Run ID: SRR3732700
Sample name:
Date: 04-04-2023 05:38:02
Number of reads: 826472
Percentage reads mapped: 99.57
Strain: lineage2.2
Drug-resistance: Other
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 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
ethA | 4327348 | c.125delG | frameshift_variant | 0.25 | ethionamide, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5107 | c.-133C>A | upstream_gene_variant | 0.12 |
gyrB | 5407 | c.168G>A | synonymous_variant | 0.25 |
gyrB | 5425 | c.186A>G | synonymous_variant | 0.25 |
gyrB | 6283 | p.Asp348Glu | missense_variant | 0.33 |
gyrB | 6562 | p.Lys441Asn | missense_variant | 0.29 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7699 | p.Arg133Gln | missense_variant | 0.4 |
gyrA | 8721 | c.1420C>A | synonymous_variant | 0.5 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 0.9 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620523 | c.633G>T | synonymous_variant | 0.22 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 760433 | p.Asp209Glu | missense_variant | 0.25 |
rpoB | 762120 | p.Asp772Asn | missense_variant | 0.29 |
rpoB | 762681 | p.Glu959Lys | missense_variant | 0.33 |
rpoB | 762697 | p.Ala964Asp | missense_variant | 0.4 |
rpoB | 762712 | p.Pro969Gln | missense_variant | 0.29 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764652 | p.Ser428Leu | missense_variant | 0.4 |
rpoC | 764987 | p.Gln540Lys | missense_variant | 0.25 |
rpoC | 765960 | p.Ala864Glu | missense_variant | 0.15 |
rpoC | 765992 | c.2623C>A | synonymous_variant | 0.17 |
rpoC | 766096 | c.2727G>T | synonymous_variant | 0.25 |
rpoC | 766849 | p.Gln1160His | missense_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775840 | p.Val881Leu | missense_variant | 0.67 |
mmpL5 | 776051 | p.Leu810Phe | missense_variant | 0.4 |
mmpL5 | 776066 | c.2415C>T | synonymous_variant | 0.33 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 777200 | c.1281C>T | synonymous_variant | 0.33 |
mmpL5 | 777747 | p.Gly245Val | missense_variant | 0.4 |
mmpL5 | 777937 | p.Val182Ile | missense_variant | 0.29 |
mmpL5 | 778008 | p.Gly158Val | missense_variant | 0.18 |
mmpL5 | 778416 | p.Pro22Leu | missense_variant | 0.25 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
mmpS5 | 779630 | c.-725T>C | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781435 | c.-125G>T | upstream_gene_variant | 0.33 |
rpsL | 781491 | c.-69C>A | upstream_gene_variant | 0.4 |
rpsL | 781737 | p.Gln60Lys | missense_variant | 0.25 |
rplC | 801221 | p.Ser138Ile | missense_variant | 0.22 |
fbiC | 1303268 | p.Lys113Met | missense_variant | 0.33 |
fbiC | 1303328 | p.Arg133His | missense_variant | 0.33 |
fbiC | 1303913 | p.Gly328Val | missense_variant | 0.2 |
fbiC | 1304552 | p.Gly541Val | missense_variant | 0.25 |
Rv1258c | 1406522 | c.819G>T | synonymous_variant | 0.4 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
embR | 1417120 | c.228G>T | synonymous_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673276 | c.-164G>A | upstream_gene_variant | 0.33 |
inhA | 1674929 | p.Cys243Ser | missense_variant | 0.18 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834219 | c.678C>T | synonymous_variant | 0.29 |
rpsA | 1834621 | p.Leu360Phe | missense_variant | 0.25 |
rpsA | 1834725 | c.1185delC | frameshift_variant | 0.67 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101931 | p.Ala371Asp | missense_variant | 0.29 |
katG | 2154523 | p.Ser530Tyr | missense_variant | 0.29 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2154941 | p.Glu391* | stop_gained | 0.25 |
katG | 2155229 | p.Gln295Lys | missense_variant | 0.67 |
katG | 2155781 | p.Gly111Ser | missense_variant | 0.22 |
