Run ID: SRR2101393
Sample name:
Date: 03-04-2023 23:41:27
Number of reads: 650974
Percentage reads mapped: 99.27
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 | 0.98 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 0.96 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
mshA | 576725 | p.Ile460Val | missense_variant | 0.1 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.15 |
rpoC | 766050 | p.Glu894Gly | missense_variant | 0.96 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775757 | c.2724C>A | synonymous_variant | 0.12 |
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 | 1.0 |
inhA | 1674524 | p.Phe108Tyr | missense_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154538 | p.Gln525Ser | missense_variant | 1.0 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 0.92 |
PPE35 | 2168291 | p.Leu774Phe | missense_variant | 0.11 |
PPE35 | 2169097 | c.1515delG | frameshift_variant | 0.11 |
PPE35 | 2169149 | c.1464G>C | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
folC | 2746335 | p.Gly422Cys | missense_variant | 0.11 |
ald | 3087146 | c.327T>C | synonymous_variant | 0.11 |
fbiD | 3339046 | c.-72G>T | upstream_gene_variant | 0.1 |
fbiD | 3339397 | p.Thr94Ser | missense_variant | 0.11 |
whiB7 | 3568541 | p.Pro47Ser | missense_variant | 0.11 |
fbiA | 3640397 | c.-146G>A | upstream_gene_variant | 0.12 |
fbiB | 3641991 | p.Gly153* | stop_gained | 0.11 |
clpC1 | 4039729 | p.Asp326Asn | missense_variant | 0.86 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244806 | p.Leu525Pro | missense_variant | 0.67 |
embA | 4245042 | p.Thr604Ala | missense_variant | 0.1 |
embB | 4246722 | p.Pro70Gln | missense_variant | 0.11 |
embB | 4249702 | c.3189C>A | synonymous_variant | 0.22 |
aftB | 4267417 | p.Pro474Thr | missense_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |