Run ID: ERR1950084
Sample name:
Date: 31-03-2023 15:39:24
Number of reads: 359207
Percentage reads mapped: 99.17
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 | 0.97 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5640 | p.Arg134Leu | missense_variant | 0.2 |
gyrB | 6270 | p.Asn344Thr | missense_variant | 0.25 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8749 | p.Leu483His | missense_variant | 0.25 |
gyrA | 9550 | p.Val750Gly | missense_variant | 0.33 |
fgd1 | 491008 | p.Thr76Pro | missense_variant | 0.29 |
fgd1 | 491232 | p.Phe150Leu | missense_variant | 0.5 |
mshA | 575293 | c.-55T>G | upstream_gene_variant | 0.3 |
mshA | 575711 | p.Lys122* | stop_gained | 0.22 |
mshA | 576561 | c.1215delG | frameshift_variant | 0.15 |
mshA | 576574 | p.Cys409Trp | missense_variant | 0.18 |
ccsA | 619702 | c.-189C>G | upstream_gene_variant | 0.5 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.33 |
rpoB | 759676 | c.-131A>T | upstream_gene_variant | 0.5 |
rpoB | 759727 | c.-80A>T | upstream_gene_variant | 0.5 |
rpoB | 760542 | p.Phe246Ile | missense_variant | 0.43 |
rpoB | 761073 | p.Glu423* | stop_gained | 0.33 |
rpoB | 761197 | p.Leu464Arg | missense_variant | 0.25 |
rpoB | 761596 | p.Asn597Thr | missense_variant | 0.18 |
rpoB | 762324 | p.Lys840* | stop_gained | 0.29 |
rpoB | 762382 | p.Val859Ala | missense_variant | 0.22 |
rpoC | 763944 | p.Asp192Ala | missense_variant | 0.18 |
rpoC | 764973 | p.Asp535Ala | missense_variant | 0.29 |
rpoC | 765776 | p.Val803Ile | missense_variant | 0.22 |
rpoC | 766098 | p.Leu910Arg | missense_variant | 0.29 |
rpoC | 766348 | p.Glu993Asp | missense_variant | 0.5 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775996 | p.Ile829Phe | missense_variant | 0.4 |
mmpL5 | 776443 | p.Phe680Val | missense_variant | 0.33 |
mmpL5 | 776847 | p.Gln545Leu | missense_variant | 0.29 |
mmpL5 | 776917 | p.Met522Leu | missense_variant | 0.29 |
mmpL5 | 776952 | p.Leu510Gln | missense_variant | 0.4 |
mmpL5 | 778047 | p.Lys145Met | missense_variant | 0.38 |
mmpL5 | 778078 | p.Thr135Pro | missense_variant | 0.5 |
mmpL5 | 779103 | c.-623T>A | upstream_gene_variant | 0.5 |
mmpR5 | 779440 | p.Ser151Thr | missense_variant | 0.29 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781674 | p.Thr39Pro | missense_variant | 0.38 |
rplC | 801249 | c.441T>G | synonymous_variant | 0.38 |
fbiC | 1302996 | c.66T>C | synonymous_variant | 0.33 |
fbiC | 1303038 | c.108T>C | synonymous_variant | 0.33 |
fbiC | 1305104 | p.Val725Ala | missense_variant | 0.18 |
Rv1258c | 1406206 | p.Thr379Ala | missense_variant | 0.5 |
Rv1258c | 1406987 | c.354G>A | synonymous_variant | 0.29 |
embR | 1417128 | p.Ser74Thr | missense_variant | 0.22 |
embR | 1417465 | c.-118A>G | upstream_gene_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472354 | n.509C>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472608 | n.763T>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472676 | n.831C>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472743 | n.898T>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474017 | n.360A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474226 | n.569A>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474331 | n.674A>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474935 | n.1278A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475035 | n.1378A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475050 | n.1393A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475556 | n.1899A>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475812 | n.2155T>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476088 | n.2431A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476757 | n.3100T>A | non_coding_transcript_exon_variant | 0.5 |
fabG1 | 1674089 | p.Val217Gly | missense_variant | 0.4 |
inhA | 1674892 | p.Asn231Tyr | missense_variant | 0.25 |
rpsA | 1833742 | p.Glu67Asp | missense_variant | 0.33 |
rpsA | 1833840 | p.Leu100Arg | missense_variant | 0.33 |
rpsA | 1834498 | c.957C>A | synonymous_variant | 0.67 |
rpsA | 1834505 | p.His322Asn | missense_variant | 0.67 |
rpsA | 1834518 | p.Leu326Arg | missense_variant | 0.5 |
tlyA | 1917915 | c.-25T>G | upstream_gene_variant | 0.2 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918013 | p.Glu25Val | missense_variant | 0.25 |
tlyA | 1918252 | p.Ala105Ser | missense_variant | 0.22 |
ndh | 2102321 | p.Val241Ala | missense_variant | 0.33 |
ndh | 2103077 | c.-35G>A | upstream_gene_variant | 0.5 |
katG | 2154866 | p.Ile416Leu | missense_variant | 0.67 |
PPE35 | 2167859 | c.2754T>G | synonymous_variant | 0.5 |
PPE35 | 2168195 | c.2418G>T | synonymous_variant | 0.29 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2168869 | p.Pro582Thr | missense_variant | 0.2 |
PPE35 | 2169352 | p.Ala421Thr | missense_variant | 0.33 |
PPE35 | 2169875 | p.Asn246Lys | missense_variant | 0.33 |
PPE35 | 2170022 | c.591T>G | synonymous_variant | 0.33 |
PPE35 | 2170047 | p.Leu189Arg | missense_variant | 0.6 |
PPE35 | 2170178 | c.435T>G | synonymous_variant | 0.43 |
PPE35 | 2170436 | c.177T>G | synonymous_variant | 0.17 |
Rv1979c | 2222631 | c.534T>A | synonymous_variant | 0.4 |
Rv1979c | 2222864 | p.Thr101Ser | missense_variant | 0.4 |
Rv1979c | 2222971 | p.Phe65Tyr | missense_variant | 0.38 |
Rv1979c | 2223084 | c.81A>T | synonymous_variant | 0.33 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289232 | p.Leu4Val | missense_variant | 0.25 |
kasA | 2518903 | c.789C>A | synonymous_variant | 0.29 |
kasA | 2518943 | p.Met277Leu | missense_variant | 0.25 |
kasA | 2519128 | c.1014G>C | synonymous_variant | 0.18 |
kasA | 2519131 | c.1017G>C | synonymous_variant | 0.18 |
kasA | 2519140 | c.1026G>C | synonymous_variant | 0.22 |
kasA | 2519143 | c.1029G>C | synonymous_variant | 0.22 |
kasA | 2519346 | p.Leu411Arg | missense_variant | 0.57 |
eis | 2714138 | p.Ala399Thr | missense_variant | 0.29 |
eis | 2714905 | p.Asp143Ala | missense_variant | 0.67 |
eis | 2715321 | c.12C>A | synonymous_variant | 0.2 |
ahpC | 2726108 | c.-85A>T | upstream_gene_variant | 0.2 |
ahpC | 2726160 | c.-33A>T | upstream_gene_variant | 0.18 |
ahpC | 2726303 | c.111T>A | synonymous_variant | 0.3 |
pepQ | 2860249 | p.Asp57Ala | missense_variant | 0.4 |
pepQ | 2860498 | c.-80A>G | upstream_gene_variant | 0.67 |
ribD | 2987053 | p.Asn72Thr | missense_variant | 0.5 |
ribD | 2987290 | p.Asp151Ala | missense_variant | 0.43 |
Rv2752c | 3064918 | p.Asn425Ile | missense_variant | 0.4 |
Rv2752c | 3065183 | p.Ser337Thr | missense_variant | 0.33 |
Rv2752c | 3065356 | p.Leu279Gln | missense_variant | 0.67 |
Rv2752c | 3065867 | p.Leu109Met | missense_variant | 0.67 |
thyX | 3068157 | c.-212T>G | upstream_gene_variant | 0.29 |
thyA | 3074543 | c.-72T>G | upstream_gene_variant | 1.0 |
ald | 3086887 | p.Val23Gly | missense_variant | 0.22 |
ald | 3087010 | p.Val64Gly | missense_variant | 0.22 |
ald | 3087382 | p.Asn188Ser | missense_variant | 0.4 |
fbiD | 3339386 | p.Asp90Val | missense_variant | 0.4 |
fprA | 3474247 | p.Asn81Tyr | missense_variant | 0.29 |
fprA | 3474418 | p.Phe138Ile | missense_variant | 0.25 |
fprA | 3474986 | p.Val327Gly | missense_variant | 0.5 |
Rv3236c | 3612531 | p.Phe196Val | missense_variant | 0.4 |
fbiA | 3640441 | c.-102T>A | upstream_gene_variant | 0.29 |
fbiA | 3640763 | p.Asp74Ala | missense_variant | 0.17 |
fbiB | 3641596 | p.Pro21His | missense_variant | 0.5 |
fbiB | 3641953 | p.Leu140Arg | missense_variant | 0.5 |
fbiB | 3642181 | p.Val216Gly | missense_variant | 0.4 |
alr | 3840583 | p.Ala280Ser | missense_variant | 0.33 |
alr | 3840852 | p.Leu190Arg | missense_variant | 0.43 |
alr | 3841122 | p.Leu100Arg | missense_variant | 0.4 |
alr | 3841376 | c.45A>T | synonymous_variant | 0.25 |
alr | 3841595 | c.-175T>A | upstream_gene_variant | 0.33 |
rpoA | 3877473 | p.Glu345Asp | missense_variant | 1.0 |
ddn | 3986943 | p.Gly34Arg | missense_variant | 0.29 |
clpC1 | 4038753 | p.Gln651Arg | missense_variant | 0.22 |
clpC1 | 4040249 | p.Glu152Asp | missense_variant | 0.33 |
panD | 4044209 | p.Ser25Ala | missense_variant | 0.36 |
embC | 4240733 | p.Thr291Pro | missense_variant | 0.5 |
embC | 4240890 | p.Trp343Leu | missense_variant | 0.25 |
embC | 4241803 | c.1941T>A | synonymous_variant | 0.33 |
embC | 4242204 | p.Leu781Gln | missense_variant | 0.67 |
embC | 4242240 | p.Asp793Ala | missense_variant | 1.0 |
embC | 4242252 | p.Asp797Ala | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244197 | p.Val322Gly | missense_variant | 0.25 |
embA | 4245421 | p.Leu730Arg | missense_variant | 0.5 |
embA | 4246291 | p.Leu1020Gln | missense_variant | 0.33 |
embB | 4247336 | p.Thr275Ala | missense_variant | 0.5 |
embB | 4247460 | p.Met316Lys | missense_variant | 0.5 |
embB | 4247597 | c.1086delG | frameshift_variant | 0.29 |
aftB | 4267062 | p.Leu592* | stop_gained | 0.4 |
aftB | 4268769 | p.Gln23Arg | missense_variant | 0.67 |
aftB | 4268952 | c.-116G>A | upstream_gene_variant | 0.33 |
ubiA | 4269327 | p.Lys169Asn | missense_variant | 0.5 |
ubiA | 4269800 | p.Asn12Tyr | missense_variant | 0.5 |
ethA | 4326059 | p.Lys472Met | missense_variant | 0.29 |
ethA | 4327203 | p.Met91Leu | missense_variant | 0.25 |
ethA | 4327386 | p.Lys30* | stop_gained | 0.4 |
ethR | 4327813 | p.Thr89Pro | missense_variant | 0.5 |
ethA | 4327911 | c.-438G>T | upstream_gene_variant | 0.29 |
whiB6 | 4338286 | p.Val79Gly | missense_variant | 0.2 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |