Run ID: ERR2228903
Sample name:
Date: 31-03-2023 16:25:31
Number of reads: 318768
Percentage reads mapped: 99.15
Strain: lineage4
Drug-resistance: RR-TB
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 |
---|---|---|---|---|---|
rpoB | 761136 | p.Thr444Pro | missense_variant | 0.33 | rifampicin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5429 | p.Thr64Ser | missense_variant | 0.36 |
gyrB | 5447 | p.Leu70Phe | missense_variant | 0.22 |
gyrB | 5757 | p.Phe173Cys | missense_variant | 0.18 |
gyrB | 6013 | c.774G>T | synonymous_variant | 0.25 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7666 | p.Asp122Ala | missense_variant | 0.38 |
gyrA | 7901 | c.600G>T | synonymous_variant | 0.29 |
gyrA | 8140 | p.His280Leu | missense_variant | 0.4 |
gyrA | 8148 | p.Phe283Ile | missense_variant | 0.33 |
gyrA | 8473 | p.Leu391Gln | missense_variant | 0.33 |
mshA | 576468 | p.Val374Gly | missense_variant | 0.38 |
ccsA | 619831 | c.-60T>G | upstream_gene_variant | 0.67 |
ccsA | 620160 | c.270A>T | synonymous_variant | 0.29 |
rpoB | 760168 | p.Met121Lys | missense_variant | 0.33 |
rpoB | 760309 | p.Val168Glu | missense_variant | 0.5 |
rpoB | 761869 | p.Asp688Gly | missense_variant | 0.33 |
rpoB | 763164 | p.Lys1120* | stop_gained | 0.25 |
rpoB | 763182 | p.Cys1126Ser | missense_variant | 0.29 |
rpoC | 764332 | c.963G>A | synonymous_variant | 0.5 |
rpoC | 765826 | c.2457T>A | synonymous_variant | 0.33 |
rpoC | 765941 | p.Lys858* | stop_gained | 0.29 |
rpoC | 767225 | p.Pro1286Thr | missense_variant | 0.5 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775677 | p.Lys935Met | missense_variant | 0.25 |
mmpL5 | 776781 | p.Leu567* | stop_gained | 0.4 |
mmpL5 | 777119 | p.His454Gln | missense_variant | 0.38 |
mmpL5 | 777122 | c.1359C>T | synonymous_variant | 0.43 |
mmpL5 | 777128 | c.1353A>G | synonymous_variant | 0.38 |
mmpL5 | 777219 | p.Leu421Gln | missense_variant | 0.57 |
mmpL5 | 777223 | p.Tyr420Asn | missense_variant | 0.29 |
mmpL5 | 778325 | p.Gln52His | missense_variant | 0.22 |
mmpR5 | 779054 | p.Gln22Leu | missense_variant | 0.4 |
mmpL5 | 779100 | c.-620A>C | upstream_gene_variant | 0.5 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781535 | c.-25A>G | upstream_gene_variant | 0.4 |
rplC | 801293 | p.Lys162Met | missense_variant | 0.22 |
fbiC | 1303224 | c.294C>T | synonymous_variant | 0.18 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304581 | p.Asn551Tyr | missense_variant | 0.33 |
Rv1258c | 1406559 | p.Gly261Asp | missense_variant | 0.5 |
embR | 1416337 | c.1011C>T | synonymous_variant | 0.33 |
atpE | 1461075 | p.Ile11Phe | missense_variant | 0.29 |
atpE | 1461286 | p.Lys81Met | missense_variant | 0.33 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473150 | n.1305T>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473255 | n.1410A>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473362 | n.1517C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475812 | n.2155T>A | non_coding_transcript_exon_variant | 0.5 |
rpsA | 1833728 | p.Ile63Leu | missense_variant | 0.33 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102132 | p.Gln304Leu | missense_variant | 0.4 |
ndh | 2102184 | p.Arg287Trp | missense_variant | 0.5 |
ndh | 2102919 | c.124C>T | synonymous_variant | 0.22 |
katG | 2154373 | p.Asp580Ala | missense_variant | 0.4 |
katG | 2155298 | p.Phe272Ile | missense_variant | 0.22 |
katG | 2156177 | c.-66T>A | upstream_gene_variant | 0.5 |
PPE35 | 2167813 | c.2798_2799delAC | frameshift_variant | 0.29 |
PPE35 | 2167919 | c.2694T>C | synonymous_variant | 0.22 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 0.2 |
PPE35 | 2168657 | c.1956T>A | synonymous_variant | 0.33 |
PPE35 | 2168665 | p.Thr650Ser | missense_variant | 0.33 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169476 | c.1137C>A | synonymous_variant | 0.22 |
PPE35 | 2169751 | p.Gly288* | stop_gained | 0.27 |
PPE35 | 2170035 | p.Val193Gly | missense_variant | 0.2 |
Rv1979c | 2222876 | p.Thr97Pro | missense_variant | 0.5 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289305 | c.-64T>A | upstream_gene_variant | 0.25 |
pncA | 2289306 | c.-65A>T | upstream_gene_variant | 0.25 |
pncA | 2290020 | c.-779T>A | upstream_gene_variant | 0.43 |
kasA | 2518695 | p.Val194Gly | missense_variant | 0.22 |
kasA | 2518823 | p.Phe237Val | missense_variant | 0.25 |
eis | 2715098 | p.Thr79Pro | missense_variant | 0.67 |
eis | 2715399 | c.-67T>A | upstream_gene_variant | 0.22 |
ahpC | 2726303 | c.111T>A | synonymous_variant | 0.43 |
ahpC | 2726521 | p.Met110Lys | missense_variant | 0.5 |
ahpC | 2726678 | c.486G>A | synonymous_variant | 0.18 |
pepQ | 2859730 | p.His230Leu | missense_variant | 0.75 |
ribD | 2986912 | p.Asp25Ala | missense_variant | 0.67 |
ribD | 2987417 | p.Glu193Asp | missense_variant | 0.5 |
Rv2752c | 3065645 | p.Thr183Pro | missense_variant | 0.4 |
Rv2752c | 3065732 | p.Leu154Val | missense_variant | 0.33 |
Rv2752c | 3066334 | c.-143T>G | upstream_gene_variant | 0.33 |
thyX | 3067839 | p.Val36Gly | missense_variant | 0.3 |
ald | 3086771 | c.-49T>A | upstream_gene_variant | 0.4 |
ald | 3086862 | c.43C>A | synonymous_variant | 0.2 |
ald | 3087161 | c.342A>T | synonymous_variant | 0.4 |
fbiD | 3339233 | p.Val39Gly | missense_variant | 0.5 |
fbiD | 3339431 | p.Glu105Val | missense_variant | 0.5 |
fprA | 3475370 | p.Leu455Arg | missense_variant | 0.5 |
whiB7 | 3568561 | p.Lys40Met | missense_variant | 0.33 |
Rv3236c | 3612893 | p.Leu75Gln | missense_variant | 0.29 |
Rv3236c | 3612950 | p.Glu56Val | missense_variant | 0.4 |
Rv3236c | 3612962 | p.Ala52Asp | missense_variant | 0.25 |
fbiA | 3641240 | p.Leu233Trp | missense_variant | 0.5 |
fbiB | 3641959 | p.Val142Gly | missense_variant | 0.22 |
fbiB | 3642658 | p.Val375Gly | missense_variant | 0.25 |
fbiB | 3642677 | c.1143A>C | synonymous_variant | 0.25 |
alr | 3840758 | p.Gln221His | missense_variant | 0.18 |
alr | 3841423 | c.-3T>G | upstream_gene_variant | 0.29 |
ddn | 3987066 | p.Val75Phe | missense_variant | 0.22 |
clpC1 | 4039069 | p.Ser546Ala | missense_variant | 0.38 |
clpC1 | 4039443 | p.Leu421Gln | missense_variant | 1.0 |
embC | 4240489 | c.627A>C | synonymous_variant | 0.43 |
embC | 4242147 | p.Asn762Thr | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243276 | p.Leu15Gln | missense_variant | 0.25 |
embA | 4244427 | p.Ser399Ala | missense_variant | 0.25 |
embA | 4244772 | p.Ser514Ala | missense_variant | 0.33 |
embA | 4245457 | p.Glu742Ala | missense_variant | 0.4 |
embA | 4245541 | p.Val770Gly | missense_variant | 1.0 |
embA | 4245649 | p.Ile806Thr | missense_variant | 0.67 |
embA | 4245702 | p.Ser824Ala | missense_variant | 1.0 |
embA | 4245894 | p.Tyr888Asn | missense_variant | 0.4 |
embB | 4246814 | p.Thr101Ala | missense_variant | 0.4 |
embB | 4246911 | p.Leu133* | stop_gained | 0.25 |
embB | 4246917 | p.Val135Glu | missense_variant | 0.33 |
embB | 4249356 | p.Val948Gly | missense_variant | 0.33 |
aftB | 4268236 | p.Leu201Val | missense_variant | 0.33 |
ethA | 4327086 | p.Thr130Pro | missense_variant | 0.5 |
ethR | 4327841 | p.Asp98Ala | missense_variant | 0.5 |
whiB6 | 4338261 | c.261G>C | synonymous_variant | 1.0 |
whiB6 | 4338286 | p.Val79Gly | missense_variant | 0.18 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407863 | p.Ile114Leu | missense_variant | 0.5 |
gid | 4407924 | c.279G>T | synonymous_variant | 0.33 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |