Run ID: ERR4816501
Sample name:
Date: 01-04-2023 14:27:50
Number of reads: 133252
Percentage reads mapped: 97.16
Strain:
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 7222 | p.Ser661Arg | missense_variant | 0.5 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9078 | p.Gly593Trp | missense_variant | 0.18 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9705 | p.Arg802Trp | missense_variant | 0.29 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
ccsA | 620746 | p.Gly286Cys | missense_variant | 0.67 |
rpoB | 759620 | c.-187A>C | upstream_gene_variant | 0.29 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 760015 | p.Glu70Val | missense_variant | 1.0 |
rpoB | 761357 | c.1551G>T | synonymous_variant | 0.67 |
rpoB | 761873 | c.2067A>G | synonymous_variant | 0.33 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 762617 | c.-753C>A | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763525 | c.156C>T | synonymous_variant | 0.4 |
rpoC | 764747 | p.Leu460Met | missense_variant | 0.33 |
rpoC | 765450 | p.Ala694Val | missense_variant | 0.22 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 778333 | p.Val50Leu | missense_variant | 0.18 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801253 | p.Gly149Ser | missense_variant | 0.5 |
Rv1258c | 1406683 | p.Trp220Arg | missense_variant | 0.29 |
embR | 1416790 | c.558G>T | synonymous_variant | 0.2 |
embR | 1416795 | p.Gly185Trp | missense_variant | 0.2 |
embR | 1416926 | p.Ala141Glu | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
inhA | 1674872 | p.Gln224Arg | missense_variant | 0.4 |
tlyA | 1917927 | c.-13G>T | upstream_gene_variant | 0.4 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726341 | p.Val50Gly | missense_variant | 0.5 |
ribD | 2987351 | c.513C>T | synonymous_variant | 0.4 |
ribD | 2987469 | c.631C>T | synonymous_variant | 0.33 |
Rv2752c | 3064893 | c.1299C>T | synonymous_variant | 0.4 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568421 | p.Arg87Cys | missense_variant | 0.4 |
Rv3236c | 3612429 | p.Ala230Ser | missense_variant | 0.25 |
Rv3236c | 3612861 | c.256C>T | synonymous_variant | 0.67 |
fbiB | 3642212 | c.678C>A | synonymous_variant | 0.67 |
fbiB | 3642776 | c.1242G>A | synonymous_variant | 1.0 |
alr | 3841473 | c.-53G>A | upstream_gene_variant | 1.0 |
clpC1 | 4038319 | p.Pro796Ser | missense_variant | 0.4 |
embC | 4240578 | p.Ala239Val | missense_variant | 0.5 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embB | 4247184 | p.Gly224Glu | missense_variant | 0.25 |
embB | 4247242 | p.Asp243Glu | missense_variant | 0.33 |
whiB6 | 4338208 | p.Pro105Gln | missense_variant | 0.5 |
whiB6 | 4338497 | p.Ala9Ser | missense_variant | 0.4 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |