Run ID: SRR4035961
Sample name:
Date: 04-04-2023 07:24:21
Number of reads: 493145
Percentage reads mapped: 99.64
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 | 1.0 |
lineage4.3.2 | Euro-American (LAM) | LAM3 | None | 1.0 |
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 |
rpoB | 760713 | p.Ala303Thr | missense_variant | 0.5 |
rpoB | 761837 | c.2031C>T | synonymous_variant | 0.25 |
rpoC | 763808 | p.Glu147Lys | missense_variant | 0.15 |
rpoC | 763930 | p.Glu187Asp | missense_variant | 0.33 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406849 | p.Met164Ile | missense_variant | 0.22 |
embR | 1416775 | c.573C>A | synonymous_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472337 | n.492C>T | non_coding_transcript_exon_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2169439 | c.1173dupC | frameshift_variant | 0.33 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pepQ | 2859361 | p.Glu353Gly | missense_variant | 0.22 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
thyA | 3074395 | c.76delA | frameshift_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474083 | p.Ala26Asp | missense_variant | 0.29 |
fbiA | 3640978 | p.Thr146Ser | missense_variant | 0.12 |
fbiB | 3641795 | c.261G>T | synonymous_variant | 0.22 |
alr | 3840889 | p.Ala178Thr | missense_variant | 0.14 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4038700 | p.Gly669Ser | missense_variant | 0.17 |
embC | 4241760 | p.Ser633Leu | missense_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244141 | c.909G>A | synonymous_variant | 0.17 |
embB | 4248052 | c.1539G>A | synonymous_variant | 0.17 |
embB | 4249357 | c.2846_2851delTGGCCG | disruptive_inframe_deletion | 0.22 |
aftB | 4266979 | p.Gly620Trp | missense_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407866 | p.Glu113* | stop_gained | 0.18 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |