Run ID: SRR2101395
Sample name:
Date: 03-04-2023 23:41:35
Number of reads: 529562
Percentage reads mapped: 99.76
Strain: lineage4.3.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.2 | Euro-American (LAM) | LAM3 | None | 1.0 |
lineage4.3.2.1 | Euro-American (LAM) | LAM3 | RD761 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5520 | p.Pro94Leu | missense_variant | 1.0 |
gyrB | 6377 | p.Val380Ile | missense_variant | 0.14 |
gyrA | 7222 | c.-80C>T | upstream_gene_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoB | 759784 | c.-23A>C | upstream_gene_variant | 0.18 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781572 | p.Gln5Lys | missense_variant | 0.12 |
fbiC | 1303433 | p.Asp168Val | missense_variant | 0.11 |
fbiC | 1303792 | p.Gln288* | stop_gained | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472337 | n.492C>T | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1674123 | p.Asp228Glu | missense_variant | 0.17 |
inhA | 1674924 | c.727_728dupTG | frameshift_variant | 0.22 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2156228 | c.-118delC | upstream_gene_variant | 0.21 |
Rv1979c | 2221909 | p.Leu419Pro | missense_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714639 | p.Asp232Asn | missense_variant | 0.11 |
folC | 2747325 | p.Arg92Ser | missense_variant | 0.33 |
pepQ | 2859851 | p.Phe190Leu | missense_variant | 0.2 |
ribD | 2987505 | p.Leu223Met | missense_variant | 0.1 |
thyX | 3068099 | c.-154G>A | upstream_gene_variant | 0.13 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339126 | c.9C>A | synonymous_variant | 0.12 |
Rv3083 | 3449299 | p.Arg266Trp | missense_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612693 | c.424C>A | synonymous_variant | 0.14 |
Rv3236c | 3612968 | p.Gly50Val | missense_variant | 0.1 |
fbiB | 3642473 | p.Met313Ile | missense_variant | 0.12 |
alr | 3840211 | c.1209delC | frameshift_variant | 0.11 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244049 | p.Asp273Tyr | missense_variant | 0.14 |
ethA | 4326040 | c.1434G>T | synonymous_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |