Run ID: ERR2229071
Sample name:
Date: 31-03-2023 16:36:56
Number of reads: 948755
Percentage reads mapped: 99.45
Strain: lineage4.8
Drug-resistance: Other
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 |
---|---|---|---|---|---|
mmpR5 | 779191 | p.Ser68Gly | missense_variant | 0.12 | clofazimine, bedaquiline |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
fgd1 | 491097 | c.315G>A | synonymous_variant | 0.13 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.5 |
rpoB | 760375 | p.Asp190Val | missense_variant | 0.18 |
rpoC | 764495 | p.Glu376* | stop_gained | 0.2 |
rpoC | 765996 | p.Arg876Leu | missense_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776854 | p.Thr543Ala | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1302860 | c.-71G>T | upstream_gene_variant | 0.12 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304113 | p.Gln395Lys | missense_variant | 0.22 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475014 | n.1357A>T | non_coding_transcript_exon_variant | 0.29 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.2 |
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 | 0.22 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169732 | p.Asn294Ser | missense_variant | 0.18 |
PPE35 | 2169748 | p.Ile289Phe | missense_variant | 0.12 |
PPE35 | 2169749 | c.864A>C | synonymous_variant | 0.12 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.45 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.46 |
PPE35 | 2170159 | p.Ala152Ser | missense_variant | 0.12 |
PPE35 | 2170232 | c.381T>C | synonymous_variant | 0.1 |
PPE35 | 2170235 | c.378T>C | synonymous_variant | 0.1 |
PPE35 | 2170238 | c.375T>G | synonymous_variant | 0.1 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289961 | c.-720C>A | upstream_gene_variant | 0.11 |
folC | 2747493 | p.Gln36Lys | missense_variant | 0.13 |
pepQ | 2859481 | p.Ala313Val | missense_variant | 0.14 |
pepQ | 2860104 | p.Asp105Glu | missense_variant | 0.2 |
ribD | 2987582 | c.744C>T | synonymous_variant | 0.12 |
thyX | 3067340 | c.606G>A | synonymous_variant | 0.19 |
ald | 3087105 | p.His96Asp | missense_variant | 0.12 |
ald | 3087269 | p.Met150Ile | missense_variant | 0.14 |
fprA | 3474817 | p.Phe271Ile | missense_variant | 0.14 |
fprA | 3475231 | p.Trp409Arg | missense_variant | 0.15 |
Rv3236c | 3612870 | p.Ala83Ser | missense_variant | 0.13 |
clpC1 | 4038888 | p.Glu606Ala | missense_variant | 0.29 |
clpC1 | 4038896 | c.1809C>A | synonymous_variant | 0.29 |
clpC1 | 4038899 | c.1806C>G | synonymous_variant | 0.29 |
clpC1 | 4038902 | c.1803C>T | synonymous_variant | 0.29 |
clpC1 | 4038905 | c.1800A>C | synonymous_variant | 0.29 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.25 |
clpC1 | 4039062 | p.Ser548Trp | missense_variant | 0.11 |
embC | 4241364 | p.Leu501Pro | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243484 | c.252C>A | synonymous_variant | 0.13 |
embA | 4244326 | p.Gly365Val | missense_variant | 0.17 |
embA | 4244749 | p.Thr506Ile | missense_variant | 0.12 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.13 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.18 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.18 |
embB | 4249262 | p.Val917Leu | missense_variant | 0.12 |
embB | 4249535 | p.Glu1008Lys | missense_variant | 0.13 |
aftB | 4267937 | c.900G>A | synonymous_variant | 0.4 |
aftB | 4268022 | p.Leu272Gln | missense_variant | 0.29 |
aftB | 4269270 | c.-434G>A | upstream_gene_variant | 0.12 |
ethA | 4327512 | c.-39T>C | upstream_gene_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448497 | c.-6_*1408del | transcript_ablation | 1.0 |