Run ID: ERR4814914
Sample name:
Date: 01-04-2023 13:33:42
Number of reads: 283905
Percentage reads mapped: 97.11
Strain:
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 1.0 | streptomycin |
katG | 2155090 | p.Trp341Ser | missense_variant | 0.22 | isoniazid |
gid | 4408137 | p.Tyr22* | stop_gained | 1.0 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
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 | 9658 | p.Thr786Asn | missense_variant | 0.5 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 760251 | p.Gly149Cys | missense_variant | 0.5 |
rpoB | 761034 | p.Thr410Ala | missense_variant | 0.4 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 765925 | c.2556C>T | synonymous_variant | 0.29 |
rpoC | 765963 | p.Leu865Ser | missense_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777940 | p.Gly181Ser | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304291 | p.Asp454Val | missense_variant | 0.15 |
fbiC | 1305203 | c.2277dupC | frameshift_variant | 0.33 |
embR | 1417037 | p.Ser104Asn | missense_variant | 0.5 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918262 | p.Val108Ala | missense_variant | 0.22 |
katG | 2154400 | p.Arg571His | missense_variant | 0.67 |
katG | 2155484 | p.Tyr210Asn | missense_variant | 0.4 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223222 | c.-58T>C | upstream_gene_variant | 0.4 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
pepQ | 2859468 | c.951G>A | synonymous_variant | 0.29 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339660 | c.544delT | frameshift_variant | 0.25 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
alr | 3841473 | c.-53G>A | upstream_gene_variant | 1.0 |
rpoA | 3877844 | p.Ala222Pro | missense_variant | 0.25 |
rpoA | 3878019 | c.489A>G | synonymous_variant | 0.22 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244639 | c.1407G>C | synonymous_variant | 0.2 |
embA | 4246494 | p.Gly1088Arg | missense_variant | 0.15 |
embB | 4249481 | c.2969_2970delTC | frameshift_variant | 0.25 |
aftB | 4266984 | p.Pro618His | missense_variant | 0.25 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4408019 | p.Gly62Ser | missense_variant | 0.2 |