Run ID: ERR2510813
Sample name:
Date: 31-03-2023 18:57:31
Number of reads: 1929161
Percentage reads mapped: 96.12
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 |
---|---|---|---|---|
gyrB | 6815 | p.Lys526Gln | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
rpoB | 762090 | p.Glu762* | stop_gained | 0.17 |
rpoB | 762858 | p.Thr1018Ala | missense_variant | 0.24 |
rpoC | 763665 | p.Ala99Glu | missense_variant | 0.13 |
rpoC | 767051 | p.Glu1228* | stop_gained | 0.18 |
mmpL5 | 775616 | c.2865G>A | synonymous_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801200 | p.Gly131Asp | missense_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472389 | n.544G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472390 | n.545T>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472391 | n.546C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475332 | n.1675G>T | non_coding_transcript_exon_variant | 0.12 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.3 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918377 | c.438T>C | synonymous_variant | 0.18 |
katG | 2153970 | p.Asp714Glu | missense_variant | 0.13 |
katG | 2154212 | p.Leu634Ile | missense_variant | 0.12 |
katG | 2156263 | c.-152A>G | upstream_gene_variant | 1.0 |
PPE35 | 2167963 | p.Gly884Arg | missense_variant | 0.12 |
PPE35 | 2168143 | p.Phe824Leu | missense_variant | 0.13 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.13 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.74 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.74 |
PPE35 | 2170147 | p.Ser156Ala | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519140 | c.1026G>C | synonymous_variant | 0.21 |
kasA | 2519143 | c.1029G>C | synonymous_variant | 0.2 |
eis | 2714846 | p.Val163Ile | missense_variant | 0.25 |
folC | 2746164 | c.1435C>A | synonymous_variant | 0.17 |
folC | 2746673 | p.Val309Ala | missense_variant | 0.14 |
alr | 3840764 | c.657G>C | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.21 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.25 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.24 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407902 | p.Leu101Phe | missense_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |