Run ID: SRR4034653
Sample name:
Date: 04-04-2023 06:56:57
Number of reads: 686688
Percentage reads mapped: 99.47
Strain: lineage2.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 1.0 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7992 | p.Ala231Thr | missense_variant | 0.17 |
gyrA | 8903 | c.1603delC | frameshift_variant | 0.1 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9773 | c.2472C>T | synonymous_variant | 0.29 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575549 | p.Met68Val | missense_variant | 0.14 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 759621 | c.-186C>T | upstream_gene_variant | 0.15 |
rpoB | 759994 | p.Arg63His | missense_variant | 0.13 |
rpoB | 760657 | p.Glu284Val | missense_variant | 0.22 |
rpoB | 761815 | p.Ala670Val | missense_variant | 0.17 |
rpoB | 762597 | p.Gly931Arg | missense_variant | 0.15 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 765997 | c.2628T>G | synonymous_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 778147 | p.Met112Val | missense_variant | 0.15 |
mmpL5 | 778161 | p.Ala107Val | missense_variant | 0.15 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781833 | c.278_279delTG | frameshift_variant | 0.22 |
fbiC | 1302776 | c.-155C>T | upstream_gene_variant | 0.14 |
fbiC | 1302891 | c.-40G>A | upstream_gene_variant | 0.17 |
fbiC | 1302992 | c.65delA | frameshift_variant | 0.12 |
fbiC | 1303843 | p.Ala305Thr | missense_variant | 0.12 |
fbiC | 1303953 | c.1023C>T | synonymous_variant | 0.25 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
atpE | 1461151 | p.Ile36Asn | missense_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472776 | n.931A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475612 | n.1955G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476076 | n.2419A>G | non_coding_transcript_exon_variant | 0.15 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918581 | c.642G>C | synonymous_variant | 0.14 |
ndh | 2102029 | p.Gln338His | missense_variant | 0.17 |
ndh | 2102139 | p.Arg302Trp | missense_variant | 0.14 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155431 | c.681G>T | synonymous_variant | 0.15 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169476 | c.1137C>T | synonymous_variant | 0.12 |
PPE35 | 2169682 | c.930delC | frameshift_variant | 0.11 |
PPE35 | 2170158 | p.Ala152Val | missense_variant | 0.2 |
Rv1979c | 2222778 | c.387C>T | synonymous_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290222 | c.-981C>G | upstream_gene_variant | 0.2 |
folC | 2747123 | p.Ala159Val | missense_variant | 0.12 |
pepQ | 2860094 | p.Ala109Thr | missense_variant | 0.4 |
Rv2752c | 3064711 | c.1480delT | frameshift_variant | 0.12 |
Rv2752c | 3067080 | c.-890delT | upstream_gene_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612331 | c.786G>A | synonymous_variant | 0.14 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiA | 3641332 | p.Gly264Arg | missense_variant | 1.0 |
fbiB | 3642547 | p.Gly338Val | missense_variant | 0.11 |
clpC1 | 4040174 | c.530delA | frameshift_variant | 0.14 |
clpC1 | 4040616 | p.Thr30Ile | missense_variant | 0.2 |
embC | 4241335 | c.1473G>A | synonymous_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
aftB | 4267483 | c.1354T>C | synonymous_variant | 0.25 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
ethR | 4328134 | p.Glu196Lys | missense_variant | 0.29 |
whiB6 | 4338186 | c.336T>C | synonymous_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |