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Detailed information for vg0218459437:

Variant ID: vg0218459437 (JBrowse)Variation Type: SNP
Chromosome: chr02Position: 18459437
Reference Allele: AAlternative Allele: T
Primary Allele: ASecondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


AGCTATAGATACCCATGTAGACATACCATTAAAGTAGTTTACTATTAATCTAGTCTATTGCTAAGATGTACATCTTTTATAGATAGCACCTTACTTTATC[A/T]
TTGTGGGTACTCTTACTAGAGTTATGTAGAAGCCACGTACATCAATCGTCGTTTGTACTGTATAGTATAACTAGCATGGTGGCCCGTGCAGATTACGCGG

Reverse complement sequence

CCGCGTAATCTGCACGGGCCACCATGCTAGTTATACTATACAGTACAAACGACGATTGATGTACGTGGCTTCTACATAACTCTAGTAAGAGTACCCACAA[T/A]
GATAAAGTAAGGTGCTATCTATAAAAGATGTACATCTTAGCAATAGACTAGATTAATAGTAAACTACTTTAATGGTATGTCTACATGGGTATCTATAGCT

Allele Frequencies:

Populations Population SizeFrequency of A(primary allele) Frequency of T(secondary allele) Frequency of N Frequency of DEL Frequency of others Allele
All  4726 97.60% 1.70% 0.70% 0.00% NA
All Indica  2759 96.10% 2.80% 1.05% 0.00% NA
All Japonica  1512 99.80% 0.20% 0.00% 0.00% NA
Aus  269 98.10% 0.40% 1.49% 0.00% NA
Indica I  595 87.70% 9.40% 2.86% 0.00% NA
Indica II  465 99.80% 0.20% 0.00% 0.00% NA
Indica III  913 98.60% 1.30% 0.11% 0.00% NA
Indica Intermediate  786 97.50% 1.10% 1.40% 0.00% NA
Temperate Japonica  767 100.00% 0.00% 0.00% 0.00% NA
Tropical Japonica  504 99.40% 0.60% 0.00% 0.00% NA
Japonica Intermediate  241 100.00% 0.00% 0.00% 0.00% NA
VI/Aromatic  96 100.00% 0.00% 0.00% 0.00% NA
Intermediate  90 100.00% 0.00% 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
vg0218459437 A -> T LOC_Os02g30910.1 upstream_gene_variant ; 2301.0bp to feature; MODIFIER silent_mutation Average:59.358; most accessible tissue: Zhenshan97 flower, score: 80.006 N N N N
vg0218459437 A -> T LOC_Os02g30910-LOC_Os02g30920 intergenic_region ; MODIFIER silent_mutation Average:59.358; most accessible tissue: Zhenshan97 flower, score: 80.006 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)
vg0218459437 A T -0.01 -0.01 0.0 -0.01 0.01 0.01

Putative Genotype-Phenotype Associations:

Var ID LMM P-value LR P-value Trait Subpopulation Is leadSNP Publication
vg0218459437 1.14E-07 2.93E-06 mr1719 Ind_All YES Genome-wide association analyses provide genetic and biochemical insights into natural variation in rice metabolism, Nat Genet, 46(7):714-21, PMID:24908251
vg0218459437 NA 9.10E-07 mr1735 Ind_All Not Genome-wide association analyses provide genetic and biochemical insights into natural variation in rice metabolism, Nat Genet, 46(7):714-21, PMID:24908251