Run ID: ERR2229211
Sample name:
Date: 31-03-2023 16:48:51
Number of reads: 424320
Percentage reads mapped: 99.66
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 | 8860 | p.Ile520Thr | missense_variant | 0.11 |
mshA | 575491 | c.144G>T | synonymous_variant | 0.18 |
mshA | 576488 | p.Val381His | missense_variant | 0.15 |
ccsA | 619937 | p.Trp16Leu | missense_variant | 0.29 |
rpoC | 764541 | p.Val391Gly | missense_variant | 0.13 |
rpoC | 764543 | p.Thr392Asp | missense_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1305474 | c.2544T>G | synonymous_variant | 0.22 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475640 | n.1983G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475904 | n.2247G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476393 | n.2736C>A | non_coding_transcript_exon_variant | 0.33 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.35 |
fabG1 | 1673533 | p.Ala32Ser | missense_variant | 0.14 |
fabG1 | 1673915 | p.Gly159Val | missense_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918411 | p.Ile158Val | missense_variant | 0.13 |
PPE35 | 2167865 | c.2748G>C | synonymous_variant | 0.15 |
PPE35 | 2167868 | c.2745A>C | synonymous_variant | 0.17 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2168819 | c.1794T>C | synonymous_variant | 0.15 |
PPE35 | 2169386 | c.1227C>A | synonymous_variant | 0.12 |
PPE35 | 2169394 | p.Ala407Thr | missense_variant | 0.12 |
PPE35 | 2169488 | c.1125G>C | synonymous_variant | 0.15 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.33 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.4 |
PPE35 | 2170298 | c.315A>G | synonymous_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290231 | c.-990G>A | upstream_gene_variant | 0.25 |
kasA | 2519140 | c.1026G>C | synonymous_variant | 0.15 |
kasA | 2519143 | c.1029G>C | synonymous_variant | 0.15 |
eis | 2714576 | p.Trp253Gly | missense_variant | 0.29 |
eis | 2715432 | c.-100C>T | upstream_gene_variant | 0.12 |
folC | 2747561 | p.Ser13* | stop_gained | 0.29 |
ribD | 2987309 | c.471G>A | synonymous_variant | 0.29 |
Rv2752c | 3064865 | p.Pro443Thr | missense_variant | 0.14 |
thyA | 3074648 | c.-177T>G | upstream_gene_variant | 0.42 |
Rv3236c | 3612115 | c.1002G>A | synonymous_variant | 0.11 |
fbiB | 3642084 | p.Gly184Ser | missense_variant | 0.18 |
clpC1 | 4038741 | p.Val655Ala | missense_variant | 0.29 |
clpC1 | 4038941 | c.1764G>T | synonymous_variant | 0.4 |
clpC1 | 4039157 | p.Lys516Asn | missense_variant | 0.17 |
clpC1 | 4040342 | c.363C>T | synonymous_variant | 0.2 |
panD | 4044207 | c.75G>T | synonymous_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245763 | p.Gly844Val | missense_variant | 0.2 |
embB | 4247907 | p.Ile465Thr | missense_variant | 0.13 |
embB | 4248719 | p.Gly736Cys | missense_variant | 0.15 |
ethA | 4326914 | p.Ala187Val | missense_variant | 0.12 |
ethA | 4328059 | c.-586G>A | upstream_gene_variant | 0.4 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448497 | c.-6_*1408del | transcript_ablation | 1.0 |