Run ID: ERR4817737
Sample name:
Date: 01-04-2023 15:09:53
Number of reads: 816185
Percentage reads mapped: 99.75
Strain: lineage4.4.1.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.4 | Euro-American | S;T | None | 1.0 |
lineage4.4.1 | Euro-American (S-type) | S;T | None | 1.0 |
lineage4.4.1.1 | Euro-American | S;Orphans | None | 1.0 |
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 | 9138 | p.Gln613Glu | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 575521 | c.174A>G | synonymous_variant | 1.0 |
rpoB | 760453 | p.Val216Ala | missense_variant | 0.12 |
rpoC | 766956 | p.Glu1196Ala | missense_variant | 0.1 |
rpoC | 766970 | p.Ala1201Ser | missense_variant | 0.11 |
mmpL5 | 775594 | c.2887T>C | synonymous_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776349 | p.Pro711Leu | missense_variant | 0.13 |
mmpL5 | 777182 | c.1299C>T | synonymous_variant | 0.11 |
mmpL5 | 777416 | c.1065G>T | synonymous_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1407157 | p.Ala62Pro | missense_variant | 0.12 |
atpE | 1461153 | c.111delC | frameshift_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918091 | p.Ala51Val | missense_variant | 1.0 |
ndh | 2102990 | p.Val18Ala | missense_variant | 1.0 |
ndh | 2103225 | c.-183A>C | upstream_gene_variant | 0.25 |
katG | 2155543 | p.Gln190Arg | missense_variant | 0.1 |
PPE35 | 2168479 | p.Thr712Pro | missense_variant | 1.0 |
PPE35 | 2169840 | p.Gly258Asp | missense_variant | 1.0 |
PPE35 | 2170361 | p.Glu84Asp | missense_variant | 1.0 |
Rv1979c | 2222948 | p.Arg73Gly | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289604 | c.-363T>A | upstream_gene_variant | 0.11 |
kasA | 2518061 | c.-54G>C | upstream_gene_variant | 0.1 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448608 | c.105G>A | synonymous_variant | 1.0 |
Rv3083 | 3449196 | c.693C>T | synonymous_variant | 0.15 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474223 | p.Asp73Tyr | missense_variant | 0.11 |
whiB7 | 3568779 | c.-100T>C | upstream_gene_variant | 1.0 |
Rv3236c | 3612665 | p.Val151Ala | missense_variant | 1.0 |
clpC1 | 4039729 | p.Asp326Asn | missense_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245591 | p.Val787Ile | missense_variant | 0.1 |
aftB | 4268450 | c.387A>G | synonymous_variant | 0.13 |
aftB | 4269393 | c.-557G>A | upstream_gene_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |