Run ID: ERR4815645
Sample name:
Date: 01-04-2023 13:58:53
Number of reads: 580623
Percentage reads mapped: 99.47
Strain: lineage4.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;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 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490791 | c.9A>G | synonymous_variant | 0.14 |
fgd1 | 490806 | c.27delA | frameshift_variant | 0.17 |
mshA | 575698 | c.351C>T | synonymous_variant | 1.0 |
ccsA | 620594 | p.Phe235Tyr | missense_variant | 0.5 |
rpoB | 761338 | p.Arg511His | missense_variant | 0.18 |
rpoC | 763959 | p.Val197Ala | missense_variant | 0.14 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765919 | c.2550C>T | synonymous_variant | 0.2 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776501 | c.1980A>G | synonymous_variant | 0.29 |
mmpL5 | 777310 | p.Gly391Ser | missense_variant | 1.0 |
mmpL5 | 779283 | c.-803G>A | upstream_gene_variant | 0.22 |
mmpL5 | 779298 | c.-818G>C | upstream_gene_variant | 0.2 |
mmpS5 | 779500 | c.-595G>A | upstream_gene_variant | 0.13 |
mmpS5 | 779560 | c.-655C>T | upstream_gene_variant | 0.25 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406158 | c.1181_1182delCG | frameshift_variant | 0.13 |
Rv1258c | 1406566 | p.Gln259* | stop_gained | 0.18 |
embR | 1416722 | p.Thr209Ile | missense_variant | 0.12 |
atpE | 1461168 | p.Gln42* | stop_gained | 0.2 |
rrs | 1471650 | n.-196T>C | upstream_gene_variant | 0.2 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473766 | n.109G>A | non_coding_transcript_exon_variant | 0.33 |
rpsA | 1834652 | p.Glu371Lys | missense_variant | 0.13 |
rpsA | 1834720 | c.1179C>G | synonymous_variant | 0.18 |
rpsA | 1834888 | c.1347G>T | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101780 | p.Phe421Leu | missense_variant | 0.11 |
ndh | 2102909 | p.Arg45His | missense_variant | 0.22 |
ndh | 2103075 | c.-33T>C | upstream_gene_variant | 0.15 |
PPE35 | 2168822 | c.1791G>C | synonymous_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519210 | p.Val366Ile | missense_variant | 0.11 |
eis | 2714868 | c.465C>G | synonymous_variant | 0.13 |
eis | 2715300 | c.33C>T | synonymous_variant | 0.13 |
folC | 2746591 | c.1008C>T | synonymous_variant | 0.29 |
thyA | 3074302 | p.Tyr57Cys | missense_variant | 0.18 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339576 | c.459G>T | synonymous_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474774 | c.768G>C | synonymous_variant | 1.0 |
whiB7 | 3568418 | c.250_261delGGACGTCCGCGC | conservative_inframe_deletion | 1.0 |
whiB7 | 3568510 | p.Leu57Pro | missense_variant | 0.14 |
alr | 3841505 | c.-85C>T | upstream_gene_variant | 1.0 |
rpoA | 3878247 | c.261G>A | synonymous_variant | 0.13 |
clpC1 | 4038859 | p.Arg616Cys | missense_variant | 0.14 |
clpC1 | 4039964 | c.741C>T | synonymous_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embB | 4249408 | c.2895G>A | synonymous_variant | 1.0 |
aftB | 4267540 | p.Pro433Ser | missense_variant | 0.18 |
ethA | 4326117 | p.Thr453Ser | missense_variant | 1.0 |
ethA | 4327263 | p.Gly71Arg | missense_variant | 0.33 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |