Run ID: SRR12708417
Sample name:
Date: 02-08-2023 14:57:58
Number of reads: NA
Percentage reads mapped: NA
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 | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490769 | c.-14A>G | upstream_gene_variant | 0.11 |
fgd1 | 490932 | p.His50Gln | missense_variant | 0.2 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575240 | c.-108G>T | upstream_gene_variant | 0.11 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 762140 | c.2334G>T | synonymous_variant | 0.22 |
rpoB | 762264 | p.Gly820Cys | missense_variant | 0.18 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763053 | p.Leu1083Met | missense_variant | 0.17 |
rpoB | 763222 | p.Ile1139Thr | missense_variant | 0.18 |
rpoC | 763680 | p.Ile104Asn | missense_variant | 0.29 |
rpoC | 765122 | p.Leu585Val | missense_variant | 0.14 |
rpoC | 765146 | p.Pro593Thr | missense_variant | 0.14 |
rpoC | 766128 | p.Ala920Asp | missense_variant | 0.11 |
rpoC | 766500 | p.Ala1044Val | missense_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 | 777534 | p.Thr316Asn | missense_variant | 0.14 |
mmpR5 | 779315 | p.Arg109Leu | missense_variant | 0.14 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303165 | p.Ser79Gly | missense_variant | 0.11 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1833749 | p.Ile70Leu | missense_variant | 1.0 |
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 |
PPE35 | 2168200 | p.Ala805Thr | missense_variant | 0.29 |
PPE35 | 2168745 | p.Gly623Ala | missense_variant | 0.33 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519221 | c.1107G>T | synonymous_variant | 0.14 |
eis | 2714526 | c.805_806delAC | frameshift_variant | 1.0 |
ahpC | 2726043 | c.-150C>T | upstream_gene_variant | 0.12 |
folC | 2747226 | p.Arg125Trp | missense_variant | 0.11 |
Rv2752c | 3065711 | p.Gly161Ser | missense_variant | 1.0 |
thyA | 3074143 | p.Asp110Val | missense_variant | 0.15 |
thyA | 3074610 | c.-139G>A | upstream_gene_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087116 | c.297G>A | synonymous_variant | 0.25 |
Rv3083 | 3449640 | c.1137A>G | synonymous_variant | 0.29 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
Rv3236c | 3613026 | p.Ser31Pro | missense_variant | 0.15 |
alr | 3841047 | p.Leu125Pro | missense_variant | 0.13 |
alr | 3841130 | c.291G>A | synonymous_variant | 0.11 |
rpoA | 3877884 | c.624G>A | synonymous_variant | 0.33 |
clpC1 | 4039368 | p.Lys446Met | missense_variant | 0.14 |
embC | 4241515 | c.1655delT | frameshift_variant | 0.2 |
embC | 4242035 | p.Gln725Lys | missense_variant | 0.29 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243425 | p.Gly65Trp | missense_variant | 0.13 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embB | 4248172 | c.1659G>T | synonymous_variant | 0.17 |
embB | 4248590 | p.Ala693Thr | missense_variant | 0.14 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4267782 | p.Val352Asp | missense_variant | 0.18 |
ethA | 4326454 | c.1020C>T | synonymous_variant | 0.25 |
ethA | 4327617 | c.-144G>A | upstream_gene_variant | 0.25 |
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 |