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Detailed information for vg1209262766:

Variant ID: vg1209262766 (JBrowse)Variation Type: SNP
Chromosome: chr12Position: 9262766
Reference Allele: GAlternative Allele: A
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


CTCCCGGTCCTTCACCGCAAATTCTCTCCCGGCATCTCGAGTCACCTACACATAGAACAAACAAAGAAACCATATTCCGAGACCAAGCTATCCCCAACTT[G/A]
ACTCATTAGTAGCAAACGACAGTATTACATACGCATAGTGTCCATCTAGAAGTCATAATCATGAAACAATCACGCATATCCAAACAAACAACCCGAAACC

Reverse complement sequence

GGTTTCGGGTTGTTTGTTTGGATATGCGTGATTGTTTCATGATTATGACTTCTAGATGGACACTATGCGTATGTAATACTGTCGTTTGCTACTAATGAGT[C/T]
AAGTTGGGGATAGCTTGGTCTCGGAATATGGTTTCTTTGTTTGTTCTATGTGTAGGTGACTCGAGATGCCGGGAGAGAATTTGCGGTGAAGGACCGGGAG

Allele Frequencies:

Populations Population SizeFrequency of G(primary allele) Frequency of A(secondary allele) Frequency of N Frequency of DEL Frequency of others Allele
All  4726 96.10% 2.90% 0.95% 0.00% NA
All Indica  2759 99.90% 0.10% 0.00% 0.00% NA
All Japonica  1512 88.30% 8.80% 2.91% 0.00% NA
Aus  269 99.30% 0.70% 0.00% 0.00% NA
Indica I  595 99.70% 0.30% 0.00% 0.00% NA
Indica II  465 100.00% 0.00% 0.00% 0.00% NA
Indica III  913 100.00% 0.00% 0.00% 0.00% NA
Indica Intermediate  786 100.00% 0.00% 0.00% 0.00% NA
Temperate Japonica  767 79.80% 14.70% 5.48% 0.00% NA
Tropical Japonica  504 98.40% 1.60% 0.00% 0.00% NA
Japonica Intermediate  241 94.20% 5.00% 0.83% 0.00% NA
VI/Aromatic  96 100.00% 0.00% 0.00% 0.00% NA
Intermediate  90 96.70% 2.20% 1.11% 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
vg1209262766 G -> A LOC_Os12g16200.1 downstream_gene_variant ; 910.0bp to feature; MODIFIER silent_mutation Average:69.409; most accessible tissue: Zhenshan97 young leaf, score: 91.967 N N N N
vg1209262766 G -> A LOC_Os12g16190-LOC_Os12g16200 intergenic_region ; MODIFIER silent_mutation Average:69.409; most accessible tissue: Zhenshan97 young leaf, score: 91.967 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)
vg1209262766 G A -0.01 -0.03 0.01 0.0 0.01 0.01

Putative Genotype-Phenotype Associations:

Var ID LMM P-value LR P-value Trait Subpopulation Is leadSNP Publication
vg1209262766 NA 4.95E-06 mr1648 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
vg1209262766 2.70E-10 NA mr1002_2 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
vg1209262766 1.79E-06 NA mr1002_2 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