Run ID: SRR13837473
Sample name:
Date: 03-04-2023 09:11:13
Number of reads: 891320
Percentage reads mapped: 97.08
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 |
---|---|---|---|---|
gyrB | 5192 | c.-48C>G | upstream_gene_variant | 1.0 |
gyrA | 9658 | c.2357_2358insT | frameshift_variant | 1.0 |
fgd1 | 490779 | c.-4A>T | upstream_gene_variant | 1.0 |
rpoB | 760041 | p.Gly79Arg | missense_variant | 1.0 |
rpoB | 760370 | c.564C>G | synonymous_variant | 0.13 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.14 |
rpoB | 760380 | p.Thr192Leu | missense_variant | 0.15 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.12 |
rpoB | 760412 | c.606C>G | synonymous_variant | 0.13 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.13 |
rpoB | 760652 | c.846C>A | synonymous_variant | 1.0 |
rpoB | 761122 | p.Pro439Arg | missense_variant | 0.92 |
mmpL5 | 775929 | p.Asn851Ile | missense_variant | 1.0 |
mmpS5 | 778941 | c.-36A>G | upstream_gene_variant | 1.0 |
embR | 1417376 | c.-29T>C | upstream_gene_variant | 1.0 |
rrl | 1473740 | n.83G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474574 | n.917A>T | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.12 |
rpsA | 1833940 | c.399C>G | synonymous_variant | 0.17 |
rpsA | 1833971 | c.430C>T | synonymous_variant | 0.15 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.14 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.12 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.14 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.14 |
rpsA | 1834610 | p.Arg357Gly | missense_variant | 1.0 |
ndh | 2101828 | c.1215C>T | synonymous_variant | 1.0 |
PPE35 | 2168706 | p.Ser636Phe | missense_variant | 1.0 |
pncA | 2289887 | c.-646A>C | upstream_gene_variant | 1.0 |
kasA | 2518783 | c.669T>C | synonymous_variant | 0.11 |
kasA | 2518789 | c.675G>C | synonymous_variant | 0.11 |
folC | 2746838 | p.Ala254Glu | missense_variant | 1.0 |
ribD | 2987500 | p.Gly221Asp | missense_variant | 1.0 |
thyX | 3068082 | c.-137T>C | upstream_gene_variant | 1.0 |
fbiD | 3338954 | c.-164A>G | upstream_gene_variant | 1.0 |
fbiD | 3339235 | p.Leu40Val | missense_variant | 1.0 |
fbiD | 3339406 | p.Thr97Ala | missense_variant | 1.0 |
Rv3083 | 3448625 | p.Leu41Gln | missense_variant | 0.97 |
fbiB | 3642247 | p.Asn238Thr | missense_variant | 1.0 |
fbiB | 3642283 | p.Glu250Ala | missense_variant | 1.0 |
clpC1 | 4039483 | c.1221_1222insC | frameshift_variant | 1.0 |
embC | 4240911 | p.Ala350Val | missense_variant | 0.12 |
embC | 4240921 | c.1059C>G | synonymous_variant | 0.12 |
embC | 4240924 | c.1062C>G | synonymous_variant | 0.12 |
embA | 4243843 | c.613dupG | frameshift_variant | 1.0 |
embA | 4244833 | p.Val534Ala | missense_variant | 1.0 |
embA | 4245735 | p.Ala835Ser | missense_variant | 1.0 |
embB | 4248208 | c.1695C>T | synonymous_variant | 0.14 |
embB | 4248220 | c.1707A>C | synonymous_variant | 0.13 |
aftB | 4267994 | p.Met281Ile | missense_variant | 1.0 |