Run ID: ERR2229447
Sample name:
Date: 31-03-2023 17:12:04
Number of reads: 523769
Percentage reads mapped: 99.4
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 |
fgd1 | 490605 | c.-178G>T | upstream_gene_variant | 0.2 |
rpoB | 759770 | c.-37C>A | upstream_gene_variant | 0.11 |
rpoC | 764949 | p.Leu527* | stop_gained | 0.17 |
rpoC | 765755 | p.Asp796Asn | missense_variant | 0.18 |
rpoC | 766073 | p.Ala902Thr | missense_variant | 0.2 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776018 | c.2463G>C | synonymous_variant | 0.15 |
mmpL5 | 776021 | c.2460G>C | synonymous_variant | 0.15 |
mmpL5 | 776210 | p.Tyr757* | stop_gained | 0.25 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781583 | c.24C>A | synonymous_variant | 0.13 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304330 | p.Ala467Asp | missense_variant | 0.22 |
fbiC | 1305010 | p.Val694Met | missense_variant | 0.25 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475573 | n.1921delC | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476601 | n.2944G>T | non_coding_transcript_exon_variant | 0.15 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102348 | p.Ala232Glu | missense_variant | 0.17 |
ndh | 2102685 | p.Gly120Ser | missense_variant | 0.13 |
katG | 2156151 | c.-40T>A | upstream_gene_variant | 0.18 |
katG | 2156221 | c.-110C>A | upstream_gene_variant | 0.18 |
PPE35 | 2167745 | p.Thr956Arg | missense_variant | 0.21 |
PPE35 | 2167865 | c.2748G>C | synonymous_variant | 0.23 |
PPE35 | 2167868 | c.2745A>C | synonymous_variant | 0.29 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.12 |
PPE35 | 2169879 | p.Phe245Ser | missense_variant | 0.11 |
PPE35 | 2169890 | c.723C>T | synonymous_variant | 0.13 |
PPE35 | 2169893 | c.720C>A | synonymous_variant | 0.14 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.17 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.18 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.12 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.13 |
PPE35 | 2170392 | p.Gly74Ala | missense_variant | 0.15 |
PPE35 | 2170400 | c.213G>C | synonymous_variant | 0.15 |
PPE35 | 2170415 | c.198A>G | synonymous_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289037 | p.Pro69Thr | missense_variant | 0.12 |
kasA | 2518723 | p.Glu203Asp | missense_variant | 0.5 |
eis | 2715483 | c.-151C>A | upstream_gene_variant | 0.13 |
folC | 2746367 | c.1231delG | frameshift_variant | 0.25 |
Rv2752c | 3064745 | p.Thr483Ser | missense_variant | 0.18 |
Rv2752c | 3064773 | c.1419C>T | synonymous_variant | 0.12 |
thyA | 3074038 | p.Pro145Leu | missense_variant | 0.18 |
thyA | 3074392 | p.Arg27His | missense_variant | 0.22 |
fprA | 3473978 | c.-29G>T | upstream_gene_variant | 0.13 |
Rv3236c | 3613294 | c.-178G>A | upstream_gene_variant | 0.17 |
clpC1 | 4038716 | c.1989C>T | synonymous_variant | 0.14 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.22 |
panD | 4044253 | p.Ile10Asn | missense_variant | 0.4 |
embC | 4240060 | c.198G>T | synonymous_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245711 | p.Ala827Ser | missense_variant | 0.29 |
embB | 4248552 | p.Ala680Asp | missense_variant | 0.17 |
aftB | 4267029 | p.Asp603Val | missense_variant | 0.17 |
aftB | 4267634 | c.1203G>T | synonymous_variant | 0.22 |
whiB6 | 4338352 | p.Pro57Gln | missense_variant | 0.17 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407604 | p.Ala200Val | missense_variant | 0.15 |
gid | 4407849 | c.354C>A | synonymous_variant | 0.14 |
gid | 4408474 | c.-272A>T | upstream_gene_variant | 0.12 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |