Run ID: ERR2513758
Sample name:
Date: 31-03-2023 19:53:09
Number of reads: 665550
Percentage reads mapped: 98.78
Strain: lineage4.3.1.1
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 |
lineage4.3.1 | Euro-American (LAM) | LAM9 | None | 1.0 |
lineage4.3.1.1 | Euro-American (LAM) | LAM9 | 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 | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777605 | c.876C>T | synonymous_variant | 0.1 |
mmpR5 | 779455 | c.467dupG | frameshift_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304084 | p.Gly385Val | missense_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471660 | n.-186G>A | upstream_gene_variant | 1.0 |
rrl | 1476350 | n.2693G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476357 | n.2700T>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476359 | n.2702C>T | non_coding_transcript_exon_variant | 0.22 |
fabG1 | 1673900 | p.Ala154Val | missense_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155559 | p.Phe185Leu | missense_variant | 0.17 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.11 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.11 |
PPE35 | 2169269 | c.1344A>G | synonymous_variant | 0.12 |
PPE35 | 2169272 | c.1341C>G | synonymous_variant | 0.12 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.13 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.12 |
PPE35 | 2169293 | c.1320T>C | synonymous_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714881 | p.Ala151Val | missense_variant | 0.14 |
pepQ | 2860509 | c.-91G>A | upstream_gene_variant | 0.11 |
Rv2752c | 3064666 | p.Arg509His | missense_variant | 0.1 |
thyX | 3067966 | c.-21G>A | upstream_gene_variant | 1.0 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339673 | p.Arg186Cys | missense_variant | 0.14 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiA | 3640702 | p.His54Tyr | missense_variant | 0.11 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4248731 | p.Val740Met | missense_variant | 0.12 |
aftB | 4268768 | c.69A>G | synonymous_variant | 0.15 |
ubiA | 4269046 | p.Ala263Val | missense_variant | 0.1 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |