Run ID: SRR13837504
Sample name:
Date: 03-04-2023 09:11:58
Number of reads: 589495
Percentage reads mapped: 95.3
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 | 6667 | p.Gln476His | missense_variant | 1.0 |
gyrA | 7289 | c.-13_-12insT | upstream_gene_variant | 1.0 |
rpoB | 760214 | p.Asn136Lys | missense_variant | 1.0 |
fbiC | 1304005 | p.Pro359Ser | missense_variant | 1.0 |
rrs | 1471943 | n.98T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472075 | n.230A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473066 | n.1221A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473370 | n.1525T>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.12 |
fabG1 | 1673813 | p.Arg125Leu | missense_variant | 1.0 |
inhA | 1674784 | p.Arg195Gly | missense_variant | 1.0 |
rpsA | 1833664 | c.123C>G | synonymous_variant | 0.1 |
rpsA | 1833700 | c.159C>T | synonymous_variant | 0.14 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.11 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 0.16 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.12 |
rpsA | 1834375 | c.834G>C | synonymous_variant | 0.12 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.15 |
rpsA | 1834411 | c.870T>G | synonymous_variant | 0.19 |
rpsA | 1834414 | c.873C>T | synonymous_variant | 0.18 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.17 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.17 |
rpsA | 1834429 | c.888C>T | synonymous_variant | 0.17 |
rpsA | 1834438 | c.897C>T | synonymous_variant | 0.15 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.16 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.17 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.22 |
rpsA | 1834477 | c.936C>T | synonymous_variant | 0.18 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.15 |
ndh | 2101793 | p.Trp417* | stop_gained | 1.0 |
PPE35 | 2169624 | p.Gly330Asp | missense_variant | 1.0 |
kasA | 2519223 | p.Thr370Ile | missense_variant | 1.0 |
ahpC | 2726213 | c.21C>T | synonymous_variant | 1.0 |
ribD | 2987016 | p.Gly60Arg | missense_variant | 1.0 |
Rv2752c | 3065644 | p.Thr183Ser | missense_variant | 1.0 |
thyA | 3074595 | c.-124C>A | upstream_gene_variant | 1.0 |
alr | 3841581 | c.-161T>A | upstream_gene_variant | 1.0 |
rpoA | 3878160 | c.348C>G | synonymous_variant | 0.1 |
rpoA | 3878169 | c.339G>C | synonymous_variant | 0.11 |
rpoA | 3878184 | c.324C>T | synonymous_variant | 0.14 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.14 |
rpoA | 3878196 | p.Glu104Ala | missense_variant | 0.14 |
rpoA | 3878205 | c.303T>C | synonymous_variant | 0.19 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.15 |
rpoA | 3878259 | c.249G>C | synonymous_variant | 0.1 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.14 |
rpoA | 3878283 | p.Glu75Asp | missense_variant | 0.12 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.12 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.1 |
clpC1 | 4038923 | c.1782A>T | synonymous_variant | 0.12 |
embC | 4242810 | p.Leu983Gln | missense_variant | 1.0 |
embB | 4246553 | p.Arg14Trp | missense_variant | 1.0 |
embB | 4248920 | p.Val803Met | missense_variant | 1.0 |
embB | 4249551 | p.Arg1013Leu | missense_variant | 1.0 |
ethA | 4326296 | p.Leu393Gln | missense_variant | 1.0 |