Run ID: ERR4816057
Sample name:
Date: 01-04-2023 14:12:52
Number of reads: 753345
Percentage reads mapped: 99.48
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 |
---|---|---|---|---|
gyrB | 6332 | p.Pro365Thr | missense_variant | 0.4 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7874 | c.573G>A | synonymous_variant | 0.2 |
gyrA | 7948 | p.Leu216Arg | missense_variant | 0.29 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 0.94 |
fgd1 | 491721 | c.939A>G | synonymous_variant | 0.15 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 576074 | p.Asp243Asn | missense_variant | 0.2 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 760018 | p.Arg71Gln | missense_variant | 0.2 |
rpoC | 762848 | c.-522G>A | upstream_gene_variant | 0.17 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764202 | p.Arg278Pro | missense_variant | 0.2 |
rpoC | 765340 | c.1971G>A | synonymous_variant | 0.33 |
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 |
mmpL5 | 777156 | c.1324delC | frameshift_variant | 0.13 |
mmpL5 | 777896 | p.Asp195Glu | missense_variant | 0.2 |
mmpL5 | 778330 | p.Pro51Ser | missense_variant | 0.1 |
mmpS5 | 778588 | p.Gln106His | missense_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781561 | c.2T>C | start_lost | 0.11 |
rplC | 801336 | c.528C>G | synonymous_variant | 0.15 |
fbiC | 1303292 | p.Thr121Met | missense_variant | 0.14 |
fbiC | 1303496 | p.Pro189Leu | missense_variant | 0.2 |
fbiC | 1305409 | p.Ala827Thr | missense_variant | 0.11 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_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 | 2167965 | p.Ala883Gly | missense_variant | 0.11 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.12 |
Rv1979c | 2222958 | c.207A>G | synonymous_variant | 0.1 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518395 | p.Leu94Pro | missense_variant | 0.12 |
kasA | 2518641 | p.Glu176Val | missense_variant | 0.18 |
eis | 2714641 | p.Thr231Ser | missense_variant | 0.11 |
ribD | 2986719 | c.-120G>C | upstream_gene_variant | 0.15 |
ribD | 2987120 | c.282C>G | synonymous_variant | 0.18 |
thyX | 3067493 | c.453A>G | synonymous_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087317 | c.498C>A | synonymous_variant | 0.4 |
fprA | 3473881 | c.-125delA | upstream_gene_variant | 0.13 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568864 | c.-185G>A | upstream_gene_variant | 0.15 |
Rv3236c | 3612120 | p.Arg333Trp | missense_variant | 0.18 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
Rv3236c | 3612925 | c.192C>A | synonymous_variant | 0.11 |
fbiA | 3641058 | p.Trp172Cys | missense_variant | 0.11 |
fbiB | 3641439 | c.-96C>T | upstream_gene_variant | 0.17 |
fbiB | 3642038 | c.504C>T | synonymous_variant | 0.18 |
rpoA | 3878171 | p.Pro113Thr | missense_variant | 0.15 |
clpC1 | 4038176 | c.2529G>A | synonymous_variant | 0.17 |
clpC1 | 4039666 | p.Val347Met | missense_variant | 0.11 |
embC | 4240079 | p.Pro73Thr | missense_variant | 0.11 |
embC | 4241094 | p.Cys411Phe | missense_variant | 0.2 |
embC | 4242359 | p.Asn833Asp | missense_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4243140 | p.Arg1093His | missense_variant | 0.22 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4244136 | p.Ala302Ser | missense_variant | 0.17 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.17 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.18 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.22 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.22 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.22 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.22 |
embB | 4249346 | p.Ala945Thr | missense_variant | 0.13 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268821 | c.16T>C | synonymous_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407547 | p.Ala219Val | missense_variant | 0.17 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |