Run ID: ERR9030453
Sample name:
Date: 02-04-2023 09:26:51
Number of reads: 1692866
Percentage reads mapped: 99.95
Strain: lineage3.1.1
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
lineage3.1.1 | East-African-Indian | CAS1-Kili | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761082 | c.1279_1284delACCAGC | conservative_inframe_deletion | 1.0 | rifampicin |
pncA | 2289043 | p.Ser67Pro | missense_variant | 1.0 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7544 | p.Met81Ile | missense_variant | 0.15 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576286 | c.939C>A | synonymous_variant | 0.15 |
mshA | 576413 | p.Gly356Cys | missense_variant | 0.33 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoB | 762639 | p.Gly945Trp | missense_variant | 0.18 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764944 | p.His525Gln | missense_variant | 0.98 |
rpoC | 766111 | c.2742G>T | synonymous_variant | 0.17 |
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 | 1304425 | p.Leu499Met | missense_variant | 0.33 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474980 | n.1323G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475027 | n.1370G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475105 | n.1448G>T | non_coding_transcript_exon_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918090 | p.Ala51Pro | missense_variant | 0.67 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2154851 | p.Gly421Ser | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170144 | p.Gly157Trp | missense_variant | 0.15 |
PPE35 | 2170461 | p.Gly51Glu | 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 |
kasA | 2519178 | p.Ser355Leu | missense_variant | 0.17 |
eis | 2714786 | p.Arg183Ser | missense_variant | 0.13 |
eis | 2715134 | c.199C>T | synonymous_variant | 0.2 |
eis | 2715525 | c.-193G>T | upstream_gene_variant | 0.17 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
pepQ | 2859534 | c.884delG | frameshift_variant | 0.18 |
ribD | 2987342 | c.504C>T | synonymous_variant | 0.22 |
Rv2752c | 3066286 | c.-95C>A | upstream_gene_variant | 0.15 |
Rv2752c | 3067060 | c.-869C>A | upstream_gene_variant | 0.18 |
thyX | 3067421 | c.525G>T | synonymous_variant | 0.5 |
thyX | 3067592 | c.354G>T | synonymous_variant | 0.33 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339336 | c.219C>A | synonymous_variant | 0.2 |
Rv3083 | 3448387 | c.-117C>A | upstream_gene_variant | 0.15 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiB | 3641559 | p.Ala9Thr | missense_variant | 0.13 |
fbiB | 3641628 | p.Ala32Ser | missense_variant | 0.17 |
fbiB | 3642174 | p.Val214Met | missense_variant | 0.67 |
rpoA | 3878583 | c.-76C>A | upstream_gene_variant | 0.22 |
embC | 4240172 | p.Val104Met | missense_variant | 1.0 |
embC | 4241116 | c.1254C>T | synonymous_variant | 0.14 |
embC | 4241562 | p.Arg567His | missense_variant | 1.0 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embC | 4242633 | p.Pro924Leu | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243518 | p.Gly96Ser | missense_variant | 0.5 |
embA | 4243700 | c.468C>A | synonymous_variant | 0.18 |
embA | 4244192 | c.960C>T | synonymous_variant | 0.18 |
embA | 4244968 | p.Gly579Val | missense_variant | 0.15 |
embA | 4245892 | p.Ile887Thr | missense_variant | 0.11 |
embB | 4247197 | c.684C>A | synonymous_variant | 0.22 |
embB | 4248631 | c.2118G>T | synonymous_variant | 0.33 |
aftB | 4267910 | c.927G>T | synonymous_variant | 0.2 |
aftB | 4267983 | p.Arg285His | missense_variant | 0.15 |
aftB | 4268275 | p.Glu188Lys | missense_variant | 0.12 |
aftB | 4268911 | c.-75G>A | upstream_gene_variant | 0.13 |
aftB | 4268917 | c.-81C>A | upstream_gene_variant | 0.12 |
ubiA | 4268971 | p.Ala288Glu | missense_variant | 0.14 |
ubiA | 4269993 | c.-160A>G | upstream_gene_variant | 0.11 |
whiB6 | 4338257 | p.Ala89Thr | missense_variant | 0.2 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.98 |