Run ID: ERR4821121
Sample name:
Date: 01-04-2023 17:04:18
Number of reads: 536610
Percentage reads mapped: 99.49
Strain: lineage4.1.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 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 | 8689 | p.Ala463Val | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490796 | p.Lys5Arg | missense_variant | 0.12 |
fgd1 | 490846 | p.Glu22Lys | missense_variant | 0.13 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoC | 764419 | c.1050C>A | synonymous_variant | 0.29 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 766902 | p.Gly1178Val | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781444 | c.-116C>T | upstream_gene_variant | 0.11 |
rplC | 801177 | c.369C>T | synonymous_variant | 0.17 |
fbiC | 1305489 | c.2559G>T | synonymous_variant | 0.11 |
embR | 1416222 | p.Phe376Leu | missense_variant | 0.13 |
embR | 1416232 | p.Cys372Gly | missense_variant | 0.12 |
embR | 1416878 | c.469delC | frameshift_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472069 | n.224G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1473715 | n.58G>A | non_coding_transcript_exon_variant | 0.67 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154387 | c.1725G>C | synonymous_variant | 0.25 |
PPE35 | 2168106 | p.Leu836His | missense_variant | 0.18 |
PPE35 | 2168145 | p.Pro823Arg | missense_variant | 0.2 |
PPE35 | 2168512 | p.Gly701Cys | missense_variant | 0.4 |
PPE35 | 2169911 | c.701delA | frameshift_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290066 | c.-825G>T | upstream_gene_variant | 0.15 |
pncA | 2290081 | c.-840C>A | upstream_gene_variant | 0.17 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
folC | 2747575 | c.24G>A | synonymous_variant | 0.11 |
thyX | 3067921 | p.Val9Met | missense_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448313 | c.-190delC | upstream_gene_variant | 0.14 |
Rv3083 | 3448337 | c.-167C>A | upstream_gene_variant | 0.13 |
Rv3083 | 3448342 | c.-161delC | upstream_gene_variant | 0.13 |
Rv3083 | 3448906 | p.Tyr135His | missense_variant | 0.2 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3877514 | p.Thr332Ala | missense_variant | 1.0 |
rpoA | 3877732 | p.Arg259Leu | missense_variant | 0.2 |
ddn | 3987201 | p.Ala120Ser | missense_variant | 0.12 |
clpC1 | 4038844 | p.Val621Met | missense_variant | 0.17 |
embC | 4239999 | p.Ala46Val | missense_variant | 0.1 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
aftB | 4268068 | p.Val257Met | missense_variant | 0.13 |
ubiA | 4268936 | p.Ala300Thr | missense_variant | 0.2 |
ubiA | 4269482 | p.Trp118Arg | missense_variant | 0.14 |
ethR | 4326766 | c.-783G>T | upstream_gene_variant | 0.15 |
ethR | 4327990 | p.Tyr148His | missense_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |