Run ID: SRR14164490
Sample name:
Date: 03-04-2023 09:53:48
Number of reads: 1059660
Percentage reads mapped: 98.84
Strain: lineage4.4.1.1
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 |
lineage4.4 | Euro-American | S;T | None | 1.0 |
lineage4.4.1 | Euro-American (S-type) | S;T | None | 1.0 |
lineage4.4.1.1 | Euro-American | S;Orphans | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2154376 | c.1735delA | frameshift_variant | 0.14 | isoniazid |
ahpC | 2726119 | c.-74G>A | upstream_gene_variant | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5846 | p.Gly203Trp | missense_variant | 0.15 |
gyrB | 7159 | p.Asp640Glu | missense_variant | 0.18 |
gyrA | 7178 | c.-124T>C | upstream_gene_variant | 0.17 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.5 |
mshA | 576365 | p.Phe340Leu | missense_variant | 0.11 |
ccsA | 620044 | p.Gly52Arg | missense_variant | 0.14 |
rpoB | 762487 | p.Pro894Leu | missense_variant | 0.11 |
rpoC | 764533 | c.1164C>T | synonymous_variant | 0.18 |
rpoC | 765812 | c.2443C>A | synonymous_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777262 | p.Thr407Ser | missense_variant | 0.14 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801427 | p.Met207Leu | missense_variant | 0.11 |
fbiC | 1304517 | c.1587C>T | synonymous_variant | 0.11 |
atpE | 1461001 | c.-44G>T | upstream_gene_variant | 0.15 |
atpE | 1461260 | c.216G>A | synonymous_variant | 0.5 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476609 | n.2952G>A | non_coding_transcript_exon_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918435 | p.Ala166Pro | missense_variant | 0.11 |
ndh | 2102990 | p.Val18Ala | missense_variant | 1.0 |
PPE35 | 2168417 | c.2196C>T | synonymous_variant | 0.17 |
PPE35 | 2168488 | p.Ile709Val | missense_variant | 0.18 |
PPE35 | 2168859 | p.Ser585Ile | missense_variant | 0.12 |
PPE35 | 2169840 | p.Gly258Asp | missense_variant | 1.0 |
PPE35 | 2170130 | c.481_482dupGT | frameshift_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289903 | c.-662C>T | upstream_gene_variant | 0.2 |
kasA | 2518808 | p.Lys232Glu | missense_variant | 0.22 |
eis | 2715394 | c.-62C>T | upstream_gene_variant | 0.14 |
ahpC | 2725926 | c.-267T>C | upstream_gene_variant | 0.12 |
folC | 2746198 | c.1401C>T | synonymous_variant | 0.13 |
ribD | 2987161 | p.Ala108Val | missense_variant | 0.12 |
ribD | 2987448 | p.Glu204Lys | missense_variant | 0.15 |
thyA | 3073880 | p.Glu198Lys | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339200 | p.Pro28Leu | missense_variant | 0.12 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.25 |
Rv3083 | 3448423 | c.-81C>G | upstream_gene_variant | 0.11 |
Rv3083 | 3448523 | p.Val7Asp | missense_variant | 0.2 |
Rv3083 | 3448608 | c.105G>A | synonymous_variant | 1.0 |
Rv3083 | 3448718 | p.Val72Gly | missense_variant | 0.12 |
Rv3083 | 3448743 | c.240G>C | synonymous_variant | 0.12 |
Rv3083 | 3449059 | p.Gly186Ser | missense_variant | 0.13 |
Rv3083 | 3449762 | p.Val420Ala | missense_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474590 | p.Val195Ala | missense_variant | 0.11 |
whiB7 | 3568682 | c.-3G>A | upstream_gene_variant | 0.13 |
whiB7 | 3568844 | c.-165C>G | upstream_gene_variant | 0.12 |
Rv3236c | 3612357 | p.Glu254Lys | missense_variant | 0.18 |
Rv3236c | 3612556 | c.561G>A | synonymous_variant | 0.14 |
Rv3236c | 3612665 | p.Val151Ala | missense_variant | 1.0 |
fbiA | 3640819 | p.Val93* | stop_gained | 0.11 |
fbiB | 3641782 | p.Val83Ala | missense_variant | 0.18 |
rpoA | 3877919 | p.Glu197Lys | missense_variant | 1.0 |
embC | 4240413 | p.Leu184Arg | missense_variant | 0.22 |
embC | 4241451 | p.Ser530Leu | missense_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243673 | c.441C>T | synonymous_variant | 0.29 |
embA | 4245461 | c.2229C>T | synonymous_variant | 1.0 |
embB | 4246903 | c.390G>T | synonymous_variant | 0.11 |
embB | 4249573 | c.3060T>G | synonymous_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407838 | p.Ser122Phe | missense_variant | 0.11 |