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Detailed information for vg0219343316:

Variant ID: vg0219343316 (JBrowse)Variation Type: SNP
Chromosome: chr02Position: 19343316
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


GCGGCGGCCTCTGCGGCCGCACGGGCGGCGAGGTGGGCGGGCTGTACTGGGAGGTGCGGAGGCAGCGCGTGGAGCCGGCGAACAAGGAATTCCTGCCGTT[C/T]
GAGCACTCGCCGTCGGCGGCGGACTGCGAGGTGCGGTGCGCGCGCAACTGCAGCTGCTGGGGCGCCGTCTACAGCAACGGCACGGGGTACTGCTACCTCA

Reverse complement sequence

TGAGGTAGCAGTACCCCGTGCCGTTGCTGTAGACGGCGCCCCAGCAGCTGCAGTTGCGCGCGCACCGCACCTCGCAGTCCGCCGCCGACGGCGAGTGCTC[G/A]
AACGGCAGGAATTCCTTGTTCGCCGGCTCCACGCGCTGCCTCCGCACCTCCCAGTACAGCCCGCCCACCTCGCCGCCCGTGCGGCCGCAGAGGCCGCCGC

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 97.50% 0.10% 1.82% 0.59% NA
All Indica  2759 98.70% 0.20% 0.80% 0.29% NA
All Japonica  1512 94.60% 0.00% 4.10% 1.26% NA
Aus  269 100.00% 0.00% 0.00% 0.00% NA
Indica I  595 98.20% 0.00% 1.85% 0.00% NA
Indica II  465 96.80% 0.00% 1.72% 1.51% NA
Indica III  913 99.30% 0.50% 0.11% 0.00% NA
Indica Intermediate  786 99.60% 0.00% 0.25% 0.13% NA
Temperate Japonica  767 90.00% 0.00% 7.82% 2.22% NA
Tropical Japonica  504 99.80% 0.00% 0.00% 0.20% NA
Japonica Intermediate  241 98.80% 0.00% 0.83% 0.41% NA
VI/Aromatic  96 99.00% 0.00% 0.00% 1.04% NA
Intermediate  90 97.80% 0.00% 2.22% 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
vg0219343316 C -> T LOC_Os02g32620.1 synonymous_variant ; p.Phe383Phe; LOW synonymous_codon Average:94.719; most accessible tissue: Zhenshan97 root, score: 97.104 N N N N
vg0219343316 C -> DEL LOC_Os02g32620.1 N frameshift_variant Average:94.719; most accessible tissue: Zhenshan97 root, score: 97.104 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)
vg0219343316 C T -0.01 -0.01 -0.01 -0.01 0.0 -0.01