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Detailed information for vg0233443766:

Variant ID: vg0233443766 (JBrowse)Variation Type: SNP
Chromosome: chr02Position: 33443766
Reference Allele: TAlternative Allele: G
Primary Allele: TSecondary Allele: G

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


GGCGCCGACGACGGCGGCAGCGGCAGCGGCAGCGGCACCGCGAGCGACGTGAGGTCCCGCTGCGGCAGCGGCAGCGTGAGATCCGGCCGGCGCCGCGACC[T/G]
CCCCGGCGTCCCCGGCTGCTGCTGCTGCTGCTGCTGCAGCCCCGCCCGCAAGCTCGGCGGCCCGCCCGGTCGCATCGCGACGGCGGCGAGGCGCGGCGCG

Reverse complement sequence

CGCGCCGCGCCTCGCCGCCGTCGCGATGCGACCGGGCGGGCCGCCGAGCTTGCGGGCGGGGCTGCAGCAGCAGCAGCAGCAGCAGCCGGGGACGCCGGGG[A/C]
GGTCGCGGCGCCGGCCGGATCTCACGCTGCCGCTGCCGCAGCGGGACCTCACGTCGCTCGCGGTGCCGCTGCCGCTGCCGCTGCCGCCGTCGTCGGCGCC

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 73.20% 1.10% 15.83% 9.86% NA
All Indica  2759 71.90% 1.10% 14.97% 12.11% NA
All Japonica  1512 76.70% 0.00% 16.01% 7.28% NA
Aus  269 79.20% 5.90% 14.50% 0.37% NA
Indica I  595 60.00% 0.50% 29.41% 10.08% NA
Indica II  465 58.50% 0.60% 19.14% 21.72% NA
Indica III  913 88.50% 1.40% 2.74% 7.34% NA
Indica Intermediate  786 69.50% 1.30% 15.78% 13.49% NA
Temperate Japonica  767 72.10% 0.00% 18.90% 9.00% NA
Tropical Japonica  504 84.30% 0.00% 11.11% 4.56% NA
Japonica Intermediate  241 75.50% 0.00% 17.01% 7.47% NA
VI/Aromatic  96 42.70% 5.20% 37.50% 14.58% NA
Intermediate  90 71.10% 1.10% 20.00% 7.78% NA

Allele Effect:

Var ID Var Locus snpEff Annotation CooVar Annotation Chromatin Accessibility Score PolyPhen-2 Effect PolyPhen-2 Score SIFT Effect SIFT Score
vg0233443766 T -> G LOC_Os02g54600.1 synonymous_variant ; p.Arg26Arg; LOW synonymous_codon Average:96.489; most accessible tissue: Minghui63 young leaf, score: 99.232 N N N N
vg0233443766 T -> DEL LOC_Os02g54600.1 N frameshift_variant Average:96.489; most accessible tissue: Minghui63 young leaf, score: 99.232 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)
vg0233443766 T G -0.01 -0.01 0.0 0.0 -0.01 -0.01