Run ID: SRR6832792
Sample name:
Date: 04-04-2023 17:38:43
Number of reads: 1004642
Percentage reads mapped: 98.74
Strain: lineage4.3.3
Drug-resistance: HR-TB
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 |
lineage4.3.3 | Euro-American (LAM) | LAM;T | RD115 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7715 | c.414G>C | synonymous_variant | 0.12 |
gyrA | 8024 | c.723T>A | synonymous_variant | 0.29 |
gyrA | 8040 | p.Gly247Ser | missense_variant | 0.75 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoB | 759793 | c.-14T>A | upstream_gene_variant | 0.2 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 1.0 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777031 | p.Ile484Val | missense_variant | 0.15 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800904 | c.96G>A | synonymous_variant | 0.12 |
atpE | 1461071 | c.27C>T | synonymous_variant | 0.25 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472654 | n.809G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474050 | n.393A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476705 | n.3048C>G | non_coding_transcript_exon_variant | 0.33 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.17 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.15 |
fabG1 | 1673773 | p.Asn112Asp | missense_variant | 0.2 |
fabG1 | 1674163 | p.Gly242Ser | missense_variant | 0.18 |
rpsA | 1834836 | p.Met432Thr | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155668 | c.444G>A | synonymous_variant | 0.14 |
katG | 2156196 | c.-85C>T | upstream_gene_variant | 1.0 |
katG | 2156307 | c.-196T>C | upstream_gene_variant | 0.12 |
PPE35 | 2169230 | c.1383G>A | synonymous_variant | 0.11 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.38 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.38 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
ahpC | 2726612 | c.420C>T | synonymous_variant | 0.18 |
folC | 2746340 | p.Ala420Val | missense_variant | 1.0 |
Rv2752c | 3065455 | p.Gln246Arg | missense_variant | 0.18 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568814 | c.-135T>C | upstream_gene_variant | 0.2 |
rpoA | 3878289 | c.219C>T | synonymous_variant | 0.12 |
ddn | 3987084 | c.245_246delCG | frameshift_variant | 0.1 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4038968 | c.1737G>A | synonymous_variant | 1.0 |
clpC1 | 4040438 | p.Glu89Asp | missense_variant | 0.15 |
embC | 4241667 | p.Ala602Glu | missense_variant | 0.14 |
embC | 4242305 | p.Ile815Val | missense_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243217 | c.-16C>A | upstream_gene_variant | 1.0 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.14 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.14 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.13 |
embB | 4246623 | p.Gly37Val | missense_variant | 0.14 |
ethA | 4328369 | c.-896G>A | upstream_gene_variant | 0.2 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407977 | p.Gly76Cys | missense_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |