Run ID: ERR2229255
Sample name:
Date: 31-03-2023 16:53:30
Number of reads: 1453899
Percentage reads mapped: 99.31
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 | 7362 | p.Glu21Gln | missense_variant | 0.98 |
mshA | 575153 | c.-195C>A | upstream_gene_variant | 0.15 |
mshA | 575259 | c.-89G>T | upstream_gene_variant | 0.22 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.31 |
rpoC | 765287 | p.Leu640Met | missense_variant | 0.15 |
rpoC | 765588 | p.Pro740Leu | missense_variant | 0.14 |
rpoC | 766823 | p.Lys1152* | stop_gained | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304075 | p.Ala382Val | missense_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
inhA | 1674784 | p.Arg195Trp | missense_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102965 | c.78G>T | synonymous_variant | 0.13 |
PPE35 | 2167973 | c.2640A>G | synonymous_variant | 0.14 |
PPE35 | 2168140 | p.Ala825Thr | missense_variant | 0.12 |
PPE35 | 2168143 | p.Phe824Leu | missense_variant | 0.12 |
PPE35 | 2168150 | c.2463T>C | synonymous_variant | 0.13 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.12 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.17 |
PPE35 | 2169287 | c.1326T>C | synonymous_variant | 0.14 |
PPE35 | 2169902 | c.711G>C | synonymous_variant | 0.12 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.38 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.39 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
folC | 2746816 | c.783C>G | synonymous_variant | 0.11 |
pepQ | 2859696 | c.723G>A | synonymous_variant | 0.14 |
pepQ | 2859951 | p.Asp156Glu | missense_variant | 0.12 |
thyX | 3068000 | c.-55G>T | upstream_gene_variant | 0.12 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
Rv3236c | 3612387 | p.Ala244Thr | missense_variant | 0.14 |
fbiB | 3641810 | c.276G>T | synonymous_variant | 0.12 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.19 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242655 | c.-578A>G | upstream_gene_variant | 0.12 |
embA | 4244184 | p.Ser318Arg | missense_variant | 0.14 |
aftB | 4268955 | c.-119A>G | upstream_gene_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |
Rv3236c | 3612912 | c.-454_204del | conservative_inframe_deletion | 1.0 |