Run ID: ERR4814350
Sample name:
Date: 01-04-2023 13:14:39
Number of reads: 855407
Percentage reads mapped: 99.34
Strain: lineage3
Drug-resistance: HR-TB
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 |
---|---|---|---|---|---|
katG | 2155421 | c.690delG | frameshift_variant | 0.15 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7732 | p.Glu144Gly | missense_variant | 0.1 |
gyrA | 9033 | p.Arg578Trp | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576751 | p.Lys468Asn | missense_variant | 0.27 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 759785 | c.-22T>A | upstream_gene_variant | 0.11 |
rpoB | 760819 | p.Tyr338Ser | missense_variant | 0.13 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777760 | p.Leu241Phe | missense_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473382 | n.1537T>C | splice_region_variant&non_coding_transcript_exon_variant | 0.25 |
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 | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
pncA | 2289715 | c.-474C>T | upstream_gene_variant | 0.13 |
pncA | 2289775 | c.-534C>A | upstream_gene_variant | 0.17 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726341 | p.Val50Gly | missense_variant | 0.24 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474143 | p.Trp46Tyr | missense_variant | 0.12 |
fbiB | 3642877 | p.Lys448Arg | missense_variant | 1.0 |
rpoA | 3878078 | p.Arg144Cys | missense_variant | 0.11 |
clpC1 | 4038858 | p.Arg616His | missense_variant | 0.13 |
embC | 4240655 | p.Ala265Pro | missense_variant | 0.21 |
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 |