Run ID: ERR751989
Sample name:
Date: 02-04-2023 04:52:09
Number of reads: 983610
Percentage reads mapped: 99.08
Strain: lineage4.5
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.5 | Euro-American | H;T | RD122 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5195 | c.-45C>A | upstream_gene_variant | 0.14 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7892 | c.591G>A | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9788 | p.Asp829Glu | missense_variant | 1.0 |
fgd1 | 490751 | c.-32T>G | upstream_gene_variant | 0.21 |
ccsA | 620029 | c.139C>T | synonymous_variant | 1.0 |
rpoB | 760633 | p.Arg276His | missense_variant | 0.17 |
rpoC | 763190 | c.-180C>T | upstream_gene_variant | 0.13 |
rpoC | 767157 | p.Gly1263Asp | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777266 | c.1215G>T | synonymous_variant | 0.22 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1302976 | p.Val16Ile | missense_variant | 0.12 |
fbiC | 1303904 | p.Leu325Pro | missense_variant | 0.12 |
Rv1258c | 1406570 | c.771G>A | synonymous_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1833970 | c.429G>A | synonymous_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155171 | p.Thr314Ile | missense_variant | 0.17 |
PPE35 | 2170568 | p.Ile15Met | missense_variant | 1.0 |
Rv1979c | 2221722 | c.1443C>T | synonymous_variant | 1.0 |
Rv1979c | 2223086 | c.77_78delCG | frameshift_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288815 | p.Ala143Ser | missense_variant | 0.14 |
pncA | 2289790 | c.-549C>T | upstream_gene_variant | 0.13 |
pepQ | 2860171 | p.Leu83Pro | missense_variant | 0.13 |
thyA | 3074319 | p.His51Gln | missense_variant | 0.13 |
fbiD | 3339060 | c.-58C>A | upstream_gene_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiB | 3641555 | c.21C>T | synonymous_variant | 0.83 |
rpoA | 3878575 | c.-68C>T | upstream_gene_variant | 1.0 |
clpC1 | 4038318 | p.Pro796Leu | missense_variant | 0.98 |
embC | 4242035 | p.Gln725Lys | missense_variant | 0.22 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4249132 | c.2619G>A | synonymous_variant | 0.17 |
whiB6 | 4338286 | c.235delG | frameshift_variant | 0.92 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |