Run ID: ERR2513356
Sample name:
Date: 31-03-2023 19:37:37
Number of reads: 1613720
Percentage reads mapped: 98.16
Strain: lineage4.5
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.5 | Euro-American | H;T | RD122 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.21 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5739 | p.Thr167Arg | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7892 | c.591G>A | synonymous_variant | 0.97 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
ccsA | 620029 | c.139C>T | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1305180 | c.2250G>A | synonymous_variant | 1.0 |
Rv1258c | 1406101 | p.Pro414Ser | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472681 | n.837_838delTT | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474634 | n.977T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474658 | n.1001A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474692 | n.1035G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2170568 | p.Ile15Met | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714529 | c.804C>T | synonymous_variant | 1.0 |
Rv3083 | 3449746 | p.Asp415Asn | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3878575 | c.-68C>T | upstream_gene_variant | 1.0 |
clpC1 | 4038318 | p.Pro796Leu | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
ethR | 4327994 | p.Thr149Met | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |