Run ID: ERR2229177
Sample name:
Date: 31-03-2023 16:46:45
Number of reads: 395213
Percentage reads mapped: 99.37
Strain: lineage4
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 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 |
rpoB | 760924 | p.Arg373His | missense_variant | 0.15 |
rpoB | 762136 | p.Asp777Val | missense_variant | 0.18 |
rpoC | 762854 | c.-516G>T | upstream_gene_variant | 0.18 |
rpoC | 764342 | p.Arg325Cys | missense_variant | 0.33 |
rpoC | 764900 | p.Ala511Pro | missense_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 778252 | p.His77Tyr | missense_variant | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781458 | c.-102C>T | upstream_gene_variant | 0.18 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
Rv1258c | 1406294 | c.1047C>T | synonymous_variant | 0.29 |
Rv1258c | 1406547 | p.Met265Lys | missense_variant | 0.22 |
Rv1258c | 1406597 | c.744G>A | synonymous_variant | 0.22 |
embR | 1416996 | p.Glu118* | stop_gained | 0.29 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.5 |
inhA | 1673772 | c.-430C>A | upstream_gene_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2167745 | p.Thr956Arg | missense_variant | 0.25 |
PPE35 | 2168140 | p.Ala825Thr | missense_variant | 0.29 |
PPE35 | 2168143 | p.Phe824Leu | missense_variant | 0.29 |
PPE35 | 2168150 | c.2463T>C | synonymous_variant | 0.2 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169269 | c.1344A>G | synonymous_variant | 0.26 |
PPE35 | 2169272 | c.1341C>G | synonymous_variant | 0.29 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.41 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.39 |
PPE35 | 2169287 | c.1326T>C | synonymous_variant | 0.29 |
PPE35 | 2169293 | c.1320T>C | synonymous_variant | 0.21 |
PPE35 | 2169308 | c.1305C>T | synonymous_variant | 0.18 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.44 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.45 |
PPE35 | 2170298 | c.315A>G | synonymous_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714608 | p.Arg242Lys | missense_variant | 0.12 |
ahpC | 2726529 | p.Asp113Asn | missense_variant | 0.13 |
Rv2752c | 3066136 | p.Thr19Ile | missense_variant | 0.2 |
Rv3236c | 3613120 | c.-4A>T | upstream_gene_variant | 0.33 |
fbiB | 3641855 | c.321C>T | synonymous_variant | 0.4 |
rpoA | 3877861 | p.Val216Asp | missense_variant | 0.14 |
clpC1 | 4039829 | p.Leu292Ile | missense_variant | 0.21 |
clpC1 | 4039972 | p.Lys245Glu | missense_variant | 0.22 |
clpC1 | 4040458 | p.Arg83Ser | missense_variant | 0.18 |
clpC1 | 4040502 | p.Gly68Asp | missense_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243285 | p.Val18Asp | missense_variant | 0.33 |
embA | 4243734 | p.Pro168Thr | missense_variant | 0.67 |
embA | 4245164 | p.His644Gln | missense_variant | 0.25 |
embA | 4246200 | p.Gln990Glu | missense_variant | 0.4 |
embB | 4249176 | p.Val888Glu | missense_variant | 0.25 |
embB | 4249177 | c.2665delC | frameshift_variant | 0.25 |
aftB | 4268530 | p.Gly103Ser | missense_variant | 0.5 |
ubiA | 4269879 | c.-46C>T | upstream_gene_variant | 0.18 |
ethR | 4327631 | p.Ala28Glu | missense_variant | 0.22 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448499 | c.-4_*1408del | transcript_ablation | 1.0 |