Run ID: ERR4814426
Sample name:
Date: 01-04-2023 13:17:17
Number of reads: 282026
Percentage reads mapped: 97.47
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 |
---|---|---|---|---|
gyrB | 6507 | p.Ala423Val | missense_variant | 0.18 |
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 | 575484 | p.Arg46Leu | missense_variant | 0.4 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.33 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.33 |
rpoC | 764869 | c.1500C>T | synonymous_variant | 0.4 |
rpoC | 764875 | c.1506C>A | synonymous_variant | 0.5 |
rpoC | 764887 | c.1518G>C | synonymous_variant | 0.4 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.4 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.29 |
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 |
rplC | 800633 | c.-176T>C | upstream_gene_variant | 0.18 |
fbiC | 1303107 | c.177C>T | synonymous_variant | 0.2 |
fbiC | 1303165 | p.Ser79Gly | missense_variant | 0.2 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167913 | p.Asn900Lys | missense_variant | 0.17 |
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 | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.22 |
Rv2752c | 3067183 | c.-992T>C | upstream_gene_variant | 0.5 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473820 | c.-187C>A | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568752 | c.-73C>T | upstream_gene_variant | 0.22 |
alr | 3841539 | c.-119C>T | upstream_gene_variant | 0.13 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.25 |
clpC1 | 4040476 | p.His77Tyr | missense_variant | 0.33 |
embC | 4239880 | c.18C>T | synonymous_variant | 0.14 |
embC | 4239894 | p.Ala11Val | missense_variant | 0.14 |
embC | 4240009 | c.147G>A | synonymous_variant | 1.0 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245068 | c.1836C>T | synonymous_variant | 0.22 |
embB | 4248172 | c.1659G>A | synonymous_variant | 0.25 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |