Run ID: ERR2229620
Sample name:
Date: 31-03-2023 17:21:51
Number of reads: 1091209
Percentage reads mapped: 99.02
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 | 491295 | c.513C>T | synonymous_variant | 0.13 |
mshA | 576457 | c.1110G>T | synonymous_variant | 0.13 |
mshA | 576471 | p.Gly375Val | missense_variant | 0.13 |
rpoC | 765719 | p.Glu784* | stop_gained | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775851 | p.Ser877Thr | missense_variant | 0.2 |
mmpL5 | 775857 | p.Gly875Ala | missense_variant | 0.13 |
mmpL5 | 775862 | c.2619G>C | synonymous_variant | 0.13 |
mmpL5 | 775871 | c.2610C>T | synonymous_variant | 0.12 |
mmpL5 | 776150 | p.Met777Ile | missense_variant | 0.14 |
mmpL5 | 777157 | c.1324C>A | synonymous_variant | 0.15 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304200 | p.Leu424Met | missense_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.11 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.27 |
inhA | 1674532 | p.Ala111Ser | missense_variant | 0.17 |
inhA | 1674823 | p.Gly208Ser | missense_variant | 0.13 |
rpsA | 1834079 | p.Arg180Cys | missense_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168278 | p.Ile779Phe | missense_variant | 0.17 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169287 | c.1326T>C | synonymous_variant | 0.12 |
PPE35 | 2169725 | c.888T>C | synonymous_variant | 0.13 |
PPE35 | 2169879 | p.Phe245Ser | missense_variant | 0.14 |
PPE35 | 2169882 | p.Ser244Asn | missense_variant | 0.14 |
PPE35 | 2169890 | c.723C>T | synonymous_variant | 0.26 |
PPE35 | 2169893 | c.720C>A | synonymous_variant | 0.26 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.22 |
PPE35 | 2170035 | p.Val193Ala | missense_variant | 0.12 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.36 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.33 |
PPE35 | 2170159 | p.Ala152Ser | missense_variant | 0.17 |
PPE35 | 2170392 | p.Gly74Ala | missense_variant | 0.12 |
PPE35 | 2170545 | p.Pro23Leu | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518451 | p.Gly113Ser | missense_variant | 0.12 |
kasA | 2518606 | c.492G>C | synonymous_variant | 0.31 |
kasA | 2518609 | p.Met165Ile | missense_variant | 0.27 |
kasA | 2519153 | p.Ile347Val | missense_variant | 0.13 |
eis | 2714857 | p.Gly159Val | missense_variant | 0.17 |
pepQ | 2860612 | c.-194A>G | upstream_gene_variant | 0.17 |
ribD | 2987145 | p.Arg103Ser | missense_variant | 0.14 |
Rv2752c | 3065557 | p.Gly212Val | missense_variant | 0.15 |
Rv2752c | 3065605 | p.Val196Ala | missense_variant | 0.13 |
fbiD | 3339609 | c.492G>C | synonymous_variant | 0.11 |
fprA | 3474123 | c.117G>T | synonymous_variant | 0.15 |
fprA | 3474393 | c.387C>A | synonymous_variant | 0.12 |
fprA | 3474689 | p.Ala228Glu | missense_variant | 0.14 |
Rv3236c | 3612849 | p.Leu90Met | missense_variant | 0.25 |
Rv3236c | 3613025 | p.Ser31Leu | missense_variant | 0.15 |
fbiA | 3640957 | p.Gly139Cys | missense_variant | 0.12 |
fbiB | 3641970 | p.Val146Met | missense_variant | 0.12 |
fbiB | 3642418 | p.Thr295Asn | missense_variant | 0.12 |
alr | 3840464 | p.Phe319Leu | missense_variant | 0.18 |
clpC1 | 4038638 | p.Asp689Gly | missense_variant | 0.12 |
clpC1 | 4039730 | c.975C>G | synonymous_variant | 0.18 |
embC | 4240758 | p.Thr299Ser | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244946 | p.Val572Leu | missense_variant | 0.15 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.33 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.2 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.25 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.25 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.25 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.29 |
aftB | 4266983 | c.1854C>T | synonymous_variant | 0.18 |
aftB | 4267011 | p.Glu609Gly | missense_variant | 0.14 |
ethA | 4327541 | c.-68G>A | upstream_gene_variant | 0.13 |
whiB6 | 4338261 | c.261G>C | synonymous_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448499 | c.-4_*1408del | transcript_ablation | 1.0 |