Run ID: ERR2229491
Sample name:
Date: 31-03-2023 17:14:52
Number of reads: 185107
Percentage reads mapped: 98.89
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 | 0.06 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2155529 | p.Glu195Lys | missense_variant | 0.4 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5083 | c.-157C>A | upstream_gene_variant | 0.2 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7804 | p.Ser168Asn | missense_variant | 1.0 |
gyrA | 7999 | p.Leu233Pro | missense_variant | 0.5 |
gyrA | 8165 | c.864C>A | synonymous_variant | 0.5 |
gyrA | 8977 | p.Phe559Tyr | missense_variant | 0.29 |
fgd1 | 490816 | p.Ala12Thr | missense_variant | 0.15 |
mshA | 576008 | p.Ala221Thr | missense_variant | 0.4 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775862 | c.2619G>T | synonymous_variant | 1.0 |
mmpL5 | 777164 | c.1317C>T | synonymous_variant | 0.4 |
mmpL5 | 777173 | c.1308C>T | synonymous_variant | 0.4 |
mmpL5 | 777176 | p.Glu435Asp | missense_variant | 0.4 |
mmpL5 | 777191 | c.1290C>A | synonymous_variant | 0.4 |
mmpL5 | 777196 | p.Glu429Gln | missense_variant | 0.4 |
mmpL5 | 777201 | c.1279_1280insACTTCATACCCG | conservative_inframe_insertion | 0.4 |
mmpL5 | 777482 | c.999G>A | synonymous_variant | 0.29 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
embR | 1416410 | p.Leu313Gln | missense_variant | 0.22 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.46 |
rpsA | 1833553 | c.12C>T | synonymous_variant | 0.29 |
rpsA | 1833940 | c.399C>T | synonymous_variant | 0.33 |
katG | 2154162 | c.1950C>A | synonymous_variant | 0.22 |
katG | 2154426 | c.1686C>T | synonymous_variant | 0.18 |
PPE35 | 2167919 | c.2694T>C | synonymous_variant | 0.4 |
PPE35 | 2168051 | p.Val854Ile | missense_variant | 0.5 |
PPE35 | 2168059 | p.Gln852Glu | missense_variant | 0.5 |
PPE35 | 2168702 | c.1911T>A | synonymous_variant | 0.12 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169239 | c.1374T>C | synonymous_variant | 0.17 |
PPE35 | 2169293 | c.1320T>C | synonymous_variant | 0.2 |
PPE35 | 2169308 | c.1305C>T | synonymous_variant | 0.29 |
PPE35 | 2169322 | c.1291T>C | synonymous_variant | 0.29 |
PPE35 | 2169323 | c.1290C>G | synonymous_variant | 0.29 |
PPE35 | 2169326 | c.1287C>T | synonymous_variant | 0.22 |
PPE35 | 2169351 | p.Ala421Ser | missense_variant | 0.2 |
PPE35 | 2169368 | c.1245A>C | synonymous_variant | 0.2 |
PPE35 | 2169371 | c.1242A>C | synonymous_variant | 0.2 |
PPE35 | 2169379 | p.Phe412Ile | missense_variant | 0.2 |
PPE35 | 2169380 | p.Trp411Ser | missense_variant | 0.2 |
PPE35 | 2169596 | c.1017T>C | synonymous_variant | 0.17 |
PPE35 | 2169602 | c.1011C>A | synonymous_variant | 0.15 |
PPE35 | 2169605 | p.Asn336Thr | missense_variant | 0.15 |
PPE35 | 2169608 | c.1005C>G | synonymous_variant | 0.15 |
PPE35 | 2169890 | c.723C>T | synonymous_variant | 0.29 |
PPE35 | 2169893 | c.720C>A | synonymous_variant | 0.33 |
PPE35 | 2169897 | p.Ser239Phe | missense_variant | 0.33 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.33 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.4 |
PPE35 | 2170159 | p.Ala152Ser | missense_variant | 0.4 |
PPE35 | 2170164 | p.Ala150Val | missense_variant | 0.4 |
PPE35 | 2170169 | c.444A>G | synonymous_variant | 0.4 |
PPE35 | 2170175 | p.Leu146Ile | missense_variant | 0.4 |
PPE35 | 2170178 | c.435T>C | synonymous_variant | 0.5 |
PPE35 | 2170189 | p.Glu142Gln | missense_variant | 0.4 |
PPE35 | 2170190 | c.423G>A | synonymous_variant | 0.33 |
PPE35 | 2170406 | c.207A>G | synonymous_variant | 0.67 |
PPE35 | 2170412 | c.201G>C | synonymous_variant | 0.67 |
PPE35 | 2170415 | c.198A>G | synonymous_variant | 0.67 |
PPE35 | 2170425 | p.Val63Ala | missense_variant | 0.67 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ribD | 2986869 | p.Asp11Tyr | missense_variant | 0.25 |
ribD | 2987114 | c.276C>A | synonymous_variant | 0.67 |
fprA | 3473836 | c.-171C>G | upstream_gene_variant | 0.22 |
alr | 3841501 | c.-81G>T | upstream_gene_variant | 0.14 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.18 |
clpC1 | 4039729 | p.Asp326Asn | missense_variant | 0.4 |
panD | 4043937 | c.345C>A | synonymous_variant | 0.5 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4247470 | c.957T>C | synonymous_variant | 0.29 |
embB | 4247472 | p.Phe320Tyr | missense_variant | 0.29 |
aftB | 4269768 | c.-932C>G | upstream_gene_variant | 0.5 |
ethR | 4326789 | c.-760G>A | upstream_gene_variant | 0.4 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |