Run ID: ERR3994098
Sample name:
Date: 01-04-2023 03:42:22
Number of reads: 2453114
Percentage reads mapped: 99.97
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 | 0.22 |
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 | 8727 | p.Arg476Ser | missense_variant | 0.18 |
gyrA | 8838 | p.Arg513Cys | missense_variant | 0.67 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoB | 762408 | p.Ala868Thr | missense_variant | 0.5 |
rpoB | 763173 | p.Gln1123* | stop_gained | 0.5 |
rpoC | 763846 | c.479delA | frameshift_variant | 0.4 |
rpoC | 763934 | p.Ala189Thr | missense_variant | 0.5 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775811 | c.2669delT | frameshift_variant | 0.5 |
mmpL5 | 776260 | p.Ala741Thr | missense_variant | 0.33 |
mmpL5 | 777395 | c.1086C>T | synonymous_variant | 0.4 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 0.8 |
rplC | 800817 | c.9A>C | synonymous_variant | 1.0 |
rplC | 801223 | p.His139Tyr | missense_variant | 0.67 |
fbiC | 1304710 | p.Ala594Thr | missense_variant | 0.2 |
embR | 1416304 | c.1044C>T | synonymous_variant | 1.0 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101761 | p.Gln428* | stop_gained | 0.29 |
ndh | 2103240 | c.-198C>T | upstream_gene_variant | 0.33 |
PPE35 | 2167738 | c.2875C>T | synonymous_variant | 0.67 |
PPE35 | 2168463 | p.Pro717Leu | missense_variant | 0.56 |
Rv1979c | 2221913 | p.Pro418Thr | missense_variant | 0.4 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 0.83 |
pncA | 2289724 | c.-483C>G | upstream_gene_variant | 0.18 |
eis | 2714494 | p.Thr280Asn | missense_variant | 0.67 |
eis | 2715147 | c.186G>T | synonymous_variant | 0.18 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612395 | p.Ala241Val | missense_variant | 0.17 |
Rv3236c | 3612515 | p.Arg201His | missense_variant | 0.67 |
ddn | 3986702 | c.-142G>A | upstream_gene_variant | 0.33 |
embC | 4241415 | p.Arg518Leu | missense_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 0.75 |
embA | 4243388 | p.Asp52Glu | missense_variant | 0.25 |
embA | 4243917 | c.689dupG | frameshift_variant | 0.33 |
embB | 4247423 | p.Leu304Met | missense_variant | 0.4 |
embB | 4248909 | p.Ala799Val | missense_variant | 0.67 |
embB | 4249408 | c.2895G>A | synonymous_variant | 1.0 |
embB | 4249781 | p.Ser1090Pro | missense_variant | 0.25 |
embB | 4249787 | p.Gly1092Ser | missense_variant | 0.25 |
aftB | 4267406 | p.Lys477His | missense_variant | 0.33 |
aftB | 4267411 | p.Gly476Cys | missense_variant | 0.33 |
aftB | 4267413 | p.Gly475Ala | missense_variant | 0.33 |
aftB | 4267912 | p.Pro309Ser | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408031 | p.Leu58Phe | missense_variant | 1.0 |