Run ID: ERR2229574
Sample name:
Date: 31-03-2023 17:19:48
Number of reads: 1149341
Percentage reads mapped: 99.01
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 | 7165 | c.-137C>A | upstream_gene_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7492 | p.Phe64Tyr | missense_variant | 0.12 |
fgd1 | 491026 | p.Asn82Asp | missense_variant | 0.12 |
rpoB | 761290 | p.Ser495Leu | missense_variant | 0.12 |
rpoC | 764056 | c.687G>A | synonymous_variant | 0.13 |
rpoC | 766940 | p.Arg1191Ser | missense_variant | 0.2 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776011 | p.Gln824Lys | missense_variant | 0.12 |
mmpL5 | 777149 | p.Asn444Lys | missense_variant | 0.18 |
mmpL5 | 777157 | c.1324C>A | synonymous_variant | 0.17 |
mmpL5 | 777164 | c.1317C>T | synonymous_variant | 0.17 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303492 | c.562T>C | synonymous_variant | 0.11 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304484 | c.1554C>G | synonymous_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475450 | n.1793C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476254 | n.2597C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.11 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.14 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.15 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.15 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.27 |
fabG1 | 1673629 | p.Asp64His | missense_variant | 0.11 |
inhA | 1674184 | c.-18C>T | upstream_gene_variant | 0.22 |
rpsA | 1834293 | p.Val251Ala | missense_variant | 0.14 |
tlyA | 1917928 | c.-12G>T | upstream_gene_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918088 | p.Thr50Asn | missense_variant | 0.12 |
tlyA | 1918203 | c.264C>T | synonymous_variant | 0.2 |
tlyA | 1918293 | c.354G>T | synonymous_variant | 0.17 |
ndh | 2102354 | p.Gln230Arg | missense_variant | 0.2 |
PPE35 | 2167865 | c.2748G>C | synonymous_variant | 0.15 |
PPE35 | 2167868 | c.2745A>C | synonymous_variant | 0.15 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.2 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.2 |
PPE35 | 2168225 | c.2388C>A | synonymous_variant | 0.14 |
PPE35 | 2168312 | p.Gln767His | missense_variant | 0.18 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169200 | c.1413G>A | synonymous_variant | 0.22 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.26 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.24 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.43 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.42 |
PPE35 | 2170147 | p.Ser156Ala | missense_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519116 | c.1002C>T | synonymous_variant | 0.2 |
eis | 2714864 | p.Gly157Ser | missense_variant | 0.18 |
folC | 2746374 | p.Pro409Ala | missense_variant | 0.14 |
pepQ | 2859742 | p.Val226Gly | missense_variant | 0.2 |
pepQ | 2859751 | p.Gly223Val | missense_variant | 0.18 |
pepQ | 2860399 | p.Arg7Gln | missense_variant | 0.12 |
pepQ | 2860616 | c.-198G>A | upstream_gene_variant | 0.17 |
ribD | 2987151 | p.His105Asn | missense_variant | 0.22 |
Rv2752c | 3065155 | p.Glu346Gly | missense_variant | 0.22 |
Rv2752c | 3065242 | p.Arg317Gln | missense_variant | 0.22 |
thyX | 3067594 | p.Val118Leu | missense_variant | 0.15 |
thyA | 3073770 | p.Asp234Glu | missense_variant | 0.14 |
thyA | 3073926 | c.546G>A | synonymous_variant | 0.12 |
ald | 3087485 | c.666C>T | synonymous_variant | 0.12 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
fbiA | 3641203 | p.Gly221Cys | missense_variant | 0.18 |
fbiB | 3641789 | c.255G>T | synonymous_variant | 0.13 |
fbiB | 3642509 | c.977delT | frameshift_variant | 0.14 |
alr | 3841133 | c.288G>A | synonymous_variant | 0.15 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.29 |
clpC1 | 4040032 | p.Val225Ile | missense_variant | 0.15 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.12 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.15 |
embC | 4239957 | p.Val32Ala | missense_variant | 0.11 |
embA | 4242370 | c.-863C>T | upstream_gene_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.22 |
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 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.33 |
embB | 4247034 | p.Ser174Asn | missense_variant | 0.25 |
aftB | 4267976 | c.861G>A | synonymous_variant | 0.14 |
ubiA | 4269990 | c.-157G>C | upstream_gene_variant | 0.14 |
ethA | 4326385 | c.1089C>T | synonymous_variant | 0.13 |
ethA | 4327554 | c.-81G>T | upstream_gene_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |