Run ID: SRR14782610
Sample name:
Date: 03-04-2023 11:32:28
Number of reads: 3502247
Percentage reads mapped: 99.62
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 | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 9647 | c.2346C>G | synonymous_variant | 0.21 |
mshA | 576613 | c.1266A>C | synonymous_variant | 0.23 |
rpoC | 764367 | p.Gly333Ala | missense_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777883 | p.Gly200Arg | missense_variant | 0.2 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1305096 | c.2166T>C | synonymous_variant | 0.99 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673553 | p.Asp38Glu | missense_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223204 | c.-41_-40insATCTA | upstream_gene_variant | 0.95 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519071 | p.Asp319Glu | missense_variant | 0.21 |
pepQ | 2860159 | p.Ala87Gly | missense_variant | 0.23 |
Rv2752c | 3064823 | p.Val457Leu | missense_variant | 0.15 |
Rv2752c | 3066321 | c.-130C>G | upstream_gene_variant | 1.0 |
ald | 3087818 | p.Cys333Trp | missense_variant | 0.14 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.62 |
fbiD | 3339746 | p.Ala210Gly | missense_variant | 0.4 |
fbiD | 3339751 | p.Ala212Pro | missense_variant | 0.25 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 0.67 |
fprA | 3474213 | p.Lys69Asn | missense_variant | 0.18 |
whiB7 | 3568428 | c.252A>G | synonymous_variant | 0.57 |
rpoA | 3878597 | c.-90G>C | upstream_gene_variant | 0.43 |
rpoA | 3878600 | c.-93G>C | upstream_gene_variant | 0.5 |
rpoA | 3878637 | c.-130G>C | upstream_gene_variant | 1.0 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.82 |
embC | 4240409 | p.Pro183Ala | missense_variant | 0.44 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4248324 | p.Ala604Gly | missense_variant | 0.19 |
embB | 4248328 | c.1815G>C | synonymous_variant | 0.25 |
aftB | 4267149 | p.Glu563Gly | missense_variant | 1.0 |
aftB | 4267155 | p.Gln561Arg | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |