Run ID: SRR14164484
Sample name:
Date: 03-04-2023 09:53:34
Number of reads: 897241
Percentage reads mapped: 99.56
Strain: lineage4.1.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 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 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
fgd1 | 491705 | p.Leu308Pro | missense_variant | 0.12 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.45 |
mshA | 576111 | p.Ala255Gly | missense_variant | 0.22 |
rpoB | 760074 | p.Ile90Phe | missense_variant | 0.11 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 761033 | c.1227G>A | synonymous_variant | 0.13 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304080 | p.Ala384Thr | missense_variant | 0.14 |
Rv1258c | 1407489 | c.-149G>A | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475955 | n.2298A>G | non_coding_transcript_exon_variant | 0.11 |
fabG1 | 1673546 | p.Ala36Val | missense_variant | 0.11 |
inhA | 1674960 | c.759C>G | synonymous_variant | 0.12 |
rpsA | 1834474 | c.933C>T | synonymous_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154746 | p.Ala456Thr | missense_variant | 0.11 |
katG | 2155337 | p.Asp259Asn | missense_variant | 0.11 |
PPE35 | 2169741 | p.Asn291Ser | missense_variant | 0.1 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290130 | c.-889C>T | upstream_gene_variant | 0.11 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
Rv2752c | 3066299 | c.-108C>T | upstream_gene_variant | 1.0 |
thyA | 3074613 | c.-142C>G | upstream_gene_variant | 0.11 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
clpC1 | 4038930 | p.Ser592Leu | missense_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.22 |
embB | 4246937 | p.Ser142Pro | missense_variant | 0.11 |
aftB | 4267542 | c.1294delT | frameshift_variant | 0.14 |
aftB | 4268008 | p.Gly277Arg | missense_variant | 0.11 |
ethA | 4327587 | c.-114C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |