NTI001 (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
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
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 NTI001 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
Phylos Strain SRR4450141
- Overlapping SNPs:
- 54
- Concordance:
- 32
Nearest genetic relative in Lynch dataset
Lynch Strain SRR3495250
- Overlapping SNPs:
- 3
- Concordance:
- 3
Blockchain Registration Information
- SHASUM Hash
-
3041bd32864bc1ac
b59eff3e55f47fdd f68975f8ac8a1f4a 8bfd5d17e6b9e051