katG | 2155813 | p.Pro100Leu | missense_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289445 | c.-204C>A | upstream_gene_variant | 0.25 |
pncA | 2289707 | c.-466A>T | upstream_gene_variant | 0.29 |
pncA | 2289772 | c.-531C>A | upstream_gene_variant | 0.29 |
kasA | 2518561 | c.447T>G | synonymous_variant | 0.17 |
eis | 2714813 | p.Glu174* | stop_gained | 0.25 |
ahpC | 2726246 | c.54C>A | synonymous_variant | 0.33 |
folC | 2747248 | c.351G>T | synonymous_variant | 0.17 |
pepQ | 2859964 | p.Ala152Val | missense_variant | 0.22 |
Rv2752c | 3065040 | c.1152C>A | synonymous_variant | 0.14 |
Rv2752c | 3065116 | p.Gly359Val | missense_variant | 0.22 |
Rv2752c | 3067039 | c.-848T>C | upstream_gene_variant | 0.95 |
thyX | 3067661 | c.285C>A | synonymous_variant | 0.2 |
thyX | 3068037 | c.-92C>A | upstream_gene_variant | 0.22 |
thyX | 3068128 | c.-183C>T | upstream_gene_variant | 0.25 |
thyA | 3073767 | c.705G>T | synonymous_variant | 0.5 |
thyA | 3073988 | p.Gln162Lys | missense_variant | 0.5 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087755 | c.936G>T | synonymous_variant | 1.0 |
Rv3083 | 3448560 | c.57G>A | synonymous_variant | 0.2 |
Rv3083 | 3448924 | p.Gly141Ser | missense_variant | 0.67 |
Rv3083 | 3449310 | c.807G>T | synonymous_variant | 0.33 |
fprA | 3473895 | c.-112T>A | upstream_gene_variant | 0.22 |
fprA | 3473998 | c.-9G>A | upstream_gene_variant | 1.0 |
fprA | 3474319 | p.Gly105Ser | missense_variant | 0.22 |
fprA | 3474825 | c.819C>G | synonymous_variant | 0.17 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiB | 3640794 | c.-741A>G | upstream_gene_variant | 0.2 |
fbiA | 3641158 | p.Ala206Ser | missense_variant | 0.25 |
fbiB | 3642072 | p.Arg180Cys | missense_variant | 0.13 |
fbiB | 3642729 | p.Gly399Cys | missense_variant | 0.33 |
alr | 3840548 | c.872delA | frameshift_variant | 0.12 |
alr | 3840613 | p.Gly270Trp | missense_variant | 0.12 |
rpoA | 3877801 | p.Pro236Gln | missense_variant | 0.33 |
rpoA | 3877920 | c.588G>T | synonymous_variant | 0.5 |
ddn | 3987083 | c.240C>A | synonymous_variant | 0.67 |
clpC1 | 4038578 | p.Phe709Leu | missense_variant | 0.29 |
clpC1 | 4038943 | c.1762C>A | synonymous_variant | 0.4 |
clpC1 | 4040778 | c.-74G>A | upstream_gene_variant | 0.29 |
embC | 4239950 | c.88C>A | synonymous_variant | 0.29 |
embC | 4241658 | p.Ser599* | stop_gained | 1.0 |
embC | 4241773 | c.1911C>A | synonymous_variant | 0.5 |
embC | 4242066 | p.Ser735* | stop_gained | 0.2 |
embC | 4242090 | p.Ala743Asp | missense_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243275 | p.Leu15Ile | missense_variant | 0.15 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4245183 | p.Leu651Met | missense_variant | 0.25 |
embA | 4245512 | c.2280G>T | synonymous_variant | 0.5 |
embA | 4246204 | p.Arg991Leu | missense_variant | 0.33 |
embB | 4246936 | c.423G>T | synonymous_variant | 0.15 |
embB | 4246978 | c.465C>T | synonymous_variant | 0.14 |
embB | 4247225 | p.Arg238Ser | missense_variant | 0.18 |
embB | 4247427 | p.Gly305Asp | missense_variant | 0.25 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268435 | c.402C>T | synonymous_variant | 0.33 |
ubiA | 4269736 | p.Leu33Gln | missense_variant | 0.22 |
ethA | 4326078 | c.1396C>A | synonymous_variant | 0.67 |
ethA | 4326692 | p.Arg261Leu | missense_variant | 0.13 |
ethR | 4327597 | p.Thr17Ser | missense_variant | 0.67 |
whiB6 | 4338487 | p.Cys12Phe | missense_variant | 0.29 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407726 | p.Met159Ile | missense_variant | 0.25 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |
gid | 4408031 | p.Leu58Ile | missense_variant | 0.29 |
gid | 4408281 | c.-79C>A | upstream_gene_variant | 0.5 |