Run ID: SRR2101400
Sample name:
Date: 03-04-2023 23:41:39
Number of reads: 481845
Percentage reads mapped: 99.26
Strain: lineage4.1.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.1 | Euro-American (X-type) | X1;X2;X3 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 7163 | p.Ala642Pro | missense_variant | 0.14 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7704 | p.Thr135Ala | missense_variant | 0.14 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490594 | c.-189C>A | upstream_gene_variant | 0.11 |
mshA | 576250 | c.903G>T | synonymous_variant | 0.1 |
ccsA | 619787 | c.-103delG | upstream_gene_variant | 0.15 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775690 | p.Ala931Ser | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303591 | c.661C>A | synonymous_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474920 | n.1263G>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476563 | n.2906G>T | non_coding_transcript_exon_variant | 0.12 |
fabG1 | 1674064 | p.Lys209* | stop_gained | 0.18 |
inhA | 1674440 | p.Glu80Gly | missense_variant | 0.2 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154613 | p.Gln500Arg | missense_variant | 0.14 |
katG | 2154965 | p.Ser383Thr | missense_variant | 0.12 |
PPE35 | 2167872 | p.Ser914Leu | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv1979c | 2223364 | c.-200G>A | upstream_gene_variant | 0.14 |
eis | 2714884 | p.His150Arg | missense_variant | 0.12 |
ahpC | 2726210 | c.18T>C | synonymous_variant | 1.0 |
folC | 2747576 | p.Pro8Leu | missense_variant | 0.13 |
pepQ | 2860230 | c.188delA | frameshift_variant | 0.15 |
Rv2752c | 3064568 | p.Gly542Trp | missense_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475267 | p.Ala421Ser | missense_variant | 0.11 |
fbiA | 3640425 | c.-118T>C | upstream_gene_variant | 0.12 |
fbiA | 3641447 | p.Thr302Met | missense_variant | 1.0 |
fbiB | 3642546 | p.Gly338Ser | missense_variant | 0.15 |
rpoA | 3877553 | p.Glu319Lys | missense_variant | 1.0 |
rpoA | 3877911 | c.597G>A | synonymous_variant | 0.11 |
embC | 4240266 | p.Arg135Pro | missense_variant | 0.11 |
embC | 4240685 | p.Thr275Ala | missense_variant | 0.18 |
embC | 4240897 | c.1035C>G | synonymous_variant | 1.0 |
embC | 4241704 | c.1842C>T | synonymous_variant | 0.11 |
embC | 4241939 | p.Pro693Ser | missense_variant | 0.12 |
embC | 4241965 | c.2103C>T | synonymous_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embB | 4249408 | c.2895G>A | synonymous_variant | 1.0 |
embB | 4249473 | p.Asp987Gly | missense_variant | 0.14 |
aftB | 4266970 | p.Pro623Thr | missense_variant | 0.18 |
aftB | 4267334 | c.1503T>C | synonymous_variant | 0.12 |
aftB | 4267964 | c.873T>A | synonymous_variant | 0.12 |
aftB | 4268275 | p.Glu188* | stop_gained | 0.11 |
ubiA | 4269960 | c.-127G>A | upstream_gene_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408022 | p.Arg61Gly | missense_variant | 0.1 |