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Detailed information for vg0521668548:

Variant ID: vg0521668548 (JBrowse)Variation Type: SNP
Chromosome: chr05Position: 21668548
Reference Allele: GAlternative Allele: C
Primary Allele: CSecondary Allele: G

Inferred Ancestral Allele : C (evidence from allele frequency in Oryza rufipogon: C: 0.61, G: 0.40, others allele: 0.00, population size: 109. )

Flanking Sequence (100 bp) in Reference Genome:


CTACAAGCTCCTCATCGGTTCCTCTCTGCCTCTGCTGCTGTTGCTGCAGCATAGAGCCATCGCAGCCGCCATTGTCGTCGCTGGATGAGGTGCTGTCAAG[G/C]
CTGTCATCTGGCGCGCTCCTTTTCCTCTTCTGACTCTTCCCGGAGGATTCAGCAGCATCCTCGTTGGCAAACGCAGCCGCGGTGGATGACGGCGCCGCCC

Reverse complement sequence

GGGCGGCGCCGTCATCCACCGCGGCTGCGTTTGCCAACGAGGATGCTGCTGAATCCTCCGGGAAGAGTCAGAAGAGGAAAAGGAGCGCGCCAGATGACAG[C/G]
CTTGACAGCACCTCATCCAGCGACGACAATGGCGGCTGCGATGGCTCTATGCTGCAGCAACAGCAGCAGAGGCAGAGAGGAACCGATGAGGAGCTTGTAG

Allele Frequencies:

Populations Population SizeFrequency of C(primary allele) Frequency of G(secondary allele) Frequency of N Frequency of DEL Frequency of others Allele
All  4726 64.50% 35.30% 0.19% 0.00% NA
All Indica  2759 98.50% 1.30% 0.22% 0.00% NA
All Japonica  1512 1.50% 98.30% 0.20% 0.00% NA
Aus  269 95.20% 4.80% 0.00% 0.00% NA
Indica I  595 99.50% 0.30% 0.17% 0.00% NA
Indica II  465 96.80% 3.20% 0.00% 0.00% NA
Indica III  913 99.30% 0.40% 0.22% 0.00% NA
Indica Intermediate  786 97.80% 1.80% 0.38% 0.00% NA
Temperate Japonica  767 1.40% 98.40% 0.13% 0.00% NA
Tropical Japonica  504 1.40% 98.60% 0.00% 0.00% NA
Japonica Intermediate  241 1.70% 97.50% 0.83% 0.00% NA
VI/Aromatic  96 5.20% 94.80% 0.00% 0.00% NA
Intermediate  90 53.30% 46.70% 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
vg0521668548 G -> C LOC_Os05g37080.1 missense_variant ; p.Ser227Arg; MODERATE nonsynonymous_codon ; S227R Average:84.467; most accessible tissue: Zhenshan97 root, score: 93.351 unknown unknown TOLERATED 0.63

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)
vg0521668548 G C -0.02 -0.03 -0.03 0.0 -0.02 0.0