Run ID: ERR4817111
Sample name:
Date: 01-04-2023 14:48:37
Number of reads: 886739
Percentage reads mapped: 99.61
Strain: lineage4.1.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5867 | p.Asp210Tyr | missense_variant | 0.12 |
gyrB | 5987 | p.Thr250Ala | missense_variant | 0.17 |
gyrB | 6194 | p.Gly319Cys | missense_variant | 0.11 |
gyrB | 6200 | p.Arg321Cys | missense_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8742 | p.Asp481His | missense_variant | 0.17 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490717 | c.-66C>G | upstream_gene_variant | 0.11 |
fgd1 | 491142 | c.360C>A | synonymous_variant | 0.14 |
fgd1 | 491282 | p.Asp167Val | missense_variant | 0.13 |
fgd1 | 491322 | c.540G>A | synonymous_variant | 0.12 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
ccsA | 619830 | c.-61G>T | upstream_gene_variant | 0.11 |
ccsA | 620270 | p.Val127Asp | missense_variant | 0.12 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 761285 | c.1479G>T | synonymous_variant | 0.13 |
rpoC | 763886 | c.517C>A | synonymous_variant | 0.12 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 766368 | p.Ala1000Asp | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpS5 | 778593 | p.Ala105Ser | missense_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303924 | p.Gln332* | stop_gained | 0.13 |
Rv1258c | 1406999 | c.342C>T | synonymous_variant | 0.12 |
Rv1258c | 1407371 | c.-31C>A | upstream_gene_variant | 0.12 |
embR | 1416770 | p.Glu193Gly | missense_variant | 0.11 |
embR | 1417540 | c.-193C>T | upstream_gene_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472562 | n.717C>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473281 | n.1436C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473292 | n.1447G>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476448 | n.2791G>T | non_coding_transcript_exon_variant | 0.4 |
fabG1 | 1673719 | p.Asp94Tyr | missense_variant | 0.22 |
tlyA | 1917882 | c.-58G>A | upstream_gene_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918210 | p.Ala91Thr | missense_variant | 0.14 |
tlyA | 1918311 | p.Asn124Lys | missense_variant | 0.14 |
ndh | 2101747 | c.1296C>T | synonymous_variant | 0.12 |
ndh | 2102506 | c.537C>T | synonymous_variant | 1.0 |
katG | 2154165 | c.1947C>A | synonymous_variant | 0.11 |
PPE35 | 2167673 | c.2940G>T | synonymous_variant | 0.11 |
PPE35 | 2168446 | p.Pro723Ala | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288746 | p.Asp166His | missense_variant | 0.14 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2518883 | p.Arg257Cys | missense_variant | 0.17 |
folC | 2746586 | p.Arg338Leu | missense_variant | 0.14 |
folC | 2746780 | c.819C>A | synonymous_variant | 0.13 |
folC | 2747756 | c.-158G>T | upstream_gene_variant | 0.15 |
ribD | 2987200 | p.Thr121Asn | missense_variant | 0.11 |
Rv2752c | 3064756 | p.Val479Ala | missense_variant | 0.17 |
thyA | 3073712 | p.His254Asn | missense_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448368 | c.-136C>G | upstream_gene_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568568 | p.Val38Ile | missense_variant | 0.12 |
Rv3236c | 3612037 | c.1080C>T | synonymous_variant | 0.18 |
Rv3236c | 3612255 | p.Val288Ile | missense_variant | 0.12 |
fbiB | 3641710 | p.Arg59Leu | missense_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4245786 | p.Ala852Thr | missense_variant | 1.0 |
embB | 4247795 | p.Leu428Phe | missense_variant | 0.11 |
aftB | 4268991 | c.-155C>T | upstream_gene_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |