Run ID: ERR4815555
Sample name:
Date: 01-04-2023 13:56:04
Number of reads: 4017108
Percentage reads mapped: 89.95
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 | 0.98 |
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 | 8588 | c.1287G>A | synonymous_variant | 0.13 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 0.91 |
mshA | 575679 | p.Asn111Ser | missense_variant | 0.96 |
rpoB | 760115 | c.309C>T | synonymous_variant | 0.97 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.14 |
rpoC | 763486 | c.117T>G | synonymous_variant | 0.14 |
rpoC | 763853 | p.Val162Ile | missense_variant | 0.13 |
rpoC | 764236 | c.867G>A | synonymous_variant | 0.12 |
rpoC | 764650 | c.1281G>C | synonymous_variant | 0.13 |
rpoC | 764651 | p.Ser428Thr | missense_variant | 0.13 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.13 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.16 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.15 |
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 | 1304808 | c.1878C>G | synonymous_variant | 0.18 |
fbiC | 1304811 | c.1881C>G | synonymous_variant | 0.19 |
fbiC | 1304817 | c.1887T>C | synonymous_variant | 0.24 |
fbiC | 1304829 | c.1899T>C | synonymous_variant | 0.31 |
fbiC | 1304832 | c.1902C>T | synonymous_variant | 0.3 |
fbiC | 1304856 | c.1926C>G | synonymous_variant | 0.61 |
fbiC | 1304862 | c.1932G>A | synonymous_variant | 0.28 |
fbiC | 1304869 | c.1939C>T | synonymous_variant | 0.23 |
fbiC | 1304875 | p.Ile649Val | missense_variant | 0.2 |
fbiC | 1304883 | p.Glu651Asp | missense_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473943 | n.286G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473986 | n.329T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473987 | n.330G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474009 | n.352A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474012 | n.355C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474076 | n.419C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476707 | n.3050C>T | non_coding_transcript_exon_variant | 1.0 |
inhA | 1674888 | c.687C>G | synonymous_variant | 0.14 |
inhA | 1674903 | c.702T>C | synonymous_variant | 0.15 |
inhA | 1674904 | p.Ala235Pro | missense_variant | 0.15 |
rpsA | 1833971 | c.430C>T | synonymous_variant | 0.14 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.13 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.15 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 0.99 |
thyX | 3067850 | c.96A>C | synonymous_variant | 0.12 |
thyA | 3074205 | p.Glu89Asp | missense_variant | 0.13 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
clpC1 | 4038749 | c.1956C>G | synonymous_variant | 0.14 |
clpC1 | 4038755 | c.1950G>T | synonymous_variant | 0.14 |
clpC1 | 4038770 | c.1935C>T | synonymous_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 0.95 |
embA | 4245137 | c.1905T>C | synonymous_variant | 0.14 |
embA | 4245146 | c.1914G>A | synonymous_variant | 0.14 |
embA | 4245149 | c.1917C>G | synonymous_variant | 0.16 |
embA | 4245153 | p.Ile641Val | missense_variant | 0.17 |
embA | 4245182 | c.1950T>C | synonymous_variant | 0.2 |
embA | 4245189 | c.1957C>T | synonymous_variant | 0.18 |
embA | 4245198 | p.Leu656Ile | missense_variant | 0.16 |
embA | 4245207 | c.1975T>C | synonymous_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |