Run ID: SRR13861447
Sample name:
Date: 03-04-2023 09:31:59
Number of reads: 646869
Percentage reads mapped: 10.79
Strain: lineage4.9
Drug-resistance: RR-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 |
---|---|---|---|---|---|
rpoB | 761135 | p.Leu443Phe | missense_variant | 0.15 | rifampicin |
rrs | 1472307 | n.462C>T | non_coding_transcript_exon_variant | 0.15 | streptomycin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.84 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7541 | c.240C>G | synonymous_variant | 0.13 |
gyrA | 7637 | c.336C>G | synonymous_variant | 0.13 |
gyrA | 7730 | p.Arg143Ser | missense_variant | 0.14 |
gyrA | 7877 | p.His192Gln | missense_variant | 0.94 |
gyrA | 8852 | c.1551T>C | synonymous_variant | 0.14 |
gyrA | 8858 | c.1557T>C | synonymous_variant | 0.16 |
gyrA | 8867 | c.1566A>G | synonymous_variant | 0.14 |
gyrA | 8870 | c.1569G>C | synonymous_variant | 0.14 |
gyrA | 8873 | c.1572A>C | synonymous_variant | 0.14 |
gyrA | 8897 | c.1596T>C | synonymous_variant | 0.16 |
gyrA | 8915 | c.1614A>G | synonymous_variant | 0.18 |
gyrA | 8942 | c.1641G>C | synonymous_variant | 0.12 |
mshA | 576146 | p.Val267Leu | missense_variant | 1.0 |
ccsA | 620703 | c.813G>C | synonymous_variant | 0.15 |
ccsA | 620710 | p.Val274Met | missense_variant | 0.15 |
ccsA | 620734 | c.844C>A | synonymous_variant | 0.14 |
ccsA | 620739 | c.849A>G | synonymous_variant | 0.14 |
ccsA | 620745 | c.855G>C | synonymous_variant | 0.14 |
ccsA | 620748 | c.858T>A | synonymous_variant | 0.14 |
ccsA | 620778 | c.888T>C | synonymous_variant | 0.17 |
ccsA | 620784 | c.894C>G | synonymous_variant | 0.17 |
ccsA | 620787 | c.897C>G | synonymous_variant | 0.17 |
rpoB | 759647 | c.-160T>C | upstream_gene_variant | 0.14 |
rpoB | 759659 | c.-148_-147insGA | upstream_gene_variant | 0.15 |
rpoB | 759662 | c.-145C>T | upstream_gene_variant | 0.15 |
rpoB | 759683 | c.-124T>C | upstream_gene_variant | 0.14 |
rpoB | 759869 | c.63C>T | synonymous_variant | 1.0 |
rpoB | 760514 | c.708C>T | synonymous_variant | 0.15 |
rpoB | 760522 | p.Ser239Asn | missense_variant | 0.16 |
rpoB | 760934 | c.1128C>T | synonymous_variant | 0.13 |
rpoB | 760970 | c.1164G>C | synonymous_variant | 0.14 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.13 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.14 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.2 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 0.23 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.22 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.21 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.21 |
rpoB | 761051 | c.1245G>T | synonymous_variant | 0.15 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.14 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.14 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.16 |
rpoB | 761063 | c.1257C>G | synonymous_variant | 0.17 |
rpoB | 761094 | c.1288C>T | synonymous_variant | 0.16 |
rpoB | 761097 | c.1291_1292delAGinsTC | synonymous_variant | 0.15 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.15 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.14 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.15 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.16 |
rpoC | 763158 | c.-212C>T | upstream_gene_variant | 0.17 |
rpoC | 763782 | p.Ser138* | stop_gained | 1.0 |
rpoC | 764568 | p.Lys400Thr | missense_variant | 0.95 |
rpoC | 765412 | c.2043T>C | synonymous_variant | 0.14 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.14 |
rpoC | 765451 | c.2082C>G | synonymous_variant | 0.16 |
rpoC | 765452 | p.Ala695Ser | missense_variant | 0.16 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.24 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.18 |
rpoC | 765508 | c.2139C>G | synonymous_variant | 0.19 |
rpoC | 765559 | c.2190G>C | synonymous_variant | 0.14 |
rpoC | 765578 | c.2209C>T | synonymous_variant | 0.14 |
rpoC | 765583 | c.2214G>T | synonymous_variant | 0.16 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.15 |
rpoC | 766390 | c.3021C>T | synonymous_variant | 0.14 |
rpoC | 766408 | c.3039C>T | synonymous_variant | 0.14 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.22 |
rpoC | 766447 | c.3078T>C | synonymous_variant | 0.17 |
rpoC | 766483 | c.3114G>C | synonymous_variant | 0.17 |
rpoC | 766484 | p.Val1039Ile | missense_variant | 0.17 |
rpoC | 766492 | c.3123T>C | synonymous_variant | 0.17 |
rpoC | 766495 | c.3126C>T | synonymous_variant | 0.17 |
rpoC | 766522 | c.3153C>G | synonymous_variant | 0.16 |
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 |
mmpL5 | 777073 | p.Lys470Glu | missense_variant | 1.0 |
mmpL5 | 777311 | c.1170C>T | synonymous_variant | 1.0 |
mmpL5 | 778981 | c.-501C>A | upstream_gene_variant | 0.95 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.15 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.17 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.18 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.18 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.15 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.23 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.23 |
rplC | 800648 | c.-161A>C | upstream_gene_variant | 0.25 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.24 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.13 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.16 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.16 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.16 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.17 |
rplC | 800738 | c.-71T>C | upstream_gene_variant | 0.15 |
rplC | 800771 | c.-38C>T | upstream_gene_variant | 0.14 |
rplC | 801436 | p.Ser210Arg | missense_variant | 0.97 |
fbiC | 1303686 | c.756C>G | synonymous_variant | 1.0 |
fbiC | 1304634 | c.1704C>G | synonymous_variant | 0.12 |
fbiC | 1304691 | c.1761G>C | synonymous_variant | 0.18 |
fbiC | 1304694 | c.1764A>C | synonymous_variant | 0.18 |
fbiC | 1304703 | c.1773C>G | synonymous_variant | 0.19 |
fbiC | 1304715 | c.1785G>C | synonymous_variant | 0.19 |
fbiC | 1304757 | c.1827A>G | synonymous_variant | 0.12 |
fbiC | 1304808 | c.1878C>G | synonymous_variant | 0.17 |
fbiC | 1304811 | c.1881C>G | synonymous_variant | 0.17 |
fbiC | 1305297 | c.2367G>C | synonymous_variant | 0.13 |
fbiC | 1305303 | c.2373T>C | synonymous_variant | 0.13 |
fbiC | 1305311 | p.Arg794Gln | missense_variant | 0.13 |
fbiC | 1305331 | p.Glu801Lys | missense_variant | 0.19 |
fbiC | 1305336 | c.2406T>C | synonymous_variant | 0.12 |
fbiC | 1305381 | c.2451G>C | synonymous_variant | 0.13 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472101 | n.256G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472122 | n.277G>A | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472230 | n.385C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472262 | n.417C>T | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472269 | n.424G>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472271 | n.426T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472277 | n.432C>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472505 | n.660G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472596 | n.751G>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472605 | n.760G>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472614 | n.769G>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472665 | n.820G>A | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472669 | n.824_825insTAGG | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472695 | n.850C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.66 |
rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.52 |
rrs | 1473248 | n.1403G>A | non_coding_transcript_exon_variant | 0.48 |
rrs | 1473249 | n.1404T>C | non_coding_transcript_exon_variant | 0.48 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473255 | n.1410A>G | non_coding_transcript_exon_variant | 0.48 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473260 | n.1415G>T | non_coding_transcript_exon_variant | 0.51 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.51 |
rrs | 1473281 | n.1436C>A | non_coding_transcript_exon_variant | 0.52 |
rrs | 1473282 | n.1437C>G | non_coding_transcript_exon_variant | 0.52 |
rrs | 1473288 | n.1443C>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473291 | n.1446G>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1473296 | n.1451G>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1473297 | n.1452G>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1473327 | n.1482A>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473328 | n.1483C>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475659 | n.2002G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476215 | n.2558C>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.84 |
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 | 0.19 |
rrl | 1476268 | n.2611A>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476275 | n.2618T>A | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.87 |
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 | 0.89 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476572 | n.2915G>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476595 | n.2938C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476695 | n.3038T>A | non_coding_transcript_exon_variant | 0.14 |
inhA | 1674376 | p.Pro59Ser | missense_variant | 0.95 |
rpsA | 1833619 | c.78A>C | synonymous_variant | 0.14 |
tlyA | 1917844 | c.-96C>A | upstream_gene_variant | 0.96 |
tlyA | 1918260 | p.His107Gln | missense_variant | 1.0 |
katG | 2154461 | p.Ala551Pro | missense_variant | 1.0 |
Rv1979c | 2222535 | c.630C>G | synonymous_variant | 1.0 |
kasA | 2518608 | p.Met165Thr | missense_variant | 0.89 |
eis | 2714211 | c.1122G>A | synonymous_variant | 1.0 |
ahpC | 2726250 | p.Gly20Arg | missense_variant | 0.95 |
thyX | 3067787 | c.159G>A | synonymous_variant | 0.17 |
thyX | 3067793 | c.153T>C | synonymous_variant | 0.18 |
thyX | 3067799 | c.147G>A | synonymous_variant | 0.2 |
thyX | 3067802 | c.144C>G | synonymous_variant | 0.2 |
thyX | 3067814 | c.132T>C | synonymous_variant | 0.14 |
thyX | 3067826 | c.120C>G | synonymous_variant | 0.14 |
thyX | 3067850 | c.96A>C | synonymous_variant | 0.14 |
thyA | 3073953 | c.519T>C | synonymous_variant | 0.12 |
fprA | 3473843 | c.-164C>G | upstream_gene_variant | 0.12 |
fprA | 3473848 | c.-159C>G | upstream_gene_variant | 0.12 |
fprA | 3473932 | c.-75G>A | upstream_gene_variant | 1.0 |
Rv3236c | 3612518 | p.Tyr200Ser | missense_variant | 1.0 |
fbiB | 3641684 | p.Ser50Arg | missense_variant | 1.0 |
rpoA | 3877704 | c.804G>T | synonymous_variant | 0.2 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.23 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.21 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.22 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.22 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.24 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.25 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.25 |
rpoA | 3877857 | c.651G>A | synonymous_variant | 0.15 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.14 |
rpoA | 3877872 | c.636C>T | synonymous_variant | 0.18 |
rpoA | 3877875 | c.633T>G | synonymous_variant | 0.18 |
rpoA | 3877899 | p.Ser203Thr | missense_variant | 0.18 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.17 |
rpoA | 3877908 | p.Asn200Ser | missense_variant | 0.17 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.17 |
rpoA | 3878141 | p.Met123Leu | missense_variant | 0.2 |
rpoA | 3878142 | p.Gly122Glu | missense_variant | 0.2 |
rpoA | 3878184 | c.324C>T | synonymous_variant | 0.25 |
rpoA | 3878187 | c.321C>G | synonymous_variant | 0.25 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.23 |
rpoA | 3878199 | c.309T>C | synonymous_variant | 0.23 |
rpoA | 3878202 | c.306G>C | synonymous_variant | 0.23 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.21 |
rpoA | 3878220 | c.288C>T | synonymous_variant | 0.21 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.14 |
rpoA | 3878284 | p.Glu75Ala | missense_variant | 0.14 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.2 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.2 |
rpoA | 3878304 | c.204G>C | synonymous_variant | 0.2 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 0.23 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.19 |
rpoA | 3878331 | c.177A>G | synonymous_variant | 0.2 |
rpoA | 3878334 | c.174T>C | synonymous_variant | 0.14 |
rpoA | 3878337 | c.171T>C | synonymous_variant | 0.14 |
rpoA | 3878364 | c.144A>G | synonymous_variant | 0.19 |
rpoA | 3878367 | c.141C>G | synonymous_variant | 0.18 |
rpoA | 3878370 | c.138T>C | synonymous_variant | 0.18 |
rpoA | 3878376 | c.132G>C | synonymous_variant | 0.18 |
rpoA | 3878385 | c.123C>G | synonymous_variant | 0.18 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 0.14 |
clpC1 | 4038434 | c.2271G>C | synonymous_variant | 0.17 |
clpC1 | 4038444 | p.Ala754Lys | missense_variant | 0.19 |
clpC1 | 4038446 | c.2259T>C | synonymous_variant | 0.18 |
clpC1 | 4038452 | c.2253G>C | synonymous_variant | 0.17 |
clpC1 | 4038461 | p.Ala748Asp | missense_variant | 0.19 |
clpC1 | 4038498 | p.Ser736Thr | missense_variant | 0.13 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.14 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 0.13 |
clpC1 | 4038932 | c.1773G>C | synonymous_variant | 0.17 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.12 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.15 |
clpC1 | 4039073 | c.1632C>G | synonymous_variant | 0.19 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.13 |
clpC1 | 4039103 | c.1602T>C | synonymous_variant | 0.15 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.14 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.14 |
clpC1 | 4039946 | c.759A>T | synonymous_variant | 0.17 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.14 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.14 |
clpC1 | 4039996 | p.Glu237Gln | missense_variant | 0.18 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.19 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.19 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.19 |
clpC1 | 4040036 | c.669C>G | synonymous_variant | 0.19 |
embC | 4240183 | c.321A>G | synonymous_variant | 0.13 |
embC | 4240204 | c.342T>C | synonymous_variant | 0.15 |
embC | 4240210 | c.348C>G | synonymous_variant | 0.15 |
embC | 4240216 | c.354T>C | synonymous_variant | 0.15 |
embC | 4240231 | c.369G>C | synonymous_variant | 0.15 |
embC | 4240232 | p.Gln124Val | missense_variant | 0.15 |
embC | 4240258 | c.396T>G | synonymous_variant | 0.15 |
embC | 4240263 | p.Val134Ala | missense_variant | 0.91 |
embC | 4240920 | p.Leu353Pro | missense_variant | 1.0 |
embC | 4241504 | p.Val548Met | missense_variant | 0.95 |
embA | 4244228 | c.996A>G | synonymous_variant | 0.13 |
embA | 4244233 | p.Ala334Gly | missense_variant | 0.12 |
embA | 4244267 | c.1035G>C | synonymous_variant | 0.18 |
embA | 4244276 | c.1044A>C | synonymous_variant | 0.17 |
embA | 4244284 | p.Pro351Arg | missense_variant | 0.18 |
embA | 4244298 | p.Ser356Ala | missense_variant | 0.21 |
embA | 4244309 | c.1077C>G | synonymous_variant | 0.21 |
embA | 4244312 | c.1080T>G | synonymous_variant | 0.21 |
embA | 4244315 | c.1083G>C | synonymous_variant | 0.2 |
embA | 4244324 | c.1092T>G | synonymous_variant | 0.22 |
embA | 4244327 | c.1095T>C | synonymous_variant | 0.22 |
embA | 4244337 | p.Leu369Val | missense_variant | 0.21 |
embA | 4244340 | p.Ser370Ala | missense_variant | 0.22 |
embA | 4244366 | c.1134C>G | synonymous_variant | 0.16 |
embA | 4244372 | c.1140T>G | synonymous_variant | 0.16 |
embB | 4245587 | c.-927G>C | upstream_gene_variant | 0.13 |
embB | 4248000 | p.Asp496Val | missense_variant | 0.95 |
aftB | 4267580 | c.1257G>C | synonymous_variant | 0.12 |
aftB | 4268715 | p.Leu41Pro | missense_variant | 1.0 |
ethR | 4327704 | p.Lys52Asn | missense_variant | 1.0 |