Run ID: ERR2179858
Sample name:
Date: 15-08-2022 11:57:28
Number of reads: 1323248
Percentage reads mapped: 72.32
Strain: lineage3
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 0.98 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
tlyA | 1918524 | c.589delG | frameshift_variant | 0.22 | capreomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5878 | c.639G>T | synonymous_variant | 0.17 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9385 | p.Arg695His | missense_variant | 0.13 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
ccsA | 620187 | c.297C>T | synonymous_variant | 0.18 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 767229 | p.Ser1287Leu | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777451 | p.Val344Ile | missense_variant | 0.18 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303377 | p.Asp149Glu | missense_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475658 | n.2001G>A | non_coding_transcript_exon_variant | 0.13 |
ndh | 2102038 | c.1004delG | frameshift_variant | 0.15 |
ndh | 2102233 | c.810G>A | synonymous_variant | 1.0 |
ndh | 2102875 | c.168C>T | synonymous_variant | 0.18 |
katG | 2155588 | p.Ser175Leu | missense_variant | 0.18 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 0.94 |
Rv1979c | 2221992 | c.1173C>A | synonymous_variant | 0.13 |
Rv1979c | 2222024 | p.Ala381Thr | missense_variant | 0.18 |
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 | 2289651 | c.-410T>C | upstream_gene_variant | 0.17 |
pncA | 2289909 | c.-668G>A | upstream_gene_variant | 0.15 |
eis | 2714318 | p.Arg339Trp | missense_variant | 0.18 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
folC | 2747168 | p.Lys144Thr | missense_variant | 0.13 |
ribD | 2987503 | p.Gly222Asp | missense_variant | 0.18 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087096 | p.Thr93Ala | missense_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474684 | p.Asp226Glu | missense_variant | 0.18 |
fprA | 3474842 | p.Lys279Thr | missense_variant | 0.15 |
Rv3236c | 3612074 | p.Ile348Thr | missense_variant | 0.12 |
fbiB | 3641400 | c.-135C>T | upstream_gene_variant | 0.17 |
rpoA | 3877797 | c.711G>A | synonymous_variant | 0.12 |
clpC1 | 4038634 | p.Glu691* | stop_gained | 0.2 |
clpC1 | 4040753 | c.-49G>A | upstream_gene_variant | 1.0 |
embC | 4239870 | p.Thr3Ile | missense_variant | 0.13 |
embC | 4241231 | p.Arg457Trp | missense_variant | 0.2 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4243545 | p.Leu105Met | missense_variant | 0.14 |
embB | 4246268 | c.-246G>A | upstream_gene_variant | 0.13 |
aftB | 4268511 | p.Ser109Asn | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |