Run ID: ERR2513016
Sample name:
Date: 31-03-2023 19:24:12
Number of reads: 476574
Percentage reads mapped: 99.45
Strain: lineage4.7
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.7 | Euro-American (mainly T) | T1;T5 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6358 | c.-944C>T | upstream_gene_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7379 | c.78C>G | synonymous_variant | 1.0 |
gyrA | 7470 | p.Tyr57Asn | missense_variant | 0.11 |
mshA | 576243 | p.Gly299Asp | missense_variant | 0.25 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.25 |
rpoB | 759620 | c.-187A>C | upstream_gene_variant | 0.24 |
rpoB | 760515 | p.Trp237Gly | missense_variant | 0.12 |
rpoB | 761392 | p.Glu529Val | missense_variant | 0.13 |
rpoB | 761771 | p.Met655Ile | missense_variant | 0.2 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777125 | c.1356C>T | synonymous_variant | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474294 | n.637C>G | non_coding_transcript_exon_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154820 | p.Val431Ala | missense_variant | 0.18 |
PPE35 | 2168828 | c.1785G>A | synonymous_variant | 1.0 |
PPE35 | 2169053 | c.1560T>C | synonymous_variant | 1.0 |
PPE35 | 2169059 | c.1554G>A | synonymous_variant | 0.67 |
PPE35 | 2169063 | p.Met517Thr | missense_variant | 1.0 |
PPE35 | 2169065 | p.Ala516Thr | missense_variant | 0.67 |
PPE35 | 2169068 | c.1545G>T | synonymous_variant | 0.67 |
Rv1979c | 2222412 | p.Asn251Lys | missense_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518151 | p.Ser13Arg | missense_variant | 0.25 |
kasA | 2518405 | c.291C>G | synonymous_variant | 0.18 |
folC | 2746307 | p.Arg431His | missense_variant | 0.14 |
pepQ | 2859916 | p.Thr168Ile | missense_variant | 0.2 |
Rv2752c | 3067132 | c.-941T>C | upstream_gene_variant | 0.13 |
alr | 3840831 | p.Met197Arg | missense_variant | 0.11 |
clpC1 | 4039484 | c.1221T>G | synonymous_variant | 0.38 |
clpC1 | 4039992 | p.Val238Ala | missense_variant | 0.11 |
embC | 4240648 | c.786C>T | synonymous_variant | 0.38 |
embC | 4241474 | c.1612C>T | synonymous_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4243111 | c.3252delG | frameshift_variant | 0.18 |
embA | 4244857 | c.1629delG | frameshift_variant | 0.5 |
embA | 4245885 | p.Asp885Tyr | missense_variant | 0.25 |
embB | 4247281 | c.768C>T | synonymous_variant | 0.11 |
embB | 4249732 | c.3219C>G | synonymous_variant | 1.0 |
ethA | 4326397 | p.Gln359His | missense_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |