Run ID: SRR1181412
Sample name:
Date: 03-04-2023 04:53:06
Number of reads: 3020270
Percentage reads mapped: 99.12
Strain: lineage4.8;lineage4.1.2;lineage2.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.6 |
lineage4.1 | Euro-American | T;X;H | None | 0.13 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 0.62 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 0.17 |
lineage4.1.2 | Euro-American | T;H | None | 0.13 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.62 |
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 | 0.79 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 0.85 |
fgd1 | 491100 | c.318C>T | synonymous_variant | 0.13 |
fgd1 | 491556 | c.774G>A | synonymous_variant | 0.45 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.62 |
mshA | 575907 | p.Ala187Val | missense_variant | 0.62 |
ccsA | 620625 | p.Ile245Met | missense_variant | 0.77 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.65 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.73 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 0.85 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 0.54 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 0.44 |
embR | 1417140 | p.Ala70Ser | missense_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.16 |
fabG1 | 1673249 | c.-191C>T | upstream_gene_variant | 0.2 |
inhA | 1674210 | c.9A>C | synonymous_variant | 0.57 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.63 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.54 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 0.53 |
PPE35 | 2168524 | p.Gly697Ser | missense_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
folC | 2747022 | p.Val193Ile | missense_variant | 0.2 |
Rv2752c | 3064519 | c.1672delG | frameshift_variant | 0.72 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.8 |
Rv3083 | 3448894 | p.Tyr131Asp | missense_variant | 0.29 |
Rv3083 | 3449642 | p.Asn380Ser | missense_variant | 0.24 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 0.81 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 0.68 |
fbiA | 3641164 | p.Ile208Val | missense_variant | 0.25 |
alr | 3840764 | c.657G>C | synonymous_variant | 0.1 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 0.25 |
embA | 4243460 | c.228C>T | synonymous_variant | 0.72 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 0.62 |
aftB | 4268861 | c.-25T>C | upstream_gene_variant | 0.26 |
whiB6 | 4338286 | p.Val79Ala | missense_variant | 0.85 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.61 |
gid | 4407927 | p.Glu92Asp | missense_variant | 0.52 |