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Detailed information for vg1225036027:

Variant ID: vg1225036027 (JBrowse)Variation Type: SNP
Chromosome: chr12Position: 25036027
Reference Allele: GAlternative Allele: C
Primary Allele: CSecondary Allele: G

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


GGCGCGGCGGAGGGGTCGGCGGCGGCGTGGGGTGGTTGCGGGACGGGGTGGAAGAAGAGGAGGTCGTCGAGGCTGGGGCGCACGCGGCGGGCGGCGCGGA[G/C]
CGGGGAGGCGACCGGGGGCGGGAGCGCGACGGCGGCGCGGCAGAGCGGGCACGAGGCGTGCGCGCGGAGCCAGACGTCGATGCAGTCCGCGTGGAACGCG

Reverse complement sequence

CGCGTTCCACGCGGACTGCATCGACGTCTGGCTCCGCGCGCACGCCTCGTGCCCGCTCTGCCGCGCCGCCGTCGCGCTCCCGCCCCCGGTCGCCTCCCCG[C/G]
TCCGCGCCGCCCGCCGCGTGCGCCCCAGCCTCGACGACCTCCTCTTCTTCCACCCCGTCCCGCAACCACCCCACGCCGCCGCCGACCCCTCCGCCGCGCC

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 51.90% 8.40% 25.26% 14.41% NA
All Indica  2759 58.10% 0.10% 23.81% 17.98% NA
All Japonica  1512 42.40% 25.70% 21.49% 10.38% NA
Aus  269 35.70% 0.00% 60.22% 4.09% NA
Indica I  595 49.10% 0.00% 30.42% 20.50% NA
Indica II  465 48.20% 0.20% 24.09% 27.53% NA
Indica III  913 72.00% 0.10% 17.31% 10.62% NA
Indica Intermediate  786 54.70% 0.10% 26.21% 18.96% NA
Temperate Japonica  767 4.30% 41.60% 37.55% 16.56% NA
Tropical Japonica  504 91.10% 2.00% 3.57% 3.37% NA
Japonica Intermediate  241 61.80% 24.90% 7.88% 5.39% NA
VI/Aromatic  96 71.90% 0.00% 22.92% 5.21% NA
Intermediate  90 47.80% 7.80% 31.11% 13.33% NA

Allele Effect:

Var ID Var Locus snpEff Annotation CooVar Annotation Chromatin Accessibility Score PolyPhen-2 Effect PolyPhen-2 Score SIFT Effect SIFT Score
vg1225036027 G -> C LOC_Os12g40460.1 missense_variant ; p.Leu159Val; MODERATE nonsynonymous_codon ; L159V Average:92.482; most accessible tissue: Zhenshan97 flag leaf, score: 98.182 unknown unknown TOLERATED 0.30
vg1225036027 G -> DEL LOC_Os12g40460.1 N frameshift_variant Average:92.482; most accessible tissue: Zhenshan97 flag leaf, score: 98.182 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)
vg1225036027 G C 0.02 0.02 0.02 0.02 0.02 0.03