Run ID: ERR4872203
Sample name:
Date: 01-04-2023 21:26:54
Number of reads: 326685
Percentage reads mapped: 99.41
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 |
pncA | 2289105 | p.Ala46Glu | missense_variant | 1.0 | pyrazinamide |
ahpC | 2726145 | c.-48G>A | upstream_gene_variant | 1.0 | isoniazid |
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 |
---|---|---|---|---|
gyrB | 5062 | c.-178T>C | upstream_gene_variant | 0.29 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9516 | p.Glu739* | stop_gained | 0.29 |
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 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765570 | p.Ala734Val | missense_variant | 1.0 |
rpoC | 767086 | c.3717C>T | synonymous_variant | 0.33 |
mmpL5 | 776042 | c.2438delG | frameshift_variant | 0.33 |
mmpL5 | 776303 | c.2178G>A | synonymous_variant | 0.5 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781605 | p.Ile16Val | missense_variant | 0.4 |
fbiC | 1304305 | p.Asn459Asp | missense_variant | 0.5 |
fbiC | 1304487 | c.1557C>T | synonymous_variant | 1.0 |
fbiC | 1304846 | p.Ala639Val | missense_variant | 0.25 |
Rv1258c | 1407031 | c.310C>T | synonymous_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474783 | n.1126G>A | non_coding_transcript_exon_variant | 0.5 |
tlyA | 1918161 | c.222G>A | synonymous_variant | 0.67 |
ndh | 2102949 | p.Lys32Glu | missense_variant | 1.0 |
katG | 2154679 | p.Ala478Val | missense_variant | 0.67 |
PPE35 | 2168105 | c.2508C>T | synonymous_variant | 0.67 |
PPE35 | 2168131 | p.Pro828Ser | missense_variant | 0.67 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290211 | c.-970G>A | upstream_gene_variant | 0.67 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
folC | 2746928 | p.Pro224His | missense_variant | 0.4 |
thyA | 3074124 | c.348G>A | synonymous_variant | 0.29 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087111 | p.Ala98Thr | missense_variant | 0.4 |
ald | 3087164 | c.345T>A | synonymous_variant | 0.5 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612698 | p.Leu140Pro | missense_variant | 0.5 |
ddn | 3986809 | c.-35G>A | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4244435 | c.1203G>A | synonymous_variant | 0.4 |
embB | 4248589 | c.2076C>A | synonymous_variant | 0.33 |
embB | 4249122 | p.Asp870Gly | missense_variant | 0.67 |
embB | 4249123 | c.2613delG | frameshift_variant | 0.67 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407628 | p.Gly192Asp | missense_variant | 0.67 |