Run ID: ERR2229515
Sample name:
Date: 31-03-2023 17:16:30
Number of reads: 1019249
Percentage reads mapped: 99.35
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 |
---|---|---|---|---|
gyrB | 6006 | p.Gly256Ala | missense_variant | 0.11 |
gyrB | 6101 | p.Glu288Gln | missense_variant | 0.1 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
fgd1 | 491443 | p.Ser221Ala | missense_variant | 0.14 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.36 |
ccsA | 620002 | p.Gln38Lys | missense_variant | 0.18 |
rpoB | 761599 | p.Arg598Pro | missense_variant | 0.11 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.11 |
rpoC | 766392 | p.Thr1008Ile | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775939 | p.Ala848Ser | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474901 | n.1246delT | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475188 | n.1531C>A | non_coding_transcript_exon_variant | 0.14 |
inhA | 1673883 | c.-319C>T | upstream_gene_variant | 0.12 |
rpsA | 1833961 | c.420C>G | synonymous_variant | 0.1 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.14 |
PPE35 | 2169939 | p.Gly225Ala | missense_variant | 0.1 |
PPE35 | 2169947 | c.666T>C | synonymous_variant | 0.11 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.14 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.12 |
Rv1979c | 2222184 | p.Trp327Cys | missense_variant | 0.11 |
Rv1979c | 2222962 | p.Ala68Val | missense_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289638 | c.-397C>A | upstream_gene_variant | 0.17 |
pncA | 2289678 | c.-437T>C | upstream_gene_variant | 0.13 |
pncA | 2289805 | c.-564C>A | upstream_gene_variant | 0.18 |
folC | 2746890 | p.Gln237Lys | missense_variant | 0.12 |
Rv2752c | 3065316 | c.876C>T | synonymous_variant | 0.11 |
thyA | 3074118 | c.354G>A | synonymous_variant | 0.2 |
fbiB | 3641352 | c.-183C>T | upstream_gene_variant | 0.13 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.21 |
panD | 4044338 | c.-57C>T | upstream_gene_variant | 0.11 |
embC | 4241657 | p.Ser599Ala | missense_variant | 0.25 |
embC | 4241872 | c.2010G>A | synonymous_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.17 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.4 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.5 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.5 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.4 |
aftB | 4268551 | p.Val96Leu | missense_variant | 0.14 |
aftB | 4269132 | c.-296G>T | upstream_gene_variant | 0.14 |
ethA | 4327517 | c.-44A>T | upstream_gene_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408009 | p.Val65Ala | missense_variant | 0.1 |
gid | 4408089 | c.114C>G | synonymous_variant | 0.1 |
Rv3083 | 3448497 | c.-6_*1408del | transcript_ablation | 1.0 |