Run ID: ERR9030273
Sample name:
Date: 02-04-2023 09:24:50
Number of reads: 1625033
Percentage reads mapped: 99.95
Strain: lineage4
Drug-resistance: MDR-TB
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 |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
embB | 4248003 | p.Gln497Arg | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
mshA | 575690 | p.Gly115Arg | missense_variant | 0.25 |
mshA | 575916 | c.570delC | frameshift_variant | 0.67 |
rpoC | 766488 | p.Pro1040Gln | missense_variant | 0.16 |
rpoC | 766494 | p.Gly1042Asp | missense_variant | 0.83 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471788 | n.-58G>A | upstream_gene_variant | 0.99 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2170198 | p.Ala139Thr | missense_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289037 | p.Pro69Ser | missense_variant | 1.0 |
kasA | 2518839 | p.Ala242Gly | missense_variant | 0.2 |
eis | 2714985 | c.348G>T | synonymous_variant | 0.67 |
folC | 2747024 | p.Ala192Asp | missense_variant | 0.15 |
folC | 2747028 | c.570_571insAGATA | frameshift_variant | 0.15 |
pepQ | 2859827 | p.Ala198Thr | missense_variant | 0.18 |
fbiD | 3338991 | c.-127T>C | upstream_gene_variant | 0.13 |
Rv3083 | 3448445 | c.-59G>A | upstream_gene_variant | 0.15 |
alr | 3840764 | c.657G>C | synonymous_variant | 1.0 |
embC | 4240453 | c.591C>T | synonymous_variant | 0.29 |
embC | 4241029 | p.Trp389Cys | missense_variant | 0.2 |
embA | 4244083 | p.Ala284Asp | missense_variant | 0.15 |
embB | 4245851 | c.-663G>A | upstream_gene_variant | 0.29 |
embB | 4247971 | c.1458C>T | synonymous_variant | 0.11 |
embB | 4249299 | p.Trp929Leu | missense_variant | 0.14 |
ubiA | 4269391 | p.Val148Ala | missense_variant | 1.0 |
ethA | 4327155 | c.307_318dupAAGGTGATCAGT | conservative_inframe_insertion | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407869 | c.316_333delACAGATCTGGGCGTGGCC | conservative_inframe_deletion | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |