Run ID: ERR4815984
Sample name:
Date: 01-04-2023 14:10:35
Number of reads: 590352
Percentage reads mapped: 97.39
Strain: lineage4.3.2
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.2 | Euro-American (LAM) | LAM3 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.64 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7428 | c.128delA | frameshift_variant | 0.12 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491008 | c.231delC | frameshift_variant | 0.29 |
mshA | 575332 | c.-16T>C | upstream_gene_variant | 0.14 |
ccsA | 620766 | c.876C>A | synonymous_variant | 0.15 |
rpoB | 762123 | p.Glu773Lys | missense_variant | 0.15 |
rpoC | 763794 | p.Glu142Gly | missense_variant | 0.17 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775973 | c.2508G>A | synonymous_variant | 0.22 |
mmpL5 | 776023 | p.Val820Leu | missense_variant | 0.17 |
mmpR5 | 778007 | c.-983G>A | upstream_gene_variant | 0.18 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801378 | c.570C>T | synonymous_variant | 0.13 |
fbiC | 1303723 | p.Glu265* | stop_gained | 0.13 |
Rv1258c | 1406534 | c.807C>A | synonymous_variant | 0.2 |
Rv1258c | 1407443 | c.-103C>T | upstream_gene_variant | 0.17 |
embR | 1416495 | p.Gly285Cys | missense_variant | 0.12 |
atpE | 1460931 | c.-114A>T | upstream_gene_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 1.0 |
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 | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.92 |
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 | 1.0 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1834390 | c.849G>A | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102778 | p.Val89Phe | missense_variant | 0.11 |
katG | 2155687 | p.Asp142Gly | missense_variant | 0.2 |
PPE35 | 2169415 | p.Gly400Cys | missense_variant | 0.15 |
Rv1979c | 2222798 | p.Pro123Thr | missense_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518979 | p.Arg289Trp | missense_variant | 0.14 |
ahpC | 2726084 | c.-109C>A | upstream_gene_variant | 0.12 |
folC | 2747068 | p.Met177Ile | missense_variant | 0.12 |
folC | 2747325 | p.Arg92Ser | missense_variant | 0.12 |
ribD | 2987033 | c.195C>T | synonymous_variant | 0.2 |
ribD | 2987296 | p.Arg153His | missense_variant | 0.15 |
Rv2752c | 3065753 | p.Asn147Tyr | missense_variant | 0.14 |
Rv2752c | 3066164 | p.Pro10Ser | missense_variant | 0.11 |
Rv2752c | 3066998 | c.-807G>A | upstream_gene_variant | 0.11 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087803 | c.984C>A | synonymous_variant | 0.12 |
ald | 3087865 | p.Ala349Val | missense_variant | 0.11 |
fbiD | 3339017 | c.-101C>A | upstream_gene_variant | 0.11 |
Rv3083 | 3448484 | c.-20T>G | upstream_gene_variant | 0.1 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474545 | p.Asp180Val | missense_variant | 0.13 |
fbiB | 3641175 | c.-360G>T | upstream_gene_variant | 0.29 |
fbiB | 3641639 | c.105G>A | synonymous_variant | 0.13 |
fbiB | 3642577 | p.Val348Ala | missense_variant | 0.11 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4038588 | p.Arg706Phe | missense_variant | 0.17 |
embC | 4240279 | p.Leu139Phe | missense_variant | 0.22 |
embC | 4240841 | p.Tyr327His | missense_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245131 | c.1899G>A | synonymous_variant | 1.0 |
embA | 4245280 | p.Arg683His | missense_variant | 0.18 |
embA | 4246348 | p.Thr1039Ile | missense_variant | 0.14 |
embB | 4249386 | p.Glu958Ala | missense_variant | 1.0 |
embB | 4249412 | p.Arg967Trp | missense_variant | 0.15 |
aftB | 4267214 | c.1623A>G | synonymous_variant | 0.1 |
aftB | 4267249 | p.Lys530Glu | missense_variant | 0.12 |
aftB | 4268133 | p.Leu235Pro | missense_variant | 0.12 |
ubiA | 4269239 | p.Ala199Thr | missense_variant | 0.25 |
ubiA | 4269259 | p.Arg192Leu | missense_variant | 0.25 |
ethA | 4326678 | p.Ser266Gly | missense_variant | 0.12 |
ethR | 4326679 | c.-870C>A | upstream_gene_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |