FBS044 (Fenix #2)
RSP 13261
Grower: Fenix Innovation Group Pty Ltd
General Information
- Sample Name
- NTI001_(Fenix_#2)_20241118
- Accession Date
- November 17, 2024
- Reported Plant Sex
- Female
- Report Type
- Whole-Genome Sequencing
The strain rarity visualization shows how distant the strain is from the other cultivars in the Kannapedia database. The y-axis represents genetic distance, getting farther as you go up. The width of the visualization at any position along the y-axis shows how many strains there are in the database at that genetic distance. So, a common strain will have a more bottom-heavy shape, while uncommon and rare cultivars will have a visualization that is generally shifted towards the top.
Chemical Information
Cannabinoid and terpenoid information provided by the grower.
Cannabinoids
No information provided.
Terpenoids
No information provided.
Genetic Information
- Plant Type
- Type III
File Downloads
The bell curve in the heterozygosity visualization shows the distribution of heterozygosity levels for cannabis cultivars in the Kannapedia database. The green line shows where this particular strain fits within the distribution. Heterozygosity is associated with heterosis (aka hybrid vigor) but also leads to the production of more variable offspring. When plants have two genetically different parents, heterozygosity levels will be higher than if it has been inbred or backcrossed repeatedly.
The ratio of reads mapped to Y-contigs to reads mapped to the whole Cannabis genome (Y-ratios) has been demonstrated to be strongly correlated with plant sex typing. This plot shows the distribution of Y-ratios for all samples in our database which were sequenced with the same method (panel or WGS) as this sample and where this sample falls in the distribution.
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This chart represents the Illumina sequence coverage over the Bt/Bd allele. These are the three regions in the cannabis genome that impact THCA, CBDA, CBGA production. Coverage over the Active CBDAS gene is highly correlated with Type II and Type III plants as described by Etienne de Meijer. Coverage over the THCA gene is highly correlated with Type I and Type II plants but is anti-correlated with Type III plants. Type I plants require coverage over the inactive CBDA loci and no coverage over the Active CBDA gene. Lack of coverage over the Active CBDA and Active THCA allele are presumed to be Type IV plants (CBGA dominant). While deletions of entire THCAS and CBDAS genes are the most common Bt:Bd alleles observed, it is possible to have plants with these genes where functional expression of the enzyme is disrupted by deactivating point mutations (Kojoma et al. 2006).
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This chart represents the Illumina sequence coverage over the CBCA synthase gene.
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Variants (THCAS, CBDAS, and CBCAS)
Variants (Select Genes of Interest)
EMF1-2 | c.710A>C | p.His237Pro | missense variant | moderate | contig885 | 810 | A/C | |
PHL-2 | c.35C>G | p.Thr12Arg | missense variant | moderate | contig2621 | 337604 | C/G |
|
PHL-2 | c.590T>C | p.Met197Thr | missense variant | moderate | contig2621 | 339583 | T/C |
|
PHL-2 | c.1422C>A | p.Asn474Lys | missense variant | moderate | contig2621 | 340700 | C/A |
|
PHL-2 | c.1493G>A | p.Gly498Asp | missense variant | moderate | contig2621 | 340771 | G/A |
|
PHL-2 | c.1528C>T | p.Arg510Trp | missense variant | moderate | contig2621 | 340806 | C/T |
|
PHL-2 | c.1540A>G | p.Thr514Ala | missense variant | moderate | contig2621 | 340818 | A/G | |
PHL-2 | c.1642G>A | p.Gly548Arg | missense variant | moderate | contig2621 | 340920 | G/A |
|
PHL-2 | c.2129A>G | p.His710Arg | missense variant | moderate | contig2621 | 341577 | A/G |
|
PHL-2 | c.2656C>A | p.Arg886Ser | missense variant | moderate | contig2621 | 342699 | C/A |
|
PHL-2 | c.2783G>A | p.Ser928Asn | missense variant | moderate | contig2621 | 342826 | G/A | |
PHL-2 | c.2830A>G | p.Asn944Asp | missense variant | moderate | contig2621 | 342873 | A/G |
|
PHL-2 | c.3379C>G | p.His1127Asp | missense variant | moderate | contig2621 | 343422 | C/G |
|
PHL-2 | c.3380A>G | p.His1127Arg | missense variant | moderate | contig2621 | 343423 | A/G |
|
PKSG-2b | c.31A>T | p.Thr11Ser | missense variant | moderate | contig700 | 1951851 | T/A | |
PKSG-2b | c.-2_1dupATA | start lost & conservative inframe insertion | high | contig700 | 1951880 | A/ATAT |
|
|
PKSG-4b |
c.558-16_558 |
splice acceptor variant & splice region variant & intron variant | high | contig700 | 2715036 |
TCTACATTAGAG |
|
|
PKSG-4b |
c.352_355del |
p.Thr118fs | frameshift variant | high | contig700 | 2721317 | CCTGT/C |
|
PKSG-4b | c.229G>A | p.Gly77Ser | missense variant | moderate | contig700 | 2724206 | C/T |
|
PKSG-4b | c.216G>C | p.Leu72Phe | missense variant | moderate | contig700 | 2724219 | C/G |
|
PKSG-4b | c.209G>A | p.Ser70Asn | missense variant | moderate | contig700 | 2724226 | C/T |
|
PKSG-4b | c.206T>C | p.Leu69Ser | missense variant | moderate | contig700 | 2724229 | A/G |
|
FAD2-2 | c.110C>T | p.Ala37Val | missense variant | moderate | contig83 | 1803259 | G/A |
|
FAD2-2 | c.88G>A | p.Glu30Lys | missense variant | moderate | contig83 | 1803281 | C/T |
|
ELF3 | c.358G>A | p.Gly120Arg | missense variant | moderate | contig97 | 242064 | G/A | |
ELF3 | c.757C>T | p.Pro253Ser | missense variant | moderate | contig97 | 242463 | C/T | |
ELF3 | c.772A>G | p.Ser258Gly | missense variant | moderate | contig97 | 242478 | A/G |
|
ELF3 | c.811G>A | p.Gly271Arg | missense variant | moderate | contig97 | 242517 | G/A |
|
ELF3 | c.812G>C | p.Gly271Ala | missense variant | moderate | contig97 | 242518 | G/C | |
ELF3 |
c.1803_1805d |
p.His601del | disruptive inframe deletion | moderate | contig97 | 244625 | ACAT/A |
|
ELF3 | c.1807G>C | p.Gly603Arg | missense variant | moderate | contig97 | 244638 | G/C |
|
ELF3 | c.1966C>G | p.Pro656Ala | missense variant | moderate | contig97 | 244797 | C/G | |
ELF3 | c.1982A>C | p.Asn661Thr | missense variant | moderate | contig97 | 244813 | A/C |
|
ELF3 | c.2198G>T | p.Arg733Leu | missense variant | moderate | contig97 | 245029 | G/T | |
aPT4 | c.97T>C | p.Tyr33His | missense variant | moderate | contig121 | 2828753 | T/C |
|
aPT4 | c.202T>A | p.Leu68Ile | missense variant | moderate | contig121 | 2828858 | T/A |
|
aPT1 | c.670T>A | p.Ser224Thr | missense variant | moderate | contig121 | 2840278 | T/A |
|
aPT1 | c.727G>T | p.Glu243* | stop gained | high | contig121 | 2841362 | G/T | |
AAE1-2 | c.133T>A | p.Phe45Ile | missense variant | moderate | contig81 | 209095 | T/A |
|
AAE1-2 | c.311A>G | p.Asn104Ser | missense variant | moderate | contig81 | 209273 | A/G |
|
AAE1-2 | c.331A>G | p.Asn111Asp | missense variant | moderate | contig81 | 209293 | A/G |
|
AAE1-2 | c.374A>G | p.His125Arg | missense variant | moderate | contig81 | 209336 | A/G |
|
AAE1-2 | c.563C>T | p.Thr188Ile | missense variant | moderate | contig81 | 209525 | C/T |
|
PHL-1 | c.2623A>G | p.Thr875Ala | missense variant | moderate | contig1439 | 1487174 | T/C |
|
PHL-1 | c.2551A>G | p.Thr851Ala | missense variant | moderate | contig1439 | 1487246 | T/C | |
PHL-1 | c.1387A>G | p.Thr463Ala | missense variant | moderate | contig1439 | 1489811 | T/C | |
Edestin | c.16T>C | p.Ser6Pro | missense variant | moderate | contig850 | 3065274 | A/G |
|
TFL1 | c.368G>T | p.Arg123Met | missense variant | moderate | contig1636 | 520549 | C/A |
|
TFL1 | c.358G>A | p.Gly120Arg | missense variant | moderate | contig1636 | 520559 | C/T |
|
TFL1 | c.302-1G>A | splice acceptor variant & intron variant | high | contig1636 | 520616 | C/T | ||
HDS-1 | c.1618A>G | p.Ile540Val | missense variant | moderate | contig1891 | 885936 | T/C | |
HDS-1 | c.1378G>A | p.Val460Ile | missense variant | moderate | contig1891 | 886370 | C/T |
|
HDS-1 | c.136G>A | p.Val46Ile | missense variant | moderate | contig1891 | 889256 | C/T | |
HDS-1 | c.56C>G | p.Ala19Gly | missense variant | moderate | contig1891 | 889336 | G/C | |
HDS-1 | c.35G>A | p.Cys12Tyr | missense variant | moderate | contig1891 | 889357 | C/T | |
PIE1-2 | c.5932A>G | p.Ile1978Val | missense variant | moderate | contig1460 | 1185552 | T/C | |
EMF2 | c.1205C>T | p.Ala402Val | missense variant & splice region variant | moderate | contig954 | 3055694 | C/T | |
EMF2 | c.1228A>G | p.Ser410Gly | missense variant | moderate | contig954 | 3055717 | A/G |
|
EMF2 | c.1772A>G | p.Gln591Arg | missense variant | moderate | contig954 | 3059929 | A/G | |
FT | c.240C>G | p.Asn80Lys | missense variant | moderate | contig1561 | 3124664 | C/G |
|
AAE1-3 | c.722G>A | p.Arg241Lys | missense variant | moderate | contig976 | 1083132 | C/T |
|
AAE1-3 | c.686A>G | p.Lys229Arg | missense variant | moderate | contig976 | 1083168 | T/C |
|
AAE1-3 | c.659G>A | p.Arg220Gln | missense variant | moderate | contig976 | 1083195 | C/T |
|
AAE1-3 | c.634G>C | p.Gly212Arg | missense variant | moderate | contig976 | 1083220 | C/G |
|
AAE1-3 | c.416T>C | p.Leu139Pro | missense variant | moderate | contig976 | 1083609 | A/G |
|
AAE1-3 | c.382T>C | p.Tyr128His | missense variant | moderate | contig976 | 1083643 | A/G |
|
AAE1-3 | c.293A>G | p.Asp98Gly | missense variant | moderate | contig976 | 1083732 | T/C |
|
AAE1-3 | c.215A>T | p.Glu72Val | missense variant | moderate | contig976 | 1083860 | T/A |
|
AAE1-3 | c.199A>G | p.Asn67Asp | missense variant | moderate | contig976 | 1083876 | T/C |
|
AAE1-3 | c.188A>G | p.Asn63Ser | missense variant | moderate | contig976 | 1083887 | T/C |
|
AAE1-3 | c.167A>G | p.Glu56Gly | missense variant | moderate | contig976 | 1083908 | T/C |
|
AAE1-3 | c.141A>G | p.Ile47Met | missense variant | moderate | contig976 | 1083934 | T/C |
|
AAE1-3 | c.125A>G | p.Glu42Gly | missense variant | moderate | contig976 | 1083950 | T/C |
|
AAE1-3 | c.52G>A | p.Gly18Ser | missense variant | moderate | contig976 | 1084023 | C/T |
|
PIE1-1 | c.3706A>G | p.Thr1236Ala | missense variant | moderate | contig1225 | 2285321 | A/G |
|
GGR | c.376G>C | p.Glu126Gln | missense variant | moderate | contig2282 | 549368 | G/C | |
GGR | c.382C>T | p.Leu128Phe | missense variant | moderate | contig2282 | 549374 | C/T |
|
PKSB-3 | c.1960G>A | p.Glu654Lys | missense variant | moderate | contig93 | 3340067 | G/A |
|
PKSB-3 | c.1978A>G | p.Asn660Asp | missense variant | moderate | contig93 | 3340085 | A/G |
|
Nearest genetic relatives (All Samples)
- 0.048 FBS044 Fenix 1 (RSP13260)
- 0.233 Tak-HN (RSP11618)
- 0.239 YNN (SRR14708199)
- 0.247 R4 (RSP11617)
- 0.252 KYRG-151 (RSP11052)
- 0.253 R3 (RSP11616)
- 0.255 IUL2 (SRR14708253)
- 0.256 SCN (SRR14708201)
- 0.257 GXI (SRR14708198)
- 0.258 R1 (RSP11483)
- 0.259 R2 (RSP11615)
- 0.259 Blch-Rt-RW (RSP13199)
- 0.261 IUL3 (SRR14708252)
- 0.264 Elite Hemp (RSP13222)
- 0.265 Tygra (RSP10667)
- 0.266 IUL1 (SRR14708254)
- 0.270 Jiangji (RSP10653)
- 0.271 Kyrgyz Gold (RSP11054)
- 0.273 Carmagnola (SRR14708274)
- 0.274 Squirrel Tail 31 (RSP11485)
Most genetically distant strains (All Samples)
- 0.455 Cherry Blossom (RSP11318)
- 0.453 BCH Rt-Fl (RSP13141)
- 0.439 Cherry Blossom (RSP11300)
- 0.432 Big Red (RSP13217)
- 0.429 El Gordo Dried (RSP13122)
- 0.427 Cherry Blossom (RSP11301)
- 0.424 Cherry Blossom (RSP11323)
- 0.424 Chematonic Cannatonic x Chemdawg (RSP11394)
- 0.422 Unknown- Cherry Wine - 001 (RSP11268)
- 0.421 Cherry Blossom (RSP11322)
- 0.417 Chem 91 (RSP11185)
- 0.416 Cherry Blossom (RSP11312)
- 0.416 Rainbow Belts 1 0 (RSP12911)
- 0.415 Medxotic (RSP11410)
- 0.415 EG2 Roots (RSP13096)
- 0.414 Cherry Blossom (RSP11325)
- 0.414 AVIDEKEL 2 0 (RSP11174)
- 0.413 EG2 Stems (RSP13095)
- 0.413 Wilburs Great Adventure (RSP11727)
- 0.412 EG2 Leaves (RSP13094)
Nearest genetic relative in Phylos dataset
- Overlapping SNPs:
- 54
- Concordance:
- 32
Nearest genetic relative in Lynch dataset
- Overlapping SNPs:
- 3
- Concordance:
- 3
Blockchain Registration Information
- SHASUM Hash
-
3041bd32864bc1ac
b59eff3e55f47fdd f68975f8ac8a1f4a 8bfd5d17e6b9e051