Search for Variation information by Variation ID:

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

Detailed information for vg0521668459:

Variant ID: vg0521668459 (JBrowse)Variation Type: SNP
Chromosome: chr05Position: 21668459
Reference Allele: TAlternative Allele: G
Primary Allele: TSecondary Allele: G

Inferred Ancestral Allele : T (evidence from allele frequency in Oryza rufipogon: T: 1.00, others allele: 0.00, population size: 259. )

Flanking Sequence (100 bp) in Reference Genome:


CCGTTTTCTTGAATTTACGACCGACCGTAAAATCGAATTCCTACATCAAAACCAGTCCAAAAGATCTGCCCAGTCCGTCATGCTGCACTCTACAAGCTCC[T/G]
CATCGGTTCCTCTCTGCCTCTGCTGCTGTTGCTGCAGCATAGAGCCATCGCAGCCGCCATTGTCGTCGCTGGATGAGGTGCTGTCAAGGCTGTCATCTGG

Reverse complement sequence

CCAGATGACAGCCTTGACAGCACCTCATCCAGCGACGACAATGGCGGCTGCGATGGCTCTATGCTGCAGCAACAGCAGCAGAGGCAGAGAGGAACCGATG[A/C]
GGAGCTTGTAGAGTGCAGCATGACGGACTGGGCAGATCTTTTGGACTGGTTTTGATGTAGGAATTCGATTTTACGGTCGGTCGTAAATTCAAGAAAACGG

Allele Frequencies:

Populations Population SizeFrequency of T(primary allele) Frequency of G(secondary allele) Frequency of N Frequency of DEL Frequency of others Allele
All  4726 99.50% 0.50% 0.02% 0.00% NA
All Indica  2759 99.90% 0.10% 0.00% 0.00% NA
All Japonica  1512 99.90% 0.00% 0.07% 0.00% NA
Aus  269 100.00% 0.00% 0.00% 0.00% NA
Indica I  595 100.00% 0.00% 0.00% 0.00% NA
Indica II  465 99.10% 0.90% 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 99.90% 0.00% 0.13% 0.00% NA
Tropical Japonica  504 100.00% 0.00% 0.00% 0.00% NA
Japonica Intermediate  241 100.00% 0.00% 0.00% 0.00% NA
VI/Aromatic  96 82.30% 17.70% 0.00% 0.00% NA
Intermediate  90 98.90% 1.10% 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
vg0521668459 T -> G LOC_Os05g37080.1 missense_variant ; p.Glu257Ala; MODERATE nonsynonymous_codon ; E257A Average:79.142; most accessible tissue: Callus, score: 90.999 unknown unknown TOLERATED 0.07

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)
vg0521668459 T G -0.02 -0.01 -0.02 0.03 0.01 0.02