T4R2
RSP 12662
Grower: plant genomic laboratory, medicinal plant research institute, DMSC
General Information
- Accession Date
- August 10, 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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CBDAS | c.407G>A | p.Arg136His | missense variant | moderate | contig1772 | 2082633 | G/A | |
CBDAS | c.437C>T | p.Thr146Ile | missense variant | moderate | contig1772 | 2082663 | C/T |
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CBDAS | c.442T>A | p.Trp148Arg | missense variant | moderate | contig1772 | 2082668 | T/A |
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CBDAS | c.454G>A | p.Gly152Arg | missense variant | moderate | contig1772 | 2082680 | G/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 |
|
Variants (Select Genes of Interest)
EMF1-2 | c.710A>C | p.His237Pro | missense variant | moderate | contig885 | 810 | A/C | |
PHL-2 | c.575T>C | p.Ile192Thr | missense variant | moderate | contig2621 | 339568 | T/C |
|
PHL-2 | c.841A>T | p.Ser281Cys | missense variant | moderate | contig2621 | 340119 | A/T |
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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.1115T>G | p.Val372Gly | missense variant | moderate | contig2621 | 340393 | T/G |
|
PHL-2 | c.1166C>T | p.Pro389Leu | missense variant | moderate | contig2621 | 340444 | C/T | |
PHL-2 | c.1577A>G | p.His526Arg | missense variant | moderate | contig2621 | 340855 | A/G |
|
PHL-2 | c.2783G>A | p.Ser928Asn | missense variant | moderate | contig2621 | 342826 | G/A | |
PHL-2 | c.3373A>G | p.Thr1125Ala | missense variant | moderate | contig2621 | 343416 | A/G | |
PHL-2 |
c.3556_3557d |
p.Lys1186fs | frameshift variant | high | contig2621 | 343598 | GAA/G | |
PKSG-4a | c.967G>C | p.Asp323His | missense variant | moderate | contig700 | 1938378 | G/C |
|
PKSG-2a | c.774G>A | p.Met258Ile | missense variant | moderate | contig700 | 1944616 | C/T |
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PKSG-2b | c.774G>A | p.Met258Ile | missense variant | moderate | contig700 | 1950864 | C/T | |
PKSG-2b | c.718T>A | p.Phe240Ile | missense variant | moderate | contig700 | 1950920 | A/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.352_355del |
p.Thr118fs | frameshift variant | high | contig700 | 2721317 | CCTGT/C |
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PKSG-4b | c.323A>G | p.Glu108Gly | missense variant | moderate | contig700 | 2721350 | T/C |
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DXR-2 | c.1319T>C | p.Ile440Thr | missense variant | moderate | contig380 | 285250 | A/G |
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OAC-1 | c.260C>G | p.Ser87Cys | missense variant | moderate | contig931 | 118104 | G/C |
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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.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 |
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ELF3 | c.812G>C | p.Gly271Ala | missense variant | moderate | contig97 | 242518 | G/C | |
ELF3 | c.1466G>A | p.Ser489Asn | missense variant | moderate | contig97 | 244297 | G/A |
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ELF3 | c.1473A>C | p.Lys491Asn | missense variant | moderate | contig97 | 244304 | A/C |
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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 |
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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 |
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ELF3 | c.2198G>T | p.Arg733Leu | missense variant | moderate | contig97 | 245029 | G/T | |
ELF5 | c.1162A>G | p.Thr388Ala | missense variant | moderate | contig382 | 881132 | A/G | |
aPT1 | c.670T>A | p.Ser224Thr | missense variant | moderate | contig121 | 2840278 | T/A |
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aPT1 | c.727G>T | p.Glu243* | stop gained | high | contig121 | 2841362 | G/T | |
aPT1 | c.864C>G | p.Asn288Lys | missense variant | moderate | contig121 | 2842407 | C/G | |
HDS-2 |
c.82_93delGT |
p.Val28_Thr3 |
conservative inframe deletion | moderate | contig95 | 1989748 |
CGTAACCGGAAC |
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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.99G>T | p.Glu33Asp | missense variant | moderate | contig1439 | 1493793 | C/A |
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Edestin | c.16T>C | p.Ser6Pro | missense variant | moderate | contig850 | 3065274 | A/G |
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FAD4 | c.220C>G | p.Arg74Gly | missense variant | moderate | contig784 | 1690972 | C/G |
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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.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.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.1289A>G | p.Asp430Gly | missense variant | moderate | contig1460 | 1192109 | T/C |
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PIE1-2 | c.1243G>C | p.Asp415His | missense variant | moderate | contig1460 | 1192155 | C/G |
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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.706T>C | p.Tyr236His | missense variant | moderate | contig1460 | 1193808 | A/G | |
PIE1-2 | c.665+2T>A | splice donor variant & intron variant | high | contig1460 | 1194391 | A/T |
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PIE1-2 | c.637T>A | p.Ser213Thr | missense variant | moderate | contig1460 | 1194421 | A/T | |
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 |
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FLD | c.2981T>C | p.Met994Thr | missense variant | moderate | contig1450 | 2044012 | A/G | |
FLD | c.2962G>A | p.Asp988Asn | missense variant | moderate | contig1450 | 2044031 | C/T |
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FLD | c.2840A>G | p.Asn947Ser | missense variant | moderate | contig1450 | 2044192 | T/C |
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FLD | c.2585G>A | p.Arg862Gln | missense variant | moderate | contig1450 | 2045075 | C/T |
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PIE1-1 | c.773A>G | p.Asn258Ser | missense variant & splice region variant | moderate | contig1225 | 2279897 | A/G | |
PIE1-1 | c.811T>C | p.Tyr271His | missense variant | moderate | contig1225 | 2279935 | T/C | |
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.1348G>C | p.Asp450His | missense variant | moderate | contig1225 | 2281608 | G/C |
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PIE1-1 | c.1394A>G | p.Asp465Gly | missense variant | moderate | contig1225 | 2281654 | A/G | |
PIE1-1 |
c.1548_1549i |
p.Gln516_Glu |
conservative inframe insertion | moderate | contig1225 | 2281807 | A/AGAT | |
PIE1-1 | c.3619G>A | p.Val1207Met | missense variant | moderate | contig1225 | 2285234 | G/A |
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GGR | c.53A>G | p.Asn18Ser | missense variant | moderate | contig2282 | 549045 | A/G |
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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 |
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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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GGR | c.727T>C | p.Tyr243His | missense variant | moderate | contig2282 | 549719 | T/C |
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Nearest genetic relatives (All Samples)
- 0.118 T2R4 (RSP12660)
- 0.127 T2R2 (RSP12659)
- 0.140 T4R15 (RSP12665)
- 0.159 T2R15 (RSP12661)
- 0.169 ST (RSP12666)
- 0.170 Tanao Sri-white 79 (RSP11620)
- 0.172 T4R4 (RSP12663)
- 0.178 Squirrel Tail 81 (RSP11622)
- 0.184 Squirrel Tail 31 (RSP11485)
- 0.202 Tiger Tail 78 (RSP11619)
- 0.208 Tanao Sri-white-T1 (RSP11658)
- 0.208 PK (RSP12667)
- 0.208 Tanao Sri-white 80 (RSP11621)
- 0.209 T4R6 (RSP12664)
- 0.213 Tiger Tail 30 (RSP11484)
- 0.239 Foithong-F2 (RSP11659)
- 0.263 IUL1 (SRR14708254)
- 0.265 Recon (RSP10755)
- 0.270 IBR2 (SRR14708250)
- 0.271 Tak-HN (RSP11618)
Most genetically distant strains (All Samples)
- 0.470 Cherry Blossom (RSP11318)
- 0.459 Cherry Blossom (RSP11323)
- 0.451 Cherry Blossom (RSP11301)
- 0.449 Cherry Blossom (RSP11300)
- 0.446 Cherry Blossom (RSP11331)
- 0.437 Cherry Blossom (RSP11312)
- 0.437 Cherry Blossom (RSP11328)
- 0.429 GG4 (RSP11978)
- 0.426 Cherry Blossom (RSP11302)
- 0.423 Unknown- Cherry Wine - 001 (RSP11268)
- 0.422 Cherry Blossom (RSP11325)
- 0.421 Cherry Blossom (RSP11319)
- 0.420 Cherry Blossom (RSP11310)
- 0.419 Northern Skunk (RSP11456)
- 0.417 Cherry Blossom (RSP11299)
- 0.416 Queen Dream (RSP11278)
- 0.415 Cherry Blossom (RSP11315)
- 0.415 Cherry Blossom (RSP11316)
- 0.414 Queen Dream CBG (RSP11295)
- 0.413 Cherry Blossom (RSP11306)
Nearest genetic relative in Phylos dataset
Phylos Strain SRR4448688
- Overlapping SNPs:
- 91
- Concordance:
- 64
Nearest genetic relative in Lynch dataset
Lynch Strain SRR3495192
- Overlapping SNPs:
- 5
- Concordance:
- 5
Blockchain Registration Information
- Transaction ID
-
dc37ba8740074d97
ffc5e2832ad3a2b4 bfaa72c6bfa34bc5 0089fe0a7057568f - Stamping Certificate
- Download PDF (39.5 KB)
- SHASUM Hash
-
b5aba71aa225b389
4c37a4d7af40f9dd 1c40e02d32da4b9e efa3cc87b3c3600d