Run ID: ERR4815716
Sample name:
Date: 01-04-2023 14:01:25
Number of reads: 282966
Percentage reads mapped: 60.32
Strain:
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2155433 | c.678delG | frameshift_variant | 0.29 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6124 | c.885C>T | synonymous_variant | 1.0 |
gyrB | 7124 | p.Ser629Ala | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7871 | c.572dupC | frameshift_variant | 0.4 |
gyrA | 8437 | p.Tyr379Cys | missense_variant | 0.18 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 9047 | c.1746C>T | synonymous_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9443 | c.2142G>A | synonymous_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576000 | p.Asp218Ala | missense_variant | 1.0 |
mshA | 576579 | p.Gly411Glu | missense_variant | 0.33 |
ccsA | 619916 | p.Gly9Asp | missense_variant | 0.22 |
rpoB | 760471 | p.Arg222His | missense_variant | 0.5 |
rpoB | 760490 | c.684C>T | synonymous_variant | 1.0 |
rpoB | 760929 | p.Val375Phe | missense_variant | 0.5 |
rpoB | 761279 | c.1473C>A | synonymous_variant | 0.29 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
rpoC | 764355 | p.Gln329Pro | missense_variant | 0.4 |
rpoC | 765171 | p.Pro601Leu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpR5 | 779267 | c.280dupC | frameshift_variant | 0.33 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406890 | p.Asn151Asp | missense_variant | 0.15 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1833414 | c.-127delT | upstream_gene_variant | 0.4 |
rpsA | 1833692 | p.Val51Leu | missense_variant | 0.67 |
rpsA | 1834499 | p.Leu320Met | missense_variant | 0.4 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101672 | c.1371A>G | synonymous_variant | 0.33 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167654 | p.Pro987Ser | missense_variant | 0.11 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167930 | p.Ser895Pro | missense_variant | 0.5 |
PPE35 | 2167983 | p.Gly877Asp | missense_variant | 1.0 |
PPE35 | 2169592 | p.Ile341Val | missense_variant | 0.18 |
PPE35 | 2169691 | p.Gly308Ser | missense_variant | 1.0 |
PPE35 | 2170325 | c.287delA | frameshift_variant | 0.23 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
folC | 2746633 | c.965delA | frameshift_variant | 0.4 |
folC | 2747003 | p.Ile199Thr | missense_variant | 0.2 |
ribD | 2986640 | c.-199C>T | upstream_gene_variant | 0.29 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 1.0 |
Rv2752c | 3065305 | p.Ala296Val | missense_variant | 1.0 |
Rv2752c | 3065444 | p.Asp250His | missense_variant | 0.29 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339378 | p.Asp87Glu | missense_variant | 0.29 |
Rv3083 | 3448319 | c.-185C>T | upstream_gene_variant | 0.33 |
Rv3083 | 3449018 | p.Asp172Gly | missense_variant | 0.4 |
Rv3083 | 3449323 | p.Arg274* | stop_gained | 0.67 |
Rv3083 | 3449353 | p.Ser284Gly | missense_variant | 0.4 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474102 | c.96C>A | synonymous_variant | 0.18 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
fbiB | 3640965 | c.-570C>A | upstream_gene_variant | 0.17 |
fbiB | 3642206 | c.672C>T | synonymous_variant | 0.2 |
rpoA | 3878082 | c.426T>C | synonymous_variant | 0.4 |
rpoA | 3878705 | c.-198A>G | upstream_gene_variant | 1.0 |
clpC1 | 4039071 | p.Pro545Gln | missense_variant | 0.5 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
embC | 4240126 | p.Cys88* | stop_gained | 0.25 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embA | 4242304 | c.-929G>A | upstream_gene_variant | 0.4 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242822 | c.2964delG | frameshift_variant | 0.25 |
embA | 4243848 | p.Val206Met | missense_variant | 1.0 |
embA | 4244234 | c.1003dupT | frameshift_variant | 0.18 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ubiA | 4269692 | p.Tyr48His | missense_variant | 0.25 |
ethR | 4326577 | c.-972G>T | upstream_gene_variant | 1.0 |
ethA | 4328243 | c.-770C>T | upstream_gene_variant | 0.25 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |
gid | 4407964 | p.Ala80Glu | missense_variant | 0.2 |
gid | 4407990 | c.213A>G | synonymous_variant | 0.2 |