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Detailed information for vg0224228628:

Variant ID: vg0224228628 (JBrowse)Variation Type: INDEL
Chromosome: chr02Position: 24228628
Reference Allele: CTAlternative Allele: C,TT
Primary Allele: CTSecondary Allele: TT

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


CGGTACATTATTAAGGCTAAGCTAGCTGCTAAGTATTAGAGGGGAGGTGAGAGAGAGCGAGAGAGAGAGAGATTGGTGAGTGGGGAGTAGTTCTTGTAGG[CT/C,TT]
GAGTAGTACTAGTTTTTTCAGGGGCACTGAAAAAAGAGCTTGTAGTTTCTGTCGGGAACACCGATTACTAGCTGAAACATCATCAGTTCTGTTCTTCTTC

Reverse complement sequence

GAAGAAGAACAGAACTGATGATGTTTCAGCTAGTAATCGGTGTTCCCGACAGAAACTACAAGCTCTTTTTTCAGTGCCCCTGAAAAAACTAGTACTACTC[AG/G,AA]
CCTACAAGAACTACTCCCCACTCACCAATCTCTCTCTCTCTCGCTCTCTCTCACCTCCCCTCTAATACTTAGCAGCTAGCTTAGCCTTAATAATGTACCG

Allele Frequencies:

Populations Population SizeFrequency of CT(primary allele) Frequency of TT(secondary allele) Frequency of N Frequency of DEL Frequency of others Allele
All  4726 99.10% 0.30% 0.53% 0.00% C: 0.11%
All Indica  2759 99.70% 0.10% 0.11% 0.00% C: 0.04%
All Japonica  1512 97.60% 0.70% 1.46% 0.00% C: 0.26%
Aus  269 100.00% 0.00% 0.00% 0.00% NA
Indica I  595 99.80% 0.00% 0.17% 0.00% NA
Indica II  465 99.80% 0.20% 0.00% 0.00% NA
Indica III  913 100.00% 0.00% 0.00% 0.00% NA
Indica Intermediate  786 99.40% 0.30% 0.25% 0.00% C: 0.13%
Temperate Japonica  767 95.40% 1.30% 2.87% 0.00% C: 0.39%
Tropical Japonica  504 100.00% 0.00% 0.00% 0.00% NA
Japonica Intermediate  241 99.20% 0.40% 0.00% 0.00% C: 0.41%
VI/Aromatic  96 100.00% 0.00% 0.00% 0.00% NA
Intermediate  90 100.00% 0.00% 0.00% 0.00% NA

Allele Effect:

Var ID Var Locus snpEff Annotation CooVar Annotation Chromatin Accessibility Score PolyPhen-2 Effect PolyPhen-2 Score SIFT Effect SIFT Score
vg0224228628 CT -> TT LOC_Os02g40010.1 3_prime_UTR_variant ; 331.0bp to feature; MODIFIER silent_mutation Average:82.7; most accessible tissue: Zhenshan97 panicle, score: 96.254 N N N N
vg0224228628 CT -> TT LOC_Os02g40010.2 3_prime_UTR_variant ; 331.0bp to feature; MODIFIER silent_mutation Average:82.7; most accessible tissue: Zhenshan97 panicle, score: 96.254 N N N N
vg0224228628 CT -> TT LOC_Os02g40010.3 3_prime_UTR_variant ; 331.0bp to feature; MODIFIER silent_mutation Average:82.7; most accessible tissue: Zhenshan97 panicle, score: 96.254 N N N N
vg0224228628 CT -> TT LOC_Os02g40010.4 3_prime_UTR_variant ; 331.0bp to feature; MODIFIER silent_mutation Average:82.7; most accessible tissue: Zhenshan97 panicle, score: 96.254 N N N N
vg0224228628 CT -> TT LOC_Os02g40020.1 downstream_gene_variant ; 205.0bp to feature; MODIFIER silent_mutation Average:82.7; most accessible tissue: Zhenshan97 panicle, score: 96.254 N N N N
vg0224228628 CT -> C LOC_Os02g40010.1 3_prime_UTR_variant ; 332.0bp to feature; MODIFIER silent_mutation Average:82.7; most accessible tissue: Zhenshan97 panicle, score: 96.254 N N N N
vg0224228628 CT -> C LOC_Os02g40010.2 3_prime_UTR_variant ; 332.0bp to feature; MODIFIER silent_mutation Average:82.7; most accessible tissue: Zhenshan97 panicle, score: 96.254 N N N N
vg0224228628 CT -> C LOC_Os02g40010.3 3_prime_UTR_variant ; 332.0bp to feature; MODIFIER silent_mutation Average:82.7; most accessible tissue: Zhenshan97 panicle, score: 96.254 N N N N
vg0224228628 CT -> C LOC_Os02g40010.4 3_prime_UTR_variant ; 332.0bp to feature; MODIFIER silent_mutation Average:82.7; most accessible tissue: Zhenshan97 panicle, score: 96.254 N N N N
vg0224228628 CT -> C LOC_Os02g40020.1 downstream_gene_variant ; 204.0bp to feature; MODIFIER silent_mutation Average:82.7; most accessible tissue: Zhenshan97 panicle, score: 96.254 N N N N

Effects Predicted by Deep Convolutional Neural Networks

For each variant, we constructed two sequences that contain the variation site and the sequence around it, differing only in the variation site. We then used Basenji to predict the chromatin accessibility of each tissue for the two sequences, respectively, and scored the effect of the variant by comparing the changes in chromatin accessibility corresponding to the two genotypes in the 1 kb region around the variation site. The effect score was defined as the logarithmic ratio of the predicted chromatin accessibility of the alternative genotype to the value of the reference genotype.

Var ID Ref Alt Root (RT) Young Leaf (YL) Flag Leaf (FL) Young Panicle (YP) Lemma & Palea (LP) Stamen & Pistil (SP)
vg0224228628 CT C -0.05 -0.08 -0.12 0.08 0.08 0.0
vg0224228628 CT TT 0.02 -0.01 -0.02 -0.08 -0.05 -0.05

Putative Genotype-Phenotype Associations:

Var ID LMM P-value LR P-value Trait Subpopulation Is leadSNP Publication
vg0224228628 3.31E-06 3.31E-06 mr1099 Jap_All YES Genome-wide association analyses provide genetic and biochemical insights into natural variation in rice metabolism, Nat Genet, 46(7):714-21, PMID:24908251
vg0224228628 2.62E-06 1.59E-06 mr1101 Jap_All Not Genome-wide association analyses provide genetic and biochemical insights into natural variation in rice metabolism, Nat Genet, 46(7):714-21, PMID:24908251
vg0224228628 8.70E-06 NA mr1123 Jap_All Not Genome-wide association analyses provide genetic and biochemical insights into natural variation in rice metabolism, Nat Genet, 46(7):714-21, PMID:24908251
vg0224228628 5.20E-07 8.73E-07 mr1150 Jap_All YES Genome-wide association analyses provide genetic and biochemical insights into natural variation in rice metabolism, Nat Genet, 46(7):714-21, PMID:24908251
vg0224228628 7.06E-06 NA mr1858 Jap_All Not Genome-wide association analyses provide genetic and biochemical insights into natural variation in rice metabolism, Nat Genet, 46(7):714-21, PMID:24908251
vg0224228628 7.06E-06 NA mr1859 Jap_All Not Genome-wide association analyses provide genetic and biochemical insights into natural variation in rice metabolism, Nat Genet, 46(7):714-21, PMID:24908251
vg0224228628 7.63E-06 NA mr1917 Jap_All Not Genome-wide association analyses provide genetic and biochemical insights into natural variation in rice metabolism, Nat Genet, 46(7):714-21, PMID:24908251
vg0224228628 7.08E-06 NA mr1936 Jap_All Not Genome-wide association analyses provide genetic and biochemical insights into natural variation in rice metabolism, Nat Genet, 46(7):714-21, PMID:24908251