Run ID: SRR4035804
Sample name:
Date: 04-04-2023 07:18:31
Number of reads: 1363439
Percentage reads mapped: 99.45
Strain: lineage4.1.2
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 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6186 | p.His316Arg | missense_variant | 0.1 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8061 | p.Arg254Cys | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575849 | p.Arg168Cys | missense_variant | 0.12 |
ccsA | 620450 | p.Leu187Pro | missense_variant | 0.12 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 760421 | c.617_618delTC | frameshift_variant | 0.12 |
rpoB | 761191 | p.Ala462Gly | missense_variant | 0.12 |
rpoC | 764263 | c.894G>A | synonymous_variant | 1.0 |
rpoC | 764333 | p.Pro322Ala | missense_variant | 0.12 |
rpoC | 764344 | c.975C>T | synonymous_variant | 0.12 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777320 | c.1161C>G | synonymous_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801131 | p.Asp108Gly | missense_variant | 0.12 |
fbiC | 1305006 | c.2076A>G | synonymous_variant | 0.12 |
fbiC | 1305089 | p.Val720Ala | missense_variant | 0.12 |
Rv1258c | 1406147 | c.1194C>A | synonymous_variant | 0.2 |
Rv1258c | 1406524 | p.Val273Leu | missense_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918500 | c.561G>A | synonymous_variant | 0.14 |
tlyA | 1918584 | c.645A>G | synonymous_variant | 0.12 |
katG | 2154337 | p.Asp592Val | missense_variant | 0.12 |
PPE35 | 2168094 | p.Asn840Ser | missense_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2518848 | p.Leu245Pro | missense_variant | 0.12 |
ribD | 2987245 | p.Thr136Ile | missense_variant | 0.13 |
thyX | 3067500 | p.Lys149Met | missense_variant | 0.15 |
thyX | 3067507 | c.439C>T | synonymous_variant | 0.15 |
thyA | 3074602 | c.-131G>A | upstream_gene_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.98 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3611974 | c.1143A>C | synonymous_variant | 1.0 |
alr | 3841072 | p.Gly117Ser | missense_variant | 0.13 |
embC | 4239975 | p.Leu38Pro | missense_variant | 0.11 |
embC | 4239995 | p.Ile45Phe | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4244857 | p.Ala542Val | missense_variant | 0.13 |
embA | 4244911 | p.Leu560Pro | missense_variant | 0.11 |
embA | 4245270 | c.2038C>A | synonymous_variant | 0.14 |
embA | 4245331 | p.Gly700Asp | missense_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408360 | c.-159delA | upstream_gene_variant | 0.12 |