Run ID: ERR2513847
Sample name:
Date: 31-03-2023 19:56:44
Number of reads: 986805
Percentage reads mapped: 99.47
Strain: lineage3
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 0.99 |
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 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 0.96 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 762752 | c.-618G>T | upstream_gene_variant | 0.17 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 0.93 |
mmpL5 | 776047 | p.Leu812Met | missense_variant | 0.1 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801158 | p.Thr117Asn | missense_variant | 0.11 |
fbiC | 1303557 | c.627G>A | synonymous_variant | 1.0 |
fbiC | 1303851 | c.921C>T | synonymous_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
inhA | 1674391 | p.Asp64Tyr | missense_variant | 0.11 |
rpsA | 1834894 | c.1353C>A | synonymous_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918626 | c.687G>A | synonymous_variant | 0.11 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
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 | 0.94 |
pncA | 2289361 | c.-120G>C | upstream_gene_variant | 0.11 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 0.97 |
pepQ | 2860133 | p.Gly96Cys | missense_variant | 0.18 |
ribD | 2987498 | c.660C>T | synonymous_variant | 0.11 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339411 | c.294T>C | synonymous_variant | 0.11 |
Rv3083 | 3449095 | p.Gly198Ser | missense_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474928 | p.Gly308Ser | missense_variant | 0.11 |
fprA | 3474997 | p.Gly331Arg | missense_variant | 0.13 |
Rv3236c | 3612486 | p.Thr211Ala | missense_variant | 0.11 |
Rv3236c | 3613105 | c.12G>A | synonymous_variant | 0.12 |
alr | 3841473 | c.-53G>A | upstream_gene_variant | 0.93 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242947 | p.Gly1029Arg | missense_variant | 0.1 |
embA | 4243482 | p.Ala84Thr | missense_variant | 0.11 |
embA | 4243506 | p.Thr92Ala | missense_variant | 0.17 |
embA | 4243568 | c.336C>T | synonymous_variant | 0.18 |
embA | 4243625 | c.393C>T | synonymous_variant | 0.12 |
embA | 4243656 | p.Trp142Arg | missense_variant | 0.12 |
embA | 4244185 | p.Ser318Asn | missense_variant | 0.13 |
embA | 4244284 | p.Pro351Gln | missense_variant | 0.12 |
embB | 4249634 | p.Asp1041Tyr | missense_variant | 0.12 |
aftB | 4267623 | p.Ser405Leu | missense_variant | 0.12 |
aftB | 4267901 | c.936G>T | synonymous_variant | 0.11 |
ubiA | 4270004 | c.-171G>T | upstream_gene_variant | 0.12 |
ethA | 4328437 | c.-964G>A | upstream_gene_variant | 0.13 |
ethA | 4328445 | c.-972A>C | upstream_gene_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4408272 | c.-70C>T | upstream_gene_variant | 0.12 |