Run ID: ERR2513354
Sample name:
Date: 31-03-2023 19:37:25
Number of reads: 629490
Percentage reads mapped: 97.7
Strain: lineage3
Drug-resistance: Sensitive
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 |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6340 | c.-962C>T | upstream_gene_variant | 0.12 |
gyrB | 7074 | p.Gly612Val | missense_variant | 0.14 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8457 | p.Glu386* | stop_gained | 0.25 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576534 | p.Gly396Val | missense_variant | 0.11 |
ccsA | 620407 | p.Pro173Ser | missense_variant | 0.13 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764303 | p.Met312Leu | missense_variant | 0.15 |
rpoC | 764608 | c.1239C>T | synonymous_variant | 0.15 |
rpoC | 765234 | p.Ala622Val | missense_variant | 0.11 |
rpoC | 766366 | c.2997C>A | synonymous_variant | 0.11 |
rpoC | 766817 | p.His1150Asn | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777678 | p.Val268Glu | missense_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781598 | c.39G>A | synonymous_variant | 1.0 |
fbiC | 1305349 | c.2419C>T | synonymous_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472148 | n.303T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472223 | n.378C>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472225 | n.380C>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472228 | n.383G>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167833 | p.Leu927Arg | missense_variant | 0.17 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
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 |
folC | 2746846 | c.753C>T | synonymous_variant | 0.11 |
pepQ | 2860431 | c.-13A>T | upstream_gene_variant | 0.12 |
ribD | 2987104 | p.Arg89His | missense_variant | 0.11 |
Rv2752c | 3065020 | p.Arg391His | missense_variant | 0.17 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568857 | c.-178C>T | upstream_gene_variant | 1.0 |
fbiB | 3642074 | c.541dupG | frameshift_variant | 0.2 |
fbiB | 3642083 | p.Tyr183* | stop_gained | 0.18 |
ddn | 3986738 | c.-106C>A | upstream_gene_variant | 0.12 |
clpC1 | 4039645 | p.His354Asp | missense_variant | 0.18 |
clpC1 | 4039654 | p.Thr351Ser | missense_variant | 0.22 |
clpC1 | 4040833 | c.-129G>A | upstream_gene_variant | 0.11 |
panD | 4044023 | c.259C>T | synonymous_variant | 1.0 |
embC | 4240655 | p.Ala265Pro | missense_variant | 0.18 |
embC | 4241652 | p.Ala597Val | missense_variant | 0.4 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244380 | p.Pro383Leu | missense_variant | 0.12 |
embA | 4244398 | p.Val389Glu | missense_variant | 0.12 |
embA | 4245438 | p.Ala736Pro | missense_variant | 0.15 |
embB | 4245518 | c.-996A>T | upstream_gene_variant | 0.18 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |