Run ID: SRR20139570
Sample name:
Date: 03-04-2023 21:50:44
Number of reads: 2641609
Percentage reads mapped: 99.66
Strain: lineage4.1.2.1
Drug-resistance: HR-TB
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 |
---|---|---|---|---|---|
pncA | 2288778 | p.Val155Gly | missense_variant | 1.0 | pyrazinamide |
ahpC | 2726136 | c.-57C>T | upstream_gene_variant | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6922 | c.-380G>T | upstream_gene_variant | 0.17 |
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 | 490751 | c.-32T>G | upstream_gene_variant | 0.18 |
fgd1 | 490756 | c.-27T>G | upstream_gene_variant | 0.16 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 0.99 |
mshA | 576744 | p.Val466Gly | missense_variant | 0.14 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.23 |
rpoB | 759615 | c.-192A>C | upstream_gene_variant | 0.34 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
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 | 1304159 | p.Val410Gly | missense_variant | 0.25 |
fbiC | 1304166 | c.1236A>G | synonymous_variant | 0.17 |
fbiC | 1304186 | p.Asp419Gly | missense_variant | 0.16 |
Rv1258c | 1407055 | p.Tyr96Asp | missense_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473953 | n.296T>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474039 | n.382A>G | non_coding_transcript_exon_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154403 | p.Gly570Ala | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.17 |
ahpC | 2726341 | p.Val50Gly | missense_variant | 0.25 |
ahpC | 2726350 | p.Trp53Leu | missense_variant | 0.27 |
ahpC | 2726355 | p.Lys55Glu | missense_variant | 0.16 |
thyA | 3074641 | c.-170C>T | upstream_gene_variant | 0.17 |
thyA | 3074645 | c.-174T>G | upstream_gene_variant | 0.23 |
thyA | 3074648 | c.-177T>G | upstream_gene_variant | 0.23 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embB | 4249305 | p.Asn931Thr | missense_variant | 0.21 |
embB | 4249323 | p.Ala937Glu | missense_variant | 0.2 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407963 | c.240G>T | synonymous_variant | 1.0 |
gid | 4407991 | p.Gly71Glu | missense_variant | 1.0 |