Run ID: ERR4827764
Sample name:
Date: 01-04-2023 18:18:42
Number of reads: 2094702
Percentage reads mapped: 99.68
Strain: lineage4.8;lineage2
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.05 |
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.96 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 0.93 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761161 | p.Leu452Pro | missense_variant | 0.18 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
embB | 4247429 | p.Met306Val | missense_variant | 0.16 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 9226 | p.Ser642Phe | missense_variant | 0.87 |
fgd1 | 491046 | p.Gln88His | missense_variant | 0.94 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.3 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.13 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 0.13 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 0.15 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.88 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 0.9 |
PPE35 | 2170623 | c.-11G>A | upstream_gene_variant | 0.21 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
folC | 2746448 | p.Asp384Ala | missense_variant | 0.1 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.28 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 0.3 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.17 |
clpC1 | 4039729 | p.Asp326Asn | missense_variant | 0.94 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246529 | p.Ser6Arg | missense_variant | 0.19 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.42 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.1 |
gid | 4407927 | p.Glu92Asp | missense_variant | 0.12 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |