Run ID: ERR7801186
Sample name:
Date: 02-04-2023 05:58:20
Number of reads: 738812
Percentage reads mapped: 99.46
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 | 491320 | p.Ala180Ser | missense_variant | 0.17 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575859 | p.Val171Ala | missense_variant | 0.13 |
mshA | 576436 | p.Gln363His | missense_variant | 0.1 |
ccsA | 620281 | p.Arg131Ser | missense_variant | 0.14 |
ccsA | 620367 | c.477T>C | synonymous_variant | 0.11 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 761960 | p.Met718Ile | missense_variant | 0.18 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777887 | p.Gln198His | missense_variant | 0.12 |
mmpL5 | 779160 | c.-680C>A | upstream_gene_variant | 0.14 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303403 | p.Ala158Glu | missense_variant | 0.13 |
fbiC | 1303992 | p.Trp354Cys | missense_variant | 0.13 |
fbiC | 1304706 | c.1776C>T | synonymous_variant | 0.14 |
fbiC | 1305076 | p.Pro716Thr | missense_variant | 0.13 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
embR | 1416931 | c.417G>T | synonymous_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917961 | p.Asp8His | missense_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103033 | p.Gln4* | stop_gained | 0.18 |
katG | 2154417 | c.1695G>C | synonymous_variant | 0.1 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155838 | p.Pro92Thr | missense_variant | 0.18 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168813 | c.1800C>A | synonymous_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289364 | c.-123G>T | upstream_gene_variant | 0.12 |
eis | 2715108 | c.225G>T | synonymous_variant | 0.12 |
ahpC | 2726311 | p.Ser40Ile | missense_variant | 0.12 |
ribD | 2987547 | c.709C>A | synonymous_variant | 0.2 |
thyX | 3068103 | c.-158C>A | upstream_gene_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339722 | p.Gly202Val | missense_variant | 0.2 |
Rv3083 | 3449032 | p.Gly177Cys | missense_variant | 0.2 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
alr | 3840680 | c.741G>A | synonymous_variant | 0.12 |
alr | 3840693 | p.Arg243Leu | missense_variant | 0.11 |
alr | 3841489 | c.-69T>C | upstream_gene_variant | 0.13 |
embC | 4240219 | c.357C>A | synonymous_variant | 0.14 |
embC | 4240669 | c.807G>T | synonymous_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4245936 | p.Asp902Asn | missense_variant | 0.11 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.12 |
embB | 4246561 | c.48T>C | synonymous_variant | 0.15 |
aftB | 4267337 | c.1500C>A | synonymous_variant | 0.12 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268855 | c.-19G>A | upstream_gene_variant | 0.12 |
ethA | 4326676 | p.Ser266Arg | missense_variant | 0.96 |
ethA | 4328046 | c.-573C>A | upstream_gene_variant | 0.12 |
whiB6 | 4338384 | c.138C>T | synonymous_variant | 0.13 |
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 |
gid | 4408213 | c.-11C>T | upstream_gene_variant | 0.14 |