Run ID: ERR2229764
Sample name:
Date: 31-03-2023 17:34:19
Number of reads: 825174
Percentage reads mapped: 99.53
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 | 2155795 | p.Ala106Val | missense_variant | 0.12 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
mshA | 575378 | p.Gly11Trp | missense_variant | 0.12 |
rpoB | 761482 | p.Ala559Val | missense_variant | 0.14 |
rpoB | 761929 | p.Ala708Val | missense_variant | 0.11 |
rpoC | 764541 | p.Val391Gly | missense_variant | 0.13 |
rpoC | 764543 | p.Thr392Asp | missense_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
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 | 0.14 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.15 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.15 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.31 |
tlyA | 1917830 | c.-110C>A | upstream_gene_variant | 0.13 |
tlyA | 1917934 | c.-6T>C | upstream_gene_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102875 | c.168C>T | synonymous_variant | 0.11 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169269 | c.1344A>G | synonymous_variant | 0.18 |
PPE35 | 2169272 | c.1341C>G | synonymous_variant | 0.19 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.14 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.14 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.18 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.55 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.55 |
PPE35 | 2170147 | p.Ser156Ala | missense_variant | 0.21 |
PPE35 | 2170159 | p.Ala152Ser | missense_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.27 |
Rv3236c | 3612454 | c.663G>T | synonymous_variant | 0.13 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.25 |
rpoA | 3878352 | c.156C>A | synonymous_variant | 0.11 |
clpC1 | 4039042 | p.Ser555Thr | missense_variant | 0.17 |
clpC1 | 4039730 | c.975C>G | synonymous_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243691 | p.Met153Ile | missense_variant | 0.17 |
ethR | 4327335 | c.-214A>G | upstream_gene_variant | 0.18 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |