Run ID: SRR11972189
Sample name:
Date: 03-04-2023 05:31:20
Number of reads: 128741
Percentage reads mapped: 98.42
Strain: lineage1
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrB | 6124 | c.885C>T | synonymous_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 9047 | c.1746C>T | synonymous_variant | 0.83 |
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 | 575428 | c.81G>A | synonymous_variant | 0.33 |
mshA | 576000 | p.Asp218Ala | missense_variant | 1.0 |
ccsA | 619958 | p.Val23Ala | missense_variant | 0.5 |
ccsA | 620331 | c.441C>T | synonymous_variant | 0.4 |
rpoB | 760490 | c.684C>T | synonymous_variant | 1.0 |
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 | 765171 | p.Pro601Leu | missense_variant | 1.0 |
rpoC | 765360 | p.Ala664Val | missense_variant | 0.4 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776395 | p.Phe696Leu | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1302743 | c.-188C>T | upstream_gene_variant | 0.18 |
fbiC | 1303508 | p.Pro193Leu | missense_variant | 0.29 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1674032 | p.Ile198Thr | missense_variant | 0.33 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101991 | p.Leu351Gln | missense_variant | 0.29 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167983 | p.Gly877Asp | missense_variant | 1.0 |
PPE35 | 2168657 | c.1956T>C | synonymous_variant | 0.15 |
PPE35 | 2170280 | c.333C>G | synonymous_variant | 0.22 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2518870 | c.757delC | frameshift_variant | 0.22 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
ahpC | 2726250 | p.Gly20Ser | missense_variant | 0.4 |
Rv2752c | 3064612 | p.Ile527Asn | missense_variant | 0.29 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 1.0 |
Rv2752c | 3064964 | p.Ala410Ser | missense_variant | 0.25 |
Rv2752c | 3065305 | p.Ala296Val | missense_variant | 1.0 |
Rv2752c | 3065898 | c.294C>A | synonymous_variant | 0.29 |
thyA | 3073946 | p.Phe176Leu | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
Rv3083 | 3449890 | p.Leu463Ile | missense_variant | 0.29 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 0.83 |
fbiA | 3641411 | p.Val290Ala | missense_variant | 0.29 |
fbiA | 3641514 | p.Cys324* | stop_gained | 0.18 |
fbiB | 3641633 | c.99C>T | synonymous_variant | 0.15 |
clpC1 | 4038385 | p.Arg774Trp | missense_variant | 0.17 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4240722 | p.Val287Ala | missense_variant | 0.22 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242909 | p.Phe1016Tyr | missense_variant | 0.4 |
embA | 4243641 | c.414_415delGC | frameshift_variant | 0.4 |
embA | 4243848 | p.Val206Met | missense_variant | 1.0 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embA | 4246429 | p.Ala1066Val | missense_variant | 0.22 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
aftB | 4268345 | c.492C>A | synonymous_variant | 0.29 |
ubiA | 4269106 | p.Tyr243Phe | missense_variant | 0.33 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ethA | 4326193 | c.1281A>G | synonymous_variant | 0.29 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |