Run ID: ERR9892286
Sample name:
Date: 02-04-2023 13:27:42
Number of reads: 1215905
Percentage reads mapped: 99.04
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 | 1.0 |
lineage4.1.2 | Euro-American | T;H | None | 0.97 |
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 | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
mshA | 576720 | p.Glu458Ala | missense_variant | 0.29 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777119 | p.His454Gln | missense_variant | 0.23 |
mmpL5 | 777122 | c.1359C>T | synonymous_variant | 0.24 |
mmpL5 | 777128 | c.1353A>G | synonymous_variant | 0.24 |
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 |
PPE35 | 2167745 | p.Thr956Arg | missense_variant | 0.16 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.12 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.23 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.23 |
PPE35 | 2170372 | p.Thr81Ala | missense_variant | 0.14 |
PPE35 | 2170392 | p.Gly74Ala | missense_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2518809 | p.Lys232Arg | missense_variant | 0.16 |
folC | 2746230 | p.Ala457Ser | missense_variant | 0.11 |
ribD | 2986869 | p.Asp11Asn | missense_variant | 1.0 |
thyA | 3074561 | c.-90T>C | upstream_gene_variant | 0.12 |
thyA | 3074564 | c.-93G>A | upstream_gene_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448824 | c.321C>A | synonymous_variant | 0.13 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiB | 3641968 | p.Ala145Val | missense_variant | 0.18 |
rpoA | 3878636 | c.-129C>A | upstream_gene_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242648 | p.Leu929Arg | missense_variant | 0.12 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4244885 | c.1653A>G | synonymous_variant | 0.13 |
embB | 4245716 | c.-798G>T | upstream_gene_variant | 0.12 |
embB | 4247512 | c.999T>C | synonymous_variant | 0.14 |
embB | 4247516 | p.Asn335Asp | missense_variant | 0.14 |
embB | 4247699 | p.Met396Leu | missense_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |