Run ID: ERR2229251
Sample name:
Date: 31-03-2023 16:52:50
Number of reads: 1463034
Percentage reads mapped: 99.13
Strain: lineage4.8
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 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 | 7905 | p.Phe202Leu | missense_variant | 0.12 |
fgd1 | 491115 | c.333G>C | synonymous_variant | 0.11 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.24 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775826 | c.2655G>A | synonymous_variant | 0.17 |
mmpL5 | 777482 | c.999G>A | synonymous_variant | 0.13 |
mmpL5 | 778976 | c.-496C>A | upstream_gene_variant | 0.12 |
mmpR5 | 779026 | p.Glu13* | stop_gained | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476147 | n.2490G>T | non_coding_transcript_exon_variant | 0.14 |
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 | 0.35 |
inhA | 1674478 | p.His93Asn | missense_variant | 0.22 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.19 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.52 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.48 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289976 | c.-735G>T | upstream_gene_variant | 0.17 |
folC | 2747011 | c.587delC | frameshift_variant | 0.11 |
folC | 2747040 | p.Ile187Leu | missense_variant | 0.12 |
Rv3236c | 3612589 | c.528C>A | synonymous_variant | 0.12 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.25 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.29 |
embC | 4241603 | p.Phe581Ile | missense_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.18 |
embB | 4246567 | c.54_55insT | frameshift_variant | 0.22 |
embB | 4249734 | p.Pro1074His | missense_variant | 0.14 |
aftB | 4267003 | c.1834C>A | synonymous_variant | 0.15 |
ethR | 4327327 | c.-222A>G | upstream_gene_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448497 | c.-6_*1408del | transcript_ablation | 1.0 |