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Detailed information for vg0913872114:

Variant ID: vg0913872114 (JBrowse)Variation Type: SNP
Chromosome: chr09Position: 13872114
Reference Allele: CAlternative Allele: A
Primary Allele: CSecondary Allele: A

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


GCACACGTAGAAGTGAGAAAATCATAATTAAATAAGTTTTAATTATTATAAACTTAAAAAAAGATTTATAAGATATTTTGAAAAATACATGAAATTCATC[C/A]
GTTTGAAAAACGTGCTATCGAGATGAAATAACGGGGACATGTCTTGTAACTCAAATTTTCCTGGCATAAAAAACCCTTGCATTTGAAGCTTAATTAATTA

Reverse complement sequence

TAATTAATTAAGCTTCAAATGCAAGGGTTTTTTATGCCAGGAAAATTTGAGTTACAAGACATGTCCCCGTTATTTCATCTCGATAGCACGTTTTTCAAAC[G/T]
GATGAATTTCATGTATTTTTCAAAATATCTTATAAATCTTTTTTTAAGTTTATAATAATTAAAACTTATTTAATTATGATTTTCTCACTTCTACGTGTGC

Allele Frequencies:

Populations Population SizeFrequency of C(primary allele) Frequency of A(secondary allele) Frequency of N Frequency of DEL Frequency of others Allele
All  4726 92.70% 7.30% 0.02% 0.00% NA
All Indica  2759 95.70% 4.30% 0.04% 0.00% NA
All Japonica  1512 92.50% 7.50% 0.00% 0.00% NA
Aus  269 60.60% 39.40% 0.00% 0.00% NA
Indica I  595 99.20% 0.80% 0.00% 0.00% NA
Indica II  465 98.90% 1.10% 0.00% 0.00% NA
Indica III  913 93.50% 6.50% 0.00% 0.00% NA
Indica Intermediate  786 93.50% 6.40% 0.13% 0.00% NA
Temperate Japonica  767 95.20% 4.80% 0.00% 0.00% NA
Tropical Japonica  504 94.80% 5.20% 0.00% 0.00% NA
Japonica Intermediate  241 78.80% 21.20% 0.00% 0.00% NA
VI/Aromatic  96 100.00% 0.00% 0.00% 0.00% NA
Intermediate  90 94.40% 5.60% 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
vg0913872114 C -> A LOC_Os09g23350.1 upstream_gene_variant ; 3139.0bp to feature; MODIFIER silent_mutation Average:80.403; most accessible tissue: Minghui63 panicle, score: 92.526 N N N N
vg0913872114 C -> A LOC_Os09g23340-LOC_Os09g23350 intergenic_region ; MODIFIER silent_mutation Average:80.403; most accessible tissue: Minghui63 panicle, score: 92.526 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)
vg0913872114 C A 0.0 0.0 0.0 0.0 0.0 0.0