NTI001 (Fenix #1)
RSP 13260
Grower: Fenix Innovation Group Pty Ltd
General Information
- Sample Name
- NTI001_(Fenix_#1)_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)
No variants to report
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.1166C>T | p.Pro389Leu | missense variant | moderate | contig2621 | 340444 | C/T | |
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.2564T>A | p.Phe855Tyr | missense variant | moderate | contig2621 | 342607 | T/A | |
PHL-2 | c.2578T>A | p.Leu860Ile | missense variant | moderate | contig2621 | 342621 | T/A | |
PHL-2 | c.2656C>A | p.Arg886Ser | missense variant | moderate | contig2621 | 342699 | C/A |
|
PHL-2 | c.2756A>C | p.Glu919Ala | missense variant | moderate | contig2621 | 342799 | A/C | |
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.3002A>G | p.Tyr1001Cys | missense variant | moderate | contig2621 | 343045 | A/G | |
PHL-2 | c.3027G>T | p.Lys1009Asn | missense variant | moderate | contig2621 | 343070 | G/T | |
PHL-2 | c.3033T>G | p.Cys1011Trp | missense variant | moderate | contig2621 | 343076 | T/G | |
PHL-2 | c.3467A>G | p.Gln1156Arg | missense variant | moderate | contig2621 | 343510 | A/G | |
PHL-2 | c.3552delG | p.Lys1185fs | frameshift variant | high | contig2621 | 343593 | CG/C |
|
PHL-2 |
c.3556_3557d |
p.Lys1186fs | frameshift variant | high | contig2621 | 343598 | GAA/G | |
PKSG-2b | c.-2_1dupATA | start lost & conservative inframe insertion | high | contig700 | 1951880 | A/ATAT |
|
|
PKSG-4b |
c.352_355del |
p.Thr118fs | frameshift variant | high | contig700 | 2721317 | CCTGT/C |
|
PKSG-4b |
c.353_354ins |
p.Gly119fs | frameshift variant | high | contig700 | 2721319 | T/TGG |
|
PKSG-4b | c.323A>G | p.Glu108Gly | missense variant | moderate | contig700 | 2721350 | T/C |
|
PKSG-4b | c.316+2T>A | splice donor variant & intron variant | high | contig700 | 2723818 | A/T | ||
DXR-2 | c.1319T>C | p.Ile440Thr | missense variant | moderate | contig380 | 285250 | A/G |
|
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.574A>G | p.Asn192Asp | missense variant | moderate | contig97 | 242280 | A/G | |
ELF3 | c.757C>T | p.Pro253Ser | missense variant | moderate | contig97 | 242463 | C/T | |
ELF3 | c.1630A>G | p.Thr544Ala | missense variant | moderate | contig97 | 244461 | A/G | |
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.2198G>T | p.Arg733Leu | missense variant | moderate | contig97 | 245029 | G/T | |
aPT1 | c.670T>A | p.Ser224Thr | missense variant | moderate | contig121 | 2840278 | T/A |
|
aPT1 | c.864C>G | p.Asn288Lys | missense variant | moderate | contig121 | 2842407 | C/G | |
AAE1-2 | c.563C>T | p.Thr188Ile | missense variant | moderate | contig81 | 209525 | C/T |
|
AAE1-2 | c.1541T>C | p.Val514Ala | missense variant | moderate | contig81 | 210503 | T/C |
|
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 | |
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.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 | |
PIE1-2 | c.6653A>G | p.Asn2218Ser | missense variant | moderate | contig1460 | 1184434 | T/C | |
PIE1-2 | c.6535T>G | p.Ser2179Ala | missense variant | moderate | contig1460 | 1184552 | A/C |
|
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.1315G>C | p.Ala439Pro | missense variant | moderate | contig954 | 3055804 | G/C | |
EMF2 | c.1742C>G | p.Thr581Ser | missense variant | moderate | contig954 | 3059899 | C/G |
|
EMF2 | c.1772A>G | p.Gln591Arg | missense variant | moderate | contig954 | 3059929 | A/G | |
AAE1-3 | c.722G>A | p.Arg241Lys | missense variant | moderate | contig976 | 1083132 | C/T |
|
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.125A>G | p.Glu42Gly | missense variant | moderate | contig976 | 1083950 | T/C |
|
AAE1-3 | c.79A>G | p.Thr27Ala | missense variant | moderate | contig976 | 1083996 | T/C |
|
AAE1-3 | c.52G>A | p.Gly18Ser | missense variant | moderate | contig976 | 1084023 | C/T |
|
PIE1-1 | c.1222C>G | p.Gln408Glu | missense variant | moderate | contig1225 | 2281482 | C/G | |
PIE1-1 | c.3706A>G | p.Thr1236Ala | missense variant | moderate | contig1225 | 2285321 | A/G |
|
GGR | c.456T>A | p.His152Gln | missense variant | moderate | contig2282 | 549448 | T/A |
|
GGR | c.460G>A | p.Asp154Asn | missense variant | moderate | contig2282 | 549452 | G/A |
|
GGR | c.704A>T | p.His235Leu | missense variant | moderate | contig2282 | 549696 | A/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 2 (RSP13261)
- 0.228 Tak-HN (RSP11618)
- 0.234 R4 (RSP11617)
- 0.238 YNN (SRR14708199)
- 0.247 R3 (RSP11616)
- 0.250 KYRG-151 (RSP11052)
- 0.251 IUL2 (SRR14708253)
- 0.252 R1 (RSP11483)
- 0.253 IUL3 (SRR14708252)
- 0.254 Blch-Rt-RW (RSP13199)
- 0.255 R2 (RSP11615)
- 0.256 GXI (SRR14708198)
- 0.256 IUL1 (SRR14708254)
- 0.257 SCN (SRR14708201)
- 0.259 Elite Hemp (RSP13222)
- 0.261 Tygra (RSP10667)
- 0.262 Tisza (RSP10659)
- 0.264 IBR3 (SRR14708249)
- 0.266 PID2 (SRR14708247)
- 0.267 Tisza (RSP11045)
Most genetically distant strains (All Samples)
- 0.460 BCH Rt-Fl (RSP13141)
- 0.459 Cherry Blossom (RSP11318)
- 0.434 El Gordo Dried (RSP13122)
- 0.433 Cherry Blossom (RSP11300)
- 0.432 Big Red (RSP13217)
- 0.427 Cherry Blossom (RSP11301)
- 0.426 Chematonic Cannatonic x Chemdawg (RSP11394)
- 0.422 Cherry Blossom (RSP11323)
- 0.420 Jamaican Lion (RSP12916)
- 0.418 Cherry Blossom (RSP11322)
- 0.417 Unknown- Cherry Wine - 001 (RSP11268)
- 0.416 El Gordo (RSP12938)
- 0.416 EG2 Roots (RSP13096)
- 0.416 Rainbow Belts 1 0 (RSP12911)
- 0.416 Medxotic (RSP11410)
- 0.415 EG2 Leaves (RSP13094)
- 0.415 Chem 91 (RSP11185)
- 0.415 Cherry Blossom (RSP11325)
- 0.413 Wilburs Great Adventure (RSP11727)
- 0.413 EG2 Stems (RSP13095)
Nearest genetic relative in Phylos dataset
Phylos Strain SRR4450141
- Overlapping SNPs:
- 54
- Concordance:
- 34
Nearest genetic relative in Lynch dataset
Lynch Strain SRR3495250
- Overlapping SNPs:
- 3
- Concordance:
- 3
Blockchain Registration Information
- SHASUM Hash
-
f2a5f4082f48968c
d223dcc415a65a63 ce8d72e9b0c8ab5b 53080edacd3113cc