Run ID: ERR4820918
Sample name:
Date: 01-04-2023 16:57:25
Number of reads: 214403
Percentage reads mapped: 60.81
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 | 0.97 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7909 | p.Trp203* | stop_gained | 0.29 |
mshA | 576456 | p.Val370Ala | missense_variant | 0.5 |
rpoC | 766746 | c.3382delC | frameshift_variant | 0.18 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776117 | p.Phe788Leu | missense_variant | 0.4 |
mmpS5 | 778965 | c.-60G>A | upstream_gene_variant | 0.5 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800679 | c.-130T>G | upstream_gene_variant | 0.33 |
embR | 1416864 | p.Phe162Leu | missense_variant | 0.33 |
atpE | 1460912 | c.-133C>T | upstream_gene_variant | 0.67 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472123 | n.278A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472150 | n.305T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474228 | n.571T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474275 | n.618T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476229 | n.2572C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101877 | p.Gly389Asp | missense_variant | 0.67 |
katG | 2155233 | c.879G>T | synonymous_variant | 0.5 |
katG | 2155907 | p.Ala69Ser | missense_variant | 0.5 |
katG | 2155941 | c.171G>A | synonymous_variant | 0.33 |
PPE35 | 2169179 | c.1434C>T | synonymous_variant | 0.29 |
Rv1979c | 2222671 | c.493delA | frameshift_variant | 0.4 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518403 | p.Ser97Thr | missense_variant | 0.5 |
pepQ | 2860373 | p.Ala16Ser | missense_variant | 0.29 |
pepQ | 2860459 | c.-41T>C | upstream_gene_variant | 0.25 |
ribD | 2986882 | p.Arg15Lys | missense_variant | 1.0 |
thyX | 3067279 | p.Ala223Thr | missense_variant | 0.22 |
thyA | 3073895 | p.Gly193Ser | missense_variant | 1.0 |
Rv3083 | 3449457 | c.954C>T | synonymous_variant | 0.4 |
fbiA | 3640723 | p.Asp61Asn | missense_variant | 0.33 |
alr | 3840696 | p.Ala242Val | missense_variant | 0.67 |
ddn | 3987104 | p.Met87Ile | missense_variant | 1.0 |
clpC1 | 4040234 | c.471C>T | synonymous_variant | 0.67 |
panD | 4044284 | c.-3C>A | upstream_gene_variant | 1.0 |
panD | 4044435 | c.-154C>T | upstream_gene_variant | 0.67 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245034 | p.Arg601Leu | missense_variant | 0.2 |
aftB | 4269393 | c.-557G>T | upstream_gene_variant | 0.29 |
ethA | 4328358 | c.-885C>T | upstream_gene_variant | 0.4 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408000 | c.202delA | frameshift_variant | 0.29 |