Run ID: ERR2229695
Sample name:
Date: 31-03-2023 17:27:56
Number of reads: 1694282
Percentage reads mapped: 99.21
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 | 1.0 |
rpoB | 760926 | p.Thr374Ser | missense_variant | 0.11 |
rpoC | 762737 | c.-633C>T | upstream_gene_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777590 | c.891G>A | synonymous_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475263 | n.1606G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475346 | n.1689C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475714 | n.2057G>A | non_coding_transcript_exon_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.52 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.5 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
thyX | 3067361 | p.Phe195Leu | missense_variant | 0.1 |
fprA | 3474370 | p.Ser122Gly | missense_variant | 0.13 |
alr | 3840402 | p.Arg340Gln | missense_variant | 0.15 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.15 |
panD | 4044283 | c.-2T>C | upstream_gene_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.15 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.36 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.39 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.39 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.2 |
embB | 4246567 | c.54G>T | synonymous_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 |