Run ID: SRR13861397
Sample name:
Date: 03-04-2023 09:30:41
Number of reads: 684593
Percentage reads mapped: 22.84
Strain: lineage4.9
Drug-resistance: HR-TB
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 | 1472307 | n.462C>T | non_coding_transcript_exon_variant | 0.23 | streptomycin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.76 | streptomycin |
katG | 2154798 | c.1313_1314insT | frameshift_variant | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5906 | p.Val223Leu | missense_variant | 1.0 |
gyrB | 6011 | p.Val258Met | missense_variant | 1.0 |
gyrA | 6307 | c.-995T>G | upstream_gene_variant | 0.17 |
gyrA | 6319 | c.-983G>C | upstream_gene_variant | 0.17 |
gyrA | 6325 | c.-977C>G | upstream_gene_variant | 0.15 |
gyrB | 6678 | p.Pro480Arg | missense_variant | 0.96 |
gyrA | 8453 | c.1152A>C | synonymous_variant | 0.12 |
gyrA | 8516 | c.1215T>C | synonymous_variant | 0.15 |
gyrA | 8519 | c.1218A>C | synonymous_variant | 0.15 |
fgd1 | 490676 | c.-107G>C | upstream_gene_variant | 1.0 |
fgd1 | 491043 | c.261T>A | synonymous_variant | 0.15 |
fgd1 | 491049 | c.267T>C | synonymous_variant | 0.19 |
fgd1 | 491063 | p.Gly94Ala | missense_variant | 0.17 |
fgd1 | 491077 | p.Asn99Gly | missense_variant | 0.21 |
fgd1 | 491082 | c.300T>C | synonymous_variant | 0.22 |
fgd1 | 491083 | p.Val101Ile | missense_variant | 0.22 |
fgd1 | 491091 | c.309T>C | synonymous_variant | 0.28 |
fgd1 | 491094 | c.312C>G | synonymous_variant | 0.28 |
fgd1 | 491106 | c.324T>C | synonymous_variant | 0.28 |
fgd1 | 491121 | c.339A>G | synonymous_variant | 0.25 |
fgd1 | 491137 | p.Glu119Gln | missense_variant | 0.26 |
fgd1 | 491144 | p.Ala121Glu | missense_variant | 0.26 |
fgd1 | 491166 | c.384G>C | synonymous_variant | 0.25 |
fgd1 | 491181 | c.399T>C | synonymous_variant | 0.27 |
fgd1 | 491191 | p.Gly137Arg | missense_variant | 0.25 |
fgd1 | 491194 | c.412_414delCTAinsTTG | synonymous_variant | 0.17 |
fgd1 | 491202 | c.420G>C | synonymous_variant | 0.19 |
fgd1 | 491203 | p.Gln141Glu | missense_variant | 0.19 |
fgd1 | 491212 | p.Ser144Arg | missense_variant | 0.19 |
fgd1 | 491217 | c.435T>C | synonymous_variant | 0.17 |
fgd1 | 491232 | c.450T>C | synonymous_variant | 0.19 |
fgd1 | 491241 | p.Asp153Glu | missense_variant | 0.18 |
fgd1 | 491244 | c.462T>C | synonymous_variant | 0.18 |
fgd1 | 491259 | c.477T>C | synonymous_variant | 0.18 |
fgd1 | 491286 | c.504G>C | synonymous_variant | 0.16 |
fgd1 | 491292 | c.510G>C | synonymous_variant | 0.17 |
fgd1 | 491295 | c.513C>G | synonymous_variant | 0.17 |
fgd1 | 491296 | p.Val172Ile | missense_variant | 0.17 |
fgd1 | 491301 | c.519C>T | synonymous_variant | 0.17 |
ccsA | 620028 | c.138G>C | synonymous_variant | 1.0 |
rpoB | 759638 | c.-169T>A | upstream_gene_variant | 1.0 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.15 |
rpoB | 760283 | c.477G>C | synonymous_variant | 0.16 |
rpoB | 760307 | c.501T>C | synonymous_variant | 0.17 |
rpoB | 760328 | c.522G>C | synonymous_variant | 0.19 |
rpoB | 760331 | c.525G>C | synonymous_variant | 0.2 |
rpoB | 760337 | c.531C>G | synonymous_variant | 0.22 |
rpoB | 760340 | c.534G>C | synonymous_variant | 0.22 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.22 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.22 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.19 |
rpoB | 760418 | c.612G>C | synonymous_variant | 0.19 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.16 |
rpoB | 760454 | c.650delG | frameshift_variant | 0.84 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.15 |
rpoB | 760481 | c.675G>C | synonymous_variant | 0.16 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.15 |
rpoB | 760522 | p.Ser239Asn | missense_variant | 0.14 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.21 |
rpoB | 760611 | c.805T>C | synonymous_variant | 0.19 |
rpoB | 760634 | c.828T>C | synonymous_variant | 0.16 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.15 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.16 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.16 |
rpoB | 760670 | c.864G>C | synonymous_variant | 0.17 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.18 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.18 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.18 |
rpoB | 760718 | c.912C>G | synonymous_variant | 0.16 |
rpoB | 760721 | c.915C>G | synonymous_variant | 0.16 |
rpoB | 760724 | c.918T>C | synonymous_variant | 0.17 |
rpoB | 760730 | c.924T>C | synonymous_variant | 0.17 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.14 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.14 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.21 |
rpoB | 761360 | c.1554T>C | synonymous_variant | 0.13 |
rpoB | 761362 | p.Ser519Thr | missense_variant | 0.13 |
rpoB | 761373 | p.Val523His | missense_variant | 0.17 |
rpoB | 761414 | c.1608A>G | synonymous_variant | 0.18 |
rpoB | 761423 | c.1617T>C | synonymous_variant | 0.14 |
rpoB | 761435 | c.1629T>C | synonymous_variant | 0.12 |
rpoB | 761437 | p.Ala544Glu | missense_variant | 0.12 |
rpoB | 761441 | p.Asp545Glu | missense_variant | 0.12 |
rpoB | 761452 | p.Val549Ala | missense_variant | 0.13 |
rpoB | 761459 | c.1653G>C | synonymous_variant | 0.12 |
rpoB | 762014 | c.2208C>T | synonymous_variant | 0.13 |
rpoB | 762027 | c.2221_2223delCTCinsTTG | synonymous_variant | 0.14 |
rpoB | 762032 | c.2226C>G | synonymous_variant | 0.14 |
rpoB | 762035 | c.2229G>C | synonymous_variant | 0.14 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.17 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.17 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.17 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.14 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.13 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.13 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 0.16 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.17 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.14 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.17 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.21 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.21 |
rpoB | 762218 | c.2412T>G | synonymous_variant | 0.27 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.21 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.2 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.17 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.17 |
rpoC | 764161 | c.792G>C | synonymous_variant | 0.13 |
rpoC | 764188 | c.819A>G | synonymous_variant | 0.19 |
rpoC | 764195 | p.Ser276Gln | missense_variant | 0.15 |
rpoC | 764203 | c.834G>T | synonymous_variant | 0.15 |
rpoC | 764206 | c.837T>C | synonymous_variant | 0.14 |
rpoC | 764266 | c.897T>C | synonymous_variant | 0.13 |
rpoC | 765487 | p.Met706Ile | missense_variant | 1.0 |
rpoC | 766327 | c.2958C>G | synonymous_variant | 0.15 |
rpoC | 766345 | c.2976T>C | synonymous_variant | 0.16 |
rpoC | 766348 | c.2979A>G | synonymous_variant | 0.15 |
rpoC | 766363 | c.2994G>C | synonymous_variant | 0.15 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.14 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.17 |
rpoC | 766390 | c.3021C>T | synonymous_variant | 0.17 |
rpoC | 766408 | c.3039C>T | synonymous_variant | 0.13 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.14 |
rpoC | 766447 | c.3078T>C | synonymous_variant | 0.13 |
rpoC | 766483 | c.3114G>C | synonymous_variant | 0.13 |
rpoC | 766484 | p.Val1039Ile | missense_variant | 0.13 |
rpoC | 766492 | c.3123T>C | synonymous_variant | 0.16 |
rpoC | 766495 | c.3126C>T | synonymous_variant | 0.15 |
rpoC | 766522 | c.3153C>G | synonymous_variant | 0.18 |
rpoC | 766528 | c.3159T>C | synonymous_variant | 0.19 |
rpoC | 766531 | c.3162G>T | synonymous_variant | 0.19 |
rpoC | 766543 | c.3174C>T | synonymous_variant | 0.16 |
rpoC | 766549 | c.3180G>C | synonymous_variant | 0.16 |
rpoC | 766573 | c.3204T>C | synonymous_variant | 0.15 |
rpoC | 766583 | p.Gly1072Ser | missense_variant | 0.16 |
rpoC | 766588 | c.3219G>A | synonymous_variant | 0.13 |
rpoC | 766609 | p.Ile1080Met | missense_variant | 0.15 |
rpoC | 767014 | c.3645G>C | synonymous_variant | 0.12 |
rpoC | 767033 | p.Ser1222Thr | missense_variant | 0.12 |
rpoC | 767074 | c.3705T>C | synonymous_variant | 0.15 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.19 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.18 |
rpoC | 767134 | c.3765C>G | synonymous_variant | 0.14 |
rpoC | 767158 | c.3789T>C | synonymous_variant | 0.14 |
rpoC | 767167 | c.3798C>G | synonymous_variant | 0.14 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.14 |
mmpL5 | 775864 | p.Ala873Ser | missense_variant | 0.14 |
mmpL5 | 775865 | c.2616T>G | synonymous_variant | 0.19 |
mmpL5 | 775904 | c.2577G>A | synonymous_variant | 0.13 |
mmpL5 | 775909 | p.Leu858Phe | missense_variant | 0.14 |
mmpL5 | 775912 | c.2569C>A | synonymous_variant | 0.13 |
mmpL5 | 775916 | c.2565T>G | synonymous_variant | 0.14 |
mmpL5 | 775937 | c.2544G>C | synonymous_variant | 0.14 |
rpsL | 781409 | c.-151T>A | upstream_gene_variant | 1.0 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.13 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.24 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.24 |
rplC | 800648 | c.-161A>C | upstream_gene_variant | 0.29 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.23 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.21 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.27 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.22 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.23 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.22 |
rplC | 800738 | c.-71T>C | upstream_gene_variant | 0.22 |
rplC | 800747 | c.-62C>G | upstream_gene_variant | 0.24 |
rplC | 800771 | c.-38C>T | upstream_gene_variant | 0.25 |
rplC | 800814 | c.6A>G | synonymous_variant | 0.25 |
rplC | 800817 | c.9A>T | synonymous_variant | 0.23 |
rplC | 800844 | c.36T>C | synonymous_variant | 0.29 |
rplC | 800865 | c.57A>G | synonymous_variant | 0.12 |
rplC | 800867 | p.Ser20Asn | missense_variant | 0.12 |
rplC | 800889 | c.81C>G | synonymous_variant | 0.17 |
fbiC | 1302873 | c.-58A>T | upstream_gene_variant | 1.0 |
fbiC | 1303575 | c.645G>C | synonymous_variant | 0.2 |
fbiC | 1303584 | c.654C>G | synonymous_variant | 0.2 |
fbiC | 1303590 | c.660A>G | synonymous_variant | 0.2 |
fbiC | 1303602 | c.672A>G | synonymous_variant | 0.16 |
fbiC | 1303605 | c.675C>G | synonymous_variant | 0.15 |
fbiC | 1303608 | c.678G>A | synonymous_variant | 0.15 |
fbiC | 1303611 | c.681G>C | synonymous_variant | 0.15 |
fbiC | 1303614 | c.684C>T | synonymous_variant | 0.15 |
fbiC | 1303617 | c.687C>G | synonymous_variant | 0.15 |
fbiC | 1303632 | c.702T>G | synonymous_variant | 0.14 |
fbiC | 1303638 | c.708A>G | synonymous_variant | 0.14 |
fbiC | 1303674 | c.744C>G | synonymous_variant | 0.16 |
fbiC | 1303686 | c.756C>G | synonymous_variant | 0.19 |
fbiC | 1303695 | c.765T>C | synonymous_variant | 0.19 |
fbiC | 1303708 | c.778T>C | synonymous_variant | 0.19 |
fbiC | 1303728 | c.798G>A | synonymous_variant | 0.13 |
fbiC | 1303730 | p.Leu267Pro | missense_variant | 0.13 |
fbiC | 1303737 | c.807G>A | synonymous_variant | 0.13 |
fbiC | 1305231 | c.2301C>G | synonymous_variant | 0.12 |
fbiC | 1305237 | c.2307A>G | synonymous_variant | 0.12 |
fbiC | 1305240 | c.2310T>C | synonymous_variant | 0.12 |
fbiC | 1305244 | c.2314T>C | synonymous_variant | 0.12 |
rrs | 1471874 | n.29A>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472101 | n.256G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472122 | n.277G>A | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472230 | n.385C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472262 | n.417C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472596 | n.751G>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472614 | n.769G>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472665 | n.820G>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472669 | n.824_825insTAGG | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472695 | n.850C>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.51 |
rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473248 | n.1403G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473249 | n.1404T>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473255 | n.1410A>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473260 | n.1415G>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473281 | n.1436C>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473282 | n.1437C>G | non_coding_transcript_exon_variant | 0.24 |
rrs | 1473288 | n.1443C>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473291 | n.1446G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473296 | n.1451G>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473297 | n.1452G>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473327 | n.1482A>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473328 | n.1483C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1473937 | n.280C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473944 | n.287G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473945 | n.288T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474009 | n.352A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474012 | n.355C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474051 | n.394T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474054 | n.397T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474056 | n.399T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474104 | n.447G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474111 | n.454T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474112 | n.455T>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474376 | n.719T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476215 | n.2558C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476263 | n.2606C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476268 | n.2611A>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476275 | n.2618T>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476572 | n.2915G>A | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476595 | n.2938C>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476596 | n.2939C>T | non_coding_transcript_exon_variant | 0.13 |
inhA | 1674756 | c.555T>C | synonymous_variant | 0.15 |
inhA | 1674771 | c.570C>G | synonymous_variant | 0.14 |
inhA | 1674774 | c.573A>G | synonymous_variant | 0.14 |
inhA | 1674780 | c.579T>G | synonymous_variant | 0.18 |
inhA | 1674786 | c.585G>C | synonymous_variant | 0.15 |
inhA | 1674799 | p.Ser200Ala | missense_variant | 0.14 |
inhA | 1674803 | p.Ala201Gly | missense_variant | 0.13 |
inhA | 1674816 | c.615T>C | synonymous_variant | 0.14 |
inhA | 1674818 | p.Ala206Val | missense_variant | 0.13 |
rpsA | 1833811 | c.270G>C | synonymous_variant | 0.14 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.14 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.14 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.14 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.17 |
rpsA | 1833940 | c.399C>G | synonymous_variant | 0.2 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.14 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.17 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.17 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.14 |
ndh | 2102559 | p.Ser162Arg | missense_variant | 0.17 |
ndh | 2102566 | c.477A>G | synonymous_variant | 0.17 |
ndh | 2102572 | c.471A>G | synonymous_variant | 0.18 |
ndh | 2102575 | c.468G>A | synonymous_variant | 0.18 |
ndh | 2102581 | c.462T>G | synonymous_variant | 0.17 |
ndh | 2102589 | c.454T>C | synonymous_variant | 0.17 |
ndh | 2102590 | c.453A>C | synonymous_variant | 0.16 |
ndh | 2102593 | c.450C>G | synonymous_variant | 0.15 |
ndh | 2102596 | c.447C>G | synonymous_variant | 0.15 |
ndh | 2102599 | c.444T>C | synonymous_variant | 0.15 |
ndh | 2102604 | p.Leu147Val | missense_variant | 0.15 |
ndh | 2102608 | c.433_435delTTGinsCTC | synonymous_variant | 0.17 |
ndh | 2102635 | c.408C>G | synonymous_variant | 0.14 |
ndh | 2102638 | c.405A>G | synonymous_variant | 0.13 |
katG | 2154654 | p.Ser486Arg | missense_variant | 1.0 |
katG | 2154882 | c.1230G>A | synonymous_variant | 1.0 |
katG | 2155857 | c.255C>A | synonymous_variant | 1.0 |
PPE35 | 2170198 | p.Ala139Ser | missense_variant | 1.0 |
pncA | 2290069 | c.-828C>T | upstream_gene_variant | 1.0 |
kasA | 2518714 | c.600A>C | synonymous_variant | 0.14 |
kasA | 2518717 | c.603C>T | synonymous_variant | 0.14 |
kasA | 2518723 | p.Glu203Asp | missense_variant | 0.14 |
kasA | 2518732 | c.618C>G | synonymous_variant | 0.14 |
eis | 2714922 | c.411G>A | synonymous_variant | 1.0 |
thyA | 3074067 | c.405C>G | synonymous_variant | 0.96 |
alr | 3840223 | c.1198A>C | synonymous_variant | 0.96 |
alr | 3840711 | p.Ser237Leu | missense_variant | 1.0 |
rpoA | 3877953 | c.555G>A | synonymous_variant | 0.16 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.13 |
rpoA | 3877986 | c.522G>C | synonymous_variant | 0.14 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.18 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.21 |
rpoA | 3878031 | c.477T>C | synonymous_variant | 0.13 |
rpoA | 3878040 | c.468T>C | synonymous_variant | 0.17 |
rpoA | 3878046 | c.462T>C | synonymous_variant | 0.16 |
rpoA | 3878049 | c.459G>C | synonymous_variant | 0.17 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.18 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.19 |
rpoA | 3878067 | c.441C>G | synonymous_variant | 0.19 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.19 |
rpoA | 3878082 | c.426T>C | synonymous_variant | 0.24 |
rpoA | 3878094 | c.414C>G | synonymous_variant | 0.15 |
rpoA | 3878100 | c.408C>G | synonymous_variant | 0.15 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.14 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.14 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.23 |
rpoA | 3878141 | p.Met123Leu | missense_variant | 0.17 |
rpoA | 3878142 | p.Gly122Glu | missense_variant | 0.17 |
rpoA | 3878169 | c.339G>C | synonymous_variant | 0.15 |
rpoA | 3878184 | c.324C>T | synonymous_variant | 0.18 |
rpoA | 3878187 | c.321C>G | synonymous_variant | 0.17 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.17 |
rpoA | 3878199 | c.309T>C | synonymous_variant | 0.17 |
rpoA | 3878202 | c.306G>C | synonymous_variant | 0.17 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.16 |
rpoA | 3878220 | c.288C>T | synonymous_variant | 0.2 |
clpC1 | 4038398 | c.2307G>T | synonymous_variant | 0.12 |
clpC1 | 4038419 | c.2286T>C | synonymous_variant | 0.14 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.17 |
clpC1 | 4039073 | c.1632C>G | synonymous_variant | 0.17 |
clpC1 | 4039085 | c.1620A>G | synonymous_variant | 0.18 |
clpC1 | 4039090 | c.1615C>T | synonymous_variant | 0.18 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.16 |
clpC1 | 4039103 | c.1602T>C | synonymous_variant | 0.17 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.17 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.17 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.18 |
clpC1 | 4039124 | c.1581C>G | synonymous_variant | 0.18 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.17 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.18 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.17 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.17 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.17 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.17 |
clpC1 | 4039187 | c.1518G>C | synonymous_variant | 0.14 |
clpC1 | 4039190 | c.1515C>G | synonymous_variant | 0.15 |
clpC1 | 4039208 | c.1497C>G | synonymous_variant | 0.14 |
clpC1 | 4039226 | c.1479T>C | synonymous_variant | 0.15 |
clpC1 | 4039268 | c.1437C>G | synonymous_variant | 0.18 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.22 |
clpC1 | 4039286 | c.1419T>C | synonymous_variant | 0.23 |
clpC1 | 4039289 | c.1416T>C | synonymous_variant | 0.14 |
clpC1 | 4039295 | c.1410A>C | synonymous_variant | 0.15 |
clpC1 | 4039319 | c.1386T>C | synonymous_variant | 0.17 |
clpC1 | 4039322 | c.1383T>C | synonymous_variant | 0.17 |
clpC1 | 4039328 | c.1377A>G | synonymous_variant | 0.16 |
clpC1 | 4039334 | c.1371G>C | synonymous_variant | 0.16 |
clpC1 | 4039337 | p.Thr456Gln | missense_variant | 0.16 |
clpC1 | 4039388 | c.1317C>A | synonymous_variant | 0.18 |
clpC1 | 4039391 | c.1314T>G | synonymous_variant | 0.18 |
clpC1 | 4039409 | c.1296T>C | synonymous_variant | 0.17 |
clpC1 | 4039412 | c.1293T>G | synonymous_variant | 0.17 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.12 |
clpC1 | 4039648 | p.Glu353Gln | missense_variant | 1.0 |
clpC1 | 4040168 | c.537G>C | synonymous_variant | 0.15 |
clpC1 | 4040201 | c.504C>G | synonymous_variant | 0.14 |
clpC1 | 4040213 | c.490_492delTCTinsAGC | synonymous_variant | 0.14 |
clpC1 | 4040225 | c.480A>C | synonymous_variant | 0.15 |
clpC1 | 4040228 | c.477G>C | synonymous_variant | 0.15 |
clpC1 | 4040234 | c.471C>G | synonymous_variant | 0.17 |
clpC1 | 4040237 | c.468C>T | synonymous_variant | 0.16 |
clpC1 | 4040249 | c.456A>G | synonymous_variant | 0.16 |
clpC1 | 4040273 | c.432T>C | synonymous_variant | 0.16 |
clpC1 | 4040354 | c.351A>G | synonymous_variant | 0.2 |
clpC1 | 4040363 | c.342A>C | synonymous_variant | 0.18 |
clpC1 | 4040369 | c.336C>G | synonymous_variant | 0.18 |
clpC1 | 4040380 | c.325T>C | synonymous_variant | 0.19 |
clpC1 | 4040381 | c.324T>C | synonymous_variant | 0.19 |
clpC1 | 4040387 | c.318A>G | synonymous_variant | 0.2 |
clpC1 | 4040393 | c.312G>C | synonymous_variant | 0.22 |
clpC1 | 4040411 | c.294T>C | synonymous_variant | 0.21 |
clpC1 | 4040423 | c.282A>G | synonymous_variant | 0.17 |
clpC1 | 4040426 | c.279T>C | synonymous_variant | 0.17 |
clpC1 | 4040441 | c.264C>G | synonymous_variant | 0.14 |
clpC1 | 4040444 | c.261C>G | synonymous_variant | 0.14 |
clpC1 | 4040459 | c.246C>G | synonymous_variant | 0.14 |
clpC1 | 4040465 | c.240T>C | synonymous_variant | 0.16 |
embC | 4242023 | p.Val721Leu | missense_variant | 1.0 |
embA | 4245071 | c.1839G>A | synonymous_variant | 0.89 |
embB | 4248070 | c.1557T>C | synonymous_variant | 0.14 |
embB | 4248085 | c.1572T>C | synonymous_variant | 0.15 |
embB | 4248097 | c.1584C>G | synonymous_variant | 0.16 |
embB | 4248142 | c.1629T>C | synonymous_variant | 0.14 |
embB | 4248143 | c.1630T>C | synonymous_variant | 0.14 |
embB | 4248206 | p.Ser565Gly | missense_variant | 0.17 |
embB | 4248220 | c.1707A>G | synonymous_variant | 0.19 |
embB | 4248241 | c.1728C>T | synonymous_variant | 0.17 |
embB | 4248265 | c.1752C>T | synonymous_variant | 0.18 |
embB | 4248266 | c.1753C>T | synonymous_variant | 0.18 |
embB | 4248277 | c.1764G>C | synonymous_variant | 0.2 |
embB | 4248304 | c.1791G>T | synonymous_variant | 0.17 |
ethA | 4327364 | p.Lys37Arg | missense_variant | 1.0 |