Carmagnola_garden
RSP 11603
Grower: Kevin McKernan
General Information
- Accession Date
- June 23, 2020
- Reported Plant Sex
- not reported
- Report Type
- CannSNP90
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
Summary of Deletions
THCAS
- Correlation:
- 0.95
- Call:
- deleted
CBDAS
- Correlation:
- -0.1
- Call:
- intact
CBCAS
- Correlation:
- -0.05
- Call:
- intact
Plant Sex
- Correlation:
- 0.9
- Call:
- female
Variants (THCAS, CBDAS, and CBCAS)
Variants (Select Genes of Interest)
EMF1-2 | c.634G>C | p.Val212Leu | missense variant | moderate | contig885 | 734 | G/C | |
EMF1-2 | c.710A>C | p.His237Pro | missense variant | moderate | contig885 | 810 | A/C | |
EMF1-2 | c.1384A>C | p.Lys462Gln | missense variant | moderate | contig885 | 2270 | A/C | |
PHL-2 | c.44G>A | p.Arg15Lys | missense variant | moderate | contig2621 | 337613 | G/A | |
PHL-2 | c.932T>C | p.Leu311Pro | missense variant | moderate | contig2621 | 340210 | T/C | |
PHL-2 | c.1057A>G | p.Arg353Gly | missense variant | moderate | contig2621 | 340335 | A/G | |
PHL-2 | c.1096G>A | p.Ala366Thr | missense variant | moderate | contig2621 | 340374 | G/A | |
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.2624C>T | p.Ser875Phe | missense variant | moderate | contig2621 | 342667 | C/T | |
PHL-2 | c.2783G>A | p.Ser928Asn | missense variant | moderate | contig2621 | 342826 | G/A | |
PHL-2 | c.2933G>T | p.Arg978Leu | missense variant | moderate | contig2621 | 342976 | G/T | |
PHL-2 | c.3209A>G | p.Gln1070Arg | missense variant | moderate | contig2621 | 343252 | A/G | |
PHL-2 | c.3467A>G | p.Gln1156Arg | missense variant | moderate | contig2621 | 343510 | A/G | |
PKSG-4a | c.1000T>C | p.Tyr334His | missense variant | moderate | contig700 | 1938411 | T/C | |
PKSG-2a | c.1152T>A | p.Asn384Lys | missense variant | moderate | contig700 | 1944238 | A/T | |
PKSG-2a | c.1117A>G | p.Ile373Val | missense variant | moderate | contig700 | 1944273 | T/C | |
PKSG-2a | c.224A>G | p.Lys75Arg | missense variant | moderate | contig700 | 1945166 | T/C | |
PKSG-2a | c.67T>A | p.Phe23Ile | missense variant | moderate | contig700 | 1945567 | A/T | |
PKSG-2a | c.31A>T | p.Thr11Ser | missense variant | moderate | contig700 | 1945603 | T/A | |
PKSG-2b | c.1152T>A | p.Asn384Lys | missense variant | moderate | contig700 | 1950486 | A/T | |
PKSG-2b | c.1117A>G | p.Ile373Val | missense variant | moderate | contig700 | 1950521 | T/C | |
PKSG-2b | c.774G>A | p.Met258Ile | missense variant | moderate | contig700 | 1950864 | C/T | |
PKSG-2b | c.224A>G | p.Lys75Arg | missense variant | moderate | contig700 | 1951414 | T/C | |
PKSG-2b | c.167C>G | p.Thr56Ser | missense variant | moderate | contig700 | 1951471 | G/C | |
PKSG-2b | c.31A>T | p.Thr11Ser | missense variant | moderate | contig700 | 1951851 | T/A | |
PKSG-4b | c.496A>G | p.Lys166Glu | missense variant | moderate | contig700 | 2721177 | T/C | |
PKSG-4b | c.489delT | p.Phe163fs | frameshift variant | high | contig700 | 2721183 | CA/C | |
PKSG-4b | c.485A>G | p.Lys162Arg | missense variant | moderate | contig700 | 2721188 | T/C | |
PKSG-4b | c.431T>G | p.Val144Gly | missense variant | moderate | contig700 | 2721242 | A/C | |
PKSG-4b | c.419A>G | p.Asp140Gly | missense variant | moderate | contig700 | 2721254 | T/C | |
PKSG-4b | c.316+2T>A | splice donor variant & intron variant | high | contig700 | 2723818 | A/T | ||
OAC-2 | c.52G>T | p.Ala18Ser | missense variant | moderate | contig931 | 110287 | C/A |
|
OAC-1 | c.220A>G | p.Ile74Val | missense variant | moderate | contig931 | 118144 | T/C | |
ELF3 | c.358G>A | p.Gly120Arg | missense variant | moderate | contig97 | 242064 | G/A | |
ELF3 | c.520A>C | p.Asn174His | missense variant | moderate | contig97 | 242226 | A/C | |
ELF3 | c.752G>T | p.Gly251Val | missense variant | moderate | contig97 | 242458 | G/T | |
ELF3 | c.812G>C | p.Gly271Ala | missense variant | moderate | contig97 | 242518 | G/C | |
ELF3 |
c.1230-2_123 |
splice acceptor variant & intron variant | high | contig97 | 243676 | TAG/T | ||
ELF3 | c.1966C>G | p.Pro656Ala | missense variant | moderate | contig97 | 244797 | C/G | |
ELF3 | c.2198delG | p.Arg733fs | frameshift variant | high | contig97 | 245028 | CG/C | |
ELF3 | c.2198G>T | p.Arg733Leu | missense variant | moderate | contig97 | 245029 | G/T | |
ELF5 | c.853C>T | p.Pro285Ser | missense variant | moderate | contig382 | 880715 | C/T | |
aPT1 | c.629C>T | p.Thr210Ile | missense variant | moderate | contig121 | 2840237 | 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.1393G>A | p.Ala465Thr | missense variant & splice region variant | moderate | contig1891 | 886355 | 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.5932A>G | p.Ile1978Val | missense variant | moderate | contig1460 | 1185552 | T/C | |
PIE1-2 | c.5884G>A | p.Gly1962Ser | missense variant | moderate | contig1460 | 1185715 | C/T | |
PIE1-2 | c.5132T>C | p.Ile1711Thr | missense variant | moderate | contig1460 | 1186607 | A/G |
|
PIE1-2 | c.4721T>C | p.Val1574Ala | missense variant | moderate | contig1460 | 1187319 | A/G |
|
PIE1-2 | c.3554G>A | p.Arg1185Lys | missense variant | moderate | contig1460 | 1188486 | C/T | |
PIE1-2 | c.3506A>C | p.Glu1169Ala | missense variant | moderate | contig1460 | 1188534 | T/G | |
PIE1-2 | c.2188G>A | p.Ala730Thr | missense variant | moderate | contig1460 | 1189852 | C/T | |
PIE1-2 |
c.2083_2085d |
p.Val695del | conservative inframe deletion | moderate | contig1460 | 1189954 | GGAC/G | |
PIE1-2 | c.2072A>G | p.His691Arg | missense variant | moderate | contig1460 | 1189968 | T/C | |
PIE1-2 | c.2027A>T | p.Gln676Leu | missense variant | moderate | contig1460 | 1190013 | T/A | |
PIE1-2 | c.1872T>A | p.Asp624Glu | missense variant | moderate | contig1460 | 1190252 | A/T | |
PIE1-2 | c.1630G>C | p.Ala544Pro | missense variant | moderate | contig1460 | 1191600 | C/G | |
PIE1-2 | c.1156T>G | p.Trp386Gly | missense variant | moderate | contig1460 | 1192242 | A/C | |
PIE1-2 | c.1117C>G | p.Gln373Glu | missense variant | moderate | contig1460 | 1192281 | G/C | |
PIE1-2 | c.1093G>A | p.Gly365Ser | missense variant | moderate | contig1460 | 1192305 | C/T | |
PIE1-2 | c.982G>A | p.Glu328Lys | missense variant | moderate | contig1460 | 1192416 | C/T | |
PIE1-2 | c.710C>T | p.Pro237Leu | missense variant | moderate | contig1460 | 1193804 | G/A | |
PIE1-2 | c.637T>A | p.Ser213Thr | missense variant | moderate | contig1460 | 1194421 | A/T | |
PIE1-2 | c.349C>T | p.Pro117Ser | missense variant & splice region variant | moderate | contig1460 | 1195017 | G/A |
|
EMF2 | c.722C>T | p.Thr241Ile | missense variant | moderate | contig954 | 3050302 | C/T | |
EMF2 | c.1205C>T | p.Ala402Val | missense variant & splice region variant | moderate | contig954 | 3055694 | C/T | |
EMF2 | c.1315G>C | p.Ala439Pro | missense variant | moderate | contig954 | 3055804 | G/C | |
EMF2 |
c.1418_1419i |
p.Ser473_His |
disruptive inframe insertion | moderate | contig954 | 3056605 | C/CACA | |
EMF2 | c.1772A>G | p.Gln591Arg | missense variant | moderate | contig954 | 3059929 | A/G | |
EMF1-1 | c.470C>A | p.Ser157Tyr | missense variant | moderate | contig883 | 269959 | C/A | |
EMF1-1 | c.605A>T | p.His202Leu | missense variant | moderate | contig883 | 270210 | A/T | |
FLD | c.2981T>C | p.Met994Thr | missense variant | moderate | contig1450 | 2044012 | A/G | |
FLD | c.2964C>A | p.Asp988Glu | missense variant | moderate | contig1450 | 2044029 | G/T | |
FLD | c.2686G>A | p.Ala896Thr | missense variant | moderate | contig1450 | 2044848 | C/T | |
FLD | c.2681T>C | p.Ile894Thr | missense variant | moderate | contig1450 | 2044853 | A/G | |
AAE1-3 | c.3G>A | p.Met1? | start lost | high | contig976 | 1084072 | C/T | |
PIE1-1 | c.742T>A | p.Ser248Thr | missense variant | moderate | contig1225 | 2279320 | T/A | |
PIE1-1 | c.773A>G | p.Asn258Ser | missense variant & splice region variant | moderate | contig1225 | 2279897 | A/G | |
PIE1-1 | c.815C>T | p.Pro272Leu | missense variant | moderate | contig1225 | 2279939 | C/T | |
PIE1-1 | c.1222C>G | p.Gln408Glu | missense variant | moderate | contig1225 | 2281482 | C/G | |
PIE1-1 | c.1394A>G | p.Asp465Gly | missense variant | moderate | contig1225 | 2281654 | A/G | |
PIE1-1 | c.1454T>C | p.Val485Ala | missense variant | moderate | contig1225 | 2281714 | T/C |
|
PIE1-1 |
c.1548_1549i |
p.Gln516_Glu |
conservative inframe insertion | moderate | contig1225 | 2281807 | A/AGAT | |
PIE1-1 | c.2174A>G | p.His725Arg | missense variant | moderate | contig1225 | 2283789 | A/G |
|
PIE1-1 |
c.2185_2187d |
p.Val729del | conservative inframe deletion | moderate | contig1225 | 2283796 | AGTC/A |
|
PIE1-1 | c.3608A>C | p.Glu1203Ala | missense variant | moderate | contig1225 | 2285223 | A/C | |
PIE1-1 | c.3656G>A | p.Arg1219Lys | missense variant | moderate | contig1225 | 2285271 | G/A | |
PIE1-1 | c.3869A>C | p.Asn1290Thr | missense variant | moderate | contig1225 | 2285484 | A/C | |
PIE1-1 | c.4823T>C | p.Val1608Ala | missense variant | moderate | contig1225 | 2286438 | T/C |
|
PIE1-1 | c.5234T>C | p.Ile1745Thr | missense variant | moderate | contig1225 | 2287152 | T/C |
|
PIE1-1 | c.6041T>C | p.Met2014Thr | missense variant | moderate | contig1225 | 2288214 | T/C |
|
PIE1-1 | c.6738G>T | p.Glu2246Asp | missense variant | moderate | contig1225 | 2289303 | G/T |
|
GGR | c.376G>C | p.Glu126Gln | missense variant | moderate | contig2282 | 549368 | G/C | |
GGR | c.581C>T | p.Ala194Val | missense variant | moderate | contig2282 | 549573 | C/T |
Nearest genetic relatives (All Samples)
- 0.119 Cbot-2019-003 (RSP11131)
- 0.132 Electra (RSP11366)
- 0.136 Cbot-2019-001 (RSP11129)
- 0.139 AVIDEKEL 2 0 (RSP11174)
- 0.147 Lift (RSP11378)
- 0.147 BlueBerry Cheesecake x JL Male (RSP11201)
- 0.148 Unknown- Cherry Wine - 005 (RSP11272)
- 0.150 Cbot-2019-005 (RSP11133)
- 0.153 Chematonic Cannatonic x Chemdawg (RSP11394)
- 0.153 Joy (RSP11380)
- 0.154 Cbot-2019-002 (RSP11130)
- 0.154 AVIDEKEL USA (RSP11169)
- 0.154 Cold Weather Cherry (RSP11414)
- 0.158 Calm (RSP11379)
- 0.159 Herijuana (RSP11181)
- 0.160 Lifter (RSP11365)
- 0.160 Charlotte Dream (RSP11412)
- 0.161 JL Cross 78 (RSP11579)
- 0.162 RAPHAEL 2 (RSP11172)
- 0.162 Sangria (RSP11631)
Most genetically distant strains (All Samples)
- 0.243 80E (RSP11212)
- 0.238 80E (RSP11213)
- 0.236 80E (RSP11211)
- 0.227 Feral (RSP11205)
- 0.223 JL 3rd Gen Father (RSP11196)
- 0.219 JL 4th Gen 6 (RSP11200)
- 0.216 Arcata Trainwreck (RSP11176)
- 0.213 Goomendaze (RSP11462)
- 0.213 Red Eye OG (RSP11190)
- 0.212 JL 4th Gen 1 (RSP11193)
- 0.211 TI-7 (RSP11601)
- 0.210 JL Cross 33 (RSP11534)
- 0.210 Deadhead OG (RSP11463)
- 0.208 Fedora 17 (RSP11203)
- 0.208 Feral (RSP11206)
- 0.207 Tiborszallasie (RSP11210)
- 0.207 unknown (RSP11432)
- 0.207 Carmaleonte (RSP11207)
- 0.207 JL 4th Gen 2 (RSP11194)
- 0.206 Chem 91 (RSP11185)
Nearest genetic relative in Phylos dataset
Phylos Strain SRR4448691
- Overlapping SNPs:
- 86
- Concordance:
- 59
Nearest genetic relative in Lynch dataset
Lynch Strain SRR3495194
- Overlapping SNPs:
- 9
- Concordance:
- 8
Blockchain Registration Information
- SHASUM Hash
-
fa38eb027d178397
676d1f2a16eac66b 4791220f42f5e3d2 13493acbcec2fa85