Run ID: SRR023453
Sample name:
Date: 02-04-2023 14:11:46
Number of reads: 7634501
Percentage reads mapped: 92.18
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 | 0.99 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 0.99 |
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 | 490751 | c.-32T>G | upstream_gene_variant | 0.32 |
fgd1 | 491014 | p.Thr78Pro | missense_variant | 0.32 |
fgd1 | 491324 | p.Val181Gly | missense_variant | 0.26 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 0.98 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
rpoB | 759816 | p.Ser4Pro | missense_variant | 0.19 |
rpoB | 759831 | p.Thr9Pro | missense_variant | 0.29 |
rpoB | 760115 | c.309C>T | synonymous_variant | 0.97 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 0.92 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777028 | p.Thr485Pro | missense_variant | 0.26 |
mmpL5 | 777502 | p.Thr327Pro | missense_variant | 0.27 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 0.99 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918058 | p.Val40Gly | missense_variant | 0.21 |
katG | 2154685 | p.Ala476Val | missense_variant | 0.33 |
katG | 2155726 | p.Phe129Ser | missense_variant | 0.74 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 0.98 |
eis | 2715098 | p.Thr79Pro | missense_variant | 0.19 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.27 |
ahpC | 2726341 | p.Val50Gly | missense_variant | 0.28 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474986 | p.Val327Gly | missense_variant | 0.37 |
fbiB | 3642049 | p.Val172Gly | missense_variant | 0.19 |
embC | 4240461 | p.Val200Gly | missense_variant | 0.25 |
embC | 4240646 | p.Phe262Val | missense_variant | 0.33 |
embC | 4241429 | p.Phe523Val | missense_variant | 0.29 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4243963 | p.Val244Gly | missense_variant | 0.31 |
embA | 4244002 | p.Val257Gly | missense_variant | 0.22 |
embA | 4244217 | p.Thr329Pro | missense_variant | 0.22 |
embA | 4244641 | p.Val470Gly | missense_variant | 0.31 |
embA | 4244905 | p.Val558Gly | missense_variant | 0.24 |
embB | 4248614 | p.Ala701Thr | missense_variant | 1.0 |
ubiA | 4269317 | p.Ser173Ala | missense_variant | 0.58 |