Run ID: ERR2229345
Sample name:
Date: 31-03-2023 17:05:41
Number of reads: 1349853
Percentage reads mapped: 98.91
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 | 7266 | c.-36A>G | upstream_gene_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7598 | p.Met99Ile | missense_variant | 0.15 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.29 |
mshA | 576111 | p.Ala255Gly | missense_variant | 0.13 |
mshA | 576661 | c.1314G>A | synonymous_variant | 0.17 |
rpoB | 759802 | c.-5G>T | upstream_gene_variant | 0.17 |
rpoB | 762275 | c.2469C>T | synonymous_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775704 | p.Thr926Lys | missense_variant | 0.17 |
mmpL5 | 775927 | c.2554C>T | synonymous_variant | 0.12 |
mmpL5 | 776027 | c.2454G>A | synonymous_variant | 0.29 |
mmpL5 | 776030 | c.2451G>A | synonymous_variant | 0.29 |
mmpL5 | 776036 | c.2445G>T | synonymous_variant | 0.29 |
mmpL5 | 776848 | p.Gln545Lys | missense_variant | 0.18 |
mmpL5 | 779076 | c.-596G>A | upstream_gene_variant | 0.13 |
mmpL5 | 779175 | c.-695G>A | upstream_gene_variant | 0.25 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304077 | p.Glu383Lys | missense_variant | 0.12 |
embR | 1416802 | c.546C>T | synonymous_variant | 0.12 |
atpE | 1461145 | p.Ala34Gly | missense_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472102 | n.257G>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472565 | n.720A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473179 | n.1334C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474413 | n.756A>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475317 | n.1660G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475475 | n.1818C>A | non_coding_transcript_exon_variant | 0.2 |
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 | 0.38 |
inhA | 1673658 | c.-544G>C | upstream_gene_variant | 0.1 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155737 | c.375C>A | synonymous_variant | 0.17 |
PPE35 | 2167878 | p.Ser912Asn | missense_variant | 0.12 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.2 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.2 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.65 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.67 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288972 | c.270C>T | synonymous_variant | 0.12 |
kasA | 2518606 | c.492G>C | synonymous_variant | 0.15 |
kasA | 2518609 | p.Met165Ile | missense_variant | 0.17 |
kasA | 2518809 | p.Lys232Arg | missense_variant | 0.11 |
kasA | 2518864 | c.750G>C | synonymous_variant | 0.12 |
folC | 2746858 | c.741C>A | synonymous_variant | 0.13 |
pepQ | 2860184 | c.229_234delCGCGCG | conservative_inframe_deletion | 0.17 |
pepQ | 2860200 | c.219G>A | synonymous_variant | 0.17 |
pepQ | 2860201 | c.216_217delAG | frameshift_variant | 0.2 |
pepQ | 2860207 | c.211_212insGCGCGC | conservative_inframe_insertion | 0.22 |
pepQ | 2860564 | c.-146A>G | upstream_gene_variant | 0.17 |
thyX | 3067340 | c.606G>A | synonymous_variant | 0.17 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
fprA | 3475185 | c.1179C>A | synonymous_variant | 0.12 |
fprA | 3475326 | c.1320C>G | synonymous_variant | 0.22 |
Rv3236c | 3612455 | p.Arg221Leu | missense_variant | 0.15 |
Rv3236c | 3612642 | p.Asp159Tyr | missense_variant | 0.12 |
fbiB | 3642226 | p.Gln231Pro | missense_variant | 0.12 |
fbiB | 3642229 | p.Leu232Gln | missense_variant | 0.12 |
fbiB | 3642232 | p.Leu233Gln | missense_variant | 0.12 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.24 |
ddn | 3987034 | p.Leu64His | missense_variant | 0.14 |
ddn | 3987093 | p.Lys84* | stop_gained | 0.12 |
clpC1 | 4038752 | p.Gln651His | missense_variant | 0.17 |
clpC1 | 4039730 | c.975C>G | synonymous_variant | 0.12 |
embC | 4241156 | p.Gly432Cys | missense_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243414 | p.Pro61Leu | missense_variant | 0.13 |
embA | 4245122 | c.1894delG | frameshift_variant | 0.22 |
embA | 4246168 | p.Met979Lys | missense_variant | 0.18 |
embA | 4246288 | p.Asn1019Ser | missense_variant | 0.12 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.5 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.45 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.45 |
embB | 4247160 | p.Thr216Met | missense_variant | 0.15 |
embB | 4249404 | p.Thr964Asn | missense_variant | 0.14 |
aftB | 4269252 | c.-416C>A | upstream_gene_variant | 0.15 |
ethA | 4328378 | c.-905G>T | upstream_gene_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |