Run ID: ERR4822268
Sample name:
Date: 01-04-2023 17:43:54
Number of reads: 161425
Percentage reads mapped: 96.02
Strain: lineage4.8
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 0.16 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
tlyA | 1918618 | c.681dupC | frameshift_variant | 0.67 | capreomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 9581 | c.2281delA | frameshift_variant | 0.15 |
rpoC | 763402 | c.33C>G | synonymous_variant | 0.33 |
rpoC | 763411 | c.42T>G | synonymous_variant | 0.29 |
rpoC | 763414 | c.45T>C | synonymous_variant | 0.29 |
rpoC | 763771 | p.Tyr134* | stop_gained | 0.25 |
rpoC | 764239 | c.870T>C | synonymous_variant | 0.4 |
rpoC | 766876 | c.3507C>T | synonymous_variant | 0.4 |
rpoC | 766882 | c.3513C>T | synonymous_variant | 0.4 |
rpoC | 766894 | c.3525T>C | synonymous_variant | 0.4 |
rpoC | 766895 | c.3526T>C | synonymous_variant | 0.4 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.4 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpS5 | 778579 | c.326delG | frameshift_variant | 0.5 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.5 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.5 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.5 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.5 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.5 |
rpsA | 1833748 | c.207C>G | synonymous_variant | 0.5 |
rpsA | 1834465 | c.924T>C | synonymous_variant | 0.5 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.5 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.4 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101907 | p.Val379Ala | missense_variant | 1.0 |
ndh | 2102780 | p.Asn88Ser | missense_variant | 0.75 |
katG | 2154015 | c.2097G>A | synonymous_variant | 0.5 |
PPE35 | 2169615 | p.Asn333Ser | missense_variant | 0.5 |
PPE35 | 2169937 | p.Asn226Asp | missense_variant | 0.4 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
gid | 4407678 | c.525G>C | synonymous_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |