Run ID: SRR13861324
Sample name:
Date: 03-04-2023 09:28:58
Number of reads: 156794
Percentage reads mapped: 3.92
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 | 0.92 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6655 | c.-647T>C | upstream_gene_variant | 0.67 |
gyrA | 6670 | c.-632G>C | upstream_gene_variant | 0.67 |
gyrA | 6673 | c.-629A>C | upstream_gene_variant | 0.67 |
gyrA | 6700 | c.-602T>C | upstream_gene_variant | 0.67 |
gyrA | 6703 | c.-599G>C | upstream_gene_variant | 0.67 |
gyrA | 6706 | c.-596G>A | upstream_gene_variant | 0.67 |
gyrA | 6709 | c.-593A>G | upstream_gene_variant | 0.67 |
gyrA | 6712 | c.-590G>C | upstream_gene_variant | 0.67 |
gyrA | 6727 | c.-575G>T | upstream_gene_variant | 0.67 |
gyrA | 6730 | c.-572A>G | upstream_gene_variant | 0.67 |
gyrA | 6745 | c.-557T>G | upstream_gene_variant | 0.67 |
gyrA | 6760 | c.-542G>C | upstream_gene_variant | 0.67 |
gyrA | 6778 | c.-524C>T | upstream_gene_variant | 0.67 |
gyrA | 6793 | c.-509T>C | upstream_gene_variant | 0.67 |
gyrB | 6797 | p.Gly520Thr | missense_variant | 0.67 |
gyrA | 6824 | c.-478C>T | upstream_gene_variant | 0.67 |
gyrA | 6841 | c.-461T>C | upstream_gene_variant | 0.67 |
gyrA | 6844 | c.-458T>G | upstream_gene_variant | 0.67 |
gyrA | 6853 | c.-449A>G | upstream_gene_variant | 1.0 |
gyrA | 6856 | c.-446T>C | upstream_gene_variant | 1.0 |
gyrA | 6859 | c.-443T>C | upstream_gene_variant | 1.0 |
gyrA | 6862 | c.-440C>G | upstream_gene_variant | 1.0 |
gyrA | 6878 | c.-424T>C | upstream_gene_variant | 0.67 |
gyrA | 6881 | c.-421T>C | upstream_gene_variant | 0.67 |
gyrA | 8324 | c.1023T>C | synonymous_variant | 0.5 |
mshA | 576184 | c.837A>C | synonymous_variant | 0.33 |
rpoB | 760139 | c.333A>G | synonymous_variant | 0.2 |
rpoB | 760142 | c.336C>G | synonymous_variant | 0.2 |
rpoB | 760181 | c.375T>C | synonymous_variant | 0.3 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.38 |
rpoB | 760196 | c.390C>G | synonymous_variant | 0.33 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.36 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.33 |
rpoB | 760283 | c.477G>C | synonymous_variant | 0.4 |
rpoB | 760307 | c.501T>C | synonymous_variant | 0.38 |
rpoB | 760328 | c.522G>C | synonymous_variant | 0.44 |
rpoB | 760331 | c.525G>C | synonymous_variant | 0.44 |
rpoB | 760337 | c.531C>G | synonymous_variant | 0.5 |
rpoB | 760340 | c.534G>C | synonymous_variant | 0.5 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.4 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.22 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.33 |
rpoB | 760418 | c.612G>C | synonymous_variant | 0.33 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.33 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.33 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.22 |
rpoB | 760481 | c.675G>C | synonymous_variant | 0.25 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.25 |
rpoB | 760514 | c.708C>T | synonymous_variant | 0.33 |
rpoB | 760522 | p.Ser239Asn | missense_variant | 0.4 |
rpoB | 760919 | c.1113C>G | synonymous_variant | 0.33 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.33 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 0.33 |
rpoB | 760934 | c.1128C>T | synonymous_variant | 0.29 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.25 |
rpoB | 760970 | c.1164G>C | synonymous_variant | 0.29 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.29 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.29 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.29 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.29 |
rpoB | 761094 | c.1288C>T | synonymous_variant | 0.29 |
rpoB | 761097 | c.1291_1292delAGinsTC | synonymous_variant | 0.29 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.29 |
rpoB | 761133 | c.1327_1329delTTGinsCTC | synonymous_variant | 0.29 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.29 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.29 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.29 |
rpoB | 761171 | c.1365C>T | synonymous_variant | 0.29 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.25 |
rpoB | 761492 | c.1686G>C | synonymous_variant | 0.4 |
rpoB | 761510 | c.1704T>C | synonymous_variant | 0.4 |
rpoB | 761531 | c.1725C>G | synonymous_variant | 0.4 |
rpoB | 761534 | c.1728G>A | synonymous_variant | 0.4 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.4 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.4 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.4 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.4 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.4 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.4 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.4 |
rpoC | 765383 | p.Met672Leu | missense_variant | 0.33 |
rpoC | 765404 | p.Leu679Val | missense_variant | 0.33 |
rpoC | 765409 | c.2040T>C | synonymous_variant | 0.33 |
rpoC | 765412 | c.2043T>C | synonymous_variant | 0.33 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.33 |
rpoC | 765451 | c.2082C>G | synonymous_variant | 0.33 |
rpoC | 765452 | p.Ala695Ser | missense_variant | 0.29 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.33 |
rpoC | 765508 | c.2139C>G | synonymous_variant | 0.33 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.67 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.67 |
rplC | 800648 | c.-161A>C | upstream_gene_variant | 0.67 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472101 | n.256G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472122 | n.277G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472230 | n.385C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472262 | n.417C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472269 | n.424G>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472271 | n.426T>C | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472277 | n.432C>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472505 | n.660G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472596 | n.751G>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472614 | n.769G>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472665 | n.820G>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472669 | n.824_825insTAGG | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472695 | n.850C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473191 | n.1346C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473206 | n.1361G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473248 | n.1403G>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473249 | n.1404T>C | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473255 | n.1410A>G | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473260 | n.1415G>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473281 | n.1436C>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473282 | n.1437C>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473288 | n.1443C>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473291 | n.1446G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473296 | n.1451G>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473297 | n.1452G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473327 | n.1482A>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473328 | n.1483C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476215 | n.2558C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476268 | n.2611A>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476275 | n.2618T>A | non_coding_transcript_exon_variant | 0.96 |
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 | 0.97 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.97 |
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 | 0.98 |
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 | 0.8 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 1.0 |
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 | 0.94 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476572 | n.2915G>A | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476595 | n.2938C>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476596 | n.2939C>T | non_coding_transcript_exon_variant | 0.43 |
rpsA | 1833851 | p.Lys104Gln | missense_variant | 1.0 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.5 |
rpsA | 1834555 | c.1014T>C | synonymous_variant | 0.5 |
rpsA | 1834558 | c.1017C>G | synonymous_variant | 0.5 |
rpsA | 1834606 | c.1065C>G | synonymous_variant | 0.33 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.33 |
rpsA | 1834622 | c.1081_1083delTCGinsAGC | synonymous_variant | 0.33 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.4 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.4 |
rpsA | 1834666 | c.1125G>C | synonymous_variant | 0.33 |
rpsA | 1834669 | c.1128G>C | synonymous_variant | 0.33 |
Rv1979c | 2223241 | c.-77C>G | upstream_gene_variant | 1.0 |
pncA | 2289811 | c.-570C>T | upstream_gene_variant | 1.0 |
pncA | 2289994 | c.-753A>C | upstream_gene_variant | 1.0 |
ahpC | 2726564 | c.372C>T | synonymous_variant | 0.2 |
ahpC | 2726579 | c.387T>C | synonymous_variant | 0.2 |
ahpC | 2726591 | c.399C>G | synonymous_variant | 0.2 |
ahpC | 2726593 | p.Val134Ala | missense_variant | 0.2 |
ahpC | 2726600 | c.408T>C | synonymous_variant | 0.2 |
ahpC | 2726612 | c.420C>G | synonymous_variant | 0.2 |
ahpC | 2726638 | p.Ala149Val | missense_variant | 0.22 |
ahpC | 2726645 | c.453C>G | synonymous_variant | 0.25 |
ahpC | 2726657 | c.465A>C | synonymous_variant | 0.25 |
ahpC | 2726669 | p.Asp159Glu | missense_variant | 0.25 |
ahpC | 2726672 | c.480G>A | synonymous_variant | 0.25 |
ahpC | 2726675 | c.483A>G | synonymous_variant | 0.29 |
ahpC | 2726681 | c.489A>G | synonymous_variant | 0.29 |
ahpC | 2726687 | c.495C>G | synonymous_variant | 0.33 |
ahpC | 2726690 | c.498C>T | synonymous_variant | 0.33 |
ahpC | 2726693 | c.501C>G | synonymous_variant | 0.33 |
ahpC | 2726696 | c.504C>G | synonymous_variant | 0.33 |
folC | 2747355 | p.Val82Ile | missense_variant | 0.33 |
folC | 2747359 | c.240C>G | synonymous_variant | 0.33 |
folC | 2747362 | c.237G>C | synonymous_variant | 0.33 |
pepQ | 2859859 | p.Ala187Glu | missense_variant | 1.0 |
Rv2752c | 3064886 | p.Ala436Pro | missense_variant | 1.0 |
Rv2752c | 3065258 | p.Met312Val | missense_variant | 1.0 |
Rv2752c | 3066315 | c.-124C>A | upstream_gene_variant | 0.4 |
Rv3083 | 3449104 | p.Pro201Ala | missense_variant | 1.0 |
fprA | 3474141 | c.135C>G | synonymous_variant | 0.25 |
Rv3236c | 3612337 | c.779delG | frameshift_variant | 1.0 |
fbiB | 3641723 | c.189T>C | synonymous_variant | 1.0 |
rpoA | 3877507 | p.Gly334Ala | missense_variant | 0.5 |
rpoA | 3877515 | c.993G>C | synonymous_variant | 0.5 |
rpoA | 3877542 | c.966C>T | synonymous_variant | 0.5 |
rpoA | 3877553 | p.Glu319Gln | missense_variant | 0.5 |
rpoA | 3877557 | c.951C>G | synonymous_variant | 0.5 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.5 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.5 |
rpoA | 3877740 | c.768G>T | synonymous_variant | 1.0 |
rpoA | 3878031 | c.477T>C | synonymous_variant | 0.5 |
rpoA | 3878040 | c.468T>C | synonymous_variant | 0.5 |
rpoA | 3878046 | c.462T>C | synonymous_variant | 0.5 |
rpoA | 3878049 | c.459G>C | synonymous_variant | 0.5 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.4 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.4 |
rpoA | 3878067 | c.441C>G | synonymous_variant | 0.4 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.4 |
rpoA | 3878094 | c.414C>G | synonymous_variant | 0.4 |
rpoA | 3878100 | c.408C>G | synonymous_variant | 0.4 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.4 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.4 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.29 |
rpoA | 3878141 | p.Met123Leu | missense_variant | 0.29 |
rpoA | 3878142 | p.Gly122Glu | missense_variant | 0.29 |
rpoA | 3878169 | c.339G>C | synonymous_variant | 0.25 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.2 |
rpoA | 3878220 | c.288C>T | synonymous_variant | 0.2 |
clpC1 | 4038293 | c.2412G>C | synonymous_variant | 0.4 |
clpC1 | 4038302 | c.2403C>G | synonymous_variant | 0.4 |
clpC1 | 4038308 | p.Val799Ile | missense_variant | 0.4 |
clpC1 | 4038317 | c.2388G>C | synonymous_variant | 0.33 |
clpC1 | 4038347 | c.2358G>C | synonymous_variant | 0.33 |
clpC1 | 4038356 | c.2349T>C | synonymous_variant | 0.33 |
clpC1 | 4038359 | c.2346A>G | synonymous_variant | 0.33 |
clpC1 | 4038368 | c.2337T>C | synonymous_variant | 0.33 |
clpC1 | 4038388 | c.2317T>C | synonymous_variant | 0.43 |
clpC1 | 4038398 | c.2307G>T | synonymous_variant | 0.38 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 0.38 |
clpC1 | 4038419 | c.2286T>C | synonymous_variant | 0.5 |
clpC1 | 4038434 | c.2271G>C | synonymous_variant | 0.43 |
clpC1 | 4038444 | p.Ala754Lys | missense_variant | 0.5 |
clpC1 | 4038446 | c.2259T>C | synonymous_variant | 0.44 |
clpC1 | 4038452 | c.2253G>C | synonymous_variant | 0.44 |
clpC1 | 4038461 | p.Ala748Asp | missense_variant | 0.5 |
clpC1 | 4038498 | p.Ser736Thr | missense_variant | 0.43 |
clpC1 | 4038530 | p.Glu725Asp | missense_variant | 0.43 |
clpC1 | 4038536 | c.2169C>T | synonymous_variant | 0.43 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.33 |
clpC1 | 4038611 | c.2094C>T | synonymous_variant | 0.5 |
clpC1 | 4038623 | c.2082A>G | synonymous_variant | 0.33 |
clpC1 | 4038640 | p.Asp689Asn | missense_variant | 0.5 |
clpC1 | 4038653 | c.2052C>T | synonymous_variant | 0.43 |
clpC1 | 4038658 | p.Lys683Gln | missense_variant | 0.43 |
clpC1 | 4038661 | p.Ser682Thr | missense_variant | 0.43 |
clpC1 | 4038662 | c.2043T>C | synonymous_variant | 0.43 |
clpC1 | 4038671 | c.2034T>C | synonymous_variant | 0.43 |
clpC1 | 4038683 | c.2022T>C | synonymous_variant | 0.38 |
clpC1 | 4038695 | c.2010C>G | synonymous_variant | 0.29 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.29 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.4 |
clpC1 | 4039748 | c.957G>C | synonymous_variant | 0.33 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.33 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.33 |
clpC1 | 4039760 | c.945T>C | synonymous_variant | 0.33 |
clpC1 | 4039766 | c.939T>C | synonymous_variant | 0.4 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.4 |
clpC1 | 4039781 | c.924G>C | synonymous_variant | 0.4 |
clpC1 | 4039787 | c.916_918delTCGinsAGC | synonymous_variant | 0.4 |
clpC1 | 4039793 | c.912C>G | synonymous_variant | 0.4 |
clpC1 | 4039817 | c.888A>T | synonymous_variant | 0.33 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.33 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.33 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.33 |
clpC1 | 4039928 | c.775_777delAGCinsTCG | synonymous_variant | 0.33 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.29 |
clpC1 | 4039946 | c.759A>T | synonymous_variant | 0.33 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.33 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.4 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.33 |
clpC1 | 4040201 | c.504C>G | synonymous_variant | 0.29 |
clpC1 | 4040207 | c.498T>C | synonymous_variant | 0.33 |
embC | 4241005 | c.1143G>T | synonymous_variant | 1.0 |
embC | 4241081 | c.1220delT | frameshift_variant | 1.0 |
embC | 4242746 | p.Pro962Ser | missense_variant | 1.0 |
embA | 4243969 | p.Val246Ala | missense_variant | 1.0 |
embB | 4247629 | c.1116C>G | synonymous_variant | 0.4 |
embB | 4247632 | c.1119C>G | synonymous_variant | 0.4 |
embB | 4247646 | p.Glu378Ala | missense_variant | 0.33 |