Run ID: SRR4033131
Sample name:
Date: 04-04-2023 05:50:41
Number of reads: 1078859
Percentage reads mapped: 99.15
Strain: lineage4.1.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 0.96 |
lineage4.1.2 | Euro-American | T;H | None | 0.94 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8061 | p.Arg254Cys | missense_variant | 0.97 |
gyrA | 9286 | p.Ala662Val | missense_variant | 0.13 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575755 | c.408G>T | synonymous_variant | 0.17 |
ccsA | 620355 | p.Trp155* | stop_gained | 0.2 |
ccsA | 620382 | p.Met164Ile | missense_variant | 0.18 |
ccsA | 620499 | c.609G>T | synonymous_variant | 0.13 |
ccsA | 620625 | p.Ile245Met | missense_variant | 0.2 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 761025 | p.Thr407Ala | missense_variant | 0.13 |
rpoB | 763246 | c.3442delG | frameshift_variant | 0.13 |
rpoC | 764263 | c.894G>A | synonymous_variant | 0.96 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765972 | p.Ala868Val | missense_variant | 0.14 |
rpoC | 767180 | p.Ala1271Ser | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775761 | p.Gly907Asp | missense_variant | 0.29 |
mmpL5 | 777260 | c.1221C>A | synonymous_variant | 0.17 |
mmpL5 | 777320 | c.1161C>G | synonymous_variant | 0.86 |
mmpS5 | 778545 | p.Glu121Lys | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781596 | c.37C>A | synonymous_variant | 0.18 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 0.17 |
embR | 1416543 | p.Thr269Ala | missense_variant | 0.15 |
rrs | 1471655 | n.-191G>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473596 | n.-62G>T | upstream_gene_variant | 0.11 |
inhA | 1674209 | p.Gly3Glu | missense_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102070 | p.Ala325Ser | missense_variant | 0.13 |
ndh | 2102115 | p.Ser310Pro | missense_variant | 0.13 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.23 |
Rv1979c | 2222334 | c.831C>T | synonymous_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
ahpC | 2725954 | c.-239C>T | upstream_gene_variant | 0.12 |
folC | 2746597 | c.1002C>A | synonymous_variant | 0.17 |
thyX | 3067288 | p.Ala220Thr | missense_variant | 0.11 |
ald | 3086653 | c.-167C>A | upstream_gene_variant | 0.18 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448726 | p.Leu75Ile | missense_variant | 0.17 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474320 | p.Gly105Asp | missense_variant | 0.22 |
Rv3236c | 3611974 | c.1143A>C | synonymous_variant | 1.0 |
fbiA | 3640529 | c.-14T>C | upstream_gene_variant | 0.13 |
fbiA | 3641453 | p.Arg304Leu | missense_variant | 0.4 |
clpC1 | 4038306 | c.2398delG | frameshift_variant | 0.14 |
clpC1 | 4039458 | p.Thr416Ile | missense_variant | 0.15 |
clpC1 | 4039987 | p.Glu240* | stop_gained | 0.12 |
embC | 4242039 | p.Ala726Glu | missense_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 0.86 |
embA | 4243340 | c.108G>A | synonymous_variant | 0.18 |
embA | 4243530 | p.Thr100Ala | missense_variant | 0.18 |
embA | 4245699 | p.Gly823Trp | missense_variant | 0.18 |
embB | 4247738 | p.Ala409Ser | missense_variant | 0.13 |
embB | 4247746 | c.1233C>A | synonymous_variant | 0.14 |
aftB | 4268442 | p.Arg132His | missense_variant | 0.11 |
aftB | 4268485 | p.Leu118Phe | missense_variant | 0.13 |
aftB | 4268507 | c.330G>A | synonymous_variant | 0.15 |
ubiA | 4269748 | p.Asn29Ser | missense_variant | 0.2 |
ethR | 4326955 | c.-594G>A | upstream_gene_variant | 0.13 |
ethA | 4327656 | c.-183A>C | upstream_gene_variant | 0.18 |
ethR | 4327975 | p.Gln143* | stop_gained | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |