Run ID: SRR5535712
Sample name:
Date: 04-04-2023 10:38:52
Number of reads: 3424734
Percentage reads mapped: 98.88
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 | 0.99 |
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 | 9138 | p.Gln613Glu | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
ccsA | 620050 | p.Val54Met | missense_variant | 0.18 |
ccsA | 620606 | p.Val239Gly | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777416 | c.1065G>T | synonymous_variant | 0.98 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303836 | c.906G>T | synonymous_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472635 | n.790G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473956 | n.299G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474517 | n.860C>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474848 | n.1191G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475164 | n.1507C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475801 | n.2144G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475824 | n.2167G>T | non_coding_transcript_exon_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102990 | p.Val18Ala | missense_variant | 1.0 |
PPE35 | 2168479 | p.Thr712Pro | missense_variant | 1.0 |
PPE35 | 2169840 | p.Gly258Asp | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518636 | c.522C>A | synonymous_variant | 0.13 |
folC | 2747012 | p.Pro196Gln | missense_variant | 0.16 |
Rv2752c | 3065023 | p.Pro390Leu | missense_variant | 1.0 |
thyX | 3067241 | c.705G>T | synonymous_variant | 0.21 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448522 | p.Val7Phe | missense_variant | 1.0 |
Rv3083 | 3448608 | c.105G>A | synonymous_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474259 | p.Gly85Cys | missense_variant | 0.14 |
whiB7 | 3568779 | c.-100T>C | upstream_gene_variant | 1.0 |
Rv3236c | 3612665 | p.Val151Ala | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4245563 | c.-951G>C | upstream_gene_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |