Run ID: ERR4819473
Sample name:
Date: 01-04-2023 16:07:44
Number of reads: 1004713
Percentage reads mapped: 99.46
Strain: lineage4.4
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.4 | Euro-American | S;T | None | 1.0 |
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 | 7979 | c.678G>T | synonymous_variant | 0.14 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491406 | p.Met208Ile | missense_variant | 0.13 |
fgd1 | 491448 | c.666C>G | synonymous_variant | 0.15 |
mshA | 575845 | c.498C>T | synonymous_variant | 0.12 |
mshA | 576337 | c.990G>A | synonymous_variant | 0.13 |
rpoB | 760848 | p.Thr348Ala | missense_variant | 0.12 |
rpoB | 762562 | p.Arg919Gln | missense_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777602 | p.Gln293His | missense_variant | 1.0 |
rpsL | 781372 | c.-188T>C | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303123 | p.Val65Met | missense_variant | 0.12 |
Rv1258c | 1407270 | p.Gly24Ala | missense_variant | 0.1 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673585 | p.Ser49Phe | missense_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154719 | p.Ser465Pro | missense_variant | 0.12 |
PPE35 | 2170558 | p.Ala19Pro | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289734 | c.-493C>T | upstream_gene_variant | 0.12 |
eis | 2714523 | p.His270Gln | missense_variant | 1.0 |
folC | 2746617 | p.Ala328Thr | missense_variant | 0.22 |
Rv2752c | 3065715 | c.477T>C | synonymous_variant | 1.0 |
thyX | 3067228 | p.Glu240* | stop_gained | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.96 |
ald | 3087690 | p.His291Tyr | missense_variant | 0.11 |
Rv3083 | 3448325 | c.-179G>C | upstream_gene_variant | 0.11 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612140 | p.Ala326Val | missense_variant | 0.14 |
Rv3236c | 3612529 | c.588C>T | synonymous_variant | 0.25 |
fbiA | 3641078 | p.Gln179Arg | missense_variant | 0.11 |
fbiB | 3641091 | c.-444C>T | upstream_gene_variant | 0.11 |
fbiB | 3642706 | p.Arg391Leu | missense_variant | 0.11 |
embC | 4241105 | c.1243C>A | synonymous_variant | 0.17 |
embC | 4242408 | p.Pro849Leu | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243324 | p.Val31Ala | missense_variant | 1.0 |
embA | 4244732 | c.1500G>A | synonymous_variant | 1.0 |
embA | 4244931 | p.Pro567Ala | missense_variant | 0.15 |
embA | 4245680 | p.Lys816Asn | missense_variant | 0.11 |
embB | 4247548 | c.1035C>T | synonymous_variant | 1.0 |
aftB | 4268460 | p.Ile126Thr | missense_variant | 1.0 |
aftB | 4268569 | p.Leu90Val | missense_variant | 0.2 |
aftB | 4268928 | c.-92C>T | upstream_gene_variant | 1.0 |
aftB | 4269375 | c.-539G>A | upstream_gene_variant | 1.0 |
whiB6 | 4338289 | p.Gly78Ala | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |