Feral
RSP 11206
General Information
- Sample Name
- IdaliaFT_1_CSU
- Accession Date
- June 26, 2019
- Reported Plant Sex
- not reported
- Report Type
- StrainSEEK v2 3.2Mb
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)
CBDAS | c.8G>A | p.Cys3Tyr | missense variant | moderate | contig1772 | 2082234 | G/A |
|
CBDAS | c.1420A>C | p.Lys474Gln | missense variant | moderate | contig1772 | 2083646 | A/C | |
CBDAS | c.1628G>A | p.Arg543His | missense variant | moderate | contig1772 | 2083854 | G/A |
|
CBCAS | c.1420C>T | p.Pro474Ser | missense variant | moderate | contig756 | 3100726 | C/T |
|
Variants (Select Genes of Interest)
PKSA-3b | c.298G>A | p.Ala100Thr | missense variant | moderate | contig705 | 2271640 | C/T | |
GPPs1 | c.160A>G | p.Lys54Glu | missense variant | moderate | contig676 | 168409 | A/G |
|
GPPs1 | c.472T>A | p.Leu158Met | missense variant | moderate | contig676 | 168721 | T/A |
|
GPPs1 | c.744C>G | p.Asp248Glu | missense variant | moderate | contig676 | 168993 | C/G |
|
GPPs1 |
c.807_814del |
p.His270fs | frameshift variant | high | contig676 | 169595 | GTGCATTTT/G |
|
GPPs1 |
c.845_848del |
p.Glu282fs | frameshift variant | high | contig676 | 169629 | TGAAA/T |
|
GPPs1 |
c.857_864del |
p.Ala286fs | frameshift variant | high | contig676 | 169645 | GGCGAAAGA/G |
|
GPPs1 |
c.866_877del |
p.Leu289_Glu |
stop gained & disruptive inframe deletion | high | contig676 | 169655 |
TTACTAGAGCTA |
|
GPPs1 | c.896A>G | p.Asn299Ser | missense variant | moderate | contig676 | 169772 | A/G |
|
GPPs1 |
c.923_927+5d |
p.Val308fs | frameshift variant & splice donor variant & splice region variant & intron variant | high | contig676 | 169798 |
GTTTTGGTACT/ |
|
GPPs1 | c.931delT | p.Ter311fs | frameshift variant & stop lost & splice region variant | high | contig676 | 169840 | AT/A |
|
EMF1-2 | c.3G>T | p.Met1? | start lost | high | contig885 | 103 | G/T |
|
EMF1-2 | c.349G>A | p.Asp117Asn | missense variant | moderate | contig885 | 449 | G/A |
|
EMF1-2 | c.572A>G | p.Asn191Ser | missense variant | moderate | contig885 | 672 | A/G |
|
EMF1-2 | c.710A>C | p.His237Pro | missense variant | moderate | contig885 | 810 | A/C | |
EMF1-2 | c.1148C>T | p.Ala383Val | missense variant | moderate | contig885 | 2034 | C/T |
|
EMF1-2 | c.1187T>C | p.Leu396Ser | missense variant | moderate | contig885 | 2073 | T/C |
|
EMF1-2 | c.1189G>A | p.Ala397Thr | missense variant | moderate | contig885 | 2075 | G/A |
|
EMF1-2 | c.1199G>A | p.Arg400Lys | missense variant | moderate | contig885 | 2085 | G/A |
|
EMF1-2 | c.1331G>A | p.Ser444Asn | missense variant | moderate | contig885 | 2217 | G/A |
|
EMF1-2 | c.1409G>A | p.Arg470Lys | missense variant | moderate | contig885 | 2295 | G/A |
|
EMF1-2 | c.1828A>G | p.Ile610Val | missense variant | moderate | contig885 | 2714 | A/G |
|
EMF1-2 | c.2008C>T | p.Pro670Ser | missense variant | moderate | contig885 | 2894 | C/T |
|
EMF1-2 | c.2256A>T | p.Lys752Asn | missense variant | moderate | contig885 | 3142 | A/T |
|
EMF1-2 | c.2653A>G | p.Thr885Ala | missense variant | moderate | contig885 | 3539 | A/G |
|
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.2830A>C | p.Asn944His | missense variant | moderate | contig2621 | 342873 | A/C |
|
PHL-2 | c.2933G>T | p.Arg978Leu | missense variant | moderate | contig2621 | 342976 | G/T | |
PHL-2 | c.2936T>G | p.Val979Gly | missense variant | moderate | contig2621 | 342979 | T/G |
|
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.37C>G | p.Gln13Glu | missense variant | moderate | contig700 | 1936734 | C/G |
|
PKSG-4a |
c.49_50insTG |
p.Glu16_Gly1 |
disruptive inframe insertion | moderate | contig700 | 1936744 | A/AGGT |
|
PKSG-4a | c.493G>A | p.Gly165Ser | missense variant | moderate | contig700 | 1937904 | G/A |
|
PKSG-2a | c.1117A>G | p.Ile373Val | missense variant | moderate | contig700 | 1944273 | T/C | |
PKSG-2a | c.948T>G | p.Asp316Glu | missense variant | moderate | contig700 | 1944442 | A/C |
|
PKSG-2a | c.945T>G | p.Ser315Arg | missense variant | moderate | contig700 | 1944445 | A/C |
|
PKSG-2a | c.944G>A | p.Ser315Asn | missense variant | moderate | contig700 | 1944446 | C/T |
|
PKSG-2a | c.934C>G | p.His312Asp | missense variant | moderate | contig700 | 1944456 | G/C |
|
PKSG-2b | c.1132C>G | p.Leu378Val | missense variant | moderate | contig700 | 1950506 | G/C |
|
PKSG-2b | c.1117A>G | p.Ile373Val | missense variant | moderate | contig700 | 1950521 | T/C | |
PKSG-2b | c.948T>G | p.Asp316Glu | missense variant | moderate | contig700 | 1950690 | A/C |
|
PKSG-2b | c.945T>G | p.Ser315Arg | missense variant | moderate | contig700 | 1950693 | A/C |
|
PKSG-2b | c.944G>A | p.Ser315Asn | missense variant | moderate | contig700 | 1950694 | C/T |
|
PKSG-2b | c.934C>G | p.His312Asp | missense variant | moderate | contig700 | 1950704 | G/C |
|
PKSG-2b | c.774G>A | p.Met258Ile | missense variant | moderate | contig700 | 1950864 | C/T | |
PKSG-2b | c.67A>T | p.Ile23Phe | missense variant | moderate | contig700 | 1951815 | T/A | |
PKSG-2b | c.31A>T | p.Thr11Ser | missense variant | moderate | contig700 | 1951851 | T/A | |
PKSG-4b | c.557+2T>C | splice donor variant & intron variant | high | contig700 | 2721114 | A/G |
|
|
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 |
|
PKSG-4b | c.347C>A | p.Thr116Asn | missense variant | moderate | contig700 | 2721326 | G/T |
|
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 | ||
AAE1-1 | c.1580A>G | p.Asn527Ser | missense variant | moderate | contig606 | 3242691 | T/C |
|
AAE1-1 | c.1504G>A | p.Asp502Asn | missense variant | moderate | contig606 | 3242767 | C/T |
|
AAE1-1 | c.946G>A | p.Ala316Thr | missense variant | moderate | contig606 | 3243325 | C/T |
|
AAE1-1 | c.454A>G | p.Lys152Glu | missense variant | moderate | contig606 | 3243817 | T/C |
|
DXR-2 | c.1319T>C | p.Ile440Thr | missense variant | moderate | contig380 | 285250 | A/G |
|
OAC-2 | c.220A>G | p.Ile74Val | missense variant | moderate | contig931 | 110019 | T/C | |
OAC-2 | c.185C>T | p.Thr62Ile | missense variant | moderate | contig931 | 110054 | G/A |
|
OAC-1 | c.260C>G | p.Ser87Cys | missense variant | moderate | contig931 | 118104 | G/C |
|
ELF3 | c.772A>G | p.Ser258Gly | missense variant | moderate | contig97 | 242478 | A/G |
|
ELF3 | c.812G>C | p.Gly271Ala | missense variant | moderate | contig97 | 242518 | G/C | |
ELF3 | c.1366T>G | p.Leu456Val | missense variant | moderate | contig97 | 244197 | T/G |
|
ELF3 | c.1466G>A | p.Ser489Asn | missense variant | moderate | contig97 | 244297 | G/A |
|
ELF3 | c.1571C>T | p.Pro524Leu | missense variant | moderate | contig97 | 244402 | 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.1966C>G | p.Pro656Ala | missense variant | moderate | contig97 | 244797 | C/G | |
ELF3 | c.2198G>T | p.Arg733Leu | missense variant | moderate | contig97 | 245029 | G/T | |
ELF3 | c.2207A>T | p.His736Leu | missense variant | moderate | contig97 | 245038 | A/T |
|
ELF5 | c.520A>G | p.Thr174Ala | missense variant | moderate | contig382 | 880382 | A/G | |
aPT4 | c.97T>C | p.Tyr33His | missense variant | moderate | contig121 | 2828753 | T/C |
|
aPT4 | c.153A>C | p.Lys51Asn | missense variant | moderate | contig121 | 2828809 | A/C |
|
aPT4 | c.517A>T | p.Ile173Leu | missense variant & splice region variant | moderate | contig121 | 2830795 | A/T |
|
aPT4 | c.757G>T | p.Val253Leu | missense variant | moderate | contig121 | 2831364 | G/T |
|
aPT4 | c.1168T>C | p.Tyr390His | missense variant | moderate | contig121 | 2833503 | T/C |
|
aPT1 |
c.95_97delGT |
p.Cys32del | disruptive inframe deletion | moderate | contig121 | 2835800 | ATGT/A | |
aPT1 | c.406A>G | p.Ile136Val | missense variant | moderate | contig121 | 2839605 | A/G | |
aPT1 | c.727G>T | p.Glu243* | stop gained | high | contig121 | 2841362 | G/T | |
HDS-2 |
c.82_93delGT |
p.Val28_Thr3 |
conservative inframe deletion | moderate | contig95 | 1989748 |
CGTAACCGGAAC |
|
HDS-2 | c.127T>C | p.Ser43Pro | missense variant | moderate | contig95 | 1989794 | T/C |
|
HDS-2 | c.127T>G | p.Ser43Ala | missense variant | moderate | contig95 | 1989794 | T/G |
|
AAE1-2 | c.205T>A | p.Ser69Thr | missense variant | moderate | contig81 | 209167 | T/A |
|
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.409C>T | p.Arg137Cys | missense variant | moderate | contig81 | 209371 | C/T |
|
AAE1-2 |
c.948_949ins |
p.Asp317fs | frameshift variant | high | contig81 | 209910 | C/CA |
|
AAE1-2 | c.952delC | p.Gln318fs | frameshift variant | high | contig81 | 209912 | AC/A |
|
AAE1-2 | c.953A>G | p.Gln318Arg | missense variant | moderate | contig81 | 209915 | A/G |
|
AAE1-2 | c.955C>T | p.Arg319Cys | missense variant | moderate | contig81 | 209917 | C/T |
|
AAE1-2 | c.1006A>G | p.Lys336Glu | missense variant | moderate | contig81 | 209968 | A/G |
|
AAE1-2 | c.1415G>A | p.Ser472Asn | missense variant | moderate | contig81 | 210377 | G/A |
|
AAE1-2 | c.1417A>G | p.Thr473Ala | missense variant | moderate | contig81 | 210379 | A/G |
|
AAE1-2 | c.1434G>T | p.Glu478Asp | missense variant | moderate | contig81 | 210396 | G/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.40G>A | p.Ala14Thr | missense variant | moderate | contig850 | 3065250 | C/T |
|
Edestin | c.17C>T | p.Ser6Leu | missense variant | moderate | contig850 | 3065273 | G/A |
|
Edestin | c.16T>C | p.Ser6Pro | missense variant | moderate | contig850 | 3065274 | A/G |
|
TFL1 | c.304G>A | p.Asp102Asn | missense variant & splice region variant | moderate | contig1636 | 520613 | 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.109G>A | p.Val37Ile | missense variant | moderate | contig1891 | 889283 | C/T |
|
HDS-1 | c.56C>G | p.Ala19Gly | missense variant | moderate | contig1891 | 889336 | G/C | |
HDS-1 |
c.-108+1_-10 |
splice donor variant & intron variant | high | contig1891 | 889975 | A/AC |
|
|
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 |
|
PIE1-2 |
c.1019_1048d |
p.Asn340_Asp |
conservative inframe insertion | moderate | contig1460 | 1192349 |
C/CTATCCTCCA |
|
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.637T>A | p.Ser213Thr | missense variant | moderate | contig1460 | 1194421 | A/T | |
EMF2 | c.434C>T | p.Ser145Phe | missense variant | moderate | contig954 | 3049270 | C/T | |
EMF2 | c.1772A>G | p.Gln591Arg | missense variant | moderate | contig954 | 3059929 | A/G | |
EMF1-1 | c.62C>G | p.Thr21Ser | missense variant | moderate | contig883 | 268910 | C/G |
|
EMF1-1 | c.389G>A | p.Arg130Gln | missense variant | moderate | contig883 | 269878 | G/A |
|
EMF1-1 | c.476A>T | p.Asn159Ile | missense variant | moderate | contig883 | 269965 | A/T |
|
EMF1-1 | c.590A>T | p.Lys197Ile | missense variant | moderate | contig883 | 270079 | A/T |
|
FT | c.13C>G | p.Leu5Val | missense variant | moderate | contig1561 | 3124437 | C/G | |
FT |
c.41_43dupAT |
p.Asn14dup | disruptive inframe insertion | moderate | contig1561 | 3124441 | T/TTAA |
|
FT |
c.43_44insAT |
p.Asn14_Ser1 |
disruptive inframe insertion | moderate | contig1561 | 3124441 |
T/TTAATAATAA |
|
FT |
c.43_44insAT |
p.Asn14_Ser1 |
disruptive inframe insertion | moderate | contig1561 | 3124441 |
T/TTAATAATAA |
|
FT | c.175C>G | p.Leu59Val | missense variant | moderate | contig1561 | 3124599 | C/G |
|
FT | c.196A>G | p.Ile66Val | missense variant | moderate | contig1561 | 3124620 | A/G | |
FT | c.240C>G | p.Asn80Lys | missense variant | moderate | contig1561 | 3124664 | C/G |
|
FT | c.420C>A | p.Ser140Arg | missense variant | moderate | contig1561 | 3126659 | C/A |
|
FLD | c.2869C>T | p.His957Tyr | missense variant | moderate | contig1450 | 2044163 | G/A |
|
FLD | c.2831A>G | p.Glu944Gly | missense variant | moderate | contig1450 | 2044201 | T/C |
|
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.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 |
|
FAD7A-1 |
c.*341_*343- |
splice donor variant & splice region variant & 3 prime UTR variant & intron variant | high | contig510 | 71468 |
TATATATATATA |
|
|
PIE1-1 | c.1222C>G | p.Gln408Glu | missense variant | moderate | contig1225 | 2281482 | C/G | |
PIE1-1 | c.3619G>A | p.Val1207Met | missense variant | moderate | contig1225 | 2285234 | G/A |
|
GGR | c.317C>T | p.Pro106Leu | missense variant | moderate | contig2282 | 549309 | C/T | |
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 |
|
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.514A>T | p.Ile172Phe | missense variant | moderate | contig2282 | 549506 | A/T |
|
GGR | c.581C>T | p.Ala194Val | missense variant | moderate | contig2282 | 549573 | C/T | |
GGR | c.704A>T | p.His235Leu | missense variant | moderate | contig2282 | 549696 | A/T |
|
GGR | c.746G>A | p.Gly249Glu | missense variant | moderate | contig2282 | 549738 | G/A |
|
GGR | c.810A>C | p.Glu270Asp | missense variant | moderate | contig2282 | 549802 | A/C |
|
GGR | c.826A>G | p.Arg276Gly | missense variant | moderate | contig2282 | 549818 | A/G |
|
PKSB-3 | c.188A>T | p.Tyr63Phe | missense variant | moderate | contig93 | 3333945 | A/T |
|
PKSB-3 | c.1652A>G | p.Glu551Gly | missense variant | moderate | contig93 | 3339759 | A/G |
|
PKSB-3 |
c.1880_1891d |
p.His627_Gly |
disruptive inframe deletion | moderate | contig93 | 3339981 |
CTGGCCATGGCC |
|
PKSB-3 | c.1901C>G | p.Ala634Gly | missense variant | moderate | contig93 | 3340008 | C/G |
|
Nearest genetic relatives (All Samples)
- 0.227 Tiborszallasie (RSP11210)
- 0.227 Fedora 17 (RSP11203)
- 0.236 VIR 37 - Novgorod-Seversky - cv (SRR14708234)
- 0.237 Carmagnola USO 31 (RSP11204)
- 0.239 Feral (RSP10892)
- 0.239 Carmagnola (RSP10982)
- 0.241 Feral (RSP11205)
- 0.242 Futura 75 (RSP10664)
- 0.242 Feral (RSP10890)
- 0.242 VIR 483 (SRR14708239)
- 0.242 Carmagnola (RSP11039)
- 0.243 Carmagnola (RSP11202)
- 0.243 Santhica27 (RSP11046)
- 0.243 Carmagnola (RSP10980)
- 0.244 Santhica 27 (RSP10665)
- 0.246 Eletta Campana (RSP11209)
- 0.246 Tisza (RSP11045)
- 0.247 Tisza (RSP11044)
- 0.247 VIR 469 (SRR14708243)
- 0.248 Delta-llosa (SRR14708272)
Most genetically distant strains (All Samples)
- 0.472 JL yellow (RSP11075)
- 0.471 JL 3rd Gen Mother (RSP11197)
- 0.465 Cherry Blossom (RSP11323)
- 0.464 Cherry Blossom (RSP11301)
- 0.462 JL 3rd Gen Mother (RSP11214)
- 0.455 JL x NSPM1 4 (RSP11482)
- 0.441 Northern Skunk (RSP11456)
- 0.439 Cherry Blossom (RSP11300)
- 0.438 Cherry Blossom (RSP11318)
- 0.438 Charlotte Dream (RSP11412)
- 0.434 AVIDEKEL 2 0 (RSP11174)
- 0.434 Wilburs Great Adventure (RSP11727)
- 0.434 Ringo s Gift -Katie s Cut- (RSP11624)
- 0.432 JL 4th Gen 5 (RSP11199)
- 0.432 Cherry Blossom (RSP11328)
- 0.432 UP Wendigo (RSP11261)
- 0.431 Cherry Blossom (RSP11298)
- 0.431 Queen Dream (RSP11278)
- 0.429 Cherry Blossom (RSP11331)
- 0.429 JL 4th Gen 4 (RSP11198)
Nearest genetic relative in Phylos dataset
Phylos Strain SRR4450138
- Overlapping SNPs:
- 9
- Concordance:
- 6
Nearest genetic relative in Lynch dataset
Lynch Strain SRR3495319
- Overlapping SNPs:
- 12
- Concordance:
- 9
Blockchain Registration Information
- Transaction ID
-
a54b7c1f586d0561
6a66abaeef3e0d60 737ed6766c3dff2f f1edf5be2ddd9c32 - Stamping Certificate
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992243bd5792d18d
9a9dd956bb1bad1b d2adf03be7291bc8 41d2d5f01a9909c5