R3in134
SRR 14708218
General Information
- Sample Name
- NEB4
- Accession Date
- May 31, 2021
- Reported Plant Sex
- not reported
- 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 I
File Downloads
Variants (THCAS, CBDAS, and CBCAS)
Variants (Select Genes of Interest)
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/ |
|
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.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.2653A>G | p.Thr885Ala | missense variant | moderate | contig885 | 3539 | A/G |
|
PHL-2 | c.280T>C | p.Phe94Leu | missense variant | moderate | contig2621 | 338845 | T/C |
|
PHL-2 | c.722G>A | p.Gly241Glu | missense variant | moderate | contig2621 | 339860 | G/A |
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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.2834A>G | p.Asn945Ser | missense variant | moderate | contig2621 | 342877 | A/G |
|
PKSG-4b | c.558-1G>A | splice acceptor variant & intron variant | high | contig700 | 2715037 | C/T |
|
|
PKSG-4b | c.323A>G | p.Glu108Gly | missense variant | moderate | contig700 | 2721350 | T/C |
|
PKSG-2a | c.241G>A | p.Val81Met | missense variant | moderate | contig700 | 1945149 | C/T |
|
PKSG-2a | c.240T>G | p.Asp80Glu | missense variant | moderate | contig700 | 1945150 | A/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-2a | c.-2_1delATA | p.Met1del | start lost & conservative inframe deletion | high | contig700 | 1945632 | ATAT/A |
|
AAE1-1 | c.1481C>T | p.Ala494Val | missense variant | moderate | contig606 | 3242790 | G/A |
|
AAE1-1 | c.454A>G | p.Lys152Glu | missense variant | moderate | contig606 | 3243817 | T/C |
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ELF3 | c.365A>T | p.Lys122Met | missense variant | moderate | contig97 | 242071 | A/T |
|
ELF3 | c.499T>G | p.Tyr167Asp | missense variant | moderate | contig97 | 242205 | T/G |
|
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 |
|
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.1966C>G | p.Pro656Ala | missense variant | moderate | contig97 | 244797 | C/G | |
ELF3 | c.2156T>G | p.Ile719Arg | missense variant | moderate | contig97 | 244987 | T/G |
|
aPT1 | c.727G>T | p.Glu243* | stop gained | high | contig121 | 2841362 | G/T | |
aPT1 | c.938C>T | p.Thr313Ile | missense variant | moderate | contig121 | 2842584 | C/T |
|
aPT1 | c.958G>A | p.Gly320Ser | missense variant | moderate | contig121 | 2842731 | G/A |
|
AAE1-2 | c.331A>G | p.Asn111Asp | missense variant | moderate | contig81 | 209293 | A/G |
|
AAE1-2 | c.384G>C | p.Glu128Asp | missense variant | moderate | contig81 | 209346 | G/C |
|
AAE1-2 | c.688G>A | p.Asp230Asn | missense variant | moderate | contig81 | 209650 | G/A |
|
AAE1-2 | c.1006A>G | p.Lys336Glu | missense variant | moderate | contig81 | 209968 | A/G |
|
AAE1-2 | c.1102C>A | p.His368Asn | missense variant | moderate | contig81 | 210064 | C/A |
|
AAE1-2 | c.1118C>G | p.Thr373Ser | missense variant | moderate | contig81 | 210080 | C/G |
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AAE1-2 | c.1415G>A | p.Ser472Asn | missense variant | moderate | contig81 | 210377 | G/A |
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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 |
|
AAE1-2 | c.1541T>C | p.Val514Ala | missense variant | moderate | contig81 | 210503 | T/C |
|
PHL-1 | c.2551A>G | p.Thr851Ala | missense variant | moderate | contig1439 | 1487246 | T/C | |
PKSG-2b | c.1152T>A | p.Asn384Lys | missense variant | moderate | contig700 | 1950486 | A/T | |
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.-2_1dupATA | start lost & conservative inframe insertion | high | contig700 | 1951880 | A/ATAT |
|
|
TFL1 | c.302-1G>A | splice acceptor variant & intron variant | high | contig1636 | 520616 | 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 | |
HDS-1 |
c.-108+1_-10 |
splice donor variant & intron variant | high | contig1891 | 889975 | A/AC |
|
|
PIE1-2 | c.5932A>G | p.Ile1978Val | missense variant | moderate | contig1460 | 1185552 | T/C | |
PIE1-2 | c.1872T>A | p.Asp624Glu | missense variant | moderate | contig1460 | 1190252 | A/T | |
PIE1-2 | c.710C>T | p.Pro237Leu | missense variant | moderate | contig1460 | 1193804 | G/A | |
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.590A>T | p.Lys197Ile | missense variant | moderate | contig883 | 270079 | A/T |
|
FT |
c.173_181del |
p.Leu58_Asn6 |
disruptive inframe deletion | moderate | contig1561 | 3124595 | ACTTCTCAAC/A |
|
FT | c.240C>G | p.Asn80Lys | missense variant | moderate | contig1561 | 3124664 | C/G |
|
FT |
c.259+1_259+ |
splice donor variant & intron variant | high | contig1561 | 3124684 | G/GTA | ||
FT | c.364A>G | p.Ile122Val | missense variant | moderate | contig1561 | 3126401 | A/G |
|
FT |
c.421_422dup |
p.Leu142fs | frameshift variant | high | contig1561 | 3126659 | C/CTA |
|
FT | c.424C>A | p.Leu142Ile | missense variant | moderate | contig1561 | 3126663 | C/A |
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aPT4 | c.80A>G | p.Lys27Arg | missense variant | moderate | contig121 | 2828736 | A/G |
|
aPT4 | c.202T>A | p.Leu68Ile | missense variant | moderate | contig121 | 2828858 | T/A |
|
aPT4 |
c.235_236del |
p.Val79fs | frameshift variant | high | contig121 | 2829030 | ATG/A |
|
aPT4 | c.238delT | p.Ser80fs | frameshift variant | high | contig121 | 2829034 | AT/A |
|
aPT4 | c.916C>T | p.His306Tyr | missense variant & splice region variant | moderate | contig121 | 2832711 | C/T |
|
aPT4 | c.1168T>C | p.Tyr390His | missense variant | moderate | contig121 | 2833503 | T/C |
|
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.2069G>A | p.Arg690Gln | missense variant | moderate | contig1450 | 2045671 | C/T |
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AAE1-3 | c.695C>T | p.Thr232Ile | missense variant | moderate | contig976 | 1083159 | G/A |
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AAE1-3 | c.634G>C | p.Gly212Arg | missense variant | moderate | contig976 | 1083220 | C/G |
|
AAE1-3 |
c.586-28_608 |
p.Ser196fs | frameshift variant & splice acceptor variant & splice region variant & intron variant | high | contig976 | 1083245 |
ATCACCACTGAC |
|
AAE1-3 | c.382T>C | p.Tyr128His | missense variant | moderate | contig976 | 1083643 | A/G |
|
AAE1-3 |
c.338_339del |
p.Pro113fs | frameshift variant | high | contig976 | 1083685 | TAG/T |
|
AAE1-3 | c.8C>T | p.Ser3Leu | missense variant | moderate | contig976 | 1084067 | G/A |
|
AAE1-3 | c.3G>A | p.Met1? | start lost | high | contig976 | 1084072 | C/T | |
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 |
|
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)
- 0.206 R3in134 (SRR14708220)
- 0.209 R3in134 (SRR14708235)
- 0.218 R3in134 (SRR14708219)
- 0.241 Kyrgyz Gold (RSP11054)
- 0.244 QHI (SRR14708202)
- 0.253 R2in135 (SRR14708221)
- 0.256 IMA (SRR14708203)
- 0.256 KYRG-11 (RSP11051)
- 0.256 R2in135 (SRR14708224)
- 0.258 Jiangji (RSP10653)
- 0.258 KYRG-151 (RSP11052)
- 0.260 Carmagnola (SRR14708274)
- 0.261 R2in135 (SRR14708223)
- 0.263 Santhica27 (RSP10056)
- 0.263 R2in135 (SRR14708236)
- 0.264 Tisza (RSP11045)
- 0.264 Tisza (RSP11044)
- 0.267 Tak-HN (RSP11618)
- 0.269 XUM1 (SRR14708205)
- 0.272 XBL1 (SRR14708207)
Most genetically distant strains (All Samples)
- 0.491 Cherry Blossom (RSP11318)
- 0.469 Cherry Blossom (RSP11323)
- 0.460 Cherry Blossom (RSP11300)
- 0.455 Cherry Blossom (RSP11325)
- 0.453 Cherry Blossom (RSP11312)
- 0.452 Cherry Blossom (RSP11301)
- 0.451 Cherry Blossom (RSP11331)
- 0.451 Cherry Blossom (RSP11328)
- 0.445 Unknown--Cherry Wine---001- (RSP11268)
- 0.442 Cherry Blossom (RSP11306)
- 0.442 Cherry Blossom (RSP11322)
- 0.441 Cherry Blossom (RSP11311)
- 0.441 Cherry Blossom (RSP11299)
- 0.439 Cherry Blossom (RSP11332)
- 0.438 Cherry Blossom (RSP11315)
- 0.438 Cherry Blossom (RSP11302)
- 0.434 Wife (RSP11148)
- 0.433 Cherry Blossom (RSP11319)
- 0.432 Cherry Blossom (RSP11321)
- 0.432 Cherry Blossom (RSP11316)
Nearest genetic relative in Phylos dataset
Phylos Strain SRR8349269
- Overlapping SNPs:
- 12
- Concordance:
- 10
Nearest genetic relative in Lynch dataset
Lynch Strain SRR3495181
- Overlapping SNPs:
- 3
- Concordance:
- 3