Run ID: ERR4821413
Sample name:
Date: 01-04-2023 17:14:28
Number of reads: 323435
Percentage reads mapped: 88.21
Strain: La3
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
La3 | M.orygis | None | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.96 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5495 | p.Val86Phe | missense_variant | 0.29 |
gyrB | 5516 | p.Ile93Val | missense_variant | 1.0 |
gyrB | 6446 | p.Ala403Ser | missense_variant | 1.0 |
gyrB | 6717 | p.Ile493Thr | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7775 | c.474C>T | synonymous_variant | 1.0 |
gyrA | 8930 | c.1629C>T | synonymous_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490661 | c.-122_-121insGCGAGC | upstream_gene_variant | 0.83 |
fgd1 | 490932 | p.His50Gln | missense_variant | 0.33 |
fgd1 | 491453 | p.Gly224Val | missense_variant | 0.33 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
fgd1 | 491749 | p.Leu323Phe | missense_variant | 1.0 |
mshA | 575347 | c.-1G>A | upstream_gene_variant | 0.14 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.38 |
rpoB | 762042 | p.Ile746Val | missense_variant | 0.5 |
rpoB | 762352 | c.2557_2562dupGACGAG | conservative_inframe_insertion | 0.83 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764420 | p.Asn351Asp | missense_variant | 0.22 |
rpoC | 765659 | p.Ala764Thr | missense_variant | 0.22 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776726 | c.1755C>T | synonymous_variant | 0.2 |
mmpL5 | 776732 | c.1749C>T | synonymous_variant | 0.18 |
mmpL5 | 776735 | c.1746C>T | synonymous_variant | 0.2 |
mmpL5 | 776738 | c.1743C>T | synonymous_variant | 0.18 |
mmpL5 | 776741 | c.1740C>G | synonymous_variant | 0.2 |
mmpL5 | 776744 | c.1735_1737delCGCinsAGG | synonymous_variant | 0.22 |
mmpL5 | 778093 | p.Trp130Gly | missense_variant | 0.38 |
mmpL5 | 778275 | p.Ala69Val | missense_variant | 0.67 |
mmpS5 | 778641 | p.Ser89Pro | missense_variant | 0.15 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781878 | p.Val107Ile | missense_variant | 0.29 |
rplC | 800701 | c.-108G>A | upstream_gene_variant | 0.22 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 1.0 |
fbiC | 1305055 | p.Met709Val | missense_variant | 0.33 |
fbiC | 1305101 | p.Asn724Ser | missense_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_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 | 1.0 |
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 | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473161 | n.1316A>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473164 | n.1319C>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1473610 | n.-48C>A | upstream_gene_variant | 0.4 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476229 | n.2572C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.67 |
inhA | 1673680 | c.-522C>G | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154134 | p.Asn660Asp | missense_variant | 0.25 |
katG | 2154567 | c.1545C>T | synonymous_variant | 0.29 |
katG | 2154707 | p.Val469Leu | missense_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155503 | c.609C>T | synonymous_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169279 | c.1312_1333delAACAATGGTGTCTTTTACCGTG | frameshift_variant | 1.0 |
PPE35 | 2169615 | p.Asn333Ser | missense_variant | 0.33 |
PPE35 | 2170669 | c.-57G>A | upstream_gene_variant | 1.0 |
Rv1979c | 2221789 | p.Val459Ala | missense_variant | 0.18 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223130 | p.His12Leu | missense_variant | 0.2 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289978 | c.-737T>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
ahpC | 2726378 | c.186T>A | synonymous_variant | 1.0 |
ahpC | 2726487 | p.Gln99Glu | missense_variant | 0.4 |
folC | 2746391 | p.Val403Ala | missense_variant | 1.0 |
folC | 2747486 | p.Trp38Ser | missense_variant | 0.33 |
Rv2752c | 3064964 | p.Ala410Ser | missense_variant | 0.67 |
Rv2752c | 3065133 | p.Asp353Glu | missense_variant | 0.25 |
Rv2752c | 3065977 | p.Asp72Val | missense_variant | 0.33 |
Rv2752c | 3067009 | c.-818A>G | upstream_gene_variant | 1.0 |
thyX | 3067223 | c.723G>A | synonymous_variant | 0.33 |
thyX | 3067812 | p.Gln45Arg | missense_variant | 1.0 |
thyX | 3067866 | p.Thr27Asn | missense_variant | 0.22 |
ald | 3086728 | c.-92C>T | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087084 | c.266delA | frameshift_variant | 1.0 |
fbiD | 3339402 | c.285C>A | synonymous_variant | 0.22 |
Rv3083 | 3448551 | c.48C>T | synonymous_variant | 0.25 |
Rv3083 | 3449167 | p.Ala222Ser | missense_variant | 0.29 |
Rv3083 | 3449359 | p.Phe286Leu | missense_variant | 0.29 |
Rv3083 | 3449435 | p.Ser311* | stop_gained | 0.29 |
Rv3083 | 3449692 | p.Leu397Met | missense_variant | 0.5 |
Rv3083 | 3449757 | p.Tyr418* | stop_gained | 0.33 |
fprA | 3473919 | c.-88A>G | upstream_gene_variant | 0.2 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474557 | p.Glu184Gly | missense_variant | 0.29 |
fprA | 3474993 | c.987G>T | synonymous_variant | 0.22 |
fprA | 3475113 | c.1107G>A | synonymous_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
fprA | 3475323 | c.1317T>C | synonymous_variant | 1.0 |
Rv3236c | 3612694 | c.423T>C | synonymous_variant | 1.0 |
fbiB | 3641584 | p.Val17Ala | missense_variant | 1.0 |
fbiB | 3641782 | p.Val83Ala | missense_variant | 0.25 |
alr | 3841468 | c.-49_-48insAGC | upstream_gene_variant | 0.33 |
alr | 3841522 | c.-102T>C | upstream_gene_variant | 0.22 |
clpC1 | 4039853 | c.852G>A | synonymous_variant | 1.0 |
embC | 4239793 | c.-70A>C | upstream_gene_variant | 0.22 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244154 | p.Thr308Ala | missense_variant | 1.0 |
embA | 4244220 | c.988C>T | synonymous_variant | 1.0 |
embA | 4244679 | p.Ala483Pro | missense_variant | 0.25 |
embA | 4244701 | p.Gly490Val | missense_variant | 0.33 |
embA | 4244783 | c.1551C>A | synonymous_variant | 0.2 |
embB | 4246864 | c.351C>T | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4248923 | p.Met804Val | missense_variant | 0.14 |
aftB | 4267635 | p.Arg401Leu | missense_variant | 0.4 |
aftB | 4268799 | c.37delG | frameshift_variant | 0.22 |
aftB | 4269351 | c.-515C>T | upstream_gene_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ethA | 4327042 | p.Asp144Asn | missense_variant | 1.0 |
ethR | 4327829 | p.Pro94Leu | missense_variant | 0.4 |
ethA | 4328211 | c.-738A>G | upstream_gene_variant | 1.0 |
whiB6 | 4338269 | p.Gly85Ser | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407800 | p.Val135Met | missense_variant | 1.0 |
gid | 4408214 | c.-12G>T | upstream_gene_variant | 0.33 |