Run ID: ERR2229098
Sample name:
Date: 31-03-2023 16:38:32
Number of reads: 486944
Percentage reads mapped: 99.4
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 |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7545 | p.Gly82Ser | missense_variant | 0.12 |
gyrA | 8661 | p.Asp454Tyr | missense_variant | 0.17 |
fgd1 | 491736 | c.954C>A | synonymous_variant | 0.2 |
mshA | 575322 | c.-26C>T | upstream_gene_variant | 0.33 |
rpoB | 761464 | p.Val553Gly | missense_variant | 0.25 |
rpoC | 762584 | c.-786G>A | upstream_gene_variant | 0.29 |
rpoC | 764458 | c.1089G>A | synonymous_variant | 0.22 |
rpoC | 765373 | c.2004G>T | synonymous_variant | 0.22 |
rpoC | 765383 | p.Met672Leu | missense_variant | 0.2 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776019 | p.Leu821Gln | missense_variant | 0.17 |
mmpL5 | 776036 | c.2445G>T | synonymous_variant | 0.17 |
mmpL5 | 777358 | p.Arg375Trp | missense_variant | 0.29 |
mmpL5 | 777837 | p.Ile215Thr | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781718 | c.159C>T | synonymous_variant | 0.12 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
Rv1258c | 1407407 | c.-67G>T | upstream_gene_variant | 0.13 |
embR | 1416721 | c.627A>T | synonymous_variant | 0.14 |
embR | 1417274 | p.Gly25Asp | missense_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476118 | n.2461G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476704 | n.3053delC | non_coding_transcript_exon_variant | 0.13 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.12 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.12 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.26 |
inhA | 1674887 | p.Gly229Asp | missense_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918142 | p.His68Leu | missense_variant | 0.17 |
tlyA | 1918325 | p.Val129Glu | missense_variant | 0.15 |
katG | 2155233 | c.879G>T | synonymous_variant | 0.18 |
PPE35 | 2167745 | p.Thr956Arg | missense_variant | 0.12 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169095 | p.Leu506Phe | missense_variant | 0.4 |
PPE35 | 2169269 | c.1344A>G | synonymous_variant | 0.17 |
PPE35 | 2169272 | c.1341C>G | synonymous_variant | 0.18 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.2 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.2 |
PPE35 | 2169581 | c.1032C>G | synonymous_variant | 0.13 |
PPE35 | 2169587 | c.1026G>A | synonymous_variant | 0.12 |
PPE35 | 2169902 | c.711G>C | synonymous_variant | 0.12 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.36 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.36 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289034 | p.Pro70Ser | missense_variant | 0.18 |
pncA | 2290026 | c.-785C>A | upstream_gene_variant | 0.2 |
eis | 2714337 | c.996G>A | synonymous_variant | 0.15 |
eis | 2714433 | c.900C>T | synonymous_variant | 0.14 |
eis | 2714773 | p.Pro187Leu | missense_variant | 0.33 |
folC | 2746290 | p.Arg437Ser | missense_variant | 0.33 |
folC | 2746324 | c.1275C>T | synonymous_variant | 0.22 |
pepQ | 2859858 | c.561G>T | synonymous_variant | 0.4 |
pepQ | 2860376 | p.Ala15Thr | missense_variant | 0.15 |
Rv2752c | 3066385 | c.-194T>C | upstream_gene_variant | 0.14 |
thyA | 3074619 | c.-148C>A | upstream_gene_variant | 0.15 |
fprA | 3474711 | c.705C>T | synonymous_variant | 0.17 |
Rv3236c | 3612789 | p.Leu110Ile | missense_variant | 0.25 |
fbiA | 3641444 | p.Val301Ala | missense_variant | 0.22 |
fbiB | 3642582 | p.Pro350Ala | missense_variant | 0.15 |
rpoA | 3877492 | p.Gln339Leu | missense_variant | 0.12 |
clpC1 | 4038685 | p.Ser674Thr | missense_variant | 0.11 |
clpC1 | 4038814 | p.His631Asn | missense_variant | 0.14 |
clpC1 | 4040691 | p.Phe5Tyr | missense_variant | 0.18 |
embA | 4242520 | c.-713G>A | upstream_gene_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4246366 | p.Tyr1045Cys | missense_variant | 0.15 |
embB | 4246555 | c.42G>C | synonymous_variant | 1.0 |
embB | 4246556 | p.Ala15Pro | missense_variant | 1.0 |
embB | 4248988 | c.2475C>A | synonymous_variant | 0.13 |
embB | 4249341 | p.Ala943Val | missense_variant | 0.12 |
aftB | 4268776 | c.60delG | frameshift_variant | 0.18 |
ubiA | 4269409 | p.Leu142Pro | missense_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |