Run ID: ERR4814330
Sample name:
Date: 01-04-2023 13:13:53
Number of reads: 829910
Percentage reads mapped: 98.89
Strain: lineage4.6.2.2
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.6 | Euro-American | T;LAM | None | 0.99 |
lineage4.6.2 | Euro-American | T;LAM | RD726 | 1.0 |
lineage4.6.2.2 | Euro-American (Cameroon) | LAM10-CAM | RD726 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
ethA | 4326881 | c.592delG | frameshift_variant | 0.13 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5052 | c.-188A>G | upstream_gene_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8894 | c.1593C>G | synonymous_variant | 0.29 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
ccsA | 620365 | p.Asn159Asp | missense_variant | 0.13 |
rpoC | 762797 | c.-573C>T | upstream_gene_variant | 0.14 |
rpoC | 766861 | c.3492G>T | synonymous_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776104 | p.Ile793Leu | missense_variant | 0.18 |
mmpL5 | 777204 | p.Pro426Leu | missense_variant | 0.17 |
mmpR5 | 778298 | c.-692C>T | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
embR | 1416498 | p.Ser284Ala | missense_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473953 | n.296T>G | non_coding_transcript_exon_variant | 0.33 |
inhA | 1674403 | p.Glu68Lys | missense_variant | 0.22 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918070 | p.Thr44Asn | missense_variant | 0.4 |
ndh | 2102302 | c.741G>T | synonymous_variant | 0.25 |
PPE35 | 2169999 | p.Ala205Gly | missense_variant | 0.29 |
PPE35 | 2170004 | p.Ile203Asn | missense_variant | 0.25 |
Rv1979c | 2221746 | c.1416_1418dupCCG | disruptive_inframe_insertion | 0.96 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714620 | p.Val238Asp | missense_variant | 0.2 |
folC | 2746503 | p.Leu366Met | missense_variant | 0.13 |
pepQ | 2860125 | p.Glu98Asp | missense_variant | 0.15 |
Rv3083 | 3448567 | p.His22Asp | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612627 | p.Ala164Thr | missense_variant | 0.25 |
rpoA | 3878542 | c.-35T>C | upstream_gene_variant | 0.14 |
clpC1 | 4039399 | p.Glu436* | stop_gained | 0.12 |
embC | 4241540 | p.Thr560Ala | missense_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
aftB | 4267272 | p.Lys522Arg | missense_variant | 1.0 |
ethR | 4326739 | c.-810G>C | upstream_gene_variant | 1.0 |
ethA | 4328004 | c.-531C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |