Run ID: ERR6866850
Sample name:
Date: 02-04-2023 03:39:26
Number of reads: 2123491
Percentage reads mapped: 99.41
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 | 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 | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.17 |
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 | 0.98 |
Rv3236c | 3612665 | p.Val151Ala | missense_variant | 1.0 |
ddn | 3986977 | p.Pro45Leu | missense_variant | 1.0 |
panD | 4044225 | c.57C>T | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243129 | c.-104G>A | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |