Run ID: SRR13861428
Sample name:
Date: 03-04-2023 09:31:33
Number of reads: 341028
Percentage reads mapped: 8.53
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 | 0.93 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5333 | p.Met32Val | missense_variant | 1.0 |
gyrA | 6388 | c.-914T>C | upstream_gene_variant | 0.13 |
gyrA | 6400 | c.-902C>G | upstream_gene_variant | 0.13 |
gyrA | 6403 | c.-899T>C | upstream_gene_variant | 0.14 |
gyrA | 8288 | c.987T>C | synonymous_variant | 0.18 |
gyrA | 8294 | c.993T>C | synonymous_variant | 0.18 |
gyrA | 8324 | c.1023T>C | synonymous_variant | 0.18 |
gyrA | 8342 | c.1041G>C | synonymous_variant | 0.2 |
gyrA | 8366 | c.1065G>C | synonymous_variant | 0.15 |
gyrA | 8375 | c.1074G>C | synonymous_variant | 0.15 |
gyrA | 8391 | p.Tyr364His | missense_variant | 0.15 |
gyrA | 8399 | c.1098T>C | synonymous_variant | 0.15 |
gyrA | 8420 | c.1119T>C | synonymous_variant | 0.13 |
gyrA | 8423 | c.1122G>C | synonymous_variant | 0.14 |
mshA | 575746 | c.399C>G | synonymous_variant | 0.14 |
mshA | 575771 | p.Val142Ser | missense_variant | 0.14 |
mshA | 575779 | c.432A>G | synonymous_variant | 0.14 |
ccsA | 620331 | c.441C>T | synonymous_variant | 0.25 |
ccsA | 620340 | c.450C>G | synonymous_variant | 0.2 |
ccsA | 620349 | c.459A>G | synonymous_variant | 0.18 |
ccsA | 620362 | p.Ala158Thr | missense_variant | 0.17 |
ccsA | 620367 | c.477T>C | synonymous_variant | 0.17 |
ccsA | 620373 | c.483C>G | synonymous_variant | 0.15 |
ccsA | 620509 | p.Thr207Ser | missense_variant | 1.0 |
ccsA | 620749 | p.Trp287Arg | missense_variant | 1.0 |
rpoB | 760337 | c.531C>G | synonymous_variant | 0.22 |
rpoB | 760340 | c.534G>C | synonymous_variant | 0.2 |
rpoB | 760670 | c.864G>C | synonymous_variant | 0.21 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.21 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.23 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.23 |
rpoB | 760718 | c.912C>G | synonymous_variant | 0.21 |
rpoB | 760721 | c.915C>G | synonymous_variant | 0.23 |
rpoB | 760724 | c.918T>C | synonymous_variant | 0.25 |
rpoB | 760730 | c.924T>C | synonymous_variant | 0.27 |
rpoB | 760751 | c.945G>C | synonymous_variant | 0.22 |
rpoB | 760757 | c.951T>C | synonymous_variant | 0.2 |
rpoB | 760759 | p.Val318Ala | missense_variant | 0.2 |
rpoB | 760763 | c.957C>T | synonymous_variant | 0.18 |
rpoB | 760769 | c.963C>G | synonymous_variant | 0.17 |
rpoB | 760775 | c.969G>C | synonymous_variant | 0.17 |
rpoB | 760776 | c.970_972delTCGinsAGC | synonymous_variant | 0.17 |
rpoB | 760793 | c.987A>G | synonymous_variant | 0.2 |
rpoB | 760805 | c.999G>C | synonymous_variant | 0.27 |
rpoB | 760830 | c.1024T>C | synonymous_variant | 0.2 |
rpoB | 760845 | p.Thr347Pro | missense_variant | 0.17 |
rpoB | 760859 | c.1053T>C | synonymous_variant | 0.17 |
rpoB | 760869 | p.Val355Ile | missense_variant | 0.18 |
rpoB | 760886 | c.1080A>G | synonymous_variant | 0.17 |
rpoB | 760919 | c.1113C>G | synonymous_variant | 0.14 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.13 |
rpoB | 760934 | c.1128C>T | synonymous_variant | 0.13 |
rpoC | 762836 | c.-534C>G | upstream_gene_variant | 0.15 |
rpoC | 764131 | c.762T>C | synonymous_variant | 0.2 |
rpoC | 764161 | c.792G>C | synonymous_variant | 0.3 |
rpoC | 764188 | c.819A>G | synonymous_variant | 0.25 |
rpoC | 764195 | p.Ser276Gln | missense_variant | 0.25 |
rpoC | 764203 | c.834G>T | synonymous_variant | 0.25 |
rpoC | 764206 | c.837T>C | synonymous_variant | 0.22 |
rpoC | 764257 | c.888G>C | synonymous_variant | 0.22 |
rpoC | 764269 | c.900G>C | synonymous_variant | 0.22 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.14 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.15 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.15 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.14 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.14 |
rpoC | 765559 | c.2190G>C | synonymous_variant | 0.14 |
rpoC | 765583 | c.2214G>T | synonymous_variant | 0.14 |
rpoC | 765613 | p.His748Gln | missense_variant | 0.2 |
rpoC | 765625 | c.2256C>G | synonymous_variant | 0.27 |
rpoC | 765628 | c.2259G>C | synonymous_variant | 0.14 |
rpoC | 765631 | p.Asp754Glu | missense_variant | 0.14 |
rpoC | 765658 | c.2289C>T | synonymous_variant | 0.14 |
rpoC | 766954 | c.3586delG | frameshift_variant | 0.92 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.17 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.15 |
rpoC | 767158 | c.3789T>C | synonymous_variant | 0.17 |
rpoC | 767167 | c.3798C>G | synonymous_variant | 0.23 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.17 |
rpoC | 767191 | c.3822C>G | synonymous_variant | 0.17 |
rpoC | 767206 | c.3837C>G | synonymous_variant | 0.22 |
rpoC | 767209 | c.3840T>C | synonymous_variant | 0.2 |
rpoC | 767212 | c.3843G>C | synonymous_variant | 0.18 |
rpoC | 767221 | c.3852C>G | synonymous_variant | 0.18 |
mmpL5 | 776029 | c.2452C>T | synonymous_variant | 0.2 |
mmpL5 | 776080 | p.Ala801Pro | missense_variant | 0.89 |
mmpS5 | 779649 | c.-744T>A | upstream_gene_variant | 1.0 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.22 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.25 |
rplC | 801220 | p.Ser138Gly | missense_variant | 0.91 |
fbiC | 1303494 | p.Leu188Phe | missense_variant | 1.0 |
rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1471969 | n.124T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472044 | n.199G>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472101 | n.256G>A | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472122 | n.277G>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.92 |
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 | 0.93 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472230 | n.385C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472262 | n.417C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472269 | n.424G>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472271 | n.426T>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472277 | n.432C>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472505 | n.660G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472596 | n.751G>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472614 | n.769G>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472665 | n.820G>A | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472669 | n.824_825insTAGG | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472695 | n.850C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.65 |
rrs | 1473248 | n.1403G>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473249 | n.1404T>C | non_coding_transcript_exon_variant | 0.61 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.61 |
rrs | 1473255 | n.1410A>G | non_coding_transcript_exon_variant | 0.61 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1473260 | n.1415G>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.58 |
rrs | 1473281 | n.1436C>A | non_coding_transcript_exon_variant | 0.61 |
rrs | 1473282 | n.1437C>G | non_coding_transcript_exon_variant | 0.61 |
rrs | 1473288 | n.1443C>A | non_coding_transcript_exon_variant | 0.66 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473291 | n.1446G>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1473296 | n.1451G>C | non_coding_transcript_exon_variant | 0.63 |
rrs | 1473297 | n.1452G>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.63 |
rrs | 1473327 | n.1482A>G | non_coding_transcript_exon_variant | 0.63 |
rrs | 1473328 | n.1483C>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474904 | n.1247G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474991 | n.1334T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475006 | n.1349A>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475015 | n.1358C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476215 | n.2558C>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476263 | n.2606C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476268 | n.2611A>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476275 | n.2618T>A | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.98 |
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 | 0.98 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476572 | n.2915G>A | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476595 | n.2938C>G | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476596 | n.2939C>T | non_coding_transcript_exon_variant | 0.41 |
fabG1 | 1673622 | p.Asp61Glu | missense_variant | 1.0 |
fabG1 | 1673718 | c.279_280insT | frameshift_variant&stop_gained | 0.9 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.22 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.22 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.22 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.22 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.2 |
rpsA | 1833790 | c.249T>A | synonymous_variant | 0.2 |
rpsA | 1833799 | c.258C>G | synonymous_variant | 0.2 |
katG | 2155998 | p.Trp38Cys | missense_variant | 1.0 |
katG | 2156285 | c.-174T>G | upstream_gene_variant | 1.0 |
ahpC | 2726085 | c.-108G>A | upstream_gene_variant | 0.9 |
folC | 2746308 | p.Arg431Ser | missense_variant | 0.14 |
folC | 2746321 | c.1278A>C | synonymous_variant | 0.13 |
folC | 2746328 | p.Arg424Gln | missense_variant | 0.14 |
folC | 2746335 | p.Gly422Arg | missense_variant | 0.15 |
folC | 2746336 | c.1263C>G | synonymous_variant | 0.15 |
folC | 2746345 | c.1254G>C | synonymous_variant | 0.17 |
folC | 2746351 | p.Ala416Ser | missense_variant | 0.17 |
folC | 2746360 | c.1239T>C | synonymous_variant | 0.15 |
folC | 2746375 | c.1224G>C | synonymous_variant | 0.14 |
folC | 2746390 | c.1209G>C | synonymous_variant | 0.14 |
folC | 2746393 | c.1206C>G | synonymous_variant | 0.14 |
folC | 2746396 | c.1203C>G | synonymous_variant | 0.14 |
folC | 2746402 | p.Asp399His | missense_variant | 0.14 |
folC | 2746416 | p.Glu395Gln | missense_variant | 0.15 |
folC | 2746420 | c.1179A>G | synonymous_variant | 0.14 |
folC | 2746438 | c.1161G>C | synonymous_variant | 0.23 |
ribD | 2987458 | p.Val207Ala | missense_variant | 1.0 |
thyA | 3073872 | p.Ile200Val | missense_variant | 0.25 |
thyA | 3073878 | c.594G>A | synonymous_variant | 0.22 |
thyA | 3073892 | c.580T>C | synonymous_variant | 0.25 |
thyA | 3073893 | c.579C>G | synonymous_variant | 0.27 |
thyA | 3073925 | c.547T>C | synonymous_variant | 0.23 |
thyA | 3073926 | c.546G>C | synonymous_variant | 0.23 |
thyA | 3073929 | c.543T>C | synonymous_variant | 0.23 |
thyA | 3073953 | c.519T>C | synonymous_variant | 0.31 |
thyA | 3073977 | c.495A>G | synonymous_variant | 0.25 |
thyA | 3073989 | c.483T>C | synonymous_variant | 0.23 |
thyA | 3074001 | c.471C>G | synonymous_variant | 0.18 |
thyA | 3074004 | c.468T>C | synonymous_variant | 0.18 |
thyA | 3074010 | c.462C>G | synonymous_variant | 0.18 |
ald | 3087895 | p.Leu359Pro | missense_variant | 0.2 |
Rv3236c | 3612721 | c.395delT | frameshift_variant | 1.0 |
alr | 3840445 | p.Leu326Met | missense_variant | 1.0 |
alr | 3841156 | p.Leu89Val | missense_variant | 1.0 |
rpoA | 3877966 | p.Thr181Asn | missense_variant | 1.0 |
rpoA | 3878046 | c.462T>C | synonymous_variant | 0.2 |
rpoA | 3878284 | p.Glu75Ala | missense_variant | 0.17 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.17 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.17 |
rpoA | 3878304 | c.204G>C | synonymous_variant | 0.17 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 0.15 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.15 |
rpoA | 3878331 | c.177A>G | synonymous_variant | 0.14 |
rpoA | 3878334 | c.174T>C | synonymous_variant | 0.13 |
rpoA | 3878337 | c.171T>C | synonymous_variant | 0.13 |
rpoA | 3878346 | c.162T>C | synonymous_variant | 0.13 |
rpoA | 3878364 | c.144A>G | synonymous_variant | 0.17 |
rpoA | 3878367 | c.141C>G | synonymous_variant | 0.17 |
rpoA | 3878370 | c.138T>C | synonymous_variant | 0.17 |
rpoA | 3878376 | c.132G>C | synonymous_variant | 0.17 |
rpoA | 3878385 | c.123C>G | synonymous_variant | 0.18 |
rpoA | 3878391 | c.117T>C | synonymous_variant | 0.2 |
rpoA | 3878396 | c.112C>T | synonymous_variant | 0.2 |
clpC1 | 4038623 | c.2082A>G | synonymous_variant | 0.2 |
clpC1 | 4038640 | p.Asp689Asn | missense_variant | 0.17 |
clpC1 | 4038653 | c.2052C>T | synonymous_variant | 0.17 |
clpC1 | 4038658 | p.Lys683Gln | missense_variant | 0.17 |
clpC1 | 4038661 | p.Ser682Thr | missense_variant | 0.17 |
clpC1 | 4038662 | c.2043T>C | synonymous_variant | 0.16 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 0.14 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.17 |
clpC1 | 4038815 | c.1890G>T | synonymous_variant | 0.17 |
clpC1 | 4038851 | c.1854G>A | synonymous_variant | 0.17 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.18 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.17 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 0.18 |
clpC1 | 4038932 | c.1773G>C | synonymous_variant | 0.3 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.2 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.18 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.18 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.18 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.2 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.2 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.25 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.22 |
clpC1 | 4039073 | c.1632C>G | synonymous_variant | 0.22 |
clpC1 | 4040237 | c.468C>T | synonymous_variant | 0.25 |
clpC1 | 4040249 | c.456A>G | synonymous_variant | 0.22 |
clpC1 | 4040273 | c.432T>C | synonymous_variant | 0.25 |
clpC1 | 4040354 | c.351A>G | synonymous_variant | 0.2 |
clpC1 | 4040363 | c.342A>C | synonymous_variant | 0.2 |
clpC1 | 4040369 | c.336C>G | synonymous_variant | 0.2 |
clpC1 | 4040380 | c.325T>C | synonymous_variant | 0.2 |
clpC1 | 4040381 | c.324T>C | synonymous_variant | 0.2 |
clpC1 | 4040411 | c.294T>C | synonymous_variant | 0.18 |
clpC1 | 4040423 | c.282A>G | synonymous_variant | 0.2 |
clpC1 | 4040426 | c.279T>C | synonymous_variant | 0.18 |
clpC1 | 4040431 | c.274T>C | synonymous_variant | 0.18 |
clpC1 | 4040441 | c.264C>G | synonymous_variant | 0.2 |
clpC1 | 4040444 | c.261C>G | synonymous_variant | 0.18 |
clpC1 | 4040450 | c.255A>G | synonymous_variant | 0.18 |
clpC1 | 4040459 | c.246C>G | synonymous_variant | 0.18 |
clpC1 | 4040465 | c.240T>C | synonymous_variant | 0.18 |
clpC1 | 4040471 | c.234T>C | synonymous_variant | 0.18 |
clpC1 | 4040477 | c.228G>A | synonymous_variant | 0.18 |
clpC1 | 4040480 | c.225T>C | synonymous_variant | 0.18 |
panD | 4044216 | c.65_66insT | frameshift_variant | 1.0 |
embB | 4247289 | p.Ala259Gly | missense_variant | 1.0 |
embB | 4249154 | p.Gly881Arg | missense_variant | 1.0 |
ubiA | 4270024 | c.-191T>G | upstream_gene_variant | 1.0 |