Run ID: ERR4819794
Sample name:
Date: 01-04-2023 16:18:33
Number of reads: 713573
Percentage reads mapped: 99.76
Strain: lineage4.8
Drug-resistance: Sensitive
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 |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
ccsA | 619818 | c.-73G>A | upstream_gene_variant | 0.17 |
ccsA | 619831 | c.-60T>G | upstream_gene_variant | 0.33 |
rpoB | 762275 | c.2469C>T | synonymous_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775689 | p.Ala931Val | missense_variant | 0.11 |
mmpL5 | 777157 | c.1324C>A | synonymous_variant | 0.11 |
mmpL5 | 777164 | c.1317C>T | synonymous_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304136 | c.1206C>G | synonymous_variant | 0.33 |
fbiC | 1305407 | p.Ser826Leu | missense_variant | 0.12 |
Rv1258c | 1406539 | p.Ala268Thr | missense_variant | 0.1 |
Rv1258c | 1407479 | c.-139A>G | upstream_gene_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
inhA | 1674693 | c.492C>G | synonymous_variant | 0.11 |
inhA | 1674703 | c.502T>C | synonymous_variant | 0.11 |
rpsA | 1834185 | p.Val215Asp | missense_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
PPE35 | 2169985 | p.Ala210Thr | missense_variant | 0.11 |
PPE35 | 2170327 | p.Glu96Lys | missense_variant | 1.0 |
Rv1979c | 2222116 | p.Met350Thr | missense_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289141 | p.Tyr34Phe | missense_variant | 0.22 |
kasA | 2518329 | p.Met72Thr | missense_variant | 1.0 |
kasA | 2519281 | c.1167G>A | synonymous_variant | 1.0 |
thyA | 3074633 | c.-163delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
Rv3083 | 3448500 | c.-4A>G | upstream_gene_variant | 1.0 |
Rv3236c | 3612237 | p.Ala294Thr | missense_variant | 0.22 |
fbiA | 3641311 | p.Asp257Asn | missense_variant | 0.13 |
fbiB | 3641884 | p.Glu117Gly | missense_variant | 0.14 |
rpoA | 3878354 | p.Thr52Ser | missense_variant | 0.18 |
clpC1 | 4039645 | p.His354Asp | missense_variant | 0.11 |
clpC1 | 4039654 | p.Thr351Ser | missense_variant | 0.11 |
clpC1 | 4039805 | c.900C>T | synonymous_variant | 0.2 |
embC | 4240648 | c.786C>T | synonymous_variant | 0.2 |
embC | 4242422 | p.Trp854Gly | missense_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |