Run ID: SRR10809127
Sample name:
Date: 02-04-2023 19:24:21
Number of reads: 700791
Percentage reads mapped: 99.47
Strain: lineage4.2
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 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6415 | c.-887G>T | upstream_gene_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8563 | p.Leu421Pro | missense_variant | 0.1 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491114 | p.Leu111Pro | missense_variant | 0.18 |
fgd1 | 491310 | c.528C>G | synonymous_variant | 0.22 |
mshA | 576077 | c.730C>T | synonymous_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.18 |
rpoB | 759638 | c.-169T>A | upstream_gene_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304826 | c.1900delT | frameshift_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.25 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.11 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.11 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.11 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.35 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103077 | c.-35G>A | upstream_gene_variant | 0.11 |
PPE35 | 2168175 | p.Gln813Arg | missense_variant | 0.15 |
PPE35 | 2169198 | p.Val472Ala | missense_variant | 0.18 |
PPE35 | 2169442 | p.Ala391Thr | missense_variant | 0.12 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.39 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.39 |
Rv1979c | 2221741 | p.Gly475Asp | missense_variant | 0.14 |
Rv1979c | 2222288 | p.Ala293Thr | missense_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518241 | p.Ile43Phe | missense_variant | 0.11 |
eis | 2714575 | p.Trp253Leu | missense_variant | 0.15 |
Rv2752c | 3066280 | c.-89C>T | upstream_gene_variant | 1.0 |
thyX | 3067340 | c.606G>A | synonymous_variant | 0.13 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086870 | c.51C>T | synonymous_variant | 0.17 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612469 | c.648A>G | synonymous_variant | 1.0 |
Rv3236c | 3613061 | p.Ala19Gly | missense_variant | 0.15 |
alr | 3841567 | c.-147A>G | upstream_gene_variant | 1.0 |
rpoA | 3878184 | c.324C>A | synonymous_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243576 | p.Val115Asp | missense_variant | 0.15 |
embA | 4246512 | p.Pro1094Ser | missense_variant | 1.0 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.33 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.5 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.5 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |