Run ID: ERR4800111
Sample name:
Date: 01-04-2023 09:35:40
Number of reads: 2030781
Percentage reads mapped: 61.91
Strain: lineage3.1.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 0.99 |
lineage3.1 | East-African-Indian | Non-CAS1-Delhi | RD750 | 1.0 |
lineage3.1.2 | East-African-Indian | CAS;CAS2 | RD750 | 0.98 |
lineage3.1.2.1 | East-African-Indian | CAS2 | RD750 | 0.96 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
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 | 0.99 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.98 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 0.95 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775946 | c.2535C>T | synonymous_variant | 0.98 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.99 |
mmpL5 | 777053 | c.1428G>A | synonymous_variant | 0.95 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472669 | n.824_825insTGGG | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472678 | n.833T>G | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472679 | n.834T>C | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472695 | n.850C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472697 | n.852T>A | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.12 |
fabG1 | 1673221 | c.-219C>A | upstream_gene_variant | 0.98 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.94 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168604 | p.Pro670Leu | missense_variant | 0.94 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 0.98 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 0.98 |
ribD | 2986890 | p.Ser18Arg | missense_variant | 0.96 |
thyA | 3073693 | p.Pro260Arg | missense_variant | 0.9 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | 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 |