Run ID: SRR6832157
Sample name:
Date: 04-04-2023 17:15:49
Number of reads: 633561
Percentage reads mapped: 99.56
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 |
---|---|---|---|---|
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 |
mshA | 575422 | c.75C>T | synonymous_variant | 0.29 |
mshA | 575583 | p.Leu79Gln | missense_variant | 0.33 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 761575 | p.Phe590Ser | missense_variant | 0.1 |
rpoB | 762324 | p.Lys840* | stop_gained | 0.13 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763700 | p.Pro111Ser | missense_variant | 0.13 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 0.88 |
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 | 776832 | p.Thr550Ile | missense_variant | 0.18 |
mmpL5 | 778159 | p.Phe108Val | missense_variant | 0.18 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781906 | c.349delT | frameshift_variant | 0.15 |
fbiC | 1304160 | c.1230G>T | synonymous_variant | 0.25 |
fbiC | 1305242 | c.2315delT | frameshift_variant | 0.2 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1407372 | c.-32C>T | upstream_gene_variant | 0.25 |
embR | 1417170 | p.Trp60Arg | missense_variant | 0.22 |
embR | 1417171 | c.176delT | frameshift_variant | 0.22 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475060 | n.1403A>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476659 | n.3002A>G | non_coding_transcript_exon_variant | 0.2 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
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 |
kasA | 2519104 | c.990T>C | synonymous_variant | 0.33 |
Rv2752c | 3066074 | p.Leu40Met | missense_variant | 0.33 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339330 | c.213G>A | synonymous_variant | 0.33 |
fbiD | 3339688 | p.Thr191Pro | missense_variant | 0.18 |
Rv3083 | 3448795 | p.Ile98Val | missense_variant | 0.2 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474743 | p.Lys246Arg | missense_variant | 0.18 |
Rv3236c | 3612301 | c.816G>A | synonymous_variant | 0.5 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.12 |
rpoA | 3878215 | p.Arg98His | missense_variant | 0.12 |
embC | 4239858 | c.-5G>A | upstream_gene_variant | 0.17 |
embC | 4240774 | c.912C>T | synonymous_variant | 0.25 |
embC | 4241798 | p.Phe646Leu | missense_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embB | 4248071 | p.Thr520Ala | missense_variant | 0.15 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
ethA | 4326342 | p.Pro378Ser | missense_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338606 | c.-85G>T | upstream_gene_variant | 0.15 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |