Run ID: ERR4819425
Sample name:
Date: 01-04-2023 16:06:28
Number of reads: 7447988
Percentage reads mapped: 99.09
Strain: lineage3
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.24 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6415 | c.-887G>C | upstream_gene_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 | 0.99 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 766582 | c.3213C>A | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406188 | c.1153C>T | synonymous_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472123 | n.278A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472150 | n.305T>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472396 | n.551A>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472426 | n.581T>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472438 | n.593T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472439 | n.594C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472447 | n.602C>T | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472450 | n.605A>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472484 | n.639_640insC | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.1 |
rrl | 1475066 | n.1409C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475902 | n.2245T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.29 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
ahpC | 2726105 | c.-88G>A | 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 |
alr | 3841473 | c.-53G>A | upstream_gene_variant | 1.0 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |