Run ID: SRR4034514
Sample name:
Date: 04-04-2023 06:51:19
Number of reads: 1130949
Percentage reads mapped: 99.64
Strain: lineage4.3.2.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | 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 |
---|---|---|---|---|---|
tlyA | 1918237 | c.299delT | frameshift_variant | 0.11 | capreomycin |
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 |
mshA | 575929 | c.582C>A | synonymous_variant | 0.11 |
rpoB | 761230 | p.Gly475Val | missense_variant | 0.12 |
rpoB | 761291 | c.1485G>A | synonymous_variant | 0.15 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 779187 | c.-707C>A | upstream_gene_variant | 0.12 |
mmpR5 | 779278 | p.Pro97Ser | missense_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303536 | c.606G>C | synonymous_variant | 1.0 |
fbiC | 1303990 | c.1064delG | frameshift_variant | 0.15 |
embR | 1416536 | p.Ala271Val | missense_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472294 | n.449G>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472337 | n.492C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473090 | n.1245G>T | non_coding_transcript_exon_variant | 0.29 |
fabG1 | 1674093 | c.658delG | frameshift_variant | 0.11 |
inhA | 1674182 | c.-20G>A | upstream_gene_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2167685 | c.2927delA | frameshift_variant | 0.2 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289788 | c.-548dupC | upstream_gene_variant | 0.11 |
pncA | 2290107 | c.-866T>A | upstream_gene_variant | 1.0 |
kasA | 2518506 | p.Ala131Val | missense_variant | 0.12 |
ahpC | 2726644 | p.Ala151Asp | missense_variant | 0.12 |
pepQ | 2859541 | p.Gly293Val | missense_variant | 0.14 |
Rv2752c | 3064680 | c.1512C>T | synonymous_variant | 0.18 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
thyA | 3074025 | c.446delT | frameshift_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473942 | c.-65C>T | upstream_gene_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568570 | p.Glu37Gly | missense_variant | 0.12 |
fbiA | 3640932 | p.Glu130Asp | missense_variant | 0.12 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
embC | 4239704 | c.-159C>A | upstream_gene_variant | 0.17 |
embC | 4239740 | c.-123C>A | upstream_gene_variant | 0.11 |
embC | 4241160 | p.Ala433Val | missense_variant | 0.12 |
embC | 4241182 | c.1320G>T | synonymous_variant | 0.12 |
embC | 4241259 | p.Arg466Gln | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245478 | p.Met749Thr | missense_variant | 0.15 |
embB | 4249009 | c.2496G>A | synonymous_variant | 0.4 |
embB | 4249271 | p.Asp920Tyr | missense_variant | 0.12 |
aftB | 4267401 | p.Ala479Val | missense_variant | 0.14 |
ethA | 4328327 | c.-855delC | upstream_gene_variant | 0.17 |
ethA | 4328376 | c.-903G>T | upstream_gene_variant | 0.14 |
whiB6 | 4338416 | p.Gln36Lys | missense_variant | 0.15 |
whiB6 | 4338429 | c.93C>A | synonymous_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |