Run ID: ERR2229422
Sample name:
Date: 31-03-2023 17:10:28
Number of reads: 192945
Percentage reads mapped: 99.28
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 | 2154746 | c.1365dupT | frameshift_variant | 0.33 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5630 | p.Leu131Ile | missense_variant | 0.21 |
gyrB | 6162 | p.Ile308Asn | missense_variant | 0.4 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
fgd1 | 491771 | p.Pro330Leu | missense_variant | 0.29 |
rpoB | 759614 | c.-193C>T | upstream_gene_variant | 0.67 |
rpoB | 761440 | p.Asp545Gly | missense_variant | 0.33 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775726 | c.2755C>T | synonymous_variant | 0.5 |
mmpL5 | 775727 | c.2754C>G | synonymous_variant | 0.5 |
mmpL5 | 775736 | c.2745C>G | synonymous_variant | 0.4 |
mmpL5 | 775741 | c.2740C>T | synonymous_variant | 0.4 |
mmpL5 | 775742 | c.2739C>T | synonymous_variant | 0.4 |
mmpL5 | 777134 | p.Met449Ile | missense_variant | 0.5 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800694 | c.-115C>T | upstream_gene_variant | 0.2 |
fbiC | 1303148 | p.Ala73Asp | missense_variant | 0.67 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.75 |
rpsA | 1834583 | c.1045_1047delATC | conservative_inframe_deletion | 0.2 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154499 | p.Val538Ala | missense_variant | 0.29 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169302 | p.Met437Phe | missense_variant | 0.4 |
PPE35 | 2169884 | c.729T>C | synonymous_variant | 0.33 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ahpC | 2726617 | p.Asn142Thr | missense_variant | 0.25 |
folC | 2746441 | c.1158C>T | synonymous_variant | 0.67 |
thyX | 3067909 | p.Ala13Thr | missense_variant | 0.29 |
thyA | 3074395 | p.Thr26Asn | missense_variant | 0.5 |
ald | 3086776 | c.-44G>A | upstream_gene_variant | 0.22 |
whiB7 | 3568800 | c.-121C>T | upstream_gene_variant | 0.5 |
Rv3236c | 3613303 | c.-187C>T | upstream_gene_variant | 0.29 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.38 |
rpoA | 3878093 | p.Val139Ile | missense_variant | 0.33 |
clpC1 | 4040482 | p.Ser75Thr | missense_variant | 0.33 |
embC | 4242531 | p.Arg890Gln | missense_variant | 0.4 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |