Run ID: ERR2229762
Sample name:
Date: 31-03-2023 17:33:29
Number of reads: 709101
Percentage reads mapped: 99.5
Strain: lineage4.8
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 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2155229 | c.882delG | frameshift_variant | 0.12 | isoniazid |
embB | 4247703 | p.Pro397Gln | missense_variant | 0.2 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7352 | c.51G>A | synonymous_variant | 0.13 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 9749 | c.2448G>C | synonymous_variant | 0.12 |
rpoB | 761152 | p.Leu449Gln | missense_variant | 0.18 |
rpoC | 766197 | c.2830delC | frameshift_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777157 | c.1324C>A | synonymous_variant | 0.29 |
mmpL5 | 777164 | c.1317C>T | synonymous_variant | 0.33 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
embR | 1417400 | c.-53C>T | upstream_gene_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.11 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.12 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.12 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.31 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169269 | c.1344A>G | synonymous_variant | 0.29 |
PPE35 | 2169272 | c.1341C>G | synonymous_variant | 0.29 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.19 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.2 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.44 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.43 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2715399 | c.-67T>A | upstream_gene_variant | 0.11 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.23 |
thyA | 3074648 | c.-177T>G | upstream_gene_variant | 0.3 |
fprA | 3474143 | p.Trp46Tyr | missense_variant | 0.19 |
fprA | 3474165 | c.159C>G | synonymous_variant | 0.13 |
fbiB | 3641826 | p.Arg98* | stop_gained | 0.12 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.12 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.15 |
panD | 4044087 | c.195C>A | synonymous_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.18 |
aftB | 4268340 | p.Pro166Gln | missense_variant | 0.12 |
ethR | 4326883 | c.-666C>A | upstream_gene_variant | 0.15 |
ethR | 4326964 | c.-585G>A | upstream_gene_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448497 | c.-6_*1408del | transcript_ablation | 1.0 |