Run ID: ERR2229064
Sample name:
Date: 31-03-2023 16:34:46
Number of reads: 970299
Percentage reads mapped: 99.51
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 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.3 |
ccsA | 619842 | c.-49G>T | upstream_gene_variant | 0.12 |
rpoC | 764541 | p.Val391Gly | missense_variant | 0.12 |
rpoC | 764543 | p.Thr392Asp | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777561 | c.919delG | frameshift_variant | 0.11 |
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 |
rrs | 1473367 | n.1522G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473375 | n.1530T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476083 | n.2426T>C | non_coding_transcript_exon_variant | 0.11 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.14 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.14 |
rpsA | 1834983 | p.Ala481Asp | missense_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102829 | p.Thr72Ser | missense_variant | 0.12 |
PPE35 | 2167815 | p.Tyr933Phe | missense_variant | 0.14 |
PPE35 | 2167885 | p.Gly910Ser | missense_variant | 0.12 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.28 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ribD | 2987347 | p.Pro170Leu | missense_variant | 0.13 |
ribD | 2987488 | p.Pro217His | missense_variant | 0.12 |
thyX | 3067534 | p.Ala138Pro | missense_variant | 0.18 |
thyX | 3067603 | c.343C>A | synonymous_variant | 0.14 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
fprA | 3474230 | p.Arg75Leu | missense_variant | 0.12 |
Rv3236c | 3611973 | p.Val382Leu | missense_variant | 0.11 |
Rv3236c | 3612506 | p.His204Arg | missense_variant | 0.12 |
fbiB | 3640782 | c.-753C>G | upstream_gene_variant | 0.12 |
alr | 3840778 | c.642delG | frameshift_variant | 0.11 |
alr | 3840828 | p.Val198Asp | missense_variant | 0.14 |
embC | 4240562 | p.Met234Leu | missense_variant | 0.14 |
embC | 4241967 | p.Gly702Val | missense_variant | 0.17 |
embA | 4242442 | c.-791G>T | upstream_gene_variant | 0.15 |
embC | 4242453 | c.2592delG | frameshift_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
aftB | 4269183 | c.-347T>C | upstream_gene_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408429 | c.-227A>C | upstream_gene_variant | 0.11 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |