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Detailed information for vg0207034728:

Variant ID: vg0207034728 (JBrowse)Variation Type: INDEL
Chromosome: chr02Position: 7034728
Reference Allele: AAlternative Allele: AG
Primary Allele: AGSecondary Allele: A

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


CGACGACAAGGCCCGACGCCATGGCCGGCAATCTCGATCTGAAAATCTCCTACGGAGTGTAGTTAAGTCAGCTGATGGAGGAGACGGGAGGGAGCAAGGC[A/AG]
GGGGTGGAGAAAGGGGTCCGCCGCCGCCGGCGCCGCCGAATCGCCGGTGACTTTCCGGCCGCCGGAGCCACTTCTGCGCCTGGGTGGGAAGACTTGGGAA

Reverse complement sequence

TTCCCAAGTCTTCCCACCCAGGCGCAGAAGTGGCTCCGGCGGCCGGAAAGTCACCGGCGATTCGGCGGCGCCGGCGGCGGCGGACCCCTTTCTCCACCCC[T/CT]
GCCTTGCTCCCTCCCGTCTCCTCCATCAGCTGACTTAACTACACTCCGTAGGAGATTTTCAGATCGAGATTGCCGGCCATGGCGTCGGGCCTTGTCGTCG

Allele Frequencies:

Populations Population SizeFrequency of AG(primary allele) Frequency of A(secondary allele) Frequency of N Frequency of DEL Frequency of others Allele
All  4726 55.40% 44.30% 0.34% 0.00% NA
All Indica  2759 79.40% 20.10% 0.43% 0.00% NA
All Japonica  1512 3.20% 96.80% 0.07% 0.00% NA
Aus  269 97.80% 2.20% 0.00% 0.00% NA
Indica I  595 72.10% 27.40% 0.50% 0.00% NA
Indica II  465 89.20% 10.10% 0.65% 0.00% NA
Indica III  913 81.30% 18.60% 0.11% 0.00% NA
Indica Intermediate  786 77.10% 22.30% 0.64% 0.00% NA
Temperate Japonica  767 2.10% 97.90% 0.00% 0.00% NA
Tropical Japonica  504 3.80% 96.00% 0.20% 0.00% NA
Japonica Intermediate  241 5.40% 94.60% 0.00% 0.00% NA
VI/Aromatic  96 66.70% 33.30% 0.00% 0.00% NA
Intermediate  90 54.40% 42.20% 3.33% 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
vg0207034728 A -> AG LOC_Os02g13200.1 5_prime_UTR_variant ; 80.0bp to feature; MODIFIER silent_mutation Average:89.534; most accessible tissue: Zhenshan97 flower, score: 93.832 N N N N
vg0207034728 A -> AG LOC_Os02g13210.1 downstream_gene_variant ; 4320.0bp to feature; MODIFIER silent_mutation Average:89.534; most accessible tissue: Zhenshan97 flower, score: 93.832 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)
vg0207034728 A AG -0.04 -0.07 -0.07 -0.04 -0.04 -0.04