Run ID: SRR6046308
Sample name:
Date: 04-04-2023 12:14:54
Number of reads: 649769
Percentage reads mapped: 99.66
Strain: lineage4.9
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 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
fgd1 | 491777 | p.Leu332Ser | missense_variant | 0.11 |
mshA | 576751 | p.Lys468Asn | missense_variant | 0.22 |
rpoB | 760038 | p.Gly78Ser | missense_variant | 0.14 |
rpoB | 763231 | p.Arg1142His | missense_variant | 0.1 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 778072 | p.Thr137Ser | missense_variant | 0.1 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800644 | c.-165G>A | upstream_gene_variant | 0.14 |
fbiC | 1303825 | p.Glu299* | stop_gained | 0.15 |
fbiC | 1304986 | p.Pro686Ser | missense_variant | 0.33 |
Rv1258c | 1407154 | p.Gly63Ser | missense_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473043 | n.1202delC | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1834531 | p.His330Gln | missense_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102540 | p.Ala168Gly | missense_variant | 0.38 |
katG | 2154410 | p.Thr568Ala | missense_variant | 0.12 |
PPE35 | 2168026 | p.Ala863Thr | missense_variant | 0.21 |
PPE35 | 2168243 | c.2370C>T | synonymous_variant | 0.1 |
PPE35 | 2169132 | p.Ala494Val | missense_variant | 0.12 |
PPE35 | 2169269 | c.1344A>G | synonymous_variant | 0.2 |
PPE35 | 2169272 | c.1341C>G | synonymous_variant | 0.2 |
Rv1979c | 2222441 | p.Ala242Thr | missense_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714569 | p.Ala255Gly | missense_variant | 0.18 |
eis | 2714670 | c.663C>T | synonymous_variant | 1.0 |
eis | 2714933 | p.Ala134Ser | missense_variant | 0.11 |
eis | 2715167 | p.Ser56Thr | missense_variant | 0.13 |
ahpC | 2726334 | c.142C>A | synonymous_variant | 0.11 |
folC | 2746545 | p.Ala352Ser | missense_variant | 0.17 |
ribD | 2986726 | c.-113G>T | upstream_gene_variant | 0.14 |
ribD | 2987525 | c.687G>A | synonymous_variant | 0.17 |
thyA | 3074654 | c.-183T>G | upstream_gene_variant | 0.23 |
ald | 3086981 | c.162C>T | synonymous_variant | 0.12 |
fbiD | 3339273 | c.156T>G | synonymous_variant | 0.29 |
fbiD | 3339688 | p.Thr191Pro | missense_variant | 0.4 |
Rv3236c | 3612494 | p.Arg208Leu | missense_variant | 0.22 |
Rv3236c | 3612835 | c.282T>G | synonymous_variant | 0.25 |
fbiA | 3640562 | p.Ala7Val | missense_variant | 0.13 |
fbiB | 3641758 | p.Arg75His | missense_variant | 0.11 |
rpoA | 3877536 | c.972C>T | synonymous_variant | 1.0 |
aftB | 4268164 | p.Gln225* | stop_gained | 0.12 |
ethR | 4327884 | p.Glu112Asp | missense_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408405 | c.-203G>T | upstream_gene_variant | 0.15 |