Run ID: ERR4817488
Sample name:
Date: 01-04-2023 15:01:09
Number of reads: 1604033
Percentage reads mapped: 95.84
Strain: lineage4.3.4.2.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.4 | Euro-American (LAM) | LAM | RD174 | 1.0 |
lineage4.3.4.2 | Euro-American (LAM) | LAM1;LAM4;LAM11 | RD174 | 1.0 |
lineage4.3.4.2.1 | Euro-American (LAM) | LAM11 | RD174 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.38 | streptomycin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.38 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.12 | kanamycin, capreomycin, aminoglycosides, amikacin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6140 | p.Val301Leu | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472076 | n.231G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472549 | n.704G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472597 | n.752G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472674 | n.829T>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472675 | n.830T>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473262 | n.1417T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473264 | n.1419A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473294 | n.1449A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473300 | n.1455C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473677 | n.20C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473695 | n.39_40delTC | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473700 | n.43G>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473702 | n.45_46insGA | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473717 | n.60G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473718 | n.61G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473744 | n.87T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473746 | n.89T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473748 | n.91A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473751 | n.94C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473753 | n.96A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473756 | n.99G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473782 | n.125A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2170066 | p.Ala183Thr | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
folC | 2746731 | p.Tyr290His | missense_variant | 0.1 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612009 | p.Ala370Thr | missense_variant | 1.0 |
alr | 3840719 | c.702A>G | synonymous_variant | 1.0 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |