Run ID: ERR2229368
Sample name:
Date: 31-03-2023 17:06:53
Number of reads: 689560
Percentage reads mapped: 98.78
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 | 5710 | c.471C>A | synonymous_variant | 0.14 |
gyrA | 6739 | c.-563C>A | upstream_gene_variant | 0.18 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8808 | p.Gly503* | stop_gained | 0.17 |
gyrA | 9374 | c.2073G>A | synonymous_variant | 0.18 |
fgd1 | 491290 | p.Val170Leu | missense_variant | 0.22 |
ccsA | 620112 | p.Glu74Asp | missense_variant | 0.29 |
rpoC | 765689 | c.2320C>T | synonymous_variant | 0.22 |
rpoC | 766211 | p.Glu948* | stop_gained | 0.14 |
rpoC | 766283 | p.Thr972Ser | missense_variant | 0.4 |
rpoC | 766447 | c.3080delG | frameshift_variant | 0.4 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775829 | c.2652C>A | synonymous_variant | 0.29 |
mmpL5 | 775883 | c.2598C>T | synonymous_variant | 0.22 |
mmpL5 | 775955 | p.Ile842Val | missense_variant | 0.2 |
mmpL5 | 776009 | c.2472A>G | synonymous_variant | 0.22 |
mmpL5 | 776018 | c.2463G>C | synonymous_variant | 0.18 |
mmpL5 | 776021 | c.2460G>C | synonymous_variant | 0.18 |
mmpL5 | 776080 | p.Ala801Ser | missense_variant | 0.22 |
mmpL5 | 776081 | c.2400G>A | synonymous_variant | 0.22 |
mmpR5 | 779008 | p.Val7Ile | missense_variant | 0.15 |
mmpR5 | 779046 | p.Phe19Leu | missense_variant | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781481 | c.-79C>A | upstream_gene_variant | 0.29 |
fbiC | 1303302 | c.372A>G | synonymous_variant | 0.12 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304844 | c.1914C>T | synonymous_variant | 0.29 |
Rv1258c | 1407056 | c.285G>A | synonymous_variant | 0.2 |
embR | 1417373 | c.-26G>A | upstream_gene_variant | 0.29 |
atpE | 1461280 | p.Pro79Leu | missense_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472178 | n.333C>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473156 | n.1311A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473477 | n.-181T>C | upstream_gene_variant | 0.12 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474544 | n.887G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.25 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.16 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.19 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.14 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.16 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.16 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.36 |
rpsA | 1833733 | c.192C>A | synonymous_variant | 0.25 |
rpsA | 1833909 | p.Asp123Val | missense_variant | 0.17 |
tlyA | 1917874 | c.-66G>T | upstream_gene_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101974 | p.Ala357Ser | missense_variant | 0.22 |
ndh | 2102371 | p.Met224Ile | missense_variant | 0.33 |
ndh | 2102890 | p.Phe51Leu | missense_variant | 0.25 |
ndh | 2103165 | c.-123G>A | upstream_gene_variant | 0.2 |
katG | 2155191 | c.921A>C | synonymous_variant | 0.15 |
PPE35 | 2167833 | p.Leu927Arg | missense_variant | 0.22 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.27 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.31 |
PPE35 | 2169287 | c.1326T>C | synonymous_variant | 0.35 |
PPE35 | 2169293 | c.1320T>C | synonymous_variant | 0.2 |
PPE35 | 2169302 | p.Met437Ile | missense_variant | 0.12 |
PPE35 | 2169308 | c.1305C>T | synonymous_variant | 0.12 |
PPE35 | 2169457 | p.His386Asp | missense_variant | 0.15 |
PPE35 | 2169488 | c.1125G>C | synonymous_variant | 0.16 |
PPE35 | 2169902 | c.711G>C | synonymous_variant | 0.17 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.78 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.8 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289521 | c.-280G>T | upstream_gene_variant | 0.2 |
pncA | 2290069 | c.-828C>T | upstream_gene_variant | 0.17 |
kasA | 2518204 | c.90G>A | synonymous_variant | 0.25 |
kasA | 2518481 | p.Val123Ile | missense_variant | 0.29 |
kasA | 2518809 | p.Lys232Arg | missense_variant | 0.18 |
eis | 2714673 | c.660C>A | synonymous_variant | 0.33 |
eis | 2714837 | p.Val166Phe | missense_variant | 0.2 |
ahpC | 2726009 | c.-184T>A | upstream_gene_variant | 0.2 |
ahpC | 2726515 | p.Phe108Ser | missense_variant | 0.18 |
folC | 2747384 | p.Thr72Ile | missense_variant | 0.25 |
folC | 2747797 | c.-199T>A | upstream_gene_variant | 0.3 |
pepQ | 2860303 | p.Ser39Tyr | missense_variant | 0.29 |
Rv2752c | 3065198 | p.Asp332Tyr | missense_variant | 0.17 |
thyX | 3067306 | p.Glu214Lys | missense_variant | 0.15 |
thyA | 3074375 | p.Gln33Lys | missense_variant | 0.29 |
fprA | 3474663 | p.Asp219Glu | missense_variant | 0.25 |
Rv3236c | 3612086 | p.Ala344Gly | missense_variant | 0.18 |
Rv3236c | 3612958 | c.159C>A | synonymous_variant | 0.25 |
Rv3236c | 3613264 | c.-148G>A | upstream_gene_variant | 0.33 |
Rv3236c | 3613266 | c.-150G>T | upstream_gene_variant | 0.33 |
alr | 3840422 | c.999A>G | synonymous_variant | 0.33 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.37 |
rpoA | 3877549 | p.Val320Ala | missense_variant | 0.13 |
rpoA | 3878486 | p.Thr8Pro | missense_variant | 0.29 |
clpC1 | 4038313 | p.Gln798Glu | missense_variant | 0.33 |
clpC1 | 4039645 | p.His354Asp | missense_variant | 0.17 |
clpC1 | 4039654 | p.Thr351Ser | missense_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245469 | p.Asn746Ser | missense_variant | 0.5 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.38 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.5 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.64 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.64 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.38 |
embB | 4248215 | p.Arg568Ser | missense_variant | 0.14 |
embB | 4249045 | p.Leu844Phe | missense_variant | 0.5 |
aftB | 4267087 | p.Leu584Met | missense_variant | 0.2 |
aftB | 4268493 | c.343delG | frameshift_variant | 0.13 |
aftB | 4268937 | c.-101T>A | upstream_gene_variant | 0.33 |
aftB | 4269516 | c.-680G>C | upstream_gene_variant | 0.25 |
ethA | 4326386 | p.Ile363Thr | missense_variant | 0.12 |
ethA | 4328379 | c.-906C>T | upstream_gene_variant | 0.25 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |