Run ID: SRR5341248
Sample name:
Date: 04-04-2023 10:10:26
Number of reads: 955559
Percentage reads mapped: 99.57
Strain: lineage4.4
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.4 | Euro-American | S;T | None | 1.0 |
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 |
ccsA | 620018 | p.Gly43Val | missense_variant | 0.14 |
rpoB | 761152 | p.Leu449Gln | missense_variant | 0.19 |
rpoC | 767316 | p.Arg1316His | missense_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
atpE | 1461042 | c.-3G>T | upstream_gene_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474817 | n.1160G>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475168 | n.1511G>C | non_coding_transcript_exon_variant | 0.13 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.11 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.12 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.12 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.26 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.88 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.88 |
PPE35 | 2170558 | p.Ala19Pro | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518606 | c.492G>C | synonymous_variant | 0.22 |
kasA | 2518609 | p.Met165Ile | missense_variant | 0.15 |
eis | 2714523 | p.His270Gln | missense_variant | 1.0 |
Rv2752c | 3064677 | p.Glu505Asp | missense_variant | 0.2 |
Rv2752c | 3065715 | c.477T>C | synonymous_variant | 1.0 |
Rv2752c | 3065797 | c.394delC | frameshift_variant | 0.15 |
thyX | 3067340 | c.606G>A | synonymous_variant | 0.12 |
thyX | 3068027 | c.-82C>T | upstream_gene_variant | 0.12 |
thyA | 3074648 | c.-177T>G | upstream_gene_variant | 0.25 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339741 | c.624G>T | synonymous_variant | 0.12 |
fbiD | 3339744 | c.627A>C | synonymous_variant | 0.11 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568525 | p.Cys52Tyr | missense_variant | 1.0 |
fbiB | 3642154 | p.Gly207Asp | missense_variant | 0.13 |
alr | 3841161 | p.Ala87Val | missense_variant | 0.12 |
embC | 4240501 | p.Ser213Arg | missense_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243324 | p.Val31Ala | missense_variant | 1.0 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.12 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.15 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.2 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.21 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.1 |
embB | 4247548 | c.1035C>T | synonymous_variant | 1.0 |
aftB | 4268928 | c.-92C>T | upstream_gene_variant | 1.0 |
aftB | 4269375 | c.-539G>A | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407606 | c.597C>T | synonymous_variant | 1.0 |
gid | 4408195 | p.Pro3Gln | missense_variant | 0.13 |