Run ID: ERR4818306
Sample name:
Date: 01-04-2023 15:29:06
Number of reads: 628101
Percentage reads mapped: 99.63
Strain: lineage3
Drug-resistance: Other
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 |
---|---|---|---|---|
gyrB | 5224 | c.-15_-12delGAGA | upstream_gene_variant | 0.14 |
gyrB | 6276 | p.Thr346Ile | missense_variant | 1.0 |
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 | 490717 | c.-66C>T | upstream_gene_variant | 1.0 |
fgd1 | 490738 | c.-45C>G | upstream_gene_variant | 0.17 |
fgd1 | 491383 | p.Glu201* | stop_gained | 0.22 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576000 | p.Asp218Gly | missense_variant | 0.1 |
mshA | 576226 | c.879G>C | synonymous_variant | 0.11 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 761501 | c.1698delC | frameshift_variant | 0.18 |
rpoB | 761671 | p.Thr622Ile | missense_variant | 0.11 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoB | 762505 | p.Phe900Ser | missense_variant | 0.22 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764889 | p.Leu507Ser | missense_variant | 0.13 |
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 |
fbiC | 1303485 | c.555C>A | synonymous_variant | 0.15 |
fbiC | 1303776 | p.Lys282Asn | missense_variant | 0.15 |
fbiC | 1303851 | c.921C>T | synonymous_variant | 0.2 |
fbiC | 1303854 | c.924T>C | synonymous_variant | 0.2 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918474 | p.Pro179Ala | missense_variant | 0.12 |
katG | 2153949 | c.2163G>C | synonymous_variant | 0.13 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155622 | p.Leu164Met | missense_variant | 0.11 |
PPE35 | 2167869 | p.Gly915Val | missense_variant | 0.5 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168685 | p.Thr643Asn | missense_variant | 0.18 |
Rv1979c | 2222201 | p.Gly322Arg | missense_variant | 0.18 |
Rv1979c | 2222265 | p.Phe300Leu | missense_variant | 0.17 |
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 |
pncA | 2289433 | c.-192C>T | upstream_gene_variant | 0.13 |
eis | 2714498 | c.834delG | frameshift_variant | 0.22 |
eis | 2715265 | p.Ser23Thr | missense_variant | 0.12 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
pepQ | 2859342 | c.1077G>A | synonymous_variant | 0.13 |
pepQ | 2860219 | p.Gln67Leu | missense_variant | 0.17 |
thyX | 3067999 | c.-54G>C | upstream_gene_variant | 0.1 |
thyA | 3074418 | c.54A>G | synonymous_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087254 | c.435C>T | synonymous_variant | 0.29 |
Rv3083 | 3449820 | c.1317G>T | synonymous_variant | 0.25 |
fprA | 3473820 | c.-187C>A | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612998 | p.Gly40Asp | missense_variant | 0.15 |
Rv3236c | 3613137 | c.-22delA | upstream_gene_variant | 0.15 |
fbiB | 3642517 | p.Ala328Asp | missense_variant | 0.11 |
fbiB | 3642830 | c.1296G>A | synonymous_variant | 1.0 |
alr | 3840672 | p.Leu250Pro | missense_variant | 0.17 |
clpC1 | 4040626 | p.Tyr27His | missense_variant | 0.14 |
embC | 4239720 | c.-142_-141delCC | upstream_gene_variant | 0.12 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245234 | c.2003delT | frameshift_variant | 0.11 |
aftB | 4268352 | c.482_484delCGC | disruptive_inframe_deletion | 0.15 |
ubiA | 4269307 | p.Phe176Ser | missense_variant | 0.14 |
ethA | 4326958 | p.Asp172Glu | missense_variant | 0.29 |
ethR | 4327858 | p.Arg104Ser | missense_variant | 0.2 |
ethA | 4328417 | c.-944G>T | upstream_gene_variant | 0.11 |
ethA | 4328457 | c.-984C>T | upstream_gene_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |