Search for Variation information by Variation ID:

Please input a variation ID (e.g., vg0722097923 , STR0500036000 ).

Detailed information for vg0620020791:

Variant ID: vg0620020791 (JBrowse)Variation Type: SNP
Chromosome: chr06Position: 20020791
Reference Allele: GAlternative Allele: A
Primary Allele: ASecondary Allele: G

Inferred Ancestral Allele : G (evidence from allele frequency in Oryza rufipogon: G: 0.90, A: 0.10, others allele: 0.00, population size: 81. )

Flanking Sequence (100 bp) in Reference Genome:


CCACCGTGGCGGGCGCCGTCGCCGTCGCGGTCGCGCTCCTCCTGCTGGCGCTCGCCGGCAGGCTGGCGCAGACGACGGGAGGAGGCTCCGCCGCGGCGGC[G/A]
GCGTCGGGGCGGCGGCGGCGGCTGCTGAGCTGCCCGTGCGCGTGCGGGCTGATGGCGCCCGGCGCGGGGGGGATCGGCGTGCTGCCGGCGTTCGCGTACG

Reverse complement sequence

CGTACGCGAACGCCGGCAGCACGCCGATCCCCCCCGCGCCGGGCGCCATCAGCCCGCACGCGCACGGGCAGCTCAGCAGCCGCCGCCGCCGCCCCGACGC[C/T]
GCCGCCGCGGCGGAGCCTCCTCCCGTCGTCTGCGCCAGCCTGCCGGCGAGCGCCAGCAGGAGGAGCGCGACCGCGACGGCGACGGCGCCCGCCACGGTGG

Allele Frequencies:

Populations Population SizeFrequency of A(primary allele) Frequency of G(secondary allele) Frequency of N Frequency of DEL Frequency of others Allele
All  4726 58.00% 16.90% 18.71% 6.39% NA
All Indica  2759 83.30% 1.60% 11.74% 3.44% NA
All Japonica  1512 4.50% 46.60% 35.38% 13.56% NA
Aus  269 100.00% 0.00% 0.00% 0.00% NA
Indica I  595 71.10% 1.50% 23.53% 3.87% NA
Indica II  465 71.80% 2.40% 17.63% 8.17% NA
Indica III  913 98.80% 0.50% 0.44% 0.22% NA
Indica Intermediate  786 81.20% 2.30% 12.47% 4.07% NA
Temperate Japonica  767 2.70% 29.50% 49.15% 18.64% NA
Tropical Japonica  504 7.50% 58.50% 23.61% 10.32% NA
Japonica Intermediate  241 3.70% 75.90% 16.18% 4.15% NA
VI/Aromatic  96 64.60% 34.40% 1.04% 0.00% NA
Intermediate  90 48.90% 22.20% 26.67% 2.22% NA

Allele Effect:

Var ID Var Locus snpEff Annotation CooVar Annotation Chromatin Accessibility Score PolyPhen-2 Effect PolyPhen-2 Score SIFT Effect SIFT Score
vg0620020791 G -> A LOC_Os06g34400.1 synonymous_variant ; p.Ala314Ala; LOW synonymous_codon Average:90.147; most accessible tissue: Minghui63 panicle, score: 98.021 N N N N
vg0620020791 G -> A LOC_Os06g34400.1 synonymous_variant ; p.Ala314Ala; LOW nonsynonymous_codon ; A314E Average:90.147; most accessible tissue: Minghui63 panicle, score: 98.021 unknown unknown DELETERIOUS 0.01
vg0620020791 G -> DEL LOC_Os06g34400.1 N frameshift_variant Average:90.147; most accessible tissue: Minghui63 panicle, score: 98.021 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)
vg0620020791 G A -0.02 -0.04 -0.03 -0.02 -0.01 0.0