Run ID: ERR552159
Sample name:
Date: 02-08-2023 08:40:43
Number of reads: NA
Percentage reads mapped: NA
Strain: lineage4.1
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 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6507 | p.Ala423Val | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9656 | c.2355C>G | synonymous_variant | 1.0 |
ccsA | 619831 | c.-60T>G | upstream_gene_variant | 0.21 |
ccsA | 620314 | c.424C>T | synonymous_variant | 1.0 |
ccsA | 620626 | p.Phe246Leu | missense_variant | 0.12 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765187 | c.1818C>T | synonymous_variant | 1.0 |
rpoC | 766012 | c.2643C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpS5 | 778816 | c.85_89delCGCAC | frameshift_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781421 | c.-139C>A | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1834764 | p.Glu408Gly | missense_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102702 | p.Ser114Ile | missense_variant | 1.0 |
katG | 2156007 | c.105C>T | synonymous_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289387 | c.-146C>G | upstream_gene_variant | 0.11 |
eis | 2714308 | p.Pro342Leu | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474109 | p.Ala35Thr | missense_variant | 1.0 |
Rv3236c | 3612078 | c.1038delC | frameshift_variant | 0.11 |
Rv3236c | 3612621 | c.496T>C | synonymous_variant | 0.1 |
alr | 3840871 | p.Ala184Thr | missense_variant | 1.0 |
clpC1 | 4039382 | c.1323C>T | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4244854 | p.Val541Ala | missense_variant | 0.18 |
embA | 4244858 | c.1626G>T | synonymous_variant | 0.18 |
embA | 4244861 | c.1629G>C | synonymous_variant | 0.18 |
embA | 4244863 | p.Leu544Gln | missense_variant | 0.18 |
embA | 4244865 | p.Ala545Pro | missense_variant | 0.17 |
embA | 4244868 | p.Ser546Arg | missense_variant | 0.17 |
embA | 4244871 | p.Gly547His | missense_variant | 0.17 |
embB | 4249323 | p.Ala937Glu | missense_variant | 0.27 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |