Run ID: SRR19406438
Sample name:
Date: 03-04-2023 21:37:08
Number of reads: 1513234
Percentage reads mapped: 99.53
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 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576781 | c.1434G>A | synonymous_variant | 0.17 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 0.99 |
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 | 1303147 | p.Ala73Thr | missense_variant | 0.14 |
Rv1258c | 1406349 | p.Ile331Ser | missense_variant | 0.97 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917971 | p.Leu11Pro | missense_variant | 0.4 |
tlyA | 1918530 | c.591G>T | synonymous_variant | 0.12 |
ndh | 2102231 | p.Ser271Leu | missense_variant | 0.12 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170182 | p.Trp144* | stop_gained | 0.18 |
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 | 2518755 | p.Arg214Leu | missense_variant | 0.4 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
folC | 2746606 | c.993C>T | synonymous_variant | 0.67 |
folC | 2746849 | c.750G>A | synonymous_variant | 0.12 |
pepQ | 2859884 | p.Leu179Met | missense_variant | 0.25 |
ribD | 2986690 | c.-149C>A | upstream_gene_variant | 0.12 |
ribD | 2987409 | p.Leu191Ile | missense_variant | 0.13 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3338960 | c.-158C>A | upstream_gene_variant | 0.12 |
fbiD | 3339234 | c.117G>T | synonymous_variant | 0.12 |
fbiD | 3339270 | c.153G>T | synonymous_variant | 0.15 |
fbiD | 3339452 | p.Val112Glu | missense_variant | 0.14 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474990 | c.984C>T | synonymous_variant | 0.2 |
fbiA | 3641462 | p.Pro307Gln | missense_variant | 0.15 |
fbiB | 3641546 | c.12C>A | synonymous_variant | 0.2 |
fbiB | 3642745 | p.Ala404Val | missense_variant | 0.12 |
embC | 4241128 | c.1266G>T | synonymous_variant | 0.15 |
embC | 4241240 | p.Leu460Val | missense_variant | 0.11 |
embC | 4241554 | c.1692G>A | synonymous_variant | 0.11 |
embC | 4241562 | p.Arg567His | missense_variant | 0.89 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242325 | c.-908C>A | upstream_gene_variant | 0.17 |
embC | 4242686 | p.Gln942Lys | missense_variant | 1.0 |
embA | 4244133 | p.Glu301Gln | missense_variant | 0.13 |
embA | 4244398 | p.Val389Ala | missense_variant | 0.25 |
embA | 4244472 | p.Val414Leu | missense_variant | 0.5 |
embA | 4244899 | p.Thr556Met | missense_variant | 0.12 |
embB | 4245590 | c.-924G>T | upstream_gene_variant | 0.17 |
embA | 4245656 | p.Asp808Glu | missense_variant | 0.25 |
embA | 4245816 | p.Arg862Ser | missense_variant | 0.25 |
embB | 4247201 | p.Val230Phe | missense_variant | 0.2 |
aftB | 4267793 | c.1044C>A | synonymous_variant | 0.14 |
aftB | 4268300 | c.537C>G | synonymous_variant | 0.14 |
aftB | 4268476 | p.Gly121Trp | missense_variant | 0.15 |
whiB6 | 4338269 | p.Gly85Arg | missense_variant | 0.2 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |