Run ID: SRR6896381
Sample name:
Date: 04-04-2023 18:04:22
Number of reads: 577689
Percentage reads mapped: 97.84
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 | 0.99 |
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 | 7271 | c.-31A>T | upstream_gene_variant | 0.15 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8721 | c.1420C>A | synonymous_variant | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491390 | p.Tyr203Cys | missense_variant | 0.11 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.87 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 761010 | p.Asp402Tyr | missense_variant | 0.11 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
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 | 778762 | c.-282G>A | upstream_gene_variant | 0.12 |
mmpS5 | 778869 | p.Leu13Ile | missense_variant | 0.11 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1407282 | p.Ala20Asp | missense_variant | 0.12 |
atpE | 1460904 | c.-141C>T | upstream_gene_variant | 0.11 |
atpE | 1460939 | c.-106G>T | upstream_gene_variant | 0.12 |
atpE | 1461008 | c.-37G>C | upstream_gene_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476468 | n.2811C>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.22 |
fabG1 | 1674182 | c.743G>T | stop_lost&splice_region_variant | 0.13 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834846 | p.Phe435Leu | missense_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102340 | c.703C>A | synonymous_variant | 0.12 |
ndh | 2102354 | p.Gln230Arg | missense_variant | 0.13 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.91 |
katG | 2155283 | p.Gly277Cys | missense_variant | 0.2 |
katG | 2155651 | p.Lys154Arg | missense_variant | 0.12 |
PPE35 | 2167682 | c.2931G>A | synonymous_variant | 0.12 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168058 | p.Gln852Arg | missense_variant | 0.1 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv1979c | 2223336 | c.-172G>A | upstream_gene_variant | 0.11 |
kasA | 2518637 | p.Ser175Pro | missense_variant | 0.11 |
folC | 2746250 | p.Ala450Val | missense_variant | 0.18 |
folC | 2746855 | c.744A>G | synonymous_variant | 0.1 |
pepQ | 2859593 | p.Ala276Thr | missense_variant | 0.14 |
Rv2752c | 3066090 | c.101delT | frameshift_variant | 0.1 |
thyX | 3067913 | c.33G>T | synonymous_variant | 0.22 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087425 | c.606C>T | synonymous_variant | 0.12 |
ald | 3087431 | c.612T>C | synonymous_variant | 0.12 |
fbiD | 3339688 | c.576delC | frameshift_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475149 | c.1143C>A | synonymous_variant | 0.13 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiA | 3640811 | p.Gln90Arg | missense_variant | 0.11 |
ddn | 3986934 | p.Arg31Ser | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4244104 | p.Ala291Gly | missense_variant | 0.11 |
embA | 4244185 | p.Ser318Thr | missense_variant | 0.2 |
embA | 4245346 | p.Met705Lys | missense_variant | 0.14 |
embB | 4249739 | p.Ala1076Thr | missense_variant | 0.29 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407620 | p.Tyr195His | missense_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |