Run ID: ERR2503379
Sample name:
Date: 31-03-2023 18:25:30
Number of reads: 524514
Percentage reads mapped: 99.55
Strain: lineage4.1.2
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
ethR | 4327876 | p.Phe110Leu | missense_variant | 1.0 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9206 | c.1905C>G | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575310 | c.-38G>T | upstream_gene_variant | 0.13 |
ccsA | 619831 | c.-60T>G | upstream_gene_variant | 0.31 |
ccsA | 620327 | p.Leu146Pro | missense_variant | 0.11 |
ccsA | 620436 | c.546T>C | synonymous_variant | 0.11 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 766746 | c.3382delC | frameshift_variant | 0.1 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800889 | c.81C>A | synonymous_variant | 1.0 |
Rv1258c | 1406887 | p.Leu152Met | missense_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475313 | n.1656G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475392 | n.1735C>A | non_coding_transcript_exon_variant | 0.18 |
inhA | 1674147 | c.-55C>T | upstream_gene_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918377 | c.438T>C | synonymous_variant | 0.11 |
ndh | 2102690 | p.Ala118Gly | missense_variant | 0.1 |
PPE35 | 2168303 | c.2310G>T | synonymous_variant | 1.0 |
PPE35 | 2169776 | p.Phe279Leu | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2518618 | c.504G>T | synonymous_variant | 0.11 |
kasA | 2518761 | p.Met216Thr | missense_variant | 0.12 |
kasA | 2519269 | c.1155C>G | synonymous_variant | 0.11 |
folC | 2746673 | p.Val309Ala | missense_variant | 0.17 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474145 | p.Gly47Trp | missense_variant | 0.12 |
alr | 3840263 | c.1158C>T | synonymous_variant | 1.0 |
embC | 4240168 | p.Lys102Asn | missense_variant | 1.0 |
embC | 4240793 | p.Ala311Ser | missense_variant | 0.13 |
embC | 4240801 | c.939C>T | synonymous_variant | 0.14 |
embC | 4240803 | p.Tyr314Phe | missense_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4243780 | p.Pro183Leu | missense_variant | 0.11 |
embB | 4249051 | c.2538C>G | synonymous_variant | 0.11 |
aftB | 4267891 | c.943_945delATC | conservative_inframe_deletion | 0.2 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |