Martins's 90's Sensi
RSP 12701
Grower: Robert Martin
General Information
- Accession Date
- August 24, 2022
- Reported Plant Sex
- not reported
- Report Type
- StrainSEEK v3 10Mb
- DNA Extracted From
- Unknown
Chemical Information
Cannabinoid and terpenoid information provided by the grower.
Cannabinoids
No information provided.
Terpenoids
No information provided.
Genetic Information
- Plant Type
- Type II
File Downloads
Variants (THCAS, CBDAS, and CBCAS)
CBDAS | c.323G>A | p.Arg108Gln | missense variant | moderate | contig1772 | 2082549 | G/A |
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CBDAS | c.329G>A | p.Arg110Gln | missense variant | moderate | contig1772 | 2082555 | G/A |
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CBDAS | c.347C>A | p.Ser116Tyr | missense variant | moderate | contig1772 | 2082573 | C/A | |
CBDAS | c.377C>A | p.Pro126Gln | missense variant | moderate | contig1772 | 2082603 | C/A |
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THCAS | c.1229G>A | p.Gly410Glu | missense variant | moderate | contig741 | 4416599 | C/T |
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THCAS | c.373G>C | p.Val125Leu | missense variant | moderate | contig741 | 4417455 | C/G |
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Variants (Select Genes of Interest)
PHL-2 | c.575T>C | p.Ile192Thr | missense variant | moderate | contig2621 | 339568 | T/C |
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PHL-2 | c.1837G>A | p.Glu613Lys | missense variant | moderate | contig2621 | 341115 | G/A |
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PHL-2 | c.2834A>G | p.Asn945Ser | missense variant | moderate | contig2621 | 342877 | A/G |
|
PHL-2 |
c.2903_2905d |
p.Ser968dup | disruptive inframe insertion | moderate | contig2621 | 342939 | T/TGCA | |
PHL-2 | c.3379C>G | p.His1127Asp | missense variant | moderate | contig2621 | 343422 | C/G |
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PHL-2 | c.3380A>G | p.His1127Arg | missense variant | moderate | contig2621 | 343423 | A/G |
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PHL-2 | c.3381T>A | p.His1127Gln | missense variant | moderate | contig2621 | 343424 | T/A |
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PHL-2 | c.3457A>G | p.Thr1153Ala | missense variant | moderate | contig2621 | 343500 | A/G |
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PHL-2 |
c.3556_3557d |
p.Lys1186fs | frameshift variant | high | contig2621 | 343598 | GAA/G | |
PKSG-2a | c.774G>A | p.Met258Ile | missense variant | moderate | contig700 | 1944616 | C/T |
|
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 |
|
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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.352_355del |
p.Thr118fs | frameshift variant | high | contig700 | 2721317 | CCTGT/C |
|
PKSG-4b | c.323A>G | p.Glu108Gly | missense variant | moderate | contig700 | 2721350 | T/C |
|
DXR-2 | c.1319T>C | p.Ile440Thr | missense variant | moderate | contig380 | 285250 | A/G |
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FAD2-2 | c.196T>C | p.Phe66Leu | missense variant | moderate | contig83 | 1803173 | A/G |
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FAD2-2 | c.172G>T | p.Asp58Tyr | missense variant | moderate | contig83 | 1803197 | C/A |
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FAD2-2 | c.161T>A | p.Leu54His | missense variant | moderate | contig83 | 1803208 | A/T |
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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.574A>G | p.Asn192Asp | missense variant | moderate | contig97 | 242280 | A/G | |
ELF3 | c.772A>G | p.Ser258Gly | missense variant | moderate | contig97 | 242478 | A/G |
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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.1466G>A | p.Ser489Asn | missense variant | moderate | contig97 | 244297 | G/A |
|
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.1966C>G | p.Pro656Ala | missense variant | moderate | contig97 | 244797 | C/G | |
ELF3 | c.2141C>G | p.Pro714Arg | missense variant | moderate | contig97 | 244972 | C/G | |
ELF3 | c.2156T>G | p.Ile719Arg | missense variant | moderate | contig97 | 244987 | T/G |
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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.406A>G | p.Ile136Val | missense variant | moderate | contig121 | 2839605 | A/G | |
aPT1 | c.629C>T | p.Thr210Ile | missense variant | moderate | contig121 | 2840237 | C/T | |
HDS-2 |
c.82_93delGT |
p.Val28_Thr3 |
conservative inframe deletion | moderate | contig95 | 1989748 |
CGTAACCGGAAC |
|
HDS-2 | c.127T>G | p.Ser43Ala | missense variant | moderate | contig95 | 1989794 | T/G |
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PHL-1 | c.2623A>G | p.Thr875Ala | missense variant | moderate | contig1439 | 1487174 | T/C |
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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 | |
PHL-1 | c.932C>T | p.Ala311Val | missense variant | moderate | contig1439 | 1490266 | G/A |
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Edestin | c.16T>C | p.Ser6Pro | missense variant | moderate | contig850 | 3065274 | A/G |
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TFL1 |
c.314_315del |
p.Thr105fs | frameshift variant | high | contig1636 | 520601 | CTG/C | |
HDS-1 | c.1618A>G | p.Ile540Val | missense variant | moderate | contig1891 | 885936 | T/C | |
HDS-1 | c.1475C>A | p.Pro492Gln | missense variant | moderate | contig1891 | 886162 | G/T |
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HDS-1 | c.1393G>A | p.Ala465Thr | missense variant & splice region variant | moderate | contig1891 | 886355 | C/T | |
HDS-1 | c.1378G>A | p.Val460Ile | missense variant | moderate | contig1891 | 886370 | C/T |
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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.6653A>G | p.Asn2218Ser | missense variant | moderate | contig1460 | 1184434 | T/C | |
PIE1-2 | c.5884G>A | p.Gly1962Ser | missense variant | moderate | contig1460 | 1185715 | C/T | |
PIE1-2 | c.2027A>T | p.Gln676Leu | missense variant | moderate | contig1460 | 1190013 | T/A | |
PIE1-2 | c.1846A>G | p.Lys616Glu | missense variant | moderate | contig1460 | 1190278 | T/C |
|
PIE1-2 | c.1156T>G | p.Trp386Gly | missense variant | moderate | contig1460 | 1192242 | A/C | |
PIE1-2 | c.982G>A | p.Glu328Lys | missense variant | moderate | contig1460 | 1192416 | C/T | |
EMF2 | c.1772A>G | p.Gln591Arg | missense variant | moderate | contig954 | 3059929 | A/G | |
FT | c.194A>T | p.His65Leu | missense variant | moderate | contig1561 | 3124618 | A/T |
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FT | c.196A>G | p.Ile66Val | missense variant | moderate | contig1561 | 3124620 | A/G | |
FLD | c.2869C>T | p.His957Tyr | missense variant | moderate | contig1450 | 2044163 | G/A |
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FLD | c.2831A>G | p.Glu944Gly | missense variant | moderate | contig1450 | 2044201 | T/C |
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FLD |
c.2598-2_259 |
splice acceptor variant & intron variant | high | contig1450 | 2044937 | C/CT |
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PIE1-1 | c.3607G>A | p.Glu1203Lys | missense variant | moderate | contig1225 | 2285222 | G/A |
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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 | |
GGR | c.86C>G | p.Ala29Gly | missense variant | moderate | contig2282 | 549078 | C/G |
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GGR | c.307G>A | p.Glu103Lys | missense variant | moderate | contig2282 | 549299 | G/A |
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GGR | c.312C>G | p.His104Gln | missense variant | moderate | contig2282 | 549304 | C/G |
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GGR | c.317C>T | p.Pro106Leu | missense variant | moderate | contig2282 | 549309 | C/T | |
GGR | c.456T>A | p.His152Gln | missense variant | moderate | contig2282 | 549448 | T/A |
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GGR | c.460G>A | p.Asp154Asn | missense variant | moderate | contig2282 | 549452 | G/A |
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GGR | c.704A>T | p.His235Leu | missense variant | moderate | contig2282 | 549696 | A/T |
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Nearest genetic relatives (All Samples)
- 0.225 Black Jack (RSP10603)
- 0.228 Serious Happiness (RSP10763)
- 0.228 Doug s Varin (RSP11243)
- 0.230 Durban Poison 1 (RSP11013)
- 0.231 RKM-2018-025 (RSP11117)
- 0.232 RKM-2018-016 (RSP11108)
- 0.236 RKM-2018-027 (RSP11119)
- 0.240 Strawberry Cough (RSP11356)
- 0.240 BLACK JACK (RSP11346)
- 0.240 Gold Cracker (RSP11048)
- 0.240 Gold Cracker (RSP11041)
- 0.244 Electra (RSP11366)
- 0.245 Blue Dream (RSP11006)
- 0.245 Domnesia (RSP11184)
- 0.246 Blue Dream (RSP11017)
- 0.246 Recon (RSP10755)
- 0.246 Blue Dream (RSP11007)
- 0.247 Durban Poison 1 (RSP10996)
- 0.248 Blue Dream (RSP11009)
- 0.249 Kimbo Slice (RSP10997)
Most genetically distant strains (All Samples)
- 0.471 Cherry Blossom (RSP11328)
- 0.462 Cherry Blossom (RSP11323)
- 0.434 Chematonic Cannatonic x Chemdawg (RSP11394)
- 0.429 Cherry Blossom (RSP11318)
- 0.426 Cherry Blossom (RSP11301)
- 0.415 Chem 91 (RSP11185)
- 0.411 Cherry Blossom (RSP11298)
- 0.410 Cherry Blossom (RSP11330)
- 0.405 Cherry Blossom (RSP11309)
- 0.404 Cherry Blossom (RSP11334)
- 0.404 Unknown- Cherry Wine - 001 (RSP11268)
- 0.402 Cherry Blossom (RSP11312)
- 0.401 80E (RSP11213)
- 0.398 Cherry Blossom (RSP11300)
- 0.398 Cherry Blossom (RSP11311)
- 0.391 CS (RSP11208)
- 0.389 Swiss Dream (RSP11408)
- 0.388 Cherry Blossom (RSP11325)
- 0.387 RKM-2018-012 (RSP11103)
- 0.387 Fatso (RSP11741)
Nearest genetic relative in Phylos dataset
Phylos Strain SRR4448627
- Overlapping SNPs:
- 87
- Concordance:
- 50
Nearest genetic relative in Lynch dataset
Lynch Strain SRR3495180
- Overlapping SNPs:
- 6
- Concordance:
- 5
Blockchain Registration Information
- Transaction ID
-
d24b2462ef5eb1f7
8a7c021f9af1f2a3 128e853ad1b6aa15 5c7ae1bff1023438 - Stamping Certificate
- Download PDF (39.5 KB)
- SHASUM Hash
-
9fb91eb2c343b4d2
fa18e53ecb68ee35 c44fce6b247a487c 0b805f671d32567e