Run ID: ERR2229490
Sample name:
Date: 31-03-2023 17:14:48
Number of reads: 256864
Percentage reads mapped: 98.94
Strain: lineage4
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 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 | 9535 | p.Arg745His | missense_variant | 0.5 |
fgd1 | 490932 | p.His50Gln | missense_variant | 0.4 |
rpoB | 760272 | p.Glu156Lys | missense_variant | 0.2 |
rpoC | 767146 | c.3777G>A | synonymous_variant | 0.4 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776018 | c.2463G>C | synonymous_variant | 0.5 |
mmpL5 | 776021 | c.2460G>C | synonymous_variant | 0.5 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801066 | c.258G>T | synonymous_variant | 0.29 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1305127 | p.Thr733Pro | missense_variant | 0.33 |
Rv1258c | 1407513 | c.-174delG | upstream_gene_variant | 0.33 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472436 | n.591G>A | non_coding_transcript_exon_variant | 0.5 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.4 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101706 | p.Ala446Val | missense_variant | 0.4 |
PPE35 | 2168185 | p.Thr810Ala | missense_variant | 0.67 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2168760 | p.Pro618His | missense_variant | 0.22 |
PPE35 | 2169488 | c.1125G>C | synonymous_variant | 0.4 |
PPE35 | 2169491 | c.1122T>C | synonymous_variant | 0.4 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.25 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.2 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.33 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.35 |
PPE35 | 2170513 | p.Leu34Val | missense_variant | 0.18 |
PPE35 | 2170528 | p.Ser29Ala | missense_variant | 0.22 |
PPE35 | 2170529 | c.84G>C | synonymous_variant | 0.22 |
PPE35 | 2170535 | c.78G>T | synonymous_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518751 | p.Met213Leu | missense_variant | 0.22 |
ribD | 2987047 | p.Val70Ala | missense_variant | 1.0 |
ribD | 2987540 | c.702G>T | synonymous_variant | 0.25 |
Rv2752c | 3065739 | c.453G>A | synonymous_variant | 0.33 |
thyX | 3067865 | c.81C>A | synonymous_variant | 1.0 |
thyA | 3074355 | c.117G>T | synonymous_variant | 0.33 |
fbiA | 3640834 | p.Gln98Lys | missense_variant | 0.29 |
clpC1 | 4039645 | p.His354Asp | missense_variant | 0.29 |
clpC1 | 4040855 | c.-151G>A | upstream_gene_variant | 0.5 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246548 | p.Pro12Gln | missense_variant | 1.0 |
embB | 4246555 | c.42G>C | synonymous_variant | 1.0 |
embB | 4246556 | p.Ala15Pro | missense_variant | 1.0 |
embB | 4249592 | p.Thr1027Pro | missense_variant | 0.4 |
embB | 4249628 | p.Ile1039Val | missense_variant | 0.29 |
embB | 4249673 | p.Ser1054Thr | missense_variant | 0.29 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |