Run ID: ERR11081471
Sample name:
Date: 08-04-2023 23:03:15
Number of reads: 4090758
Percentage reads mapped: 99.57
Strain: lineage4
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5103 | c.-137C>T | 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 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.18 |
mshA | 576113 | p.Arg256Gly | missense_variant | 0.36 |
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 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154915 | c.1197A>G | synonymous_variant | 1.0 |
PPE35 | 2168875 | p.Asn580Asp | missense_variant | 1.0 |
PPE35 | 2169031 | p.Asp528Asn | missense_variant | 0.17 |
PPE35 | 2169041 | c.1572G>A | synonymous_variant | 0.35 |
PPE35 | 2169044 | c.1569G>C | synonymous_variant | 0.39 |
PPE35 | 2169047 | p.Ile522Val | missense_variant | 0.39 |
PPE35 | 2169053 | c.1560T>C | synonymous_variant | 1.0 |
PPE35 | 2169056 | c.1557A>G | synonymous_variant | 0.39 |
PPE35 | 2169059 | c.1554G>A | synonymous_variant | 0.61 |
PPE35 | 2169063 | p.Met517Thr | missense_variant | 1.0 |
PPE35 | 2169065 | p.Ala516Ile | missense_variant | 0.61 |
PPE35 | 2169068 | c.1545G>T | synonymous_variant | 0.61 |
PPE35 | 2169071 | c.1542A>G | synonymous_variant | 0.36 |
PPE35 | 2170065 | p.Ala183Gly | missense_variant | 0.24 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2715205 | c.127delG | frameshift_variant | 1.0 |
pepQ | 2860159 | p.Ala87Gly | missense_variant | 0.24 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087455 | c.636C>T | synonymous_variant | 1.0 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.71 |
fbiD | 3339746 | p.Ala210Gly | missense_variant | 0.5 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 0.99 |
rpoA | 3878608 | c.-101C>G | upstream_gene_variant | 0.29 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.42 |
clpC1 | 4039140 | p.Glu522Gly | missense_variant | 1.0 |
embC | 4240409 | p.Pro183Ala | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246527 | p.Ala5Gly | missense_variant | 0.17 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.17 |
embB | 4248324 | p.Ala604Gly | missense_variant | 0.2 |
embB | 4248328 | c.1815G>C | synonymous_variant | 0.16 |
aftB | 4267226 | c.1611G>A | synonymous_variant | 1.0 |
whiB6 | 4338208 | p.Pro105Gln | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |