Run ID: ERR2229704
Sample name:
Date: 31-03-2023 17:27:25
Number of reads: 739782
Percentage reads mapped: 99.34
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 |
gyrA | 7726 | p.Leu142Pro | missense_variant | 0.13 |
mshA | 575949 | c.603delC | frameshift_variant | 0.12 |
rpoB | 760088 | c.282C>T | synonymous_variant | 0.12 |
rpoC | 763515 | p.Glu49Val | missense_variant | 0.13 |
rpoC | 765062 | p.Ile565Phe | missense_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777245 | c.1236G>A | synonymous_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1305389 | p.Ala820Asp | missense_variant | 0.12 |
Rv1258c | 1407243 | p.Leu33Gln | missense_variant | 0.17 |
embR | 1416453 | p.Arg299Cys | missense_variant | 0.22 |
atpE | 1460890 | c.-155G>A | upstream_gene_variant | 0.33 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475965 | n.2308A>T | non_coding_transcript_exon_variant | 0.5 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.1 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.1 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.19 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.19 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.19 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.19 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102361 | p.Leu228Val | missense_variant | 0.13 |
ndh | 2102530 | c.513G>A | synonymous_variant | 0.17 |
ndh | 2103034 | c.9C>T | synonymous_variant | 0.33 |
PPE35 | 2167814 | c.2799C>T | synonymous_variant | 0.25 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169013 | p.Val534Leu | missense_variant | 0.3 |
PPE35 | 2169178 | c.1434delC | frameshift_variant | 0.33 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.59 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.59 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518494 | p.Asp127Val | missense_variant | 0.12 |
kasA | 2518831 | p.Phe239Leu | missense_variant | 0.13 |
ribD | 2987358 | p.Asp174Tyr | missense_variant | 0.12 |
thyX | 3067340 | c.606G>A | synonymous_variant | 0.15 |
fprA | 3474039 | c.36delG | frameshift_variant | 0.22 |
fprA | 3475216 | p.Asp404His | missense_variant | 0.17 |
fbiA | 3640491 | c.-52T>A | upstream_gene_variant | 0.14 |
clpC1 | 4038699 | p.Gly669Ala | missense_variant | 0.25 |
clpC1 | 4039107 | p.Arg533Gln | missense_variant | 0.12 |
clpC1 | 4040284 | p.Leu141Met | missense_variant | 0.17 |
clpC1 | 4040447 | c.257delA | frameshift_variant | 0.14 |
embC | 4241633 | p.Gly591Trp | missense_variant | 0.22 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244324 | c.1092T>C | synonymous_variant | 0.22 |
embA | 4244706 | p.Thr492Ala | missense_variant | 0.17 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.3 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.22 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.29 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.29 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.18 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.18 |
embB | 4246747 | p.Asp78Glu | missense_variant | 0.13 |
ethR | 4327742 | p.Phe65Ser | missense_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448497 | c.-6_*1408del | transcript_ablation | 1.0 |