Run ID: ERR4872202
Sample name:
Date: 01-04-2023 21:26:53
Number of reads: 345643
Percentage reads mapped: 99.5
Strain: lineage4.1.2
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289105 | p.Ala46Glu | missense_variant | 1.0 | pyrazinamide |
ahpC | 2726145 | c.-48G>A | upstream_gene_variant | 1.0 | isoniazid |
embA | 4243222 | c.-11C>A | upstream_gene_variant | 1.0 | ethambutol |
embB | 4247431 | p.Met306Ile | missense_variant | 1.0 | ethambutol |
ethA | 4326452 | p.Ala341Val | missense_variant | 1.0 | ethionamide |
gid | 4407851 | c.351delG | frameshift_variant | 1.0 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 760618 | p.Ile271Asn | missense_variant | 0.5 |
rpoB | 761638 | p.Pro611Leu | missense_variant | 0.33 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765570 | p.Ala734Val | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777538 | p.Leu315Met | missense_variant | 0.25 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303799 | c.870delG | frameshift_variant | 0.4 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475573 | n.1921delC | non_coding_transcript_exon_variant | 0.33 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102949 | p.Lys32Glu | missense_variant | 1.0 |
ndh | 2102993 | p.Val17Asp | missense_variant | 0.29 |
katG | 2156366 | c.-255G>A | upstream_gene_variant | 0.5 |
PPE35 | 2168237 | c.2376G>A | synonymous_variant | 0.33 |
PPE35 | 2168246 | c.2367C>T | synonymous_variant | 0.4 |
PPE35 | 2168701 | p.Val638Phe | missense_variant | 0.4 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518072 | c.-43A>G | upstream_gene_variant | 0.4 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
folC | 2746326 | p.Phe425Leu | missense_variant | 0.33 |
folC | 2746374 | p.Pro409Ser | missense_variant | 0.33 |
folC | 2746928 | p.Pro224His | missense_variant | 0.4 |
Rv2752c | 3065286 | p.Leu302Phe | missense_variant | 0.4 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087111 | p.Ala98Thr | missense_variant | 0.4 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612791 | p.Trp109Leu | missense_variant | 0.67 |
fbiA | 3641470 | p.Met310Val | missense_variant | 0.5 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4244435 | c.1203G>A | synonymous_variant | 0.25 |
embA | 4245834 | p.Leu868Met | missense_variant | 0.67 |
embB | 4248589 | c.2076C>A | synonymous_variant | 0.25 |
embB | 4249662 | p.Ala1050Val | missense_variant | 0.33 |
aftB | 4268593 | p.Val82Met | missense_variant | 0.5 |
aftB | 4268602 | p.Leu79Val | missense_variant | 0.5 |
aftB | 4269207 | c.-371G>A | upstream_gene_variant | 0.5 |
whiB6 | 4338238 | p.Leu95Gln | missense_variant | 0.33 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407614 | p.Arg197Cys | missense_variant | 0.67 |
gid | 4407628 | p.Gly192Asp | missense_variant | 0.5 |