Run ID: ERR4818288
Sample name:
Date: 01-04-2023 15:28:27
Number of reads: 384897
Percentage reads mapped: 95.73
Strain: lineage3
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2154205 | p.Ala636Glu | missense_variant | 0.1 | isoniazid |
katG | 2155169 | c.942delC | frameshift_variant | 0.12 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6162 | p.Ile308Thr | missense_variant | 0.2 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8283 | p.Ile328Val | missense_variant | 0.11 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575259 | c.-89G>A | upstream_gene_variant | 1.0 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.38 |
rpoB | 759615 | c.-192A>C | upstream_gene_variant | 0.18 |
rpoB | 760511 | c.705G>A | synonymous_variant | 1.0 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763911 | p.Leu181Pro | missense_variant | 0.18 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpS5 | 779647 | c.-742G>A | upstream_gene_variant | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781699 | p.Ser47* | stop_gained | 0.12 |
fbiC | 1305494 | p.Ala855Val | missense_variant | 0.17 |
atpE | 1460950 | c.-95T>C | upstream_gene_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472954 | n.1110delC | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472958 | n.1113_1114insC | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472969 | n.1125_1126delCG | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472975 | n.1130T>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472977 | n.1132G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472982 | n.1137G>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472987 | n.1141_1142insA | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472989 | n.1145A>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472996 | n.1151T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473002 | n.1157G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473004 | n.1159T>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473008 | n.1163C>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473009 | n.1164T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473026 | n.1181T>C | non_coding_transcript_exon_variant | 0.2 |
rpsA | 1834668 | p.Ala376Val | missense_variant | 1.0 |
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 | 2170096 | p.Arg173Trp | missense_variant | 0.25 |
Rv1979c | 2223060 | c.105T>A | synonymous_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726350 | p.Trp53Leu | missense_variant | 0.25 |
ahpC | 2726519 | c.327G>A | synonymous_variant | 0.17 |
folC | 2746893 | p.Arg236Cys | missense_variant | 0.25 |
Rv2752c | 3065930 | p.Gly88Trp | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474190 | p.Ser62Thr | missense_variant | 0.15 |
fbiB | 3640731 | c.-804C>T | upstream_gene_variant | 0.18 |
fbiB | 3642367 | p.Ala278Val | missense_variant | 0.15 |
alr | 3841194 | p.Arg76Leu | missense_variant | 0.12 |
clpC1 | 4039731 | p.Leu325His | missense_variant | 0.12 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
aftB | 4268003 | c.834G>A | synonymous_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |