Run ID: ERR2229007
Sample name:
Date: 31-03-2023 16:30:41
Number of reads: 1034278
Percentage reads mapped: 99.45
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 |
fgd1 | 491765 | p.Leu328Pro | missense_variant | 0.12 |
mshA | 575420 | p.Thr25Ser | missense_variant | 0.2 |
mshA | 576089 | c.750_769delTGATCGGCGCGCGGCCCGGG | frameshift_variant | 0.33 |
ccsA | 619700 | c.-191C>T | upstream_gene_variant | 0.14 |
ccsA | 620060 | p.Asp57Gly | missense_variant | 0.15 |
ccsA | 620154 | c.267delG | frameshift_variant | 0.14 |
rpoB | 762646 | p.Pro947Leu | missense_variant | 0.12 |
rpoB | 763050 | p.Leu1082Met | missense_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776446 | p.Ala679Ser | missense_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304456 | p.Cys509Tyr | missense_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473051 | n.1206T>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473073 | n.1228A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474952 | n.1295A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476254 | n.2597C>T | non_coding_transcript_exon_variant | 0.17 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.11 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.11 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.21 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.22 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.22 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.47 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2168850 | p.Ser588Leu | missense_variant | 0.11 |
PPE35 | 2169732 | p.Asn294Ser | missense_variant | 0.11 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.29 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.26 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289919 | c.-678C>A | upstream_gene_variant | 0.13 |
eis | 2715014 | p.Arg107Cys | missense_variant | 0.12 |
fprA | 3474795 | c.789A>T | synonymous_variant | 0.11 |
fbiA | 3640612 | p.Gly24Ser | missense_variant | 0.11 |
alr | 3841114 | p.Asp103Asn | missense_variant | 0.12 |
clpC1 | 4040002 | p.His235Asp | missense_variant | 0.11 |
embC | 4240911 | p.Ala350Gly | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244220 | p.Leu330Met | missense_variant | 0.12 |
embA | 4244823 | p.Val531Leu | missense_variant | 0.13 |
embB | 4246151 | c.-363A>G | upstream_gene_variant | 0.11 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.31 |
embB | 4246856 | p.Phe115Leu | missense_variant | 0.11 |
embB | 4249765 | c.3252C>G | synonymous_variant | 0.17 |
aftB | 4267908 | p.Ala310Val | missense_variant | 0.25 |
aftB | 4268799 | p.Val13Ala | missense_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |