Run ID: SRR19428627
Sample name:
Date: 03-04-2023 21:42:51
Number of reads: 272589
Percentage reads mapped: 99.82
Strain: lineage4.3.4.2
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 |
lineage4.3.4 | Euro-American (LAM) | LAM | RD174 | 1.0 |
lineage4.3.4.2 | Euro-American (LAM) | LAM1;LAM4;LAM11 | RD174 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6140 | p.Val301Leu | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8661 | p.Asp454Tyr | missense_variant | 0.13 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490650 | c.-133G>T | upstream_gene_variant | 0.18 |
mshA | 575379 | p.Gly11Val | missense_variant | 0.15 |
mshA | 575552 | p.Asn69Asp | missense_variant | 0.11 |
mshA | 576781 | c.1434G>T | synonymous_variant | 0.25 |
rpoB | 760117 | p.Pro104His | missense_variant | 0.12 |
rpoB | 760478 | c.672C>T | synonymous_variant | 1.0 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776185 | p.Lys766* | stop_gained | 0.14 |
mmpS5 | 779588 | c.-683C>A | upstream_gene_variant | 0.18 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304242 | p.Pro438Ser | missense_variant | 1.0 |
fbiC | 1305494 | c.2565_*55delGGCCTAGCCCCGGCGACGATGCCGGGTCGCGGGATGCGGCCCGTTGAGGAGCGGGGCAATCT | frameshift_variant&stop_lost&splice_region_variant | 0.67 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473376 | n.1531C>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475829 | n.2172C>T | non_coding_transcript_exon_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154051 | c.2061G>T | synonymous_variant | 0.14 |
PPE35 | 2167837 | p.Gly926Trp | missense_variant | 0.5 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
folC | 2747319 | p.Gly94Cys | missense_variant | 0.22 |
pepQ | 2859335 | c.1084T>C | synonymous_variant | 0.1 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339708 | c.591C>A | synonymous_variant | 0.17 |
Rv3083 | 3449728 | p.Leu409Val | missense_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612009 | p.Ala370Thr | missense_variant | 1.0 |
Rv3236c | 3613142 | c.-26A>T | upstream_gene_variant | 0.13 |
alr | 3840412 | p.Gly337Cys | missense_variant | 0.14 |
rpoA | 3877977 | p.Lys177Asn | missense_variant | 0.18 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4040360 | p.Glu115Asp | missense_variant | 0.12 |
embC | 4239871 | c.9C>A | synonymous_variant | 0.15 |
embC | 4239887 | p.Arg9Ser | missense_variant | 0.14 |
embC | 4241086 | c.1224G>T | synonymous_variant | 0.22 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246830 | p.Gly106Val | missense_variant | 0.14 |
embB | 4246941 | p.Pro143Arg | missense_variant | 1.0 |
embB | 4249316 | p.Ala935Ser | missense_variant | 0.5 |
aftB | 4266966 | p.Pro624Leu | missense_variant | 0.13 |
ethA | 4328019 | c.-546G>A | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |
fbiC | 1305494 | c.2565_*56delCNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNN | frameshift_variant&stop_lost&splice_region_variant | 1.0 |