Run ID: SRR21677877
Sample name:
Date: 04-04-2023 02:49:11
Number of reads: 89223
Percentage reads mapped: 96.15
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 | 8103 | p.Ser268Thr | missense_variant | 0.29 |
gyrA | 8984 | p.Cys561* | stop_gained | 0.22 |
fgd1 | 491196 | c.414A>T | synonymous_variant | 1.0 |
mshA | 576255 | p.Gly303Val | missense_variant | 0.5 |
mshA | 576351 | p.Asp335Ala | missense_variant | 0.5 |
rpoB | 759762 | c.-45T>C | upstream_gene_variant | 0.5 |
rpoB | 761018 | p.Glu404Asp | missense_variant | 0.67 |
rpoB | 761897 | c.2091C>A | synonymous_variant | 0.5 |
rpoC | 763655 | p.Glu96Gln | missense_variant | 1.0 |
rpoC | 765256 | c.1887G>T | synonymous_variant | 0.5 |
rpoC | 766481 | p.Arg1038Trp | missense_variant | 0.5 |
mmpL5 | 775825 | c.2656C>T | synonymous_variant | 0.67 |
mmpL5 | 776834 | c.1647C>G | synonymous_variant | 0.67 |
mmpL5 | 778615 | c.-135G>T | upstream_gene_variant | 0.25 |
mmpR5 | 779180 | p.Ser64Ile | missense_variant | 0.5 |
fbiC | 1303823 | p.Lys298Arg | missense_variant | 0.25 |
Rv1258c | 1406481 | p.Arg287Leu | missense_variant | 0.2 |
atpE | 1460926 | c.-119C>A | upstream_gene_variant | 0.33 |
rrs | 1472056 | n.211G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473671 | n.14A>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473725 | n.68G>A | non_coding_transcript_exon_variant | 0.67 |
fabG1 | 1673569 | p.Val44Ile | missense_variant | 0.67 |
rpsA | 1833566 | p.Pro9Ser | missense_variant | 0.25 |
rpsA | 1834496 | p.Gly319Arg | missense_variant | 0.4 |
tlyA | 1917926 | c.-14G>T | upstream_gene_variant | 0.33 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918230 | c.291C>A | synonymous_variant | 0.33 |
ndh | 2103024 | p.Pro7Thr | missense_variant | 0.29 |
PPE35 | 2168297 | c.2316G>T | synonymous_variant | 0.18 |
PPE35 | 2168378 | c.2235C>T | synonymous_variant | 0.25 |
PPE35 | 2168746 | p.Gly623Arg | missense_variant | 0.67 |
PPE35 | 2169002 | c.1610delT | frameshift_variant | 0.5 |
PPE35 | 2169050 | c.1563C>T | synonymous_variant | 1.0 |
PPE35 | 2169768 | p.Ala282Gly | missense_variant | 0.29 |
Rv1979c | 2223364 | c.-200G>A | upstream_gene_variant | 0.5 |
ahpC | 2726749 | p.Asp186Gly | missense_variant | 1.0 |
folC | 2746422 | p.Ala393Ser | missense_variant | 0.67 |
Rv2752c | 3065694 | c.498G>A | synonymous_variant | 0.33 |
ald | 3086638 | c.-182G>A | upstream_gene_variant | 0.25 |
ald | 3087426 | p.Lys203Glu | missense_variant | 0.29 |
ald | 3087470 | c.651T>A | synonymous_variant | 0.25 |
fbiD | 3339137 | p.Asp7Gly | missense_variant | 0.4 |
fprA | 3473979 | c.-28C>A | upstream_gene_variant | 0.2 |
fbiB | 3640719 | c.-816C>T | upstream_gene_variant | 0.33 |
alr | 3840688 | c.731_732dupCC | frameshift_variant | 0.5 |
alr | 3841240 | p.Leu61Met | missense_variant | 0.33 |
ddn | 3987170 | c.327T>C | synonymous_variant | 0.5 |
clpC1 | 4038691 | p.Asp672His | missense_variant | 0.5 |
embC | 4240701 | p.Val280Ala | missense_variant | 1.0 |
embC | 4242089 | p.Ala743Ser | missense_variant | 0.5 |
embA | 4244475 | p.Ala415Pro | missense_variant | 0.5 |
embA | 4244996 | c.1764C>G | synonymous_variant | 0.33 |
embB | 4249300 | p.Trp929* | stop_gained | 0.4 |
ethA | 4326840 | p.Ile212Val | missense_variant | 0.67 |
whiB6 | 4338275 | p.Glu83Lys | missense_variant | 0.22 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407556 | p.Ala216Glu | missense_variant | 0.25 |