Run ID: ERR3597006
Sample name:
Date: 01-04-2023 02:38:05
Number of reads: 3855101
Percentage reads mapped: 97.27
Strain:
Drug-resistance: Sensitive
| Drug | Resistance | Supporting mutations |
|---|
| Lineage | Family | Main Spoligotype | RDs | Frequency |
|---|
| Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
|---|
| Gene | Chromosome position | Mutation | Type | Estimated fraction |
|---|---|---|---|---|
| gyrB | 5207 | c.-33A>C | upstream_gene_variant | 1.0 |
| gyrB | 5440 | c.201A>G | synonymous_variant | 1.0 |
| gyrB | 5452 | c.213G>A | synonymous_variant | 1.0 |
| gyrB | 5770 | c.531C>T | synonymous_variant | 1.0 |
| gyrB | 6001 | c.762G>A | synonymous_variant | 1.0 |
| gyrB | 6004 | c.765T>C | synonymous_variant | 1.0 |
| gyrB | 6286 | c.1047T>C | synonymous_variant | 0.99 |
| gyrA | 6433 | c.-869C>T | upstream_gene_variant | 1.0 |
| gyrA | 6436 | c.-866C>T | upstream_gene_variant | 1.0 |
| gyrA | 7256 | c.-46C>T | upstream_gene_variant | 1.0 |
| gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
| gyrA | 7523 | c.222C>G | synonymous_variant | 1.0 |
| gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
| gyrA | 8288 | c.987T>C | synonymous_variant | 1.0 |
| gyrA | 8654 | c.1353C>T | synonymous_variant | 1.0 |
| gyrA | 9074 | c.1773G>A | synonymous_variant | 1.0 |
| gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
| gyrA | 9218 | c.1917C>T | synonymous_variant | 1.0 |
| gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
| gyrA | 9377 | c.2076A>G | synonymous_variant | 1.0 |
| gyrA | 9716 | c.2415T>C | synonymous_variant | 1.0 |
| gyrA | 9740 | c.2439G>A | synonymous_variant | 1.0 |
| gyrA | 9776 | c.2475T>C | synonymous_variant | 1.0 |
| fgd1 | 490666 | c.-117G>T | upstream_gene_variant | 0.97 |
| fgd1 | 490679 | c.-105_-104insG | upstream_gene_variant | 1.0 |
| fgd1 | 490687 | c.-96T>C | upstream_gene_variant | 1.0 |
| fgd1 | 491406 | p.Met208Ile | missense_variant | 1.0 |
| fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
| mshA | 575665 | c.318G>C | synonymous_variant | 1.0 |
| mshA | 575971 | c.624C>T | synonymous_variant | 1.0 |
| mshA | 576285 | p.Val313Ala | missense_variant | 1.0 |
| mshA | 576757 | c.1410C>G | synonymous_variant | 1.0 |
| ccsA | 620256 | c.366C>G | synonymous_variant | 1.0 |
| ccsA | 620257 | p.Ile123Ala | missense_variant | 1.0 |
| ccsA | 620415 | c.525T>C | synonymous_variant | 1.0 |
| ccsA | 620490 | c.600A>C | synonymous_variant | 1.0 |
| ccsA | 620808 | c.918T>C | synonymous_variant | 1.0 |
| rpoB | 759741 | c.-66C>T | upstream_gene_variant | 1.0 |
| rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
| rpoC | 763660 | c.291T>C | synonymous_variant | 1.0 |
| rpoC | 764152 | c.783C>T | synonymous_variant | 1.0 |
| rpoC | 765478 | c.2109T>C | synonymous_variant | 1.0 |
| rpoC | 766912 | c.3543C>T | synonymous_variant | 1.0 |
| mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
| mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.99 |
| mmpL5 | 778057 | p.Ser142Gly | missense_variant | 1.0 |
| mmpL5 | 778573 | c.-93C>G | upstream_gene_variant | 1.0 |
| mmpL5 | 779283 | c.-803G>A | upstream_gene_variant | 0.99 |
| mmpL5 | 779295 | c.-815A>G | upstream_gene_variant | 1.0 |
| mmpR5 | 779431 | p.Asn148Gln | missense_variant | 1.0 |
| mmpL5 | 779472 | c.-992G>A | upstream_gene_variant | 1.0 |
| mmpS5 | 779523 | c.-618T>A | upstream_gene_variant | 1.0 |
| mmpS5 | 779538 | c.-633A>C | upstream_gene_variant | 1.0 |
| mmpS5 | 779539 | c.-634C>A | upstream_gene_variant | 1.0 |
| rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
| rpsL | 781456 | c.-104A>G | upstream_gene_variant | 1.0 |
| fbiC | 1302810 | c.-121C>T | upstream_gene_variant | 1.0 |
| fbiC | 1302860 | c.-71G>A | upstream_gene_variant | 1.0 |
| fbiC | 1302870 | c.-61G>C | upstream_gene_variant | 1.0 |
| fbiC | 1302948 | c.18T>C | synonymous_variant | 1.0 |
| fbiC | 1303288 | p.Ser120Gly | missense_variant | 1.0 |
| fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
| fbiC | 1303860 | c.930A>G | synonymous_variant | 1.0 |
| fbiC | 1304064 | c.1134G>A | synonymous_variant | 1.0 |
| fbiC | 1304141 | p.Ala404Gly | missense_variant | 1.0 |
| fbiC | 1304330 | p.Ala467Asp | missense_variant | 1.0 |
| fbiC | 1304707 | p.Val593Ile | missense_variant | 1.0 |
| fbiC | 1304907 | c.1977C>A | synonymous_variant | 1.0 |
| Rv1258c | 1406466 | p.Ser292Leu | missense_variant | 1.0 |
| Rv1258c | 1406492 | p.Ile283Met | missense_variant | 1.0 |
| Rv1258c | 1407008 | c.333C>A | synonymous_variant | 1.0 |
| embR | 1416462 | p.Ala296Ser | missense_variant | 1.0 |
| embR | 1417294 | c.54A>G | synonymous_variant | 1.0 |
| embR | 1417493 | c.-146T>G | upstream_gene_variant | 1.0 |
| rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
| rrs | 1471845 | n.4dupT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473420 | n.-238A>T | upstream_gene_variant | 1.0 |
| rrl | 1474615 | n.958A>C | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1475266 | n.1609T>C | non_coding_transcript_exon_variant | 1.0 |
| inhA | 1673499 | c.-703T>C | upstream_gene_variant | 1.0 |
| fabG1 | 1674079 | p.Pro214Ala | missense_variant | 1.0 |
| inhA | 1674384 | c.183C>T | synonymous_variant | 1.0 |
| inhA | 1674405 | c.204G>A | synonymous_variant | 1.0 |
| inhA | 1674471 | c.270G>C | synonymous_variant | 1.0 |
| inhA | 1674480 | c.279T>C | synonymous_variant | 1.0 |
| inhA | 1674483 | c.282G>C | synonymous_variant | 1.0 |
| inhA | 1674486 | c.285T>C | synonymous_variant | 1.0 |
| inhA | 1674603 | c.402G>A | synonymous_variant | 1.0 |
| inhA | 1674620 | p.Pro140Gln | missense_variant | 1.0 |
| inhA | 1674780 | c.579T>C | synonymous_variant | 1.0 |
| rpsA | 1833381 | c.-161T>C | upstream_gene_variant | 1.0 |
| rpsA | 1833554 | p.Thr5Ala | missense_variant | 1.0 |
| rpsA | 1833568 | c.27G>C | synonymous_variant | 1.0 |
| rpsA | 1833596 | c.55_56delAGinsTC | synonymous_variant | 1.0 |
| rpsA | 1833790 | c.249T>C | synonymous_variant | 0.99 |
| rpsA | 1833907 | c.366G>A | synonymous_variant | 1.0 |
| rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.99 |
| rpsA | 1834648 | c.1107C>T | synonymous_variant | 1.0 |
| rpsA | 1834912 | c.1371A>G | synonymous_variant | 1.0 |
| tlyA | 1917807 | c.-133T>G | upstream_gene_variant | 1.0 |
| tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
| tlyA | 1918149 | c.210A>C | synonymous_variant | 1.0 |
| tlyA | 1918150 | p.Val71Leu | missense_variant | 1.0 |
| tlyA | 1918242 | c.303G>C | synonymous_variant | 1.0 |
| tlyA | 1918587 | p.Gln216His | missense_variant | 1.0 |
| tlyA | 1918604 | p.Ser222Thr | missense_variant | 1.0 |
| ndh | 2101777 | c.1266C>G | synonymous_variant | 1.0 |
| ndh | 2101876 | c.1167C>G | synonymous_variant | 1.0 |
| ndh | 2101990 | c.1053G>T | synonymous_variant | 1.0 |
| ndh | 2102005 | c.1038G>C | synonymous_variant | 1.0 |
| ndh | 2102164 | c.879A>G | synonymous_variant | 1.0 |
| ndh | 2102302 | c.741G>C | synonymous_variant | 1.0 |
| ndh | 2102366 | p.Ala226Glu | missense_variant | 1.0 |
| ndh | 2102377 | c.666A>G | synonymous_variant | 1.0 |
| ndh | 2102420 | p.Lys208Arg | missense_variant | 1.0 |
| ndh | 2102443 | c.600A>G | synonymous_variant | 1.0 |
| ndh | 2102482 | c.561A>T | synonymous_variant | 1.0 |
| ndh | 2102638 | c.405A>G | synonymous_variant | 1.0 |
| ndh | 2102644 | c.399A>G | synonymous_variant | 1.0 |
| ndh | 2102680 | c.363T>C | synonymous_variant | 1.0 |
| ndh | 2102791 | c.252A>G | synonymous_variant | 1.0 |
| ndh | 2103028 | p.Gln5His | missense_variant | 1.0 |
| ndh | 2103173 | c.-132_-131insG | upstream_gene_variant | 1.0 |
| katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
| katG | 2156055 | c.57C>T | synonymous_variant | 1.0 |
| PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
| PPE35 | 2167934 | c.2679G>A | synonymous_variant | 1.0 |
| PPE35 | 2168269 | p.Gly782Ser | missense_variant | 1.0 |
| PPE35 | 2168342 | c.2271T>C | synonymous_variant | 1.0 |
| PPE35 | 2168567 | c.2046A>G | synonymous_variant | 1.0 |
| PPE35 | 2168612 | c.2001C>T | synonymous_variant | 1.0 |
| PPE35 | 2168882 | c.1731T>C | synonymous_variant | 1.0 |
| PPE35 | 2169263 | c.1350C>T | synonymous_variant | 1.0 |
| PPE35 | 2169304 | p.Met437Leu | missense_variant | 0.98 |
| PPE35 | 2169686 | c.927T>C | synonymous_variant | 1.0 |
| PPE35 | 2169717 | p.Asn299Ile | missense_variant | 1.0 |
| PPE35 | 2170178 | c.435T>A | synonymous_variant | 1.0 |
| PPE35 | 2170232 | c.381T>C | synonymous_variant | 0.99 |
| PPE35 | 2170394 | c.219G>C | synonymous_variant | 1.0 |
| PPE35 | 2170440 | p.Gln58Arg | missense_variant | 1.0 |
| PPE35 | 2170452 | p.Gly54Asp | missense_variant | 1.0 |
| PPE35 | 2170485 | p.Val43Ala | missense_variant | 1.0 |
| PPE35 | 2170499 | c.114A>G | synonymous_variant | 1.0 |
| PPE35 | 2170764 | c.-152C>T | upstream_gene_variant | 1.0 |
| Rv1979c | 2221723 | p.Arg481His | missense_variant | 1.0 |
| Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
| Rv1979c | 2222357 | p.Thr270Ala | missense_variant | 1.0 |
| Rv1979c | 2222504 | p.Met221Leu | missense_variant | 1.0 |
| Rv1979c | 2222598 | c.567C>T | synonymous_variant | 1.0 |
| Rv1979c | 2222897 | p.Ile90Val | missense_variant | 1.0 |
| Rv1979c | 2223146 | p.Arg7Gly | missense_variant | 1.0 |
| Rv1979c | 2223255 | c.-91A>G | upstream_gene_variant | 1.0 |
| Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
| pncA | 2289104 | c.138A>G | synonymous_variant | 1.0 |
| pncA | 2289700 | c.-459T>C | upstream_gene_variant | 1.0 |
| pncA | 2289827 | c.-586A>G | upstream_gene_variant | 1.0 |
| kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
| kasA | 2519287 | c.1173T>C | synonymous_variant | 1.0 |
| folC | 2746174 | c.1425A>C | synonymous_variant | 1.0 |
| folC | 2747204 | p.Ala132Gln | missense_variant | 1.0 |
| folC | 2747572 | c.27T>C | synonymous_variant | 1.0 |
| folC | 2747575 | c.24G>C | synonymous_variant | 1.0 |
| folC | 2747628 | c.-30G>C | upstream_gene_variant | 1.0 |
| folC | 2747631 | c.-33C>G | upstream_gene_variant | 1.0 |
| folC | 2747691 | c.-93A>G | upstream_gene_variant | 1.0 |
| pepQ | 2859490 | p.Val310Ala | missense_variant | 1.0 |
| pepQ | 2860159 | p.Ala87Gly | missense_variant | 0.19 |
| ribD | 2987614 | c.766delA | frameshift_variant | 1.0 |
| Rv2752c | 3064627 | p.Asn522Ser | missense_variant | 1.0 |
| Rv2752c | 3065573 | p.Glu207Gln | missense_variant | 1.0 |
| thyX | 3067239 | p.Ala236Asp | missense_variant | 1.0 |
| thyX | 3067355 | c.591A>C | synonymous_variant | 1.0 |
| thyX | 3067439 | c.507A>G | synonymous_variant | 1.0 |
| thyX | 3067980 | c.-35T>C | upstream_gene_variant | 1.0 |
| thyA | 3074160 | c.312A>G | synonymous_variant | 1.0 |
| thyA | 3074445 | c.27C>T | synonymous_variant | 1.0 |
| thyA | 3074529 | c.-58G>C | upstream_gene_variant | 1.0 |
| thyA | 3074580 | c.-109T>C | upstream_gene_variant | 1.0 |
| ald | 3086623 | c.-197A>G | upstream_gene_variant | 1.0 |
| ald | 3086661 | c.-159G>A | upstream_gene_variant | 1.0 |
| ald | 3086671 | c.-149T>C | upstream_gene_variant | 1.0 |
| ald | 3086707 | c.-113G>C | upstream_gene_variant | 1.0 |
| ald | 3086733 | c.-87G>A | upstream_gene_variant | 1.0 |
| ald | 3086737 | c.-83T>C | upstream_gene_variant | 1.0 |
| ald | 3086744 | c.-76A>T | upstream_gene_variant | 1.0 |
| ald | 3086753 | c.-67A>G | upstream_gene_variant | 1.0 |
| ald | 3086760 | c.-60A>T | upstream_gene_variant | 1.0 |
| ald | 3086771 | c.-49T>C | upstream_gene_variant | 1.0 |
| ald | 3086773 | c.-47A>G | upstream_gene_variant | 1.0 |
| ald | 3086788 | c.-32T>A | upstream_gene_variant | 1.0 |
| ald | 3086797 | c.-23G>A | upstream_gene_variant | 1.0 |
| ald | 3086803 | c.-17T>C | upstream_gene_variant | 1.0 |
| ald | 3087020 | c.201C>T | synonymous_variant | 1.0 |
| ald | 3087065 | c.246C>T | synonymous_variant | 1.0 |
| ald | 3087070 | p.Arg84Leu | missense_variant | 1.0 |
| ald | 3087074 | c.255G>A | synonymous_variant | 1.0 |
| ald | 3087077 | c.258A>C | synonymous_variant | 1.0 |
| ald | 3087079 | p.His87Arg | missense_variant | 1.0 |
| ald | 3087140 | c.321G>A | synonymous_variant | 1.0 |
| ald | 3087149 | c.330C>T | synonymous_variant | 1.0 |
| ald | 3087152 | c.333C>T | synonymous_variant | 1.0 |
| ald | 3087155 | c.336C>A | synonymous_variant | 1.0 |
| ald | 3087158 | c.339G>C | synonymous_variant | 1.0 |
| ald | 3087164 | c.345T>C | synonymous_variant | 1.0 |
| ald | 3087316 | p.Val166Ala | missense_variant | 1.0 |
| ald | 3087344 | c.525C>T | synonymous_variant | 1.0 |
| ald | 3087380 | c.561C>G | synonymous_variant | 1.0 |
| ald | 3087381 | p.Asn188Gly | missense_variant | 1.0 |
| ald | 3087401 | c.582T>C | synonymous_variant | 1.0 |
| ald | 3087500 | c.681T>C | synonymous_variant | 1.0 |
| ald | 3087512 | c.693T>C | synonymous_variant | 1.0 |
| ald | 3087527 | c.708T>C | synonymous_variant | 1.0 |
| ald | 3087533 | c.714C>A | synonymous_variant | 1.0 |
| ald | 3087554 | c.735G>A | synonymous_variant | 1.0 |
| ald | 3087560 | c.741C>T | synonymous_variant | 1.0 |
| ald | 3087644 | c.825C>T | synonymous_variant | 1.0 |
| ald | 3087653 | c.834A>G | synonymous_variant | 1.0 |
| ald | 3087743 | c.924G>A | synonymous_variant | 1.0 |
| ald | 3087758 | c.939G>A | synonymous_variant | 1.0 |
| ald | 3087800 | p.His327Gln | missense_variant | 1.0 |
| ald | 3087833 | c.1014A>G | synonymous_variant | 1.0 |
| ald | 3087857 | c.1038C>T | synonymous_variant | 1.0 |
| fbiD | 3339049 | c.-69C>T | upstream_gene_variant | 1.0 |
| fbiD | 3339402 | c.285C>T | synonymous_variant | 1.0 |
| fbiD | 3339568 | c.451C>T | synonymous_variant | 1.0 |
| fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.57 |
| fbiD | 3339746 | p.Ala210Gly | missense_variant | 0.3 |
| Rv3083 | 3448474 | c.-30G>T | upstream_gene_variant | 1.0 |
| Rv3083 | 3448611 | c.108A>G | synonymous_variant | 1.0 |
| Rv3083 | 3449305 | c.802T>C | synonymous_variant | 1.0 |
| Rv3083 | 3449400 | c.897C>G | synonymous_variant | 1.0 |
| Rv3083 | 3449454 | c.951G>A | synonymous_variant | 1.0 |
| Rv3083 | 3449868 | c.1365C>A | synonymous_variant | 1.0 |
| Rv3083 | 3449877 | c.1374T>C | synonymous_variant | 1.0 |
| Rv3083 | 3449885 | p.Arg461Lys | missense_variant | 1.0 |
| fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
| fprA | 3475059 | c.1053C>T | synonymous_variant | 1.0 |
| fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
| Rv3236c | 3611968 | c.1149T>G | synonymous_variant | 1.0 |
| Rv3236c | 3612208 | c.909G>C | synonymous_variant | 1.0 |
| Rv3236c | 3612250 | c.867A>G | synonymous_variant | 1.0 |
| Rv3236c | 3612319 | c.798G>C | synonymous_variant | 1.0 |
| Rv3236c | 3612322 | c.795G>C | synonymous_variant | 1.0 |
| Rv3236c | 3613038 | c.79C>A | synonymous_variant | 1.0 |
| Rv3236c | 3613056 | c.61C>T | synonymous_variant | 1.0 |
| fbiB | 3640899 | c.-636G>A | upstream_gene_variant | 1.0 |
| fbiB | 3640980 | c.-555C>T | upstream_gene_variant | 1.0 |
| fbiB | 3641909 | c.375T>C | synonymous_variant | 1.0 |
| fbiB | 3642467 | c.933T>C | synonymous_variant | 1.0 |
| fbiB | 3642599 | c.1065C>T | synonymous_variant | 1.0 |
| alr | 3840226 | p.Thr399Ala | missense_variant | 1.0 |
| alr | 3840527 | c.894A>C | synonymous_variant | 1.0 |
| alr | 3840719 | c.702A>G | synonymous_variant | 1.0 |
| alr | 3840914 | c.507G>C | synonymous_variant | 1.0 |
| alr | 3840994 | p.His143Asp | missense_variant | 1.0 |
| alr | 3841112 | c.309T>C | synonymous_variant | 1.0 |
| alr | 3841116 | p.Ala102Gly | missense_variant | 1.0 |
| alr | 3841172 | c.249A>C | synonymous_variant | 1.0 |
| alr | 3841199 | c.222T>C | synonymous_variant | 1.0 |
| alr | 3841419 | p.Val1Ala | missense_variant | 1.0 |
| rpoA | 3877886 | c.622C>T | synonymous_variant | 1.0 |
| rpoA | 3878001 | c.507A>G | synonymous_variant | 1.0 |
| rpoA | 3878043 | c.465G>T | synonymous_variant | 1.0 |
| rpoA | 3878124 | c.384G>A | synonymous_variant | 1.0 |
| rpoA | 3878619 | c.-113delC | upstream_gene_variant | 1.0 |
| rpoA | 3878630 | c.-124_-123insCC | upstream_gene_variant | 1.0 |
| ddn | 3986805 | c.-39G>C | upstream_gene_variant | 1.0 |
| ddn | 3987050 | c.207C>T | synonymous_variant | 1.0 |
| ddn | 3987287 | c.444T>C | synonymous_variant | 1.0 |
| clpC1 | 4038227 | c.2478G>T | synonymous_variant | 1.0 |
| clpC1 | 4038443 | c.2262G>A | synonymous_variant | 1.0 |
| clpC1 | 4038683 | c.2022T>C | synonymous_variant | 1.0 |
| clpC1 | 4038746 | c.1959C>T | synonymous_variant | 1.0 |
| clpC1 | 4038779 | c.1926C>T | synonymous_variant | 1.0 |
| clpC1 | 4038848 | c.1857C>T | synonymous_variant | 1.0 |
| clpC1 | 4038860 | c.1845G>C | synonymous_variant | 1.0 |
| clpC1 | 4038878 | c.1827A>G | synonymous_variant | 1.0 |
| clpC1 | 4038974 | c.1731T>C | synonymous_variant | 1.0 |
| clpC1 | 4039046 | c.1659C>T | synonymous_variant | 1.0 |
| clpC1 | 4039058 | c.1647C>T | synonymous_variant | 1.0 |
| clpC1 | 4039094 | c.1611C>T | synonymous_variant | 1.0 |
| clpC1 | 4039100 | c.1605C>T | synonymous_variant | 1.0 |
| clpC1 | 4039274 | c.1431G>C | synonymous_variant | 1.0 |
| clpC1 | 4039336 | c.1369C>T | synonymous_variant | 1.0 |
| clpC1 | 4039352 | c.1353C>T | synonymous_variant | 1.0 |
| clpC1 | 4039448 | c.1257A>G | synonymous_variant | 1.0 |
| clpC1 | 4039454 | c.1251A>G | synonymous_variant | 0.99 |
| clpC1 | 4039502 | c.1203C>T | synonymous_variant | 1.0 |
| clpC1 | 4039682 | c.1023C>A | synonymous_variant | 1.0 |
| clpC1 | 4039700 | c.1005C>T | synonymous_variant | 1.0 |
| clpC1 | 4039718 | c.987C>T | synonymous_variant | 1.0 |
| clpC1 | 4039817 | c.888A>C | synonymous_variant | 1.0 |
| clpC1 | 4039820 | c.885T>C | synonymous_variant | 1.0 |
| clpC1 | 4039823 | c.882T>G | synonymous_variant | 1.0 |
| clpC1 | 4040045 | c.660C>G | synonymous_variant | 1.0 |
| clpC1 | 4040048 | c.657C>T | synonymous_variant | 1.0 |
| clpC1 | 4040063 | c.642G>C | synonymous_variant | 1.0 |
| clpC1 | 4040090 | c.615T>C | synonymous_variant | 1.0 |
| clpC1 | 4040093 | c.612C>G | synonymous_variant | 1.0 |
| clpC1 | 4040147 | c.558A>G | synonymous_variant | 1.0 |
| clpC1 | 4040159 | c.546G>A | synonymous_variant | 0.99 |
| clpC1 | 4040162 | c.543G>C | synonymous_variant | 1.0 |
| clpC1 | 4040213 | c.492T>C | synonymous_variant | 1.0 |
| clpC1 | 4040267 | c.438A>G | synonymous_variant | 1.0 |
| clpC1 | 4040273 | c.432T>C | synonymous_variant | 1.0 |
| clpC1 | 4040276 | c.429C>G | synonymous_variant | 1.0 |
| clpC1 | 4040279 | c.426C>G | synonymous_variant | 1.0 |
| clpC1 | 4040363 | c.342A>G | synonymous_variant | 1.0 |
| clpC1 | 4040393 | c.312G>C | synonymous_variant | 1.0 |
| clpC1 | 4040411 | c.294T>C | synonymous_variant | 1.0 |
| clpC1 | 4040423 | c.282A>G | synonymous_variant | 1.0 |
| clpC1 | 4040450 | c.255A>G | synonymous_variant | 1.0 |
| clpC1 | 4040471 | c.234T>C | synonymous_variant | 1.0 |
| clpC1 | 4040480 | c.225T>C | synonymous_variant | 1.0 |
| clpC1 | 4040534 | c.171A>G | synonymous_variant | 1.0 |
| clpC1 | 4040551 | c.154T>C | synonymous_variant | 1.0 |
| clpC1 | 4040573 | c.132T>C | synonymous_variant | 1.0 |
| clpC1 | 4040657 | c.48T>G | synonymous_variant | 1.0 |
| panD | 4043932 | p.Met117Thr | missense_variant | 1.0 |
| panD | 4044243 | c.39C>G | synonymous_variant | 1.0 |
| embC | 4240060 | c.198G>C | synonymous_variant | 1.0 |
| embC | 4240106 | p.Leu82Met | missense_variant | 0.99 |
| embC | 4240237 | c.375G>C | synonymous_variant | 1.0 |
| embC | 4240499 | p.Ser213Arg | missense_variant | 1.0 |
| embC | 4240533 | p.Ser224Thr | missense_variant | 1.0 |
| embC | 4240559 | p.Ala233Thr | missense_variant | 1.0 |
| embC | 4240587 | p.Gly242Ala | missense_variant | 1.0 |
| embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
| embC | 4241698 | c.1836G>C | synonymous_variant | 1.0 |
| embC | 4241710 | c.1848G>A | synonymous_variant | 1.0 |
| embC | 4241758 | c.1896G>A | synonymous_variant | 1.0 |
| embC | 4241920 | c.2058C>T | synonymous_variant | 0.99 |
| embC | 4241921 | p.Gly687Arg | missense_variant | 0.99 |
| embC | 4242092 | c.2230T>C | synonymous_variant | 1.0 |
| embA | 4242325 | c.-908C>T | upstream_gene_variant | 1.0 |
| embA | 4242460 | c.-773G>C | upstream_gene_variant | 1.0 |
| embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
| embA | 4242655 | c.-578A>G | upstream_gene_variant | 1.0 |
| embA | 4242946 | c.-287T>C | upstream_gene_variant | 1.0 |
| embA | 4243628 | c.396A>G | synonymous_variant | 1.0 |
| embA | 4243649 | c.417G>C | synonymous_variant | 1.0 |
| embA | 4243690 | p.Met153Thr | missense_variant | 0.99 |
| embA | 4243961 | c.729G>A | synonymous_variant | 1.0 |
| embA | 4244154 | p.Thr308Pro | missense_variant | 1.0 |
| embA | 4244177 | c.945G>C | synonymous_variant | 1.0 |
| embA | 4244178 | p.Ala316Thr | missense_variant | 1.0 |
| embA | 4244312 | c.1080T>G | synonymous_variant | 1.0 |
| embA | 4244846 | c.1614C>G | synonymous_variant | 1.0 |
| embA | 4245023 | c.1791A>G | synonymous_variant | 1.0 |
| embB | 4245764 | c.-750G>T | upstream_gene_variant | 1.0 |
| embB | 4246193 | c.-321C>T | upstream_gene_variant | 1.0 |
| embA | 4246443 | p.Asp1071Asn | missense_variant | 1.0 |
| embB | 4246584 | p.Arg24Pro | missense_variant | 0.2 |
| embB | 4247590 | c.1077A>G | synonymous_variant | 1.0 |
| embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
| embB | 4247815 | c.1302C>T | synonymous_variant | 1.0 |
| embB | 4248070 | c.1557T>C | synonymous_variant | 1.0 |
| embB | 4248206 | p.Ser565Gly | missense_variant | 1.0 |
| embB | 4248226 | c.1713G>A | synonymous_variant | 1.0 |
| aftB | 4268331 | p.Gln169Pro | missense_variant | 1.0 |
| aftB | 4268810 | c.27G>T | synonymous_variant | 1.0 |
| ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
| aftB | 4269588 | c.-752G>A | upstream_gene_variant | 1.0 |
| aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
| ubiA | 4269811 | p.Gln8Arg | missense_variant | 1.0 |
| ethA | 4326463 | c.1011C>T | synonymous_variant | 1.0 |
| ethA | 4326740 | p.Arg245His | missense_variant | 1.0 |
| ethA | 4327547 | c.-75_-74insT | upstream_gene_variant | 1.0 |
| whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
| gid | 4407568 | p.Ala212Val | missense_variant | 1.0 |
| gid | 4407572 | p.Ile211Val | missense_variant | 1.0 |
| gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
| gid | 4407703 | p.Ala167Val | missense_variant | 1.0 |
| gid | 4407705 | c.498G>T | synonymous_variant | 1.0 |
| gid | 4407782 | p.Ala141Thr | missense_variant | 1.0 |
| gid | 4407822 | c.381A>G | synonymous_variant | 0.99 |
| gid | 4407943 | p.Gln87Arg | missense_variant | 1.0 |
| gid | 4407951 | c.252G>T | synonymous_variant | 1.0 |
| gid | 4408008 | c.195C>G | synonymous_variant | 1.0 |
| gid | 4408110 | p.Val31Ala | missense_variant | 1.0 |
| gid | 4408113 | c.90T>C | synonymous_variant | 1.0 |
| gid | 4408153 | p.Gly17Asp | missense_variant | 1.0 |
| gid | 4408176 | c.27T>C | synonymous_variant | 1.0 |
| gid | 4408228 | c.-28_-27delCA | upstream_gene_variant | 0.98 |
| gyrA | 9817 | c.2517_*53delANNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNN | frameshift_variant&stop_lost&splice_region_variant | 1.0 |
| alr | 3841405 | c.-1147_15del | conservative_inframe_deletion | 1.0 |
