Run ID: ERR4820652
Sample name:
Date: 01-04-2023 16:48:04
Number of reads: 1682545
Percentage reads mapped: 95.23
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 | 1.0 |
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 | 0.29 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_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 |
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 |
Rv1258c | 1406294 | c.1047C>T | synonymous_variant | 1.0 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472033 | n.188A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472584 | n.739A>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472686 | n.841G>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472687 | n.843dupT | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472988 | n.1143T>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.24 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475892 | n.2235A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475897 | n.2240T>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475938 | n.2281C>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475995 | n.2338G>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475997 | n.2340A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475998 | n.2341C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476007 | n.2350T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476523 | n.2866T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476528 | n.2871A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.12 |
rpsA | 1834319 | p.Val260Ile | missense_variant | 0.98 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167983 | p.Gly877Asp | missense_variant | 0.97 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
eis | 2715028 | p.Ala102Val | missense_variant | 1.0 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 1.0 |
Rv2752c | 3065605 | p.Val196Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
rpoA | 3878630 | c.-124delC | upstream_gene_variant | 1.0 |
ddn | 3986745 | c.-99A>C | upstream_gene_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 | 4243848 | p.Val206Met | missense_variant | 1.0 |
embA | 4244096 | c.864C>T | synonymous_variant | 1.0 |
embA | 4245969 | p.Pro913Ser | missense_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 |
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 |