Run ID: ERR2517265
Sample name:
Date: 31-03-2023 22:04:03
Number of reads: 1619282
Percentage reads mapped: 99.33
Strain: lineage4.1.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 7256 | p.Leu673Met | missense_variant | 0.12 |
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 |
mshA | 576256 | c.909C>A | synonymous_variant | 0.29 |
mshA | 576575 | p.Ala410Ser | missense_variant | 0.14 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 762011 | c.2205G>C | synonymous_variant | 1.0 |
rpoB | 762097 | p.Thr764Ile | missense_variant | 0.14 |
rpoC | 764203 | c.834G>T | synonymous_variant | 0.13 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 766382 | p.Glu1005* | stop_gained | 0.2 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775919 | c.2562G>A | synonymous_variant | 0.22 |
mmpL5 | 777724 | p.His253Tyr | missense_variant | 0.12 |
mmpL5 | 778711 | c.-231T>C | upstream_gene_variant | 0.2 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781737 | p.Gln60Lys | missense_variant | 0.17 |
rpsL | 781813 | p.Gly85Val | missense_variant | 0.25 |
embR | 1416577 | p.Gln257His | missense_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1476521 | n.2864C>A | non_coding_transcript_exon_variant | 0.12 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.13 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.13 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.12 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.33 |
rpsA | 1833761 | p.Val74Ile | missense_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101791 | p.Thr418Pro | missense_variant | 0.12 |
ndh | 2102820 | p.Val75Met | missense_variant | 0.12 |
katG | 2153970 | p.Asp714Glu | missense_variant | 0.12 |
katG | 2156332 | c.-221C>T | upstream_gene_variant | 0.14 |
PPE35 | 2167959 | p.Pro885Gln | missense_variant | 0.12 |
PPE35 | 2168105 | c.2508C>A | synonymous_variant | 0.13 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.61 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.62 |
PPE35 | 2170316 | c.297T>C | synonymous_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290067 | c.-826C>T | upstream_gene_variant | 0.33 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
ribD | 2987243 | c.405G>T | synonymous_variant | 0.12 |
Rv2752c | 3065975 | p.Asp73Tyr | missense_variant | 0.12 |
thyA | 3074139 | p.Gln111His | missense_variant | 0.29 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086937 | p.Gly40* | stop_gained | 0.12 |
fbiD | 3339155 | p.Ile13Ser | missense_variant | 0.11 |
Rv3083 | 3448400 | c.-104G>T | upstream_gene_variant | 0.14 |
Rv3083 | 3448656 | c.153G>T | synonymous_variant | 0.17 |
Rv3083 | 3448722 | p.Lys73Asn | missense_variant | 0.22 |
Rv3083 | 3449712 | c.1209C>A | synonymous_variant | 0.15 |
Rv3083 | 3449959 | p.Ala486Thr | missense_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474425 | p.Gln140Leu | missense_variant | 0.15 |
fprA | 3475165 | p.Gly387Cys | missense_variant | 0.12 |
fbiA | 3641486 | p.Ala315Gly | missense_variant | 0.11 |
rpoA | 3878582 | c.-75C>T | upstream_gene_variant | 1.0 |
ddn | 3987058 | p.Arg72Leu | missense_variant | 0.25 |
embC | 4242108 | p.Cys749Tyr | missense_variant | 0.33 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4244071 | p.Val280Ala | missense_variant | 0.4 |
embA | 4244299 | p.Ser356Phe | missense_variant | 0.25 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.45 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.27 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.33 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.33 |
embB | 4246567 | c.54_55insT | frameshift_variant | 0.4 |
embB | 4247478 | p.Trp322Leu | missense_variant | 0.2 |
embB | 4249587 | p.Thr1025Ile | missense_variant | 0.18 |
ethA | 4326025 | p.Arg483Ser | missense_variant | 0.14 |
ethR | 4327931 | p.Arg128Met | missense_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408102 | p.Gly34Val | missense_variant | 0.17 |