Run ID: ERR2229105
Sample name:
Date: 31-03-2023 16:39:15
Number of reads: 572821
Percentage reads mapped: 99.35
Strain: lineage4.8
Drug-resistance: HR-TB
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 |
---|---|---|---|---|---|
katG | 2154685 | c.1426delG | frameshift_variant | 0.14 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8923 | p.Gly541Asp | missense_variant | 0.2 |
fgd1 | 490972 | p.Arg64Ser | missense_variant | 0.12 |
mshA | 576482 | p.Val379Leu | missense_variant | 0.25 |
ccsA | 620491 | p.Ser201Thr | missense_variant | 0.12 |
rpoB | 759896 | c.90A>G | synonymous_variant | 0.13 |
rpoB | 761358 | p.Val518Ile | missense_variant | 0.14 |
rpoB | 762149 | c.2343G>T | synonymous_variant | 0.13 |
rpoC | 763771 | c.402C>T | synonymous_variant | 0.18 |
rpoC | 765302 | p.Glu645* | stop_gained | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776816 | c.1665T>A | synonymous_variant | 0.4 |
mmpL5 | 777391 | p.Phe364Leu | missense_variant | 0.29 |
mmpL5 | 778272 | p.Pro70Arg | missense_variant | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303179 | c.249G>T | synonymous_variant | 0.23 |
fbiC | 1303551 | c.621G>T | synonymous_variant | 0.22 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
Rv1258c | 1406377 | p.Gly322Ser | missense_variant | 0.15 |
Rv1258c | 1407021 | p.Ala107Asp | missense_variant | 0.13 |
embR | 1416827 | p.His174Arg | missense_variant | 0.2 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473410 | n.-248G>T | upstream_gene_variant | 0.17 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474781 | n.1124C>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475938 | n.2281C>T | non_coding_transcript_exon_variant | 0.13 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.12 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.11 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.39 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103165 | c.-123G>T | upstream_gene_variant | 0.12 |
katG | 2154465 | p.Cys549* | stop_gained | 0.13 |
katG | 2154559 | p.Ile518Asn | missense_variant | 0.12 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169269 | c.1344A>G | synonymous_variant | 0.13 |
PPE35 | 2169351 | p.Ala421Gly | missense_variant | 0.12 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.28 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.27 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.36 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.42 |
PPE35 | 2170147 | p.Ser156Ala | missense_variant | 0.16 |
Rv1979c | 2222036 | p.Leu377Met | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518879 | c.765A>G | synonymous_variant | 0.18 |
kasA | 2518882 | c.768C>A | synonymous_variant | 0.18 |
kasA | 2519140 | c.1026G>C | synonymous_variant | 0.15 |
kasA | 2519143 | c.1029G>C | synonymous_variant | 0.17 |
ahpC | 2726211 | p.Gly7Cys | missense_variant | 0.12 |
ahpC | 2726560 | p.Gly123Val | missense_variant | 0.13 |
folC | 2747122 | c.477G>T | synonymous_variant | 0.22 |
folC | 2747163 | p.Gly146Cys | missense_variant | 0.33 |
pepQ | 2859960 | c.459G>T | synonymous_variant | 0.15 |
fbiD | 3339516 | c.399C>A | synonymous_variant | 0.18 |
fprA | 3475240 | p.Ala412Ser | missense_variant | 0.12 |
fprA | 3475267 | p.Ala421Ser | missense_variant | 0.15 |
whiB7 | 3568434 | c.246G>T | synonymous_variant | 0.14 |
fbiB | 3641674 | c.142dupG | frameshift_variant | 0.14 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.25 |
clpC1 | 4040831 | c.-128delG | upstream_gene_variant | 0.11 |
panD | 4044357 | c.-77dupA | upstream_gene_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243966 | p.Arg245Pro | missense_variant | 0.14 |
embA | 4244240 | p.Trp336* | stop_gained | 0.22 |
embA | 4244313 | p.Val361Leu | missense_variant | 0.18 |
embA | 4245280 | p.Arg683Leu | missense_variant | 0.18 |
embB | 4247573 | p.Asp354Tyr | missense_variant | 0.15 |
aftB | 4267020 | p.Pro606Leu | missense_variant | 0.22 |
ethR | 4326961 | c.-588G>C | upstream_gene_variant | 0.14 |
ethR | 4326964 | c.-585G>A | upstream_gene_variant | 0.14 |
ethR | 4326970 | c.-579G>T | upstream_gene_variant | 0.13 |
whiB6 | 4338219 | c.303C>A | synonymous_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448499 | c.-4_*1408del | transcript_ablation | 1.0 |