Run ID: ERR245650
Sample name:
Date: 31-03-2023 18:12:12
Number of reads: 13074508
Percentage reads mapped: 99.56
Strain: lineage4.9.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
lineage4.9.1 | Euro-American (H37Rv-like) | T1 | 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 | 7493 | c.192C>T | synonymous_variant | 0.35 |
gyrA | 8978 | c.1677C>T | synonymous_variant | 1.0 |
mshA | 575309 | c.-39C>G | upstream_gene_variant | 0.29 |
mshA | 576751 | p.Lys468Asn | missense_variant | 0.24 |
ccsA | 620407 | p.Pro173Ala | missense_variant | 0.22 |
rpoB | 762249 | p.Leu815Val | missense_variant | 0.17 |
rpoC | 762836 | c.-534C>G | upstream_gene_variant | 0.24 |
rpoC | 764725 | p.Phe452Leu | missense_variant | 0.19 |
rpoC | 767305 | p.Tyr1312* | stop_gained | 0.16 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
embR | 1417136 | p.Ser71Ile | missense_variant | 0.17 |
atpE | 1461019 | c.-26C>A | upstream_gene_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475363 | n.1706C>A | non_coding_transcript_exon_variant | 0.21 |
inhA | 1674952 | p.Pro251Ala | missense_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102540 | p.Ala168Gly | missense_variant | 0.19 |
ndh | 2102891 | p.Phe51Ser | missense_variant | 0.18 |
PPE35 | 2169379 | p.Phe412Val | missense_variant | 0.21 |
PPE35 | 2169866 | c.747G>C | synonymous_variant | 0.23 |
Rv1979c | 2223145 | p.Arg7Lys | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289138 | p.Leu35Arg | missense_variant | 1.0 |
pncA | 2289448 | c.-207G>A | upstream_gene_variant | 1.0 |
eis | 2714366 | p.Val323Leu | missense_variant | 0.19 |
eis | 2715586 | c.-254G>C | upstream_gene_variant | 0.47 |
folC | 2746186 | c.1413G>C | synonymous_variant | 0.24 |
pepQ | 2859381 | c.1038C>G | synonymous_variant | 0.17 |
Rv2752c | 3064741 | p.Gly484Ala | missense_variant | 0.27 |
Rv2752c | 3067191 | c.-1000G>A | upstream_gene_variant | 1.0 |
thyA | 3073817 | p.Gln219Glu | missense_variant | 0.2 |
fbiD | 3339385 | p.Asp90Asn | missense_variant | 1.0 |
Rv3236c | 3611982 | p.Ala379Pro | missense_variant | 0.33 |
fbiB | 3641955 | p.Gly141Arg | missense_variant | 0.32 |
fbiB | 3642734 | c.1200G>C | synonymous_variant | 0.22 |
ddn | 3987013 | p.Gly57Ala | missense_variant | 0.21 |
clpC1 | 4038857 | c.1848C>A | synonymous_variant | 0.19 |
clpC1 | 4039932 | p.Gly258Val | missense_variant | 0.31 |
embC | 4241056 | c.1194C>G | synonymous_variant | 0.26 |
embC | 4242476 | p.Pro872Ala | missense_variant | 0.23 |
embC | 4242822 | p.Val987Gly | missense_variant | 0.39 |
embC | 4242827 | p.Leu989Val | missense_variant | 0.24 |
embA | 4244375 | c.1143C>G | synonymous_variant | 0.34 |
embB | 4247041 | c.528C>T | synonymous_variant | 0.23 |
ubiA | 4269529 | p.Ala102Gly | missense_variant | 0.19 |
ethA | 4327672 | c.-199G>A | upstream_gene_variant | 0.2 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |