Run ID: SRR14088360
Sample name:
Date: 03-04-2023 09:45:36
Number of reads: 1335753
Percentage reads mapped: 98.5
Strain: lineage3
Drug-resistance: Sensitive
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 |
---|
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 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 759620 | c.-187A>C | upstream_gene_variant | 0.27 |
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 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775981 | p.Leu834Met | missense_variant | 0.15 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777820 | c.661C>T | synonymous_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801005 | p.Leu66Pro | missense_variant | 0.13 |
rplC | 801396 | c.588T>C | synonymous_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473537 | n.-121C>T | upstream_gene_variant | 0.12 |
rrl | 1474496 | n.839C>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474497 | n.840G>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474520 | n.863A>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474551 | n.894G>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474558 | n.901G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474584 | n.927C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475871 | n.2214T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475877 | n.2220C>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475880 | n.2223C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.1 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918606 | p.Val223Ile | missense_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167763 | p.Ile950Val | missense_variant | 0.1 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168651 | p.Leu654Phe | missense_variant | 1.0 |
PPE35 | 2169287 | c.1326T>C | synonymous_variant | 0.19 |
PPE35 | 2169293 | c.1320T>C | synonymous_variant | 0.2 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.13 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.34 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.34 |
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 |
kasA | 2518685 | p.Asp191Tyr | missense_variant | 0.12 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
pepQ | 2860399 | p.Arg7Gln | missense_variant | 1.0 |
Rv2752c | 3065672 | c.519delC | frameshift_variant | 0.13 |
Rv2752c | 3065688 | c.504C>A | synonymous_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449053 | p.Gly184Cys | missense_variant | 0.22 |
Rv3083 | 3449286 | p.Trp261Cys | missense_variant | 0.17 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
alr | 3841473 | c.-53G>A | upstream_gene_variant | 1.0 |
rpoA | 3878559 | c.-53delC | upstream_gene_variant | 0.29 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245031 | c.1800delA | frameshift_variant | 0.11 |
ethA | 4326153 | p.Arg441Cys | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |