Run ID: SRR13861400
Sample name:
Date: 03-04-2023 09:30:55
Number of reads: 1561918
Percentage reads mapped: 52.11
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 | 0.98 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.46 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7697 | c.396C>G | synonymous_variant | 0.15 |
gyrA | 7760 | c.459C>T | synonymous_variant | 0.15 |
gyrA | 7763 | c.462T>C | synonymous_variant | 0.15 |
gyrA | 7799 | c.498A>G | synonymous_variant | 0.17 |
gyrA | 7835 | c.534A>G | synonymous_variant | 0.17 |
gyrA | 7838 | c.537C>G | synonymous_variant | 0.14 |
gyrA | 8399 | c.1098T>C | synonymous_variant | 0.14 |
gyrA | 8597 | c.1296C>G | synonymous_variant | 0.14 |
gyrA | 8603 | c.1302A>G | synonymous_variant | 0.16 |
gyrA | 8619 | c.1318T>C | synonymous_variant | 0.16 |
gyrA | 8624 | c.1323G>C | synonymous_variant | 0.15 |
gyrA | 8627 | c.1326C>G | synonymous_variant | 0.15 |
gyrA | 8636 | c.1335A>G | synonymous_variant | 0.17 |
gyrA | 8642 | c.1341A>G | synonymous_variant | 0.18 |
gyrA | 8645 | c.1344C>G | synonymous_variant | 0.18 |
gyrA | 8672 | c.1371A>G | synonymous_variant | 0.18 |
gyrA | 8693 | c.1392T>C | synonymous_variant | 0.15 |
gyrA | 8699 | c.1398A>G | synonymous_variant | 0.17 |
gyrA | 8711 | c.1410A>C | synonymous_variant | 0.15 |
gyrA | 8714 | c.1413A>G | synonymous_variant | 0.15 |
gyrA | 8717 | c.1416C>G | synonymous_variant | 0.15 |
gyrA | 8720 | c.1419G>A | synonymous_variant | 0.15 |
gyrA | 8729 | c.1428T>C | synonymous_variant | 0.16 |
gyrA | 8732 | c.1431G>C | synonymous_variant | 0.16 |
gyrA | 8747 | c.1446A>G | synonymous_variant | 0.15 |
gyrA | 8762 | c.1461G>C | synonymous_variant | 0.14 |
gyrA | 8765 | p.Asp488Glu | missense_variant | 0.16 |
gyrA | 8767 | p.Arg489Lys | missense_variant | 0.15 |
gyrA | 8780 | p.Asp493Glu | missense_variant | 0.15 |
gyrA | 8786 | c.1485T>C | synonymous_variant | 0.14 |
gyrA | 8796 | p.Ile499Val | missense_variant | 0.16 |
gyrA | 8801 | c.1500G>C | synonymous_variant | 0.16 |
gyrA | 8810 | c.1509A>C | synonymous_variant | 0.17 |
gyrA | 8816 | c.1515C>T | synonymous_variant | 0.15 |
gyrA | 8880 | p.Lys527Gln | missense_variant | 0.94 |
mshA | 575713 | c.366G>A | synonymous_variant | 0.13 |
mshA | 575719 | c.372C>T | synonymous_variant | 0.13 |
mshA | 575752 | c.405G>A | synonymous_variant | 0.12 |
rpoB | 760181 | c.375T>C | synonymous_variant | 0.15 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.14 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.15 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.15 |
rpoB | 760307 | c.501T>C | synonymous_variant | 0.16 |
rpoB | 760328 | c.522G>C | synonymous_variant | 0.15 |
rpoB | 760337 | c.531C>G | synonymous_variant | 0.16 |
rpoB | 760340 | c.534G>C | synonymous_variant | 0.16 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.19 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.16 |
rpoB | 760418 | c.612G>C | synonymous_variant | 0.19 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.19 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.2 |
rpoB | 760514 | c.708C>T | synonymous_variant | 0.13 |
rpoB | 760533 | p.Val243Thr | missense_variant | 0.13 |
rpoB | 760547 | c.741G>C | synonymous_variant | 0.14 |
rpoB | 760972 | p.Arg389Leu | missense_variant | 0.9 |
rpoB | 762218 | c.2412T>G | synonymous_variant | 0.14 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.15 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.16 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.17 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.17 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.18 |
rpoB | 762329 | c.2523G>C | synonymous_variant | 0.16 |
rpoB | 762338 | c.2532T>C | synonymous_variant | 0.14 |
rpoC | 763945 | c.576T>C | synonymous_variant | 0.14 |
rpoC | 763960 | c.591T>C | synonymous_variant | 0.18 |
rpoC | 763967 | p.Gly200Ser | missense_variant | 0.15 |
rpoC | 765111 | p.Met581Lys | missense_variant | 0.96 |
rpoC | 765161 | p.Glu598Lys | missense_variant | 1.0 |
rpoC | 765404 | p.Leu679Val | missense_variant | 0.15 |
rpoC | 765540 | p.Ala724Val | missense_variant | 0.88 |
rpoC | 766390 | c.3021C>T | synonymous_variant | 0.15 |
rpoC | 766408 | c.3039C>T | synonymous_variant | 0.15 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.16 |
rpoC | 766483 | c.3114G>C | synonymous_variant | 0.14 |
rpoC | 766486 | c.3117A>C | synonymous_variant | 0.14 |
rpoC | 766495 | c.3126C>T | synonymous_variant | 0.13 |
rpoC | 767068 | c.3699G>T | synonymous_variant | 0.94 |
mmpR5 | 778439 | c.-551C>A | upstream_gene_variant | 1.0 |
rplC | 801357 | p.His183Gln | missense_variant | 1.0 |
fbiC | 1303911 | c.981G>C | synonymous_variant | 0.14 |
fbiC | 1304229 | c.1301delC | frameshift_variant | 1.0 |
fbiC | 1304832 | c.1902C>G | synonymous_variant | 0.13 |
fbiC | 1304853 | c.1923C>G | synonymous_variant | 0.15 |
fbiC | 1304856 | c.1926C>G | synonymous_variant | 0.15 |
fbiC | 1304872 | c.1942_1944delAGCinsTCG | synonymous_variant | 0.15 |
fbiC | 1304877 | c.1947T>C | synonymous_variant | 0.15 |
fbiC | 1304878 | c.1948_1950delCGCinsAGG | synonymous_variant | 0.15 |
fbiC | 1304893 | p.Gly655Ser | missense_variant | 0.15 |
fbiC | 1305331 | p.Glu801Asn | missense_variant | 0.14 |
rrs | 1472044 | n.199G>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472122 | n.277G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472262 | n.417C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472288 | n.444delT | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472596 | n.751G>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472614 | n.769G>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472665 | n.820G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472669 | n.824_825insTAGG | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472695 | n.850C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473813 | n.156C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475006 | n.1349A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475015 | n.1358C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475088 | n.1431A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475199 | n.1542G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475206 | n.1549C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475209 | n.1552G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475369 | n.1712G>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475638 | n.1981C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475659 | n.2002G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476268 | n.2611A>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476275 | n.2618T>A | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.49 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.49 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476572 | n.2915G>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.46 |
inhA | 1674756 | c.555T>C | synonymous_variant | 0.15 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.14 |
rpsA | 1834225 | c.684C>G | synonymous_variant | 0.15 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.18 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.2 |
rpsA | 1834261 | c.720A>C | synonymous_variant | 0.19 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.2 |
rpsA | 1834297 | c.756C>G | synonymous_variant | 0.18 |
rpsA | 1834303 | c.762T>G | synonymous_variant | 0.17 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.17 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.16 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.16 |
rpsA | 1834375 | c.834G>A | synonymous_variant | 0.14 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.15 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.14 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.14 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.14 |
rpsA | 1834474 | c.933C>G | synonymous_variant | 0.14 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.15 |
rpsA | 1834498 | c.957C>T | synonymous_variant | 0.15 |
tlyA | 1917989 | p.Ala17Gly | missense_variant | 0.98 |
ndh | 2102525 | p.Phe173Tyr | missense_variant | 0.98 |
ndh | 2102538 | c.504_505insT | frameshift_variant | 0.98 |
Rv1979c | 2222978 | p.Ile63Phe | missense_variant | 1.0 |
Rv1979c | 2223052 | p.Glu38Val | missense_variant | 1.0 |
pncA | 2289415 | c.-174C>G | upstream_gene_variant | 1.0 |
kasA | 2518057 | c.-58A>C | upstream_gene_variant | 1.0 |
kasA | 2518799 | p.Pro229Ser | missense_variant | 0.94 |
eis | 2714983 | p.Ala117Glu | missense_variant | 1.0 |
thyX | 3067304 | c.642A>G | synonymous_variant | 0.15 |
thyX | 3067316 | c.630A>G | synonymous_variant | 0.16 |
thyX | 3067325 | c.621A>G | synonymous_variant | 0.15 |
thyX | 3067355 | c.591A>C | synonymous_variant | 0.17 |
thyX | 3067367 | c.579G>C | synonymous_variant | 0.16 |
thyX | 3067376 | c.570G>C | synonymous_variant | 0.17 |
thyX | 3067391 | c.555G>C | synonymous_variant | 0.16 |
thyX | 3067394 | c.552G>C | synonymous_variant | 0.15 |
thyX | 3067412 | c.534C>G | synonymous_variant | 0.18 |
thyX | 3067439 | c.507A>G | synonymous_variant | 0.19 |
thyX | 3067445 | c.501C>G | synonymous_variant | 0.18 |
thyX | 3067451 | c.495G>A | synonymous_variant | 0.18 |
thyX | 3067457 | c.489C>G | synonymous_variant | 0.17 |
thyX | 3067463 | p.Ile161Val | missense_variant | 0.16 |
thyX | 3067466 | c.480G>C | synonymous_variant | 0.16 |
thyX | 3067470 | p.Asn159Ser | missense_variant | 0.15 |
thyX | 3067493 | c.453A>G | synonymous_variant | 0.16 |
thyX | 3067500 | p.Lys149Arg | missense_variant | 0.17 |
thyX | 3067515 | p.Ser144Thr | missense_variant | 0.14 |
fbiA | 3640404 | c.-139C>A | upstream_gene_variant | 1.0 |
fbiB | 3642056 | c.522C>G | synonymous_variant | 1.0 |
rpoA | 3877967 | p.Thr181Ser | missense_variant | 0.92 |
rpoA | 3877972 | c.535delG | frameshift_variant | 0.93 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.16 |
rpoA | 3878067 | c.441C>G | synonymous_variant | 0.16 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.16 |
rpoA | 3878082 | c.426T>C | synonymous_variant | 0.14 |
clpC1 | 4038748 | p.Arg653Cys | missense_variant | 0.14 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.15 |
clpC1 | 4039524 | p.Phe394Tyr | missense_variant | 0.15 |
clpC1 | 4039547 | c.1158C>G | synonymous_variant | 0.17 |
clpC1 | 4039553 | c.1152C>G | synonymous_variant | 0.17 |
clpC1 | 4039562 | c.1143C>G | synonymous_variant | 0.17 |
clpC1 | 4039565 | c.1140G>C | synonymous_variant | 0.17 |
clpC1 | 4039576 | p.Ala377Ser | missense_variant | 0.14 |
clpC1 | 4039586 | c.1119G>C | synonymous_variant | 0.16 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.15 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.15 |
clpC1 | 4039622 | c.1083C>G | synonymous_variant | 0.15 |
clpC1 | 4039682 | c.1023C>G | synonymous_variant | 0.17 |
clpC1 | 4039685 | c.1020C>T | synonymous_variant | 0.16 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.14 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.18 |
clpC1 | 4039777 | c.927_928insG | frameshift_variant | 1.0 |
clpC1 | 4039789 | p.Ser306Thr | missense_variant | 0.13 |
clpC1 | 4040363 | c.342A>C | synonymous_variant | 0.14 |
clpC1 | 4040369 | c.336C>G | synonymous_variant | 0.14 |
embB | 4247545 | p.Ser344Arg | missense_variant | 0.94 |
aftB | 4268812 | p.Ser9Pro | missense_variant | 1.0 |