Run ID: ERR1194812
Sample name:
Date: 31-03-2023 12:34:29
Number of reads: 656128
Percentage reads mapped: 99.09
Strain: lineage2.2.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.99 |
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 |
---|---|---|---|---|---|
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5791 | p.Glu184Asp | missense_variant | 0.18 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8988 | p.Thr563Ala | missense_variant | 0.2 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.43 |
mshA | 576535 | c.1188T>G | synonymous_variant | 0.4 |
ccsA | 619913 | p.Val8Gly | missense_variant | 0.29 |
ccsA | 619955 | p.Val22Gly | missense_variant | 0.29 |
ccsA | 620298 | c.408G>A | synonymous_variant | 0.22 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 761152 | p.Leu449Gln | missense_variant | 0.2 |
rpoB | 762283 | p.Val826Gly | missense_variant | 0.33 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763848 | p.Lys160Thr | missense_variant | 0.22 |
rpoC | 763917 | p.Glu183Ala | missense_variant | 0.22 |
rpoC | 765445 | c.2076G>T | synonymous_variant | 0.17 |
rpoC | 766428 | p.Val1020Gly | missense_variant | 0.43 |
rpoC | 766641 | p.His1091Leu | missense_variant | 0.22 |
rpoC | 766645 | p.Glu1092Asp | 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 |
mmpR5 | 779132 | p.Pro48His | missense_variant | 0.33 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303519 | p.Ser197Arg | missense_variant | 0.18 |
Rv1258c | 1406238 | p.Gly368Asp | missense_variant | 0.18 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
embR | 1416498 | p.Ser284Ala | missense_variant | 0.21 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473396 | n.-262A>T | upstream_gene_variant | 0.91 |
inhA | 1674624 | c.423A>G | synonymous_variant | 0.2 |
inhA | 1674960 | c.759C>A | synonymous_variant | 0.22 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834861 | c.1320G>T | synonymous_variant | 0.4 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918718 | p.Val260Glu | missense_variant | 0.22 |
katG | 2154161 | p.Glu651Gln | missense_variant | 0.2 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2156284 | c.-173C>T | upstream_gene_variant | 0.13 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168882 | c.1731T>A | synonymous_variant | 0.17 |
PPE35 | 2169056 | c.1557A>T | synonymous_variant | 0.22 |
PPE35 | 2169886 | p.Gly243Cys | missense_variant | 0.67 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.2 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.2 |
PPE35 | 2170147 | p.Ser156Ala | missense_variant | 0.29 |
PPE35 | 2170159 | p.Ala152Ser | missense_variant | 0.29 |
Rv1979c | 2222203 | p.Phe321Cys | missense_variant | 0.2 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289753 | c.-512T>C | upstream_gene_variant | 1.0 |
kasA | 2518541 | p.Gln143* | stop_gained | 0.29 |
folC | 2746628 | p.Asp324Ala | missense_variant | 0.25 |
folC | 2747066 | p.Gly178Asp | missense_variant | 0.22 |
folC | 2747491 | p.Gln36His | missense_variant | 0.29 |
Rv2752c | 3065305 | p.Ala296Val | missense_variant | 0.25 |
Rv2752c | 3065500 | p.Gly231Val | missense_variant | 1.0 |
Rv2752c | 3066186 | p.Asp2Glu | missense_variant | 0.17 |
Rv2752c | 3066335 | c.-144T>G | upstream_gene_variant | 0.22 |
Rv2752c | 3066359 | c.-168G>T | upstream_gene_variant | 0.29 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
Rv3236c | 3613189 | c.-73G>A | upstream_gene_variant | 0.4 |
fbiB | 3640566 | c.-969T>G | upstream_gene_variant | 0.22 |
clpC1 | 4039404 | p.Glu434Val | missense_variant | 0.4 |
embC | 4240251 | p.Leu130Gln | missense_variant | 0.2 |
embC | 4241032 | c.1172delC | frameshift_variant | 0.22 |
embC | 4241539 | c.1677T>G | synonymous_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4243824 | p.Thr198Ser | missense_variant | 0.67 |
embA | 4244905 | p.Val558Gly | missense_variant | 0.29 |
embB | 4248902 | p.Thr797Pro | missense_variant | 0.25 |
embB | 4249113 | p.Lys867Thr | missense_variant | 0.33 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
ubiA | 4269247 | p.Leu196Arg | missense_variant | 0.67 |
ubiA | 4269716 | p.Leu40Val | missense_variant | 0.2 |
ubiA | 4269799 | p.Asn12Thr | missense_variant | 0.29 |
ubiA | 4269840 | c.-7A>G | upstream_gene_variant | 0.33 |
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 |