Run ID: SRR6785547
Sample name:
Date: 04-04-2023 16:03:06
Number of reads: 1162669
Percentage reads mapped: 99.37
Strain: lineage4.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.2 | Euro-American | H;T;LAM | None | 1.0 |
lineage4.2.1 | Euro-American (TUR) | H3;H4 | None | 0.99 |
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 | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491247 | c.465C>T | synonymous_variant | 1.0 |
rpoB | 761152 | p.Leu449Gln | missense_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 778312 | p.Gly57Arg | missense_variant | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304944 | c.2014C>T | synonymous_variant | 0.14 |
Rv1258c | 1407518 | c.-178C>G | upstream_gene_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475299 | n.1642G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475910 | n.2253A>T | non_coding_transcript_exon_variant | 0.29 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154970 | p.Asp381Ala | missense_variant | 0.12 |
PPE35 | 2170308 | p.Leu102Ala | missense_variant | 1.0 |
PPE35 | 2170313 | c.300G>C | synonymous_variant | 1.0 |
PPE35 | 2170392 | p.Gly74Ala | missense_variant | 0.11 |
PPE35 | 2170400 | c.213G>C | synonymous_variant | 0.12 |
PPE35 | 2170406 | c.207A>G | synonymous_variant | 0.14 |
PPE35 | 2170412 | c.201G>C | synonymous_variant | 0.12 |
PPE35 | 2170415 | c.198A>G | synonymous_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519140 | c.1026G>C | synonymous_variant | 0.13 |
kasA | 2519143 | c.1029G>C | synonymous_variant | 0.13 |
ribD | 2986910 | c.72C>A | synonymous_variant | 1.0 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086987 | p.Gln56His | missense_variant | 0.13 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612936 | p.Gly61Ser | missense_variant | 0.2 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.16 |
rpoA | 3878490 | c.18C>G | synonymous_variant | 0.32 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.33 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.38 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.6 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.6 |
embB | 4247512 | c.999T>C | synonymous_variant | 0.14 |
embB | 4247516 | p.Asn335Asp | missense_variant | 0.12 |
embB | 4249594 | c.3081G>A | synonymous_variant | 1.0 |
ubiA | 4269254 | p.Ala194Ser | missense_variant | 0.17 |
ethR | 4326961 | c.-588G>C | upstream_gene_variant | 0.16 |
ethR | 4326964 | c.-585G>A | upstream_gene_variant | 0.16 |
ethR | 4326970 | c.-579G>T | upstream_gene_variant | 0.17 |
ethR | 4326982 | c.-567C>G | upstream_gene_variant | 0.11 |
ethA | 4328376 | c.-903G>C | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
PPE35 | 2167034 | c.336_*614del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |