Run ID: ERR4821368
Sample name:
Date: 01-04-2023 17:12:50
Number of reads: 342805
Percentage reads mapped: 25.45
Strain: lineage1.1.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 1.0 |
lineage1.1 | Indo-Oceanic | EAI3;EAI4;EAI5;EAI6 | RD239 | 0.99 |
lineage1.1.1 | Indo-Oceanic | EAI4;EAI5 | RD239 | 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 | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrB | 6416 | p.Thr393Ser | missense_variant | 0.67 |
gyrA | 6439 | c.-863C>G | upstream_gene_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7853 | c.552C>T | synonymous_variant | 1.0 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
ccsA | 620280 | c.390C>T | synonymous_variant | 1.0 |
ccsA | 620463 | c.573C>A | synonymous_variant | 1.0 |
rpoB | 760772 | c.966C>T | synonymous_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
rpoC | 765171 | p.Pro601Leu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800864 | c.58_66dupAGCAACAGA | conservative_inframe_insertion | 1.0 |
fbiC | 1302898 | c.-33G>A | upstream_gene_variant | 1.0 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
embR | 1417297 | c.51A>G | synonymous_variant | 0.25 |
atpE | 1461127 | p.Asp28Gly | missense_variant | 0.29 |
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 | 0.95 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473147 | n.1302G>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473150 | n.1305T>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473161 | n.1316A>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473164 | n.1319C>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473172 | n.1327T>C | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473191 | n.1346C>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473193 | n.1348G>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473204 | n.1359C>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473206 | n.1361G>C | non_coding_transcript_exon_variant | 0.38 |
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 | 0.5 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.27 |
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 | 1.0 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.33 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102044 | c.999G>T | synonymous_variant | 0.14 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167983 | p.Gly877Asp | missense_variant | 1.0 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223124 | p.Leu14Arg | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086987 | p.Gln56His | missense_variant | 1.0 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
Rv3083 | 3449262 | c.759G>A | synonymous_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474342 | c.336G>A | synonymous_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243129 | c.-104G>A | upstream_gene_variant | 1.0 |
embA | 4243848 | p.Val206Met | missense_variant | 1.0 |
embA | 4244696 | c.1464G>A | synonymous_variant | 0.2 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embA | 4246225 | p.Gly998Val | missense_variant | 1.0 |
embA | 4246441 | p.Pro1070Arg | missense_variant | 0.17 |
embB | 4247254 | c.741A>G | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ethA | 4326029 | p.Lys482Ile | missense_variant | 1.0 |
whiB6 | 4338242 | p.Gln94Glu | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |