Run ID: ERR5908178
Sample name:
Date: 02-04-2023 00:52:23
Number of reads: 3214969
Percentage reads mapped: 99.75
Strain: lineage4.4.1.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.4 | Euro-American | S;T | None | 1.0 |
lineage4.4.1 | Euro-American (S-type) | S;T | None | 1.0 |
lineage4.4.1.1 | Euro-American | S;Orphans | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6826 | c.-476G>A | upstream_gene_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | 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 | 1472452 | n.607G>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473029 | n.1184C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474571 | n.914G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474768 | n.1111C>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475257 | n.1600C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475906 | n.2249C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475962 | n.2305G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476520 | n.2863G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476706 | n.3049C>T | non_coding_transcript_exon_variant | 0.15 |
rpsA | 1833510 | c.-32C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102990 | p.Val18Ala | missense_variant | 1.0 |
PPE35 | 2169840 | p.Gly258Asp | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448608 | c.105G>A | synonymous_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612665 | p.Val151Ala | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244583 | p.Gly451Arg | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |