Run ID: ERR551135
Sample name:
Date: 15-08-2022 10:52:13
Number of reads: 440966
Percentage reads mapped: 99.46
Strain:
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6446 | p.Ala403Ser | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
ccsA | 620389 | c.499C>T | synonymous_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 766073 | p.Ala902Thr | missense_variant | 0.11 |
rpoC | 766409 | c.3043_3046delTTCC | frameshift_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777835 | p.Ile216Val | missense_variant | 0.12 |
mmpS5 | 778854 | p.Val18Leu | missense_variant | 1.0 |
mmpS5 | 779685 | c.-780T>C | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473094 | n.1249T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473277 | n.1432G>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475104 | n.1450dupG | non_coding_transcript_exon_variant | 0.15 |
inhA | 1674520 | p.Pro107Ser | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155503 | c.609C>T | synonymous_variant | 1.0 |
katG | 2156056 | p.Gly19Val | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167946 | c.2667C>T | synonymous_variant | 1.0 |
PPE35 | 2168460 | p.Asn718Ser | missense_variant | 1.0 |
Rv1979c | 2223077 | p.Ala30Ser | missense_variant | 0.15 |
Rv1979c | 2223128 | p.Lys13Glu | missense_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
eis | 2715001 | p.Ser111Phe | missense_variant | 1.0 |
ald | 3086728 | c.-92C>T | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086954 | c.135C>A | synonymous_variant | 0.17 |
ald | 3087084 | c.266delA | frameshift_variant | 1.0 |
fprA | 3474123 | c.117G>A | synonymous_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
Rv3236c | 3612933 | p.Ala62Thr | missense_variant | 0.12 |
Rv3236c | 3613160 | c.-44C>T | upstream_gene_variant | 0.13 |
ddn | 3987111 | p.Leu90Val | missense_variant | 1.0 |
embC | 4242476 | p.Pro872Ala | missense_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242881 | p.Pro1007Thr | missense_variant | 0.2 |
embA | 4244220 | c.988C>T | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
ubiA | 4269130 | p.Leu235Pro | missense_variant | 0.12 |
aftB | 4269351 | c.-515C>T | upstream_gene_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ethA | 4326990 | p.Ile162Val | missense_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
Rv1979c | 2220946 | c.277_*772del | stop_lost&conservative_inframe_deletion&splice_region_variant | 1.0 |