Run ID: ERR4813354
Sample name:
Date: 01-04-2023 12:41:47
Number of reads: 3719667
Percentage reads mapped: 99.51
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 | 0.99 |
lineage4.1.2 | Euro-American | T;H | None | 0.98 |
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 | 491591 | p.Lys270Met | missense_variant | 0.98 |
mshA | 575436 | p.Pro30Gln | missense_variant | 0.33 |
mshA | 575679 | p.Asn111Ser | missense_variant | 0.95 |
ccsA | 619774 | c.-117C>T | upstream_gene_variant | 0.29 |
ccsA | 619835 | c.-56G>T | upstream_gene_variant | 0.22 |
rpoB | 760115 | c.309C>T | synonymous_variant | 0.99 |
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 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
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 |
kasA | 2518712 | p.Gly200* | stop_gained | 0.15 |
eis | 2715050 | p.Gly95Ser | missense_variant | 0.17 |
thyX | 3067400 | c.546C>T | synonymous_variant | 0.5 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3877824 | c.684G>A | synonymous_variant | 0.97 |
embC | 4240555 | p.Met231Ile | missense_variant | 0.25 |
embC | 4242803 | p.Val981Leu | missense_variant | 0.99 |
embA | 4244597 | c.1365G>T | synonymous_variant | 0.11 |
embA | 4245786 | p.Ala852Ser | missense_variant | 0.14 |
embB | 4247014 | c.501G>A | synonymous_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |