Run ID: ERR4818322
Sample name:
Date: 01-04-2023 15:29:33
Number of reads: 346535
Percentage reads mapped: 89.95
Strain: lineage4.1.2.1
Drug-resistance: Other
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 | 0.96 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.86 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
mshA | 576104 | p.Arg253Ser | missense_variant | 0.25 |
rpoB | 760072 | p.Pro89Leu | missense_variant | 0.25 |
rpoB | 760106 | c.300G>A | synonymous_variant | 1.0 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 762477 | p.Lys891Glu | missense_variant | 0.4 |
rpoB | 762984 | p.Gln1060* | stop_gained | 0.25 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 767279 | p.Ala1304Thr | missense_variant | 0.18 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776585 | c.1896C>T | synonymous_variant | 0.2 |
mmpL5 | 776688 | p.Trp598* | stop_gained | 0.33 |
mmpL5 | 778299 | p.Ala61Val | missense_variant | 0.18 |
mmpS5 | 779638 | c.-733C>T | upstream_gene_variant | 0.2 |
mmpS5 | 779640 | c.-735G>C | upstream_gene_variant | 0.22 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781576 | p.Gln6Arg | missense_variant | 0.14 |
fbiC | 1303287 | c.357C>T | synonymous_variant | 0.33 |
fbiC | 1304531 | p.Ser534Leu | missense_variant | 0.33 |
fbiC | 1305025 | p.Glu699Lys | missense_variant | 0.29 |
Rv1258c | 1407137 | p.Tyr68* | stop_gained | 0.2 |
embR | 1416222 | p.Phe376Leu | missense_variant | 0.29 |
embR | 1416232 | p.Cys372Gly | missense_variant | 0.22 |
embR | 1416299 | p.Val350Glu | missense_variant | 0.22 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471850 | n.5G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472983 | n.1138A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102089 | c.954C>T | synonymous_variant | 0.5 |
ndh | 2102602 | p.Leu147Phe | missense_variant | 0.33 |
ndh | 2103117 | c.-75G>A | upstream_gene_variant | 0.29 |
PPE35 | 2169479 | c.1134C>T | synonymous_variant | 0.33 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.67 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.67 |
PPE35 | 2170213 | p.Ala134Pro | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289341 | c.-100G>T | upstream_gene_variant | 0.22 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
eis | 2714698 | p.Arg212His | missense_variant | 0.4 |
ahpC | 2726389 | p.Ala66Val | missense_variant | 0.25 |
Rv2752c | 3066150 | c.42C>T | synonymous_variant | 0.25 |
Rv2752c | 3066241 | c.-50C>T | upstream_gene_variant | 0.2 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339556 | p.Gly147Ser | missense_variant | 0.18 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiB | 3642417 | p.Thr295Ser | missense_variant | 0.2 |
alr | 3840397 | p.Cys342Ser | missense_variant | 0.18 |
alr | 3841282 | p.His47Asn | missense_variant | 0.15 |
panD | 4044275 | p.Arg3Trp | missense_variant | 0.33 |
embC | 4240369 | c.507C>T | synonymous_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4243158 | c.-75G>A | upstream_gene_variant | 0.25 |
embA | 4243184 | c.-49G>A | upstream_gene_variant | 0.18 |
embA | 4244000 | c.768G>T | synonymous_variant | 0.17 |
embB | 4248846 | c.2336delC | frameshift_variant | 0.25 |
aftB | 4267094 | c.1743G>A | synonymous_variant | 0.14 |
aftB | 4267160 | c.1677C>T | synonymous_variant | 0.11 |
aftB | 4267782 | c.1054delG | frameshift_variant | 0.2 |
aftB | 4268035 | p.Val268Leu | missense_variant | 0.25 |
aftB | 4268871 | c.-35G>T | upstream_gene_variant | 0.5 |
ethA | 4327319 | p.Gly52Glu | missense_variant | 0.25 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |