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Detailed information for vg0727745937:

Variant ID: vg0727745937 (JBrowse)Variation Type: SNP
Chromosome: chr07Position: 27745937
Reference Allele: CAlternative Allele: T,G
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele : C (evidence from allele frequency in Oryza rufipogon: C: 0.71, T: 0.29, others allele: 0.00, population size: 66. )

Flanking Sequence (100 bp) in Reference Genome:


TATGATAGGTGGCATCAGATAACTATTGTATGAATTGGCCATTAAAATGACTACATATAATTTAGAGTTAGCAGTTGGCTATAGCCCATGAGCTGCATGC[C/T,G]
AGGATTTAGTTCACACATGCCATATGGGCACCTCCATGCAAAGACATTTTTCTCCTCTCCTTCAGCTGTCCATGCAAAAATTCTCATCGGATTTCGAGGG

Reverse complement sequence

CCCTCGAAATCCGATGAGAATTTTTGCATGGACAGCTGAAGGAGAGGAGAAAAATGTCTTTGCATGGAGGTGCCCATATGGCATGTGTGAACTAAATCCT[G/A,C]
GCATGCAGCTCATGGGCTATAGCCAACTGCTAACTCTAAATTATATGTAGTCATTTTAATGGCCAATTCATACAATAGTTATCTGATGCCACCTATCATA

Allele Frequencies:

Populations Population SizeFrequency of C(primary allele) Frequency of T(secondary allele) Frequency of N Frequency of DEL Frequency of others Allele
All  4726 93.20% 5.20% 1.57% 0.00% G: 0.04%
All Indica  2759 96.10% 3.10% 0.76% 0.00% NA
All Japonica  1512 86.20% 10.40% 3.31% 0.00% G: 0.07%
Aus  269 100.00% 0.00% 0.00% 0.00% NA
Indica I  595 95.80% 1.80% 2.35% 0.00% NA
Indica II  465 99.10% 0.60% 0.22% 0.00% NA
Indica III  913 98.50% 1.50% 0.00% 0.00% NA
Indica Intermediate  786 91.90% 7.40% 0.76% 0.00% NA
Temperate Japonica  767 73.10% 20.50% 6.39% 0.00% NA
Tropical Japonica  504 100.00% 0.00% 0.00% 0.00% NA
Japonica Intermediate  241 98.80% 0.40% 0.41% 0.00% G: 0.41%
VI/Aromatic  96 99.00% 0.00% 0.00% 0.00% G: 1.04%
Intermediate  90 96.70% 0.00% 3.33% 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
vg0727745937 C -> G LOC_Os07g46480.1 upstream_gene_variant ; 371.0bp to feature; MODIFIER silent_mutation Average:85.941; most accessible tissue: Zhenshan97 panicle, score: 97.577 N N N N
vg0727745937 C -> G LOC_Os07g46470.1 downstream_gene_variant ; 1044.0bp to feature; MODIFIER silent_mutation Average:85.941; most accessible tissue: Zhenshan97 panicle, score: 97.577 N N N N
vg0727745937 C -> G LOC_Os07g46470-LOC_Os07g46480 intergenic_region ; MODIFIER silent_mutation Average:85.941; most accessible tissue: Zhenshan97 panicle, score: 97.577 N N N N
vg0727745937 C -> T LOC_Os07g46480.1 upstream_gene_variant ; 371.0bp to feature; MODIFIER silent_mutation Average:85.941; most accessible tissue: Zhenshan97 panicle, score: 97.577 N N N N
vg0727745937 C -> T LOC_Os07g46470.1 downstream_gene_variant ; 1044.0bp to feature; MODIFIER silent_mutation Average:85.941; most accessible tissue: Zhenshan97 panicle, score: 97.577 N N N N
vg0727745937 C -> T LOC_Os07g46470-LOC_Os07g46480 intergenic_region ; MODIFIER silent_mutation Average:85.941; most accessible tissue: Zhenshan97 panicle, score: 97.577 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)
vg0727745937 C G -0.03 -0.02 -0.02 -0.03 -0.03 -0.04
vg0727745937 C T 0.01 -0.01 -0.03 0.0 -0.01 -0.02

Putative Genotype-Phenotype Associations:

Var ID LMM P-value LR P-value Trait Subpopulation Is leadSNP Publication
vg0727745937 3.71E-07 1.48E-12 Heading_date All YES Breeding signatures of rice improvement revealed by a genomic variation map from a large germplasm collection, Proc Natl Acad Sci USA, 112(39): E5411-E5419, PMID:26358652