Run ID: ERR2229429
Sample name:
Date: 31-03-2023 17:10:48
Number of reads: 351914
Percentage reads mapped: 99.41
Strain: lineage4.8
Drug-resistance: HR-TB
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 |
---|---|---|---|---|---|
katG | 2154859 | p.Arg418Gln | missense_variant | 0.29 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8689 | p.Ala463Val | missense_variant | 0.25 |
gyrA | 9666 | p.Arg789Ser | missense_variant | 0.17 |
rpoB | 759670 | c.-137C>T | upstream_gene_variant | 0.2 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.25 |
rpoC | 765075 | p.Ala569Val | missense_variant | 0.22 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777246 | p.Arg412Gln | missense_variant | 0.4 |
mmpL5 | 777499 | p.Arg328Gly | missense_variant | 0.25 |
mmpL5 | 778933 | c.-453G>T | upstream_gene_variant | 0.18 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781692 | p.Pro45Ser | missense_variant | 0.29 |
fbiC | 1303343 | p.Phe138Ser | missense_variant | 0.17 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304490 | c.1560C>T | synonymous_variant | 0.33 |
fbiC | 1304578 | p.Arg550Gly | missense_variant | 0.33 |
embR | 1417271 | p.Thr26Ile | missense_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472125 | n.280G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.12 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.2 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.21 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.21 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.21 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102401 | c.642T>C | synonymous_variant | 0.17 |
katG | 2156362 | c.-251C>A | upstream_gene_variant | 0.13 |
PPE35 | 2167745 | p.Thr956Arg | missense_variant | 0.17 |
PPE35 | 2167865 | c.2748G>C | synonymous_variant | 0.22 |
PPE35 | 2167868 | c.2745A>C | synonymous_variant | 0.2 |
PPE35 | 2168568 | p.Thr682Lys | missense_variant | 0.12 |
PPE35 | 2168640 | p.Ile658Thr | missense_variant | 0.12 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169044 | c.1569G>C | synonymous_variant | 0.25 |
PPE35 | 2169145 | p.Val490Leu | missense_variant | 0.17 |
PPE35 | 2169365 | p.Ser416Asn | missense_variant | 0.18 |
PPE35 | 2169488 | c.1125G>C | synonymous_variant | 0.15 |
PPE35 | 2169491 | c.1122T>C | synonymous_variant | 0.15 |
PPE35 | 2169581 | c.1032C>G | synonymous_variant | 0.12 |
PPE35 | 2169587 | c.1026G>A | synonymous_variant | 0.13 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.17 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.15 |
PPE35 | 2170159 | p.Ala152Ser | missense_variant | 0.13 |
PPE35 | 2170463 | c.150C>T | synonymous_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289967 | c.-726C>T | upstream_gene_variant | 0.2 |
pncA | 2289993 | c.-752C>T | upstream_gene_variant | 0.2 |
kasA | 2518064 | c.-51G>T | upstream_gene_variant | 0.17 |
ahpC | 2726591 | c.399C>A | synonymous_variant | 0.12 |
Rv2752c | 3064908 | c.1284C>T | synonymous_variant | 0.2 |
Rv2752c | 3066132 | c.60G>T | synonymous_variant | 0.29 |
thyA | 3073919 | p.Thr185Pro | missense_variant | 0.25 |
ald | 3086644 | c.-176G>A | upstream_gene_variant | 0.2 |
ald | 3086765 | c.-55G>T | upstream_gene_variant | 0.13 |
fprA | 3475230 | p.Asp408Glu | missense_variant | 0.4 |
fprA | 3475297 | c.1291C>A | synonymous_variant | 0.25 |
Rv3236c | 3612324 | p.Pro265Thr | missense_variant | 0.18 |
fbiB | 3640558 | c.-977C>T | upstream_gene_variant | 0.25 |
alr | 3841416 | p.Lys2Ile | missense_variant | 0.22 |
rpoA | 3878189 | p.Ala107Thr | missense_variant | 0.13 |
ddn | 3986814 | c.-30T>A | upstream_gene_variant | 0.12 |
clpC1 | 4038752 | c.1953G>A | synonymous_variant | 0.18 |
clpC1 | 4040402 | p.Asn101Lys | missense_variant | 0.2 |
panD | 4044208 | p.Ser25* | stop_gained | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4247028 | p.Leu172Arg | missense_variant | 0.33 |
embB | 4249279 | c.2766C>T | synonymous_variant | 0.17 |
aftB | 4266991 | p.Asp616Tyr | missense_variant | 0.22 |
aftB | 4267280 | p.Glu519Asp | missense_variant | 0.2 |
aftB | 4267310 | c.1527G>C | synonymous_variant | 0.18 |
ubiA | 4269430 | p.Gln135Arg | missense_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407982 | p.Leu74Ser | missense_variant | 0.15 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |