n.1173A>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475713 | n.2056C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475747 | n.2090A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475757 | n.2101_2104delACCC | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475764 | n.2107A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475765 | n.2108A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475766 | n.2109G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475781 | n.2124T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476130 | n.2473G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476186 | n.2529T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476253 | n.2596A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476308 | n.2651G>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.36 |
rpsA | 1833668 | p.Ile43Val | missense_variant | 0.18 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.16 |
rpsA | 1833685 | c.144G>C | synonymous_variant | 0.2 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.24 |
rpsA | 1833697 | c.156C>G | synonymous_variant | 0.27 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.4 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.35 |
rpsA | 1833733 | c.192C>G | synonymous_variant | 0.33 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.33 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.36 |
rpsA | 1833763 | c.222C>G | synonymous_variant | 0.36 |
rpsA | 1833769 | c.228C>G | synonymous_variant | 0.29 |
rpsA | 1833770 | p.Asn77Asp | missense_variant | 0.29 |
rpsA | 1833781 | c.240T>G | synonymous_variant | 0.24 |
rpsA | 1833782 | p.Ser81Ala | missense_variant | 0.24 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.24 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.24 |
rpsA | 1833794 | p.Glu85Thr | missense_variant | 0.24 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.25 |
rpsA | 1833811 | c.270G>C | synonymous_variant | 0.3 |
rpsA | 1833829 | c.288A>G | synonymous_variant | 0.37 |
rpsA | 1833835 | c.294C>T | synonymous_variant | 0.36 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.34 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.34 |
rpsA | 1833850 | c.309C>G | synonymous_variant | 0.31 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.3 |
rpsA | 1833862 | c.321G>C | synonymous_variant | 0.27 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.25 |
rpsA | 1833884 | p.Thr115Asp | missense_variant | 0.18 |
rpsA | 1833893 | p.Ala118Lys | missense_variant | 0.16 |
rpsA | 1833896 | p.Leu119Ile | missense_variant | 0.17 |
rpsA | 1833905 | p.Lys122Glu | missense_variant | 0.17 |
rpsA | 1833912 | p.Glu124Gly | missense_variant | 0.18 |
rpsA | 1833915 | p.Ala125Val | missense_variant | 0.18 |
rpsA | 1833920 | p.Lys127Glu | missense_variant | 0.19 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.19 |
rpsA | 1833940 | c.399C>G | synonymous_variant | 0.17 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.21 |
rpsA | 1833955 | c.414G>C | synonymous_variant | 0.12 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.2 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.18 |
rpsA | 1833985 | c.444G>C | synonymous_variant | 0.15 |
rpsA | 1833988 | c.447C>G | synonymous_variant | 0.15 |
rpsA | 1833994 | c.453G>C | synonymous_variant | 0.14 |
rpsA | 1833997 | c.456G>C | synonymous_variant | 0.13 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.19 |
rpsA | 1834025 | p.Gln162Ala | missense_variant | 0.19 |
rpsA | 1834040 | p.Lys167Gln | missense_variant | 0.19 |
rpsA | 1834043 | p.Glu168Lys | missense_variant | 0.19 |
rpsA | 1834046 | p.Ile169Leu | missense_variant | 0.2 |
rpsA | 1834054 | c.513C>G | synonymous_variant | 0.2 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.13 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 0.13 |
rpsA | 1834213 | c.672G>C | synonymous_variant | 0.22 |
rpsA | 1834219 | c.678C>G | synonymous_variant | 0.31 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.32 |
rpsA | 1834225 | c.684C>G | synonymous_variant | 0.32 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 0.34 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.35 |
rpsA | 1834243 | c.702G>C | synonymous_variant | 0.36 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.5 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.59 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.59 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.57 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.57 |
rpsA | 1834303 | c.762T>G | synonymous_variant | 0.52 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.54 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.54 |
rpsA | 1834327 | c.786G>C | synonymous_variant | 0.47 |
rpsA | 1834333 | p.Asp264Glu | missense_variant | 0.45 |
rpsA | 1834336 | c.795C>G | synonymous_variant | 0.41 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.26 |
rpsA | 1834354 | c.813G>T | synonymous_variant | 0.25 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 0.24 |
rpsA | 1834360 | c.819G>C | synonymous_variant | 0.24 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.22 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.26 |
rpsA | 1834369 | c.828C>G | synonymous_variant | 0.29 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.32 |
rpsA | 1834384 | c.843A>G | synonymous_variant | 0.33 |
rpsA | 1834395 | p.Arg285Gln | missense_variant | 0.29 |
rpsA | 1834398 | p.His286Leu | missense_variant | 0.28 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.24 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.26 |
rpsA | 1834418 | p.Ile293Leu | missense_variant | 0.25 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.26 |
rpsA | 1834427 | p.Ile296Val | missense_variant | 0.26 |
rpsA | 1834451 | c.910_912delTTGinsCTC | synonymous_variant | 0.26 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.23 |
rpsA | 1834465 | c.924T>C | synonymous_variant | 0.22 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.18 |
rpsA | 1834486 | p.Glu315Asp | missense_variant | 0.16 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.16 |
rpsA | 1834501 | c.960G>C | synonymous_variant | 0.19 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155173 | c.939C>T | synonymous_variant | 0.15 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.12 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.12 |
PPE35 | 2169475 | p.Gly380Ser | missense_variant | 0.15 |
PPE35 | 2169602 | c.1011C>A | synonymous_variant | 0.14 |
PPE35 | 2169995 | p.Ser206Arg | missense_variant | 0.22 |
PPE35 | 2170196 | p.Ala139Glu | missense_variant | 0.25 |
PPE35 | 2170202 | c.411A>G | synonymous_variant | 0.29 |
PPE35 | 2170398 | p.Tyr72Cys | missense_variant | 0.13 |
Rv1979c | 2222025 | c.1140C>T | synonymous_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
kasA | 2518879 | c.765A>G | synonymous_variant | 0.18 |
kasA | 2518882 | c.768C>A | synonymous_variant | 0.2 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.29 |
thyA | 3074648 | c.-177T>G | upstream_gene_variant | 0.3 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086987 | p.Gln56His | missense_variant | 1.0 |
Rv3083 | 3448873 | p.Ala124Thr | missense_variant | 0.18 |
Rv3083 | 3449562 | c.1059G>A | synonymous_variant | 0.14 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474143 | p.Trp46Tyr | missense_variant | 0.17 |
fprA | 3474165 | c.159C>G | synonymous_variant | 0.15 |
fbiB | 3642877 | p.Lys448Arg | missense_variant | 1.0 |
rpoA | 3877935 | p.Lys191Arg | missense_variant | 0.23 |
rpoA | 3877959 | c.549C>A | synonymous_variant | 0.21 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.21 |
rpoA | 3877971 | p.Asp179Glu | missense_variant | 0.22 |
rpoA | 3877974 | c.534G>C | synonymous_variant | 0.26 |
rpoA | 3877981 | p.Tyr176Phe | missense_variant | 0.23 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.26 |
rpoA | 3877995 | c.513G>C | synonymous_variant | 0.22 |
rpoA | 3878001 | c.507A>C | synonymous_variant | 0.2 |
clpC1 | 4038863 | c.1842G>C | synonymous_variant | 0.12 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.2 |
clpC1 | 4038899 | c.1806C>G | synonymous_variant | 0.15 |
clpC1 | 4039714 | p.Tyr331His | missense_variant | 0.14 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.23 |
clpC1 | 4039730 | c.975C>G | synonymous_variant | 0.29 |
clpC1 | 4039748 | c.957G>C | synonymous_variant | 0.39 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.38 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.35 |
clpC1 | 4039766 | c.939T>C | synonymous_variant | 0.33 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.37 |
clpC1 | 4039773 | p.Lys311Met | missense_variant | 0.37 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.35 |
clpC1 | 4039781 | c.924G>C | synonymous_variant | 0.34 |
clpC1 | 4039787 | c.916_918delTCGinsAGC | synonymous_variant | 0.37 |
clpC1 | 4039814 | c.891C>G | synonymous_variant | 0.43 |
clpC1 | 4039817 | c.888A>T | synonymous_variant | 0.39 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.36 |
clpC1 | 4039823 | c.882T>G | synonymous_variant | 0.36 |
clpC1 | 4039829 | c.874_876delTTGinsCTC | synonymous_variant | 0.38 |
clpC1 | 4039838 | p.Leu289Ile | missense_variant | 0.35 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.38 |
clpC1 | 4039865 | c.840T>G | synonymous_variant | 0.48 |
clpC1 | 4039871 | c.834C>G | synonymous_variant | 0.48 |
clpC1 | 4039875 | p.Asn277Arg | missense_variant | 0.42 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.25 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.27 |
clpC1 | 4039916 | c.789T>C | synonymous_variant | 0.12 |
clpC1 | 4040009 | c.696C>G | synonymous_variant | 0.19 |
clpC1 | 4040015 | c.690G>C | synonymous_variant | 0.29 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.25 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.31 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.34 |
clpC1 | 4040063 | c.642G>C | synonymous_variant | 0.47 |
clpC1 | 4040069 | c.636G>C | synonymous_variant | 0.45 |
clpC1 | 4040087 | c.618G>C | synonymous_variant | 0.38 |
clpC1 | 4040090 | c.615T>C | synonymous_variant | 0.36 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4248781 | p.Glu756Asp | missense_variant | 0.12 |
aftB | 4268217 | p.Trp207* | stop_gained | 0.17 |
ubiA | 4269280 | p.Leu185Pro | missense_variant | 0.22 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |