Run ID: ERR4815060
Sample name:
Date: 01-04-2023 13:38:48
Number of reads: 1811197
Percentage reads mapped: 95.14
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 | 0.74 | streptomycin |
gid | 4407967 | p.Leu79Ser | missense_variant | 1.0 | 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 |
gyrA | 9596 | c.2295G>T | synonymous_variant | 1.0 |
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 | 762957 | c.-413C>T | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764181 | p.Asp271Gly | missense_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 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472150 | n.305T>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473148 | n.1303G>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473163 | n.1318C>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102275 | c.768C>T | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155772 | p.Arg114Cys | missense_variant | 0.12 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.12 |
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 |
folC | 2747792 | c.-194G>T | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449066 | c.565delG | frameshift_variant | 1.0 |
Rv3083 | 3449260 | p.Lys253* | stop_gained | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
panD | 4044291 | c.-10G>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 |