Run ID: ERR2228897
Sample name:
Date: 31-03-2023 16:25:08
Number of reads: 386385
Percentage reads mapped: 98.44
Strain: lineage4
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5055 | c.-185A>T | upstream_gene_variant | 0.17 |
gyrB | 7093 | c.1856delA | frameshift_variant | 0.15 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
mshA | 576114 | p.Arg256Pro | missense_variant | 0.5 |
ccsA | 620494 | c.604C>A | synonymous_variant | 0.5 |
rpoB | 761573 | c.1769delT | frameshift_variant | 0.22 |
rpoB | 762032 | c.2226C>T | synonymous_variant | 0.18 |
rpoB | 762550 | p.Gly915Asp | missense_variant | 0.12 |
rpoB | 763075 | p.Thr1090Ile | missense_variant | 0.22 |
rpoC | 764009 | p.Arg214Ser | missense_variant | 0.22 |
rpoC | 766481 | c.3112C>A | synonymous_variant | 0.33 |
rpoC | 766536 | p.Glu1056Gly | missense_variant | 0.4 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776146 | p.Ala779Thr | missense_variant | 0.5 |
mmpL5 | 777119 | p.His454Gln | missense_variant | 0.17 |
mmpL5 | 777122 | c.1359C>T | synonymous_variant | 0.17 |
mmpL5 | 777128 | c.1353A>G | synonymous_variant | 0.17 |
mmpR5 | 778037 | c.-953G>A | upstream_gene_variant | 0.29 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1305096 | p.His722Gln | missense_variant | 0.29 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471910 | n.65T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472852 | n.1007G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476062 | n.2408dupA | non_coding_transcript_exon_variant | 0.4 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918662 | c.723G>T | synonymous_variant | 0.25 |
ndh | 2103178 | c.-136G>C | upstream_gene_variant | 0.5 |
katG | 2154372 | p.Asp580Glu | missense_variant | 0.17 |
katG | 2156131 | c.-20C>A | upstream_gene_variant | 0.17 |
katG | 2156558 | c.-447G>A | upstream_gene_variant | 0.33 |
PPE35 | 2167760 | c.2853G>A | synonymous_variant | 0.4 |
PPE35 | 2167763 | p.Ile950Val | missense_variant | 0.4 |
PPE35 | 2168252 | c.2361G>A | synonymous_variant | 0.67 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169308 | c.1305C>T | synonymous_variant | 0.13 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.27 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.2 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.31 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.36 |
PPE35 | 2170284 | p.Val110Ala | missense_variant | 0.14 |
Rv1979c | 2221720 | c.1445A>T | stop_lost&splice_region_variant | 0.12 |
Rv1979c | 2223175 | c.-11G>T | upstream_gene_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518250 | p.Leu46Ile | missense_variant | 0.25 |
kasA | 2518552 | c.441delC | frameshift_variant | 0.25 |
eis | 2714179 | p.Arg385Leu | missense_variant | 0.18 |
eis | 2714560 | p.Gly258Ala | missense_variant | 0.17 |
pepQ | 2859581 | p.Leu280Met | missense_variant | 0.25 |
Rv3236c | 3612279 | c.838C>T | synonymous_variant | 0.5 |
fbiA | 3640640 | p.Ala33Val | missense_variant | 0.29 |
fbiA | 3640845 | p.Trp101* | stop_gained | 0.29 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.24 |
rpoA | 3877589 | p.Ser307Thr | missense_variant | 0.25 |
ddn | 3986982 | p.Ala47Ser | missense_variant | 0.33 |
ddn | 3987089 | c.246G>C | synonymous_variant | 0.14 |
clpC1 | 4039077 | p.Lys543Arg | missense_variant | 0.25 |
clpC1 | 4039468 | p.Arg413Ser | missense_variant | 0.14 |
clpC1 | 4040010 | p.Ala232Arg | missense_variant | 0.22 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244505 | p.Gly425Trp | missense_variant | 0.2 |
embA | 4244761 | p.Asn510Ile | missense_variant | 0.5 |
embA | 4244942 | p.Trp570Cys | missense_variant | 0.33 |
embB | 4248401 | p.Ala630Thr | missense_variant | 0.2 |
aftB | 4267919 | c.917_918insTA | frameshift_variant | 0.25 |
aftB | 4268153 | c.684G>T | synonymous_variant | 0.2 |
ubiA | 4269110 | c.723delC | frameshift_variant | 0.33 |
ubiA | 4269116 | p.Arg240Ser | missense_variant | 0.33 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448497 | c.-6_*1408del | transcript_ablation | 1.0 |