Run ID: SRR14088361
Sample name:
Date: 03-04-2023 09:45:36
Number of reads: 807300
Percentage reads mapped: 99.54
Strain: lineage3.1
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
lineage3.1 | East-African-Indian | Non-CAS1-Delhi | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761110 | p.Asp435Gly | missense_variant | 1.0 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
embB | 4247431 | p.Met306Ile | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6658 | c.-644G>A | upstream_gene_variant | 0.11 |
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 |
mshA | 576751 | p.Lys468Asn | missense_variant | 0.25 |
ccsA | 620092 | c.202C>A | synonymous_variant | 0.14 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 761277 | p.Ile491Leu | missense_variant | 1.0 |
rpoB | 762259 | p.Ile818Thr | missense_variant | 0.11 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 766917 | p.Arg1183Leu | missense_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775736 | c.2745C>G | synonymous_variant | 0.12 |
mmpL5 | 776003 | c.2478C>T | synonymous_variant | 0.15 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776192 | c.2289G>T | synonymous_variant | 0.11 |
mmpR5 | 779109 | p.Leu40Phe | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303251 | c.321C>T | synonymous_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1834950 | p.Leu470Pro | missense_variant | 0.1 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.14 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.13 |
PPE35 | 2169287 | c.1326T>C | synonymous_variant | 0.1 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.14 |
Rv1979c | 2223047 | p.Ile40Phe | missense_variant | 0.12 |
Rv1979c | 2223113 | p.Ser18Gly | missense_variant | 0.15 |
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 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726116 | c.-77T>G | upstream_gene_variant | 1.0 |
folC | 2747645 | c.-47G>A | upstream_gene_variant | 0.11 |
Rv2752c | 3064529 | p.Val555Ile | missense_variant | 0.12 |
thyX | 3067351 | p.Arg199Trp | missense_variant | 0.14 |
thyA | 3074648 | c.-177T>G | upstream_gene_variant | 0.29 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612700 | p.Asp139Glu | missense_variant | 0.18 |
rpoA | 3877850 | p.Gly220Ser | missense_variant | 0.11 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.17 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.13 |
embC | 4241651 | p.Ala597Thr | missense_variant | 0.18 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embC | 4242308 | p.Thr816Ala | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4249535 | p.Glu1008* | stop_gained | 0.13 |
aftB | 4267716 | p.Ala374Glu | missense_variant | 0.18 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407703 | p.Ala167Asp | missense_variant | 1.0 |