Run ID: ERR2513058
Sample name:
Date: 31-03-2023 19:26:27
Number of reads: 5783888
Percentage reads mapped: 99.66
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 | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9318 | p.Leu673Val | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575283 | c.-65C>G | upstream_gene_variant | 1.0 |
mshA | 575325 | c.-23G>A | upstream_gene_variant | 0.14 |
mshA | 575397 | p.Arg17His | missense_variant | 0.18 |
mshA | 576581 | p.Pro412Ser | missense_variant | 0.14 |
ccsA | 619999 | p.Ala37Thr | missense_variant | 0.17 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 0.99 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 762719 | c.-651C>T | upstream_gene_variant | 0.15 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
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 | 1304437 | p.Glu503Lys | missense_variant | 0.22 |
embR | 1416814 | c.534G>A | synonymous_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1917992 | p.Arg18Gln | missense_variant | 0.33 |
tlyA | 1918120 | p.Ala61Thr | missense_variant | 0.17 |
tlyA | 1918207 | p.Gly90Cys | missense_variant | 0.18 |
tlyA | 1918217 | p.Thr93Ile | missense_variant | 0.12 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170453 | p.Gly54Ser | missense_variant | 0.12 |
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 |
kasA | 2518654 | c.540C>T | synonymous_variant | 0.13 |
kasA | 2518677 | p.Gly188Asp | missense_variant | 0.12 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
pepQ | 2860146 | c.273C>T | synonymous_variant | 0.67 |
thyX | 3067483 | p.Ala155Pro | missense_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474966 | c.960G>A | synonymous_variant | 0.14 |
whiB7 | 3568857 | c.-178C>T | upstream_gene_variant | 1.0 |
fbiB | 3641990 | p.Met152Ile | missense_variant | 0.25 |
fbiB | 3642005 | c.471C>A | synonymous_variant | 0.22 |
fbiB | 3642074 | c.540C>T | synonymous_variant | 0.14 |
fbiB | 3642163 | p.Thr210Ile | missense_variant | 0.12 |
fbiB | 3642239 | c.705G>A | synonymous_variant | 0.2 |
panD | 4044023 | c.259C>T | synonymous_variant | 1.0 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243948 | p.Arg239Gln | missense_variant | 0.12 |
embA | 4244575 | p.Ala448Glu | missense_variant | 0.29 |
embB | 4246731 | p.Ser73Leu | missense_variant | 0.4 |
embB | 4246739 | p.Pro76Ser | missense_variant | 0.25 |
embB | 4246751 | p.Thr80Ala | missense_variant | 0.25 |
embB | 4247060 | p.Pro183Ser | missense_variant | 0.12 |
embB | 4247855 | p.Gly448Ser | missense_variant | 0.4 |
embB | 4247870 | p.Ala453Thr | missense_variant | 0.67 |
embB | 4247889 | p.Gly459Asp | missense_variant | 0.33 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |