Run ID: ERR2229127
Sample name:
Date: 31-03-2023 16:42:14
Number of reads: 347245
Percentage reads mapped: 99.42
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 | 6526 | c.-776T>C | upstream_gene_variant | 0.15 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8030 | c.729C>A | synonymous_variant | 0.12 |
rpoB | 761152 | p.Leu449Gln | missense_variant | 0.2 |
rpoC | 764500 | c.1131C>T | synonymous_variant | 0.4 |
rpoC | 765769 | c.2400C>A | synonymous_variant | 0.5 |
rpoC | 766839 | p.Ile1157Asn | missense_variant | 0.33 |
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 |
embR | 1416779 | p.Val190Glu | missense_variant | 0.29 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472378 | n.533G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476224 | n.2568delT | non_coding_transcript_exon_variant | 0.29 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.12 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.53 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154929 | p.Arg395Ser | missense_variant | 0.33 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.25 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.25 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2168882 | c.1731T>A | synonymous_variant | 0.33 |
PPE35 | 2169378 | p.Phe412Tyr | missense_variant | 0.15 |
PPE35 | 2169623 | c.990T>C | synonymous_variant | 0.2 |
PPE35 | 2169879 | p.Phe245Ser | missense_variant | 0.12 |
PPE35 | 2169882 | p.Ser244Asn | missense_variant | 0.12 |
PPE35 | 2169890 | c.723C>T | synonymous_variant | 0.13 |
PPE35 | 2169893 | c.720C>A | synonymous_variant | 0.13 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.23 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.31 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.33 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289128 | c.114G>T | synonymous_variant | 0.22 |
eis | 2715278 | c.55C>T | synonymous_variant | 0.22 |
thyX | 3067701 | p.Ile82Thr | missense_variant | 0.22 |
thyX | 3067754 | c.192C>T | synonymous_variant | 0.2 |
Rv3236c | 3612290 | p.Leu276Pro | missense_variant | 0.22 |
alr | 3841283 | c.138A>G | synonymous_variant | 0.25 |
rpoA | 3877876 | p.Ala211Asp | missense_variant | 0.2 |
rpoA | 3877912 | p.Lys199Arg | missense_variant | 0.22 |
embC | 4240135 | c.273C>T | synonymous_variant | 0.29 |
embC | 4241191 | c.1329C>A | synonymous_variant | 0.33 |
embA | 4242529 | c.-704G>A | upstream_gene_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4247024 | p.Pro171Ala | missense_variant | 0.33 |
aftB | 4268737 | p.Val34Phe | missense_variant | 0.18 |
ubiA | 4269430 | p.Gln135Arg | missense_variant | 0.22 |
ethA | 4326314 | p.Thr387Ser | missense_variant | 0.15 |
ethR | 4326937 | c.-612G>C | upstream_gene_variant | 0.33 |
ethA | 4327068 | p.Leu136Val | missense_variant | 0.22 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |