Run ID: ERR3994110
Sample name:
Date: 01-04-2023 03:42:37
Number of reads: 457394
Percentage reads mapped: 99.56
Strain: lineage4.1.1
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 |
lineage4.1.1 | Euro-American (X-type) | X1;X2;X3 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 7157 | p.Asp640Tyr | missense_variant | 0.13 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7438 | p.Asp46Gly | missense_variant | 0.33 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7683 | c.384delG | frameshift_variant | 0.29 |
gyrA | 8745 | p.Glu482Lys | missense_variant | 0.1 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491128 | p.Thr116Ser | missense_variant | 0.17 |
fgd1 | 491751 | c.969C>T | synonymous_variant | 0.11 |
mshA | 576188 | c.843_844delCA | frameshift_variant | 0.11 |
mshA | 576768 | p.Pro474Leu | missense_variant | 0.12 |
mshA | 576783 | p.Gly479Val | missense_variant | 0.12 |
rpoB | 760354 | c.549delG | frameshift_variant | 0.1 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765414 | c.2046_2048delGTT | disruptive_inframe_deletion | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 778149 | p.Gln111Arg | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303597 | p.Phe223Ile | missense_variant | 0.1 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473005 | n.1160C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475265 | n.1608G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475994 | n.2337G>T | non_coding_transcript_exon_variant | 0.13 |
rpsA | 1834893 | p.Ala451Gly | missense_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv1979c | 2223307 | c.-143T>C | upstream_gene_variant | 0.12 |
pncA | 2288950 | p.Ala98Thr | missense_variant | 0.15 |
pncA | 2290122 | c.-882dupG | upstream_gene_variant | 0.14 |
kasA | 2518294 | p.Ile60Met | missense_variant | 0.2 |
kasA | 2518709 | p.Glu199Gln | missense_variant | 0.13 |
kasA | 2518817 | p.Asp235Asn | missense_variant | 0.12 |
eis | 2715549 | c.-217G>A | upstream_gene_variant | 0.22 |
ahpC | 2726081 | c.-112C>T | upstream_gene_variant | 0.11 |
ahpC | 2726210 | c.18T>C | synonymous_variant | 1.0 |
folC | 2746222 | c.1377C>T | synonymous_variant | 0.25 |
folC | 2746866 | c.731_732delTG | frameshift_variant | 0.12 |
Rv2752c | 3067177 | c.-986G>T | upstream_gene_variant | 0.18 |
thyA | 3073848 | c.624C>A | synonymous_variant | 0.1 |
thyA | 3074561 | c.-90T>C | upstream_gene_variant | 0.13 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449723 | p.Cys407Tyr | missense_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475286 | p.Asp427Gly | missense_variant | 0.1 |
Rv3236c | 3612720 | c.395_396dupTG | frameshift_variant | 0.25 |
fbiA | 3641398 | p.Asp286Asn | missense_variant | 0.25 |
fbiA | 3641447 | p.Thr302Met | missense_variant | 1.0 |
fbiB | 3642170 | c.636G>T | synonymous_variant | 0.2 |
fbiB | 3642273 | p.Glu247Lys | missense_variant | 0.29 |
rpoA | 3877553 | p.Glu319Lys | missense_variant | 1.0 |
embC | 4240260 | p.Val133Ala | missense_variant | 0.14 |
embC | 4240897 | c.1035C>G | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4243245 | p.Gly5Cys | missense_variant | 0.17 |
embA | 4244593 | p.Ala454Glu | missense_variant | 0.17 |
embA | 4245858 | p.Ala876Pro | missense_variant | 0.14 |
embB | 4247082 | p.Thr190Ile | missense_variant | 0.13 |
embB | 4249408 | c.2895G>A | synonymous_variant | 1.0 |
aftB | 4266995 | c.1842G>A | synonymous_variant | 0.11 |
aftB | 4267644 | p.Asp398Gly | missense_variant | 0.12 |
aftB | 4268848 | c.-13delT | upstream_gene_variant | 0.12 |
ubiA | 4269397 | p.Ala146Glu | missense_variant | 0.18 |
ethA | 4327452 | p.Val8Ile | missense_variant | 0.17 |
ethA | 4328327 | c.-855delC | upstream_gene_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408456 | c.-254C>G | upstream_gene_variant | 1.0 |