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Detailed information for vg0620019499:

Variant ID: vg0620019499 (JBrowse)Variation Type: SNP
Chromosome: chr06Position: 20019499
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele : C (evidence from allele frequency in Oryza rufipogon: C: 0.96, T: 0.04, others allele: 0.00, population size: 74. )

Flanking Sequence (100 bp) in Reference Genome:


GCTACGGCATCGTGGTGGCGTGCGTGTCGCTGCTGCTGCTGTGCGCGCTCGTCTCCGCCGTCGGCGTCGCCAGGGCCTTCGCCGCCACCGGGGTGCTCGT[C/T]
CTGCTGCTCGGCCTCGCCGGCTGGCTCGCGCCCACGGACGCCTTCGCCGTCGCGCTGGCCCCCGAGCTCTACGCGGGGAACGCCGGCGGCGGCGGCGGTA

Reverse complement sequence

TACCGCCGCCGCCGCCGGCGTTCCCCGCGTAGAGCTCGGGGGCCAGCGCGACGGCGAAGGCGTCCGTGGGCGCGAGCCAGCCGGCGAGGCCGAGCAGCAG[G/A]
ACGAGCACCCCGGTGGCGGCGAAGGCCCTGGCGACGCCGACGGCGGAGACGAGCGCGCACAGCAGCAGCAGCGACACGCACGCCACCACGATGCCGTAGC

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 40.90% 24.10% 18.26% 16.78% NA
All Indica  2759 43.70% 28.30% 13.12% 14.90% NA
All Japonica  1512 44.80% 2.10% 29.03% 24.07% NA
Aus  269 0.40% 98.10% 1.12% 0.37% NA
Indica I  595 43.70% 12.80% 22.86% 20.67% NA
Indica II  465 37.20% 16.10% 16.99% 29.68% NA
Indica III  913 44.80% 47.80% 5.15% 2.30% NA
Indica Intermediate  786 46.30% 24.60% 12.72% 16.41% NA
Temperate Japonica  767 24.60% 1.00% 40.68% 33.64% NA
Tropical Japonica  504 64.90% 4.20% 17.06% 13.89% NA
Japonica Intermediate  241 67.20% 0.80% 17.01% 14.94% NA
VI/Aromatic  96 13.50% 52.10% 31.25% 3.12% NA
Intermediate  90 37.80% 14.40% 32.22% 15.56% NA

Allele Effect:

Var ID Var Locus snpEff Annotation CooVar Annotation Chromatin Accessibility Score PolyPhen-2 Effect PolyPhen-2 Score SIFT Effect SIFT Score
vg0620019499 C -> T LOC_Os06g34400.1 synonymous_variant ; p.Val60Val; LOW synonymous_codon Average:91.543; most accessible tissue: Minghui63 panicle, score: 98.182 N N N N
vg0620019499 C -> DEL LOC_Os06g34400.1 N frameshift_variant Average:91.543; most accessible tissue: Minghui63 panicle, score: 98.182 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)
vg0620019499 C T -0.02 -0.03 -0.04 -0.02 -0.02 -0.01