Run ID: ERR2229609
Sample name:
Date: 31-03-2023 17:21:25
Number of reads: 915616
Percentage reads mapped: 99.25
Strain: lineage4.8
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6559 | c.-743C>G | upstream_gene_variant | 0.11 |
gyrA | 6595 | c.-707G>A | upstream_gene_variant | 0.11 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8874 | p.Tyr525His | missense_variant | 0.12 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.22 |
mshA | 576766 | c.1419G>C | synonymous_variant | 0.13 |
mshA | 576772 | c.1425T>A | synonymous_variant | 0.13 |
rpoB | 760790 | c.984C>T | synonymous_variant | 0.13 |
rpoC | 764767 | c.1398G>T | synonymous_variant | 0.12 |
rpoC | 766833 | p.Glu1155Val | missense_variant | 0.18 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776755 | p.Asp576Asn | missense_variant | 0.18 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303510 | p.Gly194Arg | missense_variant | 0.18 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
Rv1258c | 1406410 | c.931C>T | synonymous_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1833611 | p.Ala24Ser | missense_variant | 0.16 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918024 | p.Ala29Pro | missense_variant | 0.12 |
ndh | 2102539 | c.504C>A | synonymous_variant | 0.12 |
katG | 2155114 | p.Leu333Pro | missense_variant | 0.11 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169022 | p.Gly531Arg | missense_variant | 0.14 |
PPE35 | 2169287 | c.1326T>C | synonymous_variant | 0.13 |
PPE35 | 2169902 | c.711G>C | synonymous_variant | 0.12 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.64 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.62 |
PPE35 | 2170392 | p.Gly74Ala | missense_variant | 0.1 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289640 | c.-399C>A | upstream_gene_variant | 0.14 |
eis | 2714737 | p.Glu199Gly | missense_variant | 0.11 |
folC | 2746959 | p.Gly214Trp | missense_variant | 0.12 |
ribD | 2987026 | p.Ala63Val | missense_variant | 0.12 |
thyX | 3067206 | p.Ala247Gly | missense_variant | 0.14 |
fbiB | 3641568 | p.Ile12Phe | missense_variant | 0.14 |
fbiB | 3641941 | p.Leu136Pro | missense_variant | 0.12 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.23 |
rpoA | 3878599 | c.-92C>G | upstream_gene_variant | 1.0 |
clpC1 | 4038561 | p.Asp715Val | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244184 | p.Ser318Leu | missense_variant | 0.12 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.18 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.18 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.22 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.22 |
embB | 4247028 | p.Leu172Arg | missense_variant | 0.21 |
embB | 4249759 | c.3246C>T | synonymous_variant | 0.17 |
aftB | 4268624 | c.213C>G | synonymous_variant | 0.25 |
ubiA | 4269040 | p.Asp265Gly | missense_variant | 0.11 |
ubiA | 4269149 | p.Val229Met | missense_variant | 0.33 |
ubiA | 4269347 | p.Ala163Thr | missense_variant | 0.12 |
ethR | 4327909 | p.Thr121Ala | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |