Run ID: SRR6896146
Sample name:
Date: 04-04-2023 17:56:57
Number of reads: 266116
Percentage reads mapped: 99.65
Strain: lineage2.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
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 |
---|---|---|---|---|
gyrB | 5910 | p.Ser224Asn | missense_variant | 0.25 |
gyrB | 6770 | p.Thr511Ala | missense_variant | 0.25 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
fgd1 | 491758 | p.Ser326Thr | missense_variant | 0.2 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 760013 | c.207C>G | synonymous_variant | 0.14 |
rpoB | 761673 | p.Gly623Trp | missense_variant | 0.11 |
rpoB | 761999 | c.2193G>T | synonymous_variant | 0.18 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763147 | p.Ser1114* | stop_gained | 0.25 |
rpoC | 763355 | c.-15G>T | upstream_gene_variant | 0.15 |
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 | 777207 | p.Leu425Pro | missense_variant | 0.17 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781646 | p.Gln29His | missense_variant | 0.11 |
fbiC | 1303380 | c.450T>C | synonymous_variant | 0.12 |
fbiC | 1303581 | c.651G>C | synonymous_variant | 0.14 |
Rv1258c | 1406133 | p.Leu403Pro | missense_variant | 0.29 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472077 | n.232C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1473428 | n.-230A>T | upstream_gene_variant | 0.11 |
rrl | 1474339 | n.682C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474721 | n.1064G>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476780 | n.3123C>T | non_coding_transcript_exon_variant | 0.22 |
inhA | 1674747 | c.546C>T | synonymous_variant | 0.2 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834628 | p.Lys363* | stop_gained | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289776 | c.-535C>T | upstream_gene_variant | 0.25 |
folC | 2746286 | c.1311_1312delCG | frameshift_variant | 0.22 |
ribD | 2986746 | c.-93G>A | upstream_gene_variant | 0.15 |
ribD | 2986881 | p.Arg15Trp | missense_variant | 0.15 |
thyX | 3067988 | c.-44delC | upstream_gene_variant | 0.17 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087426 | p.Lys203Glu | missense_variant | 0.15 |
fbiD | 3339000 | c.-117_-116delCA | upstream_gene_variant | 0.18 |
Rv3083 | 3449844 | c.1341C>T | synonymous_variant | 0.11 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiA | 3640865 | p.Asp108Val | missense_variant | 0.29 |
alr | 3840522 | p.Ile300Ser | missense_variant | 0.17 |
alr | 3841427 | c.-8delA | upstream_gene_variant | 0.12 |
clpC1 | 4040646 | p.Ala20Val | missense_variant | 0.12 |
clpC1 | 4040722 | c.-18G>A | upstream_gene_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243238 | c.6C>T | synonymous_variant | 0.17 |
embA | 4243312 | p.Leu27Pro | missense_variant | 0.18 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4245232 | p.Arg667Leu | missense_variant | 0.13 |
embB | 4247150 | p.Arg213Trp | missense_variant | 0.22 |
aftB | 4267295 | p.Leu514Phe | missense_variant | 0.11 |
aftB | 4267456 | p.Asp461Asn | missense_variant | 0.15 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268857 | c.-21C>A | upstream_gene_variant | 0.22 |
aftB | 4269024 | c.-188G>A | upstream_gene_variant | 0.11 |
ethA | 4327283 | p.Phe64Ser | missense_variant | 0.15 |
ethR | 4327583 | p.Pro12Leu | missense_variant | 0.1 |
ethA | 4327998 | c.-525G>A | upstream_gene_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 |