Run ID: ERR4816213
Sample name:
Date: 01-04-2023 14:18:10
Number of reads: 744865
Percentage reads mapped: 93.26
Strain: lineage3
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
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 | 575895 | p.Val183Ala | missense_variant | 0.2 |
mshA | 576517 | c.1171delT | frameshift_variant | 0.14 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 761454 | p.Glu550* | stop_gained | 0.17 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763222 | p.Ile1139Thr | missense_variant | 0.11 |
rpoC | 766585 | c.3216T>C | synonymous_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775690 | p.Ala931Thr | missense_variant | 0.13 |
mmpL5 | 775768 | p.Gln905* | stop_gained | 0.15 |
mmpL5 | 776032 | p.Gly817Trp | missense_variant | 0.1 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpS5 | 778527 | p.Thr127Ala | missense_variant | 0.1 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800917 | p.Thr37Ala | missense_variant | 0.13 |
fbiC | 1303575 | c.645G>A | synonymous_variant | 0.11 |
Rv1258c | 1406769 | p.Leu191Gln | missense_variant | 0.12 |
embR | 1416469 | c.879C>T | synonymous_variant | 0.11 |
atpE | 1461031 | c.-14A>T | upstream_gene_variant | 0.12 |
atpE | 1461179 | c.135G>T | synonymous_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476693 | n.3036G>A | non_coding_transcript_exon_variant | 0.33 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918276 | p.Val113Ile | missense_variant | 0.11 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155402 | p.Gly237Asp | missense_variant | 0.29 |
katG | 2156075 | p.Thr13Ala | missense_variant | 0.1 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.18 |
PPE35 | 2169745 | p.Ala290Thr | missense_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288729 | c.513G>A | synonymous_variant | 0.14 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ribD | 2986844 | c.6C>T | synonymous_variant | 0.12 |
ribD | 2987538 | p.Val234Met | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087917 | c.1099delG | frameshift_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612963 | p.Ala52Thr | missense_variant | 0.12 |
fbiA | 3641218 | p.Val226Phe | missense_variant | 0.17 |
fbiB | 3641828 | c.294A>T | synonymous_variant | 0.2 |
rpoA | 3878672 | c.-165A>G | upstream_gene_variant | 0.17 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embC | 4242534 | p.Phe891Ser | missense_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4249341 | p.Ala943Gly | missense_variant | 0.13 |
ethA | 4326579 | p.Gly299Ser | missense_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |