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Detailed information for vg1107084198:

Variant ID: vg1107084198 (JBrowse)Variation Type: SNP
Chromosome: chr11Position: 7084198
Reference Allele: AAlternative Allele: G
Primary Allele: ASecondary Allele: G

Inferred Ancestral Allele: Not determined.

Flanking Sequence (100 bp) in Reference Genome:


ACGCCCAACTTTCTTTGCGTAGTGGTGGTAGTACTTTGGTATGATGCCATGTTGCTTTTTGTCCAGTTTTATATATCTGTTCTGATCCTTACACTACTAC[A/G]
CAAAATGGGAATAGTGTCGGTTTTCTCAACCAGCACAAGAGAGATGGCACAGATTGCAAATCAAAAAGGTGCCAGGTTCGAGGAATAAAAAAACAGCCGG

Reverse complement sequence

CCGGCTGTTTTTTTATTCCTCGAACCTGGCACCTTTTTGATTTGCAATCTGTGCCATCTCTCTTGTGCTGGTTGAGAAAACCGACACTATTCCCATTTTG[T/C]
GTAGTAGTGTAAGGATCAGAACAGATATATAAAACTGGACAAAAAGCAACATGGCATCATACCAAAGTACTACCACCACTACGCAAAGAAAGTTGGGCGT

Allele Frequencies:

Populations Population SizeFrequency of A(primary allele) Frequency of G(secondary allele) Frequency of N Frequency of DEL Frequency of others Allele
All  4726 90.40% 9.60% 0.00% 0.00% NA
All Indica  2759 99.70% 0.30% 0.00% 0.00% NA
All Japonica  1512 74.90% 25.10% 0.00% 0.00% NA
Aus  269 95.20% 4.80% 0.00% 0.00% NA
Indica I  595 99.70% 0.30% 0.00% 0.00% NA
Indica II  465 99.80% 0.20% 0.00% 0.00% NA
Indica III  913 99.80% 0.20% 0.00% 0.00% NA
Indica Intermediate  786 99.70% 0.30% 0.00% 0.00% NA
Temperate Japonica  767 76.00% 24.00% 0.00% 0.00% NA
Tropical Japonica  504 70.00% 30.00% 0.00% 0.00% NA
Japonica Intermediate  241 81.30% 18.70% 0.00% 0.00% NA
VI/Aromatic  96 53.10% 46.90% 0.00% 0.00% NA
Intermediate  90 88.90% 11.10% 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
vg1107084198 A -> G LOC_Os11g12610.1 downstream_gene_variant ; 119.0bp to feature; MODIFIER silent_mutation Average:77.562; most accessible tissue: Zhenshan97 panicle, score: 95.381 N N N N
vg1107084198 A -> G LOC_Os11g12600-LOC_Os11g12610 intergenic_region ; MODIFIER silent_mutation Average:77.562; most accessible tissue: Zhenshan97 panicle, score: 95.381 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)
vg1107084198 A G 0.0 -0.01 -0.01 -0.01 -0.01 -0.01

Putative Genotype-Phenotype Associations:

Var ID LMM P-value LR P-value Trait Subpopulation Is leadSNP Publication
vg1107084198 9.73E-07 5.97E-07 mr1044 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
vg1107084198 2.64E-06 NA mr1715 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
vg1107084198 1.90E-07 NA mr1715 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