Run ID: SRR4034228
Sample name:
Date: 04-04-2023 06:39:02
Number of reads: 493614
Percentage reads mapped: 99.61
Strain: lineage4.3.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 0.99 |
lineage4.3.2.1 | Euro-American (LAM) | LAM3 | RD761 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5520 | p.Pro94Leu | missense_variant | 1.0 |
gyrA | 7222 | c.-80C>T | upstream_gene_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 |
fgd1 | 491699 | c.919dupC | frameshift_variant | 0.4 |
rpoB | 759854 | p.Ser16Arg | missense_variant | 0.15 |
rpoC | 764931 | p.Ala521Asp | missense_variant | 0.25 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 765770 | p.Thr801Ala | missense_variant | 0.29 |
rpoC | 766128 | p.Ala920Val | missense_variant | 0.14 |
rpoC | 767265 | p.Ala1299Val | missense_variant | 0.22 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 778660 | c.-180C>T | upstream_gene_variant | 0.2 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801338 | p.Val177Asp | missense_variant | 0.14 |
rplC | 801391 | p.Lys195Glu | missense_variant | 0.25 |
fbiC | 1303147 | p.Ala73Ser | missense_variant | 0.2 |
embR | 1416368 | p.Arg327His | missense_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471725 | n.-121C>A | upstream_gene_variant | 0.17 |
rrs | 1472337 | n.492C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473496 | n.-162G>C | upstream_gene_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154239 | p.Thr625Ala | missense_variant | 0.18 |
Rv1979c | 2222315 | p.Ala284Thr | missense_variant | 0.18 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289368 | c.-128dupC | upstream_gene_variant | 0.14 |
folC | 2746246 | c.1353C>T | synonymous_variant | 0.22 |
pepQ | 2860420 | c.-2T>C | upstream_gene_variant | 0.2 |
Rv2752c | 3067071 | c.-880G>T | upstream_gene_variant | 0.17 |
thyX | 3067463 | c.483C>T | synonymous_variant | 0.4 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086750 | c.-70A>G | upstream_gene_variant | 0.17 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449968 | p.Ala489Thr | missense_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474064 | p.Ala20Thr | missense_variant | 0.2 |
rpoA | 3877502 | p.Tyr336His | missense_variant | 0.25 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4040667 | p.Val13Ala | missense_variant | 0.13 |
embC | 4240693 | c.831T>C | synonymous_variant | 1.0 |
embC | 4241156 | p.Gly432Ser | missense_variant | 0.22 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
ethR | 4326679 | c.-870C>T | upstream_gene_variant | 0.2 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |