Run ID: ERR2229693
Sample name:
Date: 31-03-2023 17:26:29
Number of reads: 543621
Percentage reads mapped: 99.14
Strain: lineage4
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 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2154921 | p.Trp397* | stop_gained | 0.17 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5724 | p.Ala162Val | missense_variant | 0.18 |
gyrB | 6219 | p.Val327Ala | missense_variant | 0.18 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8462 | c.1161A>G | synonymous_variant | 0.2 |
gyrA | 9054 | p.Pro585Thr | missense_variant | 0.12 |
ccsA | 620667 | p.Trp259Cys | missense_variant | 0.18 |
ccsA | 620795 | p.Ala302Asp | missense_variant | 0.17 |
rpoB | 759939 | p.Pro45Ser | missense_variant | 0.17 |
rpoC | 764460 | p.Glu364Val | missense_variant | 0.17 |
rpoC | 765635 | p.Val756Phe | missense_variant | 0.22 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776361 | p.Gln707Arg | missense_variant | 0.14 |
mmpL5 | 777091 | p.Val464Leu | missense_variant | 0.2 |
mmpR5 | 779237 | p.Leu83Arg | missense_variant | 0.25 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781438 | c.-122A>T | upstream_gene_variant | 0.17 |
rpsL | 781758 | p.Ile67Val | missense_variant | 0.15 |
fbiC | 1303509 | c.579G>T | synonymous_variant | 0.22 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
Rv1258c | 1406514 | p.Leu276Pro | missense_variant | 0.5 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473542 | n.-116C>A | upstream_gene_variant | 0.17 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.39 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103173 | c.-132delG | upstream_gene_variant | 0.2 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.22 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.25 |
PPE35 | 2168475 | p.Pro713Gly | missense_variant | 0.12 |
PPE35 | 2168482 | p.Val711Leu | missense_variant | 0.15 |
PPE35 | 2168596 | p.Phe673Leu | missense_variant | 0.12 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169044 | c.1569G>C | synonymous_variant | 0.25 |
PPE35 | 2169269 | c.1344A>G | synonymous_variant | 0.17 |
PPE35 | 2169272 | c.1341C>G | synonymous_variant | 0.17 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.18 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.18 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.18 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.14 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.62 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.64 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288992 | p.Ser84Gly | missense_variant | 0.17 |
kasA | 2518606 | c.492G>C | synonymous_variant | 0.4 |
kasA | 2518609 | p.Met165Ile | missense_variant | 0.4 |
kasA | 2519220 | p.Pro369Gln | missense_variant | 0.4 |
kasA | 2519240 | p.Pro376Thr | missense_variant | 0.25 |
eis | 2715175 | p.Gly53Asp | missense_variant | 0.18 |
ahpC | 2725938 | c.-255_-254insA | upstream_gene_variant | 0.14 |
ahpC | 2726470 | c.281dupT | frameshift_variant | 0.15 |
ribD | 2986702 | c.-137G>T | upstream_gene_variant | 0.17 |
ribD | 2986703 | c.-136A>T | upstream_gene_variant | 0.18 |
Rv2752c | 3064896 | c.1296T>C | synonymous_variant | 0.29 |
Rv2752c | 3065438 | p.Ala252Thr | missense_variant | 0.15 |
thyX | 3068023 | c.-78C>T | upstream_gene_variant | 0.25 |
thyA | 3073881 | c.591C>T | synonymous_variant | 0.15 |
ald | 3086673 | c.-147G>T | upstream_gene_variant | 0.18 |
fprA | 3474626 | p.Phe207Ser | missense_variant | 0.29 |
fprA | 3475061 | p.Pro352His | missense_variant | 0.29 |
Rv3236c | 3612623 | p.Tyr165Phe | missense_variant | 0.29 |
fbiB | 3640872 | c.-663C>T | upstream_gene_variant | 0.4 |
fbiB | 3642807 | p.Ala425Ser | missense_variant | 0.22 |
alr | 3840948 | p.Val158Ala | missense_variant | 0.25 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.19 |
ddn | 3987017 | p.Gln58His | missense_variant | 0.17 |
ddn | 3987205 | p.Glu121Gly | missense_variant | 0.13 |
clpC1 | 4040137 | p.Val190Ile | missense_variant | 0.14 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.13 |
embC | 4241728 | p.Phe622Leu | missense_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242648 | p.Leu929Arg | missense_variant | 0.29 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.6 |
embB | 4247046 | p.Asp178Ala | missense_variant | 0.5 |
aftB | 4268045 | p.Tyr264* | stop_gained | 0.2 |
ethA | 4326340 | c.1134C>A | synonymous_variant | 0.14 |
ethA | 4326394 | c.1080A>G | synonymous_variant | 0.25 |
ethA | 4328240 | c.-767T>C | upstream_gene_variant | 0.14 |
ethA | 4328458 | c.-985C>T | upstream_gene_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408204 | c.-2T>C | upstream_gene_variant | 0.18 |