Run ID: ERR4821550
Sample name:
Date: 01-04-2023 17:19:01
Number of reads: 492178
Percentage reads mapped: 64.7
Strain: lineage2.2.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 1.0 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.5 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.67 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.5 | kanamycin, capreomycin, aminoglycosides, amikacin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
ccsA | 620754 | c.864G>A | synonymous_variant | 0.18 |
rpoB | 761554 | p.Val583Ala | missense_variant | 0.13 |
rpoB | 761564 | c.1758G>C | synonymous_variant | 0.12 |
rpoB | 761565 | p.Met587Leu | missense_variant | 0.13 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.12 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.12 |
rpoB | 761600 | c.1794T>C | synonymous_variant | 0.13 |
rpoB | 761603 | c.1797C>G | synonymous_variant | 0.13 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.12 |
rpoB | 761615 | c.1809A>G | synonymous_variant | 0.12 |
rpoB | 762003 | p.Asn733Gln | missense_variant | 0.2 |
rpoB | 762017 | c.2211A>G | synonymous_variant | 0.22 |
rpoB | 762026 | c.2220G>C | synonymous_variant | 0.2 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.18 |
rpoB | 762057 | p.Ile751Val | missense_variant | 0.18 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.18 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.18 |
rpoC | 762818 | c.-552C>G | upstream_gene_variant | 0.2 |
rpoC | 762827 | c.-543G>C | upstream_gene_variant | 0.22 |
rpoB | 762832 | p.Ser1009Thr | missense_variant | 0.22 |
rpoB | 762849 | p.Tyr1015Asp | missense_variant | 0.2 |
rpoC | 762857 | c.-513C>G | upstream_gene_variant | 0.22 |
rpoB | 762858 | p.Thr1018Ser | missense_variant | 0.22 |
rpoC | 762863 | c.-507T>G | upstream_gene_variant | 0.27 |
rpoB | 762878 | p.Ile1024Met | missense_variant | 0.27 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.27 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.2 |
rpoC | 762926 | c.-444C>G | upstream_gene_variant | 0.2 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.2 |
rpoC | 762947 | c.-423C>G | upstream_gene_variant | 0.18 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.18 |
rpoC | 762995 | c.-375G>C | upstream_gene_variant | 0.2 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.88 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.2 |
rpoC | 763483 | c.114G>C | synonymous_variant | 0.23 |
rpoC | 763486 | c.117T>G | synonymous_variant | 0.21 |
rpoC | 763492 | c.123G>C | synonymous_variant | 0.14 |
rpoC | 763504 | c.135C>A | synonymous_variant | 0.25 |
rpoC | 763507 | c.138G>C | synonymous_variant | 0.29 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.32 |
rpoC | 763531 | c.162G>C | synonymous_variant | 0.24 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.27 |
rpoC | 763537 | c.168C>T | synonymous_variant | 0.27 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.27 |
rpoC | 763550 | p.Tyr61Ala | missense_variant | 0.25 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.26 |
rpoC | 763622 | p.Ala85Ser | missense_variant | 0.22 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.25 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.25 |
rpoC | 763639 | p.Glu90Asp | missense_variant | 0.24 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.24 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.33 |
rpoC | 763663 | c.294C>T | synonymous_variant | 0.14 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.27 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.33 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.33 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.25 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.25 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.18 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.17 |
rpoC | 764344 | c.975C>T | synonymous_variant | 0.14 |
rpoC | 764359 | c.990C>G | synonymous_variant | 0.14 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 0.14 |
rpoC | 764377 | c.1008C>G | synonymous_variant | 0.14 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.16 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 0.11 |
rpoC | 764404 | c.1035C>T | synonymous_variant | 0.19 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.2 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.27 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.29 |
rpoC | 764435 | c.1066A>C | synonymous_variant | 0.29 |
rpoC | 764441 | p.Ile358Leu | missense_variant | 0.31 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.31 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.31 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.29 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.33 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.33 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.31 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.42 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.36 |
rpoC | 764635 | c.1266C>G | synonymous_variant | 0.36 |
rpoC | 764650 | c.1281G>C | synonymous_variant | 0.36 |
rpoC | 764665 | c.1296C>G | synonymous_variant | 0.31 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 0.31 |
rpoC | 764671 | c.1302G>C | synonymous_variant | 0.31 |
rpoC | 764695 | c.1326T>C | synonymous_variant | 0.33 |
rpoC | 764701 | c.1332C>G | synonymous_variant | 0.3 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.45 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.36 |
rpoC | 764749 | c.1380G>C | synonymous_variant | 0.33 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.36 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.46 |
rpoC | 764780 | c.1411_1412delAGinsTC | synonymous_variant | 0.42 |
rpoC | 764804 | p.Gln479Phe | missense_variant | 0.3 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.3 |
rpoC | 764812 | c.1443C>G | synonymous_variant | 0.3 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.27 |
rpoC | 764818 | c.1449G>C | synonymous_variant | 0.27 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 0.33 |
rpoC | 764833 | c.1464A>G | synonymous_variant | 0.43 |
rpoC | 764843 | p.Ala492Thr | missense_variant | 0.43 |
rpoC | 764857 | c.1488G>C | synonymous_variant | 0.29 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.2 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 777805 | p.Ile226Phe | missense_variant | 0.4 |
mmpS5 | 778588 | p.Gln106His | missense_variant | 1.0 |
mmpR5 | 779188 | p.Ile67Val | missense_variant | 0.2 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.13 |
rpsL | 781658 | c.99A>G | synonymous_variant | 0.12 |
rpsL | 781682 | c.123T>C | synonymous_variant | 0.11 |
rpsL | 781700 | c.141G>C | synonymous_variant | 0.1 |
rpsL | 781739 | c.180G>A | synonymous_variant | 0.15 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.12 |
rpsL | 781790 | c.231C>T | synonymous_variant | 0.14 |
rpsL | 781796 | p.Met79Ile | missense_variant | 0.12 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.12 |
rpsL | 781805 | c.246G>C | synonymous_variant | 0.13 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.13 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.13 |
rpsL | 781933 | c.374G>T | stop_lost&splice_region_variant | 0.12 |
fbiC | 1304802 | c.1872G>T | synonymous_variant | 0.18 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
embR | 1416409 | c.939G>A | synonymous_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472213 | n.368G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472223 | n.378C>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472228 | n.383G>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472235 | n.390G>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472236 | n.391C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472240 | n.395G>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472242 | n.397C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472266 | n.421C>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472389 | n.544G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472674 | n.829T>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472686 | n.841G>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472812 | n.967A>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472973 | n.1128A>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472974 | n.1129A>G | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472996 | n.1151T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473022 | n.1177G>A | non_coding_transcript_exon_variant | 0.58 |
rrs | 1473026 | n.1181T>C | non_coding_transcript_exon_variant | 0.58 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473089 | n.1244A>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473122 | n.1277T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473317 | n.1472G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474155 | n.498G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474164 | n.507C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474186 | n.529A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474202 | n.545T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474627 | n.970G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474662 | n.1005C>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474688 | n.1031G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475713 | n.2056C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475747 | n.2090A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475757 | n.2101_2110delACCCGCAAGG | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475769 | n.2112_2113insAGTCTTTGACTGC | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475781 | n.2124T>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.5 |
rpsA | 1833653 | p.Ile38Leu | missense_variant | 0.2 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.2 |
rpsA | 1833668 | p.Ile43Val | missense_variant | 0.18 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.15 |
rpsA | 1833685 | c.144G>C | synonymous_variant | 0.14 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.13 |
rpsA | 1833697 | c.156C>G | synonymous_variant | 0.12 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.13 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.2 |
rpsA | 1833985 | c.444G>C | synonymous_variant | 0.14 |
rpsA | 1833994 | c.453G>C | synonymous_variant | 0.15 |
rpsA | 1833997 | c.456G>C | synonymous_variant | 0.15 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.15 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.14 |
rpsA | 1834024 | c.483G>C | synonymous_variant | 0.13 |
rpsA | 1834034 | p.Ile165Val | missense_variant | 0.12 |
rpsA | 1834040 | p.Lys167Gln | missense_variant | 0.2 |
rpsA | 1834043 | p.Glu168Lys | missense_variant | 0.13 |
rpsA | 1834046 | p.Ile169Leu | missense_variant | 0.13 |
rpsA | 1834054 | c.513C>G | synonymous_variant | 0.14 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834213 | c.672G>C | synonymous_variant | 0.15 |
rpsA | 1834219 | c.678C>G | synonymous_variant | 0.14 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.14 |
rpsA | 1834225 | c.684C>G | synonymous_variant | 0.14 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 0.14 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.12 |
rpsA | 1834243 | c.702G>C | synonymous_variant | 0.12 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.18 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.22 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.2 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.18 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.12 |
rpsA | 1834303 | c.762T>G | synonymous_variant | 0.12 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.12 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.12 |
rpsA | 1834327 | c.786G>C | synonymous_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102709 | p.Tyr112Asn | missense_variant | 0.11 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2222617 | p.Trp183Ser | missense_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ahpC | 2726613 | p.Asn141Asp | missense_variant | 0.18 |
folC | 2746895 | p.Gly235Ala | missense_variant | 0.17 |
ribD | 2987445 | p.Val203Ile | missense_variant | 0.18 |
thyA | 3074035 | c.436delT | frameshift_variant | 0.22 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449396 | c.894delC | frameshift_variant | 0.14 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475118 | p.Asn371Ser | missense_variant | 0.25 |
Rv3236c | 3612506 | p.His204Leu | missense_variant | 0.29 |
Rv3236c | 3612717 | p.Ala134Thr | missense_variant | 0.18 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
alr | 3841442 | c.-22G>T | upstream_gene_variant | 0.13 |
clpC1 | 4039730 | c.975C>G | synonymous_variant | 0.22 |
clpC1 | 4039789 | p.Ser306Thr | missense_variant | 0.18 |
clpC1 | 4039977 | p.Lys243Arg | missense_variant | 0.2 |
clpC1 | 4039988 | c.717C>G | synonymous_variant | 0.18 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 0.17 |
clpC1 | 4039994 | p.Glu237Asp | missense_variant | 0.17 |
clpC1 | 4040001 | p.His235Arg | missense_variant | 0.15 |
clpC1 | 4040003 | p.Val234Asp | missense_variant | 0.15 |
clpC1 | 4040009 | c.696C>G | synonymous_variant | 0.18 |
clpC1 | 4040013 | p.Gln231Leu | missense_variant | 0.11 |
clpC1 | 4040015 | c.690G>C | synonymous_variant | 0.16 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.16 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.26 |
clpC1 | 4040032 | p.Val225Ile | missense_variant | 0.11 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.17 |
clpC1 | 4040036 | c.669C>G | synonymous_variant | 0.12 |
clpC1 | 4040051 | c.654C>G | synonymous_variant | 0.11 |
clpC1 | 4040072 | c.633C>T | synonymous_variant | 0.12 |
embC | 4240277 | c.415T>C | synonymous_variant | 0.15 |
embC | 4241822 | p.Phe654Leu | missense_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268215 | p.Arg208Cys | missense_variant | 0.22 |
ubiA | 4269946 | c.-113G>T | upstream_gene_variant | 0.14 |
ubiA | 4270001 | c.-168C>T | upstream_gene_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |