Run ID: ERR4831068
Sample name:
Date: 01-04-2023 20:39:41
Number of reads: 2558529
Percentage reads mapped: 99.39
Strain: lineage4.1;lineage3
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 0.93 |
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.07 |
lineage4.1 | Euro-American | T;X;H | None | 0.05 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5339 | p.Ile34Val | missense_variant | 0.9 |
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 | 0.95 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 0.88 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 0.94 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.87 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 0.99 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.93 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472866 | n.1021C>T | non_coding_transcript_exon_variant | 0.92 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.92 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 0.96 |
PPE35 | 2170065 | p.Ala183Gly | missense_variant | 0.24 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 0.96 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 0.95 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 0.12 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 0.94 |
ribD | 2986835 | c.-4G>A | upstream_gene_variant | 0.92 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.33 |
fbiD | 3339744 | c.627A>T | synonymous_variant | 0.22 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3878613 | c.-106A>C | upstream_gene_variant | 0.2 |
rpoA | 3878637 | c.-130G>C | upstream_gene_variant | 0.3 |
rpoA | 3878640 | c.-133G>C | upstream_gene_variant | 0.12 |
panD | 4044219 | p.His21Gln | missense_variant | 0.95 |
embC | 4242075 | p.Arg738Gln | missense_variant | 0.96 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.57 |
embB | 4248324 | p.Ala604Gly | missense_variant | 0.22 |
embB | 4248575 | p.Phe688Val | missense_variant | 0.95 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.9 |