Run ID: SRR3675570
Sample name:
Date: 04-04-2023 05:34:08
Number of reads: 1204
Percentage reads mapped: 23.69
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 | 7670 | c.369A>G | synonymous_variant | 1.0 |
gyrA | 7676 | c.375G>C | synonymous_variant | 1.0 |
gyrA | 7683 | c.382A>C | synonymous_variant | 1.0 |
gyrA | 7694 | c.393A>G | synonymous_variant | 1.0 |
gyrA | 7697 | c.396C>G | synonymous_variant | 1.0 |
gyrA | 7710 | c.409T>C | synonymous_variant | 1.0 |
gyrA | 7715 | c.414G>C | synonymous_variant | 1.0 |
gyrA | 7728 | c.427_429delAGGinsCGC | synonymous_variant | 1.0 |
gyrA | 7760 | c.459C>T | synonymous_variant | 1.0 |
gyrA | 7763 | c.462T>C | synonymous_variant | 1.0 |
gyrA | 7799 | c.498A>G | synonymous_variant | 1.0 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 1.0 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 1.0 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 1.0 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 1.0 |
rpoB | 762114 | p.Ile770Val | missense_variant | 1.0 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 1.0 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 1.0 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 1.0 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 1.0 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 1.0 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 1.0 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 1.0 |
rpoB | 762218 | c.2412T>G | synonymous_variant | 1.0 |
rpsL | 781793 | c.234G>C | synonymous_variant | 1.0 |
rpsL | 781832 | c.273T>C | synonymous_variant | 1.0 |
rpsL | 781841 | c.282C>G | synonymous_variant | 1.0 |
rpsL | 781859 | c.300T>C | synonymous_variant | 1.0 |
rpsL | 781868 | c.309T>C | synonymous_variant | 1.0 |
rpsL | 781871 | c.312G>C | synonymous_variant | 1.0 |
rpsL | 781892 | c.333A>G | synonymous_variant | 1.0 |
rpsL | 781898 | c.339A>T | synonymous_variant | 1.0 |
rpsL | 781916 | c.357T>C | synonymous_variant | 1.0 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 1.0 |
thyX | 3067682 | c.264G>C | synonymous_variant | 1.0 |
thyX | 3067685 | c.261A>G | synonymous_variant | 1.0 |
thyX | 3067688 | c.258G>C | synonymous_variant | 1.0 |
thyX | 3067694 | c.252G>C | synonymous_variant | 1.0 |
thyX | 3067718 | c.228C>G | synonymous_variant | 1.0 |
thyX | 3067721 | c.225T>C | synonymous_variant | 1.0 |
thyX | 3067724 | c.222G>A | synonymous_variant | 1.0 |
thyX | 3067727 | c.219A>C | synonymous_variant | 1.0 |
thyX | 3067739 | c.207T>C | synonymous_variant | 1.0 |
thyX | 3067742 | c.204A>C | synonymous_variant | 1.0 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 1.0 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 1.0 |
rpoA | 3878067 | c.441C>G | synonymous_variant | 1.0 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 1.0 |
rpoA | 3878082 | c.426T>C | synonymous_variant | 1.0 |
rpoA | 3878094 | c.414C>G | synonymous_variant | 1.0 |
rpoA | 3878100 | c.408C>G | synonymous_variant | 1.0 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 1.0 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 1.0 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 1.0 |
rpoA | 3878141 | p.Met123Leu | missense_variant | 1.0 |
rpoA | 3878142 | p.Gly122Glu | missense_variant | 1.0 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 1.0 |
rpoA | 3878284 | p.Glu75Ala | missense_variant | 1.0 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 1.0 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 1.0 |
rpoA | 3878304 | c.204G>C | synonymous_variant | 1.0 |