Run ID: ERR4815754
Sample name:
Date: 01-04-2023 14:02:56
Number of reads: 5315169
Percentage reads mapped: 98.72
Strain: lineage2.2.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 1.0 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.73 | 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 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476083 | n.2426T>G | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.99 |
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 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |