Run ID: ERR10796614
Sample name:
Date: 31-03-2023 11:12:33
Number of reads: 554556
Percentage reads mapped: 100.0
Strain: lineage4
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
pncA | 2288818 | p.Thr142Ala | missense_variant | 0.1 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5982 | p.Ser248Ile | missense_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8438 | p.Tyr379* | stop_gained | 0.14 |
gyrA | 8477 | c.1176C>A | synonymous_variant | 0.15 |
gyrA | 8650 | p.Arg450His | missense_variant | 0.11 |
gyrA | 9087 | p.Val596Met | missense_variant | 0.12 |
fgd1 | 491739 | c.957G>T | synonymous_variant | 0.1 |
mshA | 576185 | p.Pro280Thr | missense_variant | 0.5 |
rpoB | 759793 | c.-14T>C | upstream_gene_variant | 0.2 |
rpoB | 760762 | p.Gly319Asp | missense_variant | 0.14 |
rpoB | 761270 | c.1464C>T | synonymous_variant | 0.4 |
rpoB | 762022 | p.Asp739Gly | missense_variant | 0.1 |
rpoC | 766168 | c.2799C>A | synonymous_variant | 0.18 |
rpoC | 766770 | p.Leu1134Pro | missense_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775741 | p.Leu914Met | missense_variant | 0.1 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801256 | p.Ser150Thr | missense_variant | 0.22 |
Rv1258c | 1406189 | c.1152A>T | synonymous_variant | 0.22 |
embR | 1416663 | p.Arg229Ser | missense_variant | 0.15 |
embR | 1417460 | c.-113G>A | upstream_gene_variant | 0.25 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673244 | c.-196T>C | upstream_gene_variant | 0.13 |
inhA | 1674617 | c.420delC | frameshift_variant | 0.25 |
inhA | 1674670 | p.Ala157Ser | missense_variant | 0.17 |
rpsA | 1833356 | c.-186A>C | upstream_gene_variant | 0.5 |
rpsA | 1833396 | c.-146T>C | upstream_gene_variant | 0.2 |
rpsA | 1833438 | c.-104C>T | upstream_gene_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101789 | c.1254G>T | synonymous_variant | 0.25 |
ndh | 2102502 | p.Thr181Ser | missense_variant | 0.11 |
katG | 2155441 | p.Gln224Arg | missense_variant | 0.1 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv1979c | 2223350 | c.-186T>C | upstream_gene_variant | 0.11 |
pncA | 2289531 | c.-290G>A | upstream_gene_variant | 0.11 |
folC | 2747561 | p.Ser13Leu | missense_variant | 0.25 |
ribD | 2986990 | p.Gly51Asp | missense_variant | 0.12 |
ribD | 2987208 | p.Gly124Ser | missense_variant | 0.29 |
ribD | 2987531 | c.693C>T | synonymous_variant | 0.17 |
thyA | 3073747 | p.Thr242Ile | missense_variant | 0.1 |
thyA | 3074343 | c.129G>T | synonymous_variant | 0.11 |
ald | 3087126 | p.Cys103Arg | missense_variant | 0.15 |
ald | 3087774 | p.Pro319Ser | missense_variant | 0.12 |
fprA | 3474116 | p.Asp37Gly | missense_variant | 0.15 |
fprA | 3474703 | p.Ile233Phe | missense_variant | 0.22 |
Rv3236c | 3612237 | p.Ala294Thr | missense_variant | 0.15 |
Rv3236c | 3612909 | p.Leu70Val | missense_variant | 0.22 |
Rv3236c | 3612962 | p.Ala52Val | missense_variant | 0.12 |
fbiA | 3641072 | p.Arg177His | missense_variant | 0.13 |
fbiB | 3642666 | p.Gly378Arg | missense_variant | 0.29 |
alr | 3840198 | p.Arg408His | missense_variant | 0.25 |
alr | 3841308 | p.Ala38Val | missense_variant | 0.11 |
clpC1 | 4039729 | p.Asp326Asn | missense_variant | 1.0 |
panD | 4043979 | p.Tyr101* | stop_gained | 0.11 |
panD | 4044324 | c.-43C>A | upstream_gene_variant | 0.12 |
embC | 4240210 | c.348C>T | synonymous_variant | 0.18 |
embA | 4242955 | c.-278C>T | upstream_gene_variant | 0.13 |
embB | 4246879 | c.366C>G | synonymous_variant | 0.2 |
embB | 4247377 | c.864G>C | synonymous_variant | 0.17 |
embB | 4248686 | p.Gly725Arg | missense_variant | 0.13 |
embB | 4248954 | p.Asp814Gly | missense_variant | 0.67 |
embB | 4249674 | p.Ser1054Tyr | missense_variant | 0.11 |
aftB | 4268731 | p.Arg36Trp | missense_variant | 0.17 |
aftB | 4268855 | c.-19G>T | upstream_gene_variant | 0.22 |
ubiA | 4269025 | p.Leu270Gln | missense_variant | 0.18 |
ubiA | 4269728 | p.Pro36Ser | missense_variant | 0.18 |
ethR | 4326559 | c.-990A>G | upstream_gene_variant | 0.29 |
ethA | 4326951 | p.Ala175Thr | missense_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407690 | c.513A>T | synonymous_variant | 0.14 |
gid | 4408413 | c.-211C>T | upstream_gene_variant | 0.22 |