Run ID: ERR2229643
Sample name:
Date: 31-03-2023 17:23:13
Number of reads: 770077
Percentage reads mapped: 99.29
Strain: lineage4.8
Drug-resistance: Other
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 |
---|---|---|---|---|---|
panD | 4043931 | p.Met117Ile | missense_variant | 0.14 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8666 | c.1365G>T | synonymous_variant | 0.12 |
fgd1 | 491254 | p.Lys158* | stop_gained | 0.17 |
mshA | 576623 | p.Ala426Pro | missense_variant | 0.14 |
mshA | 576661 | p.Leu438Phe | missense_variant | 0.15 |
ccsA | 620321 | p.Pro144Gln | missense_variant | 0.12 |
rpoB | 762496 | p.Asp897Gly | missense_variant | 0.15 |
rpoC | 766831 | c.3462C>T | synonymous_variant | 0.18 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777478 | p.Leu335Ile | missense_variant | 0.14 |
mmpL5 | 777535 | p.Thr316Pro | missense_variant | 0.12 |
mmpL5 | 779116 | c.-636G>A | upstream_gene_variant | 0.2 |
mmpL5 | 779376 | c.-896C>T | upstream_gene_variant | 0.11 |
mmpS5 | 779591 | c.-686C>A | upstream_gene_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781447 | c.-113A>T | upstream_gene_variant | 0.14 |
rplC | 801011 | p.Gly68Val | missense_variant | 0.17 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
atpE | 1461077 | c.33C>A | synonymous_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472326 | n.481T>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475145 | n.1488C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476005 | n.2348T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476059 | n.2402G>T | non_coding_transcript_exon_variant | 0.12 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.12 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.13 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.12 |
inhA | 1673805 | c.-397G>A | upstream_gene_variant | 0.17 |
inhA | 1674949 | p.Leu250Met | missense_variant | 0.12 |
rpsA | 1833751 | c.210C>T | synonymous_variant | 0.13 |
rpsA | 1834353 | p.Arg271Leu | missense_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102259 | p.Ser262Pro | missense_variant | 0.2 |
ndh | 2102653 | p.His130Glu | missense_variant | 0.14 |
katG | 2155771 | p.Arg114Leu | missense_variant | 0.17 |
PPE35 | 2168332 | c.2281C>T | synonymous_variant | 0.22 |
PPE35 | 2168333 | c.2280C>T | synonymous_variant | 0.15 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2168870 | c.1743G>T | synonymous_variant | 0.14 |
PPE35 | 2168925 | p.Val563Ala | missense_variant | 0.12 |
PPE35 | 2169695 | c.918A>G | synonymous_variant | 0.19 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.16 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.61 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.65 |
Rv1979c | 2223083 | p.Ile28Val | missense_variant | 0.18 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289897 | c.-656G>T | upstream_gene_variant | 0.29 |
kasA | 2519140 | c.1026G>C | synonymous_variant | 0.26 |
kasA | 2519143 | c.1029G>C | synonymous_variant | 0.28 |
kasA | 2519155 | p.Ile347Met | missense_variant | 0.11 |
kasA | 2519167 | c.1053T>C | synonymous_variant | 0.1 |
kasA | 2519171 | p.Leu353Val | missense_variant | 0.1 |
folC | 2746410 | p.Val397Met | missense_variant | 0.15 |
folC | 2747170 | c.429T>C | synonymous_variant | 0.17 |
pepQ | 2859512 | p.His303Asn | missense_variant | 0.17 |
pepQ | 2860222 | p.Ser66* | stop_gained | 0.17 |
ribD | 2986796 | c.-43C>T | upstream_gene_variant | 0.15 |
ribD | 2987249 | c.411G>A | synonymous_variant | 0.2 |
Rv2752c | 3064892 | p.Gly434Ser | missense_variant | 0.33 |
Rv2752c | 3067166 | c.-975G>T | upstream_gene_variant | 0.14 |
thyA | 3073966 | p.Asp169Val | missense_variant | 0.15 |
fbiD | 3339125 | p.Gly3Val | missense_variant | 0.12 |
fbiD | 3339491 | p.Leu125Pro | missense_variant | 0.18 |
fprA | 3474127 | p.Met41Val | missense_variant | 0.13 |
fprA | 3474259 | p.Gly85Ser | missense_variant | 0.22 |
fprA | 3474616 | p.Gln204Lys | missense_variant | 0.14 |
fprA | 3474700 | p.Gly232Cys | missense_variant | 0.13 |
Rv3236c | 3613057 | c.60G>T | synonymous_variant | 0.2 |
alr | 3841612 | c.-193_-192insC | upstream_gene_variant | 0.22 |
rpoA | 3878554 | c.-47C>A | upstream_gene_variant | 0.33 |
ddn | 3986911 | p.Arg23Gln | missense_variant | 0.12 |
ddn | 3987016 | p.Gln58Arg | missense_variant | 0.12 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.11 |
clpC1 | 4039508 | c.1197G>C | synonymous_variant | 0.15 |
clpC1 | 4039682 | c.1023C>T | synonymous_variant | 0.12 |
clpC1 | 4040087 | c.618G>T | synonymous_variant | 0.18 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.18 |
clpC1 | 4040230 | p.Gly159Arg | missense_variant | 0.2 |
panD | 4043901 | p.Asn127Lys | missense_variant | 0.13 |
embC | 4240650 | p.Leu263Pro | missense_variant | 0.11 |
embC | 4241104 | p.Glu414Asp | missense_variant | 0.14 |
embC | 4242501 | p.Ala880Glu | missense_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243247 | c.15T>C | synonymous_variant | 0.12 |
embA | 4244268 | c.1036C>A | synonymous_variant | 0.12 |
embA | 4244519 | c.1287G>T | synonymous_variant | 0.14 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.21 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.14 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.13 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.13 |
embB | 4248478 | c.1965G>T | synonymous_variant | 0.12 |
aftB | 4267826 | c.1011G>T | synonymous_variant | 0.13 |
ubiA | 4269467 | p.Asn123His | missense_variant | 0.12 |
aftB | 4269471 | c.-635C>G | upstream_gene_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |