Run ID: ERR2228806
Sample name:
Date: 31-03-2023 16:21:35
Number of reads: 564084
Percentage reads mapped: 99.29
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 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5536 | c.297G>T | synonymous_variant | 0.25 |
gyrB | 7083 | p.Glu615Val | missense_variant | 0.22 |
gyrB | 7094 | p.Lys619* | stop_gained | 0.2 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7738 | p.Asp146Ala | missense_variant | 0.25 |
gyrA | 7948 | p.Leu216Gln | missense_variant | 0.29 |
fgd1 | 490590 | c.-193A>C | upstream_gene_variant | 0.25 |
fgd1 | 490781 | c.-2T>A | upstream_gene_variant | 0.42 |
mshA | 576074 | p.Asp243Tyr | missense_variant | 0.2 |
mshA | 576477 | p.Leu377Arg | missense_variant | 0.18 |
ccsA | 619844 | c.-47T>G | upstream_gene_variant | 0.4 |
rpoB | 762328 | p.Val841Gly | missense_variant | 0.43 |
rpoB | 762745 | p.Gln980Leu | missense_variant | 0.43 |
rpoC | 763360 | c.-10A>T | upstream_gene_variant | 0.29 |
rpoC | 764708 | p.Met447Leu | missense_variant | 0.36 |
rpoC | 765273 | p.Val635Ala | missense_variant | 0.2 |
rpoC | 766794 | p.Tyr1142Ser | missense_variant | 0.15 |
rpoC | 766926 | p.Phe1186Cys | missense_variant | 0.33 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776427 | p.Asn685Thr | missense_variant | 0.18 |
mmpL5 | 776449 | p.Glu678Gln | missense_variant | 0.17 |
mmpL5 | 777592 | p.Ser297Ala | missense_variant | 0.29 |
mmpL5 | 778204 | p.Ile93Phe | missense_variant | 0.18 |
mmpS5 | 778625 | p.Thr94Asn | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 0.94 |
fbiC | 1303545 | p.Lys205Asn | missense_variant | 0.33 |
fbiC | 1303607 | p.Lys226Met | missense_variant | 0.29 |
fbiC | 1303613 | p.Leu228Pro | missense_variant | 0.25 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1303808 | p.Gln293Leu | missense_variant | 0.22 |
fbiC | 1305033 | c.2103T>G | synonymous_variant | 0.15 |
Rv1258c | 1406130 | p.Asp404Val | missense_variant | 0.2 |
Rv1258c | 1406558 | c.783T>C | synonymous_variant | 0.5 |
Rv1258c | 1406583 | p.Asp253Ala | missense_variant | 0.67 |
Rv1258c | 1406972 | c.369T>G | synonymous_variant | 0.17 |
Rv1258c | 1407039 | p.Val101Gly | missense_variant | 0.4 |
embR | 1417516 | c.-169T>A | upstream_gene_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472484 | n.639A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1473459 | n.-199G>T | upstream_gene_variant | 0.38 |
rrl | 1473903 | n.246A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474161 | n.504A>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474175 | n.518A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474321 | n.664T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474806 | n.1149A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474914 | n.1257A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476067 | n.2410A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476579 | n.2922T>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476692 | n.3035T>A | non_coding_transcript_exon_variant | 0.25 |
inhA | 1674655 | p.Ser152Arg | missense_variant | 0.33 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918558 | p.Ser207Ala | missense_variant | 0.31 |
tlyA | 1918607 | p.Val223Gly | missense_variant | 0.36 |
ndh | 2101703 | p.Glu447Ala | missense_variant | 0.38 |
katG | 2155785 | c.327T>C | synonymous_variant | 0.18 |
katG | 2155897 | p.Asp72Ala | missense_variant | 0.22 |
PPE35 | 2167969 | p.Pro882Thr | missense_variant | 0.4 |
PPE35 | 2168265 | p.Gly783Val | missense_variant | 0.33 |
PPE35 | 2168657 | c.1956T>A | synonymous_variant | 0.33 |
PPE35 | 2168661 | p.Ile651Lys | missense_variant | 0.4 |
PPE35 | 2168675 | c.1938T>A | synonymous_variant | 0.33 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2168943 | p.Gln557Leu | missense_variant | 0.4 |
PPE35 | 2169215 | p.Glu466Asp | missense_variant | 0.22 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.31 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.31 |
PPE35 | 2170056 | p.Val186Gly | missense_variant | 0.33 |
PPE35 | 2170153 | p.Tyr154Asp | missense_variant | 0.29 |
PPE35 | 2170336 | p.Met93Leu | missense_variant | 0.18 |
PPE35 | 2170601 | c.12A>T | synonymous_variant | 0.18 |
Rv1979c | 2221762 | p.Tyr468Phe | missense_variant | 0.18 |
Rv1979c | 2221962 | c.1203A>T | synonymous_variant | 0.43 |
Rv1979c | 2222588 | p.Tyr193Asn | missense_variant | 0.33 |
Rv1979c | 2223070 | p.Ile32Ser | missense_variant | 0.4 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv1979c | 2223320 | c.-156T>G | upstream_gene_variant | 0.17 |
pncA | 2289654 | c.-413A>C | upstream_gene_variant | 0.4 |
kasA | 2518066 | c.-49A>G | upstream_gene_variant | 0.22 |
kasA | 2519062 | c.948T>G | synonymous_variant | 0.14 |
kasA | 2519097 | p.Val328Gly | missense_variant | 0.2 |
ahpC | 2725965 | c.-228T>A | upstream_gene_variant | 0.25 |
ahpC | 2726303 | c.111T>A | synonymous_variant | 0.36 |
ahpC | 2726318 | p.Glu42Asp | missense_variant | 0.25 |
ahpC | 2726320 | p.His43Pro | missense_variant | 0.25 |
ahpC | 2726341 | p.Val50Glu | missense_variant | 0.5 |
ahpC | 2726428 | p.Asp79Ala | missense_variant | 0.4 |
folC | 2746439 | p.Val387Glu | missense_variant | 0.29 |
folC | 2747036 | p.Asn188Thr | missense_variant | 0.5 |
folC | 2747695 | c.-97C>T | upstream_gene_variant | 0.15 |
pepQ | 2860192 | p.Glu76Ala | missense_variant | 0.25 |
ribD | 2986662 | c.-177T>G | upstream_gene_variant | 0.33 |
ribD | 2987086 | p.Val83Gly | missense_variant | 0.5 |
Rv2752c | 3065496 | c.696G>T | synonymous_variant | 0.29 |
thyX | 3067363 | p.Phe195Ile | missense_variant | 0.18 |
thyX | 3067863 | p.Asp28Ala | missense_variant | 0.6 |
thyX | 3068104 | c.-159C>A | upstream_gene_variant | 0.5 |
ald | 3087619 | p.Ile267Lys | missense_variant | 0.21 |
ald | 3087928 | p.Leu370Arg | missense_variant | 0.22 |
fbiD | 3339230 | p.Val38Gly | missense_variant | 0.35 |
fbiD | 3339744 | c.627A>C | synonymous_variant | 0.2 |
fprA | 3474507 | c.501C>A | synonymous_variant | 0.33 |
whiB7 | 3568462 | p.Gln73Leu | missense_variant | 0.2 |
Rv3236c | 3612572 | p.Val182Gly | missense_variant | 0.5 |
Rv3236c | 3612581 | p.Leu179Arg | missense_variant | 0.6 |
Rv3236c | 3612643 | p.Glu158Asp | missense_variant | 0.4 |
Rv3236c | 3613138 | c.-22A>T | upstream_gene_variant | 0.4 |
fbiA | 3640512 | c.-31T>C | upstream_gene_variant | 0.25 |
fbiB | 3641911 | p.Asp126Ala | missense_variant | 0.18 |
fbiB | 3642047 | c.513G>C | synonymous_variant | 0.18 |
fbiB | 3642060 | p.Tyr176Asn | missense_variant | 0.22 |
fbiB | 3642498 | p.Thr322Pro | missense_variant | 0.29 |
alr | 3841595 | c.-175T>A | upstream_gene_variant | 0.2 |
ddn | 3987059 | c.216G>T | synonymous_variant | 0.23 |
clpC1 | 4040170 | p.Thr179Pro | missense_variant | 0.18 |
clpC1 | 4040259 | p.Glu149Ala | missense_variant | 0.5 |
embC | 4241450 | p.Ser530Ala | missense_variant | 0.25 |
embC | 4242032 | p.Thr724Pro | missense_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244298 | p.Ser356Ala | missense_variant | 0.2 |
embA | 4244308 | p.Val359Ala | missense_variant | 0.2 |
embA | 4244362 | p.Asn377Thr | missense_variant | 0.22 |
embA | 4245066 | p.Phe612Ile | missense_variant | 0.29 |
embA | 4245844 | p.Val871Gly | missense_variant | 0.29 |
embB | 4246589 | p.Thr26Pro | missense_variant | 0.4 |
embB | 4246638 | p.Val42Ala | missense_variant | 0.3 |
embB | 4247039 | p.Phe176Val | missense_variant | 0.2 |
embB | 4249182 | p.His890Pro | missense_variant | 0.25 |
aftB | 4267203 | p.Lys545Met | missense_variant | 0.18 |
aftB | 4268253 | p.Leu195Arg | missense_variant | 0.27 |
aftB | 4268865 | c.-29T>G | upstream_gene_variant | 0.4 |
ethA | 4327366 | p.Glu36Asp | missense_variant | 0.29 |
ethR | 4328021 | p.Asp158Ala | missense_variant | 0.17 |
ethA | 4328324 | c.-851A>G | upstream_gene_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338676 | c.-155T>G | upstream_gene_variant | 0.25 |
gid | 4407973 | p.Val77Gly | missense_variant | 0.38 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |