Run ID: SRR13861720
Sample name:
Date: 03-04-2023 09:38:52
Number of reads: 242604
Percentage reads mapped: 4.05
Strain: lineage4.9
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.96 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7018 | c.-284G>T | upstream_gene_variant | 1.0 |
gyrA | 7427 | c.126G>C | synonymous_variant | 0.13 |
gyrA | 7472 | c.171T>C | synonymous_variant | 0.14 |
gyrA | 7475 | c.174A>C | synonymous_variant | 0.14 |
gyrA | 7484 | c.183T>C | synonymous_variant | 0.15 |
gyrA | 7487 | c.186C>G | synonymous_variant | 0.14 |
gyrA | 7523 | c.222C>G | synonymous_variant | 0.14 |
gyrA | 7532 | c.231T>C | synonymous_variant | 0.19 |
gyrA | 7541 | c.240C>G | synonymous_variant | 0.2 |
gyrA | 7571 | c.270G>C | synonymous_variant | 0.27 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 0.23 |
gyrA | 7595 | c.294C>G | synonymous_variant | 0.21 |
gyrA | 7607 | c.306C>G | synonymous_variant | 0.23 |
gyrA | 7626 | c.325C>T | synonymous_variant | 0.23 |
gyrA | 7631 | c.330G>C | synonymous_variant | 0.2 |
gyrA | 7637 | c.336C>G | synonymous_variant | 0.21 |
gyrA | 7649 | c.348C>T | synonymous_variant | 0.2 |
gyrA | 7652 | c.351C>T | synonymous_variant | 0.2 |
gyrA | 7658 | c.357A>G | synonymous_variant | 0.2 |
gyrA | 7664 | c.363T>C | synonymous_variant | 0.14 |
gyrA | 7670 | c.369A>G | synonymous_variant | 0.15 |
gyrA | 7676 | c.375G>C | synonymous_variant | 0.15 |
mshA | 576668 | c.1322dupA | frameshift_variant&stop_gained | 1.0 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.17 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.17 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.17 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.17 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.18 |
rpoB | 761645 | c.1839C>G | synonymous_variant | 0.18 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.17 |
rpoB | 761657 | c.1851C>G | synonymous_variant | 0.18 |
rpoB | 761675 | c.1869G>C | synonymous_variant | 0.14 |
rpoB | 761687 | c.1881C>T | synonymous_variant | 0.15 |
rpoB | 761690 | c.1884G>C | synonymous_variant | 0.18 |
rpoB | 761765 | c.1959T>C | synonymous_variant | 0.18 |
rpoB | 761772 | p.His656Ala | missense_variant | 0.18 |
rpoB | 761778 | p.Asn658Asp | missense_variant | 0.17 |
rpoB | 761791 | p.Arg662His | missense_variant | 0.15 |
rpoB | 761813 | c.2007T>C | synonymous_variant | 0.17 |
rpoB | 761815 | p.Ala670Glu | missense_variant | 0.17 |
rpoB | 761834 | c.2028T>C | synonymous_variant | 0.22 |
rpoB | 761847 | p.Cys681Ser | missense_variant | 0.25 |
rpoB | 761852 | c.2046C>G | synonymous_variant | 0.25 |
rpoB | 761864 | c.2058G>C | synonymous_variant | 0.25 |
rpoB | 761873 | c.2067A>G | synonymous_variant | 0.25 |
rpoB | 761885 | c.2079T>C | synonymous_variant | 0.25 |
rpoB | 761891 | c.2085G>C | synonymous_variant | 0.25 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.18 |
rpoB | 762329 | c.2523G>C | synonymous_variant | 0.25 |
rpoB | 762338 | c.2532T>C | synonymous_variant | 0.15 |
rpoB | 762347 | c.2541T>C | synonymous_variant | 0.14 |
rpoB | 762362 | p.Glu852Asp | missense_variant | 0.2 |
rpoB | 762369 | c.2563T>C | synonymous_variant | 0.18 |
rpoC | 762374 | c.-996G>C | upstream_gene_variant | 0.17 |
rpoC | 762380 | c.-990T>G | upstream_gene_variant | 0.15 |
rpoC | 762395 | c.-975G>C | upstream_gene_variant | 0.17 |
rpoC | 762398 | c.-972T>C | upstream_gene_variant | 0.17 |
rpoC | 762401 | c.-969G>C | upstream_gene_variant | 0.18 |
rpoC | 762404 | c.-966T>C | upstream_gene_variant | 0.18 |
rpoC | 762410 | c.-960T>C | upstream_gene_variant | 0.17 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 0.18 |
rpoC | 762443 | c.-927G>C | upstream_gene_variant | 0.23 |
rpoC | 765100 | c.1731G>C | synonymous_variant | 1.0 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.17 |
rpoC | 765734 | c.2365T>C | synonymous_variant | 0.15 |
rpoC | 765739 | c.2370G>C | synonymous_variant | 0.15 |
rpoC | 765751 | c.2382C>G | synonymous_variant | 0.12 |
rpoC | 765753 | p.Asp795Ala | missense_variant | 0.12 |
rpoC | 765772 | c.2403C>G | synonymous_variant | 0.13 |
rpoC | 765784 | c.2415C>G | synonymous_variant | 0.14 |
rpoC | 765811 | c.2442T>C | synonymous_variant | 0.15 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.14 |
rpoC | 766843 | c.3474T>C | synonymous_variant | 0.2 |
mmpL5 | 776059 | p.Val808Met | missense_variant | 0.83 |
fbiC | 1304599 | p.Ile557Phe | missense_variant | 1.0 |
embR | 1417348 | c.-1A>T | upstream_gene_variant | 1.0 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472101 | n.256G>A | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472122 | n.277G>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472230 | n.385C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472262 | n.417C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472269 | n.424G>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472271 | n.426T>C | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472277 | n.432C>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472505 | n.660G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472596 | n.751G>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472614 | n.769G>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472665 | n.820G>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472669 | n.824_825insTAGG | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472695 | n.850C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473080 | n.1235C>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473248 | n.1403G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473249 | n.1404T>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473255 | n.1410A>G | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473260 | n.1415G>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473281 | n.1436C>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473282 | n.1437C>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473288 | n.1443C>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473291 | n.1446G>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473296 | n.1451G>C | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473297 | n.1452G>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473327 | n.1482A>G | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473328 | n.1483C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1473631 | n.-27T>C | upstream_gene_variant | 1.0 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476215 | n.2558C>A | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476268 | n.2611A>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476275 | n.2618T>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476572 | n.2915G>A | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476595 | n.2938C>G | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476596 | n.2939C>T | non_coding_transcript_exon_variant | 0.41 |
inhA | 1673748 | c.-454A>G | upstream_gene_variant | 0.22 |
rpsA | 1833855 | p.Lys105Thr | missense_variant | 0.9 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.17 |
PPE35 | 2170030 | p.Met195Leu | missense_variant | 1.0 |
kasA | 2518276 | p.Trp54* | stop_gained | 1.0 |
kasA | 2518352 | p.Met80Val | missense_variant | 1.0 |
kasA | 2519116 | c.1002C>G | synonymous_variant | 0.13 |
kasA | 2519137 | c.1023T>C | synonymous_variant | 0.15 |
kasA | 2519167 | c.1053T>C | synonymous_variant | 0.17 |
kasA | 2519173 | c.1059C>G | synonymous_variant | 0.17 |
kasA | 2519197 | c.1083G>C | synonymous_variant | 0.15 |
eis | 2714478 | c.855C>A | synonymous_variant | 1.0 |
pepQ | 2860170 | c.248_249insA | frameshift_variant | 1.0 |
Rv2752c | 3065335 | p.Leu286Arg | missense_variant | 1.0 |
thyX | 3067500 | p.Lys149Arg | missense_variant | 0.33 |
thyX | 3067515 | p.Ser144Thr | missense_variant | 0.29 |
thyX | 3067526 | c.420C>G | synonymous_variant | 0.29 |
thyX | 3067530 | p.Ala139Ser | missense_variant | 0.29 |
thyX | 3067545 | p.Glu134Ala | missense_variant | 0.38 |
thyX | 3067549 | p.Thr133Ala | missense_variant | 0.38 |
thyX | 3067556 | p.His130Gln | missense_variant | 0.29 |
thyX | 3067559 | p.Arg129Gln | missense_variant | 0.29 |
thyX | 3067565 | p.Asp127Glu | missense_variant | 0.25 |
thyX | 3067570 | p.Ala126Pro | missense_variant | 0.22 |
thyX | 3067571 | c.375C>T | synonymous_variant | 0.22 |
thyX | 3067577 | p.Glu123Asp | missense_variant | 0.22 |
thyX | 3067582 | p.Met122Leu | missense_variant | 0.22 |
thyX | 3067586 | c.360C>G | synonymous_variant | 0.22 |
thyX | 3067601 | c.345G>C | synonymous_variant | 0.25 |
thyX | 3067604 | c.342G>C | synonymous_variant | 0.25 |
thyX | 3067610 | p.Lys112Asn | missense_variant | 0.22 |
thyX | 3067613 | c.333G>A | synonymous_variant | 0.3 |
thyX | 3067619 | c.327A>C | synonymous_variant | 0.3 |
thyX | 3067640 | c.306G>C | synonymous_variant | 0.27 |
thyX | 3067643 | c.303C>T | synonymous_variant | 0.27 |
thyX | 3067652 | c.294T>C | synonymous_variant | 0.2 |
thyX | 3067661 | c.285C>G | synonymous_variant | 0.25 |
thyX | 3067682 | c.264G>C | synonymous_variant | 0.27 |
thyX | 3067685 | c.261A>G | synonymous_variant | 0.27 |
thyX | 3067688 | c.258G>C | synonymous_variant | 0.27 |
thyX | 3067694 | c.252G>C | synonymous_variant | 0.27 |
thyX | 3067718 | c.228C>G | synonymous_variant | 0.3 |
thyX | 3067721 | c.225T>C | synonymous_variant | 0.3 |
thyX | 3067724 | c.222G>A | synonymous_variant | 0.3 |
thyX | 3067727 | c.219A>C | synonymous_variant | 0.3 |
thyX | 3067739 | c.207T>C | synonymous_variant | 0.25 |
thyX | 3067742 | c.204A>C | synonymous_variant | 0.25 |
thyX | 3067761 | p.Arg62Lys | missense_variant | 0.18 |
thyX | 3067765 | p.Leu61Ile | missense_variant | 0.2 |
thyX | 3067781 | c.165C>G | synonymous_variant | 0.2 |
thyX | 3067787 | c.159G>A | synonymous_variant | 0.2 |
thyX | 3067793 | c.153T>C | synonymous_variant | 0.22 |
thyX | 3067799 | c.147G>A | synonymous_variant | 0.22 |
thyX | 3067802 | c.144C>G | synonymous_variant | 0.22 |
fbiB | 3641019 | c.-516G>A | upstream_gene_variant | 1.0 |
fbiB | 3641941 | p.Leu136Gln | missense_variant | 1.0 |
rpoA | 3878335 | p.Gly58Asp | missense_variant | 0.33 |
ddn | 3986771 | c.-73A>C | upstream_gene_variant | 0.29 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.2 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.22 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.25 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 0.38 |
clpC1 | 4038932 | c.1773G>C | synonymous_variant | 0.22 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.22 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.2 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.2 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.25 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.29 |
clpC1 | 4040380 | c.325T>C | synonymous_variant | 0.33 |
embC | 4241292 | p.Leu477Gln | missense_variant | 1.0 |
embC | 4242011 | p.Leu717Val | missense_variant | 1.0 |
embB | 4245764 | c.-750G>C | upstream_gene_variant | 0.29 |
embA | 4245771 | p.Asn847Ser | missense_variant | 0.29 |
embB | 4245807 | c.-707_-705delTTAinsCTG | upstream_gene_variant | 0.33 |
embA | 4245820 | p.Ser863Thr | missense_variant | 0.29 |
embB | 4245830 | c.-684G>C | upstream_gene_variant | 0.29 |
embB | 4245845 | c.-669T>G | upstream_gene_variant | 0.29 |
embB | 4245848 | c.-666C>G | upstream_gene_variant | 0.29 |
embB | 4245860 | c.-654C>G | upstream_gene_variant | 0.29 |
embB | 4248720 | p.Gly736Ala | missense_variant | 1.0 |
embB | 4249432 | c.2919A>G | synonymous_variant | 0.18 |
embB | 4249444 | c.2931T>C | synonymous_variant | 0.22 |
embB | 4249676 | p.Arg1055Cys | missense_variant | 1.0 |
aftB | 4267622 | c.1215G>C | synonymous_variant | 0.29 |
aftB | 4267927 | p.Ala304Ser | missense_variant | 1.0 |
whiB6 | 4338314 | p.Ala70Thr | missense_variant | 0.29 |