Run ID: ERR4820241
Sample name:
Date: 01-04-2023 16:34:07
Number of reads: 1115226
Percentage reads mapped: 99.74
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 | 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 | 8771 | c.1470C>T | synonymous_variant | 0.11 |
fgd1 | 491202 | c.420G>C | synonymous_variant | 0.11 |
fgd1 | 491204 | p.Gln141Arg | missense_variant | 0.11 |
mshA | 575405 | p.Arg20Cys | missense_variant | 0.11 |
mshA | 576710 | c.1367delG | frameshift_variant | 0.1 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776318 | p.Ser721Arg | missense_variant | 0.1 |
mmpL5 | 778932 | c.-452A>G | upstream_gene_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406479 | p.Arg288Cys | missense_variant | 0.18 |
Rv1258c | 1406594 | c.747A>G | synonymous_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471977 | n.132C>A | non_coding_transcript_exon_variant | 0.2 |
inhA | 1674508 | p.Met103Leu | missense_variant | 0.1 |
inhA | 1674703 | c.502T>C | synonymous_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918362 | c.423G>A | synonymous_variant | 0.11 |
tlyA | 1918643 | p.Gly235Asp | missense_variant | 0.12 |
ndh | 2102881 | c.162G>T | synonymous_variant | 0.1 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pepQ | 2860499 | c.-81C>T | upstream_gene_variant | 0.14 |
Rv2752c | 3066104 | p.Asn30Asp | missense_variant | 0.1 |
thyX | 3067592 | c.354G>A | synonymous_variant | 0.11 |
Rv3083 | 3448365 | c.-139T>C | upstream_gene_variant | 0.12 |
fprA | 3474858 | c.852G>T | synonymous_variant | 0.12 |
embC | 4242350 | p.Pro830Ser | missense_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243262 | c.30C>T | synonymous_variant | 0.12 |
embB | 4247072 | p.Gly187Arg | missense_variant | 0.11 |
embB | 4247155 | c.642G>T | synonymous_variant | 0.11 |
embB | 4249354 | c.2841G>C | synonymous_variant | 1.0 |
embB | 4249574 | p.Lys1021* | stop_gained | 0.13 |
aftB | 4267735 | p.Gly368Cys | missense_variant | 0.12 |
aftB | 4268910 | c.-74T>A | upstream_gene_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338598 | c.-77G>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |