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Detailed information for vg0302707462:

Variant ID: vg0302707462 (JBrowse)Variation Type: SNP
Chromosome: chr03Position: 2707462
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


AACGTGGGGGCCGCATGCAGCGAAAGTACCCGAAGTCGCGAACCAGTCCACTTTGATCCGCGCGGGGCAGCCGAAGAAAGCGCCCAACCCCCGCCCTTTT[C/T]
TTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCCTCTCTCACTTTTCCAAACCATCAACGTGCCCTTCTATTTCCTTCTTCCCTTCCTCCGAGGGCTTCT

Reverse complement sequence

AGAAGCCCTCGGAGGAAGGGAAGAAGGAAATAGAAGGGCACGTTGATGGTTTGGAAAAGTGAGAGAGGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAA[G/A]
AAAAGGGCGGGGGTTGGGCGCTTTCTTCGGCTGCCCCGCGCGGATCAAAGTGGACTGGTTCGCGACTTCGGGTACTTTCGCTGCATGCGGCCCCCACGTT

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 97.20% 1.30% 1.48% 0.00% NA
All Indica  2759 95.80% 1.80% 2.36% 0.00% NA
All Japonica  1512 99.60% 0.30% 0.13% 0.00% NA
Aus  269 97.80% 1.90% 0.37% 0.00% NA
Indica I  595 94.60% 0.80% 4.54% 0.00% NA
Indica II  465 95.50% 1.50% 3.01% 0.00% NA
Indica III  913 96.20% 3.00% 0.88% 0.00% NA
Indica Intermediate  786 96.60% 1.40% 2.04% 0.00% NA
Temperate Japonica  767 100.00% 0.00% 0.00% 0.00% NA
Tropical Japonica  504 98.80% 0.80% 0.40% 0.00% NA
Japonica Intermediate  241 100.00% 0.00% 0.00% 0.00% NA
VI/Aromatic  96 97.90% 1.00% 1.04% 0.00% NA
Intermediate  90 98.90% 0.00% 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
vg0302707462 C -> T LOC_Os03g05470.1 upstream_gene_variant ; 1.0bp to feature; MODIFIER silent_mutation Average:94.951; most accessible tissue: Callus, score: 99.017 N N N N
vg0302707462 C -> T LOC_Os03g05460-LOC_Os03g05470 intergenic_region ; MODIFIER silent_mutation Average:94.951; most accessible tissue: Callus, score: 99.017 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)
vg0302707462 C T -0.01 -0.01 0.01 -0.01 0.0 0.02