Run ID: ERR4816115
Sample name:
Date: 01-04-2023 14:14:51
Number of reads: 1053113
Percentage reads mapped: 99.66
Strain: lineage4.6.4
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.6 | Euro-American | T;LAM | None | 1.0 |
lineage4.6.4 | Euro-American | T;LAM | 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 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9121 | p.Arg607His | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoB | 761499 | p.Val565Met | missense_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 778176 | p.Gly102Asp | missense_variant | 0.2 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471890 | n.45G>A | non_coding_transcript_exon_variant | 0.5 |
inhA | 1673916 | c.-286A>C | upstream_gene_variant | 0.11 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.11 |
rpsA | 1833727 | c.186G>A | synonymous_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102273 | p.Ile257Thr | missense_variant | 0.11 |
katG | 2154301 | p.Leu604Ser | missense_variant | 0.13 |
katG | 2155053 | p.Tyr353* | stop_gained | 0.13 |
katG | 2155065 | c.1047C>A | synonymous_variant | 1.0 |
katG | 2155120 | p.Ser331Asn | missense_variant | 0.15 |
katG | 2155644 | c.468C>T | synonymous_variant | 1.0 |
PPE35 | 2170300 | p.Val105Leu | missense_variant | 0.1 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289274 | c.-33G>A | upstream_gene_variant | 1.0 |
kasA | 2517995 | c.-120C>T | upstream_gene_variant | 0.11 |
eis | 2714393 | p.Val314Leu | missense_variant | 1.0 |
eis | 2714822 | p.His171Asn | missense_variant | 0.13 |
folC | 2746660 | c.938delT | frameshift_variant | 0.11 |
folC | 2747293 | c.306G>A | synonymous_variant | 0.1 |
pepQ | 2859622 | p.Pro266Gln | missense_variant | 0.11 |
Rv2752c | 3065588 | p.Asp202Asn | missense_variant | 0.14 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474322 | p.Ala106Thr | missense_variant | 0.14 |
Rv3236c | 3613235 | c.-119G>A | upstream_gene_variant | 0.11 |
clpC1 | 4038634 | p.Glu691Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244852 | c.1620G>A | synonymous_variant | 0.13 |
embB | 4248624 | p.Thr704Lys | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |