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Detailed information for vg0825017138:

Variant ID: vg0825017138 (JBrowse)Variation Type: SNP
Chromosome: chr08Position: 25017138
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


ATGACGGGGTCGTCGGCCTCGCCGCGGAGGGTGAGGTCGGCGACGCGGCCGGTGGTGGGATCGCAGCTCACGCCGTACCAGCTGGTGCAGCAGTCGGTGC[C/T]
CGTCCACGACGAGAACACCCCGAGGTGCGCCTCCGACAGCGCCGCCCGGATCGCCAGCAGCGCGTCCCGGTCGCCCGCGGAGCACGCGGCGGCGGAGGCG

Reverse complement sequence

CGCCTCCGCCGCCGCGTGCTCCGCGGGCGACCGGGACGCGCTGCTGGCGATCCGGGCGGCGCTGTCGGAGGCGCACCTCGGGGTGTTCTCGTCGTGGACG[G/A]
GCACCGACTGCTGCACCAGCTGGTACGGCGTGAGCTGCGATCCCACCACCGGCCGCGTCGCCGACCTCACCCTCCGCGGCGAGGCCGACGACCCCGTCAT

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 93.90% 6.10% 0.00% 0.00% NA
All Indica  2759 89.70% 10.30% 0.00% 0.00% NA
All Japonica  1512 99.90% 0.10% 0.00% 0.00% NA
Aus  269 100.00% 0.00% 0.00% 0.00% NA
Indica I  595 99.80% 0.20% 0.00% 0.00% NA
Indica II  465 87.10% 12.90% 0.00% 0.00% NA
Indica III  913 78.20% 21.80% 0.00% 0.00% NA
Indica Intermediate  786 97.10% 2.90% 0.00% 0.00% NA
Temperate Japonica  767 99.90% 0.10% 0.00% 0.00% NA
Tropical Japonica  504 100.00% 0.00% 0.00% 0.00% NA
Japonica Intermediate  241 99.60% 0.40% 0.00% 0.00% NA
VI/Aromatic  96 100.00% 0.00% 0.00% 0.00% NA
Intermediate  90 97.80% 2.20% 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
vg0825017138 C -> T LOC_Os08g39550.1 missense_variant ; p.Gly61Ser; MODERATE nonsynonymous_codon ; G61S Average:89.188; most accessible tissue: Zhenshan97 panicle, score: 97.512 unknown unknown DELETERIOUS 0.04

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)
vg0825017138 C T -0.05 -0.04 -0.05 0.0 -0.02 -0.04