Run ID: ERR4820297
Sample name:
Date: 01-04-2023 16:36:03
Number of reads: 1068343
Percentage reads mapped: 96.96
Strain: lineage4.2.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.2 | Euro-American | H;T;LAM | None | 1.0 |
lineage4.2.1 | Euro-American (TUR) | H3;H4 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.47 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 576258 | p.Ser304Ile | missense_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406400 | p.Ile314Thr | missense_variant | 1.0 |
atpE | 1461101 | c.57T>G | synonymous_variant | 0.23 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472673 | n.828T>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472681 | n.837_838delTT | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472687 | n.843dupT | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473148 | n.1303G>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473163 | n.1318C>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474931 | n.1274G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2169879 | p.Phe245Cys | missense_variant | 1.0 |
PPE35 | 2170143 | p.Gly157Val | missense_variant | 0.12 |
PPE35 | 2170147 | p.Ser156Ala | missense_variant | 0.12 |
Rv1979c | 2223284 | c.-120C>T | upstream_gene_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474511 | p.Asp169Asn | missense_variant | 1.0 |
Rv3236c | 3612595 | c.522A>G | synonymous_variant | 1.0 |
fbiB | 3640914 | c.-621C>G | upstream_gene_variant | 1.0 |
rpoA | 3878531 | c.-24A>G | upstream_gene_variant | 0.22 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407767 | p.Thr146Ala | missense_variant | 1.0 |
gid | 4408149 | c.54T>C | synonymous_variant | 1.0 |