Run ID: ERR2652993
Sample name:
Date: 31-03-2023 22:26:07
Number of reads: 475141
Percentage reads mapped: 96.6
Strain: lineage4.7
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.7 | Euro-American (mainly T) | T1;T5 | None | 0.96 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 0.96 | rifampicin |
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 0.94 | isoniazid, ethionamide |
katG | 2155167 | p.Ser315Thr | missense_variant | 0.11 | isoniazid |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
ethA | 4326109 | c.1363_1364delTG | frameshift_variant | 0.15 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
mshA | 576123 | p.Leu259Arg | missense_variant | 0.17 |
rpoC | 764298 | p.Met310Thr | missense_variant | 0.12 |
rpoC | 764558 | p.Arg397Cys | missense_variant | 0.11 |
rpoC | 764817 | p.Val483Gly | missense_variant | 1.0 |
rpoC | 765996 | p.Arg876His | missense_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775715 | c.2766G>A | synonymous_variant | 1.0 |
mmpL5 | 779244 | c.-764G>C | upstream_gene_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303487 | p.Gly186Val | missense_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472803 | n.958T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472998 | n.1153C>T | non_coding_transcript_exon_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102840 | c.202delA | frameshift_variant | 0.12 |
katG | 2155012 | p.Pro367Gln | missense_variant | 0.18 |
PPE35 | 2167881 | p.Asn911Ser | missense_variant | 0.14 |
Rv1979c | 2221783 | p.Ala461Gly | missense_variant | 0.13 |
Rv1979c | 2222697 | c.468C>T | synonymous_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289070 | p.Phe58Val | missense_variant | 0.93 |
pncA | 2290179 | c.-938G>A | upstream_gene_variant | 0.12 |
fbiD | 3339535 | p.Val140Ile | missense_variant | 0.12 |
Rv3083 | 3448669 | p.Asp56Asn | missense_variant | 0.12 |
Rv3083 | 3449448 | c.945G>A | synonymous_variant | 0.13 |
alr | 3841071 | p.Gly117Asp | missense_variant | 1.0 |
rpoA | 3878599 | c.-92C>G | upstream_gene_variant | 0.13 |
clpC1 | 4040525 | c.180C>T | synonymous_variant | 1.0 |
clpC1 | 4040621 | c.84C>A | synonymous_variant | 0.17 |
embC | 4240599 | c.739delG | frameshift_variant | 0.14 |
embC | 4241289 | p.Ile476Thr | missense_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243977 | p.Ala249Thr | missense_variant | 1.0 |
embA | 4244798 | c.1566G>A | synonymous_variant | 0.17 |
embA | 4245703 | p.Ser824Trp | missense_variant | 0.11 |
embB | 4249732 | c.3219C>G | synonymous_variant | 0.95 |
ethA | 4327295 | p.Tyr60Cys | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407590 | p.Ala205Thr | missense_variant | 1.0 |