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Detailed information for vg1225035494:

Variant ID: vg1225035494 (JBrowse)Variation Type: SNP
Chromosome: chr12Position: 25035494
Reference Allele: AAlternative Allele: G
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


TCGGATCTCGGAGCGCAGCCGGCGGCGAGGCCTACCGGCTGAGCCGGTCCGGCGAGAGGAGGGCCTCGGGGTCGCCGCACCGGAGCCGGCTGGACGCGGC[A/G]
GCGGCGGCGCTGGCGCGCCTCGCCGCGGCGAGGATGGAGGGTGGCTCTGACGCGAGCGACATGAAGAACCCGCCTCCGGGGGCGGTGGCGCCGCCGGGGC

Reverse complement sequence

GCCCCGGCGGCGCCACCGCCCCCGGAGGCGGGTTCTTCATGTCGCTCGCGTCAGAGCCACCCTCCATCCTCGCCGCGGCGAGGCGCGCCAGCGCCGCCGC[T/C]
GCCGCGTCCAGCCGGCTCCGGTGCGGCGACCCCGAGGCCCTCCTCTCGCCGGACCGGCTCAGCCGGTAGGCCTCGCCGCCGGCTGCGCTCCGAGATCCGA

Allele Frequencies:

Populations Population SizeFrequency of G(primary allele) Frequency of A(secondary allele) Frequency of N Frequency of DEL Frequency of others Allele
All  4726 79.40% 17.50% 1.27% 1.84% NA
All Indica  2759 94.90% 0.10% 2.07% 2.94% NA
All Japonica  1512 46.20% 53.40% 0.20% 0.20% NA
Aus  269 99.60% 0.00% 0.00% 0.37% NA
Indica I  595 95.50% 0.00% 2.86% 1.68% NA
Indica II  465 88.20% 0.20% 3.87% 7.74% NA
Indica III  913 98.40% 0.10% 0.99% 0.55% NA
Indica Intermediate  786 94.40% 0.10% 1.65% 3.82% NA
Temperate Japonica  767 6.30% 93.40% 0.26% 0.13% NA
Tropical Japonica  504 97.40% 2.60% 0.00% 0.00% NA
Japonica Intermediate  241 66.40% 32.40% 0.41% 0.83% NA
VI/Aromatic  96 99.00% 0.00% 0.00% 1.04% NA
Intermediate  90 80.00% 18.90% 0.00% 1.11% NA

Allele Effect:

Var ID Var Locus snpEff Annotation CooVar Annotation Chromatin Accessibility Score PolyPhen-2 Effect PolyPhen-2 Score SIFT Effect SIFT Score
vg1225035494 A -> DEL LOC_Os12g40460.1 N frameshift_variant Average:97.954; most accessible tissue: Zhenshan97 panicle, score: 99.563 N N N N
vg1225035494 A -> G LOC_Os12g40460.1 synonymous_variant ; p.Ala288Ala; LOW synonymous_codon Average:97.954; most accessible tissue: Zhenshan97 panicle, score: 99.563 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)
vg1225035494 A G -0.01 0.0 0.0 -0.02 -0.01 0.0