Run ID: ERR4820947
Sample name:
Date: 01-04-2023 16:58:28
Number of reads: 163428
Percentage reads mapped: 99.24
Strain: lineage4
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | 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 | 490863 | c.81C>A | synonymous_variant | 0.22 |
fgd1 | 490869 | c.87C>T | synonymous_variant | 0.22 |
fgd1 | 490890 | c.108C>G | synonymous_variant | 0.17 |
fgd1 | 490896 | c.114C>T | synonymous_variant | 0.17 |
mshA | 575357 | p.Val4Met | missense_variant | 1.0 |
rpoB | 760384 | p.Leu193Pro | missense_variant | 0.67 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776526 | p.Met652Thr | missense_variant | 0.29 |
mmpL5 | 777731 | c.750C>G | synonymous_variant | 0.67 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303307 | p.Asp126Gly | missense_variant | 0.5 |
fbiC | 1304159 | p.Val410Gly | missense_variant | 0.4 |
fbiC | 1304925 | c.1995G>A | synonymous_variant | 1.0 |
Rv1258c | 1406700 | p.Glu214Gly | missense_variant | 0.22 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473288 | n.1443C>A | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673684 | p.Val82Asp | missense_variant | 0.33 |
rpsA | 1834118 | p.Gln193* | stop_gained | 0.29 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102852 | p.Ser64Tyr | missense_variant | 0.22 |
katG | 2156521 | c.-410C>A | upstream_gene_variant | 0.25 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
folC | 2747265 | p.Gly112Ser | missense_variant | 0.67 |
ald | 3086997 | p.Thr60Gly | missense_variant | 0.4 |
fprA | 3474368 | p.Gly121Asp | missense_variant | 1.0 |
fbiA | 3640443 | c.-100A>G | upstream_gene_variant | 0.5 |
rpoA | 3878142 | c.366C>T | synonymous_variant | 0.33 |
clpC1 | 4039645 | p.His354Asp | missense_variant | 1.0 |
embC | 4242749 | p.Pro963Thr | missense_variant | 0.22 |
embC | 4243104 | p.Thr1081Asn | missense_variant | 0.67 |
embA | 4243159 | c.-74C>A | upstream_gene_variant | 0.4 |
embB | 4249562 | p.Asp1017Tyr | missense_variant | 0.25 |
aftB | 4267010 | c.1827A>G | synonymous_variant | 0.33 |
ubiA | 4269238 | p.Ala199Val | missense_variant | 0.4 |
whiB6 | 4338198 | p.Asp108Glu | missense_variant | 0.25 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338705 | c.-184A>T | upstream_gene_variant | 0.29 |
gid | 4408370 | c.-168G>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448497 | c.-6_*1408del | transcript_ablation | 1.0 |