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Detailed information for vg0914106818:

Variant ID: vg0914106818 (JBrowse)Variation Type: SNP
Chromosome: chr09Position: 14106818
Reference Allele: GAlternative Allele: A
Primary Allele: GSecondary Allele: A

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


CCTTCGCGACCGCCTCGGCGAGGGGGTCCTTGGGCTTAGGCGGGCGGCCACGGGGGCGCGGCGAGGAGGCCGCCGGCGCCGCGGGCGCGGGCGCCGGTGC[G/A]
GCGGCGGCGGCGGCGGCGTCCTTGGGCTTGGGCGGCCTGCCGCGGCCGCGCTTGGGCGGGAGGGACGGGTCGTCGCCGCGGAAGTAGTTGTTCTTGGAGA

Reverse complement sequence

TCTCCAAGAACAACTACTTCCGCGGCGACGACCCGTCCCTCCCGCCCAAGCGCGGCCGCGGCAGGCCGCCCAAGCCCAAGGACGCCGCCGCCGCCGCCGC[C/T]
GCACCGGCGCCCGCGCCCGCGGCGCCGGCGGCCTCCTCGCCGCGCCCCCGTGGCCGCCCGCCTAAGCCCAAGGACCCCCTCGCCGAGGCGGTCGCGAAGG

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 71.60% 7.90% 14.75% 5.76% NA
All Indica  2759 53.80% 13.50% 23.16% 9.57% NA
All Japonica  1512 96.30% 0.00% 3.31% 0.40% NA
Aus  269 100.00% 0.00% 0.00% 0.00% NA
Indica I  595 33.60% 8.10% 42.18% 16.13% NA
Indica II  465 53.80% 9.90% 21.94% 14.41% NA
Indica III  913 68.30% 17.70% 10.41% 3.50% NA
Indica Intermediate  786 52.00% 14.90% 24.30% 8.78% NA
Temperate Japonica  767 93.10% 0.00% 6.26% 0.65% NA
Tropical Japonica  504 99.80% 0.00% 0.00% 0.20% NA
Japonica Intermediate  241 99.20% 0.00% 0.83% 0.00% NA
VI/Aromatic  96 100.00% 0.00% 0.00% 0.00% NA
Intermediate  90 86.70% 2.20% 8.89% 2.22% NA

Allele Effect:

Var ID Var Locus snpEff Annotation CooVar Annotation Chromatin Accessibility Score PolyPhen-2 Effect PolyPhen-2 Score SIFT Effect SIFT Score
vg0914106818 G -> DEL LOC_Os09g23730.1 N frameshift_variant Average:93.766; most accessible tissue: Minghui63 flag leaf, score: 98.184 N N N N
vg0914106818 G -> A LOC_Os09g23730.1 synonymous_variant ; p.Ala115Ala; LOW synonymous_codon Average:93.766; most accessible tissue: Minghui63 flag leaf, score: 98.184 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)
vg0914106818 G A -0.01 -0.01 0.0 0.0 0.01 0.01