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Detailed information for vg0700322812:

Variant ID: vg0700322812 (JBrowse)Variation Type: SNP
Chromosome: chr07Position: 322812
Reference Allele: CAlternative Allele: T
Primary Allele: CSecondary Allele: T

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


AGGCGGTCGAGGACGGCGTCATAGCCATCCCCCAGATCTACCGGCGCCCGCCAGCTGGAGGCCTGCGCCGGGGGCTGGCTCGGAAGTCGGAGGCGCGCTT[C/T]
GTCGGCGACGGGGGTGTAGAACCAGTCGCTCTTCTAGTCATCCCACTTCTTGCGGAGGACGCAGGGGATGTAGCGGTTCAGCACCGGCCCCCGCGGCTGG

Reverse complement sequence

CCAGCCGCGGGGGCCGGTGCTGAACCGCTACATCCCCTGCGTCCTCCGCAAGAAGTGGGATGACTAGAAGAGCGACTGGTTCTACACCCCCGTCGCCGAC[G/A]
AAGCGCGCCTCCGACTTCCGAGCCAGCCCCCGGCGCAGGCCTCCAGCTGGCGGGCGCCGGTAGATCTGGGGGATGGCTATGACGCCGTCCTCGACCGCCT

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 90.60% 1.10% 3.83% 4.51% NA
All Indica  2759 90.70% 0.00% 3.62% 5.65% NA
All Japonica  1512 88.40% 3.40% 5.03% 3.17% NA
Aus  269 98.10% 0.00% 0.74% 1.12% NA
Indica I  595 94.10% 0.00% 2.52% 3.36% NA
Indica II  465 90.10% 0.00% 4.30% 5.59% NA
Indica III  913 91.70% 0.00% 3.07% 5.26% NA
Indica Intermediate  786 87.40% 0.00% 4.71% 7.89% NA
Temperate Japonica  767 92.80% 1.70% 2.87% 2.61% NA
Tropical Japonica  504 83.90% 2.80% 7.74% 5.56% NA
Japonica Intermediate  241 83.80% 10.00% 6.22% 0.00% NA
VI/Aromatic  96 97.90% 0.00% 1.04% 1.04% NA
Intermediate  90 92.20% 0.00% 2.22% 5.56% NA

Allele Effect:

Var ID Var Locus snpEff Annotation CooVar Annotation Chromatin Accessibility Score PolyPhen-2 Effect PolyPhen-2 Score SIFT Effect SIFT Score
vg0700322812 C -> DEL LOC_Os07g01510.1 N frameshift_variant Average:4.21; most accessible tissue: Minghui63 panicle, score: 7.125 N N N N
vg0700322812 C -> T LOC_Os07g01510.1 missense_variant ; p.Glu154Lys; MODERATE nonsynonymous_codon ; E154K Average:4.21; most accessible tissue: Minghui63 panicle, score: 7.125 benign 1.487 DELETERIOUS 0.01

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)
vg0700322812 C T -0.01 -0.02 -0.02 -0.01 -0.01 -0.01

Putative Genotype-Phenotype Associations:

Var ID LMM P-value LR P-value Trait Subpopulation Is leadSNP Publication
vg0700322812 NA 6.44E-06 mr1070_2 Jap_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
vg0700322812 2.81E-06 3.65E-07 mr1224_2 Jap_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