Run ID: ERR405218
Sample name:
Date: 01-04-2023 04:29:50
Number of reads: 3661809
Percentage reads mapped: 82.04
Strain: lineage3.1.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
lineage3.1 | East-African-Indian | Non-CAS1-Delhi | RD750 | 1.0 |
lineage3.1.1 | East-African-Indian | CAS1-Kili | RD750 | 0.99 |
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 | 1.0 |
fgd1 | 490751 | c.-32T>G | upstream_gene_variant | 0.27 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 0.99 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 0.98 |
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 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476339 | n.2682G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476356 | n.2699C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476384 | n.2727G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476470 | n.2813C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.16 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 0.99 |
PPE35 | 2170461 | p.Gly51Glu | missense_variant | 0.97 |
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 | 0.98 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 0.99 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.25 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.21 |
embC | 4240172 | p.Val104Met | missense_variant | 1.0 |
embC | 4241562 | p.Arg567His | missense_variant | 0.99 |
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 | 0.99 |