Run ID: ERR4828357
Sample name:
Date: 01-04-2023 18:50:02
Number of reads: 1424816
Percentage reads mapped: 99.44
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 | 5286 | p.Ser16Phe | missense_variant | 0.12 |
gyrB | 5730 | p.Thr164Asn | missense_variant | 0.14 |
gyrB | 5925 | p.Ala229Val | missense_variant | 0.14 |
gyrB | 5959 | c.720C>T | synonymous_variant | 0.12 |
gyrB | 6497 | p.Ala420Thr | missense_variant | 0.13 |
gyrB | 6635 | p.Ser466Thr | missense_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7949 | c.648G>A | synonymous_variant | 0.13 |
gyrA | 9065 | c.1764C>A | synonymous_variant | 0.17 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491371 | p.Gly197Cys | missense_variant | 0.2 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.55 |
mshA | 576499 | c.1152G>A | synonymous_variant | 0.15 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763174 | p.Gln1123Arg | missense_variant | 0.1 |
rpoC | 763657 | p.Glu96Asp | missense_variant | 0.11 |
rpoC | 764104 | c.735C>T | synonymous_variant | 0.22 |
rpoC | 764132 | p.Ala255Ser | missense_variant | 0.25 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.15 |
rpoC | 765139 | c.1770C>G | synonymous_variant | 0.11 |
rpoC | 767284 | c.3915C>A | synonymous_variant | 0.29 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776806 | p.Gly559Trp | missense_variant | 0.12 |
mmpL5 | 776964 | p.Thr506Ile | missense_variant | 0.11 |
mmpL5 | 777542 | c.939G>C | synonymous_variant | 0.11 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303283 | p.Gly118Asp | missense_variant | 0.14 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
atpE | 1461225 | p.Glu61* | stop_gained | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
inhA | 1674571 | p.Ala124Ser | missense_variant | 0.17 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101931 | p.Ala371Val | missense_variant | 0.17 |
ndh | 2103226 | c.-184C>A | upstream_gene_variant | 0.12 |
katG | 2154042 | c.2070C>G | synonymous_variant | 0.14 |
katG | 2154270 | c.1842G>A | synonymous_variant | 0.12 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2156274 | c.-163G>A | upstream_gene_variant | 0.13 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168975 | c.1638C>T | synonymous_variant | 0.16 |
PPE35 | 2168985 | p.Thr543Met | missense_variant | 0.19 |
PPE35 | 2168987 | p.Thr542Ala | missense_variant | 0.11 |
PPE35 | 2168990 | c.1623T>G | synonymous_variant | 0.1 |
PPE35 | 2169902 | c.711G>C | synonymous_variant | 0.14 |
PPE35 | 2169939 | p.Gly225Ala | missense_variant | 0.18 |
PPE35 | 2169941 | c.672C>T | synonymous_variant | 0.12 |
PPE35 | 2169944 | c.669G>C | synonymous_variant | 0.11 |
PPE35 | 2169947 | c.666T>C | synonymous_variant | 0.11 |
Rv1979c | 2222407 | p.Pro253Leu | missense_variant | 0.13 |
Rv1979c | 2223113 | p.Ser18Gly | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv1979c | 2223358 | c.-194C>T | upstream_gene_variant | 0.11 |
eis | 2714271 | p.Asp354Glu | missense_variant | 0.12 |
eis | 2714856 | c.477T>C | synonymous_variant | 0.15 |
eis | 2715237 | c.96A>G | synonymous_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086890 | p.Ala24Val | missense_variant | 0.12 |
fbiD | 3339678 | c.561C>T | synonymous_variant | 1.0 |
Rv3083 | 3448905 | c.402T>C | synonymous_variant | 0.17 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiA | 3640371 | c.-172G>A | upstream_gene_variant | 0.12 |
rpoA | 3877557 | c.951C>A | synonymous_variant | 0.17 |
embC | 4240607 | p.His249Tyr | missense_variant | 0.18 |
embC | 4241850 | p.Thr663Ile | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embB | 4245911 | c.-603A>G | upstream_gene_variant | 0.2 |
embB | 4247033 | p.Ser174Arg | missense_variant | 0.2 |
aftB | 4267539 | p.Pro433Gln | missense_variant | 0.14 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4267695 | p.Gly381Glu | missense_variant | 0.13 |
aftB | 4267873 | p.Gln322* | stop_gained | 0.12 |
ubiA | 4268993 | p.Asp281Tyr | missense_variant | 0.12 |
ubiA | 4269854 | c.-21G>T | upstream_gene_variant | 0.12 |
ethA | 4326676 | p.Ser266Arg | missense_variant | 1.0 |
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 |