Run ID: ERR4769551
Sample name:
Date: 01-04-2023 06:44:16
Number of reads: 374572
Percentage reads mapped: 27.04
Strain: La1.3
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
La1 | M.bovis | None | None | 1.0 |
La1.3 | M.bovis | None | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.12 | 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 | 8285 | c.984C>T | synonymous_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.11 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.11 |
rpoB | 761261 | c.1455G>C | synonymous_variant | 0.12 |
rpoB | 761273 | c.1467T>C | synonymous_variant | 0.12 |
rpoB | 761294 | c.1488G>C | synonymous_variant | 0.13 |
rpoB | 761300 | c.1494G>C | synonymous_variant | 0.15 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.22 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.25 |
rpoC | 763492 | c.123G>C | synonymous_variant | 0.25 |
rpoC | 763507 | c.138G>C | synonymous_variant | 0.2 |
rpoC | 764611 | c.1242G>C | synonymous_variant | 0.18 |
rpoC | 764646 | p.Gly426Ala | missense_variant | 0.15 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.17 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.25 |
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 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472297 | n.453_465delGTCCGGGTTCTCT | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472599 | n.754G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472686 | n.841G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472951 | n.1106T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472953 | n.1108G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473026 | n.1181T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473082 | n.1237G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.42 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473099 | n.1254T>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473129 | n.1284C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.47 |
rrs | 1473282 | n.1437C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473717 | n.60G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1473731 | n.74T>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1473756 | n.99G>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1473757 | n.100T>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1473814 | n.157A>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1473815 | n.158T>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1473830 | n.173T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1473832 | n.175C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1473833 | n.176_177insT | non_coding_transcript_exon_variant | 0.24 |
rrl | 1473844 | n.187C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474740 | n.1083G>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474747 | n.1090C>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474790 | n.1133C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474803 | n.1146G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475443 | n.1786G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475460 | n.1803A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475481 | n.1824C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475482 | n.1825A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476110 | n.2453G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476297 | n.2640C>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476298 | n.2641C>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476300 | n.2643G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476728 | n.3071T>C | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1833894 | p.Ala118Glu | missense_variant | 0.29 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.29 |
rpsA | 1834340 | p.Met267Leu | missense_variant | 0.12 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.2 |
rpsA | 1834354 | c.813G>C | synonymous_variant | 0.21 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 0.2 |
rpsA | 1834360 | c.819G>C | synonymous_variant | 0.14 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.21 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.21 |
rpsA | 1834375 | c.834G>A | synonymous_variant | 0.14 |
rpsA | 1834378 | c.837T>G | synonymous_variant | 0.2 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.18 |
rpsA | 1834396 | c.855G>T | synonymous_variant | 0.13 |
rpsA | 1834399 | p.His286Gln | missense_variant | 0.13 |
rpsA | 1834411 | c.870T>G | synonymous_variant | 0.14 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.14 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.14 |
rpsA | 1834447 | c.906C>G | synonymous_variant | 0.13 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.12 |
rpsA | 1834540 | c.999G>T | synonymous_variant | 0.18 |
rpsA | 1834543 | c.1002C>G | synonymous_variant | 0.18 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.2 |
rpsA | 1834552 | c.1011G>T | synonymous_variant | 0.2 |
rpsA | 1834555 | c.1014T>C | synonymous_variant | 0.2 |
rpsA | 1834557 | p.Ala339Gly | missense_variant | 0.2 |
rpsA | 1834570 | c.1029C>T | synonymous_variant | 0.22 |
rpsA | 1834573 | c.1032G>A | synonymous_variant | 0.25 |
rpsA | 1834574 | p.Met345Leu | missense_variant | 0.25 |
rpsA | 1834600 | c.1059G>C | synonymous_variant | 0.22 |
rpsA | 1834606 | c.1065C>T | synonymous_variant | 0.18 |
rpsA | 1834612 | c.1071G>T | synonymous_variant | 0.18 |
rpsA | 1834619 | c.1078T>C | synonymous_variant | 0.17 |
rpsA | 1834627 | c.1086C>G | synonymous_variant | 0.23 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.15 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.14 |
rpsA | 1834645 | c.1104C>T | synonymous_variant | 0.15 |
rpsA | 1834650 | p.Thr370Asn | missense_variant | 0.17 |
rpsA | 1834859 | p.Ala440Thr | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102017 | c.1026C>T | synonymous_variant | 0.13 |
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 |
katG | 2156465 | c.-354C>T | upstream_gene_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168011 | p.Ser868Arg | 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 |
ahpC | 2726636 | c.444G>C | synonymous_variant | 0.22 |
ahpC | 2726638 | p.Ala149Val | missense_variant | 0.22 |
ahpC | 2726642 | c.450C>A | synonymous_variant | 0.2 |
ahpC | 2726651 | c.459G>C | synonymous_variant | 0.22 |
ahpC | 2726654 | c.462G>C | synonymous_variant | 0.22 |
ahpC | 2726657 | c.465A>C | synonymous_variant | 0.18 |
ahpC | 2726660 | c.468C>T | synonymous_variant | 0.18 |
ahpC | 2726669 | c.477T>C | synonymous_variant | 0.17 |
ahpC | 2726675 | c.483A>T | synonymous_variant | 0.17 |
ahpC | 2726678 | c.486G>C | synonymous_variant | 0.15 |
ahpC | 2726681 | c.489A>C | synonymous_variant | 0.18 |
ahpC | 2726684 | c.492G>C | synonymous_variant | 0.18 |
ahpC | 2726693 | c.501C>T | synonymous_variant | 0.18 |
ahpC | 2726700 | c.508_509delTCinsAG | synonymous_variant | 0.18 |
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 |
rpoA | 3878630 | c.-124delC | upstream_gene_variant | 1.0 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 1.0 |
clpC1 | 4039382 | c.1323C>G | synonymous_variant | 0.14 |
clpC1 | 4039391 | c.1314T>G | synonymous_variant | 0.17 |
clpC1 | 4039394 | c.1311G>C | synonymous_variant | 0.17 |
clpC1 | 4039397 | c.1308A>G | synonymous_variant | 0.15 |
clpC1 | 4039406 | c.1299G>C | synonymous_variant | 0.15 |
clpC1 | 4039412 | c.1293T>G | synonymous_variant | 0.15 |
clpC1 | 4039415 | p.Glu430Asp | missense_variant | 0.23 |
clpC1 | 4039424 | p.Lys427Arg | missense_variant | 0.17 |
clpC1 | 4039427 | p.Glu426Asp | missense_variant | 0.17 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.17 |
clpC1 | 4039436 | c.1269G>A | synonymous_variant | 0.18 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.18 |
clpC1 | 4039448 | c.1257A>G | synonymous_variant | 0.18 |
clpC1 | 4039457 | c.1248C>T | synonymous_variant | 0.15 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 0.15 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.15 |
clpC1 | 4039472 | c.1233G>C | synonymous_variant | 0.15 |
clpC1 | 4039478 | c.1227G>A | synonymous_variant | 0.18 |
clpC1 | 4039481 | c.1224T>G | synonymous_variant | 0.17 |
clpC1 | 4039484 | c.1221T>C | synonymous_variant | 0.18 |
clpC1 | 4039499 | c.1206G>C | synonymous_variant | 0.18 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241384 | p.Pro508Thr | missense_variant | 0.4 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242760 | c.-473G>A | upstream_gene_variant | 0.15 |
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 |
embB | 4249640 | c.3127T>C | synonymous_variant | 0.23 |
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 |