Run ID: ERR4819623
Sample name:
Date: 01-04-2023 16:12:50
Number of reads: 2236
Percentage reads mapped: 19.22
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 | 8966 | c.1665C>G | synonymous_variant | 1.0 |
gyrA | 8967 | p.Ala556Arg | missense_variant | 1.0 |
gyrA | 8981 | c.1680G>C | synonymous_variant | 1.0 |
rpoB | 760611 | c.805T>C | synonymous_variant | 1.0 |
rpoB | 760634 | c.828T>C | synonymous_variant | 1.0 |
rpoB | 760646 | c.840C>G | synonymous_variant | 1.0 |
rpoB | 760655 | c.849A>G | synonymous_variant | 1.0 |
rpoB | 760661 | c.855A>G | synonymous_variant | 1.0 |
rpoB | 760670 | c.864G>C | synonymous_variant | 1.0 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 1.0 |
rpoB | 761165 | c.1359G>T | synonymous_variant | 1.0 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 1.0 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 1.0 |
rpoB | 761183 | c.1377T>G | synonymous_variant | 1.0 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 1.0 |
rpoB | 761192 | c.1386C>G | synonymous_variant | 1.0 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 1.0 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 1.0 |
rpoC | 764923 | c.1554A>G | synonymous_variant | 1.0 |
rpoC | 764932 | c.1563C>A | synonymous_variant | 1.0 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 1.0 |
rpoC | 764962 | c.1593G>C | synonymous_variant | 1.0 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 1.0 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpsL | 781631 | c.72G>C | synonymous_variant | 1.0 |
rpsL | 781655 | c.96T>C | synonymous_variant | 1.0 |
rpsL | 781658 | c.99A>G | synonymous_variant | 1.0 |
rpsL | 781682 | c.123T>C | synonymous_variant | 1.0 |
rpsL | 781709 | c.150G>C | synonymous_variant | 1.0 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 1.0 |
inhA | 1674762 | c.561T>C | synonymous_variant | 1.0 |
inhA | 1674765 | c.564C>T | synonymous_variant | 1.0 |
inhA | 1674774 | c.573A>C | synonymous_variant | 1.0 |
inhA | 1674780 | c.579T>G | synonymous_variant | 1.0 |
inhA | 1674795 | c.594G>C | synonymous_variant | 1.0 |
Rv2752c | 3066054 | c.138T>G | synonymous_variant | 1.0 |
Rv2752c | 3066066 | p.Ile42Val | missense_variant | 1.0 |
Rv2752c | 3066075 | c.117A>T | synonymous_variant | 1.0 |
Rv2752c | 3066087 | c.105A>G | synonymous_variant | 1.0 |
Rv2752c | 3066090 | p.Phe34Leu | missense_variant | 1.0 |
Rv2752c | 3066093 | c.99T>C | synonymous_variant | 1.0 |